TMEM183A
SNP - dbSNP
dbSNPTypeAllelesHetSe(het)Fxn-classGene NameAssemblyChr-posSequenceEntrez Gene
rs14197snpC/T0.4540610.144427upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variantPPFIA4, TMEM183AGRCh38.p71:203024720GGGACTGTGCTTCTC[C/T]CCTCCTGCCTCAAAG92703
rs782784snpA/G0.0306650.119967intron-variantTMEM183AGRCh38.p71:203019612aaataatatataaat[A/G]tattGACAAAGTAAA92703
rs782785snpA/G0.4971820.037434intron-variantTMEM183AGRCh38.p71:203018878aggcctttataagag[A/G]gtcttcacactaggc92703
rs782786snpG/T0.4017470.198678intron-variantTMEM183AGRCh38.p71:203018853ctaggctcagcccct[G/T]ttggcattccacctt92703
rs782787snpC/T0.4442670.157354intron-variantTMEM183AGRCh38.p71:203018668ttctttttaagttac[C/T]cagaatctgtggtac92703
rs782788snpA/G0.4544230.143914intron-variantTMEM183AGRCh38.p71:203018642ggtactgttatagca[A/G]cacaaacagactaag92703
rs782789snpG/T0.4501050.149859intron-variantTMEM183AGRCh38.p71:203009681gcctaggcaacatag[G/T]gagacccctgtctct92703
rs968085snpC/T00intron-variant, upstream-variant-2KBTMEM183A, LOC100506747GRCh38.p71:203008946CCCACTACCAAGGTT[C/T]TTAGGGAGAGCCAAG92703
rs1046529snpC/T0.1645460.234942utr-variant-3-prime, nc-transcript-variantTMEM183AGRCh38.p71:203023826CTGACCCAGGTCTTT[C/T]TGTTGTACCATAAGT92703
rs1046532snpG/T0.451980.147323utr-variant-3-prime, downstream-variant-500B, nc-transcript-variantTMEM183AGRCh38.p71:203024070CTTCTAACAGTTCAA[G/T]GAAAGGGTCACTATC92703
rs1046538snpA/C0.496810.0398085utr-variant-3-prime, downstream-variant-500B, nc-transcript-variantTMEM183AGRCh38.p71:203024486GTAAAAAAAAAAAAA[A/C]AAAAATGTGAATTTA92703
rs1046542snpA/G0.2498860.25upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variantPPFIA4, TMEM183AGRCh38.p71:203024763TGAACTAAAGATGCC[A/G]TGGAGCAGGAGTGTC92703
rs1046543snpG/T0.0843640.187256upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variantPPFIA4, TMEM183AGRCh38.p71:203024771AGATGCCATGGAGCA[G/T]GAGTGTCTTGGTGCA92703
rs1418444snpC/G0.4967780.0400063intron-variant, upstream-variant-2KBTMEM183A, LOC100506747GRCh38.p71:203008904GGAGGAGATATAAGA[C/G]GTGATACCAGGAGAG92703
rs1623171snpA/G0.4997410.0113788upstream-variant-2KB, intron-variantTMEM183A, LOC100506747GRCh38.p71:203005569ACCCAAATCCTATAA[A/G]ACGGCCCCACCCTTA92703
rs1690821snpC/G0.3685290.220116upstream-variant-2KB, downstream-variant-500BPPFIA4, TMEM183AGRCh38.p71:203024974TGAAGCCAAGATAAC[C/G]ACTGGTAACACATTT92703
rs1690833snpA/G0.4556210.142197intron-variantTMEM183AGRCh38.p71:203012642TTTTCTGTCTTTAGA[A/G]ACAAAATTTAGTAAA92703
rs1774836snpC/T0.3979940.201489upstream-variant-2KB, intron-variantTMEM183A, LOC100506747GRCh38.p71:203005977ATTTTTTCTTTTTCT[C/T]CTTTTTTTTTTTTTG92703
rs1774846snpC/G0.3675030.220665upstream-variant-2KB, downstream-variant-500BPPFIA4, TMEM183AGRCh38.p71:203025246AGGCTATTAAGTTTT[C/G]GGGCAGTCAAAAGTC92703
rs1774847snpA/G0.4999680.00399348upstream-variant-2KB, downstream-variant-500BPPFIA4, TMEM183AGRCh38.p71:203025140ACAGAGCAAAATCAC[A/G]GTATATAACCTGTAG92703
rs1989009snpG/T0.00239330.0345097upstream-variant-2KB, intron-variantTMEM183A, LOC100506747GRCh38.p71:203006442GACCCTGGGGTTGTT[G/T]GCTGGTTAATTTTGC92703
rs2211394snpC/T0.2314820.249313upstream-variant-2KB, intron-variantTMEM183A, LOC100506747GRCh38.p71:203006728ttcttccgcctcagc[C/T]tcccgagtagctggg92703
rs2298131snpC/T00intron-variantTMEM183AGRCh38.p71:203018096CACCAGGCAAGATGA[C/T]ACAAGGCCATAAGGT92703
rs2796184snpA/T00intron-variantTMEM183AGRCh38.p71:203012150ACCCCCCACTCCATC[A/T]CACACACACACACAC92703
rs3041263in-del-/A/AA0.4088710.193029intron-variantTMEM183AGRCh38.p71:203010138TCTCAAAAAAAAAAA[-/A/AA]GAAAAAAATAATAGT92703
rs3834027in-del-/A0.5014050.0328711intron-variant, upstream-variant-2KBTMEM183A, LOC100506747GRCh38.p71:203008537TTCAGGAAAGGGGGG[-/A]AAAAAAAACATCGTT92703
rs4950873snpC/T0.04410950.141807intron-variantTMEM183AGRCh38.p71:203021877CACAATGAAAGTAGC[C/T]TTTTTAAAATGGTAA92703
rs4950903snpA/G0.1182350.212457upstream-variant-2KB, intron-variantTMEM183A, LOC100506747GRCh38.p71:203006430agctaatatgtggca[A/G]aattaaccagcaaac92703
rs4950904snpA/G0.1009440.200705upstream-variant-2KB, nc-transcript-variantTMEM183A, LOC100506747GRCh38.p71:203007001GACTCTTACAGACCT[A/G]TGTTAGACTAGCAGG92703
rs4950905snpC/T0.04449080.142359utr-variant-3-prime, downstream-variant-500B, nc-transcript-variantTMEM183AGRCh38.p71:203024167TAAGCACTTAGCGAC[C/T]TTGCTCTGCCCTGTA92703
rs6427988snpC/T0.02406430.107019intron-variantTMEM183AGRCh38.p71:203010490ctcgaccaataagta[C/T]ggtcaagatattcca92703
rs6662717snpC/T00utr-variant-3-prime, nc-transcript-variantTMEM183AGRCh38.p71:203023811TGCAGAGCCAAGATT[C/T]TGACCCAGGTCTTTT92703
rs6678040snpA/G0.2078680.246424missense, upstream-variant-2KB, nc-transcript-variantTMEM183A, LOC100506747GRCh38.p71:203008681GCCTCTCAGGTTCCT[A/G]CAGAGGAAGCTCTTT92703
rs6690103snpC/T0.129320.218944intron-variant, upstream-variant-2KBTMEM183A, LOC100506747GRCh38.p71:203008122TCTTGGTTATTAATC[C/T]CTTTGCTGTAGTTCA92703
rs6694591snpG/T0.1599510.233219intron-variantTMEM183AGRCh38.p71:203013160ATAAGAATTAGAAAA[G/T]ATGATGATGTTTTAG92703
rs7520580snpA/G0.4563320.141164intron-variantTMEM183AGRCh38.p71:203017186ATGCCGGGAGAGTAG[A/G]ATTTCACCCAGCAGC92703
rs7533550snpA/G0.01348610.0810011intron-variantTMEM183AGRCh38.p71:203021323agtgtgagccactgc[A/G]ttcagctTTTTTATA92703
rs7555847snpA/T0.03143850.121371intron-variantTMEM183AGRCh38.p71:203011961TAAAAGCCTTTTTTT[A/T]AATGaaacatgtaga92703
rs10159437snpA/G0.2777780.248452intron-variantTMEM183AGRCh38.p71:203021253ctgaggcttgtctca[A/G]actcctagcctcaag92703
rs10692558in-del-/ATC/CATintron-variantTMEM183AGRCh38.p71:203012314AGATATACCATCATC[-/ATC/CAT]TTTGTAAATATTTTA92703
rs10920545snpC/T0.01702510.090679intron-variantTMEM183AGRCh38.p71:203011942TGTATTTTTCTTCTT[C/T]TTTTAAAAGCCTTTT92703
rs11582753snpA/G0.4535750.145111intron-variantTMEM183AGRCh38.p71:203014166CTGGAATTCGGAGTC[A/G]GAAACTCTTGGTTCT92703
rs11584217snpC/T0.1030820.202275intron-variantTMEM183AGRCh38.p71:203013112AGACATGGTAGACTG[C/T]GTCTTGCATGATTAC92703
rs11584549snpC/T00intron-variantTMEM183AGRCh38.p71:203018966ctcttaatactattg[C/T]gttggagattaagtg92703
rs12035390snpA/Gintron-variantTMEM183AGRCh38.p71:203021050tttttttttttttaa[A/G]agacgtggtctcact92703
rs12035391snpA/Gintron-variantTMEM183AGRCh38.p71:203021052tttttttttttaaga[A/G]acgtggtctcactct92703
rs12073340snpC/T0.1272540.217792intron-variantTMEM183AGRCh38.p71:203009306TATGTCTAATAAGTA[C/T]TGTGGGAAATAGAAA92703
rs12088413snpC/T0.01111960.0737302intron-variantTMEM183AGRCh38.p71:203009435AGATTCTGGGTTTTC[C/T]TTcagacttaatgag92703
rs12133328snpA/G0.1791050.239737intron-variantTMEM183AGRCh38.p71:203016563TAATGCAACCTTGAC[A/G]TCAGGGATTCCCCTT92703
rs12134231snpA/G0.1645460.234942intron-variantTMEM183AGRCh38.p71:203016897CACCTTTGGCAAACA[A/G]GGTTACTCTGTTCCT92703
rs12135724snpC/Gupstream-variant-2KB, intron-variantTMEM183A, LOC100506747GRCh38.p71:203006241tgctctgcaactctt[C/G]tccttcccccaagcc92703
rs12135786snpC/Tupstream-variant-2KB, intron-variantTMEM183A, LOC100506747GRCh38.p71:203006388ataaacaaactttac[C/T]tacaccctcctgtaa92703
rs12407486snpG/T00intron-variantTMEM183AGRCh38.p71:203021084tcactcaggctgaag[G/T]gcagtgatggaatca92703
rs12727457snpC/T0.4320630.171327intron-variantTMEM183AGRCh38.p71:203022617ctgaggcacaagaat[C/T]gtttgatcccaggag92703
rs12728556snpA/C/G0.0003992810.0141238intron-variantTMEM183AGRCh38.p71:203009932caaggtcaggagttc[A/C/G]agaccatcctggcca92703
rs12732873snpG/Tupstream-variant-2KBTMEM183A, LOC100506747GRCh38.p71:203007281AGCTTGATTCGCGGG[G/T]GCCGGATGATGACGT92703
rs13375755snpC/T0.2084740.246527upstream-variant-2KBTMEM183A, LOC100506747GRCh38.p71:203007275GGACCCAGCTTGATT[C/T]GCGGGTGCCGGATGA92703
rs16850904snpA/G0.020160.0983543intron-variantTMEM183AGRCh38.p71:203017522TAGAATGAAAACTAA[A/G]GTCTTAATCCAGATA92703
rs28429376snpC/Tmissense, synonymous-codon, nc-transcript-variantTMEM183AGRCh38.p71:203022908AGTGAGACTGGTGTT[C/T]CAAGATTCCCCTGTC92703
rs28540464snpA/Cintron-variantTMEM183AGRCh38.p71:203013812GCCACCGTGCCCGGC[A/C]TAAGTGCCATCTCAG92703
rs34779153in-del-/Tintron-variantTMEM183AGRCh38.p71:203021047TTTTTTTTTTTTTTT[-/T]AAGAGACGTGGTCTC92703
rs34999883in-del-/Cintron-variant, upstream-variant-2KBTMEM183A, LOC100506747GRCh38.p71:203008626GCCATCTCATTCTCC[-/C]TTTTATTTTCTTCTA92703
rs35154916in-del-/Cintron-variant, nc-transcript-variantTMEM183AGRCh38.p71:203017827CTTAAAGCCAAGCCC[-/C]ATTAATTTTGATGGA92703
rs35300902in-del-/Gintron-variantTMEM183AGRCh38.p71:203017671GCGTGGCATTCAGGG[-/G]AGTTGCCAGCATGCC92703
rs35395088in-del-/Tintron-variant, upstream-variant-2KBTMEM183A, LOC100506747GRCh38.p71:203008471TTTTTTTTTTTTTTT[-/T]GTATTTAAAATACTA92703
rs35405836in-del-/T00utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant, upstream-variant-2KBTMEM183A, PPFIA4GRCh38.p71:203024499TTTTTTTTTTTTTTT[-/T]ACCATCTTCCCTAGG92703
rs35556394in-del-/Cintron-variantTMEM183AGRCh38.p71:203016999ATGATTCTTCTCCCC[-/C]TAGTTTAGCTCTAGG92703
rs35622497in-del-/Tintron-variantTMEM183AGRCh38.p71:203015681AGGACAGGTTCTTTT[-/T]GAGCAGCTAAAGCAT92703
rs35679231in-del-/Cutr-variant-3-prime, nc-transcript-variantTMEM183AGRCh38.p71:203023670GATGACTTTATACCC[-/C]TTGGTACTATACTAG92703
rs36026867in-del-/Tintron-variantTMEM183AGRCh38.p71:203013295GGTGTAGGGGCTTTT[-/T]CCCCAGGAAGGAAGA92703
rs55745312in-del-/TTintron-variant, upstream-variant-2KBTMEM183A, LOC100506747GRCh38.p71:203008470TTTTTTTTTTTTTTT[-/TT]GTATTTAAAATACTA92703
rs56743654in-del-/ACACintron-variantTMEM183AGRCh38.p71:203012275CACACACACACACAC[-/ACAC]GGTTATTTTGAAACA92703
rs56821871snpC/T0.03568150.128715utr-variant-3-prime, nc-transcript-variantTMEM183AGRCh38.p71:203023420TATGGATCAGAGGAA[C/T]CTTAGAGGCCTGAAA92703
rs57295287snpC/G0.03606630.129354intron-variantTMEM183AGRCh38.p71:203011750TTCTTTATCTATTCA[C/G]ATTACTAGTCACTTA92703
rs57610948snpC/G0.02094210.100162upstream-variant-2KB, nc-transcript-variantTMEM183A, LOC100506747GRCh38.p71:203007181GTGGGCTATGGTTCT[C/G]AGACACCATTCATCT92703
rs57850884snpA/C0.03568150.128715intron-variantTMEM183AGRCh38.p71:203019899TATATTCTTATGTGG[A/C]ATTATGAGCAGATAT92703
rs58503894in-del-/ACACACACACACACACACACACACACintron-variantTMEM183AGRCh38.p71:203012278CACACACACACACAC[-/ACACACACACACACACACACACACAC]GGTTATTTTGAAACA92703
rs58763803in-del-/Gintron-variantTMEM183AGRCh38.p71:203010471GATTTTCGATTAGGG[-/G]CTGCTCGACCAATAA92703
rs59153551in-del-/ACintron-variantTMEM183AGRCh38.p71:203012277CACACACACACACAC[-/AC]GGTTATTTTGAAACA92703
rs59277778snpC/G0.01623980.0886349intron-variantTMEM183AGRCh38.p71:203015363CTAGAATGTTTAAAG[C/G]TACAGATGCCTATCT92703
rs59850833snpA/G0.03568150.128715intron-variantTMEM183AGRCh38.p71:203017037TATCCTACCTAATAC[A/G]TATTAATTAAAAGGG92703
rs60471086in-del-/AC/ACACintron-variantTMEM183AGRCh38.p71:203012185CACACACACACACAC[-/AC/ACAC]GGTTATTTTGAAACG92703
rs60726502in-del-/Gupstream-variant-2KB, intron-variantTMEM183A, LOC100506747GRCh38.p71:203006801TTAGTAGAGACGGGG[-/G]TTTCACCGTGTTAGC92703
rs61822699snpA/Gupstream-variant-2KB, intron-variantTMEM183A, LOC100506747GRCh38.p71:203006677CAGTGACCCGATCTC[A/G]GCTCACTGCAAGCTC92703
rs71142584in-del-/T0.4997840.0103811intron-variantTMEM183AGRCh38.p71:203014625TTAACTTTTTTTTTT[-/T]GGGACAGAGTCTCAC92703
rs71142585in-del-/Aintron-variantTMEM183AGRCh38.p71:203020983AAAAAAAAAAAAAAA[-/A]GGAGCTGAGAATGAC92703
rs71716134in-del-/CT0.007559070.0610114upstream-variant-2KB, downstream-variant-500BPPFIA4, TMEM183AGRCh38.p71:203024924TAGATACTGCCTCAG[-/CT]CTCTCTCAGCATAAT92703
rs71781221in-del-/CACAintron-variantTMEM183AGRCh38.p71:203012236TACTCCCCACTCCAT[-/CACA]CACACACACACACAC92703
rs72754732snpA/G0.1864210.24178upstream-variant-2KB, intron-variantTMEM183A, LOC100506747GRCh38.p71:203005762GAATGTCATCAGTTA[A/G]GGCGGGGCAGGGCAT92703
rs72754737snpC/T0.50intron-variantTMEM183AGRCh38.p71:203011885TTTTTTTTTTTTTTT[C/T]TTTTTAAATTTCTTT92703
rs72754738snpA/G0.1889460.24243intron-variantTMEM183AGRCh38.p71:203014745CAGCTAGGATGAGCA[A/G]GAAATGATAAGTTTG92703
rs73073811snpC/T0.03568150.128715utr-variant-3-prime, downstream-variant-500B, nc-transcript-variantTMEM183AGRCh38.p71:203024412TTACCTGGATATTGC[C/T]AGGAGGTGGGCATTA92703
rs73091378snpA/T0.03568150.128715intron-variantTMEM183AGRCh38.p71:203010967ATAGTCTTTTGCATG[A/T]AGCTTCTTTCATTTA92703
rs73091382snpA/G0.03568150.128715intron-variantTMEM183AGRCh38.p71:203014677TAGTTGTTAAATAAA[A/G]GCCTTAAGAACAAAA92703
rs73091383snpC/G/T0.003986910.0444912intron-variantTMEM183AGRCh38.p71:203015149CTCTTTTCACTTTCT[C/G/T]TACTCCATGTCTGGG92703
rs74136931snpA/G0.0007984030.0199641intron-variantTMEM183AGRCh38.p71:203020689AGAGAAGATAAAAGT[A/G]TATCTCACTAGCTTT92703
rs74136932snpC/T0.03568150.128715utr-variant-3-prime, downstream-variant-500B, nc-transcript-variantTMEM183AGRCh38.p71:203024400GTGAGCTGGATATTA[C/T]CTGGATATTGCCAGG92703
rs74341968snpC/T0.06521440.168387intron-variantTMEM183AGRCh38.p71:203013043GGAAATTTTAATAGT[C/T]GTTTGCCTTCTCTTT92703
rs74821472snpA/C0.001197370.0244387intron-variantTMEM183AGRCh38.p71:203015457GTTTTTGTATTTATG[A/C]AGCCTTATGTATAGT92703
rs75329371snpC/G/T0.01091430.0730628intron-variantTMEM183AGRCh38.p71:203016199ATGGTAGGCCTGTTA[C/G/T]CATGGCTTGTCTCCA92703
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