SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs2303761 | snp | C/T | | | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660341 | GGCGCGGGGTGTACG[C/T]GGGCGGGGCCTCCTC | 50855 |
rs3178281 | snp | G/T | | | utr-variant-3-prime, upstream-variant-2KB, intron-variant, downstream-variant-500B | PARD6A, ACD, ENKD1 | GRCh38.p7 | 16:67662758 | CTGGGGAACATTAAA[G/T]GTTTTCTACAAATAC | 50855 |
rs3179914 | snp | A/C | | | utr-variant-3-prime, upstream-variant-2KB, intron-variant, downstream-variant-500B | PARD6A, ACD, ENKD1 | GRCh38.p7 | 16:67662773 | GGTTTTCTACAAATA[A/C]AGTCATGGTCCTTGT | 50855 |
rs7204371 | snp | A/G | | | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659894 | CCAGAGCCGCGCGGG[A/G]CCTCTCACCAGTCCG | 50855 |
rs8058187 | snp | C/T | 0.095531 | 0.196569 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659534 | GGCGGAGGCATCACT[C/T]ACCAACCAGGCACCC | 50855 |
rs11555862 | snp | C/T | 0 | 0 | missense, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661046 | GGAGTCCTCTGCGGC[C/T]GGGCCATGGCGGGGC | 50855 |
rs13331943 | snp | A/T | 0.0043906 | 0.0466478 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659180 | TAAGGTTAAGGCTGG[A/T]GAGATCACTGCACAG | 50855 |
rs28521023 | snp | C/T | 0.20111 | 0.245173 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660685 | TACACAGTGCACGGT[C/T]TTGTAAGGCCAGTGG | 50855 |
rs35356834 | snp | A/G | 0.0615833 | 0.164314 | missense, upstream-variant-2KB, intron-variant, downstream-variant-500B | PARD6A, ACD, ENKD1 | GRCh38.p7 | 16:67662462 | GACAGCAGTGACCTG[A/G]TCATTGAGAACCGCC | 50855 |
rs59443695 | snp | A/G | 0.0249278 | 0.108823 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659099 | GGACAGGGGACCATG[A/G]GATGAGTCAAGGCTT | 50855 |
rs61741302 | snp | C/T | 0.00259399 | 0.0359203 | downstream-variant-500B, missense, nc-transcript-variant | PARD6A, ENKD1 | GRCh38.p7 | 16:67663277 | CTCTCAGTGAGTCTG[C/T]CCCAGCAGGCAGCAG | 50855 |
rs72547496 | snp | C/T | 0.0298908 | 0.118541 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660703 | GTGTGTGTGCTCTTA[C/T]TTCCACTGGCCTTAC | 50855 |
rs72547497 | snp | A/C | 0.0102561 | 0.0708723 | upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67660841 | GAAACGGAGCCGTGG[A/C]TGGAGAGGAGCCGTC | 50855 |
rs73597595 | snp | A/G | 0.0031125 | 0.0393264 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660317 | CTCCTTCGCTGGGCG[A/G]GGCCGGAGGAGGAGG | 50855 |
rs75040366 | snp | C/G | | | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | PARD6A, ENKD1 | GRCh38.p7 | 16:67663030 | TGACTGGGAAGAGTG[C/G]TCTAGGGACACTGGC | 50855 |
rs79241223 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661882 | ATCTCAACATCCCCC[C/T]TCTTCTGCAGCAGAA | 50855 |
rs112282767 | snp | C/T | 0.5 | 0 | utr-variant-3-prime, upstream-variant-2KB, intron-variant, downstream-variant-500B | PARD6A, ACD, ENKD1 | GRCh38.p7 | 16:67662707 | GCAGGGACTTCACAG[C/T]GGGGGTTTTTAGCTG | 50855 |
rs112600026 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB, missense | PARD6A, ACD | GRCh38.p7 | 16:67661701 | GGGTACAGTGGGCAG[C/T]CTCTGTGGGGTAAGG | 50855 |
rs112770259 | snp | A/G | 0.0119091 | 0.0762411 | upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67660909 | TGCCCCCTTGACGTC[A/G]CGCTCCGGATGGGAA | 50855 |
rs115108685 | snp | C/T | 0.0117731 | 0.0758153 | synonymous-codon, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67662443 | TGAGCCTGATAGTGA[C/T]GATGACAGCAGTGAC | 50855 |
rs115805613 | snp | C/G | 0.0225045 | 0.103662 | upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67660912 | CCCCTTGACGTCACG[C/G]TCCGGATGGGAAGGC | 50855 |
rs116715291 | snp | C/T | 0.00201345 | 0.031665 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | PARD6A, ENKD1 | GRCh38.p7 | 16:67663144 | TGGAGCTCCTTGCCA[C/T]TGTCCCCCAAAGGGG | 50855 |
rs138202882 | snp | A/T | 0.000153988 | 0.00877328 | missense, upstream-variant-2KB, intron-variant, downstream-variant-500B | PARD6A, ACD, ENKD1 | GRCh38.p7 | 16:67662616 | GCTGGGGGAGTCGCA[A/T]TCGAGGAGATGGTAG | 50855 |
rs138527794 | snp | A/G | 0.00497694 | 0.0496357 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660013 | AGGGGCGTGGGATGG[A/G]CCCGCGACCGCGGCC | 50855 |
rs139372052 | snp | C/T | 0.00333756 | 0.0407141 | synonymous-codon, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661580 | ACTTGGCTATACGGA[C/T]GCTCATGGCGACCTG | 50855 |
rs139438549 | snp | C/T | 0.00295464 | 0.0383222 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67658960 | AGGCAGCCCAGTGGG[C/T]GACAGGGGGTGCTGT | 50855 |
rs139574276 | snp | C/G | 0.000181685 | 0.00952939 | missense, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67662029 | CCAAGATTTCCGCCA[C/G]GTTTCCTCAGTCATA | 50855 |
rs140078781 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661837 | TACAGTGCCCCCTGT[A/G]AACAGCCCAAGTCGG | 50855 |
rs140546833 | snp | A/G | 0.00206004 | 0.0320277 | synonymous-codon, upstream-variant-2KB, intron-variant, downstream-variant-500B | PARD6A, ACD, ENKD1 | GRCh38.p7 | 16:67662515 | GTCTCAGGGGCCCCC[A/G]TGCTGGGACCTGCAC | 50855 |
rs141113896 | snp | C/G | 1.68303e-05 | 0.00290084 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67659607 | CCTGGAGATAGAACT[C/G]TGCGGGCTGGAGGAG | 50855 |
rs141258993 | snp | A/G | 0.000396242 | 0.01407 | synonymous-codon, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67662236 | TACAGGGCTGCTGGC[A/G]GTCAGTGATGAGATC | 50855 |
rs142115585 | snp | A/G | 3.29516e-05 | 0.00405891 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67659257 | GGTGGACTCTGAAAG[A/G]TGCTCCCTACAGGAA | 50855 |
rs142507451 | snp | C/T | 0.00499192 | 0.0497096 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660141 | AGCAGCTGCCCGGCT[C/T]GTGGACTGGAGGGTG | 50855 |
rs142662151 | snp | C/T | 0.000761367 | 0.0194963 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660036 | CCGCGGCCTCGGCGT[C/T]CTGTAGTACCTGACG | 50855 |
rs142762905 | snp | A/G/T | 9.86818e-05 | 0.00702374 | upstream-variant-2KB, missense, synonymous-codon, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660401 | TGTGTGCAGACTCCC[A/G/T]CTGGTCCACCCCGCT | 50855 |
rs142866742 | snp | C/T | 1.65151e-05 | 0.00287355 | downstream-variant-500B, missense, nc-transcript-variant | PARD6A, ENKD1 | GRCh38.p7 | 16:67663234 | ACCTGCACCAGCTTC[C/T]GGTCCAGCTCAGCAC | 50855 |
rs143279803 | in-del | -/C | | | frameshift-variant, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661635 | TGCACCGGGCCCTGG[-/C]CCAGCGGGCCCCCGC | 50855 |
rs144087853 | snp | A/G | 1.65168e-05 | 0.00287369 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67658992 | CAAGGGCCCTCCAGT[A/G]TCAGGCAGCTTTCAG | 50855 |
rs144160135 | snp | A/C/T | 0.000177925 | 0.00943042 | missense, synonymous-codon, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661909 | AGAAGCTGACTCCAG[A/C/T]GGCCTGGCTTTTGCC | 50855 |
rs144415548 | snp | A/C | | | upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67660942 | CGGGGCGTGTGCTAC[A/C]GCCAGGGGCGGGGCG | 50855 |
rs145007645 | snp | A/C/T | 0.00016513 | 0.00908522 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67659046 | TGCTCCTGGTCCTCC[A/C/T]GCATTTCATCCAGAA | 50855 |
rs145012859 | snp | C/T | 6.61813e-05 | 0.00575207 | stop-gained, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67662375 | CGCAATAACGTGGTG[C/T]GAGGGGCATCTGGGC | 50855 |
rs145510507 | snp | C/G/T | 0.00102335 | 0.0225973 | missense, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67662154 | GCGTGCGTGTGGCTC[C/G/T]CCAGGGCCTGGAGCG | 50855 |
rs146071407 | snp | A/G | 0.00082434 | 0.0202852 | synonymous-codon, upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67661095 | CATCGTCGAGGTGAA[A/G]AGCAAAGTAAGGGCT | 50855 |
rs146598152 | snp | A/G | 0.00303032 | 0.0388069 | intron-variant, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661447 | TCTCCCCCAACCCCG[A/G]CTTCCAGTTTGACGC | 50855 |
rs146699133 | snp | C/T | 5.56798e-05 | 0.00527606 | upstream-variant-2KB, missense, splice-acceptor-variant, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660038 | GCGGCCTCGGCGTCC[C/T]GTAGTACCTGACGGC | 50855 |
rs146942923 | snp | A/C/T | 1.7042e-05 | 0.00291903 | upstream-variant-2KB, synonymous-codon, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67659783 | CCCGCGGAAGCCGAA[A/C/T]TCCTTCTCCTCCCTG | 50855 |
rs147566572 | snp | A/G/T | 0.000364127 | 0.0134883 | missense, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67662388 | TGCGAGGGGCATCTG[A/G/T]GCGTTTGACAGGTCC | 50855 |
rs148124985 | snp | A/G | 5.21698e-05 | 0.00510707 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660240 | ACGGCTACACCCAGC[A/G]GATGCAACGGGCCCG | 50855 |
rs148341217 | snp | A/G | 0.000233528 | 0.0108032 | missense, upstream-variant-2KB, intron-variant, downstream-variant-500B | PARD6A, ACD, ENKD1 | GRCh38.p7 | 16:67662493 | AGCCTCCCAGTTCCA[A/G]TGGGCTGTCTCAGGG | 50855 |
rs149051014 | snp | A/C/G | 0.000378888 | 0.0137588 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67659240 | GTACCTGCATTGGAC[A/C/G]AGGTGGACTCTGAAA | 50855 |
rs149365469 | snp | C/T | 0.00162346 | 0.0284446 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660199 | TCCAGGGCCGTAGGA[C/T]CAGCCTCCCCGAACC | 50855 |
rs149729712 | snp | A/C/G | 4.95473e-05 | 0.00497711 | missense, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67662145 | ATGGCATGAGCGTGC[A/C/G]TGTGGCTCCCCAGGG | 50855 |
rs150549185 | snp | A/G | 0.000153988 | 0.00877328 | missense, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661941 | CCAACTCTCTGCAGC[A/G]GCGCAAGAAAGGGCT | 50855 |
rs151132164 | snp | A/C/G | 0.000577558 | 0.0169839 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67659389 | CTCAAGGCAGTCATA[A/C/G]AGCTTTTTCTGAACA | 50855 |
rs181609307 | snp | A/C | | | upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67660940 | GGCGGGGCGTGTGCT[A/C]CCGCCAGGGGCGGGG | 50855 |
rs184089323 | snp | C/T | 0.00716266 | 0.059414 | intron-variant, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661156 | TCCCTCTTTCTCCCC[C/T]TCCCAGCTCCTTGGT | 50855 |
rs184418769 | snp | C/T | | | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | PARD6A, ENKD1 | GRCh38.p7 | 16:67663094 | TGGGATTGGGTCCAA[C/T]CCTGTCCTTTGCAGC | 50855 |
rs185153202 | snp | C/G | | | intron-variant, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661364 | GCTGCCGCAAAAGCG[C/G]CAGCCGCATCTTTCC | 50855 |
rs187837649 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660586 | GGCCGAGTGCCGTCC[A/G]AGCGAGTTGACTCGA | 50855 |
rs187847017 | snp | A/G | 0.00278067 | 0.0371834 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659290 | GAGTGGCCAGGACTC[A/G]GGAACCATGCTGAGG | 50855 |
rs188017607 | snp | C/T | | | synonymous-codon, upstream-variant-2KB, intron-variant, downstream-variant-500B | PARD6A, ACD, ENKD1 | GRCh38.p7 | 16:67662638 | AGATGGTAGTGGCTT[C/T]AGCCTCTGACAGTCA | 50855 |
rs188685722 | snp | C/G | | | synonymous-codon, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661643 | GGCCCTGGCCAGCGG[C/G]CCCCCGCCACTGCGC | 50855 |
rs189195547 | snp | C/T | 0.000270316 | 0.0116226 | utr-variant-3-prime, upstream-variant-2KB, intron-variant, downstream-variant-500B | PARD6A, ACD, ENKD1 | GRCh38.p7 | 16:67662648 | GGCTTCAGCCTCTGA[C/T]AGTCAGGATGAAGCC | 50855 |
rs192207041 | snp | A/G | 0.0178422 | 0.092751 | utr-variant-3-prime, upstream-variant-2KB, intron-variant, downstream-variant-500B | PARD6A, ACD, ENKD1 | GRCh38.p7 | 16:67662668 | AGGATGAAGCCCCAT[A/G]CCACTCCACACTGCT | 50855 |
rs192803767 | snp | C/G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660643 | GAACGGTTCAGCACA[C/G/T]ATTTATTATGACTCA | 50855 |
rs193208247 | snp | A/C/T | 6.66711e-05 | 0.00577331 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659694 | CCCAAGGCAGTCTCA[A/C/T]CACTCACCGCGCCGC | 50855 |
rs199612237 | snp | C/T | 4.04253e-05 | 0.00449566 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660363 | CCCCGCGCCTGCGCA[C/T]GAGGGCGTCCTGCTC | 50855 |
rs199626332 | snp | A/G | 0.0002636 | 0.0114774 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659222 | CACTGGTCAAGCTCT[A/G]CAGTACCTGCATTGG | 50855 |
rs199739793 | snp | A/G | 0.000103075 | 0.00717822 | missense, upstream-variant-2KB, intron-variant, downstream-variant-500B | PARD6A, ACD, ENKD1 | GRCh38.p7 | 16:67662556 | GACATCCTGGTACCC[A/G]CAGCTCTCTGCCCTC | 50855 |
rs200163503 | snp | A/G | 4.95593e-05 | 0.00497767 | missense, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67662127 | TGGGCTTCTACATCC[A/G]AGATGGCATGAGCGT | 50855 |
rs200365807 | snp | C/G/T | 0.000190308 | 0.00975295 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660175 | CTGACCCCAGAATCA[C/G/T]CTCCCGAATCCAGGG | 50855 |
rs200880184 | snp | A/G | 3.30704e-05 | 0.00406622 | missense, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67662351 | GTCACTGTCAAGCCC[A/G]CCAACCAGCGCAATA | 50855 |
rs200909340 | snp | C/G/T | 8.25258e-05 | 0.00642315 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67659387 | CACTCAAGGCAGTCA[C/G/T]AGAGCTTTTTCTGAA | 50855 |
rs201069165 | snp | C/T | 1.65282e-05 | 0.00287469 | missense, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67662093 | GTGCGGCTGCACAAG[C/T]ATGGTTCAGACCGCC | 50855 |
rs201232409 | snp | C/G | 0.00199797 | 0.0315435 | missense, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661045 | GGCCCCGCCATGGCC[C/G]GGCCGCAGAGGACTC | 50855 |
rs201234158 | snp | C/T | 0.000105264 | 0.00725404 | missense, upstream-variant-2KB, intron-variant, downstream-variant-500B | PARD6A, ACD, ENKD1 | GRCh38.p7 | 16:67662612 | TCTGGCTGGGGGAGT[C/T]GCATTCGAGGAGATG | 50855 |
rs201635871 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661871 | GCAGGTCTCTGATCT[C/T]AACATCCCCCCTCTT | 50855 |
rs201685459 | snp | C/G | 0.000106502 | 0.00729655 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660470 | GTCACTCTGACAGCG[C/G]CCAGGCATTTGGGCC | 50855 |
rs201736719 | snp | C/G | 0.000632953 | 0.0177785 | missense, upstream-variant-2KB, intron-variant, downstream-variant-500B | PARD6A, ACD, ENKD1 | GRCh38.p7 | 16:67662484 | AGAACCGCCAGCCTC[C/G]CAGTTCCAATGGGCT | 50855 |
rs201948166 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659617 | GAACTCTGCGGGCTG[A/G]AGGAGTTCGGGGGGA | 50855 |
rs367821436 | snp | A/C/G | 3.29534e-05 | 0.00405904 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659268 | AAAGGTGCTCCCTAC[A/C/G]GGAAGAGAGTGGCCA | 50855 |
rs367827389 | snp | C/T | 1.83646e-05 | 0.00303018 | intron-variant, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661869 | GAGCAGGTCTCTGAT[C/T]TCAACATCCCCCCTC | 50855 |
rs367886829 | snp | A/G | 1.65224e-05 | 0.00287418 | downstream-variant-500B, synonymous-codon, nc-transcript-variant | PARD6A, ENKD1 | GRCh38.p7 | 16:67663251 | GTCCAGCTCAGCACG[A/G]TGGCTCTGGGCTCTC | 50855 |
rs368053306 | snp | C/G | | | intron-variant, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661114 | AAAGTAAGGGCTCCT[C/G]CGGCCTCGGCCCTAG | 50855 |
rs368080665 | snp | C/T | 8.26685e-05 | 0.00642864 | synonymous-codon, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67662350 | TGTCACTGTCAAGCC[C/T]GCCAACCAGCGCAAT | 50855 |
rs368191589 | snp | A/G | 3.3042e-05 | 0.00406447 | downstream-variant-500B, missense, nc-transcript-variant | PARD6A, ENKD1 | GRCh38.p7 | 16:67663250 | GGTCCAGCTCAGCAC[A/G]GTGGCTCTGGGCTCT | 50855 |
rs368212170 | snp | C/T | 0.000153988 | 0.00877327 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67659707 | CACCACTCACCGCGC[C/T]GCCCTCAGCGACCTG | 50855 |
rs368387402 | snp | A/C/G | 7.33777e-05 | 0.00605677 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67659970 | TCCCGTCAGACACAA[A/C/G]CAGCGTGGCCCCGAC | 50855 |
rs368510441 | snp | C/T | 5.66963e-05 | 0.005324 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659896 | AGAGCCGCGCGGGGC[C/T]TCTCACCAGTCCGAG | 50855 |
rs368511393 | snp | A/G | 1.77647e-05 | 0.00298027 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67660101 | TCCGCCTCGGTCTCC[A/G]GGCCCTGAATGGGGG | 50855 |
rs368752643 | snp | A/G | 0.000153988 | 0.00877327 | intron-variant, upstream-variant-2KB, missense | PARD6A, ACD | GRCh38.p7 | 16:67661699 | AGGGGTACAGTGGGC[A/G]GCCTCTGTGGGGTAA | 50855 |
rs368882788 | snp | A/G | 1.6534e-05 | 0.00287519 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659090 | TAGGCCTGGGGACAG[A/G]GGACCATGGGATGAG | 50855 |
rs368923570 | snp | A/T | 1.65501e-05 | 0.00287659 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659106 | GGACCATGGGATGAG[A/T]CAAGGCTTAAAGGGG | 50855 |
rs369005864 | snp | A/C/G | 5.14146e-05 | 0.00507002 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | PARD6A, ENKD1 | GRCh38.p7 | 16:67663118 | TTGCAGCCATGTGGC[A/C/G]ATCCTCAGCATGGAG | 50855 |
rs369026483 | snp | C/T | 3.37747e-05 | 0.00410928 | intron-variant, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661430 | GCTGTCCTGACTCCT[C/T]CTCTCCCCCAACCCC | 50855 |
rs369046068 | snp | C/T | 0.000460348 | 0.0151645 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67660104 | GCCTCGGTCTCCGGG[C/T]CCTGAATGGGGGCTC | 50855 |
rs369086013 | snp | A/G | 0.00199481 | 0.0315187 | upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67660830 | CAAGAGCGGAGGACG[A/G]CTCCTCTCCATCCAC | 50855 |
rs369698525 | snp | A/G | 1.92084e-05 | 0.00309901 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660414 | CCGCTGGTCCACCCC[A/G]CTGGTGCACGGGATG | 50855 |
rs369703324 | snp | A/G | | | downstream-variant-500B | PARD6A, ENKD1 | GRCh38.p7 | 16:67662891 | GCAATCAAGCAGCAG[A/G]AGGGCCACCAGGCTT | 50855 |
rs370302172 | snp | C/T | 5.03098e-05 | 0.00501521 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659653 | GGGTCTCAGAATCGT[C/T]ACGAAGAGTCATGCC | 50855 |
rs370512338 | snp | C/T | 0.000181221 | 0.00951722 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67659234 | TCTACAGTACCTGCA[C/T]TGGACGAGGTGGACT | 50855 |
rs370613482 | snp | A/G | 5.03461e-05 | 0.00501702 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659648 | AGGGGGGGTCTCAGA[A/G]TCGTCACGAAGAGTC | 50855 |
rs371007556 | snp | G/T | 0.000571928 | 0.0169008 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659635 | GAGTTCGGGGGGAAG[G/T]GGGGGTCTCAGAATC | 50855 |
rs371109252 | snp | A/G | | | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660455 | TACTCTCATCGCGGC[A/G]TCACTCTGACAGCGG | 50855 |
rs371121940 | snp | A/C/T | 5.32281e-05 | 0.00515865 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660501 | GTTCGTCAAGATTCC[A/C/T]GTGGTACCGGTAGGG | 50855 |
rs371131781 | snp | A/C | 1.65143e-05 | 0.00287348 | missense, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67662249 | GCGGTCAGTGATGAG[A/C]TCCTCGAGGTCAATG | 50855 |
rs371282916 | snp | A/G | 1.65875e-05 | 0.00287984 | synonymous-codon, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67662422 | CTCTGCAGGGCCTGG[A/G]CCTGCTGAGCCTGAT | 50855 |
rs371315332 | snp | C/T | 1.64787e-05 | 0.00287038 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659209 | AGCGTGTTAGGATCA[C/T]TGGTCAAGCTCTACA | 50855 |
rs371619272 | snp | C/T | 0.000301412 | 0.0122725 | synonymous-codon, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661604 | CGACCTGCTGCCCCT[C/T]ACCAACGACGACAGC | 50855 |
rs371791290 | snp | C/G | 1.84126e-05 | 0.00303414 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67659983 | AAGCAGCGTGGCCCC[C/G]ACGTCGGACGTATCA | 50855 |
rs371831536 | snp | A/G | 0.000104206 | 0.0072175 | synonymous-codon, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661062 | GCCGCAGAGGACTCC[A/G]GCGCGCAGTCCCGAT | 50855 |
rs371862939 | snp | C/T | 6.60644e-05 | 0.00574698 | synonymous-codon, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67662278 | TGGCATTGAAGTAGC[C/T]GGGAAGACCTTGGAC | 50855 |
rs372161745 | snp | A/G | 1.77893e-05 | 0.00298234 | missense, upstream-variant-2KB, intron-variant, downstream-variant-500B | PARD6A, ACD, ENKD1 | GRCh38.p7 | 16:67662579 | CTGCCCTCCCTGGAT[A/G]ACCAGGAGCAGGCCA | 50855 |
rs372700670 | snp | C/G/T | 6.61599e-05 | 0.00575119 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659424 | AGTCTTGGTTGCTAA[C/G/T]AAAAAGAGAAGGGTA | 50855 |
rs372927331 | snp | C/T | 1.89209e-05 | 0.00307573 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660421 | TCCACCCCGCTGGTG[C/T]ACGGGATGCTGGCCC | 50855 |
rs373593390 | snp | C/G | 7.13636e-05 | 0.005973 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660459 | CTCATCGCGGCGTCA[C/G]TCTGACAGCGGCCAG | 50855 |
rs373776491 | snp | A/G | 0.000115623 | 0.00760251 | missense, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67662141 | CGAGATGGCATGAGC[A/G]TGCGTGTGGCTCCCC | 50855 |
rs373883261 | snp | C/T | | | downstream-variant-500B, synonymous-codon, nc-transcript-variant | PARD6A, ENKD1 | GRCh38.p7 | 16:67663275 | GGCTCTCAGTGAGTC[C/T]GCCCCAGCAGGCAGC | 50855 |
rs373997623 | snp | C/G | 0.000134585 | 0.0082021 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659636 | AGTTCGGGGGGAAGG[C/G]GGGGTCTCAGAATCG | 50855 |
rs374019081 | snp | C/T | 1.69565e-05 | 0.00291169 | intron-variant, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661421 | GGGGCGCAGGCTGTC[C/T]TGACTCCTCCTCTCC | 50855 |
rs374095852 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67662341 | TAACCTCATTGTCAC[C/T]GTCAAGCCCGCCAAC | 50855 |
rs374417270 | snp | G/T | 4.04482e-05 | 0.00449694 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660360 | ACACCCCGCGCCTGC[G/T]CACGAGGGCGTCCTG | 50855 |
rs374564303 | snp | C/T | 5.02677e-05 | 0.00501311 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67659753 | GTCCTGCAGCAGCAG[C/T]AGCCGGCCCTCTGTC | 50855 |
rs374662096 | snp | C/T | 1.67747e-05 | 0.00289605 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659652 | GGGGTCTCAGAATCG[C/T]CACGAAGAGTCATGC | 50855 |
rs374675451 | snp | C/T | 1.65293e-05 | 0.00287479 | missense, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67662109 | ATGGTTCAGACCGCC[C/T]CCTGGGCTTCTACAT | 50855 |
rs374746019 | snp | C/T | 1.72053e-05 | 0.00293298 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | PARD6A, ENKD1 | GRCh38.p7 | 16:67663117 | TTTGCAGCCATGTGG[C/T]GATCCTCAGCATGGA | 50855 |
rs374903966 | snp | A/G | 4.95372e-05 | 0.00497656 | missense, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67662202 | TCTCCCGCCTGGTAC[A/G]TGGGGGTCTGGCTGA | 50855 |
rs374942246 | snp | C/G/T | 3.34954e-05 | 0.00409228 | intron-variant, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661132 | GCCTCGGCCCTAGGC[C/G/T]CTCCCAATTCCCTCT | 50855 |
rs375059830 | snp | C/G | 3.34018e-05 | 0.00408654 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659489 | CGTCTGCCAGCGCCG[C/G]CCAGGCTGGGGTGGG | 50855 |
rs375082471 | snp | A/C | 1.64762e-05 | 0.00287016 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659267 | GAAAGGTGCTCCCTA[A/C]AGGAAGAGAGTGGCC | 50855 |
rs375257354 | snp | A/G | 1.87682e-05 | 0.00306329 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67659912 | TCTCACCAGTCCGAG[A/G]TGTCCAGGGCCTCCC | 50855 |
rs375500965 | snp | C/T | 6.60469e-05 | 0.00574622 | synonymous-codon, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67662254 | CAGTGATGAGATCCT[C/T]GAGGTCAATGGCATT | 50855 |
rs375557408 | snp | A/G | 0.0217236 | 0.101931 | downstream-variant-500B, upstream-variant-2KB, intron-variant | PARD6A, ACD, ENKD1 | GRCh38.p7 | 16:67662781 | ACAAATACAGTCATG[A/G]TCCTTGTGTGTCCCA | 50855 |
rs375559289 | snp | A/G | 0.000153988 | 0.00877328 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659440 | AAAAAGAGAAGGGTA[A/G]TTAATGGGGGCCCAA | 50855 |
rs375672468 | snp | C/G | 8.85826e-05 | 0.00665458 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660495 | TGGGCCGTTCGTCAA[C/G]ATTCCTGTGGTACCG | 50855 |
rs375973362 | snp | A/G | | | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659280 | TACAGGAAGAGAGTG[A/G]CCAGGACTCAGGAAC | 50855 |
rs376038080 | snp | C/G/T | 0.000145098 | 0.00851656 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67660074 | GCGGCGTCAATCCCA[C/G/T]CACCCCGGGCCTCCG | 50855 |
rs376086019 | snp | A/G | 0.00036336 | 0.013474 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67658982 | GGGTGCTGTGCAAGG[A/G]CCCTCCAGTGTCAGG | 50855 |
rs376240019 | snp | C/G | 0.000329511 | 0.0128315 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659314 | GCTGAGGCCTGTCTA[C/G]CTAGATACACCATCC | 50855 |
rs376391633 | snp | C/G | 1.64784e-05 | 0.00287035 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659207 | ACAGCGTGTTAGGAT[C/G]ACTGGTCAAGCTCTA | 50855 |
rs376678105 | snp | A/C/T | 1.66211e-05 | 0.00288275 | missense, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661576 | TGCTACTTGGCTATA[A/C/T]GGATGCTCATGGCGA | 50855 |
rs376761311 | snp | A/G | 0.000198128 | 0.00995111 | missense, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67662186 | GTTCCAGGAATCTTC[A/G]TCTCCCGCCTGGTAC | 50855 |
rs376813282 | snp | A/G | 1.9987e-05 | 0.00316119 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660391 | CTCGGGGGCCTGTGT[A/G]CAGACTCCCGCTGGT | 50855 |
rs376867217 | snp | C/T | 1.65132e-05 | 0.00287339 | missense, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67662235 | GTACAGGGCTGCTGG[C/T]GGTCAGTGATGAGAT | 50855 |
rs377118118 | snp | C/G | 0.000507679 | 0.0159242 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660444 | GCTGGCCCGTTTACT[C/G]TCATCGCGGCGTCAC | 50855 |
rs377247506 | snp | A/C/G | 6.92849e-05 | 0.00588543 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660229 | CTGCCATCCCCACGG[A/C/G]TACACCCAGCGGATG | 50855 |
rs377289629 | snp | A/G | 1.64762e-05 | 0.00287016 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67659231 | AGCTCTACAGTACCT[A/G]CATTGGACGAGGTGG | 50855 |
rs377328316 | snp | A/G | 8.41036e-05 | 0.00648419 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659639 | TCGGGGGGAAGGGGG[A/G]GTCTCAGAATCGTCA | 50855 |
rs377701284 | snp | A/C | 1.68357e-05 | 0.00290131 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67659610 | GGAGATAGAACTCTG[A/C]GGGCTGGAGGAGTTC | 50855 |
rs386791764 | multinucleotide-polymorphism | GGT/TGA | | | cds-indel, upstream-variant-2KB, intron-variant, downstream-variant-500B | PARD6A, ACD, ENKD1 | GRCh38.p7 | 16:67662446 | GCCTGATAGTGACGA[GGT/TGA]CAGCAGTGACCTGGT | 50855 |
rs397839864 | snp | G/T | | | upstream-variant-2KB, missense, intron-variant, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660044 | GGCAGCTGCTTGAGG[G/T]ACTACAGGACGCCGA | 50855 |
rs527307806 | snp | C/T | | | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660372 | TGCGCACGAGGGCGT[C/T]CTGCTCGGGGGCCTG | 50855 |
rs527604584 | snp | A/G | 0.00199481 | 0.0315187 | downstream-variant-500B | PARD6A, ENKD1 | GRCh38.p7 | 16:67662824 | TCCCTGGTCTCACCA[A/G]CTTGCCTTCTGCTCT | 50855 |
rs529619143 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-5-prime, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67660986 | GGCCGGGCTGTGCAC[C/T]TGCGCCTCGGCGGGC | 50855 |
rs530732740 | snp | C/G | | | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67659749 | CGCAGTCCTGCAGCA[C/G]CAGCAGCCGGCCCTC | 50855 |
rs531513202 | snp | A/G | 1.65124e-05 | 0.00287331 | missense, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67662217 | GTGGGGGTCTGGCTG[A/G]GAGTACAGGGCTGCT | 50855 |
rs531552544 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661317 | GACCTTGGACAGCGT[C/T]CCTGGTACTGGAGCT | 50855 |
rs531928488 | snp | C/T | 1.77146e-05 | 0.00297607 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660480 | CAGCGGCCAGGCATT[C/T]GGGCCGTTCGTCAAG | 50855 |
rs531965174 | snp | A/C/G | 0.000104716 | 0.00723522 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659809 | CCCTGCAACAAGCAG[A/C/G]ATCCTCACTGCCGGG | 50855 |
rs533804108 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659148 | GGTGAGGGGGAAGAC[A/G]GCTTATTGAGGAAGC | 50855 |
rs534010648 | snp | C/G | 0.000209532 | 0.0102338 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660249 | CCCAGCGGATGCAAC[C/G]GGCCCGGGTTTCCCG | 50855 |
rs535866499 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67660820 | CGTGATGACGCAAGA[A/G]CGGAGGACGGCTCCT | 50855 |
rs535895567 | snp | C/T | 1.85269e-05 | 0.00304354 | upstream-variant-2KB, splice-acceptor-variant, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67660047 | GCGTCCTGTAGTACC[C/T]GACGGCGGCGAGCGG | 50855 |
rs537272237 | snp | A/G | 0.000399281 | 0.0141238 | missense, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661929 | TGGCTTTTGCCTCCA[A/G]CTCTCTGCAGCGGCG | 50855 |
rs538093955 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660786 | TGCTCCCCAGACTCC[A/G]GGGGCGCGCGGACCT | 50855 |
rs541841503 | snp | A/G | 5.14672e-05 | 0.00507257 | missense, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661070 | GGACTCCGGCGCGCA[A/G]TCCCGATAGCATCGT | 50855 |
rs542303427 | snp | C/T | 3.96503e-05 | 0.00445237 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660398 | GCCTGTGTGCAGACT[C/T]CCGCTGGTCCACCCC | 50855 |
rs542440448 | snp | C/G | 6.68472e-05 | 0.00578093 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659500 | GCCGGCCAGGCTGGG[C/G]TGGGGAGAGCTGCTG | 50855 |
rs543708587 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660567 | TTCCAGGGCCGGAGG[C/G]TGAGGCCGAGTGCCG | 50855 |
rs545843775 | snp | G/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, upstream-variant-2KB, intron-variant, downstream-variant-500B | PARD6A, ACD, ENKD1 | GRCh38.p7 | 16:67662712 | GACTTCACAGTGGGG[G/T]TTTTTAGCTGGCTCA | 50855 |
rs545849312 | snp | A/C/T | 0.000115592 | 0.00760155 | missense, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67662192 | GGAATCTTCATCTCC[A/C/T]GCCTGGTACGTGGGG | 50855 |
rs546076920 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67660873 | TAGGAAACGTGGACT[C/T]CGCGTTCCACTCTGC | 50855 |
rs547328991 | snp | A/G | | | downstream-variant-500B | PARD6A, ENKD1 | GRCh38.p7 | 16:67662903 | CAGGAGGGCCACCAG[A/G]CTTGGCATTTTTAGG | 50855 |
rs547641566 | snp | G/T | 1.65214e-05 | 0.0028741 | downstream-variant-500B, synonymous-codon, nc-transcript-variant | PARD6A, ENKD1 | GRCh38.p7 | 16:67663206 | CCGAGAAAAGATCTT[G/T]ATGGCCTCCTCTACC | 50855 |
rs550036587 | snp | C/G | 1.65701e-05 | 0.00287833 | synonymous-codon, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67662407 | TTTGACAGGTCCTCC[C/G]TCTGCAGGGCCTGGG | 50855 |
rs550200963 | snp | A/G | 1.83596e-05 | 0.00302976 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67659954 | CATCGGACACTGTGG[A/G]TCCCGTCAGACACAA | 50855 |
rs551436578 | snp | C/T | 8.55805e-05 | 0.00654087 | missense, upstream-variant-2KB, intron-variant, downstream-variant-500B | PARD6A, ACD, ENKD1 | GRCh38.p7 | 16:67662555 | CGACATCCTGGTACC[C/T]GCAGCTCTCTGCCCT | 50855 |
rs551991549 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661291 | CCTGAGTACCTGGAG[A/G]GCGGTAAGAAGACCT | 50855 |
rs552391590 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660718 | ATAAGAGCACACACA[C/G]AGCGCTAAATAAATG | 50855 |
rs552560232 | snp | A/G | 5.0497e-05 | 0.00502453 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659631 | GGAGGAGTTCGGGGG[A/G]AAGGGGGGGTCTCAG | 50855 |
rs553408387 | snp | A/G | 0.000398387 | 0.014108 | utr-variant-3-prime, upstream-variant-2KB, intron-variant, downstream-variant-500B | PARD6A, ACD, ENKD1 | GRCh38.p7 | 16:67662678 | CCCATGCCACTCCAC[A/G]CTGCTGGGACATGGC | 50855 |
rs554184479 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661731 | GTGTCTGTGGGGCAG[G/T]TCTACAAGGGTTAGT | 50855 |
rs554250511 | snp | G/T | 0.00128943 | 0.0253584 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659102 | CAGGGGACCATGGGA[G/T]GAGTCAAGGCTTAAA | 50855 |
rs554258142 | snp | C/G/T | 0.000174688 | 0.00934443 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660410 | ACTCCCGCTGGTCCA[C/G/T]CCCGCTGGTGCACGG | 50855 |
rs554388576 | snp | A/G | 9.93575e-05 | 0.00704761 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659125 | GGCTTAAAGGGGAGG[A/G]CCAGGAGGGTGAGGG | 50855 |
rs554684021 | snp | A/G | | | intron-variant, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661176 | AGCTCCTTGGTCCCC[A/G]CCACCTCTTCCCTCT | 50855 |
rs555590208 | snp | A/C/G | 4.27234e-05 | 0.00462171 | missense, upstream-variant-2KB, intron-variant, downstream-variant-500B | PARD6A, ACD, ENKD1 | GRCh38.p7 | 16:67662613 | CTGGCTGGGGGAGTC[A/C/G]CATTCGAGGAGATGG | 50855 |
rs555623024 | snp | A/G | 5.04494e-05 | 0.00502217 | missense, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661944 | ACTCTCTGCAGCGGC[A/G]CAAGAAAGGGCTCTT | 50855 |
rs556507924 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660797 | CTCCGGGGGCGCGCG[C/G]ACCTCAGCGTGATGA | 50855 |
rs556642707 | snp | A/G/T | 2.01039e-05 | 0.00317042 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660381 | GGGCGTCCTGCTCGG[A/G/T]GGCCTGTGTGCAGAC | 50855 |
rs558547634 | snp | C/T | 1.7625e-05 | 0.00296854 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660262 | ACGGGCCCGGGTTTC[C/T]CGCGGGCGCCCAGGC | 50855 |
rs558828025 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659158 | AAGACAGCTTATTGA[A/G]GAAGCATAAGGTTAA | 50855 |
rs560657972 | snp | A/G | | | upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67660904 | GTCGCTGCCCCCTTG[A/G]CGTCACGCTCCGGAT | 50855 |
rs561823135 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | PARD6A, ENKD1 | GRCh38.p7 | 16:67663048 | TAGGGACACTGGCCA[C/G]CCCCCTGCTCCTGTC | 50855 |
rs561960251 | snp | A/G | 1.65913e-05 | 0.00288017 | missense, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67662426 | GCAGGGCCTGGGCCT[A/G]CTGAGCCTGATAGTG | 50855 |
rs562063556 | snp | A/G | 0.00286591 | 0.0377458 | utr-variant-5-prime, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67660954 | TACCGCCAGGGGCGG[A/G]GCGGCGCGGGCGGGC | 50855 |
rs562102617 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660568 | TCCAGGGCCGGAGGC[G/T]GAGGCCGAGTGCCGT | 50855 |
rs563809910 | snp | A/G | 0.000198249 | 0.00995415 | synonymous-codon, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67662302 | CTTGGACCAAGTGAC[A/G]GACATGATGGTTGCC | 50855 |
rs564156197 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B, upstream-variant-2KB, intron-variant | PARD6A, ACD, ENKD1 | GRCh38.p7 | 16:67662779 | CTACAAATACAGTCA[C/T]GGTCCTTGTGTGTCC | 50855 |
rs564824437 | snp | A/G | 1.66687e-05 | 0.00288688 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67659705 | CTCACCACTCACCGC[A/G]CCGCCCTCAGCGACC | 50855 |
rs565942092 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661809 | GCTTGACCTCTAAGT[C/G]GTAGGAAATAGCTAC | 50855 |
rs566079044 | snp | G/T | 0.00015158 | 0.00870443 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659623 | TGCGGGCTGGAGGAG[G/T]TCGGGGGGAAGGGGG | 50855 |
rs568204079 | in-del | -/GCGGC | 0.0506381 | 0.150847 | utr-variant-5-prime, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67660954 | ACCGCCAGGGGCGGG[-/GCGGC]GCGGCGCGGGCGGGC | 50855 |
rs568393136 | snp | C/T | 1.66059e-05 | 0.00288144 | missense, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661521 | TTCCAGGAGTTCTCG[C/T]GGTTGCTGCGGGCGG | 50855 |
rs568431673 | snp | A/G | 0.00398564 | 0.0444627 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660812 | GACCTCAGCGTGATG[A/G]CGCAAGAGCGGAGGA | 50855 |
rs570622120 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661301 | TGGAGGGCGGTAAGA[A/C]GACCTTGGACAGCGT | 50855 |
rs570757495 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660777 | GCGGAGCCCTGCTCC[A/C]CAGACTCCGGGGGCG | 50855 |
rs571980503 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, upstream-variant-2KB, intron-variant, downstream-variant-500B | PARD6A, ACD, ENKD1 | GRCh38.p7 | 16:67662697 | CTGGGACATGGCAGG[C/G]ACTTCACAGTGGGGG | 50855 |
rs572519785 | snp | C/G/T | 3.82902e-05 | 0.00437537 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660415 | CGCTGGTCCACCCCG[C/G/T]TGGTGCACGGGATGC | 50855 |
rs572542621 | snp | C/T | 0.00795532 | 0.062565 | upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67660837 | GGAGGACGGCTCCTC[C/T]CCATCCACGGCTCCG | 50855 |
rs572997289 | snp | A/C/G | 0.000148942 | 0.0086286 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659129 | TAAAGGGGAGGACCA[A/C/G]GAGGGTGAGGGGGAA | 50855 |
rs574032470 | snp | C/T | 1.65556e-05 | 0.00287707 | synonymous-codon, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661984 | AGTGGCACCCCTGCG[C/T]ACCCGGCCACCCTTG | 50855 |
rs574838122 | snp | C/G | | | intron-variant, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661368 | CCGCAAAAGCGGCAG[C/G]CGCATCTTTCCCATT | 50855 |
rs574891736 | snp | C/G/T | 0.000140661 | 0.00838525 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660383 | GCGTCCTGCTCGGGG[C/G/T]CCTGTGTGCAGACTC | 50855 |
rs576237919 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67660910 | GCCCCCTTGACGTCA[C/T]GCTCCGGATGGGAAG | 50855 |
rs745340618 | snp | A/C/T | 3.29942e-05 | 0.00406155 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659350 | CCAAACAACACGTGG[A/C/T]CCCCGAGCCCAACCC | 50855 |
rs745428657 | snp | A/G | 1.64757e-05 | 0.00287012 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67659252 | GACGAGGTGGACTCT[A/G]AAAGGTGCTCCCTAC | 50855 |
rs745443998 | snp | A/C/G | 3.3024e-05 | 0.00406336 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67659018 | TTCAGCCAGGCACAC[A/C/G]AGTGCCCCCTGATGC | 50855 |
rs745488500 | snp | A/C | 2.29003e-05 | 0.00338373 | utr-variant-5-prime, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661025 | GCACCGTCCCCGGCC[A/C]GCCCGGCCCCGCCAT | 50855 |
rs745504473 | snp | C/T | 2.14186e-05 | 0.00327243 | synonymous-codon, upstream-variant-2KB, intron-variant, downstream-variant-500B | PARD6A, ACD, ENKD1 | GRCh38.p7 | 16:67662614 | TGGCTGGGGGAGTCG[C/T]ATTCGAGGAGATGGT | 50855 |
rs745562541 | in-del | -/CT | 1.71683e-05 | 0.00292982 | frameshift-variant, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661930 | GGCTTTTGCCTCCAA[-/CT]CTCTGCAGCGGCGCA | 50855 |
rs745595083 | snp | A/C | 3.66529e-05 | 0.00428078 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67659956 | TCGGACACTGTGGGT[A/C]CCGTCAGACACAAGC | 50855 |
rs745664221 | in-del | -/G | 3.37436e-05 | 0.00410739 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659633 | GGAGTTCGGGGGGAA[-/G]GGGGGGGTCTCAGAA | 50855 |
rs745789392 | snp | C/T | 1.85993e-05 | 0.00304947 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660029 | CCCGCGACCGCGGCC[C/T]CGGCGTCCTGTAGTA | 50855 |
rs745891027 | snp | C/G | 1.68131e-05 | 0.00289935 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67659596 | GAAGCGGTCCACCTG[C/G]AGATAGAACTCTGCG | 50855 |
rs745972649 | snp | C/G/T | 0.000273355 | 0.0116879 | upstream-variant-2KB, stop-gained, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660407 | CAGACTCCCGCTGGT[C/G/T]CACCCCGCTGGTGCA | 50855 |
rs746191157 | snp | A/G | 9.9346e-05 | 0.00704721 | missense, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661983 | CAGTGGCACCCCTGC[A/G]CACCCGGCCACCCTT | 50855 |
rs746215226 | snp | C/T | | | missense, upstream-variant-2KB, intron-variant, downstream-variant-500B | PARD6A, ACD, ENKD1 | GRCh38.p7 | 16:67662483 | GAGAACCGCCAGCCT[C/T]CCAGTTCCAATGGGC | 50855 |
rs746215992 | snp | C/G | | | downstream-variant-500B, upstream-variant-2KB, intron-variant | PARD6A, ACD, ENKD1 | GRCh38.p7 | 16:67662810 | CAGTTCCAGCCTCCT[C/G]CCTGGTCTCACCAGC | 50855 |
rs746251847 | snp | C/T | 1.83024e-05 | 0.00302504 | intron-variant, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661878 | TCTGATCTCAACATC[C/T]CCCCTCTTCTGCAGC | 50855 |
rs746308650 | snp | A/G | | | intron-variant, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661294 | GAGTACCTGGAGGGC[A/G]GTAAGAAGACCTTGG | 50855 |
rs746445437 | snp | A/T | 3.47947e-05 | 0.00417087 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660243 | GCTACACCCAGCGGA[A/T]GCAACGGGCCCGGGT | 50855 |
rs746541344 | snp | A/G | 1.73135e-05 | 0.00294218 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660169 | GTGTCTCTGACCCCA[A/G]AATCAGCTCCCGAAT | 50855 |
rs746541439 | snp | A/C | 1.65765e-05 | 0.00287888 | missense, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661976 | CTGCGGCCAGTGGCA[A/C]CCCTGCGCACCCGGC | 50855 |
rs746636700 | snp | A/G | 3.32408e-05 | 0.00407668 | missense, upstream-variant-2KB, intron-variant, downstream-variant-500B | PARD6A, ACD, ENKD1 | GRCh38.p7 | 16:67662454 | GTGACGATGACAGCA[A/G]TGACCTGGTCATTGA | 50855 |
rs746663656 | snp | C/T | 3.29527e-05 | 0.00405898 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67659239 | AGTACCTGCATTGGA[C/T]GAGGTGGACTCTGAA | 50855 |
rs746721657 | snp | A/G | 0.000154655 | 0.00879225 | utr-variant-5-prime, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661007 | CTCGGCGGGCCGCCT[A/G]GGGCACCGTCCCCGG | 50855 |
rs746828389 | snp | A/G | 0.000101543 | 0.0071247 | missense, upstream-variant-2KB, intron-variant, downstream-variant-500B | PARD6A, ACD, ENKD1 | GRCh38.p7 | 16:67662541 | TGCACCCTGGCTGCC[A/G]ACATCCTGGTACCCG | 50855 |
rs746919859 | snp | A/G | 1.77584e-05 | 0.00297974 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659823 | GGATCCTCACTGCCG[A/G]GCCCACCTGAACACA | 50855 |
rs746958614 | snp | C/T | 1.70365e-05 | 0.00291855 | intron-variant, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661410 | GCGGTGAGAAAGGGG[C/T]GCAGGCTGTCCTGAC | 50855 |
rs747035693 | snp | C/G | 3.30622e-05 | 0.00406571 | missense, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67662315 | ACGGACATGATGGTT[C/G]CCAACAGCCATAACC | 50855 |
rs747050159 | snp | A/C | 2.02206e-05 | 0.00317961 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660378 | CGAGGGCGTCCTGCT[A/C]GGGGGCCTGTGTGCA | 50855 |
rs747150355 | snp | A/G | 1.65181e-05 | 0.00287381 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67658981 | GGGGTGCTGTGCAAG[A/G]GCCCTCCAGTGTCAG | 50855 |
rs747172616 | in-del | -/C | 1.66436e-05 | 0.00288471 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659464 | GCCCAAGCCCTCCTA[-/C]CCCCATAGGCGTCTG | 50855 |
rs747339054 | snp | A/T | 3.30382e-05 | 0.00406423 | downstream-variant-500B, missense, nc-transcript-variant | PARD6A, ENKD1 | GRCh38.p7 | 16:67663208 | GAGAAAAGATCTTGA[A/T]GGCCTCCTCTACCTG | 50855 |
rs747377996 | snp | A/G | 1.68091e-05 | 0.00289901 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67659586 | GCAGCAGGCTGAAGC[A/G]GTCCACCTGGAGATA | 50855 |
rs747479522 | snp | C/T | 1.83937e-05 | 0.00303257 | intron-variant, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661862 | AGTCGGGGAGCAGGT[C/T]TCTGATCTCAACATC | 50855 |
rs747553547 | snp | A/C | 1.83239e-05 | 0.00302682 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67660060 | CCTGACGGCGGCGAG[A/C]GGCGTCAATCCCACC | 50855 |
rs747598378 | snp | C/T | 1.97967e-05 | 0.0031461 | intron-variant, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661720 | TGTGGGGTAAGGTGT[C/T]TGTGGGGCAGGTCTA | 50855 |
rs747685311 | snp | A/G | 1.65282e-05 | 0.00287469 | downstream-variant-500B, synonymous-codon, nc-transcript-variant | PARD6A, ENKD1 | GRCh38.p7 | 16:67663260 | AGCACGGTGGCTCTG[A/G]GCTCTCAGTGAGTCT | 50855 |
rs747830238 | snp | A/G | 3.4862e-05 | 0.0041749 | upstream-variant-2KB, stop-gained, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660142 | GCAGCTGCCCGGCTC[A/G]TGGACTGGAGGGTGT | 50855 |
rs748091478 | snp | C/T | 1.65974e-05 | 0.0028807 | synonymous-codon, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67662437 | GCCTGCTGAGCCTGA[C/T]AGTGACGATGACAGC | 50855 |
rs748287317 | snp | C/G | 1.65119e-05 | 0.00287327 | missense, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67662165 | GCTCCCCAGGGCCTG[C/G]AGCGGGTTCCAGGAA | 50855 |
rs748292548 | in-del | -/GC | 0.000102095 | 0.00714401 | intron-variant, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661409 | TGCGGTGAGAAAGGG[-/GC]GCAGGCTGTCCTGAC | 50855 |
rs748312961 | snp | C/T | 1.84126e-05 | 0.00303414 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67659939 | TCCCGCGTCACCAGG[C/T]ATCGGACACTGTGGG | 50855 |
rs748459722 | snp | A/C/G | 6.67996e-05 | 0.00577892 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659488 | GCGTCTGCCAGCGCC[A/C/G]GCCAGGCTGGGGTGG | 50855 |
rs748460235 | snp | A/G | 1.65296e-05 | 0.00287481 | synonymous-codon, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67662092 | GGTGCGGCTGCACAA[A/G]CATGGTTCAGACCGC | 50855 |
rs748543340 | snp | A/G | 2.02128e-05 | 0.003179 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660370 | CCTGCGCACGAGGGC[A/G]TCCTGCTCGGGGGCC | 50855 |
rs748628507 | snp | C/G | 1.65239e-05 | 0.00287431 | downstream-variant-500B, missense, nc-transcript-variant | PARD6A, ENKD1 | GRCh38.p7 | 16:67663203 | GGGCCGAGAAAAGAT[C/G]TTGATGGCCTCCTCT | 50855 |
rs748654119 | snp | C/T | 6.7175e-05 | 0.00579508 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67659568 | GCCGGGGCTGCTCCG[C/T]GGGCAGCAGGCTGAA | 50855 |
rs748690010 | snp | A/C | 5.02812e-05 | 0.00501379 | intron-variant, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661448 | CTCCCCCAACCCCGA[A/C]TTCCAGTTTGACGCC | 50855 |
rs748777136 | snp | C/T | 8.26576e-05 | 0.00642822 | downstream-variant-500B, missense, nc-transcript-variant | PARD6A, ENKD1 | GRCh38.p7 | 16:67663192 | ACGAAGACTTTGGGC[C/T]GAGAAAAGATCTTGA | 50855 |
rs748784167 | snp | A/G | 2.38797e-05 | 0.00345533 | missense, upstream-variant-2KB, intron-variant, downstream-variant-500B | PARD6A, ACD, ENKD1 | GRCh38.p7 | 16:67662627 | CGCATTCGAGGAGAT[A/G]GTAGTGGCTTCAGCC | 50855 |
rs748798721 | snp | A/T | 1.66436e-05 | 0.00288471 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659464 | GGCCCAAGCCCTCCT[A/T]CCCCATAGGCGTCTG | 50855 |
rs748909414 | snp | G/T | | | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659130 | AAAGGGGAGGACCAG[G/T]AGGGTGAGGGGGAAG | 50855 |
rs748967256 | snp | A/G | 3.31912e-05 | 0.00407363 | missense, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661552 | TGCACCAGATCCCGG[A/G]CCTGGACGTGCTACT | 50855 |
rs749050643 | snp | C/T | 1.6517e-05 | 0.00287372 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67658985 | TGCTGTGCAAGGGCC[C/T]TCCAGTGTCAGGCAG | 50855 |
rs749195770 | snp | A/T | 1.6525e-05 | 0.00287441 | missense, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67662326 | GGTTGCCAACAGCCA[A/T]AACCTCATTGTCACT | 50855 |
rs749224903 | snp | A/G | 1.65419e-05 | 0.00287588 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659098 | GGGACAGGGGACCAT[A/G]GGATGAGTCAAGGCT | 50855 |
rs749300002 | snp | C/G | 1.75016e-05 | 0.00295813 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659812 | TGCAACAAGCAGGAT[C/G]CTCACTGCCGGGCCC | 50855 |
rs749387075 | snp | A/C | 1.65537e-05 | 0.0028769 | downstream-variant-500B, missense, nc-transcript-variant | PARD6A, ENKD1 | GRCh38.p7 | 16:67663178 | AGTCGTCCATCTTCA[A/C]GAAGACTTTGGGCCG | 50855 |
rs749408120 | snp | A/G | 3.59486e-05 | 0.00423946 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660528 | AGGGAACAGAACAAG[A/G]GCTGGTCCCGTCCCT | 50855 |
rs749490861 | snp | A/G | 9.92802e-05 | 0.00704487 | missense, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661989 | CACCCCTGCGCACCC[A/G]GCCACCCTTGCTAAT | 50855 |
rs749600273 | snp | A/C/G | 3.79451e-05 | 0.00435561 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660309 | AGAGGAAGCTCCTTC[A/C/G]CTGGGCGGGGCCGGA | 50855 |
rs749685291 | in-del | -/GCA | 6.68617e-05 | 0.00578155 | upstream-variant-2KB, cds-indel, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67659743 | GAACCCCGCAGTCCT[-/GCA]GCAGCAGCAGCCGGC | 50855 |
rs749692596 | in-del | -/T | 9.16196e-05 | 0.00676767 | intron-variant, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661875 | TCTCTGATCTCAACA[-/T]TCCCCCCTCTTCTGC | 50855 |
rs749694197 | snp | A/G | 3.30589e-05 | 0.00406551 | missense, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67662082 | CCCACCGACGGGTGC[A/G]GCTGCACAAGCATGG | 50855 |
rs749787512 | snp | A/G | 4.94939e-05 | 0.00497439 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659355 | CAACACGTGGCCCCC[A/G]AGCCCAACCCCAGAC | 50855 |
rs749911340 | snp | C/T | 2.01173e-05 | 0.00317147 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660355 | CACGTACACCCCGCG[C/T]CTGCGCACGAGGGCG | 50855 |
rs749999364 | snp | C/T | 3.30371e-05 | 0.00406417 | missense, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67662144 | GATGGCATGAGCGTG[C/T]GTGTGGCTCCCCAGG | 50855 |
rs750057739 | snp | C/T | 2.00515e-05 | 0.00316629 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660386 | TCCTGCTCGGGGGCC[C/T]GTGTGCAGACTCCCG | 50855 |
rs750088453 | snp | A/G | 1.65908e-05 | 0.00288012 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659449 | AGGGTAGTTAATGGG[A/G]GCCCAAGCCCTCCTA | 50855 |
rs750170883 | snp | A/G | 1.65151e-05 | 0.00287355 | downstream-variant-500B, missense, nc-transcript-variant | PARD6A, ENKD1 | GRCh38.p7 | 16:67663235 | CCTGCACCAGCTTCC[A/G]GTCCAGCTCAGCACG | 50855 |
rs750180592 | snp | A/C/G | 0.000149389 | 0.00864151 | synonymous-codon, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661535 | GCGGTTGCTGCGGGC[A/C/G]GTGCACCAGATCCCG | 50855 |
rs750373039 | snp | A/G | 1.81836e-05 | 0.00301521 | missense, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661675 | TACTGGTGCAGAAGC[A/G]GGGTGAGGAGGGGTA | 50855 |
rs750483117 | snp | A/G | 1.64765e-05 | 0.00287019 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659270 | AGGTGCTCCCTACAG[A/G]AAGAGAGTGGCCAGG | 50855 |
rs750571306 | snp | A/G | 3.29565e-05 | 0.00405921 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659212 | GTGTTAGGATCACTG[A/G]TCAAGCTCTACAGTA | 50855 |
rs750631382 | snp | A/G | 1.77979e-05 | 0.00298306 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660510 | GATTCCTGTGGTACC[A/G]GTAGGGAACAGAACA | 50855 |
rs750637588 | snp | C/T | 0.000189272 | 0.00972626 | missense, upstream-variant-2KB, intron-variant, downstream-variant-500B | PARD6A, ACD, ENKD1 | GRCh38.p7 | 16:67662598 | AGGAGCAGGCCAGTT[C/T]TGGCTGGGGGAGTCG | 50855 |
rs750713830 | snp | A/G | 3.74763e-05 | 0.0043286 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659868 | CGCGCTCTCCTGCCG[A/G]ACTCCGACCTCCAGA | 50855 |
rs750839783 | snp | A/G | 5.22234e-05 | 0.00510969 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659808 | TCCCTGCAACAAGCA[A/G]GATCCTCACTGCCGG | 50855 |
rs751017242 | snp | C/T | 1.65154e-05 | 0.00287358 | missense, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67662058 | TAGACGTGGACCTAC[C/T]GCCTGAGACCCACCG | 50855 |
rs751146938 | snp | C/T | 1.85958e-05 | 0.00304919 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659858 | CCGCCCACCTCGCGC[C/T]CTCCTGCCGGACTCC | 50855 |
rs751203648 | snp | G/T | 1.79606e-05 | 0.00299666 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660286 | CCCAGGCCCCGCCTT[G/T]CCTCGGAAGAGGAAG | 50855 |
rs751391813 | snp | C/T | 1.64931e-05 | 0.00287163 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659328 | ACCTAGATACACCAT[C/T]CCCTCACCAAACAAC | 50855 |
rs751398085 | snp | A/G | 1.99754e-05 | 0.00316027 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660343 | GGAGGCCCCGCCCAC[A/G]TACACCCCGCGCCTG | 50855 |
rs751398766 | snp | A/C | 1.64996e-05 | 0.0028722 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659363 | GGCCCCCGAGCCCAA[A/C]CCCAGACTCACTCAA | 50855 |
rs751400558 | in-del | -/ATT | 1.66403e-05 | 0.00288442 | cds-indel, upstream-variant-2KB, intron-variant, downstream-variant-500B | PARD6A, ACD, ENKD1 | GRCh38.p7 | 16:67662465 | AGCAGTGACCTGGTC[-/ATT]GAGAACCGCCAGCCT | 50855 |
rs751536397 | snp | C/G | 1.68332e-05 | 0.00290109 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | PARD6A, ENKD1 | GRCh38.p7 | 16:67663142 | CATGGAGCTCCTTGC[C/G]ACTGTCCCCCAAAGG | 50855 |
rs751542254 | snp | C/G | 1.65291e-05 | 0.00287476 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659083 | ACAGTGATAGGCCTG[C/G]GGACAGGGGACCATG | 50855 |
rs751731124 | snp | A/G | 7.09585e-05 | 0.00595602 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67660102 | CCGCCTCGGTCTCCG[A/G]GCCCTGAATGGGGGC | 50855 |
rs751778776 | snp | A/G | 4.96759e-05 | 0.00498352 | missense, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67662391 | GAGGGGCATCTGGGC[A/G]TTTGACAGGTCCTCC | 50855 |
rs751811734 | snp | A/G | 1.64792e-05 | 0.00287042 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659203 | CTGCACAGCGTGTTA[A/G]GATCACTGGTCAAGC | 50855 |
rs751834607 | snp | A/G | 5.32864e-05 | 0.00516143 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660505 | GTCAAGATTCCTGTG[A/G]TACCGGTAGGGAACA | 50855 |
rs751841867 | in-del | -/CCCGGCCCG | 3.3757e-05 | 0.00410821 | utr-variant-5-prime, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661017 | GCCTGGGGCACCGTC[-/CCCGGCCCG]CCCGGCCCGCCCGGC | 50855 |
rs752006255 | snp | C/T | 1.84008e-05 | 0.00303316 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660436 | CACGGGATGCTGGCC[C/T]GTTTACTCTCATCGC | 50855 |
rs752019137 | snp | G/T | 0.000135575 | 0.00823219 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67659777 | CTCTGTCCCGCGGAA[G/T]CCGAACTCCTTCTCC | 50855 |
rs752200943 | snp | C/G | 3.38032e-05 | 0.00411102 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67659771 | CCGGCCCTCTGTCCC[C/G]CGGAAGCCGAACTCC | 50855 |
rs752337933 | snp | A/G | | | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659169 | TTGAGGAAGCATAAG[A/G]TTAAGGCTGGAGAGA | 50855 |
rs752339028 | snp | C/T | 5.1721e-05 | 0.00508506 | missense, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661926 | GCCTGGCTTTTGCCT[C/T]CAACTCTCTGCAGCG | 50855 |
rs752481347 | snp | C/T | 1.65217e-05 | 0.00287412 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660235 | TCCCCACGGCTACAC[C/T]CAGCGGATGCAACGG | 50855 |
rs752493893 | snp | A/C | 1.77059e-05 | 0.00297533 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660269 | CGGGTTTCCCGCGGG[A/C]GCCCAGGCCCCGCCT | 50855 |
rs752533462 | snp | A/G | 1.65165e-05 | 0.00287367 | synonymous-codon, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67662038 | CCGCCAGGTTTCCTC[A/G]GTCATAGACGTGGAC | 50855 |
rs752647489 | snp | C/G/T | 3.38073e-05 | 0.00411129 | missense, synonymous-codon, upstream-variant-2KB, intron-variant, downstream-variant-500B | PARD6A, ACD, ENKD1 | GRCh38.p7 | 16:67662539 | CCTGCACCCTGGCTG[C/G/T]CGACATCCTGGTACC | 50855 |
rs752683720 | snp | C/G | 1.86253e-05 | 0.0030516 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660017 | GCGTGGGATGGGCCC[C/G]CGACCGCGGCCTCGG | 50855 |
rs752698276 | snp | A/G | 1.64773e-05 | 0.00287026 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659292 | GTGGCCAGGACTCAG[A/G]AACCATGCTGAGGCC | 50855 |
rs752771656 | snp | A/G | 1.66078e-05 | 0.00288161 | synonymous-codon, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661520 | CTTCCAGGAGTTCTC[A/G]CGGTTGCTGCGGGCG | 50855 |
rs752787230 | snp | A/C | 1.69467e-05 | 0.00291085 | missense, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661620 | ACCAACGACGACAGC[A/C]TGCACCGGGCCCTGG | 50855 |
rs752926001 | snp | A/G | 4.95782e-05 | 0.00497862 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67658964 | AGCCCAGTGGGTGAC[A/G]GGGGGTGCTGTGCAA | 50855 |
rs752935070 | snp | A/G | 1.65449e-05 | 0.00287614 | synonymous-codon, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67662377 | CAATAACGTGGTGCG[A/G]GGGGCATCTGGGCGT | 50855 |
rs752980678 | snp | C/G | 1.80033e-05 | 0.00300022 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67660084 | TCCCACCACCCCGGG[C/G]CTCCGCCTCGGTCTC | 50855 |
rs753040978 | snp | A/G | 7.93919e-05 | 0.00629997 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660395 | GGGGCCTGTGTGCAG[A/G]CTCCCGCTGGTCCAC | 50855 |
rs753239056 | snp | A/G | 1.90601e-05 | 0.00308702 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660417 | CTGGTCCACCCCGCT[A/G]GTGCACGGGATGCTG | 50855 |
rs753350385 | snp | C/G | 3.35706e-05 | 0.00409685 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67659557 | AGGCACCCGTAGCCG[C/G]GGCTGCTCCGTGGGC | 50855 |
rs753367228 | snp | A/C | 5.51303e-05 | 0.00524996 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660300 | TTCCTCGGAAGAGGA[A/C]GCTCCTTCGCTGGGC | 50855 |
rs753395988 | snp | A/G | | | missense, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67662361 | AGCCCGCCAACCAGC[A/G]CAATAACGTGGTGCG | 50855 |
rs753448266 | snp | A/G | 1.68346e-05 | 0.00290121 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659629 | CTGGAGGAGTTCGGG[A/G]GGAAGGGGGGGTCTC | 50855 |
rs753600700 | snp | C/T | 3.51346e-05 | 0.00419119 | missense, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661914 | CTGACTCCAGCGGCC[C/T]GGCTTTTGCCTCCAA | 50855 |
rs753635377 | in-del | -/G | 1.65168e-05 | 0.00287369 | upstream-variant-2KB, frameshift-variant, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67658992 | CAAGGGCCCTCCAGT[-/G]TCAGGCAGCTTTCAG | 50855 |
rs753646356 | snp | G/T | 1.74799e-05 | 0.00295629 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660133 | TCACCTCAAGCAGCT[G/T]CCCGGCTCGTGGACT | 50855 |
rs753666055 | in-del | -/C | 3.9803e-05 | 0.00446093 | upstream-variant-2KB, frameshift-variant, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660342 | AGGAGGCCCCGCCCA[-/C]GTACACCCCGCGCCT | 50855 |
rs753936561 | snp | C/T | 1.65083e-05 | 0.00287296 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67659395 | GCAGTCATAGAGCTT[C/T]TTCTGAACATCTAAG | 50855 |
rs754074047 | snp | G/T | 1.66308e-05 | 0.00288359 | missense, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661497 | CTGCCTCGCGCTTCG[G/T]TGAGCGGCTTCCAGG | 50855 |
rs754155392 | snp | C/G | 1.65318e-05 | 0.002875 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67658955 | TCGTGAGGCAGCCCA[C/G]TGGGTGACAGGGGGT | 50855 |
rs754238984 | snp | A/G | 5.52542e-05 | 0.00525586 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67659991 | TGGCCCCGACGTCGG[A/G]CGTATCAGGGGCGTG | 50855 |
rs754351563 | snp | C/T | 1.65127e-05 | 0.00287334 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67659037 | GCCCCCTGATGCTCC[C/T]GGTCCTCCCGCATTT | 50855 |
rs754391891 | snp | A/G | 1.65141e-05 | 0.00287346 | missense, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67662261 | GAGATCCTCGAGGTC[A/G]ATGGCATTGAAGTAG | 50855 |
rs754452675 | snp | A/G | 1.67866e-05 | 0.00289707 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67659559 | GCACCCGTAGCCGGG[A/G]CTGCTCCGTGGGCAG | 50855 |
rs754474146 | snp | A/C/G | 1.65304e-05 | 0.00287488 | downstream-variant-500B, missense, nc-transcript-variant | PARD6A, ENKD1 | GRCh38.p7 | 16:67663193 | CGAAGACTTTGGGCC[A/C/G]AGAAAAGATCTTGAT | 50855 |
rs754617378 | snp | C/G | 3.73539e-05 | 0.00432152 | intron-variant, upstream-variant-2KB, stop-gained | PARD6A, ACD | GRCh38.p7 | 16:67661691 | GGGTGAGGAGGGGTA[C/G]AGTGGGCAGCCTCTG | 50855 |
rs754742811 | snp | C/T | 1.74017e-05 | 0.00294967 | missense, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661920 | CCAGCGGCCTGGCTT[C/T]TGCCTCCAACTCTCT | 50855 |
rs754743715 | snp | C/G/T | 0.000159758 | 0.00893619 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660503 | TCGTCAAGATTCCTG[C/G/T]GGTACCGGTAGGGAA | 50855 |
rs754815475 | snp | C/G | 1.74671e-05 | 0.00295521 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660136 | CCTCAAGCAGCTGCC[C/G]GGCTCGTGGACTGGA | 50855 |
rs754832869 | snp | A/G | 8.29621e-05 | 0.00644004 | missense, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67662429 | GGGCCTGGGCCTGCT[A/G]AGCCTGATAGTGACG | 50855 |
rs755096451 | snp | C/G | 1.67452e-05 | 0.0028935 | intron-variant, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661146 | CGCTCCCAATTCCCT[C/G]TTTCTCCCCTTCCCA | 50855 |
rs755121514 | in-del | -/G | 1.67368e-05 | 0.00289277 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659501 | CGGCCAGGCTGGGGT[-/G]GGGGAGAGCTGCTGG | 50855 |
rs755166756 | snp | C/G | 3.6972e-05 | 0.00429938 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660002 | TCGGACGTATCAGGG[C/G]CGTGGGATGGGCCCG | 50855 |
rs755262674 | snp | C/T | 1.89045e-05 | 0.00307439 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659897 | GAGCCGCGCGGGGCC[C/T]CTCACCAGTCCGAGG | 50855 |
rs755371076 | snp | G/T | 0.000181853 | 0.0095338 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67658956 | CGTGAGGCAGCCCAG[G/T]GGGTGACAGGGGGTG | 50855 |
rs755492638 | snp | A/G | 1.98821e-05 | 0.00315288 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660393 | CGGGGGCCTGTGTGC[A/G]GACTCCCGCTGGTCC | 50855 |
rs755523137 | snp | A/C | 0.000115614 | 0.0076022 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67659060 | CCGCATTTCATCCAG[A/C]AGCTGGGACAGTGAT | 50855 |
rs755584473 | snp | G/T | 2.01262e-05 | 0.00317217 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660357 | CGTACACCCCGCGCC[G/T]GCGCACGAGGGCGTC | 50855 |
rs755751410 | snp | G/T | 3.30775e-05 | 0.00406665 | downstream-variant-500B, missense, nc-transcript-variant | PARD6A, ENKD1 | GRCh38.p7 | 16:67663186 | ATCTTCACGAAGACT[G/T]TGGGCCGAGAAAAGA | 50855 |
rs755769548 | snp | C/T | 5.03149e-05 | 0.00501547 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67659545 | CACTTACCAACCAGG[C/T]ACCCGTAGCCGGGGC | 50855 |
rs755780326 | snp | A/G | 1.65957e-05 | 0.00288055 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659450 | GGGTAGTTAATGGGG[A/G]CCCAAGCCCTCCTAC | 50855 |
rs755878423 | snp | C/T | 3.30393e-05 | 0.0040643 | downstream-variant-500B, missense, nc-transcript-variant | PARD6A, ENKD1 | GRCh38.p7 | 16:67663247 | TCCGGTCCAGCTCAG[C/T]ACGGTGGCTCTGGGC | 50855 |
rs756100252 | in-del | -/AGG | 3.32436e-05 | 0.00407685 | cds-indel, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661510 | CGGTGAGCGGCTTCC[-/AGG]AGTTCTCGCGGTTGC | 50855 |
rs756187203 | snp | C/G | 0.000671476 | 0.0183108 | synonymous-codon, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661676 | ACTGGTGCAGAAGCG[C/G]GGTGAGGAGGGGTAC | 50855 |
rs756189227 | snp | C/G | 7.43992e-05 | 0.00609869 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660031 | CGCGACCGCGGCCTC[C/G]GCGTCCTGTAGTACC | 50855 |
rs756232775 | snp | A/G | 1.67905e-05 | 0.00289741 | missense, upstream-variant-2KB, intron-variant, downstream-variant-500B | PARD6A, ACD, ENKD1 | GRCh38.p7 | 16:67662522 | GGGCCCCCGTGCTGG[A/G]ACCTGCACCCTGGCT | 50855 |
rs756280387 | snp | C/G | 1.6748e-05 | 0.00289374 | intron-variant, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661131 | GGCCTCGGCCCTAGG[C/G]GCTCCCAATTCCCTC | 50855 |
rs756396872 | snp | A/C | 1.78163e-05 | 0.0029846 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660518 | TGGTACCGGTAGGGA[A/C]CAGAACAAGGGCTGG | 50855 |
rs756476640 | snp | C/T | 3.75312e-05 | 0.00433177 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659871 | GCTCTCCTGCCGGAC[C/T]CCGACCTCCAGAGCC | 50855 |
rs756596405 | snp | G/T | 5.55818e-05 | 0.00527141 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660303 | CTCGGAAGAGGAAGC[G/T]CCTTCGCTGGGCGGG | 50855 |
rs756725846 | snp | A/G | 3.30595e-05 | 0.00406554 | missense, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67662076 | CTGAGACCCACCGAC[A/G]GGTGCGGCTGCACAA | 50855 |
rs756735352 | snp | A/G | 1.65228e-05 | 0.00287422 | synonymous-codon, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67662065 | GGACCTACTGCCTGA[A/G]ACCCACCGACGGGTG | 50855 |
rs756810885 | in-del | -/A | | | utr-variant-3-prime, upstream-variant-2KB, intron-variant, downstream-variant-500B | PARD6A, ACD, ENKD1 | GRCh38.p7 | 16:67662648 | GCTTCAGCCTCTGAC[-/A]AGTCAGGATGAAGCC | 50855 |
rs756878832 | snp | C/T | 1.6495e-05 | 0.0028718 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659335 | TACACCATCCCCTCA[C/T]CAAACAACACGTGGC | 50855 |
rs756883228 | snp | A/C | 6.01136e-05 | 0.00548208 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660348 | CCCCGCCCACGTACA[A/C]CCCGCGCCTGCGCAC | 50855 |
rs756960132 | in-del | -/T | 1.65127e-05 | 0.00287334 | upstream-variant-2KB, frameshift-variant, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67659028 | CACACGAGTGCCCCC[-/T]GATGCTCCTGGTCCT | 50855 |
rs756973095 | snp | C/T | 1.79774e-05 | 0.00299806 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660287 | CCAGGCCCCGCCTTT[C/T]CTCGGAAGAGGAAGC | 50855 |
rs757072954 | snp | C/T | 1.65806e-05 | 0.00287924 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659445 | GAGAAGGGTAGTTAA[C/T]GGGGGCCCAAGCCCT | 50855 |
rs757084527 | in-del | -/CCCGCTGGTCCAC | 3.9657e-05 | 0.00445274 | upstream-variant-2KB, frameshift-variant, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660398 | GCCTGTGTGCAGACT[-/CCCGCTGGTCCAC]CCCGCTGGTGCACGG | 50855 |
rs757097343 | snp | C/T | 1.83421e-05 | 0.00302832 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67659951 | AGGCATCGGACACTG[C/T]GGGTCCCGTCAGACA | 50855 |
rs757298220 | snp | G/T | 1.69651e-05 | 0.00291243 | intron-variant, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661419 | AAGGGGCGCAGGCTG[G/T]CCTGACTCCTCCTCT | 50855 |
rs757319727 | snp | A/C | 0.010998 | 0.0733351 | missense, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67662319 | ACATGATGGTTGCCA[A/C]CAGCCATAACCTCAT | 50855 |
rs757375976 | snp | A/G | 1.82081e-05 | 0.00301724 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660441 | GATGCTGGCCCGTTT[A/G]CTCTCATCGCGGCGT | 50855 |
rs757564601 | snp | G/T | 1.64741e-05 | 0.00286998 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659640 | CGGGGGGAAGGGGGG[G/T]TCTCAGAATCGTCAC | 50855 |
rs757647052 | snp | C/T | 1.77565e-05 | 0.00297958 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660506 | TCAAGATTCCTGTGG[C/T]ACCGGTAGGGAACAG | 50855 |
rs757659133 | snp | A/G | | | utr-variant-3-prime, upstream-variant-2KB, intron-variant, downstream-variant-500B | PARD6A, ACD, ENKD1 | GRCh38.p7 | 16:67662708 | CAGGGACTTCACAGT[A/G]GGGGTTTTTAGCTGG | 50855 |
rs757745319 | snp | C/T | 1.65729e-05 | 0.00287857 | missense, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661977 | TGCGGCCAGTGGCAC[C/T]CCTGCGCACCCGGCC | 50855 |
rs757994924 | snp | C/T | 1.65154e-05 | 0.00287358 | synonymous-codon, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67662047 | TTCCTCAGTCATAGA[C/T]GTGGACCTACTGCCT | 50855 |
rs758017018 | snp | C/G | 1.73507e-05 | 0.00294535 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660236 | CCCCACGGCTACACC[C/G]AGCGGATGCAACGGG | 50855 |
rs758189246 | snp | A/G | 1.77143e-05 | 0.00297605 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660270 | GGGTTTCCCGCGGGC[A/G]CCCAGGCCCCGCCTT | 50855 |
rs758226980 | snp | C/G | 2.14521e-05 | 0.00327499 | utr-variant-5-prime, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67660998 | CACCTGCGCCTCGGC[C/G]GGCCGCCTGGGGCAC | 50855 |
rs758329179 | snp | C/G | 3.29554e-05 | 0.00405914 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659309 | ACCATGCTGAGGCCT[C/G]TCTACCTAGATACAC | 50855 |
rs758505693 | snp | C/G | 1.65233e-05 | 0.00287426 | missense, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67662305 | GGACCAAGTGACGGA[C/G]ATGATGGTTGCCAAC | 50855 |
rs758513965 | snp | C/T | 3.72245e-05 | 0.00431403 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660021 | GGGATGGGCCCGCGA[C/T]CGCGGCCTCGGCGTC | 50855 |
rs758515562 | snp | A/G | 1.65154e-05 | 0.00287358 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67659047 | GCTCCTGGTCCTCCC[A/G]CATTTCATCCAGAAG | 50855 |
rs758609206 | snp | C/T | 1.77995e-05 | 0.00298319 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67660098 | GCCTCCGCCTCGGTC[C/T]CCGGGCCCTGAATGG | 50855 |
rs758700674 | snp | A/G | 8.26248e-05 | 0.00642694 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67658966 | CCCAGTGGGTGACAG[A/G]GGGTGCTGTGCAAGG | 50855 |
rs758832394 | snp | A/G | 4.95839e-05 | 0.0049789 | downstream-variant-500B, missense, nc-transcript-variant | PARD6A, ENKD1 | GRCh38.p7 | 16:67663261 | GCACGGTGGCTCTGG[A/G]CTCTCAGTGAGTCTG | 50855 |
rs759044581 | snp | C/G | 1.68035e-05 | 0.00289853 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67659584 | GGGCAGCAGGCTGAA[C/G]CGGTCCACCTGGAGA | 50855 |
rs759083028 | snp | C/T | 1.66996e-05 | 0.00288956 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67659741 | ATGAACCCCGCAGTC[C/T]TGCAGCAGCAGCAGC | 50855 |
rs759118228 | snp | C/T | 1.66427e-05 | 0.00288462 | missense, upstream-variant-2KB, intron-variant, downstream-variant-500B | PARD6A, ACD, ENKD1 | GRCh38.p7 | 16:67662466 | GCAGTGACCTGGTCA[C/T]TGAGAACCGCCAGCC | 50855 |
rs759257949 | in-del | -/G | 1.84306e-05 | 0.00303562 | upstream-variant-2KB, frameshift-variant, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67659993 | GCCCCGACGTCGGAC[-/G]TATCAGGGGCGTGGG | 50855 |
rs759315599 | snp | C/T | 1.77398e-05 | 0.00297818 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660500 | CGTTCGTCAAGATTC[C/T]TGTGGTACCGGTAGG | 50855 |
rs759365615 | snp | A/C/T | 6.6127e-05 | 0.00574976 | missense, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67662105 | AAGCATGGTTCAGAC[A/C/T]GCCCCCTGGGCTTCT | 50855 |
rs759423471 | snp | C/T | 1.79486e-05 | 0.00299566 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659831 | ACTGCCGGGCCCACC[C/T]GAACACAAGGCCCGC | 50855 |
rs759493487 | snp | A/C/G | 3.52535e-05 | 0.00419827 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660263 | CGGGCCCGGGTTTCC[A/C/G]GCGGGCGCCCAGGCC | 50855 |
rs759553652 | snp | A/C/G | 3.34651e-05 | 0.00409043 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659526 | TGCTGGAGGGCGGAG[A/C/G]CATCACTTACCAACC | 50855 |
rs759583879 | snp | A/C | 4.95577e-05 | 0.00497759 | synonymous-codon, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67662026 | GCCCCAAGATTTCCG[A/C]CAGGTTTCCTCAGTC | 50855 |
rs759619436 | in-del | -/GGCCCT | | | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67660102 | CCGCCTCGGTCTCCG[-/GGCCCT]GAATGGGGGCTCACC | 50855 |
rs759840101 | snp | A/G | 4.95356e-05 | 0.00497648 | upstream-variant-2KB, stop-gained, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67659038 | CCCCCTGATGCTCCT[A/G]GTCCTCCCGCATTTC | 50855 |
rs759902558 | snp | C/T | 1.6516e-05 | 0.00287362 | downstream-variant-500B, missense, nc-transcript-variant | PARD6A, ENKD1 | GRCh38.p7 | 16:67663226 | CCTCCTCTACCTGCA[C/T]CAGCTTCCGGTCCAG | 50855 |
rs759971683 | snp | C/T | 1.81204e-05 | 0.00300996 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67660075 | CGGCGTCAATCCCAC[C/T]ACCCCGGGCCTCCGC | 50855 |
rs760222002 | snp | C/G | 1.93127e-05 | 0.0031074 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660412 | TCCCGCTGGTCCACC[C/G]CGCTGGTGCACGGGA | 50855 |
rs760251332 | in-del | -/AG | 1.67293e-05 | 0.00289212 | frameshift-variant, upstream-variant-2KB, intron-variant, downstream-variant-500B | PARD6A, ACD, ENKD1 | GRCh38.p7 | 16:67662505 | CCAATGGGCTGTCTC[-/AG]GGGCCCCCGTGCTGG | 50855 |
rs760272736 | snp | A/G | 1.65121e-05 | 0.00287329 | missense, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67662255 | AGTGATGAGATCCTC[A/G]AGGTCAATGGCATTG | 50855 |
rs760441780 | snp | C/G | 2.00042e-05 | 0.00316255 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660387 | CCTGCTCGGGGGCCT[C/G]TGTGCAGACTCCCGC | 50855 |
rs760468921 | snp | A/G | 1.65392e-05 | 0.00287564 | missense, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67662366 | GCCAACCAGCGCAAT[A/G]ACGTGGTGCGAGGGG | 50855 |
rs760567176 | in-del | -/A | 1.95251e-05 | 0.00312445 | upstream-variant-2KB, frameshift-variant, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660324 | GCTGGGCGGGGCCGG[-/A]GGAGGAGGCCCCGCC | 50855 |
rs760846129 | snp | A/G | 1.9258e-05 | 0.003103 | missense, upstream-variant-2KB, intron-variant, downstream-variant-500B | PARD6A, ACD, ENKD1 | GRCh38.p7 | 16:67662601 | AGCAGGCCAGTTCTG[A/G]CTGGGGGAGTCGCAT | 50855 |
rs760871431 | snp | C/G | 1.64768e-05 | 0.00287021 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659285 | GAAGAGAGTGGCCAG[C/G]ACTCAGGAACCATGC | 50855 |
rs761031862 | snp | C/T | 1.66518e-05 | 0.00288542 | missense, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661485 | CGACGCTTCGCGCTG[C/T]CTCGCGCTTCGGTGA | 50855 |
rs761136320 | snp | C/T | 1.81694e-05 | 0.00301403 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67660069 | GGCGAGCGGCGTCAA[C/T]CCCACCACCCCGGGC | 50855 |
rs761225834 | snp | A/C/G | 3.33418e-05 | 0.00408289 | missense, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661590 | ACGGATGCTCATGGC[A/C/G]ACCTGCTGCCCCTCA | 50855 |
rs761226246 | snp | A/C/G | 7.36106e-05 | 0.00606629 | upstream-variant-2KB, missense, synonymous-codon, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67659986 | CAGCGTGGCCCCGAC[A/C/G]TCGGACGTATCAGGG | 50855 |
rs761367992 | snp | A/G | 3.30229e-05 | 0.0040633 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67659006 | TGTCAGGCAGCTTTC[A/G]GCCAGGCACACGAGT | 50855 |
rs761408466 | snp | A/G | 3.67444e-05 | 0.00428613 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67659977 | AGACACAAGCAGCGT[A/G]GCCCCGACGTCGGAC | 50855 |
rs761598301 | snp | C/T | 1.65209e-05 | 0.00287405 | synonymous-codon, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67662140 | CCGAGATGGCATGAG[C/T]GTGCGTGTGGCTCCC | 50855 |
rs761628896 | snp | A/C/G | 0.000100245 | 0.00707914 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660385 | GTCCTGCTCGGGGGC[A/C/G]TGTGTGCAGACTCCC | 50855 |
rs761646044 | in-del | -/TGGC | 1.65224e-05 | 0.00287418 | downstream-variant-500B, frameshift-variant, nc-transcript-variant | PARD6A, ENKD1 | GRCh38.p7 | 16:67663251 | TCCAGCTCAGCACGG[-/TGGC]TGGCTCTGGGCTCTC | 50855 |
rs761793893 | snp | G/T | 4.95438e-05 | 0.00497689 | downstream-variant-500B, missense, nc-transcript-variant | PARD6A, ENKD1 | GRCh38.p7 | 16:67663231 | TCTACCTGCACCAGC[G/T]TCCGGTCCAGCTCAG | 50855 |
rs761803222 | snp | C/G | 1.65304e-05 | 0.00287488 | missense, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67662000 | ACCCGGCCACCCTTG[C/G]TAATCAGCCTGCCCC | 50855 |
rs761974295 | snp | G/T | 1.67379e-05 | 0.00289287 | missense, upstream-variant-2KB, intron-variant, downstream-variant-500B | PARD6A, ACD, ENKD1 | GRCh38.p7 | 16:67662508 | ATGGGCTGTCTCAGG[G/T]GCCCCCGTGCTGGGA | 50855 |
rs762014701 | snp | C/T | 1.73108e-05 | 0.00294195 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660226 | AACCTGCCATCCCCA[C/T]GGCTACACCCAGCGG | 50855 |
rs762170932 | snp | A/G | 1.81283e-05 | 0.00301061 | missense, upstream-variant-2KB, intron-variant, downstream-variant-500B | PARD6A, ACD, ENKD1 | GRCh38.p7 | 16:67662585 | TCCCTGGATGACCAG[A/G]AGCAGGCCAGTTCTG | 50855 |
rs762184098 | snp | G/T | 1.75597e-05 | 0.00296303 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660256 | GATGCAACGGGCCCG[G/T]GTTTCCCGCGGGCGC | 50855 |
rs762194053 | snp | A/T | 1.86447e-05 | 0.0030532 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659863 | CACCTCGCGCTCTCC[A/T]GCCGGACTCCGACCT | 50855 |
rs762278947 | snp | C/T | 1.66918e-05 | 0.00288888 | synonymous-codon, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661469 | GTTTGACGCCGAGTT[C/T]CGACGCTTCGCGCTG | 50855 |
rs762285636 | snp | C/G | 0.000307529 | 0.0123964 | synonymous-codon, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661074 | TCCGGCGCGCAGTCC[C/G]GATAGCATCGTCGAG | 50855 |
rs762367216 | snp | C/T | 8.89996e-05 | 0.00667022 | utr-variant-3-prime, upstream-variant-2KB, intron-variant, downstream-variant-500B | PARD6A, ACD, ENKD1 | GRCh38.p7 | 16:67662662 | ACAGTCAGGATGAAG[C/T]CCCATGCCACTCCAC | 50855 |
rs762492642 | snp | C/G | 1.84137e-05 | 0.00303422 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659846 | TGAACACAAGGCCCG[C/G]CCACCTCGCGCTCTC | 50855 |
rs762558706 | snp | C/T | 3.48068e-05 | 0.00417159 | missense, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661061 | GGCCGCAGAGGACTC[C/T]GGCGCGCAGTCCCGA | 50855 |
rs762580062 | snp | A/C | 1.69166e-05 | 0.00290827 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67659772 | CGGCCCTCTGTCCCG[A/C]GGAAGCCGAACTCCT | 50855 |
rs762614167 | snp | C/G | 1.64768e-05 | 0.00287021 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659269 | AAGGTGCTCCCTACA[C/G]GAAGAGAGTGGCCAG | 50855 |
rs762709603 | in-del | -/CTC | 8.39116e-05 | 0.00647679 | intron-variant, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661109 | AGAGCAAAGTAAGGG[-/CTC]CTCCGGCCTCGGCCC | 50855 |
rs762912962 | snp | C/T | 1.65094e-05 | 0.00287305 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67659399 | TCATAGAGCTTTTTC[C/T]GAACATCTAAGTCTT | 50855 |
rs763133981 | snp | A/G | 3.43377e-05 | 0.00414339 | synonymous-codon, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661628 | CGACAGCCTGCACCG[A/G]GCCCTGGCCAGCGGG | 50855 |
rs763160982 | snp | C/G | 1.64768e-05 | 0.00287021 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67659263 | CTCTGAAAGGTGCTC[C/G]CTACAGGAAGAGAGT | 50855 |
rs763204816 | snp | G/T | 1.72889e-05 | 0.0029401 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660196 | GAATCCAGGGCCGTA[G/T]GACCAGCCTCCCCGA | 50855 |
rs763325696 | snp | A/G | 1.648e-05 | 0.0028705 | intron-variant, upstream-variant-2KB, splice-acceptor-variant | PARD6A, ACD | GRCh38.p7 | 16:67661892 | CCCCCCTCTTCTGCA[A/G]CAGAAGCTGACTCCA | 50855 |
rs763396372 | snp | C/G | 3.29576e-05 | 0.00405928 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659197 | AGATCACTGCACAGC[C/G]TGTTAGGATCACTGG | 50855 |
rs763439747 | snp | C/T | 1.66604e-05 | 0.00288616 | missense, upstream-variant-2KB, intron-variant, downstream-variant-500B | PARD6A, ACD, ENKD1 | GRCh38.p7 | 16:67662480 | ATTGAGAACCGCCAG[C/T]CTCCCAGTTCCAATG | 50855 |
rs763451945 | in-del | -/C | 1.67576e-05 | 0.00289457 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | PARD6A, ENKD1 | GRCh38.p7 | 16:67663148 | GCTCCTTGCCACTGT[-/C]CCCCAAAGGGGCTCA | 50855 |
rs763498443 | snp | C/T | 1.75526e-05 | 0.00296243 | synonymous-codon, upstream-variant-2KB, intron-variant, downstream-variant-500B | PARD6A, ACD, ENKD1 | GRCh38.p7 | 16:67662572 | CAGCTCTCTGCCCTC[C/T]CTGGATGACCAGGAG | 50855 |
rs763648763 | snp | C/G | | | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659275 | CTCCCTACAGGAAGA[C/G]AGTGGCCAGGACTCA | 50855 |
rs763681096 | snp | C/T | 1.65239e-05 | 0.00287431 | synonymous-codon, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67662125 | CCTGGGCTTCTACAT[C/T]CGAGATGGCATGAGC | 50855 |
rs763681510 | snp | A/G | 7.42997e-05 | 0.00609462 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659856 | GCCCGCCCACCTCGC[A/G]CTCTCCTGCCGGACT | 50855 |
rs763682845 | snp | A/C | 1.77385e-05 | 0.00297808 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660271 | GGTTTCCCGCGGGCG[A/C]CCAGGCCCCGCCTTT | 50855 |
rs763764694 | snp | A/G | 1.65149e-05 | 0.00287353 | missense, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67662048 | TCCTCAGTCATAGAC[A/G]TGGACCTACTGCCTG | 50855 |
rs763876886 | snp | C/T | 0.000119928 | 0.00774272 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660342 | AGGAGGCCCCGCCCA[C/T]GTACACCCCGCGCCT | 50855 |
rs764120026 | in-del | -/C | 7.95672e-05 | 0.00630692 | upstream-variant-2KB, frameshift-variant, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660338 | GAGGAGGAGGCCCCG[-/C]CCACGTACACCCCGC | 50855 |
rs764181425 | snp | A/G | 3.29576e-05 | 0.00405928 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659202 | ACTGCACAGCGTGTT[A/G]GGATCACTGGTCAAG | 50855 |
rs764264611 | snp | C/T | 1.79787e-05 | 0.00299817 | synonymous-codon, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661900 | TTCTGCAGCAGAAGC[C/T]GACTCCAGCGGCCTG | 50855 |
rs764626146 | snp | A/G | 1.69315e-05 | 0.00290955 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67659774 | GCCCTCTGTCCCGCG[A/G]AAGCCGAACTCCTTC | 50855 |
rs764838880 | snp | A/G | 1.68898e-05 | 0.00290596 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659634 | GGAGTTCGGGGGGAA[A/G]GGGGGGTCTCAGAAT | 50855 |
rs765015240 | in-del | -/CCCGCTGGTCCAC | 3.9657e-05 | 0.00445274 | upstream-variant-2KB, frameshift-variant, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660397 | GCCTGTGTGCAGACT[-/CCCGCTGGTCCAC]CCCGCTGGTCCACCC | 50855 |
rs765074184 | snp | C/T | 3.4577e-05 | 0.0041578 | synonymous-codon, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661924 | CGGCCTGGCTTTTGC[C/T]TCCAACTCTCTGCAG | 50855 |
rs765105630 | snp | G/T | 1.65573e-05 | 0.00287721 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660264 | GGGCCCGGGTTTCCC[G/T]CGGGCGCCCAGGCCC | 50855 |
rs765151223 | snp | A/G | | | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660323 | CGCTGGGCGGGGCCG[A/G]AGGAGGAGGCCCCGC | 50855 |
rs765313953 | snp | C/G | 1.80732e-05 | 0.00300604 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67660079 | GTCAATCCCACCACC[C/G]CGGGCCTCCGCCTCG | 50855 |
rs765326647 | snp | C/T | 1.66073e-05 | 0.00288156 | missense, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661519 | GCTTCCAGGAGTTCT[C/T]GCGGTTGCTGCGGGC | 50855 |
rs765378545 | snp | C/T | 1.65157e-05 | 0.0028736 | downstream-variant-500B, synonymous-codon, nc-transcript-variant | PARD6A, ENKD1 | GRCh38.p7 | 16:67663227 | CTCCTCTACCTGCAC[C/T]AGCTTCCGGTCCAGC | 50855 |
rs765403804 | snp | A/G | 1.68886e-05 | 0.00290586 | missense, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661614 | CCCCTCACCAACGAC[A/G]ACAGCCTGCACCGGG | 50855 |
rs765492921 | snp | A/G | 1.65165e-05 | 0.00287367 | synonymous-codon, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67662281 | CATTGAAGTAGCCGG[A/G]AAGACCTTGGACCAA | 50855 |
rs765603105 | snp | C/T | 1.66496e-05 | 0.00288522 | missense, upstream-variant-2KB, intron-variant, downstream-variant-500B | PARD6A, ACD, ENKD1 | GRCh38.p7 | 16:67662474 | CTGGTCATTGAGAAC[C/T]GCCAGCCTCCCAGTT | 50855 |
rs765771729 | snp | A/G | 1.64811e-05 | 0.00287059 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659183 | GGTTAAGGCTGGAGA[A/G]ATCACTGCACAGCGT | 50855 |
rs765775407 | snp | C/T | 1.99316e-05 | 0.00315681 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660390 | GCTCGGGGGCCTGTG[C/T]GCAGACTCCCGCTGG | 50855 |
rs765801423 | snp | A/G | 1.65449e-05 | 0.00287614 | missense, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67662376 | GCAATAACGTGGTGC[A/G]AGGGGCATCTGGGCG | 50855 |
rs765955687 | snp | C/T | 1.65416e-05 | 0.00287586 | synonymous-codon, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67662368 | CAACCAGCGCAATAA[C/T]GTGGTGCGAGGGGCA | 50855 |
rs765971010 | snp | C/T | 1.67809e-05 | 0.00289658 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67659549 | TACCAACCAGGCACC[C/T]GTAGCCGGGGCTGCT | 50855 |
rs765992071 | snp | A/G | 1.68499e-05 | 0.00290253 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659627 | GGCTGGAGGAGTTCG[A/G]GGGGAAGGGGGGGTC | 50855 |
rs766042933 | snp | A/G | 1.65121e-05 | 0.00287329 | missense, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67662258 | GATGAGATCCTCGAG[A/G]TCAATGGCATTGAAG | 50855 |
rs766076324 | snp | C/T | 1.92992e-05 | 0.00310632 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660413 | CCCGCTGGTCCACCC[C/T]GCTGGTGCACGGGAT | 50855 |
rs766256998 | snp | C/T | 8.25975e-05 | 0.00642588 | downstream-variant-500B, missense, nc-transcript-variant | PARD6A, ENKD1 | GRCh38.p7 | 16:67663249 | CGGTCCAGCTCAGCA[C/T]GGTGGCTCTGGGCTC | 50855 |
rs766257662 | snp | A/C | 1.76428e-05 | 0.00297003 | synonymous-codon, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661912 | AGCTGACTCCAGCGG[A/C]CTGGCTTTTGCCTCC | 50855 |
rs766279518 | snp | C/T | 3.30409e-05 | 0.0040644 | missense, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67662024 | CTGCCCCAAGATTTC[C/T]GCCAGGTTTCCTCAG | 50855 |
rs766360608 | snp | C/G | 1.73285e-05 | 0.00294346 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660228 | CCTGCCATCCCCACG[C/G]CTACACCCAGCGGAT | 50855 |
rs766452239 | snp | C/T | 1.66493e-05 | 0.0028852 | missense, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661488 | CGCTTCGCGCTGCCT[C/T]GCGCTTCGGTGAGCG | 50855 |
rs766459239 | snp | A/C/G/T | 0.000380262 | 0.0137844 | missense, upstream-variant-2KB, intron-variant, downstream-variant-500B | PARD6A, ACD, ENKD1 | GRCh38.p7 | 16:67662607 | CCAGTTCTGGCTGGG[A/C/G/T]GAGTCGCATTCGAGG | 50855 |
rs766536462 | snp | A/G | 0.000112082 | 0.00748523 | utr-variant-3-prime, upstream-variant-2KB, intron-variant, downstream-variant-500B | PARD6A, ACD, ENKD1 | GRCh38.p7 | 16:67662692 | CACTGCTGGGACATG[A/G]CAGGGACTTCACAGT | 50855 |
rs766834225 | snp | C/T | 3.3024e-05 | 0.00406336 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67659024 | CAGGCACACGAGTGC[C/T]CCCTGATGCTCCTGG | 50855 |
rs767099534 | snp | C/T | 2.01254e-05 | 0.00317211 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660351 | CGCCCACGTACACCC[C/T]GCGCCTGCGCACGAG | 50855 |
rs767179130 | snp | A/G | 1.6513e-05 | 0.00287336 | missense, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67662193 | GAATCTTCATCTCCC[A/G]CCTGGTACGTGGGGG | 50855 |
rs767192332 | in-del | -/GCCTCGGCGTCCTGTA | 1.86135e-05 | 0.00305064 | upstream-variant-2KB, frameshift-variant, intron-variant, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660026 | GGGCCCGCGACCGCG[-/GCCTCGGCGTCCTGTA]GTACCTGACGGCGGC | 50855 |
rs767285943 | snp | C/G/T | 3.3487e-05 | 0.00409177 | upstream-variant-2KB, splice-donor-variant | PARD6A, ACD | GRCh38.p7 | 16:67659536 | CGGAGGCATCACTTA[C/G/T]CAACCAGGCACCCGT | 50855 |
rs767398992 | snp | C/T | 1.66396e-05 | 0.00288436 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | PARD6A, ENKD1 | GRCh38.p7 | 16:67663160 | TGTCCCCCAAAGGGG[C/T]TCAGTCGTCCATCTT | 50855 |
rs767507409 | snp | C/T | 1.74309e-05 | 0.00295214 | synonymous-codon, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661658 | GCCCCCGCCACTGCG[C/T]CTACTGGTGCAGAAG | 50855 |
rs767670382 | snp | C/T | 1.77963e-05 | 0.00298292 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660509 | AGATTCCTGTGGTAC[C/T]GGTAGGGAACAGAAC | 50855 |
rs767699575 | snp | C/T | 1.75903e-05 | 0.00296561 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660260 | CAACGGGCCCGGGTT[C/T]CCCGCGGGCGCCCAG | 50855 |
rs767758296 | snp | C/T | 1.67649e-05 | 0.0028952 | missense, upstream-variant-2KB, intron-variant, downstream-variant-500B | PARD6A, ACD, ENKD1 | GRCh38.p7 | 16:67662514 | TGTCTCAGGGGCCCC[C/T]GTGCTGGGACCTGCA | 50855 |
rs767844152 | snp | C/G | 1.83933e-05 | 0.00303255 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67659979 | ACACAAGCAGCGTGG[C/G]CCCGACGTCGGACGT | 50855 |
rs767864839 | snp | G/T | 3.4121e-05 | 0.00413029 | missense, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661075 | CCGGCGCGCAGTCCC[G/T]ATAGCATCGTCGAGG | 50855 |
rs768119178 | snp | C/G | 5.62024e-05 | 0.00530076 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659866 | CTCGCGCTCTCCTGC[C/G]GGACTCCGACCTCCA | 50855 |
rs768199238 | snp | C/G | 3.34902e-05 | 0.00409194 | intron-variant, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661451 | CCCCAACCCCGACTT[C/G]CAGTTTGACGCCGAG | 50855 |
rs768234505 | snp | A/T | 1.65979e-05 | 0.00288074 | missense, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661558 | AGATCCCGGGCCTGG[A/T]CGTGCTACTTGGCTA | 50855 |
rs768395580 | snp | A/C/T | 3.67345e-05 | 0.00428557 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67659971 | CCCGTCAGACACAAG[A/C/T]AGCGTGGCCCCGACG | 50855 |
rs768687740 | snp | C/T | 4.95921e-05 | 0.00497932 | synonymous-codon, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67662344 | CCTCATTGTCACTGT[C/T]AAGCCCGCCAACCAG | 50855 |
rs768738227 | snp | A/T | 1.76459e-05 | 0.00297029 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659818 | AAGCAGGATCCTCAC[A/T]GCCGGGCCCACCTGA | 50855 |
rs768926429 | snp | C/T | | | intron-variant, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661728 | AAGGTGTCTGTGGGG[C/T]AGGTCTACAAGGGTT | 50855 |
rs768931747 | snp | A/G | 4.95847e-05 | 0.00497895 | synonymous-codon, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67662083 | CCACCGACGGGTGCG[A/G]CTGCACAAGCATGGT | 50855 |
rs768960565 | snp | C/T | 1.75446e-05 | 0.00296176 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660252 | AGCGGATGCAACGGG[C/T]CCGGGTTTCCCGCGG | 50855 |
rs769050563 | snp | A/G | 1.654e-05 | 0.00287571 | synonymous-codon, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661993 | CCTGCGCACCCGGCC[A/G]CCCTTGCTAATCAGC | 50855 |
rs769084659 | snp | A/C | 1.64993e-05 | 0.00287218 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659361 | GTGGCCCCCGAGCCC[A/C]ACCCCAGACTCACTC | 50855 |
rs769087929 | snp | C/T | 3.08247e-05 | 0.00392574 | missense, upstream-variant-2KB, intron-variant, downstream-variant-500B | PARD6A, ACD, ENKD1 | GRCh38.p7 | 16:67662642 | GGTAGTGGCTTCAGC[C/T]TCTGACAGTCAGGAT | 50855 |
rs769159666 | snp | C/G/T | 6.65606e-05 | 0.00576858 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659466 | CCCAAGCCCTCCTAC[C/G/T]CCATAGGCGTCTGCC | 50855 |
rs769345731 | snp | C/T | 3.43519e-05 | 0.00414424 | synonymous-codon, upstream-variant-2KB, intron-variant, downstream-variant-500B | PARD6A, ACD, ENKD1 | GRCh38.p7 | 16:67662557 | ACATCCTGGTACCCG[C/T]AGCTCTCTGCCCTCC | 50855 |
rs769382877 | snp | A/C | 2.20587e-05 | 0.00332098 | synonymous-codon, upstream-variant-2KB, intron-variant, downstream-variant-500B | PARD6A, ACD, ENKD1 | GRCh38.p7 | 16:67662618 | TGGGGGAGTCGCATT[A/C]GAGGAGATGGTAGTG | 50855 |
rs769528493 | snp | C/T | 1.81665e-05 | 0.00301378 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659837 | GGGCCCACCTGAACA[C/T]AAGGCCCGCCCACCT | 50855 |
rs769535005 | snp | C/T | 1.6851e-05 | 0.00290263 | intron-variant, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661435 | CCTGACTCCTCCTCT[C/T]CCCCAACCCCGACTT | 50855 |
rs769623291 | snp | A/C | 1.92561e-05 | 0.00310285 | utr-variant-5-prime, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661033 | CCCGGCCCGCCCGGC[A/C]CCGCCATGGCCCGGC | 50855 |
rs769728392 | snp | C/T | 1.83474e-05 | 0.00302876 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67659958 | GGACACTGTGGGTCC[C/T]GTCAGACACAAGCAG | 50855 |
rs769774717 | snp | A/G | 1.68136e-05 | 0.0028994 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67659598 | AGCGGTCCACCTGGA[A/G]ATAGAACTCTGCGGG | 50855 |
rs769875441 | snp | G/T | 1.80426e-05 | 0.00300349 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660448 | GCCCGTTTACTCTCA[G/T]CGCGGCGTCACTCTG | 50855 |
rs769996618 | snp | A/T | 1.64885e-05 | 0.00287123 | intron-variant, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661883 | TCTCAACATCCCCCC[A/T]CTTCTGCAGCAGAAG | 50855 |
rs770184750 | snp | A/G | 1.72889e-05 | 0.0029401 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660189 | AGCTCCCGAATCCAG[A/G]GCCGTAGGACCAGCC | 50855 |
rs770234764 | snp | C/G | 1.6476e-05 | 0.00287014 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67659256 | AGGTGGACTCTGAAA[C/G]GTGCTCCCTACAGGA | 50855 |
rs770307409 | in-del | -/G | 3.37436e-05 | 0.00410739 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659634 | GGAGTTCGGGGGGAA[-/G]GGGGGGTCTCAGAAT | 50855 |
rs770309489 | snp | A/G | 1.66302e-05 | 0.00288355 | missense, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661500 | CCTCGCGCTTCGGTG[A/G]GCGGCTTCCAGGAGT | 50855 |
rs770445581 | snp | A/G | 0.00013931 | 0.00834479 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660244 | CTACACCCAGCGGAT[A/G]CAACGGGCCCGGGTT | 50855 |
rs770621727 | snp | A/T | 1.66671e-05 | 0.00288674 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67659712 | CTCACCGCGCCGCCC[A/T]CAGCGACCTGGACAT | 50855 |
rs770637236 | snp | G/T | 1.70127e-05 | 0.00291652 | synonymous-codon, upstream-variant-2KB, intron-variant, downstream-variant-500B | PARD6A, ACD, ENKD1 | GRCh38.p7 | 16:67662548 | TGGCTGCCGACATCC[G/T]GGTACCCGCAGCTCT | 50855 |
rs770637260 | snp | A/G | 1.7731e-05 | 0.00297744 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660481 | AGCGGCCAGGCATTT[A/G]GGCCGTTCGTCAAGA | 50855 |
rs770725154 | snp | A/C | 9.97573e-05 | 0.00706178 | missense, upstream-variant-2KB, intron-variant, downstream-variant-500B | PARD6A, ACD, ENKD1 | GRCh38.p7 | 16:67662458 | CGATGACAGCAGTGA[A/C]CTGGTCATTGAGAAC | 50855 |
rs770831462 | snp | G/T | 5.99215e-05 | 0.00547331 | utr-variant-5-prime, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661010 | GGCGGGCCGCCTGGG[G/T]CACCGTCCCCGGCCC | 50855 |
rs770945138 | snp | C/G | 1.78382e-05 | 0.00298643 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659825 | ATCCTCACTGCCGGG[C/G]CCACCTGAACACAAG | 50855 |
rs771094112 | snp | C/G | 3.34454e-05 | 0.0040892 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659507 | AGGCTGGGGTGGGGA[C/G]AGCTGCTGGAGGGCG | 50855 |
rs771126954 | snp | C/T | 1.65198e-05 | 0.00287395 | downstream-variant-500B, missense, nc-transcript-variant | PARD6A, ENKD1 | GRCh38.p7 | 16:67663211 | AAAAGATCTTGATGG[C/T]CTCCTCTACCTGCAC | 50855 |
rs771130884 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660692 | TGCACGGTCTTGTAA[A/G]GCCAGTGGAAATAAG | 50855 |
rs771131495 | snp | C/G | 3.36157e-05 | 0.0040996 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67659589 | GCAGGCTGAAGCGGT[C/G]CACCTGGAGATAGAA | 50855 |
rs771143147 | in-del | -/G | 5.31552e-05 | 0.00515507 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659822 | AGGATCCTCACTGCC[-/G]GGCCCACCTGAACAC | 50855 |
rs771383605 | snp | A/T | 1.73048e-05 | 0.00294144 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660174 | TCTGACCCCAGAATC[A/T]GCTCCCGAATCCAGG | 50855 |
rs771388310 | snp | C/T | 7.35335e-05 | 0.00606311 | intron-variant, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661864 | TCGGGGAGCAGGTCT[C/T]TGATCTCAACATCCC | 50855 |
rs771454646 | snp | C/T | | | synonymous-codon, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67662353 | CACTGTCAAGCCCGC[C/T]AACCAGCGCAATAAC | 50855 |
rs771489203 | in-del | -/C | 1.83337e-05 | 0.00302762 | intron-variant, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661876 | CTCTGATCTCAACAT[-/C]CCCCCCTCTTCTGCA | 50855 |
rs771555619 | snp | C/T | 3.6897e-05 | 0.00429501 | intron-variant, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661850 | GTAAACAGCCCAAGT[C/T]GGGGAGCAGGTCTCT | 50855 |
rs771559899 | snp | A/C | 1.65364e-05 | 0.0028754 | missense, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67662360 | AAGCCCGCCAACCAG[A/C]GCAATAACGTGGTGC | 50855 |
rs771578447 | snp | C/T | 3.31142e-05 | 0.00406891 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659114 | GGATGAGTCAAGGCT[C/T]AAAGGGGAGGACCAG | 50855 |
rs771597100 | snp | A/G | 1.82754e-05 | 0.0030228 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67660061 | CTGACGGCGGCGAGC[A/G]GCGTCAATCCCACCA | 50855 |
rs771660128 | snp | A/G | 3.4776e-05 | 0.00416974 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660150 | CCGGCTCGTGGACTG[A/G]AGGGTGTCTCTGACC | 50855 |
rs771799486 | snp | A/G | 6.60469e-05 | 0.00574622 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67659014 | AGCTTTCAGCCAGGC[A/G]CACGAGTGCCCCCTG | 50855 |
rs771818424 | in-del | -/GGTCAATGGCATTGAAGTAGCCG | 1.65119e-05 | 0.00287327 | frameshift-variant, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67662257 | TGATGAGATCCTCGA[-/GGTCAATGGCATTGAAGTAGCCG]GGAAGACCTTGGACC | 50855 |
rs771958170 | snp | A/T | 1.66704e-05 | 0.00288703 | upstream-variant-2KB, splice-donor-variant | PARD6A, ACD | GRCh38.p7 | 16:67659700 | GCAGTCTCACCACTC[A/T]CCGCGCCGCCCTCAG | 50855 |
rs772095808 | snp | G/T | 1.77915e-05 | 0.00298252 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660462 | ATCGCGGCGTCACTC[G/T]GACAGCGGCCAGGCA | 50855 |
rs772377460 | snp | C/G | 4.04187e-05 | 0.0044953 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660376 | CACGAGGGCGTCCTG[C/G]TCGGGGGCCTGTGTG | 50855 |
rs772469759 | snp | C/G | 1.9365e-05 | 0.00311161 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660318 | TCCTTCGCTGGGCGG[C/G]GCCGGAGGAGGAGGC | 50855 |
rs772586530 | snp | G/T | 1.65231e-05 | 0.00287424 | downstream-variant-500B, missense, nc-transcript-variant | PARD6A, ENKD1 | GRCh38.p7 | 16:67663204 | GGCCGAGAAAAGATC[G/T]TGATGGCCTCCTCTA | 50855 |
rs772587736 | snp | G/T | | | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659151 | GAGGGGGAAGACAGC[G/T]TATTGAGGAAGCATA | 50855 |
rs772588545 | snp | C/T | 1.66738e-05 | 0.00288732 | synonymous-codon, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661475 | CGCCGAGTTCCGACG[C/T]TTCGCGCTGCCTCGC | 50855 |
rs772774457 | snp | A/G | 1.82327e-05 | 0.00301927 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67660064 | ACGGCGGCGAGCGGC[A/G]TCAATCCCACCACCC | 50855 |
rs772904127 | snp | C/T | 8.26836e-05 | 0.00642923 | synonymous-codon, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67662362 | GCCCGCCAACCAGCG[C/T]AATAACGTGGTGCGA | 50855 |
rs772943251 | snp | A/G | 1.68397e-05 | 0.00290165 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659619 | ACTCTGCGGGCTGGA[A/G]GAGTTCGGGGGGAAG | 50855 |
rs772952702 | snp | A/G | 1.65575e-05 | 0.00287724 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659124 | AGGCTTAAAGGGGAG[A/G]ACCAGGAGGGTGAGG | 50855 |
rs773029984 | snp | C/T | 1.66685e-05 | 0.00288686 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67659704 | TCTCACCACTCACCG[C/T]GCCGCCCTCAGCGAC | 50855 |
rs773098268 | snp | A/C | 1.93812e-05 | 0.00311291 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660411 | CTCCCGCTGGTCCAC[A/C]CCGCTGGTGCACGGG | 50855 |
rs773180799 | snp | A/G | 1.66103e-05 | 0.00288182 | missense, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67662444 | GAGCCTGATAGTGAC[A/G]ATGACAGCAGTGACC | 50855 |
rs773291286 | snp | A/G/T | 0.000489361 | 0.0156358 | upstream-variant-2KB, synonymous-codon, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660322 | TCGCTGGGCGGGGCC[A/G/T]GAGGAGGAGGCCCCG | 50855 |
rs773306733 | snp | C/T | 0.000100749 | 0.00709677 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660377 | ACGAGGGCGTCCTGC[C/T]CGGGGGCCTGTGTGC | 50855 |
rs773378464 | snp | A/G | 1.65282e-05 | 0.00287469 | missense, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67662094 | TGCGGCTGCACAAGC[A/G]TGGTTCAGACCGCCC | 50855 |
rs773494827 | snp | C/T | 0.000145205 | 0.00851946 | utr-variant-3-prime, upstream-variant-2KB, intron-variant, downstream-variant-500B | PARD6A, ACD, ENKD1 | GRCh38.p7 | 16:67662672 | TGAAGCCCCATGCCA[C/T]TCCACACTGCTGGGA | 50855 |
rs773506628 | snp | A/G | | | upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67660869 | TTCCTAGGAAACGTG[A/G]ACTCCGCGTTCCACT | 50855 |
rs773524092 | snp | G/T | 1.66532e-05 | 0.00288554 | synonymous-codon, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661484 | CCGACGCTTCGCGCT[G/T]CCTCGCGCTTCGGTG | 50855 |
rs773553890 | in-del | -/GTCATGCCCGGTAACCC | 1.67351e-05 | 0.00289263 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659661 | GAATCGTCACGAAGA[-/GTCATGCCCGGTAACCC]GCCCAAGGCAGTCTC | 50855 |
rs773575928 | snp | A/T | 1.65053e-05 | 0.0028727 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67659388 | ACTCAAGGCAGTCAT[A/T]GAGCTTTTTCTGAAC | 50855 |
rs773720724 | snp | C/T | 4.99913e-05 | 0.00499931 | synonymous-codon, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661589 | TACGGATGCTCATGG[C/T]GACCTGCTGCCCCTC | 50855 |
rs773751514 | snp | A/G | | | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659166 | TTATTGAGGAAGCAT[A/G]AGGTTAAGGCTGGAG | 50855 |
rs773801371 | snp | A/G | 1.66938e-05 | 0.00288905 | synonymous-codon, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661466 | CCAGTTTGACGCCGA[A/G]TTCCGACGCTTCGCG | 50855 |
rs774058030 | snp | C/G | 3.7024e-05 | 0.0043024 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67660052 | CTGTAGTACCTGACG[C/G]CGGCGAGCGGCGTCA | 50855 |
rs774085628 | snp | A/C | 2.00704e-05 | 0.00316778 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660384 | CGTCCTGCTCGGGGG[A/C]CTGTGTGCAGACTCC | 50855 |
rs774149870 | in-del | -/C | 1.89252e-05 | 0.00307608 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659889 | ACCTCCAGAGCCGCG[-/C]CGGGGCCTCTCACCA | 50855 |
rs774274068 | snp | A/G | 3.34644e-05 | 0.00409036 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659528 | CTGGAGGGCGGAGGC[A/G]TCACTTACCAACCAG | 50855 |
rs774278103 | snp | C/G | 0.000253325 | 0.0112516 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660408 | AGACTCCCGCTGGTC[C/G]ACCCCGCTGGTGCAC | 50855 |
rs774346517 | snp | A/G | 3.30322e-05 | 0.00406387 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67658996 | GGCCCTCCAGTGTCA[A/G]GCAGCTTTCAGCCAG | 50855 |
rs774524526 | snp | A/C | 9.92293e-05 | 0.00704307 | missense, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661994 | CTGCGCACCCGGCCA[A/C]CCTTGCTAATCAGCC | 50855 |
rs774659557 | snp | C/T | 1.78995e-05 | 0.00299156 | synonymous-codon, upstream-variant-2KB, intron-variant, downstream-variant-500B | PARD6A, ACD, ENKD1 | GRCh38.p7 | 16:67662581 | GCCCTCCCTGGATGA[C/T]CAGGAGCAGGCCAGT | 50855 |
rs774720294 | snp | C/G | 1.75372e-05 | 0.00296113 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660254 | CGGATGCAACGGGCC[C/G]GGGTTTCCCGCGGGC | 50855 |
rs774816085 | snp | G/T | 1.75628e-05 | 0.00296329 | missense, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661055 | TGGCCCGGCCGCAGA[G/T]GACTCCGGCGCGCAG | 50855 |
rs774843116 | in-del | -/A | 1.81708e-05 | 0.00301414 | intron-variant, upstream-variant-2KB, splice-acceptor-variant | PARD6A, ACD | GRCh38.p7 | 16:67661890 | TCCCCCCTCTTCTGC[-/A]AGCAGAAGCTGACTC | 50855 |
rs774906138 | snp | A/C | 1.73836e-05 | 0.00294813 | missense, upstream-variant-2KB, intron-variant, downstream-variant-500B | PARD6A, ACD, ENKD1 | GRCh38.p7 | 16:67662567 | ACCCGCAGCTCTCTG[A/C]CCTCCCTGGATGACC | 50855 |
rs774922687 | snp | G/T | 3.8503e-05 | 0.00438748 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660316 | GCTCCTTCGCTGGGC[G/T]GGGCCGGAGGAGGAG | 50855 |
rs775116847 | in-del | -/A | 3.46512e-05 | 0.00416226 | upstream-variant-2KB, frameshift-variant, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660232 | CATCCCCACGGCTAC[-/A]ACCCAGCGGATGCAA | 50855 |
rs775223665 | snp | A/G | 1.65323e-05 | 0.00287505 | missense, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67662106 | AGCATGGTTCAGACC[A/G]CCCCCTGGGCTTCTA | 50855 |
rs775283151 | snp | C/T | 1.83636e-05 | 0.00303009 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659843 | ACCTGAACACAAGGC[C/T]CGCCCACCTCGCGCT | 50855 |
rs775299013 | snp | A/C | 3.94058e-05 | 0.00443862 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660330 | CGGGGCCGGAGGAGG[A/C]GGCCCCGCCCACGTA | 50855 |
rs775590382 | snp | A/C/G | 1.66288e-05 | 0.00288343 | synonymous-codon, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661577 | GCTACTTGGCTATAC[A/C/G]GATGCTCATGGCGAC | 50855 |
rs775602659 | snp | C/T | 1.68204e-05 | 0.00289999 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67659600 | CGGTCCACCTGGAGA[C/T]AGAACTCTGCGGGCT | 50855 |
rs775693267 | snp | C/T | 1.64798e-05 | 0.00287047 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659188 | AGGCTGGAGAGATCA[C/T]TGCACAGCGTGTTAG | 50855 |
rs775708629 | snp | A/G | | | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659430 | GGTTGCTAAGAAAAA[A/G]AGAAGGGTAGTTAAT | 50855 |
rs775763406 | snp | C/G | 1.65162e-05 | 0.00287365 | downstream-variant-500B, missense, nc-transcript-variant | PARD6A, ENKD1 | GRCh38.p7 | 16:67663229 | CCTCTACCTGCACCA[C/G]CTTCCGGTCCAGCTC | 50855 |
rs775787415 | snp | A/G | 0.000155622 | 0.00881968 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660193 | CCCGAATCCAGGGCC[A/G]TAGGACCAGCCTCCC | 50855 |
rs775871868 | snp | C/G | 1.81734e-05 | 0.00301436 | intron-variant, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661889 | CATCCCCCCTCTTCT[C/G]CAGCAGAAGCTGACT | 50855 |
rs775903443 | snp | A/G/T | 0.000122322 | 0.00781968 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660251 | CAGCGGATGCAACGG[A/G/T]CCCGGGTTTCCCGCG | 50855 |
rs776054580 | snp | A/G | 3.33072e-05 | 0.00408075 | missense, upstream-variant-2KB, intron-variant, downstream-variant-500B | PARD6A, ACD, ENKD1 | GRCh38.p7 | 16:67662475 | TGGTCATTGAGAACC[A/G]CCAGCCTCCCAGTTC | 50855 |
rs776065821 | snp | C/T | 3.31005e-05 | 0.00406807 | synonymous-codon, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661987 | GGCACCCCTGCGCAC[C/T]CGGCCACCCTTGCTA | 50855 |
rs776272296 | snp | C/G | 1.78204e-05 | 0.00298494 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659826 | TCCTCACTGCCGGGC[C/G]CACCTGAACACAAGG | 50855 |
rs776330045 | snp | A/G | 1.65446e-05 | 0.00287612 | synonymous-codon, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67662374 | GCGCAATAACGTGGT[A/G]CGAGGGGCATCTGGG | 50855 |
rs776418775 | snp | G/T | 1.65206e-05 | 0.00287403 | missense, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67662025 | TGCCCCAAGATTTCC[G/T]CCAGGTTTCCTCAGT | 50855 |
rs776559555 | snp | A/G | 1.66654e-05 | 0.00288659 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67659715 | ACCGCGCCGCCCTCA[A/G]CGACCTGGACATGAA | 50855 |
rs776631387 | in-del | -/TT | 1.65403e-05 | 0.00287574 | downstream-variant-500B, frameshift-variant, nc-transcript-variant | PARD6A, ENKD1 | GRCh38.p7 | 16:67663185 | CATCTTCACGAAGAC[-/TT]TGGGCCGAGAAAAGA | 50855 |
rs776631563 | snp | G/T | 5.33447e-05 | 0.00516425 | utr-variant-5-prime, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661021 | TGGGGCACCGTCCCC[G/T]GCCCGCCCGGCCCCG | 50855 |
rs776666988 | snp | C/G | | | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660277 | CCGCGGGCGCCCAGG[C/G]CCCGCCTTTCCTCGG | 50855 |
rs776703975 | snp | C/T | 1.65165e-05 | 0.00287367 | downstream-variant-500B, missense, nc-transcript-variant | PARD6A, ENKD1 | GRCh38.p7 | 16:67663217 | TCTTGATGGCCTCCT[C/T]TACCTGCACCAGCTT | 50855 |
rs776746215 | snp | A/G | 3.34521e-05 | 0.00408961 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659520 | GAGAGCTGCTGGAGG[A/G]CGGAGGCATCACTTA | 50855 |
rs776746986 | snp | A/T | 1.68131e-05 | 0.00289935 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67659594 | CTGAAGCGGTCCACC[A/T]GGAGATAGAACTCTG | 50855 |
rs776842448 | snp | A/G | 2.0087e-05 | 0.00316908 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660382 | GGCGTCCTGCTCGGG[A/G]GCCTGTGTGCAGACT | 50855 |
rs776898651 | snp | C/T | 1.67234e-05 | 0.00289161 | missense, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661600 | ATGGCGACCTGCTGC[C/T]CCTCACCAACGACGA | 50855 |
rs777238079 | snp | A/G | 1.6476e-05 | 0.00287014 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67659236 | TACAGTACCTGCATT[A/G]GACGAGGTGGACTCT | 50855 |
rs777239730 | snp | C/G | 1.73192e-05 | 0.00294267 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660166 | AGGGTGTCTCTGACC[C/G]CAGAATCAGCTCCCG | 50855 |
rs777239811 | snp | A/G | 1.67486e-05 | 0.00289379 | missense, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661947 | CTCTGCAGCGGCGCA[A/G]GAAAGGGCTCTTGCT | 50855 |
rs777327701 | snp | G/T | 1.84028e-05 | 0.00303333 | intron-variant, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661860 | CAAGTCGGGGAGCAG[G/T]TCTCTGATCTCAACA | 50855 |
rs777476880 | in-del | -/AG | 4.95774e-05 | 0.00497858 | upstream-variant-2KB, frameshift-variant, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67658964 | AGCCCAGTGGGTGAC[-/AG]GGGGTGCTGTGCAAG | 50855 |
rs777661999 | snp | A/C | 1.69117e-05 | 0.00290785 | synonymous-codon, upstream-variant-2KB, intron-variant, downstream-variant-500B | PARD6A, ACD, ENKD1 | GRCh38.p7 | 16:67662540 | CTGCACCCTGGCTGC[A/C]GACATCCTGGTACCC | 50855 |
rs777662654 | snp | C/T | 1.65108e-05 | 0.00287317 | synonymous-codon, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67662188 | TCCAGGAATCTTCAT[C/T]TCCCGCCTGGTACGT | 50855 |
rs777707916 | snp | A/G | 3.3042e-05 | 0.00406447 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67658971 | TGGGTGACAGGGGGT[A/G]CTGTGCAAGGGCCCT | 50855 |
rs777769637 | snp | C/T | 0.000142929 | 0.00845245 | utr-variant-5-prime, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661002 | TGCGCCTCGGCGGGC[C/T]GCCTGGGGCACCGTC | 50855 |
rs777856228 | snp | A/G | 0.000181813 | 0.00953275 | synonymous-codon, upstream-variant-2KB, intron-variant, downstream-variant-500B | PARD6A, ACD, ENKD1 | GRCh38.p7 | 16:67662608 | CAGTTCTGGCTGGGG[A/G]AGTCGCATTCGAGGA | 50855 |
rs777972235 | snp | C/G | 1.88269e-05 | 0.00306808 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660424 | ACCCCGCTGGTGCAC[C/G]GGATGCTGGCCCGTT | 50855 |
rs778058811 | snp | G/T | 1.6528e-05 | 0.00287467 | missense, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67662312 | GTGACGGACATGATG[G/T]TTGCCAACAGCCATA | 50855 |
rs778156397 | snp | C/T | 1.65329e-05 | 0.0028751 | downstream-variant-500B, missense, nc-transcript-variant | PARD6A, ENKD1 | GRCh38.p7 | 16:67663264 | CGGTGGCTCTGGGCT[C/T]TCAGTGAGTCTGCCC | 50855 |
rs778255016 | snp | C/T | 1.97924e-05 | 0.00314576 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660399 | CCTGTGTGCAGACTC[C/T]CGCTGGTCCACCCCG | 50855 |
rs778255734 | snp | A/C | 1.68086e-05 | 0.00289896 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67659585 | GGCAGCAGGCTGAAG[A/C]GGTCCACCTGGAGAT | 50855 |
rs778342079 | snp | A/G | 1.65274e-05 | 0.00287462 | downstream-variant-500B, stop-gained, nc-transcript-variant | PARD6A, ENKD1 | GRCh38.p7 | 16:67663259 | CAGCACGGTGGCTCT[A/G]GGCTCTCAGTGAGTC | 50855 |
rs778357408 | in-del | -/A | 0.000120739 | 0.00776884 | intron-variant, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661729 | AGGTGTCTGTGGGGC[-/A]GGTCTACAAGGGTTA | 50855 |
rs778432021 | snp | C/G | 1.65244e-05 | 0.00287436 | downstream-variant-500B, missense, nc-transcript-variant | PARD6A, ENKD1 | GRCh38.p7 | 16:67663200 | TTTGGGCCGAGAAAA[C/G]ATCTTGATGGCCTCC | 50855 |
rs778432528 | snp | G/T | 1.90384e-05 | 0.00308526 | intron-variant, upstream-variant-2KB, missense | PARD6A, ACD | GRCh38.p7 | 16:67661700 | GGGGTACAGTGGGCA[G/T]CCTCTGTGGGGTAAG | 50855 |
rs778443589 | snp | G/T | 1.68213e-05 | 0.00290006 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659638 | TTCGGGGGGAAGGGG[G/T]GGTCTCAGAATCGTC | 50855 |
rs778709455 | snp | C/G | 3.74806e-05 | 0.00432884 | | | GRCh38.p7 | 16:67662595 | ACCAGGAGCAGGCCA[C/G]TTCTGGCTGGGGGAG | 50855 |
rs778737223 | snp | C/T | 1.73321e-05 | 0.00294376 | | | GRCh38.p7 | 16:67660234 | ATCCCCACGGCTACA[C/T]CCAGCGGATGCAACG | 50855 |
rs778914962 | snp | C/T | 1.67402e-05 | 0.00289306 | intron-variant, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661153 | AATTCCCTCTTTCTC[C/T]CCTTCCCAGCTCCTT | 50855 |
rs778915531 | snp | A/T | 1.65968e-05 | 0.00288065 | missense, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67662436 | GGCCTGCTGAGCCTG[A/T]TAGTGACGATGACAG | 50855 |
rs779018015 | snp | C/G | 1.64765e-05 | 0.00287019 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659225 | TGGTCAAGCTCTACA[C/G]TACCTGCATTGGACG | 50855 |
rs779109543 | snp | A/G | 7.10593e-05 | 0.00596025 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659822 | AGGATCCTCACTGCC[A/G]GGCCCACCTGAACAC | 50855 |
rs779289719 | snp | C/G | 4.96849e-05 | 0.00498397 | missense, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67662087 | CGACGGGTGCGGCTG[C/G]ACAAGCATGGTTCAG | 50855 |
rs779383442 | snp | A/C | 6.91539e-05 | 0.00587981 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660203 | GGGCCGTAGGACCAG[A/C]CTCCCCGAACCTGCC | 50855 |
rs779396245 | snp | A/G | 4.03494e-05 | 0.00449145 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660364 | CCCGCGCCTGCGCAC[A/G]AGGGCGTCCTGCTCG | 50855 |
rs779400583 | snp | A/C | 1.6513e-05 | 0.00287336 | missense, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67662162 | GTGGCTCCCCAGGGC[A/C]TGGAGCGGGTTCCAG | 50855 |
rs779507435 | snp | A/C | 1.67956e-05 | 0.00289784 | upstream-variant-2KB, stop-gained, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67659565 | GTAGCCGGGGCTGCT[A/C]CGTGGGCAGCAGGCT | 50855 |
rs779567500 | snp | A/G | 4.44208e-05 | 0.00471258 | missense, upstream-variant-2KB, intron-variant, downstream-variant-500B | PARD6A, ACD, ENKD1 | GRCh38.p7 | 16:67662619 | GGGGGAGTCGCATTC[A/G]AGGAGATGGTAGTGG | 50855 |
rs779581984 | snp | C/T | 1.65356e-05 | 0.00287533 | downstream-variant-500B, synonymous-codon, nc-transcript-variant | PARD6A, ENKD1 | GRCh38.p7 | 16:67663191 | CACGAAGACTTTGGG[C/T]CGAGAAAAGATCTTG | 50855 |
rs779585739 | snp | C/T | 3.32397e-05 | 0.00407661 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659458 | AATGGGGGCCCAAGC[C/T]CTCCTACCCCATAGG | 50855 |
rs779591340 | snp | C/G | 1.98841e-05 | 0.00315304 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660394 | GGGGGCCTGTGTGCA[C/G]ACTCCCGCTGGTCCA | 50855 |
rs779770932 | snp | G/T | 1.65941e-05 | 0.00288041 | missense, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661551 | GTGCACCAGATCCCG[G/T]GCCTGGACGTGCTAC | 50855 |
rs779771226 | snp | C/T | | | missense, upstream-variant-2KB, intron-variant, downstream-variant-500B | PARD6A, ACD, ENKD1 | GRCh38.p7 | 16:67662511 | GGCTGTCTCAGGGGC[C/T]CCCGTGCTGGGACCT | 50855 |
rs779870155 | snp | A/G/T | 5.55441e-05 | 0.00526967 | intron-variant, upstream-variant-2KB, synonymous-codon | PARD6A, ACD | GRCh38.p7 | 16:67661688 | GCGGGGTGAGGAGGG[A/G/T]TACAGTGGGCAGCCT | 50855 |
rs780062970 | snp | C/T | 1.68644e-05 | 0.00290378 | missense, upstream-variant-2KB, intron-variant, downstream-variant-500B | PARD6A, ACD, ENKD1 | GRCh38.p7 | 16:67662532 | GCTGGGACCTGCACC[C/T]TGGCTGCCGACATCC | 50855 |
rs780070020 | snp | C/T | 1.65389e-05 | 0.00287562 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659097 | GGGGACAGGGGACCA[C/T]GGGATGAGTCAAGGC | 50855 |
rs780077204 | snp | A/G | 1.66813e-05 | 0.00288797 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659685 | GGTAACCCGCCCAAG[A/G]CAGTCTCACCACTCA | 50855 |
rs780085368 | snp | A/G | 1.65075e-05 | 0.00287289 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660523 | CCGGTAGGGAACAGA[A/G]CAAGGGCTGGTCCCG | 50855 |
rs780160617 | snp | A/C | 1.6517e-05 | 0.00287372 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67658983 | GGTGCTGTGCAAGGG[A/C]CCTCCAGTGTCAGGC | 50855 |
rs780164453 | snp | C/T | 1.75406e-05 | 0.00296142 | upstream-variant-2KB, splice-donor-variant | PARD6A, ACD | GRCh38.p7 | 16:67660121 | CTGAATGGGGGCTCA[C/T]CTCAAGCAGCTGCCC | 50855 |
rs780167082 | snp | A/G | 0.000125758 | 0.00792863 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660452 | GTTTACTCTCATCGC[A/G]GCGTCACTCTGACAG | 50855 |
rs780193271 | snp | C/T | 1.88244e-05 | 0.00306787 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659877 | CTGCCGGACTCCGAC[C/T]TCCAGAGCCGCGCGG | 50855 |
rs780272705 | in-del | -/A | 0.000232833 | 0.0107871 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659463 | GGCCCAAGCCCTCCT[-/A]ACCCCATAGGCGTCT | 50855 |
rs780367517 | snp | C/T | 6.59837e-05 | 0.00574348 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659352 | AAACAACACGTGGCC[C/T]CCGAGCCCAACCCCA | 50855 |
rs780457506 | snp | C/T | 0.000112196 | 0.00748901 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660305 | CGGAAGAGGAAGCTC[C/T]TTCGCTGGGCGGGGC | 50855 |
rs780528072 | snp | C/G | | | downstream-variant-500B | PARD6A, ENKD1 | GRCh38.p7 | 16:67662902 | GCAGGAGGGCCACCA[C/G]GCTTGGCATTTTTAG | 50855 |
rs780545113 | snp | C/T | 1.65321e-05 | 0.00287502 | missense, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67662081 | ACCCACCGACGGGTG[C/T]GGCTGCACAAGCATG | 50855 |
rs780553842 | snp | C/T | 2.02288e-05 | 0.00318025 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660359 | TACACCCCGCGCCTG[C/T]GCACGAGGGCGTCCT | 50855 |
rs780723982 | snp | A/G | 1.83377e-05 | 0.00302795 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660299 | TTTCCTCGGAAGAGG[A/G]AGCTCCTTCGCTGGG | 50855 |
rs780754740 | snp | C/G | 1.65861e-05 | 0.00287972 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659446 | AGAAGGGTAGTTAAT[C/G]GGGGCCCAAGCCCTC | 50855 |
rs780815813 | snp | A/C/T | 3.30492e-05 | 0.00406494 | synonymous-codon, missense, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67662075 | CCTGAGACCCACCGA[A/C/T]GGGTGCGGCTGCACA | 50855 |
rs780842633 | snp | C/T | 1.64953e-05 | 0.00287182 | upstream-variant-2KB, intron-variant | PARD6A, ACD | GRCh38.p7 | 16:67659336 | ACACCATCCCCTCAC[C/T]AAACAACACGTGGCC | 50855 |
rs780935998 | snp | C/G | 1.86249e-05 | 0.00305158 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660022 | GGATGGGCCCGCGAC[C/G]GCGGCCTCGGCGTCC | 50855 |
rs780989111 | snp | C/T | 4.95356e-05 | 0.00497648 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67659017 | TTTCAGCCAGGCACA[C/T]GAGTGCCCCCTGATG | 50855 |
rs781229512 | snp | C/T | 1.96701e-05 | 0.00313603 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660402 | GTGTGCAGACTCCCG[C/T]TGGTCCACCCCGCTG | 50855 |
rs781239912 | in-del | -/CTT | 8.38821e-05 | 0.00647565 | upstream-variant-2KB, cds-indel, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67659550 | CCAACCAGGCACCCG[-/CTT]TAGCCGGGGCTGCTC | 50855 |
rs781292039 | in-del | -/CT | 0.000117185 | 0.00765368 | intron-variant, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661144 | GGCGCTCCCAATTCC[-/CT]CTTTCTCCCCTTCCC | 50855 |
rs781313616 | snp | C/G | 1.65993e-05 | 0.00288086 | synonymous-codon, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661529 | GTTCTCGCGGTTGCT[C/G]CGGGCGGTGCACCAG | 50855 |
rs781320342 | snp | A/G | 1.65244e-05 | 0.00287436 | missense, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67662325 | TGGTTGCCAACAGCC[A/G]TAACCTCATTGTCAC | 50855 |
rs781404876 | snp | C/T | 1.70621e-05 | 0.00292074 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67659786 | GCGGAAGCCGAACTC[C/T]TTCTCCTCCCTGCAA | 50855 |
rs781424953 | snp | C/G | 1.81708e-05 | 0.00301414 | upstream-variant-2KB, missense, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67660442 | ATGCTGGCCCGTTTA[C/G]TCTCATCGCGGCGTC | 50855 |
rs781455847 | snp | C/T | | | utr-variant-3-prime, upstream-variant-2KB, intron-variant, downstream-variant-500B | PARD6A, ACD, ENKD1 | GRCh38.p7 | 16:67662754 | CAGCCTGGGGAACAT[C/T]AAAGGTTTTCTACAA | 50855 |
rs781558045 | snp | C/T | 4.96866e-05 | 0.00498406 | missense, upstream-variant-2KB | PARD6A, ACD | GRCh38.p7 | 16:67661982 | CCAGTGGCACCCCTG[C/T]GCACCCGGCCACCCT | 50855 |
rs797045144 | in-del | -/AAG | | | upstream-variant-2KB, cds-indel, nc-transcript-variant | PARD6A, ACD | GRCh38.p7 | 16:67659786 | TGTTGCAGGGAGGAG[-/AAG]GAGTTCGGCTTCCGC | 50855 |