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Category   Symbol Source: HGNC EntrezGene Ensembl GeneCards RNA genes CroW21
GIFtS

TSPAN32 Gene

protein-coding   GIFtS: 49
GCID: GC11P002323

Tetraspanin 32

(Previous name: pan-hematopoietic expression)
(Previous symbols: TSSC6, PHEMX)
Microbiology & Infectious Diseases Congress
  See related diseases
at  

(According to 1HGNC, 2Entrez Gene,
3UniProtKB/Swiss-Prot, 4UniProtKB/TrEMBL, 5OMIM, 6GeneLoc, 7Ensembl, 8DME, 9miRBase, 10fRNAdb, 12H-InvDB, 13NCBI, 14NONCODE, and/or 15RNAdb)
About This Section

Aliases
Tetraspanin 321 2     Pan-Hematopoietic Expression Protein2
PHEMX1 2 3 5     tetraspanin-322
TSSC61 2 3 5     tspan-322
Protein Phemx2 3     Tumor-Suppressing STF CDNA 62
Pan-Hematopoietic Expression1     Tumor-Suppressing Subchromosomal Transferable Fragment CDNA 62
ART12     Tumor-Suppressing Subtransferable Candidate 62
PHMX2     Tspan-323

External Ids:    HGNC: 134101   Entrez Gene: 100772   Ensembl: ENSG000000642017   OMIM: 6038535   UniProtKB: Q96QS13   

Export aliases for TSPAN32 gene to outside databases

Previous GC identifers: GC11P002280 GC11P002113


(According to Entrez Gene, Tocris Bioscience, Wikipedia's Gene Wiki, PharmGKB,
UniProtKB/Swiss-Prot, and/or UniProtKB/TrEMBL)
About This Section

Entrez Gene summary for TSPAN32 Gene:
This gene, which is a member of the tetraspanin superfamily, is one of several tumor-suppressing subtransferable
fragments located in the imprinted gene domain of chromosome 11p15.5, an important tumor-suppressor gene region.
Alterations in this region have been associated with Beckwith-Wiedemann syndrome, Wilms tumor, rhabdomyosarcoma,
adrenocortical carcinoma, and lung, ovarian and breast cancers. This gene is located among several imprinted
genes; however, this gene, as well as the tumor-suppressing subchromosomal transferable fragment 4, escapes
imprinting. This gene may play a role in malignancies and diseases that involve this region, and it is also
involved in hematopoietic cell function. Alternatively spliced transcript variants have been described, but their
biological validity has not been determined. (provided by RefSeq, Jul 2008)

GeneCards Summary for TSPAN32 Gene: 
TSPAN32 (tetraspanin 32) is a protein-coding gene. Diseases associated with TSPAN32 include adrenocortical carcinoma, and mental retardation epilepsy. GO annotations related to this gene include molecular_function.

Gene Wiki entry for TSPAN32 Gene


(According to GeneLoc and/or HGNC, and/or
Entrez Gene (NCBI build 37),
and/or miRBase,
Genomic Views according to UCSC (hg19) and Ensembl (release 73), Regulatory elements and Epigenetics data according to QIAGEN, SABiosciences, and/or SwitchGear Genomics)
About This Section
RefSeq DNA sequence:
NC_000011.9  NT_009237.18  NC_018922.2  
Regulatory elements:
   SABiosciences Regulatory transcription factor binding sites in the TSPAN32 gene promoter:
         Elk-1   RP58   GATA-3   NCX/Ncx   MyoD   CREB   GATA-6   deltaCREB   HOXA5   TGIF   
         Other transcription factors

SwitchGear Promoter luciferase reporter plasmids (see all 2): TSPAN32 promoter sequence
   Search SABiosciences Chromatin IP Primers for TSPAN32

Epigenetics:
QIAGEN PyroMark CpG Assay predesigned Pyrosequencing DNA Methylation assays in human, mouse, rat TSPAN32


Genomic Location:
Genomic View: UCSC Golden Path with GeneCards custom track

Entrez Gene cytogenetic band: 11p15.5   Ensembl cytogenetic band:  11p15.5   HGNC cytogenetic band: 11p15

TSPAN32 Gene in genomic location: bands according to Ensembl, locations according to (and/or Entrez Gene and/or Ensembl if different)
TSPAN32 gene location

GeneLoc information about chromosome 11         GeneLoc Exon Structure

GeneLoc location for GC11P002323:  view genomic region     (about GC identifiers)

Start:
2,323,227 bp from pter      End:
2,339,430 bp from pter
Size:
16,204 bases      Orientation:
plus strand

(According to UniProtKB, HORDE, neXtProt, Ensembl, and/or Reactome, Modification sites according to PhosphoSitePlus, Specific Peptides from DME, Protein expression images according to data from SPIRE 1MOPED, 2PaxDb, and 3MAXQB RefSeq according to NCBI, PDB rendering according to OCA and/or Proteopedia, Recombinant Proteins from EMD Millipore, R&D Systems, GenScript, Enzo Life Sciences, OriGene, Novus Biologicals, Sino Biological, ProSpec, and/or Cloud-Clone Corp.,
Biochemical Assays by EMD Millipore, R&D Systems, OriGene, GenScript, Cell Signaling Technology, Enzo Life Sciences, and/or Cloud-Clone Corp., Ontologies according to Gene Ontology Consortium 01 Oct 2013 and Entrez Gene, Antibodies by EMD Millipore, R&D Systems, GenScript, Cell Signaling Technology, OriGene, Novus Biologicals, Thermo Fisher Scientific, LSBio, Abcam, and/or Cloud-Clone Corp.)
About This Section

UniProtKB/Swiss-Prot: TSN32_HUMAN, Q96QS1 (See protein sequence)
Recommended Name: Tetraspanin-32  
Size: 320 amino acids; 34631 Da
Subcellular location: Membrane; Multi-pass membrane protein (Potential)
Developmental stage: Expressed from early embryogenesis through to adulthood
Secondary accessions: Q96KX4 Q9HC50 Q9HC51 Q9Y5U1
Alternative splicing: 5 isoforms:  Q96QS1-1   Q96QS1-2   Q96QS1-3   Q96QS1-4   Q96QS1-5   (May be produced at very low levels due to a premature stop codon in the mRNA, leading to nonsense-mediated mRNA decay)

Explore the universe of human proteins at neXtProt for TSPAN32: NX_Q96QS1

Explore proteomics data for TSPAN32 at MOPED 

Post-translational modifications:

  • View modification sites using PhosphoSitePlus
  • View neXtProt modification sites for NX_Q96QS1

  • TSPAN32 Protein expression data from MOPED1, PaxDb2 and MAXQB3 :    About this image 

    TSPAN32 Protein Expression
    REFSEQ proteins: NP_620591.3  
    ENSEMBL proteins: 
     ENSP00000405001   ENSP00000182290   ENSP00000395018   ENSP00000370513   ENSP00000343285  
     ENSP00000405205   ENSP00000370509  

    Human Recombinant Protein Products for TSPAN32: 
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    Browse Sino Biological Cell Lysates 
    Browse ProSpec Recombinant Proteins
    Cloud-Clone Corp. Proteins for TSPAN32 

    Gene Ontology (GO): 4 cellular component terms (GO ID links to tree view):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0005622intracellular IEA--
    GO:0009986cell surface IEA--
    GO:0016021integral to membrane NAS--
    GO:0070442alphaIIb-beta3 integrin complex IEA--

    TSPAN32 for ontologies           About GeneDecksing



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    (According to HGNC, IUPHAR, InterPro, ProtoNet, UniProtKB, and/or BLOCKS, Sets of similar genes according to GeneDecks)
    About This Section
    HGNC Gene Families: 
    TSPAN: Tetraspanins

    3 InterPro protein domains:
     IPR018499 Tetraspanin/Peripherin
     IPR000301 Tetraspanin
     IPR008952 Tetraspanin_EC2

    Graphical View of Domain Structure for InterPro Entry Q96QS1

    ProtoNet protein and cluster: Q96QS1

    UniProtKB/Swiss-Prot: TSN32_HUMAN, Q96QS1
    Similarity: Belongs to the tetraspanin (TM4SF) family


    TSPAN32 for domains           About GeneDecksing


    (According to 1UniProtKB, Genatlas, LifeMap Discovery™, IUBMB, and/or 2DME, Human phenotypes from GenomeRNAi, Animal models from MGI Mar 06 2013, inGenious Targeting Laboratory, genOway,
    bound targets from SABiosciences, miRNA Gene Targets from miRTarBase, shRNA from OriGene, RNAi from EMD Millipore, siRNAs from OriGene, QIAGEN, microRNA from QIAGEN, Gene Editing from DNA2.0, Sirion Biotech, Clones from EMD Millipore, OriGene, SwitchGear Genomics, GenScript, Sino Biological, DNA2.0, Vector BioLabs, and Sirion Biotech, Cell Lines from GenScript, LifeMap BioReagents, In Situ Hybridization Assays from Advanced Cell Diagnostics, Ontologies according to Gene Ontology Consortium 01 Oct 2013 via Entrez Gene.)
    About This Section

         Gene Ontology (GO): 1 molecular function term (GO ID links to tree view):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0003674molecular_function ND--
         
    TSPAN32 for ontologies           About GeneDecksing


    Phenotypes:
         3 MGI mutant phenotypes (inferred from 1 allele(MGI details for Tspan32):
     cellular  hematopoietic system  immune system 

    TSPAN32 for phenotypes           About GeneDecksing

    Animal Models:
       inGenious Targeting Laboratory - Custom generated mouse model solutions for TSPAN32 
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       genOway customized KO model: permanent, tissue-specific or time-controlled inactivation for TSPAN32 
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    Inhib. RNA
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    (Pathways according to EMD Millipore, R&D Systems, Cell Signaling Technology, KEGG, PharmGKB, BioSystems, Sino Biological, Reactome, Tocris Bioscience, GeneGo (Thomson Reuters), QIAGEN, and/or UniProtKB, Sets of similar genes according to GeneDecks, Interaction Networks according to SABiosciences, and/or STRING, Interactions according to 1UniProtKB, 2MINT, 3I2D, and/or 4STRING, with links to IntAct and Ensembl, Ontologies according to Gene Ontology Consortium 01 Oct 2013 via Entrez Gene).
    About This Section



    Interactions:

        Search SABiosciences Gene Network CentralTM Interacting Genes and Proteins Networks for TSPAN32

    Gene Ontology (GO): 5/10 biological process terms (GO ID links to tree view) (see all 10):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0007010cytoskeleton organization IEA--
    GO:0007229integrin-mediated signaling pathway IEA--
    GO:0007267cell-cell signaling TAS10950922
    GO:0007596blood coagulation ----
    GO:0007599hemostasis ----

    TSPAN32 for ontologies           About GeneDecksing



    (Chemical Compounds according to UniProtKB, Enzo Life Sciences, EMD Millipore, Tocris Bioscience HMDB, BitterDB, and/or Novoseek, Ligands according to IUPHAR, and Drugs according to DrugBank, Enzo Life Sciences, and/or PharmGKB, with drugs/clinical trials/news search links to CenterWatch)
    About This Section

    TSPAN32 for compounds           About GeneDecksing

    Browse Small Molecules at EMD Millipore
    Browse drugs & compounds from Enzo Life Sciences

    Browse Tocris compounds for TSPAN32 (TSN32)

    7 Novoseek inferred chemical compound relationships for TSPAN32 gene    About this table
    Compound   -log (P-Val)   Hits   PubMed IDs for Articles with Shared Sentences (# sentences)
    ganglioside 44.3 4 15334254 (1), 12068006 (1), 15710618 (1), 19559406 (1)
    tyrosine 31 6 10427099 (1), 12938224 (1), 12110679 (1), 19166707 (1) (see all 5)
    lipid 27.3 9 15454569 (1), 15496196 (1), 16785325 (1), 19497983 (1) (see all 9)
    phosphatidylinositol 23.4 2 12110679 (1), 11739647 (1)
    cysteine 23.2 5 20171294 (2), 11907260 (1), 14556650 (1), 12575999 (1)
    cholesterol 5.22 23 12938224 (5), 15184367 (2), 15454569 (1), 19497983 (1) (see all 5)
    polysaccharide 0 1 12701754 (1)

    Search CenterWatch for drugs/clinical trials and news about TSPAN32 / TSN32

    (Secondary structures according to fRNAdb,
    GenBank/EMBL/DDBJ Accessions according to
    Unigene (Build 236 Homo sapiens; Apr 25 2013) or GenBank,
    RefSeq according to Entrez Gene,
    DOTS (version 10), and/or AceView, transcript ids from Ensembl with links to UCSC,
    Conferences by KenesGroup, exon structure from GeneLoc, alternative splicing isoforms according to ASD and/or ECgene,
    RNAi Products from EMD Millipore,
    siRNAs from OriGene, QIAGEN, shRNA from OriGene, microRNA from QIAGEN,
    Tagged/untagged cDNA clones from OriGene, SwitchGear Genomics, GenScript, DNA2.0, Vector BioLabs, Sirion Biotech, Primers from OriGene, SABiosciences, and/or QIAGEN )
    About This Section

    REFSEQ mRNAs for TSPAN32 gene (3 alternative transcripts): 
    NM_139022.2  NM_005705.4  NM_139024.3  

    Unigene Cluster for TSPAN32:

    Tetraspanin 32
    Hs.271954  [show with all ESTs]
    Unigene Representative Sequence: AK298692
    16 Ensembl transcripts including schematic representations, and UCSC links where relevant:
    ENST00000437313 ENST00000461200(uc001lvx.1 uc009ydk.1 uc010qxk.2 uc001lvy.1 uc009ydl.1 uc001lwb.1 uc001lwc.1 uc001lwd.1)
    ENST00000182290 ENST00000446063 ENST00000493924 ENST00000484104 ENST00000479508
    ENST00000498313 ENST00000483227 ENST00000381121 ENST00000493948 ENST00000339046
    ENST00000451520(uc001lvz.1) ENST00000381117 ENST00000484523 ENST00000486011

    Congresses - knowledge worth sharing:  
    European Congress of Clinical Microbiology and Infectious Diseases (ECCMID) 10 - 13 May 2014

    miRNA
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    Inhib. RNA
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    Additional mRNA sequence: 

    AF176071.1 AK298692.1 AK307638.1 AK310116.1 AY039001.1 AY303780.1 BC016693.1 

    11 DOTS entries:

    DT.95168325  DT.111418  DT.95094062  DT.111419  DT.91648803  DT.97812022  DT.91656368  DT.120684722 
    DT.95168321  DT.95168322  DT.40314344 

    24/49 AceView cDNA sequences (see all 49):

    AF176070 NM_139022 AA701395 CR606621 AY039001 AW440888 BI906333 NM_139024 
    BX117724 N99620 BI909447 AA694062 AA777339 BE243068 AF176071 BG506933 
    BI909345 AY303780 NM_005705 AA913945 AK128812 BI907377 BC016693 BV196160 

    GeneLoc Exon Structure

    5/12 Alternative Splicing Database (ASD) splice patterns (SP) for TSPAN32 (see all 12)    About this scheme

    ExUns: 1a · 1b · 1c ^ 2a · 2b · 2c · 2d ^ 3 ^ 4 ^ 5 ^ 6 ^ 7a · 7b ^ 8a · 8b ^ 9a · 9b ^ 10 ^ 11 ^ 12 ^ 13 ^ 14a · 14b · 14c
    SP1:              -     -     -                 -           -                             -     -     -                                             
    SP2:              -     -     -                 -           -                             -     -     -           -                                 
    SP3:                                            -           -                 -           -     -     -                                             
    SP4:                                            -           -                             -     -     -                                             
    SP5:                                            -           -     -                       -     -     -                                             


    ECgene alternative splicing isoforms for TSPAN32

    (RNA expression data according to H-InvDB, NONCODE, miRBase, and RNAdb, Expression images according to data from BioGPS, Illumina Human BodyMap, and CGAP SAGE, Sets of similar genes according to GeneDecks, in vivo and in vitro expression data from LifeMap Discovery™, plus additional links to Genevestigator, and/or SOURCE, and/or BioGPS, and/or UniProtKB,
    PCR Arrays from SABiosciences, Primers from OriGene, SABiosciences, and/or QIAGEN, In Situ Hybridization Assays from Advanced Cell Diagnostics)
    About This Section

    TSPAN32 expression in normal human tissues (normalized intensities)      TSPAN32 embryonic expression: see
    See probesets specificity/sensitivity at GeneAnnot
    About this imageBioGPS <intensity>2/3
    CGAP TAG: GCTGTAGGAC
    TSPAN32 Expression
    About this image


    TSPAN32 expression in embryonic tissues and stem cells    About this table
    Data from LifeMap, the Embryonic Development and Stem Cells Database 
     5/6 selected tissues (see all 6) fully expand
     
     Blood (Hematopoietic System)    fully expand to see all 5 entries
             Hematopoietic Stem Cells Hematopoietic Bone Marrow
             cd8+ t cell   
     
     Umbilical Cord (Extraembryonic Tissues)
             cord blood   
     
     Liver (Hepatobiliary System)
             Hematopoietic Stem Cells Liver Bud
     
     Bone (Muscoskeletal System)
             Chondrocytes Zeugopod Epiphyseal End
     
     Cartilage (Muscoskeletal System)
             Chondrocytes Zeugopod Epiphyseal End

    See TSPAN32 Protein Expression from SPIRE MOPED and PaxDB
    Genevestigator expression for TSPAN32

    SOURCE GeneReport for Unigene cluster: Hs.271954

    UniProtKB/Swiss-Prot: TSN32_HUMAN, Q96QS1
    Tissue specificity: Expressed ubiquitously at low levels. High levels of expression are confined to hematopoietic
    tissues including peripheral blood leukocytes, thymus and spleen

        SABiosciences Custom PCR Arrays for TSPAN32
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    In Situ
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    Advanced Cell Diagnostics RNAscope RNA in situ hybridization assays for TSPAN32

    (Orthologs according to 1,2HomoloGene (2older version, for species not in 1newer version), 3euGenes, 4SGD , 5MGI Mar 06 2013, with possible further links to Flybase and/or WormBase, and/or 6Ensembl pan taxonomic compara , Gene Trees according to Ensembl and TreeFam)
    About This Section

    This gene was present in the common ancestor of chordates.

    Orthologs for TSPAN32 gene from 3/8 species (see all 8)    About this table
    Organism Taxonomic
    classification
    Gene Description Human
    Similarity
    Orthology
    Type
    Details
    mouse
    (Mus musculus)
    Mammalia Tspan321 , 5 tetraspanin 321, 5 76.02(n)1
    64.03(a)1
      7 (88.09 cM)5
    270271  NM_001128080.21  NP_001121552.11 
     1430050465 
    chicken
    (Gallus gallus)
    Aves TSPAN321 tetraspanin 32 59.82(n)
    47.49(a)
      395087  XM_421025.2  XP_421025.2 
    lizard
    (Anolis carolinensis)
    Reptilia TSPAN326
    Uncharacterized protein
    52(a)
    1 ↔ 1
    1(69690114-69698244)


    ENSEMBL Gene Tree for TSPAN32 (if available)
    TreeFam Gene Tree for TSPAN32 (if available)

    (Paralogs according to 1HomoloGene,
    2Ensembl, and 3SIMAP, Pseudogenes according to 4Pseudogene.org Build 68)
    About This Section
    Paralogs for TSPAN32 gene
    1 SIMAP similar gene for TSPAN32 using alignment to 5 protein entries:     TSN32_HUMAN (see all proteins):
    PHEMX

    TSPAN32 for paralogs           About GeneDecksing



    (SNPs/Variants according to the 1NCBI SNP Database, 2Ensembl, 3PupaSUITE, 4UniProtKB, and DNA2.0, Linkage Disequilibrium by HapMap, Structural Variations(CNVs/InDels/Inversions) from the Database of Genomic Variants, Mutations from the Human Gene Mutation Database (HGMD) and the Locus Specific Mutation Databases (LSDB), Blood group antigen gene mutations by BGMUT, Resequencing Primers from QIAGEN, Cancer Mutation PCR Arrays and Assays and Copy Number PCR Arrays from SABiosciences)
    About This Section

    368/419 SNPs in TSPAN32 are shown (see all 419)    About this table     
    Genomic DataTranscription Related DataAllele Frequencies
    SNP IDValidClinical
    significance
    Chr 11 posSequence#AA
    Chg
    TypeMore#Allele
    freq
    PopTotal
    sample
    More
    ----------
    rs1833384091,2
    --2325165(+) AGTCCC/TACCTC 1 -- int10--------
    rs1176003571,2
    C,F--2325192(+) GGGCCG/ATCTGA 1 -- int11Minor allele frequency- A:0.05NA 120
    rs22342951,2
    C,F--2325239(+) CCTCAC/TGGCCC 1 -- int11Minor allele frequency- T:0.03NA 120
    rs2021894711,2
    C--2325290(+) TCAGGA/GCCTGT 1 -- int10--------
    rs2015309101,2
    --2325347(+) TCTGCA/GGGGTT 2 A syn10--------
    rs2006317811,2
    --2325378(+) CTCTGA/GGAGCC 2 R G mis10--------
    rs22342961,2
    C,F,H--2325384(+) GAGCCG/ATGCTG 2 /M /V mis1 ese38Minor allele frequency- A:0.01NS EA CSA NA EU 4985
    rs1996509871,2
    --2325392(+) CTGAGC/TGCTGC 2 S syn10--------
    rs2016344191,2
    C--2325393(+) TGAGCA/GCTGCA 2 T A mis10--------
    rs2006246621,2
    C--2325414(+) GGGAGG/TCCCAG 2 A S mis10--------
    rs617449291,2
    C,F--2325427(+) CCTCAT/CGGCAG 2 /T /M mis15Minor allele frequency- C:0.01NS NA EU 4371
    rs767230041,2
    C--2325436(+) AGGGGG/TGAGTT 1 -- spd10--------
    rs2001177051,2
    --2325468(+) GGCCCC/GCAGAA 1 -- int10--------
    rs1134162931,2
    C--2325490(+) AGGAGG/TGAAGA 1 -- int11Minor allele frequency- T:0.50CSA 2
    rs754725351,2
    C--2325518(+) CCACCC/TCCACA 1 -- int10--------
    rs20740231,2
    C,F,A,H--2325581(+) CCCCAC/TGTCAA 1 -- int121Minor allele frequency- T:0.27EA NS NA WA 3818
    rs1458417531,2
    C--2325708(+) ACGCCC/TAACAA 1 -- int10--------
    rs1387392271,2
    C--2325729(+) AGGAGA/CTCTGA 1 -- int10--------
    rs26518251,2
    H--2325746(+) GAGACG/AGCCCT 1 -- int14Minor allele frequency- A:0.00NS EA 396
    rs563446181,2
    C--2325798(+) GGTTC-/TATGCC 1 -- int11Minor allele frequency- T:0.00NA 2
    rs562953181,2
    C--2325800(+) GTTCA-/TTGCCC 1 -- int11Minor allele frequency- T:0.00NA 2
    rs25212711,2
    C,F,A,H--2325868(+) CAGGCA/TCAGGA 1 -- int117Minor allele frequency- T:0.26NS EA NA WA CSA 764
    rs128070611,2
    C,F,A--2325901(+) CTGGGT/CTCTCC 1 -- int112Minor allele frequency- C:0.27NA WA CSA EA 374
    rs588339301,2
    C,F--2325997(+) GTGGCC/TTCTTG 1 -- int14Minor allele frequency- T:0.17WA NA 242
    rs1124987471,2
    C,F--2326081(+) CCTGGC/AGGCAG 1 -- int12Minor allele frequency- A:0.09CSA WA 120
    rs108317371,2
    C,A--2326129(+) CCCTCC/TTCTCT 1 -- int1 trp313Minor allele frequency- T:0.25NA WA CSA EA 375
    rs728441981,2
    C--2326364(+) AATGAC/TCCTGG 1 -- int10--------
    rs781634281,2
    C--2326405(+) GTCACC/TTCCTG 1 -- int10--------
    rs1144208431,2
    C--2326422(+) CTGCCA/GGGCCA 1 -- int10--------
    rs20771121,2
    C,A,H--2326451(+) CATGGG/TGGGCA 1 -- int111Minor allele frequency- T:0.24NA WA CSA EA 375
    rs2019915241,2
    --2326605(+) CCCCC-/CGCCCCC 1 -- int10--------
    rs745238691,2
    C--2326608(+) CCCCC-/ACCCAG 1 -- int10--------
    rs285376081,2
    F--2326612(+) CCCCCC/AGAGGG 1 -- int11Minor allele frequency- A:0.50NA 4
    rs118236821,2
    C,F,H--2326614(+) CCCAGA/GGGGTG 1 -- int14Minor allele frequency- G:0.25NA WA 246
    rs20771131,2
    C,F,A,H--2326657(+) AAAGGC/TTGGCA 1 -- int114Minor allele frequency- T:0.24NA WA CSA EA 381
    rs20771141,2
    C,F,A,H--2326714(+) GAACCG/AGCGCT 1 -- int114Minor allele frequency- A:0.43NA WA CSA EA 381
    rs1389431861,2
    --2326734(+) GTACCA/GTCCAC 1 -- int10--------
    rs755516201,2
    C,F--2326742(+) CACCAG/AGGGGT 1 -- int12Minor allele frequency- A:0.10CSA WA 120
    rs790645321,2
    F--2326800(+) GCCACG/AGGGCT 1 -- int12Minor allele frequency- A:0.04CSA WA 120
    rs9376141,2
    C,F,A,H--2326920(+) GTGTCC/GCCAGC 1 -- int116Minor allele frequency- G:0.30EA NA NS WA CSA 926
    rs25212721,2
    C,A--2327151(+) CCTGCC/TCCATT 1 -- int113Minor allele frequency- T:0.25NA WA CSA EA 375
    rs26518191,2
    C,A--2327188(+) GGTGAA/GCCTAT 1 -- int17Minor allele frequency- G:0.00NA WA CSA 12
    rs49300781,2
    C,F,A--2327190(+) TGAGCT/CTATGT 1 -- int13Minor allele frequency- C:0.33NA 6
    rs1141120481,2
    F--2327202(+) TATGCG/ATGTGC 1 -- int11Minor allele frequency- A:0.01WA 118
    rs1822287971,2
    --2327209(+) GTGCAA/CATATA 1 -- int10--------
    rs2011562831,2
    --2327216(+) TATAC-/ATGTGTG 1 -- int10--------
    rs49299771,2
    H--2327222(+) tgtgtG/Atgtgc 1 -- int14Minor allele frequency- A:0.00NS EA 416
    rs1468126941,2
    C--2327238(+) CATGA-/GTGTGTG 1 -- int10--------
    rs1483860171,2
    C--2327276(+) GCCTC-/TGTGTG/
    TGTGTGTGTG
    TGTGT
    2 -- int1 cds10--------
    rs1864624291,2
    --2327338(+) GTTGCC/TATACG 1 -- int10--------
    rs122759441,2
    C--2327393(+) CTGCAC/TGCATG 1 -- int10--------
    rs1494421301,2
    --2327394(+) TGCACA/GCATGA 1 -- int10--------
    rs1446703711,2
    --2327454(+) TCCAAG/TGGGCT 1 -- int10--------
    rs618715771,2
    C,F--2327511(+) CCCTCC/TGGCCT 1 -- int12Minor allele frequency- T:0.06NA 122
    rs21886591,2
    C,A,H--2327587(+) AGCGCT/CGCCCA 1 -- int111Minor allele frequency- C:0.25NA WA CSA EA 372
    rs49300791,2
    C,F,A--2327601(+) AAGCAC/GATTCA 1 -- int15Minor allele frequency- G:0.22NA EA 246
    rs1917629301,2
    --2327678(+) CCTGAA/CCACCC 1 -- int10--------
    rs22378581,2
    C--2327706(+) AAGGCC/TCTGGG 1 -- int10--------
    rs2009546521,2
    --2327778(+) GGGAG-/AGA   
       GAGAA
    AGAGA
    1 -- int10--------
    rs1380750641,2
    C--2327782(+) GAGAG-/AGAA  
            
    AGAGA
    1 -- int10--------
    rs714641791,2
    C--2327785(+) AGAGAAAGA/-  
            
    GAGAA
    1 -- int11Minor allele frequency- -:0.50NA 2
    rs728457061,2
    C--2327785(+) AGAGAG/AAGAGA 1 -- int11Minor allele frequency- A:0.50WA 2
    rs1392606321,2
    C--2328067(+) AGGGG-/GAGGGA
            
    GAGGG
    1 -- int10--------
    rs1171673951,2
    C,F--2328105(+) AGGGAG/AGGGGA 1 -- int11Minor allele frequency- A:0.12NA 120
    rs1118839751,2
    C--2328156(+) GGAGAT/AGGAGG 1 -- int13Minor allele frequency- A:0.37WA NA 240
    rs561469261,2
    C--2328188(+) GAGGGG/AGAAGG 1 -- int13Minor allele frequency- A:0.06CSA WA NA 239
    rs22378591,2
    C,A--2328364(+) CCATGA/CGGAGC 1 -- int110Minor allele frequency- C:0.48EA NA WA CSA 1831
    rs1824033141,2
    --2328572(+) TGGGGA/CCCCAG 1 -- int10--------
    rs601329011,2
    F--2328628(+) CAGGCG/AGGCAC 1 -- int12Minor allele frequency- A:0.04CSA WA 120
    rs1460823341,2
    --2328656(+) CTGGCA/GTTTCA 1 -- int10--------
    rs1869368821,2
    C--2328667(+) CCGGGA/GCCTCA 1 -- int10--------
    rs22378601,2
    C,A--2328693(+) CTGCCT/CGGTCG 1 -- int112Minor allele frequency- C:0.26NA WA CSA EA 373
    rs22378611,2
    C,A--2328707(+) GCTAGG/ACTCAC 1 -- int113Minor allele frequency- A:0.25NA WA CSA EA 375
    rs1931853241,2
    C--2328759(+) AAGGCA/GGCTGC 1 -- int10--------
    rs1406499471,2
    C--2328764(+) GGCTG-/CCCAGA 1 -- int10--------
    rs22378621,2
    C,F--2328795(+) CCAGGG/ATTCTT 1 -- int18Minor allele frequency- A:0.06EA NA WA CSA 1652
    rs7569251,2
    C,F,A--2328948(+) AGTGCT/CGGGGG 1 -- int112Minor allele frequency- C:0.38NA WA CSA EA 376
    rs1400834591,2
    C--2329007(+) GGCACA/GGGCAT 1 -- int10--------
    rs7569261,2
    C,F,A,H--2329078(+) GAAAGG/TGAGGT 1 -- int125Minor allele frequency- T:0.38NS EA NA WA CSA 3836
    rs7569271,2
    C,A--2329119(+) GGCCAT/CAGCAT 1 -- int114Minor allele frequency- C:0.50EA NA WA CSA 1313
    rs79354831,2
    C,H--2329423(+) AGCGCC/AGGGGA 1 -- int1 trp310Minor allele frequency- A:0.25NA WA CSA EA 370
    rs49950511,2
    C,F--2329694(+) GCCCCA/C/GAACAG 1 -- int11NA 2
    rs1908056461,2
    --2329706(+) GACCAC/GCCCCC 1 -- int10--------
    rs1930237321,2
    --2329714(+) CCCCAC/TAGTGA 1 -- int10--------
    rs127987991,2
    A--2329739(+) TGACCA/GGCCCC 1 -- int10--------
    rs1837884361,2
    --2329762(+) GCCCCC/GAACAG 1 -- int10--------
    rs1881778321,2
    --2329774(+) GACCAC/GCCCCC 1 -- int10--------
    rs1813291801,2
    --2329782(+) CCCCAC/TAGTGA 1 -- int10--------
    rs1858105091,2
    --2329818(+) CCGCAA/GTGACC 1 -- int10--------
    rs349751241,2
    C--2329830(+) GCCCCG/CAACAG 1 -- int11Minor allele frequency- C:0.00NA 2
    rs127969571,2
    C,F--2329880(+) GGCCCC/GCCCAC 1 -- int11Minor allele frequency- G:0.00NA 2
    rs344006241,2
    C--2329895(+) ACCGG-/CCCCCC 1 -- int11Minor allele frequency- C:0.00NA 2
    rs1865744131,2
    --2329908(+) AGCAGC/TGACCA 1 -- int10--------
    rs2019407061,2
    C--2329941(+) CAACAC/GTGACC 1 -- int10--------
    rs115549471,2
    C,F--2329995(+) TTCTGA/C/G/
            
    GCACA
    4 * C W stg1 mis1 syn1 ese311NS NA CSA WA EA EU 4310
    rs22342971,2
    C,A--2330077(+) AGGGTG/CCCCCA 1 -- int17Minor allele frequency- C:0.42NA CSA WA EA 366
    rs1922982551,2
    --2330165(+) GTGGGC/GTGGGG 1 -- int10--------
    rs1433288741,2
    C--2330246(+) GCAGCC/TCCCTG 1 -- int10--------
    rs25212731,2
    C,A--2330400(+) CCTTAA/GGGGTT 1 -- int112Minor allele frequency- G:0.24NA WA CSA EA 374
    rs25212741,2
    C,A--2330479(+) CAGACA/GGTACC 1 -- int111Minor allele frequency- G:0.25NA WA CSA EA 371
    rs71088981,2
    C--2330518(+) ACTGGG/AGTGTC 1 -- int15Minor allele frequency- A:0.08NA CSA WA EA 361
    rs25212751,2
    C,F,A--2330563(+) CCTTCT/CGTCCT 1 -- int110Minor allele frequency- C:0.41NA WA CSA EA 372
    rs71129191,2
    C,F--2330596(+) GGGTCC/TGGCCT 1 -- int15Minor allele frequency- T:0.10NA CSA WA EA 362
    rs1512058681,2
    --2330634(+) GTCCCA/CGTGGA 1 -- int10--------
    rs1391904581,2
    --2330647(+) GGCCAG/TCAGCT 1 -- int10--------
    rs1129807121,2
    C,F--2330766(+) CGGGCG/AGCACC 1 -- int12Minor allele frequency- A:0.03CSA WA 119
    rs789425211,2
    F--2330801(+) GGAGTG/AGGGCA 1 -- int11Minor allele frequency- A:0.01NA 120
    rs1499641241,2
    C--2330865(+) TAGTGA/GCCTCG 1 -- int10--------
    rs1831355081,2
    --2330896(+) CCCAGA/GGCCCT 1 -- int10--------
    rs740482461,2
    C,F--2330919(+) TGGCCA/CTGAGA 1 -- int14Minor allele frequency- C:0.07WA CSA EA 242
    rs26518211,2
    C,F,A,H--2330930(-) GCCTCA/GGTATC 1 -- int117Minor allele frequency- G:0.27NS EA NA WA CSA 785
    rs25212761,2
    C,A--2330977(+) GGGCCT/CGCTGT 1 -- int112Minor allele frequency- C:0.47EA NA WA CSA 1651
    rs25212771,2
    C,A--2331050(+) GGGGAA/CTCAGG 1 -- int18Minor allele frequency- C:0.25NA WA EA 368
    rs22517111,2
    C,A--2331053(-) GGGCCC/TGAGTC 1 -- int19Minor allele frequency- T:0.27NA WA EA 370
    rs25212781,2
    C,A--2331096(+) GCAGTG/ACCGGG 1 -- int114Minor allele frequency- A:0.47EA NA WA CSA 1859
    rs25212791,2
    C,A--2331214(+) ATTTTA/CTCAGG 1 -- int112Minor allele frequency- C:0.47EA WA NA CSA 1855
    rs25212801,2
    C,F,A--2331307(+) GAGCTC/GGGCCA 1 -- int113Minor allele frequency- G:0.25NA WA CSA EA 376
    rs1851306301,2
    --2331409(+) ACAGCG/TGCCAG 1 -- int10--------
    rs110222181,2
    C,F--2331416(+) CCAGGG/ATTCCC 1 -- int15Minor allele frequency- A:0.06WA CSA EA 244
    rs25212811,2
    C,F,A,H--2331444(+) GCTGCT/GGCCCA 1 -- int111Minor allele frequency- G:0.40NA WA CSA EA 374
    rs15484321,2
    C,F,A,H--2331547(+) CTGGGA/GCCTGC 1 -- int112Minor allele frequency- G:0.43MN WA NA CSA EA 558
    rs757943411,2
    C,F--2331597(+) CAGCCG/AGGCTC 1 -- int11Minor allele frequency- A:0.17EA 120
    rs1451122321,2
    --2331662(+) TGGCCA/CGTGCG 1 -- int10--------
    rs1419260071,2
    --2331709(+) GCCTGA/GCCCCA 1 -- int10--------
    rs740482601,2
    C,F--2331771(+) CAGTGG/AGTCTT 1 -- int12Minor allele frequency- A:0.04WA 120
    rs1457776051,2
    C--2331865(+) TGGGCC/TGCCCT 1 -- int10--------
    rs1149636691,2
    F--2331868(+) GCCGCC/TCTTGG 1 -- int11Minor allele frequency- T:0.01WA 118
    rs1477852561,2
    --2331872(+) CCCTTA/GGGCAA 1 -- int10--------
    rs1898386681,2
    --2331930(+) ACCAAC/GATCCA 1 -- int10--------
    rs1412771421,2
    --2331960(+) TGGCCA/CGGTGT 1 -- int10--------
    rs8089631,2
    C,F,A,H--2332037(+) AGGACA/GTGGGA 1 -- int122Minor allele frequency- G:0.49MN NS EA NA WA CSA 2255
    rs1160256391,2
    F--2332115(+) GGGGCG/AGCTGC 1 -- int11Minor allele frequency- A:0.03WA 118
    rs1433375791,2
    --2332387(+) CCTGCA/GGATGG 1 -- int10--------
    rs1134321531,2
    C,F--2332422(+) GGGACC/AAGCCA 1 -- int12Minor allele frequency- A:0.02CSA WA 120
    rs734067831,2
    C--2332462(+) GACCCG/AGGCCC 1 -- int11Minor allele frequency- A:0.50WA 2
    rs796627541,2
    F--2332619(+) CTCCTC/TGAGGG 1 -- int11Minor allele frequency- T:0.01WA 118
    rs1483600251,2
    C--2332666(+) CTGACG/TAGTCT 1 -- int10--------
    rs3718297541,2
    C--2332677(+) GCTTCA/GGAATA 1 -- int10--------
    rs801201621,2
    C,F--2332694(+) TGCTCA/GAATTA 1 -- int17Minor allele frequency- G:0.13NA WA CSA EA 365
    rs734067851,2
    C--2332726(+) GCCTCG/ATCCTC 1 -- int14Minor allele frequency- A:0.08NA WA EA 360
    rs1821389661,2
    --2333024(+) TCCCCC/TAGGTG 1 -- int10--------
    rs8001391,2
    C,F,A,H--2333124(+) CCGTGG/AAGAGC 1 -- int111Minor allele frequency- A:0.40EA NA WA CSA 1875
    rs1415645211,2
    --2333303(+) AGGCAA/GGGCAG 1 -- int10--------
    rs1161795431,2
    F--2333460(+) GGGAGG/AGAAGC 1 -- int11Minor allele frequency- A:0.02WA 118
    rs1504754661,2
    --2333491(+) ACCCCA/CGGGCC 1 -- int10--------
    rs1384891541,2
    C--2333610(+) GCCCCC/TGCCCT 1 -- int10--------
    rs8001401,2
    C,F,A,H--2333675(+) AGGACA/GAGGCT 1 -- int122Minor allele frequency- G:0.42EA NS NA WA 3084
    rs1427254181,2
    C--2333732(+) CATCAA/GTGGGA 1 -- int10--------
    rs22831451,2
    C--2333846(+) ACTGCC/TCGCCC 1 -- int10--------
    rs22831461,2
    C,F--2333860(+) TGGCCG/ACTGTC 1 -- int16Minor allele frequency- A:0.23NA WA EA 364
    rs1884611451,2
    --2333910(+) CCGCCA/GTAAGC 1 -- int10--------
    rs1124678231,2
    C--2333966(+) TGGGGC/-TTCCA 1 -- int11Minor allele frequency- -:0.50CSA 2
    rs79368571,2
    C,F--2333987(+) GCCCTT/CTGGGG 1 -- int11Minor allele frequency- C:0.02WA 118
    rs49300801,2
    C,F,A--2334039(+) TGGCAT/CTTGGG 1 -- int16Minor allele frequency- C:0.10NA WA CSA EA 364
    rs1400715001,2
    --2334130(+) ACCAGC/TGACTC 1 -- int10--------
    rs768728071,2
    C--2334315(+) CTTCAC/TCCCCT 1 -- int12Minor allele frequency- T:0.08CSA WA 120
    rs753143311,2
    F--2334336(+) GGCCTC/TGTCCA 1 -- int11Minor allele frequency- T:0.03WA 118
    rs756663431,2
    F--2334404(+) CAGCTG/ACCCGG 1 -- int11Minor allele frequency- A:0.02EA 120
    rs1493857341,2
    --2334407(+) CTGCCC/TGGGCT 1 -- int10--------
    rs1926855981,2
    --2334525(+) CCCATC/TCCCCA 1 -- int10--------
    rs1174093741,2
    F--2334550(+) GTAGCG/ATGCTG 1 -- int11Minor allele frequency- A:0.01NA 120
    rs1445353561,2
    --2334574(+) GCCAAA/CCTTGT 1 -- int10--------
    rs1484473101,2
    C--2334667(+) GGCCAC/TTGTGT 1 -- int10--------
    rs7395461,2
    C,F,A--2334740(+) TTTGGA/GGAGAT 1 -- int114Minor allele frequency- G:0.48NA EA MN WA CSA 786
    rs22342991,2
    --2334828(+) GGGGGA/CTGTGT 1 -- int10--------
    rs22343001,2
    C--2334892(+) GAGGAC/TGCCAT 2 D syn1 ese30--------
    rs22343011,2
    C--2334893(+) AGGACG/ACCATG 2 /T /A mis1 ese32Minor allele frequency- A:0.00EA NA 4574
    rs1476304811,2
    --2334910(+) ACCTAC/TGACCT 2 Y syn10--------
    rs1124559171,2
    C,F--2334939(+) GAAAGG/TTACGT 2 G V mis12Minor allele frequency- T:0.00CSA NA 4425
    rs1381294691,2
    C--2334954(+) CGTCCG/AGCGGC 2 /Q /R mis11Minor allele frequency- A:0.00NA 4350
    rs22343021,2
    C,F--2334957(+) CCGGCG/AGCAGG 2 /Q /R mis1 ese31Minor allele frequency- A:0.00NA 4324
    rs22343031,2
    C,H--2334991(+) GTGAGA/C/TGTGGG 1 -- int14NS EA 408
    rs2004394081,2
    C--2334995(+) GCGTGA/GGGACG 1 -- int10--------
    rs22343041,2
    C,F--2335015(+) CAGGGC/TGGTCA 1 -- int11Minor allele frequency- T:0.12WA 118
    rs557561781,2
    C,F--2335054(+) CAGGCG/ACAGGG 1 -- int12Minor allele frequency- A:0.03WA 120
    rs1837180801,2
    --2335187(+) ATTCTC/TGAGGC 1 -- int10--------
    rs1170352091,2
    C,F--2335188(+) TTCTCG/AAGGCC 1 -- int11Minor allele frequency- A:0.01NA 120
    rs1155702561,2
    C,F--2335195(+) GGCCCA/CGTGCA 1 -- int11Minor allele frequency- C:0.05WA 118
    rs1881919111,2
    --2335204(+) CAAAAC/TGAGAG 1 -- int10--------
    rs1925896891,2
    --2335219(+) GGGCCC/TTGTAT 1 -- int10--------
    rs1406130751,2
    --2335266(+) AATACA/GGGGCC 1 -- int10--------
    rs1123627421,2
    F--2335279(+) ACATAG/ATGGCT 1 -- int12Minor allele frequency- A:0.04CSA WA 119
    rs1847741441,2
    --2335343(+) AGCCCA/GGGAGT 1 -- int10--------
    rs2001115741,2
    C--2335409(-) CTTTTC/TTNNNN 1 -- int10--------
    rs792974921,2
    C,F--2335436(+) TACAGC/TGCACA 1 -- int12Minor allele frequency- T:0.02WA 120
    rs7395471,2
    C,F,A,H--2335444(-) ACAGGC/GCCTGT 1 -- int111Minor allele frequency- G:0.49WA NA CSA EA 372
    rs1441968331,2
    C--2335489(+) NNNNCC/TGTCAC 1 -- int10--------
    rs784375861,2
    C,F--2335541(+) GGGCCC/TGGCTG 1 -- int11Minor allele frequency- T:0.03EA 120
    rs740482611,2
    C,F--2335560(+) CTGGAG/ACCCCA 1 -- int11Minor allele frequency- A:0.50WA 2
    rs1412136121,2
    --2335625(+) CTGGAG/TACTTG 1 -- int10--------
    rs2020944881,2
    C--2335678(+) TCTCGC/GGAGCA 1 -- int10--------
    rs1486013111,2
    C,F--2335748(+) TCAGCC/TGTCTG 2 R C mis12Minor allele frequency- T:0.00NA EU 4627
    rs1420568901,2
    C,F--2335749(+) CAGCCG/ATCTGG 2 /H /R mis11Minor allele frequency- A:0.00NA 4480
    rs2004782991,2
    --2335795(+) GCGGCA/GAGAGA 2 A syn10--------
    rs1995723861,2
    C--2335807(+) GTGAGG/TGGGGG 1 -- int10--------
    rs1916044361,2
    C--2335809(+) GAGGGA/GGGGAC 1 -- int10--------
    rs22343051,2
    C,H--2335840(+) ACCCTC/TGGGGG 1 -- int15Minor allele frequency- T:0.01NS EA WA 520
    rs762411111,2
    F--2336042(+) CCTTTG/CCCCAG 1 -- int11Minor allele frequency- C:0.12WA 118
    rs1503311621,2
    --2336106(+) GACTTC/GCCAAG 1 -- int10--------
    rs1141484801,2
    C,F--2336124(+) AAGTCC/TACAGA 1 -- int11Minor allele frequency- T:0.02WA 118
    rs1837461461,2
    --2336164(+) TGTGCC/TAAGGG 1 -- int10--------
    rs1449587001,2
    --2336217(+) CAGGCA/GTCCTG 1 -- int10--------
    rs74827551,2
    H--2336240(+) AGGAGT/ATGAAG 1 -- int14Minor allele frequency- A:0.00NS EA 420
    rs1898767381,2
    --2336246(+) TGAAGA/GGCACT 1 -- int10--------
    rs1810910061,2
    --2336432(+) CCGCTC/TCCCTC 1 -- int10--------
    rs1853640531,2
    --2336618(+) CGGCAC/TTGGGG 1 -- int10--------
    rs1898435461,2
    --2336680(+) CCCCCC/GACTGA 1 -- int10--------
    rs1163706181,2
    C,F--2336835(+) GCAGAC/ACTGCC 1 -- int11Minor allele frequency- A:0.03WA 118
    rs110222521,2
    C,H--2337012(+) AGGAAC/GCTGGG 1 -- int112Minor allele frequency- G:0.00NA WA CSA 141
    rs740482621,2
    C,F--2337022(+) GACTGT/CGCGGG 1 -- int12Minor allele frequency- C:0.04WA 120
    rs1814764361,2
    --2337211(+) GGAGAC/TGGCAC 1 -- int10--------
    rs125768241,2
    C,F,H--2337218(+) GCACCG/AGCCGG 1 -- int11Minor allele frequency- A:0.27EA 120
    rs1437700321,2
    --2337221(+) CCGGCC/TGGGCC 1 -- int10--------
    rs755746771,2
    C,F--2337272(+) CACTGG/AGCTTC 1 -- int11Minor allele frequency- A:0.16WA 118
    rs22343061,2
    C,F--2337334(+) CCGCAC/TCCGCC 1 -- int11Minor allele frequency- T:0.03WA 118
    rs1507314131,2
    F--2337506(+) CAGGTC/TGCCTC 2 V syn11Minor allele frequency- T:0.00NA 4322
    rs2014003871,2
    --2337534(+) GCCTGG/TCCCTC 2 A S mis10--------
    rs22343071,2
    C,F--2337650(+) TTGAGC/TCTCAC 1 -- int11Minor allele frequency- T:0.02NA 120
    rs22343081,2
    C,F,A--2337693(+) GACAGG/AGCCTG 1 -- int16Minor allele frequency- A:0.12NA CSA WA EA 364
    rs22343091,2
    C,F--2337758(+) AGGGGC/TGCCCG 1 -- int11Minor allele frequency- T:0.06WA 118
    rs1119548341,2
    C--2337787(+) CAGCCA/GCGGGT 1 -- int10--------
    rs2006782681,2
    --2337820(+) TTGCTC/GTTCAG 2 L syn10--------
    rs2000260821,2
    --2337848(+) CCATCC/TGCTGT 2 R C mis10--------
    rs1431121751,2
    --2337858(+) TGGCTA/GCAGCT 2 Y C mis10--------
    rs1863723891,2
    --2338000(+) CCAAGA/CCCCAG 1 -- int10--------
    rs22343101,2
    C,F--2338038(+) GGGTGG/ACTGAG 1 -- int13Minor allele frequency- A:0.10CSA WA NA 239
    rs22343111,2
    C,F--2338043(+) GCTGAG/ACACCA 1 -- int11Minor allele frequency- A:0.06WA 118
    rs22343131,2
    C--2338091(+) TGCACC/TGCACC 1 -- int10--------
    rs1908909321,2
    --2338109(+) CCACAA/TGGGGA 1 -- int10--------
    rs1388271481,2
    C--2338156(+) GGAGAG/TGGATG 1 -- int10--------
    rs110222581,2
    C,F,A,H--2338240(+) GGGGCT/AGGGAG 1 -- int113Minor allele frequency- A:0.50NA WA CSA EA 381
    rs110222591,2
    C,F,A,H--2338256(+) AACCCG/ACAGCC 1 -- int113Minor allele frequency- A:0.29NA WA CSA EA 379
    rs1810078571,2
    --2338296(+) GGCCCA/GTCTCT 1 -- int10--------
    rs1158722251,2
    C,F--2338381(+) CTACAA/GTAGCC 1 -- int11Minor allele frequency- G:0.06WA 118
    rs773625671,2
    F--2338386(+) ATAGCC/TTCACA 1 -- int11Minor allele frequency- T:0.03WA 118
    rs1152630151,2
    C,F--2338397(+) GTCCCG/ATCTAG 1 -- int11Minor allele frequency- A:0.07WA 118
    rs22343141,2
    C--2338469(+) CCAGAA/TCATTC 1 -- int10--------
    rs595482601,2
    C--2338529(+) GTCCCG/CTGTAG 1 -- int11Minor allele frequency- C:0.50WA 2
    rs1857993411,2
    --2338542(+) CATTCA/CACCAC 1 -- int10--------
    rs31801601,2
    H--2338615(+) GAGATG/TCTCCC 2 C F mis1 ese34Minor allele frequency- T:0.00NS EA 402
    rs1390818151,2
    C,F--2338621(+) CTCCCA/TGGGTG 2 Q L mis12Minor allele frequency- T:0.00NA EU 4877
    rs1468377541,2
    F--2338639(+) ACATTG/ATCTCC 2 /Y /C mis11Minor allele frequency- A:0.00NA 4362
    rs347452341,2
    C,F--2338677(+) GAGGAT/CGCTCG 2 /R /C mis12Minor allele frequency- C:0.00NA 4500
    rs1492303961,2
    C--2338681(+) ATGCTC/TGGGTA 2 S L mis11Minor allele frequency- T:0.00NA 4400
    rs1432253481,2
    C--2338692(+) GTCTTC/TGGTGG 2 R W mis11Minor allele frequency- T:0.00NA 4354
    rs2017805961,2
    C--2338705(+) GCAGGA/TGAGCG 2 E V mis11Minor allele frequency- T:0.00EU 509
    rs1914386511,2
    C--2338709(+) GAGAGC/TGATGC 2 S syn10--------
    rs2003480921,2
    --2338730(+) CCCCTC/TTCCTG 2 L syn10--------
    rs2019664611,2
    --2338776(+) CTGTCA/GGCCCT 1 -- int10--------
    rs1508413431,2
    C--2338797(+) CTGAGA/GGGAGG 1 -- int10--------
    rs1828592751,2
    --2338810(+) CCGAGC/GTGTGA 1 -- int10--------
    rs1382243441,2
    --2338977(+) ACACTA/GGTGGC 1 -- int10--------
    rs22343151,2
    C,F--2339041(+) CGTAAG/CAAGCA 1 -- int13Minor allele frequency- C:0.10CSA WA NA 240
    rs1404776751,2
    C,F--2339111(+) AAGTCA/G/TCGGTG 3 H R L mis12NA EU 5069
    rs1470632271,2
    C--2339137(+) CTGAGC/TGGGGT 2 R W mis12Minor allele frequency- T:0.00NA EU 5013
    rs1997407951,2
    C--2339138(+) TGAGCA/GGGGTC 2 Q R mis10--------
    rs22343161,2
    C--2339195(+) GCTCCG/AGGGAA 1 -- ut31 ese32Minor allele frequency- A:0.04WA 120
    rs1887238791,2
    --2339416(+) CACATC/TGTTGT 1 -- ut310--------
    rs1472047271,2
    --2339488(+) CAGTAA/TACACC 1 -- ds50010--------
    rs1907729611,2
    --2339513(+) GCCCCA/GGTCCC 1 -- ds50010--------
    rs1155895081,2
    F--2339520(+) TCCCTG/CGCACC 1 -- ds50011Minor allele frequency- C:0.02WA 118
    rs791884321,2
    C,F--2339635(+) TTATGT/CCCATA 1 -- ds50015Minor allele frequency- C:0.16NA CSA WA EA 362
    rs1146999201,2
    C,F--2339703(+) TTCCCA/GTCATC 1 -- ds50011Minor allele frequency- G:0.05WA 118
    rs2007985541,2
    C--2339709(+) TCATCC/TCACAG 1 -- ds50010--------
    rs25212821,2
    C,F,O,A,H--2339737(+) AAGGCG/AGGACA 1 -- ds500133Minor allele frequency- A:0.32NS EA NA WA CSA 2920
    rs49300811,2
    C,F,H--2339822(+) GATGAC/TGAATT 1 -- ds500134Minor allele frequency- T:0.20EA NA NS WA CSA 3405
    rs1406000551,2
    --2339928(+) GAAGCC/TGACAA 1 -- ds50010--------
    rs3693211221,2
    ----2337759(+) GGGGCA/GCCCGC 1 -- int10--------
    rs3743136741,2
    ----2339885(+) GGGTGA/GAACGC 1 -- ds50010--------
    rs3767632371,2
    ----2337477(+) GCATCC/TGGAGC 2 R W mis10--------
    rs3695050041,2
    ----2335627(+) GGATAC/TTGTGG 1 -- int10--------
    rs1115621371,2
    ----2336066(+) CCATGT/CGCCAT 1 -- int11Minor allele frequency- C:0.00CSA 1
    rs3676022241,2
    ----2335289(+) TCACAA/CCTGTA 1 -- int10--------
    rs3719402321,2
    ----2326609(+) CCCCC-/ACCAGA 1 -- int10--------
    rs3764676221,2
    ----2333254(+) GCAGGA/CAGAGC 1 -- int10--------
    rs3713216421,2
    ----2332562(+) GAGGCA/GGGACC 1 -- int10--------
    rs3690331901,2
    ----2337503(+) CAGCAG/TGTCGC 2 Q H mis10--------
    rs1121142061,2
    ----2335474(+) CCTGGC/TTCCAG 1 -- int11Minor allele frequency- T:0.50CSA 2
    rs3701229201,2
    ----2336490(+) CCTGGC/TGACCC 1 -- int10--------
    rs30346951,2
    ----2326600(-) GGGGG-/GGGCAGAC 1 -- cds1 trp30--------
    rs3723278441,2
    ----2334838(+) TCCCCA/GGATCT 1 -- int10--------
    rs3700903671,2
    ----2337553(+) CTCTCA/GCCTCC 1 -- int10--------
    rs3678512241,2
    ----2338672(+) TCCAAC/GAGGAT 2 T R mis10--------
    rs3722465961,2
    ----2329984(+) TCTCCA/CTGGCG 2 M L mis10--------
    rs3688727151,2
    ----2334949(+) TCCCAC/TGTCCG 2 H syn10--------
    rs1444608791,2
    ----2338671(+) GTCCAA/GGAGGA 2 R G mis11Minor allele frequency- G:0.00NA 4432
    rs3690852021,2
    ----2338103(+) CATGGC/TCACAT 1 -- int10--------
    rs3753398331,2
    ----2338806(+) GGGTCC/TGAGCT 1 -- int10--------
    rs26518181,2
    ----2339265(-) TGGGAA/TCCTCA 1 -- ut31 ese30--------
    rs767400231,2
    ----2325238(+) CCCTCG/ACGGCC 1 -- int11Minor allele frequency- A:0.50NA 2
    rs3684105331,2
    ----2337337(+) CACCCA/GCCGCC 1 -- int10--------
    rs3772308991,2
    ----2335705(+) CTTCTG/TTTCCT 1 -- int10--------
    rs3769262771,2
    ----2339172(+) GTGGGC/TTGCAC 1 -- ut310--------
    rs1443879871,2
    ----2325801(+) TCTATC/TGCCCA 1 -- int10--------
    rs3708567831,2
    ----2337371(+) GTGGGA/CGCTGC 1 -- int10--------
    rs123636891,2
    ----2328285(+) gagagA/Tgaaga 1 -- int1 trp30--------
    rs1136413901,2
    ----2327189(+) GTGAGC/TCTATG 1 -- int10--------
    rs3719793151,2
    ----2337451(+) TGCCCC/TCTCAC 1 -- int10--------
    rs717592631,2
    ----2327292(+) GTGTG-/GTGTGT
            
    TGTGT
    1 -- cds10--------
    rs3736647421,2
    ----2336725(+) GGGATG/TGCAGG 1 -- int10--------
    rs1409011191,2
    ----2328204(+) GAAAGA/GGAAAA 1 -- int10--------
    rs3691903651,2
    ----2334883(+) GTGCAA/GGTGGA 1 -- spa10--------
    rs3744733481,2
    ----2334953(+) ACGTCC/TGGCGG 2 R W mis10--------
    rs355931861,2
    ----2330338(+) TGATG-/CCCCTC 1 -- int10--------
    rs347007251,2
    ----2334737(+) GCTTT-/GGGGGA 1 -- int10--------
    rs3702342561,2
    ----2337802(+) CCCTCC/GCAGGT 1 -- int10--------
    rs759804781,2
    ----2328921(+) AAGCCC/TTGACC 1 -- int11Minor allele frequency- T:0.50NA 2
    rs3772259521,2
    ----2335949(+) GGAAGA/GTCTGA 1 -- int10--------
    rs1125212281,2
    ----2326395(+) TAGGAG/ATAGAG 1 -- int11Minor allele frequency- A:0.50CSA 2
    rs3703081011,2
    ----2335683(+) GGAGCA/TCATCA 1 -- int10--------
    rs3765620781,2
    ----2330035(+) GCCCCA/GCCCAG 2 T A mis10--------
    rs593609241,2
    ----2328207(+) GGAAA-/GAGAA 
            
    AAGAG
    1 -- int10--------
    rs121465941,2
    ----2336429(+) tccccC/Gctccc 1 -- int10--------
    rs3706917131,2
    ----2327136(+) ACCCCA/CTCAAG 1 -- int10--------
    rs1435813241,2
    ----2328201(+) GAGGA-/AAGAG 
            
    AAAAG
    1 -- int10--------
    rs3753636561,2
    ----2328983(+) AGAACA/GCCCAC 1 -- int10--------
    rs49299781,2
    ----2327243(+) gtgtgC/Tgtgtg 1 -- int10--------
    rs3698125241,2
    ----2337856(+) TGTGGC/TGCAGC 2 G syn10--------
    rs3704969911,2
    ----2328982(+) GAGAAC/TGCCCC 1 -- int10--------
    rs3712324761,2
    ----2325292(+)