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 |
rs4982051 | snp | A/G | 0.0183315 | 0.0939665 | missense, intron-variant, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20401004 | AGTTCCTCCCAGACC[A/G]ACGCTTTGTTCCCCC | 7011 |
rs4987229 | snp | C/G | 0.0150584 | 0.0854545 | intron-variant | TEP1 | GRCh38.p7 | 14:20404807 | AGCTACGGGAGGAGT[C/G]ACTGAGATTCTAGTC | 7011 |
rs4987230 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | TEP1 | GRCh38.p7 | 14:20404847 | ATACAGGCACACTCA[A/G]TCAGCAAGTAATTTC | 7011 |
rs6145261 | in-del | -/TGTGTGTGTGTGTGTGTATGTG | | | intron-variant | TEP1 | GRCh38.p7 | 14:20372363 | GAAGCCCCAGGAATA[-/TGTGTGTGTGTGTGTGTATGTG]TGTGTGTGTGTGTGT | 7011 |
rs6413437 | snp | C/T | 0.121071 | 0.21419 | intron-variant, synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20404704 | CTTGGCCATTGCTGC[C/T]TTCTTGCCGGCGTGT | 7011 |
rs7143219 | snp | C/T | 0.47802 | 0.102502 | intron-variant | TEP1 | GRCh38.p7 | 14:20397600 | aatttgtaagcttct[C/T]acccaatttcttcta | 7011 |
rs7144446 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | TEP1 | GRCh38.p7 | 14:20412535 | TTTCACAGTTTCTAT[A/G]CATATGCAAATACAT | 7011 |
rs7148946 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | TEP1 | GRCh38.p7 | 14:20387095 | ATGAGCCACCACACC[C/T]GGCTAATTTTGTATT | 7011 |
rs7149378 | snp | A/C | 0 | 0 | intron-variant | TEP1 | GRCh38.p7 | 14:20379497 | GCAATTTACAAATTT[A/C]CCAGGAACATTCCCC | 7011 |
rs7150689 | snp | C/T | 0.418491 | 0.184691 | intron-variant | TEP1 | GRCh38.p7 | 14:20374805 | gtctacataaaggac[C/T]taggctgggcacggt | 7011 |
rs7150966 | snp | A/G | 0.224709 | 0.248717 | intron-variant | TEP1 | GRCh38.p7 | 14:20397205 | GTTTCTAAACTTTTT[A/G]GATGGCCAAAAGAGA | 7011 |
rs7157027 | snp | C/T | 0.428484 | 0.175052 | upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20414905 | tcctcctaccttggc[C/T]tcccaaagtgcttgg | 7011 |
rs7158979 | snp | A/C | | | intron-variant | TEP1 | GRCh38.p7 | 14:20375096 | aactctgtctcaaaa[A/C]aaaaaaaaaaaaaag | 7011 |
rs7493569 | snp | A/G | 0 | 0 | | | GRCh38.p7 | 14:20416440 | actggaactacctgg[A/G]gatcttttaaaaatt | 7011 |
rs8004136 | snp | A/G | 0.00962273 | 0.0686933 | intron-variant | TEP1 | GRCh38.p7 | 14:20368927 | GAAAGGGGAGAGCAG[A/G]ATGGTGAGTTCTCAG | 7011 |
rs8005679 | snp | C/T | 0.311369 | 0.242351 | intron-variant | TEP1 | GRCh38.p7 | 14:20405869 | AGATACAAAAATTAG[C/T]CAGGCATGGCAGTGC | 7011 |
rs8007377 | snp | C/T | 0.0360663 | 0.129354 | downstream-variant-500B | TEP1 | GRCh38.p7 | 14:20365366 | gcaacctctgccccc[C/T]gagttcaagcgattc | 7011 |
rs8009925 | snp | A/C | 0.462744 | 0.131301 | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20403486 | TTCAAAAAAAGGGAA[A/C]TGGCTGTCCTTGAAG | 7011 |
rs8010863 | snp | A/G | 0.35894 | 0.225016 | intron-variant | TEP1 | GRCh38.p7 | 14:20393289 | tctgatagttttatg[A/G]aagtctattaatatt | 7011 |
rs8011749 | snp | C/T | 0.00732591 | 0.0600773 | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20368423 | GGGTATCATTATTCC[C/T]GAGTGGCACATCTTC | 7011 |
rs8011851 | snp | C/G | 0.346811 | 0.230494 | intron-variant | TEP1 | GRCh38.p7 | 14:20412896 | AACTCCTGACCTCAG[C/G]TGATCCCCAACCTCC | 7011 |
rs8011960 | snp | C/T | 0.00728184 | 0.059899 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20368557 | GCATCGGAACAGGCC[C/T]AGCTACGATGGGAAC | 7011 |
rs8013332 | snp | A/G | 0.0337553 | 0.125452 | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20367021 | GTTAAGCAAAGGCTA[A/G]CCTGCTCAATAGATT | 7011 |
rs8014515 | snp | C/G | 0.0376037 | 0.131863 | downstream-variant-500B | TEP1 | GRCh38.p7 | 14:20365303 | tttttgaccaagttt[C/G]attcttgttgcccag | 7011 |
rs8014644 | snp | A/C | 0.0360663 | 0.129354 | downstream-variant-500B | TEP1 | GRCh38.p7 | 14:20365356 | tcggctcactgcaac[A/C]tctgccccctgagtt | 7011 |
rs8018816 | snp | A/G | 0.0360663 | 0.129354 | downstream-variant-500B | TEP1 | GRCh38.p7 | 14:20365367 | caacctctgccccct[A/G]agttcaagcgattct | 7011 |
rs8018974 | snp | A/G | 0.0368353 | 0.130617 | downstream-variant-500B | TEP1 | GRCh38.p7 | 14:20365495 | ggccaggctcgcctc[A/G]aactccagaccccag | 7011 |
rs8020335 | snp | G/T | 0.00959384 | 0.0685921 | intron-variant | TEP1 | GRCh38.p7 | 14:20368757 | TGGGATAGGTGTGCA[G/T]GCGcacgcacacaca | 7011 |
rs8022805 | snp | C/T | 0.0941053 | 0.19544 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20378791 | ACGGTGGCTAGCAGC[C/T]GGCAGTCTGGGCTCA | 7011 |
rs9796387 | snp | A/G | 0.0368353 | 0.130617 | intron-variant | TEP1 | GRCh38.p7 | 14:20404351 | caagagtgaaactcc[A/G]tctccaaaaaaaaaa | 7011 |
rs9888571 | snp | A/T | 0.147991 | 0.228242 | intron-variant | TEP1 | GRCh38.p7 | 14:20405150 | TCTTTGCTTCAGAAA[A/T]GTTCACTATCTAATA | 7011 |
rs9888590 | snp | A/G | 0.147991 | 0.228242 | intron-variant | TEP1 | GRCh38.p7 | 14:20405146 | CTCTTCTTTGCTTCA[A/G]AAATGTTCACTATCT | 7011 |
rs10083536 | snp | A/G | 0.054954 | 0.156388 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20408030 | TACAAATCAGCTTGC[A/G]TCATGTGAGATATCT | 7011 |
rs10130536 | snp | G/T | 0.0221141 | 0.102801 | intron-variant | TEP1 | GRCh38.p7 | 14:20385993 | TCATAGTTGCAGGGT[G/T]TCTGACAGAGTGTGG | 7011 |
rs10131170 | snp | C/T | 0.0329836 | 0.124112 | intron-variant | TEP1 | GRCh38.p7 | 14:20410719 | tgctgggattacagg[C/T]gtgagccactgtgcc | 7011 |
rs10139437 | snp | C/T | 0.000197788 | 0.00994258 | intron-variant | TEP1 | GRCh38.p7 | 14:20371176 | TAAAAACACTGGTCC[C/T]AGACGAATGTTTGCT | 7011 |
rs10151816 | snp | C/G | 0.0304689 | 0.119608 | intron-variant | TEP1 | GRCh38.p7 | 14:20378570 | AATCAGGATGCTGAA[C/G]AGAGATGCCTGAACT | 7011 |
rs10220580 | snp | C/T | 0 | 0 | intron-variant | TEP1 | GRCh38.p7 | 14:20398260 | gtggtcgcctgtaat[C/T]tcagctaatcaggag | 7011 |
rs10220660 | snp | A/C | 0.414576 | 0.188188 | intron-variant | TEP1 | GRCh38.p7 | 14:20398318 | gggaggcggaggttg[A/C]agtgagccgaggtcg | 7011 |
rs10556159 | in-del | -/CA | 0.497241 | 0.037038 | intron-variant | TEP1 | GRCh38.p7 | 14:20413006 | TCTAGCACATTTAAG[-/CA]CAGTCTGGGTTTCTA | 7011 |
rs10567609 | in-del | -/GAG | | | intron-variant | TEP1 | GRCh38.p7 | 14:20393004 | CGGGCAGATCACAAG[-/GAG]ATCGAGACCATCCTG | 7011 |
rs10717377 | in-del | -/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20412702 | TTTTTTTTTTTTTTT[-/T]GAGGCGGAGTCTGGC | 7011 |
rs10873456 | snp | C/T | | | downstream-variant-500B | TEP1 | GRCh38.p7 | 14:20365276 | TGCTTTCTTTTTTTT[C/T]TTTTTTTTTTTTTTT | 7011 |
rs11160462 | snp | A/G | 0.33303 | 0.235809 | intron-variant | TEP1 | GRCh38.p7 | 14:20400592 | TTTCTGTATCAATGT[A/G]GGCAAATTACCTAAA | 7011 |
rs11160511 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20408890 | CATGCCTTCTCATAA[A/G]AAGGTAAAGGAGACC | 7011 |
rs11347840 | in-del | -/T | 0.0256215 | 0.110247 | intron-variant | TEP1 | GRCh38.p7 | 14:20408915 | GAGACCCAACCCCCC[-/T]GACCCCCGCTGCAGG | 7011 |
rs11385254 | in-del | -/T | 0.0263992 | 0.111815 | intron-variant | TEP1 | GRCh38.p7 | 14:20404396 | TCCAGAATAAGACCA[-/T]TTTTTTTTTCTCAAA | 7011 |
rs11504652 | snp | C/T | | | downstream-variant-500B | TEP1 | GRCh38.p7 | 14:20365263 | CCTCTCTCTTTCTTG[C/T]TTTCTTTTTTTTCTT | 7011 |
rs11555902 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20366192 | CAACAAGACTGAATC[C/T]ATTGAGCCCATTGGT | 7011 |
rs11555903 | snp | C/T | 0.00874735 | 0.0655527 | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20366176 | TTCAAGTGGGCCTGG[C/T]CAACAAGACTGAATC | 7011 |
rs11555904 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20366201 | TGAATCCATTGAGCC[C/T]ATTGGTCAAGTTAGC | 7011 |
rs11555905 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20366229 | AGCCTTTGCCCAACT[C/T]TCCCCAACCCCTTCA | 7011 |
rs11850456 | snp | A/G | 0.138854 | 0.223934 | intron-variant | TEP1 | GRCh38.p7 | 14:20382104 | CTCATCTAACCATAC[A/G]GTGTCCCCGCCCCCA | 7011 |
rs11851028 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | TEP1 | GRCh38.p7 | 14:20372446 | AGTCAGTCTGAATAG[C/T]GCTGCTGGTTTAAAT | 7011 |
rs12433941 | snp | A/G | 0.100872 | 0.200651 | intron-variant | TEP1 | GRCh38.p7 | 14:20381695 | TAGCAAACTGTCCTC[A/G]TGTGAGGAAGGGAGA | 7011 |
rs12435166 | snp | A/G | 0.3512 | 0.228601 | intron-variant | TEP1 | GRCh38.p7 | 14:20393700 | gggagtctgaggcac[A/G]agaatcacttgaaca | 7011 |
rs12436041 | snp | A/G | 0.0618563 | 0.164627 | intron-variant | TEP1 | GRCh38.p7 | 14:20381781 | CCCCCCTCAAATAGC[A/G]GAAACTGGAGCAGCT | 7011 |
rs12880583 | snp | C/T | 1.64901e-05 | 0.00287137 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20386079 | GTCTGCCTTACCCAG[C/T]GGAAGTGTGGATGGT | 7011 |
rs12882604 | snp | A/G | 0.35445 | 0.227135 | intron-variant | TEP1 | GRCh38.p7 | 14:20393669 | tggtggtatgcacct[A/G]taatcccagctactt | 7011 |
rs12884945 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20400162 | aaaaaaaaaaaaaaa[A/G]gaaTTATCTACATAT | 7011 |
rs12885739 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20398209 | acggtgaaaccccat[C/T]tctactaaaaataca | 7011 |
rs12886088 | snp | C/G/T | 1.65034e-05 | 0.00287253 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20382711 | TTCACCAGCAGCAGT[C/G/T]GCATCTGGCAAGACT | 7011 |
rs12887006 | snp | G/T | 0 | 0 | upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20415125 | ttaaatactatatgt[G/T]tagatatgtaaatgt | 7011 |
rs12888864 | snp | G/T | 0.157311 | 0.232183 | intron-variant | TEP1 | GRCh38.p7 | 14:20389005 | ATACAAAAATTAGCC[G/T]GGCATGGTGGTGCAT | 7011 |
rs12891617 | snp | A/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20410052 | aaaaaaaaaaaaaaa[A/T]aaaatgcctacctca | 7011 |
rs12891902 | snp | A/C/T | | | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20403001 | atctctactaaaaac[A/C/T]caaaaattagccaag | 7011 |
rs12893533 | snp | A/G | 0.374 | 0.217081 | intron-variant | TEP1 | GRCh38.p7 | 14:20397927 | ctggctaatttttgt[A/G]tttttagtagagacg | 7011 |
rs12894059 | snp | A/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20398213 | tgaaaccccatctct[A/T]ctaaaaatacaaaaa | 7011 |
rs12895477 | snp | A/G | 0.169435 | 0.236663 | intron-variant | TEP1 | GRCh38.p7 | 14:20385853 | CACCTAAGCAGACCC[A/G]CCCTCTTACTTTTGC | 7011 |
rs17111188 | snp | A/C | 0.0259733 | 0.11096 | missense, upstream-variant-2KB, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20401546 | GAACCTTGGAGGATT[A/C]TTTTTCTCTGACACT | 7011 |
rs17111211 | snp | C/T | 0.162909 | 0.23434 | intron-variant | TEP1 | GRCh38.p7 | 14:20404497 | CTGTCTGGGCACCAA[C/T]GCTGAGGAAAGCTGA | 7011 |
rs17211348 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | TEP1 | GRCh38.p7 | 14:20372652 | GACCTAGTTCAGAAG[C/T]AGAAGTGCAGTAATT | 7011 |
rs28397796 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | TEP1 | GRCh38.p7 | 14:20376455 | CGAGTGTGTACATAG[A/G]ACGGGAACGTGCGGC | 7011 |
rs28404466 | snp | C/G | 0.00455361 | 0.0474981 | intron-variant | TEP1 | GRCh38.p7 | 14:20384567 | CCTCTCACCACATCT[C/G]TGTACAGGTGCTCCC | 7011 |
rs28445031 | snp | A/G/T | 0.468485 | 0.121508 | intron-variant | TEP1 | GRCh38.p7 | 14:20369918 | CAATCAAGTGCGCAA[A/G/T]TTTTTTTTTTTTTGA | 7011 |
rs28552679 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20376353 | GGAGCGGCCATGGGG[A/G]CTGAGGGTGACACCT | 7011 |
rs28566032 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | TEP1 | GRCh38.p7 | 14:20376457 | AGTGTGTACATAGGA[A/C]GGGAACGTGCGGCAC | 7011 |
rs34000493 | in-del | -/A/AA | 0 | 0 | intron-variant | TEP1 | GRCh38.p7 | 14:20404373 | AAAAAAAAAAAAAAA[-/A/AA]GCATGAGGTCCAGAA | 7011 |
rs34008567 | snp | A/G | 0.00103925 | 0.0227716 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20391621 | ATGCAGACAGGCTCT[A/G]TCCAAAGAGCAACCC | 7011 |
rs34009596 | in-del | -/A | | | upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20413729 | TCCCCCTCTACCAAA[-/A]TTCGTCTCCTCTGGC | 7011 |
rs34045896 | in-del | -/G | | | | | GRCh38.p7 | 14:20416091 | ATATTGAGGAGAAGG[-/G]AAGTGAGGGGAGGGA | 7011 |
rs34157844 | in-del | -/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20381798 | AACTGGAGCAGCTGG[-/G]AGCAGTAGCTCATTC | 7011 |
rs34179031 | snp | A/G | 0.0120152 | 0.0765718 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20386510 | GAGCGGCCCCTCACC[A/G]TATCAGCCTTCACGG | 7011 |
rs34204758 | snp | G/T | 0 | 0 | intron-variant | TEP1 | GRCh38.p7 | 14:20410614 | CTTTTTTTTTTTTTG[G/T]ATTTTTAGTAAGAGA | 7011 |
rs34307293 | in-del | -/A | | | | | GRCh38.p7 | 14:20416111 | AGGGGAGGGATTGAA[-/A]GGAGTCCACACAGGG | 7011 |
rs34401320 | snp | A/G | 0.0151092 | 0.0855938 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20380256 | GGCTTAATAAACCCC[A/G]GACCATGAAAAATCA | 7011 |
rs34455090 | in-del | -/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20413098 | GCACACAGGGCAAGG[-/G]AAGTAAGAGGGGATG | 7011 |
rs34475416 | in-del | -/C | | | intron-variant | TEP1 | GRCh38.p7 | 14:20374403 | TTCCAGAGACCCCCC[-/C]AGTGGGATCTCCATT | 7011 |
rs34633175 | in-del | -/A | 0 | 0 | intron-variant | TEP1 | GRCh38.p7 | 14:20411957 | ATTTAAAAAAAAAAA[-/A]GGAATGTATTTTCTT | 7011 |
rs34734346 | in-del | -/TATA | | | intron-variant | TEP1 | GRCh38.p7 | 14:20392416 | CTTAAATAGTATATA[-/TATA]GGATCACCTATGAAC | 7011 |
rs34739214 | in-del | -/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20373629 | GGGACGGAGCAGGGG[-/G]AGAAAAGAAGAGACA | 7011 |
rs34770935 | snp | A/G | 0.00209031 | 0.0322612 | intron-variant, missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20403842 | CTGGTGCCCCTGCCC[A/G]CCTGTCTCCGTACTG | 7011 |
rs34811735 | snp | G/T | 0.00271464 | 0.0367417 | missense, intron-variant, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20372843 | GGCTCCAGGCCACAT[G/T]GGTGCTCTGATCTGG | 7011 |
rs34816712 | in-del | -/AAA/AAAAAAAAAAAAAAAA | 0.430732 | 0.172731 | intron-variant | TEP1 | GRCh38.p7 | 14:20387551 | GCGAGACTCCGTCTC[-/AAA/AAAAAAAAAAAAAAAA]AAAAAAAAAAAGAAA | 7011 |
rs34817105 | snp | A/G | 8.23906e-05 | 0.00641783 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20391052 | TGGGATGATGATCAC[A/G]AGGGCGGAGCAGGTG | 7011 |
rs34818507 | in-del | -/CA | | | intron-variant | TEP1 | GRCh38.p7 | 14:20413007 | CTAGCACATTTAAGC[-/CA]AGTCTGGGTTTCTAT | 7011 |
rs34895824 | snp | A/G | 0.00560256 | 0.0526298 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20377611 | GCATTAGGATCTACA[A/G]AATCTCTTCAGGTAC | 7011 |
rs34947952 | in-del | -/C | | | intron-variant | TEP1 | GRCh38.p7 | 14:20404183 | TCATGGTGAAACCCC[-/C]ATCACTACTAACAAT | 7011 |
rs34985552 | in-del | -/C | | | intron-variant | TEP1 | GRCh38.p7 | 14:20396062 | ACAAAATGAACTTAG[-/C]ACAAGAGATATAGAA | 7011 |
rs35038379 | in-del | -/GA | | | intron-variant | TEP1 | GRCh38.p7 | 14:20393006 | GGCAGATCACAAGGA[-/GA]TCGAGACCATCCTGA | 7011 |
rs35081660 | in-del | -/A | 0.403158 | 0.197592 | intron-variant | TEP1 | GRCh38.p7 | 14:20398506 | ATTAAAAAAAAAAAA[-/A]GAGTGAAGGGGTGAC | 7011 |
rs35099769 | snp | C/T | 0.00121849 | 0.0246528 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20384474 | GGTGTGGCAGCTGGC[C/T]GGCCCTATGTTGGCG | 7011 |
rs35159459 | in-del | -/G | 0.254385 | 0.249962 | intron-variant | TEP1 | GRCh38.p7 | 14:20370240 | TCTTAAATGTACATC[-/G]GCGATGTATTTTTAC | 7011 |
rs35165628 | snp | A/G | 0.00660988 | 0.0571074 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20374454 | TCCTGGGTCATCAGA[A/G]TGCTGTGAGCGCTGT | 7011 |
rs35202386 | snp | A/G | 0.157972 | 0.232445 | intron-variant | TEP1 | GRCh38.p7 | 14:20388320 | ACTTGCTGTTGGGCC[A/G]GGGCAACGGGGTAGG | 7011 |
rs35259162 | snp | C/T | 0.344815 | 0.231323 | intron-variant | TEP1 | GRCh38.p7 | 14:20408922 | AACCCCCCTGACCCC[C/T]GCTGCAGGACTATCA | 7011 |
rs35384067 | snp | A/T | 0.256061 | 0.249927 | intron-variant | TEP1 | GRCh38.p7 | 14:20390304 | AATAATTTTACTACA[A/T]TTTACTATTATCTAC | 7011 |
rs35446613 | in-del | -/TT | | | intron-variant | TEP1 | GRCh38.p7 | 14:20410612 | TCTTTTTTTTTTTTT[-/TT]GTATTTTTAGTAAGA | 7011 |
rs35504244 | in-del | -/T | 0.496416 | 0.0421803 | intron-variant | TEP1 | GRCh38.p7 | 14:20392487 | AATGCCCAGTGAACA[-/T]AAAACAGAAAAACAA | 7011 |
rs35517499 | snp | C/G | 0.00901223 | 0.0665199 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20378768 | GCCACCGTGTGCTTG[C/G]GAGGATGCCTAAAGG | 7011 |
rs35520880 | in-del | -/G | | | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20367083 | AAGTTCTTTTATGGG[-/G]CCGGGCACAATGGCT | 7011 |
rs35751351 | in-del | -/G | | | frameshift-variant, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20382272 | GGGAAGGACATCAGG[-/G]CCCGTGCTCCTTCTC | 7011 |
rs35793276 | snp | C/G | 0.215747 | 0.247642 | intron-variant | TEP1 | GRCh38.p7 | 14:20392942 | AGAAAATGTAAGCCG[C/G]GCACGGTGGCTCACG | 7011 |
rs35817012 | in-del | -/C | | | intron-variant | TEP1 | GRCh38.p7 | 14:20413295 | CGCCAGGCACTTCCC[-/C]ACCCAGCTCTCAGCC | 7011 |
rs35878867 | in-del | -/AC/CA | 0.5 | 0 | intron-variant | TEP1 | GRCh38.p7 | 14:20368765 | CACACACACACACAC[-/AC/CA]TTACCAGCTGCATAC | 7011 |
rs35929175 | snp | G/T | 0.00324138 | 0.0401271 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20373034 | ATCTTGTGGCAGGAA[G/T]CTAAGGCTGTGGCCA | 7011 |
rs35993125 | in-del | -/C | | | intron-variant | TEP1 | GRCh38.p7 | 14:20407434 | ACAATCTCGCCTCCC[-/C]GGTTTAAGCAATTCT | 7011 |
rs36087440 | in-del | -/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20375427 | CCAAAGTGCTGGGAT[-/T]ACAGGTGTGAGCCAC | 7011 |
rs41301453 | snp | A/G | 0.0553534 | 0.156884 | utr-variant-5-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20408462 | ACTCAGCTTGTATAT[A/G]CCTAGAAGGAGAGAA | 7011 |
rs41310936 | snp | A/G | 0.0262822 | 0.111581 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20408123 | CACCGGTTCTCCAAG[A/G]AGAGGATGTCTGGGT | 7011 |
rs45527036 | snp | G/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20382414 | AGAAGCAGCTTGGCT[G/T]GTGGGATAGGGAAGG | 7011 |
rs45565241 | snp | A/G | 1.64846e-05 | 0.0028709 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20380980 | CAGACCCAATTCCAA[A/G]TGTGCAGCCACCACA | 7011 |
rs45573241 | snp | C/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20384837 | CTCCTGACTCCAGCA[C/G]CAAGGCTGACGTGGG | 7011 |
rs45616833 | snp | C/T | 0.095934 | 0.196885 | intron-variant | TEP1 | GRCh38.p7 | 14:20376035 | GGAAGCAATGGGAAA[C/T]GGGTTGTTAAGAAAT | 7011 |
rs55790286 | snp | A/G | 0.214628 | 0.247485 | intron-variant | TEP1 | GRCh38.p7 | 14:20403687 | GCCCTTCCTGGAGAA[A/G]AGGGGCGTGGGTCGA | 7011 |
rs55871117 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20372378 | TGTGTGTGTGTGTGT[A/G]TATGTGTGTGTGTGT | 7011 |
rs55980977 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20367324 | GCTGAGATTGCACCA[C/T]TGCACTCCAGCCTAG | 7011 |
rs56035710 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20367299 | ACCCAGGAAGCAGAG[C/G]TTGCACTGAGCTGAG | 7011 |
rs56079164 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | TEP1 | GRCh38.p7 | 14:20371774 | CCTGTTCCACTTTCT[A/G]GTTTTTGTTTTTTAA | 7011 |
rs56214328 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20367325 | CTGAGATTGCACCAT[C/T]GCACTCCAGCCTAGG | 7011 |
rs56321004 | snp | A/G | 0.115075 | 0.210464 | intron-variant | TEP1 | GRCh38.p7 | 14:20368766 | TGTGCAGGCGCACGC[A/G]CACACACACACACAC | 7011 |
rs56327775 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20367311 | GAGGTTGCACTGAGC[C/T]GAGATTGCACCATTG | 7011 |
rs56343177 | snp | C/G | 0.187685 | 0.242109 | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20368014 | TCCCTCATTCTTTCC[C/G]GATGAACTGAAAGGT | 7011 |
rs56383822 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20367305 | GAAGCAGAGGTTGCA[C/G]TGAGCTGAGATTGCA | 7011 |
rs56406322 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20367292 | CGCTTGAACCCAGGA[A/G]GCAGAGGTTGCACTG | 7011 |
rs56987263 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20411238 | ACCTCCCAGCATCAT[C/T]TCTCACTAACACCCC | 7011 |
rs57417133 | snp | A/G | 0.444444 | 0.157135 | intron-variant | TEP1 | GRCh38.p7 | 14:20372380 | TGTGTGTGTGTGTGT[A/G]TGTGTGTGTGTGTGT | 7011 |
rs57766160 | snp | C/T | 0.0460142 | 0.144533 | intron-variant | TEP1 | GRCh38.p7 | 14:20371081 | GTCCTAAATTAGAAC[C/T]GCTCCAGTTGAAGGA | 7011 |
rs57797321 | in-del | -/T | 0.5 | 0 | intron-variant | TEP1 | GRCh38.p7 | 14:20369931 | AATTTTTTTTTTTTT[-/T]GAGACGGAGTCTCAC | 7011 |
rs58121179 | in-del | -/AAAAAAAAAAAA | 0.490673 | 0.0676508 | intron-variant | TEP1 | GRCh38.p7 | 14:20400138 | GCAAAACTCCGTCTC[-/AAAAAAAAAAAA]AAAAAAAAAAAAAGA | 7011 |
rs58157853 | in-del | -/GT/TGTGTA/TGTGTGTT | | | intron-variant | TEP1 | GRCh38.p7 | 14:20372412 | GTGTGTGTGTGTGTG[-/GT/TGTGTA/TGTGTGTT]TATCTTCATTATAGC | 7011 |
rs58425542 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | TEP1 | GRCh38.p7 | 14:20371371 | GAGAGGTAAAGAGAA[A/G]AACACCTCTCTTTAA | 7011 |
rs58748313 | snp | A/G | 0.342358 | 0.232314 | intron-variant | TEP1 | GRCh38.p7 | 14:20400253 | AAGAAGAGGCTGTCA[A/G]CTGGGGGCAGGTGTG | 7011 |
rs58782901 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20403013 | AACACAAAAATTAGC[C/T]AAGCGTGGTGGCACA | 7011 |
rs59298133 | snp | C/G | 0.0228947 | 0.104514 | intron-variant | TEP1 | GRCh38.p7 | 14:20371103 | GTTGAAGGAGGATAA[C/G]AGGATTTGCAGCCAA | 7011 |
rs59329010 | in-del | -/GT/GTGT | | | intron-variant | TEP1 | GRCh38.p7 | 14:20372413 | TGTGTGTGTGTGTGT[-/GT/GTGT]ATCTTCATTATAGCA | 7011 |
rs59352262 | in-del | -/ATGTGTGTGTGTGTGTGTGTGT | 0 | 0 | intron-variant | TEP1 | GRCh38.p7 | 14:20372380 | TGTGTGTGTGTGTGT[-/ATGTGTGTGTGTGTGTGTGTGT]GTGTGTGTGTGTATC | 7011 |
rs59358068 | snp | A/G | 0.352721 | 0.227922 | intron-variant | TEP1 | GRCh38.p7 | 14:20393417 | AATTAAATCAAATTA[A/G]ACTTAAATTATACAC | 7011 |
rs59435534 | snp | C/T | 0.375797 | 0.216044 | intron-variant | TEP1 | GRCh38.p7 | 14:20387049 | AAGCAATTCTCCCAC[C/T]TCAGCCTCCCCAGTA | 7011 |
rs59497578 | snp | A/G | 0.335559 | 0.234904 | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20402360 | CTTTCAGCATCTTCT[A/G]TGGCAGAAGAACTAA | 7011 |
rs59667471 | in-del | -/GTCTT/GTCTTT | | | intron-variant | TEP1 | GRCh38.p7 | 14:20369917 | CAATCAAGTGCGCAA[-/GTCTT/GTCTTT]ATTTTTTTTTTTTTG | 7011 |
rs60087138 | in-del | -/TT | | | intron-variant | TEP1 | GRCh38.p7 | 14:20369886 | ATTTTTTTTTTTTTT[-/TT]AACTACAACTTAGAT | 7011 |
rs60285926 | in-del | -/A | 0.413914 | 0.188765 | intron-variant | TEP1 | GRCh38.p7 | 14:20411683 | GGAGCTTTTTCACAG[-/A]AAAAAAAAAAGTATA | 7011 |
rs61030625 | snp | C/G | 0.0225045 | 0.103662 | intron-variant | TEP1 | GRCh38.p7 | 14:20369835 | AGTCAACTTGTACCA[C/G]ACAAAACAACAGTTT | 7011 |
rs61142604 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | TEP1 | GRCh38.p7 | 14:20370996 | AGGTTTATGGTTTCC[C/T]ATGGCTTTCTAAAAC | 7011 |
rs61351655 | snp | C/G/T | 0.0333695 | 0.124785 | intron-variant | TEP1 | GRCh38.p7 | 14:20375924 | GAAGGATGGGAACCC[C/G/T]GGAGCCATTTCAGGC | 7011 |
rs61367803 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | TEP1 | GRCh38.p7 | 14:20371011 | TATGGCTTTCTAAAA[C/T]GGTAGAGTCCTTTCT | 7011 |
rs61465318 | in-del | -/AA | 0.483345 | 0.0897213 | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20403180 | AAAAAAAAAAAAAAA[-/AA]TACAATACCAAGGAG | 7011 |
rs61594645 | snp | A/G | 0.163564 | 0.234582 | intron-variant | TEP1 | GRCh38.p7 | 14:20411425 | CTTTCCTCTCACTCT[A/G]CAGACTTCAGTTTCA | 7011 |
rs61662364 | in-del | -/TTTTTTTTTTT | | | intron-variant | TEP1 | GRCh38.p7 | 14:20410817 | GTTTTTTTTTTTTTT[-/TTTTTTTTTTT]GCTTTTTGTTTTTTG | 7011 |
rs61734876 | snp | C/T | 0.0478777 | 0.147128 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20406252 | TTTTCCTGAAGGACA[C/T]GGTCAGTAGGCTCTG | 7011 |
rs61739723 | snp | C/T | 1.65282e-05 | 0.00287469 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20381929 | TGCGCAGACTCTGGA[C/T]GAGGCAGGCAAACGG | 7011 |
rs61740505 | snp | A/G | 0.000580407 | 0.0170255 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20376223 | CTGCCTTGTGTGGCC[A/G]CGTCAGCAGCTGCCT | 7011 |
rs61996761 | snp | A/C | 0.5 | 0 | intron-variant | TEP1 | GRCh38.p7 | 14:20376718 | CACAGCAAAGTCTCC[A/C]ACGGGGCAGAAACTC | 7011 |
rs61996762 | snp | G/T | 0.5 | 0 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20380258 | ATTTTTCATGGTCCG[G/T]GGTTTATTAAGCCAT | 7011 |
rs61996763 | snp | C/G/T | 1.64743e-05 | 0.00287 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20386189 | CCCAAGGCACACTTC[C/G/T]AGTTGTCTGTAGGCA | 7011 |
rs61996764 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20387339 | ATCACCTGAGGTCGG[A/G]AGTTCAAGGTTAGCC | 7011 |
rs61996766 | snp | A/G | 0.405603 | 0.195673 | intron-variant | TEP1 | GRCh38.p7 | 14:20398000 | TACAGTGATCTGCCT[A/G]CCTCGGCCTCCCAAA | 7011 |
rs61996767 | snp | A/C | 0.5 | 0 | intron-variant | TEP1 | GRCh38.p7 | 14:20398374 | CAAAGTGAGACTCCG[A/C]CCAAAAAAAAAAAAA | 7011 |
rs61996768 | snp | C/T | 0.34101 | 0.232846 | intron-variant | TEP1 | GRCh38.p7 | 14:20400132 | AAAAGAGCAAAACTC[C/T]GTCTCAAAAAAAAAA | 7011 |
rs61996770 | snp | C/T | 0.0368353 | 0.130617 | intron-variant | TEP1 | GRCh38.p7 | 14:20400335 | TCATGCCTATAATTC[C/T]AGCACTTTGGGAGGC | 7011 |
rs61996771 | snp | C/T | 0.161924 | 0.233971 | intron-variant | TEP1 | GRCh38.p7 | 14:20410731 | AGGTGTGAGCCACTG[C/T]GCCTGGCGGACTCCT | 7011 |
rs67683135 | in-del | -/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20392488 | ATGCCCAGTGAACAA[-/T]AAACAGAAAAACAAG | 7011 |
rs71108598 | in-del | -/AAAAAAAAAAAA | 0.149665 | 0.228982 | intron-variant | TEP1 | GRCh38.p7 | 14:20400498 | AGGTAAAAGTAGACC[-/AAAAAAAAAAAA]AAAAAAAAAAAAACA | 7011 |
rs71410230 | snp | A/G | 0.188 | 0.24219 | intron-variant | TEP1 | GRCh38.p7 | 14:20375572 | TCTACTTTACAGGGT[A/G]TTGTAAAGATTAAGT | 7011 |
rs71416941 | in-del | -/TATA | 0.242775 | 0.249896 | intron-variant | TEP1 | GRCh38.p7 | 14:20392410 | GTCCCACTTAAATAG[-/TATA]TATATAGGATCACCT | 7011 |
rs71416942 | in-del | -/G | 0.5 | 0 | intron-variant | TEP1 | GRCh38.p7 | 14:20397772 | TTTTCTTTTTTTTTT[-/G]AGACGGAGTCTCACT | 7011 |
rs71416944 | in-del | -/A | 0.5 | 0 | intron-variant | TEP1 | GRCh38.p7 | 14:20399632 | GAGGCCCTGTTTCTT[-/A]AAAAAAAAAAAAAAA | 7011 |
rs71416945 | in-del | -/AA | 0.5 | 0 | intron-variant | TEP1 | GRCh38.p7 | 14:20404357 | TGAAACTCCGTCTCC[-/AA]AAAAAAAAAAAAAAA | 7011 |
rs71416946 | in-del | -/C | 0.5 | 0 | intron-variant | TEP1 | GRCh38.p7 | 14:20408800 | GGTGAAACCTCATCT[-/C]TACAAAGTTTTAAAA | 7011 |
rs72671282 | snp | C/G | 0.0232489 | 0.10528 | intron-variant | TEP1 | GRCh38.p7 | 14:20383654 | AGGCTTCTGTACATG[C/G]AGAGGAAGTCAGGGT | 7011 |
rs72671291 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | TEP1 | GRCh38.p7 | 14:20394062 | ATTGCACTCCAGCCT[G/T]GGTGATGGGAATAAA | 7011 |
rs72671293 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | TEP1 | GRCh38.p7 | 14:20396169 | GAAGGAGCCCCGTTT[A/C]TTTTAAGACTCCCTC | 7011 |
rs73585163 | snp | A/C | 0.00128437 | 0.0253088 | intron-variant | TEP1 | GRCh38.p7 | 14:20371456 | GGTTTCCTTTTTCCC[A/C]AGCTCAGGAGGAAAT | 7011 |
rs73585164 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | TEP1 | GRCh38.p7 | 14:20371804 | ACATTAGTATTCATC[A/G]GTGCCATCCCATTAC | 7011 |
rs73585167 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | TEP1 | GRCh38.p7 | 14:20372271 | GTTCCCTTCTCTTAC[C/T]GGTCCAGAAAACTCC | 7011 |
rs73585168 | snp | C/T | 6.59217e-05 | 0.00574078 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20373400 | GGTGTGGGTTTGGCA[C/T]ACCTAGGAGGAAGGG | 7011 |
rs73585169 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20374596 | CAGCATTTTGGTATA[A/T]CTGTAGTGTAGGGTG | 7011 |
rs73585176 | snp | A/G | 0.00425757 | 0.0459419 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20380302 | GGAGGTGCCATCTCC[A/G]GGAGAGCAGCGAGGC | 7011 |
rs73585181 | snp | A/G | 0.00247703 | 0.0351052 | intron-variant | TEP1 | GRCh38.p7 | 14:20384279 | GTGCCATGCTCCTCA[A/G]CACTCCCAGGCTAAA | 7011 |
rs73585190 | snp | A/G | 0.499992 | 0.00199679 | intron-variant | TEP1 | GRCh38.p7 | 14:20387276 | AACTGGTCAGGCGCG[A/G]TGGCTCACGCCTGTA | 7011 |
rs73587007 | snp | A/G | 0.0766824 | 0.180169 | intron-variant | TEP1 | GRCh38.p7 | 14:20398561 | AGATTGTGGATGCTC[A/G]GAAAACCTCAACTAT | 7011 |
rs73587012 | snp | A/G | 0.0755793 | 0.179102 | intron-variant | TEP1 | GRCh38.p7 | 14:20401226 | GAGTCATGTTTACAG[A/G]GCATGTCTGCCCAAA | 7011 |
rs73587024 | snp | A/G | 0.0232847 | 0.105357 | | | GRCh38.p7 | 14:20415821 | CAAAGTTAAAGATGC[A/G]GAAATGTCACTCATT | 7011 |
rs74336549 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | TEP1 | GRCh38.p7 | 14:20375693 | AAAAGGACGAGGTGG[A/G]GAGTGTTGTCTTGCC | 7011 |
rs74346293 | in-del | -/AA | | | intron-variant | TEP1 | GRCh38.p7 | 14:20389160 | CTTAAAAAAAAAAAA[-/AA]GTGACTGGAGTAGAG | 7011 |
rs74348618 | snp | C/G | 0.00816365 | 0.0633654 | intron-variant | TEP1 | GRCh38.p7 | 14:20386673 | GATGATTCCCACCCC[C/G]CATCCATAGACACTG | 7011 |
rs74358663 | snp | A/G | 0.0170251 | 0.090679 | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20366593 | GGAAACCAGGGCATT[A/G]GATAGAAATAAAGTC | 7011 |
rs74369960 | snp | C/T | 0.0403056 | 0.136119 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20383597 | CCAGGATGCAGGGAC[C/T]CAGCAGACTTGGGCA | 7011 |
rs74516589 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20415251 | ATACAGGCATTATAA[C/T]GGCGATTCAAATACC | 7011 |
rs74518626 | snp | C/T | 0.0110355 | 0.0734572 | intron-variant | TEP1 | GRCh38.p7 | 14:20391138 | AAAGCTCCCCTGCTT[C/T]GGAATTCACCCTTGC | 7011 |
rs74655993 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20402446 | CGTTTTTTCTTATAA[C/T]GCTAATATATATTTT | 7011 |
rs74713131 | snp | A/G | 0 | 0 | intron-variant | TEP1 | GRCh38.p7 | 14:20400163 | AAAAAAAAAAAAAAA[A/G]AATTATCTACATATA | 7011 |
rs74743908 | snp | G/T | 0.0295035 | 0.117819 | intron-variant | TEP1 | GRCh38.p7 | 14:20379717 | AAATCCTGTGTTTCT[G/T]GCAACGCTTAGCACA | 7011 |
rs74903356 | snp | A/C | 0.116838 | 0.211584 | intron-variant | TEP1 | GRCh38.p7 | 14:20396442 | GATTTACTGAACCCC[A/C]AAACTTATCTCCCTC | 7011 |
rs75239938 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | TEP1 | GRCh38.p7 | 14:20375574 | TACTTTACAGGGTGT[C/T]GTAAAGATTAAGTGA | 7011 |
rs75264494 | snp | A/G | 0.0563947 | 0.158168 | intron-variant | TEP1 | GRCh38.p7 | 14:20368764 | GGTGTGCAGGCGCAC[A/G]CACACACACACACAC | 7011 |
rs75272856 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | TEP1 | GRCh38.p7 | 14:20370842 | TTTGGCACACTCAAT[A/C]CAAAAAGTGTTGAAC | 7011 |
rs75341419 | snp | C/T | 0.0376037 | 0.131863 | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20366946 | TCTAGTTGTCTGTCT[C/T]CCATGCTCTGAAAAT | 7011 |
rs75479437 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | TEP1 | GRCh38.p7 | 14:20403943 | CAACCCTCCAAAACA[A/G]AACGAGATCACTTCA | 7011 |
rs75503338 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | TEP1 | GRCh38.p7 | 14:20413177 | CCTCCTCCTTTCTCA[C/T]CTCCCCTTTCACGCA | 7011 |
rs75543112 | snp | C/G | 0.0376037 | 0.131863 | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20366313 | CAAATAGAGCTTCCT[C/G]CTGCAATTGGCCCAA | 7011 |
rs75634627 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TEP1 | GRCh38.p7 | 14:20371867 | CTTTTCCTTCCCTCT[C/T]TACCTCCAACTCACC | 7011 |
rs75722927 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | TEP1 | GRCh38.p7 | 14:20374301 | GGGTCTTCCTATGTT[C/G]CCTAATCTCTAGGTA | 7011 |
rs75730889 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | TEP1 | GRCh38.p7 | 14:20410670 | TGGTCTCGAACTCCT[A/G]ACCTTGTGATCCACC | 7011 |
rs75747313 | snp | C/T | 0.0376037 | 0.131863 | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20366825 | CAGAAGACATTTCCT[C/T]CTTCTTTAACCCTCA | 7011 |
rs75786003 | snp | C/T | 0.084728 | 0.187577 | intron-variant | TEP1 | GRCh38.p7 | 14:20396836 | AGACAGAAGGATCAC[C/T]TGAGCCCAGAACCCA | 7011 |
rs75830725 | snp | A/T | 0.0236746 | 0.106192 | intron-variant | TEP1 | GRCh38.p7 | 14:20371782 | ACTTTCTGGTTTTTG[A/T]TTTTTAACATTAGTA | 7011 |
rs75883250 | snp | C/T | 4.9516e-05 | 0.00497549 | missense, intron-variant, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20401112 | CCAGGAAGGCGACTT[C/T]GAGAAAAGAGCTGTA | 7011 |
rs75932631 | snp | C/T | 0.20111 | 0.245173 | upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20414896 | CTCAAATAGTCCTCC[C/T]ACCTTGGCCTCCCAA | 7011 |
rs76335370 | snp | A/G | 0.0372196 | 0.131242 | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20367489 | GAGTAAGACACTTTC[A/G]TGATCTCTTCTGAGA | 7011 |
rs76394311 | snp | A/G | 0.116838 | 0.211584 | intron-variant | TEP1 | GRCh38.p7 | 14:20396190 | AGACTCCCTCTGGGC[A/G]GGGTGTGGTAGCTCA | 7011 |
rs76466486 | snp | C/G | 0.00385978 | 0.0437877 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20396622 | CCCCTCACACATACC[C/G]CATGCTGGAGTCTCT | 7011 |
rs76513246 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | TEP1 | GRCh38.p7 | 14:20386727 | GCACAAGCCAGGTAC[A/G]ACAGACAGCAGATGG | 7011 |
rs76575764 | snp | C/T | 0.0741063 | 0.177655 | intron-variant | TEP1 | GRCh38.p7 | 14:20388168 | TCCAGGTTTGGTGAC[C/T]AGTTAAGTCAAGCTC | 7011 |
rs76626967 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | TEP1 | GRCh38.p7 | 14:20394917 | AAGTGTAAGATACTG[A/G]TGAACCACTTAAAAA | 7011 |
rs76654054 | snp | C/G | 0.000296848 | 0.0121793 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20378464 | CTGCCCCTCTGGGTG[C/G]AAGGCAACACAGTTC | 7011 |
rs77029003 | snp | A/G | 0.0325976 | 0.123435 | intron-variant | TEP1 | GRCh38.p7 | 14:20391333 | TAGTGAGGTGAAAGT[A/G]AGACATATTTTGGTG | 7011 |
rs77084680 | snp | A/T | 0 | 0 | intron-variant | TEP1 | GRCh38.p7 | 14:20392488 | AATGCCCAGTGAACA[A/T]AAACAGAAAAACAAG | 7011 |
rs77084946 | snp | C/T | 0.415727 | 0.187175 | intron-variant | TEP1 | GRCh38.p7 | 14:20398246 | AGCCGGGCGTGGTGG[C/T]GGTCGCCTGTAATCT | 7011 |
rs77092051 | snp | C/G | 0.0441095 | 0.141807 | intron-variant | TEP1 | GRCh38.p7 | 14:20406091 | AAAGAAAAAAGAAAA[C/G]GGGATTAGGAAGTGA | 7011 |
rs77096275 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | TEP1 | GRCh38.p7 | 14:20375656 | CAAATATTAGCTATC[A/G]CTATTATTAATGGGT | 7011 |
rs77377906 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | TEP1 | GRCh38.p7 | 14:20409570 | TTTCTCCTTCTCATA[C/T]CTCTGCCCCAAATCC | 7011 |
rs77475121 | snp | A/C/G | 0.5 | 0 | intron-variant | TEP1 | GRCh38.p7 | 14:20376080 | GGCTATGGGACCCCA[A/C/G]GGTTGCATCCTTCTG | 7011 |
rs77508080 | snp | A/G | 0.5 | 0 | intron-variant | TEP1 | GRCh38.p7 | 14:20398518 | AATTAAAAAAAAAAA[A/G]GAGTGAAGGGGTGAC | 7011 |
rs77515776 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | TEP1 | GRCh38.p7 | 14:20390543 | GCACACCACTGGGTA[A/G]GGGGTTGTAGCCAGT | 7011 |
rs77605789 | snp | C/T | 0.0376037 | 0.131863 | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20366388 | GATGATGCCATGCCA[C/T]AGTTCGCTGCAGGAT | 7011 |
rs77610051 | snp | A/G | 0.109814 | 0.206997 | intron-variant | TEP1 | GRCh38.p7 | 14:20396561 | CTCTAAAGCAGCAGT[A/G]GCCTCTCCACGTGCA | 7011 |
rs77642753 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | TEP1 | GRCh38.p7 | 14:20413246 | GCAGGGTGGATGCAC[C/T]CCTAGCTGAGTCTCG | 7011 |
rs77667434 | snp | A/T | 0.5 | 0 | intron-variant | TEP1 | GRCh38.p7 | 14:20410036 | AAAAAAAAAAAAAAA[A/T]AAAAAAAAAAAAAAA | 7011 |
rs77685269 | snp | C/T | 0.0333695 | 0.124785 | intron-variant | TEP1 | GRCh38.p7 | 14:20392183 | CCATACAATCTATTT[C/T]CGGGTAACTAAATAA | 7011 |
rs77737638 | snp | C/T | 7.04399e-05 | 0.00593422 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20383643 | GCTCCCACACCAGGC[C/T]TCTGTACATGGAGAG | 7011 |
rs77761240 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | TEP1 | GRCh38.p7 | 14:20390420 | TCAGTAGCATCATGT[C/T]GATAGCTTGAAATCA | 7011 |
rs77782248 | snp | C/T | 0.0376037 | 0.131863 | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20365722 | CTTTTTAAATTCCTA[C/T]ACAGTTTCTAAATGG | 7011 |
rs77893109 | snp | A/G | | | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20369498 | TGCCACATGTTACCT[A/G]TGGTCCATTCTCCTT | 7011 |
rs78092551 | snp | C/T | 0.0310518 | 0.120672 | intron-variant | TEP1 | GRCh38.p7 | 14:20385366 | ACCTTTGATTTTTTT[C/T]TATTTTTTATTTTTT | 7011 |
rs78098090 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | TEP1 | GRCh38.p7 | 14:20398556 | CCCTCAGATTGTGGA[A/T]GCTCAGAAAACCTCA | 7011 |
rs78121357 | snp | C/T | 0 | 0 | intron-variant | TEP1 | GRCh38.p7 | 14:20369920 | ATCAAGTGCGCAAAT[C/T]TTTTTTTTTTTGAGA | 7011 |
rs78224652 | snp | A/G | 0.00453327 | 0.0473929 | intron-variant | TEP1 | GRCh38.p7 | 14:20396572 | CAGTGGCCTCTCCAC[A/G]TGCACATCTAGTTGC | 7011 |
rs78398678 | snp | G/T | 1.64817e-05 | 0.00287064 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20373093 | GCCATGGAACCATCT[G/T]GTGCCCAAGCCACAG | 7011 |
rs78523095 | snp | C/T | | | upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20415006 | ACGGCCATACCACCC[C/T]GAACGCGCCCGATCT | 7011 |
rs78530407 | snp | G/T | 0.5 | 0 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20391060 | CCGCCCTCGTGATCA[G/T]CATCCCAATCAACAG | 7011 |
rs78636530 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20366199 | ACTGAATCTATTGAG[C/T]CTATTGGTCAAGTTA | 7011 |
rs78675309 | snp | C/G | 0.0329836 | 0.124112 | intron-variant | TEP1 | GRCh38.p7 | 14:20375472 | GGCTTTCTTATTAGA[C/G]AGTTCCCTGGCTCAG | 7011 |
rs78793842 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | TEP1 | GRCh38.p7 | 14:20372945 | ATATGCAACCTCTAA[C/T]GCCCAGTAAATACAC | 7011 |
rs78998246 | snp | A/G | 0.5 | 0 | intron-variant | TEP1 | GRCh38.p7 | 14:20398519 | ATTAAAAAAAAAAAA[A/G]AGTGAAGGGGTGACA | 7011 |
rs79000256 | snp | A/T | 0.0240643 | 0.107019 | intron-variant | TEP1 | GRCh38.p7 | 14:20372136 | CCCCAGTTTATCTAT[A/T]CAATTCCATTTCCCT | 7011 |
rs79167882 | snp | C/T | 0.00251775 | 0.0353912 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20369695 | CAGGTTTGGCTTGAG[C/T]TATCGATATTAGGGT | 7011 |
rs79372750 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | TEP1 | GRCh38.p7 | 14:20408963 | TACTTAGTAGAGAGG[A/C]CTCGCAATATAATCT | 7011 |
rs79485112 | snp | A/G | 0 | 0 | intron-variant | TEP1 | GRCh38.p7 | 14:20411957 | TATTTAAAAAAAAAA[A/G]GGAATGTATTTTCTT | 7011 |
rs79501816 | in-del | -/TTTTTTTTTTTT | | | intron-variant | TEP1 | GRCh38.p7 | 14:20410816 | GGTTTTTTTTTTTTT[-/TTTTTTTTTTTT]GCTTTTTGTTTTTTG | 7011 |
rs79714188 | snp | A/C/G | 0.0551236 | 0.156703 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20413478 | GGAAGGGTGGCAGCC[A/C/G]GGGGAGGAGCCGGAT | 7011 |
rs79819533 | snp | C/T | 0.251014 | 0.249998 | intron-variant | TEP1 | GRCh38.p7 | 14:20411262 | ACACCCCGATCTAAC[C/T]CTCAGCACTCTAAGC | 7011 |
rs80138238 | snp | G/T | 0.00731164 | 0.0600197 | intron-variant | TEP1 | GRCh38.p7 | 14:20400942 | TGTGGAGGCATAAAT[G/T]GGGAAGAGAAGGAGG | 7011 |
rs80203186 | snp | A/C | 0.0156206 | 0.0869845 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20379079 | AGCAGAGATTCCATC[A/C]CAGCCACTCACCACA | 7011 |
rs80222924 | snp | A/C | 0.5 | 0 | intron-variant | TEP1 | GRCh38.p7 | 14:20396892 | ATAGCAAGACTGTCT[A/C]AAAAAAAAAAAGCAA | 7011 |
rs80241338 | snp | A/T | 0.5 | 0 | | | GRCh38.p7 | 14:20416215 | AGACCTCGTAGTCTG[A/T]GACTCTCTGTGGGAA | 7011 |
rs80301852 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | TEP1 | GRCh38.p7 | 14:20400907 | TCATTCCACAGAAAT[A/C]TTCTAGTGAGGATCT | 7011 |
rs111250999 | snp | C/T | 0.00102083 | 0.0225693 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20408012 | TTGCTGTTGTTCACA[C/T]GGTACAAATCAGCTT | 7011 |
rs111273734 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | TEP1 | GRCh38.p7 | 14:20378317 | ATGCTGCTGTCTGTC[A/G]TCTGCCACCCTCCAC | 7011 |
rs111288907 | snp | A/C | 0.00949599 | 0.0682482 | intron-variant | TEP1 | GRCh38.p7 | 14:20395974 | AAAGGAGGGAGGGGT[A/C]ATGAGCACAGGAGCC | 7011 |
rs111292071 | snp | C/T | 0.0494327 | 0.149241 | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20402117 | TTGAGACCAGTCTGA[C/T]CAACATGGTGAAACC | 7011 |
rs111321870 | snp | A/T | 0.084728 | 0.187577 | intron-variant | TEP1 | GRCh38.p7 | 14:20397662 | ATAGGTGAAAAAGAT[A/T]TGCACTGGAGATAGA | 7011 |
rs111437998 | snp | A/G | 0.5 | 0 | intron-variant | TEP1 | GRCh38.p7 | 14:20368595 | GGGGAGGTCAGGGCT[A/G]CAAGCCTCCTTACTA | 7011 |
rs111439724 | snp | A/G | 0.5 | 0 | intron-variant | TEP1 | GRCh38.p7 | 14:20410979 | AGTGCCTGCCACCAC[A/G]CCCAGCTAATTTTTG | 7011 |
rs111442503 | snp | A/C | 0.000543671 | 0.0164785 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20377675 | CATCTGGGCTGAGTG[A/C]CACAGAGAGGGCAGG | 7011 |
rs111482622 | snp | A/G | 0.0520787 | 0.152732 | intron-variant | TEP1 | GRCh38.p7 | 14:20405636 | AGGTAACAAGGACCA[A/G]CTTAAGCATCCATGC | 7011 |
rs111506517 | snp | C/T | 0.077417 | 0.180873 | intron-variant | TEP1 | GRCh38.p7 | 14:20388578 | ATAGACATAATTTTC[C/T]CTGGATCAAGAATTG | 7011 |
rs111542111 | snp | A/C | 0 | 0 | intron-variant | TEP1 | GRCh38.p7 | 14:20393606 | AGAGCAGCCTGGCCA[A/C]CAGGGTGAAACCCTG | 7011 |
rs111542385 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | TEP1 | GRCh38.p7 | 14:20398372 | ATCAAAGTGAGACTC[C/T]GCCCAAAAAAAAAAA | 7011 |
rs111557692 | snp | C/T | 0.5 | 0 | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20367080 | AATAAAGTTCTTTTA[C/T]GGGCCGGGCACAATG | 7011 |
rs111569552 | snp | A/T | 0.0741063 | 0.177655 | intron-variant | TEP1 | GRCh38.p7 | 14:20400443 | TAAAAAGAAAAGTAA[A/T]AATTTTATAAAGTAA | 7011 |
rs111629125 | snp | C/T | 0.077417 | 0.180873 | intron-variant | TEP1 | GRCh38.p7 | 14:20388433 | ATGTGCCTGAGGCTT[C/T]CTCATAGGAGTTGAG | 7011 |
rs111632717 | snp | C/T | 0.5 | 0 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20378845 | TGGTGAGCCTTAGTC[C/T]GCAGCACCCTATCCC | 7011 |
rs111645233 | snp | C/T | 0.0603597 | 0.1629 | intron-variant | TEP1 | GRCh38.p7 | 14:20387729 | TAGAGAAAGGAAGGG[C/T]TTGCTCACAATCTGA | 7011 |
rs111675106 | snp | A/G | 0.175897 | 0.238765 | intron-variant | TEP1 | GRCh38.p7 | 14:20405381 | GCTAGTCACCACCCC[A/G]CCACACACCATAACC | 7011 |
rs111675866 | snp | A/G | 0.171057 | 0.237209 | intron-variant | TEP1 | GRCh38.p7 | 14:20387131 | TAGAGACAGGGTTTA[A/G]TCATGTTGGACAGGC | 7011 |
rs111751048 | snp | A/G | 0.0836354 | 0.186609 | intron-variant | TEP1 | GRCh38.p7 | 14:20389441 | AGGGTGGACTCTCAC[A/G]GAGGGGTACAGAGTT | 7011 |
rs111757501 | snp | C/T | 0.0379877 | 0.132479 | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20402200 | GTACTCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 7011 |
rs111857408 | snp | A/G | 0.0448719 | 0.142907 | intron-variant | TEP1 | GRCh38.p7 | 14:20369133 | CTGCCTCAGACTCCC[A/G]AGTAGCTGGGACTAC | 7011 |
rs111873622 | snp | C/T | 0.0839998 | 0.186933 | intron-variant | TEP1 | GRCh38.p7 | 14:20388274 | AGAGAAGCCCAGCTC[C/T]AGCCCCTCCTGCTGT | 7011 |
rs111891244 | snp | C/T | 0.00713309 | 0.0592931 | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20401593 | CAAACTGTGGAAACA[C/T]CCCCAAGTCCCACAG | 7011 |
rs111894686 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TEP1 | GRCh38.p7 | 14:20404442 | TCTCAATCACATTCT[C/T]CATGCTGGACAACCC | 7011 |
rs111900934 | snp | C/T | 0.5 | 0 | intron-variant | TEP1 | GRCh38.p7 | 14:20397401 | CTAATCCCAGCCACT[C/T]GAAAGGCTGAGTCAG | 7011 |
rs111904261 | snp | C/T | 0.00156638 | 0.0279417 | intron-variant | TEP1 | GRCh38.p7 | 14:20395633 | AAGGGCAATGCTGTA[C/T]GATGACAGGTAAATT | 7011 |
rs111916789 | snp | A/C | 0.103082 | 0.202275 | intron-variant | TEP1 | GRCh38.p7 | 14:20397720 | TTATTGTTCCCTTGT[A/C]CCTGTGTTATTAATA | 7011 |
rs111974142 | snp | A/G | 0.00090567 | 0.0212606 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20384409 | CAGGTAGAGCTTCTG[A/G]ATCATATTCCATACA | 7011 |
rs112016824 | snp | C/T | 0.0543475 | 0.155628 | intron-variant | TEP1 | GRCh38.p7 | 14:20399917 | CTATAATCCCAGCAC[C/T]TTGGGAGGCCGAGGC | 7011 |
rs112024184 | in-del | -/CACA | 0.5 | 0 | intron-variant | TEP1 | GRCh38.p7 | 14:20368764 | GGTGTGCAGGCGCAC[-/CACA]ACACACACACACACA | 7011 |
rs112044157 | in-del | -/A | 0.368529 | 0.220116 | intron-variant | TEP1 | GRCh38.p7 | 14:20383681 | GGGTCAGTGGGAGAG[-/A]AAAAAAAAGCAGGGG | 7011 |
rs112075916 | snp | C/G | 0.5 | 0 | intron-variant | TEP1 | GRCh38.p7 | 14:20405891 | TGGCAGTGCACGCCT[C/G]TAATTCCAGCTACTC | 7011 |
rs112093513 | snp | A/T | 0.0763149 | 0.179815 | intron-variant | TEP1 | GRCh38.p7 | 14:20397686 | AGATAGAATTTCACC[A/T]CTGACCTCTGTCACT | 7011 |
rs112117454 | snp | C/T | 0.0566069 | 0.158427 | intron-variant | TEP1 | GRCh38.p7 | 14:20394572 | GCAACCTCCGCCTCC[C/T]GGGTTCAAGTGATTC | 7011 |
rs112128160 | snp | A/G | 0.0737376 | 0.17729 | intron-variant | TEP1 | GRCh38.p7 | 14:20385459 | CTCACAGCAACCTCC[A/G]CCTCCTCGGTTCAAG | 7011 |
rs112148434 | snp | A/T | 0 | 0 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20374491 | CAAGCCGCTGTCCTG[A/T]CTCTGGGTCCCAGAG | 7011 |
rs112150591 | snp | A/G | 0.0543475 | 0.155628 | intron-variant | TEP1 | GRCh38.p7 | 14:20399177 | GGATTACAGGCGTGA[A/G]CCATGGTGCCTGGCC | 7011 |
rs112229470 | snp | A/G | 0 | 0 | intron-variant | TEP1 | GRCh38.p7 | 14:20412979 | CTCACTCTTCAAGTG[A/G]CTGTATGGTAGTCTA | 7011 |
rs112339390 | snp | C/T | 0.5 | 0 | intron-variant | TEP1 | GRCh38.p7 | 14:20388200 | TTAAGAAGAGGACCA[C/T]AAGCAGTTTATGCAG | 7011 |
rs112340232 | snp | C/T | 0.084728 | 0.187577 | intron-variant | TEP1 | GRCh38.p7 | 14:20397999 | CTACAGTGATCTGCC[C/T]GCCTCGGCCTCCCAA | 7011 |
rs112374310 | snp | A/C | 0.0267878 | 0.112589 | intron-variant | TEP1 | GRCh38.p7 | 14:20403942 | CCAACCCTCCAAAAC[A/C]AAACGAGATCACTTC | 7011 |
rs112417669 | snp | A/G | 0.077417 | 0.180873 | intron-variant | TEP1 | GRCh38.p7 | 14:20388292 | CCCCTCCTGCTGTGC[A/G]TGGTAATCACAAACT | 7011 |
rs112421104 | snp | A/G | 0.5 | 0 | intron-variant | TEP1 | GRCh38.p7 | 14:20396991 | CAAGATAGAGGAAGT[A/G]AGGAATTCACATACA | 7011 |
rs112423176 | snp | A/G | 0.000247278 | 0.0111166 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20368506 | CAGGGTGGAGTTAGC[A/G]CCCAGCCAAGGTTCC | 7011 |
rs112458527 | snp | C/G | 0.5 | 0 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20377476 | ATCCAGTGCCTGACC[C/G]TGAGCCCCCTGGGAA | 7011 |
rs112477401 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | TEP1 | GRCh38.p7 | 14:20407630 | ACAGGCATGAGCCAC[C/T]GCACCCAGCCAGGAC | 7011 |
rs112505852 | snp | A/T | 0.5 | 0 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20391001 | TGCCTTAAGCACTGC[A/T]GTCTTCAGAGTGTCA | 7011 |
rs112507326 | snp | A/G | 0.0722614 | 0.17581 | intron-variant | TEP1 | GRCh38.p7 | 14:20400552 | ACTGAAGATAACTTG[A/G]TCCTCCTCTATTTGA | 7011 |
rs112557532 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | TEP1 | GRCh38.p7 | 14:20411146 | CTTTACTGAAATACA[A/G]CTCCTTAAGGTAAGG | 7011 |
rs112695023 | in-del | -/T | 0.410737 | 0.191478 | intron-variant | TEP1 | GRCh38.p7 | 14:20369872 | TGGGCTGGTCAGGAA[-/T]TTTTTTTTTTTTTTA | 7011 |
rs112715748 | snp | C/T | 0.5 | 0 | upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20414352 | CTATTGCCACCAGTC[C/T]CAACACTCCCTGCAA | 7011 |
rs112730924 | snp | A/G | 0.0726307 | 0.176182 | intron-variant | TEP1 | GRCh38.p7 | 14:20400133 | AAAGAGCAAAACTCC[A/G]TCTCAAAAAAAAAAA | 7011 |
rs112755259 | in-del | -/AGG | 0.395453 | 0.203331 | intron-variant | TEP1 | GRCh38.p7 | 14:20393002 | GGCGGGCAGATCACA[-/AGG]AGATCGAGACCATCC | 7011 |
rs112782955 | snp | A/G | 0.0494327 | 0.149241 | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20402018 | TGGTGGCTCATGCCT[A/G]TAAACCTAACACTTT | 7011 |
rs112784545 | snp | A/G | 0.5 | 0 | intron-variant | TEP1 | GRCh38.p7 | 14:20396845 | GATCACTTGAGCCCA[A/G]AACCCAGGAATTAGA | 7011 |
rs112881080 | snp | C/T | 0.000905775 | 0.0212619 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20408278 | CTTCAGGTCAGGAAG[C/T]GTGGCTAGGCACTGG | 7011 |
rs112882241 | snp | C/T | 0.5 | 0 | intron-variant | TEP1 | GRCh38.p7 | 14:20387530 | GTACCCCAGACTGGG[C/T]GACACAGCGAGACTC | 7011 |
rs112895188 | snp | C/T | 0.5 | 0 | intron-variant | TEP1 | GRCh38.p7 | 14:20412192 | TGATGGCTTCTGTGC[C/T]CAATACACTTTGCTC | 7011 |
rs112939447 | snp | A/G | 0.0832709 | 0.186283 | intron-variant | TEP1 | GRCh38.p7 | 14:20388862 | CTTTAAAAAAGAAGT[A/G]ACTGGAGCCGGGTGC | 7011 |
rs112993019 | snp | A/G | 0.00358779 | 0.0422022 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20413471 | GCCGGTGGGAAGGGT[A/G]GCAGCCGGGGGAGGA | 7011 |
rs113044856 | snp | G/T | 0.0722614 | 0.17581 | intron-variant | TEP1 | GRCh38.p7 | 14:20400485 | AAGAGCCTGCTATAG[G/T]TAAAAGTAGACCAAA | 7011 |
rs113110653 | snp | C/T | 0.0134518 | 0.080901 | intron-variant | TEP1 | GRCh38.p7 | 14:20369299 | AGGTGTGAGCCACTG[C/T]TCCCAGCCCTCCCCT | 7011 |
rs113134604 | snp | C/T | 0.5 | 0 | intron-variant | TEP1 | GRCh38.p7 | 14:20388224 | TATGCAGACTTAAAA[C/T]AAATGAGGATGCAGA | 7011 |
rs113174358 | snp | C/T | 0.000181241 | 0.00951777 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20373318 | AACCATCCTCAGAGG[C/T]GGTCAGCATGAGGCC | 7011 |
rs113176194 | snp | A/G | 0.108755 | 0.206276 | intron-variant | TEP1 | GRCh38.p7 | 14:20390556 | TAGGGGGTTGTAGCC[A/G]GTAGAGCTGATCTGA | 7011 |
rs113216635 | snp | A/G | 0.00303234 | 0.0388198 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20384150 | GGCCGGGCAGGACTC[A/G]GTGGCTTCTGCAGCT | 7011 |
rs113261665 | snp | A/T | 0.5 | 0 | intron-variant, missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20403805 | TGGTACTCGTCAAAC[A/T]GGGCAAATTTGTCCG | 7011 |
rs113279100 | snp | A/T | 0.0490535 | 0.14873 | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20401934 | ATCACTAAGACTCTT[A/T]ATAGATAAATAGAGA | 7011 |
rs113347557 | snp | A/G | 0.5 | 0 | intron-variant | TEP1 | GRCh38.p7 | 14:20381903 | GGGAGCTCTGCTGGG[A/G]CACCTGTACCTGCGC | 7011 |
rs113381912 | snp | A/G | 0.0543475 | 0.155628 | intron-variant | TEP1 | GRCh38.p7 | 14:20399507 | TATCTTATATTTTAT[A/G]CTTATATCTTTTTTT | 7011 |
rs113410039 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TEP1 | GRCh38.p7 | 14:20387531 | TACCCCAGACTGGGC[A/G]ACACAGCGAGACTCC | 7011 |
rs113549012 | snp | G/T | 0.170084 | 0.236883 | intron-variant | TEP1 | GRCh38.p7 | 14:20387135 | GACAGGGTTTAGTCA[G/T]GTTGGACAGGCTAAC | 7011 |
rs113652647 | snp | C/T | 0.000812481 | 0.020139 | intron-variant | TEP1 | GRCh38.p7 | 14:20395414 | CCAGGGTAGCCCCGA[C/T]TGCCCACCCTTGGCT | 7011 |
rs113754762 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | TEP1 | GRCh38.p7 | 14:20405127 | GAAGATATTTCCCAC[C/T]GCGCTCTTCTTTGCT | 7011 |
rs113769448 | snp | A/G | 0.5 | 0 | intron-variant | TEP1 | GRCh38.p7 | 14:20391280 | TGGAGGGAGGAAAAG[A/G]GGAGCCAGGATCCCT | 7011 |
rs113787476 | snp | A/G | 0.084728 | 0.187577 | intron-variant | TEP1 | GRCh38.p7 | 14:20397790 | ACGGAGTCTCACTCT[A/G]TCACCCAGGCTAGAG | 7011 |
rs113796281 | snp | A/G/T | 1.6473e-05 | 0.00286988 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20371520 | CATCCCCTGGCTTCA[A/G/T]GCAAAGTAACTTCAA | 7011 |
rs113860426 | snp | A/G | 0.0106347 | 0.0721407 | intron-variant | TEP1 | GRCh38.p7 | 14:20391785 | ACATGCAAGAAAGAC[A/G]CAGACACAGGGGCTC | 7011 |
rs113888026 | snp | A/C/G | 0.5 | 0 | intron-variant | TEP1 | GRCh38.p7 | 14:20390044 | ACATTAAATTGTATA[A/C/G]ATTTAAAAAATTAAA | 7011 |
rs113891865 | snp | C/G | 0.0256215 | 0.110247 | intron-variant | TEP1 | GRCh38.p7 | 14:20410637 | GTAAGAGACAGGGTT[C/G]CACTATGCTGGCCAG | 7011 |
rs113977788 | snp | A/G | 0.5 | 0 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20375833 | GTGGATCAAAACAGG[A/G]GTTTTGGGTGTCCTC | 7011 |
rs113979333 | snp | C/T | 0.108755 | 0.206276 | intron-variant | TEP1 | GRCh38.p7 | 14:20390481 | TTTAGCAGATGCTAC[C/T]AACCAAGGCTTATTT | 7011 |
rs113979348 | snp | C/G | 0.0810805 | 0.184299 | intron-variant | TEP1 | GRCh38.p7 | 14:20390110 | TGACACACACCAGTA[C/G]TCCCAGCTACTTGGG | 7011 |
rs114064016 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20402577 | CTTTATGACAACCTA[A/G]CAATGTAGGTTCTGC | 7011 |
rs114207117 | snp | A/G | 0.084728 | 0.187577 | intron-variant | TEP1 | GRCh38.p7 | 14:20398057 | CATGCCCAGCCCATA[A/G]TTTCTTAATAATAAT | 7011 |
rs114236487 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | TEP1 | GRCh38.p7 | 14:20389384 | CCAAGATGAAAACCC[C/T]ACTTCTGCACCTTTA | 7011 |
rs114245100 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20396189 | AAGACTCCCTCTGGG[C/T]AGGGTGTGGTAGCTC | 7011 |
rs114345839 | snp | G/T | 0.00313924 | 0.0394939 | intron-variant | TEP1 | GRCh38.p7 | 14:20378704 | AACAAATTCACGAGG[G/T]TGAGTCATGGCTCAG | 7011 |
rs114387285 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20399499 | TTACATTTTATCTTA[C/T]ATTTTATACTTATAT | 7011 |
rs114410153 | snp | A/G | 0.00159661 | 0.0282092 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20369540 | TTGGCCAGGTTCCAT[A/G]GGATCCCATCAGAGC | 7011 |
rs114715663 | snp | C/G | 0.0178098 | 0.0926698 | upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20414689 | AGCCACCCGGTCTAC[C/G]GTAATTTGTTATAGC | 7011 |
rs114848862 | snp | A/G | 0.0532157 | 0.154195 | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20402806 | TCCTGTGAAAGGTAT[A/G]TATTTCATAATGTTT | 7011 |
rs114886085 | snp | C/T | 0.00327205 | 0.0403152 | intron-variant | TEP1 | GRCh38.p7 | 14:20373844 | ATCAGAGCAGAGTCA[C/T]ATTGAGCAGGACATG | 7011 |
rs114892169 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | TEP1 | GRCh38.p7 | 14:20371868 | TTTTCCTTCCCTCTC[C/T]ACCTCCAACTCACCA | 7011 |
rs115075975 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | TEP1 | GRCh38.p7 | 14:20382543 | CAAGACAGCAAAGGA[C/T]GTGGGATAGGGATGA | 7011 |
rs115090941 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | TEP1 | GRCh38.p7 | 14:20376918 | TTAGTGTCTTTAAAA[A/G]GAACAGTGATTTGTG | 7011 |
rs115205401 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | TEP1 | GRCh38.p7 | 14:20394788 | CGTGAGCCACCACAC[C/T]CAGCCAGGCTTGATT | 7011 |
rs115218239 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TEP1 | GRCh38.p7 | 14:20381243 | GGTGGAGATGGTAAC[A/G]GGGAGAGGGGTCTCA | 7011 |
rs115285379 | snp | C/T | 0.02016 | 0.0983543 | upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20414730 | AAAACATTTCCTTTT[C/T]ATAACAAATATTTTA | 7011 |
rs115334953 | snp | C/G | 0.003241 | 0.0401248 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20373510 | GCAGGAACTCACCAA[C/G]AGTGGATGCCATAAC | 7011 |
rs115406424 | snp | C/G | 0.0310518 | 0.120672 | intron-variant | TEP1 | GRCh38.p7 | 14:20380166 | CTGGTCATCCTTATT[C/G]CTCAGTTTCAGAAAG | 7011 |
rs115648209 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TEP1 | GRCh38.p7 | 14:20392774 | TTTTTAGTTTTGTCA[A/G]GTATATTAATGACAT | 7011 |
rs115694001 | snp | C/T | 0.0019881 | 0.0314658 | intron-variant | TEP1 | GRCh38.p7 | 14:20380909 | TATCTCAGAGAAGAA[C/T]CCAGCCAGTGACTCA | 7011 |
rs115768422 | snp | C/G | 0.0123036 | 0.0774623 | intron-variant | TEP1 | GRCh38.p7 | 14:20370920 | CTTGCCCTCAAGATG[C/G]TATTATTCATAGGGG | 7011 |
rs115792343 | snp | A/C | 0.0376037 | 0.131863 | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20366521 | CTTGGCATGAGGCAC[A/C]TAAGAGAAGACAGAA | 7011 |
rs115962044 | snp | A/G | 0.00676609 | 0.0577691 | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20367526 | ATTACCATATTGACT[A/G]AAGTTGAAAGTCGTG | 7011 |
rs116033258 | snp | A/G | 0.00887202 | 0.0660098 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20396659 | TGAGCTCATGGTGGC[A/G]GGAACTGATTCCAAC | 7011 |
rs116204233 | snp | A/C | 0.0162398 | 0.0886349 | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20402040 | TAACACTTTGGGAGG[A/C]CAAGGCAGGTGGATC | 7011 |
rs116352524 | snp | A/G | 0.000364184 | 0.0134892 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20380033 | GTAGGGGATGAGGAA[A/G]CTGCCAGAGACAGGC | 7011 |
rs116446902 | snp | C/T | 0.0349115 | 0.127424 | intron-variant | TEP1 | GRCh38.p7 | 14:20389548 | CTATGCTTTGGCAGG[C/T]GTAGAGAGGAAATGT | 7011 |
rs116544464 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | TEP1 | GRCh38.p7 | 14:20383976 | CCTGAGCTCCCTGTG[C/T]CTTACCTCCTTAGCC | 7011 |
rs116586162 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TEP1 | GRCh38.p7 | 14:20405338 | AGAAATCCTTCCTAA[A/G]AGAAGCTCCTCCCAC | 7011 |
rs116606143 | snp | C/T | 0.0479149 | 0.147179 | intron-variant | TEP1 | GRCh38.p7 | 14:20405310 | CCACAGGGACTAGGC[C/T]GCAGACTCACCCAGA | 7011 |
rs116638042 | snp | A/T | 0.0352966 | 0.128072 | intron-variant | TEP1 | GRCh38.p7 | 14:20388525 | GATGGAGAGACAGAT[A/T]AAAAAAACGTGAAAA | 7011 |
rs116848433 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | TEP1 | GRCh38.p7 | 14:20382962 | TCATCCCCTCACCCC[A/G]AGAGGCCCTGGAAAG | 7011 |
rs117467335 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | TEP1 | GRCh38.p7 | 14:20412722 | CGGAGTCTGGCTCTG[C/T]TGTTCAGCTCACTGC | 7011 |
rs117495369 | snp | G/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20381224 | GGGTAATGGCGGCGG[G/T]GATGGTGGAGATGGT | 7011 |
rs117498872 | snp | A/G/T | 0.00451655 | 0.047308 | intron-variant | TEP1 | GRCh38.p7 | 14:20385152 | TAGTCCTAGGCCACA[A/G/T]TGACCCTCCCTCCAG | 7011 |
rs117775572 | snp | C/T | 0.00325875 | 0.0402337 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20383549 | TGGTCCACTAACCTA[C/T]CAGCCCCATCGATGA | 7011 |
rs117997034 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20397543 | AAGTTCACCATTTAT[A/G]ATGACGAATGTATGT | 7011 |
rs118050610 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | TEP1 | GRCh38.p7 | 14:20370059 | GCTGGGAACACCGGC[A/G]TGCGCCACCACACCC | 7011 |
rs118078325 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20409080 | CTCTTTAACCAACTA[A/G]ATGGGATTCTGTCCC | 7011 |
rs118189645 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | TEP1 | GRCh38.p7 | 14:20392750 | ACAGATGATTTCACC[A/G]AGGAATTATTTTTAG | 7011 |
rs137911183 | snp | C/T | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20396704 | ACAGGTTCCGAAGCA[C/T]GGCCATGAAGGGAAG | 7011 |
rs137916490 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20392623 | AGGTTAAAAGTGACA[C/T]AACAGACTTAACAAC | 7011 |
rs137919088 | snp | A/G | 0.000477976 | 0.0154518 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20385049 | GCAGACGTTGGTTCC[A/G]GTTCAGGAACTGCAT | 7011 |
rs137928960 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20414516 | CTCATAAGGAGAGAC[A/G]GAAGAGCTAGCTAGC | 7011 |
rs137952698 | snp | A/T | 0.000365135 | 0.0135068 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20383865 | AAAGTGGAAGAAGAC[A/T]AATGATGCCACCTTG | 7011 |
rs138032035 | snp | A/G | 9.89218e-05 | 0.00703215 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20379019 | GAGCTCCAGGAGCCC[A/G]TCGAAGGCAGTAAGA | 7011 |
rs138145344 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20408047 | CATGTGAGATATCTG[C/T]AGACTCTGGAACAAG | 7011 |
rs138145541 | in-del | -/GT | | | intron-variant | TEP1 | GRCh38.p7 | 14:20400264 | GTCAACTGGGGGCAG[-/GT]GTGTGTGTGTATGTG | 7011 |
rs138173061 | snp | C/G/T | 4.99048e-05 | 0.00499499 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20391600 | TTTTGTTTTCTTACC[C/G/T]CTTGTGGGTTGCTCT | 7011 |
rs138182761 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20402855 | TTTACTGACATGTCA[C/G]CCGGCAGTAAAGTAC | 7011 |
rs138200133 | snp | A/G | 0.00208001 | 0.032182 | intron-variant | TEP1 | GRCh38.p7 | 14:20384733 | CCACCAAAGACCCCA[A/G]AAGTTGGAATAGACT | 7011 |
rs138288297 | snp | C/T | 1.65029e-05 | 0.00287248 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20377475 | CATCCAGTGCCTGAC[C/T]CTGAGCCCCCTGGGA | 7011 |
rs138309066 | snp | A/C | 1.65004e-05 | 0.00287227 | stop-gained, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20369770 | CAAACTCTCCTGATT[A/C]CTTTTGCCTCTGTGA | 7011 |
rs138309889 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | TEP1 | GRCh38.p7 | 14:20380530 | GACCCCATTAGCCCC[A/T]GCACCAAATAAAACC | 7011 |
rs138349769 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TEP1 | GRCh38.p7 | 14:20377025 | GTTCGAGACCAGCAT[A/G]ACCAACATGGTGAAA | 7011 |
rs138588448 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | TEP1 | GRCh38.p7 | 14:20397458 | AGGTTGCAGTGAACC[A/G]AGATCACGCCACTGC | 7011 |
rs138589824 | snp | A/G | 0.000181218 | 0.00951714 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20373360 | AAACAGCAGCAGCAC[A/G]GACTGGGCCGCTGTG | 7011 |
rs138617409 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20393195 | GCACTCCAGCCTGGG[C/T]GACAGAGCAAGACTC | 7011 |
rs138668014 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | TEP1 | GRCh38.p7 | 14:20410486 | GGAGTGCAATGGCAC[A/G]ATCTTGGCTCACTGC | 7011 |
rs138692547 | snp | A/G | | | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20403078 | AGGAGAATCGCTTGA[A/G]CCTGTGAGGTGGAGG | 7011 |
rs138722240 | snp | G/T | 1.6477e-05 | 0.00287024 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20377666 | CCCGATCACCATCTG[G/T]GCTGAGTGCCACAGA | 7011 |
rs138800320 | snp | A/G | 0.000165961 | 0.00910786 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20373802 | GCTCACAGACACCAC[A/G]TGCTCCTCCTGCCCA | 7011 |
rs138848717 | snp | A/C/G | 0.000247077 | 0.0111125 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20408013 | TGCTGTTGTTCACAC[A/C/G]GTACAAATCAGCTTG | 7011 |
rs138866009 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20409098 | GGGATTCTGTCCCCA[C/T]CAGTCCACAAGTCCT | 7011 |
rs138892488 | snp | C/T | 0.00198177 | 0.0314158 | intron-variant, missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20404675 | GCACAGAAATATCGT[C/T]GCAGGTGGGGGCGAC | 7011 |
rs138897266 | snp | A/G | 1.64727e-05 | 0.00286986 | intron-variant, synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20403792 | GTACTTAGCCAGCTG[A/G]TACTCGTCAAACTGG | 7011 |
rs138899774 | snp | A/G | 0.084728 | 0.187577 | intron-variant | TEP1 | GRCh38.p7 | 14:20397973 | GGCCAGGCTGGTCTC[A/G]AACTCCCGATCTACA | 7011 |
rs138928722 | snp | C/T | 0.000402334 | 0.0141776 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20383743 | TTGGGGGATACCCAC[C/T]GGTAGGTGCTGGGGA | 7011 |
rs138959092 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | TEP1 | GRCh38.p7 | 14:20388340 | AACGGGGTAGGGAAA[A/G]GTGTAAAGATTAAAG | 7011 |
rs138962979 | snp | A/G | 0.00687864 | 0.0582409 | missense, intron-variant, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20401035 | GTAGGCTCAGCTCCC[A/G]CTCCCAGGTCTCTGG | 7011 |
rs138966593 | snp | A/C/G | 0.000230667 | 0.010737 | stop-gained, synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20390711 | AGCCAGAGACAGCAG[A/C/G]TATTTCCCAAAAGTA | 7011 |
rs138978001 | in-del | -/CCACCATAACCCACCACACA | 0.17654 | 0.238964 | intron-variant | TEP1 | GRCh38.p7 | 14:20405377 | GAAGCTAGTCACCAC[-/CCACCATAACCCACCACACA]CCCGCCACACACCAT | 7011 |
rs139053673 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | TEP1 | GRCh38.p7 | 14:20400696 | GGAATGAGTTACAGA[G/T]ATATCGATATGAGTA | 7011 |
rs139068844 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20401848 | CTTGTGAGAAACAAG[A/G]TGGGGATAGAATGAA | 7011 |
rs139071292 | snp | A/C | 0.0193772 | 0.0965046 | intron-variant | TEP1 | GRCh38.p7 | 14:20375344 | TATCTTTAGTAGAGA[A/C]AGGGTTTCTCCATGT | 7011 |
rs139113206 | snp | C/G | 0.0101177 | 0.0704023 | intron-variant | TEP1 | GRCh38.p7 | 14:20386637 | ATCTGGGGATAAGCA[C/G]AGAGCTGGGCTCAGT | 7011 |
rs139150954 | in-del | -/T | | | downstream-variant-500B | TEP1 | GRCh38.p7 | 14:20365268 | CTCTTTCTTGCTTTC[-/T]TTTTTTTCTTTTTTT | 7011 |
rs139170754 | in-del | -/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20368639 | CACATTAATGCCTTT[-/T]ATTTAGAAACAGGTT | 7011 |
rs139217125 | in-del | -/GGGGG | | | intron-variant | TEP1 | GRCh38.p7 | 14:20406417 | GGGGTAGTAGTGGCA[-/GGGGG]GTTATGAATCACAGC | 7011 |
rs139320181 | snp | C/T | 0.00108877 | 0.0233066 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20395555 | TGGCAAAGAAACCTC[C/T]GCCTGGGACGGTTCT | 7011 |
rs139323601 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | TEP1 | GRCh38.p7 | 14:20374790 | TGTGGGGCTGAGTGC[A/G]TCTACATAAAGGACT | 7011 |
rs139362330 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | TEP1 | GRCh38.p7 | 14:20371012 | ATGGCTTTCTAAAAC[A/G]GTAGAGTCCTTTCTT | 7011 |
rs139365971 | snp | C/T | 0.000198413 | 0.00995826 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20381029 | TTCGAAAGAAGTCCA[C/T]GGTTCCCGCTCTGGA | 7011 |
rs139379093 | snp | C/T | 0.00874735 | 0.0655527 | downstream-variant-500B | TEP1 | GRCh38.p7 | 14:20365564 | ATAGGCGTGAGCCAC[C/T]GTGCCTGGCCTGTTT | 7011 |
rs139380767 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20402393 | TTAGGATATATTAAT[A/C]GGATGAAGAGAAAAG | 7011 |
rs139455016 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | TEP1 | GRCh38.p7 | 14:20403580 | CTGCCCTGCACCATA[G/T]GCCCATGAGCTCTAC | 7011 |
rs139477494 | snp | C/T | 0.000330491 | 0.0128505 | intron-variant | TEP1 | GRCh38.p7 | 14:20378271 | TGGAAACGTGAAGAC[C/T]TGCTCTCAGCAAAAT | 7011 |
rs139483027 | in-del | -/TGGTTTTTTTTT | | | intron-variant | TEP1 | GRCh38.p7 | 14:20410800 | ATTGTTTCTCCTTTG[-/TGGTTTTTTTTT]TTTTTTTTTTTTTTT | 7011 |
rs139492867 | snp | G/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 14:20416638 | AGGAGGGATTAAGTC[G/T]TGAGAGCAGAGCCCT | 7011 |
rs139494450 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20403969 | CTTCATGGAGATACA[C/T]GAGAGCACAGAGTAG | 7011 |
rs139497310 | snp | C/G | 3.30251e-05 | 0.00406343 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20382242 | TCCGTGTGACTTCTA[C/G]GGCAGTCAAGGCCTG | 7011 |
rs139512373 | snp | A/C | 1.65269e-05 | 0.00287457 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20369777 | TCCTGATTCCTTTTG[A/C]CTCTGTGAAAGAATA | 7011 |
rs139517350 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20410849 | TGTTTTTTGAAACGG[A/G]GTCTCACTCTATTGC | 7011 |
rs139519365 | snp | A/G | 0.00138497 | 0.0262787 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20378105 | GCCATGGTGGGCAGG[A/G]AAGGCAGCCAGCCGT | 7011 |
rs139537263 | snp | C/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 14:20415890 | ATCCTGGGCCCTACC[C/T]ATTTAAATGTGTAAA | 7011 |
rs139580248 | snp | A/G | 0.0558544 | 0.157504 | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20367193 | ACATGGTGAAACTTC[A/G]TCTCTACTGAAATAC | 7011 |
rs139605910 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20407075 | CCTTGTCCCTCAACC[C/T]GAAACACAAGTATAT | 7011 |
rs139621392 | snp | A/C | 0.0123036 | 0.0774623 | intron-variant | TEP1 | GRCh38.p7 | 14:20393877 | GGATCGCTTGAGCTC[A/C]GGGGTTTGAAACCAG | 7011 |
rs139716447 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TEP1 | GRCh38.p7 | 14:20389424 | TGTGGTAGGCTAGGG[C/T]TAGGGTGGACTCTCA | 7011 |
rs139781911 | snp | C/G | 0.000452075 | 0.0150277 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20383793 | TTGGCCACGCAGATA[C/G]GTACAGAGGCGTCTG | 7011 |
rs139869929 | snp | A/G | 8.44759e-05 | 0.00649852 | intron-variant, missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20404739 | TATTGGCCACATTCC[A/G]GACGTTCAGCTGCTG | 7011 |
rs139927238 | snp | C/T | 0.00478085 | 0.0486577 | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20366609 | GATAGAAATAAAGTC[C/T]CTCAGGTTATTTCTC | 7011 |
rs139949220 | snp | C/G | 0.00161924 | 0.0284078 | synonymous-codon, intron-variant, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20401120 | GCGACTTCGAGAAAA[C/G]AGCTGTAGGTTGGAG | 7011 |
rs140013777 | snp | A/G | 0.00055992 | 0.0167226 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20371278 | GCCATACTCCTTGTG[A/G]GTGGACAATATCATA | 7011 |
rs140020170 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20401480 | CAGCAGGGCTTGAAC[A/G]TGCTGGGCAGGCTTG | 7011 |
rs140029752 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TEP1 | GRCh38.p7 | 14:20389460 | GGGTACAGAGTTAGG[C/T]TAAAGTATCCACCTG | 7011 |
rs140039705 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | TEP1 | GRCh38.p7 | 14:20411696 | AGAAAAAAAAAAAGT[A/G]TATACTGTTTTGTGC | 7011 |
rs140076747 | snp | A/G | 0.00680338 | 0.0579259 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20375851 | TTTGGGTGTCCTCAC[A/G]TCCCAGCAGAGGAGA | 7011 |
rs140077951 | snp | A/G | 0.00060943 | 0.0174454 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20408279 | TTCAGGTCAGGAAGC[A/G]TGGCTAGGCACTGGT | 7011 |
rs140158708 | snp | A/C/T | 4.99765e-05 | 0.00499862 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20395611 | CATCAGTGTTATATT[A/C/T]GAAGGAAAGGGCAAT | 7011 |
rs140162328 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 14:20416491 | CAGACCAATTAAATC[A/G]CAATCACCCAGAGTA | 7011 |
rs140332121 | snp | C/G | 4.96282e-05 | 0.00498113 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20377342 | GGCTTCTGGAATCTG[C/G]ACAGGAGCCAGAGGG | 7011 |
rs140348892 | snp | C/T | 0.00103958 | 0.0227752 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20382030 | AGTGTCCGCCACACA[C/T]TCAGCACTCCGTGCA | 7011 |
rs140399456 | snp | C/G/T | 0.000131776 | 0.00811621 | intron-variant, missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20403797 | TAGCCAGCTGGTACT[C/G/T]GTCAAACTGGGCAAA | 7011 |
rs140418621 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | TEP1 | GRCh38.p7 | 14:20392131 | TCTGAAAACTGGCAA[A/T]TAAAGGAGAATAAAT | 7011 |
rs140427855 | snp | A/C | 8.24056e-05 | 0.00641841 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20378837 | TTTGGTACTGGTGAG[A/C]CTTAGTCTGCAGCAC | 7011 |
rs140444610 | snp | C/G/T | 0.0376037 | 0.131863 | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20367650 | AGAGTCTCGCTCTGT[C/G/T]GCCCAGGCTGGAGTG | 7011 |
rs140474592 | snp | G/T | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20383263 | CAGAGGCCTCCAGAG[G/T]CCCCAAGGCCAGCAC | 7011 |
rs140490257 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20379849 | CAGAGTGATAACAGG[C/T]GTGTTTGGCTCATCT | 7011 |
rs140499790 | snp | C/T | 4.94368e-05 | 0.00497152 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20391640 | GCCTGTCTGCATTAG[C/T]ATCTGTCAGATAGAC | 7011 |
rs140522200 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TEP1 | GRCh38.p7 | 14:20387615 | GGCAAAGCCACAATG[A/G]AAAAGCCAGAACCTG | 7011 |
rs140581428 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | TEP1 | GRCh38.p7 | 14:20376954 | GGCGCAATGGCTCAC[A/G]TCTGTAATCCCAGCA | 7011 |
rs140582756 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TEP1 | GRCh38.p7 | 14:20412152 | AATATCTCACTGGAC[A/G]TCAGTGTGACAAACA | 7011 |
rs140613583 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20409285 | TTCTTAAAACTATTC[C/T]GACTAGATCTTCTGA | 7011 |
rs140689511 | snp | A/G | 0.000181215 | 0.00951706 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20391034 | TCCACACAGCACGAC[A/G]TCCACCTGCTCCGCC | 7011 |
rs140696200 | snp | C/T | 3.32624e-05 | 0.004078 | stop-gained, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20378530 | CCCACGGACTGTGTC[C/T]CACAGCTGAGGGAGA | 7011 |
rs140773101 | snp | A/G | 6.70219e-05 | 0.00578848 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20386522 | ATACGGTGAGGGGCC[A/G]CTCGGGCCTGCAGTG | 7011 |
rs140782313 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20397398 | CCTCTAATCCCAGCC[A/G]CTCGAAAGGCTGAGT | 7011 |
rs140817770 | snp | A/G | 3.35509e-05 | 0.00409564 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20407917 | CAGAGATGGATTTCA[A/G]GGCTATAGGGCAGGT | 7011 |
rs140821977 | snp | C/T | 8.24165e-05 | 0.00641883 | synonymous-codon, nc-transcript-variant, intron-variant | TEP1 | GRCh38.p7 | 14:20381572 | AATGAGGATGTGTGC[C/T]GTGTCCTCTAGCCCT | 7011 |
rs140918593 | snp | C/G/T | 0.00109676 | 0.0233919 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20380349 | GAGTCCAGGGGCTGG[C/G/T]TGGCTGCCTGCTGGG | 7011 |
rs140974086 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | TEP1 | GRCh38.p7 | 14:20405615 | AGAGGGAAGAAATGA[A/G]AAGAGAGGTAACAAG | 7011 |
rs141032284 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TEP1 | GRCh38.p7 | 14:20369046 | AGAGTCTCGCTCTGT[C/T]GCCCAGGCTGGAGTG | 7011 |
rs141077549 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20379254 | AGCACACGTTCAAGT[G/T]GGGGCCTCGTGATCC | 7011 |
rs141111607 | snp | C/T | 0.000148286 | 0.00860936 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20373115 | AAGCCACAGCAGTGA[C/T]GGCTGCAGAACTCCT | 7011 |
rs141172994 | snp | C/T | 0.00441581 | 0.0467804 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20386466 | TCCTACGGGTCTCCT[C/T]CTCAGTGACGCCCCA | 7011 |
rs141252226 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TEP1 | GRCh38.p7 | 14:20370449 | TGAAATCATATAGTA[C/T]GTACTCCTTTGTAAC | 7011 |
rs141252741 | snp | C/T | 0.000165369 | 0.00909158 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20376153 | TCAGTGCTGAAACTA[C/T]AGCAGCTCACAGGGC | 7011 |
rs141282395 | snp | A/G | 0.000378835 | 0.0137577 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20391711 | ACAGAGAGGTTCACA[A/G]CTGTCTCTAGGGCCT | 7011 |
rs141318575 | snp | C/T | 1.64925e-05 | 0.00287158 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20381385 | GGCATCAGCGTCACA[C/T]GTCTTCCAGAGCTGA | 7011 |
rs141322334 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20380646 | GCCCCACTCCAAACC[C/T]AGGAAACCAGAATAT | 7011 |
rs141340526 | snp | A/G | 4.94678e-05 | 0.00497307 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20384662 | TGAGATCCGACGTGC[A/G]GCCTCTTCAGACTCA | 7011 |
rs141409257 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20402573 | TAATCTTTATGACAA[C/T]CTAACAATGTAGGTT | 7011 |
rs141445002 | snp | A/G | 0.000938588 | 0.0216429 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20387963 | CCAGTGGCCGGAGAG[A/G]CTGGACCCCTGTCTT | 7011 |
rs141509875 | snp | A/G | 9.91408e-05 | 0.00703993 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20382043 | CACTCAGCACTCCGT[A/G]CAGCTGGTCCACAGT | 7011 |
rs141742706 | snp | A/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20410047 | AAAAAAAAAAAAAAA[A/T]AAAAAAAAATGCCTA | 7011 |
rs141772830 | snp | A/C/G | 0.0023933 | 0.0345097 | intron-variant | TEP1 | GRCh38.p7 | 14:20409971 | AGCTTGCAGTGAGCC[A/C/G]AGATTGGCCACTGCA | 7011 |
rs141773683 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20403087 | GCTTGAGCCTGTGAG[A/G]TGGAGGTTGTAGTGA | 7011 |
rs141820005 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TEP1 | GRCh38.p7 | 14:20372912 | GCCAGGATGCACCAT[C/T]TTTTCCCTCCCAGGC | 7011 |
rs141830967 | snp | A/G | 0.00182747 | 0.0301728 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20373297 | GAACCTGCCAGAGCC[A/G]TACAGAACCATCCTC | 7011 |
rs141928410 | snp | C/G | 0.000148762 | 0.00862315 | intron-variant, missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20404680 | GAAATATCGTCGCAG[C/G]TGGGGGCGACACGCC | 7011 |
rs141943004 | snp | A/G | 0.000214251 | 0.0103479 | intron-variant, missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20403743 | AGCGGGGTGGCCGGC[A/G]GGGGTGTCTCTTGGC | 7011 |
rs142047187 | snp | A/G | 0.000196004 | 0.00989765 | intron-variant | TEP1 | GRCh38.p7 | 14:20374384 | TCCCAAAGCCCCCTT[A/G]GCCCTTCCAGAGACC | 7011 |
rs142049486 | snp | A/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20408024 | ACACGGTACAAATCA[A/G]CTTGCGTCATGTGAG | 7011 |
rs142056330 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20375144 | GGCACACAGTGAGCA[C/T]ATAATAAATGGTAGC | 7011 |
rs142076659 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20406892 | GCAAAATGCAAAGCC[C/G]TAAATCAATGTAAGA | 7011 |
rs142149161 | snp | C/T | 6.84967e-05 | 0.00585181 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20383202 | GGTGACTCCTCCAGC[C/T]GCTTCCCGTACAGGG | 7011 |
rs142149466 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TEP1 | GRCh38.p7 | 14:20391519 | TGCCTGGGAAAACCA[A/G]CTCTGGGAACAGGAT | 7011 |
rs142239675 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | TEP1 | GRCh38.p7 | 14:20387807 | CCTTCATGAAGAGAA[C/T]AAGCGGCACCTCACC | 7011 |
rs142333924 | snp | C/G | 0.000596891 | 0.0172653 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20383311 | GCTCAAGGGTCTCCC[C/G]TAGGCCTGCATCACT | 7011 |
rs142420008 | snp | A/G | 0.000507823 | 0.0159265 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20383279 | CCCCAAGGCCAGCAC[A/G]TGGGCACCCTGGCTC | 7011 |
rs142469251 | snp | C/T | 6.58935e-05 | 0.00573955 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20386161 | CCACAAACAGCTGTG[C/T]GTTCTCCACCTCCCC | 7011 |
rs142510515 | snp | C/T | 0.000857887 | 0.0206932 | intron-variant, synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20403879 | CTTATCTCCCTCAGC[C/T]AGGCTCTGTCAAAGA | 7011 |
rs142545980 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TEP1 | GRCh38.p7 | 14:20377072 | AATATAAAATTAGCC[A/G]GGCGTGGAGGCGCAT | 7011 |
rs142564652 | snp | C/T | 6.60033e-05 | 0.00574433 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20378208 | TTGAAGGCCAAGGTA[C/T]GGATAGAGGCTCCGG | 7011 |
rs142580077 | in-del | -/CAATAGTAAGTCT | | | intron-variant | TEP1 | GRCh38.p7 | 14:20380560 | CATATGGTGTGTCTA[-/CAATAGTAAGTCT]CAAAGTGTGGCCCTC | 7011 |
rs142604447 | snp | A/C | 0.00795532 | 0.062565 | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20402168 | AAAAAATTAGCTGGG[A/C]ATGGTGGTGGATGTC | 7011 |
rs142639682 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20374796 | GCTGAGTGCGTCTAC[A/G]TAAAGGACTTAGGCT | 7011 |
rs142708166 | snp | A/G | 0.00131701 | 0.0256275 | missense, utr-variant-5-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20396716 | GCATGGCCATGAAGG[A/G]AAGCTTCCCATTTTC | 7011 |
rs142740802 | snp | A/C/T | 0.000131888 | 0.00811961 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20373683 | GTTTTGTTACCTGCA[A/C/T]GGGGCTCCATGGCAG | 7011 |
rs142826334 | snp | A/G | 0.000115316 | 0.00759243 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20387923 | TGCTGGGAAACAGGA[A/G]CCAAGGGGCTTGGAG | 7011 |
rs142875402 | snp | A/G | 0.00874735 | 0.0655527 | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20366968 | TCTGAAAATTCTACA[A/G]AACACCCCAGCTAAG | 7011 |
rs142901031 | snp | C/G | 0.0225045 | 0.103662 | upstream-variant-2KB, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20413530 | GCGGGCGGAGACTCT[C/G]GGGCCCGGGCGGGGC | 7011 |
rs142940095 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | TEP1 | GRCh38.p7 | 14:20411318 | TTATTAATTGCCAAG[A/G]TATCTCTTGACTACG | 7011 |
rs142976796 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant, missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20404709 | CCGGCAAGAAAGCAG[C/T]AATGGCCAAGATGTT | 7011 |
rs142983753 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | TEP1 | GRCh38.p7 | 14:20389440 | TAGGGTGGACTCTCA[C/T]AGAGGGGTACAGAGT | 7011 |
rs142984380 | snp | G/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20366044 | AAACCTAAATTGATT[G/T]TCCCTTCAACTCCTT | 7011 |
rs143001671 | snp | C/G | 1.95223e-05 | 0.00312422 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20383834 | GGGCAAGACCCTGGT[C/G]AGGACGAGCCCCAGA | 7011 |
rs143081526 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20400708 | AGAGATATCGATATG[A/C]GTACAATGAGAGAGA | 7011 |
rs143088473 | snp | A/G | 0.000626618 | 0.0176894 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20368450 | CTTCATTCCCAATTC[A/G]GAAAGTACACATTGC | 7011 |
rs143109919 | snp | A/G | 0.0036377 | 0.0424925 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20380958 | GGGCCTCCAAGAGCC[A/G]AGAGACCAGACCCAA | 7011 |
rs143114193 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TEP1 | GRCh38.p7 | 14:20399523 | CTTATATCTTTTTTT[A/G]TATTTCCTTTTATTT | 7011 |
rs143154274 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | TEP1 | GRCh38.p7 | 14:20413086 | CCCCTTTCGATGGGC[A/G]CACAGGGCAAGGAAG | 7011 |
rs143286405 | snp | C/T | 3.2993e-05 | 0.00406145 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20379990 | GCCCACAGCTGCTCT[C/T]TGCCCATTGGTGGAG | 7011 |
rs143407981 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | TEP1 | GRCh38.p7 | 14:20381854 | CTATACAGAGGGCCC[C/T]GGCTCAAAGAAGGGA | 7011 |
rs143456437 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20391091 | CAGTGCATAGTTCAG[C/T]GGGGGCTGATTGGAC | 7011 |
rs143467572 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | TEP1 | GRCh38.p7 | 14:20388842 | AAGAGGAGTGAACTA[C/T]CTCACTTTAAAAAAG | 7011 |
rs143496437 | snp | C/T | 0.000329435 | 0.01283 | splice-acceptor-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20403450 | GGAGGCTCCATCCCC[C/T]GTAGGGACAGGAGAA | 7011 |
rs143498164 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | TEP1 | GRCh38.p7 | 14:20401382 | GGTTTGAGAACTACT[A/G]GGATGGGGGCCACGG | 7011 |
rs143508077 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | TEP1 | GRCh38.p7 | 14:20399988 | ATGGTGAAACGCCGT[C/G]TCTACTAAAAATACA | 7011 |
rs143540555 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | TEP1 | GRCh38.p7 | 14:20411858 | TGGCTCACACCTGTA[A/G]TCCTAGCATTTTGGG | 7011 |
rs143541421 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | TEP1 | GRCh38.p7 | 14:20411110 | CAGGCGTGAGCCACC[A/G]CACCCAGCCTAATTG | 7011 |
rs143599402 | snp | A/T | 0.00148642 | 0.0272214 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20406385 | CTTTCTTCTCTTCTG[A/T]ATCAAACCAACGACC | 7011 |
rs143634087 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TEP1 | GRCh38.p7 | 14:20405316 | GGACTAGGCCGCAGA[C/G]TCACCCAGAAATCCT | 7011 |
rs143659617 | snp | A/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20410042 | AAAAAAAAAAAAAAA[A/T]AAAAAAAAAAAAAAT | 7011 |
rs143730670 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TEP1 | GRCh38.p7 | 14:20384847 | CAGCACCAAGGCTGA[C/T]GTGGGGCTGCAAAGG | 7011 |
rs143779670 | snp | A/G | 6.59228e-05 | 0.00574083 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20395909 | GCATCATGGGCGTTA[A/G]GAAATCTGAATGGAA | 7011 |
rs143847342 | snp | A/G | 0.000592905 | 0.0172076 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20386162 | CACAAACAGCTGTGC[A/G]TTCTCCACCTCCCCA | 7011 |
rs143898219 | snp | A/G | 3.33422e-05 | 0.00408289 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20395612 | ATCAGTGTTATATTC[A/G]AAGGAAAGGGCAATG | 7011 |
rs143928751 | in-del | -/GT | | | intron-variant | TEP1 | GRCh38.p7 | 14:20400298 | TTTGTGTGTGGGTGC[-/GT]GTGTGTGTGTGTGCA | 7011 |
rs143943859 | snp | A/G | 0.000131863 | 0.00811875 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20380419 | GCCTCAGGAAGGTGC[A/G]AAACACTGCAACGTC | 7011 |
rs143988875 | snp | A/G | 0.0221141 | 0.102801 | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20367832 | GCCAGGATGGTCTTG[A/G]TCTCCTGACCTCGTG | 7011 |
rs144008371 | snp | A/G | 0.00116728 | 0.0241304 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20382341 | TGGCAGGCAGGGTCC[A/G]GAGTCTCTCAGACAC | 7011 |
rs144062570 | snp | A/G | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20369459 | GTCCCTGGAGTTTGG[A/G]TTTCTGGAGTGTTTG | 7011 |
rs144107831 | snp | A/C/T | 0.000214138 | 0.0103454 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20380312 | TCTCCGGGAGAGCAG[A/C/T]GAGGCTTGGTGGCAA | 7011 |
rs144150517 | snp | C/G | 0.00453942 | 0.047456 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20381030 | TCGAAAGAAGTCCAC[C/G]GTTCCCGCTCTGGAG | 7011 |
rs144161373 | snp | C/T | 3.34236e-05 | 0.00408787 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20405585 | AGCTCAGTAGAGCCA[C/T]CTGGGAATTGAGAAA | 7011 |
rs144201146 | snp | C/T | 0.00139815 | 0.0264031 | intron-variant | TEP1 | GRCh38.p7 | 14:20383935 | TGCATGGGACAGGAA[C/T]AGAAAACATGGTCAC | 7011 |
rs144229259 | snp | A/C | 1.6473e-05 | 0.00286988 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20371224 | AGGACTTACCAAGAA[A/C]GAAAGAACTCCAGGA | 7011 |
rs144244427 | snp | A/G | 0.000164872 | 0.00907794 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20373694 | TGCACGGGGCTCCAT[A/G]GCAGCTGCACAGTGG | 7011 |
rs144273794 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TEP1 | GRCh38.p7 | 14:20370081 | ACCACACCCAGCTGA[C/T]TTTTTTATTTTTAGT | 7011 |
rs144321430 | snp | A/G | 3.295e-05 | 0.00405881 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20382667 | GATCGGTGACCAAGC[A/G]CAGGTAGAGCGGCCG | 7011 |
rs144340778 | snp | A/G | 0.00874735 | 0.0655527 | | | GRCh38.p7 | 14:20416286 | TTCCATCATATTCCC[A/G]TAAATATCAGACCTG | 7011 |
rs144403421 | snp | C/T | 0.0107246 | 0.0724382 | downstream-variant-500B | TEP1 | GRCh38.p7 | 14:20365494 | TGGCCAGGCTCGCCT[C/T]GAACTCCAGACCCCA | 7011 |
rs144424113 | snp | A/C/G | 0.00042894 | 0.0146387 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20378209 | TGAAGGCCAAGGTAC[A/C/G]GATAGAGGCTCCGGG | 7011 |
rs144451613 | snp | C/G | 0.000131941 | 0.00812116 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20391626 | GCTCTTTGGACAGAG[C/G]CTGTCTGCATTAGCA | 7011 |
rs144557772 | snp | A/G | 0.000153988 | 0.00877328 | missense, intron-variant, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20401107 | AAGGCCCAGGAAGGC[A/G]ACTTCGAGAAAAGAG | 7011 |
rs144626723 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TEP1 | GRCh38.p7 | 14:20397440 | CTTGAAACCAAAATG[C/T]GAAGGTTGCAGTGAA | 7011 |
rs144650901 | snp | C/G | 6.60208e-05 | 0.00574509 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20384135 | TCCTGAAGAAGGCGT[C/G]GCCGGGCAGGACTCG | 7011 |
rs144651230 | snp | C/G | 0.0138799 | 0.0821421 | intron-variant | TEP1 | GRCh38.p7 | 14:20393080 | AAATTAGCCGGGCGT[C/G]GTGGTGGGTGCCTGC | 7011 |
rs144678962 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | TEP1 | GRCh38.p7 | 14:20390121 | AGTACTCCCAGCTAC[C/T]TGGGAGGCTGAGGCA | 7011 |
rs144724013 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | TEP1 | GRCh38.p7 | 14:20400759 | GATAAAAACTTGTAC[A/G]TCACCTAACTACATC | 7011 |
rs144750938 | in-del | -/C | 0.030278 | 0.119257 | intron-variant | TEP1 | GRCh38.p7 | 14:20386698 | ACACTGCTGTGATCA[-/C]CCTTTAGCACTGAGC | 7011 |
rs144769892 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | TEP1 | GRCh38.p7 | 14:20411148 | TTACTGAAATACAAC[C/T]CCTTAAGGTAAGGGC | 7011 |
rs144774738 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TEP1 | GRCh38.p7 | 14:20407139 | AACTGTATACTAAAT[A/G]TAGGCATGTAGATGT | 7011 |
rs144833222 | snp | C/T | 0.00073215 | 0.0191191 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20378026 | TCTGCAAGCTGACCT[C/T]GCCATCCTCTCCAGC | 7011 |
rs144854568 | snp | C/T | 6.78967e-05 | 0.00582613 | intron-variant, missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20404742 | TGGCCACATTCCGGA[C/T]GTTCAGCTGCTGCCT | 7011 |
rs144863730 | snp | A/G | 7.07827e-05 | 0.00594864 | intron-variant | TEP1 | GRCh38.p7 | 14:20404784 | ATGCCTAGGACACAG[A/G]GTGAGAGGACTAGAA | 7011 |
rs144898570 | snp | C/T | 1.65795e-05 | 0.00287914 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20376222 | TCTGCCTTGTGTGGC[C/T]GCGTCAGCAGCTGCC | 7011 |
rs145042167 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | TEP1 | GRCh38.p7 | 14:20405649 | CAACTTAAGCATCCA[C/T]GCAGACTAACTTACA | 7011 |
rs145064396 | snp | G/T | 0.00117087 | 0.0241674 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20408382 | GCATAGCCAGGCACC[G/T]GTTCTCCAAGGAGAG | 7011 |
rs145081736 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20398845 | GATGTAAGTCTTATT[C/T]GAATTATAGCTGGAA | 7011 |
rs145088591 | snp | C/G | 6.60928e-05 | 0.00574822 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20389280 | AGTGTCACATCATTG[C/G]GATTCAAATCTGTTG | 7011 |
rs145122151 | snp | C/T | 3.30486e-05 | 0.00406487 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20385003 | AGGAAGCTGGAATCC[C/T]GGAAGTAGATGAGAG | 7011 |
rs145146246 | snp | G/T | 0.0329836 | 0.124112 | intron-variant | TEP1 | GRCh38.p7 | 14:20375401 | CCTCGTGATCCACTC[G/T]CCTCGGCCTCCCAAA | 7011 |
rs145200939 | snp | A/G | 4.96693e-05 | 0.00498319 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20395592 | TTCTAGTTAGTATCC[A/G]CCTCATCAGTGTTAT | 7011 |
rs145204534 | snp | C/G | 0.000951657 | 0.0217927 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20386512 | GTGAAGGCTGATACG[C/G]TGAGGGGCCGCTCGG | 7011 |
rs145271356 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | TEP1 | GRCh38.p7 | 14:20412808 | GGATTACAGGCGCCC[A/G]CCACCATGCCCGGCT | 7011 |
rs145356843 | snp | A/C/T | 0.000198051 | 0.00994954 | missense, upstream-variant-2KB, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20401569 | CTGACACTGTATCAC[A/C/T]GGCCTTCTCAAACTG | 7011 |
rs145376137 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TEP1 | GRCh38.p7 | 14:20395015 | CTATCTTTGTGTGTA[C/T]TTCAAAATACACACA | 7011 |
rs145400735 | snp | A/G | 0.000912979 | 0.0213461 | intron-variant | TEP1 | GRCh38.p7 | 14:20376061 | GAAATCTAGGAACTA[A/G]AGAGGCTATGGGACC | 7011 |
rs145411510 | snp | G/T | 0.0146728 | 0.0844358 | intron-variant | TEP1 | GRCh38.p7 | 14:20409749 | ATGCTGGCCGGGCGC[G/T]GTGGCTCACGCCTGT | 7011 |
rs145413343 | snp | C/T | 1.64817e-05 | 0.00287064 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20378847 | GTGAGCCTTAGTCTG[C/T]AGCACCCTATCCCAG | 7011 |
rs145421229 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | TEP1 | GRCh38.p7 | 14:20408680 | AGAGCAGAGAAATTA[A/G]GAAAAGGCCAGGTGC | 7011 |
rs145454699 | in-del | -/TTTCTAAATGCCCTGA | 0.00914312 | 0.0669923 | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20367961 | ACAGAAACATAGCTC[-/TTTCTAAATGCCCTGA]TGCATGACTGACTTA | 7011 |
rs145462743 | snp | A/C/G/T | 0.00315493 | 0.039611 | intron-variant | TEP1 | GRCh38.p7 | 14:20390644 | TGCAGAGGAAAATGT[A/C/G/T]GGGGAGGGAGAGGGT | 7011 |
rs145504517 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20371897 | CAGTAAGGCCTGTGG[A/C]TGCAACACATGCCTA | 7011 |
rs145548620 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | TEP1 | GRCh38.p7 | 14:20378916 | CCCTCCTCATTTCCT[C/T]CTCCTGGGGCTTCCA | 7011 |
rs145567037 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20396539 | CTGCCCCCTGAAAAA[A/G]CCTGGCCTCTAAAGC | 7011 |
rs145594272 | snp | A/G | 6.65857e-05 | 0.00576961 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20376112 | AGCTCACCCGATCCC[A/G]GCCCCCGGTGGCCAG | 7011 |
rs145657579 | snp | C/T | 0.00463695 | 0.0479274 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20380373 | TGCTGGGGCAGGAGC[C/T]GGGGGTACTGGCTGA | 7011 |
rs145695515 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TEP1 | GRCh38.p7 | 14:20379673 | TCTCCCAACAAAACT[A/G]ACCACTTGGTGGGCA | 7011 |
rs145715378 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20412455 | AAAGTTAAAGTTCCG[A/T]CCCCACTTCCATCTC | 7011 |
rs145717418 | snp | A/G | 0.0681886 | 0.171594 | intron-variant | TEP1 | GRCh38.p7 | 14:20376996 | CGAGGTGGGTGGATC[A/G]CCTATGGTCAGGAGT | 7011 |
rs145722439 | snp | A/G | 3.29772e-05 | 0.00406048 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20385040 | CAGAGGGCTGCAGAC[A/G]TTGGTTCCGGTTCAG | 7011 |
rs145747576 | snp | A/G | 0.000231447 | 0.010755 | missense, nc-transcript-variant, intron-variant | TEP1 | GRCh38.p7 | 14:20381661 | GCCGGGCACCAGGGC[A/G]CTCCAGAGGGCCCTC | 7011 |
rs145784365 | snp | A/C/G | 3.81119e-05 | 0.00436515 | | | GRCh38.p7 | 14:20386605 | AGTGGATGAAATGAA[A/C/G]AGCCGGATGCTGCGC | 7011 |
rs145795987 | snp | C/T | 0.000477653 | 0.0154466 | intron-variant, missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20403760 | GGGTGTCTCTTGGCC[C/T]GGTGCTTCCGAGGGT | 7011 |
rs145820200 | snp | A/G | 1.64727e-05 | 0.00286986 | synonymous-codon, intron-variant, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20372807 | ATCAGCACTGAGGAC[A/G]AAAAAGGTGTGTGCC | 7011 |
rs145944940 | snp | G/T | 0.000331362 | 0.0128674 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20384096 | CTCAGCCTTCCGTGG[G/T]GCAGCATCAGCCGTT | 7011 |
rs146024505 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | TEP1 | GRCh38.p7 | 14:20374846 | TGTAATCCCAATACT[C/T]TGGGAGGCCGAGGCA | 7011 |
rs146106964 | snp | A/C/G | 0.000829179 | 0.0203453 | missense, intron-variant, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20401127 | CGAGAAAAGAGCTGT[A/C/G]GGTTGGAGGGGTATC | 7011 |
rs146168346 | snp | A/G | 6.60939e-05 | 0.00574827 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20382272 | GGGGAAGGACATCAG[A/G]CCCGTGCTCCTTCTC | 7011 |
rs146208574 | snp | C/G | 0.00164036 | 0.0285918 | intron-variant | TEP1 | GRCh38.p7 | 14:20387862 | TCCCAAGGTTTGACT[C/G]CAGCCCCTCCCAATT | 7011 |
rs146209972 | snp | A/G | 5.8372e-05 | 0.00540209 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20383840 | GACCCTGGTCAGGAC[A/G]AGCCCCAGAAAAGTG | 7011 |
rs146231909 | snp | C/T | 0.0176667 | 0.0923105 | intron-variant | TEP1 | GRCh38.p7 | 14:20374398 | TAGCCCTTCCAGAGA[C/T]CCCCCAGTGGGATCT | 7011 |
rs146257325 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20406172 | GACCTGGTTCAAGTA[C/G]TCCACCACCAACCTC | 7011 |
rs146257508 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | TEP1 | GRCh38.p7 | 14:20370695 | TTTCTCTTAGGTATA[C/T]ATTTAGGAGTGGAAT | 7011 |
rs146268772 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TEP1 | GRCh38.p7 | 14:20403572 | AAAGAAGACTGCCCT[A/G]CACCATATGCCCATG | 7011 |
rs146288286 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | TEP1 | GRCh38.p7 | 14:20400568 | TCCTCCTCTATTTGA[C/G]TTTTTTTTTTTCTGT | 7011 |
rs146306984 | snp | A/G/T | 0.000280973 | 0.0118495 | intron-variant, missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20404682 | AATATCGTCGCAGGT[A/G/T]GGGGCGACACGCCGG | 7011 |
rs146330073 | snp | C/T | 0.000148303 | 0.00860985 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20373526 | AGTGGATGCCATAAC[C/T]GTGTGGCCCCATCTA | 7011 |
rs146350871 | snp | G/T | 0.00221188 | 0.033182 | intron-variant | TEP1 | GRCh38.p7 | 14:20389307 | GTTGACCTGGCAAAG[G/T]AAGAAGCAGTCATTA | 7011 |
rs146378910 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20386921 | TTATCTCCATTTTAG[A/C]AATCAAGAAACGATA | 7011 |
rs146413291 | snp | C/T | 0.000131874 | 0.00811909 | intron-variant | TEP1 | GRCh38.p7 | 14:20371180 | AACACTGGTCCTAGA[C/T]GAATGTTTGCTTTAG | 7011 |
rs146424991 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20367905 | TGAGCCACCATGCCC[A/G]GCCTCCTCTGGGTAG | 7011 |
rs146511904 | snp | A/G | 4.94539e-05 | 0.00497238 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20382694 | GCCGGCCTGATTCCC[A/G]CTTCACCAGCAGCAG | 7011 |
rs146530626 | snp | A/G | 0.000199243 | 0.00997907 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20381037 | AAGTCCACGGTTCCC[A/G]CTCTGGAGCTGAGAA | 7011 |
rs146656308 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20401820 | ACACAAGCAGTTAAC[A/G]TGGGTTGACTGGCTT | 7011 |
rs146667495 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TEP1 | GRCh38.p7 | 14:20399764 | ATGGGCATTTGCCTC[A/G]ACCAGGATAAATGAC | 7011 |
rs146669383 | snp | A/C | 9.89315e-05 | 0.00703249 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20381012 | GGAGGTTGGTAAGGA[A/C]CTTCGAAAGAAGTCC | 7011 |
rs146778977 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 14:20416587 | TCATGTTGAAACTCA[A/G]TCTGCGATGTGATAA | 7011 |
rs146790532 | snp | A/G | 0.030278 | 0.119257 | intron-variant | TEP1 | GRCh38.p7 | 14:20411906 | TCACTTGAGGTCAGG[A/G]GTTCAAGACCAGCCT | 7011 |
rs146872301 | snp | C/T | 9.88484e-05 | 0.00702954 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20401510 | GTGGATGTGCAGTCG[C/T]TGAACCAGCTTCTTC | 7011 |
rs146890821 | snp | C/T | 9.89413e-05 | 0.00703284 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20395880 | TTCTGAGTTGAGCCT[C/T]GAGGGCATCAATGGC | 7011 |
rs146921827 | snp | A/G | 0.00438332 | 0.0466095 | upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20414355 | TTGCCACCAGTCCCA[A/G]CACTCCCTGCAATGG | 7011 |
rs146938823 | snp | A/G/T | 6.59093e-05 | 0.0057403 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20373141 | CTCCTTGGTATACAT[A/G/T]TGTCATCTGGAGGAG | 7011 |
rs147008163 | snp | A/C/G | 3.33645e-05 | 0.00408425 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20368814 | AGCTGCATACTGGGT[A/C/G]TCTCCCATAGCTTAA | 7011 |
rs147025855 | snp | A/T | 1.65603e-05 | 0.00287747 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20381919 | CACCTGTACCTGCGC[A/T]GACTCTGGACGAGGC | 7011 |
rs147119551 | snp | C/T | 1.64806e-05 | 0.00287054 | intron-variant | TEP1 | GRCh38.p7 | 14:20373007 | CAAGGGTACACCGAC[C/T]CACCTGTGCTGTGGC | 7011 |
rs147151688 | snp | A/G | 0.00895149 | 0.0662994 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20382012 | CTCTTAGTCCCCTTC[A/G]GTAGTGTCCGCCACA | 7011 |
rs147161769 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | TEP1 | GRCh38.p7 | 14:20378591 | TGCCTGAACTTCTCA[A/G]TCCCAGACCTCCAGG | 7011 |
rs147180226 | snp | C/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20391629 | CTTTGGACAGAGCCT[C/G]TCTGCATTAGCATCT | 7011 |
rs147196720 | snp | A/G | 0.0003347 | 0.0129321 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20386517 | GGCTGATACGGTGAG[A/G]GGCCGCTCGGGCCTG | 7011 |
rs147269209 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20395185 | CATACATCAGCATAA[C/T]TAAAAGAAAGGAATC | 7011 |
rs147276664 | in-del | -/AATCATTTTCAGT/AATCGTTTTCAGT | 0.0921334 | 0.197066 | intron-variant | TEP1 | GRCh38.p7 | 14:20400860 | AGACCTTATAAATCA[-/AATCATTTTCAGT/AATCGTTTTCAGT]AATACAACAACCAGG | 7011 |
rs147286683 | snp | A/G | 0.000428209 | 0.014626 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20380326 | GCGAGGCTTGGTGGC[A/G]AAGAGGTGAGTCCAG | 7011 |
rs147374863 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | TEP1 | GRCh38.p7 | 14:20406937 | ATCCTGATAACAACC[A/C]TGTGAAGTAGATTTT | 7011 |
rs147469507 | snp | A/G | 0.00716266 | 0.059414 | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20366165 | ACAAAAAACCCTTCA[A/G]GTGGGCCTGGCCAAC | 7011 |
rs147513845 | snp | C/T | | | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20408208 | CCAGGCACTGGTTCT[C/T]CAAGGAGAGGATGTC | 7011 |
rs147582486 | snp | C/G/T | 4.94298e-05 | 0.0049712 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20405488 | AGGAGGGCAAGTTCA[C/G/T]GACAGATTTCAAAAA | 7011 |
rs147598692 | snp | A/G | 6.59457e-05 | 0.00574182 | intron-variant, missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20403740 | GAGAGCGGGGTGGCC[A/G]GCGGGGGTGTCTCTT | 7011 |
rs147608083 | snp | G/T | 3.29636e-05 | 0.00405964 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20390690 | ACTCACAGGAACCCT[G/T]TGGCCAGCCAGAGAC | 7011 |
rs147616762 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | TEP1 | GRCh38.p7 | 14:20387728 | GTAGAGAAAGGAAGG[A/G]CTTGCTCACAATCTG | 7011 |
rs147687706 | snp | C/T | 0.00366712 | 0.0426628 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20384459 | CAAACTCCTCCAGCC[C/T]GCCAACATAGGGCCG | 7011 |
rs147704289 | snp | A/G | 1.79787e-05 | 0.00299817 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20383304 | TGGCTCTGCTCAAGG[A/G]TCTCCCCTAGGCCTG | 7011 |
rs147712532 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | TEP1 | GRCh38.p7 | 14:20404230 | CGTGGTGGCGCACGC[C/T]TGTAATCCCAGCTAC | 7011 |
rs147722126 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20402145 | ACCCCGTCTCTACTA[A/G]AACTACAAAAAAATT | 7011 |
rs147792517 | snp | C/G/T | 6.65528e-05 | 0.00576824 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20376114 | CTCACCCGATCCCGG[C/G/T]CCCCGGTGGCCAGGC | 7011 |
rs147809260 | snp | C/G | 3.29538e-05 | 0.00405904 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20373102 | CCATCTGGTGCCCAA[C/G]CCACAGCAGTGACGG | 7011 |
rs147848458 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | TEP1 | GRCh38.p7 | 14:20391973 | AGGATTCTTCTAATC[C/T]ACACTCATGGTAGGA | 7011 |
rs147932685 | snp | A/G | 0.00264957 | 0.036301 | intron-variant | TEP1 | GRCh38.p7 | 14:20372879 | TACACAACAAGTTCA[A/G]TTCAGTGCTTCTGAT | 7011 |
rs147955793 | snp | C/T | 0.00212869 | 0.0325548 | intron-variant | TEP1 | GRCh38.p7 | 14:20404822 | CACTCCTCCCGTAGC[C/T]TTCTGCCCTGAAATT | 7011 |
rs148006830 | snp | C/T | 0.0766824 | 0.180169 | intron-variant | TEP1 | GRCh38.p7 | 14:20388845 | AGGAGTGAACTACCT[C/T]ACTTTAAAAAAGAAG | 7011 |
rs148038396 | snp | C/G | 0.0174175 | 0.0916809 | intron-variant | TEP1 | GRCh38.p7 | 14:20409925 | TACTCGGGAGGCTGA[C/G]GCAGGAGAATGGCGT | 7011 |
rs148069631 | snp | C/T | 0.00027771 | 0.0117804 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20407890 | AAGTTGCTTCCTGAG[C/T]TGTCTCTGTGGCAGA | 7011 |
rs148090256 | snp | A/G | 0.00350625 | 0.0417233 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20405536 | TCAGATGTATTGTTC[A/G]TGTTTACTTCTGAGA | 7011 |
rs148140542 | snp | A/G/T | 0.000904709 | 0.02125 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20383804 | GATAGGTACAGAGGC[A/G/T]TCTGAGCAGAGTGAG | 7011 |
rs148173887 | snp | C/T | 0.000379091 | 0.0137623 | intron-variant | TEP1 | GRCh38.p7 | 14:20373163 | CTGGAGGAGAAAGGA[C/T]GTGTTTCATTAGGAG | 7011 |
rs148176617 | snp | A/C | 0.0256215 | 0.110247 | intron-variant | TEP1 | GRCh38.p7 | 14:20398046 | GCGTGAGCCACCATG[A/C]CCAGCCCATAGTTTC | 7011 |
rs148192913 | snp | C/G/T | 0.000272747 | 0.0116752 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20386458 | ACACCTGTTCCTACG[C/G/T]GTCTCCTCCTCAGTG | 7011 |
rs148207836 | in-del | -/C/CC | 0.00597247 | 0.0543191 | intron-variant | TEP1 | GRCh38.p7 | 14:20394086 | AATAAAATCCTGTCT[-/C/CC]CAAAAAAAAAAGGGA | 7011 |
rs148250661 | snp | C/T | 0.00106658 | 0.0230684 | intron-variant | TEP1 | GRCh38.p7 | 14:20381060 | GCTGAGAAGGTCAGA[C/T]TGAATTCATTAGGGA | 7011 |
rs148283523 | snp | A/G | 0.000232473 | 0.0107788 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20376229 | TGTGTGGCCGCGTCA[A/G]CAGCTGCCTTGGCCA | 7011 |
rs148302230 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TEP1 | GRCh38.p7 | 14:20376467 | TAGGACGGGAACGTG[C/T]GGCACTCCCAGCTCC | 7011 |
rs148363839 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TEP1 | GRCh38.p7 | 14:20394046 | GAGCTGGGATTGTGC[C/T]ATTGCACTCCAGCCT | 7011 |
rs148523039 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | TEP1 | GRCh38.p7 | 14:20390300 | TCCTAATAATTTTAC[C/T]ACATTTTACTATTAT | 7011 |
rs148524029 | snp | A/G | 0.000115554 | 0.00760025 | stop-gained, intron-variant, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20401113 | CAGGAAGGCGACTTC[A/G]AGAAAAGAGCTGTAG | 7011 |
rs148544268 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | TEP1 | GRCh38.p7 | 14:20400827 | AGGTACCACTGTTTA[C/T]TTTGGTGTAGTCAAT | 7011 |
rs148553668 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | TEP1 | GRCh38.p7 | 14:20411219 | CAAAACCCGACTTCC[A/G]GTCACCTCCCAGCAT | 7011 |
rs148617556 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20406689 | GCATGGGGCTCTTCA[C/G]ACACCTTTTAGGATA | 7011 |
rs148696839 | snp | A/G | 8.25266e-05 | 0.00642312 | stop-gained, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20382712 | TCACCAGCAGCAGTC[A/G]CATCTGGCAAGACTC | 7011 |
rs148699881 | snp | C/T | 0.0715223 | 0.175059 | intron-variant | TEP1 | GRCh38.p7 | 14:20375044 | TGCAGTGAGCAGAGA[C/T]TGCGCCACTGCACTC | 7011 |
rs148711061 | snp | C/G | 0.0980852 | 0.198549 | intron-variant | TEP1 | GRCh38.p7 | 14:20387312 | AGCACTTTGGGAGGT[C/G]GAGGCGGGCAGATCA | 7011 |
rs148752202 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20370439 | TTCATTTAGGTGAAA[C/T]CATATAGTATGTACT | 7011 |
rs148776761 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TEP1 | GRCh38.p7 | 14:20382897 | TCTGCCCAGCCAGCC[C/T]TGCCAGAAAACCCCT | 7011 |
rs148787322 | snp | C/T | 4.95094e-05 | 0.00497517 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20373747 | GGATGCTGGTCAGCT[C/T]CACGCCTTGATGGTC | 7011 |
rs148837253 | snp | C/G | 0.000593462 | 0.0172157 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20406359 | ATAAGAAGGCATTTG[C/G]GTCTCTGCCCCTTTC | 7011 |
rs148838117 | snp | A/C/T | 0.00011531 | 0.00759228 | missense, upstream-variant-2KB, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20403406 | CTCTGAGAAACCCTA[A/C/T]GTACCTTGGAAAACA | 7011 |
rs148872333 | snp | C/G | 0.00371868 | 0.0429594 | intron-variant | TEP1 | GRCh38.p7 | 14:20384340 | CCCCAGGACAACCCA[C/G]ACCACCCCATGTCCC | 7011 |
rs148892799 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20396540 | TGCCCCCTGAAAAAG[C/T]CTGGCCTCTAAAGCA | 7011 |
rs148926124 | snp | A/G | 0.000137583 | 0.00829291 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20386610 | ATGAAATGAAAAGCC[A/G]GATGCTGCGCCATCT | 7011 |
rs148959670 | snp | A/C | 1.65861e-05 | 0.00287972 | missense, nc-transcript-variant, intron-variant | TEP1 | GRCh38.p7 | 14:20381672 | GGGCGCTCCAGAGGG[A/C]CCTCCCCTAGCAAAC | 7011 |
rs149049108 | snp | A/G | 0.0023933 | 0.0345097 | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20368118 | AGGGTCCTAGGGCCC[A/G]CGAGTGATGCAAGAA | 7011 |
rs149050411 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20392778 | TAGTTTTGTCAGGTA[C/T]ATTAATGACATTCTC | 7011 |
rs149072596 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20401971 | CACAATGCAGGCTAC[A/G]AGGAGTTTAAAAACT | 7011 |
rs149106689 | in-del | -/TGTG | | | intron-variant | TEP1 | GRCh38.p7 | 14:20372403 | TGTGTGTGTGTGTGT[-/TGTG]GTGTGTGTGTATCTT | 7011 |
rs149133823 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | TEP1 | GRCh38.p7 | 14:20408923 | ACCCCCCTGACCCCC[A/G]CTGCAGGACTATCAG | 7011 |
rs149230338 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | TEP1 | GRCh38.p7 | 14:20376346 | AAAGACAGGAGCGGC[C/T]ATGGGGGCTGAGGGT | 7011 |
rs149239555 | snp | A/G | 3.29587e-05 | 0.00405934 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20391053 | ACCTGCTCCGCCCTC[A/G]TGATCATCATCCCAA | 7011 |
rs149273269 | snp | A/G | 0.000148595 | 0.00861831 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20382252 | TTCTAGGGCAGTCAA[A/G]GCCTGGGGAAGGACA | 7011 |
rs149326341 | snp | A/G | 0.00337173 | 0.0409206 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20377632 | ATCCTAATGCCATCC[A/G]CTCGATATCCAACAG | 7011 |
rs149401651 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20386645 | ATAAGCAGAGAGCTG[A/G]GCTCAGTCTAGGGAT | 7011 |
rs149434806 | snp | A/G | 0.000197072 | 0.00992456 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20383786 | CTTTTAGTTGGCCAC[A/G]CAGATAGGTACAGAG | 7011 |
rs149521092 | snp | A/C/T | 0.000280055 | 0.0118304 | intron-variant, missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20403832 | TCCGTCATGGCAGTA[A/C/T]GGAGACAGGCGGGCA | 7011 |
rs149539721 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20406572 | CTGTCTGACTTACTG[C/T]TCTCACACACCACCT | 7011 |
rs149614257 | snp | C/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 14:20416190 | GCCTTAGATAATAAT[C/T]CCAACCTCAAGACCT | 7011 |
rs149674201 | snp | A/G | 1.64738e-05 | 0.00286995 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20371557 | TTTGGCCAAGATGAG[A/G]AAGTGACCATCAGGA | 7011 |
rs149695872 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20382499 | GAAGTGAGGCGAGGT[A/G]TGAGGCGAGGATAGG | 7011 |
rs149697045 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | TEP1 | GRCh38.p7 | 14:20404119 | CAGCACTTAGGGAGG[A/C]CAAGGCCAGTGGATC | 7011 |
rs149726033 | snp | A/G | 0.0372196 | 0.131242 | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20367202 | AACTTCGTCTCTACT[A/G]AAATACAAAAATTAG | 7011 |
rs149746485 | snp | A/G | 0.000742629 | 0.0192552 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20384131 | TGTGTCCTGAAGAAG[A/G]CGTGGCCGGGCAGGA | 7011 |
rs149770370 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TEP1 | GRCh38.p7 | 14:20389549 | TATGCTTTGGCAGGC[A/G]TAGAGAGGAAATGTA | 7011 |
rs149817039 | snp | C/T | 0.00097586 | 0.0220676 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20371607 | GCACCCCTAAGTCCT[C/T]CTGTAGAATTCGGTT | 7011 |
rs149856742 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20379454 | ACTATTAGCCTCCCA[C/T]AAGCACGCTGTGCTG | 7011 |
rs149869458 | snp | A/G | 0.000594982 | 0.0172377 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20376181 | GGCCCTCATGTCCCC[A/G]CAGCTCAGTGCCACA | 7011 |
rs149888080 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20401904 | AGGGGAAAGGGAAAA[C/T]CAGCTCCGATTTAAA | 7011 |
rs149939907 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | TEP1 | GRCh38.p7 | 14:20398729 | AGAGGTGCATTCAAA[A/C]CACTTTAGAGGCCAG | 7011 |
rs149975035 | snp | C/T | 6.62087e-05 | 0.00575326 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20395591 | TTTCTAGTTAGTATC[C/T]GCCTCATCAGTGTTA | 7011 |
rs150026634 | snp | C/T | 0.00145138 | 0.0268995 | missense, upstream-variant-2KB, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20401568 | TCTGACACTGTATCA[C/T]CGGCCTTCTCAAACT | 7011 |
rs150066759 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20408494 | GACAGGAGATGAGCA[C/T]CTGGCTGCACTGAGC | 7011 |
rs150089919 | in-del | -/AG | 0.0376037 | 0.131863 | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20366994 | TAAGGCTGGAGTAAC[-/AG]AGAGGAGGAAAGTTA | 7011 |
rs150130034 | snp | A/G | 0.00274804 | 0.0369658 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20373319 | ACCATCCTCAGAGGC[A/G]GTCAGCATGAGGCCT | 7011 |
rs150148697 | snp | A/G | 3.29669e-05 | 0.00405984 | missense, nc-transcript-variant, intron-variant | TEP1 | GRCh38.p7 | 14:20381573 | ATGAGGATGTGTGCC[A/G]TGTCCTCTAGCCCTG | 7011 |
rs150161561 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | TEP1 | GRCh38.p7 | 14:20410485 | TGGAGTGCAATGGCA[C/T]GATCTTGGCTCACTG | 7011 |
rs150202894 | snp | C/T | 0.0176419 | 0.0922481 | intron-variant | TEP1 | GRCh38.p7 | 14:20373457 | ACAACAGAAGGTTAT[C/T]CCGCATACCTTCCCC | 7011 |
rs150224948 | snp | A/G | 0.00370085 | 0.0428571 | intron-variant | TEP1 | GRCh38.p7 | 14:20384251 | AGGGTAAATGGGTCA[A/G]TGACTATCCATGGTG | 7011 |
rs150284912 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TEP1 | GRCh38.p7 | 14:20392299 | GAAACAATTGGTTCA[A/C]GCAAAGATCACCAAT | 7011 |
rs150286483 | snp | C/T | 1.93265e-05 | 0.00310851 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20396697 | AGGTTGCACAGGTTC[C/T]GAAGCATGGCCATGA | 7011 |
rs150336838 | snp | G/T | 0.0197687 | 0.0974348 | intron-variant | TEP1 | GRCh38.p7 | 14:20387667 | CGCCCTGGCCATACG[G/T]CCATGATGTCTGCCG | 7011 |
rs150338133 | snp | A/C | 9.88321e-05 | 0.00702896 | intron-variant, missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20403809 | ACTCGTCAAACTGGG[A/C]AAATTTGTCCGTCAT | 7011 |
rs150481718 | snp | C/G/T | 0.000181215 | 0.00951738 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20384641 | GCTTAGGTAGCTCTT[C/G/T]AGTTCTGAGATCCGA | 7011 |
rs150531447 | snp | G/T | 0.0329836 | 0.124112 | | | GRCh38.p7 | 14:20415637 | GGGAGACTGAGGCAG[G/T]AGAATGGCTTGAACC | 7011 |
rs150552948 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20367101 | GGGCACAATGGCTCA[C/T]GCCTGTAATCCCAGA | 7011 |
rs150573285 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | TEP1 | GRCh38.p7 | 14:20377083 | AGCCGGGCGTGGAGG[C/T]GCATGCCTGTAATCC | 7011 |
rs150739818 | snp | A/G | 0.000329419 | 0.0128297 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20386131 | GAATGTATCCATAAC[A/G]GGAGCCCAGAATCCC | 7011 |
rs150792015 | snp | A/T | 1.65002e-05 | 0.00287225 | intron-variant | TEP1 | GRCh38.p7 | 14:20381409 | GAGCTGAGCTGCATG[A/T]ACAGATATTGAGAAA | 7011 |
rs150794249 | snp | A/C/G/T | 0.000967988 | 0.0219796 | missense, synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20386497 | GCGGAGGTCGATTCC[A/C/G/T]TGAAGGCTGATACGG | 7011 |
rs150814897 | snp | A/C | 0.0221141 | 0.102801 | intron-variant | TEP1 | GRCh38.p7 | 14:20394748 | ATCCACCTGCCTCGG[A/C]CTCCCAAAGTTCTGG | 7011 |
rs150965591 | snp | A/T | 0.0562307 | 0.157967 | intron-variant | TEP1 | GRCh38.p7 | 14:20399994 | AAACGCCGTCTCTAC[A/T]AAAAATACAAAATTA | 7011 |
rs151017274 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | TEP1 | GRCh38.p7 | 14:20397193 | TCTAGAGCAAAGGTT[C/T]CTAAACTTTTTAGAT | 7011 |
rs151082585 | snp | A/C/G | 9.89583e-05 | 0.00703352 | missense, stop-gained, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20368547 | CTGACCCTTCGCATC[A/C/G]GAACAGGCCCAGCTA | 7011 |
rs151109514 | snp | A/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20387957 | CCTCTTCCAGTGGCC[A/G]GAGAGACTGGACCCC | 7011 |
rs151111908 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20371253 | GATCCTTGGGCTGCA[A/G]GACAAATATGCCATA | 7011 |
rs151113456 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | TEP1 | GRCh38.p7 | 14:20411535 | ATATGTCCCCTATCA[C/T]AGAGCACATCACCTG | 7011 |
rs151143858 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20375177 | TTGTCCATATTATTA[C/T]TGTTATTATTTTGAG | 7011 |
rs151250357 | snp | A/C/T | 0.000477723 | 0.0154481 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20384603 | CCCTCAGCTCACCTG[A/C/T]GGCAGGTGATCCCTT | 7011 |
rs151271261 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | TEP1 | GRCh38.p7 | 14:20387408 | AAAAAAAAAATTAGC[C/T]GGGCATGGTGGCAGG | 7011 |
rs180812417 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TEP1 | GRCh38.p7 | 14:20406796 | ACCTCTCTGAACCTC[A/G]GCTTTCTCTCATTCA | 7011 |
rs180813895 | snp | A/G | 0.00373804 | 0.0430703 | intron-variant | TEP1 | GRCh38.p7 | 14:20383395 | AAGGTAGAAAGAAAA[A/G]GAGAACCACATTGGA | 7011 |
rs180821744 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | TEP1 | GRCh38.p7 | 14:20393664 | GGGTGTGGTGGTATG[C/T]ACCTGTAATCCCAGC | 7011 |
rs180846042 | snp | G/T | 0.0023933 | 0.0345097 | upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20415362 | ATCATCCCATGATTT[G/T]CATGGTAGTTGCATC | 7011 |
rs180890074 | snp | C/T | 1.66902e-05 | 0.00288874 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20368843 | AACATCTCTGTCCTT[C/T]GAAGCTGTCACCAGC | 7011 |
rs181095772 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | TEP1 | GRCh38.p7 | 14:20369196 | GTATTTTTTAGTAGA[A/G]ATGGGGTTTCACCGT | 7011 |
rs181098171 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20382494 | GGAGGGAAGTGAGGC[A/G/T]AGGTATGAGGCGAGG | 7011 |
rs181098353 | snp | A/C/T | 0.00159649 | 0.0282165 | intron-variant | TEP1 | GRCh38.p7 | 14:20404825 | TCCTCCCGTAGCTTT[A/C/T]TGCCCTGAAATTACT | 7011 |
rs181160505 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20394103 | AAAAAAAAAAGGGAC[A/G]GGGTCTTCCTCTGTT | 7011 |
rs181183963 | snp | A/T | 0.00119737 | 0.0244387 | | | GRCh38.p7 | 14:20415741 | ACTCAAAAAAAAAAT[A/T]AAAAAATTAAGTTAG | 7011 |
rs181330550 | snp | G/T | 0.000160074 | 0.0089449 | intron-variant | TEP1 | GRCh38.p7 | 14:20374405 | TCCAGAGACCCCCCA[G/T]TGGGATCTCCATTGC | 7011 |
rs181363045 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | TEP1 | GRCh38.p7 | 14:20412213 | CACTTTGCTCATGTC[G/T]TTGCCCTATATAAGC | 7011 |
rs181378556 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TEP1 | GRCh38.p7 | 14:20400048 | GTAATCCCAGCTACT[C/T]GGGAGACTGAGGCAG | 7011 |
rs181534108 | snp | C/T | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20389277 | GAGAGTGTCACATCA[C/T]TGGGATTCAAATCTG | 7011 |
rs181578744 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20400545 | AGAGAAAACTGAAGA[C/T]AACTTGATCCTCCTC | 7011 |
rs181720630 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20388291 | GCCCCTCCTGCTGTG[A/C]GTGGTAATCACAAAC | 7011 |
rs181736834 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TEP1 | GRCh38.p7 | 14:20389062 | CGGAGGCAGGAGGAT[C/T]GCTTGAACCCAGGAG | 7011 |
rs181787527 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20412023 | GTAAATATTTTGGGA[A/G]TAATATTGTTAAGTC | 7011 |
rs181788066 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TEP1 | GRCh38.p7 | 14:20374664 | CCTGGGTTCAAATCC[C/T]AGCTCTGTCACTCAT | 7011 |
rs182257757 | snp | A/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20406039 | AAAGAAAAGGAAAAG[A/G]GAGAAAGAAAGGAAA | 7011 |
rs182283308 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | TEP1 | GRCh38.p7 | 14:20400859 | GCAGACCTTATAAAT[C/G]AAATACAACAACCAG | 7011 |
rs182405039 | snp | G/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20371150 | TATCCTCCATGACGG[G/T]CCCCAAGGTGTAAAA | 7011 |
rs182414575 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | TEP1 | GRCh38.p7 | 14:20396908 | AAAAAAAAAAAGCAA[A/G]TGAGGGATGATTAGA | 7011 |
rs182512605 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TEP1 | GRCh38.p7 | 14:20382830 | GAGTCCCCAGCAGAC[A/G]CCAGGTCCATGGCAT | 7011 |
rs182617380 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20396336 | ACTCCTTCTGAAATC[A/G]GTTACATCACACAAG | 7011 |
rs182637714 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20401855 | GAAACAAGGTGGGGA[C/T]AGAATGAACACAGGA | 7011 |
rs182640472 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20376469 | GGACGGGAACGTGCG[A/G]CACTCCCAGCTCCAG | 7011 |
rs182884500 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | TEP1 | GRCh38.p7 | 14:20370243 | TAAATGTACATCGGC[A/G]ATGTATTTTTACATG | 7011 |
rs183012079 | snp | C/G | 0.000798403 | 0.0199641 | downstream-variant-500B | TEP1 | GRCh38.p7 | 14:20365607 | TGTCACGGAATAATA[C/G]TTTTATAAAATATAA | 7011 |
rs183061887 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TEP1 | GRCh38.p7 | 14:20390467 | TTACACCATGGAAAT[G/T]TAGCAGATGCTACTA | 7011 |
rs183131971 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TEP1 | GRCh38.p7 | 14:20407377 | GGCTTTCATTTTTTT[A/G]AGACACAGTCTCTCT | 7011 |
rs183210531 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20367048 | GATTCTTCCATATGA[C/T]TGAATTTTAGAAATA | 7011 |
rs183215625 | snp | A/C | | | upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20414241 | CCTTAGAGAGGTACC[A/C]TTGAGTCTCAGGTAA | 7011 |
rs183258806 | snp | A/C/G | 0.000198825 | 0.00996872 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20391092 | AGTGCATAGTTCAGC[A/C/G]GGGGCTGATTGGACA | 7011 |
rs183272235 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20413904 | AACTCCTTAAAAGGA[A/G]ACGGAAAGCGGAAAG | 7011 |
rs183284244 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20366895 | ATCTTTTGCCTTTTG[C/T]TCTCCTAAAAGCATG | 7011 |
rs183461821 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20391992 | CTCATGGTAGGAGAG[A/G]GGAAGTCACCTGTAG | 7011 |
rs183498478 | snp | C/T | 3.39202e-05 | 0.00411812 | intron-variant | TEP1 | GRCh38.p7 | 14:20395445 | CCCAGACAGTGCATA[C/T]ATACCTGGCCTTGTG | 7011 |
rs183502043 | snp | A/G | 0.000181188 | 0.00951636 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20369538 | ATTTGGCCAGGTTCC[A/G]TAGGATCCCATCAGA | 7011 |
rs183504026 | snp | G/T | 0.00597247 | 0.0543191 | | | GRCh38.p7 | 14:20416561 | TATGGTCTGAATATG[G/T]CCCCCAAAATTCATG | 7011 |
rs183705624 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TEP1 | GRCh38.p7 | 14:20412625 | TGCTATTCTGCACTT[A/G]GTATATCTCAGAGAC | 7011 |
rs183722794 | snp | A/G | 0.000478321 | 0.0154574 | intron-variant | TEP1 | GRCh38.p7 | 14:20377785 | GGGCTTAAGGATACC[A/G]CCTCCACCACGCGGT | 7011 |
rs183725884 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TEP1 | GRCh38.p7 | 14:20375635 | CCTGGCACATATCAA[C/G]TTTGACAAATATTAG | 7011 |
rs183789957 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20409902 | TGGCGGGCACCTGTA[G/T]TCCCAGCTACTCGGG | 7011 |
rs184068106 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20400106 | TGCGCCATTGCATTC[C/T]GGCCTGGGCAAAAAG | 7011 |
rs184075325 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20409227 | CTCTCTCATTAAAAC[C/T]CTCTCTTCCTTTGCT | 7011 |
rs184310234 | snp | C/T | 1.65477e-05 | 0.00287638 | intron-variant, missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20404658 | AAGGCAGCTGGACAA[C/T]GGCACAGAAATATCG | 7011 |
rs184316992 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20380583 | AGTCTCAAAGTGTGG[A/C]CCTCTGGCCCTATAT | 7011 |
rs184339147 | snp | G/T | 0.00795532 | 0.062565 | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20368335 | ACTTCATTTTTATAA[G/T]TATCAAGAAATTATT | 7011 |
rs184356317 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TEP1 | GRCh38.p7 | 14:20392941 | AAGAAAATGTAAGCC[A/G]GGCACGGTGGCTCAC | 7011 |
rs184408601 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20415016 | CACCCCGAACGCGCC[C/T]GATCTCCTCTGATCT | 7011 |
rs184434999 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | TEP1 | GRCh38.p7 | 14:20398835 | TTGTAAAGGGGATGT[A/G]AGTCTTATTTGAATT | 7011 |
rs184494742 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | TEP1 | GRCh38.p7 | 14:20374092 | ATTTTCTTTTTCTCT[C/T]TTTTTTTTTTTTAAA | 7011 |
rs184621539 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20415132 | CTATATGTTTAGATA[A/T]GTAAATGTTTGTGTA | 7011 |
rs184653018 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20393375 | AATCAGTAGTCTTCC[C/G]AGCACTATCCAATAG | 7011 |
rs184674859 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TEP1 | GRCh38.p7 | 14:20387771 | GGTAGAGAAACCTCC[A/G]CCTGAGAAAGAGGAA | 7011 |
rs184824849 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20410220 | CTCAGTGTCTCTCAG[A/G]TCTATCCAATTCTCT | 7011 |
rs184854073 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20388610 | ACAGAAGCCACAGTG[A/G]CATGGCCAACTCTTG | 7011 |
rs184873103 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TEP1 | GRCh38.p7 | 14:20397559 | ATGACGAATGTATGT[A/G]AATCCATATTTGAAA | 7011 |
rs184888653 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TEP1 | GRCh38.p7 | 14:20407045 | TTGGCAGAGACAGAA[A/G]AGGGTTCAGATTAGC | 7011 |
rs184926559 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | TEP1 | GRCh38.p7 | 14:20383418 | ACATTGGAGAGGCCT[C/G]TCTCCTCCGTGCCGT | 7011 |
rs185139000 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | TEP1 | GRCh38.p7 | 14:20412046 | GTTAAGTCAACCACC[A/T]AAACTTAGTGTGAAA | 7011 |
rs185167057 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20389085 | CCCAGGAGATGGAGG[C/T]TGCAGTGAGCCAAGA | 7011 |
rs185269201 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20405033 | TCCTTCTTTGGAAGA[C/T]CTCCTGCATCAACAG | 7011 |
rs185363760 | snp | C/T | 3.29549e-05 | 0.00405911 | intron-variant | TEP1 | GRCh38.p7 | 14:20382588 | AGAGAGAATGGGAAG[C/T]AGTGATTAGGACTTG | 7011 |
rs185421912 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | TEP1 | GRCh38.p7 | 14:20379763 | GGTGTGCAGCAAATA[C/T]TTGCTGTGTGATTGA | 7011 |
rs185614346 | snp | A/G | 0.000560196 | 0.0167268 | intron-variant, missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20403856 | GCGGGCAGGGGCACC[A/G]GCTTATTCTTATCTC | 7011 |
rs185616022 | snp | A/G | 3.74855e-05 | 0.00432913 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20374528 | AGAGCCATCACTGGA[A/G]CAGGATATCTACAGA | 7011 |
rs185718229 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20411451 | TTTCATCAACTCCTC[C/T]AAAAAGCCTGTGCTG | 7011 |
rs185748950 | snp | A/G | 0.000345978 | 0.013148 | intron-variant | TEP1 | GRCh38.p7 | 14:20372870 | AGCCTGGTGTACACA[A/G]CAAGTTCAATTCAGT | 7011 |
rs185783223 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20415419 | CTACGCATAAAATGC[C/T]TTGTGTTTATATTTA | 7011 |
rs185906801 | snp | A/G | 3.29984e-05 | 0.00406179 | intron-variant | TEP1 | GRCh38.p7 | 14:20390765 | ATCAAACTCCTGAAG[A/G]AAAGAGACTTCATGT | 7011 |
rs185917587 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TEP1 | GRCh38.p7 | 14:20412818 | CGCCCACCACCATGC[C/T]CGGCTAATTTTTTTG | 7011 |
rs185918146 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TEP1 | GRCh38.p7 | 14:20393763 | CACCAGCCTGGGTGA[C/T]GAAGTGGGACTTTGT | 7011 |
rs186145316 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | TEP1 | GRCh38.p7 | 14:20394771 | AGTTCTGGGATTACA[A/G]GCGTGAGCCACCACA | 7011 |
rs186165866 | snp | C/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 14:20416054 | TGAAAGAAAGGGTTA[C/T]GTGAGGTGACTACAG | 7011 |
rs186179795 | snp | A/G | 1.67908e-05 | 0.00289743 | intron-variant | TEP1 | GRCh38.p7 | 14:20369316 | CCCAGCCCTCCCCTA[A/G]TATTTCTGACCCTTC | 7011 |
rs186180641 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TEP1 | GRCh38.p7 | 14:20382914 | GCCAGAAAACCCCTG[C/T]GGCTCGGCCTACCCC | 7011 |
rs186268366 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20390281 | ATACTCAAAATGTAT[A/G]ACTTCCTAATAATTT | 7011 |
rs186432140 | snp | G/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 14:20416606 | GCGATGTGATAATAT[G/T]AAGGGTTGGGGTCTT | 7011 |
rs186514617 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20412356 | GACTGTCCTATCCTT[A/T]AAAGGACAGTCTCAC | 7011 |
rs186516685 | snp | A/G | 0.00222445 | 0.0332758 | intron-variant | TEP1 | GRCh38.p7 | 14:20368911 | AGTGAATCTCAAAGA[A/G]GAAAGGGGAGAGCAG | 7011 |
rs186574608 | snp | C/T | | | intron-variant | TEP1 | GRCh38.p7 | 14:20374842 | TGCCTGTAATCCCAA[C/T]ACTTTGGGAGGCCGA | 7011 |
rs186671881 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TEP1 | GRCh38.p7 | 14:20387120 | TGTATTTTTAGTAGA[A/G]ACAGGGTTTAGTCAT | 7011 |
rs186684467 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | TEP1 | GRCh38.p7 | 14:20409965 | AGGCGGAGCTTGCAG[C/T]GAGCCCAGATTGGCC | 7011 |
rs186820082 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20400737 | GAAGGTACTTTTGTC[A/G]TATGTTGATAAAAAC | 7011 |
rs186891058 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | TEP1 | GRCh38.p7 | 14:20404223 | AGCCAGGCGTGGTGG[C/T]GCACGCCTGTAATCC | 7011 |
rs186914100 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TEP1 | GRCh38.p7 | 14:20391312 | CCCAAGTTCAACACC[A/G]GGATGTAGTGAGGTG | 7011 |
rs186927974 | snp | C/T | 1.69605e-05 | 0.00291204 | intron-variant | TEP1 | GRCh38.p7 | 14:20380089 | AAGGGAGGAAATAAA[C/T]GAGAGAATGCAAACA | 7011 |
rs186936062 | snp | A/C | 0.00159617 | 0.0282053 | upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20413918 | AGACGGAAAGCGGAA[A/C]GCAACCGCCTGTAAC | 7011 |
rs187011024 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20401996 | AAAACTAAAAGTAGG[A/C]AGGGCGTGGTGGCTC | 7011 |
rs187016543 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | TEP1 | GRCh38.p7 | 14:20376953 | AGGCGCAATGGCTCA[C/T]GTCTGTAATCCCAGC | 7011 |
rs187165526 | snp | C/T | 7.00624e-05 | 0.0059183 | intron-variant | TEP1 | GRCh38.p7 | 14:20395673 | GGCAGCTTCTATTCC[C/T]TCATCTTTTCCTACC | 7011 |
rs187282467 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TEP1 | GRCh38.p7 | 14:20406486 | GCAGCACCAGGCCAC[A/G]GGAAAAGTCTACATC | 7011 |
rs187374984 | snp | C/T | 0.00141599 | 0.0265704 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20369699 | TTTGGCTTGAGTTAT[C/T]GATATTAGGGTCCTA | 7011 |
rs187388036 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20365979 | TCATCCAGCCTTTGG[C/G]AGACACTGAAACTCC | 7011 |
rs187433651 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20370452 | AATCATATAGTATGT[A/T]CTCCTTTGTAACTGG | 7011 |
rs187488183 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TEP1 | GRCh38.p7 | 14:20397385 | GTGGTGTCTGGTGCC[C/T]CTAATCCCAGCCACT | 7011 |
rs187493757 | snp | A/C | 0.00217235 | 0.0328855 | intron-variant | TEP1 | GRCh38.p7 | 14:20371669 | ACAGAGAAAGATCCT[A/C]TTTTAGTTAACCTTT | 7011 |
rs187697681 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20396486 | TCCCAGATCTACTTA[C/G]AGCCCACATGGAAAC | 7011 |
rs187712836 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20367028 | AAAGGCTAACCTGCT[C/G]AATAGATTCTTCCAT | 7011 |
rs187850567 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TEP1 | GRCh38.p7 | 14:20409811 | GGATCACAAGGTCAG[C/G]AGATCGAGACCATCC | 7011 |
rs187856632 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | TEP1 | GRCh38.p7 | 14:20384777 | GCCTCCCTCCACCAA[A/C]CACCAGACATAGCTG | 7011 |
rs187950110 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | TEP1 | GRCh38.p7 | 14:20392381 | CTGATCAACATTAGC[A/G]TTACTGAGTAGTGGT | 7011 |
rs188089622 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TEP1 | GRCh38.p7 | 14:20412061 | TAAACTTAGTGTGAA[A/G]AAGCTTAGGGACAAA | 7011 |
rs188176364 | snp | C/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20374394 | CCCTTAGCCCTTCCA[C/G]AGACCCCCCAGTGGG | 7011 |
rs188191764 | snp | C/T | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20379021 | GCTCCAGGAGCCCGT[C/T]GAAGGCAGTAAGAAA | 7011 |
rs188222816 | snp | A/G | 0.0111196 | 0.0737302 | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20367710 | GCCTCCTGGGTTCAC[A/G]CCATTCTCCTGCCTC | 7011 |
rs188231267 | snp | C/T | 0.00517822 | 0.0506191 | upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20414343 | TAGAAACCTCTATTG[C/T]CACCAGTCCCAACAC | 7011 |
rs188708863 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20380682 | CCCAAGGATCTGCAA[C/T]TTGAACAAGTTTCCT | 7011 |
rs188717243 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | TEP1 | GRCh38.p7 | 14:20369071 | GGAGTGCAGTGGCGC[A/G]ATCTCGGCTCACCGC | 7011 |
rs188723191 | snp | G/T | 1.75093e-05 | 0.00295877 | intron-variant | TEP1 | GRCh38.p7 | 14:20404776 | ATACAAAGATGCCTA[G/T]GACACAGGGTGAGAG | 7011 |
rs188800430 | snp | A/G | 0.00557542 | 0.0525036 | upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20415060 | GGGTTGGGCTTGGTT[A/G]GTACTTGGATGGGAG | 7011 |
rs188816293 | snp | C/G/T | 4.94656e-05 | 0.00497301 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20368481 | CCTGCACGTCTCCCA[C/G/T]GGCAAGCTGCAGGGT | 7011 |
rs188831195 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | TEP1 | GRCh38.p7 | 14:20393089 | GGGCGTGGTGGTGGG[C/T]GCCTGCAGTCCCAGC | 7011 |
rs189249561 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | TEP1 | GRCh38.p7 | 14:20400167 | AAAAAAAAAAAGAAT[C/T]ATCTACATATACCGG | 7011 |
rs189255885 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20374618 | TGTAGGGTGGAAGGC[A/G]GTTAGCCACGTAATT | 7011 |
rs189317786 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20399436 | AAAAAAATGTTAATG[A/C]GTTATTAATGAGATC | 7011 |
rs189331785 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TEP1 | GRCh38.p7 | 14:20411704 | AAAAAGTATATACTG[C/T]TTTGTGCTCAATTTT | 7011 |
rs189349422 | snp | A/C | 0.00438332 | 0.0466095 | upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20415188 | TACTCAGATATATGC[A/C]TCTGTATATAAAATC | 7011 |
rs189367961 | snp | C/G | | | intron-variant | TEP1 | GRCh38.p7 | 14:20388839 | TAAAAGAGGAGTGAA[C/G]TACCTCACTTTAAAA | 7011 |
rs189573113 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TEP1 | GRCh38.p7 | 14:20393541 | TTACGCCTGTAATCC[C/T]AGTACTTTGGGAGGC | 7011 |
rs189583632 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TEP1 | GRCh38.p7 | 14:20393775 | TGACGAAGTGGGACT[C/T]TGTCTCAATTAAAAA | 7011 |
rs189644175 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20376408 | GCAGGGAGTCACAAG[A/G]CTGTGGAGAGGCCCT | 7011 |
rs189653961 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20401203 | AAATAACTCAGAAAA[C/G]GAAAGGTGAGTCATG | 7011 |
rs189841330 | snp | C/G | 4.94319e-05 | 0.00497127 | intron-variant | TEP1 | GRCh38.p7 | 14:20382592 | AGAATGGGAAGTAGT[C/G]ATTAGGACTTGGAAG | 7011 |
rs189849835 | snp | G/T | 0.00358779 | 0.0422022 | upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20415457 | ATTATGGTCAGGCAC[G/T]GTGGCTCACGCCTGT | 7011 |
rs189904831 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20406542 | TCTCCCTTCACACAC[C/T]AGCACTGATGTGTCC | 7011 |
rs189909748 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | TEP1 | GRCh38.p7 | 14:20383079 | GAAAACAAAGGAGCA[C/G]GTCTGTGCAAGGCAG | 7011 |
rs189943888 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | TEP1 | GRCh38.p7 | 14:20402316 | TCGTCTCAAAAATAA[A/G]TAAATAAATAAAAAC | 7011 |
rs190100327 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TEP1 | GRCh38.p7 | 14:20410267 | CACCTTTGTTGAAAC[C/T]CTCTAATCCATGTGG | 7011 |
rs190117064 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20405669 | ACTAACTTACAAAGT[C/T]AAGGACAGAGAGAAT | 7011 |
rs190186120 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TEP1 | GRCh38.p7 | 14:20407076 | CTTGTCCCTCAACCC[A/G]AAACACAAGTATATA | 7011 |
rs190338989 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TEP1 | GRCh38.p7 | 14:20388141 | CGAAAAGGGCAGGGG[A/G]AAAAAGATATGTCCA | 7011 |
rs190419608 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20398757 | CAGGCCGGTCAGTCC[A/G]TCACCATGCCTTGTG | 7011 |
rs190503710 | snp | A/C/G/T | 0.000115415 | 0.00759581 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20369351 | AAACTCACCTTTCTA[A/C/G/T]GCTGCCGTGTCTTTA | 7011 |
rs190563782 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20395240 | AGATAATAGAGTGGA[A/G]GTCCAGGAGTAGACT | 7011 |
rs190585482 | snp | A/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 14:20416276 | ATGCAAGCCCTTCCA[A/T]CATATTCCCATAAAT | 7011 |
rs190651718 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | TEP1 | GRCh38.p7 | 14:20389137 | TGAGCGACAGAGTGA[A/G]ATTCTGTCTTAAAAA | 7011 |
rs190667354 | snp | A/G | 0.00581333 | 0.0535992 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20377720 | AACCCAGGTGCCCAC[A/G]GGGCCGACCCAGAGA | 7011 |
rs190909161 | snp | A/G | 0.00835141 | 0.0640778 | downstream-variant-500B | TEP1 | GRCh38.p7 | 14:20365337 | GGAGTGCAATGATGC[A/G]ATCTCGGCTCACTGC | 7011 |
rs190937584 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TEP1 | GRCh38.p7 | 14:20370017 | CTCCTGGGTTCAAGC[A/G]ATTATCCTGCCTCAG | 7011 |
rs191049329 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20366170 | AAACCCTTCAAGTGG[A/G]CCTGGCCAACAAGAC | 7011 |
rs191125999 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20413107 | GGCAAGGAAGTAAGA[C/G]GGGATGATTCTTACG | 7011 |
rs191407353 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | TEP1 | GRCh38.p7 | 14:20404228 | GGCGTGGTGGCGCAC[A/G]CCTGTAATCCCAGCT | 7011 |
rs191411803 | snp | C/G/T | 6.61949e-05 | 0.00575271 | missense, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20380440 | CTGCAACGTCAGCCT[C/G/T]GGGGAGCTTTTGTTC | 7011 |
rs191436526 | snp | A/G | 0.00019971 | 0.00999076 | synonymous-codon, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20383560 | CCTATCAGCCCCATC[A/G]ATGATCAGGACCTGG | 7011 |
rs191507131 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | TEP1 | GRCh38.p7 | 14:20367758 | GGACTACAGGTGCCC[A/G]CCGCCACACCTGGCT | 7011 |
rs191518531 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TEP1 | GRCh38.p7 | 14:20384264 | CAGTGACTATCCATG[A/G]TGCCATGCTCCTCAG | 7011 |
rs191737612 | snp | C/G | 1.77347e-05 | 0.00297776 | intron-variant | TEP1 | GRCh38.p7 | 14:20408467 | GCTTGTATATGCCTA[C/G]AAGGAGAGAAAGACA | 7011 |