TEP1
SNP - dbSNP
dbSNPTypeAllelesHetSe(het)Fxn-classGene NameAssemblyChr-posSequenceEntrez Gene
rs872072snpA/G0.4993540.0179596intron-variantTEP1GRCh38.p714:20390854TCAGAACTGTGTATT[A/G]TCTGTGCCTTTACCA7011
rs872073snpC/T0.3474630.230219intron-variantTEP1GRCh38.p714:20390925TTTGGATGGTGGGTG[C/T]TGAGTGTCTGACCTG7011
rs872074snpC/T0.2795720.248245synonymous-codon, nc-transcript-variantTEP1GRCh38.p714:20391046GACGTCCACCTGCTC[C/T]GCCCTCGTGATCATC7011
rs938886snpC/G0.387330.208903missense, nc-transcript-variantTEP1GRCh38.p714:20369542GGCCAGGTTCCATAG[C/G]ATCCCATCAGAGCTG7011
rs938887snpA/G0.366760.221059synonymous-codon, nc-transcript-variantTEP1GRCh38.p714:20379043AGTAAGAAAGAGTGT[A/G]TCATCGGAGAGGAAC7011
rs938892snpC/T0.4068140.194704intron-variantTEP1GRCh38.p714:20399330GGACTTAATTTCTTA[C/T]CGAAAATGATCTAGA7011
rs945009snpC/T0.3797460.213696intron-variantTEP1GRCh38.p714:20395099TTTTCTGTGACATGT[C/T]TGTTTTTCTTTTTGT7011
rs945010snpC/G0.3267410.23793intron-variantTEP1GRCh38.p714:20394983TACCATCAGCAGGCT[C/G]AAAGACAGATGTACC7011
rs945011snpC/T0.01632760.0888696synonymous-codon, nc-transcript-variantTEP1GRCh38.p714:20386575TTTCCGAGACATGCA[C/T]GGGGAGCGGGACCTG7011
rs1108613snpC/T0.435980.167067intron-variantTEP1GRCh38.p714:20380804TTGGCATTTTCAACT[C/T]GAAATGGAAATTTGA7011
rs1108614snpC/G0.4516080.147832intron-variantTEP1GRCh38.p714:20380843TCCCTGACACCCACA[C/G]CCCTGCCCCAACCCT7011
rs1112141snpA/G0.0003992810.0141238GRCh38.p714:20416515cagagtaggacccag[A/G]catcagtagtttttg7011
rs1618089snpC/T0.3570240.225933intron-variantTEP1GRCh38.p714:20397486AGTCTTGCTTTGTCA[C/T]CCAGGCTGCAGTGCA7011
rs1713417snpC/T0.2367010.249646intron-variantTEP1GRCh38.p714:20395652AGAAGCTGCCTAACT[C/T]GGAAATTTACCTGTC7011
rs1713418snpC/T0.4980090.0314867utr-variant-3-prime, nc-transcript-variantTEP1GRCh38.p714:20366650GAGTTTTACTCTCAC[C/T]GTACCCTGATTCCAG7011
rs1713419snpC/T0.4999370.0055907utr-variant-3-prime, nc-transcript-variantTEP1GRCh38.p714:20366389AATCCTGCAGCGAAC[C/T]ATGGCATGGCATCAT7011
rs1713423snpC/T0.4732660.112482intron-variantTEP1GRCh38.p714:20391914CCCAGTCCTCTACAC[C/T]AGAAATGGAGTGGGC7011
rs1713424snpC/T0.4948550.0504572intron-variantTEP1GRCh38.p714:20392831ttaaagaaacacaca[C/T]gaaataaggaaaggt7011
rs1713425snpA/G0.4983920.028309intron-variantTEP1GRCh38.p714:20390015GGGCAGTTGTTAAAG[A/G]TGGACATTATTAAAC7011
rs1713434snpC/T0.4835630.0891524intron-variantTEP1GRCh38.p714:20413368CCTGCGCTCGGACCC[C/T]ACCTTAGACTGGGGC7011
rs1713435snpA/G0.1930280.243422GRCh38.p714:20415771gatcctaattaaaac[A/G]agttttcagctacat7011
rs1713436snpC/T0.2294290.249152GRCh38.p714:20415790TTTCAGCTACATGAA[C/T]GACTGGCAAGTTATT7011
rs1713438snpC/T0.06372350.166737intron-variantTEP1GRCh38.p714:20407814GTATGCTCTTGTCTC[C/T]AGCTTTCAGTGTCTC7011
rs1713439snpA/G0.4429260.158996intron-variantTEP1GRCh38.p714:20407591CACTTTGGGAGGCCA[A/G]GGCGGGCGGATCACT7011
rs1713440snpA/T0.4978030.033074intron-variantTEP1GRCh38.p714:20407110TTCAGAATCACTAGA[A/T]AGACACACATTGCTT7011
rs1713441snpC/T0.4119140.190483intron-variant, upstream-variant-2KBTEP1GRCh38.p714:20403014GTGTGCCACCACGCT[C/T]GGCTAATTTTTGTGT7011
rs1713442snpA/Gutr-variant-3-prime, nc-transcript-variantTEP1GRCh38.p714:20367632tttttttttttttta[A/G]acagagtctcgctct7011
rs1713443snpA/G0.4339630.169285intron-variantTEP1GRCh38.p714:20369120tcacaccattctcct[A/G]cctcagactcccgag7011
rs1713444snpA/C0.4339630.169285intron-variantTEP1GRCh38.p714:20369121CACACCATTCTCCTG[A/C]CTCAGACTCCCGAGT7011
rs1713446snpC/T0.4487080.151707intron-variantTEP1GRCh38.p714:20369976TGGAGTGCAGTGGCG[C/T]GATCTCGGTTCACTG7011
rs1713447snpC/T0.4345430.168653intron-variantTEP1GRCh38.p714:20370257CGATGTATTTTTACA[C/T]GTGCATCCACCCATG7011
rs1713448snpA/G0.3994670.200399intron-variantTEP1GRCh38.p714:20373154ATGTGTCATCTGGAG[A/G]AGAAAGGACGTGTTT7011
rs1713449snpC/T0.382810.211806missense, nc-transcript-variantTEP1GRCh38.p714:20373548CCCCATCTAGCCCGA[C/T]GGTTACCACCAGAAG7011
rs1713455snpA/G0.2618840.249717intron-variantTEP1GRCh38.p714:20381855TATACAGAGGGCCCC[A/G]GCTCAAAGAAGGGAA7011
rs1713456snpC/T0.3243470.238689missense, nc-transcript-variantTEP1GRCh38.p714:20381934AGACTCTGGACGAGG[C/T]AGGCAAACGGGCCCA7011
rs1713457snpC/G0.1062790.204562missense, nc-transcript-variantTEP1GRCh38.p714:20381997ACTGCTTCTTCCCAG[C/G]TCTTAGTCCCCTTCG7011
rs1713458snpG/T0.2985420.245242synonymous-codon, nc-transcript-variantTEP1GRCh38.p714:20384611TCACCTGCGGCAGGT[G/T]ATCCCTTTCTGTCTG7011
rs1760889snpA/C0.1989440.244731GRCh38.p714:20416141GCCTTATAAAGCTGG[A/C]CTTCAGAAGAAAGGC7011
rs1760890snpG/T0.2450610.249951upstream-variant-2KBTEP1GRCh38.p714:20413630GGCCCCAGAAAAGGC[G/T]GCAGGGGTCCTGGGC7011
rs1760891snpA/C0.3248550.23853intron-variantTEP1GRCh38.p714:20413265GGGCCGGTTAGGAAC[A/C]ACCCGAGACTCAGCT7011
rs1760892snpA/G0.4390850.163545intron-variantTEP1GRCh38.p714:20412775GTTACTCGGAAGGCT[A/G]AGGCAGGAGAATCGC7011
rs1760893snpG/T0.2487550.249997intron-variantTEP1GRCh38.p714:20412501TTAGTATAAAACTGT[G/T]AGCAATGTTTACTTC7011
rs1760894snpA/G0.4368340.166111intron-variantTEP1GRCh38.p714:20408955TTGCGAGGCCTCTCT[A/G]CTAAGTAGGGATCAA7011
rs1760895snpA/G0.379550.213815intron-variantTEP1GRCh38.p714:20408948GCCTCTCTACTAAGT[A/G]GGGATCAAACTGATA7011
rs1760896snpG/T0.4948960.0502606intron-variantTEP1GRCh38.p714:20408844CCATTCCTTTTTGTT[G/T]TTTTTTTTTTTAAGA7011
rs1760897snpC/T0.4447060.156811missense, nc-transcript-variantTEP1GRCh38.p714:20408094TGCCTGGCCACCCTC[C/T]CTAGTCTAAAGAGCA7011
rs1760898snpA/C0.409390.1926intron-variant, missense, nc-transcript-variantTEP1GRCh38.p714:20404722GAATGTGGCCAATAA[A/C]ATCTTGGCCATTGCT7011
rs1760899snpA/G0.405950.195396intron-variantTEP1GRCh38.p714:20399863TATGAAGATAATTCT[A/G]TATGCACCCATCTCC7011
rs1760900snpC/T0.4157270.187175intron-variantTEP1GRCh38.p714:20399539AAAAATAAATATAAA[C/T]AAATAAAAGGAAATA7011
rs1760901snpC/G0.3899030.207189intron-variantTEP1GRCh38.p714:20396287GAGATGGGGTTTTGC[C/G]ATGTTGGCAAGGCTG7011
rs1760903snpC/T0.4979120.0322408missense, nc-transcript-variantTEP1GRCh38.p714:20384658TCTGAAGAGGCCGCA[C/T]GTCGGATCTCAGAAC7011
rs1760904snpC/T0.4921490.0621596missense, nc-transcript-variantTEP1GRCh38.p714:20383870GGGGCCAAGGTGGCA[C/T]CATTAGTCTTCTTCC7011
rs1760906snpC/T0.4429260.158996intron-variantTEP1GRCh38.p714:20376859GTATGAAAATACACA[C/T]GTGCGATTTTGTTTT7011
rs1760907snpA/G0.439780.162738intron-variantTEP1GRCh38.p714:20376700AGACTTTGCTGTGAA[A/G]AGGGATAGGTTTCCC7011
rs1760908snpC/T0.3862390.209628intron-variantTEP1GRCh38.p714:20375730GGGCCAGGGGTGGCA[C/T]AGAGCCCAGCTGGGT7011
rs1760909snpA/G0.382170.212205intron-variantTEP1GRCh38.p714:20373003CAGCACAGGTGAGTC[A/G]GTGTACCCTTGGTTC7011
rs1760910snpA/G0.005972470.0543191utr-variant-3-prime, nc-transcript-variantTEP1GRCh38.p714:20366658AGGGCACTGAGTTTT[A/G]CTCTCACTGTACCCT7011
rs1760911snpA/Gdownstream-variant-500BTEP1GRCh38.p714:20365275aaaaaaaaaaaaaag[A/G]aaaaaaagaaaGCAA7011
rs1878704snpC/T0.02149390.101416intron-variantTEP1GRCh38.p714:20405622GTTGGTCCTTGTTAC[C/T]TCTCTTCTCATTTCT7011
rs2104977snpC/T0.2208430.248294intron-variantTEP1GRCh38.p714:20370554tacaatggaatacta[C/T]atggcaaaaaaatta7011
rs2104978snpA/G0.1052230.203813missense, nc-transcript-variantTEP1GRCh38.p714:20368874CTGTCACAGCCCTCC[A/G]TGTGCTACCTGAGTT7011
rs2151753snpC/T0.2749290.248754intron-variantTEP1GRCh38.p714:20412169AGCCATCATTTTTTA[C/T]GTGTTTGTCACACTG7011
rs2184282snpA/G0.2532640.249979intron-variantTEP1GRCh38.p714:20412001AATATTTACATATGA[A/G]TGAGAGATTAGCCTT7011
rs2228026snpC/T0.09226160.193955synonymous-codon, nc-transcript-variantTEP1GRCh38.p714:20395890CGCCCATGATGCCAT[C/T]GATGCCCTCGAGGCT7011
rs2228030snpA/G0.02115780.100654synonymous-codon, nc-transcript-variantTEP1GRCh38.p714:20382053TTCAGGTTTGACTGT[A/G]GACCAGCTGCACGGA7011
rs2228034snpA/G0.02258130.104149synonymous-codon, nc-transcript-variantTEP1GRCh38.p714:20368894CTTTGAGATTCACTC[A/G]GGCTCTGTCACAGCC7011
rs2228035snpA/G0.1128240.209004intron-variant, missense, nc-transcript-variantTEP1GRCh38.p714:20403814CTGCCATGACGGACA[A/G]ATTTGCCCAGTTTGA7011
rs2228036snpG/T0.3980840.201435synonymous-codon, nc-transcript-variantTEP1GRCh38.p714:20395518CCGTCAGCAGCTTCG[G/T]ATGGCAATGAGGATA7011
rs2228039snpC/T0.1148090.210294synonymous-codon, nc-transcript-variantTEP1GRCh38.p714:20381010ACTTCTTTCGAAGTT[C/T]CTTACCAACCTCCAT7011
rs2228041snpA/G0.09907440.199302missense, nc-transcript-variantTEP1GRCh38.p714:20384108AGGACACAGTGCAAC[A/G]GCTGATGCTGCCCCA7011
rs2228042snpA/G0.1054980.204008synonymous-codon, nc-transcript-variantTEP1GRCh38.p714:20376224AAGGCAGCTGCTGAC[A/G]CGGCCACACAAGGCA7011
rs2229100snpA/G0.007247120.0597582missense, nc-transcript-variantTEP1GRCh38.p714:20382275CTGGAGAAGGAGCAC[A/G]GGCCTGATGTCCTTC7011
rs2229101snpG/T0.1156860.210855synonymous-codon, nc-transcript-variantTEP1GRCh38.p714:20377362CAAGGAATGCTCCCT[G/T]CAGTCCCTCTGGCTC7011
rs2275009snpC/T0.2692840.249255intron-variantTEP1GRCh38.p714:20404581TCCCTGAGCTTGGGC[C/T]TTCACTTCATTCCTT7011
rs2297612snpA/T0.3401080.233197intron-variant, upstream-variant-2KBTEP1GRCh38.p714:20401660AGGGATCGGATGGTC[A/T]TACAATCTGCTTTAT7011
rs2297613snpA/T0.0002800910.0118308missense, nc-transcript-variantTEP1GRCh38.p714:20391641GGTCTATCTGACAGA[A/T]GCTAATGCAGACAGG7011
rs2297614snpC/T0.4957710.0457907intron-variantTEP1GRCh38.p714:20383681CCCCTGCTTTTTTTT[C/T]CTCTCCCACTGACCC7011
rs2297615snpA/T0.3801130.213473intron-variantTEP1GRCh38.p714:20378362AAGAAGGTCCAGTGT[A/T]GCTCTTGGGGGAAGC7011
rs2319193snpG/T0.4158910.18703intron-variantTEP1GRCh38.p714:20398748TTTAGAGGCCAGGCC[G/T]GTCAGTCCGTCACCA7011
rs2319194snpA/C0.3265060.238006intron-variantTEP1GRCh38.p714:20400038GCATGCGCCTGTAAT[A/C]CCAGCTACTCGGGAG7011
rs2678685snpG/T0.4959630.0447464intron-variantTEP1GRCh38.p714:20411152TGAAATACAACTCCT[G/T]AAGGTAAGGGCTCCT7011
rs2781364snpC/Tintron-variantTEP1GRCh38.p714:20394664GGTGAAACCCCCTGT[C/T]TACTAAAAATACAAA7011
rs2781365snpC/Tintron-variantTEP1GRCh38.p714:20394499agagtgagactctgt[C/T]tcaaaaaaaaaaaaa7011
rs2945461snpA/G0.3380690.233974intron-variantTEP1GRCh38.p714:20394911AAAAATAAGTGTAAG[A/G]TACTGATGAACCACT7011
rs3220660microsatellite(CA)14/24/25/26/27/28/290.7589640.120738intron-variantTEP1GRCh38.p714:20372411GCTATAATGANGATA[(CA)14/24/25/26/27/28/29]ATATTCCTGGGGCTT7011
rs3748336snpA/G0.006403980.0562226synonymous-codon, nc-transcript-variantTEP1GRCh38.p714:20408146GTCTGGGTGGGCAGA[A/G]ACATGTCCATGTGGT7011
rs3762145snpC/T0.2602270.249791intron-variantTEP1GRCh38.p714:20405129AGATATTTCCCACCG[C/T]GCTCTTCTTTGCTTC7011
rs3762146snpA/G0.379550.213815intron-variantTEP1GRCh38.p714:20405365CCACCCCCAACATGA[A/G]GCTAGTCACCACCCC7011
rs3818768snpA/G0.01820190.0936463intron-variantTEP1GRCh38.p714:20370952ATTGCATTTTTTCCC[A/G]TGTCTCTCTTGTCTT7011
rs4246977snpC/T0.4455920.155704upstream-variant-2KBTEP1GRCh38.p714:20414432cccaatgcgatggta[C/T]ttagggtgggatctc7011
rs4280143snpA/C0.425740.177808intron-variantTEP1GRCh38.p714:20398532AAGAGTGAAGGGGTG[A/C]CATTAATGCCCTCAG7011
rs4981171snpC/T0.09470690.195918intron-variantTEP1GRCh38.p714:20390785AGACTTCATGTTATG[C/T]GGTTGCACAGTAAGC7011
rs4981173snpG/T0.08509190.187897intron-variantTEP1GRCh38.p714:20397438CGCTTGAAACCAAAA[G/T]GCGAAGGTTGCAGTG7011
rs4981175snpA/G0.4852550.0845871intron-variant, upstream-variant-2KBTEP1GRCh38.p714:20402930TTGGGAGGTCAAGGC[A/G]GGTGGATCACGAGGT7011
rs4981176snpG/T0.01151440.0749975intron-variant, upstream-variant-2KBTEP1GRCh38.p714:20402962AGGAGTTCGAGACCA[G/T]CCTGGCCAACATGGT7011
rs4982007snpA/C6.85025e-050.00585206intron-variantTEP1GRCh38.p714:20368786CACACACACACACAC[A/C]CACACACTTACCAGC7011
rs4982017snpA/G0.07152230.175059intron-variantTEP1GRCh38.p714:20376776CAGAATGAAGGTGAA[A/G]GAATGAGTGGAAACA7011
rs4982038snpA/G0.3509820.228698intron-variantTEP1GRCh38.p714:20394383tgtctcaactcagac[A/G]tcactagcatatttc7011
rs4982039snpG/T0.05660690.158427intron-variantTEP1GRCh38.p714:20394967AGCCTACAAAACAGA[G/T]GGTACATCTGTCTTT7011
rs4982042snpC/G0.0847280.187577intron-variantTEP1GRCh38.p714:20396849ACTTGAGCCCAGAAC[C/G]CAGGAATTAGAGTCC7011
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