SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs872072 | snp | A/G | 0.499354 | 0.0179596 | intron-variant | TEP1 | GRCh38.p7 | 14:20390854 | TCAGAACTGTGTATT[A/G]TCTGTGCCTTTACCA | 7011 |
rs872073 | snp | C/T | 0.347463 | 0.230219 | intron-variant | TEP1 | GRCh38.p7 | 14:20390925 | TTTGGATGGTGGGTG[C/T]TGAGTGTCTGACCTG | 7011 |
rs872074 | snp | C/T | 0.279572 | 0.248245 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20391046 | GACGTCCACCTGCTC[C/T]GCCCTCGTGATCATC | 7011 |
rs938886 | snp | C/G | 0.38733 | 0.208903 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20369542 | GGCCAGGTTCCATAG[C/G]ATCCCATCAGAGCTG | 7011 |
rs938887 | snp | A/G | 0.36676 | 0.221059 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20379043 | AGTAAGAAAGAGTGT[A/G]TCATCGGAGAGGAAC | 7011 |
rs938892 | snp | C/T | 0.406814 | 0.194704 | intron-variant | TEP1 | GRCh38.p7 | 14:20399330 | GGACTTAATTTCTTA[C/T]CGAAAATGATCTAGA | 7011 |
rs945009 | snp | C/T | 0.379746 | 0.213696 | intron-variant | TEP1 | GRCh38.p7 | 14:20395099 | TTTTCTGTGACATGT[C/T]TGTTTTTCTTTTTGT | 7011 |
rs945010 | snp | C/G | 0.326741 | 0.23793 | intron-variant | TEP1 | GRCh38.p7 | 14:20394983 | TACCATCAGCAGGCT[C/G]AAAGACAGATGTACC | 7011 |
rs945011 | snp | C/T | 0.0163276 | 0.0888696 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20386575 | TTTCCGAGACATGCA[C/T]GGGGAGCGGGACCTG | 7011 |
rs1108613 | snp | C/T | 0.43598 | 0.167067 | intron-variant | TEP1 | GRCh38.p7 | 14:20380804 | TTGGCATTTTCAACT[C/T]GAAATGGAAATTTGA | 7011 |
rs1108614 | snp | C/G | 0.451608 | 0.147832 | intron-variant | TEP1 | GRCh38.p7 | 14:20380843 | TCCCTGACACCCACA[C/G]CCCTGCCCCAACCCT | 7011 |
rs1112141 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 14:20416515 | cagagtaggacccag[A/G]catcagtagtttttg | 7011 |
rs1618089 | snp | C/T | 0.357024 | 0.225933 | intron-variant | TEP1 | GRCh38.p7 | 14:20397486 | AGTCTTGCTTTGTCA[C/T]CCAGGCTGCAGTGCA | 7011 |
rs1713417 | snp | C/T | 0.236701 | 0.249646 | intron-variant | TEP1 | GRCh38.p7 | 14:20395652 | AGAAGCTGCCTAACT[C/T]GGAAATTTACCTGTC | 7011 |
rs1713418 | snp | C/T | 0.498009 | 0.0314867 | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20366650 | GAGTTTTACTCTCAC[C/T]GTACCCTGATTCCAG | 7011 |
rs1713419 | snp | C/T | 0.499937 | 0.0055907 | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20366389 | AATCCTGCAGCGAAC[C/T]ATGGCATGGCATCAT | 7011 |
rs1713423 | snp | C/T | 0.473266 | 0.112482 | intron-variant | TEP1 | GRCh38.p7 | 14:20391914 | CCCAGTCCTCTACAC[C/T]AGAAATGGAGTGGGC | 7011 |
rs1713424 | snp | C/T | 0.494855 | 0.0504572 | intron-variant | TEP1 | GRCh38.p7 | 14:20392831 | ttaaagaaacacaca[C/T]gaaataaggaaaggt | 7011 |
rs1713425 | snp | A/G | 0.498392 | 0.028309 | intron-variant | TEP1 | GRCh38.p7 | 14:20390015 | GGGCAGTTGTTAAAG[A/G]TGGACATTATTAAAC | 7011 |
rs1713434 | snp | C/T | 0.483563 | 0.0891524 | intron-variant | TEP1 | GRCh38.p7 | 14:20413368 | CCTGCGCTCGGACCC[C/T]ACCTTAGACTGGGGC | 7011 |
rs1713435 | snp | A/G | 0.193028 | 0.243422 | | | GRCh38.p7 | 14:20415771 | gatcctaattaaaac[A/G]agttttcagctacat | 7011 |
rs1713436 | snp | C/T | 0.229429 | 0.249152 | | | GRCh38.p7 | 14:20415790 | TTTCAGCTACATGAA[C/T]GACTGGCAAGTTATT | 7011 |
rs1713438 | snp | C/T | 0.0637235 | 0.166737 | intron-variant | TEP1 | GRCh38.p7 | 14:20407814 | GTATGCTCTTGTCTC[C/T]AGCTTTCAGTGTCTC | 7011 |
rs1713439 | snp | A/G | 0.442926 | 0.158996 | intron-variant | TEP1 | GRCh38.p7 | 14:20407591 | CACTTTGGGAGGCCA[A/G]GGCGGGCGGATCACT | 7011 |
rs1713440 | snp | A/T | 0.497803 | 0.033074 | intron-variant | TEP1 | GRCh38.p7 | 14:20407110 | TTCAGAATCACTAGA[A/T]AGACACACATTGCTT | 7011 |
rs1713441 | snp | C/T | 0.411914 | 0.190483 | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20403014 | GTGTGCCACCACGCT[C/T]GGCTAATTTTTGTGT | 7011 |
rs1713442 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20367632 | tttttttttttttta[A/G]acagagtctcgctct | 7011 |
rs1713443 | snp | A/G | 0.433963 | 0.169285 | intron-variant | TEP1 | GRCh38.p7 | 14:20369120 | tcacaccattctcct[A/G]cctcagactcccgag | 7011 |
rs1713444 | snp | A/C | 0.433963 | 0.169285 | intron-variant | TEP1 | GRCh38.p7 | 14:20369121 | CACACCATTCTCCTG[A/C]CTCAGACTCCCGAGT | 7011 |
rs1713446 | snp | C/T | 0.448708 | 0.151707 | intron-variant | TEP1 | GRCh38.p7 | 14:20369976 | TGGAGTGCAGTGGCG[C/T]GATCTCGGTTCACTG | 7011 |
rs1713447 | snp | C/T | 0.434543 | 0.168653 | intron-variant | TEP1 | GRCh38.p7 | 14:20370257 | CGATGTATTTTTACA[C/T]GTGCATCCACCCATG | 7011 |
rs1713448 | snp | A/G | 0.399467 | 0.200399 | intron-variant | TEP1 | GRCh38.p7 | 14:20373154 | ATGTGTCATCTGGAG[A/G]AGAAAGGACGTGTTT | 7011 |
rs1713449 | snp | C/T | 0.38281 | 0.211806 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20373548 | CCCCATCTAGCCCGA[C/T]GGTTACCACCAGAAG | 7011 |
rs1713455 | snp | A/G | 0.261884 | 0.249717 | intron-variant | TEP1 | GRCh38.p7 | 14:20381855 | TATACAGAGGGCCCC[A/G]GCTCAAAGAAGGGAA | 7011 |
rs1713456 | snp | C/T | 0.324347 | 0.238689 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20381934 | AGACTCTGGACGAGG[C/T]AGGCAAACGGGCCCA | 7011 |
rs1713457 | snp | C/G | 0.106279 | 0.204562 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20381997 | ACTGCTTCTTCCCAG[C/G]TCTTAGTCCCCTTCG | 7011 |
rs1713458 | snp | G/T | 0.298542 | 0.245242 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20384611 | TCACCTGCGGCAGGT[G/T]ATCCCTTTCTGTCTG | 7011 |
rs1760889 | snp | A/C | 0.198944 | 0.244731 | | | GRCh38.p7 | 14:20416141 | GCCTTATAAAGCTGG[A/C]CTTCAGAAGAAAGGC | 7011 |
rs1760890 | snp | G/T | 0.245061 | 0.249951 | upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20413630 | GGCCCCAGAAAAGGC[G/T]GCAGGGGTCCTGGGC | 7011 |
rs1760891 | snp | A/C | 0.324855 | 0.23853 | intron-variant | TEP1 | GRCh38.p7 | 14:20413265 | GGGCCGGTTAGGAAC[A/C]ACCCGAGACTCAGCT | 7011 |
rs1760892 | snp | A/G | 0.439085 | 0.163545 | intron-variant | TEP1 | GRCh38.p7 | 14:20412775 | GTTACTCGGAAGGCT[A/G]AGGCAGGAGAATCGC | 7011 |
rs1760893 | snp | G/T | 0.248755 | 0.249997 | intron-variant | TEP1 | GRCh38.p7 | 14:20412501 | TTAGTATAAAACTGT[G/T]AGCAATGTTTACTTC | 7011 |
rs1760894 | snp | A/G | 0.436834 | 0.166111 | intron-variant | TEP1 | GRCh38.p7 | 14:20408955 | TTGCGAGGCCTCTCT[A/G]CTAAGTAGGGATCAA | 7011 |
rs1760895 | snp | A/G | 0.37955 | 0.213815 | intron-variant | TEP1 | GRCh38.p7 | 14:20408948 | GCCTCTCTACTAAGT[A/G]GGGATCAAACTGATA | 7011 |
rs1760896 | snp | G/T | 0.494896 | 0.0502606 | intron-variant | TEP1 | GRCh38.p7 | 14:20408844 | CCATTCCTTTTTGTT[G/T]TTTTTTTTTTTAAGA | 7011 |
rs1760897 | snp | C/T | 0.444706 | 0.156811 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20408094 | TGCCTGGCCACCCTC[C/T]CTAGTCTAAAGAGCA | 7011 |
rs1760898 | snp | A/C | 0.40939 | 0.1926 | intron-variant, missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20404722 | GAATGTGGCCAATAA[A/C]ATCTTGGCCATTGCT | 7011 |
rs1760899 | snp | A/G | 0.40595 | 0.195396 | intron-variant | TEP1 | GRCh38.p7 | 14:20399863 | TATGAAGATAATTCT[A/G]TATGCACCCATCTCC | 7011 |
rs1760900 | snp | C/T | 0.415727 | 0.187175 | intron-variant | TEP1 | GRCh38.p7 | 14:20399539 | AAAAATAAATATAAA[C/T]AAATAAAAGGAAATA | 7011 |
rs1760901 | snp | C/G | 0.389903 | 0.207189 | intron-variant | TEP1 | GRCh38.p7 | 14:20396287 | GAGATGGGGTTTTGC[C/G]ATGTTGGCAAGGCTG | 7011 |
rs1760903 | snp | C/T | 0.497912 | 0.0322408 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20384658 | TCTGAAGAGGCCGCA[C/T]GTCGGATCTCAGAAC | 7011 |
rs1760904 | snp | C/T | 0.492149 | 0.0621596 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20383870 | GGGGCCAAGGTGGCA[C/T]CATTAGTCTTCTTCC | 7011 |
rs1760906 | snp | C/T | 0.442926 | 0.158996 | intron-variant | TEP1 | GRCh38.p7 | 14:20376859 | GTATGAAAATACACA[C/T]GTGCGATTTTGTTTT | 7011 |
rs1760907 | snp | A/G | 0.43978 | 0.162738 | intron-variant | TEP1 | GRCh38.p7 | 14:20376700 | AGACTTTGCTGTGAA[A/G]AGGGATAGGTTTCCC | 7011 |
rs1760908 | snp | C/T | 0.386239 | 0.209628 | intron-variant | TEP1 | GRCh38.p7 | 14:20375730 | GGGCCAGGGGTGGCA[C/T]AGAGCCCAGCTGGGT | 7011 |
rs1760909 | snp | A/G | 0.38217 | 0.212205 | intron-variant | TEP1 | GRCh38.p7 | 14:20373003 | CAGCACAGGTGAGTC[A/G]GTGTACCCTTGGTTC | 7011 |
rs1760910 | snp | A/G | 0.00597247 | 0.0543191 | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20366658 | AGGGCACTGAGTTTT[A/G]CTCTCACTGTACCCT | 7011 |
rs1760911 | snp | A/G | | | downstream-variant-500B | TEP1 | GRCh38.p7 | 14:20365275 | aaaaaaaaaaaaaag[A/G]aaaaaaagaaaGCAA | 7011 |
rs1878704 | snp | C/T | 0.0214939 | 0.101416 | intron-variant | TEP1 | GRCh38.p7 | 14:20405622 | GTTGGTCCTTGTTAC[C/T]TCTCTTCTCATTTCT | 7011 |
rs2104977 | snp | C/T | 0.220843 | 0.248294 | intron-variant | TEP1 | GRCh38.p7 | 14:20370554 | tacaatggaatacta[C/T]atggcaaaaaaatta | 7011 |
rs2104978 | snp | A/G | 0.105223 | 0.203813 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20368874 | CTGTCACAGCCCTCC[A/G]TGTGCTACCTGAGTT | 7011 |
rs2151753 | snp | C/T | 0.274929 | 0.248754 | intron-variant | TEP1 | GRCh38.p7 | 14:20412169 | AGCCATCATTTTTTA[C/T]GTGTTTGTCACACTG | 7011 |
rs2184282 | snp | A/G | 0.253264 | 0.249979 | intron-variant | TEP1 | GRCh38.p7 | 14:20412001 | AATATTTACATATGA[A/G]TGAGAGATTAGCCTT | 7011 |
rs2228026 | snp | C/T | 0.0922616 | 0.193955 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20395890 | CGCCCATGATGCCAT[C/T]GATGCCCTCGAGGCT | 7011 |
rs2228030 | snp | A/G | 0.0211578 | 0.100654 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20382053 | TTCAGGTTTGACTGT[A/G]GACCAGCTGCACGGA | 7011 |
rs2228034 | snp | A/G | 0.0225813 | 0.104149 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20368894 | CTTTGAGATTCACTC[A/G]GGCTCTGTCACAGCC | 7011 |
rs2228035 | snp | A/G | 0.112824 | 0.209004 | intron-variant, missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20403814 | CTGCCATGACGGACA[A/G]ATTTGCCCAGTTTGA | 7011 |
rs2228036 | snp | G/T | 0.398084 | 0.201435 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20395518 | CCGTCAGCAGCTTCG[G/T]ATGGCAATGAGGATA | 7011 |
rs2228039 | snp | C/T | 0.114809 | 0.210294 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20381010 | ACTTCTTTCGAAGTT[C/T]CTTACCAACCTCCAT | 7011 |
rs2228041 | snp | A/G | 0.0990744 | 0.199302 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20384108 | AGGACACAGTGCAAC[A/G]GCTGATGCTGCCCCA | 7011 |
rs2228042 | snp | A/G | 0.105498 | 0.204008 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20376224 | AAGGCAGCTGCTGAC[A/G]CGGCCACACAAGGCA | 7011 |
rs2229100 | snp | A/G | 0.00724712 | 0.0597582 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20382275 | CTGGAGAAGGAGCAC[A/G]GGCCTGATGTCCTTC | 7011 |
rs2229101 | snp | G/T | 0.115686 | 0.210855 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20377362 | CAAGGAATGCTCCCT[G/T]CAGTCCCTCTGGCTC | 7011 |
rs2275009 | snp | C/T | 0.269284 | 0.249255 | intron-variant | TEP1 | GRCh38.p7 | 14:20404581 | TCCCTGAGCTTGGGC[C/T]TTCACTTCATTCCTT | 7011 |
rs2297612 | snp | A/T | 0.340108 | 0.233197 | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20401660 | AGGGATCGGATGGTC[A/T]TACAATCTGCTTTAT | 7011 |
rs2297613 | snp | A/T | 0.000280091 | 0.0118308 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20391641 | GGTCTATCTGACAGA[A/T]GCTAATGCAGACAGG | 7011 |
rs2297614 | snp | C/T | 0.495771 | 0.0457907 | intron-variant | TEP1 | GRCh38.p7 | 14:20383681 | CCCCTGCTTTTTTTT[C/T]CTCTCCCACTGACCC | 7011 |
rs2297615 | snp | A/T | 0.380113 | 0.213473 | intron-variant | TEP1 | GRCh38.p7 | 14:20378362 | AAGAAGGTCCAGTGT[A/T]GCTCTTGGGGGAAGC | 7011 |
rs2319193 | snp | G/T | 0.415891 | 0.18703 | intron-variant | TEP1 | GRCh38.p7 | 14:20398748 | TTTAGAGGCCAGGCC[G/T]GTCAGTCCGTCACCA | 7011 |
rs2319194 | snp | A/C | 0.326506 | 0.238006 | intron-variant | TEP1 | GRCh38.p7 | 14:20400038 | GCATGCGCCTGTAAT[A/C]CCAGCTACTCGGGAG | 7011 |
rs2678685 | snp | G/T | 0.495963 | 0.0447464 | intron-variant | TEP1 | GRCh38.p7 | 14:20411152 | TGAAATACAACTCCT[G/T]AAGGTAAGGGCTCCT | 7011 |
rs2781364 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20394664 | GGTGAAACCCCCTGT[C/T]TACTAAAAATACAAA | 7011 |
rs2781365 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20394499 | agagtgagactctgt[C/T]tcaaaaaaaaaaaaa | 7011 |
rs2945461 | snp | A/G | 0.338069 | 0.233974 | intron-variant | TEP1 | GRCh38.p7 | 14:20394911 | AAAAATAAGTGTAAG[A/G]TACTGATGAACCACT | 7011 |
rs3220660 | microsatellite | (CA)14/24/25/26/27/28/29 | 0.758964 | 0.120738 | intron-variant | TEP1 | GRCh38.p7 | 14:20372411 | GCTATAATGANGATA[(CA)14/24/25/26/27/28/29]ATATTCCTGGGGCTT | 7011 |
rs3748336 | snp | A/G | 0.00640398 | 0.0562226 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20408146 | GTCTGGGTGGGCAGA[A/G]ACATGTCCATGTGGT | 7011 |
rs3762145 | snp | C/T | 0.260227 | 0.249791 | intron-variant | TEP1 | GRCh38.p7 | 14:20405129 | AGATATTTCCCACCG[C/T]GCTCTTCTTTGCTTC | 7011 |
rs3762146 | snp | A/G | 0.37955 | 0.213815 | intron-variant | TEP1 | GRCh38.p7 | 14:20405365 | CCACCCCCAACATGA[A/G]GCTAGTCACCACCCC | 7011 |
rs3818768 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | TEP1 | GRCh38.p7 | 14:20370952 | ATTGCATTTTTTCCC[A/G]TGTCTCTCTTGTCTT | 7011 |
rs4246977 | snp | C/T | 0.445592 | 0.155704 | upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20414432 | cccaatgcgatggta[C/T]ttagggtgggatctc | 7011 |
rs4280143 | snp | A/C | 0.42574 | 0.177808 | intron-variant | TEP1 | GRCh38.p7 | 14:20398532 | AAGAGTGAAGGGGTG[A/C]CATTAATGCCCTCAG | 7011 |
rs4981171 | snp | C/T | 0.0947069 | 0.195918 | intron-variant | TEP1 | GRCh38.p7 | 14:20390785 | AGACTTCATGTTATG[C/T]GGTTGCACAGTAAGC | 7011 |
rs4981173 | snp | G/T | 0.0850919 | 0.187897 | intron-variant | TEP1 | GRCh38.p7 | 14:20397438 | CGCTTGAAACCAAAA[G/T]GCGAAGGTTGCAGTG | 7011 |
rs4981175 | snp | A/G | 0.485255 | 0.0845871 | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20402930 | TTGGGAGGTCAAGGC[A/G]GGTGGATCACGAGGT | 7011 |
rs4981176 | snp | G/T | 0.0115144 | 0.0749975 | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20402962 | AGGAGTTCGAGACCA[G/T]CCTGGCCAACATGGT | 7011 |
rs4982007 | snp | A/C | 6.85025e-05 | 0.00585206 | intron-variant | TEP1 | GRCh38.p7 | 14:20368786 | CACACACACACACAC[A/C]CACACACTTACCAGC | 7011 |
rs4982017 | snp | A/G | 0.0715223 | 0.175059 | intron-variant | TEP1 | GRCh38.p7 | 14:20376776 | CAGAATGAAGGTGAA[A/G]GAATGAGTGGAAACA | 7011 |
rs4982038 | snp | A/G | 0.350982 | 0.228698 | intron-variant | TEP1 | GRCh38.p7 | 14:20394383 | tgtctcaactcagac[A/G]tcactagcatatttc | 7011 |
rs4982039 | snp | G/T | 0.0566069 | 0.158427 | intron-variant | TEP1 | GRCh38.p7 | 14:20394967 | AGCCTACAAAACAGA[G/T]GGTACATCTGTCTTT | 7011 |
rs4982042 | snp | C/G | 0.084728 | 0.187577 | intron-variant | TEP1 | GRCh38.p7 | 14:20396849 | ACTTGAGCCCAGAAC[C/G]CAGGAATTAGAGTCC | 7011 |