SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs146496899 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246867499 | ATTTCACTTTTAAAG[A/G]TTTTTAAAAATTCTT | 25909 |
rs146535830 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246914953 | TTATTTACCTGAATG[C/G]CAATAGTCTACTTGT | 25909 |
rs146554120 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246920654 | GGGCGCCTGTAGTTC[C/T]AGCTACTCGGGAGGC | 25909 |
rs146587251 | snp | C/T | 0.0345262 | 0.126772 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246873574 | ATACTAGAGACAATA[C/T]ACTAGTCAATTTCTC | 25909 |
rs146607238 | snp | C/T | 0.0024552 | 0.034951 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246863895 | AGCCATCTAGTTTGA[C/T]TGTGAACGCTAGATG | 25909 |
rs146651670 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246861567 | ACTGAAAGGTTCCTA[C/T]TAACCTACAGTGGAC | 25909 |
rs146653142 | snp | C/G/T | 0.00795532 | 0.062565 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246929789 | CCGGGCGCGGTGGCT[C/G/T]ACGCCTGTAATCCCA | 25909 |
rs146669369 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246864501 | AAATTCATTAACATG[C/T]AAAATATCCATTCAC | 25909 |
rs146669497 | snp | A/G | 3.35903e-05 | 0.00409805 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246877268 | TCAACCTATTGCAAT[A/G]TTGCCGCAAAAAATT | 25909 |
rs146672252 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246933027 | AGCAGCCTCGAACTC[A/G]TGGGCTCAAATGATC | 25909 |
rs146716812 | snp | G/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868846 | GTGTGTGTGTTTTTT[G/T]TTTTTTTTTTTTTTT | 25909 |
rs146724486 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246878871 | TATTCCCTAAAAATT[C/T]ACATCTGAAATTGCC | 25909 |
rs146724760 | in-del | -/TTGCAGTGAGCCGAGA | 0.34101 | 0.232846 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246854236 | CCTGGGAGGCGGAGC[-/TTGCAGTGAGCCGAGA]TTGCACCACTGCACT | 25909 |
rs146736366 | in-del | -/A | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246845366 | AAGCATATGATTCTT[-/A]AAAAAAAAGAAAAAT | 25909 |
rs146740751 | in-del | -/ATT | 0.0898077 | 0.191933 | cds-indel, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246839708 | GTTTCTAGATAATCA[-/ATT]ATTAATAGTCCATTC | 25909 |
rs146772110 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246880435 | TGGTCATGGTGGCAC[A/G]TGCCTATAATCCCAG | 25909 |
rs146772616 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246875923 | AGCAATATCTCCAAG[G/T]CATGCCTGTATGTGT | 25909 |
rs146780498 | snp | C/T | 5.06205e-05 | 0.00503068 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246853247 | AGAGACAATAGGACC[C/T]TCAGAGATAGTGAGC | 25909 |
rs146791176 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246879006 | CCAAAATCTAGAAAC[A/G]TTAAAAGCAGAACAT | 25909 |
rs146824779 | snp | G/T | 0.0030839 | 0.0391464 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246840993 | GCACTTTCTTTTTCT[G/T]TGTTTCTGAAAAAAA | 25909 |
rs146913959 | snp | A/C/G | 0.0248531 | 0.10867 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246849641 | CTTGGAACTTCTGAC[A/C/G]CTGGAGAAAATAAAG | 25909 |
rs146950666 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246880997 | CAGACTGAAAACCCA[C/T]CCTGTGGCAAACTCT | 25909 |
rs147054466 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246899689 | AACAAACCTATTACA[C/T]AGCAAAACAAGAAAA | 25909 |
rs147084849 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246843239 | TCTGTTGGGAGGAAT[A/G]CCTGTCTCCTCTAAC | 25909 |
rs147100873 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246846423 | AAGGAGTGAATACTC[A/C]TAAGAACCCCTGTAA | 25909 |
rs147113268 | snp | C/T | 1.66493e-05 | 0.0028852 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246900169 | ATATCCAAGATGCCA[C/T]GTGGAGAAGTCCTAC | 25909 |
rs147139190 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246913756 | AGATGAAATAACCTG[A/G]GGCTTAGAAAGTCAG | 25909 |
rs147140439 | snp | A/T | 0.00700672 | 0.058773 | synonymous-codon, nc-transcript-variant, intron-variant | AHCTF1 | GRCh38.p7 | 1:246843876 | GATGACAAACTGAGA[A/T]GATAAATCCGAAACT | 25909 |
rs147142698 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246916923 | TATTATTCTATCCCT[A/G]AAGAGTTCACAGTCC | 25909 |
rs147143321 | snp | C/G | 3.29951e-05 | 0.00406159 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850919 | CTCACTAAAGGTATT[C/G]TTTCATGAATGGACT | 25909 |
rs147232579 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246928661 | ATAAATCAGTTTTCT[A/G]TGTGAAATACACAAA | 25909 |
rs147238273 | snp | A/G | 4.99654e-05 | 0.00499802 | missense, nc-transcript-variant, intron-variant | AHCTF1 | GRCh38.p7 | 1:246842718 | TGTTTTGTTTTTGAC[A/G]TCCTGATTCGTTTCG | 25909 |
rs147242943 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246860249 | CTCCAGCCTGGGCAA[A/C]AGAGTGAGACTCTGT | 25909 |
rs147246074 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246862844 | TAACCAAATTATGTA[G/T]CAGAATCCTCTGAAG | 25909 |
rs147249071 | snp | A/C | 0.0517044 | 0.152246 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246931781 | GGCCACCTCAGAGCC[A/C]CACGCCCCCGAGAGT | 25909 |
rs147351671 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246873101 | ACTAGGTTCGACTTA[C/T]TCCTATAAGCCAGTC | 25909 |
rs147355371 | snp | A/G | 0.00163586 | 0.0285527 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246877181 | TGTCTGTAAATGGTA[A/G]CTTCAGTAAATCTTC | 25909 |
rs147399261 | snp | G/T | 3.30753e-05 | 0.00406652 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246877178 | CAGTGTCTGTAAATG[G/T]TAACTTCAGTAAATC | 25909 |
rs147455910 | snp | C/G/T | 0.000104242 | 0.0072188 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246891945 | TAAAAGAAAAGATAA[C/G/T]TTTCCATACAGTAAA | 25909 |
rs147459267 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246896778 | GGTTTAATATCACAG[C/G]AACCTATTAATTTCA | 25909 |
rs147575288 | in-del | -/A | 0.0126979 | 0.078662 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246874174 | ACTCCAGTTTCTAGT[-/A]TATACAAGTAGACAT | 25909 |
rs147620319 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246903304 | AGACGCGTATGTCCT[C/T]TTATAAAAATCACCC | 25909 |
rs147643285 | snp | C/T | 0.0883596 | 0.190715 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246928057 | GTGCGGTGGCTCACG[C/T]CTGTAATCCCAAGGC | 25909 |
rs147650038 | snp | A/T | 0.0603597 | 0.1629 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246909124 | ATTTATATATATATA[A/T]AATTCAGCCAGGTGA | 25909 |
rs147658943 | snp | C/T | 0.0358925 | 0.129066 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246877229 | GACAGACTTCATACA[C/T]GTGCTTCAGTAACTC | 25909 |
rs147722911 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246853025 | TAGATTTGAACTACT[G/T]TGTCTTGAAACAACT | 25909 |
rs147723200 | snp | G/T | 0.000477408 | 0.0154427 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246916301 | AGGCTGTTCATTGAC[G/T]CCACTGAATCTGTAA | 25909 |
rs147739591 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246925605 | AGCCTGGGCAAGATC[C/T]TGTTTCTAAAAATAT | 25909 |
rs147752536 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246858400 | ATTCAAAAAAAGTAG[A/G]TAAGAAAACTGAAGC | 25909 |
rs147755684 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246927331 | TCTCTACTAAAAACA[A/G]GAAATGTAGCAGCCA | 25909 |
rs147811792 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246909827 | CTATCCTGTACACTG[C/T]AGGACGCTAAGCCAC | 25909 |
rs147859788 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869679 | ACAGCATGGTTTACC[A/G]AATATTTTAAGCCTA | 25909 |
rs147898082 | in-del | -/TT | 0.0596104 | 0.162024 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246921008 | AGGCAGGAGAATCGC[-/TT]TTGAACCTGGGAGAA | 25909 |
rs147918616 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246927460 | TGCCACTACACTCCA[C/G]CCTCAGCAACACAGC | 25909 |
rs147931881 | snp | C/T | 3.31565e-05 | 0.0040715 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850313 | ATCATTCTGCTAGGA[C/T]TTGTTACCGTACTAA | 25909 |
rs147935233 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246928768 | AGCAAACATTTCTAT[A/T]AACCACTTTGTATGC | 25909 |
rs147936400 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246884692 | TTATTATGTAAATGA[C/G]AAATACACTGATTAG | 25909 |
rs147966769 | snp | C/T | 0.000177399 | 0.00941638 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246888545 | AAAAATTAAGACTTA[C/T]TTAATATCACTGTTA | 25909 |
rs147968469 | snp | A/T | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850104 | TTCTAGGTATGGCAG[A/T]CATATCAAATTCTGC | 25909 |
rs147981044 | snp | A/G | 0.00413666 | 0.0452904 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850807 | TTTGGAGGAAACCAC[A/G]TCATCAACCTGGCTG | 25909 |
rs148019871 | snp | C/T | 0.00230211 | 0.033849 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246916339 | ATCGCTCTCCTGTTA[C/T]AGAGTTTACTACCTC | 25909 |
rs148056251 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246931056 | TTAAATCTCCTTGAT[A/C]TGACCAATCGGGTGA | 25909 |
rs148060665 | snp | C/T | 0.14933 | 0.228835 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246922952 | TGCACCACTGCACTC[C/T]AGCCTGGGCGACAGA | 25909 |
rs148103547 | snp | A/G | 9.88419e-05 | 0.00702931 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246849746 | TTAGTGAAGGAAGCT[A/G]TGGCGAGCAATCTTT | 25909 |
rs148129004 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246872103 | AACCTAGGGTGGTCT[C/G]TAACTAAATATGGTC | 25909 |
rs148243382 | snp | C/T | 0.00116933 | 0.0241516 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246902615 | TACTCGTCTGTCCCC[C/T]CAAAGGGAACATGCC | 25909 |
rs148267610 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246895427 | TGTGTGTGTGTATGT[A/G]TGTGAAGAGTAACAG | 25909 |
rs148290282 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246904773 | GAATTTTACTACTAG[C/T]TGATCCCTTTTAATA | 25909 |
rs148319631 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246867986 | TTTTTTTCTTTTAGA[C/T]CAGTCTTGCTGTGTC | 25909 |
rs148340536 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B | AHCTF1 | GRCh38.p7 | 1:246838693 | ATGTTGTTCTGTCAA[C/G]CAAGTCTTGATCGAC | 25909 |
rs148341363 | snp | A/C/G | 0.0360663 | 0.129354 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246912378 | ATCTCAGCTACTCAG[A/C/G]AGGCTGAGGCAGGAG | 25909 |
rs148366852 | snp | C/T | 1.79464e-05 | 0.00299548 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246885643 | TGCCATGACAAAGGT[C/T]TTGCAGTAGCTGGAT | 25909 |
rs148394860 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246907992 | TATTTAAAAATTCTC[C/T]CAGTACATCTCAAAT | 25909 |
rs148424307 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868827 | TATTGTGCTTTGCTT[A/C]ATTGTGTGTGTGTTT | 25909 |
rs148463078 | snp | G/T | 0.0225045 | 0.103662 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246914424 | CAGGCTGTAACTTAC[G/T]ACAGACAAAAGCCTG | 25909 |
rs148581930 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246863598 | TGATAGAAGAAATAA[C/T]AGCATAATGATATCA | 25909 |
rs148584080 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246932655 | TCATGGCCAAAAATG[C/T]TCGCGCAGCCTAGCC | 25909 |
rs148587670 | in-del | -/TTAGT | 0.293807 | 0.246132 | downstream-variant-500B | AHCTF1 | GRCh38.p7 | 1:246839004 | ATGATACTAAGCACC[-/TTAGT]TTAACCAATGCTTTG | 25909 |
rs148600466 | snp | A/T | 0.00755907 | 0.0610114 | splice-acceptor-variant, intron-variant | AHCTF1 | GRCh38.p7 | 1:246843930 | CTCTATTTTTTTAGC[A/T]AAAAAAAGTTGAAAA | 25909 |
rs148636241 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246902203 | AAGACAACCAAGGCA[C/T]GTATGCCATACATGG | 25909 |
rs148657554 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246873501 | GTACTAGAGACAATA[C/T]ACTAGTCAATTTCTC | 25909 |
rs148727145 | snp | C/G/T | 0.000233063 | 0.0107926 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246862043 | AGACCTTCCAGGTGA[C/G/T]GGAGAGGGAGATGCT | 25909 |
rs148778024 | snp | A/C/T | 1.66363e-05 | 0.00288407 | synonymous-codon, missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246860960 | ATCTTTATCTCCATC[A/C/T]TTTTCAGTTTGTTCA | 25909 |
rs148792915 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246897246 | TGAACCCAGGAGGTT[A/G]GAGGTTGCAGTGAGC | 25909 |
rs148853953 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246927482 | CAACACAGCCTGACT[A/G]TCTCAAAAAGAAAAA | 25909 |
rs148902945 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246899190 | ACTTCATTTCCTCAT[A/C]AGCTTTCTGAGGAGA | 25909 |
rs148921577 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246879320 | CATAGCATACGGTAA[C/T]TGAGAGGAGGATTAA | 25909 |
rs148954903 | snp | A/C/G/T | 0.0968282 | 0.198216 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869066 | GGCCAGGATGGTCTC[A/C/G/T]ATCTCCTGACCTCGT | 25909 |
rs149009595 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246925052 | CACATTGTTACTATG[C/T]TGTTTTCCCCTCTGA | 25909 |
rs149058862 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246929189 | CGAGGTGGGCAGATC[A/G]TCTGAGCTCAGGAGT | 25909 |
rs149130949 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246845765 | GGAGTTCAAAAGGCC[C/T]AGGTTCAAACCCAAC | 25909 |
rs149164047 | snp | C/T | 0.0592355 | 0.161582 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246904329 | TCCTTCCTCAATGGT[C/T]ATACTCTACTTAAAC | 25909 |
rs149188418 | in-del | -/AAAG | 0.0341408 | 0.126114 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246918169 | TTTCTTCTTCCACAT[-/AAAG]AAACTATAATATATA | 25909 |
rs149219566 | snp | C/T | 0.000395537 | 0.0140575 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246851121 | TATCATTTTCCCCAC[C/T]GCATACAAGTTTTTC | 25909 |
rs149221187 | snp | C/T | 0.0322114 | 0.122752 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246883809 | AGACTTTTTCCAACT[C/T]AAGAGAAATAAGGTT | 25909 |
rs149239782 | in-del | -/TT | 0.0588605 | 0.161139 | upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246933785 | CTTTTGGAAATGTAA[-/TT]TTCTTTTTTCTGTAA | 25909 |
rs149252201 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246847348 | CATAAGTAGGGGGAC[A/C]AAAGCAGAATATATG | 25909 |
rs149307588 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246857179 | AACATAAACTGACAC[A/T]CTCACCAATCTGCTT | 25909 |
rs149320039 | snp | A/C/G | 0.000249847 | 0.0111746 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850784 | ATACGTTGACCTCTC[A/C/G]TACGAGTTTTGGAGG | 25909 |
rs149380779 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246859713 | CCTGAGTAGCTAGGA[A/C]TACAAGTGCATGCTA | 25909 |
rs149383055 | snp | A/G | 0.0433465 | 0.140692 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246928118 | CATCCTGGCTAACAC[A/G]GTGAAACCCCATCTC | 25909 |
rs149412849 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246915398 | ATAAGGCCATTCACA[A/G]TCTAAAACCTAACGT | 25909 |
rs149419984 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246901038 | AGGAAATAGGAAGAA[C/T]GGGGAATAAGAGAGA | 25909 |
rs149429737 | in-del | -/TACTACTGA | 0.154661 | 0.231107 | downstream-variant-500B | AHCTF1 | GRCh38.p7 | 1:246838899 | GTACATTGTTTACCT[-/TACTACTGA]TACTAAGTATCTTTC | 25909 |
rs149437187 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246863293 | GAGAACCCAGGGACA[A/G]TGGGGAGGGGTGAGG | 25909 |
rs149453680 | in-del | -/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246895051 | AAAAGGTCAATTTTT[-/T]GAAAGACAAAGTGAC | 25909 |
rs149466120 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246881428 | TTAAAACCATGCAAC[A/G]AACAAACTTGATCAT | 25909 |
rs149538294 | snp | A/T | 1.6842e-05 | 0.00290184 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246851359 | CTGAAGCTTAAGTGT[A/T]CCAGAGGGATATAAC | 25909 |
rs149543044 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246926749 | AATCCCAGCTACTTT[A/G]GGAGGCTGAGGCAGG | 25909 |
rs149594899 | snp | C/T | 0.0535932 | 0.154675 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246890247 | AGTGAGAAAATGATC[C/T]GTCATGAAAGTCTAA | 25909 |
rs149611336 | in-del | -/CTTT | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246857963 | TGCTAACACTTTCTT[-/CTTT]CTTTTTTTTTTTTTG | 25909 |
rs149623746 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246876294 | TCCAAAAAATCTTCC[C/G]CCTACCTACATATCC | 25909 |
rs149645831 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246897079 | AGCACTTTGGGAGGC[C/T]GAGGAGGGCAGATCA | 25909 |
rs149650242 | in-del | -/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246848391 | GATAATTTCTTTGTA[-/T]TTTTTTTTAGTAGTG | 25909 |
rs149690307 | snp | C/T | 0.000412919 | 0.0143628 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246904023 | GATGCAAACTCAAAA[C/T]ATCCCCTTCACTGAA | 25909 |
rs149713465 | in-del | -/A | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246870279 | TGAGGCCCTCTCTAC[-/A]AAAAATACCCAGGCA | 25909 |
rs149732454 | snp | C/T | 0.00438332 | 0.0466095 | utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246839901 | TCCCAACCTCAATAA[C/T]CTGTGCCTGAGGTCC | 25909 |
rs149783282 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246851871 | CTTTTCTAAATAGCA[C/T]GATCCCCGTAAGGTT | 25909 |
rs149784740 | snp | A/T | 0.0170251 | 0.090679 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246924463 | TAAAATCAATAATTA[A/T]AGAATTTTAAAACAT | 25909 |
rs149818118 | in-del | -/GTACT | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246927570 | AAACACCTACGTTCA[-/GTACT]GTACAAAATTAAACA | 25909 |
rs149818912 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246893377 | GAATAACTTAACTTA[C/T]ATTGTGAAAAGCTAT | 25909 |
rs149835592 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246858430 | CCTAAGGTTATACTG[C/T]GTATCCCAGCTCATG | 25909 |
rs149892420 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869360 | TGTTCATGTGAAAGG[A/G]GGAGTCACATGTCTA | 25909 |
rs149899496 | snp | C/T | 0.000843735 | 0.0205221 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850293 | TAGTACTTCTCAATT[C/T]TCTGATCATTCTGCT | 25909 |
rs149944020 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246919759 | GTTATTTTCAGGTTC[A/G]TTGCTCCAAGCAATC | 25909 |
rs149947550 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246873455 | TCTCCTGCATCATAG[C/T]GAAGGGAAAGAATCC | 25909 |
rs149979310 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246927315 | ACATGGTGAAACCCC[A/G]TCTCTACTAAAAACA | 25909 |
rs149995687 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246883284 | GACTTTTAGTTCAAA[C/T]TTCCCAAATGTAACC | 25909 |
rs150032385 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246929079 | AGGTACATATGCTGT[A/G]AGATCCCAGTAAAAA | 25909 |
rs150088180 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246886143 | CAAGACCAGCCTGGT[C/G]AACATGGTGAAACCT | 25909 |
rs150104510 | snp | C/T | 0.327445 | 0.237702 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246847107 | GCTTGGCCAACATGG[C/T]GAAACCCTGTCTCTA | 25909 |
rs150123190 | snp | A/G/T | 4.04132e-05 | 0.00449503 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246861259 | CTGCACATTTTTTAG[A/G/T]TGTAGTAAATACTTC | 25909 |
rs150139369 | snp | A/G | 0.000904334 | 0.021245 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246931103 | TGAGCCCCGAGTCCA[A/G]CTTCTTCCCCGCCAG | 25909 |
rs150290650 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246866061 | ATATGATGTACCCAC[A/G]GATGTTATCTATTCT | 25909 |
rs150298389 | snp | C/G | 0.00175125 | 0.0295391 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246855821 | GGACTTCTGGGTGAA[C/G]ATTTTCCTTTAGAAA | 25909 |
rs150299020 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246926531 | CTTTTCCAATTTAAG[C/T]ACACTACAGAGAACA | 25909 |
rs150348172 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246895679 | CATACTGTGGGCAAA[C/T]GTGCTAAAGGGGGTG | 25909 |
rs150394496 | snp | C/T | 0.00115354 | 0.0239883 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850143 | TCAACTGAGATGACT[C/T]AAGGTTGGAGTCTTC | 25909 |
rs150403067 | snp | A/G | | | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246900119 | GTGGATATGAAGGAG[A/G]GACTCCTCTATTTAA | 25909 |
rs150420552 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246870219 | GAGGCCAAGGTGGGA[A/G]GATCACTTGAGGCCA | 25909 |
rs150473634 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246875933 | CCAAGGCATGCCTGT[A/G]TGTGTTAGCGAAAGT | 25909 |
rs150504092 | snp | C/T | 9.89674e-05 | 0.00703377 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246903970 | TAAGATTTGTCCTGA[C/T]GCCAAACACTTTCTA | 25909 |
rs150543674 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246872325 | GGAAAAGACTGACAA[A/G]AAGACTTTACAGTGA | 25909 |
rs150565789 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246923228 | GAGACCAGCCTGACT[A/G]ACATGATGAAACCCC | 25909 |
rs150578707 | in-del | -/TTCAA | 0.00941842 | 0.0679743 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246899420 | AAGATCTGACTTCAG[-/TTCAA]TTAAGAAATCACTAG | 25909 |
rs150596968 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246877577 | AAGACAAAAAACTAA[C/T]GTGGCCTGGATAGAG | 25909 |
rs150612389 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246900724 | CTTGTTTTCAGTTAA[C/T]ACTTGAGCAACGTTG | 25909 |
rs150619640 | snp | C/T | 0.000264275 | 0.0114921 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246888179 | CTTAAAAGGATACAA[C/T]AGAGTGTTTGGCTGC | 25909 |
rs150710000 | snp | G/T | 0.000247641 | 0.0111247 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850260 | GCTTATTTCCTGTAT[G/T]TTCAGAAGCATCTAA | 25909 |
rs150742902 | in-del | -/TA | 0.0228947 | 0.104514 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246912839 | ATATGCCAAGAACAC[-/TA]TGTTAGATCCTACAT | 25909 |
rs150752133 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246912539 | AGTCAAAATTTTTTC[A/G]GGTCAAATACTCCTT | 25909 |
rs150761910 | snp | A/C/T | 0.000115495 | 0.00759843 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246849889 | AGAGCTCATCACCAT[A/C/T]GAAAGTTCCTCGTTT | 25909 |
rs150768350 | in-del | -/GC | 0.394171 | 0.204242 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246927870 | TAGCTGGGCGCGGTA[-/GC]GCGCTGTAGTCCCAG | 25909 |
rs150772980 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246859678 | CCTCCTGGGTCCAAG[C/T]GATCCTCCCCTCTCA | 25909 |
rs150790555 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246844236 | TTAATCCGTACTGCT[C/G]CTCAAGCATTCTGGG | 25909 |
rs150807473 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246918504 | AAAATCTGGTTACAA[A/G]ATACATATTGGCCAG | 25909 |
rs150822349 | snp | C/T | 0.0528381 | 0.153711 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868253 | CCTGCCTTAGCCTCC[C/T]GAGTAGCTGGGACTA | 25909 |
rs150874772 | snp | C/T | 0.0520825 | 0.152737 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869134 | AGGCGTGAGCCACCA[C/T]GCCCGGCCGTGTGTT | 25909 |
rs150972308 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246870045 | ATTAAAAGGAGTTTG[C/T]AAGAAGGTGATTCCA | 25909 |
rs150987118 | in-del | -/AGAT | 0.00517822 | 0.0506191 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869910 | AGCTATAGCTGTCAC[-/AGAT]AGATAGTGATTCCTC | 25909 |
rs150987151 | snp | A/G | 3.29777e-05 | 0.00406051 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246855799 | CTTCGTCCAACACTG[A/G]TACCTTGGACTTCTG | 25909 |
rs151038417 | snp | C/G | 1.64852e-05 | 0.00287094 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246861040 | TGAAAACAGTCTCTT[C/G]AAGGTCTTCCGGTGA | 25909 |
rs151093519 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246892589 | GCCTCCCAAAGTCCT[A/G]GGATTACAGGCATGA | 25909 |
rs151129973 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246902776 | GTTCACACAATACAA[A/C]GAAAACAATTTAGAC | 25909 |
rs151137571 | in-del | -/AAATA | 0.372592 | 0.217879 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246843712 | AAATCATTAAAATTT[-/AAATA]AAATAATTTTATTAA | 25909 |
rs151148585 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246889554 | GTCATTCTAAAGCAC[C/T]GGTTCCCACAATTGC | 25909 |
rs151269714 | in-del | -/TACTGA | 0.0755793 | 0.179102 | downstream-variant-500B | AHCTF1 | GRCh38.p7 | 1:246838902 | CATTGTTTACCTTAC[-/TACTGA]TACTAAGTATCTTTC | 25909 |
rs151285382 | snp | A/G | 0 | 0 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246914724 | TGAACTTTTGAAAGT[A/G]TCTATCGCTACTCCC | 25909 |
rs151288253 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246897623 | ACTGTGCTGAATACT[A/G]TAAGCAACTGTAACA | 25909 |
rs151296376 | snp | C/T | 9.90949e-05 | 0.0070383 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246899468 | CCTTCTGAAAGCCAG[C/T]ACAAGTTAAATGAAC | 25909 |
rs151336952 | snp | A/G/T | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246920824 | GGCACGGTGCCTCAC[A/G/T]CCTATAATCCCAGCA | 25909 |
rs180712612 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246918658 | GGGCGACAGAGCAAA[A/G]TCCAGTCTTAAAAAC | 25909 |
rs180729263 | snp | C/T | 0.0596104 | 0.162024 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246930005 | TGCAGTGAGCCAAGA[C/T]TGTGCCACTGCACTC | 25909 |
rs180970667 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246896613 | GCATAGAACTTTCTT[C/T]AGAAGTAATAAAAAT | 25909 |
rs180975219 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246878381 | CAGCCTGGCAGACAG[A/G]GCAAGATTCTGTCTC | 25909 |
rs181009716 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246842871 | TAGAGCCAAACACTG[A/C]TGAATTCAAACTCGC | 25909 |
rs181022038 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246861791 | CTTAGCCAATGGCCC[C/T]AGTGTTTCTTTCAGA | 25909 |
rs181049550 | snp | C/T | | | intron-variant, downstream-variant-500B | AHCTF1 | GRCh38.p7 | 1:246842454 | AGGTGTGGTGGTGGG[C/T]ACCTGTAGTCCCAGC | 25909 |
rs181151873 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246877862 | ATTTAAATGAAGGAG[G/T]GTTTCTTACACAGAA | 25909 |
rs181167824 | snp | A/G/T | 8.2485e-05 | 0.00642157 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246861089 | TAAGGTAGTCTCATC[A/G/T]GATGTGATTGAAACA | 25909 |
rs181168192 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246896172 | GGCGGTTTCTCAGTA[G/T]GCTAAACATAGACTT | 25909 |
rs181204573 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246873083 | GCCCTCAGATCAGGC[A/G]CTACTAGGTTCGACT | 25909 |
rs181212014 | snp | A/G | 0.000149911 | 0.0086564 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246900099 | ATTAAAAAACTGCTC[A/G]GGAGGTGGATATGAA | 25909 |
rs181213354 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246858633 | AGGAGTTCGAGACCA[A/G]CCTGGCCAACATGGT | 25909 |
rs181213986 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246924208 | GTGTTTAACTTTAAA[A/C]AATTTATAAAGAAAT | 25909 |
rs181218878 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246892021 | CACTCAAAAGAATTA[C/T]TCTATTCATTATGAG | 25909 |
rs181257988 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246929932 | TGGCGTGCGCCTGTA[A/G]TCCCAGCTACTCAGG | 25909 |
rs181261627 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246839717 | TAATCAATTATTAAT[A/G]GTCCATTCATTACAC | 25909 |
rs181264158 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246852152 | CATTTTCCCACTCCC[C/G]AAACATTCAGTGAGA | 25909 |
rs181264780 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869091 | CCTCGTGATCCGCCC[A/G]CCTTGGCCTCCCAAA | 25909 |
rs181270182 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246906906 | TTATTAAGCTGTTAC[C/T]TTACACAGATGATGA | 25909 |
rs181304177 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246912742 | TTCTATTTTAGGATG[C/T]TATTTTGTGAGAAAG | 25909 |
rs181308771 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246886663 | ATGGACACAGAGGGC[C/T]GATGGTATACAAGAG | 25909 |
rs181337564 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246916049 | ATTGTAAATGTTGCG[C/G]GTCAGTGAAATTTCA | 25909 |
rs181351945 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246846685 | AGATGAAATGCCAAT[A/C]TGAAAAAAAAAGAAA | 25909 |
rs181358439 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246881406 | AATTATTCAGGACAC[A/G]GAAAGATTAAAACCA | 25909 |
rs181398266 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246927095 | AGGAGGGAGAATGGC[A/G]TGAACCCGGGAGGCG | 25909 |
rs181469028 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246866793 | CAATCACAATTTCAT[C/G]TTGGATACAAAACTT | 25909 |
rs181484078 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246901741 | GAGAATTGGTTGAGC[A/C]CAGAAGGTCAAGGCT | 25909 |
rs181492346 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246882601 | ATCATTATCCAACCT[C/G]AGTTAAAAGGACAGC | 25909 |
rs181492771 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246921511 | AATGCAGCACAAAGG[C/G]ATGAGTAGTTTTAAA | 25909 |
rs181522177 | snp | A/C/T | 0.035 | 0.128084 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246926990 | CCATCCTGGCTAACA[A/C/T]GGTGAAATCCCGTCT | 25909 |
rs181712276 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868285 | AGGAATGTGCCACCA[C/T]GCTAATTTTTGTATT | 25909 |
rs181717914 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246847451 | AATGGTGATTCTTTC[A/G]ATGGCTGGATTATAT | 25909 |
rs181820068 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246927564 | CACATGAAACACCTA[C/T]GTTCAGTACTGTACA | 25909 |
rs181830472 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246856518 | ACTAGTTAGCCAAGA[C/T]AGTGAATATGCACCC | 25909 |
rs181863748 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246893369 | TCTACTAAGAATAAC[C/T]TAACTTACATTGTGA | 25909 |
rs181867609 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246890826 | GAAAAGAAGGTTAAG[A/C]ATAAATTAAATTAAG | 25909 |
rs181903693 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246846908 | AGGTGCAGCCACCAC[A/G]TGCCCAAATCATTAA | 25909 |
rs181928886 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246885944 | GTAATCTCCGCACTT[C/T]GGGAGGCCAAGACAA | 25909 |
rs181934968 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246923567 | ATGGTAAAAAGCTAT[C/T]TGGATATTTCAATTC | 25909 |
rs181937950 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246906524 | GAAGTGGAGGTTGCA[A/G]TGAGCCAAGATCGTG | 25909 |
rs181990187 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869026 | ACTTTTTCTATTTTT[A/G]GTAGAGACGGGGTTT | 25909 |
rs182073822 | snp | A/G | 0.000581693 | 0.0170443 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246867850 | TTAAGTGCATCTCTA[A/G]CAAACGGGAATTTAA | 25909 |
rs182082990 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246901355 | AAAAAAACAAAAACA[A/G]GCCAGGTGCGGTGGC | 25909 |
rs182086025 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869421 | GCCAGTTAGCCAAGT[C/T]GTAAATGCAAAAAAG | 25909 |
rs182092266 | snp | A/G | 0.0119091 | 0.0762411 | upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246932013 | GAGGGGAGAACCGGC[A/G]GGAGATCGCGGCTGC | 25909 |
rs182105118 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | AHCTF1 | GRCh38.p7 | 1:246838757 | TTCTATCTACATCTA[A/G]GAAGCCTTCAAGATC | 25909 |
rs182116179 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246872257 | AATAATACTCAGATC[A/G]GGCTCCCTTGTGACT | 25909 |
rs182119624 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246911645 | TGCGCCACCACACCT[A/G]GCTAATTTTATATTT | 25909 |
rs182142878 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246878784 | ACTTTTGTTGTTCTG[G/T]AACTAGAGTATTTCC | 25909 |
rs182169249 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246919009 | ATATCTTTTGCAGGA[C/T]AGAAATAATATAGGC | 25909 |
rs182170969 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246919895 | ATGCCTGTAACACCA[A/C]TTTGGGAGGCCAAGG | 25909 |
rs182359090 | snp | C/T | 0.0566069 | 0.158427 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246882142 | AGCTGGGACTACAGG[C/T]GTGCACCACCTCGCC | 25909 |
rs182396126 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246921278 | TTTGAGAGAGAAAGC[A/G]GAAGAATATACGAGG | 25909 |
rs182419335 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246862269 | GCGGATCACCAGGTC[A/G]GGAGATCGAGACCAT | 25909 |
rs182425396 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246896876 | GAGGGAATTACATAA[C/T]GGTCCACAAAACCTA | 25909 |
rs182432605 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246930658 | GTTCAAGCGATCCTC[A/C]CGCCTCAGCCTCTCA | 25909 |
rs182436998 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246863307 | AATGGGGAGGGGTGA[A/G]GGAGAAATAAAGCTT | 25909 |
rs182444981 | snp | A/G/T | 4.9504e-05 | 0.00497493 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246888190 | ACAATAGAGTGTTTG[A/G/T]CTGCTTCAGTAACGC | 25909 |
rs182446433 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246924815 | AAGTCATCAAAAGTA[G/T]AAGTTTGCTTTTTAT | 25909 |
rs182467447 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246897543 | ACACAAACTTAGATG[A/G]TGTAGTCAACTACAT | 25909 |
rs182584442 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246896976 | GTCTGCTACTAACAT[C/T]ATTACCTATAGTTTA | 25909 |
rs182595360 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246878928 | ATCATTGTAACTTGG[A/G]TGTAGAAGAGTGTTC | 25909 |
rs182659630 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246845347 | ACACAGTAGGTGTAT[A/T]TATAAGCATATGATT | 25909 |
rs182664647 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246862646 | TATACGTAAGTCTAC[A/G]AAACATAAAACTGCA | 25909 |
rs182676473 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246844870 | AATATAATTACAGAC[A/G]AGCACAGTTCAGTTT | 25909 |
rs182678161 | snp | A/C | 0.000951873 | 0.0217952 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246907506 | GTACAAGCTATATGC[A/C]AAAAAACTACCTATA | 25909 |
rs182698462 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246879742 | CTGAGGCAGGAAAAT[C/T]GGCTTGAACCCAGGA | 25909 |
rs182702045 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246859864 | CAGCCTGAACATTTA[C/T]TTTCATTGTCCAGTG | 25909 |
rs182712900 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246875605 | ACTTCACTGTGTCAT[C/T]GTAAGAAACTGTCAC | 25909 |
rs182714808 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246841073 | GCTTCCCAACATGTT[A/G]AGAAAAACCTTAGGG | 25909 |
rs182716933 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246922794 | GAGACCATCCTGGAT[A/G]ACACGGTGAAACCCT | 25909 |
rs182718588 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246903342 | TAATGCTTGATATGT[C/T]AGAGCAACAAAGTGG | 25909 |
rs182792508 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246884079 | AAATGAAAAAAAAAT[G/T]TATATGCTGGTTTCC | 25909 |
rs182811610 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246894117 | GCTGAGGCAGGAGGA[C/T]GACTTGGGCTCAAAA | 25909 |
rs182814086 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246922092 | GGGCTGGGCACAGTG[A/G]CTCACGCCTGTAATC | 25909 |
rs182826139 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246913890 | TCCTAAGAGTAAAAA[C/T]TAATCATTCCAGAAA | 25909 |
rs182906051 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246870262 | TAGCCTGGGCGACAT[A/G]GTGAGGCCCTCTCTA | 25909 |
rs182909280 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246909715 | ATAAGGAAAAATCAT[A/G]ATGTGTGCAGGGTTC | 25909 |
rs183003094 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246848033 | AAAACATAGGTCTAA[A/C]CACACTTTTCTAACA | 25909 |
rs183038891 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246882815 | GCCACAGTTGTGATG[C/G]TATGTCCATATATAT | 25909 |
rs183160573 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868747 | GAAAGGCTTACATTT[C/G]TTGGGTTACAGAGCA | 25909 |
rs183185973 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246889615 | TTAAAGTACTGATTC[A/C]CAGGTGATTCAGGTG | 25909 |
rs183189293 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246853685 | TCTGGGCTTTGATAC[A/C]ACTAGGATAAAGAAT | 25909 |
rs183221658 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246848533 | TATAAGGTCCTGAAC[A/T]GCTTTGCTGAAATTC | 25909 |
rs183225743 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246925809 | GTTTAAAGCCAGGCA[C/T]GGTGGCTCCCAGCAC | 25909 |
rs183236322 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246873830 | TCCCCTCCACAAAAA[C/T]GTTCCCTGTGTCACC | 25909 |
rs183267333 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869781 | ACCCAGGAGCCCTGA[C/T]GATGTACAGGGAGAC | 25909 |
rs183277579 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246852964 | TTTTTTGAACCCATA[C/T]TTTTATAAATAAGTT | 25909 |
rs183278800 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246889114 | TACCATAAAGCCCAG[C/T]GTAGTGAAAATAATG | 25909 |
rs183286893 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868400 | TGCTGGGATTACAGG[C/T]GTGAGCCACTGCGCC | 25909 |
rs183315071 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246902419 | AATTCCGTTAATTAC[C/T]ATTCCAATTTTCTGA | 25909 |
rs183317877 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246893815 | TAGTAAATTAAACTC[C/T]TAAGACCAAAAGACA | 25909 |
rs183319280 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246927873 | CTGGGCGCGGTAGCG[C/T]GCTGTAGTCCCAGCT | 25909 |
rs183420176 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246925259 | TCCATGATCCCTATA[C/T]TTCAATCAAAATCAT | 25909 |
rs183426083 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246908683 | ACAAGGTCAGGAGAT[G/T]GAGACCATCCTGGCT | 25909 |
rs183433112 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246928091 | TGGATCACGAGGTCA[A/G]GAGATCGAGACCATC | 25909 |
rs183540050 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246840120 | AAGGTTGCAAGTGAG[C/T]AGTGAACCGGTCAAT | 25909 |
rs183542698 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246874423 | AACTTGCTAAACCTT[C/T]TGACTTATCTGTCCC | 25909 |
rs183602106 | snp | A/G | 0.000247519 | 0.011122 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246889994 | CAAACTTCTGTCGAC[A/G]ACTGGTGTAGTAGTT | 25909 |
rs183618308 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246910171 | CGAAAATGATACCAC[A/T]TGAAAGCACAGTTAA | 25909 |
rs183686187 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246870717 | CTAAAAGAGGGTATA[A/T]AACCTCAAAAAAAAA | 25909 |
rs183691939 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246855327 | GCTCATTGGATTAAA[A/C]AAAAAATTCCATATA | 25909 |
rs183784916 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246903154 | AAACCCGTTTCTATA[C/T]GCCTCCAACATTAGG | 25909 |
rs183822958 | snp | C/G | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246839953 | AAACCTGAATATTAA[C/G]GGATTTCTGTGGTTC | 25909 |
rs183850010 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246928640 | AGATACTAAAAACAG[A/C]ATACTATAAATCAGT | 25909 |
rs183853630 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246885925 | GGCACGGTGGCTCAC[A/G]CCTGTAATCTCCGCA | 25909 |
rs183898548 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246846470 | TTCATTCTAGGAGGA[A/G]GAAACAAGGCTCATA | 25909 |
rs183915973 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246866267 | AACTTCTATTATTGC[C/T]CCCCGCAACCTCAGA | 25909 |
rs183923158 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246899671 | TTCATCCTAAGAATA[A/G]ATAACAAACCTATTA | 25909 |
rs183940591 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246881209 | ATTAACAAGTATTCA[A/T]AATAAAGAAGGTTAC | 25909 |
rs183980650 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246882998 | GAGTCCAAAGATTTT[A/G]CTCTTAACATCTTTG | 25909 |
rs183993127 | snp | A/C/T | 0.0182236 | 0.0938726 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246922753 | TTTGGGAGGCCAAGG[A/C/T]GGGCGGATCACGAGG | 25909 |
rs184044269 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246859119 | TGCTATTTATGGGCA[C/T]GGTCCTAAAGTTCTT | 25909 |
rs184092347 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246916630 | CTGCACTCCAGCCTG[C/T]GTGACAGAGCAAGAC | 25909 |
rs184099934 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246867025 | AACTTCACTCCTGTC[C/T]ACTAAGCAGTCTGAA | 25909 |
rs184101022 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246929938 | GCGCCTGTAATCCCA[A/G]CTACTCAGGAGGCTG | 25909 |
rs184125630 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246926274 | TCCTTTATAGCAACA[C/T]AGGCTAACGTATTTC | 25909 |
rs184136551 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246900536 | ATCACCTCAACAGAA[C/T]TATAGCAAGATTTTC | 25909 |
rs184154525 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246861370 | TAAGCTACCCATCCC[A/T]ATCATACCCATACTT | 25909 |
rs184155920 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246896245 | AGAAACAAAAATACA[C/T]GCCCAAACAAAAATT | 25909 |
rs184166984 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246878301 | ATTCAGTAGGCTAAG[A/G]TGGGAGGATTGCTTG | 25909 |
rs184229649 | snp | C/T | | | intron-variant, downstream-variant-500B | AHCTF1 | GRCh38.p7 | 1:246842236 | GCTTAATTTCCTTTT[C/T]GTAAAATTAAGGGTC | 25909 |
rs184229946 | snp | A/G | 0.00318978 | 0.0398085 | upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246932634 | TTCTAGCATCCTCCT[A/G]TGCTTTCATGGCCAA | 25909 |
rs184231153 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868876 | TTGAGATGGAGTCTC[A/G]CTCTGTCACCCAGGT | 25909 |
rs184240348 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246849461 | CTCAAACTTTGAAAC[A/G]TGAAACCTTTAAACT | 25909 |
rs184265555 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246846706 | AAAAAAGAAATATTA[C/T]GTTTAAGATTTTGAA | 25909 |
rs184265883 | snp | A/T | 0.0325976 | 0.123435 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246881531 | GTCTTACCAAAAAAA[A/T]TTTTTTTAAATAGAA | 25909 |
rs184289545 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246921160 | TGACATTTATATAAG[C/G]TTAAAAAGACACGCA | 25909 |
rs184383099 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246920642 | GAGCGTGGTGGCGGG[C/T]GCCTGTAGTTCCAGC | 25909 |
rs184398832 | snp | A/G | 0.00874735 | 0.0655527 | upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246933334 | AGACAGGGTTTCACC[A/G]TGTTGGCCAGGATGG | 25909 |
rs184401387 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246905270 | TTTGGGAGGCTGAGG[C/T]GGGCAGATCATGAGG | 25909 |
rs184538425 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246923392 | TGCACTCCAGCCTAG[C/G]TGACAGCAAGACTCT | 25909 |
rs184736382 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246846095 | CGATATATGAATGTC[A/C]TGTATCTAGTATGGC | 25909 |
rs184839925 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246894917 | CCACACCACGGAGCA[C/T]GTCATTTCAGGTAAT | 25909 |
rs184854150 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246914470 | CAGTATACAAAACAT[C/T]ACTCAGTGTTTCTAA | 25909 |
rs184863324 | snp | A/G | 0.00170055 | 0.0291099 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850274 | TTTTCAGAAGCATCT[A/G]AATTAGTACTTCTCA | 25909 |
rs184882761 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246839739 | TCATTACACACTATC[A/G]ATTACCTGTTATAAA | 25909 |
rs184910478 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246873429 | TACTAGAGACAATAC[A/G]CTAGTCAATTTCTCC | 25909 |
rs184922441 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246892724 | GCACTCTCAAACTCC[C/T]GGGCTCAAGTGTTCC | 25909 |
rs184938859 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246885070 | CAATTTGGCGCCCCT[C/T]CCTTTTATTCAAGGT | 25909 |
rs184991582 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246895602 | AAGAAGGTAGGTATG[A/G]CTGTAACGGCAGCAT | 25909 |
rs184999493 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246929879 | CAATATGGTGAAACC[C/T]CGTCTCTACTAAAAA | 25909 |
rs185020099 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246926949 | GGAGGCTAAGGCGGG[C/T]GGATCACGAGGTCAG | 25909 |
rs185036978 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246927156 | GCACTCCAGCCTGGG[C/T]GACAGAGCGAGACTC | 25909 |
rs185038690 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246912835 | AACAATATGCCAAGA[A/G]CACTATGTTAGATCC | 25909 |
rs185059329 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246860809 | ACAGTACCTGGCTAG[A/G]ATGCTTTTCTTATGG | 25909 |
rs185069810 | snp | A/G | 0.000186651 | 0.00965871 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246904059 | AATTAACGAAGACAC[A/G]CTAAATATATTAATA | 25909 |
rs185087376 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246876971 | ATTAATCTTCAGAGT[C/T]TGGTTCAGCTTCAAG | 25909 |
rs185088150 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246890778 | ACTGTGTGTCAGGCA[C/T]AGGATGAAGATACAA | 25909 |
rs185088223 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246907815 | ACAGCATTAAAAGCA[A/G]ATATGTCATCCATTA | 25909 |
rs185111717 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246910672 | ATTAATATAACCACT[A/G]TGCAAGAGCAGATTC | 25909 |
rs185115457 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246915681 | ACCAAGTTCAATTTA[C/T]TCATCCTGGGAATCT | 25909 |
rs185139212 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246852597 | CAAGGATGCATGGGG[C/T]GGGGGTGTCAATCCT | 25909 |
rs185156779 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869482 | GTGAACACATGAATG[A/G]AGAAGTCAATGCCTG | 25909 |
rs185156945 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246918893 | CAGAAAAAAGAAAAA[C/G]TGATTGGTGTCTTTT | 25909 |
rs185164100 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246930071 | AAAAAAAAAGATGTA[G/T]CTGTACCTATGAAAA | 25909 |
rs185168576 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246888288 | CAGTCATTCATTCAT[C/T]CATGCTTCTTGTTTT | 25909 |
rs185236694 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246912220 | TGGTGGCTCACACCT[A/G]TAATCCCAGCACTTG | 25909 |
rs185360018 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246927020 | TCTACTAAAAATACA[A/G]AAACAAAATTAGCAG | 25909 |
rs185481876 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246841700 | AGGTAAACCATCCCA[C/T]TTCCCTTTCCTACTT | 25909 |
rs185492707 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246876364 | TTTTATCAATCCTTA[C/T]CCATCAATAAATTCC | 25909 |
rs185593558 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246859946 | AATTATAGAAACTTA[A/G]AACTGGTGGATAAGT | 25909 |
rs185625524 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | AHCTF1 | GRCh38.p7 | 1:246842589 | TCTGTCTCAAAAAAA[A/T]TAAATAAAAATAAAA | 25909 |
rs185705768 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246880846 | TTCTCTTGCTTCCTA[C/T]AGAAGACAATAATGA | 25909 |
rs185736704 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246920498 | TTAAACCAGCCGGGC[A/G]TGGTGGCTCACGCCT | 25909 |
rs185852705 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246898032 | AGTTATGGCCTATTG[A/G]GTATTAGGAATAGGA | 25909 |
rs185871975 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246871721 | TGCATTTTTTTTTGA[A/G]GCCTCCTGACTGCAG | 25909 |
rs185910751 | snp | A/C/G | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869056 | TCACCATGTTGGCCA[A/C/G]GATGGTCTCGATCTC | 25909 |
rs185922053 | snp | A/G | 0.0715223 | 0.175059 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246862353 | GGCGGGGTGGCGGGC[A/G]CCTGTAGTCCCAGCT | 25909 |
rs185924135 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246886113 | AGGTGGGCAGATCAG[G/T]TGAGGTCAGGAGTTC | 25909 |
rs185927135 | snp | C/T | 1.65581e-05 | 0.00287728 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246902544 | ATTCACGCCTTCCTC[C/T]CTGTCACCATGAGAT | 25909 |
rs185939446 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246924023 | GCAAAAGAGAGATCC[A/G]AGGTACAAGTCATTA | 25909 |
rs185941658 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246844267 | GAGGGAAAGCATTAA[A/T]CCTATATGTAACCTG | 25909 |
rs185947811 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246906565 | CCAGCCTGGGCAACA[C/G]AGTGAGACCCCACCC | 25909 |
rs186019261 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246842977 | ATTCCTACAATTCAA[C/T]TAATCTCCAAGTTAT | 25909 |
rs186023684 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246878446 | TGAAACAATGAATTA[C/T]GATGTAGCCCTATAT | 25909 |
rs186037126 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246882906 | ATGAGGAAACTCAGG[C/T]TCAGAGAGGATAACT | 25909 |
rs186065934 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246922419 | AACAGTATTCTGTTG[C/T]GGTTTTTTGGGTTGT | 25909 |
rs186087215 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246924924 | CAAAACCCTCATGAG[A/G]GTCCTATACTCAAGC | 25909 |
rs186156007 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246861910 | ACTTGTCAGAGCTAA[C/T]ACATTCTTATTAAAA | 25909 |
rs186159570 | snp | C/T | 0.0513262 | 0.151752 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868340 | TGGCCAGGCTGGTCT[C/T]GAACTCCTGACCTCA | 25909 |
rs186170215 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246896738 | ATATCTCAATAAAGC[C/T]GATATTTTGAAAATC | 25909 |
rs186176782 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246882634 | AATAAACCCACCTAA[C/G]AAAGAGGAAAAATTA | 25909 |
rs186183900 | snp | A/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246922045 | TGGTATATTTTAGAC[A/T]TTGTTACATATCCAT | 25909 |
rs186187248 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246902281 | TTCAGACTAGGGATC[A/G]CCTGTTTTGAGAACT | 25909 |
rs186278955 | snp | A/C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246839224 | ATGATCTACATTCAC[A/C/G]GAGGGGGGAAAAAAA | 25909 |
rs186397371 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246913013 | TACTTGAGAACATAT[G/T]AACACCTGATCAACA | 25909 |
rs186414551 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246927648 | AAAGTAATTTACTAA[C/G]TTTCAATTCCTTTCC | 25909 |
rs186442971 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246857482 | TCTGCCTCAATTTAC[C/T]GTGTCTCTGTATATT | 25909 |
rs186471654 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246887767 | AACATTAGCACAAAA[A/T]TATTATCACAAAGAC | 25909 |
rs186494073 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246924382 | ATTCACAAAACATTA[C/G]TGCCGTTTATTTTTG | 25909 |
rs186523367 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246852255 | ACTAAAAGAACTGGA[A/G]CTTTACTCATCTATT | 25909 |
rs186590574 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246882243 | ACCTCGTGATCCACC[C/T]GCCTCAGCCTCCCAA | 25909 |
rs186593933 | snp | A/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246847280 | GGTAACAACAGCCAA[A/T]CTCCATCTCAAAAAA | 25909 |
rs186595371 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868100 | CCCAAGTAGATGGGA[C/T]TACAGGCATGGCCAC | 25909 |
rs186674151 | snp | G/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869116 | CCCAAAGTGCTGGAT[G/T]ACAGGCGTGAGCCAC | 25909 |
rs186689763 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246907411 | AATGCCATGAAAAAT[C/T]AGTCATCTCAATCAT | 25909 |
rs186693546 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246928235 | ATGAACCCGGGAGGC[A/G]GACCTGGCAGTGAGC | 25909 |
rs186711914 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246896960 | GGGACAAAACAGAAA[C/T]GTCTGCTACTAACAT | 25909 |
rs186720154 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246930901 | CAGATAGTATGAACC[C/T]CGTAAGCTTTGAGAA | 25909 |
rs186748646 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246859922 | AGAATGAAATTCTTA[A/T]TTTCTGAGAATTATA | 25909 |
rs186759246 | snp | G/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246875678 | AGCCATCAACATTGA[G/T]ACAAGATCCTTTATT | 25909 |
rs186766834 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246841499 | ATAAAATGCATTCAC[A/G]TGTGCTTTTATTGAA | 25909 |
rs186771516 | snp | C/G/T | 0.000610833 | 0.0174657 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246851330 | AACTGTTGGTCAATA[C/G/T]TATCAAAATTGTACT | 25909 |
rs186777873 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246894443 | GCCGAGCGTAGTGGC[A/G]GGCAGGAGAATGGCG | 25909 |
rs186792622 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246914184 | TTTCCTTCAGTTTCC[C/T]ATTAATTCATAAAAA | 25909 |
rs186810407 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246872438 | CACAAAAAGACAAAT[G/T]AGGTGGTCAGAGCTT | 25909 |
rs186815694 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246878828 | GGCTTATACAGGCCA[A/G]CAACTCAAGAAGTAC | 25909 |
rs186818267 | snp | C/G | | | upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246932359 | GGACTCTCTTGTCAC[C/G]TAATCGTGTGGCCCT | 25909 |
rs186829124 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246926781 | GAATCACTTGAACCC[A/G]GGAGGCGGAGATTGC | 25909 |
rs186937330 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246919221 | AGCCTAGGACAAAGA[C/G]AACTAATAAGCTCAT | 25909 |
rs187039849 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246931832 | TGCAGACCGCTCAGC[A/G]GCTAAAACGCAGTCG | 25909 |
rs187040324 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246891279 | CTCCAAAATGCTAAA[A/G]TAAGTAAGTCACTCC | 25909 |
rs187265771 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246862966 | AACAAATTACTGAAT[C/T]CCATTAGATCATAAT | 25909 |
rs187287311 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246845047 | AACAATGTGTGGCAG[C/G]GTAGGTGGTAAGTGC | 25909 |
rs187290811 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246897080 | GCACTTTGGGAGGCC[A/G]AGGAGGGCAGATCAC | 25909 |
rs187301522 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246878991 | TCATTTTTCCCTAAA[C/T]CAAAATCTAGAAACG | 25909 |
rs187305429 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246919777 | GCTCCAAGCAATCCA[C/T]GGAAACAACCACATA | 25909 |
rs187323713 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246893505 | ACAGTGCAACTGTAT[A/C]CCTACTAGTACTTTT | 25909 |
rs187328040 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246859202 | TTCAGTGGACTCTCA[C/T]CTTAAACTACTTAAG | 25909 |
rs187329758 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246921441 | AATACTCAACAAAAA[C/T]AAACTCAAAGGATAA | 25909 |
rs187334222 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246846267 | TATAGTATACCTATA[A/C]CCAGTCTTCTCGGCA | 25909 |
rs187342418 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246889209 | ATTCCTTCACTCGAA[C/T]ATCTATTGCTGAGTG | 25909 |
rs187348029 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246881053 | TATGCATTATGAAAT[A/G]CACGGTGGAGACCAC | 25909 |
rs187354153 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246864982 | CAACTTTAAGATTCT[A/G]CTACAAGGTTTTCCG | 25909 |
rs187355551 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246909009 | ACAGTTTCACTCTCC[A/G]ATTTCCGTTACCTGT | 25909 |
rs187362828 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246925320 | AATCCAAAGTCCAAA[G/T]GATAACACACAAAAA | 25909 |
rs187393305 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246884363 | TGTAGATCTTACCCT[C/T]TTATCCGTAGAAGTA | 25909 |
rs187399426 | snp | A/T | 0.0232847 | 0.105357 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246922797 | ACCATCCTGGATAAC[A/T]CGGTGAAACCCTGTC | 25909 |
rs187401056 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246903539 | TTCAATATAAGAATC[C/G]CTTTTCACAGCCAGG | 25909 |
rs187566134 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868499 | GCCTCAAGTGATCCT[C/T]CCTCCTCGGCCTCTC | 25909 |
rs187579199 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246901408 | TGGGGAGGCCGAGGC[A/G]GGTGGATCATGAGGT | 25909 |
rs187592476 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246840674 | GAGTTACTTTACTTA[C/T]TGAAGACCTTCTGTT | 25909 |
rs187596244 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246873961 | AACACAGACTTACTA[C/T]GCTGACATAAGATCT | 25909 |
rs187599383 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246880486 | GGAGAATCACTTGAA[C/T]CCGGGAGGTGGAGGT | 25909 |
rs187607280 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246920004 | ATAAATTAGCCGGGC[A/G]TGGAGGCATACGCTT | 25909 |
rs187662148 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246845379 | TTAAAAAAAAGAAAA[A/G]TAGAGTTGATATCAG | 25909 |
rs187665741 | snp | A/G | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246839991 | AGCTCCTTCACAGCA[A/G]TATTATAAAAATTTG | 25909 |
rs187705607 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246848257 | ATTATTTGGCCCCCC[A/G]GGCTGGAATACAGTG | 25909 |
rs187782843 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246929623 | GTTAACATATGAGGA[C/T]AGACAGTAGCATATA | 25909 |
rs187843206 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246889685 | TGTTATATGCTTTGT[A/G]ATTTTGTCACTGCAA | 25909 |
rs187847727 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246925924 | AAAATAATTAGCCAG[C/G]TGTGGTGGCGCCTGC | 25909 |
rs187865569 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246848588 | GTCAACTACATGGCT[A/G]GGTGTGGTGGCTCAC | 25909 |
rs187883865 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246897824 | TGTCTCTACCAAAAA[A/G]AAAAAGGGCTAAGCA | 25909 |
rs187886155 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868781 | AATAAAAAAGTACCA[C/T]GTGATGAATGAGTAC | 25909 |
rs187897007 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246903155 | AACCCGTTTCTATAC[C/G]CCTCCAACATTAGGT | 25909 |
rs187904910 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246883267 | TGCAGCTTAACTTCT[C/T]GGACTTTTAGTTCAA | 25909 |
rs187955343 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246863845 | CGTATCAGTTATAAA[C/T]TGCTTATTTTTCTCC | 25909 |
rs188067542 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246896465 | ACAAAAGACTTCATA[C/T]TATTTGACCCATTTA | 25909 |
rs188072806 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246861410 | TTTTTACCCAAATTC[A/T]CTCCTTAATAAAAAT | 25909 |
rs188076710 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246878380 | CCAGCCTGGCAGACA[A/G]AGCAAGATTCTGTCT | 25909 |
rs188081396 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246917349 | TGGTAACTTCTAAAT[C/T]TGAGATGTCCATCAA | 25909 |
rs188101913 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246929973 | AGGAGAATCGCTTGA[A/G]CCTGGGAGACGGAGG | 25909 |
rs188119537 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246909782 | TGGAATGTATCCCTC[A/G]CAGATAAGGGGGAAC | 25909 |
rs188124954 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246854338 | ACATACTTCTGGACC[C/T]AACAAGTCCATGGTT | 25909 |
rs188287011 | snp | A/G | 0.000214297 | 0.010349 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246855788 | AGATGTTAATCCTTC[A/G]TCCAACACTGGTACC | 25909 |
rs188296183 | snp | G/T | 0.00438332 | 0.0466095 | upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246932944 | GTGCTTTTTAAATTT[G/T]TTTATTTTTGAGACA | 25909 |
rs188299946 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246870718 | TAAAAGAGGGTATAA[A/G]ACCTCAAAAAAAAAA | 25909 |
rs188314650 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246890355 | GCAAGAAATGTTCAC[C/T]ACAAATCAAAATCTA | 25909 |
rs188329084 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246910213 | GGAACATTCTATCAG[A/G]TAACTTCAGCAAGTC | 25909 |
rs188352840 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869845 | CATTCTGTAACCCTG[A/G]ATCACAGTAATCGCA | 25909 |
rs188370119 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246898396 | AATAATCAAATTTAA[A/G]ATTAATTAATTACAC | 25909 |
rs188398068 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246913120 | TTTTTATAGATAGGA[A/G]GATATCTTTTATTTT | 25909 |
rs188399805 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246839402 | TCATTTAACAAGTTC[A/G]TTTAAATAAGTTCAA | 25909 |
rs188403784 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246866585 | AAAATTCAGAGTCTT[G/T]TAATGATTATTTATA | 25909 |
rs188408747 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246870276 | TAGTGAGGCCCTCTC[C/T]ACAAAAAATACCCAG | 25909 |
rs188410138 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246858518 | GTGTTGTATGAAACC[C/T]CACCCACCACAAACA | 25909 |
rs188420758 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246881342 | ACATCCACCATTAGC[A/G]TCAGCAACTCTGCAT | 25909 |
rs188425011 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246920728 | TGAGCCGAGATCGCA[C/G]CACTGCACTCCAGCC | 25909 |
rs188434258 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246899848 | TAATTCCTTTATAAA[A/G]CATATAAATACTAAA | 25909 |
rs188448163 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246933868 | AGGTATTGGACCAAG[C/T]TGTGATAGAAACAGT | 25909 |
rs188468889 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246874826 | TAAAAAGTTACAAAA[A/C]AACCTGACCTCCGGC | 25909 |
rs188573798 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246920526 | CCTGTAACCCCAGCA[A/C]TTTGGGAGGCTGAGG | 25909 |
rs188627042 | snp | A/G | 5.09628e-05 | 0.00504765 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246853228 | CCTGGTTAAGCCTGC[A/G]CTCAGAGACAATAGG | 25909 |
rs188628781 | snp | C/G/T | 0.00279162 | 0.0372561 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246922778 | ACGAGGTCAGGAGAT[C/G/T]GAGACCATCCTGGAT | 25909 |
rs188651412 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246895041 | TTTAAAAAAAAAAAG[A/G]TCAATTTTTTGAAAG | 25909 |
rs188662158 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868938 | CAAGTTCTGCCTCCC[A/G]GGTTCACGCCATTCT | 25909 |
rs188666437 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246894024 | GCCTAGGCAATATAG[C/T]GAGACCATGTCTCTA | 25909 |
rs188674087 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246927908 | GGGAGGCTGAGGCAG[A/G]AGAATCGCTTGAACC | 25909 |
rs188912240 | snp | C/T | 0.000100299 | 0.00708093 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246876921 | TCCTTATTCTCTTAT[C/T]CCCCATAATAAGACA | 25909 |
rs188923148 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246914582 | TCAGTGAGGAGTAGC[A/G]AATCTAAGTTTACAT | 25909 |
rs188943142 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | AHCTF1 | GRCh38.p7 | 1:246842411 | ACATGATAAAATGCC[A/G]TCTCTACTAAAAATA | 25909 |
rs188964345 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246877489 | AATGTCAGTAAAATG[A/G]CACGTTTAAAGAATT | 25909 |
rs188976481 | snp | A/C/T | 1.64868e-05 | 0.00287109 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246861022 | TTTTGGGCTTAGAGG[A/C/T]CGTGAAAACAGTCTC | 25909 |
rs188988862 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246911387 | TTTTGCTCATCAATT[A/C]TTTTCATTTAAACTT | 25909 |
rs188999284 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246901700 | GTGTGTGCCGGCAGT[C/T]CCAGTTACTTGGGAG | 25909 |
rs189008391 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246926950 | GAGGCTAAGGCGGGC[A/G]GATCACGAGGTCAGG | 25909 |
rs189073335 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246904120 | TTAGTTTGCTTGCAA[C/T]GTTGAGTGCATGTGA | 25909 |
rs189171214 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868948 | CTCCCGGGTTCACGC[A/C]ATTCTCCTGCCTCAG | 25909 |
rs189212609 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246846746 | CATATACATATATAT[A/T]TTTTTTGGGGGGATG | 25909 |
rs189243217 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246906642 | GAGAGTTGAGATACA[C/T]TTCCTATAAGATAAA | 25909 |
rs189251390 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246924152 | ACTATCAAACTGAAA[C/T]CTGTGGTAAAATAAC | 25909 |
rs189341214 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246921277 | ATTTGAGAGAGAAAG[C/T]GGAAGAATATACGAG | 25909 |
rs189350958 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246885938 | ACGCCTGTAATCTCC[A/G]CACTTTGGGAGGCCA | 25909 |
rs189357861 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246923491 | ATATAGGCTAGTAAT[A/G]GACAAACAGGTCAAC | 25909 |
rs189364695 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246905998 | GTGGATGCATTCATG[C/T]CTGTGTAAACTGGTC | 25909 |
rs189375706 | snp | A/C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246927034 | AGAAACAAAATTAGC[A/C/T]GGGCGTGGTGACGGG | 25909 |
rs189379174 | snp | A/C | 0.0126979 | 0.078662 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246923176 | TCCCAGCACTTTGGG[A/C]GGCCGAGGTGGGCAG | 25909 |
rs189445466 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246885349 | CACTGTATTTTCAAT[C/G]TGAATTTGATGCAGA | 25909 |
rs189451209 | snp | A/G | 0.000115497 | 0.00759837 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850231 | CAGCTGCTTGTCACT[A/G]GATTTATCATCTTGC | 25909 |
rs189465346 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246891559 | TAATAATCATTAACT[G/T]CAGAATTTCCCAAGC | 25909 |
rs189505574 | snp | A/G | 8.28998e-05 | 0.00643763 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246867311 | GCAGCTCTGGAGCTG[A/G]GAGCGAATACACTAT | 25909 |
rs189614656 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246900612 | ACGCATTTCTATCAT[G/T]TGTATGTAAGACCAG | 25909 |
rs189625267 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246852308 | GATGAGTATGGATAA[C/T]GATGACATTTTTATG | 25909 |
rs189727244 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246872711 | TCGCACTATCATGGG[C/T]GCTGAAAGGGAATGG | 25909 |
rs189737862 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246912415 | TTGAACACGGGAGGC[A/G]GAGGTTGCAGTGAGC | 25909 |
rs189746436 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246839872 | TTTCTCCTTTTCTAC[A/G]TCTACTCACTCTCTC | 25909 |
rs189863713 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246873598 | ATTTCTCCTGCATCA[C/T]AGCAAAGGGAAAGAA | 25909 |
rs189878097 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246858884 | ATAATGCTATGAACA[C/T]TCTTTTAACAGCTAC | 25909 |
rs189898503 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246912866 | TACATTGCTGGGTAA[C/T]TTCATATTGGCTGAT | 25909 |
rs189899676 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246872049 | AGATGAACTATTAAT[A/G]ACAAAAAAAAAAAAA | 25909 |
rs189906202 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246927369 | CTGCATACGCTTGTC[A/C]TCCCGACTACTTGGG | 25909 |
rs189979929 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246846629 | AAAGCAATTCAAATA[A/C]CCAACAGAAGAGGGT | 25909 |
rs189986694 | snp | A/G | 0 | 0 | downstream-variant-500B | AHCTF1 | GRCh38.p7 | 1:246838658 | AATCCATTGTAGCCC[A/G]TTCAGGACCAGGTCT | 25909 |
rs190017354 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246851535 | ACCCTTGGCTGTGTG[C/T]CTTTTAAAACATAAA | 25909 |
rs190050935 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246882786 | CATGGTTAATTTGCA[C/T]GTAAAACAGCCACGC | 25909 |
rs190062366 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246922057 | GACTTTGTTACATAT[C/T]CATGTTGAAAACATA | 25909 |
rs190062580 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246875368 | TCCTTACTTAGAAGC[C/T]AAATAATAAAAAGTC | 25909 |
rs190141871 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246886282 | GCTGCAGTGAGACAA[C/G]ATCGTGCCACTGCAC | 25909 |
rs190143995 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246890825 | AGAAAAGAAGGTTAA[A/G]CATAAATTAAATTAA | 25909 |
rs190144338 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246915765 | GGTAAAAACATTTTA[A/T]AAATTGAATAGTAAT | 25909 |
rs190181851 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246921471 | AGTAAAAAAGTAAAC[C/T]AGAAAGCCCCCAAAA | 25909 |
rs190222228 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246856331 | TTCCTTTAATATTCT[A/C]ATCTGACCTTTCTCA | 25909 |
rs190276696 | snp | A/G | 0.0573587 | 0.15934 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869080 | CGATCTCCTGACCTC[A/G]TGATCCGCCCGCCTT | 25909 |
rs190284983 | snp | G/T | 0.00180009 | 0.0299467 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246895826 | TTTTACTTGTTATCA[G/T]AATCTTACCTTCTGT | 25909 |
rs190302654 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246879314 | AAAAGACATAGCATA[C/T]GGTAATTGAGAGGAG | 25909 |
rs190307524 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246919810 | CTCTGGAATCTCAAA[G/T]AATTCTTAAAGAATT | 25909 |
rs190315672 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246897521 | CAATCATGGTAAGAG[C/T]GTACTTACACAAACT | 25909 |
rs190330401 | snp | C/T | 0.00318978 | 0.0398085 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246931926 | CGGCCCCGCTCTGCG[C/T]ATTACCCTGCGCCGA | 25909 |
rs190391748 | snp | G/T | 0.021333 | 0.101051 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246929922 | CCGGGTGTGGTGGCG[G/T]GCGCCTGTAATCCCA | 25909 |
rs190518781 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246860089 | ATATGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 25909 |
rs190558581 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868283 | ACAGGAATGTGCCAC[A/C]ACGCTAATTTTTGTA | 25909 |
rs190558770 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246847286 | AACAGCCAAACTCCA[C/T]CTCAAAAAAAAAAAA | 25909 |
rs190571948 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246882352 | AAGGTCAGGTACCAC[A/G]TGGATCACATTATGT | 25909 |
rs190699404 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869517 | CAAAGGACAGGGTGA[C/T]TCTGCTGTTAGTGGT | 25909 |
rs190711324 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246852665 | TATGACTAAAAAAAC[C/T]TTTCATTTGAACCAG | 25909 |
rs190714025 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869225 | CCATTTTTCCAACAG[C/T]GTGTACTTACTCCAC | 25909 |
rs190717664 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246888293 | ATTCATTCATTCATG[C/T]TTCTTGTTTTCCCAA | 25909 |
rs190725384 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246907451 | CATTAATCTACCCAC[A/C]CTTTTCTCACTATGC | 25909 |
rs190725635 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246925200 | GCAGTAGCTTTTTAC[A/G]AAGTGTATTCAGAAG | 25909 |
rs190729662 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246908539 | AAATTATTCTTTACA[C/T]TGACAGAACATAAAA | 25909 |
rs190731597 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246845248 | ATATAAAAATGTTTT[C/T]TGTGGGTACACAGTA | 25909 |
rs190783816 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246841714 | ACTTCCCTTTCCTAC[G/T]TTTTCTGCAAAAACC | 25909 |
rs190787258 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246862582 | ATATCAATAGAAATA[C/T]TTATTCCAGATTTCT | 25909 |
rs190797902 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246878917 | TAGACGGTGGAATCA[C/T]TGTAACTTGGGTGTA | 25909 |
rs190806283 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246844447 | GAGAAAGTGCCAGGT[A/G]CAGTGGCTCACAATT | 25909 |
rs190814904 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246896974 | ACGTCTGCTACTAAC[A/T]TTATTACCTATAGTT | 25909 |
rs190889533 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246922645 | GCAATCCTCCTGCCT[C/T]GGCCTCCCAAAGTGC | 25909 |
rs190937167 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246848497 | TGAGCCACCGTGACC[A/G]GCCAAGTCATCTACT | 25909 |
rs190953927 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246882956 | TTCACAAAGTGGCAT[A/C/T]GTTTAGATTTAAATC | 25909 |
rs190964992 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246927864 | AAAAATTAGCTGGGC[A/G]CGGTAGCGCGCTGTA | 25909 |
rs190966275 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246863138 | AAAAATACTATACTG[A/C]ATATTTTAAATTATT | 25909 |
rs190979521 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246888037 | TCTGAGCCCAAACAA[C/G]AGATCCTGGGTTAAC | 25909 |
rs191013572 | snp | G/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246894114 | GAGGCTGAGGCAGGA[G/T]GATGACTTGGGCTCA | 25909 |
rs191021623 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246927994 | ACAGAGCAAGACTCC[A/G]CCACCAAAAAATTAA | 25909 |
rs191071031 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868367 | CTCATGTGATCCACC[C/T]GCCTTGGCCTCCCAA | 25909 |
rs191211409 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868729 | AACAGTCAAATCTTC[G/T]AAGAAAGGCTTACAT | 25909 |
rs191217193 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246902774 | TTGTTCACACAATAC[A/G]AAGAAAACAATTTAG | 25909 |
rs191269569 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246913855 | CTTAAACAGCTACTC[C/T]AGGATTCTATGGCCT | 25909 |
rs191300745 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246847810 | TTACTGAGATGTTTG[C/T]TAAGCTCTAACAAAA | 25909 |
rs191481947 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246924385 | CACAAAACATTAGTG[C/T]CGTTTATTTTTGTGT | 25909 |
rs191491397 | snp | A/G | 0.00478085 | 0.0486577 | utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246840001 | CAGCAATATTATAAA[A/G]ATTTGTTCAGACATC | 25909 |
rs191537632 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246876253 | CTGTAATTCTATATT[C/T]ACCATTTAAAATAAA | 25909 |
rs191539806 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246914451 | CCTGGCTCTTTCTCT[A/G]TATCAGTATACAAAA | 25909 |
rs191557274 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246928416 | ATTCGACAAGGTCAC[A/G]GTGCCTTTGGACTAA | 25909 |
rs191599931 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246859936 | AATTTCTGAGAATTA[C/T]AGAAACTTAAAACTG | 25909 |
rs191616291 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246859833 | TGCTGGTATTACAGG[C/T]GTGAGCCACTTTACC | 25909 |
rs191629276 | snp | G/T | 0.00500552 | 0.0497765 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246841037 | GTAAGAATAAACACA[G/T]TATGCTATAAAATAA | 25909 |
rs191651108 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246922808 | TAACACGGTGAAACC[C/T]TGTCTCTACTAAAAA | 25909 |
rs191686839 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246921009 | AGGCAGGAGAATCGC[C/T]TGAACCTGGGAGAAG | 25909 |
rs191696447 | snp | G/T | 0.00755907 | 0.0610114 | upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246933882 | GTTGTGATAGAAACA[G/T]TTAAAAAGAGTACTG | 25909 |
rs191784203 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246859232 | GATGCAGATTTTTAT[A/G]TAAGTATGTAGTTTT | 25909 |
rs191786121 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246919590 | TGGTGGCACACACCT[A/G]TAGTCTCACCTACTC | 25909 |
rs191798900 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246896840 | AAAAGGAATCCCATG[A/G]ATGTAAGTTGAACAG | 25909 |
rs191802152 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246930618 | GGGTCTCGCCATGTT[C/G]CTCAGGCTGGTCTCA | 25909 |
rs191840221 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246870414 | TGTGACAGACAAAGA[C/T]CTTGTCTCTTAAAAA | 25909 |
rs191842864 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246855165 | GATTAAATGAGTTAA[C/T]AGACACAAGATGATC | 25909 |
rs191877319 | snp | C/T | 6.32798e-05 | 0.00562458 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246862197 | CATTAAAAGTGCTTA[C/T]AGGCCGGGCGCGGTG | 25909 |
rs192004954 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246913089 | CAATAAAAAAGATTT[A/T]AAAATACCTTTTTTT | 25909 |
rs192026887 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246849219 | CTTAGTAAAAAGCTA[C/T]TGGTGTTTCCCTTCA | 25909 |
rs192092296 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246918927 | AAAATCACTTCTTCA[C/G]TAAAGGGGGAGAAAG | 25909 |
rs192176344 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246843693 | AAATAATAAACAAAA[C/T]TTAAAATCATTAAAA | 25909 |
rs192178517 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246878628 | GTAATGATCAATCTG[G/T]CAGTTAAAATTTTTG | 25909 |
rs192209774 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246865254 | TGCCAAAGTGGCTCA[C/T]CTGAGAATAACCAGA | 25909 |
rs192216242 | snp | A/G | 0.00225249 | 0.0334839 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246899424 | TCTGACTTCAGTTCA[A/G]TTAAGAAATCACTAG | 25909 |
rs192224437 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246925478 | TTTAAACTGTGGCCA[A/G]ACATGATGGCTTATG | 25909 |
rs192224759 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246881139 | GGAGTAAAGTAAAAA[C/G]ACTGGGGAAATATAC | 25909 |
rs192235151 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246920580 | TCGAGACCATCCTGG[C/T]TAACAAGGTGAAACC | 25909 |
rs192282630 | snp | A/G/T | 0.00159617 | 0.0282053 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246846304 | TCCCTATGTAAAAAC[A/G/T]AAGTTTAGAATATAA | 25909 |
rs192356034 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246893526 | TAGTACTTTTTAGCC[C/T]TATTTTTGCACTAAC | 25909 |
rs192374185 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246855948 | TTCAGAGAATTCAAT[A/G]CAACTCAAGCTCATT | 25909 |
rs192383171 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246871160 | ACTTGACATGGTGGC[A/C/T]ACCAAAAGGCCCCCA | 25909 |
rs192453653 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246885877 | GCAGACTGAACTAAG[G/T]GCAGATAGAAAACAT | 25909 |
rs192469264 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246923273 | TACAAAAATTAGCTG[G/T]GCATGGTGACATGCG | 25909 |
rs192484331 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246890591 | GAAATATTAGTCAGT[A/G]ACCATATTAAAAGGA | 25909 |
rs192499008 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246910591 | TATGGGAACTCTTGT[A/T]TTCTTCTAACTATCT | 25909 |
rs192506408 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246926814 | TCAGCCGACACTGCA[C/T]CATTGCACTCCAGCC | 25909 |
rs192547227 | snp | A/C | 0.0138799 | 0.0821421 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868944 | CTGCCTCCCGGGTTC[A/C]CGCCATTCTCCTGCC | 25909 |
rs192556235 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868875 | TTTGAGATGGAGTCT[C/T]GCTCTGTCACCCAGG | 25909 |
rs192568024 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246903182 | AGGTTCAGAAAAGTC[A/G]GTTCTAGAGACAGGT | 25909 |
rs192572159 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246883858 | TTAGTGTTTGTTTAC[C/T]ATATGGCAAAGGTAA | 25909 |
rs192578090 | snp | A/C | 0.0433465 | 0.140692 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246922792 | TCGAGACCATCCTGG[A/C]TAACACGGTGAAACC | 25909 |
rs192744256 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246910156 | TAATTTGCAGAAAAT[C/T]GAAAATGATACCACA | 25909 |
rs192775568 | snp | C/G/T | 0.0418435 | 0.138591 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868967 | CTCCTGCCTCAGCCT[C/G/T]CTGAGTAGCTGGGAC | 25909 |
rs192780663 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246905030 | ACATTCAAGTAAGTC[C/T]GCACAATTTCTTCTG | 25909 |
rs192812338 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246841615 | TTTTAGTGCTTTCTG[A/T]AAAATAATTGCAGGA | 25909 |
rs192835030 | snp | C/G | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850122 | TATCAAATTCTGCTT[C/G]AACAGTCAACTGAGA | 25909 |
rs192835938 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246884393 | ACATGCTATTTAACC[A/G]AAGAGAACCAAGAAA | 25909 |
rs192955815 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246889841 | AATAAAATAGTAATG[C/G]TAATAGCAAATTCTG | 25909 |
rs192957816 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246925934 | GCCAGGTGTGGTGGC[A/G]CCTGCCTGTAGTCCC | 25909 |
rs192996276 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246889563 | AAGCACTGGTTCCCA[C/G]AATTGCCATGCATCA | 25909 |
rs192999096 | snp | C/T | 3.92249e-05 | 0.00442842 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246853297 | CAAGGACATCAGCCA[C/T]AGCTGAAAGAAAAAT | 25909 |
rs193020663 | snp | C/G | 6.59315e-05 | 0.0057412 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246863907 | TGATTGTGAACGCTA[C/G]ATGCGTAAATACTAA | 25909 |
rs193024688 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246897890 | GGGCTGGGGTGGGAA[A/G]ATCGCTTAAGCCCAA | 25909 |
rs193078851 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246932542 | ATCTTGGCTCACTAC[A/C]ACCTGTGCTCCCGCT | 25909 |
rs193112182 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246842061 | GCCTCCCAAAGTGCT[C/G]GGATTACAGGCGTGA | 25909 |
rs193119424 | snp | G/T | 3.33483e-05 | 0.00408327 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246876930 | TCTTATCCCCCATAA[G/T]AAGACAACTTTAATC | 25909 |
rs193122083 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246915285 | CAGTGAGCTGAGATC[A/G]TGCCACTGCACTCCA | 25909 |
rs193190820 | snp | C/T | | | upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246933056 | TCCTCCTACCTCAGC[C/T]CTCCAAGTAGCTGGG | 25909 |
rs193203753 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246870232 | GAGGATCACTTGAGG[C/T]CATGAGTTTGAGAAT | 25909 |
rs193205214 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246845656 | CATGCAAAAATAGCC[G/T]CCACCATTTTTTCCA | 25909 |
rs193211316 | snp | C/T | 0 | 0 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246880842 | ACTATTCTCTTGCTT[C/T]CTACAGAAGACAATA | 25909 |
rs193243252 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246920029 | ACGCTTGTAATTCCA[G/T]CTACTCAGGAGGCTG | 25909 |
rs193253623 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246929828 | GGAGGCCAAGGCGGG[C/T]GGATCACGAGGTCAG | 25909 |
rs193268311 | snp | C/G/T | 0.00795532 | 0.062565 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246860126 | TTAGCCAGTCATGGT[C/G/T]GGGGGCGACTATAGT | 25909 |
rs193278154 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246895476 | GGATGAATTCCTAGA[A/G/T]AATTTTGCTGAGTAA | 25909 |
rs199542478 | snp | C/T | 8.25212e-05 | 0.00642291 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850939 | ATGAATGGACTGTTC[C/T]ATTGTATCTGAAGTA | 25909 |
rs199556608 | snp | C/G | 0.00226712 | 0.0335919 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246876199 | CATTCTATTAAACAT[C/G]AAAATTGGTAAAAAA | 25909 |
rs199608908 | in-del | -/GC | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246860198 | CTGGTTGGGGGGGGG[-/GC]GGAGGTTGCAGTGAG | 25909 |
rs199612083 | in-del | -/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246891484 | GAAAAAATTTATGAG[-/T]TCTTTGAATAAAAAA | 25909 |
rs199635904 | snp | C/T | 0.00178324 | 0.0298067 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246904025 | TGCAAACTCAAAACA[C/T]CCCCTTCACTGAAAC | 25909 |
rs199638572 | snp | A/C | 0.000153988 | 0.00877328 | missense, nc-transcript-variant, intron-variant | AHCTF1 | GRCh38.p7 | 1:246843796 | CATGCATTTCTTACC[A/C]GTTCATCTTCAAGCT | 25909 |
rs199639157 | snp | A/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246892810 | CTAATTAAAAAAAAG[A/T]TTTTTTTTTGGTTTT | 25909 |
rs199686540 | in-del | -/TT | 0.00557542 | 0.0525036 | utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246839246 | GGAAAAAAAGTACAC[-/TT]ATTAAAAACAGGTAC | 25909 |
rs199694321 | snp | A/G | 6.66678e-05 | 0.00577317 | intron-variant, downstream-variant-500B | AHCTF1 | GRCh38.p7 | 1:246842684 | TCAAGAACAGAACAG[A/G]AAGTCATACTTGCTT | 25909 |
rs199729275 | in-del | -/CT/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246903662 | TGAGACCCCCCCCCC[-/CT/T]TCCGTCTCTGCTAAA | 25909 |
rs199732006 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869028 | TTTTTCTATTTTTAG[C/T]AGAGACGGGGTTTCA | 25909 |
rs199739670 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246903743 | ACTCCAGAGGCTGAG[A/G]CAGAGAATTGCTTGA | 25909 |
rs199771528 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246911210 | CATATTGACTTGAAG[A/G]GAGTTTTAATTACGA | 25909 |
rs199837370 | snp | A/G/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246904191 | TTTTATAAAAATGTA[A/G/T]TCCTTTGAAATAATA | 25909 |
rs199870359 | in-del | -/A | 0.00993419 | 0.0697739 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246884068 | AGGTACATGCAAATG[-/A]AAAAAAAAATTTATA | 25909 |
rs199923661 | in-del | -/A | | | intron-variant, downstream-variant-500B | AHCTF1 | GRCh38.p7 | 1:246842589 | CTGTCTCAAAAAAAA[-/A]TAAATAAAAATAAAA | 25909 |
rs199987898 | in-del | -/ATAAATAAATAC | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246923421 | CTGTCCCAAAAATAA[-/ATAAATAAATAC]ATAAATAAATACATA | 25909 |
rs200010862 | snp | C/T | 0.00199806 | 0.0315443 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246855727 | CAAAATTATTATACA[C/T]ACATTTATTGTCATT | 25909 |
rs200042860 | in-del | -/G | 0.0737376 | 0.17729 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869111 | GCCTCCCAAAGTGCT[-/G]GGATTACAGGCGTGA | 25909 |
rs200059115 | snp | A/T | 0.43221 | 0.171171 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246864592 | AAAGACTAGACTGAC[A/T]TGGGAGGCCGAGGCG | 25909 |
rs200085237 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246896097 | GACGTGTTAAAACTG[C/G]AACTCTCATACACTG | 25909 |
rs200147070 | snp | C/T | 0.000215077 | 0.0103678 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246891838 | ACTATATTAAGATTG[C/T]TAAGAAGCAAATAGC | 25909 |
rs200147170 | in-del | -/TTAA | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246899949 | TAAGTTATCCATATG[-/TTAA]CTAACAGTGAGATAC | 25909 |
rs200148859 | in-del | -/GG | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246910786 | CTTTTTCAGAGAAGA[-/GG]GATTAGATTTTGCCA | 25909 |
rs200165532 | in-del | -/ATTT | | | upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246933152 | TTTATTTATTTATTT[-/ATTT]GAGACGGAGTCTCGC | 25909 |
rs200166495 | in-del | -/TTAT | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246845970 | AACAACACATCTTAC[-/TTAT]TCCCTGGGTGATGTG | 25909 |
rs200171102 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868066 | CTCCTGGGTTCAAGC[A/G]ATTCTCCTGCCTCAG | 25909 |
rs200194769 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246928227 | AGAATGGCATGAACC[C/T]GGGAGGCGGACCTGG | 25909 |
rs200231734 | in-del | -/TCTT | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246845964 | CTCTAGAACAACACA[-/TCTT]ACTTATTCCCTGGGT | 25909 |
rs200254086 | in-del | -/AATT | 0.0130921 | 0.0798413 | utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246839753 | CGATTACCTGTTATA[-/AATT]ATTTTACAACACTTA | 25909 |
rs200283654 | snp | A/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246852394 | GTTTTTTATCCAAAT[A/T]TCTATAAATAATTAG | 25909 |
rs200284512 | in-del | -/TAGAG | 0.00755907 | 0.0610114 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246913522 | ATAGATTTAAGACTA[-/TAGAG]TAAATTTGCATTTGA | 25909 |
rs200325446 | in-del | -/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246871709 | CATGCCTACAGTGCA[-/T]TTTTTTTTTGAGGCC | 25909 |
rs200338789 | snp | C/G/T | 0.00067552 | 0.018367 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246907587 | TTCCAAAGTGCTAGA[C/G/T]AGCCATCAGAAAAAC | 25909 |
rs200355866 | snp | G/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246875045 | AGGCCAACAACTTAT[G/T]TTATAGATAAACCAG | 25909 |
rs200363705 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246920582 | GAGACCATCCTGGCT[A/G]ACAAGGTGAAACCCT | 25909 |
rs200512569 | snp | C/T | 0.0039921 | 0.0444985 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246930947 | TCTCAAAACAAAACA[C/T]CCAAACCAAAACAGT | 25909 |
rs200513694 | in-del | -/G | 0.0596104 | 0.162024 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246922435 | GTTTTTTGGGTTGTT[-/G]TTTTTTTTTTGACAG | 25909 |
rs200537262 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246908323 | AAATTCACAGGGATA[A/C]AAAAAAAAAAAAAAA | 25909 |
rs200562886 | in-del | -/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246860199 | TGGTTGGGGGGGGGG[-/C]GGAGGTTGCAGTGAG | 25909 |
rs200582408 | snp | G/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246883729 | CATTTTGAGTGGTTG[G/T]TTTTATTTCTGTATT | 25909 |
rs200604228 | in-del | -/A | 0.0225045 | 0.103662 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246882476 | CCGTAATGAAAATTT[-/A]AAAGATACTTAGAAC | 25909 |
rs200641823 | snp | C/T | 4.2983e-05 | 0.00463569 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246851442 | TTTCTTGTTCAATCA[C/T]CTAAATGAATTAAAG | 25909 |
rs200680433 | in-del | -/AG | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246910783 | TGTCTTTTTCAGAGA[-/AG]AGAGATTAGATTTTG | 25909 |
rs200701729 | snp | C/T | 0.000197821 | 0.0099434 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246877045 | ATTCATGATTCTGAA[C/T]GCTGGCACTGGACTG | 25909 |
rs200702767 | snp | C/T | 0.000449749 | 0.0149891 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246891031 | AGATGAGGTGGGAAA[C/T]CACAAACTTATTGCT | 25909 |
rs200743124 | in-del | -/AC | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246847294 | ACTCCATCTCAAAAA[-/AC]AAAAAAACAAACAAA | 25909 |
rs200751034 | in-del | -/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246852484 | TTTGGTATAATAGAA[-/T]TTTTTTTTTTAAAAA | 25909 |
rs200762494 | snp | G/T | 0.00199798 | 0.0315436 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246849602 | AAACTGTTTTGCAGA[G/T]AAAGAAAAGTACCTT | 25909 |
rs200792896 | snp | A/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246864886 | AAAAAAAAAAAAAAA[A/T]AAAGACTAGACTGAC | 25909 |
rs200888196 | in-del | -/AC | | | downstream-variant-500B | AHCTF1 | GRCh38.p7 | 1:246838886 | AGTATCTTTCTGAGT[-/AC]ATTGTTTACCTTACT | 25909 |
rs200903359 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246892808 | AGCTAATTAAAAAAA[A/G]GATTTTTTTTTGGTT | 25909 |
rs200912155 | snp | A/G | 3.30819e-05 | 0.00406692 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246918276 | TTTCCACGAAGCACA[A/G]ATTCTAATGTTATTT | 25909 |
rs201013631 | snp | A/C/T | 0.161924 | 0.233971 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246852389 | AGTTGGTTTTTTATC[A/C/T]AAATTTCTATAAATA | 25909 |
rs201021519 | snp | A/C | 0.00019858 | 0.00996246 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246849956 | ACATCAACATTTTCA[A/C]TTTTAGCTGGGGTAT | 25909 |
rs201022449 | snp | A/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246862720 | AAAAGTGCCAATTAG[A/T]AAGATAAATTACTTA | 25909 |
rs201045015 | in-del | -/T | 0.0127029 | 0.0786772 | utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246839513 | TTCAACAAGGCAGCG[-/T]TAACATCCATCACTA | 25909 |
rs201109397 | snp | C/T | 0.000667234 | 0.018253 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246887187 | TAATTCATGAAAGTT[C/T]ATGCTGTAAGTGAAT | 25909 |
rs201113359 | snp | A/G | 3.29538e-05 | 0.00405904 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246898288 | GATTATAACCATCAG[A/G]AATGAGTTCATTGAG | 25909 |
rs201117355 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246884365 | TAGATCTTACCCTCT[C/T]ATCCGTAGAAGTACA | 25909 |
rs201139530 | in-del | -/G | 0.0566069 | 0.158427 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246911847 | AATCAAATTTTTTCA[-/G]GTCTGATTTTGCATA | 25909 |
rs201150652 | in-del | -/TTC | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246857958 | CAGACTGCTAACACT[-/TTC]TTCTTCTTTTTTTTT | 25909 |
rs201179961 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246928006 | TCCGCCACCAAAAAA[A/T]TAATTAATTAATTAA | 25909 |
rs201238439 | snp | A/C | 0.00199798 | 0.0315436 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850661 | TCAGAAGCTTCAGAA[A/C]TTTCTTTTGCCTTCC | 25909 |
rs201253679 | in-del | -/TCCT | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246906860 | TTTGATTTTTAAAAA[-/TCCT]TTTTTTTCCCTCTCA | 25909 |
rs201266735 | snp | C/T | 1.65389e-05 | 0.00287562 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246890056 | GACAACTGCACAGAA[C/T]CATCTAGATTTTTAA | 25909 |
rs201276411 | snp | C/T | 0.000160571 | 0.00895878 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246867827 | CTGTAAAATGAAGAA[C/T]GCTGGAATTAAGTGC | 25909 |
rs201308457 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246906768 | CACAAATTAACTTAG[A/C]TACAAAGTATCAATA | 25909 |
rs201321125 | in-del | -/A | 0.00113992 | 0.0238466 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246841001 | TTTTCTGTGTTTCTG[-/A]AAAAAAAAAGATATG | 25909 |
rs201338008 | in-del | -/AAC/AC/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246847305 | AAAAAAAAAAACAAA[-/AAC/AC/C]CAAAAAAAAAACTGA | 25909 |
rs201346302 | in-del | -/ATATAC | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246846725 | AAGATTTTGAAATAT[-/ATATAC]ATATACATATACATA | 25909 |
rs201354601 | snp | A/C | 0.330482 | 0.236691 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246867905 | CACCCCCCCCCCCAC[A/C]CACACACACACACAC | 25909 |
rs201407224 | snp | A/G | 3.29516e-05 | 0.00405891 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246851250 | TGCTTTGAGCCACAA[A/G]AAGTTCCCCATCTAC | 25909 |
rs201421761 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246920586 | CCATCCTGGCTAACA[A/C]GGTGAAACCCTGTCT | 25909 |
rs201449234 | in-del | -/AA | 0.425586 | 0.17796 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246930052 | GCAAGACCCCGTCTC[-/AA]AAAAAAAAAAAGATG | 25909 |
rs201481584 | snp | C/T | 0.00183889 | 0.0302665 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246903938 | AAACCCATAGTCCAA[C/T]GACCATTTACCTCAT | 25909 |
rs201498481 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246920920 | GTGAATCCACATCTC[C/T]ACTAATAATACCAAA | 25909 |
rs201559540 | in-del | -/TAT | 0.222035 | 0.248431 | downstream-variant-500B | AHCTF1 | GRCh38.p7 | 1:246838988 | TGTTTACCTTACTAC[-/TAT]GATACTAAGCACCTT | 25909 |
rs201638378 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869236 | ACAGCGTGTACTTAC[C/T]CCACTGACTAACTGT | 25909 |
rs201652739 | in-del | -/A | 0.00874735 | 0.0655527 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246921663 | CCAATGAATCCTAGG[-/A]ACTACCAAAAAAGAG | 25909 |
rs201657362 | snp | A/C | 0.00181402 | 0.0300619 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246900134 | GGACTCCTCTATTTA[A/C]ACTTCTCTCATGTAC | 25909 |
rs201673996 | in-del | -/A | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869915 | ATAGCTGTCACAGAT[-/A]AGTGATTCCTCTGAG | 25909 |
rs201677476 | snp | A/C/T | 3.30246e-05 | 0.0040634 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246877120 | AAACTACCAATTTAT[A/C/T]TTGAATTTCTGACAA | 25909 |
rs201706489 | in-del | -/TCTT | 0.0205511 | 0.0992634 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246915517 | TTTTCCATGCTAGTC[-/TCTT]TATCTAAAATGTCCA | 25909 |
rs201718431 | in-del | -/TAAC | 0.0290542 | 0.116974 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246899950 | AAGTTATCCATATGT[-/TAAC]TAACAGTGAGATACA | 25909 |
rs201746803 | snp | A/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246852393 | GGTTTTTTATCCAAA[A/T]TTCTATAAATAATTA | 25909 |
rs201761552 | snp | A/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246854968 | TGATCGGCTTTTTAC[A/T]TGTTAGACAATTCTC | 25909 |
rs201763321 | in-del | -/ACTA | 0.0209421 | 0.100162 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246926666 | TTCAAGACCAGCCTC[-/ACTA]ACAGGGTGAAATCCC | 25909 |
rs201767677 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246894400 | ACACGGTGAAACCCC[A/G]TCTCTACTAAAAAAT | 25909 |
rs201781867 | snp | A/C | 0.268452 | 0.249318 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246847308 | AAAAAAAAACAAACA[A/C]AAAAAAAACTGAAAA | 25909 |
rs201805140 | snp | A/C | 0.00199792 | 0.0315431 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246888378 | TCTAAATGATAGCAC[A/C]TTACTGCAAACCTAC | 25909 |
rs201815383 | in-del | -/CGGGG | | | downstream-variant-500B | AHCTF1 | GRCh38.p7 | 1:246838618 | GTGGGCGGGGCGGGG[-/CGGGG]GGAAGACCTCATATA | 25909 |
rs201853355 | snp | A/C/T | 0.000179009 | 0.00945918 | missense, nc-transcript-variant, intron-variant | AHCTF1 | GRCh38.p7 | 1:246843863 | AAGCAGGAGGTGAGA[A/C/T]GACAAACTGAGAAGA | 25909 |
rs201868046 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246892809 | GCTAATTAAAAAAAA[A/G]ATTTTTTTTTGGTTT | 25909 |
rs201879215 | snp | A/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246852390 | GTTGGTTTTTTATCC[A/T]AATTTCTATAAATAA | 25909 |
rs201904837 | snp | C/T | 0.00199802 | 0.0315439 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246918286 | GCACAGATTCTAATG[C/T]TATTTCGTCTTCTCC | 25909 |
rs201947289 | in-del | -/TG | 0.00716266 | 0.059414 | upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246933585 | TATTTTTGTAGAGAC[-/TG]TGTCTTGCTGTGTTG | 25909 |
rs201962947 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246922779 | CGAGGTCAGGAGATC[A/G]AGACCATCCTGGATA | 25909 |
rs201974813 | snp | A/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246848713 | TCTACAAATACAAAA[A/T]ATTAGCCAGGCCTGT | 25909 |
rs201984673 | snp | C/G | 2.01888e-05 | 0.0031771 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246861258 | ACTGCACATTTTTTA[C/G]GTGTAGTAAATACTT | 25909 |
rs202058646 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246920523 | ACGCCTGTAACCCCA[A/G]CACTTTGGGAGGCTG | 25909 |
rs202069305 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246917544 | ACAGAATAGTGGCTA[A/C]TTAGAAAAAAGTTTT | 25909 |
rs202106757 | snp | C/T | 0.00034628 | 0.0131537 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246867730 | ATTTTAGATAACACA[C/T]TGTTGATGAAAACAG | 25909 |
rs202199548 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246864913 | TGACAACCCACACCC[A/C]CCACCACAACCAAAA | 25909 |
rs202231152 | snp | A/G | 1.65545e-05 | 0.00287697 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246894713 | TCCACGTCCATTCAA[A/G]AACAAAGCGCAAATT | 25909 |
rs267598462 | snp | A/G | 1.64876e-05 | 0.00287116 | AHCTF1 | 1 | allele_origin=G(germline)/A(somatic) | 1:246850151 | GATGACTCAAGGTTG[A/G]AGTCTTCTCTCACAT | 25909 |
rs367564374 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246922617 | CATGATGGTCTTGAA[C/T]TCCTGGGTTCCAGCA | 25909 |
rs367585265 | in-del | -/C | 0.00795532 | 0.062565 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246886685 | ATACAAGAGGATGTG[-/C]ATAGGGTATATGCAA | 25909 |
rs367665479 | snp | C/T | 0.000535854 | 0.0163597 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246867855 | TGCATCTCTAACAAA[C/T]GGGAATTTAATAAAA | 25909 |
rs367694906 | snp | C/T | 0.000383107 | 0.013835 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850783 | GATACGTTGACCTCT[C/T]GTACGAGTTTTGGAG | 25909 |
rs367723662 | snp | C/T | 0.000332419 | 0.0128879 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246887194 | TGAAAGTTTATGCTG[C/T]AAGTGAATAGACTTA | 25909 |
rs367757339 | snp | A/G | 4.94368e-05 | 0.00497152 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246902626 | CCCCTCAAAGGGAAC[A/G]TGCCACCTGTCAGGT | 25909 |
rs367757583 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246885807 | TAAGCTGAAAAAATC[G/T]ACTTTAATCTGTGCT | 25909 |
rs367758846 | snp | A/G/T | 6.59374e-05 | 0.00574151 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246861043 | AAACAGTCTCTTCAA[A/G/T]GTCTTCCGGTGACGG | 25909 |
rs367764687 | snp | G/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246899605 | AGACTGCAAGGCAAG[G/T]TGTCAAATTATTACA | 25909 |
rs367765009 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246907777 | AAACCACAAATTAGA[C/T]AAATGAAGTTAAAAA | 25909 |
rs367768011 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246924130 | ATTCTCACAGAAGAG[A/G]ATCAATACTATCAAA | 25909 |
rs367769249 | snp | G/T | 1.81253e-05 | 0.00301037 | missense, nc-transcript-variant, intron-variant | AHCTF1 | GRCh38.p7 | 1:246843857 | TCCTTAAAGCAGGAG[G/T]TGAGATGACAAACTG | 25909 |
rs367799840 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246920643 | AGCGTGGTGGCGGGC[A/G]CCTGTAGTTCCAGCT | 25909 |
rs367848739 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246857848 | AGAATATTATTTATG[C/T]TAAATATTTAGTGAT | 25909 |
rs367872349 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246923998 | CCCAAAGGCGTAGAA[C/T]ATAAATCTGGCAAAA | 25909 |
rs367920072 | snp | C/T | 4.99147e-05 | 0.00499549 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246900396 | AAAAAGCCCCAAATA[C/T]ACAGAAGGCTTTCCC | 25909 |
rs367924006 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869096 | TGATCCGCCCGCCTT[A/G]GCCTCCCAAAGTGCT | 25909 |
rs367958551 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246861777 | GATGATGGGTTTGGC[C/T]TAGCCAATGGCCCTA | 25909 |
rs367972100 | multinucleotide-polymorphism | AA/GG | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246919871 | TCACAGAGCCAGGCA[AA/GG]GTGGCTCATGCCTGT | 25909 |
rs368025192 | in-del | -/T | 0.00716266 | 0.059414 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246877740 | GCTTGGTAGTAGATG[-/T]TTTTTGGTTGATTTG | 25909 |
rs368063328 | in-del | -/GTTTTAC | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246892295 | ATCAAATTCTAATTT[-/GTTTTAC]TTTTTTTTTTTTTTT | 25909 |
rs368072334 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246920724 | GCAGTGAGCCGAGAT[C/T]GCACCACTGCACTCC | 25909 |
rs368107849 | snp | C/T | 6.61781e-05 | 0.00575193 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246891850 | TTGCTAAGAAGCAAA[C/T]AGCATTGCTGGATAG | 25909 |
rs368119622 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246843236 | TACTCTGTTGGGAGG[A/G]ATGCCTGTCTCCTCT | 25909 |
rs368120677 | snp | A/G | 1.66338e-05 | 0.00288386 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850795 | TCTCGTACGAGTTTT[A/G]GAGGAAACCACGTCA | 25909 |
rs368123846 | snp | A/G | 0.000275824 | 0.0117404 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246862203 | AAGTGCTTATAGGCC[A/G]GGCGCGGTGGCTCAC | 25909 |
rs368127317 | snp | G/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246874248 | GACCATCTTTGAGGT[G/T]GGCCTCTGTCTCCCT | 25909 |
rs368212406 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246930435 | AGACAACGTAGACTT[C/T]CCATAGCGCTTGGCA | 25909 |
rs368230093 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246848423 | AGCCAGGATGGTCTC[A/G]ATCTCCTGATCTCGT | 25909 |
rs368246638 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869256 | TGACTAACTGTTCCC[C/T]CGCGTCTCTCCCTTT | 25909 |
rs368307524 | snp | A/C | 1.65792e-05 | 0.00287912 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246840950 | CAAGGGGGAAATCAG[A/C]CGAATTTCTATGGGA | 25909 |
rs368320933 | snp | A/G | 1.65002e-05 | 0.00287225 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246861123 | CTGTTTCCTTTGCTC[A/G]CATCCAGTTTCTCTA | 25909 |
rs368370413 | snp | A/G | 1.64841e-05 | 0.00287085 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246851107 | AATTTGTCCATGATT[A/G]TCATTTTCCCCACTG | 25909 |
rs368383090 | snp | G/T | 1.65573e-05 | 0.00287721 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246918305 | TTCGTCTTCTCCAAG[G/T]GCTTGAAGAGTCACT | 25909 |
rs368385143 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246929881 | ATATGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 25909 |
rs368425692 | in-del | -/A | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246867891 | TGAAAGAATGATTAC[-/A]CCCCCCCCCCCACAC | 25909 |
rs368425839 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246848795 | GCACATGTTGCAGTG[A/T]GCCGAGATCATGCCA | 25909 |
rs368431815 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246855266 | ATCCTATCTTCCTCA[C/T]CTCTGTATAGCCAGG | 25909 |
rs368445746 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246918106 | GCTTATAGATGTTAT[A/G]TATGTAACTGTAGAT | 25909 |
rs368523532 | snp | A/G | 1.65312e-05 | 0.00287495 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246867757 | ACAGATCTTGTCAAC[A/G]CAGTTCCTGTTACAA | 25909 |
rs368537882 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246900886 | GATGAACCTTAGCTG[A/G]GAAGGACTTATCCAG | 25909 |
rs368548624 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246927730 | CTGTTCATGGCCGGG[C/T]GCGGTAGCTCAAGCC | 25909 |
rs368558758 | snp | A/G/T | 3.43284e-05 | 0.00414286 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246899526 | ATCTAAAAAAAAGAT[A/G/T]TAAAAAATAATCCAC | 25909 |
rs368600987 | snp | C/T | 5.00931e-05 | 0.0050044 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246885548 | TACCACTGGACACTG[C/T]TGGCTTCATTGTCTG | 25909 |
rs368629914 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246928052 | GCCGGGTGCGGTGGC[G/T]CACGCCTGTAATCCC | 25909 |
rs368632848 | snp | C/T | | | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246905590 | AGCAATTCCGAGGAT[C/T]ATTCTCAGGTTCTTG | 25909 |
rs368654840 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868916 | GTGGTGTGATCTCGG[C/T]TCACTGCAAGTTCTG | 25909 |
rs368702933 | snp | A/C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246877662 | TCAGTGGGAAGCGTG[A/C/T]GAAAGACTGAGATCT | 25909 |
rs368716204 | in-del | -/AAAAA | 0.0228903 | 0.104504 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246845366 | AAGCATATGATTCTT[-/AAAAA]AAAGAAAAATAGAGT | 25909 |
rs368742330 | snp | C/T | 0.000304961 | 0.0123445 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246904058 | AAATTAACGAAGACA[C/T]GCTAAATATATTAAT | 25909 |
rs368754778 | snp | A/G | 3.8552e-05 | 0.00439027 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246861226 | CTTTGCTCTTCAGCC[A/G]TTCAGTTTCCACTGG | 25909 |
rs368769884 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246883832 | ATAAGGTTTAGAAAT[C/T]AAACTATTTATTAGT | 25909 |
rs368778976 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868905 | GTTGGAGTGCAGTGG[C/T]GTGATCTCGGCTCAC | 25909 |
rs368802357 | snp | C/T | 3.30447e-05 | 0.00406464 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246905645 | TTGTCCACTTTCCAA[C/T]TGTATGTAATATCTG | 25909 |
rs368802989 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246928404 | TTATTCCTGGGCATT[C/T]GACAAGGTCACAGTG | 25909 |
rs368823025 | snp | A/C/T | 3.4329e-05 | 0.00414289 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246877298 | TCCAGGCTTCAACCA[A/C/T]ACACCTGAAAGCAGT | 25909 |
rs368827923 | snp | A/C | 1.71714e-05 | 0.00293008 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246862128 | AATCCAGAAGTAGTA[A/C]CTGACATGGCCAAAC | 25909 |
rs368902281 | snp | C/T | 1.65034e-05 | 0.00287253 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246877101 | AAAGAACAAAATAGA[C/T]TGTAAACTACCAATT | 25909 |
rs368941568 | snp | A/C | 0.104504 | 0.2033 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246867901 | ATTACACCCCCCCCC[A/C]CACACACACACACAC | 25909 |
rs368950744 | snp | C/T | 0.00024729 | 0.0111168 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246895934 | GTTCTTCCTAAACCA[C/T]GCATTACAGAAAGGA | 25909 |
rs368970530 | snp | C/G | 1.67939e-05 | 0.0028977 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246916348 | CTGTTATAGAGTTTA[C/G]TACCTCAAGTTGTGG | 25909 |
rs368992959 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246849173 | CCAGTTTGTGGGCAA[C/T]AGTGAATATGGATTG | 25909 |
rs368999735 | snp | C/T | 1.65551e-05 | 0.00287702 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850064 | ACATCTTCAGATGGA[C/T]TGATTTTTCTTGGTC | 25909 |
rs369048405 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246926465 | AAATGTTTAATAAAG[C/T]TTTTCAAATTTAACA | 25909 |
rs369072844 | snp | C/T | 4.94344e-05 | 0.00497139 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246898299 | TCAGGAATGAGTTCA[C/T]TGAGTGATGGACCTG | 25909 |
rs369090058 | in-del | -/ACAT | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246864522 | TCCATTCACCTACAT[-/ACAT]GTAATATATATAATG | 25909 |
rs369090958 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246866336 | CAGAAAAAAAAATCC[A/G]AACTATTGGTAGAAA | 25909 |
rs369099199 | snp | C/T | 3.2969e-05 | 0.00405998 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246855782 | TTCAACAGATGTTAA[C/T]CCTTCGTCCAACACT | 25909 |
rs369119391 | snp | A/G | 8.70193e-05 | 0.00659561 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246853206 | TCTTTTAAGTTCAGC[A/G]CTACTTCCTGGTTAA | 25909 |
rs369166034 | snp | C/G/T | 0.000764551 | 0.0195369 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246889923 | CTATTCTGAGAAACT[C/G/T]TGACTTCTTACAGAT | 25909 |
rs369212124 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246902436 | TTCCAATTTTCTGAA[C/T]TGCCAGGAGTATGAA | 25909 |
rs369213429 | snp | A/G/T | 0.00024652 | 0.0110996 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246876087 | GGCTTAGCTCGTTCA[A/G/T]TGGCTAATTTTCGAT | 25909 |
rs369259650 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246891258 | CCAAAATGATGTCAA[A/G]CAAACCTCCAAAATG | 25909 |
rs369278200 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246893798 | TCCATCATCAGTATA[C/T]TTAGTAAATTAAACT | 25909 |
rs369343018 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246910794 | AGAGAAGAGATTAGA[C/T]TTTGCCACAACAAAC | 25909 |
rs369355157 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246911479 | CTATCTATGAAGATT[C/T]TTTTTTTTTTTTTTT | 25909 |
rs369427665 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246888825 | TAAGGAAGGAGGATC[A/G]TTGGAGCCCAGGAGT | 25909 |
rs369433989 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246916017 | TAAGAGTAACACATT[C/T]ACATAAAAGTATACA | 25909 |
rs369507349 | snp | C/T | 1.64844e-05 | 0.00287087 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246849660 | GAGAAAATAAAGGCT[C/T]ATTGTTTGGTTCAGA | 25909 |
rs369528671 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246915717 | ATATTTTCCATAATG[C/T]TCCAATCCAAGACTA | 25909 |
rs369612509 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246918508 | TCTGGTTACAAAATA[A/C]ATATTGGCCAGATGC | 25909 |
rs369612701 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869034 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCATGT | 25909 |
rs369643786 | snp | C/T | 0.410399 | 0.191761 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246897884 | TTGCGGGGGCTGGGG[C/T]GGGAAGATCGCTTAA | 25909 |
rs369646906 | snp | G/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246844225 | GTCTATTTCTTTTAA[G/T]CCGTACTGCTCCTCA | 25909 |
rs369650473 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246848216 | TGTATCAGTACAACA[A/G]GTCATCTACTTTATT | 25909 |
rs369678601 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246886890 | ATCACCAATTTCATA[C/T]ATCAAGGCCAAATCT | 25909 |
rs369696763 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246908374 | AAGCCTACCCTCCCC[A/C]CCTACAAAAGACCTT | 25909 |
rs369757901 | snp | C/T | 0.000165096 | 0.00908408 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246888358 | CCCTCCCCAGCTTTG[C/T]AGACTCTAAATGATA | 25909 |
rs369759637 | snp | A/C/T | 8.23708e-05 | 0.00641712 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246849826 | TGATACTGAGTGCAA[A/C/T]GAACGTTTTTGGCTT | 25909 |
rs369797943 | snp | C/T | 1.64808e-05 | 0.00287057 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246864004 | CTTTTAATTGCGAAC[C/T]TGAGGGCAGTGAACG | 25909 |
rs369798428 | snp | C/T | 6.59729e-05 | 0.005743 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246876999 | AAGGCAGGCACATAA[C/T]TGGCACGCTGCAAAT | 25909 |
rs369839183 | snp | A/C | 0.000153988 | 0.00877327 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246900485 | CTGGAAGAAAAAGAT[A/C]ATTTTTAAAAACAGA | 25909 |
rs369872645 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246906163 | GATGAGTTAGAAACT[A/G]AAGAGTTCCCATAAA | 25909 |
rs369881206 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246896713 | ATATCTGAACTGCAC[A/G]GTGTATGAAATATCT | 25909 |
rs369897027 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246879955 | AATTAGCACCAAACT[A/G]AAGTGAAAAAAGTAT | 25909 |
rs369907900 | in-del | -/CAAAAAA | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246848708 | CTGTCTCTACAAATA[-/CAAAAAA]TTAGCCAGGCCTGTA | 25909 |
rs369910717 | snp | A/C | 0.000179424 | 0.00946993 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246891959 | AGTTTCCATACAGTA[A/C]ATCTAAATAAATTAG | 25909 |
rs369954768 | snp | C/T | 8.65314e-05 | 0.0065771 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246867384 | TAACTTCTGATGTAT[C/T]ACAAGGAGCACTGAT | 25909 |
rs369978816 | snp | G/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246908346 | AAAAAAAAAGAGGGG[G/T]GGGGCAAGGGGGAAG | 25909 |
rs369984833 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246925665 | CTGTCCCCTCCCAAT[C/T]TCATACTGAAATGTG | 25909 |
rs369995299 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246846807 | TCACCTGGGCTGGAG[C/T]ACAGTGGTGTGATGG | 25909 |
rs369995931 | snp | A/G | 0.000101612 | 0.00712712 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246907779 | ACCACAAATTAGACA[A/G]ATGAAGTTAAAAAAC | 25909 |
rs370055569 | in-del | -/AA | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246880567 | GTGAGACTCCAGCTC[-/AA]AAAAAAAAAAAAAAA | 25909 |
rs370081948 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246921636 | ACACACCGATTCCCT[A/G]AGTCAGGAAGTCCAA | 25909 |
rs370087175 | snp | C/T | 0.0479149 | 0.147179 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868969 | CCTGCCTCAGCCTGC[C/T]GAGTAGCTGGGACTA | 25909 |
rs370105401 | snp | G/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246929755 | CGTTTTGCTTCCTCT[G/T]AAAATATATCTGTAC | 25909 |
rs370118612 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246929404 | ACAAAGTGAGACTCC[A/G]TCTCAAAAAAATAAA | 25909 |
rs370142896 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246898665 | ACACACACACACACA[C/G]GAAAACTCCTGCAGT | 25909 |
rs370145552 | snp | A/C | 4.97682e-05 | 0.00498815 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246900333 | GAAAAAAAAAGAATC[A/C]TACCTTAACGAATCT | 25909 |
rs370165641 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246924168 | CTGTGGTAAAATAAC[A/G]GGATAACAGCCACTT | 25909 |
rs370220535 | in-del | -/AT | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246912840 | TATGCCAAGAACACT[-/AT]GTTAGATCCTACATT | 25909 |
rs370281990 | snp | G/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246854490 | GTTAAGCATGTAACA[G/T]CTACACTACAAAACA | 25909 |
rs370291964 | snp | C/T | 0.000164902 | 0.00907876 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246913278 | CAAGTCATCCAAACA[C/T]AGGTCAACAAGAAGG | 25909 |
rs370302054 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246909781 | TTGGAATGTATCCCT[C/T]GCAGATAAGGGGGAA | 25909 |
rs370331065 | snp | C/T | 1.78784e-05 | 0.00298979 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246857849 | GAATATTATTTATGC[C/T]AAATATTTAGTGATT | 25909 |
rs370331510 | snp | C/T | 0.000100189 | 0.00707703 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246902693 | GTAACATAAAATACA[C/T]GCAAATATTAATCTG | 25909 |
rs370390882 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246927045 | TAGCAGGGCGTGGTG[A/G]CGGGAACCTGTAGTC | 25909 |
rs370392677 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246904674 | ACAAAGTGAAGATAC[C/T]AAATCAACCCTGTAG | 25909 |
rs370396851 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246873239 | ACTCATTACTCTTCT[A/G]TAAAAGAAAAAAATC | 25909 |
rs370404844 | snp | A/G | 8.26125e-05 | 0.00642646 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246877146 | GACAAGTTTACATCG[A/G]TAAGTAATTACCTGC | 25909 |
rs370406323 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246854571 | AAATGTCTTAAATAT[A/G]TTACATGAGAAAAGA | 25909 |
rs370448826 | snp | A/T | 1.86565e-05 | 0.00305416 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246861911 | CTTGTCAGAGCTAAT[A/T]CATTCTTATTAAAAA | 25909 |
rs370453312 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246907432 | TCTCAATCATTCATT[C/G]AATCATTAATCTACC | 25909 |
rs370475593 | snp | C/G | 0.000324867 | 0.0127408 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850614 | GTATTTGCTGGTTCT[C/G]AGATAGTCCTCTGAC | 25909 |
rs370510911 | in-del | -/TC | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246846842 | TGCAACCTCAACCTC[-/TC]CCGGGCTCAAGCCAT | 25909 |
rs370532111 | snp | C/T | 6.61649e-05 | 0.00575135 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246891830 | AGCTCAAGACTATAT[C/T]AAGATTGCTAAGAAG | 25909 |
rs370568528 | snp | A/G | 1.75459e-05 | 0.00296186 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246918219 | TTACAAATCAATTGT[A/G]TTAGTAAATGTTCAG | 25909 |
rs370593480 | snp | A/T | 3.3083e-05 | 0.00406699 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246895822 | AACATTTTACTTGTT[A/T]TCAGAATCTTACCTT | 25909 |
rs370639205 | snp | A/C/G | 0.000165678 | 0.00910009 | missense, utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246840823 | ACAGCATTTTTCTGC[A/C/G]TAAAATTTGCTTTGG | 25909 |
rs370684422 | snp | A/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246871741 | CCTGACTGCAGACTA[A/T]AAGGAGGTTAATAAT | 25909 |
rs370800805 | snp | G/T | 0.000153988 | 0.00877328 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246862160 | TTTAGCTTTCTATAG[G/T]AAAGAGCAAATGGAA | 25909 |
rs370808320 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246867075 | AAGTATACTACTACC[C/T]GATGTAAAATTTCCT | 25909 |
rs370829910 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246922861 | GGTGGCAGGCGCCTG[C/T]AGTCCCAGCTACTCG | 25909 |
rs370847036 | in-del | -/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246903855 | AAAAAAAAAAAAAAA[-/G]AATCACTTTTCAATA | 25909 |
rs370907992 | snp | A/C | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246891011 | AACCACTTGTGCATA[A/C]TGACAGATGAGGTGG | 25909 |
rs371036535 | snp | A/C | 5.49486e-05 | 0.0052413 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246877342 | TAGTTTTAGAAAAAG[A/C]TATTTAAATGTACAA | 25909 |
rs371058434 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246904316 | CTTTCTCAAATATTC[C/T]TTCCTCAATGGTTAT | 25909 |
rs371074920 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246903430 | ATTGTAGAGGAAAAC[A/G]GTATCTGAGAAGTTA | 25909 |
rs371075057 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246872265 | TCAGATCGGGCTCCC[C/T]TGTGACTCCACTAAC | 25909 |
rs371095250 | snp | G/T | 7.03977e-05 | 0.00593245 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246849595 | AGATGAAAAACTGTT[G/T]TGCAGAGAAAGAAAA | 25909 |
rs371099999 | snp | C/G | 1.66427e-05 | 0.00288462 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246900198 | ACTTACAACAGACTC[C/G]AATGACCACAGTGCA | 25909 |
rs371100178 | snp | C/T | 1.65111e-05 | 0.0028732 | missense, utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246840897 | GTCACTTCTGTAGTT[C/T]TTCTTGGTTTGCTCT | 25909 |
rs371107812 | snp | C/G | 0.000346761 | 0.0131628 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246857753 | CGGGCTTAAGTGATT[C/G]AATTCTGAAAATGCC | 25909 |
rs371134556 | snp | A/G | 3.34874e-05 | 0.00409177 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246891730 | TCGTTTCTCTTAGTC[A/G]AGAAGTAAAATTTAA | 25909 |
rs371134950 | in-del | -/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246864462 | AGAAAACAGGACAAG[-/G]CTTCCCTGGCAATCT | 25909 |
rs371157124 | snp | A/C/T | 1.66067e-05 | 0.00288151 | synonymous-codon, missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850741 | TGCTGATGCTTCCTG[A/C/T]TGTGCTGATTTGACA | 25909 |
rs371220461 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246929921 | GCCGGGTGTGGTGGC[A/G]TGCGCCTGTAATCCC | 25909 |
rs371230164 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246881291 | TGTACCTAATATTCA[A/G]AATACAAAAAGCTGG | 25909 |
rs371294351 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246897409 | TAGATATCAAATAAA[C/T]ATACAAAAATGAATT | 25909 |
rs371298272 | snp | A/C | 0.00279162 | 0.0372561 | downstream-variant-500B | AHCTF1 | GRCh38.p7 | 1:246839034 | CTTTGATCATCAGAT[A/C]CATGGTTGCTACAAG | 25909 |
rs371304548 | snp | C/T | 1.77915e-05 | 0.00298252 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246913192 | TTGCATCAGAATATC[C/T]AGGTGCTCCATTTTT | 25909 |
rs371333425 | snp | A/C | 2.07372e-05 | 0.00321996 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246885459 | TTATTAACAGATACG[A/C]TAAAGACTTTATAGT | 25909 |
rs371353448 | snp | C/T | | | upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246932433 | GCTTGCATTCTGTAT[C/T]TTCTGTTCTGTGCTC | 25909 |
rs371361209 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246885867 | ATCCATATCTGCAGA[A/C]TGAACTAAGTGCAGA | 25909 |
rs371454614 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246878472 | TATATAAGGAAAATA[C/T]GTATTAACTTGGAAA | 25909 |
rs371541290 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246922331 | CACCACTGCACTCCA[C/G]CGCGGGTGACAGAGC | 25909 |
rs371546935 | snp | A/C/T | 0.000183131 | 0.00956757 | missense, nc-transcript-variant, intron-variant | AHCTF1 | GRCh38.p7 | 1:246842727 | TTTGACGTCCTGATT[A/C/T]GTTTCGCTTTTGGCT | 25909 |
rs371558157 | snp | A/G | 0.000100341 | 0.00708241 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246887370 | GGTCTTTTAAAAAGC[A/G]GATTAAGGACAATAA | 25909 |
rs371642091 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246910397 | ACATCAATTTGATTA[C/T]AGTCTAGATAACACA | 25909 |
rs371688669 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246863090 | GAACCTAGCTGTAGA[A/G]AATACAAAGTGTGAT | 25909 |
rs371688921 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246847058 | TTGGGAGGCCAAGGC[A/G]GGTGGATTATCTGAG | 25909 |
rs371700285 | snp | C/G/T | 0.000136738 | 0.00826754 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246867273 | TGATGCTTTTGAAAT[C/G/T]GGTGTTCCAAAAAAT | 25909 |
rs371700914 | snp | A/C/T | 3.32018e-05 | 0.00407431 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246891897 | ATCCATGAAATGACA[A/C/T]GAACCATCAAATAAT | 25909 |
rs371701056 | snp | C/T | 8.24804e-05 | 0.00642132 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246851059 | TACTTTTTGGGACTT[C/T]TGGTCACTAGTTACG | 25909 |
rs371712513 | snp | G/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246883881 | AAAGGTAAAGGAAAT[G/T]AGAACCTGGCAAATC | 25909 |
rs371714111 | in-del | -/G | 0.00358779 | 0.0422022 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246901115 | AAGGCCAGGTGGGCA[-/G]ATCAATTGAGCCCAG | 25909 |
rs371786127 | snp | C/T | 4.02059e-05 | 0.00448345 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246876002 | GTATCTTTTTTGATC[C/T]AATAGATTATGATAT | 25909 |
rs371835166 | snp | A/G | 1.66466e-05 | 0.00288496 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246900244 | TGTAGATATTCTCCT[A/G]ACCTAAAAGAAAATT | 25909 |
rs371877843 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246842916 | ACTCCTTTTCTCATA[C/T]CTTTTAGTAGAAACC | 25909 |
rs371888208 | snp | C/T | | | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246863984 | GGAGATGGCCTGAGG[C/T]GATCCTTTTAATTGC | 25909 |
rs371948895 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246849637 | TTTCCTTGGAACTTC[C/T]GACGCTGGAGAAAAT | 25909 |
rs371969768 | snp | G/T | 0.0166325 | 0.0896639 | upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246932873 | AGGTAGAGTAGGGAT[G/T]TTAAGAAGATGCTCT | 25909 |
rs372036407 | snp | C/T | 1.64988e-05 | 0.00287213 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246888237 | ATCAAGTACTGCCTA[C/T]AAAACAAAGGGATAA | 25909 |
rs372037901 | snp | C/T | 0.00013084 | 0.0080872 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246907501 | AATGAGTACAAGCTA[C/T]ATGCAAAAAAACTAC | 25909 |
rs372046386 | snp | A/G | 3.30134e-05 | 0.00406271 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246863875 | CTTGCTACTTGAAAA[A/G]TAAGAGCCATCTAGT | 25909 |
rs372049828 | snp | C/T | 4.95872e-05 | 0.00497907 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246904027 | CAAACTCAAAACATC[C/T]CCTTCACTGAAACAG | 25909 |
rs372066381 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246922720 | GGGCGCAGTGGCTCA[C/T]GCCTGTAATCCCAGC | 25909 |
rs372085829 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246843268 | ACCTCGGTCTATAAA[A/G]TATTTGAAGTAATTG | 25909 |
rs372110145 | snp | C/T | 1.6498e-05 | 0.00287206 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246861126 | TTTCCTTTGCTCACA[C/T]CCAGTTTCTCTAAAC | 25909 |
rs372154266 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246881862 | AACCAAAAAAAAAAA[A/C]AAAAAAAAAAGAAGA | 25909 |
rs372163053 | snp | A/C | 0.000153988 | 0.00877328 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246876140 | ATACTGGTCTAATAT[A/C]GAATTTCGAGCCAGT | 25909 |
rs372257932 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246904391 | CAGCTTCCTTTGCAG[C/T]TAAGTGCAGTACCCT | 25909 |
rs372299704 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869117 | CCAAAGTGCTGGATT[A/G]CAGGCGTGAGCCACC | 25909 |
rs372302506 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246901600 | CTGCACTGGACAGAG[C/T]GAGACTCCATCTCAA | 25909 |
rs372302812 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246920813 | AAAAGCATCCAGGCA[C/T]GGTGCCTCACGCCTA | 25909 |
rs372323719 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246908401 | CCTTATATTGAACAA[C/T]TGGAGTAACTAGGTA | 25909 |
rs372344061 | snp | C/T | 3.40524e-05 | 0.00412614 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246904061 | TTAACGAAGACACGC[C/T]AAATATATTAATACA | 25909 |
rs372392410 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868946 | GCCTCCCGGGTTCAC[A/G]CCATTCTCCTGCCTC | 25909 |
rs372396900 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246905421 | AGAATGGCATGAATC[C/T]GGGAGGCGGAGGTTG | 25909 |
rs372453230 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246898687 | TCCTGCAGTCTACTC[C/T]TCTTTATCTAATGTG | 25909 |
rs372460109 | snp | C/T | 3.45644e-05 | 0.00415704 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246916415 | AAGAAAAAAAAATTG[C/T]CTATTTTAATATTGT | 25909 |
rs372534833 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246924823 | AAAAGTAGAAGTTTG[C/T]TTTTTATTATCCAAA | 25909 |
rs372542632 | snp | A/G | 6.61365e-05 | 0.00575012 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246891798 | CTCAGTGATCTCTCG[A/G]GCTTCTGATGCAAAA | 25909 |
rs372545499 | snp | A/G | 1.64947e-05 | 0.00287177 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246864033 | CGGGATACTAGGTAC[A/G]AAGGAGATTTCATGG | 25909 |
rs372609681 | snp | A/T | 3.30393e-05 | 0.0040643 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246877142 | TTCTGACAAGTTTAC[A/T]TCGGTAAGTAATTAC | 25909 |
rs372613414 | snp | C/G | 3.29516e-05 | 0.00405891 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246851275 | ATCTACTTCAGCAAT[C/G]TCACATTCAGCAGTG | 25909 |
rs372617142 | snp | A/G | 4.9923e-05 | 0.0049959 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246918341 | AAATGGCAGGAGACC[A/G]CTAGTCACTTGAGCT | 25909 |
rs372654933 | snp | C/T | 1.85789e-05 | 0.0030478 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246861918 | GAGCTAATACATTCT[C/T]ATTAAAAAATGTCTT | 25909 |
rs372686736 | snp | C/G/T | 5.10341e-05 | 0.00505123 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246853262 | TTCAGAGATAGTGAG[C/G/T]GAGGAGTTTCCACCA | 25909 |
rs372688283 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246846081 | AAGTGGGAATCAAAC[G/T]ATATATGAATGTCAT | 25909 |
rs372696795 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868927 | TCGGCTCACTGCAAG[C/T]TCTGCCTCCCGGGTT | 25909 |
rs372742919 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246926840 | CAGCCTGGGCAACAA[A/G]AGCGAAACCCCGTTT | 25909 |
rs372748732 | snp | C/G | 7.00109e-05 | 0.00591612 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246877310 | CCATACACCTGAAAG[C/G]AGTATTTATCAAAGT | 25909 |
rs372793971 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246917389 | TACATTAGTTGGATA[C/T]GTAAGTTTATAGCTA | 25909 |
rs372843367 | in-del | -/GT | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246895411 | CAATATGCGTTTGGG[-/GT]GTGTGTGTGTATGTG | 25909 |
rs372858806 | snp | C/T | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246862020 | CTAGTTTCTTTAAGT[C/T]GTTGAGGAGACCTTC | 25909 |
rs372860043 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246889939 | TGACTTCTTACAGAT[A/G]TAATTTCTAAAATTG | 25909 |
rs372869051 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246925748 | GGACCCCTCATGAAT[A/G]GGTTGGTGTCCTCTC | 25909 |
rs372869333 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868907 | TGGAGTGCAGTGGTG[C/T]GATCTCGGCTCACTG | 25909 |
rs372894439 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246922851 | AGCCGGGCGTGGTGG[C/T]AGGCGCCTGTAGTCC | 25909 |
rs372902458 | snp | C/T | 0.000204915 | 0.01012 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246916296 | ACAGGAGGCTGTTCA[C/T]TGACTCCACTGAATC | 25909 |
rs372908744 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246845614 | CTCCATTTCAAATAT[A/G]TAAGGAAATACAAAA | 25909 |
rs372932409 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246907027 | AGGGATTCAGTCATT[G/T]TGCAAACATCATACA | 25909 |
rs372967955 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246909779 | TCTTGGAATGTATCC[C/T]TCGCAGATAAGGGGG | 25909 |
rs373007431 | snp | A/G | 3.38226e-05 | 0.0041122 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246902511 | CATGACATATTTCAA[A/G]TACTTTAACTAACCT | 25909 |
rs373012684 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868248 | ATTTTCCTGCCTTAG[C/T]CTCCCGAGTAGCTGG | 25909 |
rs373043560 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246891912 | CGAACCATCAAATAA[C/T]GGCACACCTTTCAAG | 25909 |
rs373146844 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246908902 | GACTCCGTCTCAAAA[A/G]AAAAAAAAAAAAAAG | 25909 |
rs373188474 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869035 | ATTTTTAGTAGAGAC[A/G]GGGTTTCACCATGTT | 25909 |
rs373226573 | snp | A/G | 3.29592e-05 | 0.00405938 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246863938 | CCTTAACTACAAGAG[A/G]AGTTTCAAGCAAATG | 25909 |
rs373338270 | snp | C/T | 9.9167e-05 | 0.00704086 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850085 | TTTCTTGGTCTACCA[C/T]GTTTTCTAGGTATGG | 25909 |
rs373347700 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246921791 | ATCCTTAACAAATAC[A/G]AAATATGTTTTTAGA | 25909 |
rs373392871 | snp | C/T | 0.000216557 | 0.0104034 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246900270 | AAATTTAAAACATTA[C/T]TAAGTCATTGGTCAG | 25909 |
rs373415930 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246879083 | AATCTCACAACAAGG[C/T]TGATTTCCCTAATGC | 25909 |
rs373438051 | snp | A/G | 1.64882e-05 | 0.00287121 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246877055 | CTGAACGCTGGCACT[A/G]GACTGCAAAAATTTC | 25909 |
rs373456600 | snp | A/C | 1.69804e-05 | 0.00291374 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246907784 | AAATTAGACAAATGA[A/C]GTTAAAAAACTAGAA | 25909 |
rs373464644 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246905983 | GTTAGAATTACTCAA[C/G]TGGATGCATTCATGT | 25909 |
rs373492917 | snp | C/T | 1.64942e-05 | 0.00287173 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246888448 | ATCTCGTTTCCACAA[C/T]TTCTCAATTCGCTCT | 25909 |
rs373496461 | snp | C/T | 6.59055e-05 | 0.00574007 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246849856 | TTGACTTTCAGTCTT[C/T]TTTGTAAGTTTTTTC | 25909 |
rs373549632 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246880622 | CTACACCCAGTTGAT[C/T]AGACAAACTAGCAGG | 25909 |
rs373566595 | in-del | -/A | | | upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246932169 | TCATTTACAAAAAAA[-/A]TCGGGTCTCTCCGCC | 25909 |
rs373573414 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246908609 | CCAAGAATCTTAGGC[C/T]GGGCACGGTGGCTCA | 25909 |
rs373619574 | snp | A/C/G | 4.95711e-05 | 0.0049783 | missense, synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246860992 | TTACATTAGTAGTTA[A/C/G]TGCAGTGGAAGAGCT | 25909 |
rs373667317 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246894492 | AGCCTGCAGTGAGCC[A/G]AGATCGCGCCACTGC | 25909 |
rs373708166 | in-del | -/ATTA | | | utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246839754 | GATTACCTGTTATAA[-/ATTA]TTTTACAACACTTAT | 25909 |
rs373718195 | snp | C/T | 3.29522e-05 | 0.00405894 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246907622 | AGCAAGCTGATTTGT[C/T]CTGCTTATGTAACTA | 25909 |
rs373736823 | snp | A/T | 1.67978e-05 | 0.00289804 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246913434 | AACATAATACGTGAT[A/T]TGCTTTTCTTCTGCA | 25909 |
rs373744452 | snp | A/G | 1.76805e-05 | 0.0029732 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246851396 | AATGAAAGATTCCTA[A/G]CCTCTTCTCCTGAAT | 25909 |
rs373838472 | snp | A/G | 0.000635728 | 0.0178174 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246855846 | TAGAAAAAGAAATAC[A/G]TACCTTAGTGTGTAA | 25909 |
rs373852389 | snp | C/T | 0.067446 | 0.170804 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246897919 | AAGAGGTTGAGGCTA[C/T]AGTGAGCCATGACCA | 25909 |
rs373884656 | snp | G/T | 3.30497e-05 | 0.00406494 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246857774 | TGAAAATGCCTCTGC[G/T]GCAACTAAGAGATCC | 25909 |
rs373887485 | snp | A/T | | | upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246933116 | ACGTCCCATTAATTT[A/T]TTTATTTTATTTATT | 25909 |
rs373892396 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246921138 | GCAGCAGAAAATACA[C/T]GCAAAATGACATTTA | 25909 |
rs373895205 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246892973 | AAAACACTTACTATG[C/T]TTTGTATGTTAATTA | 25909 |
rs373896111 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246927292 | TTGGTTAGAGACCAG[C/T]CTGGCCAACATGGTG | 25909 |
rs373897626 | in-del | -/A | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246877553 | GCAAAGTAGACAAAA[-/A]ATTCAAAGAAGACAA | 25909 |
rs373898965 | in-del | -/TTC | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246929550 | GAGTGGAAACATCTC[-/TTC]CACAGAATGAGTCCA | 25909 |
rs373919412 | snp | A/C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246899085 | CAAGAGCGAAACTCC[A/C/G]TCTCAAAAAGAGAAA | 25909 |
rs373928660 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246920706 | ACCTGGGAGGCGGAG[C/T]TTGCAGTGAGCCGAG | 25909 |
rs373929379 | snp | G/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246919032 | ATATAGGCATAAAGT[G/T]GTCTTTCATTTAGAA | 25909 |
rs373950211 | in-del | -/GACTAGACTGAC | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246864890 | AAAAAAAAAAAAAAA[-/GACTAGACTGAC]AACCCACACCCACCA | 25909 |
rs373954182 | snp | A/C | 1.65181e-05 | 0.00287381 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246864056 | TTTCATGGAGCTTTG[A/C]TGAATAAACTCCGAA | 25909 |
rs373975739 | snp | G/T | 4.94246e-05 | 0.0049709 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246867637 | AACAAGCAGCATGAC[G/T]ATGAAACGTGTAAGA | 25909 |
rs373981950 | in-del | -/AACAA | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246866644 | TTTTGTCTTTGATAA[-/AACAA]TCAAAAATTTCCAAA | 25909 |
rs373985621 | snp | C/T | 8.25566e-05 | 0.00642429 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246913384 | GCACTGGCTCCTCCA[C/T]GATTAATTATAGGTT | 25909 |
rs374006698 | snp | C/T | 0.000153988 | 0.00877328 | missense, utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246840873 | CTGTTCCTTCCAAGA[C/T]CTGTTCCTGTCACTT | 25909 |
rs374026609 | snp | C/T | 8.33757e-05 | 0.00645608 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246903930 | GGTAATATAAACCCA[C/T]AGTCCAATGACCATT | 25909 |
rs374030684 | snp | C/G | 0.00014845 | 0.00861411 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246861090 | AAGGTAGTCTCATCG[C/G]ATGTGATTGAAACAC | 25909 |
rs374068053 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246927630 | AGCACTGGCAACCTA[C/T]AAAAAGTAATTTACT | 25909 |
rs374148720 | in-del | -/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868846 | GTGTGTGTGTTTTTT[-/G]TTTTTTTTTTTTTTT | 25909 |
rs374195541 | snp | C/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246867745 | TTGTTGATGAAAACA[C/G]ATCTTGTCAACACAG | 25909 |
rs374213766 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246846356 | TATGGTAACAGTATA[A/C]AGGGCAGAGGAAGAC | 25909 |
rs374217782 | snp | C/T | 1.68258e-05 | 0.00290045 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246900455 | AGACTGAAACACTAG[C/T]GTCAGGCGATAGAGC | 25909 |
rs374222002 | snp | A/C/T | 3.32117e-05 | 0.00407492 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850321 | GCTAGGACTTGTTAC[A/C/T]GTACTAACTTTTAGA | 25909 |
rs374263217 | snp | A/G/T | 0.00159617 | 0.0282053 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868914 | CAGTGGTGTGATCTC[A/G/T]GCTCACTGCAAGTTC | 25909 |
rs374265942 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246913055 | TATGCAAGAAGTATC[C/T]ACTGTGCTCAGGTCC | 25909 |
rs374271779 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246840014 | AAAATTTGTTCAGAC[A/G]TCTCATCCTATCAAT | 25909 |
rs374274680 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246898935 | TCTACTAAAAATACA[A/G]AATATTAGCCGGGCG | 25909 |
rs374281941 | snp | C/T | 2.20233e-05 | 0.00331831 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246862201 | AAAAGTGCTTATAGG[C/T]CGGGCGCGGTGGCTC | 25909 |
rs374319977 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868915 | AGTGGTGTGATCTCG[A/G]CTCACTGCAAGTTCT | 25909 |
rs374352059 | snp | A/C/T | 1.7051e-05 | 0.0029198 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246899522 | TGGCATCTAAAAAAA[A/C/T]GATTTAAAAAATAAT | 25909 |
rs374422640 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246924072 | CCTCCTATCTATTGA[A/G]TACAGAAAGGACTAC | 25909 |
rs374435402 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869052 | GGTTTCACCATGTTG[A/G]CCAGGATGGTCTCGA | 25909 |
rs374471218 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246931567 | CAACCCCCTCCCTCC[C/G]TTCCCCCTACCTGAA | 25909 |
rs374482635 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246913816 | GCATAAAACGCAAAC[C/G]TAAATTGTTCTCATT | 25909 |
rs374560518 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246855230 | GCTTCCCCTGAATCC[A/C]ACTGTAAGCTCCTTA | 25909 |
rs374602603 | snp | A/C/G | 5.00124e-05 | 0.00500041 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850773 | TCACGTTTTGGATAC[A/C/G]TTGACCTCTCGTACG | 25909 |
rs374602983 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868384 | CCTTGGCCTCCCAAA[C/G]TGCTGGGATTACAGG | 25909 |
rs374608822 | snp | C/G | 0.0558544 | 0.157504 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246903660 | TGGTGAGACCCCCCC[C/G]CCTCCGTCTCTGCTA | 25909 |
rs374610979 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246922078 | TGAAAACATATACAG[A/G]GCTGGGCACAGTGGC | 25909 |
rs374627296 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246843250 | GAATGCCTGTCTCCT[C/T]TAACCTCGGTCTATA | 25909 |
rs374687125 | snp | C/T | 1.66502e-05 | 0.00288527 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850787 | CGTTGACCTCTCGTA[C/T]GAGTTTTGGAGGAAA | 25909 |
rs374710464 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246856127 | TATTTAAGCCAATTT[C/T]TAATAATCTGTGGCC | 25909 |
rs374720542 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246878700 | TGCACTGCCCTATAC[A/G]TTCTGTGAATACAAA | 25909 |
rs374757952 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246854639 | ACATTTACTAAACTT[C/T]AGGTACCAAGCGCTA | 25909 |
rs374798878 | snp | C/T | 1.65392e-05 | 0.00287564 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246877184 | CTGTAAATGGTAACT[C/T]CAGTAAATCTTCCAT | 25909 |
rs374800499 | snp | A/G | 1.65195e-05 | 0.00287393 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246888480 | CTAACTGAGAAACCA[A/G]TCCATCAATCATCAA | 25909 |
rs374821852 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246882143 | GCTGGGACTACAGGC[A/G]TGCACCACCTCGCCC | 25909 |
rs374904963 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246858147 | TGTATTTTTAGTAGA[A/G]ACGGGGTTTCACTGT | 25909 |
rs374928501 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246929779 | TCTGTACCAGCCGGG[A/C/T]GCGGTGGCTCACGCC | 25909 |
rs374936055 | snp | A/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869413 | CCTCTTATGCCAGTT[A/T]GCCAAGTTGTAAATG | 25909 |
rs374963100 | in-del | -/TTT | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246857957 | TCAGACTGCTAACAC[-/TTT]TTTCTTCTTTTTTTT | 25909 |
rs375008404 | snp | G/T | 3.29473e-05 | 0.00405864 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246898227 | CTTAAACTGGAAGGC[G/T]GAACATCAACAAATC | 25909 |
rs375048035 | snp | G/T | 0.00049613 | 0.0157423 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246918261 | TTACCTGCAGCAAAC[G/T]TTCCACGAAGCACAG | 25909 |
rs375082870 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869036 | TTTTTAGTAGAGACG[A/G]GGTTTCACCATGTTG | 25909 |
rs375097328 | snp | A/T | 0.000138882 | 0.00833196 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246891942 | GAATAAAAGAAAAGA[A/T]AAGTTTCCATACAGT | 25909 |
rs375099156 | snp | C/T | 3.2993e-05 | 0.00406145 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246851060 | ACTTTTTGGGACTTT[C/T]GGTCACTAGTTACGG | 25909 |
rs375132592 | snp | C/T | 3.50238e-05 | 0.00418458 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246913463 | CAAAGTAAGAAAATA[C/T]AATTAACACAATAAA | 25909 |
rs375145421 | snp | A/G | 0.000355556 | 0.0133286 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246843756 | AAAAAAAAAAAGTAT[A/G]TTTTAACAAACATAC | 25909 |
rs375161879 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246884137 | TTATTCAACAGTTAC[C/T]ACATTTAGCTTCTTT | 25909 |
rs375170246 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246879815 | CCTGGGTGACAAAGT[C/G]AGACTCTGTTCCCCC | 25909 |
rs375232044 | snp | A/G | 2.12836e-05 | 0.00326211 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246885449 | CAATTCCATTTTATT[A/G]ACAGATACGATAAAG | 25909 |
rs375284074 | snp | C/T | 1.7107e-05 | 0.00292459 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246857640 | ACTTCTGGTTCATAA[C/T]TTCATTAAACTTCTT | 25909 |
rs375306954 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246847420 | ATGTATCTGGAACGA[C/T]ATACAGGAAAACGTG | 25909 |
rs375335803 | snp | A/G | 1.9297e-05 | 0.00310614 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246918413 | AAACATTATTATGAC[A/G]CATTTGTAGACAATA | 25909 |
rs375354441 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246863225 | GGTATCTTTTATTCA[A/G]CTTGAAAAATAAGGA | 25909 |
rs375362186 | snp | A/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246849738 | GGGATGATTTAGTGA[A/G]GGAAGCTGTGGCGAG | 25909 |
rs375362581 | snp | C/T | 4.9534e-05 | 0.0049764 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246888283 | TTATACAGTCATTCA[C/T]TCATTCATGCTTCTT | 25909 |
rs375402511 | snp | C/T | 1.64876e-05 | 0.00287116 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246849658 | TGGAGAAAATAAAGG[C/T]TCATTGTTTGGTTCA | 25909 |
rs375441020 | snp | A/G | 1.66774e-05 | 0.00288763 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246876929 | CTCTTATCCCCCATA[A/G]TAAGACAACTTTAAT | 25909 |
rs375462884 | in-del | -/A | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246900496 | GATAATTTTTAAAAA[-/A]CAGAATAAAGAATCT | 25909 |
rs375470134 | snp | A/G | 1.68567e-05 | 0.00290312 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850382 | TCTACAGATCTTTTA[A/G]TTCTTCTAGGAGTCC | 25909 |
rs375479517 | in-del | -/TTA | | | cds-indel, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246839712 | CTAGATAATCAATTA[-/TTA]ATAGTCCATTCATTA | 25909 |
rs375482777 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246872038 | TAGATTCAGAAAGAT[A/G]AACTATTAATGACAA | 25909 |
rs375513578 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246901238 | CCCAGCTACTCAGGA[A/G]GCTGAGGTGGGAGGA | 25909 |
rs375529420 | snp | G/T | 0.000100334 | 0.00708217 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246891742 | GTCAAGAAGTAAAAT[G/T]TAATAAAACACTCAT | 25909 |
rs375584455 | snp | A/C/G | 0.000258618 | 0.0113687 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246907797 | GAAGTTAAAAAACTA[A/C/G]AAACAGCATTAAAAG | 25909 |
rs375589160 | snp | C/T | 6.61857e-05 | 0.00575226 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246864084 | GAACACTGAGAAGGC[C/T]GGGGGACAGGCTGAA | 25909 |
rs375615157 | in-del | -/CTGG | 0.00795532 | 0.062565 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246922554 | CTCGTGCCACCATGC[-/CTGG]CTAATTTTTTTTTTT | 25909 |
rs375642977 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246872352 | GTGATGCCCCAGGAC[C/T]CAAAAACTTCAGGTA | 25909 |
rs375643011 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246893776 | TTACCTAGCACATTC[C/T]GCTTACTCCATCATC | 25909 |
rs375657308 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246929867 | GACCAGCCTGGCCAA[C/T]ATGGTGAAACCCCGT | 25909 |
rs375680762 | snp | A/C | | | upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246933866 | CAAGGTATTGGACCA[A/C]GTTGTGATAGAAACA | 25909 |
rs375715157 | snp | A/G/T | 0.0213452 | 0.101169 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868990 | GCTGGGACTACAGGC[A/G/T]CCCGCCACCATGCCT | 25909 |
rs375722416 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246845544 | TAACTCTCTTCTAGG[C/T]TACCTGAAAAAACGA | 25909 |
rs375728771 | snp | A/G | 0.000183626 | 0.00958014 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246905506 | TGTCTCCAAAAAAAC[A/G]AAACAAAACAAAACA | 25909 |
rs375742788 | snp | A/G | 1.65507e-05 | 0.00287664 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246849949 | TTTTCCAACATCAAC[A/G]TTTTCACTTTTAGCT | 25909 |
rs375761312 | snp | C/G | 0.00358779 | 0.0422022 | upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246932403 | CGAGTGATAATCTTT[C/G]TCCCATAATTGGCAG | 25909 |
rs375765269 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246926180 | AGGTAGGCAGCTGCT[A/G]GTGTCATGCCTGCAC | 25909 |
rs375868677 | snp | C/T | 3.38003e-05 | 0.00411084 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246916326 | CTGTAAGCAGACAAT[C/T]GCTCTCCTGTTATAG | 25909 |
rs375884310 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868993 | GGGACTACAGGCGCC[C/T]GCCACCATGCCTGGC | 25909 |
rs375886381 | snp | C/T | 4.79145e-05 | 0.00489438 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246867336 | CACTATAGGAGATGG[C/T]TCTTCTATTTTAGAA | 25909 |
rs375910854 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246872051 | ATGAACTATTAATGA[A/C]AAAAAAAAAAAAAAA | 25909 |
rs375932279 | in-del | -/ATA | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246916555 | ATCATTACAATAATA[-/ATA]GTCATTCAGTGGCGT | 25909 |
rs375932948 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246847104 | CTAGCTTGGCCAACA[C/T]GGCGAAACCCTGTCT | 25909 |
rs375933399 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246922852 | GCCGGGCGTGGTGGC[A/G]GGCGCCTGTAGTCCC | 25909 |
rs375978705 | snp | C/T | 0.000122003 | 0.0078094 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246861262 | CACATTTTTTAGGTG[C/T]AGTAAATACTTCTAA | 25909 |
rs375999683 | snp | C/G | 0.000120355 | 0.00775647 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246851376 | CAGAGGGATATAACT[C/G]ATTAAATGAAAGATT | 25909 |
rs376018203 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246907945 | TTATCTATTTAAATG[C/T]CACAATTTAAAAAAC | 25909 |
rs376044622 | in-del | -/GATTTTAAAGTACT | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246889596 | ATTACAGCCGGCACA[-/GATTTTAAAGTACT]GATTCCCAGGTGATT | 25909 |
rs376048859 | snp | C/T | 0.000407747 | 0.0142726 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246916123 | AGAGAAATGTCCAGG[C/T]ATCTTAAACAGTACC | 25909 |
rs376055634 | snp | C/T | 1.66488e-05 | 0.00288515 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246885539 | TAACATCGTTACCAC[C/T]GGACACTGTTGGCTT | 25909 |
rs376061981 | snp | C/T | 4.94662e-05 | 0.00497299 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246867726 | TCCAATTTTAGATAA[C/T]ACATTGTTGATGAAA | 25909 |
rs376073830 | snp | A/C | 0.000699872 | 0.0186935 | intron-variant, downstream-variant-500B | AHCTF1 | GRCh38.p7 | 1:246842681 | CAATCAAGAACAGAA[A/C]AGAAAGTCATACTTG | 25909 |
rs376126499 | snp | C/G | 0.000403234 | 0.0141935 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246867851 | TAAGTGCATCTCTAA[C/G]AAACGGGAATTTAAT | 25909 |
rs376171651 | snp | C/T | 0.000131946 | 0.0081213 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850214 | CTAACATGTTTAATA[C/T]GCAGCTGCTTGTCAC | 25909 |
rs376196185 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246897185 | GGGTGTGGTGGCACA[C/T]GCCTCTAGTTCCAGC | 25909 |
rs376217768 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246909071 | TAATTCTATATCTAT[A/C]TATATCTATATCTAT | 25909 |
rs376245355 | snp | A/C | 0.00318978 | 0.0398085 | utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246839177 | TTTAAAATATATGTA[A/C]AGTTCATTTAGAACA | 25909 |
rs376278917 | snp | C/T | 1.69642e-05 | 0.00291236 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246887396 | AATAAAATACAACAA[C/T]AAAAACCTCCTACGT | 25909 |
rs376323714 | snp | C/T | 3.40426e-05 | 0.00412554 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246918366 | TGAGCTCTTAAGTCT[C/T]GCATACTTCCACTGT | 25909 |
rs376427862 | snp | A/G | 1.66801e-05 | 0.00288787 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246862052 | AGGTGATGGAGAGGG[A/G]GATGCTAAAGGTGTT | 25909 |
rs376474185 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246922798 | CCATCCTGGATAACA[C/T]GGTGAAACCCTGTCT | 25909 |
rs376513733 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246925086 | CCTTTTATATAGCTT[A/G]ATAAAACTAGTTTAA | 25909 |
rs376522295 | snp | A/G | 0.000297015 | 0.0121827 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246877099 | AAAAAGAACAAAATA[A/G]ATTGTAAACTACCAA | 25909 |
rs376540570 | snp | C/T | 5.19458e-05 | 0.0050961 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246860871 | GGACATTAATAACAA[C/T]TTTGAGTATTCAGAA | 25909 |
rs376540753 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246909886 | GTAGCACCAGCAGTA[A/G]CAATCAAAAATGTCT | 25909 |
rs376628761 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868266 | CCCGAGTAGCTGGGA[A/C]TACAGGAATGTGCCA | 25909 |
rs376641485 | snp | C/T | 2.10617e-05 | 0.00324506 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246885457 | TTTTATTAACAGATA[C/T]GATAAAGACTTTATA | 25909 |
rs376646297 | snp | A/C/G | 5.20877e-05 | 0.0051031 | synonymous-codon, missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246840977 | GGGAGGAGGTGACCA[A/C/G]GCACTTTCTTTTTCT | 25909 |
rs376685608 | snp | A/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246861201 | TTCAGGAAAAAAGAT[A/G]TGGTCCTATCTTTGC | 25909 |
rs376766906 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246922722 | GCGCAGTGGCTCACG[A/C]CTGTAATCCCAGCAC | 25909 |
rs376772059 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246894979 | AATCATGAGGAGCGA[C/T]GGCAAGCACAAACTA | 25909 |
rs376781120 | snp | C/G | 8.24858e-05 | 0.00642153 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246855747 | TTATTGTCATTTGCT[C/G]TAATTGCAGGGGTGT | 25909 |
rs376786479 | snp | C/T | 0.000442951 | 0.0148755 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246876020 | TAGATTATGATATTC[C/T]TCAATGAAATTCTTA | 25909 |
rs376794190 | snp | A/G | 4.94214e-05 | 0.00497074 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246907688 | CTGGAAACACAGATG[A/G]CGCCCTTGTCTCATT | 25909 |
rs376798744 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246896435 | AACCTTGAAAACATG[C/T]TAAATGAGACAGTCA | 25909 |
rs376806951 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246844796 | AATTAAAAGCATTTA[C/T]CACACAGACTTTTTT | 25909 |
rs376837343 | in-del | -/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246882792 | AATTTGCACGTAAAA[-/C]CAGCCACGCCACAGT | 25909 |
rs376837878 | in-del | -/AAATTTGTTGAATACTAA | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246877432 | TGAAAAGTACTTTAA[-/AAATTTGTTGAATACTAA]GTACTGCATAATAAT | 25909 |
rs376844732 | snp | G/T | 6.59228e-05 | 0.00574083 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246895911 | TGCTGACAATATAGC[G/T]TCTAACTGTTCTTCC | 25909 |
rs376888811 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246841214 | AATTTTTTCATTTTC[A/G]ATCAGAATATTTACA | 25909 |
rs376933748 | snp | G/T | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246907561 | CTTACTCTCTTTTCA[G/T]GCTTTTCATGTTCCA | 25909 |
rs376943640 | snp | A/T | 3.59357e-05 | 0.0042387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246885706 | CATGAAAAATGTTAA[A/T]TATAAATATAATCCT | 25909 |
rs377050688 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246923899 | CCAGGTCTGGAAGTC[C/T]CTAACTACATACTAT | 25909 |
rs377075707 | snp | C/T | | | upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246932666 | AATGCTCGCGCAGCC[C/T]AGCCTAATCTTTTTA | 25909 |
rs377088513 | snp | A/G | | | upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246932960 | TTTATTTTTGAGACA[A/G]TGTCTCGCTCTGTCG | 25909 |
rs377097885 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246888627 | ATCAAAGAGAGAAGA[A/G]GCTGGGCATGGTGGC | 25909 |
rs377099713 | in-del | -/GTTT | | | downstream-variant-500B | AHCTF1 | GRCh38.p7 | 1:246838891 | CTTTCTGAGTACATT[-/GTTT]ACCTTACTACTGATA | 25909 |
rs377251787 | snp | A/G | 0.000177456 | 0.00941787 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850451 | GTTTCTTCAACTGCT[A/G]GTTCCAACAGCTGAG | 25909 |
rs377257919 | snp | A/G | 3.30273e-05 | 0.00406356 | missense, utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246840891 | GTTCCTGTCACTTCT[A/G]TAGTTTTTCTTGGTT | 25909 |
rs377315376 | snp | C/T | 3.37177e-05 | 0.00410582 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246894745 | GTGGCAGAATTTGGT[C/T]GTTCTTATTTGTAAA | 25909 |
rs377345070 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868171 | TCTTGCTCTGTAGCC[C/G]AGGCTGGAGTGCAGT | 25909 |
rs377357876 | in-del | -/CT | 0.00676609 | 0.0577691 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246874607 | TTCCTTCCCTTCACC[-/CT]GTTTAACATTAACTT | 25909 |
rs377375258 | snp | A/G | 0.00011536 | 0.00759387 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246864000 | GATCCTTTTAATTGC[A/G]AACTTGAGGGCAGTG | 25909 |
rs377388249 | in-del | -/C | 0.00993419 | 0.0697739 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246919478 | CAGCACTTTGGGAGG[-/C]TGAGGCAGGCGGATC | 25909 |
rs377390554 | in-del | -/A | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246930051 | GCAAGACCCCGTCTC[-/A]AAAAAAAAAAAAAGA | 25909 |
rs377508264 | snp | A/G | 0.000155988 | 0.00883004 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246843968 | TCTGTATCTTTATAT[A/G]TGTGTGTATATATAT | 25909 |
rs377558015 | snp | C/T | 3.32851e-05 | 0.00407939 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246900299 | AGCTACACATACAAA[C/T]ACAAAGAGAAAGGAG | 25909 |
rs377563134 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246899033 | GGCAGAGGTTGCAAT[A/G]AGCCGAGATGGTGTC | 25909 |
rs377572505 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246846459 | GCACTACCACATTCA[C/T]TCTAGGAGGAGGAAA | 25909 |
rs377574206 | snp | C/T | 7.03346e-05 | 0.00592979 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246916434 | TTTTAATATTGTATA[C/T]ACACAAAACATGCAA | 25909 |
rs377608299 | snp | C/T | 1.65203e-05 | 0.002874 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246899479 | CCAGTACAAGTTAAA[C/T]GAACAACTCCCGAGT | 25909 |
rs377630628 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246919557 | TCTCTACTAAAAATA[C/T]AAAAAATTAGCCAGG | 25909 |
rs377632340 | snp | G/T | | | upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246933529 | TCAGCCTCTCAACGT[G/T]CTGGGATTACAGACA | 25909 |
rs377658506 | snp | G/T | 1.86586e-05 | 0.00305434 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246891103 | TTACTTACAAAAAAA[G/T]CAAGATGCTCCACAG | 25909 |
rs377664267 | snp | C/G | 1.64947e-05 | 0.00287177 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850703 | CTGACTGACTGCCCT[C/G]GCATCTTAGGAGTAG | 25909 |
rs377665424 | in-del | -/GTTTA | | | downstream-variant-500B | AHCTF1 | GRCh38.p7 | 1:246839007 | ATACTAAGCACCTTA[-/GTTTA]ACCAATGCTTTGATC | 25909 |
rs377698455 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246853644 | TCCTTGTAGAGTAAT[C/T]ACAGAATTACATGAG | 25909 |
rs377764344 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246908654 | GCACTTTGGAAGGCC[A/G]AGGTGGGCGGATCAC | 25909 |
rs386354762 | in-del | -/A | 0 | 0 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246877554 | CAAAGTAGACAAAAA[-/A]TTCAAAGAAGACAAA | 25909 |
rs386354763 | in-del | -/A | 0 | 0 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246879848 | CCCGCCAAAAAAAAA[-/A]GGGAGAACTAATTTA | 25909 |
rs386370367 | in-del | -/A | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246879842 | CCCAACCCCGCCAAA[-/A]AAAAAAGGGAGAACT | 25909 |
rs386641780 | multinucleotide-polymorphism | GC/TG | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868905 | GTTGGAGTGCAGTGG[GC/TG]TGATCTCGGCTCACT | 25909 |
rs386641781 | multinucleotide-polymorphism | CA/TG | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869001 | AGGCGCCCGCCACCA[CA/TG]CCTGGCTAACTTTTT | 25909 |
rs386641783 | in-del | AGG/GA | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246882480 | TAATGAAAATTTAAA[AGG/GA]TACTTAGAACAGAAT | 25909 |
rs386641784 | in-del | CC/TCT | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246891485 | AAAAAATTTATGAGT[CC/TCT]TTGAATAAAAAATAC | 25909 |
rs386641785 | in-del | CGGG/TGGGAAGATCGCTTAAGCCCAAGAGGTTGAGGCTACAGTGAGCCATGAC | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246897884 | TTGCGGGGGCTGGGG[lengthTooLong]CATGCCACTGCATTC | 25909 |
rs386641786 | multinucleotide-polymorphism | CG/TC | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246903154 | AAACCCGTTTCTATA[CG/TC]CCTCCAACATTAGGT | 25909 |
rs386641787 | in-del | C/TAAAT | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246906707 | AAATGGAGAAACAAA[C/TAAAT]TGACAACTTAAGGGC | 25909 |
rs386641788 | multinucleotide-polymorphism | CA/TG | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246920694 | AGAATGGCATGAACC[CA/TG]GGAGGCGGAGCTTGC | 25909 |
rs386641789 | multinucleotide-polymorphism | CCA/GCG | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246929778 | ATCTGTACCAGCCGG[CCA/GCG]CGGTGGCTCACGCCT | 25909 |
rs386641790 | in-del | ATCT/CCCAAGATGTGCTTTTATTTTA | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246931022 | AGGAAGGCAAAGCAC[ATCT/CCCAAGATGTGCTTTTATTTTA]AATCTCCTTGATCTG | 25909 |
rs397701939 | in-del | -/TTTAA/TTTAC | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246854967 | TGATCGGCTTTTTAC[-/TTTAA/TTTAC]ATGTTAGACAATTCT | 25909 |
rs397730569 | in-del | -/GAG | 0 | 0 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246910787 | TTTTTCAGAGAAGAG[-/GAG]ATTAGATTTTGCCAC | 25909 |
rs397776307 | in-del | -/AAAATA | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246929435 | ATAAAAATAAAAATA[-/AAAATA]CAGTGAAAACATTGG | 25909 |
rs397792946 | in-del | -/AAAA/AAAAC/AAAC | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246848865 | AACAAACAACACAAA[-/AAAA/AAAAC/AAAC]CCCCCTACATTTTGT | 25909 |
rs397821330 | in-del | -/CTG | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246842870 | TAGAGCCAAACACTG[-/CTG]ATGAATTCAAACTCG | 25909 |
rs397844557 | in-del | -/A | 0.476746 | 0.10529 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868612 | CTTTTGGTAAGTGGT[-/A]AAAAAAAAAAAAAAA | 25909 |
rs397860206 | in-del | -/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246841974 | TTTTTTTTTTTTTTT[-/T]CAGTAGAGACAGGGT | 25909 |
rs397953618 | in-del | -/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246924396 | GTGCCGTTTATTTTT[-/T]GTGTGATGCAAATTT | 25909 |
rs397973850 | in-del | -/A | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246880587 | AAAAAAAAAAAAAAA[-/A]TTCCACTTTAAACTG | 25909 |
rs397983634 | in-del | -/A | 0 | 0 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246843751 | TTTGTAAAAAAAAAA[-/A]GTATGTTTTAACAAA | 25909 |
rs397983635 | in-del | -/G | 0 | 0 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246860198 | CTGGTTGGGGGGGGG[-/G]CGGAGGTTGCAGTGA | 25909 |
rs397983636 | in-del | -/T | 0 | 0 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246870079 | TTCATGAATAACTTT[-/T]GAGGGCTTCAAGACT | 25909 |
rs397983640 | in-del | -/T | 0 | 0 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246892819 | AAAAGATTTTTTTTT[-/T]GGTTTTGCAGAGACG | 25909 |
rs397983642 | in-del | -/A | 0 | 0 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246908745 | AAAAAAAAAAAAAAA[-/A]TTAGCCGGGCATGGC | 25909 |
rs397983644 | in-del | -/A | 0 | 0 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246919717 | CAAAAAAAAAAAAAA[-/A]TCCTCAAGAGAAGAA | 25909 |
rs397983645 | in-del | -/AAA | 0 | 0 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246920168 | AAAAAAAAAAAAAAA[-/AAA]GAAAAGAAGCTCACA | 25909 |
rs397983646 | in-del | -/A | 0 | 0 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246926066 | AAAAAAAAAAAAAAA[-/A]GGCCTGGTACCTCCT | 25909 |
rs398074826 | in-del | -/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246870078 | TTTCATGAATAACTT[-/T]TGAGGGCTTCAAGAC | 25909 |
rs398090056 | in-del | -/TTATA | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246875046 | GGCCAACAACTTATA[-/TTATA]GATAAACCAGAATGA | 25909 |
rs527242743 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246911731 | TCAAGTGATCCACCC[A/G]CCTTGGCCTCCCAAA | 25909 |
rs527259881 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246870214 | TTTTGGAGGCCAAGG[G/T]GGGAGGATCACTTGA | 25909 |
rs527382500 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246904187 | TAATTTTTATAAAAA[G/T]GTAGTCCTTTGAAAT | 25909 |
rs527417305 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246904983 | AGAGAGCAGGGTACT[G/T]AGAAGGTTCCAAGGC | 25909 |
rs527428514 | snp | G/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868858 | TTTGTTTTTTTTTTT[G/T]TTTTGAGATGGAGTC | 25909 |
rs527430851 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246898411 | GATTAATTAATTACA[C/T]TTAAAATTTAAGTAA | 25909 |
rs527454255 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246898987 | CTAGCTATTCAGGTG[A/G]CGGAGGCAGAAGAAT | 25909 |
rs527480152 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246862676 | ATCCATCTTTCTAAA[A/C]GCATTATTTCCAACT | 25909 |
rs527489102 | snp | C/G/T | 0.00199481 | 0.0315187 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246892390 | TGCAATCTCAATCTC[C/G/T]GCTCACTGCAACCTC | 25909 |
rs527526293 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246849152 | AGATGAGGGCATGTA[A/G]ATGCGCCAGTTTGTG | 25909 |
rs527529078 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246901862 | AAAACTTTAAAAAGA[C/T]GTGAGCTCATGACAA | 25909 |
rs527539411 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246929880 | AATATGGTGAAACCC[C/T]GTCTCTACTAAAAAT | 25909 |
rs527548077 | in-del | -/AAAG | 0.00318978 | 0.0398085 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246845371 | TATGATTCTTAAAAA[-/AAAG]AAAAATAGAGTTGAT | 25909 |
rs527553101 | snp | A/G | 8.23784e-05 | 0.00641735 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246849804 | TCATTTCATCTGTGC[A/G]TTCTTCTGATACTGA | 25909 |
rs527678940 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246905446 | AGGTTGCAGTGAGCC[A/G]AAATCACGCCACTGC | 25909 |
rs527685517 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869280 | TCCCTTTCCCCGAGG[A/G]CCTCCCTTATTCCTT | 25909 |
rs527699910 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246878976 | TGCACAGAAATATAG[C/T]CATTTTTCCCTAAAC | 25909 |
rs527705438 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246870748 | AAAAAAAAGCCCTAG[A/G]CTATTTAATTTCTCA | 25909 |
rs527715489 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246926063 | AAAAAAAAAAAAAAA[A/G]AAAGGCCTGGTACCT | 25909 |
rs527740931 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246903152 | TGAAACCCGTTTCTA[C/T]ACGCCTCCAACATTA | 25909 |
rs527741879 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246871694 | TGCTTTCTCTGTAAT[A/C]CATGCCTACAGTGCA | 25909 |
rs527777392 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246920545 | GGGAGGCTGAGGCGG[C/T]GAATCATGAGGTCAG | 25909 |
rs527806848 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246913024 | ATATGAACACCTGAT[C/G]AACAAAACAGTATCT | 25909 |
rs527837906 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246906003 | TGCATTCATGTCTGT[G/T]TAAACTGGTCCTAAG | 25909 |
rs527888948 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246853401 | CTGCACTTGAATAGT[C/G]TATTAATAAACTATC | 25909 |
rs527918600 | snp | C/T | 1.65315e-05 | 0.00287498 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246864072 | TGAATAAACTCCGAA[C/T]ACTGAGAAGGCCGGG | 25909 |
rs527946192 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246864490 | TCTATTTACTAAAAT[C/T]CATTAACATGCAAAA | 25909 |
rs527956977 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246858304 | AGCTCAAGAGCCCCC[A/C]TTAACCTCTCGCTTT | 25909 |
rs528013816 | snp | A/G | 1.65861e-05 | 0.00287972 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246900343 | GAATCATACCTTAAC[A/G]AATCTGGCATTTGTG | 25909 |
rs528063428 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246894299 | AACTTCAGGCCAGGC[A/G]CGGTGGCTCACGCCT | 25909 |
rs528066384 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246920086 | AGGCAGTTGCAGTGA[A/G]CCGAGATTGTGCAAC | 25909 |
rs528088826 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246858687 | AAAATTGGCTGGGCA[C/T]GGTGGCACGTGCCTG | 25909 |
rs528116595 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246931068 | GATCTGACCAATCGG[A/G]TGAGCTGGAACCTCA | 25909 |
rs528127298 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246931603 | CGGGTGAGCGCGCCG[C/T]CGCGGGCCGAGTCCA | 25909 |
rs528135003 | snp | G/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246916517 | ATATTATCTCCACAT[G/T]GAAATCTTTTAATCA | 25909 |
rs528165475 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246852034 | GGAATGGTCCTTGCA[A/G]TTACCTTTTGGTAAG | 25909 |
rs528191338 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246927002 | ACAAGGTGAAATCCC[A/C/G]TCTCTACTAAAAATA | 25909 |
rs528240848 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246880244 | TATATATATAAAATA[C/T]ATAATAGGCATTATA | 25909 |
rs528294028 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246865299 | TTTGGAGCCCAGAAA[C/T]AAAAACTTGTAGTTG | 25909 |
rs528316991 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246873261 | AAAAAAATCTTAACC[A/G]GTGATAAATCACCAT | 25909 |
rs528340336 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246862971 | ATTACTGAATCCCAT[C/T]AGATCATAATAAATT | 25909 |
rs528345511 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869043 | TAGAGACGGGGTTTC[A/G]CCATGTTGGCCAGGA | 25909 |
rs528351849 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246874054 | TCACTCCTGTCCTGA[A/C]ACAATCACCATTAAT | 25909 |
rs528361259 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246922427 | TCTGTTGCGGTTTTT[C/T]GGGTTGTTTTTTTTT | 25909 |
rs528369865 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246914780 | CTCTTCCATACACCA[A/G]CCATGCATTCAACTG | 25909 |
rs528471387 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869079 | TCGATCTCCTGACCT[C/T]GTGATCCGCCCGCCT | 25909 |
rs528478549 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246865843 | CCCTGAGACCAAATA[G/T]TCTTTCAGAACTAAC | 25909 |
rs528488358 | snp | C/T | | | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246903961 | TACCTCATATAAGAT[C/T]TGTCCTGATGCCAAA | 25909 |
rs528524232 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246885281 | TTGGTCCTGCAGAGC[C/T]CATGTATATGAAAAG | 25909 |
rs528570879 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246905403 | CTCGGGAGGCTGAGC[A/G]AGAGAATGGCATGAA | 25909 |
rs528629758 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246902157 | CTGCCAGGAAAAAGC[A/G]ATGACACTAAAGAAG | 25909 |
rs528659861 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246888748 | GACCCCAGTTCTAAA[C/G]AAAATATAAAAACTA | 25909 |
rs528665408 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246896358 | TATGGTATGCTCATA[A/C]AACAGAATATTATAC | 25909 |
rs528693993 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246896911 | GGCATGACTCTAAAC[A/G]GAGACTCACTGAAGC | 25909 |
rs528702836 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246853630 | CAGACAACCAGCTAT[C/T]CTTGTAGAGTAATTA | 25909 |
rs528753166 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246927930 | GCTTGAACCTGGGAG[A/G]CAGAGGTTGCAATAA | 25909 |
rs528759613 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246847273 | CAGCCTGGGTAACAA[C/T]AGCCAAACTCCATCT | 25909 |
rs528812461 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246928088 | AGGTGGATCACGAGG[C/T]CAGGAGATCGAGACC | 25909 |
rs528818678 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246922314 | GCAGTAAGCAGAGAT[G/T]GCACCACTGCACTCC | 25909 |
rs528830532 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246899681 | GAATAGATAACAAAC[C/T]TATTACACAGCAAAA | 25909 |
rs528831515 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246882083 | GCTCACTGCAAGCTC[C/T]GCCTCCTGGGTTCAC | 25909 |
rs528881071 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246857529 | AACTACTAAATGACA[C/T]ATAACTGCACAACTA | 25909 |
rs528955164 | snp | A/G | 8.33382e-05 | 0.00645462 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850769 | ACATTCACGTTTTGG[A/G]TACGTTGACCTCTCG | 25909 |
rs528964573 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246844092 | ATGTTGGCAGAGAAA[C/T]GACAGAAAAATCCCA | 25909 |
rs528985358 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246893534 | TTTAGCCTTATTTTT[A/G]CACTAACTGGACATG | 25909 |
rs528992602 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246926464 | AAAATGTTTAATAAA[C/G]TTTTTCAAATTTAAC | 25909 |
rs529005024 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246894209 | CCATGTCTCAAAAAA[A/G]AAAATTACTTTTATC | 25909 |
rs529028951 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246886160 | ACATGGTGAAACCTC[A/G]TCTCTACTAAAAATG | 25909 |
rs529068212 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246886901 | CATATATCAAGGCCA[A/C]ATCTTGCCTTCCATG | 25909 |
rs529089515 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246908607 | ATCCAAGAATCTTAG[A/G]CCGGGCACGGTGGCT | 25909 |
rs529090895 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246880048 | TTAGTGGGAGAGGAC[A/G]TATAGGCATTTGTTG | 25909 |
rs529098780 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246844829 | TTTTTTTTAACTATA[A/G]GGCCCCCATATTAAA | 25909 |
rs529228497 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246872479 | CATCATCTTGAGGTT[C/T]TGGCTTACTCCAACC | 25909 |
rs529229231 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246913829 | ACCTAAATTGTTCTC[A/C]TTTTAAAGCTCTTAA | 25909 |
rs529266507 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246906938 | TAGGAAGGTACTTCT[C/G]AAAGAACTCATATTA | 25909 |
rs529271528 | snp | C/G | 0.43221 | 0.171171 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246864594 | AGACTAGACTGACTT[C/G]GGAGGCCGAGGCGGG | 25909 |
rs529307691 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246865751 | TCAAGACTTAATAGT[G/T]TAAAGGTTCTGAGAA | 25909 |
rs529315551 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246854411 | CACAAGAATATTCAC[C/T]GCAGAAACAGCAAAA | 25909 |
rs529332728 | snp | A/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246878046 | ACCCAATGATCCCAA[A/T]GCAAAGAATACAGTC | 25909 |
rs529368565 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246851809 | AAACAGAAACAACCC[C/G]CAAACTGTGTTTTAA | 25909 |
rs529403161 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246901165 | GCAACACAGCAAAAA[A/C]CTCATCTCTACAAAA | 25909 |
rs529415955 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246875652 | AGTAGTCACCATGCT[-/G]ATCAGTCAGCAGCCA | 25909 |
rs529419649 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246901594 | GTGCAACTGCACTGG[A/G]CAGAGCGAGACTCCA | 25909 |
rs529420324 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246908630 | CGGTGGCTCACGCCT[A/G]TAATCTCAGCACTTT | 25909 |
rs529428003 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246927190 | CTCAAAAAAAAAAAA[A/G]GAAAGAAATAGGCCA | 25909 |
rs529435715 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246910812 | TGCCACAACAAACAG[C/T]TCACACAATGGGATA | 25909 |
rs529444043 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246866418 | AAAATACCATCTTAC[A/C]AGAGTAAATAAAGGG | 25909 |
rs529479892 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246859825 | TCCCGAAGTGCTGGT[A/G]TTACAGGCGTGAGCC | 25909 |
rs529524216 | in-del | -/TCAAT | 0.00358779 | 0.0422022 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246857472 | CACCAGAGTTCTGCC[-/TCAAT]TCAATTTACCGTGTC | 25909 |
rs529534864 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246887996 | AAACAAAATTTTTCA[C/T]ATAGTTTTAGGTTGA | 25909 |
rs529549845 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246931872 | CCGCGCTTCTGGGTC[C/T]TTCCCCTTGCAACGC | 25909 |
rs529562509 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246911929 | TTTTATCACTTGCAG[-/T]TTTTTTTGTTTTTGT | 25909 |
rs529572167 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246846397 | GTCCTAGAGTGGTCA[C/T]TGCTTTGTTAAAGGA | 25909 |
rs529573143 | snp | G/T | 5.01073e-05 | 0.00500511 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246888513 | AATCGGGATTCCACT[G/T]CCCTCTGCAATCAGG | 25909 |
rs529608809 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246881469 | ATATTTGACATTTCA[C/T]CTATTAAATGGAGAA | 25909 |
rs529610844 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246889310 | TTTCTAATTGTGAAT[A/G]GCGGCAGCACTTACT | 25909 |
rs529629265 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246927413 | GGAATCGCTTGAACC[A/G]GGGAGGTGGAGGTAG | 25909 |
rs529646966 | snp | A/C/T | 0.00517997 | 0.0506535 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246882036 | GGAGTCTTGCTCTGT[A/C/T]GCCCAGGCTGGAGTG | 25909 |
rs529719084 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246922558 | TGCCACCATGCCTGG[C/T]TAATTTTTTTTTTTT | 25909 |
rs529765839 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246880864 | AAGACAATAATGATG[C/T]TAGGAAGAACAATAA | 25909 |
rs529781459 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246893775 | GTTACCTAGCACATT[C/T]CGCTTACTCCATCAT | 25909 |
rs529782106 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246915465 | CTCAGCCATTCTAAA[C/T]CAAGTCTAGTTTCCC | 25909 |
rs529793286 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246875132 | CCTTACCATGACATG[A/C]GACCTATATACTGAC | 25909 |
rs529797292 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246839823 | TTGCTTAATTGCACA[C/G]AGTTGTACTGTAGAG | 25909 |
rs529826196 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246909101 | TCTATCTATCTATCT[A/G]TCTATCTATTTATAT | 25909 |
rs529913705 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246845369 | CATATGATTCTTAAA[A/G]AAAAGAAAAATAGAG | 25909 |
rs529916101 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869433 | AGTTGTAAATGCAAA[A/G]AAGAACCTGAAGGAA | 25909 |
rs529971980 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246902955 | TAAACTGGAATAACC[A/G]TCAAAATTATATATG | 25909 |
rs529975470 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246842985 | AATTCAACTAATCTC[C/T]AAGTTATCATCAGTT | 25909 |
rs529975762 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246860657 | CTGAACACTCCCACC[A/G]TGCCTGGCTAATTTT | 25909 |
rs529975930 | snp | A/C/G | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246867897 | AATGATTACACCCCC[A/C/G]CCCCCACACACACAC | 25909 |
rs530026674 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246927143 | AGATCGTGCCACTGC[A/G]CTCCAGCCTGGGCGA | 25909 |
rs530107612 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246847688 | TACTTTTTGTAGAGA[C/T]GGGGTTTTTTTGGCC | 25909 |
rs530145691 | snp | C/G | 1.74154e-05 | 0.00295083 | utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246840756 | ATTTAATAATCCACA[C/G]TATTCTGATGACTTT | 25909 |
rs530147836 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246928771 | AAACATTTCTATAAA[C/T]CACTTTGTATGCAAT | 25909 |
rs530183820 | snp | A/T | 0 | 0 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246855107 | GTTGAGAGCATGGGC[A/T]CTAGAGTCAGATAAC | 25909 |
rs530201223 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246897619 | TGTTACTGTGCTGAA[C/T]ACTGTAAGCAACTGT | 25909 |
rs530224202 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246848305 | TGCAAGCTCTGCCTC[C/T]CAGGTTCACACCATT | 25909 |
rs530240690 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246890503 | AACAAATATAGCACA[A/G]GTCAAATACCAAAAA | 25909 |
rs530264011 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246882695 | TGTACATTTATGATC[C/G]TAAGACTGAATAATC | 25909 |
rs530312892 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246918192 | TATAATATATACTTA[C/T]TATTATTTATCTTAC | 25909 |
rs530322992 | snp | C/T | 0.000701895 | 0.0187204 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246876920 | TTCCTTATTCTCTTA[C/T]CCCCCATAATAAGAC | 25909 |
rs530324709 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246881765 | ATCGCTTGAACCTGG[A/G]AGGCAGAGGTTGCAG | 25909 |
rs530382245 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869143 | CCACCACGCCCGGCC[A/G]TGTGTTTTGTTTTTT | 25909 |
rs530409010 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246924487 | AAAACATATATATAT[A/G]AAATAAAAATGCAAC | 25909 |
rs530460357 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868977 | AGCCTGCTGAGTAGC[C/T]GGGACTACAGGCGCC | 25909 |
rs530473003 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246932299 | GTGGTAGTCTTCGCT[A/G]GGGGTCGCGCCGGGC | 25909 |
rs530483687 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246921783 | CTGAAAGGATCCTTA[A/G]CAAATACGAAATATG | 25909 |
rs530533019 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246839329 | CATACGTTGCATCCA[C/T]GTTTATTGTGCTACT | 25909 |
rs530539292 | in-del | -/AGTAGCTGGGACTAC | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868971 | TGCCTCAGCCTGCTG[-/AGTAGCTGGGACTAC]AGGCGCCCGCCACCA | 25909 |
rs530542038 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246922505 | ATCAGAGCTCAATGC[A/T]GCCTCAATCTCCTGG | 25909 |
rs530558713 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246845733 | ATTCTTTACCCATCT[C/T]TTGTTTTGAGGATTA | 25909 |
rs530559505 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246881427 | ATTAAAACCATGCAA[C/T]GAACAAACTTGATCA | 25909 |
rs530605377 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246874177 | CCAGTTTCTAGTATA[C/T]ACAAGTAGACATGCC | 25909 |
rs530641988 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246928288 | AGCCTGGGCGACAGA[C/G]CGAGACTCCGTCTCA | 25909 |
rs530658735 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246915316 | GCCTGCTGACAGAGC[A/G]ACTCTGTCTCAAAAA | 25909 |
rs530662204 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246873397 | CAAAGGGAAAGAATC[C/T]GTCCCAATACTAAAT | 25909 |
rs530693930 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246916047 | AAATTGTAAATGTTG[C/T]GGGTCAGTGAAATTT | 25909 |
rs530726178 | snp | C/G/T | 0.000100202 | 0.0070775 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246860933 | TGAAGGAGTTACTTC[C/G/T]GATGCAAATACATCT | 25909 |
rs530730609 | snp | A/C | 0 | 0 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246909631 | AGTGGTCATGCTGGC[A/C]ATTCAGATATGCCAA | 25909 |
rs530737770 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246885290 | CAGAGCCCATGTATA[C/T]GAAAAGCTGACCTTC | 25909 |
rs530768062 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246902229 | CATGGCTCAAAAAAT[A/T]CACGGGTAAACTTCA | 25909 |
rs530783547 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246866789 | CTTGCAATCACAATT[A/T]CATCTTGGATACAAA | 25909 |
rs530796841 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246883783 | CTAGTTTTCTGGGGA[A/C]TGGAAAATTGAGACT | 25909 |
rs530814285 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246908830 | GTGAATCCGGGAGGC[A/C]GAGCTTGCCGTGAGC | 25909 |
rs530836421 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246860408 | CTAAATTTCACGGCC[A/C]AATAAAAAATGTAAC | 25909 |
rs530885571 | in-del | -/A | 0.00438332 | 0.0466095 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869914 | ATAGCTGTCACAGAT[-/A]AGTGATTCCTCTGAG | 25909 |
rs530917521 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246867228 | TGTCTCTAAGAATGA[G/T]TTAATAAACTCTTAC | 25909 |
rs530918956 | in-del | -/CATATTTATG | 0.00358779 | 0.0422022 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246924517 | TTTAAAAATACAGTA[-/CATATTTATG]CATATTTATGTAGCC | 25909 |
rs530922496 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246859947 | ATTATAGAAACTTAA[A/C]ACTGGTGGATAAGTT | 25909 |
rs530956268 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869065 | TGGCCAGGATGGTCT[C/T]GATCTCCTGACCTCG | 25909 |
rs531000218 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246922034 | TAAAGATACATTGGT[A/G]TATTTTAGACTTTGT | 25909 |
rs531019800 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246896424 | TAATACAGATGAACC[C/T]TGAAAACATGCTAAA | 25909 |
rs531037589 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246854519 | CACTATTAGAGCTGT[C/T]AAAAAGAACAGGATT | 25909 |
rs531049330 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246847562 | GAGTGCAGGGGCACA[C/T]GATCATGGCTCACTG | 25909 |
rs531052781 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246889475 | ACACTTAGGAAATAA[A/C]AGATCTAGAATTTTA | 25909 |
rs531056807 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246896805 | TTCATTCATTACAGG[A/C]GCAAATTAAAAGATG | 25909 |
rs531066843 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246862471 | GGCGACAGAGCAAGA[C/T]TCCGTCTCAAAAAAA | 25909 |
rs531091423 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246889770 | CTTTGTCTATTACCT[C/T]TACTTCATTTCAAAG | 25909 |
rs531097061 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246882132 | CCTCCTGAGTAGCTG[A/G]GACTACAGGCGTGCA | 25909 |
rs531119756 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246927957 | ATAAGCCAAGATCAC[A/G]CCACTGCACTCCAGC | 25909 |
rs531147087 | snp | C/T | 3.51642e-05 | 0.00419295 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246876081 | TGATAAGGCTTAGCT[C/T]GTTCAATGGCTAATT | 25909 |
rs531177375 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246839925 | GAGGTCCTGTGAGAA[C/T]TTGCCAGTTTTAAAA | 25909 |
rs531191952 | in-del | -/G | 0.00757112 | 0.0610593 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246846752 | ATATATATATTTTTT[-/G]GGGGGGATGGGGGTG | 25909 |
rs531219727 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869797 | GATGTACAGGGAGAC[A/G]AATGCTGTTAGCAGG | 25909 |
rs531229670 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246867926 | ACACACACACATTAC[A/G]TGGTAATACTAGCTA | 25909 |
rs531232916 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246917254 | AATTGGATTTCCTTG[C/T]TGATGAATGAGACAC | 25909 |
rs531284858 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246899601 | TAACAGACTGCAAGG[C/T]AAGGTGTCAAATTAT | 25909 |
rs531313078 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246876787 | AATTACGTGGTAATA[C/T]CCTGTTCCCAATTCT | 25909 |
rs531319982 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246903679 | CCGTCTCTGCTAAAT[A/G]TACAAAAAAATTAGC | 25909 |
rs531341971 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246845574 | ATTTATTTCACTTTT[C/T]GTAATCTTCACCTAA | 25909 |
rs531345472 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | AHCTF1 | GRCh38.p7 | 1:246839070 | AGAATATCATTCATG[C/T]GCTATCCTAAAATGT | 25909 |
rs531355327 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246897756 | GATGCCAAGGTGGGA[A/G]GGTAACTTGAGGCCT | 25909 |
rs531403920 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246861812 | TTCTTTCAGAACTAA[C/T]CTTTTCTTATTTCAT | 25909 |
rs531409222 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246847310 | AAAAAAACAAACAAA[A/C]AAAAAACTGAAAATG | 25909 |
rs531460154 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246927220 | AGGCACTGTGGCTCA[C/G]ACCTGTCATCTCAGC | 25909 |
rs531489828 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246904150 | ACAAAACTAAAATCA[C/T]TGTGAAAAATTTAGT | 25909 |
rs531491950 | snp | A/C | | | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246900228 | AAAATAAGAGCAATT[A/C]TGTAGATATTCTCCT | 25909 |
rs531495595 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246890789 | GGCATAGGATGAAGA[C/T]ACAAAGTAAGGAAAA | 25909 |
rs531562139 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246884416 | CCAAGAAAATGTAAC[A/T]TTCAGAGTGCTGACA | 25909 |
rs531597731 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246885131 | ATGTTTTTCTTAACA[C/T]TGGAAGACCAATAAA | 25909 |
rs531598786 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246855927 | TTTTGGTGATGTAAA[A/C]TGAGGTTCAGAGAAT | 25909 |
rs531599964 | snp | C/T | 1.6498e-05 | 0.00287206 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850918 | GCTCACTAAAGGTAT[C/T]GTTTCATGAATGGAC | 25909 |
rs531607771 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246848512 | GGCCAAGTCATCTAC[C/T]TTATTTATAAGGTCC | 25909 |
rs531610625 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246877502 | TGACACGTTTAAAGA[A/T]TTTTATGCTGCTTTT | 25909 |
rs531628308 | snp | A/G | 0.00032943 | 0.0128299 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246898249 | CAACAAATCTTGGGG[A/G]AAGAAGGCCAGCTAC | 25909 |
rs531639802 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246849110 | ATACAGTCCTTAGCT[C/T]GTGACAATGAAGGAT | 25909 |
rs531656656 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246919342 | TCCACATTGACCATG[C/G]CTCTGAGTCTCTTAC | 25909 |
rs531779587 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246929869 | CCAGCCTGGCCAATA[C/T]GGTGAAACCCCGTCT | 25909 |
rs531780657 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | AHCTF1 | GRCh38.p7 | 1:246842400 | CAGCCTGGCCAACAT[A/G]ATAAAATGCCGTCTC | 25909 |
rs531827419 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246841475 | GTGGTATTAGCCATA[A/G]TGTCTTAAATAAAAT | 25909 |
rs531862353 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246912885 | ATATTGGCTGATAAG[C/G]CTCAAGATTTCTTAT | 25909 |
rs531871998 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246878266 | GCTGGGCATGGTGGT[G/T]TGTGCCTGTAGTCCC | 25909 |
rs531910217 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246870611 | GGAATTTTACATTTA[A/T]AAGAGAAAAGTATAA | 25909 |
rs531926072 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246899151 | CAGGCACTATACCAC[A/T]GTGCTAGGTGCCTTC | 25909 |
rs531975558 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246893328 | GCGCCATGTCTTCCT[A/G]ACGAACTTGATTGGT | 25909 |
rs532001185 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869198 | ACCCTGTGTCCAGCA[A/T]GTCTACTGGCACCAT | 25909 |
rs532011719 | snp | G/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246885910 | GAAAAAATAAGGCTG[G/T]GCACGGTGGCTCACG | 25909 |
rs532037010 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869506 | ATGCCTGGCTTCAAA[A/G]GACAGGGTGACTCTG | 25909 |
rs532043369 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246884358 | AATTTGTAGATCTTA[-/C]CCCTCTTATCCGTAG | 25909 |
rs532047442 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246905913 | ATGCATTTATGTGTG[C/T]GTGTAACTGGTCCTA | 25909 |
rs532087008 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246885325 | TATGCAGGTTTTACA[C/T]CCCATGAACACTGTA | 25909 |
rs532091281 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246917160 | CACAGAGTAGCCGCA[C/G]TGGGTGGAAGACGAC | 25909 |
rs532133843 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246903134 | GGGCCTTTACTGATT[C/T]CCTGAAACCCGTTTC | 25909 |
rs532177334 | snp | C/G | 0.000117425 | 0.00766151 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246916357 | AGTTTACTACCTCAA[C/G]TTGTGGACCACAAGC | 25909 |
rs532179526 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246840252 | ATTTGAGGTAGATTA[A/C]ACAAAATTTGTGAAA | 25909 |
rs532198828 | snp | A/C | 0.499631 | 0.0135733 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246867903 | TACACCCCCCCCCCC[A/C]CACACACACACACAC | 25909 |
rs532236432 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246861359 | AAGTCTAGTCCTAAG[C/T]TACCCATCCCAATCA | 25909 |
rs532269794 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246897096 | AGGAGGGCAGATCAC[C/T]TGAGGTCAGGAGTTT | 25909 |
rs532271611 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246903595 | AGCACTTTGGGAGTT[C/T]GAGGTGGGTGGATCA | 25909 |
rs532291262 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246910745 | AGAACAGGGCCCCCA[A/C]CCCCAAATCACTTCT | 25909 |
rs532305750 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246897653 | ACAATATGAAGTATA[C/T]GTGTATTTAAACACA | 25909 |
rs532365579 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868151 | TTTTTTTTTTTGAGA[C/T]GGAGTCTTGCTCTGT | 25909 |
rs532376052 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246890704 | CATTTTCAGGAGCTA[C/T]GTTTTCTCAAATTTG | 25909 |
rs532394440 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246922900 | AGGCAGGAGAATGGC[A/G]TGAACCCAGGAGGCG | 25909 |
rs532414695 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246883417 | AAACTTTGTTTTCTT[A/G]AATAAGTCCCTGTAA | 25909 |
rs532416126 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246854650 | ACTTCAGGTACCAAG[C/T]GCTACACAAAACACT | 25909 |
rs532427201 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246924052 | TACCGTTTCTCAGCA[C/T]TCCCCCTCCTATCTA | 25909 |
rs532476869 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246841498 | AATAAAATGCATTCA[C/T]GTGTGCTTTTATTGA | 25909 |
rs532549043 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246891437 | GGCATTTAAATGAAA[C/T]TGGCTTGTTTTTGTT | 25909 |
rs532596096 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246929365 | AGTGAGCCAAGATCA[C/T]GCCATTGCACTCTAG | 25909 |
rs532735254 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868397 | AAGTGCTGGGATTAC[A/G]GGCGTGAGCCACTGC | 25909 |
rs532750301 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868989 | AGCTGGGACTACAGG[C/T]GCCCGCCACCATGCC | 25909 |
rs532772929 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246847699 | GAGATGGGGTTTTTT[G/T]GGCCATGTTGTTGCA | 25909 |
rs532812942 | snp | A/T | 3.32674e-05 | 0.0040783 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246900219 | CCACAGTGCAAAATA[A/T]GAGCAATTATGTAGA | 25909 |
rs532830618 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246857450 | TTGGTCTTCAACAAA[A/C]ACAGAATCACCAGAG | 25909 |
rs532869171 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246858087 | GCCTCCGCCCCCCGA[A/G]TAGCTGGCACTACAG | 25909 |
rs532869215 | snp | C/G | 0.00028111 | 0.0118523 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246849989 | CTTGTAGATCTCCTT[C/G]TAATGCTGGGAGCTT | 25909 |
rs532894904 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246905099 | TAACTTTTAAAATAA[C/T]TTCAACTACTACTCA | 25909 |
rs532932126 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868807 | AGTACAGGTCTACCT[C/T]ATTTTATTGTGCTTT | 25909 |
rs532956445 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246885431 | TGCCACTGTCTATCT[C/T]ATCAATTCCATTTTA | 25909 |
rs532970100 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246862865 | TCCTCTGAAGATTTC[C/G]TATAATGAATACAAA | 25909 |
rs533017761 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246843403 | GCAGACTCATGGCAG[A/G]TAATTCAATAAATGC | 25909 |
rs533093844 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246899626 | AATTATTACATGTAA[C/T]AAATCTTTAAATAAA | 25909 |
rs533094204 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246892545 | AGGCTGGCCTCGAAC[A/T]CCTGACCTCAGGTGA | 25909 |
rs533140055 | in-del | -/T | 0.0115144 | 0.0749975 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246858661 | GTGAAACCCCGCCTC[-/T]TAATAATACAAAAAT | 25909 |
rs533151748 | in-del | -/AA | 0.000838954 | 0.0204639 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246855713 | AATAATCCTGAAGTC[-/AA]AATTATTATACATAC | 25909 |
rs533154569 | snp | A/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246878328 | CTTGATCCTAGGAGG[A/T]CAAGGCTGCAGTGAG | 25909 |
rs533158805 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246879902 | AATAATGAACTACTA[C/T]GCAATAGTTAAAAAG | 25909 |
rs533162268 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246886091 | ATCCCAGCACTTTGG[C/G]AGGCTGAGGTGGGCA | 25909 |
rs533169441 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868943 | TCTGCCTCCCGGGTT[C/T]ACGCCATTCTCCTGC | 25909 |
rs533215428 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868991 | CTGGGACTACAGGCG[C/T]CCGCCACCATGCCTG | 25909 |
rs533221198 | in-del | -/TTG | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246911901 | TGGCTCTTCCATTTC[-/TTG]TTAAGTATAGTTTTT | 25909 |
rs533223102 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246926344 | ACATGTAACATTGTG[C/T]TTTACTATATTCTGT | 25909 |
rs533231401 | snp | A/G | 0.000273947 | 0.0117004 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246843978 | TATATATGTGTGTAT[A/G]TATATAAACACAATA | 25909 |
rs533304944 | snp | C/T | 5.9783e-05 | 0.00546698 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246900509 | AAACAGAATAAAGAA[C/T]CTCAAAGTAAAATCA | 25909 |
rs533320448 | snp | A/G | 0.000431023 | 0.014674 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246907534 | ATAATCAAATAAGGG[A/G]AAAAAGTTATACTTA | 25909 |
rs533398574 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246920963 | TGGCCATGGTGGCGC[A/T]TGCCTGTAATCTCAG | 25909 |
rs533413608 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246897423 | ATATACAAAAATGAA[C/T]TGCATTTTTCCATAT | 25909 |
rs533424108 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246859217 | TCTTAAACTACTTAA[A/G]ATGCAGATTTTTATG | 25909 |
rs533473864 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246894906 | TTCTCAGTGCACCAC[A/G]CCACGGAGCACGTCA | 25909 |
rs533491894 | in-del | -/T | 0.0023933 | 0.0345097 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869153 | CGGCCGTGTGTTTTG[-/T]TTTTTTAAACAAATT | 25909 |
rs533517033 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246897347 | AACAAACAAATAAAC[G/T]AAAAAAGTCTATTAT | 25909 |
rs533561859 | snp | G/T | 1.85824e-05 | 0.00304809 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246861917 | AGAGCTAATACATTC[G/T]TATTAAAAAATGTCT | 25909 |
rs533561959 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246864561 | TTCATTTTGCCTTTA[C/T]GGTTCTGATTACAAT | 25909 |
rs533600675 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246855489 | GGATGCATTTGGCTG[C/T]GGACTAGTAATCTAA | 25909 |
rs533601614 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246858713 | GCCTGTAATCCCAGC[A/T]ACTCGGGAGGCTGAG | 25909 |
rs533630525 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246851560 | CATAAATTATATTTA[A/G]TATGGCATATACTTA | 25909 |
rs533668533 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246852195 | AATAACCTAGAAATT[A/T]GGATTCCCACTTACA | 25909 |
rs533721555 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246898439 | TAAAATTTAAAGATA[A/G]CAAGTGGAAATTATG | 25909 |
rs533745456 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246884547 | TGGTATAAAATAAGT[C/T]TAGTAAGGAATTTCA | 25909 |
rs533747523 | snp | A/C/G | 3.29789e-05 | 0.00406061 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246877066 | CACTGGACTGCAAAA[A/C/G]TTTCACTAAACATTC | 25909 |
rs533816458 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246918534 | GATGCGGAGGCTCAC[A/G]CCTTTAAGTCCCAGC | 25909 |
rs533818821 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | AHCTF1 | GRCh38.p7 | 1:246842531 | AGGTTGCAGTGAGCC[A/G]AAATCACACCACTGC | 25909 |
rs533821417 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246898743 | TACAGCATTCATCCA[C/T]ATCTGGACGATTATC | 25909 |
rs533839659 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246928542 | TAAAATCAATTTTTT[A/T]AAACTCAAGATTGGG | 25909 |
rs533852139 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246911552 | GCAATGGCGCAATCT[C/T]GGCTCACTGCAGCCT | 25909 |
rs533887274 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246870042 | CACATTAAAAGGAGT[G/T]TGTAAGAAGGTGATT | 25909 |
rs533919454 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246842085 | GGCGTGAGCCACCAC[A/G]CCCGACCTCCCATGT | 25909 |
rs533919527 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246890857 | GAGAAAAATAAGTGA[A/G]GTGGAAGAAAAGAAA | 25909 |
rs533956185 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246929075 | ATAGAGGTACATATG[A/C]TGTGAGATCCCAGTA | 25909 |
rs533988088 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246848547 | CTGCTTTGCTGAAAT[G/T]CAAATATTAAACTGT | 25909 |
rs533993175 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868868 | TTTTTTTTTTGAGAT[A/G]GAGTCTCGCTCTGTC | 25909 |
rs534010434 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246904616 | GGAAAAAATTTTTTT[A/T]AAATATGGATGTTGC | 25909 |
rs534028587 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246841646 | TTTTAAAGTGTATAA[C/T]TGTTTTTTACTAATA | 25909 |
rs534035660 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246924955 | CTTAGTTGCTCTTAT[A/G]TACACAAATGGACCC | 25909 |
rs534046734 | snp | G/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246901098 | TAATCCCAGCACTTT[G/T]GAAGGCCAGGTGGGC | 25909 |
rs534082934 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246899226 | AGCTTGAGGTTCACG[C/T]AGCTAGCATCTACAT | 25909 |
rs534179482 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246870296 | AAAATACCCAGGCAC[A/G]GTTGCAGTCTCAGCC | 25909 |
rs534229361 | snp | A/G | 1.65381e-05 | 0.00287555 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850819 | CACGTCATCAACCTG[A/G]CTGACATTCATAGTC | 25909 |
rs534240773 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246862534 | CAACTGAGTCACAAT[A/G]GTGGTTATATTCTCA | 25909 |
rs534244460 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246912161 | ATGAAAAGAGCTACA[C/G]TGATATTCTAGGCTT | 25909 |
rs534255131 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869029 | TTTTCTATTTTTAGT[A/G]GAGACGGGGTTTCAC | 25909 |
rs534256072 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246893659 | ATAACGACATCTATC[C/T]ATGGAGGACAGCAGT | 25909 |
rs534256134 | in-del | -/AG | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246848025 | CTCCATGCAAAACAT[-/AG]GTCTAACCACACTTT | 25909 |
rs534292712 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246886318 | CCTGGGTGACAGAGC[A/G]AGACTCCATCTCAAA | 25909 |
rs534298671 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246930534 | AAGTAAACCACTCTA[A/G]TTTCTTCTCTCCTAA | 25909 |
rs534319392 | in-del | -/AAGTA | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246859233 | TGCAGATTTTTATGT[-/AAGTA]AAGTATGTAGTTTTA | 25909 |
rs534355308 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246844255 | AAGCATTCTGGGGAG[A/G]GAAAGCATTAATCCT | 25909 |
rs534382479 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246856785 | TTTCTCAGGCGTAAA[C/G]CATGTGATTTAGTTC | 25909 |
rs534538497 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868997 | CTACAGGCGCCCGCC[A/G]CCATGCCTGGCTAAC | 25909 |
rs534544869 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246885746 | GACAAAGTAGGTAAA[C/T]CTAACACTAAAAACC | 25909 |
rs534559843 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246913894 | AAGAGTAAAAACTAA[C/T]CATTCCAGAAAAATT | 25909 |
rs534568398 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246864903 | AAGACTAGACTGACA[A/G]CCCACACCCACCACC | 25909 |
rs534573041 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246878749 | TGGTACCCACTGTTG[A/G]CAGATCAGGGCCATC | 25909 |
rs534579122 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246930976 | GTCAACCAGTGGCAA[A/G]AGAAACCGTCCTGTT | 25909 |
rs534608881 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246879287 | AAAAAATATCTGGTA[A/C]ACTGTGTTGATAAAA | 25909 |
rs534617037 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246920678 | GGGAGGCTGAGGCAG[A/G]AGAATGGCATGAACC | 25909 |
rs534722576 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246913483 | AACACAATAAATTTA[A/G]GTTAAAGCAGGTTAT | 25909 |
rs534727851 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246859476 | CCATTTCTACTTGAC[C/T]CACTGTTTGATCTTC | 25909 |
rs534733257 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246859628 | GGGCTGGAGTTCAGT[A/G]GCGCAATCACGGCTC | 25909 |
rs534739599 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246876662 | TACCACACAATGATC[C/T]TTGTACTATGTAACT | 25909 |
rs534755568 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246871911 | CTAAAAAGACAACAC[A/G]AACATGTGAACTTTA | 25909 |
rs534795072 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246872526 | AGAACTGCCTTCATT[A/T]ACAAAGTTACTTAGG | 25909 |
rs534803758 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246895165 | GCATGATTCTGAGCT[C/G]TCTCTACCCTCTAAA | 25909 |
rs534812893 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246845876 | CTCCTGTGGCCAATG[A/C]AAACCATGGCTGGGT | 25909 |
rs534814535 | snp | C/T | 1.65405e-05 | 0.00287576 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246918267 | GCAGCAAACTTTCCA[C/T]GAAGCACAGATTCTA | 25909 |
rs534833665 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246864362 | CGTCGTCCTCCTTCC[C/T]TTTACCTATATTTAC | 25909 |
rs534860397 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246906407 | ACAAGGTGAAAATCC[A/G]TCTCTAAAAAAAAAA | 25909 |
rs534882207 | snp | A/C/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246839353 | TGCTACTTGCGCAAA[A/C/G]GAATTGTTTACTGAA | 25909 |
rs534921674 | in-del | -/AA | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246929527 | AGGACATGAGCAAAG[-/AA]ACATCAGAGTGGAAA | 25909 |
rs534939657 | in-del | -/TCAT | 1.65388e-05 | 0.00287561 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246888275 | GTGGATCTTATACAG[-/TCAT]TCATTCATTCATTCA | 25909 |
rs534952095 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246861354 | CAGTTAAGTCTAGTC[C/G]TAAGCTACCCATCCC | 25909 |
rs534963381 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246864263 | AATCCAAAGTGCTAC[C/G]ATGCATTCAAAAAGT | 25909 |
rs534973079 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246901257 | GAGGTGGGAGGATCG[C/T]TTGAACCTGGGAAGC | 25909 |
rs534976380 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246894521 | GCACTATAGCCTGGC[A/G]ACAGAGCAAGACTCA | 25909 |
rs535013397 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246915643 | TCTTCTCCCACTAGA[A/C]TATAAGCTCTCTAAA | 25909 |
rs535024624 | snp | C/T | 0.000152219 | 0.00872274 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246931269 | GCGGCCCCGGCCGTC[C/T]GTAAAGGGACCCGAC | 25909 |
rs535032396 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246874407 | CACTGTAGCCTTGCT[A/T]AACTTGCTAAACCTT | 25909 |
rs535063943 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246917849 | AATGAAATCAGAAAA[A/C]GAGATTTTCTGAAAA | 25909 |
rs535085900 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246845325 | TATAAAAATGTTTTT[C/T]GTGGGTACACAGTAG | 25909 |
rs535116869 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246887596 | CAGCACCACAAAGGA[A/G]ATAAAGCGTATTTTT | 25909 |
rs535190603 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246904402 | GCAGCTAAGTGCAGT[A/G]CCCTGTGGTAAAGTT | 25909 |
rs535279258 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246927424 | AACCGGGGAGGTGGA[A/G]GTAGCTGTGAGCTGA | 25909 |
rs535293705 | snp | A/C/G | 0.00159617 | 0.0282053 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246915058 | CACCACTGGCCGGGC[A/C/G]TGGTGGCTCATGCCT | 25909 |
rs535295727 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246871846 | ACAAAAAAATAAAAA[A/G]TAAAAATTTGAGGTT | 25909 |
rs535297103 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246893961 | GTAATACCAACACTT[C/T]GGAAGGCCCAGGCAG | 25909 |
rs535304313 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246839404 | ATTTAACAAGTTCAT[G/T]TAAATAAGTTCAATA | 25909 |
rs535364032 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246890357 | AAGAAATGTTCACTA[C/T]AAATCAAAATCTAAG | 25909 |
rs535375841 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869062 | TGTTGGCCAGGATGG[C/T]CTCGATCTCCTGACC | 25909 |
rs535394286 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246892694 | TGGAGTGCAATGGTA[C/T]GATCACAGCTCACTG | 25909 |
rs535394308 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246884912 | CAGAGTACCATTACT[A/G]AATACAAATTCTCAA | 25909 |
rs535405377 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868947 | CCTCCCGGGTTCACG[A/C]CATTCTCCTGCCTCA | 25909 |
rs535405472 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246863831 | CAGCACTCCCCAAGC[A/G]TATCAGTTATAAATT | 25909 |
rs535429285 | in-del | -/GTAG | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246927564 | ACATGAAACACCTAC[-/GTAG]GTTCAGTACTGTACA | 25909 |
rs535484767 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246931821 | GGCTGTAGGCCTGCA[A/G]ACCGCTCAGCGGCTA | 25909 |
rs535486433 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246925673 | TCCCAATCTCATACT[A/G]AAATGTGATCCCCAG | 25909 |
rs535493006 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246926945 | TTTGGGAGGCTAAGG[C/T]GGGCGGATCACGAGG | 25909 |
rs535535680 | snp | C/T | 0.000217248 | 0.01042 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246885530 | GGTGAAGGATAACAT[C/T]GTTACCACTGGACAC | 25909 |
rs535575182 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246900539 | ACCTCAACAGAATTA[C/T]AGCAAGATTTTCTCA | 25909 |
rs535581690 | in-del | -/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246851677 | TTTAACTAGAAATTC[-/T]ACATTTCCCTAGCTA | 25909 |
rs535587769 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246886625 | CTGATCTACAGTTGA[C/T]TGAAGCCACGGATGT | 25909 |
rs535606254 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246871011 | AGTGACTGCGCTCCC[A/G]CTGTAGCCTTGCTTA | 25909 |
rs535624154 | snp | C/T | 3.31175e-05 | 0.00406911 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246887343 | ATACATAATATCAAG[C/T]AGCAAATAAATGGTC | 25909 |
rs535667245 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246851578 | TGGCATATACTTATG[A/G]GTTTACTTTACAAAA | 25909 |
rs535669100 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246922764 | AAGGAGGGCGGATCA[C/T]GAGGTCAGGAGATCG | 25909 |
rs535697511 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246912707 | AGTATTTCATTTTCT[C/T]TGAATCTGAATAGAA | 25909 |
rs535698202 | snp | A/T | | | upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246933338 | AGGGTTTCACCATGT[A/T]GGCCAGGATGGTCTT | 25909 |
rs535733833 | snp | C/T | 1.64855e-05 | 0.00287097 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246913299 | AACAAGAAGGATCTG[C/T]CCAACATCAGTGACC | 25909 |
rs535735735 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246905432 | AATCCGGGAGGCGGA[A/G]GTTGCAGTGAGCCGA | 25909 |
rs535739030 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246880478 | CTGAGGCAGGAGAAT[C/T]ACTTGAACCCGGGAG | 25909 |
rs535773551 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246906281 | GAGCAAATTCAAAGA[C/T]GAGCTGACAAACTGG | 25909 |
rs535774762 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246881056 | GCATTATGAAATGCA[C/T]GGTGGAGACCACAAT | 25909 |
rs535788696 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246922022 | TGCCTGAGAGAATAA[A/T]GATACATTGGTATAT | 25909 |
rs535802148 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246899966 | AACTAACAGTGAGAT[A/G]CAAACAGATAACACT | 25909 |
rs535840495 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246873459 | CTGCATCATAGCGAA[A/G]GGAAAGAATCCGTCC | 25909 |
rs535845380 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246841844 | TCACCCAGGCTGGAG[C/T]GCAGTGGCGTGATCT | 25909 |
rs535862446 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246858428 | AGCCTAAGGTTATAC[A/T]GCGTATCCCAGCTCA | 25909 |
rs535891301 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246914881 | TTCTGTATGTGTTCT[A/G]AATCTGCCCCATCTT | 25909 |
rs535900280 | snp | C/T | 4.94858e-05 | 0.00497398 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246851073 | TTTGGTCACTAGTTA[C/T]GGCAGATGGCAAATT | 25909 |
rs535920845 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246930714 | CACTGCGCCCAGCCA[A/G]AGACAGTTCTTAAAA | 25909 |
rs535972925 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246864211 | TTCACTGGTAACTAT[C/G]ATAGCCACATGCAAA | 25909 |
rs536016821 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246922704 | ATAGTATCAATAGGC[C/T]GGGCGCAGTGGCTCA | 25909 |
rs536037532 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, synonymous-codon, utr-variant-5-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246931206 | CGCTTCCCTCGGGGA[A/G]AGGCCCGCCAACGAG | 25909 |
rs536099250 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246921446 | TCAACAAAAACAAAC[A/T]CAAAGGATAAGTAAA | 25909 |
rs536110036 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246932900 | CTCTTTTATCAGGAA[A/G]GTTTCTACTTTTCTG | 25909 |
rs536110311 | snp | A/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246875684 | CAACATTGAGACAAG[A/T]TCCTTTATTAGCAAA | 25909 |
rs536155349 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246896077 | ACAATAACAAGCATG[C/G]TAAGGACGTGTTAAA | 25909 |
rs536162159 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B | AHCTF1 | GRCh38.p7 | 1:246838987 | TTGTTTACCTTACTA[C/T]TATGATACTAAGCAC | 25909 |
rs536177331 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246872918 | CCATATTAACCTAGA[A/G]ACCGGGTTCACCTTA | 25909 |
rs536226995 | snp | A/C | 0.00119737 | 0.0244387 | upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246933427 | GTGAGCCACCGCGCC[A/C]GGCCTTATTTTTTAT | 25909 |
rs536283277 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246839608 | CCAATTTCTCATTAT[C/T]TGTATTATTTGGTAG | 25909 |
rs536287433 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246927986 | GCCTGGCGACAGAGC[A/G]AGACTCCGCCACCAA | 25909 |
rs536357115 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246916829 | AGATCCCAAGCCTGT[C/T]TAACTCCAAAACTCA | 25909 |
rs536391378 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246875593 | TTGACATGGCCAACT[C/T]CACTGTGTCATCGTA | 25909 |
rs536396387 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246866028 | ATCAATTACATAAAT[C/T]AGCACTTCAGCCTTA | 25909 |
rs536414298 | snp | G/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246924790 | CTAAAAAGTTATGTT[G/T]GAGATTTCCAAGTCA | 25909 |
rs536438127 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246841822 | TTGAGACAGAGTCTC[-/A]AGTCTGTCACCCAGG | 25909 |
rs536459570 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246888050 | AACAGATCCTGGGTT[A/T]ACACCTCTTCTTAAG | 25909 |
rs536467115 | snp | A/C | 1.64751e-05 | 0.00287007 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246867632 | AGATTAACAAGCAGC[A/C]TGACTATGAAACGTG | 25909 |
rs536467912 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246852621 | CAATCCTGTGTAACT[A/G]TATCCATATATTTTC | 25909 |
rs536470162 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246860028 | GCACTCTGGGAGTCC[A/G]AGGCAGGCAGATCAC | 25909 |
rs536529886 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246866982 | GCAGGTAACAAGGAA[A/C]GTAAGTTAATAGTTT | 25909 |
rs536583600 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246888947 | TTGACCCTAGTTAGC[A/G]TGATGAGAACTACAG | 25909 |
rs536609093 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246880331 | GCACTTTGGGAGCCC[A/G]AGGCGGGCAGATCAC | 25909 |
rs536619589 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246881769 | CTTGAACCTGGGAGG[A/C]AGAGGTTGCAGTGAG | 25909 |
rs536626832 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246926912 | GGCCGCGGTGGCACA[C/T]GCCTGTAATCCCAGC | 25909 |
rs536627847 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246848957 | GTGTCTTAACTTTTT[A/G]GACATGTTTAAAGCA | 25909 |
rs536637019 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246891985 | ATTAGAATCACAATG[C/T]AAAATTTCTCAAACT | 25909 |
rs536641959 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868911 | GTGCAGTGGTGTGAT[C/T]TCGGCTCACTGCAAG | 25909 |
rs536644053 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246853939 | AGGACGACGAAAAAC[C/G]ACTTTACAGGCTTCT | 25909 |
rs536654879 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246882233 | CGATCTCCTGACCTC[A/G]TGATCCACCCGCCTC | 25909 |
rs536691629 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246922749 | GCACTTTGGGAGGCC[A/G]AGGAGGGCGGATCAC | 25909 |
rs536701969 | snp | G/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246898075 | ACCTAAGACCACAAC[G/T]GCTGATCACCCAGAG | 25909 |
rs536703171 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246909161 | TCATGCCTGTAATCC[C/T]AGCACTTTGGGAGGC | 25909 |
rs536759025 | in-del | -/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246924053 | ACCGTTTCTCAGCAC[-/T]CCCCCTCCTATCTAT | 25909 |
rs536767910 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246923086 | AGGAGAATGAAGAAG[A/T]AGTTATTTAATCAAA | 25909 |
rs536824683 | snp | A/G | 3.68915e-05 | 0.00429469 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246876136 | TTCCATACTGGTCTA[A/G]TATAGAATTTCGAGC | 25909 |
rs536871159 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869562 | ACTTTAAATTAAAGG[C/G]AATCACCATTCCAAA | 25909 |
rs536873977 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246865921 | AGTGGTATTTAAAAA[A/T]TTGATTTATGTAACT | 25909 |
rs536877254 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246907267 | TGACCAAAACGTTGT[-/A]AAAGTTACAAAGTCA | 25909 |
rs536892450 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246910093 | TACTCAGCACTTCCA[A/G]ACTACCTTGCCAAAA | 25909 |
rs536895019 | snp | G/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246870053 | GAGTTTGTAAGAAGG[G/T]GATTCCATCTTTCAT | 25909 |
rs536909644 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246859561 | AAAACATTTTTTGAT[C/T]ACTAAAATAATATTT | 25909 |
rs536922964 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246901295 | GCAGTGAGACGAGAT[C/T]GTGCAAGTGCACTCC | 25909 |
rs536928123 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246902759 | CTCCAAATTTAAAGA[C/T]TGTTCACACAATACA | 25909 |
rs536969059 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246903202 | TAGAGACAGGTATGT[A/G]AGGGTGAACAAAATA | 25909 |
rs536974934 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246843789 | ATAAAATCATGCATT[C/T]CTTACCAGTTCATCT | 25909 |
rs537009029 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246872120 | AACTAAATATGGTCA[C/T]AGATCATCACATTAT | 25909 |
rs537060692 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246932796 | CCCAGCGCCAAACAT[A/G]TTTCAAACAGATAGG | 25909 |
rs537093550 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246873882 | AATACTACTTACTGT[A/G]TAAGTCCTACTAAAC | 25909 |
rs537111799 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246854625 | ATTTCTAACAGCTAA[C/T]ATTTACTAAACTTCA | 25909 |
rs537123404 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246927573 | CACCTACGTTCAGTA[C/T]TGTACAAAATTAAAC | 25909 |
rs537152529 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246907199 | ACATTAAAAAGGTAC[A/G]ATCAAAATACAGTAA | 25909 |
rs537174491 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246881700 | AAAATTAGGTGGGCA[C/T]GATGGCGGGCACCTG | 25909 |
rs537213049 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246874478 | GGGGGAGCACTTACC[C/T]AAATGCTAGGACCAC | 25909 |
rs537250888 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869114 | CTCCCAAAGTGCTGG[A/G]TTACAGGCGTGAGCC | 25909 |
rs537276345 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246858956 | ATGTAGGCCAGGACC[A/G]GTGGCGCATGCCTGT | 25909 |
rs537313689 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246915702 | CTGGGAATCTAACAT[A/G]TATTTTCCATAATGC | 25909 |
rs537355035 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246895223 | CAATAAGGTCTCTAG[A/G]TTAGATAAAAGTCTT | 25909 |
rs537367523 | in-del | -/T | 0.0923359 | 0.194016 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246891487 | AAAATTTATGAGTTC[-/T]TTGAATAAAAAATAC | 25909 |
rs537373241 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246879186 | AGGTCACAAAAGAAA[C/T]AGCTCTTTAAAAAAA | 25909 |
rs537387112 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869245 | ACTTACTCCACTGAC[C/T]AACTGTTCCCCCGCG | 25909 |
rs537399062 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246888098 | CAACCTTGCAATTAG[A/G]TATGTCAGGTTTCCA | 25909 |
rs537422924 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246924276 | CTTTCAGTTTTCTTA[C/T]GAAATTAACTATTTC | 25909 |
rs537433831 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246867542 | GCCAACATAAAGAGT[C/T]TTTCTTTTTTACATA | 25909 |
rs537465278 | snp | C/T | 3.33161e-05 | 0.00408129 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246860950 | ATGCAAATACATCTT[C/T]ATCTCCATCCTTTTC | 25909 |
rs537506045 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246854168 | GCCAGGCGTGGTGGC[A/G]GGCACCTGTAGTCCC | 25909 |
rs537523130 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B | AHCTF1 | GRCh38.p7 | 1:246839090 | TCCTAAAATGTTGTA[C/G]CAACACATTTTAATG | 25909 |
rs537525250 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246896551 | ATGTAAGGCTGGGTA[C/G]GATGGGGCAGGCAGG | 25909 |
rs537545350 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246881211 | TAACAAGTATTCATA[A/T]TAAAGAAGGTTACCA | 25909 |
rs537636156 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246903550 | AATCGCTTTTCACAG[C/T]CAGGTGCGGTGGCTC | 25909 |
rs537638993 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246889476 | CACTTAGGAAATAAC[A/T]GATCTAGAATTTTAA | 25909 |
rs537667800 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246915731 | GCTCCAATCCAAGAC[A/T]ATTGTCGCAAATTTA | 25909 |
rs537683208 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246928337 | AATTACTTCTGCTTG[C/T]CTGTCTTCTCCACTA | 25909 |
rs537698570 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246922802 | CCTGGATAACACGGT[G/T]AAACCCTGTCTCTAC | 25909 |
rs537700397 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246923258 | CATCTTTACTAAAAA[C/T]ACAAAAATTAGCTGG | 25909 |
rs537705094 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246916571 | TAGTCATTCAGTGGC[A/G]TGAACCTGGGAGGTG | 25909 |
rs537713121 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246909239 | ATATGGTGAAACCTC[A/G]GCTCTACTAAAAAAA | 25909 |
rs537742814 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246882829 | GGTATGTCCATATAT[A/G]TAGCTCATAAAATTG | 25909 |
rs537759708 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246917659 | TCAAGAGAGAAATGA[C/T]TGATACATATGTTTT | 25909 |
rs537779408 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246876431 | TAAAAACAATGGTTA[C/T]TAAGCATCCATGTGT | 25909 |
rs537950963 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246912050 | ACTGGCAGTTTTAAT[C/T]GGTTTTTTTATACAC | 25909 |
rs537977194 | snp | C/G | 1.64914e-05 | 0.00287149 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246903997 | TCTATTACCAAAGGC[C/G]AGCTGCAGCAGATGC | 25909 |
rs538038542 | snp | C/T | 6.9006e-05 | 0.00587352 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246862135 | AAGTAGTAACTGACA[C/T]GGCCAAACTTTTAGC | 25909 |
rs538042010 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246854837 | TCGGGTTCAGCCCCC[C/T]GCACTCTTCAGGCAC | 25909 |
rs538073728 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246847862 | ACTATATTCCTCCAG[C/G]TCCTGAGGAGTGTAT | 25909 |
rs538108525 | snp | C/G/T | 0.000895268 | 0.0211394 | missense, utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246840951 | AAGGGGGAAATCAGC[C/G/T]GAATTTCTATGGGAG | 25909 |
rs538159056 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246926895 | ACAAAAGTGTATGGC[C/T]GGGCCGCGGTGGCAC | 25909 |
rs538242316 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246852917 | TTATTAAAGGATGTG[-/T]TTTTATATTCCACAA | 25909 |
rs538298602 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246909120 | ATCTATTTATATATA[C/T]ATAAAATTCAGCCAG | 25909 |
rs538326577 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246901863 | AAACTTTAAAAAGAC[G/T]TGAGCTCATGACAAC | 25909 |
rs538367703 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246883054 | ATTATTTGTAAGGGT[A/G]CAAATTAATAAACAA | 25909 |
rs538389332 | snp | A/G | 0.0479149 | 0.147179 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868350 | GGTCTTGAACTCCTG[A/G]CCTCATGTGATCCAC | 25909 |
rs538409265 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246929643 | AGTAGCATATACTTA[C/T]TGTAGAGACCTTTGA | 25909 |
rs538411214 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246929912 | CAAAAATTAGCCGGG[C/T]GTGGTGGCGTGCGCC | 25909 |
rs538426373 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868570 | CATTTTGTTTCATTA[C/T]AGCTATGCTGGATTT | 25909 |
rs538426654 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246870952 | AAGAAGACAAACAAT[A/G]CAACTGAGCCTTCGA | 25909 |
rs538463554 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246858651 | TGGCCAACATGGTGA[A/C]ACCCCGCCTCTAATA | 25909 |
rs538472186 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246904493 | AAAATATCCTTTATG[C/G]CTTCATCCTGGTCTC | 25909 |
rs538508710 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246898696 | CTACTCCTCTTTATC[G/T]AATGTGAAAGAGATT | 25909 |
rs538554576 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246889601 | AGCCGGCACAGATTT[C/T]AAAGTACTGATTCCC | 25909 |
rs538631897 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246922856 | GGCGTGGTGGCAGGC[A/G]CCTGTAGTCCCAGCT | 25909 |
rs538674983 | in-del | -/A | 0.00636936 | 0.0560724 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246920369 | TTTGAAAAAATTTCT[-/A]AAAAATGAAAAATTA | 25909 |
rs538692617 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246923175 | ATCCCAGCACTTTGG[A/G]AGGCCGAGGTGGGCA | 25909 |
rs538748809 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246859798 | GTCTAGGCTGGTCTC[A/G]AACTCCTGGGCTCCC | 25909 |
rs538760118 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246910662 | AGACTCATATATTAA[C/T]ATAACCACTGTGCAA | 25909 |
rs538772345 | in-del | -/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246920968 | ATGGTGGCGCATGCC[-/T]GTAATCTCAGCTACT | 25909 |
rs538791539 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246883250 | TGGGTGTTGGACTAT[C/T]ATGCAGCTTAACTTC | 25909 |
rs538834493 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246867980 | ATTAATTTTTTTTCT[C/T]TTAGACCAGTCTTGC | 25909 |
rs538995624 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246882792 | TAATTTGCACGTAAA[A/C]CAGCCACGCCACAGT | 25909 |
rs539008709 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246875708 | TAGCAAAAGGATTAC[A/G]ACTCACAGAAGGCTC | 25909 |
rs539034069 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246855645 | ATCTGAATAACACAA[C/T]AGATTATTTTGTTCT | 25909 |
rs539062848 | snp | C/G | 1.65141e-05 | 0.00287346 | missense, utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246840889 | CTGTTCCTGTCACTT[C/G]TGTAGTTTTTCTTGG | 25909 |
rs539072674 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246856194 | TTTCTATGAACTCAG[A/T]AGAGGCAAGGTTCAA | 25909 |
rs539072857 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246848608 | TGGTGGCTCACGCCT[A/G]TAATCCCAACACTTT | 25909 |
rs539184570 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869608 | AAAAATGATGGGAAA[C/T]CTACTATGCCTGTCT | 25909 |
rs539206612 | in-del | -/A | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246912312 | AACCCCATCTCTACT[-/A]AAAAAAAAAAAAATA | 25909 |
rs539249174 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246870365 | AAGGTCAAGGCTACA[A/G]TGAGCTATGATTATA | 25909 |
rs539255684 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246854874 | GTCTCCTCTTCCAAC[A/G]TATCGGGAGAAATGG | 25909 |
rs539264305 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246911109 | GAGAAATGGTTCTGA[A/T]CACAATCCAGAGACT | 25909 |
rs539298063 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246903859 | AAAAAAAAAAAGAAT[C/T]ACTTTTCAATATCTT | 25909 |
rs539304749 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868897 | TCACCCAGGTTGGAG[C/T]GCAGTGGTGTGATCT | 25909 |
rs539356998 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246897912 | TAAGCCCAAGAGGTT[A/G]AGGCTACAGTGAGCC | 25909 |
rs539368916 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246867525 | TTCTTCTCAGAAACA[C/T]AGCCAACATAAAGAG | 25909 |
rs539393137 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246898549 | TTAGCAAAAGGTAGC[C/T]TATATATTTTTATGA | 25909 |
rs539423732 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868880 | GATGGAGTCTCGCTC[C/T]GTCACCCAGGTTGGA | 25909 |
rs539487454 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246904664 | CTATCAAGACACAAA[A/G]TGAAGATACTAAATC | 25909 |
rs539492454 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246929778 | ATCTGTACCAGCCGG[C/G]CGCGGTGGCTCACGC | 25909 |
rs539499022 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246864179 | AATTTAGTATCCCAT[C/T]TAATCAGACCTCTAT | 25909 |
rs539526357 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | AHCTF1 | GRCh38.p7 | 1:246842590 | CTGTCTCAAAAAAAA[A/T]AAATAAAAATAAAAT | 25909 |
rs539526689 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246927872 | GCTGGGCGCGGTAGC[A/G]CGCTGTAGTCCCAGC | 25909 |
rs539528488 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246906208 | AAAATTGACCAAGAG[A/G]TGATAGTGTTAGAGA | 25909 |
rs539584099 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246877623 | GGTGTGACAGAGGAA[C/T]ATCAGGTTTTTAAGA | 25909 |
rs539599198 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246893836 | CCAAAAGACAAGTTA[C/T]AATCCTAAAACCTGC | 25909 |
rs539628220 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246925101 | GATAAAACTAGTTTA[A/C]TGATGAACTGAAGTT | 25909 |
rs539635710 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246858378 | ATTAACTTACTTAAT[A/C]CTCAACATTCAAAAA | 25909 |
rs539689764 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246913604 | CCATTACTCAATACA[C/T]AGAAAAATCACGCAG | 25909 |
rs539701445 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246875984 | CAGAAAAGTAATCAT[C/T]CAGTATCTTTTTTGA | 25909 |
rs539764191 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246873522 | TCAATTTCTCCTGCA[A/T]CACAGTGAAGGGAAA | 25909 |
rs539801856 | snp | A/G | | | upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246933450 | TTTTTTATTTTTTGT[A/G]GAGACTGTCTCACTG | 25909 |
rs539812932 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246921578 | AATCCCCCCAAAAAT[A/C]TAGTACTAATAGGAA | 25909 |
rs539863948 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246905402 | ACTCGGGAGGCTGAG[C/T]GAGAGAATGGCATGA | 25909 |
rs539917470 | snp | C/T | | | intron-variant, downstream-variant-500B | AHCTF1 | GRCh38.p7 | 1:246842218 | GATAATCTTTTCTGA[C/T]GAGCTTAATTTCCTT | 25909 |
rs539919650 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246922924 | GGAGGCGGAGTTTGC[A/T]GTGAGCCGAGATTGC | 25909 |
rs539938508 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246884147 | GTTACCACATTTAGC[G/T]TCTTTATTTTGTTCT | 25909 |
rs540007291 | in-del | -/ATAATG | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246916965 | TAAGACATAACTAGC[-/ATAATG]ATAGGAAGTCTCAGA | 25909 |
rs540008984 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246876565 | CCCAAGCACACAGAG[C/T]AAATGAAGAATTAGT | 25909 |
rs540024963 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869463 | AATTAAAAGTGCTAC[A/G]TCAGTGAACACATGA | 25909 |
rs540048092 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246917149 | ACAAGGAGAAGCACA[A/G]AGTAGCCGCACTGGG | 25909 |
rs540056502 | snp | A/C | 0.02016 | 0.0983543 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246867899 | TGATTACACCCCCCC[A/C]CCCACACACACACAC | 25909 |
rs540065218 | snp | C/T | 3.29587e-05 | 0.00405934 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850891 | CAATTTAGTGGGACA[C/T]ATTATGTTTTGGCTC | 25909 |
rs540081152 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246895340 | GCTACAAAAGCATGA[C/T]GGCTTATCATCAAAT | 25909 |
rs540104199 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246844292 | AACCTGAGCTAGTCT[G/T]TGCCATAACTACTGC | 25909 |
rs540114709 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246886523 | ATACCATGTAAATAA[C/T]TGTTATAGTGTAACA | 25909 |
rs540187346 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246889687 | TTATATGCTTTGTAA[C/T]TTTGTCACTGCAACT | 25909 |
rs540228112 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246927880 | CGGTAGCGCGCTGTA[C/G]TCCCAGCTACTTGGG | 25909 |
rs540250770 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246847493 | AGAGTTTTCAGTAAG[G/T]AGGCATGTATTGTTT | 25909 |
rs540258721 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246839826 | CTTAATTGCACACAG[C/T]TGTACTGTAGAGAAC | 25909 |
rs540295293 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246840191 | GCCTTTAAGCTTGCC[A/G]AATAAGAGATGCCAA | 25909 |
rs540325068 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246848415 | GTAGTGTTAGCCAGG[A/G]TGGTCTCGATCTCCT | 25909 |
rs540400834 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246925906 | GAAATCTCATCTCTA[C/T]GAAAAATAATTAGCC | 25909 |
rs540423488 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246929265 | ATACAAAAAATTAGC[C/G]GAGTGTGGCGGCGCG | 25909 |
rs540435586 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246924588 | CTTGTCATTCTTATT[C/G]TCTCCACATCTTAGT | 25909 |
rs540452970 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246917743 | TGCAATATCTTTCAT[C/T]AGAACAAGATCCATA | 25909 |
rs540495342 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246925330 | CCAAAGGATAACACA[A/C/T]AAAAAGCATTTTTTG | 25909 |
rs540500286 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246849530 | GGGAAAAATTCCCTA[C/T]AAAACCATTTTTAGG | 25909 |
rs540535301 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246842854 | CCTGAGACAAGGAAT[A/G]CTAGAGCCAAACACT | 25909 |
rs540570087 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246884994 | GCATACTAAACCCTC[A/G]GCTGTCCAGGCAGGA | 25909 |
rs540611011 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246861680 | AATTAGGAGGTTTGA[A/C]TCCTACTCCCAATTC | 25909 |
rs540617691 | in-del | -/TCTT | 0.00119737 | 0.0244387 | downstream-variant-500B | AHCTF1 | GRCh38.p7 | 1:246838875 | CTACGATACTAAGTA[-/TCTT]TCTGAGTACATTGTT | 25909 |
rs540711845 | in-del | -/ACAA | 0.00159617 | 0.0282053 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246893160 | AAAACATGAGCTCTG[-/ACAA]ACATTTTCCTCTTAA | 25909 |
rs540714202 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246920258 | CTTCAGATATTGAAA[C/T]TACCAGAGATTAGAA | 25909 |
rs540808172 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246899897 | CCTTTATAAAACATA[G/T]AAATACTAAGTTTCT | 25909 |
rs540809075 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868906 | TTGGAGTGCAGTGGT[A/G]TGATCTCGGCTCACT | 25909 |
rs540814665 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246848933 | GATGGGATCTATTCA[C/G]CCACACCAGTGTCTT | 25909 |
rs540840495 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246858045 | GCTCACTGCAAGCTC[C/T]GCCTCCCAGGTTCAC | 25909 |
rs540883028 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246858456 | TCATGACGCATACTC[A/C]GTAAGTAGCTGAGCT | 25909 |
rs540928507 | snp | C/T | 3.32662e-05 | 0.00407824 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246877244 | TGTGCTTCAGTAACT[C/T]CTCTATATTCAACCT | 25909 |
rs541026001 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246886664 | TGGACACAGAGGGCC[A/G]ATGGTATACAAGAGG | 25909 |
rs541052028 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246912355 | AGGCATGGTGGCGTG[C/T]GCCTGTAATCTCAGC | 25909 |
rs541083912 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246895609 | TAGGTATGGCTGTAA[C/T]GGCAGCATGAGGGAT | 25909 |
rs541093029 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246844596 | CAATGTGGTGGTGCA[C/T]GCCTGTGGTGTCAGC | 25909 |
rs541111401 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246881546 | TTTTTTTTAAATAGA[A/G]GCAGGGTCAGCTGGG | 25909 |
rs541124601 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246879836 | CTGTTCCCCCAACCC[C/T]GCCAAAAAAAAAGGG | 25909 |
rs541133029 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246905459 | CCGAAATCACGCCAC[C/T]GCACTCCAGCCTGGA | 25909 |
rs541141857 | in-del | -/A | 0.49706 | 0.0382258 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246881838 | GCAAGGCTCCGTCTC[-/A]AAAAAAAAAACCAAA | 25909 |
rs541161458 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246880577 | CAGCTCAAAAAAAAA[A/C]AAAAAAAAAATTCCA | 25909 |
rs541163326 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246872318 | CACGCCAGGAAAAGA[A/C]TGACAAGAAGACTTT | 25909 |
rs541196599 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246911274 | CCACAAAATACACTA[C/T]GAAACAAAAGCCTAT | 25909 |
rs541201566 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246873049 | AAAGCCATCATTCCT[C/G]AGTGAATCCTGCACC | 25909 |
rs541269835 | snp | A/G | 0.000381961 | 0.0138143 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246899550 | AATCCACTTACATAT[A/G]TTTAAAATGGCATTA | 25909 |
rs541271095 | snp | A/G | 2.55073e-05 | 0.00357113 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850549 | TTCTAGTATGTCCTG[A/G]TTAACTTCTTTCTTT | 25909 |
rs541276696 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869025 | AACTTTTTCTATTTT[C/T]AGTAGAGACGGGGTT | 25909 |
rs541296229 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246893358 | TTTAAAAATCCTCTA[C/T]TAAGAATAACTTAAC | 25909 |
rs541331381 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246900988 | AGAGACATCAACAGG[A/T]GAAGAAGAAAGTAAA | 25909 |
rs541342755 | in-del | -/T | 0.308931 | 0.249744 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246848390 | GATAATTTCTTTGTA[-/T]TTTTTTTTAGTAGTG | 25909 |
rs541399332 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246865322 | TGTAGTTGCAGTACC[C/T]TCCTTGTCATTCTAT | 25909 |
rs541444798 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246926770 | CTGAGGCAGGAGAAT[C/T]ACTTGAACCCGGGAG | 25909 |
rs541446107 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246901828 | GTGAGACCCCTGTCT[C/G]TAAATAAATAAACAA | 25909 |
rs541508402 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246926954 | CTAAGGCGGGCGGAT[C/T]ACGAGGTCAGGAGAT | 25909 |
rs541556255 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868446 | TTTTAGTAGAGACAG[C/G]GTTTCACCATGTTGG | 25909 |
rs541594533 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868761 | TCTTGGGTTACAGAG[C/T]AGCCAATAAAAAAGT | 25909 |
rs541594586 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246862276 | ACCAGGTCAGGAGAT[A/C]GAGACCATCCTGGCT | 25909 |
rs541603466 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246913616 | ACATAGAAAAATCAC[A/G]CAGTTGGACTAACAA | 25909 |
rs541620784 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246921520 | CAAAGGGATGAGTAG[C/T]TTTAAATTATAGATA | 25909 |
rs541636517 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246881100 | CAAGAGAGGTAAACA[A/C]CCAACCACTGATTTC | 25909 |
rs541716653 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246908247 | CATTACCAATGACAG[C/G]ACATTTTGGGCATCA | 25909 |
rs541735430 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246901043 | ATAGGAAGAATGGGG[A/C]ATAAGAGAGAGCATG | 25909 |
rs541763787 | snp | A/C | 8.27506e-05 | 0.00643183 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246877204 | AAATCTTCCATCAAG[A/C]CCATTTCCTGACAGA | 25909 |
rs541781154 | snp | C/T | 0.00143753 | 0.0267712 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246899490 | TAAATGAACAACTCC[C/T]GAGTTTAACAAACAA | 25909 |
rs541792335 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868965 | TTCTCCTGCCTCAGC[C/G]TGCTGAGTAGCTGGG | 25909 |
rs541794090 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246928257 | GCAGTGAGCCGACAT[C/T]GCGCCACTGCACTGT | 25909 |
rs541816014 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246893281 | TATTTCATGACAACA[C/G]TTTCATAAGTATAGT | 25909 |
rs541902567 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246870163 | AGAAGCAGAGCCTAG[C/G]CCAGGCATGATGGCT | 25909 |
rs541919623 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246911672 | ATTTTTTAGTAGAGA[C/T]GGGGTTTCTCCATGT | 25909 |
rs541956166 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246912316 | CCCATCTCTACTAAA[A/G]AAAAAAAAATACAAA | 25909 |
rs541958506 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246924628 | CAAAAAAATTTATGT[C/G]AAAAAAACATTTCAA | 25909 |
rs542016318 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246896835 | GTTCAAAAAGGAATC[C/G]CATGAATGTAAGTTG | 25909 |
rs542036794 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246926614 | TCATCCCAGCACTTC[A/G]GAAAGCTGAGGTGGG | 25909 |
rs542067808 | in-del | -/TATA | 0.00159617 | 0.0282053 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246907096 | ACCTAGGCTAGATGG[-/TATA]TATAGCCTGTTGCTC | 25909 |
rs542093008 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246898913 | GCCAACATGGTGAAA[A/C]CCCATCTCTACTAAA | 25909 |
rs542125118 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246906616 | AGAGCTGATAAAAGG[A/G]TAACAGCAAAGAGAG | 25909 |
rs542128984 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246905292 | ATCATGAGGTCAGGA[A/G]TTCAAGACCAGCCTG | 25909 |
rs542153870 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246857092 | AATCATACTGATTAG[C/T]ACAGCTGACTTTCCG | 25909 |
rs542190722 | snp | A/T | 1.6476e-05 | 0.00287014 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246849785 | TCATTTGTTTCTTTA[A/T]GTGTCATTTCATCTG | 25909 |
rs542206071 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246863148 | TACTGAATATTTTAA[A/G]TTATTGAAACCTAAT | 25909 |
rs542235757 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246929870 | CAGCCTGGCCAATAT[A/G]GTGAAACCCCGTCTC | 25909 |
rs542305190 | snp | C/G | 1.71199e-05 | 0.00292569 | missense, nc-transcript-variant, intron-variant | AHCTF1 | GRCh38.p7 | 1:246843905 | CTAATTCTTTCAGCT[C/G]TGCAGGAACCTCTAT | 25909 |
rs542343884 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246900868 | GCATTAAGGCTTTAT[C/T]ATGATGAACCTTAGC | 25909 |
rs542382513 | snp | C/T | 0.000414068 | 0.0143827 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246894721 | CATTCAAGAACAAAG[C/T]GCAAATTAGTGGCAG | 25909 |
rs542418042 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246932149 | AGCAGGGCCTGGAAG[A/G]GCGGATCATTTACAA | 25909 |
rs542445145 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246896537 | GTAGATTAGTCATTA[C/T]GTAAGGCTGGGTAGG | 25909 |
rs542446621 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868919 | GTGTGATCTCGGCTC[A/C]CTGCAAGTTCTGCCT | 25909 |
rs542459511 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246870393 | ATACCACTGTACTAG[A/G]GCATCTGTGACAGAC | 25909 |
rs542473421 | snp | A/G | 0.00358779 | 0.0422022 | downstream-variant-500B | AHCTF1 | GRCh38.p7 | 1:246838663 | ATTGTAGCCCATTCA[A/G]GACCAGGTCTTTGCA | 25909 |
rs542569750 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246910040 | ACTAATTGAAACTAC[C/T]AGACACTATGTGTCT | 25909 |
rs542623955 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246858625 | ACGAGGTCAGGAGTT[A/C]GAGACCAGCCTGGCC | 25909 |
rs542624831 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246864458 | CTAAAGAAAACAGGA[C/G]AAGGCTTCCCTGGCA | 25909 |
rs542651331 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246865195 | GTCTATCTTATGGTT[C/G]TATTTCCTAGTGGTA | 25909 |
rs542652311 | snp | A/C/G | 6.6565e-05 | 0.00576877 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246900305 | ACATACAAATACAAA[A/C/G]AGAAAGGAGAGAGAA | 25909 |
rs542663246 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869073 | ATGGTCTCGATCTCC[C/T]GACCTCGTGATCCGC | 25909 |
rs542687675 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246915206 | GTGGTGGTGCACGCC[C/T]GTAGTCCCAGCTACT | 25909 |
rs542689070 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246894245 | AATGTAAAAAGAAAT[A/G]ATTTTCTTTTGGGAC | 25909 |
rs542734687 | in-del | -/TTTA | 0.0707826 | 0.174302 | upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246933121 | CATTAATTTTTTTAT[-/TTTA]TTTATTTATTTATTT | 25909 |
rs542754130 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246866457 | TAACTAAATTTAGTC[C/T]AAAAAAAGAAAAATC | 25909 |
rs542788495 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246859002 | GAGGCTGAGGCAAGA[C/G]AAGAGGTTGCAGGAG | 25909 |
rs542792961 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246867171 | GTCTATAAAATGTTA[A/C]AGATAATTAAAAATT | 25909 |
rs542800491 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246887671 | AAATTTCTAAAGATC[A/T]AGCAAAAGATGGCAG | 25909 |
rs542854914 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246921172 | AAGGTTAAAAAGACA[C/T]GCAGAACTAAGCAAA | 25909 |
rs542865078 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246846087 | GAATCAAACGATATA[C/T]GAATGTCATGTATCT | 25909 |
rs542906059 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246853540 | CAGGAAACATTAATA[C/T]GACGACCAACTGCTT | 25909 |
rs542933106 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246896336 | CATTAATTGTAGATA[A/G]ACAAATTATGGTATG | 25909 |
rs542937639 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246880857 | CCTACAGAAGACAAT[A/G]ATGATGCTAGGAAGA | 25909 |
rs542940649 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246873245 | TACTCTTCTGTAAAA[C/G]AAAAAAATCTTAACC | 25909 |
rs542975631 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246889312 | TCTAATTGTGAATAG[C/T]GGCAGCACTTACTAC | 25909 |
rs542978299 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246916857 | TCATGCTTTAACTAC[C/T]AAGGCTTAAACGATT | 25909 |
rs542987360 | in-del | -/A | 0.350863 | 0.22875 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246843742 | ATTAAAACATTTGTA[-/A]AAAAAAAAAGTATGT | 25909 |
rs543003373 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246912872 | GCTGGGTAATTTCAT[A/G]TTGGCTGATAAGGCT | 25909 |
rs543040131 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246913576 | GAAATCTTCAGCTAT[A/T]CTAGGAATTACACCA | 25909 |
rs543098732 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868195 | GTGCAGTGGCACAAT[C/G]TTGGCTCACTGCAAC | 25909 |
rs543098808 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246840179 | AGACTTTAAAGAGCC[G/T]TTAAGCTTGCCGAAT | 25909 |
rs543113223 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246908648 | ATCTCAGCACTTTGG[A/G]AGGCCAAGGTGGGCG | 25909 |
rs543119616 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246867061 | TGAACAAAAATTTTA[A/G]GTATACTACTACCTG | 25909 |
rs543152719 | snp | A/T | 6.65779e-05 | 0.00576927 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246900255 | TCCTGACCTAAAAGA[A/T]AATTTAAAACATTAC | 25909 |
rs543153544 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246909359 | GAGGCAGAGGTTGCA[A/G]TGAGCCGAGATTGCG | 25909 |
rs543159227 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246864743 | TACTCGGGAGGCTGA[C/G]GCAGGAGAATGGCGT | 25909 |
rs543200628 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246864382 | CCTATATTTACTGAG[A/C]TCTTACTATGTGCCT | 25909 |
rs543237330 | snp | A/G/T | 0.00319074 | 0.0398324 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246858558 | TTTCTGGCCAGGCAC[A/G/T]GAGGCTCATACCTGT | 25909 |
rs543256124 | in-del | -/CTT | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246884328 | TCTATTATTAAACTT[-/CTT]TTCTTCTGCCTGAAA | 25909 |
rs543271264 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246844778 | AATTGGTTTAAAATA[A/G]GGAATTAAAAGCATT | 25909 |
rs543273134 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246851816 | AACAACCCCCAAACT[A/G]TGTTTTAATGGTATT | 25909 |
rs543287909 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246902059 | AACAGAGCTCTGAAA[A/C/T]GTTAAGCAATTTGTC | 25909 |
rs543347732 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246911880 | TAAGTTTTGTTCAGA[A/T]GATTTTGGCTCTTCC | 25909 |
rs543414896 | snp | A/G | 0.000477889 | 0.0154504 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246863912 | GTGAACGCTAGATGC[A/G]TAAATACTAACCTTA | 25909 |
rs543437329 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246878512 | TTTTTAAAAAGCAAG[C/T]TAAAAACAGTATGAA | 25909 |
rs543453026 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868971 | TGCCTCAGCCTGCTG[A/T]GTAGCTGGGACTACA | 25909 |
rs543492204 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246910742 | CCTAGAACAGGGCCC[C/G]CACCCCCAAATCACT | 25909 |
rs543498806 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246849400 | AAATAAATCTGTTAC[A/G]TGAGTTACAGGATTT | 25909 |
rs543538057 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869033 | CTATTTTTAGTAGAG[A/G]CGGGGTTTCACCATG | 25909 |
rs543556187 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246870246 | GCCATGAGTTTGAGA[A/G]TAGCCTGGGCGACAT | 25909 |
rs543581333 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246865587 | GTTTGCTCACTTTTA[C/T]ACTGAGCTATCCCAA | 25909 |
rs543619435 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246866370 | AGAATGTCGGTAATA[A/G]CGACTTTCATTTAAA | 25909 |
rs543659382 | snp | C/T | 3.29837e-05 | 0.00406088 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246877005 | GGCACATAATTGGCA[C/T]GCTGCAAATGGTGCA | 25909 |
rs543662653 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246860053 | GATCACGAGGTCAGG[A/G]GTTCGAGACCAGCCT | 25909 |
rs543665047 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246926793 | CCCGGGAGGCGGAGA[C/T]TGCAGTCAGCCGACA | 25909 |
rs543680568 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246894179 | ACTGTACTCCTGCCT[A/C/G]GGCAAAAAGTGAGAC | 25909 |
rs543694000 | in-del | -/TAAGA | 0.00953873 | 0.0683987 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246911791 | GCCCAGCTCTTCTAT[-/TAAGA]TATTTTAAAGTGCAT | 25909 |
rs543710393 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246895567 | ACAAAATTCTTGCCA[A/G]GGGTTAAGGATGGGG | 25909 |
rs543716351 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246894564 | GAAAAGAGTTTACAA[C/T]TTCAAAATGATTAAA | 25909 |
rs543719605 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246879934 | AAATCCTTTATGTAA[C/T]TATAAAATTAGCACC | 25909 |
rs543720529 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246886810 | ACTGTATTTTAAAGA[A/C]TAAAAGCTTTATAAA | 25909 |
rs543721576 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246901497 | GGCATGGTGGCGGGT[A/G]CTTGTAGCCCCAGCT | 25909 |
rs543781560 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246895433 | TGTGTATGTGTGTGA[A/C]GAGTAACAGTGATAC | 25909 |
rs543784456 | snp | C/T | 3.31131e-05 | 0.00406884 | missense, synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246891780 | AACAAAGAGCGTACC[C/T]CTCTCAGTGATCTCT | 25909 |
rs543810135 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246859750 | CCAGCTAATTTTTTT[A/G]TATTTTTTGTAGAGA | 25909 |
rs543849781 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246852935 | TTATATTCCACAAAA[G/T]ATTTATACACTTATT | 25909 |
rs543884107 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246889255 | GCAGGTATGGTCCCT[A/G]TTTCCTTTTCTTTTC | 25909 |
rs543900599 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246907770 | AGATCTAAAACCACA[A/G]ATTAGACAAATGAAG | 25909 |
rs543908057 | snp | A/G | 1.65468e-05 | 0.00287631 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246907756 | CAGTTAGAACTTCAA[A/G]ATCTAAAACCACAAA | 25909 |
rs543947162 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246921222 | CATGACAAAACTATG[-/A]AAAAAAACAAAGAAA | 25909 |
rs543972371 | in-del | -/ATG | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246921897 | TGAGAGGCAGCAAGA[-/ATG]ATGATGTCAAAGTAC | 25909 |
rs543988551 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246881897 | TCTCCTACGTTGCCC[A/G]GCCTGATCCTGGGCT | 25909 |
rs544006153 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246921798 | ACAAATACGAAATAT[C/G]TTTTTAGACAAAAAA | 25909 |
rs544051683 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868936 | TGCAAGTTCTGCCTC[C/T]CGGGTTCACGCCATT | 25909 |
rs544110138 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246881287 | CTTATGTACCTAATA[C/T]TCAAAATACAAAAAG | 25909 |
rs544134062 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246842884 | TGATGAATTCAAACT[C/T]GCCAAATGCAAAATT | 25909 |
rs544152405 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246880658 | GATAAACTTAATTTA[C/T]GATTTACCAAGTATT | 25909 |
rs544181065 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246860212 | GGCGGAGGTTGCAGT[A/G]AGCCGAGATCACGCC | 25909 |
rs544220033 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246853497 | AAGGTAAATTTCACA[A/T]TTAAAAATGATAACT | 25909 |
rs544247738 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246910675 | AATATAACCACTGTG[A/C]AAGAGCAGATTCTCT | 25909 |
rs544286361 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246847016 | TGAAGGCTGGGCACA[A/G]TGGCTCATGCCTATA | 25909 |
rs544351663 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246882308 | GGCCTATTATTACTT[C/T]TAAACAGAGCAAGTC | 25909 |
rs544384555 | snp | A/C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246845152 | CTTCAGCTACTGGGA[A/C/T]AGTCAAGAGTTCTAT | 25909 |
rs544414828 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246839763 | TTATAAATTATTTTA[C/T]AACACTTATTTATTG | 25909 |
rs544423098 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246854593 | GAGAAAAGAAAGTTG[C/T]TTTTTTGATAATGAT | 25909 |
rs544433668 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246922910 | ATGGCATGAACCCAG[A/G]AGGCGGAGTTTGCAG | 25909 |
rs544452497 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246840129 | AGTGAGCAGTGAACC[A/G]GTCAATCTAACCTGG | 25909 |
rs544453844 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246905194 | GTTCTATTTTTGACT[A/G]ATTTTTAAAGATTGT | 25909 |
rs544484095 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246928751 | TATTGCAACATGTAC[C/G]AAGCAAACATTTCTA | 25909 |
rs544545407 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246923882 | ATAACCCCAGGAAAA[C/T]TCCAGGTCTGGAAGT | 25909 |
rs544546775 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869393 | ACTTTAAATCAAAAG[C/G]TAGACCTCTTATGCC | 25909 |
rs544611103 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246876829 | GAACTGAGGATTCTC[C/T]AAGTTCAAGGTAATG | 25909 |
rs544645239 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246901440 | AGGAGATGGCTAACA[C/T]GGTGAAACCCTGTCT | 25909 |
rs544653037 | in-del | -/AA | 0.401711 | 0.198705 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246843741 | TATTAAAACATTTGT[-/AA]AAAAAAAAAGTATGT | 25909 |
rs544738016 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246861612 | TCAAAAACATATAAC[G/T]AGTTAGAAACAACAC | 25909 |
rs544773660 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246855086 | ACCAGGAACAAAGGC[A/G]TAACAGTTGAGAGCA | 25909 |
rs544774711 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246890496 | TATTCTAAACAAATA[C/T]AGCACAAGTCAAATA | 25909 |
rs544800676 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246927362 | GCCACGGCTGCATAC[A/G]CTTGTCATCCCGACT | 25909 |
rs544813018 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246922436 | GTTTTTTGGGTTGTT[G/T]TTTTTTTTTGACAGG | 25909 |
rs544814170 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246932212 | GTGGGGAGAAAGACT[A/G]CGAGTCCCACAGTGC | 25909 |
rs544829859 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246902448 | GAACTGCCAGGAGTA[C/T]GAAATCTAGAAAATA | 25909 |
rs544865242 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246846206 | CTAAGATAATTTCTT[C/T]GCTATGTTTCAATAA | 25909 |
rs544905250 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246839287 | ATATTCACCAAATTG[C/T]GTTGGTTTAAAAAAG | 25909 |
rs544916943 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246883182 | AGTGTTTGATGGTTT[A/C]AATATTAAAACTTTT | 25909 |
rs544917646 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246915627 | TAGTCTTATTCATTT[A/G]TCTTCTCCCACTAGA | 25909 |
rs544937640 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246884038 | TAGCAACACTTTAAC[A/G]TCACTAAACAGTGAG | 25909 |
rs544952974 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246921022 | GCTTGAACCTGGGAG[A/G]AGGAGGTTGCAGTGA | 25909 |
rs544963368 | in-del | -/ACTG | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869239 | GCGTGTACTTACTCC[-/ACTG]ACTAACTGTTCCCCC | 25909 |
rs545037170 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246859716 | GAGTAGCTAGGAATA[A/C]AAGTGCATGCTATCG | 25909 |
rs545047099 | in-del | -/AAAT | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246923415 | AAGACTCTGTCCCAA[-/AAAT]AAATAAATAAATACA | 25909 |
rs545073615 | snp | A/G | 0.000109242 | 0.00738979 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246867193 | TTAAAAATTACAATT[A/G]TAACTATCATCTAAC | 25909 |
rs545086786 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246863374 | GGAGATAGTATGTTT[A/G]AAAAAAAAAAAACAA | 25909 |
rs545187046 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246932939 | CATATGTGCTTTTTA[A/C]ATTTTTTTATTTTTG | 25909 |
rs545204419 | snp | G/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246882007 | ACTTTTTTTTTTGTT[G/T]TTTTTTTTGAGATGG | 25909 |
rs545211803 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246854456 | GTGATTGGCCCAAAT[G/T]TTCAGCAATAAGCAA | 25909 |
rs545248756 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246847520 | GTTTTTGTTTTGAGA[C/T]GTGGTCTTGCTCTGT | 25909 |
rs545256461 | snp | A/C | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246839699 | AAGCAGTTCGTTTCT[A/C]GATAATCAATTATTA | 25909 |
rs545276966 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246881820 | CCCAGCCTGGGTAAC[A/G]GAGCAAGGCTCCGTC | 25909 |
rs545347964 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246874846 | TGACCTCCGGCTCTC[A/G]GCCCTCAAGAATGAG | 25909 |
rs545349787 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246873699 | AGAATCTGTCCTATA[A/C]TGAATATACTAGAGA | 25909 |
rs545352662 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246889758 | CAACACCACTTTCTT[C/T]GTCTATTACCTTTAC | 25909 |
rs545389939 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246882565 | ACTTTTGTATTACAA[A/G]GAAAAAAGGCTGAAA | 25909 |
rs545410452 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246864607 | TTGGGAGGCCGAGGC[A/G]GGTGGATCATGAGGT | 25909 |
rs545413473 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246916979 | CATAATGATAGGAAG[C/T]CTCAGAACCTCTTCT | 25909 |
rs545430867 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869358 | AGTGTTCATGTGAAA[A/G]GAGGAGTCACATGTC | 25909 |
rs545451160 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246910113 | CCTTGCCAAAATACT[A/G]AACCTTCATCTATAA | 25909 |
rs545484245 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246876707 | CTACATCTTCCTCTT[C/G]TTTTCCCTGAGTGAA | 25909 |
rs545519091 | snp | C/T | 0 | 0 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246877151 | GTTTACATCGGTAAG[C/T]AATTACCTGCTCAGT | 25909 |
rs545535994 | snp | A/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246884867 | TACAAAGAATTCCAA[A/T]ACTCAAACAACCAAT | 25909 |
rs545557792 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246870083 | TGAATAACTTTTGAG[A/G]GCTTCAAGACTTCAG | 25909 |
rs545653398 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868221 | GCAACCTCTGCCTGC[A/C]AGACTCAAGTGATTT | 25909 |
rs545669849 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246910759 | ACCCCCAAATCACTT[A/C]TGCTTCTGATGTCTT | 25909 |
rs545692719 | snp | A/T | 8.23784e-05 | 0.00641735 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246898197 | AACAATAGAGTTAAA[A/T]ATCATCTCACTTGGC | 25909 |
rs545769234 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246847239 | GGTTGCAGTGAGCCA[A/G]GATCACACCATTGCA | 25909 |
rs545799428 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869978 | AAAGGATTCACCATT[A/C]TAGATGCCATTCAGC | 25909 |
rs545802508 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246848845 | ACAGAGTGAGACTCT[A/G]CCTCAAACAAACAAC | 25909 |
rs545830589 | snp | A/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869126 | TGGATTACAGGCGTG[A/T]GCCACCACGCCCGGC | 25909 |
rs545832052 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246898872 | GCAGGCGGATCATCT[A/G]AGGTCAGGAGTTCGA | 25909 |
rs545836289 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246891465 | GTTTTGAAATTGCAA[A/C]ACAGAAAAAATTTAT | 25909 |
rs545864005 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246862619 | AAAATACAAAATTCT[C/T]CCAGAGCTTTTTATA | 25909 |
rs545866503 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246918004 | CAAACATAGATAATA[C/T]TAAGATACAAAACAC | 25909 |
rs545873322 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246892175 | CTCATAACCAGCACA[A/C]ATCAAAAGACAGGGA | 25909 |
rs545986245 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246925434 | AGATGATATAGAAGT[A/C]CTAGCTCTAAGAGAA | 25909 |
rs546006224 | snp | C/G/T | 0.0023933 | 0.0345097 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246911632 | GGGATTAGAGGCATG[C/G/T]GCCACCACACCTGGC | 25909 |
rs546009836 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246918640 | GCCACTTCACTCCAG[C/G]ATGGGCGACAGAGCA | 25909 |
rs546042676 | snp | C/T | 1.76024e-05 | 0.00296663 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246904082 | TATTAATACATTAAA[C/T]ATCTCTTACTGTCCA | 25909 |
rs546059618 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246926270 | ATATTCCTTTATAGC[A/G]ACACAGGCTAACGTA | 25909 |
rs546096486 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246901365 | AAACAGGCCAGGTGC[A/G]GTGGCTCACGCCTGT | 25909 |
rs546160394 | snp | A/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246887056 | TATTCTTGCCTTCTA[A/T]AATAGTGCTTGGTAA | 25909 |
rs546204855 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246855900 | GCTTTAGTCCTACCA[A/C]CTAACCTGTCATTTT | 25909 |
rs546222713 | in-del | -/ACAAAACAC | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246920192 | CTCACAGTCCAAATA[-/ACAAAACAC]ACAAAACACACAAGG | 25909 |
rs546238144 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246874327 | TCTATCTTCAGACAA[A/G]TACGTGTCCCTCTGA | 25909 |
rs546241650 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246849048 | TATATGTGCTCCCTT[G/T]GGGGAGAGATCACCC | 25909 |
rs546243446 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246856948 | ACCCTTACTACTACT[C/T]GATAACTGAAGCTGT | 25909 |
rs546274565 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246922593 | GAAATAAGGTCTCAC[G/T]ATGTTGCCCATGATG | 25909 |
rs546280276 | snp | A/G | 4.94328e-05 | 0.00497131 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246849683 | GGTTCAGAAAGGTCC[A/G]GCAACAAGATGGCCT | 25909 |
rs546281609 | snp | A/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246928684 | TACACAAATTCCTGC[A/T]GTAACTGAATTCCAC | 25909 |
rs546291771 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246885113 | CTAGATAAAAGGTGT[G/T]GTATGTTTTTCTTAA | 25909 |
rs546294141 | snp | G/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246916633 | CACTCCAGCCTGCGT[G/T]ACAGAGCAAGACTTC | 25909 |
rs546314204 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246929863 | TCAAGACCAGCCTGG[C/T]CAATATGGTGAAACC | 25909 |
rs546376796 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869093 | TCGTGATCCGCCCGC[C/T]TTGGCCTCCCAAAGT | 25909 |
rs546383693 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246928786 | CCACTTTGTATGCAA[C/T]GGTACTTTTTTTCTT | 25909 |
rs546448150 | snp | A/C | 1.96126e-05 | 0.00313144 | missense, nc-transcript-variant, intron-variant | AHCTF1 | GRCh38.p7 | 1:246843824 | GCTTGTTCTTATTGG[A/C]TGTGTTTTTTTGTCT | 25909 |
rs546544557 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246896499 | GAAATGTCTAGAATA[A/G]GTCAATCTATAAAGA | 25909 |
rs546546201 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246871415 | CCCAGGAACTGCTCC[C/G]ACACAAATACTCAAC | 25909 |
rs546583730 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246922791 | ATCGAGACCATCCTG[A/G]ATAACACGGTGAAAC | 25909 |
rs546626384 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246933546 | TGGGATTACAGACAT[A/G]AGCCACCATGCCCAG | 25909 |
rs546654130 | snp | A/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246904609 | AGGGTGGGGAAAAAA[A/T]TTTTTTAAAATATGG | 25909 |
rs546666663 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246930978 | CAACCAGTGGCAAAA[A/G]AAACCGTCCTGTTTC | 25909 |
rs546692591 | snp | G/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246885445 | TCATCAATTCCATTT[G/T]ATTAACAGATACGAT | 25909 |
rs546723274 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246928820 | GACTAATAAAAAGAC[A/G]AATTGTCATTTAAAT | 25909 |
rs546723316 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246923095 | AAGAAGAAGTTATTT[A/C]ATCAAATAATACCAA | 25909 |
rs546745763 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246866911 | TTCAATGAGCTACCC[A/G]AGATTAATCTGTAAT | 25909 |
rs546755428 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246875777 | AAATTAAGGTATGTA[C/T]ACTGGTTTTAAGAAT | 25909 |
rs546786225 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246924006 | CGTAGAATATAAATC[C/T]GGCAAAAGAGAGATC | 25909 |
rs546821920 | snp | C/G | | | downstream-variant-500B | AHCTF1 | GRCh38.p7 | 1:246838829 | TTCCCTTACTACTAT[C/G]ATACTAAGTATCTGA | 25909 |
rs546857311 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246917491 | CTGCCACTTACCTGT[A/G]TAACTGGGATCAAAT | 25909 |
rs546867513 | snp | A/C/G | 0.00119752 | 0.0244452 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246841440 | TTTCTCACATAGATA[A/C/G]GCCAGTTTATATGTA | 25909 |
rs546883274 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246863284 | ATCCAAACAGAGAAC[C/G]CAGGGACAATGGGGA | 25909 |
rs546886375 | in-del | -/AC | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246898408 | TAAGATTAATTAATT[-/AC]ACTTAAAATTTAAGT | 25909 |
rs546951819 | snp | C/T | 1.71352e-05 | 0.00292699 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246861947 | TTTTCTCCCAATTAT[C/T]ATCAAACTTACCCCA | 25909 |
rs546954676 | snp | C/T | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246861247 | TTTCCACTGGAACTG[C/T]ACATTTTTTAGGTGT | 25909 |
rs546982841 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246922335 | ACTGCACTCCAGCGC[A/G]GGTGACAGAGCAAGA | 25909 |
rs546992531 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246855535 | AGCCACAGAATGCCT[C/T]ACAAGCAACCCACTG | 25909 |
rs546997624 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246854633 | CAGCTAACATTTACT[A/G]AACTTCAGGTACCAA | 25909 |
rs547022079 | snp | A/C | 1.65228e-05 | 0.00287422 | missense, utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246840870 | TTTCTGTTCCTTCCA[A/C]GACCTGTTCCTGTCA | 25909 |
rs547071717 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246911807 | AAGATATTTTAAAGT[C/G]CATGTATGACCATTA | 25909 |
rs547101507 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246882697 | TACATTTATGATCCT[A/T]AGACTGAATAATCAA | 25909 |
rs547165407 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246857290 | ACAAACTTAGAGTCA[C/T]GTATTGAACAAATGG | 25909 |
rs547225408 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246911074 | GCTATAAAGTCCAAC[G/T]GCTTCCAATTCTCAA | 25909 |
rs547263776 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246877605 | GAGCTGAATGGTTGG[C/T]GTGGTGTGACAGAGG | 25909 |
rs547269923 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869858 | TGGATCACAGTAATC[A/G]CAATTTTCAAGATAT | 25909 |
rs547286727 | snp | C/T | 3.29891e-05 | 0.00406122 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246849886 | CTTAGAGCTCATCAC[C/T]ATCGAAAGTTCCTCG | 25909 |
rs547298234 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868323 | AAAGGGTTTCACCAT[C/G]TTGGCCAGGCTGGTC | 25909 |
rs547315407 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246892464 | TAGCTGGGATTACAG[C/G]CATGTGCCACAACAC | 25909 |
rs547321311 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246922855 | GGGCGTGGTGGCAGG[A/C]GCCTGTAGTCCCAGC | 25909 |
rs547338108 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246870811 | TGGCTGTGTATCAAA[C/T]ACCTCCTCCTCAGAA | 25909 |
rs547432218 | in-del | -/A | 0.00398564 | 0.0444627 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246903683 | CTCTGCTAAATATAC[-/A]AAAAAATTAGCCAGG | 25909 |
rs547443701 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246904241 | TCTAATCAACTAAAT[C/T]GATGCTGTTTGCATA | 25909 |
rs547468350 | in-del | -/A | 0.00318978 | 0.0398085 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246887448 | ACAAAATGTAGCATT[-/A]AAAGAGACTTGAAAT | 25909 |
rs547484221 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246920563 | ATCATGAGGTCAGGA[A/G]ATCGAGACCATCCTG | 25909 |
rs547484959 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246871700 | CTCTGTAATCCATGC[C/T]TACAGTGCATTTTTT | 25909 |
rs547575076 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246929596 | TTCTGGAATAGCAAA[A/G]GCATAAAATTTGTTA | 25909 |
rs547577611 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246906080 | TGCCCTACAAAGAGA[C/T]GAGATACTGCCACGA | 25909 |
rs547585109 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246854570 | AAAATGTCTTAAATA[C/T]ATTACATGAGAAAAG | 25909 |
rs547609662 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246884564 | AGTAAGGAATTTCAG[A/C]TCCAAGCAATTTCTC | 25909 |
rs547646193 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246908707 | CCTGGCTAACACGGT[A/G]AAACCCAGTCTCTAC | 25909 |
rs547653574 | snp | C/T | 6.6486e-05 | 0.00576529 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246900387 | ATTTATATCAAAAAG[C/T]CCCAAATATACAGAA | 25909 |
rs547707369 | snp | G/T | | | upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246932512 | CTGTTGCCCAGGCTG[G/T]AGTGCTGTGGCACGA | 25909 |
rs547709309 | snp | A/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246906525 | AAGTGGAGGTTGCAG[A/T]GAGCCAAGATCGTGC | 25909 |
rs547749980 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246925579 | AAGCTATGATCAGGC[C/T]ACTGCACTCCAGCCT | 25909 |
rs547750705 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246867929 | CACACACATTACGTG[A/G]TAATACTAGCTAAAA | 25909 |
rs547767445 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246920015 | GGGCGTGGAGGCATA[C/T]GCTTGTAATTCCAGC | 25909 |
rs547783515 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246912484 | GAGACGCCGTCTCCA[A/G]AAAAAAAAAACAAAA | 25909 |
rs547788463 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868254 | CTGCCTTAGCCTCCC[A/G]AGTAGCTGGGACTAC | 25909 |
rs547819324 | snp | A/C | 8.28562e-05 | 0.00643593 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246857788 | CTGCAACTAAGAGAT[A/C]CTTTGTTTCTGCATC | 25909 |
rs547990470 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246896470 | AGACTTCATATTATT[C/T]GACCCATTTATATGA | 25909 |
rs548036734 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868884 | GAGTCTCGCTCTGTC[A/G]CCCAGGTTGGAGTGC | 25909 |
rs548037969 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246893670 | TATCCATGGAGGACA[A/G]CAGTGATGCATTTTT | 25909 |
rs548062404 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246891513 | AATACATATAACTTA[A/C]TTTGAAACTTTACTG | 25909 |
rs548062458 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246883540 | CCTTTTGCAAAATTA[C/T]CAGTTCAAAAATTTA | 25909 |
rs548072731 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246847754 | AGTTAAAATTAGTAG[A/G]TACAGAAATGAAAAA | 25909 |
rs548099510 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246884442 | TGACACAGAAGTGGT[A/G]ATTGGTTCATGTATA | 25909 |
rs548117279 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246930543 | ACTCTAATTTCTTCT[C/G]TCCTAAGAGACTCTA | 25909 |
rs548134730 | snp | A/G | 1.64917e-05 | 0.00287151 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246898315 | TGAGTGATGGACCTG[A/G]TTTCTTTAAAAAAGT | 25909 |
rs548149121 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246858689 | AATTGGCTGGGCATG[A/G]TGGCACGTGCCTGTA | 25909 |
rs548149162 | snp | C/T | 1.64914e-05 | 0.00287149 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850842 | TCATAGTCATTGTGC[C/T]TGTTTCCTGAGCAGT | 25909 |
rs548205223 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246918105 | AGCTTATAGATGTTA[C/T]ATATGTAACTGTAGA | 25909 |
rs548233469 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246912092 | ATTAGTTATGTTCAT[C/T]ATAAACTACATAAAA | 25909 |
rs548234416 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246849114 | AGTCCTTAGCTCGTG[A/G]CAATGAAGGATGGCC | 25909 |
rs548238413 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246903700 | AAAAATTAGCCAGGC[A/G]TGGTGGCGGGCACCT | 25909 |
rs548241470 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246910895 | AGATGTATAAGAAAC[C/T]GGTTAAGTCTGGGGA | 25909 |
rs548273008 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246897802 | CCTAGGCAACATAGC[A/G]AGACCCTGTCTCTAC | 25909 |
rs548273195 | in-del | -/AATTCAA | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246926291 | GGCTAACGTATTTCT[-/AATTCAA]ACTTTGAATCCAGGT | 25909 |
rs548298681 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246925553 | TAAGACCAGGAGTTG[C/T]AGGTTGCAGTAAGCT | 25909 |
rs548342591 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246849517 | TTGAGGGGGGAAGGG[A/G]AAAAATTCCCTATAA | 25909 |
rs548345276 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246855417 | TCAACCTTGGCCTTA[A/C]GTTATCACAAACAAA | 25909 |
rs548351031 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246919984 | TCTCTACTAAAAATA[A/C]AAAAATAAATTAGCC | 25909 |
rs548368459 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246912453 | ACGCCACTGCACTCC[A/G]GCCTGGCAACAGAGC | 25909 |
rs548390189 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246878275 | GGTGGTGTGTGCCTG[C/T]AGTCCCAGCTATTCA | 25909 |
rs548409075 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246905226 | TGTATCAGGCCAGTC[A/G]TGGTGACTCACACCT | 25909 |
rs548410265 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246912323 | CTACTAAAAAAAAAA[A/G]AATACAAAAATTAGC | 25909 |
rs548522949 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246877541 | AAATAATAAAAAAGC[A/G]AAGTAGACAAAAATT | 25909 |
rs548533981 | in-del | -/TGAC | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869513 | CTTCAAAGGACAGGG[-/TGAC]TGACTCTGCTGTTAG | 25909 |
rs548534247 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246929482 | TGAAATTTGAGTATT[A/T]AAAAAAGGAAAGATG | 25909 |
rs548536803 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246882084 | CTCACTGCAAGCTCC[A/G]CCTCCTGGGTTCACG | 25909 |
rs548584313 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246919376 | GAAAGACAACATTTT[C/G]TTTCATACAAATGTG | 25909 |
rs548590031 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246930428 | AGTACAGAGACAACG[C/T]AGACTTCCCATAGCG | 25909 |
rs548594824 | in-del | -/AAGA | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246900993 | CATCAACAGGAGAAG[-/AAGA]AAGTAAAAATCTGAA | 25909 |
rs548607907 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869230 | TTTCCAACAGCGTGT[A/G]CTTACTCCACTGACT | 25909 |
rs548657803 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246870284 | CCCTCTCTACAAAAA[A/C]TACCCAGGCACGGTT | 25909 |
rs548676248 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246879315 | AAAGACATAGCATAC[A/G]GTAATTGAGAGGAGG | 25909 |
rs548680632 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246858283 | TTCTTCTAATTCTCT[A/G]AACCTAGCTCAAGAG | 25909 |
rs548729151 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868573 | TTTGTTTCATTATAG[C/G]TATGCTGGATTTAGG | 25909 |
rs548740734 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246912474 | GCAACAGAGCGAGAC[A/G]CCGTCTCCAAAAAAA | 25909 |
rs548748821 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246893616 | AGATTAATAAAACTG[G/T]CAAGAAGGAAAATGA | 25909 |
rs548767769 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868853 | TGTTTTTTGTTTTTT[G/T]TTTTTTTTTGAGATG | 25909 |
rs548875259 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868994 | GGACTACAGGCGCCC[A/G]CCACCATGCCTGGCT | 25909 |
rs548904047 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246857530 | ACTACTAAATGACAT[A/G]TAACTGCACAACTAA | 25909 |
rs548911220 | snp | G/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246846063 | CTACACTTTACTGGG[G/T]TGAAGTGGGAATCAA | 25909 |
rs548912398 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246921151 | CACGCAAAATGACAT[C/T]TATATAAGGTTAAAA | 25909 |
rs548932136 | snp | C/G | 0.43221 | 0.171171 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246864595 | GACTAGACTGACTTG[C/G]GAGGCCGAGGCGGGT | 25909 |
rs548943647 | snp | C/T | 1.64901e-05 | 0.00287137 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246864025 | GCAGTGAACGGGATA[C/T]TAGGTACAAAGGAGA | 25909 |
rs548968818 | snp | A/C | 0.046775 | 0.145601 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246865763 | AGTTTAAAGGTTCTG[A/C]GAAATCTTTTTAAGG | 25909 |
rs548972275 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246912352 | GCCAGGCATGGTGGC[A/G]TGTGCCTGTAATCTC | 25909 |
rs549004631 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246872487 | TGAGGTTCTGGCTTA[C/T]TCCAACCAATCCAGA | 25909 |
rs549041580 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868995 | GACTACAGGCGCCCG[C/T]CACCATGCCTGGCTA | 25909 |
rs549107673 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246859382 | TACTAGTGTTCCCCT[C/G]GCCCTCTTGTTAACC | 25909 |
rs549121711 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246879267 | TACCCATGAGATGAA[A/G]AGACAAAAAATATCT | 25909 |
rs549181627 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246901221 | TGGCATGCACCTGTA[C/G]TCCCAGCTACTCAGG | 25909 |
rs549214030 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246888026 | ATCACAGGCCATCTG[A/G]GCCCAAACAACAGAT | 25909 |
rs549218484 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246895107 | ATAAAAACAATTACA[A/T]ACAAACTATTCTAGA | 25909 |
rs549227379 | snp | A/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246898148 | ATACATTTTTACTGT[A/T]ATAGAAAGCTAATAA | 25909 |
rs549270211 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246882285 | TACAGGCATGAGCCA[C/T]CGCACCTGGCCTATT | 25909 |
rs549292303 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246852347 | AACTTCCCAAATCCT[A/C]AACAAATTTCTATAA | 25909 |
rs549305502 | snp | A/G/T | 0.00438332 | 0.0466095 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246858811 | TCTCAAAAAAAAAAA[A/G/T]AAATAAATACAAATT | 25909 |
rs549391126 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246900565 | TCTCATAAATTAAGC[C/G]GTTTAATTCATATTT | 25909 |
rs549405737 | in-del | -/A | 0.494358 | 0.0528145 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246847306 | AAAAAAAAAACAAAC[-/A]AAAAAAAAAACTGAA | 25909 |
rs549500393 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246905140 | GAAAGAATTGTGTTG[C/T]CTTCACTAAAAAAGA | 25909 |
rs549546776 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246843495 | AAAACACCCAGGTAA[A/T]TCTGATGGACACTAG | 25909 |
rs549550920 | snp | C/T | 0.00070835 | 0.0188062 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850625 | TTCTGAGATAGTCCT[C/T]TGACATCAGAATAGA | 25909 |
rs549555916 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246931889 | TCCCCTTGCAACGCT[C/G]CCTGCTCGCCTCGGA | 25909 |
rs549585429 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246844026 | ATGTGTTTTAGAAAG[A/G]TGCAAACGTCCCCAA | 25909 |
rs549607674 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246846415 | CTTTGTTAAAGGAGT[C/G]AATACTCATAAGAAC | 25909 |
rs549621095 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246927113 | AACCCGGGAGGCGGA[A/G]CTTGCAGTGAGCCAA | 25909 |
rs549635392 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246922103 | AGTGGCTCACGCCTG[C/T]AATCCCAGCACTTTG | 25909 |
rs549649890 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | AHCTF1 | GRCh38.p7 | 1:246839019 | TTAGTTTAACCAATG[C/T]TTTGATCATCAGATA | 25909 |
rs549681750 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246871750 | AGACTATAAGGAGGT[G/T]AATAATATTAAAAAC | 25909 |
rs549683977 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246906036 | TCATATTTGATGTAC[A/C]CTCCTACATACTGCT | 25909 |
rs549698389 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246930221 | GCTCACTGCAACCCT[C/T]GAACTCTCAGTTTGA | 25909 |
rs549729262 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246927416 | ATCGCTTGAACCGGG[G/T]AGGTGGAGGTAGCTG | 25909 |
rs549743131 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246854116 | CACCCTGGCTAACAC[A/G]GTGAAACCCTGTCTC | 25909 |
rs549788768 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246879107 | CTAATGCATACAAAG[C/T]GGCTATAAATCAGTA | 25909 |
rs549855644 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868992 | TGGGACTACAGGCGC[A/C]CGCCACCATGCCTGG | 25909 |
rs549857001 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246842898 | TCGCCAAATGCAAAA[C/T]TGACTCCTTTTCTCA | 25909 |
rs549872357 | snp | G/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246872311 | GGGGTGGCACGCCAG[G/T]AAAAGACTGACAAGA | 25909 |
rs549873447 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246929919 | TAGCCGGGTGTGGTG[A/G]CGTGCGCCTGTAATC | 25909 |
rs549920617 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246847391 | CTGCAGGTTTTTAAA[C/T]ACCAACCATACATAT | 25909 |
rs549923160 | snp | A/G | | | upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246933227 | CAACCTCCGCCTCCC[A/G]GGTTCAAGAGGTTCT | 25909 |
rs549936851 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246925630 | AAATATAAAAAATAA[A/G]CCTAATGTGGTTTGT | 25909 |
rs550016016 | snp | A/T | 4.04187e-05 | 0.0044953 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246900513 | AGAATAAAGAATCTC[A/T]AAGTAAAATCACCTC | 25909 |
rs550038550 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246894311 | GGCGCGGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 25909 |
rs550077374 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246858740 | TGAGGCAGAGGTTGC[A/G]GTGAGCCGAGATCAC | 25909 |
rs550082448 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246887856 | CAGCACAGAGGTTAA[C/T]GCCATTGATAGTGAC | 25909 |
rs550082799 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246906368 | GTGGATCACAAGGTC[A/G]GGAGTTCGAGACCAG | 25909 |
rs550141534 | in-del | -/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246865956 | ACTTGTTAGAGCTAA[-/T]TTTTTTTTACCATAA | 25909 |
rs550154386 | in-del | -/GG | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246877628 | GACAGAGGAACATCA[-/GG]TTTTTAAGAAGTGAC | 25909 |
rs550164080 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246921867 | TCAGGTAGAATAGAG[A/T]TCAGATAGAAGGTCT | 25909 |
rs550175289 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246920991 | CAGCTACTCAGGAGG[C/T]TGAGGCAGGAGAATC | 25909 |
rs550189054 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246875401 | ATTGACCAAAACCTG[A/C]CTTCTTGTAGAGTAG | 25909 |
rs550204117 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246846808 | CACCTGGGCTGGAGC[A/G]CAGTGGTGTGATGGC | 25909 |
rs550219454 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246914853 | CAAATGATCAATGAG[C/T]GTCCATGTTTCCTTC | 25909 |
rs550234672 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246913790 | AGTTATTCAAGCCAT[A/G]AAATCATTACGCATA | 25909 |
rs550297891 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246927071 | TAGTCCCAGGTACCC[A/G]GGAGGCTGAGGAGGG | 25909 |
rs550306158 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246928125 | GCTAACACGGTGAAA[-/C]CCCATCTCTACTAAA | 25909 |
rs550330443 | snp | G/T | 0.000399281 | 0.0141238 | downstream-variant-500B | AHCTF1 | GRCh38.p7 | 1:246838934 | TTTCTGAGTATATCA[G/T]TTACCTTACTATGAT | 25909 |
rs550358275 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246915353 | AAAAAATTACTTCAC[C/T]GTTGATTTCAAAGGA | 25909 |
rs550398192 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246873445 | CTAGTCAATTTCTCC[C/T]GCATCATAGCGAAGG | 25909 |
rs550400162 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246874331 | TCTTCAGACAAATAC[A/G]TGTCCCTCTGAGGCA | 25909 |
rs550405553 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246851564 | AATTATATTTAATAT[A/G]GCATATACTTATGGG | 25909 |
rs550433746 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246909641 | CTGGCAATTCAGATA[C/T]GCCAAAGAGAAGCTG | 25909 |
rs550543839 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246845092 | CATTTGTTATTTCAA[G/T]AATATCATTTACAAA | 25909 |
rs550552540 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246927373 | ATACGCTTGTCATCC[C/T]GACTACTTGGGAAGC | 25909 |
rs550575657 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246901805 | CCTGGACTGGCCTGG[C/G]CATCAGAGTGAGACC | 25909 |
rs550576490 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246845747 | TCTTGTTTTGAGGAT[A/T]AAGGAGTTCAAAAGG | 25909 |
rs550577452 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246933360 | GATGGTCTTGAACTC[C/T]TGACCTCGTGATCCA | 25909 |
rs550615273 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246922521 | GCCTCAATCTCCTGG[A/G]CTCTAGCAATCTCTC | 25909 |
rs550633113 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246860000 | GGCGCGGTGGCTCAC[C/G]CCTGTAATCCCAGCA | 25909 |
rs550663886 | snp | A/C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246925555 | AGACCAGGAGTTGTA[A/C/G]GTTGCAGTAAGCTAT | 25909 |
rs550668340 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246874200 | GACATGCCAACAAAT[C/T]ACGATAAAATTTCAG | 25909 |
rs550671733 | snp | C/G | 3.43956e-05 | 0.00414688 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246853216 | TCAGCGCTACTTCCT[C/G]GTTAAGCCTGCGCTC | 25909 |
rs550727418 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869050 | GGGGTTTCACCATGT[C/T]GGCCAGGATGGTCTC | 25909 |
rs550744844 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246847616 | GTGATCCTCCTGCCT[C/G]AGCCTCCCAAGTAGC | 25909 |
rs550750308 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869088 | TGACCTCGTGATCCG[C/T]CCGCCTTGGCCTCCC | 25909 |
rs550785866 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246840698 | TTCTGTTTACATAAA[A/C]ATTTACAATAATTTA | 25909 |
rs550807773 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246927831 | AACATGGTGAAACCC[C/T]GTCTCTACTAAAAAT | 25909 |
rs550826337 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246927969 | CACGCCACTGCACTC[C/G]AGCCTGGCGACAGAG | 25909 |
rs550864385 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246902232 | GGCTCAAAAAATACA[C/T]GGGTAAACTTCATTC | 25909 |
rs550906757 | snp | A/G | 9.90802e-05 | 0.00703778 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246895970 | ATGGAAAGAAAGAGG[A/G]TGTGAGATCATAGGC | 25909 |
rs550921635 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246860423 | AAATAAAAAATGTAA[C/T]ACATAAGTTCTCCTC | 25909 |
rs550960873 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246853723 | TTTTGGCAGAAAGCA[C/T]TCAAATAGGTACAAA | 25909 |
rs550994077 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246900538 | CACCTCAACAGAATT[A/G]TAGCAAGATTTTCTC | 25909 |
rs551095891 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246917788 | TTAGTATGGTTCTCT[C/G]ATGTATTACACAATC | 25909 |
rs551096776 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246921221 | AACATGACAAAACTA[C/T]GAAAAAAACAAAGAA | 25909 |
rs551115640 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246889801 | GAACTAAGTAGGTTA[C/T]TCGTGTACTTTTTTA | 25909 |
rs551116619 | snp | C/T | | | upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246932631 | TTTTTCTAGCATCCT[C/T]CTGTGCTTTCATGGC | 25909 |
rs551124026 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246918164 | TGCTTTTTCTTCTTC[C/T]ACATAAAGAAACTAT | 25909 |
rs551128848 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246887144 | TTTAATACCAAATTT[A/T]AATTATGTGTATTTT | 25909 |
rs551158893 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246922970 | CCTGGGCGACAGAGC[A/G]AGACTCTGTCTCAAA | 25909 |
rs551159893 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246921750 | ACCAAAAGTAACTGC[C/G]AACATAATTATATAT | 25909 |
rs551250064 | snp | A/G | 1.75925e-05 | 0.00296579 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246876086 | AGGCTTAGCTCGTTC[A/G]ATGGCTAATTTTCGA | 25909 |
rs551254802 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246917306 | ATCAAGTACAGACTC[C/T]GAATTTCTGCTTGAG | 25909 |
rs551263477 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246858108 | GGCACTACAGATGCC[C/T]GCCACCATGCCCTGC | 25909 |
rs551288892 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869546 | GTTAATGTAGCTGAT[A/G]ACTTTAAATTAAAGG | 25909 |
rs551302347 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246914838 | TCTCAATTCCTCATC[A/C]AAATGATCAATGAGT | 25909 |
rs551339399 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246907946 | TATCTATTTAAATGC[C/G]ACAATTTAAAAAACA | 25909 |
rs551359374 | snp | A/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246909078 | ATATCTATATATATC[A/T]ATATCTATCTATCTA | 25909 |
rs551375933 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869044 | AGAGACGGGGTTTCA[C/T]CATGTTGGCCAGGAT | 25909 |
rs551401503 | in-del | -/A | 0.277867 | 0.248442 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246858799 | GCGAAACTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 25909 |
rs551407428 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246845693 | TCTATTATAGCACAG[A/G]TGAGACTTTCTTGAG | 25909 |
rs551433871 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246887806 | TCAAATAATGCCTAA[A/G]GTAGTATCACGCTAA | 25909 |
rs551438614 | in-del | -/C | 0.00159617 | 0.0282053 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246916673 | AATAATAATAATAGT[-/C]ATTCAGTAAAAGCCA | 25909 |
rs551497296 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246912550 | TTTCGGGTCAAATAC[G/T]CCTTTTCTAAAAATT | 25909 |
rs551508378 | snp | G/T | 4.06413e-05 | 0.00450766 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246853059 | CCAAAACTGAAAGAC[G/T]GATAAAGAAGTAAAA | 25909 |
rs551516154 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246872528 | AACTGCCTTCATTTA[A/C]AAAGTTACTTAGGGG | 25909 |
rs551529844 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246914216 | TAATTAGGTATGATA[C/T]ATGATAAAATGTTTG | 25909 |
rs551536958 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246853656 | AATTACAGAATTACA[A/T]GAGGAACATGCAATC | 25909 |
rs551551076 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246873270 | TTAACCGGTGATAAA[C/T]CACCATATAAAAAAA | 25909 |
rs551654589 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246912408 | GAATTGCTTGAACAC[A/G]GGAGGCGGAGGTTGC | 25909 |
rs551704985 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246839500 | AAGTCAGTGAAATTT[A/T]CAACAAGGCAGCGTA | 25909 |
rs551709168 | snp | C/T | 0.000482567 | 0.0155258 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246875997 | ATTCAGTATCTTTTT[C/T]GATCCAATAGATTAT | 25909 |
rs551727525 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246866587 | AATTCAGAGTCTTGT[A/G]ATGATTATTTATAAT | 25909 |
rs551730148 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246881542 | AAAATTTTTTTTAAA[A/T]AGAAGCAGGGTCAGC | 25909 |
rs551741951 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246908752 | AAAAAAAAATTAGCC[A/G]GGCATGGCGGCGTGC | 25909 |
rs551787847 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246901285 | AGCAGAGGTTGCAGT[C/G]AGACGAGATCGTGCA | 25909 |
rs551861782 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246895766 | AAAATAACTAAGAAA[A/G]AAATATAACAAATAG | 25909 |
rs551899529 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246909805 | GGGGGAACTACCCTG[A/C]AGAGGGCTATCCTGT | 25909 |
rs551911099 | snp | A/C | 0.0228947 | 0.104514 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246896372 | ACAACAGAATATTAT[A/C]CAGCCATAAAAGGGG | 25909 |
rs551912057 | snp | C/T | 0.0023933 | 0.0345097 | upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246933288 | ACAGGTGTGCGCCAC[C/T]ATGCCCAGCTGATTT | 25909 |
rs551914230 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246920442 | AATGAGAGTGAATCA[C/T]AGCTACATGCAACAA | 25909 |
rs551975307 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246927931 | CTTGAACCTGGGAGG[A/C]AGAGGTTGCAATAAG | 25909 |
rs551989638 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246889350 | GGTTGTCCAATGAGC[C/T]AGGCACTGCACTAGA | 25909 |
rs552001621 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868987 | GTAGCTGGGACTACA[A/G]GCGCCCGCCACCATG | 25909 |
rs552004315 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246839890 | TACTCACTCTCTCCC[A/C]ACCTCAATAATCTGT | 25909 |
rs552026840 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246882122 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGACTA | 25909 |
rs552052789 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246927172 | GACAGAGCGAGACTC[C/T]GTCTCAAAAAAAAAA | 25909 |
rs552057863 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246890770 | GTATGAGCACTGTGT[G/T]TCAGGCATAGGATGA | 25909 |
rs552112047 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246903655 | CAAGATGGTGAGACC[C/T]CCCCCCCTCCGTCTC | 25909 |
rs552178801 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246916480 | TTACATACAACTATA[C/T]GTTCATTACATAAAA | 25909 |
rs552196153 | in-del | -/A | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869429 | CCAAGTTGTAAATGC[-/A]AAAAAAGAACCTGAA | 25909 |
rs552200780 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246910351 | ATTCCAATCCAAACA[A/G]TCCAAATGTAAAAAG | 25909 |
rs552214636 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246918481 | CACCAACAAAATAAA[C/G]AAAAACTAAAATCTG | 25909 |
rs552215648 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246917173 | CACTGGGTGGAAGAC[A/G]ACACCTGCTAGGTGA | 25909 |
rs552259591 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246903156 | ACCCGTTTCTATACG[C/T]CTCCAACATTAGGTT | 25909 |
rs552264087 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246843258 | GTCTCCTCTAACCTC[A/G]GTCTATAAAGTATTT | 25909 |
rs552289844 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246929386 | TGCACTCTAGCTTGG[G/T]CTACAAAGTGAGACT | 25909 |
rs552355316 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246870065 | AGGTGATTCCATCTT[C/T]CATGAATAACTTTTG | 25909 |
rs552379009 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246926581 | GAAATAGGGGCCAGG[C/T]GCGGTGGCTCACACC | 25909 |
rs552406535 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246877436 | AAGTACTTTAAAAAT[C/T]TGTTGAATACTAAGT | 25909 |
rs552413228 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246854682 | TACATGCAAGGGGCT[G/T]AATCCTGACAACTCT | 25909 |
rs552469509 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246928970 | TCAAGAAGATAACCT[C/T]CTTCCTGACTTTAAG | 25909 |
rs552506204 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246919436 | AATCCTCAAGAGGCC[A/G]GGCGTGGTGGCTCAC | 25909 |
rs552520354 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246848121 | GTGACGAGGGGAGAG[A/G]AGGATCCCCTATAGC | 25909 |
rs552530112 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246907481 | CTAACTTTCAAATAT[C/T]AGTAAATGAGTACAA | 25909 |
rs552532258 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246928933 | TACTTTTAAAACACC[A/G]TGTTAGTAAAGGAAT | 25909 |
rs552564781 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246908094 | AGAACTACTACCTAA[A/G]TACCTTCCTTGGAGC | 25909 |
rs552570011 | snp | A/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246884681 | TGTAATAATCATTAT[A/T]ATGTAAATGACAAAT | 25909 |
rs552589908 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246848496 | GTGAGCCACCGTGAC[C/T]GGCCAAGTCATCTAC | 25909 |
rs552619830 | snp | A/G | 6.64088e-05 | 0.00576194 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246876946 | AAGACAACTTTAATC[A/G]TACCATAACATTAAT | 25909 |
rs552721597 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869912 | GCTATAGCTGTCACA[G/T]ATAGTGATTCCTCTG | 25909 |
rs552722456 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246932174 | TTACAAAAAAATCGG[A/G]TCTCTCCGCCTCCGA | 25909 |
rs552740578 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246901830 | GAGACCCCTGTCTCT[A/C]AATAAATAAACAAAT | 25909 |
rs552758230 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246870256 | TGAGAATAGCCTGGG[C/T]GACATAGTGAGGCCC | 25909 |
rs552794824 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246856516 | GAACTAGTTAGCCAA[A/G]ATAGTGAATATGCAC | 25909 |
rs552808551 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246904275 | TAGGAGATATCTTAT[C/G]TAGCAAAGACTGATT | 25909 |
rs552836382 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246932912 | GAAAGTTTCTACTTT[G/T]CTGTTACCTTTCATA | 25909 |
rs552867179 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246862463 | CCAGCCTGGGCGACA[A/G]AGCAAGACTCCGTCT | 25909 |
rs552896494 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246927731 | TGTTCATGGCCGGGC[A/G]CGGTAGCTCAAGCCT | 25909 |
rs552901416 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868544 | GAGGTGTGAGCCACC[A/G]GCCTGGCCTACATTT | 25909 |
rs552913914 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246898553 | CAAAAGGTAGCTTAT[A/C]TATTTTTATGAACTG | 25909 |
rs552917477 | snp | A/G | 1.64961e-05 | 0.00287189 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246888204 | GGCTGCTTCAGTAAC[A/G]CCGTCTAATAGGTAC | 25909 |
rs552929147 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246839670 | CTTCACATTAAAATA[C/T]TAAAAGCCCACGAAA | 25909 |
rs553052423 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246922750 | CACTTTGGGAGGCCA[A/G]GGAGGGCGGATCACG | 25909 |
rs553089426 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246921706 | AACAGTAGTAGAAAC[C/T]GCAATTCTGGAATAT | 25909 |
rs553094916 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246915802 | ATTTTTATAAACTTC[A/G]AGTGTCCTCATAGAA | 25909 |
rs553128463 | snp | A/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246895613 | TATGGCTGTAACGGC[A/T]GCATGAGGGATCCTG | 25909 |
rs553168577 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869124 | GCTGGATTACAGGCG[C/T]GAGCCACCACGCCCG | 25909 |
rs553249694 | in-del | -/C | 0.0023933 | 0.0345097 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246929801 | GCTCACGCCTGTAAT[-/C]CCAGCACTCTGGGAG | 25909 |
rs553268887 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246842136 | TTTCATGCTATTAAT[A/G]TATAAAGAAATCCAC | 25909 |
rs553271709 | snp | G/T | 0.00320191 | 0.0398836 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246846752 | CATATATATATTTTT[G/T]GGGGGGATGGGGGTG | 25909 |
rs553276755 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246861499 | CCCTAATTGGTAATA[C/T]ACCAGTATTTTCAGA | 25909 |
rs553286912 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246854348 | GGACCCAACAAGTCC[A/G]TGGTTAGGAATCTAC | 25909 |
rs553306231 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246881770 | TTGAACCTGGGAGGC[A/G]GAGGTTGCAGTGAGC | 25909 |
rs553307622 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246910597 | AACTCTTGTATTCTT[C/T]TAACTATCTGAAGAT | 25909 |
rs553315605 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246854919 | AATTCAGGAAAGACA[C/T]TTTAAATGGTTAATT | 25909 |
rs553330090 | in-del | -/TTAC | 0.00199481 | 0.0315187 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246867442 | GGGTTTTCATTCGTT[-/TTAC]TTTGTACAGTTCTGC | 25909 |
rs553340594 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246896712 | AATATCTGAACTGCA[A/C/T]GGTGTATGAAATATC | 25909 |
rs553370946 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246890637 | AGGAAAACTGAGTTA[C/T]AGAAACTATAGTTCT | 25909 |
rs553379521 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246867946 | AATACTAGCTAAAAA[C/T]TTTAATTATATATAT | 25909 |
rs553415484 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246882921 | CTCAGAGAGGATAAC[C/T]GAACTGCCTTTGATC | 25909 |
rs553434436 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246920825 | GCACGGTGCCTCACG[C/T]CTATAATCCCAGCAC | 25909 |
rs553445475 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869286 | TCCCCGAGGACCTCC[C/T]TTATTCCTTGAGACT | 25909 |
rs553494492 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246867649 | GACTATGAAACGTGT[A/G]AGAAAACATACCTAT | 25909 |
rs553495870 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246918030 | AACACATGAGATTTT[C/T]AATAAGGAAAAATTA | 25909 |
rs553570105 | in-del | -/TAGA | 0.00358779 | 0.0422022 | utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246839698 | AAAGCAGTTCGTTTC[-/TAGA]TAATCAATTATTAAT | 25909 |
rs553581557 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246910105 | CCAAACTACCTTGCC[A/C]AAATACTAAACCTTC | 25909 |
rs553586331 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246883716 | ATCTCACAAATAGCA[C/T]TTTGAGTGGTTGTTT | 25909 |
rs553589400 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246872291 | CTAACCCAAGCTGTC[C/T]AGCTGGGGTGGCACG | 25909 |
rs553636677 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246860774 | GCCTCCCAAAGTGCT[A/G]AGATTAACTAGCATG | 25909 |
rs553658305 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246903250 | CCTCCGATCTCCTCA[A/G]GAATTCAGCCAGATA | 25909 |
rs553704259 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246929976 | AGAATCGCTTGAACC[C/T]GGGAGACGGAGGTTG | 25909 |
rs553723051 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246897400 | AAAGTTATGTAGATA[C/T]CAAATAAATATACAA | 25909 |
rs553755798 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246890289 | GGGGCTTAAAATCCT[A/G]GAAACTGTTCTAAAT | 25909 |
rs553763391 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246904636 | ATGGATGTTGCCCTC[A/G]ACCATGAGAGGCCTA | 25909 |
rs553800538 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246898859 | TCGGGAGGCCGAGGC[A/G]GGCGGATCATCTGAG | 25909 |
rs553820367 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246919489 | GAGGCTGAGGCAGGC[A/G]GATCACAAGGTTAGG | 25909 |
rs553842687 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868672 | GGACATGTGCCTTCA[A/G]CTGAAATAGGAGTTC | 25909 |
rs553858912 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246912193 | CTTTAAAAATCAAGA[A/C]TGTGCCGGGTGTGGT | 25909 |
rs553872535 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246841055 | TGCTATAAAATAAAA[C/T]TGGCTTCCCAACATG | 25909 |
rs553882206 | snp | C/T | 0.000777174 | 0.0196973 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246918284 | AAGCACAGATTCTAA[C/T]GTTATTTCGTCTTCT | 25909 |
rs553904778 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246851846 | TCCCCAAATTACCTA[A/T]CTATCCACACTTTTC | 25909 |
rs553914408 | snp | C/T | 4.95552e-05 | 0.00497747 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246913255 | TCAACTTCATTTTGA[C/T]TGCATGACAAGTCAT | 25909 |
rs553934518 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246918581 | GCAGGCGGATGAACT[C/G]ATCCCAGAAGTTCGA | 25909 |
rs553967215 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246873443 | CACTAGTCAATTTCT[C/G]CTGCATCATAGCGAA | 25909 |
rs553970951 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246924360 | TTTAAACAGAGATAT[C/T]TGAAATATTCACAAA | 25909 |
rs553974106 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246909946 | CAAAATTCACCCCCT[A/G]CTGAGAACCACTAGT | 25909 |
rs553974463 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246862543 | CACAATAGTGGTTAT[A/C]TTCTCATCTCATCTC | 25909 |
rs554036982 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246907102 | GGCTAGATGGTATAG[C/T]CTGTTGCTCTTAGTC | 25909 |
rs554037057 | snp | G/T | | | upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246933401 | CCTCCCAAAGTGCTG[G/T]GATTATAGGCGTGAG | 25909 |
rs554057878 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868377 | CCACCCGCCTTGGCC[C/T]CCCAAAGTGCTGGGA | 25909 |
rs554069657 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246925827 | TGGCTCCCAGCACTT[G/T]GGGAGGCTGAGGCAG | 25909 |
rs554074041 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246911554 | AATGGCGCAATCTCG[A/G]CTCACTGCAGCCTCC | 25909 |
rs554101909 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246892954 | CCTAATCTCTAATAC[G/T]TTTAAAACACTTACT | 25909 |
rs554138480 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246885774 | ACCACAAAAATCCAG[A/G]TAAGACTCGTTTAAA | 25909 |
rs554170758 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246862207 | GCTTATAGGCCGGGC[A/G]CGGTGGCTCACGCCT | 25909 |
rs554255633 | in-del | -/GT | | | utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246839110 | ACATTTTAATGAGCA[-/GT]GTTTTTATTCAAGCT | 25909 |
rs554255767 | snp | G/T | 0 | 0 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246890177 | GTTAACCCACAGGGT[G/T]GGTATATTTAGGTAA | 25909 |
rs554292846 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246929844 | GGATCACGAGGTCAG[A/G]AGTTCAAGACCAGCC | 25909 |
rs554336031 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246892138 | GACTATGAACTCAAA[C/T]CATCTATATCTAGAG | 25909 |
rs554336903 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246897283 | CACGTCACTGCACTC[C/T]AGTCTGGGCAACAGA | 25909 |
rs554364072 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246922711 | CAATAGGCTGGGCGC[A/G]GTGGCTCACGCCTGT | 25909 |
rs554392378 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246882866 | TACCAGCATGAAGTT[A/T]TAGAGAAATGCAAAG | 25909 |
rs554410222 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246854841 | GTTCAGCCCCCTGCA[C/G]TCTTCAGGCACCGTC | 25909 |
rs554412399 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246928070 | CGCCTGTAATCCCAA[A/G]GCAGGTGGATCACGA | 25909 |
rs554549376 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246889065 | TGGTCCATCCAGCCA[A/G]TGACCATTCTATTTT | 25909 |
rs554552698 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246854191 | GTAGTCCCAGCTACT[C/T]GGGAGACTGAGGCAG | 25909 |
rs554564072 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246911403 | TTTTCATTTAAACTT[A/C]ACATAAAAATTTTAT | 25909 |
rs554581310 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246896566 | GGATGGGGCAGGCAG[A/G]AAGGTAAGGGAAAAG | 25909 |
rs554588297 | snp | C/T | 1.64904e-05 | 0.00287139 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246877014 | TTGGCACGCTGCAAA[C/T]GGTGCACTAAAAGGA | 25909 |
rs554616820 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246889486 | ATAACAGATCTAGAA[C/T]TTTAAAATATGCCTA | 25909 |
rs554625253 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246870001 | CATTCAGCACATTCA[A/C/T]AATTCCTGGGAGGAG | 25909 |
rs554688513 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246933957 | AAGAGATCTCTTCAA[A/G]CAGAAACCACCCTCT | 25909 |
rs554702140 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868913 | GCAGTGGTGTGATCT[C/T]GGCTCACTGCAAGTT | 25909 |
rs554707668 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246894977 | TTAATCATGAGGAGC[A/G]ACGGCAAGCACAAAC | 25909 |
rs554747558 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246847454 | GGTGATTCTTTCGAT[A/G]GCTGGATTATATACT | 25909 |
rs554782185 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246840170 | GACTAATTAAGACTT[C/T]AAAGAGCCTTTAAGC | 25909 |
rs554834471 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246876543 | AAAAGCAAGACTCAG[A/T]GTGTGTCCCAAGCAC | 25909 |
rs554869556 | snp | C/T | 0.00228352 | 0.0337127 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246877270 | AACCTATTGCAATGT[C/T]GCCGCAAAAAATTCC | 25909 |
rs554869863 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246856725 | CTTTCATACTGGCTT[C/T]TACTTTTTCCATGCA | 25909 |
rs554889383 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246929820 | GCACTCTGGGAGGCC[A/G]AGGCGGGCGGATCAC | 25909 |
rs554898776 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246898816 | TTTCAGGCCAGGCAC[A/G]GTGGCTCACGCTCAT | 25909 |
rs554937308 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246892053 | TTTATAAAGACAAGC[C/T]AGAAATGGCAAAACC | 25909 |
rs554963187 | in-del | -/AA | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246926047 | GAGACCCTGTCTTTA[-/AA]AAAAAAAAAAAAAAA | 25909 |
rs555034902 | in-del | -/TG | 0.00159617 | 0.0282053 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246891708 | CTAAGACATGGGAAA[-/TG]TGTTATTCGTTTCTC | 25909 |
rs555045486 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868227 | TCTGCCTGCCAGACT[C/G]AAGTGATTTTCCTGC | 25909 |
rs555091550 | snp | A/T | 0.0479149 | 0.147179 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868356 | GAACTCCTGACCTCA[A/T]GTGATCCACCCGCCT | 25909 |
rs555113444 | snp | A/G | 1.64871e-05 | 0.00287111 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246855793 | TTAATCCTTCGTCCA[A/G]CACTGGTACCTTGGA | 25909 |
rs555141999 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246898045 | TGGGTATTAGGAATA[A/G]GAATTTTAAACCAAA | 25909 |
rs555203135 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246920175 | AAAAAAAAAGAAAAG[A/C]AGCTCACAGTCCAAA | 25909 |
rs555269712 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246864344 | ATTTTTAAAAAGAGT[C/T]TGCGTCGTCCTCCTT | 25909 |
rs555312138 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246884934 | AATTCTCAATTTGTC[A/G]ACTCTATCACTTCAT | 25909 |
rs555379081 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246876458 | GTGTCAGGCAACATT[A/C]TACTTCACACACATC | 25909 |
rs555407233 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246886635 | GTTGATTGAAGCCAC[A/G]GATGTAGAATCCATG | 25909 |
rs555426521 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246870422 | ACAAAGACCTTGTCT[C/T]TTAAAAAAACAAAAA | 25909 |
rs555433194 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246852877 | ACTATGGGCACCCGC[C/T]ACAGCACCCACCTCC | 25909 |
rs555433291 | in-del | -/A | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246881384 | ACAAAACAGACTAGG[-/A]AAAAAAAATTATTCA | 25909 |
rs555450441 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246887410 | ACAAAAACCTCCTAC[A/G]TATATATTTACAATA | 25909 |
rs555451494 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246877945 | TTTTTTTTAATGCCA[C/G]TGTTCAACTCATACC | 25909 |
rs555468349 | snp | C/T | 0.000617846 | 0.0175653 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246900015 | ACGTATACATTTACA[C/T]ACTTTTGTGCATTAC | 25909 |
rs555478272 | snp | A/T | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246851096 | GGCAAATTTGCAATT[A/T]GTCCATGATTATCAT | 25909 |
rs555506890 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246893966 | ACCAACACTTTGGAA[A/G]GCCCAGGCAGGAGGA | 25909 |
rs555591245 | snp | A/G | 1.70618e-05 | 0.00292072 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246899523 | GGCATCTAAAAAAAA[A/G]ATTTAAAAAATAATC | 25909 |
rs555618531 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246905434 | TCCGGGAGGCGGAGG[C/T]TGCAGTGAGCCGAAA | 25909 |
rs555618588 | snp | C/T | 1.68875e-05 | 0.00290576 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246913441 | TACGTGATTTGCTTT[C/T]CTTCTGCAAAGTAAG | 25909 |
rs555623651 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246844499 | GCTGAGGTAGGAGGA[C/T]GGCTTAAGGCCAGGA | 25909 |
rs555626225 | in-del | -/GAGGCAGAAGAATCACCTGAACCCAG | 0.0126979 | 0.078662 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246909317 | GCTACTTGGGAGGCT[-/GAGGCAGAAGAATCACCTGAACCCAG]GAGGCAGAAGAATCA | 25909 |
rs555655328 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246906299 | GCTGACAAACTGGCA[C/G]CCGGGCGTGGTAGCT | 25909 |
rs555656253 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246864219 | TAACTATGATAGCCA[C/T]ATGCAAATACAGTCA | 25909 |
rs555688685 | in-del | -/G | 0.00318978 | 0.0398085 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246921292 | CGGAAGAATATACGA[-/G]GGACTCTGAAGTAGT | 25909 |
rs555690001 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246917428 | CACAGTTTAAGAAAG[C/T]AGCATGGTACAGTGG | 25909 |
rs555704643 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246921447 | CAACAAAAACAAACT[C/G]AAAGGATAAGTAAAA | 25909 |
rs555709344 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246848686 | GCCTGGCCAACATGG[C/T]GAAATGCTGTCTCTA | 25909 |
rs555711242 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246854106 | AGATCGAGACCACCC[C/T]GGCTAACACGGTGAA | 25909 |
rs555750081 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246848436 | TCGATCTCCTGATCT[C/T]GTGATCCACCCGCCT | 25909 |
rs555772012 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246872937 | GGGTTCACCTTAAGA[A/C]TCAAAAATCCAAATC | 25909 |
rs555810907 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869018 | CCTGGCTAACTTTTT[C/G]TATTTTTAGTAGAGA | 25909 |
rs555883756 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246930804 | TTACGTTTTGTTCTA[C/T]GAAGAACCCAGTTCT | 25909 |
rs555942778 | snp | G/T | 0.000726375 | 0.0190436 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246931236 | GTCCATCGCGTGGGA[G/T]AACAGTGGGAAAGGG | 25909 |
rs555945023 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246926724 | ACCAGGTGTGGTGGC[A/G]CATGCCTATAATCCC | 25909 |
rs555983296 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246870408 | AGCATCTGTGACAGA[A/C]AAAGACCTTGTCTCT | 25909 |
rs555990403 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246877857 | AGATCATTTAAATGA[A/C]GGAGTGTTTCTTACA | 25909 |
rs556019564 | in-del | -/ACT | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246884182 | GTAAATCTTATTGAA[-/ACT]ACAATTTTGATCTCA | 25909 |
rs556020281 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246870956 | AGACAAACAATACAA[A/C]TGAGCCTTCGAAAAA | 25909 |
rs556031325 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246896218 | AATTCCACACCTAGG[C/T]ATATACCAAAAAGAA | 25909 |
rs556050644 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246873470 | CGAAGGGAAAGAATC[C/T]GTCCCAATACTAAAT | 25909 |
rs556079169 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246929137 | CAGTGGGCTGGGTGC[A/G]GTGGTTCACGCCTGT | 25909 |
rs556132703 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246899652 | ATAAACTTTTCTAGG[C/T]ATTTTCATCCTAAGA | 25909 |
rs556136510 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246841822 | TTTGAGACAGAGTCT[C/T]AGTCTGTCACCCAGG | 25909 |
rs556184458 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246901519 | GCCCCAGCTACTTAG[C/G]GGGCTGAAGCAGGAG | 25909 |
rs556210791 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246924387 | CAAAACATTAGTGCC[A/G]TTTATTTTTGTGTGA | 25909 |
rs556359070 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246929920 | AGCCGGGTGTGGTGG[C/T]GTGCGCCTGTAATCC | 25909 |
rs556378764 | snp | C/T | 0.000176081 | 0.00938134 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246857839 | ATACAAATAAGAATA[C/T]TATTTATGCTAAATA | 25909 |
rs556385847 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246886539 | TGTTATAGTGTAACA[C/T]CTAGGGAATAATGAC | 25909 |
rs556395703 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246920089 | CAGTTGCAGTGAGCC[A/G]AGATTGTGCAACTGC | 25909 |
rs556416104 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246912247 | CTTGGGAGGCCAAGG[C/T]GGGCGGATCACAAGG | 25909 |
rs556437164 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246930659 | TTCAAGCGATCCTCC[C/T]GCCTCAGCCTCTCAA | 25909 |
rs556438963 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246906954 | AAAGAACTCATATTA[C/T]ACAAACACAGCCATG | 25909 |
rs556456915 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246912685 | TACAAGCATTTAAAG[C/G]AGAAAAAGTATTTCA | 25909 |
rs556468722 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246920799 | AATTATTAAACAATA[A/C]AAGCATCCAGGCACG | 25909 |
rs556522084 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246913577 | AAATCTTCAGCTATA[C/T]TAGGAATTACACCAT | 25909 |
rs556560775 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246914314 | CCCAGGCATTTTGGA[C/T]AGGGGATTCTCAACC | 25909 |
rs556598431 | snp | A/G | 0 | 0 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246872203 | GATCTAAAAGATAAA[A/G]CAGATCAAGGATCTA | 25909 |
rs556643290 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246861643 | AATATAAGGTAAAAA[C/G]AAAGATAAAAGAAGG | 25909 |
rs556658509 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246930006 | GCAGTGAGCCAAGAT[C/T]GTGCCACTGCACTCC | 25909 |
rs556728227 | snp | C/T | 4.96118e-05 | 0.0049803 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850284 | CATCTAAATTAGTAC[C/T]TCTCAATTTTCTGAT | 25909 |
rs556740844 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246907297 | ATGCTTTACTAGCAT[A/G]TTAAACACATGACTG | 25909 |
rs556765007 | snp | G/T | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850893 | ATTTAGTGGGACACA[G/T]TATGTTTTGGCTCAC | 25909 |
rs556800453 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246931836 | GACCGCTCAGCGGCT[A/G]AAACGCAGTCGCTGC | 25909 |
rs556837986 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246880334 | CTTTGGGAGCCCGAG[A/G]CGGGCAGATCACGAG | 25909 |
rs556844378 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246926913 | GCCGCGGTGGCACAC[A/G]CCTGTAATCCCAGCA | 25909 |
rs556845538 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246858962 | GCCAGGACCGGTGGC[A/G]CATGCCTGTAATCCA | 25909 |
rs556872080 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246900729 | TTTCAGTTAATACTT[C/G]AGCAACGTTGAGGTA | 25909 |
rs556909009 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246846078 | TTGAAGTGGGAATCA[A/G]ACGATATATGAATGT | 25909 |
rs556951238 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868983 | CTGAGTAGCTGGGAC[A/T]ACAGGCGCCCGCCAC | 25909 |
rs556959381 | in-del | -/TT | 0.00159617 | 0.0282053 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246876705 | CTCTACATCTTCCTC[-/TT]GTTTTCCCTGAGTGA | 25909 |
rs556997629 | in-del | -/AAAAC | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246866642 | AATTTTGTCTTTGAT[-/AAAAC]AATCAAAAATTTCCA | 25909 |
rs557006429 | in-del | -/CT | 0.00318978 | 0.0398085 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246920763 | TGACAGAGCAAAACA[-/CT]GTCTCAAAAAAAAAA | 25909 |
rs557078431 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246921008 | GAGGCAGGAGAATCG[C/T]TTGAACCTGGGAGAA | 25909 |
rs557080972 | snp | A/G | 0.000803535 | 0.020028 | utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246839513 | TTTCAACAAGGCAGC[A/G]TAACATCCATCACTA | 25909 |
rs557117270 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246908043 | TTTAGGGTTAACAAC[C/T]ATAAATAAAACTGAT | 25909 |
rs557120961 | snp | A/G/T | 0.00358779 | 0.0422022 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246881243 | ATAATAATTTTAAAA[A/G/T]TCATTTTAAAAAAGA | 25909 |
rs557124294 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246865173 | CTTCTCGATTTCCTA[A/T]TAAACAGTCTATCTT | 25909 |
rs557150704 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246865928 | TTTAAAAAATTGATT[C/T]ATGTAACTTTTTACT | 25909 |
rs557159367 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246873569 | TAAATATACTAGAGA[A/C]AATACACTAGTCAAT | 25909 |
rs557226262 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869261 | AACTGTTCCCCCGCG[C/T]CTCTCCCTTTCCCCG | 25909 |
rs557262592 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246867585 | TAGGCAAAGAGAGTG[C/G]ATTGTTGATGAACGC | 25909 |
rs557293266 | snp | A/G/T | 0.00159649 | 0.0282165 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246926549 | ACTACAGAGAACATC[A/G/T]AAACACTCTATTATT | 25909 |
rs557300680 | in-del | -/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246913098 | AGATTTTAAAATACC[-/T]TTTTTTTTTTTATAG | 25909 |
rs557318167 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246920268 | TGAAATTACCAGAGA[G/T]TAGAAAGTAAATGTC | 25909 |
rs557329819 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246901994 | GTGATTTAATCCTCA[C/T]AACTACCCTTTGCAA | 25909 |
rs557356657 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246920702 | ATGAACCTGGGAGGC[A/G]GAGCTTGCAGTGAGC | 25909 |
rs557363641 | snp | C/T | 0.000131796 | 0.00811668 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246867644 | AGCATGACTATGAAA[C/T]GTGTAAGAAAACATA | 25909 |
rs557415850 | in-del | -/TAAG | 0.00119737 | 0.0244387 | downstream-variant-500B | AHCTF1 | GRCh38.p7 | 1:246838869 | CCCTTACTACGATAC[-/TAAG]TATCTTTCTGAGTAC | 25909 |
rs557424396 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246864703 | AAATTAGCCGGGCGC[A/G]GTGGCGGGCGCCTGT | 25909 |
rs557436498 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246888885 | CTGCAGCCTGGGCAA[C/G]AGAGACCCTGTCTCT | 25909 |
rs557450253 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246874558 | GAAACGGCCACCCAA[A/C]AAAATATAAAACCCA | 25909 |
rs557487247 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246922806 | GATAACACGGTGAAA[C/T]CCTGTCTCTACTAAA | 25909 |
rs557489543 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246891732 | GTTTCTCTTAGTCAA[C/G]AAGTAAAATTTAATA | 25909 |
rs557531007 | in-del | -/TAC | 0.00755907 | 0.0610114 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246889606 | GCACAGATTTTAAAG[-/TAC]TGATTCCCAGGTGAT | 25909 |
rs557571183 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246915740 | CAAGACTATTGTCGC[A/T]AATTTAAAAGGTAAA | 25909 |
rs557607783 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246909283 | TTGGCCGCACATGGT[C/G]GTGTGCAACTGTAGT | 25909 |
rs557629134 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246864378 | TTTACCTATATTTAC[C/T]GAGCTCTTACTATGT | 25909 |
rs557630126 | in-del | -/AAG | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246843750 | ATTTGTAAAAAAAAA[-/AAG]TATGTTTTAACAAAC | 25909 |
rs557643676 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246906433 | AAAAAAATACAAAAA[A/C]TAGCTGGGTTCAGTG | 25909 |
rs557646597 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246909964 | GAGAACCACTAGTTT[A/C]AAGTTGATGACAGAC | 25909 |
rs557684873 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246909718 | AGGAAAAATCATAAT[A/G]TGTGCAGGGTTCAGT | 25909 |
rs557772693 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246852753 | CATGAAAACCAGTTT[A/G]TTTATTTATTTATTT | 25909 |
rs557812241 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246906648 | TGAGATACACTTCCT[A/G]TAAGATAAATTACTC | 25909 |
rs557817726 | snp | C/G | 0.000153151 | 0.0087494 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246931275 | CCGGCCGTCCGTAAA[C/G]GGACCCGACTGCCGG | 25909 |
rs557833335 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246873082 | AGCCCTCAGATCAGG[A/C]GCTACTAGGTTCGAC | 25909 |
rs557865093 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246872096 | TCCCAAAAACCTAGG[A/G]TGGTCTCTAACTAAA | 25909 |
rs557886675 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868999 | ACAGGCGCCCGCCAC[C/T]ATGCCTGGCTAACTT | 25909 |
rs557895592 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246887604 | CAAAGGAGATAAAGC[A/G]TATTTTTATGAAGTC | 25909 |
rs557970533 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246873528 | TCTCCTGCATCACAG[C/T]GAAGGGAAAGAATCC | 25909 |
rs557999988 | snp | C/T | 3.33139e-05 | 0.00408116 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246900138 | TCCTCTATTTAAACT[C/T]CTCTCATGTACTAAT | 25909 |
rs558046139 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869097 | GATCCGCCCGCCTTG[C/G]CCTCCCAAAGTGCTG | 25909 |
rs558080917 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246922786 | AGGAGATCGAGACCA[A/C/T]CCTGGATAACACGGT | 25909 |
rs558093643 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246915095 | CCAGCACTTTGGGAG[C/G]CTAAGGCAGGTGGAT | 25909 |
rs558147399 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246931932 | CGCTCTGCGCATTAC[C/T]CTGCGCCGACAAAAC | 25909 |
rs558166538 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246901882 | GCTCATGACAACATG[C/T]GCTTTTCACATATTT | 25909 |
rs558183131 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246896151 | AGCCACTCTGCAAAG[C/T]AGTTTGGCGGTTTCT | 25909 |
rs558189602 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246866271 | TCTATTATTGCTCCC[C/T]GCAACCTCAGAGCCA | 25909 |
rs558196828 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246926956 | AAGGCGGGCGGATCA[C/T]GAGGTCAGGAGATCG | 25909 |
rs558198692 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246888054 | GATCCTGGGTTAACA[A/C]CTCTTCTTAAGAAAA | 25909 |
rs558209220 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246895215 | TGGGATTTCAATAAG[C/G]TCTCTAGGTTAGATA | 25909 |
rs558237378 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246881143 | TAAAGTAAAAAGACT[A/G]GGGAAATATACATAC | 25909 |
rs558297807 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246901290 | AGGTTGCAGTGAGAC[A/G]AGATCGTGCAAGTGC | 25909 |
rs558309245 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246927164 | GCCTGGGCGACAGAG[C/T]GAGACTCTGTCTCAA | 25909 |
rs558309507 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246921559 | CTAAGATATGCCTAA[G/T]CAGAATCCCCCCAAA | 25909 |
rs558320309 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246896544 | AGTCATTATGTAAGG[C/T]TGGGTAGGATGGGGC | 25909 |
rs558355086 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246898900 | CGAGACCAGCCTGGC[A/C]AACATGGTGAAACCC | 25909 |
rs558361900 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246908443 | CTCTGAAAATTAGTA[C/T]TTAAGAAACACTAAA | 25909 |
rs558372239 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246922177 | TCAGCCCAACCAGTA[C/T]GGTGAAACCCCATCT | 25909 |
rs558417670 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246913615 | TACATAGAAAAATCA[C/T]GCAGTTGGACTAACA | 25909 |
rs558420011 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246927805 | GTCAAGAGACCCAGA[C/G]CATCCTGGCCAACAT | 25909 |
rs558463322 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246889169 | TTTCTGTTTCATCAC[C/T]TGGGTTAGTCTTTTA | 25909 |
rs558486819 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246866952 | AACAACCCTCATTTA[C/G]AGGTCTACTAACAAG | 25909 |
rs558500066 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246881861 | AAACCAAAAAAAAAA[A/C]CAAAAAAAAAAGAAG | 25909 |
rs558513389 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246917013 | CCTATTAGTCATGTT[A/T]GGATTTTACCCTGCC | 25909 |
rs558552411 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246917582 | TCCAATGAAGTCATC[A/G]TACAATGCCTGGCAT | 25909 |
rs558607049 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246928267 | GACATCGCGCCACTG[C/T]ACTGTAGCCTGGGCG | 25909 |
rs558628182 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246893905 | TGCTGCAAAATCTTG[C/G]TCAAAAATTACTTTT | 25909 |
rs558662453 | snp | C/T | 1.65138e-05 | 0.00287343 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246840890 | TGTTCCTGTCACTTC[C/T]GTAGTTTTTCTTGGT | 25909 |
rs558662773 | snp | G/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246879108 | TAATGCATACAAAGC[G/T]GCTATAAATCAGTAA | 25909 |
rs558696949 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246919170 | GGGAACCCTGATCTT[A/C]TTCTGGGCACTCTAA | 25909 |
rs558702869 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246910116 | TGCCAAAATACTAAA[C/T]CTTCATCTATAACCA | 25909 |
rs558731070 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246928040 | AAATACTGTTCGGCC[A/G]GGTGCGGTGGCTCAC | 25909 |
rs558745198 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246889602 | GCCGGCACAGATTTT[A/C]AAGTACTGATTCCCA | 25909 |
rs558759040 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246854159 | AAAAAATTAGCCAGG[C/T]GTGGTGGCGGGCACC | 25909 |
rs558818846 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246855051 | CTGCTGAAGCTTGCC[A/G]TATACCCCATTCATA | 25909 |
rs558884765 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246911285 | ACTATGAAACAAAAG[C/G]CTATCAAGCCTACTT | 25909 |
rs558897806 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246875736 | CTCAGATGATCCTTA[C/G]CATTTTTTAGCAATA | 25909 |
rs558903673 | snp | A/C/T | 3.31957e-05 | 0.00407394 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246900324 | AAGGAGAGAGAAAAA[A/C/T]AAAGAATCATACCTT | 25909 |
rs558972488 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246910665 | CTCATATATTAATAT[A/C]ACCACTGTGCAAGAG | 25909 |
rs558983340 | snp | C/T | 1.67882e-05 | 0.00289721 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246862071 | GCTAAAGGTGTTGAT[C/T]GAAGAGTAGACCTCA | 25909 |
rs559013335 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246855045 | ACTAGTCTGCTGAAG[C/T]TTGCCGTATACCCCA | 25909 |
rs559013750 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246845070 | GTAAGTGCTCTACAG[A/T]TGTTTGCATTTGTTA | 25909 |
rs559032029 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246931597 | ACGGGGCGGGTGAGC[A/G]CGCCGCCGCGGGCCG | 25909 |
rs559053589 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246915173 | CATCTCTACTAAAAA[C/T]ACAAAAATTAGCTGG | 25909 |
rs559075160 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869633 | CTGTCTTCTATCAAT[G/T]GAAAAAGCCTAGATG | 25909 |
rs559152757 | snp | A/G | 0.0509478 | 0.151255 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868341 | GGCCAGGCTGGTCTT[A/G]AACTCCTGACCTCAT | 25909 |
rs559174020 | snp | A/G | 2.87129e-05 | 0.00378888 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246851472 | GATAAGAGACTGGTT[A/G]AAGAATTTTAATACA | 25909 |
rs559230978 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246897467 | TTAATGATGGGGATA[C/T]ATTCCGATGAATGTT | 25909 |
rs559302152 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246891219 | TCTTGAACTAATTCA[C/T]CTTTGTATTTAGTTT | 25909 |
rs559355413 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246894836 | AAGCATGGCAGACAG[C/T]ACCCTAACCGAGTGA | 25909 |
rs559390473 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869037 | TTTTAGTAGAGACGG[A/G]GTTTCACCATGTTGG | 25909 |
rs559426181 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246851980 | AATTCCTAAGGCTTT[C/G]AAGTTCAGTACCTCT | 25909 |
rs559480201 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246853029 | TTTGAACTACTGTGT[A/C]TTGAAACAACTAAAC | 25909 |
rs559482166 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246860281 | TCAAAAATTAAATAA[A/G]TAAAAATTGCAATAA | 25909 |
rs559487889 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246887758 | TAAGTAACTAACATT[A/T]GCACAAAAATATTAT | 25909 |
rs559489165 | in-del | -/GA | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246894099 | GTCCAAGCTACTCAG[-/GA]GGCTGAGGCAGGAGG | 25909 |
rs559525845 | in-del | -/ATAG | 0.00358779 | 0.0422022 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246882441 | TAAAACTTCTAAATC[-/ATAG]ATAGGGAAAATAAAC | 25909 |
rs559541673 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246915190 | CAAAAATTAGCTGGG[C/T]GTGGTGGTGCACGCC | 25909 |
rs559545726 | in-del | -/A | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246852656 | TATGATCTTATGACT[-/A]AAAAAAACCTTTCAT | 25909 |
rs559604446 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246873559 | GTCCCAATAATAAAT[A/G]TACTAGAGACAATAC | 25909 |
rs559640010 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869226 | CATTTTTCCAACAGC[A/G]TGTACTTACTCCACT | 25909 |
rs559652130 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246873260 | GAAAAAAATCTTAAC[C/T]GGTGATAAATCACCA | 25909 |
rs559663632 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246915221 | TGTAGTCCCAGCTAC[G/T]CAGGAGGCTAAGGCA | 25909 |
rs559684935 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246845449 | GGCAGAAATGGCAAT[C/G]GCTAGGTCTACTGGT | 25909 |
rs559712478 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246859973 | AAGTTAAAAATTGCA[A/G]TAATTTGGCAGGGCG | 25909 |
rs559728735 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246860257 | TGGGCAACAGAGTGA[A/G]ACTCTGTCTCAAAAA | 25909 |
rs559736321 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869075 | GGTCTCGATCTCCTG[A/G]CCTCGTGATCCGCCC | 25909 |
rs559784944 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246866525 | TGTACTTCTGGCCTC[A/C]GTTGTTTGTATGACC | 25909 |
rs559822556 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246858629 | GGTCAGGAGTTCGAG[-/A]CCAGCCTGGCCAACA | 25909 |
rs559874918 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246881602 | AGCACTTTGGGAGGC[C/T]GAGGCGGGCGGATCA | 25909 |
rs559896963 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246840195 | TTAAGCTTGCCGAAT[A/G]AGAGATGCCAACATT | 25909 |
rs559910266 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246896338 | TTAATTGTAGATAAA[C/T]AAATTATGGTATGCT | 25909 |
rs559948660 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246881489 | TAAATGGAGAATACA[C/T]TGAGTACTTATCAGT | 25909 |
rs559973618 | snp | C/T | 0.00199481 | 0.0315187 | upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246933157 | TTTATTTATTTGAGA[C/T]GGAGTCTCGCTCTGT | 25909 |
rs559985033 | in-del | -/TT | 0.0146672 | 0.084371 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869143 | CACCACGCCCGGCCG[-/TT]TGTGTTTTGTTTTTT | 25909 |
rs560053448 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246917869 | TTTTCTGAAAATTTT[A/C]TAACATCTAGGGCCC | 25909 |
rs560056357 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246903570 | TGCGGTGGCTCACAC[C/T]TGTAATCCCAGCACT | 25909 |
rs560065741 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246839847 | TGTAGAGAACAGGGC[A/G]TGTGTTGTTTTTCTC | 25909 |
rs560086695 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868896 | GTCACCCAGGTTGGA[C/G]TGCAGTGGTGTGATC | 25909 |
rs560090179 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246910736 | CACTGTCCTAGAACA[C/G]GGCCCCCACCCCCAA | 25909 |
rs560098533 | in-del | -/A | 0.309399 | 0.242841 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246845370 | TATGATTCTTAAAAA[-/A]AAAGAAAAATAGAGT | 25909 |
rs560127584 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246898151 | CATTTTTACTGTAAT[A/G]GAAAGCTAATAACGT | 25909 |
rs560131762 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246903145 | GATTCCCTGAAACCC[A/G]TTTCTATACGCCTCC | 25909 |
rs560164791 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246928086 | GCAGGTGGATCACGA[A/G]GTCAGGAGATCGAGA | 25909 |
rs560173430 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868125 | GGCCACCAAGCCCGG[C/G]TAATTTTTTTTTTTT | 25909 |
rs560191260 | snp | G/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246927157 | CACTCCAGCCTGGGC[G/T]ACAGAGCGAGACTCT | 25909 |
rs560191505 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246928848 | AATGTAAACTACCAG[C/T]GGACCCAGAAACTTC | 25909 |
rs560257366 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246910275 | GAAAGAGGATTGCTG[C/T]ACGTTCAAGGAGACT | 25909 |
rs560264469 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246924774 | CATTAAGTCACAAAA[A/C]CTAAAAAGTTATGTT | 25909 |
rs560276265 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246922937 | GCAGTGAGCCGAGAT[C/T]GCACCACTGCACTCT | 25909 |
rs560339923 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246891348 | GCTACACTTTCATTT[A/C]GCTAATTCCAGAACT | 25909 |
rs560462159 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246861260 | TGCACATTTTTTAGG[C/T]GTAGTAAATACTTCT | 25909 |
rs560480961 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246855183 | ACACAAGATGATCAG[A/G]CCAATTCTGGGCATA | 25909 |
rs560503025 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246920000 | AAAAATAAATTAGCC[A/G]GGCGTGGAGGCATAC | 25909 |
rs560543120 | snp | C/T | 0.0012598 | 0.0250662 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246888501 | CAATCATCAAGCAAT[C/T]GGGATTCCACTTCCC | 25909 |
rs560551915 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246890699 | GAACTCATTTTCAGG[A/G]GCTATGTTTTCTCAA | 25909 |
rs560565502 | snp | A/G | 1.66671e-05 | 0.00288674 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246855838 | TTTTCCTTTAGAAAA[A/G]GAAATACATACCTTA | 25909 |
rs560567798 | snp | A/C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246916477 | CATTTACATACAACT[A/C/G]TATGTTCATTACATA | 25909 |
rs560585240 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246881456 | CATGGGGACAAATAT[A/G]TTTGACATTTCACCT | 25909 |
rs560585323 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246889260 | TATGGTCCCTATTTC[C/T]TTTTCTTTTCTCTTC | 25909 |
rs560601656 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246925596 | CTGCACTCCAGCCTG[A/G]GCAAGATCCTGTTTC | 25909 |
rs560622113 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246882001 | ATTATTACTTTTTTT[G/T]TTGTTTTTTTTTTTG | 25909 |
rs560670894 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246919801 | CCACATATCCTCTGG[A/C]ATCTCAAAGAATTCT | 25909 |
rs560680848 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246863229 | TCTTTTATTCAACTT[A/G]AAAAATAAGGATTCC | 25909 |
rs560689304 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246853510 | CATTTAAAAATGATA[A/C]CTGATAAACGGTATC | 25909 |
rs560693230 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246927398 | GGAAGCTGAGGCATG[A/G]GAATCGCTTGAACCG | 25909 |
rs560717556 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246896180 | CTCAGTATGCTAAAC[A/G]TAGACTTACCACACG | 25909 |
rs560733683 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246878110 | AGTATAAGAATATAC[A/G]GTAAGAGCCAGGCAT | 25909 |
rs560735966 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246880862 | AGAAGACAATAATGA[C/T]GCTAGGAAGAACAAT | 25909 |
rs560748774 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246918995 | ATCAAGTTTGGTACA[C/T]ATCTTTTGCAGGATA | 25909 |
rs560754349 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246917103 | TTATGCATGTTTTTA[A/C]ATGTTACTCCAGCTG | 25909 |
rs560767295 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246874734 | CCTATCCTGAGAGAT[A/C]CTGAAATATATTTAA | 25909 |
rs560836134 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246846345 | GGGACAGAAAGTATG[A/G]TAACAGTATAAAGGG | 25909 |
rs560836444 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246933024 | CACAGCAGCCTCGAA[C/T]TCGTGGGCTCAAATG | 25909 |
rs560848869 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868538 | GGGATAGAGGTGTGA[A/G]CCACCGGCCTGGCCT | 25909 |
rs560872835 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246847047 | ATCCCAGCACTTTGG[A/G]AGGCCAAGGCGGGTG | 25909 |
rs560876836 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246922914 | CATGAACCCAGGAGG[C/T]GGAGTTTGCAGTGAG | 25909 |
rs560880463 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246864756 | GAGGCAGGAGAATGG[C/T]GTGAACCCGGGAAGC | 25909 |
rs560891713 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246911813 | TTTTAAAGTGCATGT[A/G]TGACCATTATTTCTG | 25909 |
rs560946356 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246892528 | GTTTCACCATGTTGG[C/T]CAGGCTGGCCTCGAA | 25909 |
rs561003895 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246839808 | CTACATCAAGTACCA[C/T]TGCTTAATTGCACAC | 25909 |
rs561050067 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246875111 | CCCCAGGAGGTGCTA[C/T]GACTTCCTTACCATG | 25909 |
rs561142902 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246903462 | GAATGCTACCTGGGT[A/G]AATAGGTAAAACAGA | 25909 |
rs561151664 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246841374 | ATGTCAGAAATGTCA[A/G]TGATCAAACACAGCA | 25909 |
rs561181213 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246867895 | AGAATGATTACACCC[C/G]CCCCCCCACACACAC | 25909 |
rs561184928 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869135 | GGCGTGAGCCACCAC[A/G]CCCGGCCGTGTGTTT | 25909 |
rs561219934 | snp | C/T | 0.000131823 | 0.00811752 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246861216 | GTGGTCCTATCTTTG[C/T]TCTTCAGCCATTCAG | 25909 |
rs561227259 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246886359 | AAAAATAAAAAATAA[C/T]AGTATAATGATAAAA | 25909 |
rs561251338 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246855102 | TAACAGTTGAGAGCA[C/T]GGGCTCTAGAGTCAG | 25909 |
rs561289624 | in-del | -/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246844809 | ACCACACAGACTTTT[-/T]TTTTTTTTTTTTAAC | 25909 |
rs561314444 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246902921 | ACACAGAAGCCCTCA[C/T]GCACTACTGGTTGGT | 25909 |
rs561366581 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246840414 | GTAAAAAGAAATATC[A/G]ATACTTCAATCATCC | 25909 |
rs561421275 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246924677 | AAAATATATGAGTTA[C/T]CATTTTCTGTTCAGG | 25909 |
rs561422443 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246854598 | AAGAAAGTTGCTTTT[C/T]TGATAATGATCATTT | 25909 |
rs561457573 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246890497 | ATTCTAAACAAATAT[A/T]GCACAAGTCAAATAC | 25909 |
rs561459577 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246862308 | ACACGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 25909 |
rs561472911 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246924481 | AATTTTAAAACATAT[A/G]TATATAAAATAAAAA | 25909 |
rs561493192 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246918869 | ACCTCACCACCACCA[A/T]CCTCCCTACAGAAAA | 25909 |
rs561493827 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246883194 | TTTAAATATTAAAAC[C/T]TTTTCAGCCATTTCA | 25909 |
rs561496569 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246862657 | CTACGAAACATAAAA[A/C]TGCATCCATCTTTCT | 25909 |
rs561578273 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246870176 | AGGCCAGGCATGATG[A/G]CTCATGCCTGTAATC | 25909 |
rs561637753 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869827 | GCATGAAAACACAAC[A/G]TCCATTCTGTAACCC | 25909 |
rs561653534 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246918132 | TAGATGTTACATATT[A/T]AAGATCACTCAGGTT | 25909 |
rs561672513 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246911673 | TTTTTTAGTAGAGAC[A/G]GGGTTTCTCCATGTT | 25909 |
rs561752237 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246898917 | ACATGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 25909 |
rs561774175 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246885931 | GTGGCTCACGCCTGT[A/T]ATCTCCGCACTTTGG | 25909 |
rs561785416 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246892384 | CAGTGGTGCAATCTC[A/C]ATCTCCGCTCACTGC | 25909 |
rs561808779 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246904181 | TTTCGGTAATTTTTA[C/T]AAAAATGTAGTCCTT | 25909 |
rs561847294 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246904982 | AAGAGAGCAGGGTAC[A/T]TAGAAGGTTCCAAGG | 25909 |
rs561860295 | snp | C/T | 1.64768e-05 | 0.00287021 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246849801 | GTGTCATTTCATCTG[C/T]GCGTTCTTCTGATAC | 25909 |
rs561874548 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246855974 | TCATTCTGAACAATA[A/C]TATAAAATTTAAAAG | 25909 |
rs561878959 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246905779 | AGAATAAGTGATCTG[C/T]GGGCCATGGCCAAGT | 25909 |
rs562024548 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246875429 | TAGTTTGTTACTCAC[C/T]AGGCATTTAGAAAAT | 25909 |
rs562036679 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246927169 | GGCGACAGAGCGAGA[C/T]TCTGTCTCAAAAAAA | 25909 |
rs562037432 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246930024 | GCCACTGCACTCCAG[C/G]CTGGGCAACAGAGCA | 25909 |
rs562042629 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246871615 | CTACCTCTGTGAACC[C/T]TGACTAGATGAGCCT | 25909 |
rs562043281 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246860079 | AGCCTGGCCAATATG[A/G]TGAAACCCCGTCTCT | 25909 |
rs562069211 | snp | A/G | 0.000188999 | 0.00971924 | missense, nc-transcript-variant, intron-variant | AHCTF1 | GRCh38.p7 | 1:246843911 | CTTTCAGCTGTGCAG[A/G]AACCTCTATTTTTTT | 25909 |
rs562078405 | snp | A/G | 3.56608e-05 | 0.00422245 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850415 | TTTGTAACAGATGAA[A/G]CCTTAACTTCTTTTT | 25909 |
rs562086653 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246925557 | ACCAGGAGTTGTAGG[C/T]TGCAGTAAGCTATGA | 25909 |
rs562103173 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246893314 | AAAAACACTAGAAAG[C/T]GCCATGTCTTCCTAA | 25909 |
rs562157365 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246845822 | TTCAAAGAGAGCTCT[A/G]ATTTGCAGCATTTGC | 25909 |
rs562279053 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246896945 | TTATATTTAATACCA[C/G]GGACAAAACAGAAAC | 25909 |
rs562297831 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868409 | TACAGGCGTGAGCCA[C/T]TGCGCCTGGCAATTT | 25909 |
rs562309670 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246913603 | ACCATTACTCAATAC[A/G]TAGAAAAATCACGCA | 25909 |
rs562318858 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246841192 | GAGTTCAGGTTTCAT[A/T]AAGGGGAATTTTTTC | 25909 |
rs562355764 | snp | A/C/G | 0.000132241 | 0.00813047 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246864069 | TGCTGAATAAACTCC[A/C/G]AACACTGAGAAGGCC | 25909 |
rs562369179 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246896162 | AAAGCAGTTTGGCGG[C/T]TTCTCAGTATGCTAA | 25909 |
rs562388345 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246876778 | ACGTAAAAGAATTAC[C/G]TGGTAATACCCTGTT | 25909 |
rs562422793 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246923812 | TTCACAAAATCCAGA[C/G]AATTCTAACATCCTT | 25909 |
rs562430351 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246922800 | ATCCTGGATAACACG[A/G]TGAAACCCTGTCTCT | 25909 |
rs562437381 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246917205 | CGAATAGAGAAAAGT[A/G]GGTTGACTGGAGATT | 25909 |
rs562542569 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246898885 | CTGAGGTCAGGAGTT[C/T]GAGACCAGCCTGGCC | 25909 |
rs562542571 | snp | C/T | 0.0923359 | 0.194016 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246891485 | AAAAAATTTATGAGT[C/T]CTTTGAATAAAAAAT | 25909 |
rs562586241 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246893497 | TTTCACTTACAGTGC[A/G]ACTGTATCCCTACTA | 25909 |
rs562633843 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246862231 | CACGCCTGTAATCCC[A/T]GCACTTTGGGAGGCA | 25909 |
rs562647414 | snp | A/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246921923 | AAAGTACTGGTATAT[A/T]CACAGAAAAAAATCT | 25909 |
rs562670547 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246855901 | CTTTAGTCCTACCAC[C/G]TAACCTGTCATTTTG | 25909 |
rs562750633 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246912420 | CACGGGAGGCGGAGG[C/T]TGCAGTGAGCAGGGA | 25909 |
rs562760215 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246920483 | TGTCAGAATATATTA[C/T]TAAACCAGCCGGGCG | 25909 |
rs562812120 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246885130 | TATGTTTTTCTTAAC[A/G]TTGGAAGACCAATAA | 25909 |
rs562858915 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246856988 | GTATCCTCTACAACG[A/G]TGTTATTCAAAAGTG | 25909 |
rs562870666 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246929417 | CCGTCTCAAAAAAAT[A/T]AAAATAAAAATAAAA | 25909 |
rs562873969 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | AHCTF1 | GRCh38.p7 | 1:246842365 | GGCAGGCGGATCACT[G/T]GAGACCAGGAGTTTG | 25909 |
rs563054154 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246925890 | GCCTGGGCCACATGG[A/C]GAAATCTCATCTCTA | 25909 |
rs563055863 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246870315 | GCAGTCTCAGCCACT[C/T]GGAAAGCTGAGGCAG | 25909 |
rs563092117 | snp | A/C/T | 0.000131839 | 0.00811815 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246863999 | CGATCCTTTTAATTG[A/C/T]GAACTTGAGGGCAGT | 25909 |
rs563094999 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869139 | TGAGCCACCACGCCC[A/G]GCCGTGTGTTTTGTT | 25909 |
rs563109798 | snp | C/T | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246851186 | TCAGATGATGCAAAA[C/T]CACCTGGCTCAACTT | 25909 |
rs563118985 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246905830 | ACACGGCACAAGACA[C/T]CAAGACTATGGTCAT | 25909 |
rs563144134 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246844821 | TTTTTTTTTTTTTTT[A/T]AACTATAGGGCCCCC | 25909 |
rs563144703 | snp | A/G/T | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246878889 | ATCTGAAATTGCCTC[A/G/T]TGCTTCTCTTACTAG | 25909 |
rs563154609 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868817 | TACCTCATTTTATTG[C/T]GCTTTGCTTCATTGT | 25909 |
rs563225195 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246931459 | CCCGGCCTAGGCCCG[A/G]CGCTCGCGGGGCAGA | 25909 |
rs563230390 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246858239 | GCTGGGATTACAGGC[A/G]TGAGCCACTGCACCC | 25909 |
rs563283633 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246845511 | ACAAAAGTATTTCTA[C/T]GAAAATTATACATTC | 25909 |
rs563319898 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B | AHCTF1 | GRCh38.p7 | 1:246838601 | AGCAGCAAGTTGTAG[A/G]AGTGGGCGGGGCGGG | 25909 |
rs563359285 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246919351 | ACCATGGCTCTGAGT[C/T]TCTTACTCAGAAAGA | 25909 |
rs563360966 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246915911 | TTTTTACTCTGGAAC[A/G]TTTTAACCAATAAGA | 25909 |
rs563366137 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246864383 | CTATATTTACTGAGC[A/T]CTTACTATGTGCCTG | 25909 |
rs563383895 | in-del | -/TT | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868848 | GTGTGTGTTTTTTGT[-/TT]TTTTTTTTTTTTTGA | 25909 |
rs563410946 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246880040 | AAAAGGGTTTAGTGG[A/G]AGAGGACATATAGGC | 25909 |
rs563417229 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246926805 | AGATTGCAGTCAGCC[A/G]ACACTGCACCATTGC | 25909 |
rs563430166 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246860761 | TCCTCCAGCCTCAGC[C/T]TCCCAAAGTGCTGAG | 25909 |
rs563453463 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246928163 | AAAAAATTAGCCGGG[C/T]GTGGTGGTGGGCACC | 25909 |
rs563457069 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246865700 | GGACTGTGCAACAAA[A/C]GCTACCTACCAAGTC | 25909 |
rs563463291 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869067 | GCCAGGATGGTCTCG[A/G]TCTCCTGACCTCGTG | 25909 |
rs563467098 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246894197 | CAAAAAGTGAGACCA[C/T]GTCTCAAAAAAAAAA | 25909 |
rs563494825 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246866371 | GAATGTCGGTAATAA[C/T]GACTTTCATTTAAAA | 25909 |
rs563548738 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246887650 | ACAAGAAACAAAGAT[A/G]TACGCAAATTTCTAA | 25909 |
rs563549532 | in-del | -/A | 0.00159617 | 0.0282053 | upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246932162 | GGGCGGATCATTTAC[-/A]AAAAAAATCGGGTCT | 25909 |
rs563559405 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246911886 | TTGTTCAGATGATTT[C/T]GGCTCTTCCATTTCT | 25909 |
rs563645165 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246926988 | GACCATCCTGGCTAA[C/G]AAGGTGAAATCCCGT | 25909 |
rs563657289 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246921627 | GATTTACAGACACAC[C/T]GATTCCCTGAGTCAG | 25909 |
rs563683822 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246859293 | TAACCTTGTTAAAAA[C/T]GTGTGTAGGGTAAGA | 25909 |
rs563750796 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246873205 | ATATTCAAACTTTCT[C/T]CCTTATAGAACTCTC | 25909 |
rs563808117 | snp | A/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246896872 | CACAGAGGGAATTAC[A/T]TAATGGTCCACAAAA | 25909 |
rs563815668 | snp | A/G | 1.65974e-05 | 0.0028807 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246907761 | AGAACTTCAAGATCT[A/G]AAACCACAAATTAGA | 25909 |
rs563875061 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246859751 | CAGCTAATTTTTTTA[C/T]ATTTTTTGTAGAGAT | 25909 |
rs563966995 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246895573 | TTCTTGCCAGGGGTT[A/G]AGGATGGGGCAGAAA | 25909 |
rs563972611 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868801 | TGAATGAGTACAGGT[C/T]TACCTCATTTTATTG | 25909 |
rs563978508 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246932420 | CCCATAATTGGCAGC[C/T]TGCATTCTGTATTTT | 25909 |
rs564026255 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246883019 | AACATCTTTGCTACA[A/G]TAAGTGCTGTTTCAA | 25909 |
rs564039185 | snp | C/T | 7.37944e-05 | 0.00607386 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850558 | GTCCTGATTAACTTC[C/T]TTCTTTCTCCTTCCT | 25909 |
rs564092239 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246903018 | GTTCTCACAGAAATT[A/C]TTGCTCTAGAATAGT | 25909 |
rs564094653 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246905031 | CATTCAAGTAAGTCC[A/G]CACAATTTCTTCTGA | 25909 |
rs564179835 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246886058 | TAAACAAAAAAAGTG[C/T]AGTGGCTCATGCCTA | 25909 |
rs564201665 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246930117 | AGAAAACAAAAGTCT[C/T]AAAACTGATGTATAA | 25909 |
rs564225696 | snp | C/T | 4.94694e-05 | 0.00497316 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246905583 | AAGTAACAGCAATTC[C/T]GAGGATCATTCTCAG | 25909 |
rs564251523 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246899608 | CTGCAAGGCAAGGTG[G/T]CAAATTATTACATGT | 25909 |
rs564255285 | snp | C/G/T | 0.000320775 | 0.0126607 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246843969 | CTGTATCTTTATATA[C/G/T]GTGTGTATATATATA | 25909 |
rs564302045 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246892532 | CACCATGTTGGCCAG[C/G]CTGGCCTCGAACTCC | 25909 |
rs564364697 | snp | A/C/G | 1.66443e-05 | 0.00288477 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246900400 | AGCCCCAAATATACA[A/C/G]AAGGCTTTCCCTGTC | 25909 |
rs564368244 | snp | G/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246857262 | AGTATGTTTCAAATG[G/T]TCGTTAAAAAACACA | 25909 |
rs564398610 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246900992 | ACATCAACAGGAGAA[A/G]AAGAAAGTAAAAATC | 25909 |
rs564411863 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246926262 | AGTTTCACATATTCC[G/T]TTATAGCAACACAGG | 25909 |
rs564425974 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246920571 | GTCAGGAGATCGAGA[A/C]CATCCTGGCTAACAA | 25909 |
rs564444203 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246930903 | GATAGTATGAACCTC[C/G]TAAGCTTTGAGAACA | 25909 |
rs564455937 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246926940 | AGCACTTTGGGAGGC[C/T]AAGGCGGGCGGATCA | 25909 |
rs564471818 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246913664 | CTTACTGATACGCCA[C/G]GCATTGTGTTACCTG | 25909 |
rs564475556 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246844615 | TGTGGTGTCAGCTAC[A/G]TGGGAGGCTGAGGCA | 25909 |
rs564486797 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246920947 | CAAAAAAAAAATCAG[C/T]TGGCCATGGTGGCGC | 25909 |
rs564498034 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246886679 | GATGGTATACAAGAG[A/G]ATGTGCATAGGGTAT | 25909 |
rs564506827 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246906731 | AACTTAAGGGCCAAA[C/T]AGGCATCTATTTAAC | 25909 |
rs564528268 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246907460 | ACCCACCCTTTTCTC[A/C]CTATGCTAACTTTCA | 25909 |
rs564533724 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246879853 | CCAAAAAAAAAGGGA[G/T]AACTAATTTAAAATA | 25909 |
rs564536966 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246894880 | AGGGAGGCAACTTGG[A/G]AAAATGGACTTTCTC | 25909 |
rs564555160 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246921581 | CCCCCCAAAAATATA[A/G]TACTAATAGGAAGAA | 25909 |
rs564569167 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246864517 | AAAATATCCATTCAC[C/T]TACATGTAATATATA | 25909 |
rs564591272 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246930584 | CTCACAAAAAAACAG[C/T]TTAAAAAAAAAAAAG | 25909 |
rs564616388 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246920292 | AAATGTCTAATATAT[C/T]TGTGTAAATCAGCGA | 25909 |
rs564688347 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246914502 | TCTGAAAGCTGTAAC[C/T]TCATCACTTTTTCTT | 25909 |
rs564688944 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246855519 | AGACTTTGAATATTA[A/G]AGCCACAGAATGCCT | 25909 |
rs564690951 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246922479 | CACCCAGGCTGGAGT[A/G]CAGTGGCATTATCAG | 25909 |
rs564724191 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246901154 | GACCAGCCCAGGCAA[C/T]ACAGCAAAAACCTCA | 25909 |
rs564747241 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246915286 | AGTGAGCTGAGATCG[C/T]GCCACTGCACTCCAG | 25909 |
rs564753383 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246922757 | GGAGGCCAAGGAGGG[C/T]GGATCACGAGGTCAG | 25909 |
rs564754467 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246858690 | ATTGGCTGGGCATGG[A/T]GGCACGTGCCTGTAA | 25909 |
rs564762038 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246887810 | ATAATGCCTAAGGTA[A/G]TATCACGCTAACTTA | 25909 |
rs564800869 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246880957 | AATAAGGAATGCATG[A/G]GGGTTCTTGGCAATA | 25909 |
rs564807194 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246927046 | AGCAGGGCGTGGTGA[C/T]GGGAACCTGTAGTCC | 25909 |
rs564824158 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246845716 | TTCTTGAGTGTATGT[C/T]AATTCTTTACCCATC | 25909 |
rs564827505 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246895363 | CATCAAATGGTTCAG[A/G]AAAAAAACTATTCTC | 25909 |
rs564865739 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | AHCTF1 | GRCh38.p7 | 1:246838816 | CTGAGTATATTGTTT[C/T]CCTTACTACTATGAT | 25909 |
rs564882553 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246915962 | AGTTCCTTGAATAAC[A/G]TATCATCTTTAACCT | 25909 |
rs564973357 | snp | G/T | 0.00279162 | 0.0372561 | upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246932285 | GTGCGCAGTTGGGAG[G/T]GGTAGTCTTCGCTGG | 25909 |
rs565001167 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246881408 | TTATTCAGGACACAG[A/T]AAGATTAAAACCATG | 25909 |
rs565004581 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246846228 | TTTCAATAAAATAAA[A/G]GACCACCTCTAGCCT | 25909 |
rs565005318 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868025 | TGGAGGGCAGTGGCA[C/T]GATCTCGGCTCACTG | 25909 |
rs565034015 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246927363 | CCACGGCTGCATACG[C/T]TTGTCATCCCGACTA | 25909 |
rs565051406 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246866593 | GAGTCTTGTAATGAT[C/T]ATTTATAATCATTAT | 25909 |
rs565066569 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246839298 | ATTGCGTTGGTTTAA[A/G]AAAGTATTAACTTGA | 25909 |
rs565078282 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246908760 | ATTAGCCGGGCATGG[C/T]GGCGTGCGCCTGTAG | 25909 |
rs565096716 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246847294 | AACTCCATCTCAAAA[A/C]AAAAAAACAAACAAA | 25909 |
rs565096790 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246854496 | CATGTAACATCTACA[A/C]TACAAAACACTATTA | 25909 |
rs565135345 | in-del | -/TTGT | 0.00517822 | 0.0506191 | downstream-variant-500B | AHCTF1 | GRCh38.p7 | 1:246838889 | ATCTTTCTGAGTACA[-/TTGT]TTACCTTACTACTGA | 25909 |
rs565177797 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246865836 | TCTTCAACCCTGAGA[A/C]CAAATATTCTTTCAG | 25909 |
rs565185172 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869132 | ACAGGCGTGAGCCAC[A/C/T]ACGCCCGGCCGTGTG | 25909 |
rs565217176 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246867744 | ATTGTTGATGAAAAC[A/G]GATCTTGTCAACACA | 25909 |
rs565233790 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246847538 | GGTCTTGCTCTGTTG[C/T]CCAGGCTGGAGTGCA | 25909 |
rs565239057 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246933290 | AGGTGTGCGCCACCA[C/T]GCCCAGCTGATTTTT | 25909 |
rs565267315 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246909621 | AAAGCACAAGAGTGG[C/T]CATGCTGGCAATTCA | 25909 |
rs565270121 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246848209 | CTCAAACTGTATCAG[C/T]ACAACAAGTCATCTA | 25909 |
rs565286210 | snp | G/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246843728 | AATAAAATAATTTTA[G/T]TAAAACATTTGTAAA | 25909 |
rs565323960 | snp | C/T | 5.34402e-05 | 0.00516887 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246867203 | CAATTGTAACTATCA[C/T]CTAACATTGTGTCTC | 25909 |
rs565362563 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246860404 | TTTTCTAAATTTCAC[A/G]GCCAAATAAAAAATG | 25909 |
rs565416701 | snp | G/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246925485 | TGTGGCCAGACATGA[G/T]GGCTTATGCCTGTAC | 25909 |
rs565448434 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246883157 | GAAGGGTGAGTCCGG[A/G]GAGAGTGTTAGTGTT | 25909 |
rs565476823 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246896757 | ATTTTGAAAATCACT[C/G]AGTCTGGTTTAATAT | 25909 |
rs565510367 | snp | A/C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246885721 | ATATAAATATAATCC[A/C/T]ATACATTTAGACAAA | 25909 |
rs565511856 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246889761 | CACCACTTTCTTTGT[C/G]TATTACCTTTACTTC | 25909 |
rs565547451 | snp | G/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246874839 | AAAAACCTGACCTCC[G/T]GCTCTCAGCCCTCAA | 25909 |
rs565581835 | snp | A/G | 0.000158579 | 0.00890306 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246876008 | TTTTTGATCCAATAG[A/G]TTATGATATTCTTCA | 25909 |
rs565606579 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246840591 | TAAGCCATATTTACA[C/T]ATATAAATGTATGAA | 25909 |
rs565646183 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246893658 | AATAACGACATCTAT[A/C]CATGGAGGACAGCAG | 25909 |
rs565647307 | snp | C/G | 0.43221 | 0.171171 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246864596 | ACTAGACTGACTTGG[C/G]AGGCCGAGGCGGGTG | 25909 |
rs565661051 | snp | A/T | 0.000122095 | 0.00781233 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246885602 | GCTCGCCCTGACTCA[A/T]GAATGCCTGAATAAT | 25909 |
rs565675860 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246920663 | TAGTTCCAGCTACTC[C/G]GGAGGCTGAGGCAGG | 25909 |
rs565697875 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246886314 | CCAGCCTGGGTGACA[A/G]AGCGAGACTCCATCT | 25909 |
rs565701351 | snp | A/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246861753 | CTTCCGAGTCCTATT[A/T]ATCTGTAAGATGATG | 25909 |
rs565712480 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246913476 | TATAATTAACACAAT[A/C]AATTTAAGTTAAAGC | 25909 |
rs565728376 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246871890 | AACAACCTAAAGACA[A/C]AGCTACTAAAAAGAC | 25909 |
rs565735005 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246879283 | AGACAAAAAATATCT[A/G]GTACACTGTGTTGAT | 25909 |
rs565753193 | snp | G/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246852322 | ACGATGACATTTTTA[G/T]GAGTTAAGAAACTTC | 25909 |
rs565771335 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868954 | GGTTCACGCCATTCT[C/T]CTGCCTCAGCCTGCT | 25909 |
rs565784632 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246858830 | TAAATACAAATTTCT[A/C]TTTGAGACTGCCTAA | 25909 |
rs565784723 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246865795 | ATTTTCTAAATGAAA[C/T]GTTAAATATTGCATT | 25909 |
rs565812572 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246873452 | ATTTCTCCTGCATCA[C/T]AGCGAAGGGAAAGAA | 25909 |
rs565821328 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246859388 | TGTTCCCCTGGCCCT[A/C]TTGTTAACCAAACTG | 25909 |
rs565823182 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246854707 | AACTCTAGGAAATGG[G/T]TCTTATTAATATTCC | 25909 |
rs565870384 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246880212 | TTATTATCAAAAACA[A/G]TATGTTATTTGTTAT | 25909 |
rs565931696 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868996 | ACTACAGGCGCCCGC[C/T]ACCATGCCTGGCTAA | 25909 |
rs565942844 | snp | A/T | 5.03926e-05 | 0.00501934 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246913435 | ACATAATACGTGATT[A/T]GCTTTTCTTCTGCAA | 25909 |
rs565953181 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246913877 | CTATGGCCTCTTCTC[C/G]TAAGAGTAAAAACTA | 25909 |
rs565989494 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246881530 | AGTCTTACCAAAAAA[A/T]TTTTTTTTAAATAGA | 25909 |
rs566006509 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246906988 | CACTTAACAAAAGGG[A/G]ATCTGTTCTGAGAAA | 25909 |
rs566019791 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246906554 | GCCACTGCACTCCAG[C/T]CTGGGCAACAGAGTG | 25909 |
rs566026651 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246851626 | CAGACTTTCTCATTC[A/G]GTCAAAATAACTACA | 25909 |
rs566042366 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246907831 | ATATGTCATCCATTA[G/T]TCAAGCTGCAAATGA | 25909 |
rs566044153 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246900584 | TAATTCATATTTCAC[G/T]TGATTCATCAAAACG | 25909 |
rs566082956 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246901250 | GGAGGCTGAGGTGGG[A/G]GGATCGCTTGAACCT | 25909 |
rs566122356 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246874345 | CGTGTCCCTCTGAGG[C/T]ATGTATTCCTCTACA | 25909 |
rs566143051 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246909016 | CACTCTCCAATTTCC[A/G]TTACCTGTAGTAAAC | 25909 |
rs566159877 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246888702 | TCAACTCAAGGTCAG[A/G]AGTTCGAGACCAGCC | 25909 |
rs566179074 | snp | A/C | 0.000798403 | 0.0199641 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246931914 | CTCGGACAGCGCCGG[A/C]CCCGCTCTGCGCATT | 25909 |
rs566203399 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246895109 | AAAAACAATTACATA[C/T]AAACTATTCTAGATC | 25909 |
rs566225758 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246845839 | TTTGCAGCATTTGCT[A/G]ATTTCTAAGGTATAA | 25909 |
rs566317024 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246902383 | GCAAGAAATATCTAG[C/T]ATCTCATATAGAACT | 25909 |
rs566351542 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246896533 | GAAAGTAGATTAGTC[A/T]TTATGTAAGGCTGGG | 25909 |
rs566352318 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246927417 | TCGCTTGAACCGGGG[A/T]GGTGGAGGTAGCTGT | 25909 |
rs566357878 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246916349 | TGTTATAGAGTTTAC[C/T]ACCTCAAGTTGTGGA | 25909 |
rs566407863 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246848799 | ATGTTGCAGTGAGCC[A/G]AGATCATGCCATTGT | 25909 |
rs566409610 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246839403 | CATTTAACAAGTTCA[C/T]TTAAATAAGTTCAAT | 25909 |
rs566411191 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869171 | TTTTAAACAAATTGA[A/G]GGTCTGTGGCAACCC | 25909 |
rs566494064 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246928255 | TGGCAGTGAGCCGAC[A/G]TCGCGCCACTGCACT | 25909 |
rs566496645 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246909749 | ACTAGCTGTGGTTTC[A/G]GCATCCACTGGGGTT | 25909 |
rs566580911 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246860070 | TTCGAGACCAGCCTG[A/G]CCAATATGGTGAAAC | 25909 |
rs566603667 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246901029 | ACTACTATAAGGAAA[C/T]AGGAAGAATGGGGAA | 25909 |
rs566604021 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246923138 | AAAAAAGATAGGCTG[A/G]GCACGGTGGCCCATG | 25909 |
rs566663364 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246924040 | GGTACAAGTCATTAC[C/T]GTTTCTCAGCACTCC | 25909 |
rs566663407 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246926329 | CTAGCACTTAATAAT[A/C]CATGTAACATTGTGC | 25909 |
rs566670176 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246882981 | TAAATCCAAATCTAT[C/T]TGAGTCCAAAGATTT | 25909 |
rs566714504 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246847749 | AAAAAAGTTAAAATT[A/G]GTAGGTACAGAAATG | 25909 |
rs566717919 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246860725 | TGACCAGGCTGGTCT[G/T]GAACTCCTGGGCTCA | 25909 |
rs566719147 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246889600 | CAGCCGGCACAGATT[C/T]TAAAGTACTGATTCC | 25909 |
rs566752065 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246933552 | TACAGACATGAGCCA[A/C]CATGCCCAGCCTATT | 25909 |
rs566754833 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246854096 | TGAGGTCAGGAGATC[A/G]AGACCACCCTGGCTA | 25909 |
rs566757833 | in-del | -/ATCTAT | 0.00159617 | 0.0282053 | cds-indel, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246839268 | AAACAGGTACCACAC[-/ATCTAT]ATTCACCAAATTGCG | 25909 |
rs566769452 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246882790 | GTTAATTTGCACGTA[A/C]AACAGCCACGCCACA | 25909 |
rs566795697 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246854638 | AACATTTACTAAACT[C/T]CAGGTACCAAGCGCT | 25909 |
rs566814455 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869258 | ACTAACTGTTCCCCC[A/G]CGTCTCTCCCTTTCC | 25909 |
rs566820563 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246840028 | CATCTCATCCTATCA[A/G]TATTAGGCACATACA | 25909 |
rs566867209 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246882244 | CCTCGTGATCCACCC[A/G]CCTCAGCCTCCCAAA | 25909 |
rs566924472 | snp | A/G | 4.96266e-05 | 0.00498105 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246918285 | AGCACAGATTCTAAT[A/G]TTATTTCGTCTTCTC | 25909 |
rs566929561 | in-del | -/TA | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246880224 | CAATATGTTATTTGT[-/TA]TATATATATATATAA | 25909 |
rs566961773 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246911092 | TTCCAATTCTCAAAA[C/T]TGAGAAATGGTTCTG | 25909 |
rs566965571 | in-del | -/GCCTCCCA | 0.00835141 | 0.0640778 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246848453 | GATCCACCCGCCTTG[-/GCCTCCCA]GCCTCCCAAAGTGCT | 25909 |
rs566990494 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246917535 | CTCAGTTACACAGAA[C/T]AGTGGCTACTTAGAA | 25909 |
rs567023113 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868338 | GTTGGCCAGGCTGGT[C/T]TTGAACTCCTGACCT | 25909 |
rs567051639 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246915418 | AAACCTAACGTTTCT[A/G]GCCCCCTATTCTTCC | 25909 |
rs567059110 | snp | C/T | 8.30834e-05 | 0.00644475 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246861971 | TACCCCAGGAATCCA[C/T]TTTGGGTGGACATCT | 25909 |
rs567064643 | snp | C/G/T | 0.000618223 | 0.0175718 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246876922 | CCTTATTCTCTTATC[C/G/T]CCCATAATAAGACAA | 25909 |
rs567086295 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246867948 | TACTAGCTAAAAATT[G/T]TAATTATATATATAT | 25909 |
rs567089503 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246908926 | AAAAAAGAATCTTAA[C/T]GAATGAAACAATTAG | 25909 |
rs567100943 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869886 | TATAATTTAGAAATA[C/T]ATTTCATAAAGCTAT | 25909 |
rs567220750 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246903818 | ACTCCAGCCTGGGCG[A/C]CAGAGCGAGACTCTG | 25909 |
rs567222853 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246859176 | CTAAGTAAAGATATC[A/G]TAGTCCAAACTTCAG | 25909 |
rs567223967 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246874298 | AAGCCAAATAACATT[A/G]ACTATTAAATGTCTC | 25909 |
rs567225387 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246921971 | CAATAATAATGGCTG[G/T]GTGGAGTTTAAATAA | 25909 |
rs567251881 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246881017 | TGGCAAACTCTCTAA[A/T]CATGCTAGACCAAAT | 25909 |
rs567270390 | in-del | -/GAG | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246879324 | GCATACGGTAATTGA[-/GAG]GAGGATTAAGTTGTC | 25909 |
rs567359580 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246933421 | ATAGGCGTGAGCCAC[C/T]GCGCCCGGCCTTATT | 25909 |
rs567379852 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869090 | ACCTCGTGATCCGCC[C/T]GCCTTGGCCTCCCAA | 25909 |
rs567431372 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246928164 | AAAAATTAGCCGGGC[A/G]TGGTGGTGGGCACCT | 25909 |
rs567451599 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246839966 | AAGGGATTTCTGTGG[C/T]TCAATAGCAAGCTCC | 25909 |
rs567460838 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246901810 | ACTGGCCTGGGCATC[A/G]GAGTGAGACCCCTGT | 25909 |
rs567474886 | in-del | -/AATATTT | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246863138 | AAAAATACTATACTG[-/AATATTT]TAAATTATTGAAACC | 25909 |
rs567528111 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246860008 | GGCTCACGCCTGTAA[C/T]CCCAGCACTCTGGGA | 25909 |
rs567531980 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246896478 | TATTATTTGACCCAT[A/T]TATATGAAATGTCTA | 25909 |
rs567593409 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246895981 | GAGGGTGTGAGATCA[C/T]AGGCAAGTTCTGGTT | 25909 |
rs567691421 | in-del | -/AAAT | 0.00914312 | 0.0669923 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246871837 | GCCAGGGTCACAAAA[-/AAAT]AAAAAATAAAAATTT | 25909 |
rs567697384 | in-del | -/A | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246909423 | AAAAAAAAAAAAAAA[-/A]TTTGCATGCTGCTCT | 25909 |
rs567730698 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246922977 | GACAGAGCGAGACTC[C/T]GTCTCAAAAAAAAAA | 25909 |
rs567755757 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868258 | CTTAGCCTCCCGAGT[A/G]GCTGGGACTACAGGA | 25909 |
rs567765030 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246861481 | TAATGGTGGCTAATG[C/T]TTCCCTAATTGGTAA | 25909 |
rs567779894 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246893852 | AATCCTAAAACCTGC[C/T]ATTGTAGGCATATCA | 25909 |
rs567811541 | in-del | -/TTATTA | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246848231 | AGTCATCTACTTTAT[-/TTATTA]TTATTATTATTTGGC | 25909 |
rs567812846 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246916798 | CCCAAAGTCAAAAAG[C/T]AGCACAGGCAGAAGT | 25909 |
rs567826493 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869560 | TGACTTTAAATTAAA[C/G]GCAATCACCATTCCA | 25909 |
rs567848254 | in-del | -/A | 0.00874735 | 0.0655527 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246841277 | TGTTTCAAATGTATG[-/A]AAAAAATACTGCTGG | 25909 |
rs567853335 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246917330 | GCTTGAGCAACCAGA[C/T]GAATGGTAACTTCTA | 25909 |
rs567875042 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869276 | TCTCTCCCTTTCCCC[A/G]AGGACCTCCCTTATT | 25909 |
rs567927540 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246883632 | TGACTTTCTAGCAAC[A/C/T]CTGAAGTCATTCTCT | 25909 |
rs567964295 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246884541 | TAAAAGTGGTATAAA[A/G]TAAGTCTAGTAAGGA | 25909 |
rs567966330 | snp | A/G | 0.000461544 | 0.0151842 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246877046 | TTCATGATTCTGAAC[A/G]CTGGCACTGGACTGC | 25909 |
rs568026532 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246910920 | TGGGGAAGCTGCAGA[A/C]CAATATTTATGCTGT | 25909 |
rs568054756 | snp | C/G | 0.0356815 | 0.128715 | intron-variant, upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246931473 | GGCGCTCGCGGGGCA[C/G]AAGCCCCGCCGCCGC | 25909 |
rs568068241 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246903781 | TGGCGGAGGTTGCAG[C/T]GAGCCAAGATTGCAC | 25909 |
rs568077097 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246855435 | TATCACAAACAAACA[C/T]GAAATAACTCTTCTG | 25909 |
rs568105801 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246897807 | GCAACATAGCGAGAC[C/G]CTGTCTCTACCAAAA | 25909 |
rs568115885 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246848538 | GGTCCTGAACTGCTT[G/T]GCTGAAATTCAAATA | 25909 |
rs568201204 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246851582 | ATATACTTATGGGTT[C/T]ACTTTACAAAATTAT | 25909 |
rs568203468 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246912134 | TGTATCTATTTCTGA[C/G]CTGCTCCATAAATGA | 25909 |
rs568243525 | snp | A/C | 0.0130921 | 0.0798413 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246912463 | ACTCCAGCCTGGCAA[A/C]AGAGCGAGACGCCGT | 25909 |
rs568260320 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246891529 | TTTGAAACTTTACTG[A/C]AAATACATTAATCTT | 25909 |
rs568262591 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246906174 | AACTGAAGAGTTCCC[A/C]TAAACTGCTAAAAAA | 25909 |
rs568275417 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246924942 | CCTATACTCAAGCCT[C/T]AGTTGCTCTTATATA | 25909 |
rs568315557 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246919405 | TGTGGCCAGAATTCA[A/C]GCTAGGTTATATGGA | 25909 |
rs568333706 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246849119 | TTAGCTCGTGACAAT[G/T]AAGGATGGCCTCACT | 25909 |
rs568353997 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246841641 | CAGGATTTTAAAGTG[C/T]ATAATTGTTTTTTAC | 25909 |
rs568363176 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246929523 | ATGAAGGACATGAGC[A/G]AAGAAACATCAGAGT | 25909 |
rs568390148 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246870295 | AAAAATACCCAGGCA[C/T]GGTTGCAGTCTCAGC | 25909 |
rs568393004 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | AHCTF1 | GRCh38.p7 | 1:246842530 | GAGGTTGCAGTGAGC[C/T]GAAATCACACCACTG | 25909 |
rs568407206 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246927262 | CCAAGGCGGGAGAAT[A/G]GCTGAGGTCAGGAGT | 25909 |
rs568417707 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246929967 | TGAGGCAGGAGAATC[A/G]CTTGAACCTGGGAGA | 25909 |
rs568537121 | in-del | -/TAAG | | | downstream-variant-500B | AHCTF1 | GRCh38.p7 | 1:246838952 | ACCTTACTATGATAC[-/TAAG]TATCTCTCTGAGTAC | 25909 |
rs568551864 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868867 | TTTTTTTTTTTGAGA[C/T]GGAGTCTCGCTCTGT | 25909 |
rs568562904 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246899224 | AAAGCTTGAGGTTCA[C/T]GTAGCTAGCATCTAC | 25909 |
rs568577564 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246862526 | GATGGGGTCAACTGA[A/G]TCACAATAGTGGTTA | 25909 |
rs568591563 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246867925 | CACACACACACATTA[C/G]GTGGTAATACTAGCT | 25909 |
rs568657066 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246896546 | TCATTATGTAAGGCT[C/G]GGTAGGATGGGGCAG | 25909 |
rs568689987 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246841863 | GTGGCGTGATCTTGG[C/T]TCACTGCAACCTCCG | 25909 |
rs568694307 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246897184 | CGGGTGTGGTGGCAC[A/G]CGCCTCTAGTTCCAG | 25909 |
rs568702972 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246892801 | CCTGCCCAGCTAATT[A/T]AAAAAAAGATTTTTT | 25909 |
rs568767405 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246910358 | TCCAAACAATCCAAA[A/T]GTAAAAAGATGCTTT | 25909 |
rs568793109 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246858300 | ACCTAGCTCAAGAGC[A/C]CCCCTTAACCTCTCG | 25909 |
rs568889247 | in-del | -/TAAAAATTTGTTGAATAC | 0.00159617 | 0.0282053 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246877429 | AATTGAAAAGTACTT[-/TAAAAATTTGTTGAATAC]TAAGTACTGCATAAT | 25909 |
rs568913541 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246860820 | CTAGGATGCTTTTCT[C/T]ATGGTGGAAAAAATT | 25909 |
rs568983267 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246889244 | TGATGCAACGTGCAG[A/G]TATGGTCCCTATTTC | 25909 |
rs568991953 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246854167 | AGCCAGGCGTGGTGG[C/T]GGGCACCTGTAGTCC | 25909 |
rs569039446 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246911290 | GAAACAAAAGCCTAT[C/G]AAGCCTACTTCTTTG | 25909 |
rs569041254 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246919280 | TACATCAGCCTAAAG[A/G]TGAGCAAGAACAATA | 25909 |
rs569064730 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246928937 | TTTAAAACACCGTGT[G/T]AGTAAAGGAATGCAA | 25909 |
rs569079503 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246911999 | AGTGCAGTGGCGTGA[C/T]CTCGGTTCACTGCAG | 25909 |
rs569126251 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246924111 | CCAACACCCAGCCCA[A/G]GCCATTCTCACAGAA | 25909 |
rs569127578 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246928282 | CACTGTAGCCTGGGC[A/G]ACAGAGCGAGACTCC | 25909 |
rs569149673 | in-del | -/GG | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246860195 | AACCTGGTTGGGGGG[-/GG]GGCGGAGGTTGCAGT | 25909 |
rs569156812 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246883517 | CTCCTGGGCAATAAA[C/T]ATGGCTGCCTTTTGC | 25909 |
rs569166324 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246847825 | CTAAGCTCTAACAAA[A/G]TAACTCTCACTTTTG | 25909 |
rs569193007 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246923598 | AGAGCAGACATGTGG[A/C]CTCTTCAATCAACAT | 25909 |
rs569266035 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246849453 | TAACTGAACTCAAAC[A/T]TTGAAACATGAAACC | 25909 |
rs569346868 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869921 | GTCACAGATAGTGAT[G/T]CCTCTGAGAGATCCG | 25909 |
rs569367242 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246922674 | GCTGGGATTACAGGT[A/G]TGAGACACCTATCAA | 25909 |
rs569376880 | snp | G/T | 0.0479149 | 0.147179 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868348 | CTGGTCTTGAACTCC[G/T]GACCTCATGTGATCC | 25909 |
rs569404964 | snp | A/G/T | 4.94934e-05 | 0.0049744 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850106 | CTAGGTATGGCAGAC[A/G/T]TATCAAATTCTGCTT | 25909 |
rs569438474 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246843537 | CCTTCCACAAACAGG[G/T]AATTTAAACTGTAAC | 25909 |
rs569477043 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246844033 | TTAGAAAGATGCAAA[C/T]GTCCCCAAACCTGGA | 25909 |
rs569496651 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246898691 | GCAGTCTACTCCTCT[A/T]TATCTAATGTGAAAG | 25909 |
rs569513818 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868551 | GAGCCACCGGCCTGG[C/G]CTACATTTTGTTTCA | 25909 |
rs569551703 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246862944 | CTTGGCCTCTAAAGG[A/C]CTAGTAAACAAATTA | 25909 |
rs569580539 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246900578 | GCGGTTTAATTCATA[C/T]TTCACTTGATTCATC | 25909 |
rs569616673 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246899104 | CAAAAAGAGAAAAGT[A/G]TTTTTCAAAATTCTT | 25909 |
rs569654018 | snp | A/G | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246891899 | CCATGAAATGACACG[A/G]ACCATCAAATAATGG | 25909 |
rs569661012 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246925646 | CCTAATGTGGTTTGT[A/G]TAACTGTCCCCTCCC | 25909 |
rs569666018 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246929780 | CTGTACCAGCCGGGC[A/G]CGGTGGCTCACGCCT | 25909 |
rs569683930 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246929857 | AGAAGTTCAAGACCA[G/T]CCTGGCCAATATGGT | 25909 |
rs569691068 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246892625 | TGTGCCCGACCTAAT[C/T]TGCTTTACTTCTAAT | 25909 |
rs569727186 | snp | C/T | 0.000805737 | 0.0200554 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246885466 | CAGATACGATAAAGA[C/T]TTTATAGTTTCAAAA | 25909 |
rs569738929 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246930222 | CTCACTGCAACCCTC[C/G]AACTCTCAGTTTGAG | 25909 |
rs569749711 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246878610 | AGATATACACTAAGA[A/G]TGGTAATGATCAATC | 25909 |
rs569768638 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246859826 | CCCGAAGTGCTGGTA[-/T]TACAGGCGTGAGCCA | 25909 |
rs569786874 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246870961 | AACAATACAACTGAG[C/T]CTTCGAAAAACTAAA | 25909 |
rs569793409 | snp | A/T | 0.43221 | 0.171171 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246864593 | AAGACTAGACTGACT[A/T]GGGAGGCCGAGGCGG | 25909 |
rs569837684 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246920117 | TGCACTCCAGCCTGA[C/T]GACACAGTGAGACTC | 25909 |
rs569843891 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246912935 | ATTTACTTAAGAATA[C/G]ATCTTATTCAGGTAT | 25909 |
rs569867497 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246879143 | AATCCCAACAACACA[C/G]GAAAAAAAGCCAAAG | 25909 |
rs569893721 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246894442 | AGCCGAGCGTAGTGG[C/T]GGGCAGGAGAATGGC | 25909 |
rs569905133 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246871841 | GGGTCACAAAAAAAT[A/C]AAAAATAAAAATTTG | 25909 |
rs569930622 | snp | A/G | 0.000197954 | 0.00994676 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246887307 | AGATTCAATGGGAGT[A/G]TCTGTTTTGTTGGGA | 25909 |
rs569936812 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246894947 | TGCTGCCGCCAAAAA[C/T]GCAAAAACTGTCATT | 25909 |
rs569952182 | in-del | -/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246879029 | CAGAACATTTTTGTA[-/T]AAAGAAAAATAGAGG | 25909 |
rs569958040 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246912705 | AAAGTATTTCATTTT[A/C]TTTGAATCTGAATAG | 25909 |
rs569959238 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246889843 | TAAAATAGTAATGGT[A/G]ATAGCAAATTCTGAT | 25909 |
rs569974633 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246887931 | GTGTCTTGGACACAT[C/T]TAAGTGTCTGATAAA | 25909 |
rs569996751 | snp | C/G | 8.26112e-05 | 0.00642641 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246913253 | CTTCAACTTCATTTT[C/G]ATTGCATGACAAGTC | 25909 |
rs570008911 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246876290 | AATATCCAAAAAATC[C/T]TCCCCCTACCTACAT | 25909 |
rs570128804 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246852496 | AGAATTTTTTTTTTA[A/T]AAAAACTAAGTCTTA | 25909 |
rs570148415 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246858748 | AGGTTGCGGTGAGCC[A/G]AGATCACACCACTGC | 25909 |
rs570159320 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246855589 | AGAATACTTCTACAC[C/T]AGGAAAGCTGACCAG | 25909 |
rs570182819 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246851570 | ATTTAATATGGCATA[C/T]ACTTATGGGTTTACT | 25909 |
rs570194416 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246848606 | TGTGGTGGCTCACGC[C/T]TGTAATCCCAACACT | 25909 |
rs570232842 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246849244 | CCTTCAAAACAATTT[C/G/T]GGGTTGTGGATATCA | 25909 |
rs570246672 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246852263 | AACTGGAACTTTACT[C/T]ATCTATTTGGCAGTG | 25909 |
rs570299748 | snp | A/C | 0.000137922 | 0.00830312 | intron-variant, synonymous-codon, utr-variant-5-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246931182 | ACAGGACAGGCTCAG[A/C]ACGCCGGCCGCTTCC | 25909 |
rs570344092 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246877615 | GTTGGTGTGGTGTGA[C/T]AGAGGAACATCAGGT | 25909 |
rs570394474 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246845762 | TAAGGAGTTCAAAAG[G/T]CCTAGGTTCAAACCC | 25909 |
rs570410826 | snp | A/G | 3.31345e-05 | 0.00407016 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246891775 | GATAAAACAAAGAGC[A/G]TACCTCTCTCAGTGA | 25909 |
rs570421488 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246870849 | TTCTTGAAAATGGCC[A/G]GATTCTGTCACATAT | 25909 |
rs570436573 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246920312 | TAAATCAGCGATTTA[C/G]CTTGATAAGAAACTG | 25909 |
rs570535005 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246872195 | AGATACCTGATCTAA[A/C]AGATAAAACAGATCA | 25909 |
rs570593701 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246929907 | AAATACAAAAATTAG[A/C]CGGGTGTGGTGGCGT | 25909 |
rs570598742 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869536 | GCTGTTAGTGGTTAA[C/T]GTAGCTGATGACTTT | 25909 |
rs570601060 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246884715 | CTGATTAGAGAACAT[A/T]AAAATCTGCAAAAGG | 25909 |
rs570628060 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246925053 | ACATTGTTACTATGT[G/T]GTTTTCCCCTCTGAC | 25909 |
rs570636545 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246927173 | ACAGAGCGAGACTCT[A/G]TCTCAAAAAAAAAAA | 25909 |
rs570647315 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246870242 | TGAGGCCATGAGTTT[C/G]AGAATAGCCTGGGCG | 25909 |
rs570661578 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246903363 | AACAAAGTGGAATTA[A/T]TTTTCCTGGGTACCA | 25909 |
rs570697582 | snp | A/T | 0.0111196 | 0.0737302 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246899865 | ATATAAATACTAAAT[A/T]TCTCCAAGTCATAAT | 25909 |
rs570768132 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246905398 | AGCTACTCGGGAGGC[A/T]GAGCGAGAGAATGGC | 25909 |
rs570794200 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246930434 | GAGACAACGTAGACT[G/T]CCCATAGCGCTTGGC | 25909 |
rs570800761 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868878 | GAGATGGAGTCTCGC[C/T]CTGTCACCCAGGTTG | 25909 |
rs570827268 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246863472 | TCTCAGCTAATAACT[C/T]AGGAGATGGGAAAAG | 25909 |
rs570842934 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246846535 | GCAGAAATGAGAGAT[A/C]TCAATCCCAAGTTTC | 25909 |
rs570924995 | snp | G/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246887073 | ATAGTGCTTGGTAAA[G/T]GTACTGATTAAACTG | 25909 |
rs570972942 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246906094 | ACGAGATACTGCCAC[A/G]AGACTTTTCAGCTGT | 25909 |
rs570988052 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246883050 | TAACATTATTTGTAA[A/G]GGTGCAAATTAATAA | 25909 |
rs571048327 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246916664 | ATCTCAAATAATAAT[A/G]ATAATAGTCATTCAG | 25909 |
rs571110488 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246863497 | GAAAAGGCAGTTTAA[A/G]GAGGGATAAACCAAA | 25909 |
rs571142241 | snp | G/T | 1.64898e-05 | 0.00287135 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850843 | CATAGTCATTGTGCT[G/T]GTTTCCTGAGCAGTC | 25909 |
rs571153702 | snp | C/T | | | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246913368 | TAAATGCTGAGTGCT[C/T]GCACTGGCTCCTCCA | 25909 |
rs571182332 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246851556 | AAAACATAAATTATA[C/T]TTAATATGGCATATA | 25909 |
rs571217534 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246887153 | AAATTTAAATTATGT[A/G]TATTTTCTAAAATTC | 25909 |
rs571243890 | in-del | -/AAA | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246920142 | GACTCTGTCCCCCGC[-/AAA]AAAAAAAAAAAAAAA | 25909 |
rs571252508 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246880312 | GCTCACGCCTGTAAT[C/G]CCAGCACTTTGGGAG | 25909 |
rs571326097 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246907119 | TGTTGCTCTTAGTCT[A/G]CTAACCTGTACAGCA | 25909 |
rs571333962 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246872567 | TGCCTTGGAAATTAA[A/G]TAGAGGAGGTTACAC | 25909 |
rs571371166 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246873325 | TAGTCCCTTTTATTA[C/T]TGTGGCTGATGGTCT | 25909 |
rs571373007 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869000 | CAGGCGCCCGCCACC[A/G]TGCCTGGCTAACTTT | 25909 |
rs571390907 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246914845 | TCCTCATCCAAATGA[C/T]CAATGAGTGTCCATG | 25909 |
rs571395363 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246865109 | TTTAAACTCAAAAGT[C/G]GGGTTTTCAGGTGGT | 25909 |
rs571398206 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246845954 | GCAGTAGTAGCTCTA[C/G]AACAACACATCTTAC | 25909 |
rs571442050 | snp | A/G | | | downstream-variant-500B | AHCTF1 | GRCh38.p7 | 1:246838891 | CTTTCTGAGTACATT[A/G]TTTACCTTACTACTG | 25909 |
rs571498743 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246865916 | TCTATAGTGGTATTT[A/T]AAAAATTGATTTATG | 25909 |
rs571512366 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869045 | GAGACGGGGTTTCAC[C/T]ATGTTGGCCAGGATG | 25909 |
rs571535629 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246859522 | CACAGTAGGAGCTAA[C/G]AGGAATACATACTTC | 25909 |
rs571541144 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246874454 | ATAAAAGGAAGGGAA[C/T]AGCTAGCTGGGGGAG | 25909 |
rs571560737 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246922531 | CCTGGGCTCTAGCAA[A/C/T]CTCTCGTCTCGTGCC | 25909 |
rs571585569 | snp | C/G | 0.00318978 | 0.0398085 | upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246932008 | AGAGGGAGGGGAGAA[C/G]CGGCGGGAGATCGCG | 25909 |
rs571612551 | in-del | -/G | 0.00398564 | 0.0444627 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246926896 | CAAAAGTGTATGGCC[-/G]GGCCGCGGTGGCACA | 25909 |
rs571649723 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246895222 | TCAATAAGGTCTCTA[A/G]GTTAGATAAAAGTCT | 25909 |
rs571671165 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246888826 | AAGGAAGGAGGATCG[C/T]TGGAGCCCAGGAGTT | 25909 |
rs571716514 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246927956 | AATAAGCCAAGATCA[C/T]GCCACTGCACTCCAG | 25909 |
rs571772679 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246839507 | TGAAATTTTCAACAA[A/G]GCAGCGTAACATCCA | 25909 |
rs571781121 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246882123 | CTGCCTCAGCCTCCT[C/G]AGTAGCTGGGACTAC | 25909 |
rs571885337 | in-del | -/TT | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246899118 | TATTTTTCAAAATTC[-/TT]TTTTTTTTTCCTGTG | 25909 |
rs571886017 | in-del | -/AT | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246879038 | TTTGTATAAAGAAAA[-/AT]AGAGGATAAGATGAA | 25909 |
rs571907782 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246919773 | CGTTGCTCCAAGCAA[C/T]CCACGGAAACAACCA | 25909 |
rs571953173 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246867498 | CATTTCACTTTTAAA[A/G]GTTTTTAAAAATTCT | 25909 |
rs571954819 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869125 | CTGGATTACAGGCGT[C/G]AGCCACCACGCCCGG | 25909 |
rs571962811 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246870438 | TTAAAAAAACAAAAA[A/C]AGACTAAAGATGTGA | 25909 |
rs571979893 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246858009 | GTGTCGCCCAGGCTG[C/G]AGTGCAGTGGCGCTA | 25909 |
rs572018579 | in-del | -/A | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246894203 | GTGAGACCATGTCTC[-/A]AAAAAAAAAATTACT | 25909 |
rs572020820 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246858448 | ATCCCAGCTCATGAC[A/G]CATACTCAGTAAGTA | 25909 |
rs572053842 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246862297 | CATCCTGGCTAACAC[A/G]GTGAAACCCCGTCTC | 25909 |
rs572086643 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246878699 | TTGCACTGCCCTATA[C/T]GTTCTGTGAATACAA | 25909 |
rs572134617 | snp | C/T | | | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246863954 | AGTTTCAAGCAAATG[C/T]AATTCTGAAGCCCTG | 25909 |
rs572143382 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246901973 | TGGGATGGGTAAGTT[C/T]GCTGTGTGATTTAAT | 25909 |
rs572143526 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246912715 | ATTTTCTTTGAATCT[A/G]AATAGAATTACTTCT | 25909 |
rs572171568 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246912326 | CTAAAAAAAAAAAAA[C/T]ACAAAAATTAGCCAG | 25909 |
rs572206700 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246926977 | CAGGAGATCGAGACC[A/C]TCCTGGCTAACAAGG | 25909 |
rs572243785 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246905440 | AGGCGGAGGTTGCAG[C/T]GAGCCGAAATCACGC | 25909 |
rs572283485 | snp | G/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246848785 | AACCCAGGGGGCACA[G/T]GTTGCAGTGAGCCGA | 25909 |
rs572284221 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246880519 | CAGTGAGCCGAGATC[A/G]CGCCACTGCACTCCA | 25909 |
rs572371912 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246893983 | CCCAGGCAGGAGGAT[C/T]GCTTGAGGCCAGGAG | 25909 |
rs572376811 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246910157 | AATTTGCAGAAAATC[A/G]AAAATGATACCACAT | 25909 |
rs572439269 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246907484 | ACTTTCAAATATTAG[C/T]AAATGAGTACAAGCT | 25909 |
rs572440851 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246907202 | TTAAAAAGGTACAAT[C/G]AAAATACAGTAAAAT | 25909 |
rs572453159 | snp | G/T | 3.29745e-05 | 0.00406031 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246851097 | GCAAATTTGCAATTT[G/T]TCCATGATTATCATT | 25909 |
rs572467199 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246845252 | AAAAATGTTTTTTGT[A/G]GGTACACAGTAGGTG | 25909 |
rs572483540 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246844583 | TTAAAAGATTAGCCA[A/G]TGTGGTGGTGCACGC | 25909 |
rs572488842 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246887458 | GCATTAAAAGAGACT[G/T]GAAATGCCTGTTTTT | 25909 |
rs572500107 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246930887 | TAAAACTTTGCACAC[A/G]GATAGTATGAACCTC | 25909 |
rs572515145 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246901414 | GGCCGAGGCGGGTGG[A/G]TCATGAGGTCAGGAG | 25909 |
rs572560433 | snp | A/G | 0.000293988 | 0.0121205 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246931244 | CGTGGGAGAACAGTG[A/G]GAAAGGGTCGCGGCC | 25909 |
rs572593939 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246855053 | GCTGAAGCTTGCCGT[A/G]TACCCCATTCATAAT | 25909 |
rs572654295 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869020 | TGGCTAACTTTTTCT[A/G]TTTTTAGTAGAGACG | 25909 |
rs572687166 | snp | A/C | | | upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246933417 | GATTATAGGCGTGAG[A/C]CACCGCGCCCGGCCT | 25909 |
rs572709885 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246900943 | AGTGCTTGGATGGTG[C/G]CTGTGGAATGGAAAG | 25909 |
rs572729816 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246927348 | AAATGTAGCAGCCAG[C/T]CACGGCTGCATACGC | 25909 |
rs572742989 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869058 | ACCATGTTGGCCAGG[A/C]TGGTCTCGATCTCCT | 25909 |
rs572783870 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246866071 | CCCACGGATGTTATC[A/T]ATTCTGCCTTATTTC | 25909 |
rs572883508 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246926941 | GCACTTTGGGAGGCT[A/G]AGGCGGGCGGATCAC | 25909 |
rs572934926 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246914834 | TTCTTCTCAATTCCT[C/T]ATCCAAATGATCAAT | 25909 |
rs572936477 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246896087 | GCATGGTAAGGACGT[A/G]TTAAAACTGGAACTC | 25909 |
rs572941535 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246895425 | GGTGTGTGTGTGTAT[G/T]TGTGTGAAGAGTAAC | 25909 |
rs572954643 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246895233 | TCTAGGTTAGATAAA[A/C]GTCTTAATTTTCTTG | 25909 |
rs572974922 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246888981 | TCAAGGAGAGTTAGT[C/G]GGATAAGCCCTTAAT | 25909 |
rs572976808 | snp | A/G | 3.29913e-05 | 0.00406135 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246888207 | TGCTTCAGTAACGCC[A/G]TCTAATAGGTACATA | 25909 |
rs572983733 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246932915 | AGTTTCTACTTTTCT[C/G]TTACCTTTCATATGT | 25909 |
rs573036716 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246846828 | GGTGTGATGGCTCAC[C/T]GCAACCTCAACCTCC | 25909 |
rs573079808 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246839681 | AATATTAAAAGCCCA[C/T]GAAAGCAGTTCGTTT | 25909 |
rs573106940 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246879141 | AAAATCCCAACAACA[C/T]AGGAAAAAAAGCCAA | 25909 |
rs573120138 | snp | A/C | 0.000175512 | 0.00936619 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246853280 | GGAGTTTCCACCATC[A/C]CCAAGGACATCAGCC | 25909 |
rs573133006 | snp | A/G | 3.29679e-05 | 0.00405991 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246861033 | GAGGCCGTGAAAACA[A/G]TCTCTTCAAGGTCTT | 25909 |
rs573150454 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246915875 | AAAAAAAGAGTATCA[A/G]AACATTACATGTCAT | 25909 |
rs573210526 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246854957 | CCTAAAATGGGTGAT[C/T]GGCTTTTTACATGTT | 25909 |
rs573213082 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869298 | TCCCTTATTCCTTGA[A/G]ACTGACAATATCCAA | 25909 |
rs573221699 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869127 | GGATTACAGGCGTGA[G/T]CCACCACGCCCGGCC | 25909 |
rs573253633 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246906593 | CCCCCCAAAAAAATA[A/G]AAAAAAAAGAGCTGA | 25909 |
rs573253691 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246914369 | AAAAGAAAATATCTG[A/G]TATCAATGATTCATG | 25909 |
rs573268651 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868917 | TGGTGTGATCTCGGC[C/T]CACTGCAAGTTCTGC | 25909 |
rs573283319 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246909551 | GTTCTCAGATCAACT[A/G]TCGCAGTATTGCAGT | 25909 |
rs573291908 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246875606 | CTTCACTGTGTCATC[A/G]TAAGAAACTGTCACA | 25909 |
rs573292261 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246910111 | TACCTTGCCAAAATA[C/T]TAAACCTTCATCTAT | 25909 |
rs573351269 | snp | G/T | 0.000131804 | 0.00811695 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246867699 | TATAGGTTCTTTGCT[G/T]GCCCAAACTTCTCCA | 25909 |
rs573434409 | in-del | -/TCAA | 0.0525931 | 0.153397 | intron-variant, downstream-variant-500B | AHCTF1 | GRCh38.p7 | 1:246842653 | CAGAGCGAGACTGTC[-/TCAA]TCAATCAATCAATCA | 25909 |
rs573448373 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246902771 | AGATTGTTCACACAA[C/T]ACAAAGAAAACAATT | 25909 |
rs573488669 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246903255 | GATCTCCTCAGGAAT[C/T]CAGCCAGATAAATAG | 25909 |
rs573545734 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246872822 | AGAGGGCAGTAAAAC[A/G]TGCTGTAGATTTTTA | 25909 |
rs573644256 | snp | C/T | 4.99422e-05 | 0.00499686 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246900293 | TTGGTCAGCTACACA[C/T]ACAAATACAAAGAGA | 25909 |
rs573678661 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868984 | TGAGTAGCTGGGACT[A/G]CAGGCGCCCGCCACC | 25909 |
rs573693075 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246855445 | AAACACGAAATAACT[A/C]TTCTGAGTCCAAGAA | 25909 |
rs573715503 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246864423 | TTCAAATGAAGATGA[A/G]CTGCCAATGATTTAA | 25909 |
rs573723235 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246874241 | AGACTGAGACCATCT[C/T]TGAGGTGGGCCTCTG | 25909 |
rs573754104 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246865190 | AAACAGTCTATCTTA[C/T]GGTTGTATTTCCTAG | 25909 |
rs573754294 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246852973 | CCCATATTTTTATAA[A/G]TAAGTTTTTATATAG | 25909 |
rs573787655 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246839551 | TAAAAGGCCGCACTC[A/G]CACTGCTTTCACACT | 25909 |
rs573793093 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246859612 | TCTCATTCTCTTGCC[C/T]GGGCTGGAGTTCAGT | 25909 |
rs573827406 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246851867 | CACACTTTTCTAAAT[A/G]GCACGATCCCCGTAA | 25909 |
rs573881869 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246887653 | AGAAACAAAGATATA[C/T]GCAAATTTCTAAAGA | 25909 |
rs573947202 | in-del | -/A | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246847289 | GCCAAACTCCATCTC[-/A]AAAAAAAAAAAACAA | 25909 |
rs573962642 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246916745 | ATCACACCTCAATGT[A/G]GAGATAAGGCAGCTA | 25909 |
rs573969347 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246867597 | GTGGATTGTTGATGA[A/G]CGCTGTTGATGTCCA | 25909 |
rs574002820 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246874676 | TTCCAAATTAAAAAA[A/C]ATTCAACTACAGCTG | 25909 |
rs574015563 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246922333 | CCACTGCACTCCAGC[A/G]CGGGTGACAGAGCAA | 25909 |
rs574019766 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246905208 | TAATTTTTAAAGATT[A/G]TATGTATCAGGCCAG | 25909 |
rs574031205 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869071 | GGATGGTCTCGATCT[C/T]CTGACCTCGTGATCC | 25909 |
rs574083479 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246917581 | CTCCAATGAAGTCAT[C/T]GTACAATGCCTGGCA | 25909 |
rs574095694 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246881768 | GCTTGAACCTGGGAG[A/G]CAGAGGTTGCAGTGA | 25909 |
rs574135725 | snp | A/G | | | upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246932344 | GCTGCGATTGCAGGC[A/G]GACTCTCTTGTCACG | 25909 |
rs574142458 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869122 | GTGCTGGATTACAGG[C/T]GTGAGCCACCACGCC | 25909 |
rs574146068 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246914663 | GAAGACAAAAATAAA[C/T]ATAATGAGTGTATAC | 25909 |
rs574155585 | in-del | -/AC | 0.00199481 | 0.0315187 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868715 | TACACTAGTAAATAA[-/AC]AGTCAAATCTTCTAA | 25909 |
rs574158472 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246915202 | GGGCGTGGTGGTGCA[C/T]GCCTGTAGTCCCAGC | 25909 |
rs574231838 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246861939 | AAAATGTCTTTTCTC[A/C]CAATTATTATCAAAC | 25909 |
rs574234875 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246882355 | GTCAGGTACCACATG[C/G]ATCACATTATGTGAT | 25909 |
rs574236102 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246909344 | ATCACCTGAACCCAG[C/G]AGGCAGAGGTTGCAG | 25909 |
rs574277181 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246902745 | TAAAATTAAATATTC[C/T]CCAAATTTAAAGATT | 25909 |
rs574286082 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246853520 | TGATAACTGATAAAC[A/G]GTATCAGGAAACATT | 25909 |
rs574289533 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246884193 | TGAAACTACAATTTT[A/G]ATCTCATAAAAAATC | 25909 |
rs574305943 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246846940 | AATTTTTCTTTTGTA[C/G]AGATGGGGTCCCACT | 25909 |
rs574316233 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246896570 | GGGGCAGGCAGGAAG[G/T]TAAGGGAAAAGGAGT | 25909 |
rs574378586 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246909968 | ACCACTAGTTTAAAG[C/T]TGATGACAGACTTTA | 25909 |
rs574396670 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246854286 | CCTGGGTGACAGAGC[A/G]AGACTCTGTTTCAAA | 25909 |
rs574435293 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246847480 | ATACTTCTATTTTAG[A/C]GTTTTCAGTAAGTAG | 25909 |
rs574443710 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246911480 | TATCTATGAAGATTC[A/T]TTTTTTTTTTTTTTT | 25909 |
rs574475429 | snp | C/T | 0.0402882 | 0.136092 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246922919 | ACCCAGGAGGCGGAG[C/T]TTGCAGTGAGCCGAG | 25909 |
rs574504008 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246921713 | GTAGAAACCGCAATT[C/T]TGGAATATCTTCAGA | 25909 |
rs574552672 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246924563 | GGCAAAAATCAACCT[A/G]ACGTTCTTTCTTGTC | 25909 |
rs574563584 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246876550 | AGACTCAGAGTGTGT[A/C]CCAAGCACACAGAGT | 25909 |
rs574598386 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869676 | TTGACAGCATGGTTT[A/G]CCGAATATTTTAAGC | 25909 |
rs574605860 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246840190 | AGCCTTTAAGCTTGC[C/T]GAATAAGAGATGCCA | 25909 |
rs574620859 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246917732 | GAAAAGTCTTCTGCA[A/G]TATCTTTCATTAGAA | 25909 |
rs574644404 | snp | C/T | 7.70604e-05 | 0.00620679 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246841015 | TGAAAAAAAAAGATA[C/T]GATCAAGTAAGAATA | 25909 |
rs574690239 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246918533 | AGATGCGGAGGCTCA[C/T]GCCTTTAAGTCCCAG | 25909 |
rs574719674 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246929263 | AAATACAAAAAATTA[A/G]CCGAGTGTGGCGGCG | 25909 |
rs574765828 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246870013 | TCATAATTCCTGGGA[A/G]GAGTCAAACTATGCA | 25909 |
rs574774746 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246841933 | AGCTGGGACTACAGG[C/T]ACCCACCACCACGCC | 25909 |
rs574782924 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246929824 | TCTGGGAGGCCAAGG[C/T]GGGCGGATCACGAGG | 25909 |
rs574793164 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246925323 | CCAAAGTCCAAAGGA[A/T]AACACACAAAAAGCA | 25909 |
rs574820623 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246928234 | CATGAACCCGGGAGG[C/T]GGACCTGGCAGTGAG | 25909 |
rs574849186 | snp | C/T | 1.6489e-05 | 0.00287128 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246855800 | TTCGTCCAACACTGG[C/T]ACCTTGGACTTCTGG | 25909 |
rs574863498 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246898111 | ATTACACTACTTCAC[C/T]TATTTTTGCAGAAAT | 25909 |
rs574900740 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246896084 | CAAGCATGGTAAGGA[C/T]GTGTTAAAACTGGAA | 25909 |
rs574902460 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246891331 | AATACACTTTCACCT[C/T]AGCTACACTTTCATT | 25909 |
rs574902808 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246896160 | GCAAAGCAGTTTGGC[A/G]GTTTCTCAGTATGCT | 25909 |
rs574922326 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246861670 | AAGGACTAAAAATTA[A/G]GAGGTTTGAATCCTA | 25909 |
rs574941743 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246898826 | GGCACGGTGGCTCAC[A/G]CTCATAATCCCAACA | 25909 |
rs574949000 | in-del | -/AAGTGCAGAACTGGG | 0.0103295 | 0.0711199 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246854776 | AGAGACACAGCCCTT[-/AAGTGCAGAACTGGG]AAGTGCAGAACTGGG | 25909 |
rs574959357 | snp | C/T | 0.000156685 | 0.00884975 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246862202 | AAAGTGCTTATAGGC[C/T]GGGCGCGGTGGCTCA | 25909 |
rs574982540 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246906956 | AGAACTCATATTATA[A/C]AAACACAGCCATGTG | 25909 |
rs574996620 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246905253 | ACCTGTAATCCCAGC[A/G]CTTTGGGAGGCTGAG | 25909 |
rs575036323 | in-del | -/T | 0.415399 | 0.187465 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246844805 | ATTTACCACACAGAC[-/T]TTTTTTTTTTTTTTT | 25909 |
rs575081507 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246889604 | CGGCACAGATTTTAA[A/G]GTACTGATTCCCAGG | 25909 |
rs575089279 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246884105 | TTTCCAACCCAGTAC[C/T]AGAACTCTTAACCCA | 25909 |
rs575103170 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246901892 | ACATGTGCTTTTCAC[A/G]TATTTAACTGGATCT | 25909 |
rs575173036 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246860192 | TTGAACCTGGTTGGG[A/G]GGGGGGCGGAGGTTG | 25909 |
rs575179923 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246922908 | GAATGGCATGAACCC[A/G]GGAGGCGGAGTTTGC | 25909 |
rs575194597 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246917639 | CATTCAAGAGAATGG[C/T]GCTGTCAAGAGAGAA | 25909 |
rs575249532 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246884962 | CATTCTTCCTCTCTA[C/T]TCCTGACTCCTTTTC | 25909 |
rs575297225 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868275 | CTGGGACTACAGGAA[C/T]GTGCCACCACGCTAA | 25909 |
rs575381379 | snp | A/C | 0.0275645 | 0.114116 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246881863 | ACCAAAAAAAAAAAC[A/C]AAAAAAAAAGAAGAA | 25909 |
rs575411359 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246875752 | CATTTTTTAGCAATA[C/T]TGCATTTCAAAATTA | 25909 |
rs575420104 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246875018 | CCTACTTTGTTAAAA[C/T]CATCTCCTGACAGGC | 25909 |
rs575429415 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246846972 | AGTTGCCCAGGCTGG[C/T]TGGATTTTGAAGAAT | 25909 |
rs575462897 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246919381 | ACAACATTTTCTTTC[A/G]TACAAATGTGTGGCC | 25909 |
rs575509009 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246848256 | TATTATTTGGCCCCC[C/T]GGGCTGGAATACAGT | 25909 |
rs575588773 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246841852 | GCTGGAGTGCAGTGG[C/T]GTGATCTTGGCTCAC | 25909 |
rs575656789 | snp | A/C | 1.64999e-05 | 0.00287222 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246861148 | TCTCTAAACTTTGTG[A/C]CCCCTCATCCATTTC | 25909 |
rs575666954 | in-del | -/TTAT | 0.00597247 | 0.0543191 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246918195 | AATATATACTTATTA[-/TTAT]TTATCTTACAAATCA | 25909 |
rs575667145 | in-del | -/T | 0.00279162 | 0.0372561 | upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246933067 | AGCCCTCCAAGTAGC[-/T]TGGGACTATGGGCAT | 25909 |
rs575678159 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246903347 | CTTGATATGTTAGAG[C/T]AACAAAGTGGAATTA | 25909 |
rs575682340 | in-del | -/A | 0.00318978 | 0.0398085 | intron-variant, downstream-variant-500B | AHCTF1 | GRCh38.p7 | 1:246842271 | AAATCTAATTTTGAG[-/A]AAAAAAATGGATAAA | 25909 |
rs575683207 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246870150 | GAGAACTAGAATGAG[A/C]AGCAGAGCCTAGGCC | 25909 |
rs575686912 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246902818 | AATCATGGAAAAAGG[C/T]TCTAAAATTTTACAT | 25909 |
rs575708288 | snp | C/T | 0 | 0 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869373 | GGAGGAGTCACATGT[C/T]TAGGACTTTAAATCA | 25909 |
rs575734575 | snp | A/C | 1.737e-05 | 0.00294698 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246867818 | GTCTAGAAACTGTAA[A/C]ATGAAGAACGCTGGA | 25909 |
rs575744512 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869649 | GAAAAAGCCTAGATG[A/G]AAACACATCTGTTGA | 25909 |
rs575751647 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246925891 | CCTGGGCCACATGGC[A/G]AAATCTCATCTCTAC | 25909 |
rs575786129 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246855068 | ATACCCCATTCATAA[G/T]GTACCAGGAACAAAG | 25909 |
rs575786872 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246864741 | GCTACTCGGGAGGCT[A/G]AGGCAGGAGAATGGC | 25909 |
rs575855369 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246928742 | CAACAATTATATTGC[A/C]ACATGTACCAAGCAA | 25909 |
rs575871414 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246929146 | GGGTGCGGTGGTTCA[C/T]GCCTGTAATCCCAGC | 25909 |
rs575874515 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246897468 | TAATGATGGGGATAC[A/T]TTCCGATGAATGTTT | 25909 |
rs575891177 | in-del | -/CC | 0.00755907 | 0.0610114 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246889614 | TTTAAAGTACTGATT[-/CC]CAGGTGATTCAGGTG | 25909 |
rs575911125 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246877593 | GTGGCCTGGATAGAG[A/C]TGAATGGTTGGTGTG | 25909 |
rs575931393 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246863782 | TCCGTTTTTAGAAGA[C/T]GTGAAAACATAAAAG | 25909 |
rs575934055 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246883162 | GTGAGTCCGGGGAGA[A/G]TGTTAGTGTTTGATG | 25909 |
rs575962224 | snp | A/G | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246877201 | AGTAAATCTTCCATC[A/G]AGCCCATTTCCTGAC | 25909 |
rs575991943 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246892265 | AACTGTCTTCATTCT[A/G]AAATCCTTCTTTAAA | 25909 |
rs575992273 | snp | A/T | 0.0111196 | 0.0737302 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246865936 | ATTGATTTATGTAAC[A/T]TTTTACTTGTTAGAG | 25909 |
rs576022426 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246899685 | AGATAACAAACCTAT[C/T]ACACAGCAAAACAAG | 25909 |
rs576024774 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246906882 | TTTTCCCTCTCAACT[A/G]AGAATTCTTTATTAA | 25909 |
rs576030140 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246893140 | AATTGAGTTTAATTT[C/T]TTACAAAACATGAGC | 25909 |
rs576048129 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246891225 | ACTAATTCATCTTTG[C/T]ATTTAGTTTACTTTG | 25909 |
rs576090521 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246896673 | AGAATTCTGTGAATT[A/C]AAATCACTGAACTGT | 25909 |
rs576113682 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246873839 | CAAAAACGTTCCCTG[C/T]GTCACCTTGACTAAC | 25909 |
rs576117924 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246849399 | AAAATAAATCTGTTA[C/G/T]GTGAGTTACAGGATT | 25909 |
rs576170531 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246893916 | CTTGGTCAAAAATTA[C/G]TTTTGGCTGGATGTA | 25909 |
rs576176798 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246870117 | AGAAAACAACTGCAG[A/G]TATGGGGGAAAGAGC | 25909 |
rs576186021 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246870413 | CTGTGACAGACAAAG[A/G]CCTTGTCTCTTAAAA | 25909 |
rs576219030 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246911663 | TAATTTTATATTTTT[C/T]AGTAGAGACGGGGTT | 25909 |
rs576220958 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246919649 | ACCCAGGAGGTGGAG[A/G]TTGCAGTGAGCCTCA | 25909 |
rs576239928 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246860002 | CGCGGTGGCTCACGC[C/T]TGTAATCCCAGCACT | 25909 |
rs576259660 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246912304 | ATATGGTGAAACCCC[A/G]TCTCTACTAAAAAAA | 25909 |
rs576260540 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246857010 | TCAAAAGTGCGGACA[A/T]GCAATCTGTGTCAGT | 25909 |
rs576289524 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246898905 | CCAGCCTGGCCAACA[C/T]GGTGAAACCCCATCT | 25909 |
rs576298817 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246880855 | TTCCTACAGAAGACA[A/G]TAATGATGCTAGGAA | 25909 |
rs576362170 | in-del | -/GTA | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246877730 | GAAGAGTAGAGCTTG[-/GTA]GTAGATGTTTTTTGG | 25909 |
rs576423699 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246857868 | TATTTAGTGATTACT[A/G]ATAGTCTTGCATTAT | 25909 |
rs576440146 | snp | C/T | | | upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246933789 | GAAATGTAATTTTCT[C/T]TTTTCTGTAATTTTT | 25909 |
rs576454925 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246852842 | AGGATCCTCCCTCCT[C/T]AAACTCCCAAGTAGC | 25909 |
rs576458752 | snp | A/C | 3.37046e-05 | 0.00410502 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850381 | TTCTACAGATCTTTT[A/C]ATTCTTCTAGGAGTC | 25909 |
rs576465385 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246844159 | AATGCTTCAAACTAA[A/G]AAGTGCTACAATATA | 25909 |
rs576474243 | snp | C/T | 3.30087e-05 | 0.00406242 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850941 | GAATGGACTGTTCCA[C/T]TGTATCTGAAGTAAT | 25909 |
rs576565701 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246930013 | GCCAAGATTGTGCCA[C/T]TGCACTCCAGCCTGG | 25909 |
rs576592058 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246879488 | AGCATTGTTTAAAAT[A/G]GCTAAAGGTTGAAAC | 25909 |
rs576624513 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869765 | GATAATGCCCCTGGT[C/T]ACCCAGGAGCCCTGA | 25909 |
rs576634025 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246930713 | CCACTGCGCCCAGCC[A/C]AAGACAGTTCTTAAA | 25909 |
rs576634168 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868933 | CACTGCAAGTTCTGC[C/T]TCCCGGGTTCACGCC | 25909 |
rs576698199 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246914155 | TAACTAGTCATCCAT[A/G]TTTTATACTTGTCTT | 25909 |
rs576701636 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868368 | TCATGTGATCCACCC[A/G]CCTTGGCCTCCCAAA | 25909 |
rs576744929 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246890348 | TTTGAAAGCAAGAAA[C/T]GTTCACTACAAATCA | 25909 |
rs576809294 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246848206 | GGGCTCAAACTGTAT[C/G]AGTACAACAAGTCAT | 25909 |
rs576831934 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246883779 | TGTGCTAGTTTTCTG[A/G]GGACTGGAAAATTGA | 25909 |
rs576833228 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246898862 | GGAGGCCGAGGCAGG[A/C]GGATCATCTGAGGTC | 25909 |
rs576892207 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246917957 | ACTTCCTAATTATAA[A/G]GAAAAACTAGTTGCA | 25909 |
rs576894632 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246841710 | TCCCACTTCCCTTTC[C/T]TACTTTTTCTGCAAA | 25909 |
rs576918696 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246895404 | GAACAGACAATATGC[A/G]TTTGGGGTGTGTGTG | 25909 |
rs577004784 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246892968 | CTTTTAAAACACTTA[C/G]TATGCTTTGTATGTT | 25909 |
rs577031674 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868380 | CCCGCCTTGGCCTCC[C/T]AAAGTGCTGGGATTA | 25909 |
rs577054500 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246925375 | GTAAATGTTCTATTT[C/T]TTAGGCTGGGTGAGT | 25909 |
rs577061112 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246880911 | AAGGCTAGGCTAGCA[C/T]GTTGGCAGTAAAAGA | 25909 |
rs577070008 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246862218 | GGGCGCGGTGGCTCA[C/T]GCCTGTAATCCCTGC | 25909 |
rs577073671 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868700 | TTCTTTCATTATGCA[C/T]ACACTAGTAAATAAA | 25909 |
rs577101372 | snp | G/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246924212 | TTAACTTTAAAAAAT[G/T]TATAAAGAAATATTT | 25909 |
rs577114479 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246925870 | AGCCCAGGAATTTGA[C/T]ACCAGCCTGGGCCAC | 25909 |
rs577138816 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246904699 | CTGTAGTGAACTCAA[A/G]CACGAAGCATGCAGT | 25909 |
rs577248790 | in-del | -/CAT | 0.00119737 | 0.0244387 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246846567 | TATCCCTTCCAATCC[-/CAT]CATCTCATTCTAGCA | 25909 |
rs577351838 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246855882 | TCCCATCTGCTTTAA[C/G]CTGCTTTAGTCCTAC | 25909 |
rs577389594 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246858061 | GCCTCCCAGGTTCAC[A/G]CCATTCTCCTGCCTC | 25909 |
rs577390789 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246856896 | ACCATTTATAATGTT[G/T]TAAGTTATATTTTGT | 25909 |
rs577523820 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246912871 | TGCTGGGTAATTTCA[C/T]ATTGGCTGATAAGGC | 25909 |
rs577532215 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246851814 | GAAACAACCCCCAAA[C/T]TGTGTTTTAATGGTA | 25909 |
rs577536725 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246878146 | CTCATGCCTGTAATC[A/C]CAACACTTTGGGAGG | 25909 |
rs577654282 | in-del | -/A | 0.00120651 | 0.0245316 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246852494 | TAGAATTTTTTTTTT[-/A]AAAAAAACTAAGTCT | 25909 |
rs577659031 | snp | C/T | 1.64912e-05 | 0.00287147 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246905635 | ATACAGGAACTTGTC[C/T]ACTTTCCAATTGTAT | 25909 |
rs577670378 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246864381 | ACCTATATTTACTGA[A/G]CTCTTACTATGTGCC | 25909 |
rs577698450 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246906472 | ATGTAATCCCAGCTA[C/G]TTGGGAGGCTGAGGC | 25909 |
rs577709306 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246871295 | AAAACAGAGACACCA[C/T]TCGCTTACTGATGGG | 25909 |
rs577714473 | in-del | -/CTGGTAACTCTCATGTGATTCCTTCTCATG | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246856543 | GCACCCAGGTTCTCA[lengthTooLong]CTGGTAACTCTCATG | 25909 |
rs577813788 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869030 | TTTCTATTTTTAGTA[C/G]AGACGGGGTTTCACC | 25909 |
rs577874301 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246844737 | AGGAAGATATTCCAT[A/G]GAAAAATAAAAATGG | 25909 |
rs577884110 | snp | C/T | 6.65458e-05 | 0.00576788 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246900210 | CTCCAATGACCACAG[C/T]GCAAAATAAGAGCAA | 25909 |
rs577891160 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246931335 | GCCGCCATGTGCCGC[A/C]GCTCCTCCGGTCCGA | 25909 |
rs577907246 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246886719 | CTATGCCATTTTATA[C/T]AAGAGACATGAGCCT | 25909 |
rs577918968 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246900688 | TTAAAAAGTAGTCAC[A/T]CATCAGAAGTTATAT | 25909 |
rs577920863 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246894161 | CTGAGCCATGAACTC[A/G]CCACTGTACTCCTGC | 25909 |
rs577975446 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246862341 | AAAAATTAGGCAGGC[A/G]GGGTGGCGGGCGCCT | 25909 |
rs577994202 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246926978 | AGGAGATCGAGACCA[C/T]CCTGGCTAACAAGGT | 25909 |
rs578031491 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246894556 | CAAAAAAAGAAAAGA[C/G]TTTACAACTTCAAAA | 25909 |
rs578150552 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246922189 | GTATGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 25909 |
rs578184158 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246915148 | CAGCCTGGCCAACAG[A/G]GTGAAACCCCATCTC | 25909 |
rs578190718 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246908481 | CCTGCCTGTTCTGTA[A/G]ACATTGTGTTTCAGA | 25909 |
rs578211073 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246909184 | TGGGAGGCTGAGGCA[A/G]GCAGATCATGAAGTC | 25909 |
rs578218312 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246901493 | GCTGGGCATGGTGGC[A/G]GGTGCTTGTAGCCCC | 25909 |
rs745308809 | snp | A/G | 1.64743e-05 | 0.00287 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246849820 | TTCTTCTGATACTGA[A/G]TGCAATGAACGTTTT | 25909 |
rs745353272 | snp | C/T | 1.66579e-05 | 0.00288595 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246900096 | TGGATTAAAAAACTG[C/T]TCGGGAGGTGGATAT | 25909 |
rs745356540 | snp | A/G | 1.65031e-05 | 0.00287251 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246889992 | CTCAAACTTCTGTCG[A/G]CGACTGGTGTAGTAG | 25909 |
rs745364337 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246845575 | TTTATTTCACTTTTC[A/G]TAATCTTCACCTAAG | 25909 |
rs745387102 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246859753 | GCTAATTTTTTTATA[C/T]TTTTTGTAGAGATGG | 25909 |
rs745393529 | snp | C/T | 1.9517e-05 | 0.0031238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246876015 | TCCAATAGATTATGA[C/T]ATTCTTCAATGAAAT | 25909 |
rs745399680 | snp | C/T | 5.24654e-05 | 0.00512152 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246861200 | GTTCAGGAAAAAAGA[C/T]GTGGTCCTATCTTTG | 25909 |
rs745410574 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246907262 | TGTTGTTGACCAAAA[C/T]GTTGTAAAGTTACAA | 25909 |
rs745421117 | snp | C/T | 1.75167e-05 | 0.0029594 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246899534 | AAAAGATTTAAAAAA[C/T]AATCCACTTACATAT | 25909 |
rs745421350 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246894222 | AAAAAAATTACTTTT[A/C]TCACTTTAATGTAAA | 25909 |
rs745427412 | in-del | -/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246911479 | CTATCTATGAAGATT[-/C]TTTTTTTTTTTTTTT | 25909 |
rs745471437 | snp | A/T | 1.66671e-05 | 0.00288674 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246905657 | CAATTGTATGTAATA[A/T]CTGAAACAAATTAGT | 25909 |
rs745520896 | snp | A/C/G | 8.23684e-05 | 0.00641706 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246849723 | GAGTCCTGCTGCTGC[A/C/G]GGATGATTTAGTGAA | 25909 |
rs745530686 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246895234 | CTAGGTTAGATAAAA[C/G]TCTTAATTTTCTTGA | 25909 |
rs745554095 | snp | C/T | 1.65622e-05 | 0.00287764 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850812 | AGGAAACCACGTCAT[C/T]AACCTGGCTGACATT | 25909 |
rs745562552 | snp | G/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246846332 | TAAATAGGCACAAGG[G/T]ACAGAAAGTATGGTA | 25909 |
rs745585236 | snp | A/T | 1.81338e-05 | 0.00301108 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246867830 | TAAAATGAAGAACGC[A/T]GGAATTAAGTGCATC | 25909 |
rs745601363 | snp | A/G | 1.66081e-05 | 0.00288163 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246842786 | ATCTTTCTATGGGTT[A/G]AACATTTTAAAAGGT | 25909 |
rs745619250 | snp | C/T | 5.17451e-05 | 0.00508624 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850401 | TTCTAGGAGTCCTTT[C/T]TGTAACAGATGAAAC | 25909 |
rs745623814 | snp | A/C | 3.53432e-05 | 0.00420361 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246877318 | CTGAAAGCAGTATTT[A/C]TCAAAGTTTAGTTTT | 25909 |
rs745634334 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869246 | CTTACTCCACTGACT[A/G]ACTGTTCCCCCGCGT | 25909 |
rs745639711 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246854823 | AGGAACCCACACATT[C/G]GGGTTCAGCCCCCTG | 25909 |
rs745645765 | snp | G/T | 1.77307e-05 | 0.00297742 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246864163 | ACTGAAAAAACAAAA[G/T]AATTTAGTATCCCAT | 25909 |
rs745652905 | snp | C/G | 3.31384e-05 | 0.00407039 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246902673 | TTCACAGTATTCTAA[C/G]CCCTGTAACATAAAA | 25909 |
rs745674759 | in-del | -/A | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246905693 | TCATATTTTTAAGTT[-/A]TTTTTTAGAAAGGAA | 25909 |
rs745678766 | snp | C/T | 1.65996e-05 | 0.00288089 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246877233 | GACTTCATACATGTG[C/T]TTCAGTAACTCCTCT | 25909 |
rs745707771 | snp | C/G | 1.64803e-05 | 0.00287052 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246902596 | CATCCCAACAATTTG[C/G]TATTACTCGTCTGTC | 25909 |
rs745724348 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868482 | CTGGTCTCAAACTCC[A/G]GGCCTCAAGTGATCC | 25909 |
rs745732093 | snp | A/G | 0.000265098 | 0.0115099 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246890071 | TCATCTAGATTTTTA[A/G]GAGTTGGAAAAAAAG | 25909 |
rs745741965 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246888583 | TCAAAGCAACCAGCA[C/T]CAAAATATTAAAAGT | 25909 |
rs745798503 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246916512 | TTTACATATTATCTC[C/G]ACATTGAAATCTTTT | 25909 |
rs745805835 | snp | A/C | | | upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246933891 | GAAACAGTTAAAAAG[A/C]GTACTGCTTTTGCAG | 25909 |
rs745817083 | snp | G/T | 3.55032e-05 | 0.00421311 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246853190 | TTCTACTTCATGATC[G/T]TCTTTTAAGTTCAGC | 25909 |
rs745825077 | snp | C/T | 3.46891e-05 | 0.00416453 | utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246840765 | TCCACACTATTCTGA[C/T]GACTTTACAAATAGG | 25909 |
rs745839202 | snp | C/G | 1.6825e-05 | 0.00290038 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246916201 | GGTCATAAAGACAGA[C/G]AACACTCCCTTCTGT | 25909 |
rs745870521 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246929850 | CGAGGTCAGAAGTTC[A/G]AGACCAGCCTGGCCA | 25909 |
rs745935425 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246841878 | CTCACTGCAACCTCC[A/G]CCTCCTGGGTTCAAG | 25909 |
rs745953082 | snp | A/T | 1.67156e-05 | 0.00289093 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246913427 | CCTAGAAAACATAAT[A/T]CGTGATTTGCTTTTC | 25909 |
rs745954810 | in-del | -/TTGCAGTGAGCCGAGA | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246854235 | CCTGGGAGGCGGAGC[-/TTGCAGTGAGCCGAGA]TTGCAGTGAGCCGAG | 25909 |
rs745966646 | snp | C/T | 3.30748e-05 | 0.00406649 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246888489 | AAACCAGTCCATCAA[C/T]CATCAAGCAATCGGG | 25909 |
rs745989774 | snp | C/T | 1.64849e-05 | 0.00287092 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246913306 | AGGATCTGTCCAACA[C/T]CAGTGACCACAGCTG | 25909 |
rs746000634 | in-del | -/AT | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246854968 | TGATCGGCTTTTTAC[-/AT]GTTAGACAATTCTCT | 25909 |
rs746008613 | snp | C/T | 1.64773e-05 | 0.00287026 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246898291 | TATAACCATCAGGAA[C/T]GAGTTCATTGAGTGA | 25909 |
rs746071853 | snp | C/T | 3.29669e-05 | 0.00405984 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246851169 | CTGCTTTAGGTAACA[C/T]ATCAGATGATGCAAA | 25909 |
rs746104489 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246910018 | TCACCATGTGAATCC[A/G]CTGATCACTAATTGA | 25909 |
rs746122214 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246924566 | AAAAATCAACCTAAC[A/G]TTCTTTCTTGTCATT | 25909 |
rs746129399 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246923695 | GTGACACATTGCTTT[A/G]CATTCCTCCCCTAGT | 25909 |
rs746152606 | snp | A/G | 1.64857e-05 | 0.00287099 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246851103 | TTGCAATTTGTCCAT[A/G]ATTATCATTTTCCCC | 25909 |
rs746153217 | in-del | -/A | 0.000119253 | 0.00772091 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246905497 | CGAGACTCTGTCTCC[-/A]AAAAAAACAAAACAA | 25909 |
rs746166496 | snp | A/G | 3.3976e-05 | 0.00412151 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246857661 | TAAACTTCTTTCTAA[A/G]AGTATTTGAATTTCT | 25909 |
rs746167533 | snp | A/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246914708 | AAAACAGCTAGTAGG[A/T]TGAACTTTTGAAAGT | 25909 |
rs746177702 | snp | A/G | 1.95946e-05 | 0.00313 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246918421 | TTATGACACATTTGT[A/G]GACAATATACTTGAT | 25909 |
rs746188781 | snp | A/T | 1.65726e-05 | 0.00287855 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850732 | AGCAACATCTGCTGA[A/T]GCTTCCTGTTGTGCT | 25909 |
rs746219072 | snp | A/C | 1.65121e-05 | 0.00287329 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246864051 | GGAGATTTCATGGAG[A/C]TTTGCTGAATAAACT | 25909 |
rs746227895 | snp | A/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246912848 | GAACACTATGTTAGA[A/T]CCTACATTGCTGGGT | 25909 |
rs746232246 | in-del | -/G | | | utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246839227 | ATCTACATTCACGGA[-/G]GGGGGAAAAAAAGTA | 25909 |
rs746235389 | snp | C/T | 1.67733e-05 | 0.00289592 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246864129 | AGTCTGTAATCAGAA[C/T]GCGCATTTATTGAGT | 25909 |
rs746241299 | in-del | -/TTTCCTGAT | 0.000418155 | 0.0144535 | cds-indel, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850356 | TTATAATTTCAACAC[-/TTTCCTGAT]TTTCTACAGATCTTT | 25909 |
rs746242151 | snp | C/G | 1.65086e-05 | 0.00287298 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246855812 | TGGTACCTTGGACTT[C/G]TGGGTGAAGATTTTC | 25909 |
rs746257524 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246912294 | ATCCTGGCCAATATG[A/G]TGAAACCCCATCTCT | 25909 |
rs746328158 | in-del | -/A | | | splice-acceptor-variant, intron-variant | AHCTF1 | GRCh38.p7 | 1:246843930 | TCTATTTTTTTAGCT[-/A]AAAAAAAGTTGAAAA | 25909 |
rs746345149 | snp | A/C | 0.000200093 | 0.0100003 | intron-variant, downstream-variant-500B | AHCTF1 | GRCh38.p7 | 1:246842659 | GAGACTGTCTCAATC[A/C]ATCAATCAATCAAGA | 25909 |
rs746398092 | snp | C/G | 1.75542e-05 | 0.00296256 | missense, synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246840979 | GAGGAGGTGACCAAG[C/G]ACTTTCTTTTTCTGT | 25909 |
rs746406227 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246900654 | TGCATTTTGACTGTT[C/T]CTCAATTTTAAGGCC | 25909 |
rs746412004 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246929370 | GCCAAGATCACGCCA[C/T]TGCACTCTAGCTTGG | 25909 |
rs746416283 | snp | A/T | 1.64885e-05 | 0.00287123 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850165 | GGAGTCTTCTCTCAC[A/T]TCTGATGGACTAACT | 25909 |
rs746449054 | snp | A/G | 1.64792e-05 | 0.00287042 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246863969 | TAATTCTGAAGCCCT[A/G]GAGATGGCCTGAGGC | 25909 |
rs746463611 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246927568 | TGAAACACCTACGTT[A/C]AGTACTGTACAAAAT | 25909 |
rs746476506 | snp | A/G | 3.53632e-05 | 0.0042048 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246891079 | TAAAGAAGAGTTAAC[A/G]TCAGTTGTTTACTTA | 25909 |
rs746480416 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246880986 | TACAGCAAAGACAGA[A/C]TGAAAACCCATCCTG | 25909 |
rs746493325 | snp | C/T | 1.66338e-05 | 0.00288386 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246877245 | GTGCTTCAGTAACTC[C/T]TCTATATTCAACCTA | 25909 |
rs746530827 | snp | A/G | 1.66726e-05 | 0.00288722 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246862050 | CCAGGTGATGGAGAG[A/G]GAGATGCTAAAGGTG | 25909 |
rs746533513 | snp | A/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246914271 | GAACATCCAAATCCA[A/T]AAGTCCAAAATCTAA | 25909 |
rs746543111 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246846732 | TTGAAATATATATAC[A/G]TATACATATATATAT | 25909 |
rs746550814 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246880511 | GGAGGTTACAGTGAG[A/C]CGAGATCGCGCCACT | 25909 |
rs746557110 | snp | A/G | 1.66228e-05 | 0.0028829 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246890090 | TTGGAAAAAAAGCTG[A/G]TAATAATCCCCAAAT | 25909 |
rs746600292 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246879728 | AGCTACTTGCGAGAC[C/T]GAGGCAGGAAAATCG | 25909 |
rs746606806 | snp | C/G | 1.66546e-05 | 0.00288566 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246900120 | TGGATATGAAGGAGG[C/G]ACTCCTCTATTTAAA | 25909 |
rs746632307 | snp | C/T | 1.71149e-05 | 0.00292526 | utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246840777 | TGATGACTTTACAAA[C/T]AGGTGTACATTAAAA | 25909 |
rs746649401 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246917017 | TTAGTCATGTTTGGA[C/T]TTTACCCTGCCTGCA | 25909 |
rs746687719 | snp | A/G | 3.29489e-05 | 0.00405874 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246849831 | CTGAGTGCAATGAAC[A/G]TTTTTGGCTTTGACT | 25909 |
rs746737038 | snp | A/T | 1.90134e-05 | 0.00308323 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246876162 | CGAGCCAGTGATCTC[A/T]CCCGCAAACGAGGAT | 25909 |
rs746741909 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246903092 | AGGCTATGAGACTTC[A/G]CCCATAAAAATGCAA | 25909 |
rs746749291 | snp | G/T | 1.87675e-05 | 0.00306324 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246843956 | GAAAAAACTGTATCT[G/T]TATCTTTATATATGT | 25909 |
rs746763370 | snp | A/G/T | 3.31946e-05 | 0.00407387 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246860975 | CTTTTCAGTTTGTTC[A/G/T]GTTACATTAGTAGTT | 25909 |
rs746784410 | in-del | -/TC | 5.65254e-05 | 0.00531597 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246894628 | ATTTTAATATTAAAT[-/TC]TGTCCTACATCTAGA | 25909 |
rs746793008 | snp | C/T | 1.64811e-05 | 0.00287059 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246898175 | ATAACGTGATCCAAC[C/T]AAAAGAAACAATAGA | 25909 |
rs746802871 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246857212 | CCATACTTTGAATAC[A/G]TCATCTGGTAAAGTG | 25909 |
rs746819261 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246856033 | TTACCCATTTTCTAA[C/T]GTTTTACTCTTTTGG | 25909 |
rs746859756 | snp | A/G | 4.94727e-05 | 0.00497332 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246903999 | TATTACCAAAGGCCA[A/G]CTGCAGCAGATGCAA | 25909 |
rs746905854 | snp | A/G | 1.82241e-05 | 0.00301856 | synonymous-codon, nc-transcript-variant, intron-variant | AHCTF1 | GRCh38.p7 | 1:246843855 | GCTCCTTAAAGCAGG[A/G]GGTGAGATGACAAAC | 25909 |
rs746931903 | snp | A/C | 2.49972e-05 | 0.00353525 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850554 | GTATGTCCTGATTAA[A/C]TTCTTTCTTTCTCCT | 25909 |
rs746944451 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246904740 | AGCATAGATTCCAGA[C/G]CCACATCATCTGAAT | 25909 |
rs747017810 | snp | C/T | 1.6554e-05 | 0.00287693 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246918253 | CATTATGTTTACCTG[C/T]AGCAAACTTTCCACG | 25909 |
rs747049667 | snp | C/G/T | 4.95793e-05 | 0.00497871 | synonymous-codon, missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246864065 | GCTTTGCTGAATAAA[C/G/T]TCCGAACACTGAGAA | 25909 |
rs747061573 | in-del | -/CTC | 3.29603e-05 | 0.00405944 | cds-indel, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246851202 | CACCTGGCTCAACTT[-/CTC]CTTCTTCACCTTCCA | 25909 |
rs747070990 | snp | A/C | 1.68972e-05 | 0.0029066 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246916129 | ATGTCCAGGTATCTT[A/C]AACAGTACCTACCCT | 25909 |
rs747071652 | snp | C/T | 0.000162838 | 0.00902179 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246891963 | TCCATACAGTAAATC[C/T]AAATAAATTAGAATC | 25909 |
rs747079897 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246899942 | AATTTCCTAAGTTAT[C/T]CATATGTTAACTAAC | 25909 |
rs747097475 | snp | C/T | 1.65157e-05 | 0.0028736 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246902559 | CCTGTCACCATGAGA[C/T]CGAAATTTCTCTATA | 25909 |
rs747098059 | snp | A/G | 1.77303e-05 | 0.00297739 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246900476 | GCGATAGAGCTGGAA[A/G]AAAAAGATAATTTTT | 25909 |
rs747098665 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246844228 | TATTTCTTTTAATCC[A/G]TACTGCTCCTCAAGC | 25909 |
rs747108992 | snp | G/T | 1.65124e-05 | 0.00287331 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246877123 | CTACCAATTTATCTT[G/T]AATTTCTGACAAGTT | 25909 |
rs747140014 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246910985 | TCAGTGAAGCCTAAA[C/T]AGTTGTAATCATAAA | 25909 |
rs747152873 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246866411 | TCCATTTAAAATACC[A/G]TCTTACCAGAGTAAA | 25909 |
rs747199866 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246855606 | GGAAAGCTGACCAGA[A/G]AGAGGAATAACTGAG | 25909 |
rs747245098 | snp | A/G | 1.67368e-05 | 0.00289277 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246913429 | TAGAAAACATAATAC[A/G]TGATTTGCTTTTCTT | 25909 |
rs747264288 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246912026 | GCAGCCTCCCCTCCC[A/G]CTTCCACCACTGGCA | 25909 |
rs747265367 | snp | C/T | 3.3042e-05 | 0.00406447 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246889968 | TGTTTTACTATACCT[C/T]GATAAACGCTCAAAC | 25909 |
rs747271989 | snp | A/G | 1.65089e-05 | 0.00287301 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246851329 | AAACTGTTGGTCAAT[A/G]GTATCAAAATTGTAC | 25909 |
rs747275720 | snp | A/G | 4.95086e-05 | 0.00497512 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850931 | ATTGTTTCATGAATG[A/G]ACTGTTCCATTGTAT | 25909 |
rs747308530 | snp | C/T | 1.75965e-05 | 0.00296613 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246876058 | GAAAAACTGATGATG[C/T]TGACAGATGATAAGG | 25909 |
rs747316822 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246870724 | AGGGTATAAAACCTC[A/C]AAAAAAAAAAAAAAA | 25909 |
rs747321221 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246930263 | AAACGTTCCCCCCGC[C/T]TCAGCCTCCCAAGTA | 25909 |
rs747326267 | in-del | -/A | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246871741 | CTGACTGCAGACTAT[-/A]AAGGAGGTTAATAAT | 25909 |
rs747329452 | in-del | -/ACAC | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246898634 | AAAACACACACACAC[-/ACAC]ACACACACACACACA | 25909 |
rs747368544 | snp | A/G | 1.64768e-05 | 0.00287021 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246907607 | ATCAGAAAAACCTAC[A/G]GCAAGCTGATTTGTC | 25909 |
rs747403104 | snp | A/C | 1.64969e-05 | 0.00287196 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246887304 | GAAAGATTCAATGGG[A/C]GTGTCTGTTTTGTTG | 25909 |
rs747419980 | snp | G/T | 1.88149e-05 | 0.0030671 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246905676 | AAACAAATTAGTATA[G/T]TTCATATTTTTAAGT | 25909 |
rs747442353 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246901819 | GGCATCAGAGTGAGA[C/T]CCCTGTCTCTAAATA | 25909 |
rs747465807 | snp | A/G | 1.7009e-05 | 0.0029162 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246857820 | TCTAAATTGCCTATA[A/G]GTCATACAAATAAGA | 25909 |
rs747536430 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246906374 | CACAAGGTCAGGAGT[C/T]CGAGACCAGTCTGAC | 25909 |
rs747546536 | snp | A/G | 1.65343e-05 | 0.00287521 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850822 | GTCATCAACCTGGCT[A/G]ACATTCATAGTCATT | 25909 |
rs747557376 | snp | A/G | 0.000162774 | 0.00902 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246931295 | CCGACTGCCGGCGCA[A/G]GACGCGAACCACCAG | 25909 |
rs747582142 | snp | C/T | 1.67206e-05 | 0.00289137 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246885552 | ACTGGACACTGTTGG[C/T]TTCATTGTCTGAATA | 25909 |
rs747582879 | in-del | -/C | 3.35233e-05 | 0.00409396 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246855849 | AAAAAGAAATACATA[-/C]CTTAGTGTGTAAGAA | 25909 |
rs747587376 | snp | A/C | 1.66355e-05 | 0.002884 | missense, nc-transcript-variant, intron-variant | AHCTF1 | GRCh38.p7 | 1:246842748 | GCTTTTGGCTTTCCC[A/C]GAGTTTCTACTGATT | 25909 |
rs747596138 | snp | A/G/T | 8.80153e-05 | 0.00663333 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850583 | CTTCCTCTCCTAGGC[A/G/T]TAACAGAATTTTGAG | 25909 |
rs747597500 | snp | C/T | 5.00897e-05 | 0.00500423 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246857680 | ATTTGAATTTCTCTC[C/T]ATTAACTTACCCTTC | 25909 |
rs747603129 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246911143 | GTTATAAAATTATCC[C/T]TGTGCACCTACTGAT | 25909 |
rs747639401 | in-del | -/TCAA | 0.0525931 | 0.153397 | intron-variant, downstream-variant-500B | AHCTF1 | GRCh38.p7 | 1:246842652 | CAGAGCGAGACTGTC[-/TCAA]TCAATCAATCAATCA | 25909 |
rs747656296 | snp | A/C | 1.6525e-05 | 0.00287441 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246904026 | GCAAACTCAAAACAT[A/C]CCCTTCACTGAAACA | 25909 |
rs747664719 | snp | C/G | 1.75041e-05 | 0.00295833 | utr-variant-5-prime, missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246918376 | AGTCTCGCATACTTC[C/G]ACTGTAAATATTTTT | 25909 |
rs747683525 | snp | A/G | 1.654e-05 | 0.00287571 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246891790 | GTACCTCTCTCAGTG[A/G]TCTCTCGGGCTTCTG | 25909 |
rs747688439 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246908682 | CACAAGGTCAGGAGA[C/T]TGAGACCATCCTGGC | 25909 |
rs747717897 | snp | A/G | 2.1067e-05 | 0.00324547 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246885454 | CCATTTTATTAACAG[A/G]TACGATAAAGACTTT | 25909 |
rs747732737 | snp | A/G | 1.66291e-05 | 0.00288345 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246900312 | AATACAAAGAGAAAG[A/G]AGAGAGAAAAAAAAA | 25909 |
rs747736400 | snp | C/T | 3.61579e-05 | 0.00425178 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246891091 | AACATCAGTTGTTTA[C/T]TTACAAAAAAATCAA | 25909 |
rs747744982 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246904884 | CACTCCTTAGTCCTT[C/T]GCTGAGTACCCACCC | 25909 |
rs747745047 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246847185 | TCCCAGCTACTGGGG[A/G]GGCTGAGGCAGGAGA | 25909 |
rs747748138 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246874548 | TGGTGGTCATGAAAC[A/G]GCCACCCAAAAAAAT | 25909 |
rs747799982 | snp | C/T | | | utr-variant-5-prime, missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246918373 | TTAAGTCTCGCATAC[C/T]TCCACTGTAAATATT | 25909 |
rs747803449 | snp | A/G | 1.68357e-05 | 0.00290131 | missense, synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246840967 | GAATTTCTATGGGAG[A/G]AGGTGACCAAGCACT | 25909 |
rs747883397 | snp | A/T | 1.90569e-05 | 0.00308676 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246862186 | TGGAATTACACCATT[A/T]AAAGTGCTTATAGGC | 25909 |
rs747899069 | snp | C/G | 1.64784e-05 | 0.00287035 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246851227 | ACCTTCCAATATCAA[C/G]GTAAAGTTGCTTTGA | 25909 |
rs747933406 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246844407 | GTTCCAGCCAAAGGA[A/C]CAGAAAAGTTCATCT | 25909 |
rs747947036 | in-del | -/GCGGG | | | downstream-variant-500B | AHCTF1 | GRCh38.p7 | 1:246838607 | AAGTTGTAGAAGTGG[-/GCGGG]GCGGGGCGGGGGGAA | 25909 |
rs747960854 | snp | A/G | 1.64855e-05 | 0.00287097 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246861041 | GAAAACAGTCTCTTC[A/G]AGGTCTTCCGGTGAC | 25909 |
rs747966604 | in-del | -/AT | 4.94336e-05 | 0.00497135 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246898186 | CAACCAAAAGAAACA[-/AT]AGAGTTAAAAATCAT | 25909 |
rs747968451 | snp | G/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246877505 | CACGTTTAAAGAATT[G/T]TATGCTGCTTTTTAG | 25909 |
rs747975206 | in-del | -/ATCT | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246871632 | GACTAGATGAGCCTC[-/ATCT]TCAGGACAGGCTAAG | 25909 |
rs747994051 | in-del | -/AAAACAAAAC | 1.67594e-05 | 0.00289472 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246905501 | GACTCTGTCTCCAAA[-/AAAACAAAAC]AAAACAAAACAAAGT | 25909 |
rs748040755 | snp | A/G | 4.97203e-05 | 0.00498575 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246905530 | CAAAACAAAGTTTGT[A/G]TGAGACCTACCTATC | 25909 |
rs748045156 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246892409 | CACTGCAACCTCTAC[C/T]TCCCAGGTTCAAGGG | 25909 |
rs748058979 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246865302 | GGAGCCCAGAAATAA[A/G]AACTTGTAGTTGCAG | 25909 |
rs748068412 | snp | C/T | 3.29864e-05 | 0.00406105 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246849652 | TGACGCTGGAGAAAA[C/T]AAAGGCTCATTGTTT | 25909 |
rs748071561 | snp | C/G/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246926970 | ACGAGGTCAGGAGAT[C/G/T]GAGACCATCCTGGCT | 25909 |
rs748091418 | snp | A/G | 1.64743e-05 | 0.00287 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246867663 | TAAGAAAACATACCT[A/G]TTGAAAGGTGTGGTG | 25909 |
rs748100554 | in-del | -/GA | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246861878 | GGTATTTAAAAACTT[-/GA]TTTATCTAACTTTTT | 25909 |
rs748173691 | snp | G/T | 1.95372e-05 | 0.00312541 | missense, nc-transcript-variant, intron-variant | AHCTF1 | GRCh38.p7 | 1:246843828 | GTTCTTATTGGATGT[G/T]TTTTTTTGTCTGCTC | 25909 |
rs748192239 | in-del | -/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246918511 | GTTACAAAATACATA[-/T]TTGGCCAGATGCGGA | 25909 |
rs748209865 | in-del | -/A | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246862479 | GCAAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAG | 25909 |
rs748220523 | snp | A/G | 3.30639e-05 | 0.00406581 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246887332 | TTGGGAAAGGAATAC[A/G]TAATATCAAGTAGCA | 25909 |
rs748233484 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246855205 | CTGGGCATAGACATT[C/T]AAGGTGTCTGCTTCC | 25909 |
rs748241395 | in-del | -/CAGT | 1.64762e-05 | 0.00287016 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246877310 | CCATACACCTGAAAG[-/CAGT]ATTTATCAAAGTTTA | 25909 |
rs748241505 | snp | A/C | 0.000197827 | 0.00994356 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246895860 | CCATCTTCGGATATA[A/C]CCAGTCAAAAGTCCC | 25909 |
rs748262742 | snp | C/T | 1.64996e-05 | 0.0028722 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246902569 | TGAGATCGAAATTTC[C/T]CTATACTCTGGCATC | 25909 |
rs748270702 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246901182 | TCATCTCTACAAAAA[A/G]ATACAAAAATTAGCC | 25909 |
rs748273425 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246853835 | AGGAAAAAATATTTC[C/T]ACACTTTCAATGGAA | 25909 |
rs748273760 | in-del | -/TC | 1.67987e-05 | 0.00289811 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246857674 | AAAAGTATTTGAATT[-/TC]TCTCCATTAACTTAC | 25909 |
rs748294594 | snp | A/G | 8.24463e-05 | 0.00642 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246902647 | CCTGTCAGGTCCAGG[A/G]TGTATCTTTCTTCAC | 25909 |
rs748305600 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246886744 | GAGCCTCTGTAAATT[C/T]TGGTATGTTTCTGGA | 25909 |
rs748333026 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246853925 | TGTTTGGCAAAAAGA[C/G]GACGACGAAAAACCA | 25909 |
rs748349335 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246920306 | TTTGTGTAAATCAGC[A/G]ATTTAGCTTGATAAG | 25909 |
rs748369982 | snp | G/T | 0.0020254 | 0.0317584 | missense, nc-transcript-variant, intron-variant | AHCTF1 | GRCh38.p7 | 1:246842752 | TTGGCTTTCCCAGAG[G/T]TTCTACTGATTGTGC | 25909 |
rs748377419 | snp | A/G | 6.63328e-05 | 0.00575865 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246877228 | TGACAGACTTCATAC[A/G]TGTGCTTCAGTAACT | 25909 |
rs748408002 | snp | A/G | 1.65405e-05 | 0.00287576 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246849908 | AGTTCCTCGTTTGGC[A/G]CTAAAATGGATTTTC | 25909 |
rs748420187 | snp | C/T | 1.66944e-05 | 0.0028891 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246862055 | TGATGGAGAGGGAGA[C/T]GCTAAAGGTGTTGAT | 25909 |
rs748423421 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246930293 | AGGCGCGCGACTAGA[A/G]GCGCCACCAATTCCC | 25909 |
rs748426126 | snp | C/T | 6.61201e-05 | 0.00574941 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246864068 | TTGCTGAATAAACTC[C/T]GAACACTGAGAAGGC | 25909 |
rs748430743 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246859914 | CAGAGAGTAGAATGA[A/C]ATTCTTAATTTCTGA | 25909 |
rs748465551 | snp | A/G | | | downstream-variant-500B | AHCTF1 | GRCh38.p7 | 1:246838864 | TGTTTCCCTTACTAC[A/G]ATACTAAGTATCTTT | 25909 |
rs748484392 | snp | C/G | 3.34941e-05 | 0.00409218 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246876907 | AAAGCCTCCAGTTTT[C/G]CTTATTCTCTTATCC | 25909 |
rs748537598 | snp | C/T | 1.92959e-05 | 0.00310605 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246876167 | CAGTGATCTCTCCCG[C/T]AAACGAGGATCACGA | 25909 |
rs748571347 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246871931 | TGTGAACTTTACAAA[C/T]GACCCTGATCCCAGA | 25909 |
rs748572951 | snp | G/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246888257 | CAAAGGGATAAAACC[G/T]TCAGTGGATCTTATA | 25909 |
rs748580216 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246921155 | CAAAATGACATTTAT[A/G]TAAGGTTAAAAAGAC | 25909 |
rs748610843 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246909723 | AAATCATAATGTGTG[C/T]AGGGTTCAGTACTAG | 25909 |
rs748640066 | snp | C/T | 1.64751e-05 | 0.00287007 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246907636 | TCCTGCTTATGTAAC[C/T]AAGAGTTGAAACAGC | 25909 |
rs748652890 | snp | A/G | 1.64914e-05 | 0.00287149 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246851084 | GTTACGGCAGATGGC[A/G]AATTTGCAATTTGTC | 25909 |
rs748659437 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246921064 | GGCATTGCACTCCAG[A/C]CTGGGCAACAAGAGT | 25909 |
rs748666315 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246922239 | GCAGTATGTGCCCGT[A/G]GTCCCAGCTACTCAG | 25909 |
rs748688909 | snp | A/C/G | 4.94265e-05 | 0.00497104 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246849850 | TTGGCTTTGACTTTC[A/C/G]GTCTTTTTTGTAAGT | 25909 |
rs748692431 | in-del | -/GC | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246860804 | GAGCCACAGTACCTG[-/GC]TAGGATGCTTTTCTT | 25909 |
rs748704163 | snp | A/G | 1.66665e-05 | 0.00288669 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246860945 | TTCTGATGCAAATAC[A/G]TCTTTATCTCCATCC | 25909 |
rs748720600 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246858447 | TATCCCAGCTCATGA[C/T]GCATACTCAGTAAGT | 25909 |
rs748737238 | snp | C/T | 4.96973e-05 | 0.00498459 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246905650 | CACTTTCCAATTGTA[C/T]GTAATATCTGAAACA | 25909 |
rs748740387 | snp | C/T | 3.30098e-05 | 0.00406249 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850944 | TGGACTGTTCCATTG[C/T]ATCTGAAGTAATTTC | 25909 |
rs748742490 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246889510 | ATGCCTAGTCAATCT[C/T]CCAAGCTAATGTTCA | 25909 |
rs748765217 | snp | A/T | 1.74318e-05 | 0.00295222 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246867819 | TCTAGAAACTGTAAA[A/T]TGAAGAACGCTGGAA | 25909 |
rs748797163 | snp | A/C | 1.65034e-05 | 0.00287253 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246898328 | TGATTTCTTTAAAAA[A/C]GTCAAAGTCTGTAAC | 25909 |
rs748798833 | in-del | -/A | 1.92721e-05 | 0.00310414 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246907505 | GTACAAGCTATATGC[-/A]AAAAAAACTACCTAT | 25909 |
rs748810136 | snp | C/T | 1.64746e-05 | 0.00287002 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246867686 | GTGTGGTGCTATTTA[C/T]AGGTTCTTTGCTTGC | 25909 |
rs748832449 | in-del | -/AT | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246862719 | AAAAGTGCCAATTAG[-/AT]TAAGATAAATTACTT | 25909 |
rs748841123 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246905129 | ACTAATTCACTGAAA[C/G]AATTGTGTTGCCTTC | 25909 |
rs748845661 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246844578 | AATTTTTAAAAGATT[A/G]GCCAATGTGGTGGTG | 25909 |
rs748850182 | snp | A/G | 1.65277e-05 | 0.00287464 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246905550 | ACCTACCTATCTTGT[A/G]TAGACTGAACAGCCC | 25909 |
rs748860563 | snp | A/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246870598 | TCCAGGGATTATAGG[A/T]ATTTTACATTTAAAA | 25909 |
rs748896913 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246859660 | CTGCATCCCCAACCT[C/T]GACCTCCTGGGTCCA | 25909 |
rs748915510 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246926283 | GCAACACAGGCTAAC[A/G]TATTTCTAATTCAAA | 25909 |
rs748969270 | snp | C/T | | | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850724 | TTAGGAGTAGCAACA[C/T]CTGCTGATGCTTCCT | 25909 |
rs748997494 | snp | A/G | 1.64887e-05 | 0.00287125 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246855801 | TCGTCCAACACTGGT[A/G]CCTTGGACTTCTGGG | 25909 |
rs749008373 | snp | C/T | 1.68758e-05 | 0.00290476 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246885571 | ATTGTCTGAATATAT[C/T]TGAGGGCTTGTCTGT | 25909 |
rs749008578 | in-del | -/CTTCTCTCACATCTGATGGACTAA | 4.94605e-05 | 0.0049727 | cds-indel, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850155 | ACTCAAGGTTGGAGT[-/CTTCTCTCACATCTGATGGACTAA]CTTCTCTCCCTCTGA | 25909 |
rs749036247 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246926986 | GAGACCATCCTGGCT[A/G]ACAAGGTGAAATCCC | 25909 |
rs749043981 | snp | A/T | 3.30535e-05 | 0.00406518 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246851335 | TTGGTCAATAGTATC[A/T]AAATTGTACTGAAGC | 25909 |
rs749046482 | snp | C/T | 8.24559e-05 | 0.00642037 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850200 | TCCCTCTGACCCTTC[C/T]AACATGTTTAATACG | 25909 |
rs749063191 | snp | A/T | 2.44412e-05 | 0.00349571 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246851459 | TAAATGAATTAAAGA[A/T]AAGAGACTGGTTAAA | 25909 |
rs749085095 | snp | C/T | 1.67167e-05 | 0.00289103 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246916165 | GAAGAACAACTGCTT[C/T]AACTACTTTTGATAT | 25909 |
rs749111022 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246845514 | AAAGTATTTCTACGA[A/C]AATTATACATTCTAT | 25909 |
rs749115287 | snp | A/G | 1.66261e-05 | 0.00288319 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246861333 | GAAAAAAATTAGTAA[A/G]TATCACAGTTAAGTC | 25909 |
rs749131586 | snp | G/T | 4.95201e-05 | 0.0049757 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246889984 | GATAAACGCTCAAAC[G/T]TCTGTCGACGACTGG | 25909 |
rs749136991 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868469 | CATGTTGGCCAGACT[A/G]GTCTCAAACTCCGGG | 25909 |
rs749148447 | snp | A/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246895030 | GGCCTAATTCCTTTA[A/T]AAAAAAAAAGGTCAA | 25909 |
rs749173898 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246877734 | AGTAGAGCTTGGTAG[C/T]AGATGTTTTTTGGTT | 25909 |
rs749215652 | snp | C/T | 1.64743e-05 | 0.00287 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246849713 | TTGCTAGACCGAGTC[C/T]TGCTGCTGCGGGATG | 25909 |
rs749240210 | in-del | -/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246875928 | TATCTCCAAGGCATG[-/C]CTGTATGTGTTAGCG | 25909 |
rs749243963 | snp | C/T | 1.65121e-05 | 0.00287329 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246861157 | TTTGTGACCCCTCAT[C/T]CATTTCTTGATGCTC | 25909 |
rs749273645 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246913659 | GAGAGCTTACTGATA[C/T]GCCAGGCATTGTGTT | 25909 |
rs749304075 | snp | A/G | | | upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246932527 | GAGTGCTGTGGCACG[A/G]TCTTGGCTCACTACA | 25909 |
rs749304732 | in-del | -/TC | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246908260 | AGGACATTTTGGGCA[-/TC]AAAAACAATAAAATT | 25909 |
rs749318042 | snp | A/C | 1.64882e-05 | 0.00287121 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246851092 | AGATGGCAAATTTGC[A/C]ATTTGTCCATGATTA | 25909 |
rs749336183 | snp | C/T | 1.66252e-05 | 0.00288311 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246860965 | TATCTCCATCCTTTT[C/T]AGTTTGTTCAGTTAC | 25909 |
rs749365487 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246886907 | TCAAGGCCAAATCTT[A/G]CCTTCCATGGTTCCC | 25909 |
rs749378492 | snp | C/T | | | downstream-variant-500B | AHCTF1 | GRCh38.p7 | 1:246838990 | TTTACCTTACTACTA[C/T]GATACTAAGCACCTT | 25909 |
rs749395017 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246854588 | TACATGAGAAAAGAA[A/G]GTTGCTTTTTTGATA | 25909 |
rs749397589 | snp | A/G | 3.29647e-05 | 0.00405971 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246898165 | TAGAAAGCTAATAAC[A/G]TGATCCAACCAAAAG | 25909 |
rs749406446 | in-del | -/C | 1.95082e-05 | 0.00312309 | frameshift-variant, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246885676 | AACAAAAGATCCAAA[-/C]CACTCTGGAAATAAC | 25909 |
rs749408331 | in-del | -/TTGTTTAC | 1.7814e-05 | 0.00298441 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246891084 | AAGAGTTAACATCAG[-/TTGTTTAC]TTACAAAAAAATCAA | 25909 |
rs749427189 | in-del | -/TA | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246909078 | ATATCTATATATATC[-/TA]TATCTATCTATCTAT | 25909 |
rs749438002 | snp | A/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246894794 | AAGATTATTAATTAC[A/T]AACAGAGTTCTAAAT | 25909 |
rs749444646 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246873195 | TACTCTTGATATATT[C/T]AAACTTTCTCCCTTA | 25909 |
rs749448420 | snp | C/T | 1.64795e-05 | 0.00287045 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246895896 | ACTAGTCTGAATTGC[C/T]GCTGACAATATAGCT | 25909 |
rs749450421 | snp | A/C | 1.64893e-05 | 0.0028713 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246903977 | TGTCCTGATGCCAAA[A/C]ACTTTCTATTACCAA | 25909 |
rs749498949 | snp | G/T | 1.85273e-05 | 0.00304357 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246843949 | AAAAGTTGAAAAAAC[G/T]GTATCTGTATCTTTA | 25909 |
rs749533245 | snp | C/G | 2.07514e-05 | 0.00322107 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246867291 | TGTTCCAAAAAATGC[C/G]TCAGGCAGCTCTGGA | 25909 |
rs749535591 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246840612 | AATGTATGAAGTCTT[A/C]ATATAAAATAGAAAA | 25909 |
rs749540526 | snp | A/G | | | upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246933627 | AGTGCATGGCTATTC[A/G]CAGGCACTATGGCCT | 25909 |
rs749543190 | snp | A/G | | | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246888502 | AATCATCAAGCAATC[A/G]GGATTCCACTTCCCT | 25909 |
rs749552372 | snp | C/G | 1.91496e-05 | 0.00309426 | missense, nc-transcript-variant, intron-variant | AHCTF1 | GRCh38.p7 | 1:246843836 | TGGATGTGTTTTTTT[C/G]TCTGCTCCTTAAAGC | 25909 |
rs749557651 | snp | A/C | 1.71684e-05 | 0.00292983 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246840974 | TATGGGAGGAGGTGA[A/C]CAAGCACTTTCTTTT | 25909 |
rs749574538 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246841550 | ACAGCATAAACAAGA[C/T]ACTGTGTAACAAATA | 25909 |
rs749583750 | snp | A/G | 3.4822e-05 | 0.0041725 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246860856 | ATAAACTTTATTGAG[A/G]GACATTAATAACAAT | 25909 |
rs749584903 | in-del | -/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246904190 | TTTTATAAAAATGTA[-/G]GTCCTTTGAAATAAT | 25909 |
rs749618289 | snp | A/G/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246862567 | TCATCTCCAATAAAC[A/G/T]TATCAATAGAAATAT | 25909 |
rs749618388 | in-del | -/TTGTT | 1.66618e-05 | 0.00288628 | frameshift-variant, nc-transcript-variant, intron-variant | AHCTF1 | GRCh38.p7 | 1:246842702 | GTCATACTTGCTTGC[-/TTGTT]TTGTTTTTGACGTCC | 25909 |
rs749625852 | snp | A/G | 3.29853e-05 | 0.00406098 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246877001 | GGCAGGCACATAATT[A/G]GCACGCTGCAAATGG | 25909 |
rs749630994 | snp | C/G/T | 5.13249e-05 | 0.00506559 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246855689 | TCTTCACTCAAAACA[C/G/T]AAAAATGGAATAATC | 25909 |
rs749684159 | snp | G/T | 1.95785e-05 | 0.00312871 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246862191 | TTACACCATTAAAAG[G/T]GCTTATAGGCCGGGC | 25909 |
rs749753377 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246881334 | GAACTGAGACATCCA[C/T]CATTAGCGTCAGCAA | 25909 |
rs749756762 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246848090 | AAAATCGAAGATCCA[A/G]TTAAAAATTTTCTGA | 25909 |
rs749757853 | snp | A/G | 1.64857e-05 | 0.00287099 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246913292 | ATAGGTCAACAAGAA[A/G]GATCTGTCCAACATC | 25909 |
rs749768710 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246928417 | TTCGACAAGGTCACA[A/G]TGCCTTTGGACTAAC | 25909 |
rs749795710 | snp | A/G | 1.65143e-05 | 0.00287348 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246840920 | TTTGCTCTTGACTCC[A/G]TCAGCTGGGCTAGCC | 25909 |
rs749835821 | snp | C/T | 4.94548e-05 | 0.00497242 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246851160 | CTGTGTTAGCTGCTT[C/T]AGGTAACACATCAGA | 25909 |
rs749835998 | snp | A/G | 3.31082e-05 | 0.00406854 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246849941 | AAAGCTGGTTTTCCA[A/G]CATCAACATTTTCAC | 25909 |
rs749880184 | snp | A/G | 3.40344e-05 | 0.00412505 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246853263 | TCAGAGATAGTGAGC[A/G]AGGAGTTTCCACCAT | 25909 |
rs749886223 | snp | G/T | 1.64985e-05 | 0.0028721 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246851051 | AAAGTGTCTACTTTT[G/T]GGGACTTTTGGTCAC | 25909 |
rs749891546 | snp | G/T | 1.86218e-05 | 0.00305132 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246876146 | GTCTAATATAGAATT[G/T]CGAGCCAGTGATCTC | 25909 |
rs749933821 | snp | C/T | 1.64746e-05 | 0.00287002 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246907703 | GCGCCCTTGTCTCAT[C/T]ACACTTTCTCTAATG | 25909 |
rs749950409 | in-del | -/CTC | 1.65007e-05 | 0.00287229 | cds-indel, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246888462 | ACTTCTCAATTCGCT[-/CTC]CTAACTGAGAAACCA | 25909 |
rs749966562 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246888962 | ATGATGAGAACTACA[A/G]ACATCAAGGAGAGTT | 25909 |
rs749968334 | snp | C/G | 1.65002e-05 | 0.00287225 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246895958 | GAAAGGAAAGAAATG[C/G]AAAGAAAGAGGGTGT | 25909 |
rs750016817 | in-del | -/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246928428 | ACAGTGCCTTTGGAC[-/T]TAACAGGTCCTAAAT | 25909 |
rs750027057 | snp | C/G | 1.67203e-05 | 0.00289134 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246860925 | TGTAGGTCTGAAGGA[C/G]TTACTTCTGATGCAA | 25909 |
rs750099909 | in-del | -/TCTTTATGTTG | 1.78438e-05 | 0.0029869 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246867827 | TGTAAAATGAAGAAC[-/TCTTTATGTTG]GCTGGAATTAAGTGC | 25909 |
rs750100103 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246883155 | CAGAAGGGTGAGTCC[A/G]GGGAGAGTGTTAGTG | 25909 |
rs750108240 | snp | G/T | 5.00271e-05 | 0.0050011 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246895786 | ATAACAAATAGCAAG[G/T]TGATAACTTTAAAAA | 25909 |
rs750111395 | snp | A/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246923928 | ATGCCACAGGACCTG[A/T]GAAGAGGGCCATGTT | 25909 |
rs750113737 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246909560 | TCAACTGTCGCAGTA[C/T]TGCAGTGCTTGTGTT | 25909 |
rs750124737 | snp | C/T | 3.49034e-05 | 0.00417738 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246853278 | GAGGAGTTTCCACCA[C/T]CACCAAGGACATCAG | 25909 |
rs750128073 | snp | C/T | 1.65935e-05 | 0.00288036 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246857792 | AACTAAGAGATCCTT[C/T]GTTTCTGCATCTTCT | 25909 |
rs750150213 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246861793 | TAGCCAATGGCCCTA[C/G]TGTTTCTTTCAGAAC | 25909 |
rs750157810 | snp | A/G | 1.65012e-05 | 0.00287234 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246863888 | AAGTAAGAGCCATCT[A/G]GTTTGATTGTGAACG | 25909 |
rs750193849 | snp | A/G | 1.67399e-05 | 0.00289304 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246918234 | ATTAGTAAATGTTCA[A/G]TGACATTATGTTTAC | 25909 |
rs750195258 | in-del | -/C | 0.000120755 | 0.00776937 | utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246840773 | ATTCTGATGACTTTA[-/C]AAATAGGTGTACATT | 25909 |
rs750206531 | snp | A/C | 1.66532e-05 | 0.00288554 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246900295 | GGTCAGCTACACATA[A/C]AAATACAAAGAGAAA | 25909 |
rs750209176 | snp | C/G/T | 3.31577e-05 | 0.00407161 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246891773 | TTGATAAAACAAAGA[C/G/T]CGTACCTCTCTCAGT | 25909 |
rs750230045 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246848902 | AACCATTAACACTTT[C/T]ACAGAGAGTTACTCT | 25909 |
rs750243290 | snp | A/C/T | 3.29507e-05 | 0.00405887 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246898272 | CCAGCTACAAGACAT[A/C/T]GATTATAACCATCAG | 25909 |
rs750245602 | in-del | -/A | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246923110 | AATCAAATAATACCA[-/A]AAAAAAAAAAAAAAA | 25909 |
rs750259513 | snp | A/G | 1.69146e-05 | 0.0029081 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246913221 | TTGGTTTCAAGTAAA[A/G]AACTGATTACCTGAT | 25909 |
rs750262279 | snp | A/G | 1.72047e-05 | 0.00293293 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246891063 | AAGTCTATCAGTCCT[A/G]TAAAGAAGAGTTAAC | 25909 |
rs750274819 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246863454 | AAGTTGAGTGCTGTG[A/G]TTTCTCAGCTAATAA | 25909 |
rs750276606 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246846845 | CAACCTCAACCTCCC[A/G]GGCTCAAGCCATCCT | 25909 |
rs750328148 | in-del | -/AAAT | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246845376 | TCTTAAAAAAAAGAA[-/AAAT]AAATAGAGTTGATAT | 25909 |
rs750352407 | snp | A/G | 1.65422e-05 | 0.0028759 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246849968 | TCACTTTTAGCTGGG[A/G]TATTTCTTGTAGATC | 25909 |
rs750377497 | snp | A/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246928890 | AAATTTCTTACCAAC[A/T]TAATTCAAACATTTT | 25909 |
rs750408583 | in-del | -/CTGA | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246927476 | CCTCAGCAACACAGC[-/CTGA]CTGTCTCAAAAAGAA | 25909 |
rs750428516 | snp | A/G | 4.77829e-05 | 0.00488765 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246876214 | CAAAATTGGTAAAAA[A/G]TTTAACCTTCAAAAT | 25909 |
rs750441271 | snp | A/G | 0.000100239 | 0.0070788 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246900024 | TTTACATACTTTTGT[A/G]CATTACTTTTCTTAA | 25909 |
rs750454838 | in-del | -/TA | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246909067 | AGATAATTCTATATC[-/TA]TATATATATCTATAT | 25909 |
rs750459242 | snp | A/T | 1.64827e-05 | 0.00287073 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246851309 | TTGTTATCAGCTAAG[A/T]CACAAAACTGTTGGT | 25909 |
rs750468056 | snp | C/T | 1.65784e-05 | 0.00287905 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246889943 | TTCTTACAGATGTAA[C/T]TTCTAAAATTGTTTT | 25909 |
rs750506512 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246919072 | CCCAGAATGACTACT[C/T]CCATTATAAACAACC | 25909 |
rs750508648 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246870261 | ATAGCCTGGGCGACA[C/T]AGTGAGGCCCTCTCT | 25909 |
rs750510027 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246905405 | CGGGAGGCTGAGCGA[C/G]AGAATGGCATGAATC | 25909 |
rs750519336 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246857006 | TTATTCAAAAGTGCG[C/G]ACATGCAATCTGTGT | 25909 |
rs750535535 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246840197 | AAGCTTGCCGAATAA[A/G]AGATGCCAACATTAT | 25909 |
rs750591278 | snp | A/G | 1.64836e-05 | 0.0028708 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246905616 | TCTTGAAAAGTGACA[A/G]CATATACAGGAACTT | 25909 |
rs750623456 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246925725 | GGAGGTGTCTGGGTC[A/G]TGGGAGAGGACCCCT | 25909 |
rs750623731 | snp | C/G | 3.29506e-05 | 0.00405884 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246849688 | AGAAAGGTCCGGCAA[C/G]AAGATGGCCTTGCTA | 25909 |
rs750627497 | snp | G/T | | | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246862095 | GACCTCAGGATGGAC[G/T]GAGGAGTGAACTCAG | 25909 |
rs750634497 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246893516 | GTATCCCTACTAGTA[C/T]TTTTTAGCCTTATTT | 25909 |
rs750663479 | snp | C/G/T | 9.99978e-05 | 0.0070704 | missense, synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850774 | CACGTTTTGGATACG[C/G/T]TGACCTCTCGTACGA | 25909 |
rs750671480 | snp | C/T | 2.00749e-05 | 0.00316813 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246876000 | CAGTATCTTTTTTGA[C/T]CCAATAGATTATGAT | 25909 |
rs750710937 | snp | A/G | 3.32629e-05 | 0.00407803 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246887193 | ATGAAAGTTTATGCT[A/G]TAAGTGAATAGACTT | 25909 |
rs750719857 | snp | C/T | 1.66835e-05 | 0.00288816 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246902691 | CTGTAACATAAAATA[C/T]ACGCAAATATTAATC | 25909 |
rs750720380 | snp | A/G | 1.67304e-05 | 0.00289222 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246867793 | TTTGGAACTGCTGAT[A/G]ATGGTTTGGGTCTAG | 25909 |
rs750747706 | snp | C/G | 1.65509e-05 | 0.00287666 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246864088 | ACTGAGAAGGCCGGG[C/G]GACAGGCTGAACAAC | 25909 |
rs750750298 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246878169 | TTGGGAGGCCAGGGT[A/G]GGCAGATCACTTGAG | 25909 |
rs750768183 | in-del | -/AAAT | 2.98681e-05 | 0.00386435 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246853339 | TACATTTAAACTGAA[-/AAAT]AAATAAATCCACACA | 25909 |
rs750770271 | snp | A/G | 1.71132e-05 | 0.00292511 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246916285 | CAGCTAAAACTACAG[A/G]AGGCTGTTCATTGAC | 25909 |
rs750775634 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246874547 | ATGGTGGTCATGAAA[C/T]GGCCACCCAAAAAAA | 25909 |
rs750794098 | snp | C/G | 0.000115349 | 0.00759349 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246902622 | CTGTCCCCTCAAAGG[C/G]AACATGCCACCTGTC | 25909 |
rs750825292 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246911878 | TTTAAGTTTTGTTCA[C/G]ATGATTTTGGCTCTT | 25909 |
rs750828165 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246901694 | GTGGTGGTGTGTGCC[A/G]GCAGTCCCAGTTACT | 25909 |
rs750851570 | snp | C/T | 1.66413e-05 | 0.0028845 | synonymous-codon, nc-transcript-variant, intron-variant | AHCTF1 | GRCh38.p7 | 1:246842741 | TCGTTTCGCTTTTGG[C/T]TTTCCCAGAGTTTCT | 25909 |
rs750855690 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246926706 | ACTAAATACAGAAAA[C/G]TAACCAGGTGTGGTG | 25909 |
rs750864401 | snp | C/T | 3.35475e-05 | 0.00409544 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850365 | CAACACTTTCCTGAT[C/T]TTCTACAGATCTTTT | 25909 |
rs750919421 | snp | C/T | 2.01428e-05 | 0.00317348 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246853098 | TTTTTTACATGAATT[C/T]CTTGAGTATCAGGAG | 25909 |
rs750924356 | snp | C/T | 1.83994e-05 | 0.00303305 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246851418 | CTCCTGAATCTTGAG[C/T]TTCAAGCTTTTCTTG | 25909 |
rs750941605 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246912826 | ACAAACATAAACAAT[A/C]TGCCAAGAACACTAT | 25909 |
rs750942522 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246871565 | AAACAAGGTATACAG[C/T]GCTGTCCTCACTTGG | 25909 |
rs750975661 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246852125 | GAACATTACCACCCA[C/G]CTAGACAATGACATT | 25909 |
rs750981675 | snp | C/T | 3.55859e-05 | 0.00421802 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246862157 | ACTTTTAGCTTTCTA[C/T]AGTAAAGAGCAAATG | 25909 |
rs750982197 | snp | C/G | 1.65051e-05 | 0.00287267 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246877108 | AAAATAGATTGTAAA[C/G]TACCAATTTATCTTG | 25909 |
rs750990107 | snp | A/G | 1.65053e-05 | 0.0028727 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246890028 | AATTACAGGGTAGTT[A/G]TAGCATAACCTTGAC | 25909 |
rs751002835 | snp | G/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246928986 | CTTCCTGACTTTAAG[G/T]AGTTTACAATCTAGA | 25909 |
rs751039101 | snp | C/G | 6.21022e-05 | 0.005572 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246876237 | TTCAAAATGTTAGGT[C/G]CTGTAATTCTATATT | 25909 |
rs751048463 | snp | A/G | 1.66405e-05 | 0.00288443 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246900303 | ACACATACAAATACA[A/G]AGAGAAAGGAGAGAG | 25909 |
rs751050073 | snp | C/T | 3.30759e-05 | 0.00406655 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246849983 | GTATTTCTTGTAGAT[C/T]TCCTTCTAATGCTGG | 25909 |
rs751073668 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246863579 | CAAAGAACTAAATAG[C/T]ATTTGATAGAAGAAA | 25909 |
rs751091206 | snp | C/G | 1.6507e-05 | 0.00287284 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246913381 | CTTGCACTGGCTCCT[C/G]CATGATTAATTATAG | 25909 |
rs751094813 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246898463 | AATTATGAAAGACTA[C/T]ATTTCCTGCAAGAAA | 25909 |
rs751106321 | in-del | -/A | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246908505 | TTTCAGAGTGACCAG[-/A]AAGCCCTAATTAATG | 25909 |
rs751116630 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246925438 | GATATAGAAGTACTA[C/G]CTCTAAGAGAATAAA | 25909 |
rs751119655 | snp | A/G | 6.59446e-05 | 0.00574177 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246888403 | ACCTACATGCAGACT[A/G]GCAGGAGGATATTTT | 25909 |
rs751161621 | snp | A/G | 1.64846e-05 | 0.0028709 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246851130 | CCCCACTGCATACAA[A/G]TTTTTCTTCAGTTGC | 25909 |
rs751176388 | in-del | -/ATTTA | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246870751 | AAAAAGCCCTAGGCT[-/ATTTA]ATTTCTCAGGGACAG | 25909 |
rs751184939 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246910601 | CTTGTATTCTTCTAA[A/C]TATCTGAAGATGTCT | 25909 |
rs751251729 | multinucleotide-polymorphism | AT/GC | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869087 | CTGACCTCGTGATCC[AT/GC]CCGCCTTGGCCTCCC | 25909 |
rs751274435 | snp | A/G | 1.85903e-05 | 0.00304874 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246885662 | CAGTAGCTGGATGAA[A/G]CAAAAGATCCAAACC | 25909 |
rs751275830 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246849004 | TATTACTGCAGATAT[A/G]TTGTATATCTGTTTG | 25909 |
rs751280371 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246870367 | GGTCAAGGCTACAAT[A/G]AGCTATGATTATACC | 25909 |
rs751285402 | snp | A/G | 1.6498e-05 | 0.00287206 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850679 | TCTTTTGCCTTCCTA[A/G]TTTTCTTCCTGACTG | 25909 |
rs751287332 | snp | A/G | 1.68366e-05 | 0.00290138 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246855856 | AATACATACCTTAGT[A/G]TGTAAGAAGATCCCA | 25909 |
rs751312983 | in-del | -/TG | 7.06826e-05 | 0.00594444 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246849591 | ACTGAGATGAAAAAC[-/TG]TTTTGCAGAGAAAGA | 25909 |
rs751317888 | snp | C/T | 1.64963e-05 | 0.00287192 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246888223 | TCTAATAGGTACATA[C/T]CAAGTACTGCCTATA | 25909 |
rs751320115 | in-del | -/TTACC | | | downstream-variant-500B | AHCTF1 | GRCh38.p7 | 1:246838893 | TTCTGAGTACATTGT[-/TTACC]TTACTACTGATACTA | 25909 |
rs751325576 | snp | C/G | 1.65562e-05 | 0.00287712 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246891869 | ATTGCTGGATAGACT[C/G]TATAGTTTGTGGATC | 25909 |
rs751337087 | snp | A/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246885892 | TGCAGATAGAAAACA[A/T]TTGAAAAAATAAGGC | 25909 |
rs751345811 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246851545 | GTGTGCCTTTTAAAA[A/C]ATAAATTATATTTAA | 25909 |
rs751362444 | snp | C/G/T | 3.36006e-05 | 0.00409871 | missense, synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246918358 | TAGTCACTTGAGCTC[C/G/T]TAAGTCTCGCATACT | 25909 |
rs751388025 | snp | C/T | 1.66305e-05 | 0.00288357 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246885538 | ATAACATCGTTACCA[C/T]TGGACACTGTTGGCT | 25909 |
rs751414007 | snp | A/C | 0.000133449 | 0.00816742 | intron-variant, missense, utr-variant-5-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246931148 | GCCAGGCCCAAGCGC[A/C]TGTGGAACACACGCC | 25909 |
rs751431703 | in-del | -/AAAACAAAGAAA | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246891628 | CTGTAGCTTTTCATT[-/AAAACAAAGAAA]CAAACAAAAACCCTA | 25909 |
rs751449296 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246858149 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACTGTTT | 25909 |
rs751449578 | snp | C/G/T | 1.64939e-05 | 0.0028717 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246905577 | GCCCACAAGTAACAG[C/G/T]AATTCCGAGGATCAT | 25909 |
rs751465750 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246871110 | CCAAATGCTAGGACC[A/C]CTAAAAAAGGTGGTG | 25909 |
rs751484045 | snp | C/T | 1.64841e-05 | 0.00287085 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246855783 | TCAACAGATGTTAAT[C/T]CTTCGTCCAACACTG | 25909 |
rs751496666 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246891111 | AAAAAAATCAAGATG[C/T]TCCACAGTTTTCAAA | 25909 |
rs751521719 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246920368 | GATTTGAAAAAATTT[C/T]TAAAAATGAAAAATT | 25909 |
rs751527009 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246919427 | TTATATGGAAATCCT[C/G]AAGAGGCCGGGCGTG | 25909 |
rs751553846 | snp | C/T | 1.64836e-05 | 0.0028708 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246863904 | GTTTGATTGTGAACG[C/T]TAGATGCGTAAATAC | 25909 |
rs751554306 | snp | A/G | 1.71408e-05 | 0.00292747 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246890958 | GTAAATATTTTACCT[A/G]TGCCTTCTGGTAAAA | 25909 |
rs751573964 | snp | C/T | 3.33367e-05 | 0.00408255 | missense, stop-lost, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246840959 | AATCAGCCGAATTTC[C/T]ATGGGAGGAGGTGAC | 25909 |
rs751584930 | in-del | -/A | 0.00113992 | 0.0238466 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246841002 | TTTTCTGTGTTTCTG[-/A]AAAAAAAAGATATGA | 25909 |
rs751596748 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246881811 | CCACTGCACCCCAGC[C/T]TGGGTAACAGAGCAA | 25909 |
rs751600674 | snp | C/G | 1.65682e-05 | 0.00287817 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246877216 | AAGCCCATTTCCTGA[C/G]AGACTTCATACATGT | 25909 |
rs751603752 | snp | C/T | 1.70749e-05 | 0.00292184 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246916297 | CAGGAGGCTGTTCAT[C/T]GACTCCACTGAATCT | 25909 |
rs751614611 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246887898 | AGTATTTTAGAGCAA[C/G]TGTTGTTAACTTTTT | 25909 |
rs751625418 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246845202 | ATGATTCTTTAAAAA[A/C]ATGTTTTTTGTGGGT | 25909 |
rs751633142 | snp | A/G | 1.82048e-05 | 0.00301697 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246853129 | GGCTGTCAGAAATTG[A/G]AAGCTTTTCTTCTGG | 25909 |
rs751643886 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246859214 | TCATCTTAAACTACT[C/T]AAGATGCAGATTTTT | 25909 |
rs751673109 | snp | C/T | 3.30186e-05 | 0.00406303 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246890038 | TAGTTGTAGCATAAC[C/T]TTGACAACTGCACAG | 25909 |
rs751751409 | snp | G/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246893632 | CAAGAAGGAAAATGA[G/T]TTGCCACAATAATAA | 25909 |
rs751758088 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246879930 | AAGCAAATCCTTTAT[A/G]TAATTATAAAATTAG | 25909 |
rs751803469 | snp | C/T | 1.66134e-05 | 0.00288208 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246861973 | CCCCAGGAATCCATT[C/T]TGGGTGGACATCTTC | 25909 |
rs751816772 | snp | A/G | 4.29415e-05 | 0.00463345 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246851441 | TTTTCTTGTTCAATC[A/G]CCTAAATGAATTAAA | 25909 |
rs751821443 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246845856 | TTTCTAAGGTATAAA[C/T]GTGCCTCCTGTGGCC | 25909 |
rs751864283 | snp | A/T | 3.41711e-05 | 0.00413333 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246867369 | ATGAAAATAAAAATT[A/T]AACTTCTGATGTATC | 25909 |
rs751873184 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246910459 | TTATGTAATAAAATA[C/T]CCCTATTTGCTTTAA | 25909 |
rs751879303 | snp | C/T | 1.66966e-05 | 0.00288929 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246900044 | ACTTTTCTTAAGAGG[C/T]AATGTTAAGGAAATA | 25909 |
rs751891708 | snp | A/C | 1.66952e-05 | 0.00288917 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246860938 | GAGTTACTTCTGATG[A/C]AAATACATCTTTATC | 25909 |
rs751903122 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246902376 | CTGGAGAGCAAGAAA[C/T]ATCTAGTATCTCATA | 25909 |
rs751938802 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246853681 | GCAATCTGGGCTTTG[A/C]TACAACTAGGATAAA | 25909 |
rs751941316 | snp | C/G | 1.65214e-05 | 0.0028741 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246895974 | AAAGAAAGAGGGTGT[C/G]AGATCATAGGCAAGT | 25909 |
rs751945332 | in-del | -/TT | 4.99122e-05 | 0.00499536 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246889922 | ACTATTCTGAGAAAC[-/TT]TGACTTCTTACAGAT | 25909 |
rs751945573 | snp | C/G | 1.64819e-05 | 0.00287066 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246902635 | GGGAACATGCCACCT[C/G]TCAGGTCCAGGGTGT | 25909 |
rs751958521 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246914667 | ACAAAAATAAACATA[A/G]TGAGTGTATACTGCA | 25909 |
rs751974412 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246888103 | TTGCAATTAGATATG[C/T]CAGGTTTCCACTACT | 25909 |
rs751977393 | snp | A/G | 5.08091e-05 | 0.00504004 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246903916 | GAAAACAACAAAATG[A/G]TAATATAAACCCATA | 25909 |
rs751982201 | in-del | -/T | 1.65015e-05 | 0.00287237 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246877101 | AAAGAACAAAATAGA[-/T]TGTAAACTACCAATT | 25909 |
rs751990889 | snp | C/T | 2.00672e-05 | 0.00316752 | missense, nc-transcript-variant, intron-variant | AHCTF1 | GRCh38.p7 | 1:246843817 | TCTTCAAGCTTGTTC[C/T]TATTGGATGTGTTTT | 25909 |
rs752024333 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246903195 | TCGGTTCTAGAGACA[C/G]GTATGTGAGGGTGAA | 25909 |
rs752030285 | snp | C/T | 5.1343e-05 | 0.00506645 | synonymous-codon, nc-transcript-variant, intron-variant | AHCTF1 | GRCh38.p7 | 1:246843903 | AACTAATTCTTTCAG[C/T]TGTGCAGGAACCTCT | 25909 |
rs752039964 | snp | A/C | 1.67866e-05 | 0.00289707 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850371 | TTTCCTGATTTTCTA[A/C]AGATCTTTTAATTCT | 25909 |
rs752056188 | snp | A/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246855123 | CTAGAGTCAGATAAC[A/T]ACTATGTCATAGTAT | 25909 |
rs752056968 | snp | A/G | 2.99999e-05 | 0.00387286 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246867248 | TAAACTCTTACCTAG[A/G]AATTTTTTGTGATGC | 25909 |
rs752099901 | snp | G/T | | | downstream-variant-500B | AHCTF1 | GRCh38.p7 | 1:246838753 | ATGCTTCTATCTACA[G/T]CTAGGAAGCCTTCAA | 25909 |
rs752108126 | snp | A/G | 1.66034e-05 | 0.00288122 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246864115 | CAACCAAATCTAGCA[A/G]TCTGTAATCAGAATG | 25909 |
rs752156514 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246849343 | ATTAAAAGTCACTTA[C/T]AATTTATAAAACTCA | 25909 |
rs752173216 | in-del | -/AAAAAAACAAAACAA | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246901614 | GCGAGACTCCATCTC[-/AAAAAAACAAAACAA]AAAAAAACAAAACAC | 25909 |
rs752175047 | snp | C/T | 1.74695e-05 | 0.00295541 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246916427 | TTGCCTATTTTAATA[C/T]TGTATATACACAAAA | 25909 |
rs752175571 | in-del | -/TCC | 0.000132103 | 0.00812612 | cds-indel, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246849896 | ATCACCATCGAAAGT[-/TCC]TCGTTTGGCACTAAA | 25909 |
rs752175697 | snp | A/T | 1.65603e-05 | 0.00287747 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246891877 | ATAGACTGTATAGTT[A/T]GTGGATCCATGAAAT | 25909 |
rs752204222 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246865822 | CATTAGGTCTCAGGT[C/T]TTCAACCCTGAGACC | 25909 |
rs752224289 | snp | G/T | 1.68969e-05 | 0.00290657 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246902512 | ATGACATATTTCAAG[G/T]ACTTTAACTAACCTT | 25909 |
rs752228896 | snp | C/T | 1.66813e-05 | 0.00288797 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246900414 | AGAAGGCTTTCCCTG[C/T]CCATATATATTCACC | 25909 |
rs752260137 | snp | C/T | 1.6483e-05 | 0.00287076 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246863911 | TGTGAACGCTAGATG[C/T]GTAAATACTAACCTT | 25909 |
rs752270952 | snp | C/G | 1.64917e-05 | 0.00287151 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850118 | GACATATCAAATTCT[C/G]CTTGAACAGTCAACT | 25909 |
rs752272755 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246930746 | CTACAGGTTCTTTAG[A/G]ATATTCTGAGAATAA | 25909 |
rs752328787 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246919606 | TAGTCTCACCTACTC[C/G]GGAGGCTGAAGCAGG | 25909 |
rs752356538 | snp | C/T | 1.65211e-05 | 0.00287407 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246913394 | CTCCATGATTAATTA[C/T]AGGTTCAATAGCTGT | 25909 |
rs752357903 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246886312 | CTCCAGCCTGGGTGA[C/G]AGAGCGAGACTCCAT | 25909 |
rs752372720 | snp | G/T | 3.29587e-05 | 0.00405934 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850894 | TTTAGTGGGACACAT[G/T]ATGTTTTGGCTCACT | 25909 |
rs752382325 | snp | C/T | | | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246853245 | TCAGAGACAATAGGA[C/T]CTTCAGAGATAGTGA | 25909 |
rs752398166 | in-del | -/A | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246845528 | AAAATTATACATTCT[-/A]TAACTCTCTTCTAGG | 25909 |
rs752410972 | in-del | -/A | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246904366 | TGCCTAAAGTTCTAT[-/A]AACATCTCCCAGCTT | 25909 |
rs752412028 | snp | A/G | 1.6691e-05 | 0.00288881 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246899508 | GTTTAACAAACAAGT[A/G]GCATCTAAAAAAAAG | 25909 |
rs752425265 | snp | C/T | 1.64741e-05 | 0.00286998 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246849707 | ATGGCCTTGCTAGAC[C/T]GAGTCCTGCTGCTGC | 25909 |
rs752428674 | snp | C/T | 6.61496e-05 | 0.00575069 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246849990 | TTGTAGATCTCCTTC[C/T]AATGCTGGGAGCTTC | 25909 |
rs752434013 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246859429 | GTTTGTCAGTATAGT[C/T]CACCATGCTCTGTGT | 25909 |
rs752440524 | snp | C/T | 3.30808e-05 | 0.00406686 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246887211 | AGTGAATAGACTTAC[C/T]TCATAGTCATTATGA | 25909 |
rs752444713 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246871241 | ACAAACCATGACTCA[A/G]ACATTAATGGTCTAG | 25909 |
rs752454417 | snp | C/T | 1.64958e-05 | 0.00287187 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246876994 | GCTTCAAGGCAGGCA[C/T]ATAATTGGCACGCTG | 25909 |
rs752478555 | in-del | -/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246874911 | AGACAGAGTCTCCCA[-/G]GATTATAGAAATTTA | 25909 |
rs752493268 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246886533 | AATAATTGTTATAGT[A/G]TAACATCTAGGGAAT | 25909 |
rs752521461 | snp | A/C | 1.80719e-05 | 0.00300593 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246907524 | AAAACTACCTATAAT[A/C]AAATAAGGGAAAAAA | 25909 |
rs752525155 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246906010 | ATGTCTGTGTAAACT[A/G]GTCCTAAGAGTCATA | 25909 |
rs752533366 | in-del | -/T/TT | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246852388 | AGTTGGTTTTTTATC[-/T/TT]CAAATTTCTATAAAT | 25909 |
rs752561949 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246908065 | AAAACTGATTTATTT[A/C]TTTATTGAAATTTAG | 25909 |
rs752572727 | snp | G/T | 1.64988e-05 | 0.00287213 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246905638 | CAGGAACTTGTCCAC[G/T]TTCCAATTGTATGTA | 25909 |
rs752649856 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246907009 | TTCTGAGAAATGCTC[A/G]TCAGGGATTCAGTCA | 25909 |
rs752673510 | snp | C/T | 1.71267e-05 | 0.00292627 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246877295 | AATTCCAGGCTTCAA[C/T]CATACACCTGAAAGC | 25909 |
rs752677585 | snp | A/G/T | 8.93606e-05 | 0.00668381 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246885485 | ATAGTTTCAAAAGAT[A/G/T]TACTTACCTATTAAA | 25909 |
rs752692575 | in-del | -/T | 0.000201558 | 0.0100368 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246853081 | GAAGTAAAAAATTAA[-/T]TTTTTTTACATGAAT | 25909 |
rs752692676 | snp | G/T | 1.76599e-05 | 0.00297147 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246894641 | ATTCTGTCCTACATC[G/T]AGACCTCTAATACTT | 25909 |
rs752720979 | snp | C/T | 3.41431e-05 | 0.00413163 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246855870 | TGTGTAAGAAGATCC[C/T]ATCTGCTTTAACCTG | 25909 |
rs752725201 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246860259 | GGCAACAGAGTGAGA[A/C]TCTGTCTCAAAAATT | 25909 |
rs752738277 | snp | G/T | 0.000140125 | 0.00836915 | intron-variant, synonymous-codon, utr-variant-5-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246931199 | CGCCGGCCGCTTCCC[G/T]CGGGGAAAGGCCCGC | 25909 |
rs752739097 | snp | A/C | 2.39725e-05 | 0.00346203 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246885691 | CCACTCTGGAAATAA[A/C]ATGAAAAATGTTAAA | 25909 |
rs752739878 | snp | C/T | 1.79406e-05 | 0.00299499 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246918215 | TATCTTACAAATCAA[C/T]TGTATTAGTAAATGT | 25909 |
rs752756043 | snp | A/G | 1.65179e-05 | 0.00287379 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246903954 | GACCATTTACCTCAT[A/G]TAAGATTTGTCCTGA | 25909 |
rs752758644 | snp | C/G | 5.56127e-05 | 0.00527288 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850521 | GTAATTCTTGTTCCA[C/G]AGAACTGGTGTTTTC | 25909 |
rs752773695 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246896401 | GGATGAAGTACTGAT[A/G]CTTGCTATAATACAG | 25909 |
rs752782414 | snp | A/G | 2.60122e-05 | 0.0036063 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246867260 | TAGAAATTTTTTGTG[A/G]TGCTTTTGAAATTGG | 25909 |
rs752808083 | in-del | -/TTA | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246848234 | CATCTACTTTATTTA[-/TTA]TTATTATTATTTGGC | 25909 |
rs752835319 | snp | C/T | 3.45095e-05 | 0.00415374 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246877302 | GGCTTCAACCATACA[C/T]CTGAAAGCAGTATTT | 25909 |
rs752836580 | snp | C/T | 1.66935e-05 | 0.00288903 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246891751 | TAAAATTTAATAAAA[C/T]ACTCATTTGATAAAA | 25909 |
rs752871710 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246914801 | CATTCAACTGAGCAA[C/G]CAGTTCAGGAACCTT | 25909 |
rs752889133 | snp | G/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246907354 | AAAAATAAAGCTAAA[G/T]TCATGTGCTAAGTCA | 25909 |
rs752906596 | snp | C/G/T | 5.39353e-05 | 0.00519281 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246853170 | CTTTCTTTTAGTACA[C/G/T]CAACTTCTACTTCAT | 25909 |
rs752916069 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869184 | GAAGGTCTGTGGCAA[C/T]CCTGTGTCCAGCAAG | 25909 |
rs752919329 | snp | A/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246916088 | CACACCTATATAACC[A/T]GCAGGGGTTCAGTTT | 25909 |
rs752921619 | snp | A/G | 1.65438e-05 | 0.00287605 | missense, utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246840838 | GTAAAATTTGCTTTG[A/G]ATAGGAAGACAGTTT | 25909 |
rs752933675 | in-del | -/AAT | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246916655 | CAAGACTTCATCTCA[-/AAT]AATAATAATAATAGT | 25909 |
rs752972627 | snp | C/T | 1.70261e-05 | 0.00291766 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246916306 | GTTCATTGACTCCAC[C/T]GAATCTGTAAGCAGA | 25909 |
rs752975071 | snp | A/G | | | upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246932015 | GGGGAGAACCGGCGG[A/G]AGATCGCGGCTGCAG | 25909 |
rs752975503 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246927780 | GAGGCCGAGGCTGGC[A/G]GATCACAAGGTCAAG | 25909 |
rs753005586 | snp | C/T | 1.64933e-05 | 0.00287165 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246861083 | ATACTCTAAGGTAGT[C/T]TCATCGGATGTGATT | 25909 |
rs753006968 | snp | A/T | 1.71563e-05 | 0.0029288 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246862126 | AAAATCCAGAAGTAG[A/T]AACTGACATGGCCAA | 25909 |
rs753021392 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246845078 | TCTACAGATGTTTGC[A/G]TTTGTTATTTCAAGA | 25909 |
rs753034362 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246889206 | GTGATTCCTTCACTC[A/G]AATATCTATTGCTGA | 25909 |
rs753051830 | snp | G/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246896843 | AGGAATCCCATGAAT[G/T]TAAGTTGAACAGGCA | 25909 |
rs753092353 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246923982 | GGGAGAAAGGTGAAG[A/G]CCCAAAGGCGTAGAA | 25909 |
rs753094812 | snp | A/G | 0.000247355 | 0.0111183 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246913277 | ACAAGTCATCCAAAC[A/G]TAGGTCAACAAGAAG | 25909 |
rs753101948 | snp | A/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246856655 | TTGCAATAAATAACA[A/T]TAGTTTTCATTAAAA | 25909 |
rs753118573 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246855358 | TTTGTTAATTTCCCT[A/G]GAGAATATTCAGTCA | 25909 |
rs753121506 | in-del | -/ATACAA | 1.66551e-05 | 0.00288571 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246900292 | ATTGGTCAGCTACAC[-/ATACAA]ATACAAAGAGAAAGG | 25909 |
rs753121638 | snp | G/T | 0.000164745 | 0.00907442 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246898273 | CAGCTACAAGACATC[G/T]ATTATAACCATCAGG | 25909 |
rs753128486 | snp | A/G | 1.65015e-05 | 0.00287237 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246888248 | CCTATAAAACAAAGG[A/G]ATAAAACCTTCAGTG | 25909 |
rs753158523 | snp | C/T | | | upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246933495 | GTCTCTACTCCTGGG[C/T]TCAAGAGATCCTCCT | 25909 |
rs753158977 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246891138 | CAAAATTAATCACTT[A/G]GTAATTTACATAATT | 25909 |
rs753168710 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246903287 | CAGCCATCTAAAAGC[C/T]CAGACGCGTATGTCC | 25909 |
rs753188962 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246859387 | GTGTTCCCCTGGCCC[C/T]CTTGTTAACCAAACT | 25909 |
rs753197946 | snp | A/G | 3.30049e-05 | 0.00406219 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246861005 | TAGTGCAGTGGAAGA[A/G]CTTTTGGGCTTAGAG | 25909 |
rs753213247 | in-del | -/A | 3.31763e-05 | 0.00407272 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246890078 | ATTTTTAAGAGTTGG[-/A]AAAAAAAGCTGGTAA | 25909 |
rs753214869 | snp | A/G | 8.24273e-05 | 0.00641926 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246898160 | TGTAATAGAAAGCTA[A/G]TAACGTGATCCAACC | 25909 |
rs753224879 | snp | C/T | 3.51723e-05 | 0.00419343 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246849596 | GATGAAAAACTGTTT[C/T]GCAGAGAAAGAAAAG | 25909 |
rs753237268 | in-del | -/TAGT | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246898516 | TTAACCAATGCTTGC[-/TAGT]TGTGAATACTACTAT | 25909 |
rs753254380 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246879766 | CCCAGGAGGCAGAGG[C/T]TGCAGTGAGCCAAAA | 25909 |
rs753279915 | snp | C/G/T | 5.17088e-05 | 0.0050845 | synonymous-codon, missense, nc-transcript-variant, intron-variant | AHCTF1 | GRCh38.p7 | 1:246843915 | CAGCTGTGCAGGAAC[C/G/T]TCTATTTTTTTAGCT | 25909 |
rs753302170 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246899364 | GAAACAACTGTCAAT[A/G]TCACTAAGTAAAACT | 25909 |
rs753304186 | in-del | -/AAAAC | 3.44364e-05 | 0.00414934 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246864154 | TTGAGTTATACTGAA[-/AAAAC]AAAAGAATTTAGTAT | 25909 |
rs753307240 | snp | C/G | 1.72519e-05 | 0.00293695 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246894648 | CCTACATCTAGACCT[C/G]TAATACTTACATAGT | 25909 |
rs753314812 | snp | A/G | 1.64914e-05 | 0.00287149 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246887267 | GTTTAACTTGGCCCC[A/G]AGAAATGGCAAATAC | 25909 |
rs753352721 | snp | G/T | 0.000105442 | 0.00726015 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246894790 | AATAAAGATTATTAA[G/T]TACAAACAGAGTTCT | 25909 |
rs753359905 | in-del | -/AATTTCTTGAGT | 2.0919e-05 | 0.00323405 | cds-indel, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246853093 | AATTTTTTTTACATG[-/AATTTCTTGAGT]AATTTCTTGAGTATC | 25909 |
rs753360431 | snp | A/T | 1.6684e-05 | 0.00288821 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246902526 | GTACTTTAACTAACC[A/T]TCATTCACGCCTTCC | 25909 |
rs753371292 | snp | A/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246871449 | TACTGATAAAATGTA[A/T]TCTAGTCAAAAGGAC | 25909 |
rs753384522 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246921953 | TAAACACTGACTACA[A/C]AACAATAATAATGGC | 25909 |
rs753446458 | snp | A/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246902273 | CACACTAGTTCAGAC[A/T]AGGGATCGCCTGTTT | 25909 |
rs753463689 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246896412 | TGATACTTGCTATAA[C/T]ACAGATGAACCTTGA | 25909 |
rs753486272 | in-del | -/TATG | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246884655 | CTTTCTCACAGTTAC[-/TATG]TATGTGAGACTGTAA | 25909 |
rs753494296 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246872690 | ACTGACTAAAGCTCC[C/T]TCCCATCGCACTATC | 25909 |
rs753499425 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246922705 | TAGTATCAATAGGCT[A/G]GGCGCAGTGGCTCAC | 25909 |
rs753508974 | snp | A/T | 1.65012e-05 | 0.00287234 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850233 | GCTGCTTGTCACTGG[A/T]TTTATCATCTTGCTT | 25909 |
rs753530062 | snp | A/T | 1.65792e-05 | 0.00287912 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246861989 | TGGGTGGACATCTTC[A/T]TCCACAAATGAAATT | 25909 |
rs753534476 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246920919 | GGTGAATCCACATCT[C/G]TACTAATAATACCAA | 25909 |
rs753539284 | snp | C/G | 1.65405e-05 | 0.00287576 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246864081 | TCCGAACACTGAGAA[C/G]GCCGGGGGACAGGCT | 25909 |
rs753541025 | snp | C/T | 1.70414e-05 | 0.00291898 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246857656 | TTCATTAAACTTCTT[C/T]CTAAAAGTATTTGAA | 25909 |
rs753557086 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246846203 | ATTCTAAGATAATTT[A/C]TTCGCTATGTTTCAA | 25909 |
rs753558183 | snp | A/G | 5.00446e-05 | 0.00500198 | intron-variant, downstream-variant-500B | AHCTF1 | GRCh38.p7 | 1:246842644 | GGGTGGGGACAGAGC[A/G]AGACTGTCTCAATCA | 25909 |
rs753602111 | snp | A/G | 3.29473e-05 | 0.00405864 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246907690 | GGAAACACAGATGGC[A/G]CCCTTGTCTCATTAC | 25909 |
rs753605642 | snp | A/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246896701 | TGTACACTTGAAATA[A/T]CTGAACTGCACGGTG | 25909 |
rs753619447 | snp | G/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246913063 | AAGTATCCACTGTGC[G/T]CAGGTCCAGACAATA | 25909 |
rs753632271 | snp | A/C | 1.83296e-05 | 0.00302729 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246876128 | AAGGATTTTTCCATA[A/C]TGGTCTAATATAGAA | 25909 |
rs753642595 | snp | A/C/T | 3.29849e-05 | 0.00406098 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246849884 | TTCTTAGAGCTCATC[A/C/T]CCATCGAAAGTTCCT | 25909 |
rs753660728 | snp | C/T | 1.66413e-05 | 0.0028845 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246900185 | GTGGAGAAGTCCTAC[C/T]TACAACAGACTCCAA | 25909 |
rs753679734 | in-del | -/ATA | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246911062 | TTAATTTTTTGTGCT[-/ATA]AAGTCCAACTGCTTC | 25909 |
rs753693530 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246860403 | CTTTTCTAAATTTCA[C/T]GGCCAAATAAAAAAT | 25909 |
rs753694936 | snp | A/G | 4.94947e-05 | 0.00497443 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246851045 | TATGGTAAAGTGTCT[A/G]CTTTTTGGGACTTTT | 25909 |
rs753704921 | in-del | -/A | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246928304 | CGAGACTCCGTCTCA[-/A]AAAAAAAAAAAAAAA | 25909 |
rs753711735 | snp | A/G | 5.00254e-05 | 0.00500102 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246900072 | ATACATACCAAAATT[A/G]TAAGTGCTTGGATTA | 25909 |
rs753735512 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246898137 | GAAATTATCTAATAC[A/G]TTTTTACTGTAATAG | 25909 |
rs753746962 | snp | A/T | 3.37365e-05 | 0.00410696 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246907541 | AATAAGGGAAAAAAG[A/T]TATACTTACTCTCTT | 25909 |
rs753783368 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869317 | GACAATATCCAAAGC[C/T]AACTAATAACCCTAC | 25909 |
rs753785226 | in-del | -/TGAAG | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246914617 | CATAAAAATACTATA[-/TGAAG]TGATTAATACTATTA | 25909 |
rs753793042 | snp | C/T | 8.23798e-05 | 0.00641741 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246849803 | GTCATTTCATCTGTG[C/T]GTTCTTCTGATACTG | 25909 |
rs753802207 | in-del | -/ACAA | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246870942 | ACCCTTTTAAAGAAG[-/ACAA]ACAAACAATACAACT | 25909 |
rs753816151 | snp | C/T | 1.65441e-05 | 0.00287607 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246867761 | ATCTTGTCAACACAG[C/T]TCCTGTTACAACTTG | 25909 |
rs753829363 | snp | C/T | 1.97924e-05 | 0.00314576 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246876009 | TTTTGATCCAATAGA[C/T]TATGATATTCTTCAA | 25909 |
rs753832156 | in-del | -/G | 1.69372e-05 | 0.00291004 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246900319 | GAGAAAGGAGAGAGA[-/G]AAAAAAAAGAATCAT | 25909 |
rs753846197 | snp | C/T | 1.64808e-05 | 0.00287057 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850901 | GGACACATTATGTTT[C/T]GGCTCACTAAAGGTA | 25909 |
rs753861669 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246927280 | TGAGGTCAGGAGTTG[A/G]TTAGAGACCAGTCTG | 25909 |
rs753874920 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246847093 | GGCGTTTGAGACTAG[C/G]TTGGCCAACATGGCG | 25909 |
rs753883456 | in-del | -/TTTA | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246893007 | TTAGAGGTTTTTATT[-/TTTA]TTTTTTAAAAAACCC | 25909 |
rs753888818 | snp | C/T | 1.64765e-05 | 0.00287019 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246898284 | CATCGATTATAACCA[C/T]CAGGAATGAGTTCAT | 25909 |
rs753891876 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246844204 | AAGCAGGTACAGAAC[C/T]GTTTAGTCTATTTCT | 25909 |
rs753907727 | snp | A/T | 1.64904e-05 | 0.00287139 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246861017 | AGAGCTTTTGGGCTT[A/T]GAGGCCGTGAAAACA | 25909 |
rs753940784 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246889376 | CTAGATGTCCTGCAC[A/G]TACTATTTTATTTAG | 25909 |
rs753960874 | snp | A/G | 1.64757e-05 | 0.00287012 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246867626 | CAGTAAAGATTAACA[A/G]GCAGCATGACTATGA | 25909 |
rs753977798 | in-del | -/A | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246872052 | TGAACTATTAATGAC[-/A]AAAAAAAAAAAAAAA | 25909 |
rs754014894 | snp | C/T | 3.31307e-05 | 0.00406992 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246849633 | TTGCTTTCCTTGGAA[C/T]TTCTGACGCTGGAGA | 25909 |
rs754023078 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246904379 | TATAACATCTCCCAG[C/T]TTCCTTTGCAGCTAA | 25909 |
rs754027689 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246903316 | CCTCTTATAAAAATC[A/G]CCCTATGGCTTAATG | 25909 |
rs754035939 | snp | C/G | 5.13782e-05 | 0.00506818 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850548 | TTTCTAGTATGTCCT[C/G]ATTAACTTCTTTCTT | 25909 |
rs754040479 | snp | C/T | 1.77272e-05 | 0.00297713 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246916438 | AATATTGTATATACA[C/T]AAAACATGCAATAAC | 25909 |
rs754068157 | snp | C/T | 5.02374e-05 | 0.0050116 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850653 | AGATGTTTTCAGAAG[C/T]TTCAGAAATTTCTTT | 25909 |
rs754116711 | in-del | -/CG | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246927871 | AGCTGGGCGCGGTAG[-/CG]CGCTGTAGTCCCAGC | 25909 |
rs754132668 | snp | C/T | 1.76577e-05 | 0.00297129 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246851394 | TAAATGAAAGATTCC[C/T]AGCCTCTTCTCCTGA | 25909 |
rs754134696 | snp | A/G | 1.64898e-05 | 0.00287135 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850131 | CTGCTTGAACAGTCA[A/G]CTGAGATGACTCAAG | 25909 |
rs754188356 | snp | G/T | 1.65016e-05 | 0.00287238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246877097 | CTAAAAAGAACAAAA[G/T]AGATTGTAAACTACC | 25909 |
rs754213273 | snp | C/G | 3.34465e-05 | 0.00408927 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246900431 | CATATATATTCACCT[C/G]CCAGGTAAAGACTGA | 25909 |
rs754220071 | snp | C/G | 1.66073e-05 | 0.00288156 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246913416 | AATAGCTGTTACCTA[C/G]AAAACATAATACGTG | 25909 |
rs754220238 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246857345 | TCCCCTGTGCTCTAC[C/T]GTGTCTACCTACAAG | 25909 |
rs754238130 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246911775 | AGGCATGAGCCACGG[C/T]GCCCAGCTCTTCTAT | 25909 |
rs754239466 | snp | A/G | 1.66377e-05 | 0.00288419 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246889915 | GATGAACACTATTCT[A/G]AGAAACTTTGACTTC | 25909 |
rs754285823 | in-del | -/CCGCCG | | | intron-variant, upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246931479 | CGCGGGGCAGAAGCC[-/CCGCCG]CCGCCGCCGCCGCCG | 25909 |
rs754286535 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246891312 | AAAATAGACATTTTA[C/G]GTAAATACACTTTCA | 25909 |
rs754292006 | snp | C/G | | | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246876979 | TCAGAGTTTGGTTCA[C/G]CTTCAAGGCAGGCAC | 25909 |
rs754301581 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246874968 | TCCTGCTATTTAGCC[A/G]GTTTCTTCCTAAACC | 25909 |
rs754331331 | snp | C/G | 1.64773e-05 | 0.00287026 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246851292 | CACATTCAGCAGTGT[C/G]TTTGTTATCAGCTAA | 25909 |
rs754342974 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246854959 | TAAAATGGGTGATCG[C/G]CTTTTTACATGTTAG | 25909 |
rs754351955 | in-del | -/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246876765 | CATAAATGGCATACG[-/T]TAAAAGAATTACGTG | 25909 |
rs754368961 | snp | A/G | 3.30104e-05 | 0.00406252 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246888467 | TCAATTCGCTCTCCT[A/G]ACTGAGAAACCAGTC | 25909 |
rs754397667 | snp | A/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246912563 | ACTCCTTTTCTAAAA[A/T]TTAAGAGTAAAAAAC | 25909 |
rs754424057 | snp | A/G | 1.64833e-05 | 0.00287078 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246863906 | TTGATTGTGAACGCT[A/G]GATGCGTAAATACTA | 25909 |
rs754425825 | in-del | -/ATT | 9.27136e-05 | 0.00680795 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246918402 | TTTTTAAAAGAAAAC[-/ATT]ATTATGACACATTTG | 25909 |
rs754436495 | in-del | -/ATAAA | 1.67525e-05 | 0.00289413 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246841044 | TAAACACATTATGCT[-/ATAAA]ATAAAATTGGCTTCC | 25909 |
rs754461811 | snp | A/T | 2.20909e-05 | 0.0033234 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246853310 | CATAGCTGAAAGAAA[A/T]ATGAGTGAATTTTTT | 25909 |
rs754483583 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246863767 | ATAAATTTAATTAGC[C/T]CCGTTTTTAGAAGAT | 25909 |
rs754485817 | snp | C/T | 1.6743e-05 | 0.0028933 | missense, synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246840961 | TCAGCCGAATTTCTA[C/T]GGGAGGAGGTGACCA | 25909 |
rs754492023 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246898537 | TGAATACTACTATTA[C/G]CAAAAGGTAGCTTAT | 25909 |
rs754533644 | snp | G/T | 1.6537e-05 | 0.00287545 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246849987 | TTCTTGTAGATCTCC[G/T]TCTAATGCTGGGAGC | 25909 |
rs754545901 | snp | C/T | 3.73148e-05 | 0.00431926 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246862179 | GAGCAAATGGAATTA[C/T]ACCATTAAAAGTGCT | 25909 |
rs754546438 | in-del | -/GAC | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246928977 | GATAACCTTCTTCCT[-/GAC]TTTAAGGAGTTTACA | 25909 |
rs754567541 | snp | C/T | 1.65037e-05 | 0.00287256 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246876981 | AGAGTTTGGTTCAGC[C/T]TCAAGGCAGGCACAT | 25909 |
rs754575175 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869796 | TGATGTACAGGGAGA[C/T]GAATGCTGTTAGCAG | 25909 |
rs754595276 | snp | C/T | 1.6638e-05 | 0.00288422 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246900212 | CCAATGACCACAGTG[C/T]AAAATAAGAGCAATT | 25909 |
rs754603037 | snp | A/C | 1.65726e-05 | 0.00287855 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246876238 | TCAAAATGTTAGGTG[A/C]TGTAATTCTATATTT | 25909 |
rs754609584 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246918144 | ATTTAAGATCACTCA[C/G]GTTCTGCTTTTTCTT | 25909 |
rs754662506 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246929061 | TAAATGCTACTACAA[C/T]AGAGGTACATATGCT | 25909 |
rs754688323 | snp | C/T | | | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246900243 | ATGTAGATATTCTCC[C/T]GACCTAAAAGAAAAT | 25909 |
rs754697487 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246919454 | CGTGGTGGCTCACGC[C/T]TGTAATCCCAGCACT | 25909 |
rs754737894 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246859989 | TAATTTGGCAGGGCG[C/T]GGTGGCTCACGCCTG | 25909 |
rs754753473 | snp | A/C | 0.000135584 | 0.00823247 | intron-variant, missense, utr-variant-5-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246931166 | TGGAACACACGCCAA[A/C]ACAGGACAGGCTCAG | 25909 |
rs754758485 | snp | A/G | 1.65029e-05 | 0.00287248 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246849645 | GAACTTCTGACGCTG[A/G]AGAAAATAAAGGCTC | 25909 |
rs754779208 | snp | A/G | 4.94719e-05 | 0.00497328 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850690 | CCTAGTTTTCTTCCT[A/G]ACTGACTGCCCTGGC | 25909 |
rs754802806 | in-del | -/TATG | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246883376 | AACAAATTAGGTGAT[-/TATG]TATGACCGCAGGAGA | 25909 |
rs754804757 | snp | A/G | 1.68664e-05 | 0.00290395 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246867802 | GCTGATAATGGTTTG[A/G]GTCTAGAAACTGTAA | 25909 |
rs754813273 | snp | G/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246880201 | ATGTAAATAGCTTAT[G/T]ATCAAAAACAATATG | 25909 |
rs754833295 | in-del | -/CTC | | | cds-indel, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246913376 | GAGTGCTTGCACTGG[-/CTC]CTCCATGATTAATTA | 25909 |
rs754845976 | snp | A/G | 1.87149e-05 | 0.00305893 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246885665 | TAGCTGGATGAAACA[A/G]AAGATCCAAACCACT | 25909 |
rs754850462 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246870416 | TGACAGACAAAGACC[C/T]TGTCTCTTAAAAAAA | 25909 |
rs754853038 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246859259 | TTTTACAGCTTTAGA[A/G]TTAGGAGTTACCTTT | 25909 |
rs754857774 | snp | C/T | 1.64751e-05 | 0.00287007 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246867639 | CAAGCAGCATGACTA[C/T]GAAACGTGTAAGAAA | 25909 |
rs754868510 | snp | A/C | 1.66776e-05 | 0.00288765 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246905510 | TCCAAAAAAACAAAA[A/C]AAAACAAAACAAAGT | 25909 |
rs754869890 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246893727 | TATCAATATGTTAAA[C/T]AGAAAGTGAGTTAAG | 25909 |
rs754889894 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246905805 | CAAGTCATCTTATCT[A/G]CAAAAATACACACGG | 25909 |
rs754895393 | snp | C/G | 1.65578e-05 | 0.00287726 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246891874 | TGGATAGACTGTATA[C/G]TTTGTGGATCCATGA | 25909 |
rs754899492 | in-del | -/TTGCAGAGAAAG | 1.76111e-05 | 0.00296736 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246849595 | AGATGAAAAACTGTT[-/TTGCAGAGAAAG]AAAAGTACCTTTTGC | 25909 |
rs754936188 | snp | C/T | 0.00016484 | 0.00907704 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246855787 | CAGATGTTAATCCTT[C/T]GTCCAACACTGGTAC | 25909 |
rs755033364 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246894857 | AACCGAGTGAACATC[A/G]ACACTTCAGGGAGGC | 25909 |
rs755035822 | snp | C/T | 1.66062e-05 | 0.00288146 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246864116 | AACCAAATCTAGCAG[C/T]CTGTAATCAGAATGC | 25909 |
rs755054696 | snp | C/T | 1.65817e-05 | 0.00287933 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246877225 | TCCTGACAGACTTCA[C/T]ACATGTGCTTCAGTA | 25909 |
rs755091329 | snp | A/T | 1.66098e-05 | 0.00288177 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246861974 | CCCAGGAATCCATTT[A/T]GGGTGGACATCTTCT | 25909 |
rs755107773 | snp | A/G | 1.65116e-05 | 0.00287324 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246890041 | TTGTAGCATAACCTT[A/G]ACAACTGCACAGAAT | 25909 |
rs755132680 | snp | C/T | 3.6003e-05 | 0.00424266 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246853159 | GTAAGTCAACACTTT[C/T]TTTTAGTACACCAAC | 25909 |
rs755134725 | snp | G/T | 1.65288e-05 | 0.00287474 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850278 | CAGAAGCATCTAAAT[G/T]AGTACTTCTCAATTT | 25909 |
rs755148487 | snp | G/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246914680 | TAATGAGTGTATACT[G/T]CACCCTACCCAAAAA | 25909 |
rs755152162 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246929324 | TGAGGCACAAGAATC[A/G]CTTGAGCCCTGGAGG | 25909 |
rs755159572 | snp | A/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246877314 | ACACCTGAAAGCAGT[A/T]TTTATCAAAGTTTAG | 25909 |
rs755177349 | snp | C/G | 1.68119e-05 | 0.00289926 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246916134 | CAGGTATCTTAAACA[C/G]TACCTACCCTTCCAG | 25909 |
rs755259731 | snp | A/G | 1.66913e-05 | 0.00288883 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246900054 | AGAGGTAATGTTAAG[A/G]AAATACATACCAAAA | 25909 |
rs755274594 | snp | A/C | 3.30246e-05 | 0.0040634 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246913259 | CTTCATTTTGATTGC[A/C]TGACAAGTCATCCAA | 25909 |
rs755301955 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246920987 | ATCTCAGCTACTCAG[C/G]AGGCTGAGGCAGGAG | 25909 |
rs755317905 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246893124 | CAAAACTCAATTTAT[A/G]AATTGAGTTTAATTT | 25909 |
rs755343472 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246931061 | TCTCCTTGATCTGAC[C/T]AATCGGGTGAGCTGG | 25909 |
rs755351100 | snp | G/T | 1.65285e-05 | 0.00287471 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246895976 | AGAAAGAGGGTGTGA[G/T]ATCATAGGCAAGTTC | 25909 |
rs755356634 | snp | A/G | 1.6674e-05 | 0.00288734 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246860943 | ACTTCTGATGCAAAT[A/G]CATCTTTATCTCCAT | 25909 |
rs755411706 | snp | C/G/T | 0.000142438 | 0.00843806 | missense, synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246867252 | CTCTTACCTAGAAAT[C/G/T]TTTTGTGATGCTTTT | 25909 |
rs755445761 | in-del | -/CTT | 1.6507e-05 | 0.00287284 | cds-indel, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246889983 | TGATAAACGCTCAAA[-/CTT]CTGTCGACGACTGGT | 25909 |
rs755463546 | snp | G/T | | | downstream-variant-500B | AHCTF1 | GRCh38.p7 | 1:246838815 | TCTGAGTATATTGTT[G/T]CCCTTACTACTATGA | 25909 |
rs755483516 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246888119 | CAGGTTTCCACTACT[C/G]TTGAAATTTTATAAT | 25909 |
rs755490389 | in-del | -/TGT | 3.30617e-05 | 0.00406568 | cds-indel, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246877166 | TAATTACCTGCTCAG[-/TGT]CTGTAAATGGTAACT | 25909 |
rs755497281 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246872760 | CACTATATAGAAGAG[C/T]TTGCTTGGCATGATT | 25909 |
rs755502009 | snp | A/C | 3.29777e-05 | 0.00406051 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246895855 | GTTATCCATCTTCGG[A/C]TATAACCAGTCAAAA | 25909 |
rs755524776 | snp | C/T | 9.88843e-05 | 0.00703081 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246902636 | GGAACATGCCACCTG[C/T]CAGGTCCAGGGTGTA | 25909 |
rs755526487 | snp | G/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246922094 | GCTGGGCACAGTGGC[G/T]CACGCCTGTAATCCC | 25909 |
rs755527541 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246901581 | GTGAGCTGAGATCGT[C/G]CAACTGCACTGGACA | 25909 |
rs755532977 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246855317 | TCACAAAAATGCTCA[C/T]TGGATTAAAAAAAAA | 25909 |
rs755547499 | snp | A/G | | | upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246933368 | TGAACTCTTGACCTC[A/G]TGATCCACCTGCCTC | 25909 |
rs755557828 | snp | C/T | 1.75529e-05 | 0.00296246 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246855879 | AGATCCCATCTGCTT[C/T]AACCTGCTTTAGTCC | 25909 |
rs755569767 | snp | A/T | 1.99249e-05 | 0.00315627 | missense, nc-transcript-variant, intron-variant | AHCTF1 | GRCh38.p7 | 1:246843819 | TTCAAGCTTGTTCTT[A/T]TTGGATGTGTTTTTT | 25909 |
rs755581451 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246921135 | AAAGCAGCAGAAAAT[A/G]CACGCAAAATGACAT | 25909 |
rs755592653 | snp | G/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246892397 | TCAATCTCCGCTCAC[G/T]GCAACCTCTACCTCC | 25909 |
rs755596515 | in-del | -/TTCT/TTT | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246857961 | ACTGCTAACACTTTC[-/TTCT/TTT]TTCTTTTTTTTTTTT | 25909 |
rs755618028 | snp | A/G | 2.53913e-05 | 0.00356301 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246885694 | CTCTGGAAATAACAT[A/G]AAAAATGTTAAATAT | 25909 |
rs755618031 | in-del | -/C/T | 0.000201558 | 0.0100368 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246853080 | GAAGTAAAAAATTAA[-/C/T]TTTTTTTTACATGAA | 25909 |
rs755619681 | snp | A/G | 1.75268e-05 | 0.00296025 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246894643 | TCTGTCCTACATCTA[A/G]ACCTCTAATACTTAC | 25909 |
rs755630613 | snp | C/T | 1.64961e-05 | 0.00287189 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850708 | TGACTGCCCTGGCAT[C/T]TTAGGAGTAGCAACA | 25909 |
rs755631830 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246884676 | GAGACTGTAATAATC[A/C]TTATTATGTAAATGA | 25909 |
rs755660997 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246929208 | GAGCTCAGGAGTTCG[A/C]GATCACCCTGGGCAA | 25909 |
rs755661466 | snp | C/T | 0.000165126 | 0.0090849 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246841040 | AGAATAAACACATTA[C/T]GCTATAAAATAAAAT | 25909 |
rs755672914 | in-del | -/CTT | 1.65389e-05 | 0.00287562 | cds-indel, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246849986 | TTTCTTGTAGATCTC[-/CTT]CTAATGCTGGGAGCT | 25909 |
rs755673039 | snp | A/G | 1.65627e-05 | 0.00287769 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246891880 | GACTGTATAGTTTGT[A/G]GATCCATGAAATGAC | 25909 |
rs755738258 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246906023 | CTGGTCCTAAGAGTC[A/C]TATTTGATGTACACT | 25909 |
rs755739389 | snp | A/G | 8.32577e-05 | 0.00645151 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246900320 | GAGAAAGGAGAGAGA[A/G]AAAAAAAGAATCATA | 25909 |
rs755750960 | snp | G/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246889041 | GTCAGTCAAGGTGAG[G/T]TCCCCATGTGGTCCA | 25909 |
rs755757058 | snp | C/T | 1.6691e-05 | 0.00288881 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246900420 | CTTTCCCTGTCCATA[C/T]ATATTCACCTGCCAG | 25909 |
rs755775483 | snp | C/G | 1.65293e-05 | 0.00287479 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246913400 | GATTAATTATAGGTT[C/G]AATAGCTGTTACCTA | 25909 |
rs755779938 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246920907 | CCTGGCCAACATGGT[A/G]AATCCACATCTCTAC | 25909 |
rs755786671 | snp | A/C/G | 5.07227e-05 | 0.00503579 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246840969 | ATTTCTATGGGAGGA[A/C/G]GTGACCAAGCACTTT | 25909 |
rs755808040 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246919630 | AAGCAGGAGAATCAC[C/T]TGAACCCAGGAGGTG | 25909 |
rs755811275 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246871292 | CTAAAAACAGAGACA[C/T]CACTCGCTTACTGAT | 25909 |
rs755832750 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246840201 | TTGCCGAATAAGAGA[C/T]GCCAACATTATAGTT | 25909 |
rs755838313 | in-del | -/GT | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246923743 | TGTGCGTGCATGCGT[-/GT]GTGTGTGTGTGCGCG | 25909 |
rs755854248 | snp | C/T | 1.6492e-05 | 0.00287154 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850119 | ACATATCAAATTCTG[C/T]TTGAACAGTCAACTG | 25909 |
rs755865627 | snp | A/C | 1.64765e-05 | 0.00287019 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246849798 | TATGTGTCATTTCAT[A/C]TGTGCGTTCTTCTGA | 25909 |
rs755895293 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246893941 | GATGTAGTGGCTCAC[A/G]CCTTGTAATACCAAC | 25909 |
rs755918895 | snp | A/G | 0.000115311 | 0.00759224 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246849708 | TGGCCTTGCTAGACC[A/G]AGTCCTGCTGCTGCG | 25909 |
rs755925372 | snp | A/G | 4.69462e-05 | 0.00484467 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246861298 | TATCATCTGCAGCCT[A/G]TAAAGTAAGATTTTG | 25909 |
rs755946408 | snp | C/T | 0.00104848 | 0.0228723 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246867815 | TGGGTCTAGAAACTG[C/T]AAAATGAAGAACGCT | 25909 |
rs755976686 | snp | A/G | 1.98963e-05 | 0.00315401 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246876007 | TTTTTTGATCCAATA[A/G]ATTATGATATTCTTC | 25909 |
rs755981311 | snp | C/T | 0.000285225 | 0.0119386 | intron-variant, synonymous-codon, utr-variant-5-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246931218 | GGAAAGGCCCGCCAA[C/T]GAGTCCATCGCGTGG | 25909 |
rs755996260 | snp | A/G | 3.30082e-05 | 0.00406239 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246887226 | CTCATAGTCATTATG[A/G]TCTATCAACCAAAAC | 25909 |
rs756001393 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246879166 | AGCCAAAGATTTTAA[C/T]AGGCAGGTCACAAAA | 25909 |
rs756032571 | snp | A/G | 1.7051e-05 | 0.0029198 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246899520 | AGTGGCATCTAAAAA[A/G]AAGATTTAAAAAATA | 25909 |
rs756034691 | snp | A/G | 1.73168e-05 | 0.00294246 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246907533 | TATAATCAAATAAGG[A/G]AAAAAAGTTATACTT | 25909 |
rs756064105 | in-del | -/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246860190 | GCTTGAACCTGGTTG[-/G]GGGGGGGGCGGAGGT | 25909 |
rs756089086 | snp | C/G | 1.65051e-05 | 0.00287267 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246905641 | GAACTTGTCCACTTT[C/G]CAATTGTATGTAATA | 25909 |
rs756101765 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246845395 | TAGAGTTGATATCAG[A/G]TATCAGAAATATATA | 25909 |
rs756163414 | snp | C/G/T | 5.53193e-05 | 0.00525901 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850523 | AATTCTTGTTCCACA[C/G/T]AACTGGTGTTTTCTA | 25909 |
rs756176438 | snp | C/G | | | intron-variant, downstream-variant-500B | AHCTF1 | GRCh38.p7 | 1:246842524 | GAGGCAGAGGTTGCA[C/G]TGAGCCGAAATCACA | 25909 |
rs756205801 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246902409 | GAACTGAATAAATTC[C/T]GTTAATTACTATTCC | 25909 |
rs756231317 | in-del | -/A | | | utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246840328 | GTAACAGCCAAAAAC[-/A]AAAAAAATACATTTT | 25909 |
rs756239288 | snp | A/G | 1.73426e-05 | 0.00294466 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246877306 | TCAACCATACACCTG[A/G]AAGCAGTATTTATCA | 25909 |
rs756247847 | snp | C/T | 1.6516e-05 | 0.00287362 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246903955 | ACCATTTACCTCATA[C/T]AAGATTTGTCCTGAT | 25909 |
rs756255457 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246903294 | CTAAAAGCCCAGACG[C/T]GTATGTCCTCTTATA | 25909 |
rs756277027 | snp | G/T | 1.92665e-05 | 0.00310369 | missense, nc-transcript-variant, intron-variant | AHCTF1 | GRCh38.p7 | 1:246843833 | TATTGGATGTGTTTT[G/T]TTGTCTGCTCCTTAA | 25909 |
rs756279015 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246927105 | ATGGCGTGAACCCGG[A/G]AGGCGGAGCTTGCAG | 25909 |
rs756300836 | snp | A/G | 1.64991e-05 | 0.00287215 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246902651 | TCAGGTCCAGGGTGT[A/G]TCTTTCTTCACAGTA | 25909 |
rs756303119 | snp | A/T | 5.10347e-05 | 0.00505121 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246916310 | ATTGACTCCACTGAA[A/T]CTGTAAGCAGACAAT | 25909 |
rs756309731 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868419 | AGCCACTGCGCCTGG[A/C]AATTTTTGTATTTTT | 25909 |
rs756343520 | snp | C/G | | | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246916380 | CCACAAGCCAAGCAA[C/G]CAAGTCCATTTTTCC | 25909 |
rs756360999 | in-del | -/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246845244 | GTATATATAAAAATG[-/T]TTTTTGTGGGTACAC | 25909 |
rs756387863 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869209 | AGCAAGTCTACTGGC[A/G]CCATTTTTCCAACAG | 25909 |
rs756404764 | snp | A/G | 1.65395e-05 | 0.00287567 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246849999 | TCCTTCTAATGCTGG[A/G]AGCTTCTTTCTTCTT | 25909 |
rs756408014 | snp | C/T | 1.66838e-05 | 0.00288818 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246891034 | TGAGGTGGGAAACCA[C/T]AAACTTATTGCTTAA | 25909 |
rs756414195 | snp | A/C/G | 1.67708e-05 | 0.00289571 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246902706 | CACGCAAATATTAAT[A/C/G]TGATTCTAGGCAAAA | 25909 |
rs756417679 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246889323 | ATAGCGGCAGCACTT[A/C]CTACTCTTTGCGGTT | 25909 |
rs756440164 | snp | A/G | 1.6476e-05 | 0.00287014 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246851278 | TACTTCAGCAATGTC[A/G]CATTCAGCAGTGTCT | 25909 |
rs756445387 | snp | A/G | | | upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246933527 | CCTCAGCCTCTCAAC[A/G]TGCTGGGATTACAGA | 25909 |
rs756445992 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246917433 | TTTAAGAAAGTAGCA[C/T]GGTACAGTGGGGTCT | 25909 |
rs756471351 | snp | C/T | 1.69407e-05 | 0.00291034 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850388 | GATCTTTTAATTCTT[C/T]TAGGAGTCCTTTTTG | 25909 |
rs756482422 | snp | C/G | 8.2479e-05 | 0.00642127 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246888451 | TCGTTTCCACAACTT[C/G]TCAATTCGCTCTCCT | 25909 |
rs756531391 | in-del | -/A | 0.000305105 | 0.0123475 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246900318 | AGAGAAAGGAGAGAG[-/A]AAAAAAAAAGAATCA | 25909 |
rs756535737 | snp | C/T | 1.6476e-05 | 0.00287014 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246898278 | ACAAGACATCGATTA[C/T]AACCATCAGGAATGA | 25909 |
rs756550334 | snp | C/T | 1.65002e-05 | 0.00287225 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246861009 | GCAGTGGAAGAGCTT[C/T]TGGGCTTAGAGGCCG | 25909 |
rs756573900 | in-del | -/ATAG | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246923862 | GAAATGAAGGGGGAA[-/ATAG]ATAGATAACCCCAGG | 25909 |
rs756578879 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246907482 | TAACTTTCAAATATT[A/G]GTAAATGAGTACAAG | 25909 |
rs756587618 | snp | C/T | 1.67293e-05 | 0.00289212 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246876915 | CAGTTTTCCTTATTC[C/T]CTTATCCCCCATAAT | 25909 |
rs756596455 | snp | G/T | 4.95111e-05 | 0.00497525 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246888262 | GGATAAAACCTTCAG[G/T]GGATCTTATACAGTC | 25909 |
rs756629135 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246862206 | TGCTTATAGGCCGGG[C/T]GCGGTGGCTCACGCC | 25909 |
rs756651823 | in-del | -/CAA | 3.34694e-05 | 0.00409067 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246890110 | AATCCCCAAATATCT[-/CAA]CAATACATATTAATA | 25909 |
rs756651916 | snp | A/C | 1.64827e-05 | 0.00287073 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246898163 | AATAGAAAGCTAATA[A/C]CGTGATCCAACCAAA | 25909 |
rs756690647 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246924057 | TTTCTCAGCACTCCC[C/T]CTCCTATCTATTGAG | 25909 |
rs756727492 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246917046 | CAATGTAAAGTCATA[A/G]AGGTGACTATCTGAT | 25909 |
rs756754128 | snp | A/G | 1.97241e-05 | 0.00314032 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246876011 | TTGATCCAATAGATT[A/G]TGATATTCTTCAATG | 25909 |
rs756767919 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246887941 | CACATTTAAGTGTCT[C/G]ATAAAAGCCAAGTAC | 25909 |
rs756798263 | snp | G/T | 3.29913e-05 | 0.00406135 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850914 | TTTGGCTCACTAAAG[G/T]TATTGTTTCATGAAT | 25909 |
rs756809314 | snp | A/G | 1.64906e-05 | 0.00287142 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246887269 | TTAACTTGGCCCCAA[A/G]AAATGGCAAATACAG | 25909 |
rs756817653 | snp | C/T | | | downstream-variant-500B | AHCTF1 | GRCh38.p7 | 1:246838649 | TATAAGGTCAATCCA[C/T]TGTAGCCCATTCAGG | 25909 |
rs756841281 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246930966 | AACCAAAACAGTCAA[C/T]CAGTGGCAAAAGAAA | 25909 |
rs756851524 | snp | C/T | 4.97739e-05 | 0.00498844 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850806 | TTTTGGAGGAAACCA[C/T]GTCATCAACCTGGCT | 25909 |
rs756861258 | snp | A/G | 0.000165656 | 0.00909949 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246905651 | ACTTTCCAATTGTAT[A/G]TAATATCTGAAACAA | 25909 |
rs756865996 | in-del | -/GACT | 1.64887e-05 | 0.00287125 | frameshift-variant, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850173 | CTCTCACATCTGATG[-/GACT]AACTTCTCTCCCTCT | 25909 |
rs756867330 | in-del | -/CT | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246927169 | GGCGACAGAGCGAGA[-/CT]CTGTCTCAAAAAAAA | 25909 |
rs756870314 | snp | A/G | 1.73534e-05 | 0.00294558 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246891941 | AGAATAAAAGAAAAG[A/G]TAAGTTTCCATACAG | 25909 |
rs756870671 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246895151 | AAACAAAATACAAAG[C/T]ATGATTCTGAGCTCT | 25909 |
rs756879765 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246871608 | TAACAGCCTACCTCT[A/G]TGAACCCTGACTAGA | 25909 |
rs756885510 | in-del | -/TCT | 3.5598e-05 | 0.00421873 | cds-indel, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246853188 | ACTTCTACTTCATGA[-/TCT]TCTTTTAAGTTCAGC | 25909 |
rs756889770 | snp | C/T | 1.66485e-05 | 0.00288513 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246894675 | TAGTCTGTCAAATTC[C/T]TCTTTTGTGAGAACC | 25909 |
rs756914771 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246860421 | CCAAATAAAAAATGT[A/G]ACACATAAGTTCTCC | 25909 |
rs756917277 | snp | G/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246907194 | CTTAAACATTAAAAA[G/T]GTACAATCAAAATAC | 25909 |
rs756944550 | snp | C/T | 1.6643e-05 | 0.00288465 | missense, nc-transcript-variant, intron-variant | AHCTF1 | GRCh38.p7 | 1:246842737 | TGATTCGTTTCGCTT[C/T]TGGCTTTCCCAGAGT | 25909 |
rs756944974 | snp | C/T | 3.32441e-05 | 0.00407688 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246902534 | ACTAACCTTCATTCA[C/T]GCCTTCCTCCCTGTC | 25909 |
rs756950637 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246867598 | TGGATTGTTGATGAA[C/T]GCTGTTGATGTCCAG | 25909 |
rs756952978 | snp | A/C/T | 0.00058517 | 0.0170965 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246931242 | CGCGTGGGAGAACAG[A/C/T]GGGAAAGGGTCGCGG | 25909 |
rs756954436 | in-del | -/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869330 | GCCAACTAATAACCC[-/T]ACAAAGACCTCAAGT | 25909 |
rs756957007 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246852548 | TCAGAGTGTACAGAT[A/G]TTCAACACCAGCCAG | 25909 |
rs756983877 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246921994 | TTAAATAAACCATAC[A/G]GAGTCTTCTTACTGC | 25909 |
rs756995556 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246896716 | TCTGAACTGCACGGT[A/G]TATGAAATATCTCAA | 25909 |
rs757037085 | snp | A/C | 1.65302e-05 | 0.00287486 | missense, utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246840849 | TTTGGATAGGAAGAC[A/C]GTTTCTTTCTGTTCC | 25909 |
rs757086714 | snp | C/G | 1.66646e-05 | 0.00288652 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246861337 | AAAATTAGTAAATAT[C/G]ACAGTTAAGTCTAGT | 25909 |
rs757109050 | snp | G/T | 1.65811e-05 | 0.00287929 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246862010 | AAATGAAATTCTAGT[G/T]TCTTTAAGTCGTTGA | 25909 |
rs757139638 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246846207 | TAAGATAATTTCTTC[A/G]CTATGTTTCAATAAA | 25909 |
rs757160395 | snp | C/T | 1.67556e-05 | 0.0028944 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246907544 | AAGGGAAAAAAGTTA[C/T]ACTTACTCTCTTTTC | 25909 |
rs757167462 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246842803 | ACATTTTAAAAGGTT[A/G]AGTATTAAACACGAA | 25909 |
rs757173810 | snp | A/C/G | 0.000116496 | 0.00763122 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246900188 | GAGAAGTCCTACTTA[A/C/G]AACAGACTCCAATGA | 25909 |
rs757184477 | snp | C/T | 1.64743e-05 | 0.00287 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246907698 | AGATGGCGCCCTTGT[C/T]TCATTACACTTTCTC | 25909 |
rs757187820 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246880747 | TCCCAGTTTCCCCCA[C/T]AGCAGGAAAATACTT | 25909 |
rs757226973 | snp | C/T | 1.66746e-05 | 0.00288739 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246900073 | TACATACCAAAATTA[C/T]AAGTGCTTGGATTAA | 25909 |
rs757227077 | in-del | -/TTC | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246845701 | AGCACAGATGAGACT[-/TTC]TTGAGTGTATGTCAA | 25909 |
rs757249410 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246916454 | AAAACATGCAATAAC[A/G]GTTAGCTCATTTACA | 25909 |
rs757250019 | in-del | -/GAA | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246904932 | TCTCCAAGTATATTT[-/GAA]GAATAAGAGAGCAGG | 25909 |
rs757264547 | snp | A/G | 1.64841e-05 | 0.00287085 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246851162 | GTGTTAGCTGCTTTA[A/G]GTAACACATCAGATG | 25909 |
rs757287157 | snp | C/T | 3.30513e-05 | 0.00406504 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246849640 | CCTTGGAACTTCTGA[C/T]GCTGGAGAAAATAAA | 25909 |
rs757302709 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246915062 | ACTGGCCGGGCGTGG[C/T]GGCTCATGCCTGTAA | 25909 |
rs757316981 | snp | C/T | | | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246855786 | ACAGATGTTAATCCT[C/T]CGTCCAACACTGGTA | 25909 |
rs757335600 | snp | A/G/T | 3.29898e-05 | 0.00406128 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246861091 | AGGTAGTCTCATCGG[A/G/T]TGTGATTGAAACACT | 25909 |
rs757375264 | in-del | -/AAC | 1.70653e-05 | 0.00292102 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246903904 | ATATTTAAAATAGAA[-/AAC]AACAAAATGGTAATA | 25909 |
rs757377288 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246859686 | GTCCAAGCGATCCTC[C/T]CCTCTCAGTGTCCTG | 25909 |
rs757386569 | snp | A/C | 1.77745e-05 | 0.00298109 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246904085 | TAATACATTAAACAT[A/C]TCTTACTGTCCAAGT | 25909 |
rs757390474 | in-del | -/AACA | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246857952 | TGTTATCAGACTGCT[-/AACA]AACACTTTCTTCTTT | 25909 |
rs757402469 | snp | G/T | 1.66551e-05 | 0.00288571 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246918343 | ATGGCAGGAGACCAC[G/T]AGTCACTTGAGCTCT | 25909 |
rs757430495 | in-del | -/AAAAG | 3.41309e-05 | 0.00413089 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246891931 | ACACCTTTCAAGAAT[-/AAAAG]AAAAGATAAGTTTCC | 25909 |
rs757436317 | snp | G/T | 1.64819e-05 | 0.00287066 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246898169 | AAGCTAATAACGTGA[G/T]CCAACCAAAAGAAAC | 25909 |
rs757439221 | snp | A/G | 3.3168e-05 | 0.00407221 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246867772 | ACAGTTCCTGTTACA[A/G]CTTGCTTTGGAACTG | 25909 |
rs757478321 | snp | C/T | 1.66167e-05 | 0.00288237 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850662 | CAGAAGCTTCAGAAA[C/T]TTCTTTTGCCTTCCT | 25909 |
rs757483821 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246922810 | ACACGGTGAAACCCT[A/G]TCTCTACTAAAAATA | 25909 |
rs757489801 | snp | A/G | 1.6489e-05 | 0.00287128 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246903978 | GTCCTGATGCCAAAC[A/G]CTTTCTATTACCAAA | 25909 |
rs757492844 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246910695 | GCAGATTCTCTCATT[C/G]TTATAAAGGGGGAAA | 25909 |
rs757493168 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246874731 | CAACCTATCCTGAGA[A/G]ATCCTGAAATATATT | 25909 |
rs757496520 | snp | A/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246849109 | AATACAGTCCTTAGC[A/T]CGTGACAATGAAGGA | 25909 |
rs757513653 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246889413 | ACTGACTTTATAACT[C/T]ATATAACAAGCAGGA | 25909 |
rs757552610 | snp | C/T | 1.65089e-05 | 0.00287301 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246864046 | ACAAAGGAGATTTCA[C/T]GGAGCTTTGCTGAAT | 25909 |
rs757556837 | snp | G/T | 1.85379e-05 | 0.00304444 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246843950 | AAAGTTGAAAAAACT[G/T]TATCTGTATCTTTAT | 25909 |
rs757569758 | snp | C/T | | | intron-variant, downstream-variant-500B | AHCTF1 | GRCh38.p7 | 1:246842652 | ACAGAGCGAGACTGT[C/T]TCAATCAATCAATCA | 25909 |
rs757581822 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246925570 | GGTTGCAGTAAGCTA[C/T]GATCAGGCCACTGCA | 25909 |
rs757625854 | snp | A/G | 1.67382e-05 | 0.00289289 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246900438 | ATTCACCTGCCAGGT[A/G]AAGACTGAAACACTA | 25909 |
rs757631720 | snp | C/T | 1.7117e-05 | 0.00292544 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246916101 | CCAGCAGGGGTTCAG[C/T]TTTGAAAGAGAAATG | 25909 |
rs757635067 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246924219 | TAAAAAATTTATAAA[C/G]AAATATTTACATTAA | 25909 |
rs757636628 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246870817 | TGTATCAAATACCTC[C/T]TCCTCAGAACCAAAA | 25909 |
rs757637018 | in-del | -/TA | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246862720 | AAAAGTGCCAATTAG[-/TA]AGATAAATTACTTAA | 25909 |
rs757739903 | snp | A/T | 3.29587e-05 | 0.00405934 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246863951 | AGGAGTTTCAAGCAA[A/T]TGTAATTCTGAAGCC | 25909 |
rs757767844 | in-del | -/ACAAAAA | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246848706 | GCTGTCTCTACAAAT[-/ACAAAAA]ACAAAAAATTAGCCA | 25909 |
rs757788540 | snp | A/C/G | 1.64795e-05 | 0.00287045 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246863935 | TAACCTTAACTACAA[A/C/G]AGGAGTTTCAAGCAA | 25909 |
rs757836741 | snp | A/C | 2.49237e-05 | 0.00353004 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246876220 | TGGTAAAAAATTTAA[A/C]CTTCAAAATGTTAGG | 25909 |
rs757838911 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246911781 | GAGCCACGGCGCCCA[A/G]CTCTTCTATTAAGAT | 25909 |
rs757847395 | snp | C/T | 1.64773e-05 | 0.00287026 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246851295 | ATTCAGCAGTGTCTT[C/T]GTTATCAGCTAAGTC | 25909 |
rs757864826 | snp | A/G | 3.33506e-05 | 0.0040834 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246913422 | TGTTACCTAGAAAAC[A/G]TAATACGTGATTTGC | 25909 |
rs757898761 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246851898 | GGTTGAAGAACAATT[C/G]ACCTACATAAGCTCC | 25909 |
rs757949928 | in-del | -/AG | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246848905 | CATTAACACTTTTAC[-/AG]AGAGTTACTCTGATG | 25909 |
rs757967887 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246860573 | GCTTTCCTTCTGAGA[C/T]AGGGTCTTGCTCTGT | 25909 |
rs757968395 | snp | A/G | 1.64751e-05 | 0.00287007 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246907706 | CCCTTGTCTCATTAC[A/G]CTTTCTCTAATGTGT | 25909 |
rs757970163 | snp | C/T | 3.73741e-05 | 0.00432269 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246876147 | TCTAATATAGAATTT[C/T]GAGCCAGTGATCTCT | 25909 |
rs757985160 | in-del | -/TCAAT | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246911381 | TATTGCTTTTGCTCA[-/TCAAT]TCTTTTCATTTAAAC | 25909 |
rs757989663 | snp | C/T | 3.29891e-05 | 0.00406122 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246887300 | TTGGGAAAGATTCAA[C/T]GGGAGTGTCTGTTTT | 25909 |
rs757991360 | snp | G/T | 1.64966e-05 | 0.00287194 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246851058 | CTACTTTTTGGGACT[G/T]TTGGTCACTAGTTAC | 25909 |
rs758016958 | snp | C/G | 1.70688e-05 | 0.00292132 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246887402 | ATACAACAACAAAAA[C/G]CTCCTACGTATATAT | 25909 |
rs758022590 | in-del | -/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246863831 | AGCACTCCCCAAGCG[-/T]TATCAGTTATAAATT | 25909 |
rs758046033 | snp | G/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246880956 | TAATAAGGAATGCAT[G/T]GGGGTTCTTGGCAAT | 25909 |
rs758126238 | snp | A/G | 1.65699e-05 | 0.00287831 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246895815 | AATACCAAACATTTT[A/G]CTTGTTATCAGAATC | 25909 |
rs758126748 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246866584 | AAAAATTCAGAGTCT[C/T]GTAATGATTATTTAT | 25909 |
rs758135670 | snp | A/C | 1.67122e-05 | 0.00289064 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246860929 | GGTCTGAAGGAGTTA[A/C]TTCTGATGCAAATAC | 25909 |
rs758136091 | snp | C/T | 5.5439e-05 | 0.00526464 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246857866 | AATATTTAGTGATTA[C/T]TGATAGTCTTGCATT | 25909 |
rs758140455 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246910589 | TTTATGGGAACTCTT[A/G]TATTCTTCTAACTAT | 25909 |
rs758172343 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246916996 | TCAGAACCTCTTCTC[C/T]GCCTATTAGTCATGT | 25909 |
rs758191634 | snp | A/T | 1.6498e-05 | 0.00287206 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850920 | TCACTAAAGGTATTG[A/T]TTCATGAATGGACTG | 25909 |
rs758208623 | in-del | -/AAAAAGTGCTTATAT | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246862487 | CCGTCTCAAAAAAAA[-/AAAAAGTGCTTATAT]AAAAAAGTGCTTATA | 25909 |
rs758208803 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246857036 | TCAGTCTCGCAATGA[A/G]ACAAGGACCTCTTGC | 25909 |
rs758224918 | snp | C/G | 0.000121098 | 0.00778038 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246891068 | TATCAGTCCTGTAAA[C/G]AAGAGTTAACATCAG | 25909 |
rs758259236 | snp | A/G | 1.67019e-05 | 0.00288975 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246885531 | GTGAAGGATAACATC[A/G]TTACCACTGGACACT | 25909 |
rs758260839 | snp | G/T | 1.76555e-05 | 0.0029711 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246862153 | CCAAACTTTTAGCTT[G/T]CTATAGTAAAGAGCA | 25909 |
rs758262461 | snp | G/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246882677 | AGGATTTTTTGGCTT[G/T]CTTGTACATTTATGA | 25909 |
rs758280312 | snp | A/C | 3.32806e-05 | 0.00407912 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246900199 | CTTACAACAGACTCC[A/C]ATGACCACAGTGCAA | 25909 |
rs758282811 | snp | A/C/T | 6.64114e-05 | 0.00576211 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246918243 | TGTTCAGTGACATTA[A/C/T]GTTTACCTGCAGCAA | 25909 |
rs758285704 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246886631 | TACAGTTGATTGAAG[C/G]CACGGATGTAGAATC | 25909 |
rs758314453 | snp | A/T | 1.64789e-05 | 0.0028704 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246877323 | AGCAGTATTTATCAA[A/T]GTTTAGTTTTAGAAA | 25909 |
rs758316645 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246918053 | AAAAATTAACTATAA[C/T]CCCCCCAATCAGAGG | 25909 |
rs758320250 | in-del | -/TT | 1.65252e-05 | 0.00287443 | frameshift-variant, utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246840932 | CCGTCAGCTGGGCTA[-/TT]GCCAAGGGGGAAATC | 25909 |
rs758346249 | snp | A/C/G | 4.97998e-05 | 0.00498977 | missense, utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246840952 | AGGGGGAAATCAGCC[A/C/G]AATTTCTATGGGAGG | 25909 |
rs758364897 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869698 | ATTTTAAGCCTACTG[C/T]TGAGAACTGTTCAGA | 25909 |
rs758376059 | snp | C/T | 1.64887e-05 | 0.00287125 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850171 | TTCTCTCACATCTGA[C/T]GGACTAACTTCTCTC | 25909 |
rs758383074 | in-del | -/CT | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246930169 | AGCAACAGGTTCTCG[-/CT]CTGTCACACAGGCTG | 25909 |
rs758425751 | snp | A/C | 1.65086e-05 | 0.00287298 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246851326 | ACAAAACTGTTGGTC[A/C]ATAGTATCAAAATTG | 25909 |
rs758453114 | in-del | -/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246911275 | CACAAAATACACTAT[-/G]AAACAAAAGCCTATC | 25909 |
rs758468293 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246903432 | TGTAGAGGAAAACGG[C/T]ATCTGAGAAGTTAAG | 25909 |
rs758471853 | snp | C/T | 1.65097e-05 | 0.00287308 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246877116 | TTGTAAACTACCAAT[C/T]TATCTTGAATTTCTG | 25909 |
rs758471964 | snp | A/G | 1.65064e-05 | 0.00287279 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246890033 | CAGGGTAGTTGTAGC[A/G]TAACCTTGACAACTG | 25909 |
rs758473094 | snp | C/G | 1.88329e-05 | 0.00306857 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246851424 | AATCTTGAGCTTCAA[C/G]CTTTTCTTGTTCAAT | 25909 |
rs758476757 | snp | C/G/T | 3.34662e-05 | 0.0040905 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246913428 | CTAGAAAACATAATA[C/G/T]GTGATTTGCTTTTCT | 25909 |
rs758495293 | in-del | -/TC | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246887051 | TTTATATTCTTGCCT[-/TC]TCTAAAATAGTGCTT | 25909 |
rs758504910 | snp | G/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246905464 | ATCACGCCACTGCAC[G/T]CCAGCCTGGACAACA | 25909 |
rs758504963 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246892012 | AACTCCTATCACTCA[A/G]AAGAATTATTCTATT | 25909 |
rs758524817 | snp | A/G | 1.65633e-05 | 0.00287774 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246889950 | AGATGTAATTTCTAA[A/G]ATTGTTTTACTATAC | 25909 |
rs758562770 | snp | C/T | 1.64836e-05 | 0.0028708 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246905619 | TGAAAAGTGACAGCA[C/T]ATACAGGAACTTGTC | 25909 |
rs758571381 | snp | A/G/T | 0.000142023 | 0.00842582 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246861261 | GCACATTTTTTAGGT[A/G/T]TAGTAAATACTTCTA | 25909 |
rs758579118 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246907400 | CACATTGATTTAATG[C/T]CATGAAAAATTAGTC | 25909 |
rs758581335 | in-del | -/TC | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246875160 | GACATAGTAACTAAG[-/TC]TACACAACTGGGACC | 25909 |
rs758597231 | snp | G/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246911931 | TTTATCACTTGCAGT[G/T]TTTTTGTTTTTGTTT | 25909 |
rs758605367 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246926742 | TGCCTATAATCCCAG[C/T]TACTTTGGGAGGCTG | 25909 |
rs758621810 | in-del | -/AAAAC | 0.277778 | 0.248452 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246905501 | GACTCTGTCTCCAAA[-/AAAAC]AAAACAAAACAAAAC | 25909 |
rs758648190 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246900841 | TTCACTACCTAAAAC[A/G]GATGCTTTTGGGCAT | 25909 |
rs758655616 | snp | C/T | | | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246876180 | CGCAAACGAGGATCA[C/T]GATCATTCTATTAAA | 25909 |
rs758657807 | snp | A/G | 1.64773e-05 | 0.00287026 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246898292 | ATAACCATCAGGAAT[A/G]AGTTCATTGAGTGAT | 25909 |
rs758664218 | snp | C/T | 1.66192e-05 | 0.00288259 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246857798 | GAGATCCTTTGTTTC[C/T]GCATCTTCTAAATTG | 25909 |
rs758681386 | snp | C/T | 1.64754e-05 | 0.00287009 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246849693 | GGTCCGGCAACAAGA[C/T]GGCCTTGCTAGACCG | 25909 |
rs758709757 | snp | C/G | 4.07166e-05 | 0.00451183 | missense, nc-transcript-variant, intron-variant | AHCTF1 | GRCh38.p7 | 1:246843813 | TTCATCTTCAAGCTT[C/G]TTCTTATTGGATGTG | 25909 |
rs758717529 | snp | C/G | 1.65712e-05 | 0.00287843 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246864103 | GGACAGGCTGAACAA[C/G]CAAATCTAGCAGTCT | 25909 |
rs758732012 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246866047 | ACTTCAGCCTTACTA[C/T]ATGATGTACCCACGG | 25909 |
rs758763048 | snp | C/T | 9.98303e-05 | 0.00706436 | missense, nc-transcript-variant, intron-variant | AHCTF1 | GRCh38.p7 | 1:246842745 | TTCGCTTTTGGCTTT[C/T]CCAGAGTTTCTACTG | 25909 |
rs758780543 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246899655 | AACTTTTCTAGGTAT[C/T]TTCATCCTAAGAATA | 25909 |
rs758784240 | in-del | -/A | 7.04655e-05 | 0.0059353 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246876208 | AACATCAAAATTGGT[-/A]AAAAAATTTAACCTT | 25909 |
rs758826780 | in-del | -/ATCC | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246893741 | TAGAAAGTGAGTTAA[-/ATCC]GTACAGAAACTTCTG | 25909 |
rs758863614 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246871297 | AACAGAGACACCACT[C/T]GCTTACTGATGGGAG | 25909 |
rs758878604 | snp | C/G | 1.65165e-05 | 0.00287367 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246864055 | ATTTCATGGAGCTTT[C/G]CTGAATAAACTCCGA | 25909 |
rs758917844 | snp | A/G | 5.09221e-05 | 0.00504564 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246916124 | GAGAAATGTCCAGGT[A/G]TCTTAAACAGTACCT | 25909 |
rs758925793 | snp | G/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246852127 | ACATTACCACCCACC[G/T]AGACAATGACATTTT | 25909 |
rs758931642 | snp | C/T | 1.64958e-05 | 0.00287187 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850109 | GGTATGGCAGACATA[C/T]CAAATTCTGCTTGAA | 25909 |
rs758937842 | in-del | AAAAAAAAAAAAAA/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246909399 | CCAGCCTCTCAAAAA[AAAAAAAAAAAAAA/T]AAAAAAAAAATTTGC | 25909 |
rs758940402 | snp | A/G | 1.65474e-05 | 0.00287636 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246902547 | CACGCCTTCCTCCCT[A/G]TCACCATGAGATCGA | 25909 |
rs758941358 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246886456 | TAAGTAATCTACAGA[C/T]GATTTAAAGATCAAG | 25909 |
rs758957942 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246901719 | GTTACTTGGGAGACC[A/G]AGATGGGAGAATTGG | 25909 |
rs758986571 | snp | G/T | 1.64757e-05 | 0.00287012 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246851267 | AGTTCCCCATCTACT[G/T]CAGCAATGTCACATT | 25909 |
rs758987725 | snp | A/G | 1.65111e-05 | 0.0028732 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246913383 | TGCACTGGCTCCTCC[A/G]TGATTAATTATAGGT | 25909 |
rs759040712 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246930181 | TCGCTCTGTCACACA[C/G]GCTGAGTGCAGCGGC | 25909 |
rs759045210 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246901722 | ACTTGGGAGACCGAG[A/G]TGGGAGAATTGGTTG | 25909 |
rs759047411 | snp | A/G | 1.65979e-05 | 0.00288074 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246851348 | TCAAAATTGTACTGA[A/G]GCTTAAGTGTTCCAG | 25909 |
rs759056251 | snp | C/T | 1.66026e-05 | 0.00288115 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246898372 | AGGCATCAATCAATG[C/T]TCAATTTGAATAATC | 25909 |
rs759063345 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246899389 | AAAACTTAAATCCAT[A/C]AATCAACTATATTCT | 25909 |
rs759082090 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246876764 | AACATAAATGGCATA[C/T]GTAAAAGAATTACGT | 25909 |
rs759094026 | snp | C/T | | | upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246932461 | CTCCCACTTTTCTTT[C/T]TTTCTTTTTCTTTTT | 25909 |
rs759126391 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246844709 | AGCCTGGGTAACAGA[C/G]TGAAAAGCTAACAGG | 25909 |
rs759150696 | snp | G/T | 1.77881e-05 | 0.00298223 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246888546 | AAAATTAAGACTTAT[G/T]TAATATCACTGTTAA | 25909 |
rs759152189 | snp | C/T | 3.29641e-05 | 0.00405968 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246849663 | AAAATAAAGGCTCAT[C/T]GTTTGGTTCAGAAAG | 25909 |
rs759164168 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246851548 | TGCCTTTTAAAACAT[A/G]AATTATATTTAATAT | 25909 |
rs759206319 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246877961 | TGTTCAACTCATACC[C/G]CACCGACAGGATTAT | 25909 |
rs759207132 | snp | C/G | 1.64874e-05 | 0.00287113 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246888404 | CCTACATGCAGACTA[C/G]CAGGAGGATATTTTC | 25909 |
rs759208911 | in-del | -/TTCAGT | 1.71315e-05 | 0.00292668 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246916096 | TATAACCAGCAGGGG[-/TTCAGT]TTTGAAAGAGAAATG | 25909 |
rs759223506 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246839261 | TTATTAAAAACAGGT[A/G]CCACACATCTATATT | 25909 |
rs759235603 | snp | G/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246913941 | AAAAACAACAAAAAA[G/T]ATATTTTAAGTCCTC | 25909 |
rs759251600 | snp | A/C/G | 6.59429e-05 | 0.00574177 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246861057 | AGGTCTTCCGGTGAC[A/C/G]GTGCATCCTGATACT | 25909 |
rs759255909 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246901342 | AGACCCTGTCTCTAA[A/C]AAAACAAAAACAGGC | 25909 |
rs759257715 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246930552 | TCTTCTCTCCTAAGA[A/G]ACTCTATCAGTGAAA | 25909 |
rs759261775 | in-del | -/AAC | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246921228 | CAAAACTATGAAAAA[-/AAC]AAAGAAAAAATAAAC | 25909 |
rs759273373 | snp | A/G | 1.6531e-05 | 0.00287493 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246864070 | GCTGAATAAACTCCG[A/G]ACACTGAGAAGGCCG | 25909 |
rs759293843 | in-del | -/A | 3.54566e-05 | 0.00421035 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246853070 | GACTGATAAAGAAGT[-/A]AAAAAATTAATTTTT | 25909 |
rs759297998 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246886043 | AAACAAAAGTAAGTT[C/T]AAACAAAAAAAGTGC | 25909 |
rs759316810 | snp | C/T | 1.67167e-05 | 0.00289103 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246894740 | AATTAGTGGCAGAAT[C/T]TGGTTGTTCTTATTT | 25909 |
rs759358995 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246854215 | GAGGCAGGAGAATAG[C/T]GTGAGCCTGGGAGGC | 25909 |
rs759364965 | in-del | -/A | 7.45261e-05 | 0.00610389 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246861911 | CTTGTCAGAGCTAAT[-/A]CATTCTTATTAAAAA | 25909 |
rs759399151 | snp | A/C | | | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246916148 | AGTACCTACCCTTCC[A/C]GGAAGAACAACTGCT | 25909 |
rs759399677 | snp | G/T | 1.6896e-05 | 0.0029065 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246855862 | TACCTTAGTGTGTAA[G/T]AAGATCCCATCTGCT | 25909 |
rs759443498 | in-del | -/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246854625 | ATTTCTAACAGCTAA[-/C]ATTTACTAAACTTCA | 25909 |
rs759452268 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246902128 | CTTGGCTTAAAAAAC[C/T]GATGCAAAAAAAACT | 25909 |
rs759467078 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246839580 | CTGTCAACACTTTGC[A/G]TAGGCATTTTCACCA | 25909 |
rs759476253 | snp | A/C | 1.66601e-05 | 0.00288614 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246900405 | CAAATATACAGAAGG[A/C]TTTCCCTGTCCATAT | 25909 |
rs759481949 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246908015 | TCTCAAATATTATCT[A/C]AGATAGAATTTTTTT | 25909 |
rs759499255 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246917234 | TTCAACTTAGAGGGA[A/G]AACTAATTGGATTTC | 25909 |
rs759505841 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246931008 | CCCAGGTAGGAAAAA[A/G]GAAGGCAAAGCACCC | 25909 |
rs759510273 | snp | C/T | 1.69654e-05 | 0.00291246 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246913445 | TGATTTGCTTTTCTT[C/T]TGCAAAGTAAGAAAA | 25909 |
rs759524712 | snp | A/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246907064 | TAACACAAACCTAGA[A/T]GAGATAGCCTACTAT | 25909 |
rs759528795 | snp | A/G | 3.34868e-05 | 0.00409173 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246891731 | CGTTTCTCTTAGTCA[A/G]GAAGTAAAATTTAAT | 25909 |
rs759545917 | snp | C/T | 0.000765455 | 0.0195484 | missense, utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246840930 | ACTCCGTCAGCTGGG[C/T]TAGCCAAGGGGGAAA | 25909 |
rs759584965 | snp | A/T | 2.83821e-05 | 0.00376699 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246841020 | AAAAAAGATATGATC[A/T]AGTAAGAATAAACAC | 25909 |
rs759596600 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246873471 | GAAGGGAAAGAATCC[A/G]TCCCAATACTAAATG | 25909 |
rs759619263 | snp | C/G | | | upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246931998 | GAAAGGGCGGAGAGG[C/G]AGGGGAGAACCGGCG | 25909 |
rs759656970 | snp | C/T | 3.38828e-05 | 0.00411585 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246853258 | GACCTTCAGAGATAG[C/T]GAGCGAGGAGTTTCC | 25909 |
rs759676665 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246860133 | GTCATGGTGGGGGGC[A/G]ACTATAGTCCCAGCT | 25909 |
rs759685774 | snp | A/G | 3.42395e-05 | 0.00413746 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246862121 | CTCAGAAAATCCAGA[A/G]GTAGTAACTGACATG | 25909 |
rs759700229 | snp | G/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246845055 | GTGGCAGGGTAGGTG[G/T]TAAGTGCTCTACAGA | 25909 |
rs759702424 | snp | A/C | 1.6599e-05 | 0.00288084 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246890984 | TAAAAGCCCAGAATG[A/C]GAGAACCAAAGAACC | 25909 |
rs759719454 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246847176 | CACCTGTAATCCCAG[A/C]TACTGGGGAGGCTGA | 25909 |
rs759734529 | snp | A/G | 2.02702e-05 | 0.0031835 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246876181 | GCAAACGAGGATCAC[A/G]ATCATTCTATTAAAC | 25909 |
rs759735557 | snp | G/T | 1.6651e-05 | 0.00288535 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246900258 | TGACCTAAAAGAAAA[G/T]TTAAAACATTACTAA | 25909 |
rs759740089 | snp | G/T | 1.65688e-05 | 0.00287821 | missense, utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246840824 | CAGCATTTTTCTGCG[G/T]AAAATTTGCTTTGGA | 25909 |
rs759755437 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246928524 | AATAGGCATGTTAAA[C/T]AATAAAATCAATTTT | 25909 |
rs759788378 | snp | A/G | 1.76201e-05 | 0.00296812 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246907802 | TAAAAAACTAGAAAC[A/G]GCATTAAAAGCAAAT | 25909 |
rs759803378 | snp | G/T | 1.64817e-05 | 0.00287064 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246849873 | TTGTAAGTTTTTTCT[G/T]AGAGCTCATCACCAT | 25909 |
rs759816995 | in-del | -/TAAAT | | | utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246840716 | TTACAATAATTTATA[-/TAAAT]TATTTTCTTCCAAAC | 25909 |
rs759817313 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246880036 | TGTTAAAAGGGTTTA[C/G]TGGGAGAGGACATAT | 25909 |
rs759818901 | snp | A/G | 1.64993e-05 | 0.00287218 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246905570 | CTGAACAGCCCACAA[A/G]TAACAGCAATTCCGA | 25909 |
rs759872976 | snp | C/G | 1.6477e-05 | 0.00287024 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246867703 | GGTTCTTTGCTTGCC[C/G]AAACTTCTCCAATTT | 25909 |
rs759888265 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868506 | GTGATCCTCCCTCCT[C/T]GGCCTCTCAAAGTGC | 25909 |
rs759899385 | in-del | -/ACA | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246879074 | TCATTATTAAATCTC[-/ACA]ACAAGGTTGATTTCC | 25909 |
rs759902833 | snp | C/T | 1.6473e-05 | 0.00286988 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246885471 | ACGATAAAGACTTTA[C/T]AGTTTCAAAAGATGT | 25909 |
rs759971265 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246879487 | TAGCATTGTTTAAAA[C/T]GGCTAAAGGTTGAAA | 25909 |
rs759978109 | in-del | -/A | 1.66604e-05 | 0.00288616 | frameshift-variant, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246900086 | ATAAGTGCTTGGATT[-/A]AAAAAACTGCTCGGG | 25909 |
rs759984160 | snp | C/T | 1.72722e-05 | 0.00293867 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850637 | CCTCTGACATCAGAA[C/T]AGATGTTTTCAGAAG | 25909 |
rs759987050 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246917282 | CACAGGGAGGTGAGT[A/C]AAACAAGAATCAAGT | 25909 |
rs760018955 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246881418 | CACAGAAAGATTAAA[A/G]CCATGCAACGAACAA | 25909 |
rs760044674 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246903214 | TGTGAGGGTGAACAA[A/C]ATACAGCTATTAGCA | 25909 |
rs760095640 | in-del | -/CA | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246870723 | GAGGGTATAAAACCT[-/CA]AAAAAAAAAAAAAAA | 25909 |
rs760109268 | snp | A/C | 1.64993e-05 | 0.00287218 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850229 | CGCAGCTGCTTGTCA[A/C]TGGATTTATCATCTT | 25909 |
rs760156275 | snp | G/T | 1.68408e-05 | 0.00290175 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246902515 | ACATATTTCAAGTAC[G/T]TTAACTAACCTTCAT | 25909 |
rs760173356 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246895616 | GGCTGTAACGGCAGC[A/G]TGAGGGATCCTGGTG | 25909 |
rs760177980 | snp | C/T | 1.69321e-05 | 0.0029096 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246916214 | GAGAACACTCCCTTC[C/T]GTTTCTTCCAATCCT | 25909 |
rs760179640 | snp | C/T | 4.27451e-05 | 0.00462285 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246853051 | CAACTAAACCAAAAC[C/T]GAAAGACTGATAAAG | 25909 |
rs760182402 | snp | A/G | 1.66782e-05 | 0.0028877 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246855719 | CCTGAAGTCAAAATT[A/G]TTATACATACATTTA | 25909 |
rs760182454 | snp | A/C/G | 0.000198739 | 0.00996663 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850494 | TTTTTGATTCCCTAC[A/C/G]TGTAGTGATCTGTAA | 25909 |
rs760183202 | snp | C/T | 1.65012e-05 | 0.00287234 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246890002 | TGTCGACGACTGGTG[C/T]AGTAGTTCTGAATTA | 25909 |
rs760231960 | snp | A/G | | | upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246932899 | GCTCTTTTATCAGGA[A/G]AGTTTCTACTTTTCT | 25909 |
rs760232052 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246903046 | AGTTCTTAGACTTTT[A/G]GCTTATTGATACCTT | 25909 |
rs760237399 | snp | G/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246863746 | GTTAACTTTAAGCAG[G/T]AAGGGATAAATTTAA | 25909 |
rs760242005 | snp | A/C | 1.65348e-05 | 0.00287526 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246864074 | AATAAACTCCGAACA[A/C]TGAGAAGGCCGGGGG | 25909 |
rs760277708 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246854898 | GAAATGGGCACAGAA[A/C]ACAAAAATTCAGGAA | 25909 |
rs760281122 | snp | G/T | 8.54037e-05 | 0.00653411 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246913452 | CTTTTCTTCTGCAAA[G/T]TAAGAAAATATAATT | 25909 |
rs760344070 | snp | C/T | 1.64933e-05 | 0.00287165 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246877070 | GGACTGCAAAAATTT[C/T]ACTAAACATTCCTAA | 25909 |
rs760348708 | snp | A/T | 9.89952e-05 | 0.00703476 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246851030 | ATAGGTTCAGGCACA[A/T]ATGGTAAAGTGTCTA | 25909 |
rs760373255 | snp | A/G | 1.8053e-05 | 0.00300436 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246876110 | TTTTCGATGGACTCT[A/G]GGAAGGATTTTTCCA | 25909 |
rs760388922 | snp | G/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246887817 | CTAAGGTAGTATCAC[G/T]CTAACTTATAATGTA | 25909 |
rs760403673 | snp | A/C | 5.20784e-05 | 0.00510259 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246860866 | TTGAGGGACATTAAT[A/C]ACAATTTTGAGTATT | 25909 |
rs760415927 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869248 | TACTCCACTGACTAA[C/G]TGTTCCCCCGCGTCT | 25909 |
rs760419144 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246930794 | CCCAAAGGATTTACG[C/T]TTTGTTCTATGAAGA | 25909 |
rs760421537 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246856915 | GTTATATTTTGTGTC[A/G]GTTAATTTTACTGAA | 25909 |
rs760450121 | in-del | -/AATC | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246887690 | AAAAGATGGCAGCTT[-/AATC]AAACATCATCTAGCT | 25909 |
rs760456492 | snp | A/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246879115 | TACAAAGCGGCTATA[A/T]ATCAGTAAGAAAAAT | 25909 |
rs760457826 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869988 | CCATTCTAGATGCCA[C/T]TCAGCACATTCATAA | 25909 |
rs760500570 | snp | C/T | 1.66092e-05 | 0.00288172 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246887354 | CAAGTAGCAAATAAA[C/T]GGTCTTTTAAAAAGC | 25909 |
rs760531819 | snp | C/T | 1.64798e-05 | 0.00287047 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850896 | TAGTGGGACACATTA[C/T]GTTTTGGCTCACTAA | 25909 |
rs760549438 | in-del | -/AGG | 1.64963e-05 | 0.00287192 | cds-indel, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246864035 | GGATACTAGGTACAA[-/AGG]AGATTTCATGGAGCT | 25909 |
rs760553770 | snp | C/T | 5.78185e-05 | 0.00537642 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246894777 | ACAAAAGGGAAAAAA[C/T]AAAGATTATTAATTA | 25909 |
rs760583281 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246872489 | AGGTTCTGGCTTACT[C/T]CAACCAATCCAGAGT | 25909 |
rs760589163 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246888800 | CTGTAGTCCTAGCCA[C/T]TCAGGAGGATAAGGA | 25909 |
rs760598784 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246861475 | AAAAGTTAATGGTGG[C/G]TAATGTTTCCCTAAT | 25909 |
rs760655294 | snp | C/G | 1.77316e-05 | 0.0029775 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246885630 | AATCTTTGAATGTTG[C/G]CATGACAAAGGTTTT | 25909 |
rs760662305 | snp | A/G | 1.64803e-05 | 0.00287052 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246902605 | AATTTGGTATTACTC[A/G]TCTGTCCCCTCAAAG | 25909 |
rs760686203 | snp | C/T | 1.65809e-05 | 0.00287926 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246918323 | TTGAAGAGTCACTTC[C/T]GGAAATGGCAGGAGA | 25909 |
rs760686791 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246923451 | AATAAATACATAAAA[C/T]AATTATAATAACTGA | 25909 |
rs760694972 | snp | A/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246890122 | TCTCAACAATACATA[A/T]TAATATTTTACTGTA | 25909 |
rs760722141 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246881970 | CAGGCATGAGCCACC[A/G]TGCCTGGCCTTTATT | 25909 |
rs760727763 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246863159 | TTAAATTATTGAAAC[C/G]TAATCTTTTCAACTT | 25909 |
rs760736790 | snp | C/G | 1.6522e-05 | 0.00287414 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246857770 | ATTCTGAAAATGCCT[C/G]TGCTGCAACTAAGAG | 25909 |
rs760765068 | snp | A/G | 1.66032e-05 | 0.0028812 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246867202 | ACAATTGTAACTATC[A/G]TCTAACATTGTGTCT | 25909 |
rs760767548 | snp | G/T | 1.69934e-05 | 0.00291486 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850646 | TCAGAATAGATGTTT[G/T]CAGAAGCTTCAGAAA | 25909 |
rs760790737 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246897795 | AGACCAGCCTAGGCA[A/G]CATAGCGAGACCCTG | 25909 |
rs760820555 | snp | C/T | 3.2981e-05 | 0.00406071 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246855754 | CATTTGCTCTAATTG[C/T]AGGGGTGTAGGTTTC | 25909 |
rs760835234 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246865949 | ACTTTTTACTTGTTA[C/G]AGCTAATTTTTTTTT | 25909 |
rs760863464 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246847403 | AAATACCAACCATAC[A/G]TATGTATCTGGAACG | 25909 |
rs760867412 | in-del | -/CTGTAT | 1.82814e-05 | 0.0030233 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246843948 | AAAAAGTTGAAAAAA[-/CTGTAT]CTGTATCTTTATATA | 25909 |
rs760873512 | snp | A/C | 1.65474e-05 | 0.00287636 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246891840 | TATATTAAGATTGCT[A/C]AGAAGCAAATAGCAT | 25909 |
rs760890525 | snp | A/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246883183 | GTGTTTGATGGTTTA[A/T]ATATTAAAACTTTTT | 25909 |
rs760902458 | snp | A/G | 1.65872e-05 | 0.00287981 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246900345 | ATCATACCTTAACGA[A/G]TCTGGCATTTGTGCA | 25909 |
rs760930694 | snp | A/C | 3.32386e-05 | 0.00407654 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246891764 | AACACTCATTTGATA[A/C]AACAAAGAGCGTACC | 25909 |
rs760940178 | snp | C/T | 1.80651e-05 | 0.00300536 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246899547 | AATAATCCACTTACA[C/T]ATATTTAAAATGGCA | 25909 |
rs760949448 | snp | A/G | 1.64933e-05 | 0.00287165 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246913365 | ATGTAAATGCTGAGT[A/G]CTTGCACTGGCTCCT | 25909 |
rs760949626 | snp | C/T | 1.81965e-05 | 0.00301628 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246840984 | GGTGACCAAGCACTT[C/T]CTTTTTCTGTGTTTC | 25909 |
rs760977040 | snp | A/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246917507 | TAACTGGGATCAAAT[A/T]AATGATTTCATTCTC | 25909 |
rs760978804 | snp | C/G | 1.66515e-05 | 0.00288539 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246900280 | CATTACTAAGTCATT[C/G]GTCAGCTACACATAC | 25909 |
rs760993765 | snp | A/G | 8.26289e-05 | 0.0064271 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850086 | TTCTTGGTCTACCAC[A/G]TTTTCTAGGTATGGC | 25909 |
rs761003741 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246886317 | GCCTGGGTGACAGAG[C/T]GAGACTCCATCTCAA | 25909 |
rs761020927 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246919693 | TCGGTGACAGAGCAA[C/G]ACTCCATCTCAAAAA | 25909 |
rs761049721 | in-del | -/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246876633 | CCCTTACTGCTGGCC[-/T]CTACGTCTTCCTCTA | 25909 |
rs761052117 | in-del | -/A | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246848831 | TCCAGCCTGGGCGAC[-/A]AGAGTGAGACTCTAC | 25909 |
rs761065908 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246918801 | ATTCCCTAGATTCTT[C/T]AAACACTAGTTCAGT | 25909 |
rs761089835 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246905247 | ACTCACACCTGTAAT[C/G]CCAGCACTTTGGGAG | 25909 |
rs761094648 | snp | C/T | | | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246857693 | TCCATTAACTTACCC[C/T]TCATAGACTGATGGT | 25909 |
rs761095728 | snp | C/T | 0.000337901 | 0.0129937 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246888568 | CACTGTTAATTAATA[C/T]CAAAGCAACCAGCAT | 25909 |
rs761120104 | snp | C/G | 3.87732e-05 | 0.00440285 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246867847 | GAATTAAGTGCATCT[C/G]TAACAAACGGGAATT | 25909 |
rs761127937 | snp | A/G | 3.29783e-05 | 0.00406055 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246905584 | AGTAACAGCAATTCC[A/G]AGGATCATTCTCAGG | 25909 |
rs761128061 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246846389 | GAAGCTATGTCCTAG[A/C]GTGGTCATTGCTTTG | 25909 |
rs761142676 | in-del | -/A | 0.000503031 | 0.0158513 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246916402 | ATTTTTCCCTAGAAG[-/A]AAAAAAAAATTGCCT | 25909 |
rs761180882 | snp | A/G | 1.71231e-05 | 0.00292597 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246904066 | GAAGACACGCTAAAT[A/G]TATTAATACATTAAA | 25909 |
rs761194849 | snp | A/T | 0.000133849 | 0.00817963 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246887179 | AATTCTAGTAATTCA[A/T]GAAAGTTTATGCTGT | 25909 |
rs761247682 | snp | C/T | 1.64923e-05 | 0.00287156 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246867233 | CTAAGAATGATTTAA[C/T]AAACTCTTACCTAGA | 25909 |
rs761258194 | snp | A/G | 1.64806e-05 | 0.00287054 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246849669 | AAGGCTCATTGTTTG[A/G]TTCAGAAAGGTCCGG | 25909 |
rs761268096 | in-del | -/TC | 5.06598e-05 | 0.00503263 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246867215 | TCATCTAACATTGTG[-/TC]TCTAAGAATGATTTA | 25909 |
rs761271805 | in-del | -/AAAC | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246854658 | ACCAAGCGCTACACA[-/AAAC]AAACACTTTACATGC | 25909 |
rs761278131 | snp | A/G | 2.25966e-05 | 0.00336122 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246894798 | TTATTAATTACAAAC[A/G]GAGTTCTAAATTGTT | 25909 |
rs761289993 | in-del | -/AAG | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246877471 | CATAATAATCTTGCT[-/AAG]AATGTCAGTAAAATG | 25909 |
rs761318779 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246890161 | TTTACAGCAACCCCT[A/G]GTTAACCCACAGGGT | 25909 |
rs761353051 | snp | C/T | 0.000368596 | 0.0135706 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246867333 | ATACACTATAGGAGA[C/T]GGTTCTTCTATTTTA | 25909 |
rs761363639 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246856262 | TCAGAATAAGAGACC[A/C]ATGAAACCTGTATTA | 25909 |
rs761368770 | snp | C/G | | | upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246933046 | GCTCAAATGATCCTC[C/G]TACCTCAGCCCTCCA | 25909 |
rs761371486 | in-del | -/TCAT | 1.65388e-05 | 0.00287561 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246888276 | GTGGATCTTATACAG[-/TCAT]TCATTCATTCATGCT | 25909 |
rs761374481 | snp | A/G | 1.67371e-05 | 0.0028928 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246860921 | TTTCTGTAGGTCTGA[A/G]GGAGTTACTTCTGAT | 25909 |
rs761375620 | snp | A/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246856740 | CTACTTTTTCCATGC[A/T]GGCCTGGCAAAAATT | 25909 |
rs761375838 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246920478 | ATGAATGTCAGAATA[C/T]ATTATTAAACCAGCC | 25909 |
rs761380015 | snp | A/G | 1.64982e-05 | 0.00287208 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246895951 | CATTACAGAAAGGAA[A/G]GAAATGGAAAGAAAG | 25909 |
rs761448300 | snp | A/G | 0.000105416 | 0.00725925 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246843784 | TACAAATAAAATCAT[A/G]CATTTCTTACCAGTT | 25909 |
rs761453221 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869272 | CGCGTCTCTCCCTTT[C/T]CCCGAGGACCTCCCT | 25909 |
rs761499711 | snp | C/T | 1.66635e-05 | 0.00288643 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850337 | GTACTAACTTTTAGA[C/T]CATTTATAATTTCAA | 25909 |
rs761501192 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246874102 | ATTTAGTATTTTATA[A/G]TCTTTTTTAATATTA | 25909 |
rs761533846 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246894581 | TCAAAATGATTAAAA[A/G]TTATGTACTTAAGAC | 25909 |
rs761541791 | snp | A/T | 1.6507e-05 | 0.00287284 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246888369 | TTTGTAGACTCTAAA[A/T]GATAGCACATTACTG | 25909 |
rs761546332 | snp | C/G | 1.71176e-05 | 0.00292549 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246916245 | ATTAATAATCCAGTT[C/G]TCTTCTGCCAAGAGA | 25909 |
rs761568392 | snp | C/G | 1.76537e-05 | 0.00297095 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246913197 | TCAGAATATCCAGGT[C/G]CTCCATTTTTGGTTT | 25909 |
rs761580630 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246875262 | ACACTCCCTTACATA[A/C]AATGACACAACCTCT | 25909 |
rs761599612 | snp | C/T | 1.6884e-05 | 0.00290547 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246916394 | AGCAAGTCCATTTTT[C/T]CCTAGAAGAAAAAAA | 25909 |
rs761602641 | in-del | -/TCTT | | | downstream-variant-500B | AHCTF1 | GRCh38.p7 | 1:246838917 | TACTGATACTAAGTA[-/TCTT]TCTGAGTATATCATT | 25909 |
rs761605943 | snp | A/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246906478 | TCCCAGCTACTTGGG[A/T]GGCTGAGGCAGGAGA | 25909 |
rs761634146 | snp | G/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869061 | ATGTTGGCCAGGATG[G/T]TCTCGATCTCCTGAC | 25909 |
rs761645860 | in-del | -/TAT | | | cds-indel, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246839611 | ATTTCTCATTATCTG[-/TAT]TATTTGGTAGAAAAA | 25909 |
rs761680907 | in-del | -/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869329 | GCCAACTAATAACCC[-/T]TACAAAGACCTCAAG | 25909 |
rs761693307 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246922282 | GGAGAATTGCTTGAA[C/T]CCAGGAGGCAGAGGT | 25909 |
rs761729681 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246885893 | GCAGATAGAAAACAT[C/T]TGAAAAAATAAGGCT | 25909 |
rs761741960 | snp | C/T | 0.000409836 | 0.0143091 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246931356 | TCCGGTCCGAGATTA[C/T]GTAACGAAGCCCGGC | 25909 |
rs761749767 | snp | A/G | 1.64974e-05 | 0.00287201 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246888199 | TGTTTGGCTGCTTCA[A/G]TAACGCCGTCTAATA | 25909 |
rs761798794 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246928819 | TGACTAATAAAAAGA[C/T]GAATTGTCATTTAAA | 25909 |
rs761802779 | in-del | -/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246847920 | CCCTGCCAATAAAAT[-/G]TTTTTCATTTTAACT | 25909 |
rs761815444 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246911190 | GAAGGATGTTTTAAC[A/G]CCACCATATTGACTT | 25909 |
rs761816867 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246919177 | CTGATCTTATTCTGG[A/G]CACTCTAAGATCCAG | 25909 |
rs761871138 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246857902 | TTTTTAAAAAGTTGT[C/T]GGGTCTGCTTTTTTG | 25909 |
rs761875794 | in-del | -/CAACTTCTT | 0.000258065 | 0.0113563 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246931101 | GCTGAGCCCCGAGTC[-/CAACTTCTT]CCCCGCCAGGACTAC | 25909 |
rs761884141 | snp | C/G | 1.65154e-05 | 0.00287358 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246857734 | AAGCTTCAGTTCCTT[C/G]AACCGGGCTTAAGTG | 25909 |
rs761895894 | snp | C/T | 1.65765e-05 | 0.00287888 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246860983 | TTTGTTCAGTTACAT[C/T]AGTAGTTAGTGCAGT | 25909 |
rs761898045 | snp | C/T | 1.64991e-05 | 0.00287215 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246851048 | GGTAAAGTGTCTACT[C/T]TTTGGGACTTTTGGT | 25909 |
rs761900985 | snp | C/T | 1.64776e-05 | 0.00287028 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246849682 | TGGTTCAGAAAGGTC[C/T]GGCAACAAGATGGCC | 25909 |
rs761918399 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246917646 | GAGAATGGCGCTGTC[A/G]AGAGAGAAATGACTG | 25909 |
rs761966900 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246870195 | ATGCCTGTAATCCCA[A/G]TACTTTTGGAGGCCA | 25909 |
rs762009426 | snp | C/G | 1.6483e-05 | 0.00287076 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246905610 | TCAGGTTCTTGAAAA[C/G]TGACAGCATATACAG | 25909 |
rs762029865 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246870925 | TACAAGAGCTGGAGT[C/T]AGACCCTTTTAAAGA | 25909 |
rs762038185 | snp | A/T | 1.91419e-05 | 0.00309363 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246894613 | TAAACCAAGGTTAGT[A/T]TTTTAATATTAAATT | 25909 |
rs762045595 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246885361 | AATCTGAATTTGATG[C/T]AGAACCCACTAATAC | 25909 |
rs762057201 | in-del | -/T | 2.41999e-05 | 0.00347841 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246851458 | TAAATGAATTAAAGA[-/T]TAAGAGACTGGTTAA | 25909 |
rs762073550 | snp | C/G | 0.000146483 | 0.00855686 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246885655 | GGTTTTGCAGTAGCT[C/G]GATGAAACAAAAGAT | 25909 |
rs762104686 | snp | C/T | | | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850259 | TGCTTATTTCCTGTA[C/T]TTTCAGAAGCATCTA | 25909 |
rs762122830 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246905326 | AACATGGTGAAACCC[C/T]GTCTCTACTGAAAAT | 25909 |
rs762149312 | snp | A/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246918898 | AAAAGAAAAAGTGAT[A/T]GGTGTCTTTTAGAAA | 25909 |
rs762154451 | snp | G/T | 2.74179e-05 | 0.00370246 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246890911 | CAAAATTATAAAGAT[G/T]CAGAATGTTTTAATT | 25909 |
rs762171853 | snp | C/G/T | 3.33257e-05 | 0.0040819 | missense, splice-donor-variant, nc-transcript-variant, intron-variant | AHCTF1 | GRCh38.p7 | 1:246842697 | AGAAAGTCATACTTG[C/G/T]TTGCTTGTTTTGTTT | 25909 |
rs762203443 | snp | C/G | 1.65012e-05 | 0.00287234 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246890010 | ACTGGTGTAGTAGTT[C/G]TGAATTACAGGGTAG | 25909 |
rs762221394 | snp | C/T | 1.65408e-05 | 0.00287578 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246877185 | TGTAAATGGTAACTT[C/T]AGTAAATCTTCCATC | 25909 |
rs762224336 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246912692 | ATTTAAAGGAGAAAA[A/C]GTATTTCATTTTCTT | 25909 |
rs762237172 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246845098 | TTATTTCAAGAATAT[A/C]ATTTACAAACCCTTG | 25909 |
rs762248231 | snp | A/G | 1.82417e-05 | 0.00302002 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246861929 | TTCTTATTAAAAAAT[A/G]TCTTTTCTCCCAATT | 25909 |
rs762258506 | snp | G/T | 1.88802e-05 | 0.00307242 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246899560 | CATATATTTAAAATG[G/T]CATTAATAGAACAAA | 25909 |
rs762259468 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246894301 | CTTCAGGCCAGGCGC[A/G]GTGGCTCACGCCTGT | 25909 |
rs762263196 | snp | A/C | 3.29506e-05 | 0.00405884 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246849755 | GAAGCTGTGGCGAGC[A/C]ATCTTTCTTCCTGCT | 25909 |
rs762288950 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246893383 | CTTAACTTACATTGT[A/G]AAAAGCTATCTATAG | 25909 |
rs762292886 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246929509 | GATGGCACTCCAGGA[C/T]GAAGGACATGAGCAA | 25909 |
rs762294871 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246858960 | AGGCCAGGACCGGTG[A/G]CGCATGCCTGTAATC | 25909 |
rs762305656 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246927008 | TGAAATCCCGTCTCT[A/G]CTAAAAATACAGAAA | 25909 |
rs762311921 | snp | C/G | 1.65165e-05 | 0.00287367 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246899470 | TTCTGAAAGCCAGTA[C/G]AAGTTAAATGAACAA | 25909 |
rs762318810 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246906578 | CAGAGTGAGACCCCA[C/T]CCCCCAAAAAAATAG | 25909 |
rs762360142 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246845632 | AGGAAATACAAAAAT[A/G]TACTATCACATGCAA | 25909 |
rs762362885 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246865506 | CTTTTCTTCTAGATT[C/G]TCTTCTTTCTCTATC | 25909 |
rs762365458 | in-del | -/CAAATTTCTATAAATAATTAGAAGAGTTGGTTTTTTATC | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246852350 | TTCCCAAATCCTAAA[lengthTooLong]CAAATTTCTATAAAT | 25909 |
rs762372372 | in-del | -/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246927369 | TGCATACGCTTGTCA[-/T]TCCCGACTACTTGGG | 25909 |
rs762383722 | snp | C/G | 3.3089e-05 | 0.00406736 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246860988 | TCAGTTACATTAGTA[C/G]TTAGTGCAGTGGAAG | 25909 |
rs762451436 | in-del | -/A | 3.47102e-05 | 0.0041658 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246888529 | CCTCTGCAATCAGGG[-/A]AAAAATTAAGACTTA | 25909 |
rs762455348 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246876588 | GAATTAGTCTGACCC[C/T]TGAAGTCCAATGATC | 25909 |
rs762458531 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246872752 | TTTCCAATCACTATA[C/T]AGAAGAGCTTGCTTG | 25909 |
rs762483210 | snp | C/T | 1.64849e-05 | 0.00287092 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246861048 | GTCTCTTCAAGGTCT[C/T]CCGGTGACGGTGCAT | 25909 |
rs762509252 | snp | A/T | 3.29685e-05 | 0.00405995 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246851126 | TTTTCCCCACTGCAT[A/T]CAAGTTTTTCTTCAG | 25909 |
rs762515808 | snp | G/T | 1.65012e-05 | 0.00287234 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246888380 | TAAATGATAGCACAT[G/T]ACTGCAAACCTACAT | 25909 |
rs762536224 | in-del | -/ATTT | | | utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246839389 | TTTAGCTCTTTATTC[-/ATTT]AACAAGTTCATTTAA | 25909 |
rs762545424 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246896215 | TCCAATTCCACACCT[A/G]GGTATATACCAAAAA | 25909 |
rs762548417 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246903618 | GTGGATCACGAGGTC[A/G]GGAGTTCAAGACCAG | 25909 |
rs762577727 | snp | A/G | 2.49884e-05 | 0.00353463 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246867343 | GGAGATGGTTCTTCT[A/G]TTTTAGAACTATGAA | 25909 |
rs762607957 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246863502 | GGCAGTTTAAAGAGG[A/G]ATAAACCAAAGTAGC | 25909 |
rs762612214 | snp | A/G | 7.72171e-05 | 0.0062131 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246841002 | TTTTCTGTGTTTCTG[A/G]AAAAAAAAGATATGA | 25909 |
rs762647514 | snp | A/G | 1.65046e-05 | 0.00287264 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246895962 | GGAAAGAAATGGAAA[A/G]AAAGAGGGTGTGAGA | 25909 |
rs762653425 | snp | C/T | 3.30983e-05 | 0.00406793 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246891856 | AGAAGCAAATAGCAT[C/T]GCTGGATAGACTGTA | 25909 |
rs762663729 | in-del | -/TT | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868847 | TGTGTGTGTTTTTTG[-/TT]TTTTTTTTTTTTTTG | 25909 |
rs762669685 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246920352 | AAGGAAAAATCAAGT[A/G]GATTTGAAAAAATTT | 25909 |
rs762681626 | snp | C/G | 1.64876e-05 | 0.00287116 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246877050 | TGATTCTGAACGCTG[C/G]CACTGGACTGCAAAA | 25909 |
rs762716957 | in-del | -/A | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246845365 | AAGCATATGATTCTT[-/A]AAAAAAAAGAAAAAT | 25909 |
rs762719950 | snp | C/T | 1.71185e-05 | 0.00292557 | synonymous-codon, nc-transcript-variant, intron-variant | AHCTF1 | GRCh38.p7 | 1:246843897 | ATCCGAAACTAATTC[C/T]TTCAGCTGTGCAGGA | 25909 |
rs762722568 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246865435 | TTACTCTGTATCAAA[C/T]ACAGCTTTTAGATTT | 25909 |
rs762732890 | snp | A/T | 1.75409e-05 | 0.00296145 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246888534 | TGCAATCAGGGAAAA[A/T]TTAAGACTTATTTAA | 25909 |
rs762732976 | in-del | -/C | | | upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246933425 | GCGTGAGCCACCGCG[-/C]CCGGCCTTATTTTTT | 25909 |
rs762737502 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246928513 | CAGAGACAAGAAATA[A/G]GCATGTTAAACAATA | 25909 |
rs762826227 | in-del | -/T | 4.25677e-05 | 0.00461324 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246843980 | ATATGTGTGTATATA[-/T]TATAAACACAATAAA | 25909 |
rs762831399 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246883358 | TAGAGATGTAGGTAT[C/T]TGAACAAATTAGGTG | 25909 |
rs762848050 | in-del | -/GCTCTA | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246889661 | AACGTTTGTGGCACT[-/GCTCTA]GCTCTAAATGTTATA | 25909 |
rs762869372 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246930414 | GATCCAAAAATCACA[C/G]TACAGAGACAACGTA | 25909 |
rs762880584 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246920456 | ACAGCTACATGCAAC[A/G]ATATGAATGAATGTC | 25909 |
rs762889999 | snp | A/G | 1.68545e-05 | 0.00290292 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246913223 | GGTTTCAAGTAAAGA[A/G]CTGATTACCTGATGC | 25909 |
rs762892446 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246885782 | AATCCAGATAAGACT[C/T]GTTTAAATATAAGCT | 25909 |
rs762918430 | snp | A/G | 1.65015e-05 | 0.00287237 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246913374 | CTGAGTGCTTGCACT[A/G]GCTCCTCCATGATTA | 25909 |
rs762938117 | snp | C/T | 1.66593e-05 | 0.00288607 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246900147 | TAAACTTCTCTCATG[C/T]ACTAATATATCCAAG | 25909 |
rs762941404 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246919130 | TTTTAGCCATCTGAG[C/T]TGGTTAGCTATGAAA | 25909 |
rs762993619 | snp | A/T | 6.58946e-05 | 0.0057396 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246907661 | AACAGCTGTTCCTGT[A/T]GGACTTACTAACTGG | 25909 |
rs763016540 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246879832 | GACTCTGTTCCCCCA[A/G]CCCCGCCAAAAAAAA | 25909 |
rs763028950 | snp | C/T | 1.64762e-05 | 0.00287016 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246849782 | TGCTCATTTGTTTCT[C/T]TATGTGTCATTTCAT | 25909 |
rs763029053 | snp | C/T | 4.95119e-05 | 0.00497529 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850985 | GTGTCTTTAATTACA[C/T]CTAGTAAATTTTCTG | 25909 |
rs763029669 | snp | C/T | 1.65381e-05 | 0.00287555 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246849978 | CTGGGGTATTTCTTG[C/T]AGATCTCCTTCTAAT | 25909 |
rs763088155 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246871017 | TGCGCTCCCACTGTA[C/G]CCTTGCTTAAGTTGC | 25909 |
rs763118695 | in-del | -/A | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246841482 | TAGCCATAGTGTCTT[-/A]AATAAAATGCATTCA | 25909 |
rs763133784 | in-del | -/AAT | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246916657 | GACTTCATCTCAAAT[-/AAT]AATAATAATAATAGT | 25909 |
rs763143098 | snp | C/T | 1.67049e-05 | 0.00289002 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246900027 | ACATACTTTTGTGCA[C/T]TACTTTTCTTAAGAG | 25909 |
rs763217676 | in-del | -/AA | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246928303 | GCGAGACTCCGTCTC[-/AA]AAAAAAAAAAAAAAA | 25909 |
rs763222353 | snp | C/T | 1.64779e-05 | 0.00287031 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850875 | TAAATGCAGATTTGA[C/T]CAATTTAGTGGGACA | 25909 |
rs763228246 | snp | C/T | 3.35435e-05 | 0.0040952 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850368 | CACTTTCCTGATTTT[C/T]TACAGATCTTTTAAT | 25909 |
rs763253810 | snp | A/C | 0.000525072 | 0.0161945 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246931377 | GAAGCCCGGCGCCCG[A/C]GAGCCTGCCGTACCC | 25909 |
rs763282193 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246846701 | TGAAAAAAAAAGAAA[C/T]ATTACGTTTAAGATT | 25909 |
rs763339244 | snp | C/T | 5.57585e-05 | 0.00527978 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850479 | GAGATGATTTTAATC[C/T]TTTTGATTCCCTACC | 25909 |
rs763340545 | snp | G/T | 3.39098e-05 | 0.00411749 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246877283 | GTTGCCGCAAAAAAT[G/T]CCAGGCTTCAACCAT | 25909 |
rs763397698 | snp | G/T | 1.99193e-05 | 0.00315583 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246890943 | ATACTTATAGATTAA[G/T]TAAATATTTTACCTA | 25909 |
rs763400989 | snp | C/T | 5.13185e-05 | 0.00506523 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246916289 | TAAAACTACAGGAGG[C/T]TGTTCATTGACTCCA | 25909 |
rs763406673 | snp | A/C | 1.88457e-05 | 0.00306961 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246891104 | TACTTACAAAAAAAT[A/C]AAGATGCTCCACAGT | 25909 |
rs763417017 | snp | C/G | 1.66183e-05 | 0.00288251 | missense, utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246840811 | TCCCAAGAAATTACA[C/G]CATTTTTCTGCGTAA | 25909 |
rs763417553 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246915603 | TTAAAGTATTCACTA[C/T]ATTTATGCTAGTCTT | 25909 |
rs763452006 | snp | C/T | 3.29582e-05 | 0.00405931 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246902607 | TTTGGTATTACTCGT[C/T]TGTCCCCTCAAAGGG | 25909 |
rs763456092 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246902234 | CTCAAAAAATACACG[A/G]GTAAACTTCATTCAA | 25909 |
rs763472697 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246914595 | GCGAATCTAAGTTTA[C/T]ATTCCTCATAAAAAT | 25909 |
rs763488686 | snp | A/G | 3.8678e-05 | 0.00439744 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246843765 | AAGTATGTTTTAACA[A/G]ACATACAAATAAAAT | 25909 |
rs763501523 | snp | A/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246881404 | AAAATTATTCAGGAC[A/T]CAGAAAGATTAAAAC | 25909 |
rs763511375 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246930891 | ACTTTGCACACAGAT[A/G]GTATGAACCTCGTAA | 25909 |
rs763517206 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246914418 | TTGTTTCAGGCTGTA[A/C]CTTACTACAGACAAA | 25909 |
rs763534209 | snp | C/T | 1.7333e-05 | 0.00294384 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246894646 | GTCCTACATCTAGAC[C/T]TCTAATACTTACATA | 25909 |
rs763542495 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246853408 | TGAATAGTGTATTAA[C/T]AAACTATCACAATGC | 25909 |
rs763546245 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246854471 | GTTCAGCAATAAGCA[A/G]TTAGTTAAGCATGTA | 25909 |
rs763577728 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246879906 | ATGAACTACTATGCA[A/G]TAGTTAAAAAGCAAA | 25909 |
rs763579498 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246872784 | CATGATTGAACCTTC[A/G]AAGTGTGCTGCTGTC | 25909 |
rs763598043 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246903634 | GGAGTTCAAGACCAG[A/C]CTGGCCAAGATGGTG | 25909 |
rs763598864 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246852175 | CAGTGAGATGACAGA[C/T]TGGAAATAACCTAGA | 25909 |
rs763611636 | snp | A/G | 1.89414e-05 | 0.00307739 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246853110 | ATTTCTTGAGTATCA[A/G]GAGGGCTGTCAGAAA | 25909 |
rs763622332 | snp | A/G | 1.67899e-05 | 0.00289736 | stop-gained, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246862072 | CTAAAGGTGTTGATC[A/G]AAGAGTAGACCTCAG | 25909 |
rs763625624 | snp | A/G | 0.000182705 | 0.00955609 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850322 | CTAGGACTTGTTACC[A/G]TACTAACTTTTAGAT | 25909 |
rs763635578 | snp | A/G | | | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246887355 | AAGTAGCAAATAAAT[A/G]GTCTTTTAAAAAGCG | 25909 |
rs763670830 | in-del | -/CA | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246887844 | TGTATTCATTTCCAG[-/CA]CAGAGGTTAATGCCA | 25909 |
rs763675525 | snp | A/C | 1.64953e-05 | 0.00287182 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246877085 | CACTAAACATTCCTA[A/C]AAAGAACAAAATAGA | 25909 |
rs763691860 | in-del | -/AAC | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246847304 | CAAAAAAAAAAAACA[-/AAC]AAAAAAAAAACTGAA | 25909 |
rs763738233 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246854907 | ACAGAAAACAAAAAT[C/T]CAGGAAAGACACTTT | 25909 |
rs763745535 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246870712 | TCTAGCTAAAAGAGG[A/G]TATAAAACCTCAAAA | 25909 |
rs763768365 | snp | C/T | 6.61573e-05 | 0.00575102 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246877182 | GTCTGTAAATGGTAA[C/T]TTCAGTAAATCTTCC | 25909 |
rs763794044 | snp | A/C | 1.72065e-05 | 0.00293308 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246913455 | TTCTTCTGCAAAGTA[A/C]GAAAATATAATTAAC | 25909 |
rs763794750 | snp | A/C | 1.67956e-05 | 0.00289784 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246902518 | TATTTCAAGTACTTT[A/C]ACTAACCTTCATTCA | 25909 |
rs763810529 | snp | C/G | 6.59642e-05 | 0.00574262 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246864028 | GTGAACGGGATACTA[C/G]GTACAAAGGAGATTT | 25909 |
rs763818920 | snp | A/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246872625 | AAAGGTCAAGCATAG[A/T]AATAAAACATAAGGA | 25909 |
rs763826400 | snp | C/T | 4.95029e-05 | 0.00497484 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246890005 | CGACGACTGGTGTAG[C/T]AGTTCTGAATTACAG | 25909 |
rs763845650 | snp | A/G | 1.70046e-05 | 0.00291582 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246916225 | CTTCTGTTTCTTCCA[A/G]TCCTATTAATAATCC | 25909 |
rs763853907 | in-del | -/TTAA | 3.63861e-05 | 0.00426518 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246888558 | TATTTAATATCACTG[-/TTAA]TTAATATCAAAGCAA | 25909 |
rs763889081 | snp | A/G | 3.29598e-05 | 0.00405941 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850897 | AGTGGGACACATTAT[A/G]TTTTGGCTCACTAAA | 25909 |
rs763908611 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246887865 | GGTTAATGCCATTGA[C/T]AGTGACCACTTGGTG | 25909 |
rs763914192 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246860283 | AAAAATTAAATAAAT[A/G]AAAATTGCAATAATT | 25909 |
rs763929025 | snp | C/T | 3.29473e-05 | 0.00405864 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246907689 | TGGAAACACAGATGG[C/T]GCCCTTGTCTCATTA | 25909 |
rs763936920 | snp | C/T | 1.64917e-05 | 0.00287151 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246849880 | TTTTTTCTTAGAGCT[C/T]ATCACCATCGAAAGT | 25909 |
rs763940327 | snp | C/T | 1.6501e-05 | 0.00287232 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246888191 | CAATAGAGTGTTTGG[C/T]TGCTTCAGTAACGCC | 25909 |
rs763942410 | snp | A/G | 1.81217e-05 | 0.00301007 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246876115 | GATGGACTCTAGGAA[A/G]GATTTTTCCATACTG | 25909 |
rs763960554 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246916758 | GTAGAGATAAGGCAG[C/T]TAAACCTGAATACTG | 25909 |
rs763966450 | snp | G/T | 3.87087e-05 | 0.00439919 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246894781 | AAGGGAAAAAATAAA[G/T]ATTATTAATTACAAA | 25909 |
rs763983669 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246921871 | GTAGAATAGAGATCA[A/G]ATAGAAGGTCTGAGA | 25909 |
rs763992055 | snp | A/G | 1.64985e-05 | 0.0028721 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246851039 | GGCACATATGGTAAA[A/G]TGTCTACTTTTTGGG | 25909 |
rs763995889 | snp | C/G/T | 5.01688e-05 | 0.00500822 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246887369 | TGGTCTTTTAAAAAG[C/G/T]GGATTAAGGACAATA | 25909 |
rs764039376 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246891455 | GCTTGTTTTTGTTTT[C/G]AAATTGCAAAACAGA | 25909 |
rs764042394 | in-del | -/T | 1.69861e-05 | 0.00291424 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246864139 | CAGAATGCGCATTTA[-/T]TGAGTTATACTGAAA | 25909 |
rs764048702 | snp | G/T | 1.64917e-05 | 0.00287151 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246887262 | AATAAGTTTAACTTG[G/T]CCCCAAGAAATGGCA | 25909 |
rs764058879 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246910292 | CGTTCAAGGAGACTT[C/G]AGACTTAACTGTCAA | 25909 |
rs764060029 | snp | C/G | | | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246887252 | AAAACCCCTGAATAA[C/G]TTTAACTTGGCCCCA | 25909 |
rs764080781 | snp | C/G | 1.66109e-05 | 0.00288187 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246918332 | CACTTCTGGAAATGG[C/G]AGGAGACCACTAGTC | 25909 |
rs764107980 | snp | A/T | 1.7268e-05 | 0.00293832 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246904073 | CGCTAAATATATTAA[A/T]ACATTAAACATCTCT | 25909 |
rs764118284 | snp | G/T | 1.67764e-05 | 0.00289619 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850652 | TAGATGTTTTCAGAA[G/T]CTTCAGAAATTTCTT | 25909 |
rs764126844 | snp | G/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246881771 | TGAACCTGGGAGGCA[G/T]AGGTTGCAGTGAGCC | 25909 |
rs764135701 | snp | C/T | 8.26084e-05 | 0.00642631 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246857771 | TTCTGAAAATGCCTC[C/T]GCTGCAACTAAGAGA | 25909 |
rs764149032 | snp | A/T | 1.64765e-05 | 0.00287019 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246867615 | CTGTTGATGTCCAGT[A/T]AAGATTAACAAGCAG | 25909 |
rs764169631 | snp | A/G | 8.24463e-05 | 0.00642 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246855755 | ATTTGCTCTAATTGC[A/G]GGGGTGTAGGTTTCA | 25909 |
rs764193424 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246859565 | CATTTTTTGATCACT[A/G]AAATAATATTTTTTT | 25909 |
rs764195885 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246870126 | CTGCAGATATGGGGG[A/G]AAGAGCAAGAGAACT | 25909 |
rs764216964 | snp | A/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246879887 | TGGTACAGCCATCCA[A/T]ATAATGAACTACTAT | 25909 |
rs764235487 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246910297 | AAGGAGACTTGAGAC[C/T]TAACTGTCAAATGCA | 25909 |
rs764256014 | snp | A/G | 1.66056e-05 | 0.00288141 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246849629 | CCTTTTGCTTTCCTT[A/G]GAACTTCTGACGCTG | 25909 |
rs764287241 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246931100 | GGCTGAGCCCCGAGT[A/C]CAACTTCTTCCCCGC | 25909 |
rs764296899 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246927972 | GCCACTGCACTCCAG[C/T]CTGGCGACAGAGCAA | 25909 |
rs764298253 | snp | A/C | 3.81643e-05 | 0.00436815 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246888569 | ACTGTTAATTAATAT[A/C]AAAGCAACCAGCATC | 25909 |
rs764308177 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246891276 | AACCTCCAAAATGCT[A/G]AAATAAGTAAGTCAC | 25909 |
rs764331907 | snp | A/G | 1.7731e-05 | 0.00297744 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246885632 | TCTTTGAATGTTGCC[A/G]TGACAAAGGTTTTGC | 25909 |
rs764378835 | in-del | -/TG | 1.85393e-05 | 0.00304455 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246843949 | AAAAGTTGAAAAAAC[-/TG]TATCTGTATCTTTAT | 25909 |
rs764381152 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246847748 | GAAAAAAGTTAAAAT[C/T]AGTAGGTACAGAAAT | 25909 |
rs764383704 | snp | C/T | 3.47017e-05 | 0.00416529 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246853275 | AGCGAGGAGTTTCCA[C/T]CATCACCAAGGACAT | 25909 |
rs764386876 | snp | C/T | 5.01895e-05 | 0.00500921 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246885527 | TGAGGTGAAGGATAA[C/T]ATCGTTACCACTGGA | 25909 |
rs764396291 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246904331 | CTTCCTCAATGGTTA[C/T]ACTCTACTTAAACAC | 25909 |
rs764410761 | snp | C/T | 1.65353e-05 | 0.00287531 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246913403 | TAATTATAGGTTCAA[C/T]AGCTGTTACCTAGAA | 25909 |
rs764430639 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869588 | CCAAAATTCCTAAGG[C/T]CCTTAAAAATGATGG | 25909 |
rs764433187 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246839876 | TCCTTTTCTACATCT[A/T]CTCACTCTCTCCCAA | 25909 |
rs764437889 | snp | C/T | 4.94694e-05 | 0.00497316 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850125 | CAAATTCTGCTTGAA[C/T]AGTCAACTGAGATGA | 25909 |
rs764438231 | snp | A/G | 1.65847e-05 | 0.0028796 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246891771 | ATTTGATAAAACAAA[A/G]AGCGTACCTCTCTCA | 25909 |
rs764450621 | in-del | -/ACACACACACACACAC | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246898630 | TGACAAAACACACAC[-/ACACACACACACACAC]ACACACACACACACA | 25909 |
rs764459458 | snp | G/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246861743 | TTACTTGGTGCTTCC[G/T]AGTCCTATTTATCTG | 25909 |
rs764470769 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246917573 | TTACACCACTCCAAT[A/G]AAGTCATCGTACAAT | 25909 |
rs764486093 | in-del | -/A | 1.81866e-05 | 0.00301546 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246918391 | ACTGTAAATATTTTT[-/A]AAAAGAAAACATTAT | 25909 |
rs764492933 | snp | C/G | 1.64768e-05 | 0.00287021 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246851285 | GCAATGTCACATTCA[C/G]CAGTGTCTTTGTTAT | 25909 |
rs764568360 | snp | C/T | 8.26153e-05 | 0.00642657 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246899448 | TCACTAGTTGTTACC[C/T]ACCTCCTTCTGAAAG | 25909 |
rs764582411 | snp | G/T | 1.65004e-05 | 0.00287227 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246895956 | CAGAAAGGAAAGAAA[G/T]GGAAAGAAAGAGGGT | 25909 |
rs764588456 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246888906 | CCCTGTCTCTAAAAA[C/G]AGAGAGAGAGGAGAG | 25909 |
rs764604537 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246856305 | ATAAATCCTGGAATA[C/T]GATGACAGTGTTCCT | 25909 |
rs764623442 | snp | A/C | 1.64765e-05 | 0.00287019 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246898279 | CAAGACATCGATTAT[A/C]ACCATCAGGAATGAG | 25909 |
rs764623548 | snp | A/G | 3.2975e-05 | 0.00406035 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246905587 | AACAGCAATTCCGAG[A/G]ATCATTCTCAGGTTC | 25909 |
rs764626395 | snp | A/G | 1.64781e-05 | 0.00287033 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246849677 | TTGTTTGGTTCAGAA[A/G]GGTCCGGCAACAAGA | 25909 |
rs764648316 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246875912 | GGAACCAAACCAGCA[A/G]TATCTCCAAGGCATG | 25909 |
rs764655820 | in-del | -/TC | | | downstream-variant-500B | AHCTF1 | GRCh38.p7 | 1:246838879 | GATACTAAGTATCTT[-/TC]TGAGTACATTGTTTA | 25909 |
rs764680152 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246840603 | ACATATATAAATGTA[G/T]GAAGTCTTAATATAA | 25909 |
rs764694962 | in-del | -/A | 0.000305105 | 0.0123475 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246900319 | AGAGAAAGGAGAGAG[-/A]AAAAAAAAGAATCAT | 25909 |
rs764718593 | in-del | -/A | 1.64988e-05 | 0.00287213 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246888385 | ATAGCACATTACTGC[-/A]AAACCTACATGCAGA | 25909 |
rs764733957 | snp | A/T | 5.0396e-05 | 0.00501951 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246887383 | GCGGATTAAGGACAA[A/T]AAAATACAACAACAA | 25909 |
rs764789289 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869456 | TGAAGGAAATTAAAA[C/G]TGCTACGTCAGTGAA | 25909 |
rs764801267 | snp | A/G | 2.08435e-05 | 0.00322821 | missense, nc-transcript-variant, intron-variant | AHCTF1 | GRCh38.p7 | 1:246843808 | ACCAGTTCATCTTCA[A/G]GCTTGTTCTTATTGG | 25909 |
rs764806558 | snp | C/G | 1.65507e-05 | 0.00287664 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246864085 | AACACTGAGAAGGCC[C/G]GGGGACAGGCTGAAC | 25909 |
rs764834680 | snp | C/T | 1.64982e-05 | 0.00287208 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246851050 | TAAAGTGTCTACTTT[C/T]TGGGACTTTTGGTCA | 25909 |
rs764861038 | snp | G/T | | | upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246933066 | TCAGCCCTCCAAGTA[G/T]CTGGGACTATGGGCA | 25909 |
rs764884470 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246911368 | ATTCATTTTTAGTTA[C/T]TGCTTTTGCTCATCA | 25909 |
rs764885624 | snp | G/T | 1.67267e-05 | 0.0028919 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246860923 | TCTGTAGGTCTGAAG[G/T]AGTTACTTCTGATGC | 25909 |
rs764913640 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246875275 | TACAATGACACAACC[C/T]CTCCCCTCTCCATAA | 25909 |
rs764919563 | in-del | -/A | 3.0254e-05 | 0.00388923 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246867362 | TAGAACTATGAAAAT[-/A]AAAATTTAACTTCTG | 25909 |
rs764927947 | snp | C/G | 2.25005e-05 | 0.00335406 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246894799 | TATTAATTACAAACA[C/G]AGTTCTAAATTGTTG | 25909 |
rs764937763 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246882434 | TGTAAATTAAAACTT[C/T]TAAATCATAGATAGG | 25909 |
rs764965859 | snp | A/G | 1.65312e-05 | 0.00287495 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246840850 | TTGGATAGGAAGACA[A/G]TTTCTTTCTGTTCCT | 25909 |
rs764966694 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246925554 | AAGACCAGGAGTTGT[A/G]GGTTGCAGTAAGCTA | 25909 |
rs764969740 | snp | G/T | 1.68159e-05 | 0.0028996 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246902713 | ATATTAATCTGATTC[G/T]AGGCAAAAAGTCACT | 25909 |
rs765024399 | snp | A/G | 3.29478e-05 | 0.00405867 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246898246 | CATCAACAAATCTTG[A/G]GGAAAGAAGGCCAGC | 25909 |
rs765040922 | snp | A/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246923897 | CTCCAGGTCTGGAAG[A/T]CCCTAACTACATACT | 25909 |
rs765073811 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246847464 | TCGATGGCTGGATTA[C/T]ATACTTCTATTTTAG | 25909 |
rs765076053 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246863342 | GTTTCAATCCAGAAC[A/G]TTAGTCAAGGGGCTA | 25909 |
rs765078510 | snp | C/G | 6.87628e-05 | 0.00586316 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246862129 | ATCCAGAAGTAGTAA[C/G]TGACATGGCCAAACT | 25909 |
rs765108189 | snp | C/G | 1.65438e-05 | 0.00287605 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246849967 | TTCACTTTTAGCTGG[C/G]GTATTTCTTGTAGAT | 25909 |
rs765112366 | snp | G/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246910556 | ATGTTGAAAATTAAC[G/T]TGAATTTGGGTGATG | 25909 |
rs765123555 | snp | C/T | 7.04655e-05 | 0.0059353 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246876208 | AAACATCAAAATTGG[C/T]AAAAAATTTAACCTT | 25909 |
rs765134003 | snp | G/T | 1.64743e-05 | 0.00287 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246907699 | GATGGCGCCCTTGTC[G/T]CATTACACTTTCTCT | 25909 |
rs765135473 | snp | A/T | 1.64836e-05 | 0.0028708 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246851111 | TGTCCATGATTATCA[A/T]TTTCCCCACTGCATA | 25909 |
rs765175799 | snp | C/T | | | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246916387 | CCAAGCAAGCAAGTC[C/T]ATTTTTCCCTAGAAG | 25909 |
rs765214331 | snp | C/T | 1.76263e-05 | 0.00296864 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246913198 | CAGAATATCCAGGTG[C/T]TCCATTTTTGGTTTC | 25909 |
rs765236917 | in-del | -/CAT | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246887697 | GGCAGCTTAATCAAA[-/CAT]CATCTAGCTTATAAA | 25909 |
rs765241767 | snp | A/G | 0.0002147 | 0.0103588 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246899472 | CTGAAAGCCAGTACA[A/G]GTTAAATGAACAACT | 25909 |
rs765269937 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246848747 | CCCAGCTACTAGGGA[A/G]GCTGAGGTAGGAGAA | 25909 |
rs765302345 | snp | C/T | 4.48029e-05 | 0.0047328 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246905696 | TATTTTTAAGTTATT[C/T]TTTAGAAAGGAAAAA | 25909 |
rs765328409 | snp | C/G | 0.000666356 | 0.018241 | intron-variant, missense, utr-variant-5-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246931146 | TGGCCAGGCCCAAGC[C/G]CATGTGGAACACACG | 25909 |
rs765334727 | snp | C/T | 1.64749e-05 | 0.00287005 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246849759 | CTGTGGCGAGCAATC[C/T]TTCTTCCTGCTCATT | 25909 |
rs765350660 | snp | C/T | 6.65557e-05 | 0.00576831 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246887192 | CATGAAAGTTTATGC[C/T]GTAAGTGAATAGACT | 25909 |
rs765371434 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246858982 | CCTGTAATCCAGCTA[C/T]TTGGGAGGCTGAGGC | 25909 |
rs765373073 | snp | C/T | 3.29674e-05 | 0.00405988 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246905614 | GTTCTTGAAAAGTGA[C/T]AGCATATACAGGAAC | 25909 |
rs765387503 | in-del | -/AAAG | 3.97354e-05 | 0.00445714 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246853063 | AACTGAAAGACTGAT[-/AAAG]AAGTAAAAAATTAAT | 25909 |
rs765388200 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246929819 | AGCACTCTGGGAGGC[C/T]AAGGCGGGCGGATCA | 25909 |
rs765401686 | snp | A/T | 3.82212e-05 | 0.0043714 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246894614 | AAACCAAGGTTAGTA[A/T]TTTAATATTAAATTC | 25909 |
rs765439191 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246917764 | AAGATCCATAAGAGA[A/G]AGCCTTCTTTAGTAT | 25909 |
rs765442060 | snp | G/T | | | upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246932014 | AGGGGAGAACCGGCG[G/T]GAGATCGCGGCTGCA | 25909 |
rs765502906 | snp | C/T | 1.67511e-05 | 0.00289401 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850359 | TAATTTCAACACTTT[C/T]CTGATTTTCTACAGA | 25909 |
rs765507816 | in-del | -/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869012 | CCATGCCTGGCTAAC[-/T]TTTTTCTATTTTTAG | 25909 |
rs765521877 | snp | G/T | 1.66252e-05 | 0.00288311 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246867780 | TGTTACAACTTGCTT[G/T]GGAACTGCTGATAAT | 25909 |
rs765523282 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246859373 | TCTCCCATTTACTAG[C/T]GTTCCCCTGGCCCTC | 25909 |
rs765583218 | snp | A/G | 1.85262e-05 | 0.00304348 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246885659 | TTGCAGTAGCTGGAT[A/G]AAACAAAAGATCCAA | 25909 |
rs765591066 | snp | C/T | 1.65452e-05 | 0.00287616 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246877196 | ACTTCAGTAAATCTT[C/T]CATCAAGCCCATTTC | 25909 |
rs765628964 | snp | C/T | 3.30098e-05 | 0.00406249 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850246 | GGATTTATCATCTTG[C/T]TTATTTCCTGTATTT | 25909 |
rs765694726 | snp | A/G | 1.70813e-05 | 0.00292239 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246916112 | TCAGTTTTGAAAGAG[A/G]AATGTCCAGGTATCT | 25909 |
rs765712841 | snp | A/T | 1.65026e-05 | 0.00287246 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246890016 | GTAGTAGTTCTGAAT[A/T]ACAGGGTAGTTGTAG | 25909 |
rs765721900 | snp | A/G | 1.83913e-05 | 0.00303238 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246851417 | TCTCCTGAATCTTGA[A/G]CTTCAAGCTTTTCTT | 25909 |
rs765746489 | snp | A/C | 3.29533e-05 | 0.00405901 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246867610 | GAACGCTGTTGATGT[A/C]CAGTAAAGATTAACA | 25909 |
rs765747691 | snp | A/G | 1.71525e-05 | 0.00292847 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246916272 | GAGAATTCTTTCACA[A/G]CTAAAACTACAGGAG | 25909 |
rs765761592 | snp | C/T | 1.65935e-05 | 0.00288036 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246889938 | TTGACTTCTTACAGA[C/T]GTAATTTCTAAAATT | 25909 |
rs765788804 | snp | A/G | 1.7376e-05 | 0.00294749 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246861942 | ATGTCTTTTCTCCCA[A/G]TTATTATCAAACTTA | 25909 |
rs765805897 | snp | C/T | 1.64765e-05 | 0.00287019 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246851254 | TTGAGCCACAAAAAG[C/T]TCCCCATCTACTTCA | 25909 |
rs765834434 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246878164 | ACACTTTGGGAGGCC[A/G]GGGTGGGCAGATCAC | 25909 |
rs765927841 | snp | A/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246896223 | CACACCTAGGTATAT[A/T]CCAAAAAGAAACAAA | 25909 |
rs765951256 | snp | C/G | 1.64844e-05 | 0.00287087 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246851127 | TTTCCCCACTGCATA[C/G]AAGTTTTTCTTCAGT | 25909 |
rs765970221 | snp | G/T | 1.65378e-05 | 0.00287552 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246849982 | GGTATTTCTTGTAGA[G/T]CTCCTTCTAATGCTG | 25909 |
rs765976475 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246910592 | ATGGGAACTCTTGTA[C/T]TCTTCTAACTATCTG | 25909 |
rs765984023 | snp | A/G | 5.38677e-05 | 0.0051895 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246876228 | AATTTAACCTTCAAA[A/G]TGTTAGGTGCTGTAA | 25909 |
rs766003906 | snp | G/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246863572 | AATAAACCAAAGAAC[G/T]AAATAGCATTTGATA | 25909 |
rs766006266 | snp | C/T | 1.65356e-05 | 0.00287533 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246860990 | AGTTACATTAGTAGT[C/T]AGTGCAGTGGAAGAG | 25909 |
rs766016028 | snp | G/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246923944 | GAAGAGGGCCATGTT[G/T]CAGGGAACTGTGCTG | 25909 |
rs766023815 | snp | A/G | 3.01491e-05 | 0.00388248 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246867362 | TAGAACTATGAAAAT[A/G]AAAATTTAACTTCTG | 25909 |
rs766026947 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246901298 | GTGAGACGAGATCGT[A/G]CAAGTGCACTCCAGC | 25909 |
rs766035109 | snp | A/G | | | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850268 | CCTGTATTTTCAGAA[A/G]CATCTAAATTAGTAC | 25909 |
rs766050848 | in-del | -/TACTACTGA | | | downstream-variant-500B | AHCTF1 | GRCh38.p7 | 1:246838898 | GTACATTGTTTACCT[-/TACTACTGA]TACTACTGATACTAA | 25909 |
rs766057157 | snp | A/G | 1.64993e-05 | 0.00287218 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246888381 | AAATGATAGCACATT[A/G]CTGCAAACCTACATG | 25909 |
rs766103945 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246858942 | ACATCAAAAGAGCAA[C/T]GTAGGCCAGGACCGG | 25909 |
rs766112046 | snp | C/T | 1.64969e-05 | 0.00287196 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246888221 | CGTCTAATAGGTACA[C/T]ATCAAGTACTGCCTA | 25909 |
rs766112113 | in-del | -/A | 3.29609e-05 | 0.00405948 | splice-acceptor-variant | AHCTF1 | GRCh38.p7 | 1:246899514 | AAACAAGTGGCATCT[-/A]AAAAAAAAGATTTAA | 25909 |
rs766133797 | snp | G/T | 1.65531e-05 | 0.00287686 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246891860 | GCAAATAGCATTGCT[G/T]GATAGACTGTATAGT | 25909 |
rs766150171 | snp | A/G | | | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246851377 | AGAGGGATATAACTC[A/G]TTAAATGAAAGATTC | 25909 |
rs766154627 | snp | C/T | 1.65839e-05 | 0.00287953 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850666 | AGCTTCAGAAATTTC[C/T]TTTGCCTTCCTAGTT | 25909 |
rs766156618 | snp | C/T | 1.67581e-05 | 0.00289461 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246855847 | AGAAAAAGAAATACA[C/T]ACCTTAGTGTGTAAG | 25909 |
rs766238300 | snp | C/T | 1.66994e-05 | 0.00288953 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246918350 | GAGACCACTAGTCAC[C/T]TGAGCTCTTAAGTCT | 25909 |
rs766243370 | snp | C/G/T | 0.000165334 | 0.00909074 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246876965 | CATAACATTAATCTT[C/G/T]AGAGTTTGGTTCAGC | 25909 |
rs766244419 | snp | C/T | 3.29696e-05 | 0.00406001 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246864014 | CGAACTTGAGGGCAG[C/T]GAACGGGATACTAGG | 25909 |
rs766260738 | in-del | -/TGAC | 3.55745e-05 | 0.00421734 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246849574 | TTTTAAGCTGAAGAG[-/TGAC]TGAGATGAAAAACTG | 25909 |
rs766263546 | snp | C/G | 1.65029e-05 | 0.00287248 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246913375 | TGAGTGCTTGCACTG[C/G]CTCCTCCATGATTAA | 25909 |
rs766266032 | snp | A/G | 0.000149749 | 0.00865171 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246900302 | TACACATACAAATAC[A/G]AAGAGAAAGGAGAGA | 25909 |
rs766279406 | in-del | -/TATC | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246849200 | TTGAAATAATTTCTG[-/TATC]TATCTTAGTAAAAAG | 25909 |
rs766282345 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246919289 | CTAAAGGTGAGCAAG[A/C]ACAATACCCATTGTA | 25909 |
rs766287409 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869260 | TAACTGTTCCCCCGC[A/G]TCTCTCCCTTTCCCC | 25909 |
rs766292499 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246885821 | CTACTTTAATCTGTG[C/T]TATATAGAGTTGGCT | 25909 |
rs766295291 | snp | A/C | 2.4754e-05 | 0.00351801 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246841012 | TTCTGAAAAAAAAAG[A/C]TATGATCAAGTAAGA | 25909 |
rs766307001 | snp | C/T | 1.65067e-05 | 0.00287282 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246890034 | AGGGTAGTTGTAGCA[C/T]AACCTTGACAACTGC | 25909 |
rs766350721 | in-del | -/AA | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246926048 | AGACCCTGTCTTTAA[-/AA]AAAAAAAAAAAAAAA | 25909 |
rs766418494 | snp | A/G | 8.3266e-05 | 0.00645183 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246900162 | TACTAATATATCCAA[A/G]ATGCCATGTGGAGAA | 25909 |
rs766449025 | snp | C/T | 1.6574e-05 | 0.00287867 | missense, utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246840822 | TACAGCATTTTTCTG[C/T]GTAAAATTTGCTTTG | 25909 |
rs766458120 | snp | A/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246865978 | TTACCATAATCCATA[A/T]AAAGAATGCATCCTA | 25909 |
rs766471858 | snp | C/G/T | 3.58425e-05 | 0.00423322 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246876102 | ATGGCTAATTTTCGA[C/G/T]GGACTCTAGGAAGGA | 25909 |
rs766478498 | snp | A/G | 3.29538e-05 | 0.00405904 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246849860 | CTTTCAGTCTTTTTT[A/G]TAAGTTTTTTCTTAG | 25909 |
rs766481808 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246920494 | ATTATTAAACCAGCC[C/G]GGCGTGGTGGCTCAC | 25909 |
rs766497607 | snp | G/T | 3.34029e-05 | 0.00408661 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246900031 | ACTTTTGTGCATTAC[G/T]TTTCTTAAGAGGTAA | 25909 |
rs766507698 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246845825 | AAAGAGAGCTCTGAT[C/T]TGCAGCATTTGCTGA | 25909 |
rs766512918 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246893554 | AACTGGACATGATAG[C/T]TTTTAATATTCATGA | 25909 |
rs766524220 | snp | C/G | 6.6291e-05 | 0.00575683 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246887346 | CATAATATCAAGTAG[C/G]AAATAAATGGTCTTT | 25909 |
rs766533829 | snp | C/T | 6.59022e-05 | 0.00573993 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246849783 | GCTCATTTGTTTCTT[C/T]ATGTGTCATTTCATC | 25909 |
rs766597402 | snp | A/C | 1.69911e-05 | 0.00291466 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246903911 | AAATAGAAAACAACA[A/C]AATGGTAATATAAAC | 25909 |
rs766638956 | snp | A/C/T | 5.9818e-05 | 0.00546864 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246876005 | TCTTTTTTGATCCAA[A/C/T]AGATTATGATATTCT | 25909 |
rs766639136 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246845175 | AGTTCTATCAAATTC[C/T]GCTTTTCGAGCATGA | 25909 |
rs766642670 | snp | A/G | 1.71114e-05 | 0.00292496 | synonymous-codon, nc-transcript-variant, intron-variant | AHCTF1 | GRCh38.p7 | 1:246843902 | AAACTAATTCTTTCA[A/G]CTGTGCAGGAACCTC | 25909 |
rs766659899 | in-del | -/AAAT | | | utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246839626 | TATTATTTGGTAGAA[-/AAAT]AAATGCAGAAAGCAC | 25909 |
rs766685381 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246927047 | GCAGGGCGTGGTGAC[A/G]GGAACCTGTAGTCCC | 25909 |
rs766688833 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246896041 | ATCAGTATGACCCAT[A/C]AGAAGGGCTATAATC | 25909 |
rs766695938 | snp | C/G/T | 5.58024e-05 | 0.00528192 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850482 | ATGATTTTAATCTTT[C/G/T]TGATTCCCTACCTGT | 25909 |
rs766698659 | snp | C/G | 1.64738e-05 | 0.00286995 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246907682 | TACTAACTGGAAACA[C/G]AGATGGCGCCCTTGT | 25909 |
rs766778496 | snp | C/T | 1.65737e-05 | 0.00287864 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246894689 | CCTCTTTTGTGAGAA[C/T]CACTTTATTCCACGT | 25909 |
rs766787059 | snp | A/G | 3.08228e-05 | 0.00392562 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246867246 | AATAAACTCTTACCT[A/G]GAAATTTTTTGTGAT | 25909 |
rs766787443 | snp | A/G | 4.10282e-05 | 0.00452906 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246885462 | TTAACAGATACGATA[A/G]AGACTTTATAGTTTC | 25909 |
rs766789283 | in-del | -/TGATT | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246908055 | AACCATAAATAAAAC[-/TGATT]TATTTCTTTATTGAA | 25909 |
rs766800016 | snp | C/T | 0.000881918 | 0.0209805 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246916416 | AGAAAAAAAAATTGC[C/T]TATTTTAATATTGTA | 25909 |
rs766810830 | snp | C/T | 2.02677e-05 | 0.00318331 | missense, nc-transcript-variant, intron-variant | AHCTF1 | GRCh38.p7 | 1:246843814 | TCATCTTCAAGCTTG[C/T]TCTTATTGGATGTGT | 25909 |
rs766842451 | snp | C/T | 1.70342e-05 | 0.00291836 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246877289 | GCAAAAAATTCCAGG[C/T]TTCAACCATACACCT | 25909 |
rs766863851 | snp | C/T | 1.67761e-05 | 0.00289617 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850369 | ACTTTCCTGATTTTC[C/T]ACAGATCTTTTAATT | 25909 |
rs766878377 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246855122 | TCTAGAGTCAGATAA[A/C]AACTATGTCATAGTA | 25909 |
rs766917479 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246912559 | AAATACTCCTTTTCT[A/G]AAAATTAAGAGTAAA | 25909 |
rs766925637 | snp | A/G | 1.64972e-05 | 0.00287199 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850225 | AATACGCAGCTGCTT[A/G]TCACTGGATTTATCA | 25909 |
rs766931539 | snp | A/G | 3.76541e-05 | 0.00433885 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246890947 | TTATAGATTAAGTAA[A/G]TATTTTACCTATGCC | 25909 |
rs766971054 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246865747 | ATCATCAAGACTTAA[C/T]AGTTTAAAGGTTCTG | 25909 |
rs766989944 | snp | C/T | 1.64798e-05 | 0.00287047 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246902629 | CTCAAAGGGAACATG[C/T]CACCTGTCAGGTCCA | 25909 |
rs766991103 | snp | C/T | 1.69703e-05 | 0.00291288 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246913446 | GATTTGCTTTTCTTC[C/T]GCAAAGTAAGAAAAT | 25909 |
rs767000209 | snp | A/G | 1.88603e-05 | 0.00307079 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246853111 | TTTCTTGAGTATCAG[A/G]AGGGCTGTCAGAAAT | 25909 |
rs767055835 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246911675 | TTTTAGTAGAGACGG[C/G]GTTTCTCCATGTTGG | 25909 |
rs767084936 | snp | C/T | 4.94572e-05 | 0.00497254 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246851142 | CAAGTTTTTCTTCAG[C/T]TGCTGTGTTAGCTGC | 25909 |
rs767089304 | in-del | -/AA | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246870724 | AGGGTATAAAACCTC[-/AA]AAAAAAAAAAAAAAA | 25909 |
rs767098714 | snp | A/C | 1.6495e-05 | 0.0028718 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850110 | GTATGGCAGACATAT[A/C]AAATTCTGCTTGAAC | 25909 |
rs767118712 | snp | C/T | 5.10747e-05 | 0.00505319 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246900465 | ACTAGTGTCAGGCGA[C/T]AGAGCTGGAAGAAAA | 25909 |
rs767129122 | snp | A/G | 1.65343e-05 | 0.00287521 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246841021 | AAAAAGATATGATCA[A/G]GTAAGAATAAACACA | 25909 |
rs767153999 | snp | A/G | 1.64762e-05 | 0.00287016 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246851273 | CCATCTACTTCAGCA[A/G]TGTCACATTCAGCAG | 25909 |
rs767223611 | in-del | -/AAAT | 1.7088e-05 | 0.00292296 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246916111 | TCAGTTTTGAAAGAG[-/AAAT]AAATGTCCAGGTATC | 25909 |
rs767227067 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246876324 | CATTTTTCCAAACCA[A/G]GAACTTCATCCACAT | 25909 |
rs767227682 | snp | C/G/T | 4.99042e-05 | 0.004995 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246898378 | CAATCAATGCTCAAT[C/G/T]TGAATAATCAAATTT | 25909 |
rs767247666 | snp | C/G | 1.64977e-05 | 0.00287203 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246876990 | TTCAGCTTCAAGGCA[C/G]GCACATAATTGGCAC | 25909 |
rs767253974 | snp | A/G | 1.78401e-05 | 0.00298659 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246888549 | ATTAAGACTTATTTA[A/G]TATCACTGTTAATTA | 25909 |
rs767274772 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246871195 | TTAGGACAGTGGTTA[C/G]TACTTGCCTATTAGT | 25909 |
rs767318310 | snp | A/G | 3.39225e-05 | 0.00411826 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246855865 | CTTAGTGTGTAAGAA[A/G]ATCCCATCTGCTTTA | 25909 |
rs767334206 | in-del | ACTAAGCACC/GATACTAAGCACCTTAGT | | | downstream-variant-500B | AHCTF1 | GRCh38.p7 | 1:246838991 | TTACCTTACTACTAT[ACTAAGCACC/GATACTAAGCACCTTAGT]TTAACCAATGCTTTG | 25909 |
rs767353815 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246887422 | TACGTATATATTTAC[A/G]ATAGGTAGCAACAAA | 25909 |
rs767374218 | in-del | -/ATATAC | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246846726 | AAGATTTTGAAATAT[-/ATATAC]ATATACATATATATA | 25909 |
rs767385500 | in-del | -/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246892144 | AACTCAAATCATCTA[-/T]TATCTAGAGCTTGTC | 25909 |
rs767389363 | in-del | -/TTTT | | | upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246932466 | ACTTTTCTTTTTTTC[-/TTTT]TCTTTTTTTTGGAGA | 25909 |
rs767389798 | in-del | -/TTG | 1.64768e-05 | 0.00287021 | cds-indel, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246849858 | GACTTTCAGTCTTTT[-/TTG]TAAGTTTTTTCTTAG | 25909 |
rs767415699 | snp | C/T | 1.65776e-05 | 0.00287898 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246887202 | TATGCTGTAAGTGAA[C/T]AGACTTACCTCATAG | 25909 |
rs767423089 | snp | A/C | 1.89346e-05 | 0.00307684 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246894625 | AGTATTTTAATATTA[A/C]ATTCTGTCCTACATC | 25909 |
rs767442042 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246886052 | TAAGTTTAAACAAAA[A/C]AAGTGCAGTGGCTCA | 25909 |
rs767470861 | in-del | -/AATT | 3.20067e-05 | 0.00400029 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246853074 | GATAAAGAAGTAAAA[-/AATT]AATTAATTTTTTTTA | 25909 |
rs767478107 | snp | C/T | 0.000132468 | 0.00813735 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246891876 | GATAGACTGTATAGT[C/T]TGTGGATCCATGAAA | 25909 |
rs767575909 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246881973 | GCATGAGCCACCGTG[C/T]CTGGCCTTTATTATT | 25909 |
rs767598148 | snp | C/G | 1.71237e-05 | 0.00292602 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246862122 | TCAGAAAATCCAGAA[C/G]TAGTAACTGACATGG | 25909 |
rs767601519 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246927086 | GGGAGGCTGAGGAGG[A/G]AGAATGGCGTGAACC | 25909 |
rs767614421 | snp | C/T | 1.6566e-05 | 0.00287797 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246891001 | AGAACCAAAGAACCA[C/T]TTGTGCATACTGACA | 25909 |
rs767616942 | snp | A/G | 1.65436e-05 | 0.00287602 | missense, utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246840939 | GCTGGGCTAGCCAAG[A/G]GGGAAATCAGCCGAA | 25909 |
rs767632674 | snp | G/T | 1.65037e-05 | 0.00287256 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246855744 | CATTTATTGTCATTT[G/T]CTCTAATTGCAGGGG | 25909 |
rs767668291 | snp | G/T | 4.96611e-05 | 0.00498278 | missense, utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246840831 | TTTCTGCGTAAAATT[G/T]GCTTTGGATAGGAAG | 25909 |
rs767687977 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246927770 | AGTACTTTGGGAGGC[A/C]GAGGCTGGCGGATCA | 25909 |
rs767729543 | in-del | -/TTT | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246891445 | AATGAAATTGGCTTG[-/TTT]TTGTTTTGAAATTGC | 25909 |
rs767735464 | snp | G/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246847344 | ATGACATAAGTAGGG[G/T]GACAAAAGCAGAATA | 25909 |
rs767737594 | snp | C/T | 2.04288e-05 | 0.00319593 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246876183 | AAACGAGGATCACGA[C/T]CATTCTATTAAACAT | 25909 |
rs767795810 | snp | A/G | 1.66081e-05 | 0.00288163 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246861975 | CCAGGAATCCATTTT[A/G]GGTGGACATCTTCTT | 25909 |
rs767807860 | snp | C/G | 1.79842e-05 | 0.00299863 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246853168 | CACTTTCTTTTAGTA[C/G]ACCAACTTCTACTTC | 25909 |
rs767815388 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246903244 | AGCACCCCTCCGATC[C/T]CCTCAGGAATTCAGC | 25909 |
rs767833484 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246914788 | TACACCAACCATGCA[C/T]TCAACTGAGCAACCA | 25909 |
rs767836813 | snp | A/G | 6.66112e-05 | 0.00577071 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246900262 | CTAAAAGAAAATTTA[A/G]AACATTACTAAGTCA | 25909 |
rs767886013 | snp | G/T | 1.66485e-05 | 0.00288513 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246900173 | CCAAGATGCCATGTG[G/T]AGAAGTCCTACTTAC | 25909 |
rs767901310 | snp | C/T | 1.69781e-05 | 0.00291355 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246904060 | ATTAACGAAGACACG[C/T]TAAATATATTAATAC | 25909 |
rs767928092 | snp | A/G | 1.65061e-05 | 0.00287277 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246860999 | AGTAGTTAGTGCAGT[A/G]GAAGAGCTTTTGGGC | 25909 |
rs767928528 | snp | A/T | 1.64863e-05 | 0.00287104 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246867723 | TTCTCCAATTTTAGA[A/T]AACACATTGTTGATG | 25909 |
rs767928956 | in-del | -/TAAG | 3.33225e-05 | 0.00408168 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246900270 | AATTTAAAACATTAC[-/TAAG]TAAGTCATTGGTCAG | 25909 |
rs767939920 | in-del | -/AAGATCGCTTAAGCCCAAGAGGTTGAGGCTACAGTGAGCCATGAC | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246897887 | GGGGGCTGGGGTGGG[lengthTooLong]AAGATCGCTTAAGCC | 25909 |
rs767969005 | snp | C/T | 6.62252e-05 | 0.00575397 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246918307 | CGTCTTCTCCAAGGG[C/T]TTGAAGAGTCACTTC | 25909 |
rs767981565 | snp | C/T | 1.66286e-05 | 0.0028834 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246867386 | ACTTCTGATGTATCA[C/T]AAGGAGCACTGATAA | 25909 |
rs768050688 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246889136 | AAAATAATGAAGTTC[A/G]AAGACAGAGAGTTAA | 25909 |
rs768058259 | snp | A/G | 3.29707e-05 | 0.00406008 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246898159 | CTGTAATAGAAAGCT[A/G]ATAACGTGATCCAAC | 25909 |
rs768069639 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246902245 | CACGGGTAAACTTCA[C/T]TCAAAGACTACTCAC | 25909 |
rs768090998 | snp | C/T | 1.79544e-05 | 0.00299615 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246885484 | TATAGTTTCAAAAGA[C/T]GTACTTACCTATTAA | 25909 |
rs768104236 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246915354 | AAAAATTACTTCACC[A/G]TTGATTTCAAAGGAG | 25909 |
rs768105437 | snp | A/G | 8.39328e-05 | 0.0064776 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246877266 | ATTCAACCTATTGCA[A/G]TGTTGCCGCAAAAAA | 25909 |
rs768106016 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246928367 | ACACTATGAATTCCT[A/G]AAAGGCAAAAATCAC | 25909 |
rs768127230 | in-del | -/GTAGCATAA | 3.30066e-05 | 0.00406229 | cds-indel, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246890028 | AATTACAGGGTAGTT[-/GTAGCATAA]CCTTGACAACTGCAC | 25909 |
rs768132394 | snp | A/G | 1.66718e-05 | 0.00288715 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246862051 | CAGGTGATGGAGAGG[A/G]AGATGCTAAAGGTGT | 25909 |
rs768146822 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246901549 | GAATGGCATGAACCC[C/T]GGAGGCGGAGCTTGC | 25909 |
rs768157294 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246927569 | GAAACACCTACGTTC[A/G]GTACTGTACAAAATT | 25909 |
rs768158889 | snp | A/T | 1.66543e-05 | 0.00288563 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246890096 | AAAAAGCTGGTAATA[A/T]TCCCCAAATATCTCA | 25909 |
rs768164510 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246881057 | CATTATGAAATGCAC[A/G]GTGGAGACCACAATA | 25909 |
rs768172996 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246903763 | GAATTGCTTGAATCC[A/G]GGTGGCGGAGGTTGC | 25909 |
rs768181822 | snp | G/T | 1.71687e-05 | 0.00292986 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246853217 | CAGCGCTACTTCCTG[G/T]TTAAGCCTGCGCTCA | 25909 |
rs768220585 | in-del | -/ACA | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246895451 | GTAACAGTGATACAC[-/ACA]ACAATTTGGATGAAT | 25909 |
rs768257985 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246908368 | AGGGGGAAGCCTACC[C/T]TCCCCACCTACAAAA | 25909 |
rs768264458 | snp | A/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246845579 | TTTCACTTTTCGTAA[A/T]CTTCACCTAAGCTTT | 25909 |
rs768272774 | snp | G/T | 1.79422e-05 | 0.00299513 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246891087 | AGTTAACATCAGTTG[G/T]TTACTTACAAAAAAA | 25909 |
rs768283817 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246856186 | TGGAATATTTTCTAT[A/G]AACTCAGTAGAGGCA | 25909 |
rs768295753 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246889932 | GAAACTTTGACTTCT[C/T]ACAGATGTAATTTCT | 25909 |
rs768316855 | snp | A/G | 3.33139e-05 | 0.00408116 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246900129 | AGGAGGGACTCCTCT[A/G]TTTAAACTTCTCTCA | 25909 |
rs768341840 | snp | A/G | 1.67697e-05 | 0.00289561 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246916370 | AAGTTGTGGACCACA[A/G]GCCAAGCAAGCAAGT | 25909 |
rs768357436 | in-del | -/AATA | | | utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246839714 | AGATAATCAATTATT[-/AATA]GTCCATTCATTACAC | 25909 |
rs768362297 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246929929 | TGGTGGCGTGCGCCT[A/G]TAATCCCAGCTACTC | 25909 |
rs768395794 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246858095 | CCCCCGAGTAGCTGG[C/G]ACTACAGATGCCCGC | 25909 |
rs768401964 | snp | C/T | 3.29582e-05 | 0.00405931 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246898187 | AACCAAAAGAAACAA[C/T]AGAGTTAAAAATCAT | 25909 |
rs768436703 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246878299 | CTATTCAGTAGGCTA[A/C]GGTGGGAGGATTGCT | 25909 |
rs768483433 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246844861 | GCAATTATCAATATA[A/G]TTACAGACGAGCACA | 25909 |
rs768488523 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246857257 | TTGGGAGTATGTTTC[A/C]AATGGTCGTTAAAAA | 25909 |
rs768493056 | snp | G/T | 1.70168e-05 | 0.00291687 | utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246840780 | TGACTTTACAAATAG[G/T]TGTACATTAAAATCT | 25909 |
rs768496471 | in-del | -/CT | 3.47899e-05 | 0.00417058 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246894646 | GTCCTACATCTAGAC[-/CT]CTAATACTTACATAG | 25909 |
rs768550046 | in-del | -/CAGTCATT | 1.65105e-05 | 0.00287315 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246888273 | TCAGTGGATCTTATA[-/CAGTCATT]CATTCATTCATGCTT | 25909 |
rs768550375 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246856010 | TCAGAAACAATGCTG[C/T]ACTTGTTTTACCCAT | 25909 |
rs768553760 | snp | A/T | 1.64841e-05 | 0.00287085 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246861034 | AGGCCGTGAAAACAG[A/T]CTCTTCAAGGTCTTC | 25909 |
rs768583957 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246915677 | ACAGACCAAGTTCAA[C/T]TTATTCATCCTGGGA | 25909 |
rs768604412 | snp | C/G | 3.30819e-05 | 0.00406692 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246857707 | CTTCATAGACTGATG[C/G]TGCACAAAGAGAAGC | 25909 |
rs768613394 | snp | G/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246843009 | ATCAGTTTTATTTTT[G/T]AATGTTTCCACTGTC | 25909 |
rs768616035 | snp | C/T | 3.29804e-05 | 0.00406068 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246895939 | TCCTAAACCATGCAT[C/T]ACAGAAAGGAAAGAA | 25909 |
rs768627020 | in-del | -/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246871964 | TCCTACTCCACAAGT[-/C]CCAGCCTCAGTGTTC | 25909 |
rs768646743 | snp | G/T | 1.83893e-05 | 0.00303221 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246877343 | AGTTTTAGAAAAAGC[G/T]ATTTAAATGTACAAA | 25909 |
rs768661982 | snp | A/G | 0.000167923 | 0.0091615 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246867316 | TCTGGAGCTGGGAGC[A/G]AATACACTATAGGAG | 25909 |
rs768685968 | snp | A/C/T | 4.954e-05 | 0.00497674 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246902560 | CTGTCACCATGAGAT[A/C/T]GAAATTTCTCTATAC | 25909 |
rs768704208 | snp | G/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246925033 | AGATGGAAAAGGCCA[G/T]AATCACATTGTTACT | 25909 |
rs768710998 | snp | A/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246876330 | TCCAAACCAAGAACT[A/T]CATCCACATATCTAA | 25909 |
rs768731649 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246875044 | CAGGCCAACAACTTA[C/T]ATTATAGATAAACCA | 25909 |
rs768746376 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246911007 | AATCATAAATTACTT[C/T]TGTAATCAATAAAAT | 25909 |
rs768790237 | snp | A/G | | | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246849991 | TGTAGATCTCCTTCT[A/G]ATGCTGGGAGCTTCT | 25909 |
rs768792256 | snp | C/T | 1.65927e-05 | 0.00288029 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246900361 | TCTGGCATTTGTGCA[C/T]GATACCAACGATTTA | 25909 |
rs768818251 | snp | G/T | 3.33525e-05 | 0.00408352 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246855839 | TTTCCTTTAGAAAAA[G/T]AAATACATACCTTAG | 25909 |
rs768821089 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246883185 | GTTTGATGGTTTAAA[C/T]ATTAAAACTTTTTCA | 25909 |
rs768875739 | snp | A/G | 1.65157e-05 | 0.0028736 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246877131 | TTATCTTGAATTTCT[A/G]ACAAGTTTACATCGG | 25909 |
rs768892121 | snp | A/G | 1.67593e-05 | 0.00289471 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246913431 | GAAAACATAATACGT[A/G]ATTTGCTTTTCTTCT | 25909 |
rs768900228 | snp | C/G | 1.91944e-05 | 0.00309788 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246900499 | TAATTTTTAAAAACA[C/G]AATAAAGAATCTCAA | 25909 |
rs768900701 | snp | A/C | 1.91122e-05 | 0.00309124 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246876164 | AGCCAGTGATCTCTC[A/C]CGCAAACGAGGATCA | 25909 |
rs768907322 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246865295 | ATGCTTTGGAGCCCA[C/G]AAATAAAAACTTGTA | 25909 |
rs768913266 | in-del | -/CTT | 8.23988e-05 | 0.00641815 | cds-indel, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246851205 | CTGGCTCAACTTCTC[-/CTT]CTTCACCTTCCAATA | 25909 |
rs768921798 | snp | C/T | 1.83357e-05 | 0.00302779 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246891967 | TACAGTAAATCTAAA[C/T]AAATTAGAATCACAA | 25909 |
rs768924275 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246900933 | GAAAAAGAAAAGTGC[C/T]TGGATGGTGCCTGTG | 25909 |
rs768931720 | in-del | -/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868942 | TCTGCCTCCCGGGTT[-/C]CACGCCATTCTCCTG | 25909 |
rs768940782 | snp | A/G | 1.64762e-05 | 0.00287016 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246907616 | ACCTACAGCAAGCTG[A/G]TTTGTCCTGCTTATG | 25909 |
rs768974056 | snp | C/T | 1.65343e-05 | 0.00287521 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850824 | CATCAACCTGGCTGA[C/T]ATTCATAGTCATTGT | 25909 |
rs768993508 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246867884 | AAGCATATGAAAGAA[C/T]GATTACACCCCCCCC | 25909 |
rs769005035 | snp | G/T | 0.000163412 | 0.00903766 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246931296 | CGACTGCCGGCGCAG[G/T]ACGCGAACCACCAGC | 25909 |
rs769012159 | in-del | -/TA | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246889322 | ATAGCGGCAGCACTT[-/TA]ACTACTCTTTGCGGT | 25909 |
rs769018753 | snp | A/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246870759 | CTAGGCTATTTAATT[A/T]CTCAGGGACAGGGGT | 25909 |
rs769019506 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246894238 | TCACTTTAATGTAAA[A/C]AGAAATAATTTTCTT | 25909 |
rs769049702 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246871784 | ACAGCTATTAGAGGC[A/G]GCAGTATAGCTACCT | 25909 |
rs769058490 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246929740 | GCGTGAAAGACACAA[C/T]GTTTTGCTTCCTCTT | 25909 |
rs769093519 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246920013 | CCGGGCGTGGAGGCA[C/T]ACGCTTGTAATTCCA | 25909 |
rs769107595 | snp | C/T | 1.64749e-05 | 0.00287005 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246849842 | GAACGTTTTTGGCTT[C/T]GACTTTCAGTCTTTT | 25909 |
rs769116967 | snp | A/G | 1.75286e-05 | 0.00296041 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246876068 | TGATGTTGACAGATG[A/G]TAAGGCTTAGCTCGT | 25909 |
rs769136756 | snp | A/C | 1.91551e-05 | 0.0030947 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246905680 | AAATTAGTATATTTC[A/C]TATTTTTAAGTTATT | 25909 |
rs769144566 | in-del | -/AGAATA | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246856249 | TATGATAAATGACTC[-/AGAATA]AGAGACCAATGAAAC | 25909 |
rs769148614 | snp | G/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246918880 | ACCATCCTCCCTACA[G/T]AAAAAAGAAAAAGTG | 25909 |
rs769148766 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246930279 | TCAGCCTCCCAAGTA[A/G]GCGCGCGACTAGAGG | 25909 |
rs769153631 | snp | C/T | | | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246918292 | ATTCTAATGTTATTT[C/T]GTCTTCTCCAAGGGC | 25909 |
rs769162657 | snp | C/T | 6.58989e-05 | 0.00573978 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246849750 | TGAAGGAAGCTGTGG[C/T]GAGCAATCTTTCTTC | 25909 |
rs769184545 | snp | G/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246907272 | CAAAACGTTGTAAAG[G/T]TACAAAGTCATGCTT | 25909 |
rs769230889 | snp | C/T | | | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246903986 | GCCAAACACTTTCTA[C/T]TACCAAAGGCCAGCT | 25909 |
rs769249381 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246918523 | CATATTGGCCAGATG[C/T]GGAGGCTCACGCCTT | 25909 |
rs769258589 | in-del | -/AA | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246889389 | CATACTATTTTATTT[-/AA]AGCTTTATACTGACT | 25909 |
rs769269105 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246844729 | AAGCTAACAGGAAGA[C/T]ATTCCATAGAAAAAT | 25909 |
rs769274809 | snp | C/T | 2.86389e-05 | 0.003784 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246853336 | TTTTTACATTTAAAC[C/T]GAAAAATAAATCCAC | 25909 |
rs769287506 | in-del | -/A | 1.70921e-05 | 0.00292331 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246857647 | GTTCATAATTTCATT[-/A]AACTTCTTTCTAAAA | 25909 |
rs769295979 | snp | A/G | 3.34403e-05 | 0.00408889 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246887181 | TTCTAGTAATTCATG[A/G]AAGTTTATGCTGTAA | 25909 |
rs769301786 | snp | A/G | 1.65523e-05 | 0.00287678 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246894712 | TTCCACGTCCATTCA[A/G]GAACAAAGCGCAAAT | 25909 |
rs769316985 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246903496 | CTAATTTAAATTACT[C/T]CTACTACATTATGAA | 25909 |
rs769319952 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246858314 | CCCCCCTTAACCTCT[C/T]GCTTTTCACTTTTTG | 25909 |
rs769341551 | snp | A/G | 1.64749e-05 | 0.00287005 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246867669 | AACATACCTATTGAA[A/G]GGTGTGGTGCTATTT | 25909 |
rs769345120 | snp | A/C | 3.36089e-05 | 0.00409919 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246885565 | GGCTTCATTGTCTGA[A/C]TATATCTGAGGGCTT | 25909 |
rs769360009 | snp | C/G/T | 0.000146359 | 0.00855326 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246867315 | CTCTGGAGCTGGGAG[C/G/T]GAATACACTATAGGA | 25909 |
rs769384220 | in-del | -/TCAATCAA | 3.34038e-05 | 0.00408666 | intron-variant, downstream-variant-500B | AHCTF1 | GRCh38.p7 | 1:246842653 | CAGAGCGAGACTGTC[-/TCAATCAA]TCAATCAATCAAGAA | 25909 |
rs769396623 | snp | C/G/T | 4.96121e-05 | 0.00498036 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246891795 | TCTCTCAGTGATCTC[C/G/T]CGGGCTTCTGATGCA | 25909 |
rs769419285 | snp | C/G | 2.5944e-05 | 0.00360158 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850455 | CTTCAACTGCTGGTT[C/G]CAACAGCTGAGATGA | 25909 |
rs769420501 | snp | A/G | 3.31252e-05 | 0.00406958 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246860985 | TGTTCAGTTACATTA[A/G]TAGTTAGTGCAGTGG | 25909 |
rs769453707 | snp | A/G | 5.51293e-05 | 0.00524992 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246891096 | CAGTTGTTTACTTAC[A/G]AAAAAATCAAGATGC | 25909 |
rs769485815 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246841407 | TAGCAAAGATGCACA[A/G]AATTTCACAAACTTG | 25909 |
rs769493097 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246857428 | ATGCACAGCTGTGAG[C/T]GAAATCTTGGTCTTC | 25909 |
rs769498450 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246904943 | ATTTGAAGAATAAGA[C/G]AGCAGGGTACTGAGA | 25909 |
rs769505894 | snp | A/C | 1.64982e-05 | 0.00287208 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246861127 | TTCCTTTGCTCACAT[A/C]CAGTTTCTCTAAACT | 25909 |
rs769532757 | snp | A/G | 1.70904e-05 | 0.00292316 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246916405 | TTTTCCCTAGAAGAA[A/G]AAAAAATTGCCTATT | 25909 |
rs769536393 | snp | A/G | 1.64958e-05 | 0.00287187 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246913369 | AAATGCTGAGTGCTT[A/G]CACTGGCTCCTCCAT | 25909 |
rs769538655 | snp | A/G | 5.12098e-05 | 0.00505987 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246888522 | TCCACTTCCCTCTGC[A/G]ATCAGGGAAAAATTA | 25909 |
rs769571448 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246905361 | AAATTAGCCAGGCAT[A/G]GTGACAGGCACCTGT | 25909 |
rs769581467 | snp | G/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246875658 | CACCATGCTGATCAG[G/T]CAGCAGCCATCAACA | 25909 |
rs769620370 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246844463 | CAGTGGCTCACAATT[C/G]TAATTCCAGCACTTT | 25909 |
rs769671308 | snp | A/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246872432 | GTCACACACAAAAAG[A/T]CAAATGAGGTGGTCA | 25909 |
rs769686831 | snp | A/G | 1.65045e-05 | 0.00287263 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850100 | CGTTTTCTAGGTATG[A/G]CAGACATATCAAATT | 25909 |
rs769706438 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246847550 | TTGCCCAGGCTGGAG[C/T]GCAGGGGCACACGAT | 25909 |
rs769714758 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246925290 | CTCAATACAATTTTG[C/G]AAAGATTTTCACAAA | 25909 |
rs769738929 | snp | C/T | 3.29549e-05 | 0.00405911 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246851239 | CAAGGTAAAGTTGCT[C/T]TGAGCCACAAAAAGT | 25909 |
rs769739683 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246930365 | GTTGTTTGCAAACTC[A/G]TGACAGCTTGGTAGT | 25909 |
rs769743319 | snp | A/G | 3.30136e-05 | 0.00406273 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246888370 | TTGTAGACTCTAAAT[A/G]ATAGCACATTACTGC | 25909 |
rs769753380 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246901198 | ATACAAAAATTAGCC[A/G]GGCATTGTGGCATGC | 25909 |
rs769780387 | in-del | -/A | 1.64779e-05 | 0.00287031 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246898194 | AGAAACAATAGAGTT[-/A]AAAATCATCTCACTT | 25909 |
rs769782209 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246877641 | CAGGTTTTTAAGAAG[C/T]GACACTCAGTGGGAA | 25909 |
rs769793322 | snp | A/G/T | 4.94624e-05 | 0.00497284 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246849657 | CTGGAGAAAATAAAG[A/G/T]CTCATTGTTTGGTTC | 25909 |
rs769794584 | snp | G/T | 1.64746e-05 | 0.00287002 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246898213 | ATCATCTCACTTGGC[G/T]TAAACTGGAAGGCTG | 25909 |
rs769825671 | in-del | -/T | 1.74967e-05 | 0.00295771 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246877312 | TACACCTGAAAGCAG[-/T]TATTTATCAAAGTTT | 25909 |
rs769825807 | snp | C/G | 4.94417e-05 | 0.00497176 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246895877 | CAGTCAAAAGTCCCA[C/G]GGAACTAGTCTGAAT | 25909 |
rs769826093 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246885693 | ACTCTGGAAATAACA[C/T]GAAAAATGTTAAATA | 25909 |
rs769851117 | snp | C/G/T | 1.68272e-05 | 0.00290057 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850376 | TGATTTTCTACAGAT[C/G/T]TTTTAATTCTTCTAG | 25909 |
rs769854747 | snp | C/T | 1.65048e-05 | 0.00287265 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850946 | GACTGTTCCATTGTA[C/T]CTGAAGTAATTTCTT | 25909 |
rs769866468 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246865326 | GTTGCAGTACCTTCC[C/T]TGTCATTCTATCTAT | 25909 |
rs769875584 | snp | A/G | 3.31318e-05 | 0.00406999 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246905532 | AAACAAAGTTTGTAT[A/G]AGACCTACCTATCTT | 25909 |
rs769903839 | snp | C/T | 3.62516e-05 | 0.00425729 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246857857 | TTTATGCTAAATATT[C/T]AGTGATTACTGATAG | 25909 |
rs769944202 | snp | C/T | 1.65154e-05 | 0.00287358 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246857738 | TTCAGTTCCTTGAAC[C/T]GGGCTTAAGTGATTC | 25909 |
rs769976161 | snp | A/G | 1.65392e-05 | 0.00287564 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246887334 | GGGAAAGGAATACAT[A/G]ATATCAAGTAGCAAA | 25909 |
rs770001250 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246871945 | ATGACCCTGATCCCA[A/G]ACATCCTACTCCACA | 25909 |
rs770009196 | snp | C/T | 1.69882e-05 | 0.00291441 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246864139 | CAGAATGCGCATTTA[C/T]TGAGTTATACTGAAA | 25909 |
rs770028189 | snp | C/T | 9.89642e-05 | 0.00703365 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246902573 | ATCGAAATTTCTCTA[C/T]ACTCTGGCATCCCAA | 25909 |
rs770029746 | in-del | -/A | 1.74251e-05 | 0.00295165 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246860854 | TTATAAACTTTATTG[-/A]GGGACATTAATAACA | 25909 |
rs770031454 | snp | C/G | 1.65699e-05 | 0.00287831 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246894722 | ATTCAAGAACAAAGC[C/G]CAAATTAGTGGCAGA | 25909 |
rs770034623 | snp | G/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246884631 | CTGTACTTCCAATCA[G/T]GCCATTTAGCTTTCT | 25909 |
rs770082260 | snp | C/T | 5.0176e-05 | 0.00500854 | utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246840797 | GTACATTAAAATCTT[C/T]CCAAGAAATTACAGC | 25909 |
rs770093915 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246873106 | GTTCGACTTATTCCT[A/G]TAAGCCAGTCTCTGA | 25909 |
rs770095238 | in-del | -/AGT | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246845222 | TTTTTGTGGGTACAC[-/AGT]AGGTGTATATATAAA | 25909 |
rs770121283 | snp | A/G | | | upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246932182 | AAATCGGGTCTCTCC[A/G]CCTCCGAGGAGCTGG | 25909 |
rs770125274 | in-del | -/TTC | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246911385 | GCTTTTGCTCATCAA[-/TTC]TTTTCATTTAAACTT | 25909 |
rs770166834 | in-del | -/TG | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246901880 | GAGCTCATGACAACA[-/TG]TGCTTTTCACATATT | 25909 |
rs770170583 | snp | A/G | 4.95372e-05 | 0.00497656 | missense, utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246840903 | TCTGTAGTTTTTCTT[A/G]GTTTGCTCTTGACTC | 25909 |
rs770188590 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246846992 | TTTTGAAGAATATTT[A/C]AGATTAACTGAAGGC | 25909 |
rs770208912 | snp | C/T | 3.33072e-05 | 0.00408075 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246888145 | ATAATTTTAGTAATA[C/T]ATGAAACACTGGATA | 25909 |
rs770210034 | snp | A/G/T | 3.32156e-05 | 0.00407515 | missense, nc-transcript-variant, intron-variant | AHCTF1 | GRCh38.p7 | 1:246842753 | TGGCTTTCCCAGAGT[A/G/T]TCTACTGATTGTGCA | 25909 |
rs770212670 | snp | G/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246914850 | ATCCAAATGATCAAT[G/T]AGTGTCCATGTTTCC | 25909 |
rs770214297 | snp | C/T | 4.17162e-05 | 0.00456688 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246890940 | TTAATACTTATAGAT[C/T]AAGTAAATATTTTAC | 25909 |
rs770219573 | snp | C/T | 3.30983e-05 | 0.00406793 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246849922 | CACTAAAATGGATTT[C/T]CCTAAAGCTGGTTTT | 25909 |
rs770220000 | snp | C/G | | | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246907568 | TCTTTTCATGCTTTT[C/G]ATGTTCCAAAGTGCT | 25909 |
rs770232662 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246912310 | TGAAACCCCATCTCT[A/G]CTAAAAAAAAAAAAA | 25909 |
rs770235460 | snp | C/T | 1.64743e-05 | 0.00287 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246907656 | GTTGAAACAGCTGTT[C/T]CTGTTGGACTTACTA | 25909 |
rs770260566 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246881328 | TGTGAGGAACTGAGA[C/T]ATCCACCATTAGCGT | 25909 |
rs770260735 | snp | A/G | 3.32662e-05 | 0.00407824 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246900221 | ACAGTGCAAAATAAG[A/G]GCAATTATGTAGATA | 25909 |
rs770269173 | snp | A/T | 7.61992e-05 | 0.00617202 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246862187 | GGAATTACACCATTA[A/T]AAGTGCTTATAGGCC | 25909 |
rs770277537 | snp | G/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868532 | AGTGCTGGGATAGAG[G/T]TGTGAGCCACCGGCC | 25909 |
rs770313761 | snp | C/T | 1.69378e-05 | 0.00291009 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246907781 | CACAAATTAGACAAA[C/T]GAAGTTAAAAAACTA | 25909 |
rs770318564 | in-del | -/AAT | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246871869 | TTGAGGTTATTAAAA[-/AAT]AATAACAACCTAAAG | 25909 |
rs770322398 | snp | A/T | 1.67178e-05 | 0.00289113 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246862061 | AGAGGGAGATGCTAA[A/T]GGTGTTGATCGAAGA | 25909 |
rs770357498 | snp | A/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246892788 | AGGCATGTGCCACCC[A/T]GCCCAGCTAATTAAA | 25909 |
rs770366664 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246849245 | CTTCAAAACAATTTC[A/G]GGTTGTGGATATCAC | 25909 |
rs770397897 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246897260 | TGGAGGTTGCAGTGA[A/G]CCAAGATCACGTCAC | 25909 |
rs770405647 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246906301 | TGACAAACTGGCAGC[C/T]GGGCGTGGTAGCTCA | 25909 |
rs770423744 | snp | C/T | 1.65822e-05 | 0.00287938 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850728 | GAGTAGCAACATCTG[C/T]TGATGCTTCCTGTTG | 25909 |
rs770442400 | in-del | -/AA | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246923109 | TAATCAAATAATACC[-/AA]AAAAAAAAAAAAAAA | 25909 |
rs770456149 | snp | C/T | 5.82021e-05 | 0.00539423 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246918417 | ATTATTATGACACAT[C/T]TGTAGACAATATACT | 25909 |
rs770470708 | snp | C/T | 1.65236e-05 | 0.00287429 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246905551 | CCTACCTATCTTGTG[C/T]AGACTGAACAGCCCA | 25909 |
rs770470947 | snp | C/T | 1.65206e-05 | 0.00287403 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246861160 | GTGACCCCTCATCCA[C/T]TTCTTGATGCTCCTT | 25909 |
rs770477433 | in-del | -/CTGT | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246854124 | TAACACGGTGAAACC[-/CTGT]CTGTCTCCACTAAAA | 25909 |
rs770485656 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246895423 | GGGGTGTGTGTGTGT[A/G]TGTGTGTGAAGAGTA | 25909 |
rs770489601 | snp | A/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246919831 | TTAAAGAATTCTCAA[A/T]GTTAAAGCAACAAAG | 25909 |
rs770504182 | in-del | -/T | | | utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246839197 | ATTTAGAACAGGCAA[-/T]TTTGTTTGCTTATGA | 25909 |
rs770529215 | snp | A/T | 3.6675e-05 | 0.00428208 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246885708 | TGAAAAATGTTAAAT[A/T]TAAATATAATCCTAT | 25909 |
rs770537249 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246877748 | GTAGATGTTTTTTGG[C/T]TGATTTGCAGCAAGA | 25909 |
rs770552926 | snp | C/G | 1.78131e-05 | 0.00298433 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246849566 | TAACCAAATTTTAAG[C/G]TGAAGAGTGACTGAG | 25909 |
rs770579070 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246867045 | AGCAGTCTGAAATTA[C/T]TGAACAAAAATTTTA | 25909 |
rs770582467 | snp | C/T | 0.000103313 | 0.0071865 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246885590 | GGGCTTGTCTGTGCT[C/T]GCCCTGACTCATGAA | 25909 |
rs770611406 | in-del | -/AGA | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246901743 | GAATTGGTTGAGCCC[-/AGA]AGGTCAAGGCTGCAA | 25909 |
rs770627319 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246894131 | ATGACTTGGGCTCAA[A/G]AAGTCAAGGCTGCAC | 25909 |
rs770635022 | in-del | -/TACC | 1.67461e-05 | 0.00289357 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246913228 | AAGTAAAGAACTGAT[-/TACC]TACCTGATGCTTCAA | 25909 |
rs770636944 | snp | C/T | 1.65326e-05 | 0.00287507 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246898347 | AAAGTCTGTAACAGA[C/T]AAATTAGTAAGGCAT | 25909 |
rs770647868 | snp | C/G | 1.70615e-05 | 0.00292069 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246902499 | ATCCAGCCTTCACAT[C/G]ACATATTTCAAGTAC | 25909 |
rs770648988 | snp | A/G | 0.000151295 | 0.00869624 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246904051 | GAAACAGAAATTAAC[A/G]AAGACACGCTAAATA | 25909 |
rs770650995 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246844598 | ATGTGGTGGTGCACG[C/T]CTGTGGTGTCAGCTA | 25909 |
rs770660332 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246879258 | TACCATTTTTACCCA[C/T]GAGATGAAGAGACAA | 25909 |
rs770662748 | snp | C/G | 2.67212e-05 | 0.00365512 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246851468 | TAAAGATAAGAGACT[C/G]GTTAAAGAATTTTAA | 25909 |
rs770681220 | snp | A/C/G | 3.30443e-05 | 0.00406464 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246877145 | TGACAAGTTTACATC[A/C/G]GTAAGTAATTACCTG | 25909 |
rs770741009 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246872243 | TCCAATTTGTACAAA[A/G]TAATACTCAGATCGG | 25909 |
rs770768048 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246926422 | TCTCCAGACTTCATC[A/G]TGGTGCCTAGCACAA | 25909 |
rs770776821 | snp | A/G | 1.67164e-05 | 0.00289101 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246916166 | AAGAACAACTGCTTT[A/G]ACTACTTTTGATATT | 25909 |
rs770781092 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246852957 | ACACTTATTTTTTGA[A/G]CCCATATTTTTATAA | 25909 |
rs770799142 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246928048 | TTCGGCCGGGTGCGG[C/T]GGCTCACGCCTGTAA | 25909 |
rs770799337 | in-del | -/AAGT | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246863873 | TCCTTGCTACTTGAA[-/AAGT]AAGAGCCATCTAGTT | 25909 |
rs770804565 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246913660 | AGAGCTTACTGATAC[A/G]CCAGGCATTGTGTTA | 25909 |
rs770831159 | snp | C/T | 1.65625e-05 | 0.00287766 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850304 | AATTTTCTGATCATT[C/T]TGCTAGGACTTGTTA | 25909 |
rs770845244 | in-del | -/A | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246920770 | GCAAAACACTGTCTC[-/A]AAAAAAAAAAAAAAA | 25909 |
rs770847163 | snp | C/T | 1.65425e-05 | 0.00287593 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246851339 | TCAATAGTATCAAAA[C/T]TGTACTGAAGCTTAA | 25909 |
rs770863446 | snp | A/G | 1.64857e-05 | 0.00287099 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246877052 | ATTCTGAACGCTGGC[A/G]CTGGACTGCAAAAAT | 25909 |
rs770866690 | snp | C/T | 6.73582e-05 | 0.00580298 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246913437 | ATAATACGTGATTTG[C/T]TTTTCTTCTGCAAAG | 25909 |
rs770871250 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246888580 | ATATCAAAGCAACCA[A/G]CATCAAAATATTAAA | 25909 |
rs770875798 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246886953 | TCTCTCTAATATTAA[C/T]GATCACTGTATCTGA | 25909 |
rs770884177 | snp | C/T | 3.29832e-05 | 0.00406085 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850205 | CTGACCCTTCTAACA[C/T]GTTTAATACGCAGCT | 25909 |
rs770891984 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246854599 | AGAAAGTTGCTTTTT[C/T]GATAATGATCATTTC | 25909 |
rs770902178 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868474 | TGGCCAGACTGGTCT[C/G]AAACTCCGGGCCTCA | 25909 |
rs770953764 | snp | C/T | 1.65051e-05 | 0.00287267 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246889989 | ACGCTCAAACTTCTG[C/T]CGACGACTGGTGTAG | 25909 |
rs770958397 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246872389 | AGTGTAGACACCTTT[A/G]CTGGCTAAATAAAAG | 25909 |
rs770965723 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246902051 | GATGGAGAAACAGAG[C/G]TCTGAAATGTTAAGC | 25909 |
rs770973551 | snp | C/T | 3.30371e-05 | 0.00406417 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246888344 | TAAGCATGTCTCCTC[C/T]CTCCCCAGCTTTGTA | 25909 |
rs770976823 | snp | C/T | 1.65559e-05 | 0.00287709 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246849942 | AAGCTGGTTTTCCAA[C/T]ATCAACATTTTCACT | 25909 |
rs770978831 | snp | C/T | | | upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246933723 | AGCTGGGACTACAGG[C/T]ATGGATATCATGCCT | 25909 |
rs770999570 | snp | A/G | | | upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246932571 | CTTTTCATGCCAAAG[A/G]TGGGCTCCCAGACTT | 25909 |
rs771006965 | snp | C/T | 1.75468e-05 | 0.00296194 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246888536 | CAATCAGGGAAAAAT[C/T]AAGACTTATTTAATA | 25909 |
rs771069340 | in-del | -/AAT | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246896364 | ATGCTCATACAACAG[-/AAT]ATTATACAGCCATAA | 25909 |
rs771071299 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246873307 | CTTTCTCCCTGTGCT[A/G]TTTAGTCCCTTTTAT | 25909 |
rs771083456 | snp | G/T | 3.30066e-05 | 0.00406229 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246851006 | AAATTTTCTGCAATT[G/T]CTACTTTAATAGGTT | 25909 |
rs771122251 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246879424 | ATCCTTTCACCCTAG[A/G]ATTTTATTCTATAAA | 25909 |
rs771130520 | snp | C/G | 3.29766e-05 | 0.00406045 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246907736 | TGGTACTTCAGCTGG[C/G]ATACCAGTTAGAACT | 25909 |
rs771131264 | snp | G/T | 1.66128e-05 | 0.00288204 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246860968 | CTCCATCCTTTTCAG[G/T]TTGTTCAGTTACATT | 25909 |
rs771151665 | snp | A/T | 1.65121e-05 | 0.00287329 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246888182 | AAAAGGATACAATAG[A/T]GTGTTTGGCTGCTTC | 25909 |
rs771156832 | in-del | -/TG | 1.66582e-05 | 0.00288597 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246887192 | CATGAAAGTTTATGC[-/TG]TAAGTGAATAGACTT | 25909 |
rs771169699 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246911692 | TTTCTCCATGTTGGT[C/T]AGGCTGGTCTCAAAC | 25909 |
rs771227990 | in-del | -/AAT | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246862605 | GATTTCTGCAAAGAA[-/AAT]AATACAAAATTCTTC | 25909 |
rs771297386 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246841623 | CTTTCTGTAAAATAA[C/T]TGCAGGATTTTAAAG | 25909 |
rs771300929 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246927678 | CAAAGGCTAGATAGG[C/G]AGAGCAGGAACGTTC | 25909 |
rs771310818 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869331 | CCAACTAATAACCCT[A/G]CAAAGACCTCAAGTG | 25909 |
rs771312651 | snp | A/T | 1.67444e-05 | 0.00289343 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246891728 | ATTCGTTTCTCTTAG[A/T]CAAGAAGTAAAATTT | 25909 |
rs771345651 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246909891 | ACCAGCAGTAACAAT[A/C]AAAAATGTCTTCTAA | 25909 |
rs771350796 | in-del | -/TATGTTTTAACAAACA | 4.81012e-05 | 0.00490391 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246843753 | TGTAAAAAAAAAAAG[-/TATGTTTTAACAAACA]TACAAATAAAATCAT | 25909 |
rs771352576 | snp | A/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246897322 | CTGTCTCAAAAAAAA[A/T]AAAGGTAGTAACAAA | 25909 |
rs771365960 | snp | A/G | 1.66418e-05 | 0.00288455 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246900250 | TATTCTCCTGACCTA[A/G]AAGAAAATTTAAAAC | 25909 |
rs771386830 | snp | A/G | 4.96003e-05 | 0.00497973 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246891799 | TCAGTGATCTCTCGG[A/G]CTTCTGATGCAAAAC | 25909 |
rs771398603 | snp | A/T | 1.65151e-05 | 0.00287355 | missense, utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246840921 | TTGCTCTTGACTCCG[A/T]CAGCTGGGCTAGCCA | 25909 |
rs771404535 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246928461 | AATAAATTAGGATAA[C/G]AGGATACTGTATAGC | 25909 |
rs771413639 | snp | C/T | 1.64917e-05 | 0.00287151 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246855805 | CCAACACTGGTACCT[C/T]GGACTTCTGGGTGAA | 25909 |
rs771517848 | snp | G/T | 2.04715e-05 | 0.00319927 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246862195 | ACCATTAAAAGTGCT[G/T]ATAGGCCGGGCGCGG | 25909 |
rs771528634 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246878001 | TCACTTGAGCATATC[C/T]ATAAAAATTATAATT | 25909 |
rs771532467 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246882935 | CTGAACTGCCTTTGA[C/T]CCTATTTCACAAAGT | 25909 |
rs771559628 | snp | C/T | 3.54089e-05 | 0.00420752 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246851488 | AAGAATTTTAATACA[C/T]GTTTTAACTTGAAGC | 25909 |
rs771564407 | snp | A/C | 3.45149e-05 | 0.00415406 | utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246840773 | ATTCTGATGACTTTA[A/C]AAATAGGTGTACATT | 25909 |
rs771569343 | snp | A/G | 1.697e-05 | 0.00291285 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246862101 | AGGATGGACTGAGGA[A/G]TGAACTCAGAAAATC | 25909 |
rs771598958 | snp | C/T | 1.77798e-05 | 0.00298154 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246899541 | TTAAAAAATAATCCA[C/T]TTACATATATTTAAA | 25909 |
rs771620173 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246898945 | ATACAAAATATTAGC[C/T]GGGCGTGGTGGTGAG | 25909 |
rs771649979 | snp | G/T | 1.73872e-05 | 0.00294844 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246905669 | ATATCTGAAACAAAT[G/T]AGTATATTTCATATT | 25909 |
rs771665371 | in-del | -/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246911464 | TTAAGGTATAGTGTC[-/T]TATCTATGAAGATTC | 25909 |
rs771665956 | snp | C/T | 3.52821e-05 | 0.00419998 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246861202 | TCAGGAAAAAAGATG[C/T]GGTCCTATCTTTGCT | 25909 |
rs771733558 | snp | G/T | 1.89856e-05 | 0.00308098 | synonymous-codon, nc-transcript-variant, intron-variant | AHCTF1 | GRCh38.p7 | 1:246843839 | ATGTGTTTTTTTGTC[G/T]GCTCCTTAAAGCAGG | 25909 |
rs771756939 | snp | A/C | 1.82467e-05 | 0.00302043 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246867833 | AATGAAGAACGCTGG[A/C]ATTAAGTGCATCTCT | 25909 |
rs771762552 | snp | A/G | 1.73766e-05 | 0.00294755 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246860863 | TTATTGAGGGACATT[A/G]ATAACAATTTTGAGT | 25909 |
rs771784320 | snp | A/C | 1.66771e-05 | 0.00288761 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246902686 | AACCCCTGTAACATA[A/C]AATACACGCAAATAT | 25909 |
rs771813404 | snp | C/T | 1.82774e-05 | 0.00302297 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246864168 | AAAAACAAAAGAATT[C/T]AGTATCCCATTTAAT | 25909 |
rs771815317 | snp | A/G | | | downstream-variant-500B | AHCTF1 | GRCh38.p7 | 1:246838782 | AAGATCTATCCAGGC[A/G]GAATTAACTATACTT | 25909 |
rs771819047 | in-del | -/A | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246895763 | ATTAAAATAACTAAG[-/A]AAAAAATATAACAAA | 25909 |
rs771826196 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246914070 | TATTATTTAAAGAAA[A/C]GTATACTTTAGCTAT | 25909 |
rs771827895 | in-del | -/CTG | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246898576 | ATGAACTGTATAACC[-/CTG]CTGTCTTCTCTAAAG | 25909 |
rs771828269 | in-del | -/ATG | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246930316 | CAATTCCCGGTTGAC[-/ATG]ATGTTTTAAAAATTT | 25909 |
rs771831723 | in-del | -/ATT | 0.00010459 | 0.00723076 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246861942 | ATGTCTTTTCTCCCA[-/ATT]ATTATCAAACTTACC | 25909 |
rs771873406 | snp | A/G | 1.66507e-05 | 0.00288532 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246900170 | TATCCAAGATGCCAT[A/G]TGGAGAAGTCCTACT | 25909 |
rs771906906 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869249 | ACTCCACTGACTAAC[C/T]GTTCCCCCGCGTCTC | 25909 |
rs771910866 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246844953 | TCAAGTAACTTAAAC[C/T]TGTCTGTGCATCAGT | 25909 |
rs771921644 | snp | C/G | 3.36276e-05 | 0.00410032 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246916341 | CGCTCTCCTGTTATA[C/G]AGTTTACTACCTCAA | 25909 |
rs771923466 | snp | A/G | 1.67189e-05 | 0.00289122 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246894742 | TTAGTGGCAGAATTT[A/G]GTTGTTCTTATTTGT | 25909 |
rs771924254 | snp | C/T | 4.98915e-05 | 0.00499432 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246842815 | GTTAAGTATTAAACA[C/T]GAATCCAATTTTAAA | 25909 |
rs771926650 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246902932 | CTCATGCACTACTGG[C/T]TGGTATGTAAACTGG | 25909 |
rs771930103 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246839638 | GAAAAATAAATGCAG[A/C]AAGCACACTGCATAT | 25909 |
rs771935355 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246924243 | ACATTAAAAGAACTA[C/T]TATAAATTTAACAAT | 25909 |
rs771938324 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246860517 | CTGTGCATTATGTCT[A/G]GGAACTAGTATACTG | 25909 |
rs771978599 | snp | C/T | 1.64808e-05 | 0.00287057 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246902600 | CCAACAATTTGGTAT[C/T]ACTCGTCTGTCCCCT | 25909 |
rs771979714 | snp | A/G | 1.66021e-05 | 0.0028811 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850319 | CTGCTAGGACTTGTT[A/G]CCGTACTAACTTTTA | 25909 |
rs771992145 | snp | C/G | 2.03415e-05 | 0.0031891 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246867302 | ATGCCTCAGGCAGCT[C/G]TGGAGCTGGGAGCGA | 25909 |
rs771999516 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246874827 | AAAAAGTTACAAAAA[A/C]ACCTGACCTCCGGCT | 25909 |
rs772010384 | snp | C/G | 1.69126e-05 | 0.00290792 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246916209 | AGACAGAGAACACTC[C/G]CTTCTGTTTCTTCCA | 25909 |
rs772017552 | in-del | -/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246899763 | ACACAGCAAAAAAAA[-/T]AAAAGCTACTATAAA | 25909 |
rs772033834 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246857570 | AAAACAGCCAACATT[A/G]CCAAAATGGAGATGT | 25909 |
rs772044367 | snp | C/T | 1.64776e-05 | 0.00287028 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246863987 | GATGGCCTGAGGCGA[C/T]CCTTTTAATTGCGAA | 25909 |
rs772059330 | snp | A/G/T | 8.29502e-05 | 0.00643965 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246890079 | ATTTTTAAGAGTTGG[A/G/T]AAAAAAGCTGGTAAT | 25909 |
rs772078783 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246910061 | CTATGTGTCTCCTGA[C/T]GTGATACAATATGAA | 25909 |
rs772092889 | snp | A/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246924603 | CTCTCCACATCTTAG[A/T]CCCCTCCCCCAAAAA | 25909 |
rs772094248 | snp | C/T | 1.6601e-05 | 0.00288101 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246877235 | CTTCATACATGTGCT[C/T]CAGTAACTCCTCTAT | 25909 |
rs772118212 | snp | C/T | 1.65512e-05 | 0.00287669 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246849950 | TTTCCAACATCAACA[C/T]TTTCACTTTTAGCTG | 25909 |
rs772119279 | snp | A/T | 1.76446e-05 | 0.00297018 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246840980 | AGGAGGTGACCAAGC[A/T]CTTTCTTTTTCTGTG | 25909 |
rs772146323 | snp | A/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246923433 | TAAATAAATAAATAC[A/T]TAAATAAATACATAA | 25909 |
rs772147539 | snp | G/T | 1.65255e-05 | 0.00287445 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246877154 | TACATCGGTAAGTAA[G/T]TACCTGCTCAGTGTC | 25909 |
rs772161616 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246921067 | ATTGCACTCCAGCCT[A/G]GGCAACAAGAGTGAA | 25909 |
rs772184798 | snp | A/G | 0.000313234 | 0.0125108 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246877028 | ATGGTGCACTAAAAG[A/G]AATTCATGATTCTGA | 25909 |
rs772191744 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246862664 | ACATAAAACTGCATC[C/T]ATCTTTCTAAAAGCA | 25909 |
rs772207136 | snp | C/T | 0.00014928 | 0.00863815 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246900342 | AGAATCATACCTTAA[C/T]GAATCTGGCATTTGT | 25909 |
rs772214474 | snp | C/G | 1.65307e-05 | 0.0028749 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850083 | TTTTTCTTGGTCTAC[C/G]ACGTTTTCTAGGTAT | 25909 |
rs772269675 | snp | A/C | 1.64928e-05 | 0.00287161 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246851212 | AACTTCTCCTTCTTC[A/C]CCTTCCAATATCAAG | 25909 |
rs772278086 | in-del | -/A | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246916022 | GTAACACATTTACAT[-/A]AAAGTATACAAATTG | 25909 |
rs772291127 | snp | A/G | 1.65097e-05 | 0.00287308 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246888359 | CCTCCCCAGCTTTGT[A/G]GACTCTAAATGATAG | 25909 |
rs772316562 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246899084 | ACAAGAGCGAAACTC[C/T]GTCTCAAAAAGAGAA | 25909 |
rs772322671 | snp | A/G | 1.64866e-05 | 0.00287106 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246913311 | CTGTCCAACATCAGT[A/G]ACCACAGCTGCCACT | 25909 |
rs772425996 | snp | A/C | 6.89941e-05 | 0.00587301 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246885593 | CTTGTCTGTGCTCGC[A/C]CTGACTCATGAATGC | 25909 |
rs772439185 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246883028 | GCTACAATAAGTGCT[A/G]TTTCAATAACATTAT | 25909 |
rs772459402 | snp | A/G | 1.78321e-05 | 0.00298593 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246907809 | CTAGAAACAGCATTA[A/G]AAGCAAATATGTCAT | 25909 |
rs772461108 | in-del | -/AAAA | 3.55878e-05 | 0.00421813 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246843931 | TCTATTTTTTTAGCT[-/AAAA]AAAGTTGAAAAAACT | 25909 |
rs772463946 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246917307 | TCAAGTACAGACTCC[A/G]AATTTCTGCTTGAGC | 25909 |
rs772468806 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246884940 | CAATTTGTCAACTCT[A/G]TCACTTCATTCTTCC | 25909 |
rs772516311 | snp | C/T | 1.69117e-05 | 0.00290785 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246857666 | TTCTTTCTAAAAGTA[C/T]TTGAATTTCTCTCCA | 25909 |
rs772523398 | snp | A/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868343 | CCAGGCTGGTCTTGA[A/T]CTCCTGACCTCATGT | 25909 |
rs772525534 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246918605 | AGTTCGAGGCTGCGC[C/T]TCCAGTGAGCTATGA | 25909 |
rs772530229 | snp | A/G/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246906567 | AGCCTGGGCAACAGA[A/G/T]TGAGACCCCACCCCC | 25909 |
rs772541170 | snp | A/T | 1.67668e-05 | 0.00289537 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246887167 | TGTATTTTCTAAAAT[A/T]CTAGTAATTCATGAA | 25909 |
rs772542522 | snp | A/C/T | 8.24034e-05 | 0.00641839 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246849665 | AATAAAGGCTCATTG[A/C/T]TTGGTTCAGAAAGGT | 25909 |
rs772544290 | in-del | -/TCTAAGA | 1.65938e-05 | 0.00288039 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246899401 | ATAAATCAACTATAT[-/TCTAAGA]TCTAAGATCTGACTT | 25909 |
rs772578229 | snp | A/C | 1.98687e-05 | 0.00315182 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246918424 | TGACACATTTGTAGA[A/C]AATATACTTGATTAT | 25909 |
rs772590229 | in-del | -/CTG | 4.96093e-05 | 0.00498018 | cds-indel, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850725 | TAGGAGTAGCAACAT[-/CTG]CTGATGCTTCCTGTT | 25909 |
rs772604185 | in-del | -/A | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246870725 | GGGTATAAAACCTCA[-/A]AAAAAAAAAAAAAAA | 25909 |
rs772623853 | snp | G/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246858454 | GCTCATGACGCATAC[G/T]CAGTAAGTAGCTGAG | 25909 |
rs772635772 | snp | G/T | 3.33489e-05 | 0.0040833 | intron-variant, downstream-variant-500B | AHCTF1 | GRCh38.p7 | 1:246842669 | CAATCAATCAATCAA[G/T]CAAGAACAGAACAGA | 25909 |
rs772645512 | in-del | -/A | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246907897 | AAGATTAGTGATAAC[-/A]AAAAAGTATGTTAAA | 25909 |
rs772698155 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246870613 | AATTTTACATTTAAA[A/G]GAGAAAAGTATAATA | 25909 |
rs772707243 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246890467 | ATGCAAGAAGCTGAA[A/G]GCTTTGCAAGTTATA | 25909 |
rs772728498 | snp | C/T | 1.6543e-05 | 0.00287597 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246891835 | AAGACTATATTAAGA[C/T]TGCTAAGAAGCAAAT | 25909 |
rs772750447 | snp | A/G | 2.75099e-05 | 0.00370867 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850469 | TCCAACAGCTGAGAT[A/G]ATTTTAATCTTTTTG | 25909 |
rs772799244 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246892619 | AGCCACTGTGCCCGA[C/T]CTAATTTGCTTTACT | 25909 |
rs772807345 | snp | C/T | 3.45077e-05 | 0.00415363 | synonymous-codon, nc-transcript-variant, intron-variant | AHCTF1 | GRCh38.p7 | 1:246843885 | CTGAGAAGATAAATC[C/T]GAAACTAATTCTTTC | 25909 |
rs772810059 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246843257 | TGTCTCCTCTAACCT[C/T]GGTCTATAAAGTATT | 25909 |
rs772810319 | snp | A/T | 1.64741e-05 | 0.00286998 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246898217 | TCTCACTTGGCTTAA[A/T]CTGGAAGGCTGAACA | 25909 |
rs772853775 | snp | A/C | 1.65405e-05 | 0.00287576 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246918283 | GAAGCACAGATTCTA[A/C]TGTTATTTCGTCTTC | 25909 |
rs772855007 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246912397 | CTGAGGCAGGAGAAT[C/T]GCTTGAACACGGGAG | 25909 |
rs772879630 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869881 | CAAGATATAATTTAG[A/G]AATACATTTCATAAA | 25909 |
rs772892565 | snp | A/G | 4.31295e-05 | 0.00464358 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850589 | CTCCTAGGCGTAACA[A/G]AATTTTGAGGTATTT | 25909 |
rs772893213 | snp | A/G | 0.000188251 | 0.0097 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246885458 | TTTATTAACAGATAC[A/G]ATAAAGACTTTATAG | 25909 |
rs772905226 | snp | C/T | 2.40185e-05 | 0.00346536 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246867338 | CTATAGGAGATGGTT[C/T]TTCTATTTTAGAACT | 25909 |
rs772940820 | snp | A/T | 3.19056e-05 | 0.00399397 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246853343 | ATTTAAACTGAAAAA[A/T]AAATCCACACACAAG | 25909 |
rs772969822 | snp | A/C | 6.59968e-05 | 0.00574404 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246913372 | TGCTGAGTGCTTGCA[A/C]TGGCTCCTCCATGAT | 25909 |
rs772990777 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246879026 | AAGCAGAACATTTTT[A/G]TATAAAGAAAAATAG | 25909 |
rs773004278 | snp | C/T | 1.64844e-05 | 0.00287087 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246877048 | CATGATTCTGAACGC[C/T]GGCACTGGACTGCAA | 25909 |
rs773026706 | snp | A/G | 3.32033e-05 | 0.00407438 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246900371 | GTGCATGATACCAAC[A/G]ATTTATATCAAAAAG | 25909 |
rs773032679 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246899743 | ACTCCAAGCACAGCT[A/G]AGAAACACAGCAAAA | 25909 |
rs773045140 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246865377 | AGGAGCGGTAGACCA[A/G]CACAGGTGATAATGG | 25909 |
rs773063085 | snp | G/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246876532 | TTACAGTTGATAAAA[G/T]CAAGACTCAGAGTGT | 25909 |
rs773064606 | snp | A/C/T | 3.41625e-05 | 0.00413283 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246903909 | TAAAATAGAAAACAA[A/C/T]AAAATGGTAATATAA | 25909 |
rs773188794 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246926267 | CACATATTCCTTTAT[A/G]GCAACACAGGCTAAC | 25909 |
rs773195156 | snp | A/C/G | 4.9504e-05 | 0.00497493 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850103 | TTTCTAGGTATGGCA[A/C/G]ACATATCAAATTCTG | 25909 |
rs773200330 | snp | A/G | 1.72142e-05 | 0.00293374 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246888527 | TTCCCTCTGCAATCA[A/G]GGAAAAATTAAGACT | 25909 |
rs773234744 | snp | A/G | 1.6476e-05 | 0.00287014 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246849772 | TCTTTCTTCCTGCTC[A/G]TTTGTTTCTTTATGT | 25909 |
rs773250325 | snp | C/T | 6.59055e-05 | 0.00574007 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246851245 | AAAGTTGCTTTGAGC[C/T]ACAAAAAGTTCCCCA | 25909 |
rs773255225 | in-del | -/ATATTTC | 1.81138e-05 | 0.00300941 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246905673 | CTGAAACAAATTAGT[-/ATATTTC]ATATTTTTAAGTTAT | 25909 |
rs773268034 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246871005 | ACAAAAAGTGACTGC[A/G]CTCCCACTGTAGCCT | 25909 |
rs773274163 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246886861 | CCTATCACACTATTT[C/T]ATAAGATCTTCCCAT | 25909 |
rs773286947 | snp | G/T | 4.96537e-05 | 0.00498241 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246888165 | AACACTGGATAAAAC[G/T]TAAAAGGATACAATA | 25909 |
rs773290432 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246886083 | TGCCTATAATCCCAG[A/C]ACTTTGGGAGGCTGA | 25909 |
rs773297561 | in-del | -/AGAT | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246870571 | TGATAAAGTGTAAAC[-/AGAT]AGAGGGTCTCCAGGG | 25909 |
rs773302445 | snp | A/G | 8.26945e-05 | 0.00642965 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246887335 | GGAAAGGAATACATA[A/G]TATCAAGTAGCAAAT | 25909 |
rs773311351 | snp | C/T | 1.64741e-05 | 0.00286998 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246907658 | TGAAACAGCTGTTCC[C/T]GTTGGACTTACTAAC | 25909 |
rs773327390 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246920452 | AATCACAGCTACATG[C/T]AACAATATGAATGAA | 25909 |
rs773349922 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246902001 | AATCCTCACAACTAC[C/T]CTTTGCAAAAGGTCT | 25909 |
rs773350682 | snp | C/T | 1.65034e-05 | 0.00287253 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850980 | TTCTTGTGTCTTTAA[C/T]TACATCTAGTAAATT | 25909 |
rs773351685 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246854115 | CCACCCTGGCTAACA[C/T]GGTGAAACCCTGTCT | 25909 |
rs773359458 | in-del | -/AA | 2.48592e-05 | 0.00352548 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246861305 | TGCAGCCTGTAAAGT[-/AA]GATTTTGAAAAGAAA | 25909 |
rs773359616 | snp | G/T | 1.66032e-05 | 0.0028812 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246894730 | ACAAAGCGCAAATTA[G/T]TGGCAGAATTTGGTT | 25909 |
rs773378669 | in-del | -/A | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246877929 | TATTTATTTATTTTT[-/A]TTTTTTTTAATGCCA | 25909 |
rs773380841 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246930377 | CTCGTGACAGCTTGG[C/T]AGTATGTTACTGAAG | 25909 |
rs773403571 | snp | C/T | 1.64776e-05 | 0.00287028 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850871 | GTCTTAAATGCAGAT[C/T]TGACCAATTTAGTGG | 25909 |
rs773431464 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246849514 | GGTTTGAGGGGGGAA[A/G]GGGAAAAATTCCCTA | 25909 |
rs773449168 | snp | A/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246852671 | TAAAAAAACCTTTCA[A/T]TTGAACCAGATCAGC | 25909 |
rs773454962 | snp | A/C/G | 6.60593e-05 | 0.00574682 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246857739 | TCAGTTCCTTGAACC[A/C/G]GGCTTAAGTGATTCA | 25909 |
rs773457659 | snp | C/T | 3.32912e-05 | 0.00407976 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246900231 | ATAAGAGCAATTATG[C/T]AGATATTCTCCTGAC | 25909 |
rs773471087 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246872224 | CAAGGATCTAACAGG[C/T]GTCTCCAATTTGTAC | 25909 |
rs773472072 | snp | A/T | 1.72689e-05 | 0.00293839 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246916412 | TAGAAGAAAAAAAAA[A/T]TGCCTATTTTAATAT | 25909 |
rs773480305 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246859988 | ATAATTTGGCAGGGC[A/G]CGGTGGCTCACGCCT | 25909 |
rs773488271 | snp | C/G | 3.30229e-05 | 0.0040633 | missense, utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246840904 | CTGTAGTTTTTCTTG[C/G]TTTGCTCTTGACTCC | 25909 |
rs773506033 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246860769 | CCTCAGCCTCCCAAA[C/G]TGCTGAGATTAACTA | 25909 |
rs773513235 | snp | C/T | 5.06376e-05 | 0.00503152 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246853240 | TGCGCTCAGAGACAA[C/T]AGGACCTTCAGAGAT | 25909 |
rs773520062 | snp | C/T | 3.37137e-05 | 0.00410557 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246877273 | CTATTGCAATGTTGC[C/T]GCAAAAAATTCCAGG | 25909 |
rs773523556 | snp | A/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246859025 | TGCAGGAGCTGAAAT[A/T]GCCCCACTGTACTCC | 25909 |
rs773553338 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246919504 | GGATCACAAGGTTAG[A/G]AGATCAACACCATCC | 25909 |
rs773570172 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246930250 | GAGGCTGAAGCTCAA[A/C]CGTTCCCCCCGCCTC | 25909 |
rs773575145 | snp | A/C | 2.01696e-05 | 0.0031756 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246890942 | AATACTTATAGATTA[A/C]GTAAATATTTTACCT | 25909 |
rs773635038 | snp | C/G | 0.000452796 | 0.0150397 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246931376 | CGAAGCCCGGCGCCC[C/G]CGAGCCTGCCGTACC | 25909 |
rs773664465 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246844614 | CTGTGGTGTCAGCTA[C/T]GTGGGAGGCTGAGGC | 25909 |
rs773669188 | snp | A/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246914534 | TCTAATTACTGTAAT[A/T]ATGTCTATAAATACT | 25909 |
rs773672359 | in-del | -/TG | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246910049 | AACTACTAGACACTA[-/TG]TGTCTCCTGATGTGA | 25909 |
rs773716132 | snp | C/T | 4.98898e-05 | 0.00499424 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246840809 | CTTCCCAAGAAATTA[C/T]AGCATTTTTCTGCGT | 25909 |
rs773784048 | snp | G/T | 3.34102e-05 | 0.00408705 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246861181 | GATGCTCCTTTTCAG[G/T]GCTGTTCAGGAAAAA | 25909 |
rs773785342 | snp | C/T | 3.29516e-05 | 0.00405891 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246849853 | GCTTTGACTTTCAGT[C/T]TTTTTTGTAAGTTTT | 25909 |
rs773787255 | in-del | -/AT | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868355 | TGAACTCCTGACCTC[-/AT]GTGATCCACCCGCCT | 25909 |
rs773819879 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246879743 | TGAGGCAGGAAAATC[A/G]GCTTGAACCCAGGAG | 25909 |
rs773828178 | snp | G/T | 1.66579e-05 | 0.00288595 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246900145 | TTTAAACTTCTCTCA[G/T]GTACTAATATATCCA | 25909 |
rs773838424 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246847065 | GCCAAGGCGGGTGGA[C/T]TATCTGAGGTCAGGC | 25909 |
rs773848576 | snp | A/T | 1.6476e-05 | 0.00287014 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246851266 | AAGTTCCCCATCTAC[A/T]TCAGCAATGTCACAT | 25909 |
rs773863728 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246892951 | ACACCTAATCTCTAA[C/T]ACTTTTAAAACACTT | 25909 |
rs773869209 | in-del | -/A | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246867903 | TACACCCCCCCCCCC[-/A]CACACACACACACAC | 25909 |
rs773882926 | in-del | -/A | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246881862 | ACCAAAAAAAAAAAC[-/A]AAAAAAAAAAGAAGA | 25909 |
rs773886776 | snp | C/G | 1.96957e-05 | 0.00313807 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246876174 | CTCTCCCGCAAACGA[C/G]GATCACGATCATTCT | 25909 |
rs773891099 | snp | A/C | 1.77241e-05 | 0.00297686 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246849582 | TGAAGAGTGACTGAG[A/C]TGAAAAACTGTTTTG | 25909 |
rs773921863 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246865565 | TTCGATCCAAACTTG[A/G]AAAACAGTTTGCTCA | 25909 |
rs773936757 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246843354 | ACAAGGAATTTGCCT[C/G]AATTATTCTTGTGTA | 25909 |
rs773978044 | snp | A/G | 0.000143524 | 0.00847001 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246867828 | TGTAAAATGAAGAAC[A/G]CTGGAATTAAGTGCA | 25909 |
rs773982016 | snp | C/T | 3.29734e-05 | 0.00406025 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246861056 | AAGGTCTTCCGGTGA[C/T]GGTGCATCCTGATAC | 25909 |
rs774004801 | snp | C/G | 3.31055e-05 | 0.00406837 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246898360 | GATAAATTAGTAAGG[C/G]ATCAATCAATGCTCA | 25909 |
rs774006467 | in-del | -/AAGT | 3.41099e-05 | 0.00412962 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246913450 | TGCTTTTCTTCTGCA[-/AAGT]AAGAAAATATAATTA | 25909 |
rs774015441 | snp | C/T | 3.29652e-05 | 0.00405974 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246849662 | GAAAATAAAGGCTCA[C/T]TGTTTGGTTCAGAAA | 25909 |
rs774016842 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246858695 | CTGGGCATGGTGGCA[C/T]GTGCCTGTAATCCCA | 25909 |
rs774032912 | snp | C/G | 1.6477e-05 | 0.00287024 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246867702 | AGGTTCTTTGCTTGC[C/G]CAAACTTCTCCAATT | 25909 |
rs774038545 | snp | G/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246872849 | TTTAAAAATACAAAC[G/T]CTTAAAACATGTGAA | 25909 |
rs774063591 | in-del | -/A | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246891733 | TTTCTCTTAGTCAAG[-/A]AGTAAAATTTAATAA | 25909 |
rs774095197 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246843521 | ACTAGAATTTAAAAA[C/T]CCTTCCACAAACAGG | 25909 |
rs774095825 | snp | A/G | 1.64806e-05 | 0.00287054 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246902595 | GCATCCCAACAATTT[A/G]GTATTACTCGTCTGT | 25909 |
rs774115358 | snp | C/T | 1.65141e-05 | 0.00287346 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246905556 | CTATCTTGTGTAGAC[C/T]GAACAGCCCACAAGT | 25909 |
rs774116585 | snp | A/T | 1.67576e-05 | 0.00289457 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246916191 | GATATTCCAAGGTCA[A/T]AAAGACAGAGAACAC | 25909 |
rs774128168 | snp | A/G | 3.2987e-05 | 0.00406108 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850211 | CTTCTAACATGTTTA[A/G]TACGCAGCTGCTTGT | 25909 |
rs774142521 | snp | C/G/T | 4.9464e-05 | 0.00497292 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246864018 | CTTGAGGGCAGTGAA[C/G/T]GGGATACTAGGTACA | 25909 |
rs774147102 | snp | A/G/T | 5.10385e-05 | 0.00505144 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246902502 | CAGCCTTCACATGAC[A/G/T]TATTTCAAGTACTTT | 25909 |
rs774156282 | snp | A/G/T | 5.72408e-05 | 0.00534955 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246894619 | AAGGTTAGTATTTTA[A/G/T]TATTAAATTCTGTCC | 25909 |
rs774160147 | snp | A/C | 1.65625e-05 | 0.00287766 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850731 | TAGCAACATCTGCTG[A/C]TGCTTCCTGTTGTGC | 25909 |
rs774160350 | in-del | -/AAG | 0.000236752 | 0.0108775 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246853064 | ACTGAAAGACTGATA[-/AAG]AAGTAAAAAATTAAT | 25909 |
rs774195900 | snp | C/T | 4.94605e-05 | 0.0049727 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246877053 | TTCTGAACGCTGGCA[C/T]TGGACTGCAAAAATT | 25909 |
rs774205965 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246856427 | AAAAGGTATTTGAAA[C/T]ATTTATAGATTTTAC | 25909 |
rs774208924 | in-del | -/T | 1.66996e-05 | 0.00288956 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246900035 | TGTGCATTACTTTTC[-/T]TTAAGAGGTAATGTT | 25909 |
rs774238789 | snp | A/G | 1.69928e-05 | 0.00291481 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246862103 | GATGGACTGAGGAGT[A/G]AACTCAGAAAATCCA | 25909 |
rs774260268 | snp | A/G | 3.31521e-05 | 0.00407123 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850312 | GATCATTCTGCTAGG[A/G]CTTGTTACCGTACTA | 25909 |
rs774282182 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246930456 | GCGCTTGGCACACTT[A/C]AAACATCCCTTCAAG | 25909 |
rs774340182 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246913865 | TACTCTAGGATTCTA[C/T]GGCCTCTTCTCCTAA | 25909 |
rs774352585 | snp | A/G | 1.66601e-05 | 0.00288614 | stop-gained, nc-transcript-variant, intron-variant | AHCTF1 | GRCh38.p7 | 1:246842704 | CATACTTGCTTGCTT[A/G]TTTTGTTTTTGACGT | 25909 |
rs774405773 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246839309 | TTAAAAAAGTATTAA[C/G]TTGACATACGTTGCA | 25909 |
rs774406381 | snp | A/G | 4.94597e-05 | 0.00497266 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246851101 | ATTTGCAATTTGTCC[A/G]TGATTATCATTTTCC | 25909 |
rs774430728 | snp | A/G | 0.000220125 | 0.0104888 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246876179 | CCGCAAACGAGGATC[A/G]CGATCATTCTATTAA | 25909 |
rs774455195 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869922 | TCACAGATAGTGATT[C/G]CTCTGAGAGATCCGA | 25909 |
rs774461984 | snp | G/T | 1.66076e-05 | 0.00288158 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246860970 | CCATCCTTTTCAGTT[G/T]GTTCAGTTACATTAG | 25909 |
rs774473508 | snp | A/G | 1.65542e-05 | 0.00287695 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246849943 | AGCTGGTTTTCCAAC[A/G]TCAACATTTTCACTT | 25909 |
rs774477322 | snp | C/T | 1.65037e-05 | 0.00287256 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246889990 | CGCTCAAACTTCTGT[C/T]GACGACTGGTGTAGT | 25909 |
rs774492793 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246888581 | TATCAAAGCAACCAG[C/T]ATCAAAATATTAAAA | 25909 |
rs774526938 | snp | C/T | 4.94319e-05 | 0.00497127 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246849861 | TTTCAGTCTTTTTTG[C/T]AAGTTTTTTCTTAGA | 25909 |
rs774529895 | snp | A/C/G | 0.000103397 | 0.00718951 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246885591 | GGCTTGTCTGTGCTC[A/C/G]CCCTGACTCATGAAT | 25909 |
rs774554505 | snp | C/T | 1.65446e-05 | 0.00287612 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246918289 | CAGATTCTAATGTTA[C/T]TTCGTCTTCTCCAAG | 25909 |
rs774588884 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246896085 | AAGCATGGTAAGGAC[A/G]TGTTAAAACTGGAAC | 25909 |
rs774588969 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246897519 | TGCAATCATGGTAAG[A/C]GCGTACTTACACAAA | 25909 |
rs774592486 | snp | A/G | | | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246861051 | TCTTCAAGGTCTTCC[A/G]GTGACGGTGCATCCT | 25909 |
rs774613906 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246927697 | GCAGGAACGTTCTAC[C/T]GGCTTTGAATGAAGA | 25909 |
rs774656306 | snp | C/T | 6.60131e-05 | 0.00574476 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246851007 | AATTTTCTGCAATTG[C/T]TACTTTAATAGGTTC | 25909 |
rs774695420 | in-del | -/AA | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246903838 | GCGAGACTCTGTCTC[-/AA]AAAAAAAAAAAAAAA | 25909 |
rs774705813 | in-del | -/AT | 3.72696e-05 | 0.00431665 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246843768 | TATGTTTTAACAAAC[-/AT]ACAAATAAAATCATG | 25909 |
rs774762218 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246928504 | GGATACTAGCAGAGA[C/G]AAGAAATAGGCATGT | 25909 |
rs774784059 | snp | C/T | 3.29478e-05 | 0.00405867 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246907686 | AACTGGAAACACAGA[C/T]GGCGCCCTTGTCTCA | 25909 |
rs774807322 | snp | C/T | 1.96311e-05 | 0.00313292 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246918420 | ATTATGACACATTTG[C/T]AGACAATATACTTGA | 25909 |
rs774815569 | in-del | -/AAATGCTATC | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246875520 | GAAGTTCTATGGCTA[-/AAATGCTATC]AAATGGTATCACATG | 25909 |
rs774822433 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246903512 | CTACTACATTATGAA[C/T]ACAATATTAACTTCA | 25909 |
rs774852031 | snp | G/T | 8.26125e-05 | 0.00642646 | missense, utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246840929 | GACTCCGTCAGCTGG[G/T]CTAGCCAAGGGGGAA | 25909 |
rs774852868 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246879709 | GGTGCATGCCTGTAA[C/T]CCCAGCTACTTGCGA | 25909 |
rs774867561 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246879959 | AGCACCAAACTAAAG[C/T]GAAAAAAGTATACTG | 25909 |
rs774889577 | snp | C/T | 1.69301e-05 | 0.00290942 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246916212 | CAGAGAACACTCCCT[C/T]CTGTTTCTTCCAATC | 25909 |
rs774900170 | snp | C/T | | | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246861036 | GCCGTGAAAACAGTC[C/T]CTTCAAGGTCTTCCG | 25909 |
rs774923048 | snp | A/G | 1.79194e-05 | 0.00299322 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850627 | CTGAGATAGTCCTCT[A/G]ACATCAGAATAGATG | 25909 |
rs774952115 | in-del | -/TAAG | | | downstream-variant-500B | AHCTF1 | GRCh38.p7 | 1:246838911 | CCTTACTACTGATAC[-/TAAG]TATCTTTCTGAGTAT | 25909 |
rs774980326 | snp | A/C | 1.69129e-05 | 0.00290795 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246855705 | AAAAATGGAATAATC[A/C]TGAAGTCAAAATTAT | 25909 |
rs774987774 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246928503 | AGGATACTAGCAGAG[A/G]CAAGAAATAGGCATG | 25909 |
rs775030950 | snp | C/T | 1.69123e-05 | 0.0029079 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246853255 | TAGGACCTTCAGAGA[C/T]AGTGAGCGAGGAGTT | 25909 |
rs775038567 | snp | A/C | 1.70307e-05 | 0.00291806 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246913448 | TTTGCTTTTCTTCTG[A/C]AAAGTAAGAAAATAT | 25909 |
rs775045527 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869365 | ATGTGAAAGGAGGAG[C/T]CACATGTCTAGGACT | 25909 |
rs775050161 | snp | C/T | 1.66051e-05 | 0.00288137 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246853040 | GTGTCTTGAAACAAC[C/T]AAACCAAAACTGAAA | 25909 |
rs775053557 | snp | C/T | 1.65941e-05 | 0.00288041 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246900331 | GAGAAAAAAAAAGAA[C/T]CATACCTTAACGAAT | 25909 |
rs775061402 | snp | G/T | 3.69604e-05 | 0.0042987 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246888563 | AATATCACTGTTAAT[G/T]AATATCAAAGCAACC | 25909 |
rs775073197 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246878070 | TACAGTCTACAGAAA[C/T]ACCAGCAAAAATTGC | 25909 |
rs775103193 | snp | C/G/T | 5.06311e-05 | 0.00503124 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246851361 | GAAGCTTAAGTGTTC[C/G/T]AGAGGGATATAACTC | 25909 |
rs775105289 | snp | A/C | 1.86211e-05 | 0.00305126 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246861913 | TGTCAGAGCTAATAC[A/C]TTCTTATTAAAAAAT | 25909 |
rs775132534 | snp | C/T | 1.6498e-05 | 0.00287206 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850226 | ATACGCAGCTGCTTG[C/T]CACTGGATTTATCAT | 25909 |
rs775142483 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246915255 | GAATCGGTTGAACCC[A/G]GGACACAGAGGTTGC | 25909 |
rs775185749 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246901826 | GAGTGAGACCCCTGT[C/G]TCTAAATAAATAAAC | 25909 |
rs775187221 | snp | A/G | | | downstream-variant-500B | AHCTF1 | GRCh38.p7 | 1:246838614 | AGAAGTGGGCGGGGC[A/G]GGGCGGGGGGAAGAC | 25909 |
rs775198410 | in-del | -/TCTA | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246865333 | TACCTTCCTTGTCAT[-/TCTA]TCTATCAAATGAGAG | 25909 |
rs775217695 | in-del | -/A | 3.33244e-05 | 0.0040818 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246887363 | AATAAATGGTCTTTT[-/A]AAAAGCGGATTAAGG | 25909 |
rs775223909 | snp | A/G | 1.66056e-05 | 0.00288141 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246887353 | TCAAGTAGCAAATAA[A/G]TGGTCTTTTAAAAAG | 25909 |
rs775251324 | snp | A/G | 1.6631e-05 | 0.00288362 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246842818 | AAGTATTAAACACGA[A/G]TCCAATTTTAAAACT | 25909 |
rs775267549 | snp | A/G | 3.61317e-05 | 0.00425024 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246899546 | AAATAATCCACTTAC[A/G]TATATTTAAAATGGC | 25909 |
rs775269480 | in-del | -/T | 0.000181547 | 0.00952577 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246863875 | TTGCTACTTGAAAAG[-/T]TAAGAGCCATCTAGT | 25909 |
rs775276697 | snp | C/T | 3.30398e-05 | 0.00406434 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246857767 | TCAATTCTGAAAATG[C/T]CTCTGCTGCAACTAA | 25909 |
rs775285144 | snp | A/G | 1.64743e-05 | 0.00287 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246849725 | GTCCTGCTGCTGCGG[A/G]ATGATTTAGTGAAGG | 25909 |
rs775292442 | snp | A/G | 1.73694e-05 | 0.00294693 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246860864 | TATTGAGGGACATTA[A/G]TAACAATTTTGAGTA | 25909 |
rs775338645 | in-del | -/AGTGAGCCGAGATTGC | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246854240 | GGAGGCGGAGCTTGC[-/AGTGAGCCGAGATTGC]ACCACTGCACTCTAG | 25909 |
rs775353910 | snp | C/T | 3.29587e-05 | 0.00405934 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246902604 | CAATTTGGTATTACT[C/T]GTCTGTCCCCTCAAA | 25909 |
rs775365662 | snp | A/G | 1.66776e-05 | 0.00288765 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246902690 | CCTGTAACATAAAAT[A/G]CACGCAAATATTAAT | 25909 |
rs775368022 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246903037 | CTCTAGAATAGTTCT[C/T]AGACTTTTAGCTTAT | 25909 |
rs775377191 | in-del | -/CAA | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246920212 | ACACACAAGGATATC[-/CAA]CAATAGCCAGCAGAA | 25909 |
rs775402926 | snp | A/C | 1.84367e-05 | 0.00303612 | synonymous-codon, nc-transcript-variant, intron-variant | AHCTF1 | GRCh38.p7 | 1:246843849 | TTGTCTGCTCCTTAA[A/C]GCAGGAGGTGAGATG | 25909 |
rs775418333 | in-del | -/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246857498 | TGTCTCTGTATATTT[-/C]CCGAAACTTTATAGT | 25909 |
rs775419828 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246888707 | TCAAGGTCAGGAGTT[C/T]GAGACCAGCCTGGGC | 25909 |
rs775422745 | snp | A/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246921797 | AACAAATACGAAATA[A/T]GTTTTTAGACAAAAA | 25909 |
rs775427021 | snp | C/T | | | upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246932883 | GGGATTTTAAGAAGA[C/T]GCTCTTTTATCAGGA | 25909 |
rs775438259 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246887675 | TTCTAAAGATCTAGC[A/C]AAAGATGGCAGCTTA | 25909 |
rs775474744 | snp | C/G | 1.79355e-05 | 0.00299456 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246840981 | GGAGGTGACCAAGCA[C/G]TTTCTTTTTCTGTGT | 25909 |
rs775487838 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246847367 | GCAGAATATATGCAC[A/G]TACATAAACTGCAGG | 25909 |
rs775500195 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246909885 | AGTAGCACCAGCAGT[A/G]ACAATCAAAAATGTC | 25909 |
rs775516508 | snp | A/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246910927 | GCTGCAGAACAATAT[A/T]TATGCTGTATGTTTG | 25909 |
rs775527259 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246896795 | ACCTATTAATTTCAT[C/T]CATTACAGGAGCAAA | 25909 |
rs775565615 | snp | C/G | 1.65581e-05 | 0.00287728 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246918310 | CTTCTCCAAGGGCTT[C/G]AAGAGTCACTTCTGG | 25909 |
rs775570175 | snp | G/T | 1.648e-05 | 0.0028705 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246863997 | GGCGATCCTTTTAAT[G/T]GCGAACTTGAGGGCA | 25909 |
rs775600730 | in-del | -/A | 1.80468e-05 | 0.00300384 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246843941 | AGCTAAAAAAAGTTG[-/A]AAAAAACTGTATCTG | 25909 |
rs775608939 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246897656 | ATATGAAGTATACGT[A/G]TATTTAAACACAGAA | 25909 |
rs775610326 | snp | A/G | 3.3066e-05 | 0.00406595 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246864073 | GAATAAACTCCGAAC[A/G]CTGAGAAGGCCGGGG | 25909 |
rs775638442 | snp | C/G | 3.37211e-05 | 0.00410602 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246913318 | ACATCAGTGACCACA[C/G]CTGCCACTCCAAAAA | 25909 |
rs775643208 | snp | A/G | 1.65614e-05 | 0.00287757 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246840944 | GCTAGCCAAGGGGGA[A/G]ATCAGCCGAATTTCT | 25909 |
rs775656563 | snp | C/T | 1.88724e-05 | 0.00307178 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246867844 | CTGGAATTAAGTGCA[C/T]CTCTAACAAACGGGA | 25909 |
rs775674631 | in-del | -/CAAAA | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246930935 | AATTTCCCCATCTCT[-/CAAAA]CAAAACACCCAAACC | 25909 |
rs775677246 | in-del | -/A | 0.000503031 | 0.0158513 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246916403 | ATTTTTCCCTAGAAG[-/A]AAAAAAAATTGCCTA | 25909 |
rs775719910 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246883089 | ACTAACATAAATTAA[C/T]AGTTCAAAACAGGGC | 25909 |
rs775726936 | snp | C/T | 1.66139e-05 | 0.00288213 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246876945 | TAAGACAACTTTAAT[C/T]GTACCATAACATTAA | 25909 |
rs775729601 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246881522 | GTAAATCAAGTCTTA[C/G]CAAAAAAATTTTTTT | 25909 |
rs775747148 | in-del | -/AGTG | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246899958 | CATATGTTAACTAAC[-/AGTG]AGATACAAACAGATA | 25909 |
rs775760860 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246917353 | AACTTCTAAATTTGA[A/G]ATGTCCATCAAGCAT | 25909 |
rs775796909 | snp | C/T | 1.84391e-05 | 0.00303632 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246905674 | TGAAACAAATTAGTA[C/T]ATTTCATATTTTTAA | 25909 |
rs775852735 | snp | C/T | 1.67638e-05 | 0.0028951 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246887169 | TATTTTCTAAAATTC[C/T]AGTAATTCATGAAAG | 25909 |
rs775867832 | snp | C/T | 1.64789e-05 | 0.0028704 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246851218 | TCCTTCTTCACCTTC[C/T]AATATCAAGGTAAAG | 25909 |
rs775899975 | in-del | -/CTGATTTGACAT | 3.32182e-05 | 0.00407529 | cds-indel, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850746 | ATGCTTCCTGTTGTG[-/CTGATTTGACAT]TCACGTTTTGGATAC | 25909 |
rs775960328 | snp | G/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246915138 | AGATCGAGAGCAGCC[G/T]GGCCAACAGGGTGAA | 25909 |
rs775971498 | snp | C/T | 0.000200632 | 0.0100138 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246902699 | TAAAATACACGCAAA[C/T]ATTAATCTGATTCTA | 25909 |
rs776006290 | in-del | -/TAGA | | | utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246839697 | AAAGCAGTTCGTTTC[-/TAGA]TAGATAATCAATTAT | 25909 |
rs776053931 | snp | C/T | 1.65348e-05 | 0.00287526 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850821 | CGTCATCAACCTGGC[C/T]GACATTCATAGTCAT | 25909 |
rs776059691 | in-del | -/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246849112 | ACAGTCCTTAGCTCG[-/T]GACAATGAAGGATGG | 25909 |
rs776085266 | snp | C/T | 1.66021e-05 | 0.0028811 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246855831 | GTGAAGATTTTCCTT[C/T]AGAAAAAGAAATACA | 25909 |
rs776100035 | snp | A/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246888841 | TTGGAGCCCAGGAGT[A/T]TAAAGTGAGCTATAC | 25909 |
rs776106976 | snp | C/T | 5.00271e-05 | 0.0050011 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850761 | CTGATTTGACATTCA[C/T]GTTTTGGATACGTTG | 25909 |
rs776111577 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246917056 | TCATAGAGGTGACTA[C/T]CTGATTTAAATCAAG | 25909 |
rs776158227 | snp | C/T | | | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246887357 | GTAGCAAATAAATGG[C/T]CTTTTAAAAAGCGGA | 25909 |
rs776164245 | snp | A/T | 1.71319e-05 | 0.00292672 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850640 | CTGACATCAGAATAG[A/T]TGTTTTCAGAAGCTT | 25909 |
rs776166461 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246915429 | TTCTGGCCCCCTATT[C/G]TTCCTTCCCCTCATC | 25909 |
rs776167403 | snp | C/T | 4.09996e-05 | 0.00452748 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246853058 | ACCAAAACTGAAAGA[C/T]TGATAAAGAAGTAAA | 25909 |
rs776172749 | snp | C/T | 2.02603e-05 | 0.00318273 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850434 | TAACTTCTTTTTTAG[C/T]AGTTTCTTCAACTGC | 25909 |
rs776174769 | snp | C/T | 3.5478e-05 | 0.00421162 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246843769 | ATGTTTTAACAAACA[C/T]ACAAATAAAATCATG | 25909 |
rs776183520 | snp | G/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246870616 | TTTACATTTAAAAGA[G/T]AAAAGTATAATATGT | 25909 |
rs776219616 | snp | A/G | 4.49226e-05 | 0.00473912 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246867226 | TGTGTCTCTAAGAAT[A/G]ATTTAATAAACTCTT | 25909 |
rs776234961 | snp | A/G | 1.66624e-05 | 0.00288633 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850336 | CGTACTAACTTTTAG[A/G]TCATTTATAATTTCA | 25909 |
rs776260810 | snp | C/T | 1.68476e-05 | 0.00290233 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246916392 | CAAGCAAGTCCATTT[C/T]TCCCTAGAAGAAAAA | 25909 |
rs776276508 | snp | A/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246925099 | TTGATAAAACTAGTT[A/T]AATGATGAACTGAAG | 25909 |
rs776331429 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246856238 | CCTAGAAAAAGTATG[A/G]TAAATGACTCAGAAT | 25909 |
rs776358251 | snp | A/T | 2.2186e-05 | 0.00333054 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246876198 | TCATTCTATTAAACA[A/T]CAAAATTGGTAAAAA | 25909 |
rs776358501 | snp | A/G | 1.65113e-05 | 0.00287322 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246888360 | CTCCCCAGCTTTGTA[A/G]ACTCTAAATGATAGC | 25909 |
rs776362997 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246880964 | AATGCATGGGGGTTC[C/T]TGGCAATACAGCAAA | 25909 |
rs776391663 | snp | C/T | 1.67119e-05 | 0.00289062 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246890107 | AATAATCCCCAAATA[C/T]CTCAACAATACATAT | 25909 |
rs776393882 | snp | G/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246911051 | AACCCTAAAGCTTAA[G/T]TTTTTGTGCTATAAA | 25909 |
rs776411680 | snp | A/C | 1.64988e-05 | 0.00287213 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246888198 | GTGTTTGGCTGCTTC[A/C]GTAACGCCGTCTAAT | 25909 |
rs776461417 | snp | C/T | 2.20821e-05 | 0.00332274 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246867326 | GGAGCGAATACACTA[C/T]AGGAGATGGTTCTTC | 25909 |
rs776487079 | in-del | -/TTA | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246848231 | AGTCATCTACTTTAT[-/TTA]TTATTATTATTATTT | 25909 |
rs776489117 | snp | A/G | 1.64982e-05 | 0.00287208 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246895947 | CATGCATTACAGAAA[A/G]GAAAGAAATGGAAAG | 25909 |
rs776489369 | snp | C/G | 1.64784e-05 | 0.00287035 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246898189 | CCAAAAGAAACAATA[C/G]AGTTAAAAATCATCT | 25909 |
rs776496158 | snp | A/G | 1.70249e-05 | 0.00291756 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246916230 | GTTTCTTCCAATCCT[A/G]TTAATAATCCAGTTC | 25909 |
rs776530870 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246923758 | GTGTGTGTGTGTGCG[C/T]GTAGCACACAGGAGC | 25909 |
rs776540223 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246903188 | AGAAAAGTCGGTTCT[A/G]GAGACAGGTATGTGA | 25909 |
rs776540344 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246870084 | GAATAACTTTTGAGG[C/G]CTTCAAGACTTCAGT | 25909 |
rs776555445 | snp | C/T | 1.64841e-05 | 0.00287085 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246851106 | CAATTTGTCCATGAT[C/T]ATCATTTTCCCCACT | 25909 |
rs776555868 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246875126 | CGACTTCCTTACCAT[A/G]ACATGCGACCTATAT | 25909 |
rs776556539 | snp | G/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246901698 | TGGTGTGTGCCGGCA[G/T]TCCCAGTTACTTGGG | 25909 |
rs776579708 | snp | C/G | 1.91676e-05 | 0.00309571 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246894611 | CATAAACCAAGGTTA[C/G]TATTTTAATATTAAA | 25909 |
rs776593992 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246848561 | TTCAAATATTAAACT[C/G]TAACTTAAATAGTCA | 25909 |
rs776624928 | in-del | -/A | 1.65046e-05 | 0.00287264 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246895962 | GAAAGAAATGGAAAG[-/A]AAAGAGGGTGTGAGA | 25909 |
rs776636117 | snp | C/G | | | intron-variant, missense, utr-variant-5-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246931201 | CCGGCCGCTTCCCTC[C/G]GGGAAAGGCCCGCCA | 25909 |
rs776638582 | snp | C/T | 0.000116726 | 0.00763868 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850772 | TTCACGTTTTGGATA[C/T]GTTGACCTCTCGTAC | 25909 |
rs776665163 | snp | A/G | 1.66632e-05 | 0.0028864 | synonymous-codon, splice-donor-variant, nc-transcript-variant, intron-variant | AHCTF1 | GRCh38.p7 | 1:246842696 | CAGAAAGTCATACTT[A/G]CTTGCTTGTTTTGTT | 25909 |
rs776684527 | snp | A/T | 1.6588e-05 | 0.00287988 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246860979 | TCAGTTTGTTCAGTT[A/T]CATTAGTAGTTAGTG | 25909 |
rs776737615 | snp | A/G | 1.67615e-05 | 0.0028949 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246860913 | CCCATTTGTTTCTGT[A/G]GGTCTGAAGGAGTTA | 25909 |
rs776751714 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246876338 | AAGAACTTCATCCAC[A/C]TATCTAATTTTTTTA | 25909 |
rs776751741 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246863292 | AGAGAACCCAGGGAC[A/G]ATGGGGAGGGGTGAG | 25909 |
rs776758772 | snp | G/T | 3.30409e-05 | 0.0040644 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246857721 | GGTGCACAAAGAGAA[G/T]CTTCAGTTCCTTGAA | 25909 |
rs776791923 | snp | A/T | 1.85441e-05 | 0.00304495 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246861920 | GCTAATACATTCTTA[A/T]TAAAAAATGTCTTTT | 25909 |
rs776797004 | snp | C/G | 0.001386 | 0.0262884 | intron-variant, missense, utr-variant-5-prime, upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246931315 | CGAACCACCAGCGCC[C/G]CTCCGCCGCCATGTG | 25909 |
rs776800372 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246858853 | CTGCCTAATATTGTA[A/G]GAATAATCAGTGAAG | 25909 |
rs776806795 | snp | A/T | 1.67066e-05 | 0.00289016 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246887183 | CTAGTAATTCATGAA[A/T]GTTTATGCTGTAAGT | 25909 |
rs776807947 | snp | C/T | 1.67346e-05 | 0.00289258 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246855845 | TTAGAAAAAGAAATA[C/T]ATACCTTAGTGTGTA | 25909 |
rs776810110 | snp | C/T | 6.61081e-05 | 0.00574888 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246864066 | CTTTGCTGAATAAAC[C/T]CCGAACACTGAGAAG | 25909 |
rs776818511 | snp | C/T | 3.30022e-05 | 0.00406202 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246890008 | CGACTGGTGTAGTAG[C/T]TCTGAATTACAGGGT | 25909 |
rs776874783 | in-del | -/AATT | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246928004 | ACTCCGCCACCAAAA[-/AATT]AATTAATTAATTAAA | 25909 |
rs776894710 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246870848 | ATTCTTGAAAATGGC[C/T]GGATTCTGTCACATA | 25909 |
rs776905203 | snp | C/T | 1.64751e-05 | 0.00287007 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246849848 | TTTTGGCTTTGACTT[C/T]CAGTCTTTTTTGTAA | 25909 |
rs776926702 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246929776 | ATATCTGTACCAGCC[A/G]GGCGCGGTGGCTCAC | 25909 |
rs776928750 | snp | G/T | 2.01266e-05 | 0.00317221 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246840995 | ACTTTCTTTTTCTGT[G/T]TTTCTGAAAAAAAAA | 25909 |
rs776937884 | in-del | -/A | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246903839 | CGAGACTCTGTCTCA[-/A]AAAAAAAAAAAAAAA | 25909 |
rs776939278 | snp | C/T | 1.66568e-05 | 0.00288585 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246900130 | GGAGGGACTCCTCTA[C/T]TTAAACTTCTCTCAT | 25909 |
rs776963320 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246870147 | CAAGAGAACTAGAAT[A/G]AGAAGCAGAGCCTAG | 25909 |
rs776981157 | in-del | -/A | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246894417 | TCTACTAAAAAATAC[-/A]AAAAAAATTAGCCGA | 25909 |
rs776985432 | in-del | -/AAGAT | 4.70572e-05 | 0.0048504 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246851455 | CACCTAAATGAATTA[-/AAGAT]AAGAGACTGGTTAAA | 25909 |
rs777009869 | snp | C/T | 1.64912e-05 | 0.00287147 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850195 | TTCTCTCCCTCTGAC[C/T]CTTCTAACATGTTTA | 25909 |
rs777040366 | in-del | -/TA | 2.06499e-05 | 0.00321318 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246843974 | CTTTATATATGTGTG[-/TA]TATATATATAAACAC | 25909 |
rs777048628 | snp | C/T | 3.30956e-05 | 0.00406776 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246891855 | AAGAAGCAAATAGCA[C/T]TGCTGGATAGACTGT | 25909 |
rs777073621 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246864649 | GACCATCCTGGCTAA[C/T]AAGGTGAAACCCCGT | 25909 |
rs777126355 | snp | A/G | 6.7906e-05 | 0.00582652 | utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246840782 | ACTTTACAAATAGGT[A/G]TACATTAAAATCTTC | 25909 |
rs777132046 | snp | C/T | 1.8571e-05 | 0.00304715 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246918403 | TTTTAAAAGAAAACA[C/T]TATTATGACACATTT | 25909 |
rs777147489 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246926559 | ACATCGAAACACTCT[A/C]TTATTAGAAATAGGG | 25909 |
rs777153406 | snp | C/G | 1.64749e-05 | 0.00287005 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246849751 | GAAGGAAGCTGTGGC[C/G]AGCAATCTTTCTTCC | 25909 |
rs777178026 | snp | C/T | 2.01311e-05 | 0.00317256 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246861256 | GAACTGCACATTTTT[C/T]AGGTGTAGTAAATAC | 25909 |
rs777183632 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246920101 | GCCGAGATTGTGCAA[C/T]TGCACTCCAGCCTGA | 25909 |
rs777188388 | snp | G/T | 2.08627e-05 | 0.00322969 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246905684 | TAGTATATTTCATAT[G/T]TTTAAGTTATTTTTT | 25909 |
rs777199000 | snp | C/T | 2.89457e-05 | 0.00380421 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246885700 | AAATAACATGAAAAA[C/T]GTTAAATATAAATAT | 25909 |
rs777201478 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246918553 | TTAAGTCCCAGCTAC[C/T]TGGGAGGCTGAGGCA | 25909 |
rs777204568 | snp | C/T | 6.59935e-05 | 0.0057439 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850836 | TGACATTCATAGTCA[C/T]TGTGCTTGTTTCCTG | 25909 |
rs777211448 | snp | A/G | 1.64982e-05 | 0.00287208 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850713 | GCCCTGGCATCTTAG[A/G]AGTAGCAACATCTGC | 25909 |
rs777223927 | snp | C/T | 6.67534e-05 | 0.00577687 | intron-variant, downstream-variant-500B | AHCTF1 | GRCh38.p7 | 1:246842643 | AGGGTGGGGACAGAG[C/T]GAGACTGTCTCAATC | 25909 |
rs777255162 | snp | G/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246845581 | TCACTTTTCGTAATC[G/T]TCACCTAAGCTTTCC | 25909 |
rs777322500 | snp | C/T | 1.65045e-05 | 0.00287263 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246887317 | GGAGTGTCTGTTTTG[C/T]TGGGAAAGGAATACA | 25909 |
rs777334366 | snp | C/T | 1.66944e-05 | 0.0028891 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246900422 | TTCCCTGTCCATATA[C/T]ATTCACCTGCCAGGT | 25909 |
rs777357927 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246870560 | CAGTGTTGAAATGAT[A/G]AAGTGTAAACAGATA | 25909 |
rs777373204 | snp | A/C | 1.65075e-05 | 0.00287289 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246889980 | CCTTGATAAACGCTC[A/C]AACTTCTGTCGACGA | 25909 |
rs777379821 | snp | C/G | 0.000142542 | 0.008441 | intron-variant, missense, utr-variant-5-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246931219 | GAAAGGCCCGCCAAC[C/G]AGTCCATCGCGTGGG | 25909 |
rs777380264 | snp | A/G | 1.65614e-05 | 0.00287757 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246905535 | CAAAGTTTGTATGAG[A/G]CCTACCTATCTTGTG | 25909 |
rs777383893 | in-del | -/AA | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246913948 | CAAAAAAGATATTTT[-/AA]AAGTCCTCTTTATAC | 25909 |
rs777389148 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246848934 | ATGGGATCTATTCAG[A/C]CACACCAGTGTCTTA | 25909 |
rs777391033 | snp | A/G | 1.68258e-05 | 0.00290045 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246885567 | CTTCATTGTCTGAAT[A/G]TATCTGAGGGCTTGT | 25909 |
rs777393086 | in-del | -/CTT | 6.61583e-05 | 0.00575107 | cds-indel, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850002 | TTCTAATGCTGGGAG[-/CTT]CTTTCTTCTTGGGGC | 25909 |
rs777394908 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246845426 | ATCTCTGCTCCCAGC[C/T]TGTAAATGGCAGAAA | 25909 |
rs777395525 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246930161 | TTTATTTTAGCAACA[A/G]GTTCTCGCTCTGTCA | 25909 |
rs777416743 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246877659 | CACTCAGTGGGAAGC[A/G]TGCGAAAGACTGAGA | 25909 |
rs777439526 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246847341 | CTCATGACATAAGTA[A/G]GGGGACAAAAGCAGA | 25909 |
rs777440135 | snp | C/T | 6.69658e-05 | 0.00578605 | utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246840795 | GTGTACATTAAAATC[C/T]TCCCAAGAAATTACA | 25909 |
rs777447877 | in-del | -/C | 3.33428e-05 | 0.00408293 | intron-variant, downstream-variant-500B | AHCTF1 | GRCh38.p7 | 1:246842671 | TCAATCAATCAATCA[-/C]AGAACAGAACAGAAA | 25909 |
rs777469605 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246880489 | GAATCACTTGAACCC[A/G]GGAGGTGGAGGTTAC | 25909 |
rs777497040 | snp | C/T | 3.27327e-05 | 0.0040454 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246861327 | TGAAAAGAAAAAAAT[C/T]AGTAAATATCACAGT | 25909 |
rs777582799 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246927977 | TGCACTCCAGCCTGG[C/T]GACAGAGCAAGACTC | 25909 |
rs777658602 | in-del | -/TTATAGAT | 2.4674e-05 | 0.00351232 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246890932 | TGTTTTAATTAATAC[-/TTATAGAT]TAAGTAAATATTTTA | 25909 |
rs777668786 | in-del | -/TTCT | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246884147 | GTTACCACATTTAGC[-/TTCT]TTATTTTGTTCTTAC | 25909 |
rs777697550 | snp | A/G | | | upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246932389 | TGCCAGCTGGGGGCC[A/G]AGTGATAATCTTTCT | 25909 |
rs777705950 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246902739 | TCACTCTAAAATTAA[A/G]TATTCTCCAAATTTA | 25909 |
rs777718699 | snp | A/C | 1.64741e-05 | 0.00286998 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246849712 | CTTGCTAGACCGAGT[A/C]CTGCTGCTGCGGGAT | 25909 |
rs777775870 | snp | G/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246846131 | GTATATAGCAGGCCC[G/T]TCTTAATATCTGCTG | 25909 |
rs777790686 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246913648 | TGATGTTGACTGAGA[A/G]CTTACTGATACGCCA | 25909 |
rs777864976 | snp | G/T | 1.70542e-05 | 0.00292007 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850395 | TAATTCTTCTAGGAG[G/T]CCTTTTTGTAACAGA | 25909 |
rs777880388 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246883234 | ATGTAATCAAATCAT[C/T]TGGGTGTTGGACTAT | 25909 |
rs777888853 | snp | A/C | 1.71655e-05 | 0.00292958 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246864149 | ATTTATTGAGTTATA[A/C]TGAAAAAACAAAAGA | 25909 |
rs777907891 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246877695 | AGATGGAAACAAGCA[C/T]GCTGTGTCCATGAGG | 25909 |
rs777928006 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868420 | GCCACTGCGCCTGGC[A/G]ATTTTTGTATTTTTA | 25909 |
rs777935709 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246854026 | AAAATCTGGCTGGGC[A/G]CAGTGGCTCACGCCT | 25909 |
rs777997631 | snp | A/G | 3.38055e-05 | 0.00411116 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246918229 | ATTGTATTAGTAAAT[A/G]TTCAGTGACATTATG | 25909 |
rs777998767 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246924068 | TCCCCCTCCTATCTA[C/T]TGAGTACAGAAAGGA | 25909 |
rs778023020 | snp | C/G | 1.65124e-05 | 0.00287331 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246902657 | CCAGGGTGTATCTTT[C/G]TTCACAGTATTCTAA | 25909 |
rs778026421 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246915000 | TCCTCGCTGACCCAA[C/T]CCAAGCAAGCCTTTT | 25909 |
rs778039087 | snp | A/T | 1.73228e-05 | 0.00294297 | missense, nc-transcript-variant, intron-variant | AHCTF1 | GRCh38.p7 | 1:246843919 | TGTGCAGGAACCTCT[A/T]TTTTTTTAGCTAAAA | 25909 |
rs778050607 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246855565 | GTCTGACAGCTTATA[C/T]ATCTCCTTAGAATAC | 25909 |
rs778053682 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246874628 | AACATTAACTTATCC[C/T]TACGTCTTGAACCTC | 25909 |
rs778054784 | in-del | -/TATC | 1.6477e-05 | 0.00287024 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246877317 | CCTGAAAGCAGTATT[-/TATC]AAAGTTTAGTTTTAG | 25909 |
rs778054918 | snp | C/T | 6.59141e-05 | 0.00574045 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246895892 | GGGAACTAGTCTGAA[C/T]TGCTGCTGACAATAT | 25909 |
rs778092310 | snp | G/T | 1.91889e-05 | 0.00309743 | missense, nc-transcript-variant, intron-variant | AHCTF1 | GRCh38.p7 | 1:246843835 | TTGGATGTGTTTTTT[G/T]GTCTGCTCCTTAAAG | 25909 |
rs778112639 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246841510 | TCACGTGTGCTTTTA[C/T]TGAATTCAACCATGC | 25909 |
rs778121719 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246847864 | TATATTCCTCCAGGT[C/T]CTGAGGAGTGTATAA | 25909 |
rs778132210 | snp | C/T | 3.2987e-05 | 0.00406108 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246877000 | AGGCAGGCACATAAT[C/T]GGCACGCTGCAAATG | 25909 |
rs778139678 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246873171 | TGTTAAGTAAATGTG[C/T]CCTTGCCATACTCTT | 25909 |
rs778154947 | snp | A/G | 1.65979e-05 | 0.00288074 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246900321 | AGAAAGGAGAGAGAA[A/G]AAAAAAGAATCATAC | 25909 |
rs778158536 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246893974 | TTTGGAAGGCCCAGG[C/T]AGGAGGATCGCTTGA | 25909 |
rs778160549 | snp | C/T | 3.29832e-05 | 0.00406085 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246861016 | AAGAGCTTTTGGGCT[C/T]AGAGGCCGTGAAAAC | 25909 |
rs778162111 | snp | A/C/G | 3.30919e-05 | 0.00406756 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850009 | GCTGGGAGCTTCTTT[A/C/G]TTCTTGGGGCTTCTC | 25909 |
rs778182882 | snp | C/T | 1.65081e-05 | 0.00287293 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246888269 | ACCTTCAGTGGATCT[C/T]ATACAGTCATTCATT | 25909 |
rs778202411 | snp | C/T | | | downstream-variant-500B | AHCTF1 | GRCh38.p7 | 1:246838972 | ATCTCTCTGAGTACA[C/T]TGTTTACCTTACTAC | 25909 |
rs778202544 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246855662 | GATTATTTTGTTCTA[A/C]GAACAGAAAACTCTT | 25909 |
rs778203570 | snp | A/G | 1.69608e-05 | 0.00291206 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246907782 | ACAAATTAGACAAAT[A/G]AAGTTAAAAAACTAG | 25909 |
rs778207893 | snp | C/G | 1.64906e-05 | 0.00287142 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246913280 | AGTCATCCAAACATA[C/G]GTCAACAAGAAGGAT | 25909 |
rs778213251 | snp | G/T | 3.29723e-05 | 0.00406018 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246851155 | AGTTGCTGTGTTAGC[G/T]GCTTTAGGTAACACA | 25909 |
rs778215011 | snp | C/G | 1.65589e-05 | 0.00287736 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246849939 | CTAAAGCTGGTTTTC[C/G]AACATCAACATTTTC | 25909 |
rs778216993 | snp | A/C | 1.92361e-05 | 0.00310124 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246862188 | GAATTACACCATTAA[A/C]AGTGCTTATAGGCCG | 25909 |
rs778218281 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246922358 | GAGCAAGACTCTGTC[C/T]CAAATAAAAGGGAAA | 25909 |
rs778227594 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246863889 | AGTAAGAGCCATCTA[A/G]TTTGATTGTGAACGC | 25909 |
rs778254721 | in-del | -/TTTA | | | upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246933125 | AATTTTTTTATTTTA[-/TTTA]TTTATTTATTTATTT | 25909 |
rs778270387 | snp | C/T | 1.64901e-05 | 0.00287137 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246851088 | CGGCAGATGGCAAAT[C/T]TGCAATTTGTCCATG | 25909 |
rs778282058 | snp | A/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246909879 | GTAGCAAGTAGCACC[A/T]GCAGTAACAATCAAA | 25909 |
rs778295376 | snp | A/G | 1.66671e-05 | 0.00288674 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246905656 | CCAATTGTATGTAAT[A/G]TCTGAAACAAATTAG | 25909 |
rs778299314 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246906319 | GCGTGGTAGCTCACA[C/T]CTGTAATCCCAGCAC | 25909 |
rs778313672 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246871724 | ATTTTTTTTTGAGGC[C/T]TCCTGACTGCAGACT | 25909 |
rs778325584 | snp | G/T | 1.96412e-05 | 0.00313372 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246876013 | GATCCAATAGATTAT[G/T]ATATTCTTCAATGAA | 25909 |
rs778328927 | snp | C/T | 4.94996e-05 | 0.00497467 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246888458 | CACAACTTCTCAATT[C/T]GCTCTCCTAACTGAG | 25909 |
rs778413892 | snp | A/G | 1.64901e-05 | 0.00287137 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246887271 | AACTTGGCCCCAAGA[A/G]ATGGCAAATACAGTT | 25909 |
rs778422886 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246872704 | CTTCCCATCGCACTA[C/T]CATGGGTGCTGAAAG | 25909 |
rs778443140 | snp | C/G | 3.29625e-05 | 0.00405958 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246907585 | TGTTCCAAAGTGCTA[C/G]ATAGCCATCAGAAAA | 25909 |
rs778461035 | in-del | -/T | 0.000121956 | 0.00780788 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246853319 | AGAAAAATGAGTGAA[-/T]TTTTTTACATTTAAA | 25909 |
rs778461601 | in-del | -/CTTTAAAAATGGAAAG | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246863392 | AAAAAAAAAACAAAA[-/CTTTAAAAATGGAAAG]GTTTAAAAAGGCCAC | 25909 |
rs778469454 | snp | G/T | 3.32121e-05 | 0.00407492 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246894681 | GTCAAATTCCTCTTT[G/T]GTGAGAACCACTTTA | 25909 |
rs778476183 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246897300 | GTCTGGGCAACAGAC[C/T]GAGATGCTGTCTCAA | 25909 |
rs778481874 | snp | C/T | 1.64749e-05 | 0.00287005 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246849807 | TTTCATCTGTGCGTT[C/T]TTCTGATACTGAGTG | 25909 |
rs778605979 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246896731 | GTATGAAATATCTCA[A/G]TAAAGCTGATATTTT | 25909 |
rs778606984 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246908485 | CCTGTTCTGTAGACA[C/T]TGTGTTTCAGAGTGA | 25909 |
rs778622677 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246927352 | GTAGCAGCCAGCCAC[A/G]GCTGCATACGCTTGT | 25909 |
rs778634742 | snp | C/T | 1.78404e-05 | 0.00298662 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246853185 | CCAACTTCTACTTCA[C/T]GATCTTCTTTTAAGT | 25909 |
rs778646887 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246880206 | AATAGCTTATTATCA[A/C]AAACAATATGTTATT | 25909 |
rs778667802 | snp | C/T | 3.67667e-05 | 0.00428743 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246885709 | GAAAAATGTTAAATA[C/T]AAATATAATCCTATA | 25909 |
rs778684218 | in-del | -/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246870723 | GAGGGTATAAAACCT[-/C]AAAAAAAAAAAAAAA | 25909 |
rs778765894 | snp | G/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246928041 | AATACTGTTCGGCCG[G/T]GTGCGGTGGCTCACG | 25909 |
rs778792987 | snp | C/T | 1.65938e-05 | 0.00288039 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246877231 | CAGACTTCATACATG[C/T]GCTTCAGTAACTCCT | 25909 |
rs778802070 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869616 | TGGGAAATCTACTAT[A/G]CCTGTCTTCTATCAA | 25909 |
rs778823379 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246882463 | GGGAAAATAAACAAC[C/T]GTAATGAAAATTTAA | 25909 |
rs778840802 | snp | C/T | 9.25318e-05 | 0.00680127 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246876139 | CATACTGGTCTAATA[C/T]AGAATTTCGAGCCAG | 25909 |
rs778843387 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246889438 | GCAGGATTAGAAAGC[A/G]TAACAAAGCTGCCAA | 25909 |
rs778846926 | snp | C/G | 4.71665e-05 | 0.00485603 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246861341 | TTAGTAAATATCACA[C/G]TTAAGTCTAGTCCTA | 25909 |
rs778882662 | snp | C/T | 2.87204e-05 | 0.00378937 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246851470 | AAGATAAGAGACTGG[C/T]TAAAGAATTTTAATA | 25909 |
rs778902082 | snp | A/G | 1.65323e-05 | 0.00287505 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246888487 | AGAAACCAGTCCATC[A/G]ATCATCAAGCAATCG | 25909 |
rs778912850 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246875027 | TTAAAACCATCTCCT[A/G]ACAGGCCAACAACTT | 25909 |
rs778944314 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246902880 | CTCTCAAAAATAATT[A/C]CCAACAAGTCTTCTA | 25909 |
rs778956201 | snp | C/T | 1.66701e-05 | 0.002887 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246900077 | TACCAAAATTATAAG[C/T]GCTTGGATTAAAAAA | 25909 |
rs778959386 | in-del | -/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246858815 | AAAAAAAAAAAAAAA[-/T]AAATACAAATTTCTA | 25909 |
rs778980579 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869243 | GTACTTACTCCACTG[A/G]CTAACTGTTCCCCCG | 25909 |
rs779012022 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246910913 | TTAAGTCTGGGGAAG[A/C]TGCAGAACAATATTT | 25909 |
rs779041561 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246874787 | CTCCTTTAACATCTC[C/T]AGACACATATCCCTG | 25909 |
rs779093632 | snp | G/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246841674 | ATAGTTACCTAACTT[G/T]CCTGACAAAGAGGTA | 25909 |
rs779094017 | in-del | -/C | 3.3657e-05 | 0.00410212 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246905496 | AGCGAGACTCTGTCT[-/C]CAAAAAAACAAAACA | 25909 |
rs779101629 | snp | C/T | 8.24219e-05 | 0.00641905 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246913304 | GAAGGATCTGTCCAA[C/T]ATCAGTGACCACAGC | 25909 |
rs779102208 | snp | A/G | 1.6477e-05 | 0.00287024 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246898290 | TTATAACCATCAGGA[A/G]TGAGTTCATTGAGTG | 25909 |
rs779102324 | snp | C/G | 3.30295e-05 | 0.0040637 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246888348 | CATGTCTCCTCCCTC[C/G]CCAGCTTTGTAGACT | 25909 |
rs779105377 | snp | A/G | 1.64844e-05 | 0.00287087 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246851163 | TGTTAGCTGCTTTAG[A/G]TAACACATCAGATGA | 25909 |
rs779121555 | in-del | -/GTGGTCTCTAACTAAAT | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246872096 | TCCCAAAAACCTAGG[-/GTGGTCTCTAACTAAAT]ATGGTCATAGATCAT | 25909 |
rs779122758 | snp | A/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246929446 | AAATACAGTGAAAAC[A/T]TTGGATTTAGAAGGA | 25909 |
rs779139911 | snp | G/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246911873 | GCATATTTAAGTTTT[G/T]TTCAGATGATTTTGG | 25909 |
rs779145843 | in-del | -/AAGAT | 0.00053343 | 0.0163227 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246891938 | TCAAGAATAAAAGAA[-/AAGAT]AAGTTTCCATACAGT | 25909 |
rs779151716 | snp | C/G | 1.64833e-05 | 0.00287078 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246898171 | GCTAATAACGTGATC[C/G]AACCAAAAGAAACAA | 25909 |
rs779226636 | snp | C/T | | | upstream-variant-2KB | AHCTF1 | GRCh38.p7 | 1:246932053 | AGTTCTCGCGATGGT[C/T]CCGCGCTCTAGCGCC | 25909 |
rs779243360 | snp | A/C | 1.68459e-05 | 0.00290219 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246905490 | CAACAGAGCGAGACT[A/C]TGTCTCCAAAAAAAC | 25909 |
rs779247793 | snp | A/T | 1.6643e-05 | 0.00288465 | synonymous-codon, nc-transcript-variant, intron-variant | AHCTF1 | GRCh38.p7 | 1:246842738 | GATTCGTTTCGCTTT[A/T]GGCTTTCCCAGAGTT | 25909 |
rs779264554 | in-del | -/CT | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246889284 | CTCTTCTTTTTTCCC[-/CT]CTGATTTCCTTTTCT | 25909 |
rs779268358 | snp | G/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246862574 | CAATAAACATATCAA[G/T]AGAAATATTTATTCC | 25909 |
rs779268815 | snp | C/G | 6.59152e-05 | 0.00574049 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246863953 | GAGTTTCAAGCAAAT[C/G]TAATTCTGAAGCCCT | 25909 |
rs779280036 | in-del | -/TAAAAGTGAAAATGTTGA | 1.64988e-05 | 0.00287213 | cds-indel, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850219 | TGTTTAATACGCAGC[-/TAAAAGTGAAAATGTTGA]TGCTTGTCACTGGAT | 25909 |
rs779283511 | snp | A/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246896010 | TTTAGAATTTAAAAA[A/T]TTTAAGGCTAAAAAA | 25909 |
rs779296051 | snp | G/T | 1.64751e-05 | 0.00287007 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246867633 | GATTAACAAGCAGCA[G/T]GACTATGAAACGTGT | 25909 |
rs779300922 | snp | C/T | 1.67153e-05 | 0.00289091 | intron-variant, downstream-variant-500B | AHCTF1 | GRCh38.p7 | 1:246842653 | CAGAGCGAGACTGTC[C/T]CAATCAATCAATCAA | 25909 |
rs779316068 | snp | A/G | 1.64925e-05 | 0.00287158 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246877006 | GCACATAATTGGCAC[A/G]CTGCAAATGGTGCAC | 25909 |
rs779324317 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246855090 | GGAACAAAGGCATAA[C/T]AGTTGAGAGCATGGG | 25909 |
rs779327424 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246898973 | GAGCACCTGTAATCC[C/T]AGCTATTCAGGTGGC | 25909 |
rs779358182 | snp | A/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246851888 | ATCCCCGTAAGGTTG[A/T]AGAACAATTCACCTA | 25909 |
rs779406638 | snp | A/G | 1.65111e-05 | 0.0028732 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246864048 | AAAGGAGATTTCATG[A/G]AGCTTTGCTGAATAA | 25909 |
rs779421853 | snp | C/T | 1.67832e-05 | 0.00289677 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246900449 | AGGTAAAGACTGAAA[C/T]ACTAGTGTCAGGCGA | 25909 |
rs779434747 | snp | C/G | 1.66527e-05 | 0.00288549 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246900118 | GGTGGATATGAAGGA[C/G]GGACTCCTCTATTTA | 25909 |
rs779449978 | snp | A/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246849438 | GTTAACCATACTGAA[A/T]AACTGAACTCAAACT | 25909 |
rs779458999 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246857462 | AAAAACAGAATCACC[A/G]GAGTTCTGCCTCAAT | 25909 |
rs779504666 | snp | C/T | | | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246867319 | GGAGCTGGGAGCGAA[C/T]ACACTATAGGAGATG | 25909 |
rs779507700 | snp | C/T | 1.66774e-05 | 0.00288763 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246913423 | GTTACCTAGAAAACA[C/T]AATACGTGATTTGCT | 25909 |
rs779527555 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246927555 | ACACAAACACACATG[A/C]AACACCTACGTTCAG | 25909 |
rs779543619 | snp | C/G | 1.64817e-05 | 0.00287064 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246907729 | TAATGTGTGGTACTT[C/G]AGCTGGGATACCAGT | 25909 |
rs779549133 | snp | A/C/T | 3.41968e-05 | 0.00413488 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246861948 | TTTCTCCCAATTATT[A/C/T]TCAAACTTACCCCAG | 25909 |
rs779553793 | snp | A/C | 1.89095e-05 | 0.0030748 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246876159 | TTTCGAGCCAGTGAT[A/C]TCTCCCGCAAACGAG | 25909 |
rs779567378 | snp | A/C | 1.6638e-05 | 0.00288422 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246900208 | GACTCCAATGACCAC[A/C]GTGCAAAATAAGAGC | 25909 |
rs779602859 | snp | A/G | 1.66579e-05 | 0.00288595 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246862044 | GACCTTCCAGGTGAT[A/G]GAGAGGGAGATGCTA | 25909 |
rs779606839 | snp | C/T | 3.44157e-05 | 0.00414809 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246887409 | AACAAAAACCTCCTA[C/T]GTATATATTTACAAT | 25909 |
rs779613549 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246892856 | TTGCTATATTGCTCA[A/G]GCTGGTCTTGAACTC | 25909 |
rs779707462 | snp | A/G | 3.70617e-05 | 0.00430459 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246843952 | AGTTGAAAAAACTGT[A/G]TCTGTATCTTTATAT | 25909 |
rs779735730 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246917003 | CTCTTCTCCGCCTAT[C/T]AGTCATGTTTGGATT | 25909 |
rs779736190 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246882780 | GTGCATCATGGTTAA[C/T]TTGCACGTAAAACAG | 25909 |
rs779738371 | snp | A/G | 1.64803e-05 | 0.00287052 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246907588 | TCCAAAGTGCTAGAT[A/G]GCCATCAGAAAAACC | 25909 |
rs779749038 | snp | A/G | 1.65094e-05 | 0.00287305 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246849891 | AGCTCATCACCATCG[A/G]AAGTTCCTCGTTTGG | 25909 |
rs779757812 | snp | A/C | 1.6501e-05 | 0.00287232 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850928 | GGTATTGTTTCATGA[A/C]TGGACTGTTCCATTG | 25909 |
rs779761716 | snp | A/C | 3.44988e-05 | 0.0041531 | utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246840774 | TTCTGATGACTTTAC[A/C]AATAGGTGTACATTA | 25909 |
rs779762323 | snp | C/T | 2.53926e-05 | 0.0035631 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850550 | TCTAGTATGTCCTGA[C/T]TAACTTCTTTCTTTC | 25909 |
rs779782678 | snp | C/T | 1.76375e-05 | 0.00296958 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246876056 | TCGAAAAACTGATGA[C/T]GTTGACAGATGATAA | 25909 |
rs779796793 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246880977 | TCTTGGCAATACAGC[A/C]AAGACAGACTGAAAA | 25909 |
rs779836144 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246847087 | AGGTCAGGCGTTTGA[A/G]ACTAGCTTGGCCAAC | 25909 |
rs779910929 | snp | G/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246847547 | CTGTTGCCCAGGCTG[G/T]AGTGCAGGGGCACAC | 25909 |
rs779922668 | snp | A/G | 7.13827e-05 | 0.0059738 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246853285 | TTCCACCATCACCAA[A/G]GACATCAGCCATAGC | 25909 |
rs779943622 | in-del | -/GAAA | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246877684 | TGAGATCTATAGATG[-/GAAA]GAAACAAGCACGCTG | 25909 |
rs779948316 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246844139 | CCAAATGTGTAGGAC[A/G]ATTGAATGCTTCAAA | 25909 |
rs779977730 | snp | A/G | 1.77596e-05 | 0.00297985 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246862156 | AACTTTTAGCTTTCT[A/G]TAGTAAAGAGCAAAT | 25909 |
rs779991299 | snp | A/C | 1.65165e-05 | 0.00287367 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850266 | TTCCTGTATTTTCAG[A/C]AGCATCTAAATTAGT | 25909 |
rs779999268 | snp | C/T | 1.74622e-05 | 0.00295479 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850407 | GAGTCCTTTTTGTAA[C/T]AGATGAAACCTTAAC | 25909 |
rs780009140 | snp | G/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246842932 | CTTTTAGTAGAAACC[G/T]TAGTTATGCAGGCCT | 25909 |
rs780038506 | snp | C/T | 1.69651e-05 | 0.00291243 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246916125 | AGAAATGTCCAGGTA[C/T]CTTAAACAGTACCTA | 25909 |
rs780077578 | snp | A/C | 1.76197e-05 | 0.00296809 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246891077 | TGTAAAGAAGAGTTA[A/C]CATCAGTTGTTTACT | 25909 |
rs780090219 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246904686 | TACTAAATCAACCCT[C/G]TAGTGAACTCAAGCA | 25909 |
rs780121835 | snp | C/G | 1.81125e-05 | 0.00300931 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246877335 | CAAAGTTTAGTTTTA[C/G]AAAAAGCTATTTAAA | 25909 |
rs780157059 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246924777 | TAAGTCACAAAACCT[A/G]AAAAGTTATGTTTGA | 25909 |
rs780171920 | snp | A/C | 3.33506e-05 | 0.0040834 | intron-variant, downstream-variant-500B | AHCTF1 | GRCh38.p7 | 1:246842670 | AATCAATCAATCAAT[A/C]AAGAACAGAACAGAA | 25909 |
rs780201324 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246911994 | GCTGGAGTGCAGTGG[C/T]GTGATCTCGGTTCAC | 25909 |
rs780224423 | in-del | -/A | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246887397 | ATAAAATACAACAAC[-/A]AAAACCTCCTACGTA | 25909 |
rs780228627 | snp | A/C/T | 0.000197868 | 0.0099447 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850179 | CATCTGATGGACTAA[A/C/T]TTCTCTCCCTCTGAC | 25909 |
rs780235960 | in-del | -/T | | | utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246840339 | AAACAAAAAAATACA[-/T]TTTTCTGATTAGAAA | 25909 |
rs780240138 | snp | A/G | 1.7598e-05 | 0.00296626 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246900473 | CAGGCGATAGAGCTG[A/G]AAGAAAAAGATAATT | 25909 |
rs780245922 | snp | G/T | 1.64849e-05 | 0.00287092 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246877035 | ACTAAAAGGAATTCA[G/T]GATTCTGAACGCTGG | 25909 |
rs780297258 | snp | A/T | 0.000132868 | 0.00814963 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246888506 | ATCAAGCAATCGGGA[A/T]TCCACTTCCCTCTGC | 25909 |
rs780302772 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246866372 | AATGTCGGTAATAAC[A/G]ACTTTCATTTAAAAT | 25909 |
rs780312818 | snp | C/T | 3.31148e-05 | 0.00406894 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246889952 | ATGTAATTTCTAAAA[C/T]TGTTTTACTATACCT | 25909 |
rs780317212 | snp | A/G | 1.66824e-05 | 0.00288806 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246900061 | ATGTTAAGGAAATAC[A/G]TACCAAAATTATAAG | 25909 |
rs780328113 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869837 | ACAACATCCATTCTG[C/T]AACCCTGGATCACAG | 25909 |
rs780328299 | snp | G/T | 7.9818e-05 | 0.00631685 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246851433 | CTTCAAGCTTTTCTT[G/T]TTCAATCACCTAAAT | 25909 |
rs780363517 | snp | C/T | 3.32745e-05 | 0.00407875 | missense, nc-transcript-variant, intron-variant | AHCTF1 | GRCh38.p7 | 1:246842746 | TCGCTTTTGGCTTTC[C/T]CAGAGTTTCTACTGA | 25909 |
rs780379363 | snp | C/T | 4.9525e-05 | 0.00497595 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246851328 | AAAACTGTTGGTCAA[C/T]AGTATCAAAATTGTA | 25909 |
rs780390071 | snp | C/T | 1.67089e-05 | 0.00289035 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246857679 | TATTTGAATTTCTCT[C/T]CATTAACTTACCCTT | 25909 |
rs780404998 | snp | A/G | 1.64953e-05 | 0.00287182 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246887301 | TGGGAAAGATTCAAT[A/G]GGAGTGTCTGTTTTG | 25909 |
rs780423466 | snp | A/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246852248 | CTTCCCAACTAAAAG[A/C]ACTGGAACTTTACTC | 25909 |
rs780436531 | snp | C/T | 1.64988e-05 | 0.00287213 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246861124 | TGTTTCCTTTGCTCA[C/T]ATCCAGTTTCTCTAA | 25909 |
rs780455875 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246885065 | AATCTCAATTTGGCG[C/T]CCCTCCCTTTTATTC | 25909 |
rs780496031 | in-del | -/A | 1.65016e-05 | 0.00287238 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246877097 | TAAAAAGAACAAAAT[-/A]AGATTGTAAACTACC | 25909 |
rs780505403 | snp | A/T | 1.65902e-05 | 0.00288008 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246864111 | TGAACAACCAAATCT[A/T]GCAGTCTGTAATCAG | 25909 |
rs780521481 | snp | C/T | 5.02685e-05 | 0.00501316 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246857811 | TCTGCATCTTCTAAA[C/T]TGCCTATAAGTCATA | 25909 |
rs780533964 | snp | C/G | | | downstream-variant-500B | AHCTF1 | GRCh38.p7 | 1:246838706 | AAGCAAGTCTTGATC[C/G]ACCTTTGACAAAGCC | 25909 |
rs780553243 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246930198 | CTGAGTGCAGCGGCG[C/G]GATCCTAGCTCACTG | 25909 |
rs780564661 | snp | C/G | 1.65644e-05 | 0.00287783 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246877214 | TCAAGCCCATTTCCT[C/G]ACAGACTTCATACAT | 25909 |
rs780573673 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246854888 | CATATCGGGAGAAAT[A/G]GGCACAGAAAACAAA | 25909 |
rs780623206 | snp | A/G | 4.49741e-05 | 0.00474184 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246853313 | AGCTGAAAGAAAAAT[A/G]AGTGAATTTTTTACA | 25909 |
rs780626309 | snp | A/C | 1.6546e-05 | 0.00287624 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246891786 | GAGCGTACCTCTCTC[A/C]GTGATCTCTCGGGCT | 25909 |
rs780642779 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246930984 | GTGGCAAAAGAAACC[A/G]TCCTGTTTCCCAGGT | 25909 |
rs780676123 | snp | C/T | 1.64749e-05 | 0.00287005 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246862181 | GCAAATGGAATTACA[C/T]CATTAAAAGTGCTTA | 25909 |
rs780691871 | in-del | -/AAAT | 1.66765e-05 | 0.00288756 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246855839 | TTCCTTTAGAAAAAG[-/AAAT]AAATACATACCTTAG | 25909 |
rs780704727 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246884231 | TGATTCTAGATTAAG[C/T]TATCTAAACATTTTT | 25909 |
rs780715605 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246849290 | AATGCAGCAGTACAT[C/G]GGAGATTAAAAATAT | 25909 |
rs780728492 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246928405 | TATTCCTGGGCATTC[A/G]ACAAGGTCACAGTGC | 25909 |
rs780738143 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246882887 | AAATGCAAAGATGCT[C/G]TTAATGAGGAAACTC | 25909 |
rs780755393 | snp | C/T | 1.65269e-05 | 0.00287457 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246902554 | TCCTCCCTGTCACCA[C/T]GAGATCGAAATTTCT | 25909 |
rs780758041 | snp | C/T | 1.651e-05 | 0.0028731 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246913260 | TTCATTTTGATTGCA[C/T]GACAAGTCATCCAAA | 25909 |
rs780784739 | snp | C/G/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246858279 | CTTCTTCTTCTAATT[C/G/T]TCTGAACCTAGCTCA | 25909 |
rs780790585 | in-del | -/AAAAC | 0.277778 | 0.248452 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246905500 | GACTCTGTCTCCAAA[-/AAAAC]AAAACAAAACAAAAC | 25909 |
rs780802911 | snp | A/C/G | 3.29561e-05 | 0.00405921 | synonymous-codon, missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246898298 | ATCAGGAATGAGTTC[A/C/G]TTGAGTGATGGACCT | 25909 |
rs780805476 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246888681 | TGGGAGGCCAAGGCA[C/G]GAGGATCAACTCAAG | 25909 |
rs780820447 | snp | C/T | 3.59848e-05 | 0.00424159 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246891089 | TTAACATCAGTTGTT[C/T]ACTTACAAAAAAATC | 25909 |
rs780850591 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246839527 | CGTAACATCCATCAC[C/T]AACCTGACTAAAAGG | 25909 |
rs780851394 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246898718 | AAAGAGATTTGATAT[C/T]AAGTATAAATACAGC | 25909 |
rs780870162 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246870419 | CAGACAAAGACCTTG[C/T]CTCTTAAAAAAACAA | 25909 |
rs780873479 | snp | A/G | 1.66358e-05 | 0.00288402 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246900218 | ACCACAGTGCAAAAT[A/G]AGAGCAATTATGTAG | 25909 |
rs780881893 | snp | C/T | 1.65438e-05 | 0.00287605 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246918265 | CTGCAGCAAACTTTC[C/T]ACGAAGCACAGATTC | 25909 |
rs780896259 | snp | A/G | 1.67632e-05 | 0.00289505 | missense, synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246840964 | GCCGAATTTCTATGG[A/G]AGGAGGTGACCAAGC | 25909 |
rs780900382 | snp | A/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246863710 | CCACACAGAACCCTA[A/T]ATTACCTTTAAGAAA | 25909 |
rs780905653 | snp | G/T | 1.65408e-05 | 0.00287578 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246849906 | AAAGTTCCTCGTTTG[G/T]CACTAAAATGGATTT | 25909 |
rs780913527 | snp | A/G/T | 3.39647e-05 | 0.00412085 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246867808 | AATGGTTTGGGTCTA[A/G/T]AAACTGTAAAATGAA | 25909 |
rs780965250 | snp | A/G | 8.23703e-05 | 0.00641704 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246849704 | AAGATGGCCTTGCTA[A/G]ACCGAGTCCTGCTGC | 25909 |
rs780970673 | snp | A/T | 1.99185e-05 | 0.00315577 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246885678 | CAAAAGATCCAAACC[A/T]CTCTGGAAATAACAT | 25909 |
rs780987965 | snp | A/G/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246857410 | AGCAGAGGGCATGGA[A/G/T]GTATGCACAGCTGTG | 25909 |
rs781001977 | snp | A/T | 1.6495e-05 | 0.0028718 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246849650 | TCTGACGCTGGAGAA[A/T]ATAAAGGCTCATTGT | 25909 |
rs781015187 | snp | C/T | 1.67618e-05 | 0.00289493 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246876900 | AACCAAAAAAGCCTC[C/T]AGTTTTCCTTATTCT | 25909 |
rs781031209 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246883764 | GTATAGGAGCCTTAA[C/T]GTGCTAGTTTTCTGG | 25909 |
rs781055463 | snp | C/T | 1.6492e-05 | 0.00287154 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850699 | CTTCCTGACTGACTG[C/T]CCTGGCATCTTAGGA | 25909 |
rs781085031 | snp | A/T | 3.29674e-05 | 0.00405988 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246902641 | ATGCCACCTGTCAGG[A/T]CCAGGGTGTATCTTT | 25909 |
rs781110328 | snp | G/T | 2.23917e-05 | 0.00334594 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246850578 | TTCTCCTTCCTCTCC[G/T]AGGCGTAACAGAATT | 25909 |
rs781125720 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246857610 | AAGTGAAATCTAACA[C/T]GCACAGAATATTTTA | 25909 |
rs781137876 | snp | A/G | 3.32801e-05 | 0.00407908 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246905516 | AAAACAAAACAAAAC[A/G]AAACAAAGTTTGTAT | 25909 |
rs781164297 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246844303 | GTCTGTGCCATAACT[A/G]CTGCTATTGCAGAGA | 25909 |
rs781211089 | in-del | -/AA | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246888901 | AGAGACCCTGTCTCT[-/AA]AAACAGAGAGAGAGG | 25909 |
rs781233084 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246893828 | TCCTAAGACCAAAAG[A/G]CAAGTTATAATCCTA | 25909 |
rs781242042 | snp | A/T | 1.70359e-05 | 0.0029185 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246916304 | CTGTTCATTGACTCC[A/T]CTGAATCTGTAAGCA | 25909 |
rs781300061 | in-del | -/ACA | 5.05072e-05 | 0.00502504 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246887389 | TAAGGACAATAAAAT[-/ACA]ACAACAAAAACCTCC | 25909 |
rs781304733 | in-del | -/TAAG | | | downstream-variant-500B | AHCTF1 | GRCh38.p7 | 1:246838834 | TTACTACTATGATAC[-/TAAG]TATCTGAGTATTGTT | 25909 |
rs781311198 | snp | G/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246867065 | CAAAAATTTTAAGTA[G/T]ACTACTACCTGATGT | 25909 |
rs781332869 | snp | G/T | 1.67172e-05 | 0.00289108 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246916160 | TCCAGGAAGAACAAC[G/T]GCTTTAACTACTTTT | 25909 |
rs781346872 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246912165 | AAAGAGCTACACTGA[C/T]ATTCTAGGCTTGCTT | 25909 |
rs781354440 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246866686 | GGCATATTAAGGACA[A/G]AGAATCAATACATGA | 25909 |
rs781358603 | in-del | -/TC | 3.4132e-05 | 0.00413096 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246857652 | TAATTTCATTAAACT[-/TC]TTTCTAAAAGTATTT | 25909 |
rs781445164 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246901837 | CTGTCTCTAAATAAA[C/T]AAACAAATAAAAACT | 25909 |
rs781446110 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246877396 | TTCAAAGATACTTTG[C/T]AAAGTATCTTTATAA | 25909 |
rs781454737 | snp | C/T | 1.65861e-05 | 0.00287972 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246877227 | CTGACAGACTTCATA[C/T]ATGTGCTTCAGTAAC | 25909 |
rs781454927 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246853887 | ATGTGGATACTAATA[A/G]AACAAAATGAAAAAT | 25909 |
rs781481823 | snp | A/G/T | 3.34114e-05 | 0.00408715 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246888132 | CTCTTGAAATTTTAT[A/G/T]ATTTTAGTAATACAT | 25909 |
rs781506108 | in-del | -/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246880115 | AGTTATTCACACTAC[-/T]TGGGTACTAAGAGGA | 25909 |
rs781529581 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246860663 | ACTCCCACCATGCCT[A/G]GCTAATTTTTAAATT | 25909 |
rs781552719 | in-del | -/AA | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246930586 | ACAAAAAAACAGTTT[-/AA]AAAAAAAAAAAAGGG | 25909 |
rs781554840 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246923157 | CGGTGGCCCATGCCT[A/G]TAATCCCAGCACTTT | 25909 |
rs781572081 | snp | A/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246902456 | AGGAGTATGAAATCT[A/T]GAAAATAACACCTGT | 25909 |
rs781579285 | snp | A/G | 2.27033e-05 | 0.00336914 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246851449 | TTCAATCACCTAAAT[A/G]AATTAAAGATAAGAG | 25909 |
rs781590768 | snp | A/G | 1.64885e-05 | 0.00287123 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246895857 | TATCCATCTTCGGAT[A/G]TAACCAGTCAAAAGT | 25909 |
rs781630719 | in-del | -/A | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246849131 | ATGAAGGATGGCCTC[-/A]ACTGAAGATGAGGGC | 25909 |
rs781635057 | snp | C/G | 1.65004e-05 | 0.00287227 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246888246 | TGCCTATAAAACAAA[C/G]GGATAAAACCTTCAG | 25909 |
rs781636571 | snp | A/G | 1.92978e-05 | 0.0031062 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246876166 | CCAGTGATCTCTCCC[A/G]CAAACGAGGATCACG | 25909 |
rs781642189 | snp | C/T | 1.66732e-05 | 0.00288727 | missense, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246860944 | CTTCTGATGCAAATA[C/T]ATCTTTATCTCCATC | 25909 |
rs781647629 | in-del | -/A | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246880568 | GTGAGACTCCAGCTC[-/A]AAAAAAAAAAAAAAA | 25909 |
rs781655475 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246931929 | CCCCGCTCTGCGCAT[C/T]ACCCTGCGCCGACAA | 25909 |
rs781664818 | snp | A/G | 1.6495e-05 | 0.0028718 | synonymous-codon, nc-transcript-variant | AHCTF1 | GRCh38.p7 | 1:246851074 | TTGGTCACTAGTTAC[A/G]GCAGATGGCAAATTT | 25909 |
rs781728209 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246871185 | CCCCCATGTCTTAGG[A/G]CAGTGGTTACTACTT | 25909 |
rs781739715 | in-del | -/A | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246928302 | GCGAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 25909 |
rs781775779 | in-del | -/A | 1.64749e-05 | 0.00287005 | intron-variant | AHCTF1 | GRCh38.p7 | 1:246877306 | TCAACCATACACCTG[-/A]AAGCAGTATTTATCA | 25909 |
rs796066512 | in-del | -/CT | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246909437 | AATTTGCATGCTGCT[-/CT]GAGTGGTATGATGAA | 25909 |
rs796074494 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246925933 | AGCCAGGTGTGGTGG[C/T]GCCTGCCTGTAGTCC | 25909 |
rs796144096 | in-del | -/CT | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246903662 | GTGAGACCCCCCCCC[-/CT]CCGTCTCTGCTAAAT | 25909 |
rs796224739 | in-del | -/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246920828 | GGTGCCTCACGCCTA[-/T]TAATCCCAGCACTGT | 25909 |
rs796268374 | in-del | -/A | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246903854 | AAAAAAAAAAAAAAA[-/A]GAATCACTTTTCAAT | 25909 |
rs796366579 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246907847 | TCAAGCTGCAAATGA[A/G]GTCAACTGAGTTAAA | 25909 |
rs796387208 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246869040 | TAGTAGAGACGGGGT[C/T]TCACCATGTTGGCCA | 25909 |
rs796493119 | in-del | -/A | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246923128 | AAAAAAAAAAAAAAA[-/A]GATAGGCTGGGCACG | 25909 |
rs796546047 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246902805 | ACTGAAGAGAACCAA[C/T]CATGGAAAAAGGCTC | 25909 |
rs796550402 | snp | C/T | | | synonymous-codon, nc-transcript-variant, intron-variant | AHCTF1 | GRCh38.p7 | 1:246843921 | TGCAGGAACCTCTAT[C/T]TTTTTAGCTAAAAAA | 25909 |
rs796574174 | multinucleotide-polymorphism | AT/TG | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246931052 | ATTTTAAATCTCCTT[AT/TG]TCTGACCAATCGGGT | 25909 |
rs796579076 | in-del | C/GGG | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246860195 | ACCTGGTTGGGGGGG[C/GGG]CGGAGGTTGCAGTGA | 25909 |
rs796596506 | in-del | -/A | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246930052 | GCAAGACCCCGTCTC[-/A]AAAAAAAAAAAAGAT | 25909 |
rs796630102 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246903386 | GGGTACCAATTAAGC[C/T]ACAAGCTTGAATCTA | 25909 |
rs796635621 | in-del | -/GG | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246860189 | TGCTTGAACCTGGTT[-/GG]GGGGGGGGCGGAGGT | 25909 |
rs796659823 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246903890 | AAAACAAAGACAACA[C/T]ATTTAAAATAGAAAA | 25909 |
rs796682533 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246911643 | CATGCGCCACCACAC[C/T]TGGCTAATTTTATAT | 25909 |
rs796682817 | snp | G/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246903666 | GACCCCCCCCCCTCC[G/T]TCTCTGCTAAATATA | 25909 |
rs796683714 | in-del | -/CACAC | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246867904 | ACACCCCCCCCCCCA[-/CACAC]ACACACACACACATT | 25909 |
rs796711547 | in-del | -/AAG | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246843077 | AGGCTCTCACTTTCT[-/AAG]AAGTAGACAACCAGA | 25909 |
rs796736833 | in-del | -/CTTA | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246845969 | GAACAACACATCTTA[-/CTTA]TTCCCTGGGTGATGT | 25909 |
rs796773120 | snp | A/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246865519 | TTCTCTTCTTTCTCT[A/G]TCTTGTTTGCATTTA | 25909 |
rs796794431 | in-del | -/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246899118 | TATTTTTCAAAATTC[-/T]TTTTTTTTTTCCTGT | 25909 |
rs796811689 | in-del | -/AAAC | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246854424 | ACTGCAGAAACAGCA[-/AAAC]AAACCCCAAAATGGT | 25909 |
rs796833739 | in-del | -/AC | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246847305 | AAAAAAAAAAAACAA[-/AC]AAAAAAAAAACTGAA | 25909 |
rs796835506 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246848411 | TTTAGTAGTGTTAGC[C/T]AGGATGGTCTCGATC | 25909 |
rs796836371 | snp | C/G | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246909661 | AAGAGAAGCTGTAAA[C/G]TGCTTCCTTTAAATG | 25909 |
rs796852549 | in-del | AA/C | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246930108 | AGCATAAAAAGAAAA[AA/C]AAAAGTCTCAAAACT | 25909 |
rs796888111 | in-del | -/AA | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246926047 | TGAGACCCTGTCTTT[-/AA]AAAAAAAAAAAAAAA | 25909 |
rs796909528 | in-del | -/A | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246878043 | TGACCCAATGATCCC[-/A]AATGCAAAGAATACA | 25909 |
rs796973168 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246847858 | GGTTACTATATTCCT[C/T]CAGGTCCTGAGGAGT | 25909 |
rs797009254 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246903659 | ATGGTGAGACCCCCC[C/T]CCCTCCGTCTCTGCT | 25909 |
rs797010304 | in-del | -/AA | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246866500 | AACATATGTCCATTA[-/AA]CTACACTCTGTACTT | 25909 |
rs797012157 | snp | C/T | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246873342 | GTGGCTGATGGTCTC[C/T]GGAAAGACAATTCAC | 25909 |
rs797012234 | multinucleotide-polymorphism | AAC/CAA | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246847306 | AAAAAAAAAACAAAC[AAC/CAA]AAAAAAACTGAAAAT | 25909 |
rs797016082 | in-del | -/TTTT | | | intron-variant | AHCTF1 | GRCh38.p7 | 1:246868847 | TGTGTGTGTTTTTTG[-/TTTT]TTTTTTTTTTTTGAG | 25909 |