TMEM129
SNP - dbSNP
dbSNPTypeAllelesHetSe(het)Fxn-classGene NameAssemblyChr-posSequenceEntrez Gene
rs712982snpG/T0.2032670.245593intron-variantTMEM129GRCh38.p74:1717906ACCTCCCCCAGATTC[G/T]TGGGGAGCACTCAGG92305
rs712983snpC/T0.2032670.245593intron-variantTMEM129GRCh38.p74:1718090AGAGCCAGGCTCTGG[C/T]GCCACGACCCCTGGG92305
rs743569snpG/T0.4747230.109542intron-variantTMEM129GRCh38.p74:1717893AGGGCTGCACTGTCC[G/T]GAGTGCTCCCCAAGA92305
rs798751snpA/G0.42310.180378intron-variantTMEM129GRCh38.p74:1717845CAGCCTGGGCACGGG[A/G]CGGACCTAGGAGCAA92305
rs798752snpA/C0.05768910.159739missenseTMEM129GRCh38.p74:1718585GCTTCAGAAAAGCGG[A/C]TCCACGCCCTCAGCC92305
rs798753snpA/G0.06818860.171594intron-variantTMEM129GRCh38.p74:1718741GAGTGGGTAAAGCCC[A/G]ATTACCCTGGGAGCT92305
rs798754snpA/G0.4411580.161117intron-variant, utr-variant-5-primeTMEM129GRCh38.p74:1719030GCATCCCAGAGCTGA[A/G]AAGTTATGTGCGAGA92305
rs798755snpA/G0.3610290.223992intron-variant, utr-variant-5-primeTMEM129GRCh38.p74:1719097AGAGGACACGGAGCC[A/G]GCTTCAGGGCCCTGC92305
rs812251snpC/T0.240190.249807intron-variant, upstream-variant-2KBTMEM129, TACC3GRCh38.p74:1719976GGCTGCGTCTGCCCC[C/T]GTGTCCTCCAGAGGT92305
rs1044173snpA/G00utr-variant-3-primeTMEM129GRCh38.p74:1716195TGGCTGTTTGAGGCA[A/G]AGGTGATGGACTCCG92305
rs1044202snpA/G00utr-variant-3-primeTMEM129GRCh38.p74:1716064TCAAGGGCTGCCAAA[A/G]AGGGGCAGTGGGTTG92305
rs1044221snpA/Cutr-variant-3-primeTMEM129GRCh38.p74:1715982TTGTAGCCAAATGAC[A/C]CCATATTTAATAAAA92305
rs1348869snpA/G0.2815770.247998downstream-variant-500BTMEM129GRCh38.p74:1715579GACGCAGCTGCAAAC[A/G]TAAGTGAACCGGAAA92305
rs1374467snpA/G0.240190.249807upstream-variant-2KB, intron-variantTMEM129, TACC3GRCh38.p74:1722777CGTGAGGACCTGGGC[A/G]GCCCTGGAACCTGGG92305
rs1374468snpC/T0.240190.249807upstream-variant-2KB, intron-variantTMEM129, TACC3GRCh38.p74:1722852TCAGCTCTGGGCTTC[C/T]CTTGTTTGCGCATCG92305
rs1374469snpC/T0.3670910.220884upstream-variant-2KB, intron-variantTMEM129, TACC3GRCh38.p74:1723072TGGCCCGGGCTTTTC[C/T]GTCTCTTGACTTCTG92305
rs1374470snpC/T0.2541050.249966upstream-variant-2KB, intron-variantTMEM129, TACC3GRCh38.p74:1723075CCCGGGCTTTTCCGT[C/T]TCTTGACTTCTGCTT92305
rs1665360snpA/G0.2404780.249819upstream-variant-2KB, intron-variantTMEM129, TACC3GRCh38.p74:1723280TCTGCCAAGAGACAC[A/G]TGTGGGAGGTGTGAG92305
rs1665361snpA/G0.2399020.249796upstream-variant-2KB, intron-variantTMEM129, TACC3GRCh38.p74:1723344GGTCGTGCCCCTTGC[A/G]GCAGCTGTCACGTCT92305
rs1793990snpC/T0.2361440.249616intron-variant, upstream-variant-2KB, utr-variant-5-primeTMEM129, TACC3GRCh38.p74:1720460GAGCGCGCTTAGGGG[C/T]GCCGCCGGCACTGAC92305
rs2236786snpA/G0.3369530.234391synonymous-codon, intron-variantTMEM129GRCh38.p74:1717567CCTGTTCCTGGAGAC[A/G]TTTGCCTCCCTGGTA92305
rs2236787snpA/T0.4850740.0850883utr-variant-3-primeTMEM129GRCh38.p74:1717156GGGCCTTGAGGTGAC[A/T]CTGTGTCTCCCCCCA92305
rs2236788snpC/G0.3740050.218342utr-variant-3-primeTMEM129GRCh38.p74:1717143ACTCTGTGTCTCCCC[C/G]CAAAGCCACAGGGCA92305
rs2592825snpC/GGRCh38.p74:1722385AGGGCGAAAACCTAA[C/G]CGTCGTCCGTAAGTC92305
rs2592826snpA/G0.2404780.249819GRCh38.p74:1722451GGCATCTACTCCTTG[A/G]GCTCCAGAAGCCTGT92305
rs2592827snpA/G0.2404780.249819GRCh38.p74:1722533ACAGTGGGCTTCTCA[A/G]GCTGCAGCACCGACC92305
rs2854907snpC/Gutr-variant-3-primeTMEM129GRCh38.p74:1716175GATGGACTCCGGGGG[C/G]CTGACACTTGGGATT92305
rs2854912snpA/G0.240190.249807upstream-variant-2KB, intron-variantTMEM129, TACC3GRCh38.p74:1722484GGAGGTTAAGAGCAG[A/G]AGGGAAGCAGGGAAA92305
rs2854913snpA/T0.4746340.109726upstream-variant-2KB, utr-variant-5-primeTMEM129, TACC3GRCh38.p74:1721410TCCAATGGGAAGCTG[A/T]GCCTCGCCGGCTCCG92305
rs2854914snpA/G0.06818860.171594intron-variant, upstream-variant-2KBTMEM129, TACC3GRCh38.p74:1719946CCTGGGAGGACAGAT[A/G]GCCAGTGGCTGGCCA92305
rs2854915snpC/T0.4277270.175821intron-variant, upstream-variant-2KBTMEM129, TACC3GRCh38.p74:1719927AGTGGCTGGCCAGGT[C/T]TGCCACTCTGGGGAT92305
rs2854916snpC/T0.4745440.10991intron-variant, upstream-variant-2KBTMEM129, TACC3GRCh38.p74:1719621AGACAGCACAGCTGG[C/T]CTCACAGTCGGATGT92305
rs2854917snpA/G0.4747230.109542intron-variant, utr-variant-5-primeTMEM129GRCh38.p74:1718823AGCAGCAAATTAAAA[A/G]CCTTTTCCGCTAATA92305
rs3134864snpC/T0.005178220.0506191upstream-variant-2KB, intron-variantTMEM129, TACC3GRCh38.p74:1722052GGTGTCCGCCGCAGG[C/T]GGCCTAGATGGAGTT92305
rs3134865snpA/G0.4221580.181278upstream-variant-2KB, utr-variant-5-primeTMEM129, TACC3GRCh38.p74:1721552CCGGGGGCCAAGCCT[A/G]GCTGCTACCGCCGTC92305
rs3134866snpC/T0.4223150.181128upstream-variant-2KB, utr-variant-5-primeTMEM129, TACC3GRCh38.p74:1721538TAGCTGCTACCGCCG[C/T]CGCGCTTCTAGCCCT92305
rs3806769snpA/G0.0003992810.0141238intron-variant, upstream-variant-2KBTMEM129, TACC3GRCh38.p74:1719944CCTGGCCAGCCACTG[A/G]CCATCTGTCCTCCCA92305
rs3822047snpA/G0.2692670.249256intron-variant, upstream-variant-2KBTMEM129, TACC3GRCh38.p74:1719769TGAGAGATGGATGGG[A/G]CTGAGTGGGGCTGGG92305
rs3822048snpC/T0.278930.24832intron-variant, upstream-variant-2KBTMEM129, TACC3GRCh38.p74:1720172TCCCCAGCCTCTGCC[C/T]CTGTGGCGCCCCCAA92305
rs3836608in-del-/Tintron-variant, upstream-variant-2KBTMEM129, TACC3GRCh38.p74:1719387attttttgtattttt[-/T]agtggagatggggtt92305
rs6837127snpC/Tutr-variant-5-prime, upstream-variant-2KBTMEM129, TACC3GRCh38.p74:1721064ATGGAGTcccgccgc[C/T]cggccgcccgcgggg92305
rs6837277snpC/Tutr-variant-5-prime, upstream-variant-2KBTMEM129, TACC3GRCh38.p74:1721072ccgccgcccggccgc[C/T]cgcggggcACTCTAG92305
rs6846887snpA/Gutr-variant-5-prime, upstream-variant-2KBTMEM129, TACC3GRCh38.p74:1721081ggccgcccgcggggc[A/G]cTCTAGGGCATGGAG92305
rs7695106snpA/G0.00239330.0345097intron-variant, utr-variant-5-primeTMEM129GRCh38.p74:1719280AACTAGGggccgggt[A/G]cagtggctcacacct92305
rs10030268snpA/G0.02484320.108648utr-variant-5-prime, upstream-variant-2KBTMEM129, TACC3GRCh38.p74:1721132CGGGGCGCTCTGGGA[A/G]ATGCAGTCCCCGTGC92305
rs11552262snpC/T0.347020.230407synonymous-codon, utr-variant-5-primeTMEM129GRCh38.p74:1718619CTTTGCAGGCTACTA[C/T]GTGGGCATGTGCCTT92305
rs11931848snpA/G0.04525280.143452intron-variant, upstream-variant-2KB, utr-variant-5-primeTMEM129, TACC3GRCh38.p74:1720398GACTTGGTGGGCCGG[A/G]GCATCCCTTGCCCAA92305
rs11945830snpC/T0.0004567250.0151048missenseTMEM129GRCh38.p74:1718531TGGAGGGGAGGGTCA[C/T]GGCCAGCAGCAGGAA92305
rs12331136snpC/T0.007162660.059414upstream-variant-2KB, intron-variantTMEM129, TACC3GRCh38.p74:1722916CAGCCTGGTCTTGTC[C/T]CGCTGCCTAGCCCGG92305
rs17132038snpA/G0.07115250.174681intron-variant, upstream-variant-2KBTMEM129, TACC3GRCh38.p74:1720063TCCAATCAGCTGAGA[A/G]AGGGACCTTCCAGAG92305
rs17802841snpA/G0.1371870.223099intron-variantTMEM129GRCh38.p74:1718031TGCCTGGTGTCACAC[A/G]AGCCCAGGAGTGTTG92305
rs34742489in-del-/Cupstream-variant-2KB, utr-variant-5-primeTMEM129, TACC3GRCh38.p74:1721401GAGGGAGGGCGGAGC[-/C]GGCGAGGCACAGCTT92305
rs35715226in-del-/Cutr-variant-3-primeTMEM129GRCh38.p74:1716280TGTCAGGGCTGTGCC[-/C]TGGGGCCTGGCCAAC92305
rs35731068in-del-/Tintron-variant, utr-variant-5-primeTMEM129GRCh38.p74:1719236CCAGTCACTGCATTT[-/T]CAAGGTAACATGACA92305
rs55716619snpA/G0.2821050.24793upstream-variant-2KB, intron-variantTMEM129, TACC3GRCh38.p74:1722816GAGGCTCTGATGTGG[A/G]AGTTCCTTGGCACCT92305
rs55784570snpA/G0.2689950.249277upstream-variant-2KB, intron-variantTMEM129, TACC3GRCh38.p74:1721976CTTGGCTCTTTGTTG[A/G]CTCCCAGCACGCGGA92305
rs56215097snpC/G0.50utr-variant-3-primeTMEM129GRCh38.p74:1716879TCCAGGGAATGGCTC[C/G]GGGGCAGACGCTGTG92305
rs56306836snpC/T0.2818410.247964upstream-variant-2KB, intron-variant, utr-variant-5-primeTMEM129, TACC3GRCh38.p74:1721773AAGCGTCCCCCACGG[C/T]TCCTCCTGGGGCCGC92305
rs60976521in-del-/G00upstream-variant-2KB, utr-variant-5-primeTMEM129, TACC3GRCh38.p74:1721385GGGGGGTGGGGGGGG[-/G]AGGGAGGGCGGAGCC92305
rs61337960snpA/G0.1371870.223099upstream-variant-2KB, intron-variantTMEM129, TACC3GRCh38.p74:1722579CTCTCTCTTCTCCAG[A/G]ACCCTCCCCAACTTT92305
rs61675353snpG/T0.487490.0780934intron-variant, utr-variant-5-primeTMEM129GRCh38.p74:1719067GCAAGTCTCAAAGAA[G/T]GATGGGACATGTCCA92305
rs61738628snpA/G0.0001377130.00829683missense, utr-variant-3-primeTMEM129GRCh38.p74:1717335TGGGGCGGCAGTAAC[A/G]CTGCTGGCACTCGCC92305
rs61741140snpA/C0.01371170.0816569synonymous-codon, intron-variantTMEM129GRCh38.p74:1717663GAGCTCCCCGTACTC[A/C]GTGGAGTTCAGCCTG92305
rs61745200snpA/C/G0.0001902770.00975204missenseTMEM129GRCh38.p74:1718161TCTTACCAGATGTCA[A/C/G]AGGCCTGCACAGCAG92305
rs62285072snpG/Tintron-variantTMEM129GRCh38.p74:1717720TGCAGGGCAAAGGGA[G/T]CGGAAGATGGAGGCT92305
rs62285073snpA/G0.2823690.247896intron-variantTMEM129GRCh38.p74:1717781CACCAGGACCAACCA[A/G]GAGAGATGGCCCTAA92305
rs62285100snpC/T0.2786640.248351upstream-variant-2KB, intron-variant, utr-variant-5-primeTMEM129, TACC3GRCh38.p74:1721850GACCGCCGGGCTGGG[C/T]CCCCTGGATGGTGGC92305
rs62285103snpC/T0.09844310.198823upstream-variant-2KB, intron-variantTMEM129, TACC3GRCh38.p74:1723062GGTTTCTTATTGGCC[C/T]GGGCTTTTCCGTCTC92305
rs75291711snpA/G0.06930130.172766utr-variant-3-primeTMEM129GRCh38.p74:1716396CTGGGAGACCCTAGG[A/G]GAGTGGGTAGCCTGG92305
rs75603613snpA/G0.01427360.0832652utr-variant-3-primeTMEM129GRCh38.p74:1716566TGAGAAACCCGGAGG[A/G]GCAGCCCCACAAATG92305
rs76977466snpG/T0.02678780.112589utr-variant-3-primeTMEM129GRCh38.p74:1716778GAGAATGCGGTCCAG[G/T]TCTGGCACGTAACTG92305
rs76998502snpC/T0.01652780.0893908upstream-variant-2KB, intron-variantTMEM129, TACC3GRCh38.p74:1722895TCCTCTGGGCCTTCA[C/T]CCTCTCAGCCTGGTC92305
rs77232207snpC/T0.1371870.223099upstream-variant-2KB, intron-variantTMEM129, TACC3GRCh38.p74:1722822CTGATGTGGAAGTTC[C/T]TTGGCACCTGTTGCT92305
rs77561723snpA/C0.0003992810.0141238missenseTMEM129GRCh38.p74:1718567GCCAGGCCTCAGGGG[A/C]CTGGCTGAGGGCGTG92305
rs78203006snpA/G0.07410630.177655upstream-variant-2KB, intron-variantTMEM129, TACC3GRCh38.p74:1722954GAGCAGACCAGAGCC[A/G]CTGTCCTGCTTTTCT92305
rs78251206snpA/G0.07226140.17581downstream-variant-500BTMEM129GRCh38.p74:1715881AAGGTGGCTTCTCCA[A/G]TACCCACAGGCCATT92305
rs111254096in-del-/A0.50intron-variant, upstream-variant-2KBTMEM129, TACC3GRCh38.p74:1719394TCTCCACTAAAAAAT[-/A]CAAAAAATTAGCCGG92305
rs112182776snpA/C0.2399020.249796upstream-variant-2KB, intron-variantTMEM129, TACC3GRCh38.p74:1721659GTAGGAGAGCGGCTA[A/C]ACGGCGCGGGGAGGC92305
rs112205518snpA/G00intron-variant, utr-variant-5-primeTMEM129GRCh38.p74:1719347TCACGAGGTCAGATC[A/G]AGACCATCCTGGCTA92305
rs112253035snpA/G0.50upstream-variant-2KB, intron-variantTMEM129, TACC3GRCh38.p74:1723245TCTGAAGCAAGATGG[A/G]GACTCAGTCTGAGGC92305
rs112419137snpA/G0.50upstream-variant-2KB, intron-variantTMEM129, TACC3GRCh38.p74:1723348GTGCCCCTTGCAGCA[A/G]CTGTCACGTCTGTGT92305
rs112780538snpA/C0.50intron-variantTMEM129GRCh38.p74:1717488TGGGCACCCACCCAT[A/C]CACCCGGCCCTGGCC92305
rs113172950snpC/T0.007955320.062565upstream-variant-2KB, intron-variantTMEM129, TACC3GRCh38.p74:1722110CTGCGCCGCTCCACC[C/T]TCCCCCCGCACCGCA92305
rs113260869snpC/Gutr-variant-5-prime, upstream-variant-2KB, intron-variantTMEM129, TACC3GRCh38.p74:1720871CTGTCGAGCTAGGCC[C/G]CCGCCCCGGCGCGCG92305
rs113432645snpA/G0.007955320.062565intron-variant, upstream-variant-2KBTMEM129GRCh38.p74:1719367CATCCTGGCTAACAC[A/G]GTGAAACCCCATCTC92305
rs113898361snpA/G0.50upstream-variant-2KB, intron-variantTMEM129, TACC3GRCh38.p74:1723300GGAGGTGTGAGTTCC[A/G]GAGCAATGAGCACAC92305
rs114268489snpC/T0.04829460.147699intron-variantTMEM129GRCh38.p74:1717833TGCCAGACAGCCCAG[C/T]CTGGGCACGGGACGG92305
rs114305353snpC/G0.04867410.148216intron-variant, upstream-variant-2KBTMEM129, TACC3GRCh38.p74:1720065CAATCAGCTGAGAGA[C/G]GGACCTTCCAGAGCC92305
rs114397142snpA/G0.0009065010.0212704synonymous-codon, upstream-variant-2KB, intron-variantTMEM129, TACC3GRCh38.p74:1720760GAGCCCCGCCGCGTG[A/G]AACTCGTTGGGCGTG92305
rs114623357snpA/G0.04715510.14613intron-variant, upstream-variant-2KB, utr-variant-5-primeTMEM129, TACC3GRCh38.p74:1720320CTTCTCCTGGCCACT[A/G]CCCCCAACCACGACA92305
rs114747829snpA/T0.02685090.112714missenseTMEM129GRCh38.p74:1718497TCACGGGACCAGTAG[A/T]AGATCAGGATGCAGG92305
rs115285310snpC/T0.2174570.247873intron-variant, utr-variant-5-primeTMEM129GRCh38.p74:1719275TAGGTAACTAGGGGC[C/T]GGGTGCAGTGGCTCA92305
rs115455600snpC/T0.1368470.222927upstream-variant-2KB, utr-variant-5-primeTMEM129, TACC3GRCh38.p74:1721565GCTAGGCTTGGCCCC[C/T]GGCGTGGAGCAGACG92305
rs115768485snpA/T0.02678980.112593missenseTMEM129GRCh38.p74:1718498CACGGGACCAGTAGT[A/T]GATCAGGATGCAGGC92305
rs116100549snpC/G0.05450580.156565upstream-variant-2KB, intron-variantTMEM129, TACC3GRCh38.p74:1722012CTGTTGTTCTTTGGT[C/G]CCTTCCGGCCTCCGT92305
rs116187706snpA/C0.04867410.148216utr-variant-3-primeTMEM129GRCh38.p74:1716389TCTGAGCCTGGGAGA[A/C]CCTAGGGGAGTGGGT92305
rs116792017snpC/G0.04791490.147179upstream-variant-2KB, intron-variantTMEM129, TACC3GRCh38.p74:1722170GCACCAGCCTGGGGC[C/G]GGTCCCTTCTCTGCC92305
rs117594966snpA/G0.0003992810.0141238upstream-variant-2KB, intron-variantTMEM129, TACC3GRCh38.p74:1722248AAGGCTGGGTCTGCT[A/G]CTCTCCCGAGCTCCT92305
rs138231306snpC/G1.79716e-050.00299757missenseTMEM129GRCh38.p74:1718313TCGGTAGGTGGTTAC[C/G]TTCATCACCCACGTG92305
rs138401702snpA/C/T0.0007989460.0199715missenseTMEM129GRCh38.p74:1718213TGGTGAGGAGCTGCA[A/C/T]GGGCAAGTTCGAGTC92305
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