SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs752524316 | snp | A/G | 1.66394e-05 | 0.00288434 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56719877 | GTCTTTCTTGGTGGT[A/G]AGTCCTGCTTGGGCT | 4666 |
rs752601094 | snp | C/T | 1.64768e-05 | 0.00287021 | missense | NACA | GRCh38.p7 | 12:56714660 | AGCTCTGGTACTGAT[C/T]CATCACTGTCAGATT | 4666 |
rs752651361 | snp | A/G | 3.8786e-05 | 0.00440358 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56716745 | GAGGAGCTCTTTGGG[A/G]GATGGGGCCCCTTTG | 4666 |
rs752768996 | snp | A/G | 0.000275482 | 0.0117331 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718078 | GGAGTTGCAGCTGGG[A/G]TTGTGGGGGCCCCTT | 4666 |
rs752808649 | snp | A/G | 3.32541e-05 | 0.00407749 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56720843 | TGTTGTCTGAGGAAG[A/G]GAGGCCACTCCAGAT | 4666 |
rs752844855 | snp | A/G/T | 1.68066e-05 | 0.00289879 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716143 | GGCAGAGAGACTGGT[A/G/T]GGGAGGGTGCTGCAG | 4666 |
rs752858815 | snp | A/C/T | 3.94721e-05 | 0.00444238 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718226 | CTGGGGGCATGGGGG[A/C/T]CCCTTTGGGGGATGG | 4666 |
rs752948984 | snp | G/T | 1.97307e-05 | 0.00314085 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717298 | GGAGCCTTTTTGGGG[G/T]AGAGAGGAATCACTG | 4666 |
rs752959858 | in-del | -/AC | 1.68665e-05 | 0.00290396 | intron-variant, frameshift-variant | NACA | GRCh38.p7 | 12:56716560 | CCCATTTTACATGTG[-/AC]AGAAGCTGGGGAAGT | 4666 |
rs752962711 | snp | A/T | 1.72157e-05 | 0.00293386 | intron-variant, missense | NACA | GRCh38.p7 | 12:56719047 | GCTTCAACTGGAGAA[A/T]CAGGGGATGAGAGAT | 4666 |
rs753011482 | snp | C/T | 1.96767e-05 | 0.00313655 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718604 | ATGGAGTAGCTGGAC[C/T]TCCTTTTGGGGAGGG | 4666 |
rs753016625 | in-del | -/T | | | intron-variant | NACA | GRCh38.p7 | 12:56721571 | CACTGGAGTTTAAAA[-/T]CTGACAGTCTAAGTC | 4666 |
rs753031480 | snp | A/C | 1.67103e-05 | 0.00289048 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716226 | TAGAGGGGTGGACGC[A/C]TTAGACTCAGGAGGA | 4666 |
rs753034554 | snp | A/G | 1.68383e-05 | 0.00290153 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720503 | CCCCTGTGGAAGAAT[A/G]ATCTACAGAAATGGT | 4666 |
rs753044699 | in-del | -/CA | 0.00149849 | 0.0273313 | intron-variant, frameshift-variant | NACA | GRCh38.p7 | 12:56718150 | TTGCAGCTGGGGTTG[-/CA]TGGGTGCCCCTTTGT | 4666 |
rs753050741 | snp | A/C | 1.66283e-05 | 0.00288338 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56720198 | AATTGTACAGGGGTT[A/C]GTCACCACAAGTGGG | 4666 |
rs753101609 | snp | C/T | 0.000114784 | 0.00757489 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718697 | GGGAGGGAGGAGTTG[C/T]AGCTGGGGGTGTGGG | 4666 |
rs753104893 | snp | C/T | 1.6477e-05 | 0.00287024 | missense | NACA | GRCh38.p7 | 12:56713602 | CATCTGGTTTTGTGA[C/T]GACAAAGAGGATATT | 4666 |
rs753189040 | snp | A/G | 1.7029e-05 | 0.00291791 | intron-variant, missense | NACA | GRCh38.p7 | 12:56721312 | AAAGGGGTCGAGGCA[A/G]TAGTAGAGGGGGAAG | 4666 |
rs753223384 | snp | A/T | 1.96027e-05 | 0.00313065 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716872 | GGGGAGGGAACAGTC[A/T]TAGCTGGGGGAATGA | 4666 |
rs753277917 | in-del | -/G | 9.02861e-05 | 0.00671825 | intron-variant, frameshift-variant | NACA | GRCh38.p7 | 12:56718871 | CACCACTGAAGGAGT[-/G]GGGGGTCTCTTTGGG | 4666 |
rs753286740 | snp | G/T | 1.66646e-05 | 0.00288652 | intron-variant, missense | NACA | GRCh38.p7 | 12:56719568 | AGCCACCCCGGCAGG[G/T]TCAGCACTTTCCAAA | 4666 |
rs753323983 | snp | A/G | 1.96655e-05 | 0.00313566 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56717828 | CCCTTTGGGGGATGG[A/G]GTAGCCAGACCTCCT | 4666 |
rs753411607 | snp | A/C | 3.87905e-05 | 0.00440383 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716984 | ATGGGGTAGCTGGGA[A/C]CTCTTTGGGGGAAGA | 4666 |
rs753422760 | snp | C/T | 3.67242e-05 | 0.00428494 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56715893 | GTTCTTCGTAACAGG[C/T]TGCTTGGCAGAGGGG | 4666 |
rs753514335 | snp | C/G | 3.66488e-05 | 0.00428055 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56715956 | GGGCATGTTGACGAG[C/G]ACCGACTGGAAAGGC | 4666 |
rs753519550 | snp | A/G | 1.94706e-05 | 0.00312008 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56718392 | TGGGGTAGCTGCTGG[A/G]CTTCCTTTGGGGGAG | 4666 |
rs753523188 | in-del | -/C | 0.000280156 | 0.0118321 | intron-variant | NACA | GRCh38.p7 | 12:56713025 | GAACACAATGCTATA[-/C]GGCGAGAGTTAAATT | 4666 |
rs753524245 | snp | C/T | 1.95946e-05 | 0.00313 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718322 | ATGGGGTAGCTGGAC[C/T]TCCTTTTGGGGAGGG | 4666 |
rs753564247 | snp | A/G | 1.66866e-05 | 0.00288842 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56720624 | AGAGCCCAGAGAAAT[A/G]GGAAAATCTGGGGGG | 4666 |
rs753570823 | snp | C/G/T | 5.96787e-05 | 0.00546227 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717473 | CTTTAGAGGAGGGAG[C/G/T]TGTAGCTGGGAGAGT | 4666 |
rs753584468 | snp | C/G | | | intron-variant | NACA | GRCh38.p7 | 12:56715431 | CCCTGGGCAACTGGT[C/G]ATTACTAAGTCTAAT | 4666 |
rs753604697 | snp | A/G | 1.65206e-05 | 0.00287403 | intron-variant, utr-variant-3-prime | NACA | GRCh38.p7 | 12:56712567 | CCTGTAACAGAGAAA[A/G]GATAATTAGCGGTTC | 4666 |
rs753605408 | snp | A/T | | | utr-variant-5-prime, intron-variant | NACA | GRCh38.p7 | 12:56725204 | GTCCCCGGGGCGGCT[A/T]AGCCCGAAAGAAAGG | 4666 |
rs753615586 | snp | C/T | 2.49317e-05 | 0.00353062 | utr-variant-5-prime, intron-variant | NACA | GRCh38.p7 | 12:56724549 | GGAATAAAAAGGAGG[C/T]CTAAATTGATTGGGA | 4666 |
rs753665762 | snp | C/G | 0.000178648 | 0.00944944 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717556 | TTGGGGGGTGGGGTA[C/G]CTGGGCTTCCTTTTG | 4666 |
rs753674212 | snp | C/T | 1.76095e-05 | 0.00296723 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56718836 | TGGAGTAGCTGGACC[C/T]TCTTTGGGGAAGGGC | 4666 |
rs753691485 | snp | C/T | 1.64732e-05 | 0.0028699 | missense | NACA | GRCh38.p7 | 12:56712827 | TGTTGTTCTTCAGGG[C/T]TCGGACTGCCTTTGC | 4666 |
rs753755727 | snp | C/G | 1.66432e-05 | 0.00288467 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716477 | GAGCTGGGGCAACAA[C/G]TACTTCTTTCAGAGC | 4666 |
rs753833333 | snp | A/G | | | intron-variant | NACA | GRCh38.p7 | 12:56724295 | TTACTCCAAATCCCT[A/G]AAGAAGTATCTCCAG | 4666 |
rs753843604 | snp | A/G | | | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56716598 | GTCTTTGAGGGAGGA[A/G]GGAGTCACAGGTGGG | 4666 |
rs753879408 | snp | A/G | 1.6476e-05 | 0.00287014 | missense | NACA | GRCh38.p7 | 12:56714645 | GAATCCTGTTCTTCA[A/G]GCTCTGGTACTGATT | 4666 |
rs753884893 | snp | C/T | 1.64906e-05 | 0.00287142 | synonymous-codon | NACA | GRCh38.p7 | 12:56714437 | TTCAGCTGCTGCCGC[C/T]AGCTAAGAAGATAAA | 4666 |
rs753956003 | snp | A/T | 1.66879e-05 | 0.00288855 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56721074 | AAGGTTAGGTGGAAA[A/T]GCAGAACTCTTCTGA | 4666 |
rs753960029 | snp | G/T | 1.66366e-05 | 0.0028841 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56719883 | CTTGGTGGTGAGTCC[G/T]GCTTGGGCTGGAGAG | 4666 |
rs754030503 | in-del | -/TTGGGGGTGGGGTAGCTAGACCTCCTTTTGGGGAGGGAGGAGTTGCAG | 1.97066e-05 | 0.00313893 | intron-variant, cds-indel | NACA | GRCh38.p7 | 12:56718094 | TTGTGGGGGCCCCTT[lengthTooLong]CTGGGGTTGTGGGTG | 4666 |
rs754079663 | in-del | -/GTGGGGGCCCCTTTGGGGG | 1.98635e-05 | 0.00315141 | intron-variant, frameshift-variant | NACA | GRCh38.p7 | 12:56717528 | GTTACAGCTGGGGGA[-/GTGGGGGCCCCTTTGGGGG]GTGGGGGCCCCTTTG | 4666 |
rs754112176 | snp | C/T | 1.78944e-05 | 0.00299113 | intron-variant, missense | NACA | GRCh38.p7 | 12:56719288 | CATCAACCTTTTTTG[C/T]ACCTGGAGGAGTCCC | 4666 |
rs754152445 | snp | C/T | 5.04851e-05 | 0.00502394 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56720432 | CACAGTAGCAGGAAC[C/T]ACCTCATTTCTGGAA | 4666 |
rs754174182 | in-del | -/G | 1.67398e-05 | 0.00289303 | intron-variant, frameshift-variant | NACA | GRCh38.p7 | 12:56720634 | GAAATGGGAAAATCT[-/G]GGGGGGTGTTGGGAC | 4666 |
rs754270901 | snp | A/C/T | 0.000100287 | 0.00708055 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56716223 | TGTTAGAGGGGTGGA[A/C/T]GCCTTAGACTCAGGA | 4666 |
rs754295164 | snp | C/T | 3.93337e-05 | 0.00443456 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56718581 | GGGTGTGGGGGCCCC[C/T]TTGGGGGATGGAGTA | 4666 |
rs754316696 | snp | G/T | 1.64776e-05 | 0.00287028 | missense | NACA | GRCh38.p7 | 12:56713081 | TCCTCTTCACTCTCC[G/T]CTTGTACAGTTGGAG | 4666 |
rs754331688 | snp | C/G | 6.7014e-05 | 0.00578814 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56720402 | AACAGATGGAGCCAC[C/G]ACTGGAAAGGCAGCC | 4666 |
rs754401289 | snp | A/G | 3.76868e-05 | 0.00434073 | intron-variant, missense | NACA | GRCh38.p7 | 12:56721399 | CAAGGAGGGGGGAGG[A/G]TAGGTCCAGGCTGCC | 4666 |
rs754404666 | snp | A/G | 1.67346e-05 | 0.00289258 | intron-variant | NACA | GRCh38.p7 | 12:56713490 | GTCAGCAGTGCTGAG[A/G]TTGAGAAACCCTGGT | 4666 |
rs754435675 | snp | G/T | | | intron-variant, missense | NACA | GRCh38.p7 | 12:56717250 | TCTCCTTTGGATGGG[G/T]TGGCTGCGCCTTCTC | 4666 |
rs754465833 | in-del | -/G | 3.34124e-05 | 0.00408719 | intron-variant, frameshift-variant | NACA | GRCh38.p7 | 12:56721191 | AGAGCTAAGGCAGCT[-/G]GGGGAGATGGGAGGC | 4666 |
rs754495789 | snp | C/T | 1.83206e-05 | 0.00302654 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56715959 | CATGTTGACGAGGAC[C/T]GACTGGAAAGGCACT | 4666 |
rs754500345 | snp | A/G | 1.83478e-05 | 0.00302879 | intron-variant, missense | NACA | GRCh38.p7 | 12:56715903 | ACAGGTTGCTTGGCA[A/G]AGGGGGTTGGGACAG | 4666 |
rs754500582 | snp | A/G | | | intron-variant | NACA | GRCh38.p7 | 12:56723539 | CCTATTGTCCTTCCT[A/G]GCAGCTGTATTAATC | 4666 |
rs754520380 | snp | C/T | 1.9585e-05 | 0.00312924 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718328 | TAGCTGGACCTCCTT[C/T]TGGGGAGGGAAGAGT | 4666 |
rs754581735 | snp | A/C | | | intron-variant | NACA | GRCh38.p7 | 12:56715510 | ATCTCAGGCCCAGGG[A/C]CAAGGTTAGTTAGTG | 4666 |
rs754587984 | snp | A/G | 1.65015e-05 | 0.00287237 | intron-variant | NACA | GRCh38.p7 | 12:56724412 | CCAAATGGCTTTAGG[A/G]TTAATTTTAATTAAT | 4666 |
rs754623290 | in-del | -/GT | | | upstream-variant-2KB | NACA | GRCh38.p7 | 12:56726902 | GCTTATTTATTCTAG[-/GT]GTCTGGGACCCCACC | 4666 |
rs754675822 | snp | C/T | 3.30622e-05 | 0.00406571 | intron-variant, utr-variant-3-prime | NACA | GRCh38.p7 | 12:56712577 | AGAAAAGATAATTAG[C/T]GGTTCTTATAGGCAA | 4666 |
rs754682585 | snp | C/T | 1.94668e-05 | 0.00311978 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718394 | GGGTAGCTGCTGGAC[C/T]TCCTTTGGGGGAGGG | 4666 |
rs754738427 | snp | C/G | 3.96283e-05 | 0.00445113 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717557 | TGGGGGGTGGGGTAC[C/G]TGGGCTTCCTTTTGG | 4666 |
rs754738589 | snp | G/T | 1.66302e-05 | 0.00288355 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716387 | GATCTGGGCATATAG[G/T]AGGTGAAGTAGCAGA | 4666 |
rs754796663 | in-del | -/G | 1.68353e-05 | 0.00290127 | intron-variant, frameshift-variant | NACA | GRCh38.p7 | 12:56716143 | GGCAGAGAGACTGGT[-/G]GGGAGGGTGCTGCAG | 4666 |
rs754827206 | in-del | -/CT | 6.62482e-05 | 0.00575497 | intron-variant | NACA | GRCh38.p7 | 12:56714312 | AAATAAACAGTTCCA[-/CT]CTGTATAAAGGTGCT | 4666 |
rs754828312 | snp | C/T | 1.66565e-05 | 0.00288583 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56716487 | AACAAGTACTTCTTT[C/T]AGAGCTGTGGGGCCT | 4666 |
rs754875547 | snp | G/T | | | intron-variant | NACA | GRCh38.p7 | 12:56724302 | AAATCCCTAAAGAAG[G/T]ATCTCCAGGATAGTA | 4666 |
rs754879668 | snp | C/T | 1.65015e-05 | 0.00287237 | intron-variant | NACA | GRCh38.p7 | 12:56714449 | CGCCAGCTAAGAAGA[C/T]AAAACAGCTATTAGT | 4666 |
rs754915937 | snp | C/G | 1.66496e-05 | 0.00288522 | intron-variant, missense | NACA | GRCh38.p7 | 12:56719602 | AATGCAGCCACTGTT[C/G]GGGTAATGAGAGAAC | 4666 |
rs754945472 | snp | A/G | 3.32541e-05 | 0.00407749 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720826 | GCTAGGGTAGTTGTG[A/G]GTGTTGTCTGAGGAA | 4666 |
rs755037459 | snp | C/T | 1.72136e-05 | 0.00293369 | intron-variant, missense | NACA | GRCh38.p7 | 12:56719018 | AAGAAAGACTATTCT[C/T]TGGAAGAAATGAAGC | 4666 |
rs755039444 | snp | C/G | 1.6477e-05 | 0.00287024 | missense | NACA | GRCh38.p7 | 12:56714649 | CCTGTTCTTCAAGCT[C/G]TGGTACTGATTCATC | 4666 |
rs755078945 | snp | A/T | 1.7203e-05 | 0.00293278 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56719022 | AAGACTATTCTCTGG[A/T]AGAAATGAAGCTTCA | 4666 |
rs755151581 | snp | A/T | 1.92736e-05 | 0.00310426 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717119 | TGGGGGAAGGAGGAG[A/T]CACTGCTGGGAGGGT | 4666 |
rs755171167 | snp | C/T | 3.81163e-05 | 0.0043654 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717197 | AAGTTGCTGGGGCCT[C/T]TTTGAGGGAGACAGG | 4666 |
rs755176026 | snp | C/T | 3.93229e-05 | 0.00443395 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56718068 | TGGGGAAGGAGGAGT[C/T]GCAGCTGGGGTTGTG | 4666 |
rs755205406 | snp | C/T | 1.66277e-05 | 0.00288333 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56720174 | AAAGGTAGTAGTAGG[C/T]GCTGCAGCAATTGTA | 4666 |
rs755239472 | snp | C/T | 1.70156e-05 | 0.00291677 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716065 | GATTCCAACACCAGC[C/T]CAGGAGAGGACGGCA | 4666 |
rs755261178 | snp | A/G | 3.36202e-05 | 0.00409988 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716120 | TGGGAACTGGGGAGG[A/G]AGCAAGAGGCAGAGA | 4666 |
rs755265014 | in-del | -/TAGA | 7.92464e-05 | 0.0062942 | intron-variant, frameshift-variant | NACA | GRCh38.p7 | 12:56718110 | TGGGGGTGGGGTAGC[-/TAGA]CCTCCTTTTGGGGAG | 4666 |
rs755281791 | snp | C/T | 3.90839e-05 | 0.00442045 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718490 | GGGAGGGAGGAGTCA[C/T]AGCTGGGGGTGTGGG | 4666 |
rs755291310 | snp | A/G | 1.64808e-05 | 0.00287057 | intron-variant | NACA | GRCh38.p7 | 12:56712933 | GAGAGGGAAAAAGCA[A/G]TAAATTAAAGGCAAG | 4666 |
rs755293497 | snp | A/C | 1.66283e-05 | 0.00288338 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56720090 | CATAACCAAGGCAGC[A/C]GGGGAAGTTGGTTCT | 4666 |
rs755316722 | in-del | -/ATG | 1.66294e-05 | 0.00288347 | intron-variant, cds-indel | NACA | GRCh38.p7 | 12:56720258 | GGCCACTAAAGGATA[-/ATG]ATAAGTGGCATTAGG | 4666 |
rs755381391 | snp | A/G | 1.67041e-05 | 0.00288994 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56721203 | AGCTGGGGAGATGGG[A/G]GGCCCTATTAGGTTT | 4666 |
rs755445874 | snp | A/G | 1.96678e-05 | 0.00313584 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718592 | CCCCTTTGGGGGATG[A/G]AGTAGCTGGACCTCC | 4666 |
rs755470643 | snp | A/G/T | 5.01327e-05 | 0.00500642 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56721101 | CTGAACTGAGTGGGG[A/G/T]GCCAGGGCAACCAGA | 4666 |
rs755475166 | snp | C/T | 1.67287e-05 | 0.00289207 | intron-variant | NACA | GRCh38.p7 | 12:56713491 | TCAGCAGTGCTGAGG[C/T]TGAGAAACCCTGGTC | 4666 |
rs755529022 | snp | A/G | 0.00190049 | 0.0307674 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717697 | TGGGGTGGGGTAGCT[A/G]GACCTCCTTTTAGGG | 4666 |
rs755563533 | in-del | -/TT | 0.0012696 | 0.0251633 | intron-variant, frameshift-variant | NACA | GRCh38.p7 | 12:56718148 | GAGTTGCAGCTGGGG[-/TT]GTGGGTGCCCCTTTG | 4666 |
rs755651838 | snp | A/G | 1.96883e-05 | 0.00313748 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716783 | AAGGAGTCACTGCTG[A/G]GGGACTGGAGGCCTC | 4666 |
rs755670506 | in-del | -/AG | | | utr-variant-3-prime | NACA | GRCh38.p7 | 12:56712441 | TGAATTCATCCAACA[-/AG]AGAAGCCATAACTTT | 4666 |
rs755704118 | snp | A/G | 1.66838e-05 | 0.00288818 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56720617 | CAAGATGAGAGCCCA[A/G]AGAAATGGGAAAATC | 4666 |
rs755725181 | snp | A/G | 5.05012e-05 | 0.00502475 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56720501 | GGCCCCTGTGGAAGA[A/G]TGATCTACAGAAATG | 4666 |
rs755739732 | snp | C/T | 3.69297e-05 | 0.00429691 | intron-variant | NACA | GRCh38.p7 | 12:56715827 | CGCCCAAGAGGGGTG[C/T]GGACGACAGACACAC | 4666 |
rs755741755 | snp | A/T | 1.96138e-05 | 0.00313154 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56716868 | TTTAGGGGAGGGAAC[A/T]GTCATAGCTGGGGGA | 4666 |
rs755741807 | snp | A/G | 1.77662e-05 | 0.0029804 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56719331 | AGAGGGTGAGGGCAC[A/G]GACTTTGGGATTTCA | 4666 |
rs755791574 | snp | A/G | 1.97031e-05 | 0.00313865 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718246 | TTGGGGGATGGGGTA[A/G]CTGGGCCTCCTTTTG | 4666 |
rs755812828 | snp | A/G | 3.29533e-05 | 0.00405901 | intron-variant | NACA | GRCh38.p7 | 12:56724434 | TTAATTAATGGCAAG[A/G]AGGGTAGGGAAACCT | 4666 |
rs755821081 | snp | A/G | | | intron-variant | NACA | GRCh38.p7 | 12:56723248 | TAATATAAGCCTACT[A/G]TGCAACTCAGACTAT | 4666 |
rs755823870 | snp | C/G | | | utr-variant-3-prime | NACA | GRCh38.p7 | 12:56712508 | TGCAGTTACTCCTTT[C/G]AGACACCAAAAAAAG | 4666 |
rs755839505 | snp | C/T | 1.75391e-05 | 0.00296129 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718813 | AGAGCAGGAGCCTGT[C/T]TGGGTGCTGGAGTAG | 4666 |
rs755877721 | snp | C/T | 2.04996e-05 | 0.00320146 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56717342 | GTCCCCTTTGGGAGA[C/T]GGGATAGCTGGTCCT | 4666 |
rs755879731 | snp | A/G | 1.96419e-05 | 0.00313378 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718318 | AGGGATGGGGTAGCT[A/G]GACCTCCTTTTGGGG | 4666 |
rs755939502 | in-del | -/GGA | 1.67083e-05 | 0.00289031 | intron-variant, cds-indel | NACA | GRCh38.p7 | 12:56717370 | CCTCTTTTGGGGGAG[-/GGA]GGAGTCATAGCGGGA | 4666 |
rs755984362 | in-del | -/A | 1.86197e-05 | 0.00305115 | intron-variant, frameshift-variant | NACA | GRCh38.p7 | 12:56721389 | GGCAGGAGAGCAAGG[-/A]GGGGGGAGGGTAGGT | 4666 |
rs756000997 | snp | A/G | 1.81253e-05 | 0.00301037 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56718731 | CCCTTTGGGGGATGG[A/G]GAAGCTGGGATTCCT | 4666 |
rs756015790 | snp | C/G | 1.66308e-05 | 0.00288359 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716377 | TTAGCTGAGGGATCT[C/G]GGCATATAGGAGGTG | 4666 |
rs756039990 | snp | G/T | | | upstream-variant-2KB | NACA | GRCh38.p7 | 12:56727400 | AGTGCAGTGGCGCGA[G/T]CTCAGCTTACTGCAA | 4666 |
rs756048146 | snp | A/G | | | intron-variant | NACA | GRCh38.p7 | 12:56722210 | CAAACAAGAAAACCA[A/G]CCACAAAAGGACTGT | 4666 |
rs756087720 | snp | A/G | 1.66385e-05 | 0.00288426 | intron-variant, missense | NACA | GRCh38.p7 | 12:56719878 | TCTTTCTTGGTGGTG[A/G]GTCCTGCTTGGGCTG | 4666 |
rs756104260 | snp | A/G | 1.66081e-05 | 0.00288163 | intron-variant | NACA | GRCh38.p7 | 12:56713715 | AGTATCAGGTTTTCA[A/G]CCTCTTTAGAAGCAG | 4666 |
rs756106248 | snp | C/G | 1.66435e-05 | 0.0028847 | intron-variant, missense | NACA | GRCh38.p7 | 12:56719731 | GCTGGCTTACCTATA[C/G]GGAGAGGCTCCCCAA | 4666 |
rs756175378 | snp | A/C | 1.6638e-05 | 0.00288422 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716465 | GCGTGCTTTCTGGAG[A/C]TGGGGCAACAAGTAC | 4666 |
rs756263223 | snp | C/T | 6.59533e-05 | 0.00574215 | synonymous-codon | NACA | GRCh38.p7 | 12:56714434 | AATTTCAGCTGCTGC[C/T]GCCAGCTAAGAAGAT | 4666 |
rs756345235 | in-del | -/G | 1.69843e-05 | 0.00291408 | intron-variant, frameshift-variant | NACA | GRCh38.p7 | 12:56716578 | GAAGCTGGGGAAGTA[-/G]GGGAGTCTTTGAGGG | 4666 |
rs756346049 | snp | A/G | 1.728e-05 | 0.00293933 | intron-variant, missense | NACA | GRCh38.p7 | 12:56719134 | TGAGGAGACACACTA[A/G]CCCCTAAAGGAGATG | 4666 |
rs756524132 | in-del | -/G | 7.26559e-05 | 0.00602683 | intron-variant, frameshift-variant | NACA | GRCh38.p7 | 12:56718883 | AGTGGGGGTCTCTTT[-/G]GGGGGGTAGTGTTAC | 4666 |
rs756525713 | snp | C/G | 1.7117e-05 | 0.00292544 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716048 | CAAGGGGTTTAGAGG[C/G]TGATTCCAACACCAG | 4666 |
rs756525908 | snp | A/G | 1.6628e-05 | 0.00288335 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720212 | TAGTCACCACAAGTG[A/G]GGTGGTTCCAACAGA | 4666 |
rs756549363 | snp | A/C | | | intron-variant, missense | NACA | GRCh38.p7 | 12:56716332 | AGAGGGGCTGGAGCC[A/C]CTGTGGAAAGGGGTC | 4666 |
rs756577474 | in-del | -/T | 0.000640779 | 0.017888 | intron-variant, frameshift-variant | NACA | GRCh38.p7 | 12:56718165 | GTGGGTGCCCCTTTG[-/T]GGGGTGGGGTAGCTA | 4666 |
rs756582431 | snp | C/T | 1.70429e-05 | 0.0029191 | intron-variant, missense | NACA | GRCh38.p7 | 12:56721313 | AAGGGGTCGAGGCAA[C/T]AGTAGAGGGGGAAGG | 4666 |
rs756613939 | snp | A/T | 4.9884e-05 | 0.00499395 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56720114 | TGGTTCTATGTTACT[A/T]ATGGGACCTGATGAC | 4666 |
rs756626624 | snp | A/G | 1.94433e-05 | 0.0031179 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718414 | TTGGGGGAGGGAGGA[A/G]TTGCAGCTGGGGGTG | 4666 |
rs756703844 | snp | A/C | 1.64784e-05 | 0.00287035 | missense | NACA | GRCh38.p7 | 12:56713068 | CTAGTATACCTCTTC[A/C]TCTTCACTCTCCTCT | 4666 |
rs756708588 | snp | A/G | | | intron-variant, missense | NACA | GRCh38.p7 | 12:56717419 | GGGTTGCAGCTGGGG[A/G]AGTGGGGCCCTCTTT | 4666 |
rs756716392 | snp | A/C | 1.95276e-05 | 0.00312465 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56718482 | TCCTTTGGGGGAGGG[A/C]GGAGTCACAGCTGGG | 4666 |
rs756742476 | snp | A/G | 1.67128e-05 | 0.00289069 | intron-variant, missense | NACA | GRCh38.p7 | 12:56721234 | GGTAGGAAGGTTGGG[A/G]CTTCAGGGGCAGTTC | 4666 |
rs756746371 | in-del | -/AAAT | 2.17526e-05 | 0.00329785 | intron-variant | NACA | GRCh38.p7 | 12:56713241 | TTAGCAGTCTTTGAA[-/AAAT]AAATCATATAGTTTC | 4666 |
rs756782442 | snp | C/T | 1.80117e-05 | 0.00300092 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56716643 | TTTGGGGGCTGGAGT[C/T]GCTGGGCCCTTTTCG | 4666 |
rs756802459 | snp | A/G | 1.76952e-05 | 0.00297444 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717622 | CCTTTGGGGGGTGAG[A/G]TAGCTGGGCCTCCTT | 4666 |
rs756890334 | snp | C/G | 5.87205e-05 | 0.00541819 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717683 | TGGGGGCCCCTTTGT[C/G]GGGTGGGGTAGCTAG | 4666 |
rs756941155 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime | NACA | GRCh38.p7 | 12:56725555 | TCCGCCCTCCGGTCC[A/G]CGAAGTGGCGACTGC | 4666 |
rs756960195 | snp | A/G | 1.66843e-05 | 0.00288823 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720625 | GAGCCCAGAGAAATG[A/G]GAAAATCTGGGGGGG | 4666 |
rs757032124 | snp | C/T | | | intron-variant | NACA | GRCh38.p7 | 12:56724292 | TTTTTACTCCAAATC[C/T]CTAAAGAAGTATCTC | 4666 |
rs757034980 | snp | C/T | 5.13624e-05 | 0.0050674 | intron-variant | NACA | GRCh38.p7 | 12:56714753 | GGTACTTCACCACAG[C/T]CTGCCCTGGACTAGA | 4666 |
rs757057630 | snp | A/G | 5.91139e-05 | 0.00543631 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56718086 | AGCTGGGGTTGTGGG[A/G]GCCCCTTTTGGGGGT | 4666 |
rs757091572 | snp | C/T | 2.69967e-05 | 0.00367391 | intron-variant | NACA | GRCh38.p7 | 12:56724559 | GGAGGCCTAAATTGA[C/T]TGGGATACATTCACT | 4666 |
rs757145746 | snp | C/G | 1.9143e-05 | 0.00309372 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717244 | GTGAGATCTCCTTTG[C/G]ATGGGGTGGCTGCGC | 4666 |
rs757162339 | snp | C/G | 2.0228e-05 | 0.00318018 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717325 | ACTGCTGGGGAAGTG[C/G]GGTCCCCTTTGGGAG | 4666 |
rs757181551 | snp | A/G | 2.99594e-05 | 0.00387025 | intron-variant | NACA | GRCh38.p7 | 12:56724442 | TGGCAAGGAGGGTAG[A/G]GAAACCTACCTGTCT | 4666 |
rs757248373 | snp | C/T | 1.76188e-05 | 0.00296801 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718760 | CTTTAGGGGCTGGAG[C/T]TGCTCGGGCCTTTTT | 4666 |
rs757308084 | in-del | -/T | 1.98635e-05 | 0.00315141 | intron-variant, frameshift-variant | NACA | GRCh38.p7 | 12:56717539 | GGGAGTGGGGGCCCC[-/T]TTTGGGGGGTGGGGT | 4666 |
rs757331228 | snp | A/G | 1.6691e-05 | 0.00288881 | intron-variant, missense | NACA | GRCh38.p7 | 12:56721075 | AGGTTAGGTGGAAAA[A/G]CAGAACTCTTCTGAA | 4666 |
rs757375836 | snp | C/T | 1.66291e-05 | 0.00288345 | intron-variant, missense | NACA | GRCh38.p7 | 12:56719980 | ACTGAACTGGGGAGA[C/T]TTTTGAGGTCTTCAG | 4666 |
rs757379727 | snp | C/T | 1.66946e-05 | 0.00288912 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716243 | TAGACTCAGGAGGAG[C/T]CAAGGGGCCCTTTGG | 4666 |
rs757465321 | snp | A/G | 1.6638e-05 | 0.00288422 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56719889 | GGTGAGTCCTGCTTG[A/G]GCTGGAGAGAAAGGG | 4666 |
rs757469781 | snp | A/G | 3.32414e-05 | 0.00407671 | intron-variant | NACA | GRCh38.p7 | 12:56713521 | CTGGAACAATGCCCA[A/G]GAAAAGTTTACTCAC | 4666 |
rs757497648 | snp | C/G | 2.08592e-05 | 0.00322942 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717790 | TTTGGGGAGGGAGGA[C/G]TTGCAGCTGGGGTTG | 4666 |
rs757543201 | in-del | -/TGGGGGTGGGG | 3.94139e-05 | 0.00443908 | intron-variant, frameshift-variant | NACA | GRCh38.p7 | 12:56718095 | TGTGGGGGCCCCTTT[-/TGGGGGTGGGG]TAGCTAGACCTCCTT | 4666 |
rs757566846 | in-del | -/GGT | 0.000182926 | 0.00956189 | intron-variant, cds-indel | NACA | GRCh38.p7 | 12:56720924 | ACATGGAGGGCTGGG[-/GGT]GCCTTTTGGATTAGG | 4666 |
rs757588194 | snp | C/T | 1.95345e-05 | 0.0031252 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716896 | GGAATGAGGGCCTCT[C/T]TGGGGGCTAGAGTTG | 4666 |
rs757590330 | snp | A/G | 5.89698e-05 | 0.00542968 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56717837 | GGATGGGGTAGCCAG[A/G]CCTCCTTTTGGGGAG | 4666 |
rs757612091 | snp | C/T | 1.79008e-05 | 0.00299167 | intron-variant, missense | NACA | GRCh38.p7 | 12:56719290 | TCAACCTTTTTTGTA[C/T]CTGGAGGAGTCCCAG | 4666 |
rs757622166 | snp | A/G | 6.92042e-05 | 0.00588195 | intron-variant, missense | NACA | GRCh38.p7 | 12:56719143 | ACACTAACCCCTAAA[A/G]GAGATGGGGAATCAG | 4666 |
rs757669138 | snp | C/G | 6.62866e-05 | 0.00575664 | intron-variant | NACA | GRCh38.p7 | 12:56714712 | GAAACAACTTTTACT[C/G]CTTTATAGTAGAAAT | 4666 |
rs757712107 | snp | A/G | 1.66549e-05 | 0.00288568 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720337 | GTAGCTACATTTAAG[A/G]AGCCAGAAGGGCTGC | 4666 |
rs757716622 | snp | C/G | | | intron-variant, missense | NACA | GRCh38.p7 | 12:56721321 | GAGGCAATAGTAGAG[C/G]GGGAAGGGAATGGGG | 4666 |
rs757805680 | snp | C/T | 1.71396e-05 | 0.00292737 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716042 | CAGGGGCAAGGGGTT[C/T]AGAGGGTGATTCCAA | 4666 |
rs757872257 | in-del | -/T | | | intron-variant, frameshift-variant | NACA | GRCh38.p7 | 12:56720858 | GGAGGCCACTCCAGA[-/T]TGAATAGAGGCCATG | 4666 |
rs757879793 | snp | C/T | 1.66283e-05 | 0.00288338 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720237 | AACAGAAGAAACGGG[C/T]ATTTGGGCCACTAAA | 4666 |
rs757894002 | snp | A/G | 1.64732e-05 | 0.0028699 | synonymous-codon | NACA | GRCh38.p7 | 12:56712879 | CATGACCAATTCAAT[A/G]TCCTTAACTTCTACA | 4666 |
rs757916306 | snp | A/G | 0.000178297 | 0.00944017 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56717561 | GGGTGGGGTACCTGG[A/G]CTTCCTTTTGGGGAG | 4666 |
rs757939071 | snp | C/G | | | upstream-variant-2KB, utr-variant-5-prime | NACA | GRCh38.p7 | 12:56725364 | GAGGGGGTGGGACTA[C/G]GATCCGATTCCGGGT | 4666 |
rs758001898 | snp | C/T | 1.67287e-05 | 0.00289207 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716522 | TTGCTGGAAGCCCTT[C/T]AGATGCTTGAGGAAC | 4666 |
rs758023969 | snp | C/G | 1.72142e-05 | 0.00293374 | intron-variant, missense | NACA | GRCh38.p7 | 12:56721328 | TAGTAGAGGGGGAAG[C/G]GAATGGGGAAGCCTG | 4666 |
rs758086237 | snp | A/G | 1.96616e-05 | 0.00313535 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717617 | GGGCCCCTTTGGGGG[A/G]TGAGGTAGCTGGGCC | 4666 |
rs758129325 | in-del | -/G | 1.73273e-05 | 0.00294335 | intron-variant, frameshift-variant | NACA | GRCh38.p7 | 12:56718969 | GAGGAGTGGGAGAAT[-/G]GCGTCGTGGCTGGTG | 4666 |
rs758152210 | snp | A/T | 1.65138e-05 | 0.00287343 | intron-variant | NACA | GRCh38.p7 | 12:56714460 | AAGATAAAACAGCTA[A/T]TAGTTAACCAGAATC | 4666 |
rs758174088 | snp | A/C/G | 0.000123153 | 0.0078463 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716623 | GGTGGGGAAGTGGGA[A/C/G]TCCCTTTGGGGGCTG | 4666 |
rs758203056 | snp | C/T | 5.31759e-05 | 0.00515608 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716629 | GAAGTGGGAGTCCCT[C/T]TGGGGGCTGGAGTTG | 4666 |
rs758238318 | snp | A/G | 1.64768e-05 | 0.00287021 | synonymous-codon | NACA | GRCh38.p7 | 12:56714662 | CTCTGGTACTGATTC[A/G]TCACTGTCAGATTCT | 4666 |
rs758290951 | snp | C/T | 3.91435e-05 | 0.00442383 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56717972 | GGGGGATGGGGTAGC[C/T]AGACCTCCTTTTGGG | 4666 |
rs758292297 | snp | C/T | 1.96973e-05 | 0.00313819 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718082 | TTGCAGCTGGGGTTG[C/T]GGGGGCCCCTTTTGG | 4666 |
rs758335145 | in-del | -/AAG | 1.65266e-05 | 0.00287455 | intron-variant | NACA | GRCh38.p7 | 12:56713687 | TTTGGACATAGCCTA[-/AAG]AAGAGAAAATAGTAT | 4666 |
rs758466783 | snp | C/G | 3.32579e-05 | 0.00407773 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720070 | TCTTTGGGAGCCACA[C/G]GTGCCATAACCAAGG | 4666 |
rs758513945 | in-del | -/GG | 1.98155e-05 | 0.0031476 | intron-variant, frameshift-variant | NACA | GRCh38.p7 | 12:56718102 | GCCCCTTTTGGGGGT[-/GG]GGTAGCTAGACCTCC | 4666 |
rs758521419 | snp | A/T | 3.81614e-05 | 0.00436798 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56717228 | AGTCACTGCTGGGGG[A/T]GTGAGATCTCCTTTG | 4666 |
rs758610280 | snp | A/C | 0.000107333 | 0.00732494 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718858 | GGGAAGGGCAGATTC[A/C]CCACTGAAGGAGTGG | 4666 |
rs758612309 | snp | A/C | 6.00414e-05 | 0.00547879 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717307 | TTGGGGGAGAGAGGA[A/C]TCACTGCTGGGGAAG | 4666 |
rs758642072 | snp | A/G | 3.34119e-05 | 0.00408715 | intron-variant | NACA | GRCh38.p7 | 12:56713503 | AGGTTGAGAAACCCT[A/G]GTCTGGAACAATGCC | 4666 |
rs758653483 | snp | A/G | 3.49724e-05 | 0.0041815 | synonymous-codon | NACA | GRCh38.p7 | 12:56713188 | CTGGGATAAATCTTC[A/G]ATCTACAGGGTAGAA | 4666 |
rs758661515 | snp | A/T | 0.000370084 | 0.013598 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720504 | CCCTGTGGAAGAATG[A/T]TCTACAGAAATGGTC | 4666 |
rs758729928 | snp | C/T | 1.66338e-05 | 0.00288386 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720964 | TCAGAGGGAACTTTA[C/T]TAAGATTAGTCTTTG | 4666 |
rs758742333 | snp | C/G | 3.79334e-05 | 0.00435491 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718703 | GAGGAGTTGCAGCTG[C/G]GGGTGTGGGGGCCCC | 4666 |
rs758758576 | snp | A/G | 1.97494e-05 | 0.00314234 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716812 | TCTTTGGAGGATGGG[A/G]TAGCTGGGGCTTCTT | 4666 |
rs758802708 | snp | G/T | | | missense | NACA | GRCh38.p7 | 12:56714630 | GTGGTTGCCTGGGTG[G/T]AATCCTGTTCTTCAA | 4666 |
rs758842422 | snp | G/T | 8.91591e-05 | 0.0066762 | intron-variant, missense | NACA | GRCh38.p7 | 12:56719312 | GAGTCCCAGCTGGGG[G/T]AAGAGAGGGTGAGGG | 4666 |
rs758927822 | snp | A/G | 7.01057e-05 | 0.00592013 | utr-variant-5-prime, intron-variant | NACA | GRCh38.p7 | 12:56724533 | GCATTTCTGAAGGAA[A/G]GGAATAAAAAGGAGG | 4666 |
rs758933584 | snp | A/G | 0.000116232 | 0.00762249 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716998 | ACCTCTTTGGGGGAA[A/G]AAGGAATCACAGCTG | 4666 |
rs758961821 | snp | A/T | 1.95551e-05 | 0.00312685 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716885 | TCATAGCTGGGGGAA[A/T]GAGGGCCTCTTTGGG | 4666 |
rs758965593 | in-del | -/TTG | 5.86952e-05 | 0.00541702 | intron-variant, cds-indel | NACA | GRCh38.p7 | 12:56717666 | GTTACAACTGCGGGA[-/TTG]TTGGGGGCCCCTTTG | 4666 |
rs759030727 | snp | A/C | | | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56718908 | TGTTACTCCTTTGGG[A/C]GACAGAGGAGTCACA | 4666 |
rs759039974 | snp | A/G | 3.32579e-05 | 0.00407773 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720031 | ACTGGTATCCTCAGA[A/G]TGGTTGCTACTTGAG | 4666 |
rs759109258 | snp | C/T | 1.91503e-05 | 0.00309431 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717169 | GGGGTAGCTGGGCCT[C/T]CTTTGGGGGCTGAAG | 4666 |
rs759120509 | snp | A/T | 1.75127e-05 | 0.00295906 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56718788 | TTTGGGGGAGGAAGA[A/T]GTCATGGATAGAGCA | 4666 |
rs759126400 | in-del | -/CA | 0.000137194 | 0.00828121 | intron-variant, frameshift-variant | NACA | GRCh38.p7 | 12:56717943 | TTGCAGCTGGGGTTG[-/CA]TGGGGGCCCCTTTGG | 4666 |
rs759137763 | snp | A/G | 5.791e-05 | 0.00538067 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717065 | GGGCCTTTTTGGGAG[A/G]GGAAGAAGTGGCAAC | 4666 |
rs759195707 | snp | C/T | 1.68562e-05 | 0.00290307 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56716100 | TTGCTGTTTAGGAGG[C/T]AGAGTGGGAACTGGG | 4666 |
rs759220382 | snp | C/T | 8.31871e-05 | 0.00644877 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56719853 | CTGGACTAACGGTAA[C/T]ACAGTAGGGTCTTTC | 4666 |
rs759222491 | snp | G/T | 1.94229e-05 | 0.00311626 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56718449 | TGCCCCTTTGGGGAA[G/T]GGGGTAGCTGCTGGA | 4666 |
rs759254475 | snp | G/T | 1.66607e-05 | 0.00288619 | intron-variant, missense | NACA | GRCh38.p7 | 12:56719945 | TTTGGAGGTCTTTTT[G/T]TGTTGGAAATTTAAC | 4666 |
rs759274046 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB | NACA | GRCh38.p7 | 12:56725267 | AAAGTACTTACTGTG[C/T]AGGGAACGCGGAACC | 4666 |
rs759304119 | snp | C/G | 1.66308e-05 | 0.00288359 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56720921 | TATACATGGAGGGCT[C/G]GGGGTGCCTTTTGGA | 4666 |
rs759340411 | snp | A/C | 9.99534e-05 | 0.00706871 | intron-variant, missense | NACA | GRCh38.p7 | 12:56721037 | CTGACTCAGCTACAG[A/C]CACTGAAGGAGGTGA | 4666 |
rs759347986 | snp | C/T | 1.64732e-05 | 0.0028699 | synonymous-codon | NACA | GRCh38.p7 | 12:56712846 | GACTGCCTTTGCTCT[C/T]GACACATTTGCTTGT | 4666 |
rs759418659 | snp | A/C | 1.77281e-05 | 0.00297721 | intron-variant, missense | NACA | GRCh38.p7 | 12:56719252 | AAGCAACAGGTGCCA[A/C]TGCTGAAGTATGAGA | 4666 |
rs759436476 | snp | A/G | 1.96296e-05 | 0.0031328 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718543 | GCTGGACCTCCTTTG[A/G]GGGAGGGAGGAGTTG | 4666 |
rs759535045 | in-del | -/GAA | 3.5033e-05 | 0.00418513 | intron-variant, cds-indel | NACA | GRCh38.p7 | 12:56718783 | GCCTTTTTGGGGGAG[-/GAA]GAAGTCATGGATAGA | 4666 |
rs759610429 | in-del | -/C | 1.66295e-05 | 0.00288349 | intron-variant, frameshift-variant | NACA | GRCh38.p7 | 12:56720073 | TGGGAGCCACAGGTG[-/C]CCATAACCAAGGCAG | 4666 |
rs759613700 | in-del | -/GAA | 1.91002e-05 | 0.00309026 | intron-variant, cds-indel | NACA | GRCh38.p7 | 12:56717181 | CCTCCTTTGGGGGCT[-/GAA]GTTGCTGGGGCCTTT | 4666 |
rs759676435 | snp | A/G | 1.66308e-05 | 0.00288359 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56720294 | GCTTTTGAGAATGAG[A/G]GAGGTTGTAGGAGAT | 4666 |
rs759703249 | snp | C/T | | | intron-variant | NACA | GRCh38.p7 | 12:56714982 | AAGGTCTTTGTTTCT[C/T]GGCACAGGCAAATAA | 4666 |
rs759724891 | snp | A/G | | | intron-variant, missense | NACA | GRCh38.p7 | 12:56718270 | CCTTTTGGGGAGGGA[A/G]GAGTCGCAGCTGGGG | 4666 |
rs759741895 | snp | C/G/T | 7.37455e-05 | 0.00607191 | intron-variant | NACA | GRCh38.p7 | 12:56715851 | GACACACCATGCACA[C/G/T]GGCAAACCAAGGCAA | 4666 |
rs759790877 | snp | A/C | | | intron-variant | NACA | GRCh38.p7 | 12:56713276 | CAACTCTCTGTAAAC[A/C]CATTCAGGTAACTTA | 4666 |
rs759852238 | in-del | -/AG | 1.65441e-05 | 0.00287607 | intron-variant | NACA | GRCh38.p7 | 12:56714707 | ATGAGAAACAACTTT[-/AG]TACTGCTTTATAGTA | 4666 |
rs759903795 | in-del | -/AAG | 4.94535e-05 | 0.00497236 | intron-variant | NACA | GRCh38.p7 | 12:56712946 | CAGTAAATTAAAGGC[-/AAG]AACAATTTCAGCAGT | 4666 |
rs759941331 | snp | A/G | 1.96945e-05 | 0.00313797 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718288 | GTCGCAGCTGGGGGA[A/G]TGGGGGCCCCCTTGA | 4666 |
rs759956371 | snp | C/T | 1.66374e-05 | 0.00288417 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56716316 | TTTCTGAACAGGGAG[C/T]AGAGGGGCTGGAGCC | 4666 |
rs759982850 | snp | C/T | 3.88267e-05 | 0.00440589 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718676 | GGGTAGCTGGGCCTC[C/T]TTTAGGGGAGGGAGG | 4666 |
rs760007059 | snp | A/G | | | intron-variant | NACA | GRCh38.p7 | 12:56722517 | ACATGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 4666 |
rs760049851 | snp | G/T | 1.66452e-05 | 0.00288484 | intron-variant, missense | NACA | GRCh38.p7 | 12:56719640 | AAGCGGACCAGCAGA[G/T]TCTGGGCCTGCATAA | 4666 |
rs760068751 | snp | A/G | 1.66779e-05 | 0.00288768 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56720681 | AGAGGTCACCACAGG[A/G]AGAGACTGAGTTGAA | 4666 |
rs760122245 | snp | A/T | 1.64779e-05 | 0.00287031 | missense | NACA | GRCh38.p7 | 12:56713588 | AGGGCTCTTGTAGAC[A/T]TCTGGTTTTGTGATG | 4666 |
rs760181212 | snp | A/G | 5.17139e-05 | 0.00508471 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718981 | GAATGCGTCGTGGCT[A/G]GTGAGTCTTTAGAGC | 4666 |
rs760264449 | snp | A/C | | | intron-variant | NACA | GRCh38.p7 | 12:56715403 | GATTTCTACATTTTT[A/C]TGAAAAGGGAGTCCC | 4666 |
rs760336261 | in-del | -/AGG | 0.000726694 | 0.0190478 | intron-variant, cds-indel | NACA | GRCh38.p7 | 12:56718059 | ACCTCCTTTTGGGGA[-/AGG]AGGAGTTGCAGCTGG | 4666 |
rs760401005 | snp | A/G | 0.000106255 | 0.00728808 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718930 | GGAGTCACAGCTGAG[A/G]GAGTAGGGGCCCCTT | 4666 |
rs760409545 | snp | A/G | 1.94173e-05 | 0.00311581 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716950 | GTCGCTGTTGGGGCA[A/G]TGGGGTCCCTTCTGG | 4666 |
rs760430478 | snp | C/G | | | intron-variant, utr-variant-3-prime | NACA | GRCh38.p7 | 12:56712563 | AATTCCTGTAACAGA[C/G]AAAAGATAATTAGCG | 4666 |
rs760450991 | snp | C/G | 1.66302e-05 | 0.00288355 | intron-variant, stop-gained | NACA | GRCh38.p7 | 12:56719968 | AATTTAACCAATACT[C/G]AACTGGGGAGATTTT | 4666 |
rs760497580 | snp | A/G | 3.86571e-05 | 0.00439625 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717052 | GCTGGAGTTGCTGGG[A/G]CCTTTTTGGGAGAGG | 4666 |
rs760499532 | snp | A/G | 3.66542e-05 | 0.00428086 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56715953 | GGTGGGCATGTTGAC[A/G]AGGACCGACTGGAAA | 4666 |
rs760527364 | snp | A/G | | | intron-variant | NACA | GRCh38.p7 | 12:56724214 | AGCTTCTTTTGAGGC[A/G]ACAGGCATAACATAG | 4666 |
rs760529222 | snp | A/G | 3.8975e-05 | 0.00441429 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718381 | CCTTTGGGGAGTGGG[A/G]TAGCTGCTGGACTTC | 4666 |
rs760617056 | snp | A/G | 9.91837e-05 | 0.00704145 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717548 | GGGCCCCTTTGGGGG[A/G]TGGGGTACCTGGGCT | 4666 |
rs760619114 | snp | G/T | | | intron-variant, missense | NACA | GRCh38.p7 | 12:56718441 | GGTGTGGATGCCCCT[G/T]TGGGGAATGGGGTAG | 4666 |
rs760650214 | snp | C/T | 6.58924e-05 | 0.0057395 | synonymous-codon | NACA | GRCh38.p7 | 12:56712792 | AACACTTACCATAAT[C/T]GCATTTACAATATCA | 4666 |
rs760700281 | snp | A/G | 1.66751e-05 | 0.00288744 | intron-variant, missense | NACA | GRCh38.p7 | 12:56721061 | GAGGTGAAGTAAGAA[A/G]GTTAGGTGGAAAAGC | 4666 |
rs760706959 | snp | C/T | 1.97015e-05 | 0.00313853 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717607 | GGAGGAGTGGGGGCC[C/T]CTTTGGGGGGTGAGG | 4666 |
rs760709663 | in-del | -/GGAGGGAGGA | 7.9358e-05 | 0.00629863 | intron-variant, frameshift-variant | NACA | GRCh38.p7 | 12:56718125 | TAGACCTCCTTTTGG[-/GGAGGGAGGA]GTTGCAGCTGGGGTT | 4666 |
rs760718783 | snp | A/G | 1.70435e-05 | 0.00291915 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56716583 | TGGGGAAGTAGGGGA[A/G]TCTTTGAGGGAGGAA | 4666 |
rs760725081 | snp | A/G | 3.5246e-05 | 0.00419783 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56719360 | CAGGGGCCAGCACTA[A/G]GGTAGCCAGAGGAGC | 4666 |
rs760797214 | snp | A/C | | | utr-variant-5-prime, intron-variant | NACA | GRCh38.p7 | 12:56725140 | GGAGGCCCAGGGGCG[A/C]GTAGGAACCCTGTGG | 4666 |
rs760807270 | snp | C/T | 1.6477e-05 | 0.00287024 | missense | NACA | GRCh38.p7 | 12:56714603 | AAGAGAATACCCACC[C/T]GGGCTTGTTGTGTGG | 4666 |
rs760815206 | snp | A/C | 7.13292e-05 | 0.00597156 | intron-variant, missense | NACA | GRCh38.p7 | 12:56719279 | GAGAAATACCATCAA[A/C]CTTTTTTGTACCTGG | 4666 |
rs760903215 | snp | A/G | 0.000100762 | 0.00709726 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720415 | ACCACTGGAAAGGCA[A/G]CCACAGTAGCAGGAA | 4666 |
rs760909810 | snp | C/G | 2.57981e-05 | 0.00359143 | intron-variant | NACA | GRCh38.p7 | 12:56721489 | AAGGAGATAAAGAAA[C/G]GGGGAGGGGGAGGAG | 4666 |
rs760933853 | snp | A/T | | | upstream-variant-2KB | NACA | GRCh38.p7 | 12:56726919 | GTCTGGGACCCCACC[A/T]TAAACCATGCTTTGT | 4666 |
rs760949773 | snp | A/G | 3.80757e-05 | 0.00436307 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716707 | GCCTCTTTGGGGGAA[A/G]GAGAAGTCACAGCTG | 4666 |
rs760965056 | in-del | -/AGAG | | | upstream-variant-2KB, utr-variant-5-prime | NACA | GRCh38.p7 | 12:56725856 | TTCTGTTCAATGACT[-/AGAG]AGACTCAAACGATGT | 4666 |
rs760993193 | snp | C/T | 1.66322e-05 | 0.00288371 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56720312 | GGTTGTAGGAGATAA[C/T]GAAAAAGAGGTAGCT | 4666 |
rs761002168 | snp | G/T | 2.15102e-05 | 0.00327943 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718163 | TTGTGGGTGCCCCTT[G/T]GTGGGGTGGGGTAGC | 4666 |
rs761067319 | snp | A/G | 1.96612e-05 | 0.00313532 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718061 | CTCCTTTTGGGGAAG[A/G]AGGAGTTGCAGCTGG | 4666 |
rs761089880 | snp | A/C/G | 3.91867e-05 | 0.0044263 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717287 | CTGGAGTTGCTGGAG[A/C/G]CTTTTTGGGGGAGAG | 4666 |
rs761157169 | snp | A/G | 1.86837e-05 | 0.00305639 | intron-variant, missense | NACA | GRCh38.p7 | 12:56721393 | GGAGAGCAAGGAGGG[A/G]GGAGGGTAGGTCCAG | 4666 |
rs761157368 | snp | C/T | | | intron-variant | NACA | GRCh38.p7 | 12:56723340 | TTGAATCAGATTATT[C/T]TAAATTCATCTGAAT | 4666 |
rs761158988 | snp | A/G | 1.90707e-05 | 0.00308788 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717187 | TTGGGGGCTGAAGTT[A/G]CTGGGGCCTTTTTGA | 4666 |
rs761200410 | snp | A/G | 1.66432e-05 | 0.00288467 | intron-variant, missense | NACA | GRCh38.p7 | 12:56719654 | AGTCTGGGCCTGCAT[A/G]AGAATCTGTCTTGAT | 4666 |
rs761204306 | snp | C/G | 1.96547e-05 | 0.0031348 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718567 | GGAGTTGCAGCTGGG[C/G]GTGTGGGGGCCCCTT | 4666 |
rs761285472 | snp | A/T | 1.66277e-05 | 0.00288333 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56720894 | CACACAGTGGTAAGG[A/T]ACAGTACTGACTATA | 4666 |
rs761348765 | snp | A/T | 7.86364e-05 | 0.00626993 | intron-variant | NACA | GRCh38.p7 | 12:56713227 | TCCATGTGAGTAGAT[A/T]AGCAGTCTTTGAAAA | 4666 |
rs761416885 | in-del | -/GT | 1.84643e-05 | 0.00303839 | intron-variant | NACA | GRCh38.p7 | 12:56715824 | TAGCGCCCAAGAGGG[-/GT]GTGGACGACAGACAC | 4666 |
rs761444466 | snp | A/G | 1.64814e-05 | 0.00287061 | synonymous-codon | NACA | GRCh38.p7 | 12:56713582 | TGAAGCAGGGCTCTT[A/G]TAGACATCTGGTTTT | 4666 |
rs761514563 | in-del | -/AA | 1.946e-05 | 0.00311923 | intron-variant, frameshift-variant | NACA | GRCh38.p7 | 12:56716931 | GGTCTTTTTAGAGAG[-/AA]GAGTCGCTGTTGGGG | 4666 |
rs761558420 | snp | C/T | 1.83889e-05 | 0.00303218 | intron-variant, missense | NACA | GRCh38.p7 | 12:56715876 | AGGCAAATACCCTTG[C/T]TGTTCTTCGTAACAG | 4666 |
rs761559368 | in-del | -/G | 1.95934e-05 | 0.00312991 | intron-variant, frameshift-variant | NACA | GRCh38.p7 | 12:56718503 | CACAGCTGGGGGTGT[-/G]GGGGCCCCTTTGGGG | 4666 |
rs761570763 | snp | C/T | 2.10568e-05 | 0.00324468 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717761 | CTTTGGGGGGTGGGG[C/T]AGCTGGGCCTCCTTT | 4666 |
rs761610256 | in-del | -/GGA | 0.375 | 0.216506 | intron-variant, cds-indel | NACA | GRCh38.p7 | 12:56718129 | CCTCCTTTTGGGGAG[-/GGA]GGAGTTGCAGCTGGG | 4666 |
rs761647861 | snp | A/G | | | intron-variant | NACA | GRCh38.p7 | 12:56713952 | GTTCAAGCAATTGCC[A/G]TGCCTCAGCCACCTT | 4666 |
rs761656731 | snp | G/T | 1.96868e-05 | 0.00313736 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716854 | ATTGCTGGGGTCTTT[G/T]TAGGGGAGGGAACAG | 4666 |
rs761660787 | snp | C/G | 0.000137924 | 0.0083032 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717812 | CTGGGGTTGTGGGGG[C/G]CCCTTTGGGGGATGG | 4666 |
rs761674547 | snp | A/G | 1.67835e-05 | 0.0028968 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56721272 | TAGGGCTGTTCCAGA[A/G]GATGACTGGGGAAAA | 4666 |
rs761679420 | snp | C/T | 1.72466e-05 | 0.00293649 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718990 | GTGGCTGGTGAGTCT[C/T]TAGAGCCTTGGAAAG | 4666 |
rs761756088 | in-del | -/AAG | 0.000181412 | 0.00952224 | intron-variant | NACA | GRCh38.p7 | 12:56714442 | CTGCTGCCGCCAGCT[-/AAG]AAGATAAAACAGCTA | 4666 |
rs761767192 | snp | A/G | 1.66277e-05 | 0.00288333 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56720144 | CATTGGAGGAGAAAC[A/G]CAAGTAGCTACCTCA | 4666 |
rs761769266 | snp | C/T | 1.75888e-05 | 0.00296548 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56718941 | TGAGGGAGTAGGGGC[C/T]CCTTTGGGGGATGGA | 4666 |
rs761803020 | snp | C/G | 1.83394e-05 | 0.00302809 | intron-variant, missense | NACA | GRCh38.p7 | 12:56715942 | GCAGATTTAGGGGTG[C/G]GCATGTTGACGAGGA | 4666 |
rs761829333 | snp | A/G | 1.96597e-05 | 0.0031352 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718304 | TGGGGGCCCCCTTGA[A/G]GGATGGGGTAGCTGG | 4666 |
rs761834240 | snp | A/G | 1.64746e-05 | 0.00287002 | intron-variant, utr-variant-3-prime | NACA | GRCh38.p7 | 12:56712756 | TGGTCAGGGCAGAGG[A/G]AGTCAAGGAACAAAG | 4666 |
rs761847485 | snp | C/G | 1.95299e-05 | 0.00312483 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718364 | CTGGGGTTGTGGGGG[C/G]CCCTTTGGGGAGTGG | 4666 |
rs761852636 | snp | G/T | 1.9862e-05 | 0.00315128 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56717543 | AGTGGGGGCCCCTTT[G/T]GGGGGTGGGGTACCT | 4666 |
rs761859107 | snp | C/T | 1.66291e-05 | 0.00288345 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720058 | TGAGTAGAAGGCTCT[C/T]TGGGAGCCACAGGTG | 4666 |
rs761913330 | snp | A/T | 1.67061e-05 | 0.00289011 | intron-variant, missense | NACA | GRCh38.p7 | 12:56721172 | GAGCTATCATGGGAG[A/T]GGCTAGAGCTAAGGC | 4666 |
rs761917516 | snp | A/G | 0.000101788 | 0.00713329 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56717438 | GGGGCCCTCTTTGGA[A/G]GATGGAGTAGTTGGG | 4666 |
rs761964739 | snp | G/T | 8.76908e-05 | 0.00662101 | intron-variant, missense | NACA | GRCh38.p7 | 12:56719374 | AAGGTAGCCAGAGGA[G/T]CACAGGTATTCTGGG | 4666 |
rs762054730 | snp | G/T | 0.00019999 | 0.00999775 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720583 | TGGACAGAACCAAAA[G/T]AACTCTGATGTAAAG | 4666 |
rs762130842 | snp | C/T | 3.3264e-05 | 0.0040781 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56716451 | AGCTGTGATGATTGG[C/T]GTGCTTTCTGGAGCT | 4666 |
rs762184850 | snp | A/G | 1.70107e-05 | 0.00291634 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716579 | AAGCTGGGGAAGTAG[A/G]GGAGTCTTTGAGGGA | 4666 |
rs762218766 | snp | C/T | 3.29587e-05 | 0.00405934 | synonymous-codon | NACA | GRCh38.p7 | 12:56714410 | TGCTTTACTGACTGG[C/T]TCTTCATCAATTTCA | 4666 |
rs762228216 | snp | A/G | 1.95769e-05 | 0.00312859 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717931 | GGGGAGGGAGGAGTT[A/G]CAGCTGGGGTTGTGG | 4666 |
rs762306689 | snp | C/G | 1.6483e-05 | 0.00287076 | intron-variant | NACA | GRCh38.p7 | 12:56714573 | CCCTGCTTCTTTGAC[C/G]CAATACCAGTTAGTA | 4666 |
rs762318122 | snp | C/T | 1.93015e-05 | 0.0031065 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717103 | GGGGCTGGGGGCTCC[C/T]TGGGGGAAGGAGGAG | 4666 |
rs762318187 | snp | C/T | 3.92665e-05 | 0.00443077 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718025 | TTGTGGGGGCCCCTT[C/T]TGGGGGTGGGGTAGC | 4666 |
rs762329474 | snp | A/G | 1.64738e-05 | 0.00286995 | synonymous-codon | NACA | GRCh38.p7 | 12:56724513 | GGTTTCTGTGGCTTC[A/G]CCGGGCATTTCTGAA | 4666 |
rs762419016 | snp | C/G | 2.81156e-05 | 0.00374926 | intron-variant | NACA | GRCh38.p7 | 12:56721501 | AAAGGGGGAGGGGGA[C/G]GAGAAAAAAGGTGAG | 4666 |
rs762426376 | snp | A/G | 0.000251376 | 0.0112083 | intron-variant, missense | NACA | GRCh38.p7 | 12:56719935 | GCAGGTACAGTTTGG[A/G]GGTCTTTTTGTGTTG | 4666 |
rs762515114 | in-del | -/T | 1.91386e-05 | 0.00309337 | intron-variant, frameshift-variant | NACA | GRCh38.p7 | 12:56717170 | GGTAGCTGGGCCTCC[-/T]TTTGGGGGCTGAAGT | 4666 |
rs762568208 | in-del | -/TTGT | 7.35774e-05 | 0.00606492 | intron-variant, frameshift-variant | NACA | GRCh38.p7 | 12:56715873 | CCAAGGCAAATACCC[-/TTGT]TGTTCTTCGTAACAG | 4666 |
rs762572991 | snp | A/G | 1.68269e-05 | 0.00290055 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716110 | GGAGGCAGAGTGGGA[A/G]CTGGGGAGGGAGCAA | 4666 |
rs762595843 | snp | C/T | 3.74118e-05 | 0.00432487 | intron-variant | NACA | GRCh38.p7 | 12:56713216 | GAAAATACAGATCCA[C/T]GTGAGTAGATTAGCA | 4666 |
rs762665641 | in-del | -/AA | 1.66385e-05 | 0.00288426 | intron-variant, frameshift-variant | NACA | GRCh38.p7 | 12:56719913 | GAAAGGGGCTCCTTC[-/AA]GAGAGGCAGGTACAG | 4666 |
rs762712521 | snp | A/G | 1.94022e-05 | 0.0031146 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716746 | AGGAGCTCTTTGGGG[A/G]ATGGGGCCCCTTTGT | 4666 |
rs762712966 | snp | C/T | 3.93012e-05 | 0.00443273 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56718557 | GGGGGAGGGAGGAGT[C/T]GCAGCTGGGGGTGTG | 4666 |
rs762861699 | snp | G/T | 6.33399e-05 | 0.00562725 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717751 | GTGGGGGCCCCTTTG[G/T]GGGGTGGGGTAGCTG | 4666 |
rs762895069 | in-del | -/GTT | | | intron-variant, cds-indel | NACA | GRCh38.p7 | 12:56718135 | TTTGGGGAGGGAGGA[-/GTT]GCAGCTGGGGTTGTG | 4666 |
rs762916064 | snp | A/G | 1.72794e-05 | 0.00293928 | intron-variant, missense | NACA | GRCh38.p7 | 12:56719107 | CCCTTCTTGGTTGGA[A/G]GTCTTTTAGTCTGAG | 4666 |
rs762951550 | snp | G/T | 1.9742e-05 | 0.00314175 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716849 | TTGGAATTGCTGGGG[G/T]CTTTTTAGGGGAGGG | 4666 |
rs762971611 | snp | A/C | 1.84221e-05 | 0.00303492 | intron-variant | NACA | GRCh38.p7 | 12:56715858 | CATGCACACGGCAAA[A/C]CAAGGCAAATACCCT | 4666 |
rs763003929 | snp | C/T | 0.000118147 | 0.00768504 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56718299 | GGGAGTGGGGGCCCC[C/T]TTGAGGGATGGGGTA | 4666 |
rs763025859 | in-del | -/AG | | | intron-variant | NACA | GRCh38.p7 | 12:56723796 | TCCTAAGTTTTCTAC[-/AG]AGATATGTTTTAACC | 4666 |
rs763055972 | snp | A/G | 1.6628e-05 | 0.00288335 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720163 | GTAGCTACCTCAAAG[A/G]TAGTAGTAGGTGCTG | 4666 |
rs763059463 | snp | A/T | 0.000110045 | 0.00741691 | intron-variant, missense | NACA | GRCh38.p7 | 12:56715933 | GGGATTCCAGCAGAT[A/T]TAGGGGTGGGCATGT | 4666 |
rs763092775 | snp | A/G | 3.34119e-05 | 0.00408715 | intron-variant, missense | NACA | GRCh38.p7 | 12:56721180 | ATGGGAGAGGCTAGA[A/G]CTAAGGCAGCTGGGG | 4666 |
rs763128152 | snp | A/G | | | intron-variant | NACA | GRCh38.p7 | 12:56722839 | TGGCATTCAGGAGGT[A/G]ACACAGAATTGGATC | 4666 |
rs763148328 | in-del | -/AGG | 0.000152259 | 0.0087239 | intron-variant, cds-indel | NACA | GRCh38.p7 | 12:56716706 | TGCCTCTTTGGGGGA[-/AGG]AGAAGTCACAGCTGG | 4666 |
rs763149134 | snp | A/G | 1.66324e-05 | 0.00288374 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56719952 | GTCTTTTTGTGTTGG[A/G]AATTTAACCAATACT | 4666 |
rs763300457 | in-del | -/G | 1.96713e-05 | 0.00313612 | intron-variant, frameshift-variant | NACA | GRCh38.p7 | 12:56718572 | TGCAGCTGGGGGTGT[-/G]GGGGCCCCTTTGGGG | 4666 |
rs763364058 | snp | C/T | 1.64852e-05 | 0.00287094 | synonymous-codon | NACA | GRCh38.p7 | 12:56714371 | TCTTACCTTCCGTGC[C/T]TTCTTTTCACTCCGA | 4666 |
rs763385164 | snp | A/G | 1.66682e-05 | 0.00288684 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56719550 | ACCTTTGGCAGTTGT[A/G]GGAGCCACCCCGGCA | 4666 |
rs763410829 | in-del | -/A | 1.65188e-05 | 0.00287387 | intron-variant, utr-variant-3-prime | NACA | GRCh38.p7 | 12:56712564 | ATTCCTGTAACAGAG[-/A]AAAGATAATTAGCGG | 4666 |
rs763414873 | snp | C/T | 1.64773e-05 | 0.00287026 | synonymous-codon | NACA | GRCh38.p7 | 12:56713618 | GACAAAGAGGATATT[C/T]TTAGATTTCCGGATA | 4666 |
rs763441376 | snp | A/G | 0.000138622 | 0.00832416 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56719397 | ATTCTGGGGGGATGG[A/G]GCCACAGGGCAATTT | 4666 |
rs763466919 | snp | C/G | 1.96655e-05 | 0.00313566 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717832 | TTGGGGGATGGGGTA[C/G]CCAGACCTCCTTTTG | 4666 |
rs763477499 | snp | C/G | 1.66835e-05 | 0.00288816 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56720675 | TTGAGAAGAGGTCAC[C/G]ACAGGAAGAGACTGA | 4666 |
rs763538868 | snp | A/C | | | intron-variant | NACA | GRCh38.p7 | 12:56723914 | CAGGAACTATTCCAG[A/C]ACACTAGAAGTATCT | 4666 |
rs763567276 | snp | C/T | 1.66746e-05 | 0.00288739 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720602 | TCTGATGTAAAGGTG[C/T]AAGATGAGAGCCCAG | 4666 |
rs763580591 | snp | A/C/G/T | 5.05246e-05 | 0.00502597 | intron-variant, missense, splice-acceptor-variant | NACA | GRCh38.p7 | 12:56716111 | GAGGCAGAGTGGGAA[A/C/G/T]TGGGGAGGGAGCAAG | 4666 |
rs763598462 | snp | A/G | 8.33174e-05 | 0.00645382 | intron-variant, missense | NACA | GRCh38.p7 | 12:56719567 | GAGCCACCCCGGCAG[A/G]GTCAGCACTTTCCAA | 4666 |
rs763608249 | snp | A/G | 3.93329e-05 | 0.00443451 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717620 | CCCCTTTGGGGGGTG[A/G]GGTAGCTGGGCCTCC | 4666 |
rs763628720 | snp | G/T | 1.66829e-05 | 0.00288811 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720619 | AGATGAGAGCCCAGA[G/T]AAATGGGAAAATCTG | 4666 |
rs763666769 | in-del | -/CAG | 0.000593462 | 0.0172157 | intron-variant | NACA | GRCh38.p7 | 12:56712957 | AGGCAAGAACAATTT[-/CAG]CAGTTCTTTGGAGTC | 4666 |
rs763698692 | snp | C/G | | | upstream-variant-2KB | NACA | GRCh38.p7 | 12:56728179 | AATTTTTCTTTCTTC[C/G]CCAGCAAGCCCACTT | 4666 |
rs763701258 | in-del | -/CCT | | | intron-variant | NACA | GRCh38.p7 | 12:56723776 | AAGAACTTTTCATTA[-/CCT]CCTCCTAAGTTTTCT | 4666 |
rs763705898 | snp | A/G | 0.000155951 | 0.00882901 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718475 | CTGGACTTCCTTTGG[A/G]GGAGGGAGGAGTCAC | 4666 |
rs763741400 | snp | A/G | 1.77049e-05 | 0.00297526 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718931 | GAGTCACAGCTGAGG[A/G]AGTAGGGGCCCCTTT | 4666 |
rs763794117 | in-del | -/GGAGGGA | | | intron-variant, frameshift-variant | NACA | GRCh38.p7 | 12:56718125 | TAGACCTCCTTTTGG[-/GGAGGGA]GGAGTTGCAGCTGGG | 4666 |
rs763795786 | snp | A/G | 1.9652e-05 | 0.00313458 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718558 | GGGGAGGGAGGAGTT[A/G]CAGCTGGGGGTGTGG | 4666 |
rs763878819 | snp | C/T | 1.97112e-05 | 0.0031393 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716852 | GAATTGCTGGGGTCT[C/T]TTTAGGGGAGGGAAC | 4666 |
rs763991074 | snp | G/T | 7.87991e-05 | 0.00627641 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718234 | ATGGGGGCCCCTTTG[G/T]GGGATGGGGTAGCTG | 4666 |
rs764000462 | in-del | -/CCTTTTGGGGGTGGGGTAGCTAGACCT | 1.97046e-05 | 0.00313878 | intron-variant, cds-indel | NACA | GRCh38.p7 | 12:56718090 | GGGGTTGTGGGGGCC[-/CCTTTTGGGGGTGGGGTAGCTAGACCT]CCTTTTGGGGAGGGA | 4666 |
rs764104831 | snp | A/C | 1.66299e-05 | 0.00288352 | intron-variant, missense | NACA | GRCh38.p7 | 12:56719970 | TTTAACCAATACTGA[A/C]CTGGGGAGATTTTTG | 4666 |
rs764179586 | in-del | -/GAG | 4.00858e-05 | 0.00447675 | intron-variant, cds-indel | NACA | GRCh38.p7 | 12:56717463 | GTTGGGCCTCCTTTA[-/GAG]GAGGGAGTTGTAGCT | 4666 |
rs764201021 | snp | C/G | 1.66832e-05 | 0.00288814 | intron-variant, missense | NACA | GRCh38.p7 | 12:56721067 | AAGTAAGAAGGTTAG[C/G]TGGAAAAGCAGAACT | 4666 |
rs764268404 | snp | G/T | 1.99563e-05 | 0.00315876 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717313 | GAGAGAGGAATCACT[G/T]CTGGGGAAGTGGGGT | 4666 |
rs764290784 | snp | A/G | 3.32635e-05 | 0.00407807 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56720942 | GCCTTTTGGATTAGG[A/G]ACTACCTCAGAGGGA | 4666 |
rs764338096 | snp | A/T | | | intron-variant | NACA | GRCh38.p7 | 12:56723956 | ACCCATAAACAAGTT[A/T]TCCGACCTAGGACGA | 4666 |
rs764353142 | snp | A/G | 1.64895e-05 | 0.00287132 | synonymous-codon | NACA | GRCh38.p7 | 12:56713666 | TGTAACCTGCCGAAG[A/G]CCCAGTTTGGACATA | 4666 |
rs764356514 | snp | A/G | 4.12252e-05 | 0.00453992 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717424 | GCAGCTGGGGGAGTG[A/G]GGCCCTCTTTGGAGG | 4666 |
rs764359969 | snp | G/T | 9.44421e-05 | 0.00687111 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718706 | GAGTTGCAGCTGGGG[G/T]TGTGGGGGCCCCTTT | 4666 |
rs764378596 | snp | C/T | 1.728e-05 | 0.00293933 | intron-variant, missense | NACA | GRCh38.p7 | 12:56719135 | GAGGAGACACACTAA[C/T]CCCTAAAGGAGATGG | 4666 |
rs764424669 | snp | A/G | | | intron-variant | NACA | GRCh38.p7 | 12:56715690 | GAAGTAATGAAAACC[A/G]AGATTTGGTTTCATA | 4666 |
rs764438334 | snp | A/G | | | intron-variant | NACA | GRCh38.p7 | 12:56722066 | TCTGACTCTGTTAGA[A/G]TAGTTTTGGGAAGGA | 4666 |
rs764450216 | snp | A/G | 3.32657e-05 | 0.0040782 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716342 | GAGCCACTGTGGAAA[A/G]GGGTCCTTTAGAACC | 4666 |
rs764479967 | snp | A/G | 1.87577e-05 | 0.00306243 | intron-variant, missense | NACA | GRCh38.p7 | 12:56721397 | AGCAAGGAGGGGGGA[A/G]GGTAGGTCCAGGCTG | 4666 |
rs764541118 | snp | A/C/G | 2.61825e-05 | 0.00361809 | intron-variant | NACA | GRCh38.p7 | 12:56721496 | TAAAGAAAGGGGGAG[A/C/G]GGGAGGAGAAAAAAG | 4666 |
rs764542193 | in-del | -/G | 1.67398e-05 | 0.00289303 | intron-variant, frameshift-variant | NACA | GRCh38.p7 | 12:56720633 | GAAATGGGAAAATCT[-/G]GGGGGGGTGTTGGGA | 4666 |
rs764565634 | in-del | -/CC/CCC | | | upstream-variant-2KB, utr-variant-5-prime | NACA | GRCh38.p7 | 12:56725937 | TTAGCTGTACCCCCG[-/CC/CCC]CCCCCCCCCCAAAAA | 4666 |
rs764594157 | snp | C/T | 3.29636e-05 | 0.00405964 | missense | NACA | GRCh38.p7 | 12:56714384 | GCCTTCTTTTCACTC[C/T]GACTCTGTTTTGCTT | 4666 |
rs764596433 | snp | C/T | 1.66385e-05 | 0.00288426 | intron-variant, missense | NACA | GRCh38.p7 | 12:56719809 | GAAGAGGATGTACTT[C/T]GGAAAGAAGGGGAAT | 4666 |
rs764629812 | snp | A/G | 1.96311e-05 | 0.00313292 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56717906 | GGATGGGGTAGCTAG[A/G]CCTCCTTTTGGGGAG | 4666 |
rs764643352 | snp | A/C | 1.92922e-05 | 0.00310575 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717071 | TTTTGGGAGAGGAAG[A/C]AGTGGCAACTTGTTT | 4666 |
rs764705477 | snp | A/G | 5.81311e-05 | 0.00539093 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716999 | CCTCTTTGGGGGAAG[A/G]AGGAATCACAGCTGG | 4666 |
rs764706510 | in-del | -/AACAATGCCC | 1.66879e-05 | 0.00288855 | intron-variant | NACA | GRCh38.p7 | 12:56713510 | GAAACCCTGGTCTGG[-/AACAATGCCC]AAGAAAAGTTTACTC | 4666 |
rs764731074 | snp | A/G | 1.71605e-05 | 0.00292915 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716032 | TCCTCATCAGCAGGG[A/G]CAAGGGGTTTAGAGG | 4666 |
rs764740210 | snp | A/T | | | intron-variant | NACA | GRCh38.p7 | 12:56723382 | GTATTTGTAAAATTA[A/T]GTTGTTCAATGACAC | 4666 |
rs764790765 | snp | A/G | 5.49476e-05 | 0.00524126 | intron-variant, missense | NACA | GRCh38.p7 | 12:56715960 | ATGTTGACGAGGACC[A/G]ACTGGAAAGGCACTC | 4666 |
rs764837683 | snp | C/T | 1.66421e-05 | 0.00288458 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56719664 | TGCATAAGAATCTGT[C/T]TTGATTACAGAGGCC | 4666 |
rs764938659 | snp | G/T | 1.66651e-05 | 0.00288657 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720702 | CTGAGTTGAAAGAGA[G/T]AAGGCAGCAGGTGGA | 4666 |
rs764991695 | snp | A/G | 3.88448e-05 | 0.00440691 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718450 | GCCCCTTTGGGGAAT[A/G]GGGTAGCTGCTGGAC | 4666 |
rs765004308 | snp | A/G | 1.64732e-05 | 0.0028699 | synonymous-codon | NACA | GRCh38.p7 | 12:56712872 | CTTGTGACATGACCA[A/G]TTCAATGTCCTTAAC | 4666 |
rs765031753 | snp | C/T | 1.95666e-05 | 0.00312777 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717668 | TTACAACTGCGGGAT[C/T]GGGGGCCCCTTTGTG | 4666 |
rs765095129 | in-del | -/C | | | intron-variant, frameshift-variant | NACA | GRCh38.p7 | 12:56716636 | GAGTCCCTTTGGGGG[-/C]TGGAGTTGCTGGGCC | 4666 |
rs765186587 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB | NACA | GRCh38.p7 | 12:56725270 | GTACTTACTGTGCAG[A/G]GAACGCGGAACCAAG | 4666 |
rs765191035 | snp | A/T | 1.64773e-05 | 0.00287026 | missense | NACA | GRCh38.p7 | 12:56714654 | TCTTCAAGCTCTGGT[A/T]CTGATTCATCACTGT | 4666 |
rs765191078 | snp | C/T | 1.93396e-05 | 0.00310957 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56716736 | TGGTGGAATGAGGAG[C/T]TCTTTGGGGGATGGG | 4666 |
rs765258967 | snp | C/G | 1.6708e-05 | 0.00289028 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56721173 | AGCTATCATGGGAGA[C/G]GCTAGAGCTAAGGCA | 4666 |
rs765271329 | snp | A/G | | | intron-variant | NACA | GRCh38.p7 | 12:56721536 | GCAGCCCAACTTGGT[A/G]CAACATGCCTCCTAG | 4666 |
rs765278799 | snp | C/G | 1.66471e-05 | 0.00288501 | intron-variant | NACA | GRCh38.p7 | 12:56714720 | TTTTACTGCTTTATA[C/G]TAGAAATTATAAGAG | 4666 |
rs765288760 | in-del | -/GGGTGGGGT | 1.97971e-05 | 0.00314613 | intron-variant, cds-indel | NACA | GRCh38.p7 | 12:56718098 | GGGGGCCCCTTTTGG[-/GGGTGGGGT]AGCTAGACCTCCTTT | 4666 |
rs765380933 | in-del | -/A | 1.9981e-05 | 0.00316071 | intron-variant, frameshift-variant | NACA | GRCh38.p7 | 12:56718131 | TCCTTTTGGGGAGGG[-/A]GGAGTTGCAGCTGGG | 4666 |
rs765412608 | snp | A/G | 3.93275e-05 | 0.00443421 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718069 | GGGGAAGGAGGAGTT[A/G]CAGCTGGGGTTGTGG | 4666 |
rs765468257 | snp | A/G | 6.6788e-05 | 0.00577837 | intron-variant, missense | NACA | GRCh38.p7 | 12:56721078 | TTAGGTGGAAAAGCA[A/G]AACTCTTCTGAACTG | 4666 |
rs765507888 | snp | A/G | 1.98501e-05 | 0.00315034 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56718215 | AGGAGTTGCAGCTGG[A/G]GGCATGGGGGCCCCT | 4666 |
rs765554055 | snp | A/T | 1.78838e-05 | 0.00299025 | intron-variant, missense | NACA | GRCh38.p7 | 12:56719300 | TTGTACCTGGAGGAG[A/T]CCCAGCTGGGGGAAG | 4666 |
rs765597397 | snp | A/G | 1.97225e-05 | 0.0031402 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56717297 | TGGAGCCTTTTTGGG[A/G]GAGAGAGGAATCACT | 4666 |
rs765599155 | snp | A/G | 3.34554e-05 | 0.00408982 | intron-variant | NACA | GRCh38.p7 | 12:56713493 | AGCAGTGCTGAGGTT[A/G]AGAAACCCTGGTCTG | 4666 |
rs765640599 | snp | C/T | 1.68496e-05 | 0.0029025 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720440 | CAGGAACTACCTCAT[C/T]TCTGGAAGGAAGGGG | 4666 |
rs765694039 | snp | A/G | 3.91213e-05 | 0.00442257 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56718680 | AGCTGGGCCTCCTTT[A/G]GGGGAGGGAGGAGTT | 4666 |
rs765729639 | snp | G/T | 8.33632e-05 | 0.00645559 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720593 | CAAAAGAACTCTGAT[G/T]TAAAGGTGCAAGATG | 4666 |
rs765797390 | snp | C/T | 1.64776e-05 | 0.00287028 | synonymous-codon | NACA | GRCh38.p7 | 12:56713591 | GCTCTTGTAGACATC[C/T]GGTTTTGTGATGACA | 4666 |
rs765804258 | snp | A/G | 1.9669e-05 | 0.00313594 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717827 | CCCCTTTGGGGGATG[A/G]GGTAGCCAGACCTCC | 4666 |
rs765823951 | snp | C/T | 6.25906e-05 | 0.00559387 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717770 | GTGGGGTAGCTGGGC[C/T]TCCTTTTGGGGAGGG | 4666 |
rs765890028 | snp | A/G | 3.54818e-05 | 0.00421184 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716954 | CTGTTGGGGCAATGG[A/G]GTCCCTTCTGGAGGA | 4666 |
rs765916766 | snp | A/G | 3.88659e-05 | 0.00440811 | intron-variant | NACA | GRCh38.p7 | 12:56724403 | TTTTGCCCACCAAAT[A/G]GCTTTAGGGTTAATT | 4666 |
rs766000996 | snp | A/C | 3.82482e-05 | 0.00437295 | intron-variant, missense | NACA | GRCh38.p7 | 12:56721415 | TAGGTCCAGGCTGCC[A/C]TAAGGCAGCAGTGAC | 4666 |
rs766001440 | snp | C/T | 1.66382e-05 | 0.00288424 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56719847 | GGCTGCCTGGACTAA[C/T]GGTAATACAGTAGGG | 4666 |
rs766019145 | in-del | -/AAG | 3.33461e-05 | 0.00408313 | intron-variant, cds-indel | NACA | GRCh38.p7 | 12:56721056 | TGAAGGAGGTGAAGT[-/AAG]AAGGTTAGGTGGAAA | 4666 |
rs766034451 | in-del | -/AGA | 1.91163e-05 | 0.00309156 | intron-variant, cds-indel | NACA | GRCh38.p7 | 12:56717175 | CTGGGCCTCCTTTGG[-/AGA]GGGCTGAAGTTGCTG | 4666 |
rs766052910 | snp | C/G | 3.32674e-05 | 0.0040783 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716333 | GAGGGGCTGGAGCCA[C/G]TGTGGAAAGGGGTCC | 4666 |
rs766097142 | snp | A/C | 3.32856e-05 | 0.00407942 | intron-variant, missense | NACA | GRCh38.p7 | 12:56719681 | TGATTACAGAGGCCG[A/C]GGAGTTAACACCCAG | 4666 |
rs766165248 | snp | C/G | 3.66455e-05 | 0.00428035 | intron-variant, missense | NACA | GRCh38.p7 | 12:56715955 | TGGGCATGTTGACGA[C/G]GACCGACTGGAAAGG | 4666 |
rs766220199 | snp | A/G | 1.66272e-05 | 0.00288328 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720817 | GAAGCGATGGCTAGG[A/G]TAGTTGTGGGTGTTG | 4666 |
rs766255043 | snp | A/G | 1.98301e-05 | 0.00314875 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717553 | CCTTTGGGGGGTGGG[A/G]TACCTGGGCTTCCTT | 4666 |
rs766256169 | snp | A/G | 3.43731e-05 | 0.00414552 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56716012 | GAATCAGAGGCAGCA[A/G]CTCATCCTCATCAGC | 4666 |
rs766258158 | snp | A/G | 1.65206e-05 | 0.00287403 | intron-variant, utr-variant-3-prime | NACA | GRCh38.p7 | 12:56712565 | TTCCTGTAACAGAGA[A/G]AAGATAATTAGCGGT | 4666 |
rs766310930 | snp | C/G/T | 3.44271e-05 | 0.00414881 | intron-variant, missense | NACA | GRCh38.p7 | 12:56719021 | AAAGACTATTCTCTG[C/G/T]AAGAAATGAAGCTTC | 4666 |
rs766334507 | snp | C/T | 1.7263e-05 | 0.00293789 | intron-variant, missense | NACA | GRCh38.p7 | 12:56719113 | TTGGTTGGAGGTCTT[C/T]TAGTCTGAGGAGACA | 4666 |
rs766345450 | snp | C/G/T | 3.94347e-05 | 0.00444028 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56717612 | AGTGGGGGCCCCTTT[C/G/T]GGGGGTGAGGTAGCT | 4666 |
rs766346119 | snp | A/G | 1.64732e-05 | 0.0028699 | synonymous-codon | NACA | GRCh38.p7 | 12:56712804 | AATCGCATTTACAAT[A/G]TCATTACTGTTGTTC | 4666 |
rs766352010 | in-del | -/G | 3.94042e-05 | 0.00443853 | intron-variant, frameshift-variant | NACA | GRCh38.p7 | 12:56718633 | GGAGGAGTTGCAGCT[-/G]GGGGTGTGGGGGCCC | 4666 |
rs766354403 | in-del | -/AG | 1.68179e-05 | 0.00289977 | intron-variant, frameshift-variant | NACA | GRCh38.p7 | 12:56716131 | GAGGGAGCAAGAGGC[-/AG]AGAGACTGGTGGGGA | 4666 |
rs766398764 | snp | C/T | 1.66277e-05 | 0.00288333 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720170 | CCTCAAAGGTAGTAG[C/T]AGGTGCTGCAGCAAT | 4666 |
rs766437115 | snp | C/G | 3.42354e-05 | 0.00413721 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716591 | TAGGGGAGTCTTTGA[C/G]GGAGGAAGGAGTCAC | 4666 |
rs766518411 | in-del | -/C | 3.46494e-05 | 0.00416215 | intron-variant, frameshift-variant | NACA | GRCh38.p7 | 12:56718139 | GGGAGGGAGGAGTTG[-/C]AGCTGGGGTTGTGGG | 4666 |
rs766558846 | snp | C/G | 1.96524e-05 | 0.00313461 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718064 | CTTTTGGGGAAGGAG[C/G]AGTTGCAGCTGGGGT | 4666 |
rs766561124 | snp | C/T | 1.64757e-05 | 0.00287012 | synonymous-codon | NACA | GRCh38.p7 | 12:56714611 | ACCCACCTGGGCTTG[C/T]TGTGTGGTTGCCTGG | 4666 |
rs766581752 | snp | A/G | 1.95808e-05 | 0.0031289 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717949 | GCTGGGGTTGTGGGG[A/G]CCCCTTTGGGGGATG | 4666 |
rs766602391 | snp | A/G | 1.66295e-05 | 0.00288349 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720073 | TTGGGAGCCACAGGT[A/G]CCATAACCAAGGCAG | 4666 |
rs766616951 | in-del | -/A | | | intron-variant, frameshift-variant | NACA | GRCh38.p7 | 12:56720227 | GGGTGGTTCCAACAG[-/A]AGAAACGGGCATTTG | 4666 |
rs766646895 | snp | A/C | 1.90685e-05 | 0.0030877 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717188 | TGGGGGCTGAAGTTG[A/C]TGGGGCCTTTTTGAG | 4666 |
rs766656646 | snp | A/C | 1.67105e-05 | 0.0028905 | intron-variant, missense | NACA | GRCh38.p7 | 12:56721181 | TGGGAGAGGCTAGAG[A/C]TAAGGCAGCTGGGGA | 4666 |
rs766700608 | snp | A/C/G/T | 5.58044e-05 | 0.00528201 | intron-variant, missense | NACA | GRCh38.p7 | 12:56721390 | GCAGGAGAGCAAGGA[A/C/G/T]GGGGGAGGGTAGGTC | 4666 |
rs766721815 | in-del | -/A | 3.30901e-05 | 0.00406743 | intron-variant, utr-variant-3-prime | NACA | GRCh38.p7 | 12:56712590 | GCGGTTCTTATAGGC[-/A]AAATCAGGAGAATTC | 4666 |
rs766811694 | snp | A/G | 0.000134576 | 0.00820182 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716117 | GAGTGGGAACTGGGG[A/G]GGGAGCAAGAGGCAG | 4666 |
rs766889758 | snp | A/C/T | 0.000300017 | 0.0122443 | intron-variant, missense | NACA | GRCh38.p7 | 12:56719561 | TTGTGGGAGCCACCC[A/C/T]GGCAGGGTCAGCACT | 4666 |
rs766905792 | snp | A/G | 1.67189e-05 | 0.00289122 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56716217 | AGCTGCTGTTAGAGG[A/G]GTGGACGCCTTAGAC | 4666 |
rs766939916 | snp | A/G | 1.95131e-05 | 0.00312349 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56718671 | GGATGGGGTAGCTGG[A/G]CCTCCTTTAGGGGAG | 4666 |
rs766965911 | snp | G/T | 3.93213e-05 | 0.00443386 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718568 | GAGTTGCAGCTGGGG[G/T]TGTGGGGGCCCCTTT | 4666 |
rs766995886 | snp | G/T | 2.08019e-05 | 0.00322498 | intron-variant | NACA | GRCh38.p7 | 12:56713235 | AGTAGATTAGCAGTC[G/T]TTGAAAAATAAATCA | 4666 |
rs767067855 | snp | A/G | 1.66751e-05 | 0.00288744 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720605 | GATGTAAAGGTGCAA[A/G]ATGAGAGCCCAGAGA | 4666 |
rs767149160 | snp | A/G | 3.50459e-05 | 0.0041859 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56718794 | GGAGGAAGAAGTCAT[A/G]GATAGAGCAGGAGCC | 4666 |
rs767156443 | snp | A/G | 1.66324e-05 | 0.00288374 | intron-variant, missense | NACA | GRCh38.p7 | 12:56719950 | AGGTCTTTTTGTGTT[A/G]GAAATTTAACCAATA | 4666 |
rs767202872 | snp | C/T | | | intron-variant | NACA | GRCh38.p7 | 12:56714043 | GTAGAGATGGGGTTT[C/T]GCCATGTTGGCCAGG | 4666 |
rs767225318 | snp | C/G | 1.96315e-05 | 0.00313295 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716773 | TTGTAAGTGGAAGGA[C/G]TCACTGCTGGGGGAC | 4666 |
rs767229360 | snp | C/G | 6.30855e-05 | 0.00561594 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717763 | TTGGGGGGTGGGGTA[C/G]CTGGGCCTCCTTTTG | 4666 |
rs767246715 | snp | A/G | 1.66721e-05 | 0.00288717 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56721053 | CACTGAAGGAGGTGA[A/G]GTAAGAAGGTTAGGT | 4666 |
rs767287491 | in-del | -/T | 1.95773e-05 | 0.00312862 | intron-variant, frameshift-variant | NACA | GRCh38.p7 | 12:56717954 | GGTTGTGGGGGCCCC[-/T]TTGGGGGATGGGGTA | 4666 |
rs767287665 | snp | C/T | 1.83293e-05 | 0.00302726 | intron-variant, missense | NACA | GRCh38.p7 | 12:56715948 | TTAGGGGTGGGCATG[C/T]TGACGAGGACCGACT | 4666 |
rs767315088 | snp | G/T | 1.96639e-05 | 0.00313554 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716858 | CTGGGGTCTTTTTAG[G/T]GGAGGGAACAGTCAT | 4666 |
rs767328000 | snp | A/G | 1.83842e-05 | 0.00303179 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56715878 | GCAAATACCCTTGTT[A/G]TTCTTCGTAACAGGT | 4666 |
rs767330028 | in-del | -/GCTGGA | 0.000233645 | 0.0108059 | intron-variant, cds-indel | NACA | GRCh38.p7 | 12:56717280 | CTGGTGACTGGAGTT[-/GCTGGA]GCCTTTTTGGGGGAG | 4666 |
rs767375116 | snp | A/G | 3.32773e-05 | 0.00407892 | intron-variant, missense | NACA | GRCh38.p7 | 12:56719860 | AACGGTAATACAGTA[A/G]GGTCTTTCTTGGTGG | 4666 |
rs767381664 | snp | C/T | 1.65111e-05 | 0.0028732 | utr-variant-3-prime | NACA | GRCh38.p7 | 12:56712529 | CCAAAAAAAGTTGCT[C/T]CCATATGGTTACATT | 4666 |
rs767398626 | snp | A/G | 3.93252e-05 | 0.00443408 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718307 | GGGCCCCCTTGAGGG[A/G]TGGGGTAGCTGGACC | 4666 |
rs767405121 | snp | A/G | 0.000233286 | 0.0107976 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716938 | TTAGAGAGAAGAGTC[A/G]CTGTTGGGGCAATGG | 4666 |
rs767489802 | snp | C/G | 1.66322e-05 | 0.00288371 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716353 | GAAAGGGGTCCTTTA[C/G]AACCATTCTTAGCTG | 4666 |
rs767530631 | snp | C/T | 3.45399e-05 | 0.00415557 | intron-variant, missense | NACA | GRCh38.p7 | 12:56719129 | TAGTCTGAGGAGACA[C/T]ACTAACCCCTAAAGG | 4666 |
rs767541933 | snp | A/G | | | intron-variant | NACA | GRCh38.p7 | 12:56715266 | CAATGATGATGACCT[A/G]TATCTCTAGTTTTTC | 4666 |
rs767581372 | snp | A/G | 1.77404e-05 | 0.00297824 | intron-variant, missense | NACA | GRCh38.p7 | 12:56719254 | GCAACAGGTGCCAAT[A/G]CTGAAGTATGAGAAA | 4666 |
rs767630213 | snp | G/T | 0.000277723 | 0.0117807 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717544 | GTGGGGGCCCCTTTG[G/T]GGGGTGGGGTACCTG | 4666 |
rs767752692 | in-del | -/GGA | 1.6628e-05 | 0.00288335 | intron-variant, cds-indel | NACA | GRCh38.p7 | 12:56720133 | GGACCTGATGACATT[-/GGA]GGAGAAACACAAGTA | 4666 |
rs767773830 | snp | A/G | | | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56717939 | AGGAGTTGCAGCTGG[A/G]GTTGTGGGGGCCCCT | 4666 |
rs767799043 | snp | C/G | 1.6628e-05 | 0.00288335 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720194 | CAGCAATTGTACAGG[C/G]GTTAGTCACCACAAG | 4666 |
rs767802295 | snp | A/C | | | intron-variant | NACA | GRCh38.p7 | 12:56724105 | CACAAATGCTCCGGG[A/C]TCCTTGGCCTGTGTC | 4666 |
rs767891304 | snp | A/C | 3.40472e-05 | 0.00412583 | intron-variant, missense | NACA | GRCh38.p7 | 12:56721310 | CTAAAGGGGTCGAGG[A/C]AATAGTAGAGGGGGA | 4666 |
rs767901186 | snp | A/G | 1.66441e-05 | 0.00288474 | intron-variant, missense | NACA | GRCh38.p7 | 12:56719644 | GGACCAGCAGAGTCT[A/G]GGCCTGCATAAGAAT | 4666 |
rs767959176 | snp | C/G/T | 0.000135078 | 0.00821719 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717104 | GGGCTGGGGGCTCCT[C/G/T]GGGGGAAGGAGGAGT | 4666 |
rs768048776 | snp | A/G | 1.90936e-05 | 0.00308973 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717181 | CCTCCTTTGGGGGCT[A/G]AAGTTGCTGGGGCCT | 4666 |
rs768096631 | in-del | -/GAA | 1.79345e-05 | 0.00299448 | intron-variant, cds-indel | NACA | GRCh38.p7 | 12:56718864 | GGCAGATTCACCACT[-/GAA]GGAGTGGGGGTCTCT | 4666 |
rs768140778 | snp | G/T | 1.94479e-05 | 0.00311826 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717275 | CTTCTCTGGTGACTG[G/T]AGTTGCTGGAGCCTT | 4666 |
rs768189983 | in-del | -/G | 1.74949e-05 | 0.00295756 | intron-variant, frameshift-variant | NACA | GRCh38.p7 | 12:56719386 | GAGCACAGGTATTCT[-/G]GGGGGGATGGAGCCA | 4666 |
rs768199123 | snp | G/T | 1.97272e-05 | 0.00314057 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56718260 | AGCTGGGCCTCCTTT[G/T]GGGGAGGGAGGAGTC | 4666 |
rs768210102 | in-del | -/T | | | intron-variant | NACA | GRCh38.p7 | 12:56722413 | GAATTGGAGAGCCTG[-/T]TAACAGTGGCTCATG | 4666 |
rs768229006 | snp | A/G | | | intron-variant, missense | NACA | GRCh38.p7 | 12:56717353 | GAGATGGGATAGCTG[A/G]TCCTCTTTTGGGGGA | 4666 |
rs768316820 | snp | A/T | 1.66499e-05 | 0.00288525 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716288 | CTTTGCCTTTTGCTG[A/T]CTTTGAAGAGTCTTT | 4666 |
rs768352530 | snp | G/T | 0.00181135 | 0.0300399 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56718983 | ATGCGTCGTGGCTGG[G/T]GAGTCTTTAGAGCCT | 4666 |
rs768516992 | snp | A/G | 1.6628e-05 | 0.00288335 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720137 | CTGATGACATTGGAG[A/G]AGAAACACAAGTAGC | 4666 |
rs768556967 | snp | C/T | 3.33333e-05 | 0.00408235 | intron-variant | NACA | GRCh38.p7 | 12:56713728 | CAACCTCTTTAGAAG[C/T]AGCCTAAAGAAGCAA | 4666 |
rs768558715 | snp | C/T | | | intron-variant | NACA | GRCh38.p7 | 12:56715097 | GTGAAAAAACCAAAA[C/T]CACACCGTGGAGGCA | 4666 |
rs768562171 | snp | G/T | 2.09694e-05 | 0.00323794 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56717753 | GGGGGCCCCTTTGGG[G/T]GGTGGGGTAGCTGGG | 4666 |
rs768581322 | in-del | -/AT | 5.82507e-05 | 0.00539648 | intron-variant, frameshift-variant | NACA | GRCh38.p7 | 12:56718433 | CAGCTGGGGGTGTGG[-/AT]GCCCCTTTGGGGAAT | 4666 |
rs768669414 | snp | A/T | 1.9449e-05 | 0.00311835 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56716934 | CTTTTTAGAGAGAAG[A/T]GTCGCTGTTGGGGCA | 4666 |
rs768675053 | snp | C/T | 1.66771e-05 | 0.00288761 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56719499 | AGAGACAGTTCCTTC[C/T]AGAAAAGGGCTGGCT | 4666 |
rs768708488 | snp | C/G | 1.95356e-05 | 0.00312529 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718357 | GTTGCAGCTGGGGTT[C/G]TGGGGGCCCCTTTGG | 4666 |
rs768729193 | snp | A/G | | | intron-variant, missense | NACA | GRCh38.p7 | 12:56715999 | ATTGGTTCCGGGGGA[A/G]TCAGAGGCAGCAGCT | 4666 |
rs768747570 | snp | C/T | 3.3305e-05 | 0.00408061 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720560 | TAGGACCTGTTTGAC[C/T]TAAAAGTTGGACAGA | 4666 |
rs768798461 | snp | C/T | 5.95776e-05 | 0.00545759 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717538 | GGGGGAGTGGGGGCC[C/T]CTTTGGGGGGTGGGG | 4666 |
rs768822329 | snp | A/G | 3.33784e-05 | 0.0040851 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720652 | GGGGTGTTGGGACCC[A/G]CAGTCTTTTGAGAAG | 4666 |
rs768837305 | snp | C/T | 2.14931e-05 | 0.00327812 | missense | NACA | GRCh38.p7 | 12:56724500 | CTGTAGCAGGGACGG[C/T]TTCTGTGGCTTCGCC | 4666 |
rs768875387 | snp | C/G | 1.64751e-05 | 0.00287007 | intron-variant, utr-variant-3-prime | NACA | GRCh38.p7 | 12:56712747 | ACTCATAATTGGTCA[C/G]GGCAGAGGGAGTCAA | 4666 |
rs768897154 | snp | A/G | | | intron-variant | NACA | GRCh38.p7 | 12:56724704 | TGATGTGACCCTCAC[A/G]CCTCTATCAAGGCCA | 4666 |
rs768949803 | snp | A/G | 1.66294e-05 | 0.00288347 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720007 | TCAGGGTCTGGCAGA[A/G]GAGGAGAGACTGGTA | 4666 |
rs768959574 | snp | C/T | 1.94403e-05 | 0.00311766 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56718422 | GGGAGGAGTTGCAGC[C/T]GGGGGTGTGGATGCC | 4666 |
rs769023782 | snp | C/T | | | intron-variant | NACA | GRCh38.p7 | 12:56722820 | GACAGTAAGACAGTA[C/T]CTCTGGCATTCAGGA | 4666 |
rs769047587 | snp | A/G | 0.000772147 | 0.0196336 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56717594 | AGGAGTTGCAGCTGG[A/G]GGAGTGGGGGCCCCT | 4666 |
rs769098309 | in-del | -/G | 2.10781e-05 | 0.00324633 | intron-variant, frameshift-variant | NACA | GRCh38.p7 | 12:56717750 | AGTGGGGGCCCCTTT[-/G]GGGGGTGGGGTAGCT | 4666 |
rs769114671 | snp | G/T | 7.01484e-05 | 0.00592193 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718774 | GTTGCTCGGGCCTTT[G/T]TGGGGGAGGAAGAAG | 4666 |
rs769218250 | snp | C/G | 1.6892e-05 | 0.00290615 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716563 | ATTTTACATGTGACA[C/G]AAGCTGGGGAAGTAG | 4666 |
rs769274556 | in-del | -/A | 1.93759e-05 | 0.00311249 | intron-variant, frameshift-variant | NACA | GRCh38.p7 | 12:56717015 | GGAATCACAGCTGGC[-/A]AGAGTGGGGGCCCCC | 4666 |
rs769278401 | snp | A/G | | | intron-variant, missense | NACA | GRCh38.p7 | 12:56719800 | ATCTCTGGAGAAGAG[A/G]ATGTACTTTGGAAAG | 4666 |
rs769285936 | snp | A/G | 1.96338e-05 | 0.00313313 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56718017 | AGCTGGGGTTGTGGG[A/G]GCCCCTTTTGGGGGT | 4666 |
rs769307925 | snp | C/G | 1.64838e-05 | 0.00287083 | intron-variant | NACA | GRCh38.p7 | 12:56714562 | GCCCTGATCAACCCT[C/G]CTTCTTTGACCCAAT | 4666 |
rs769325048 | snp | C/G | 1.66286e-05 | 0.0028834 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720898 | CAGTGGTAAGGAACA[C/G]TACTGACTATACATG | 4666 |
rs769374150 | snp | C/T | 1.98344e-05 | 0.00314909 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718121 | TAGCTAGACCTCCTT[C/T]TGGGGAGGGAGGAGT | 4666 |
rs769394015 | snp | A/G | 1.64961e-05 | 0.00287189 | intron-variant | NACA | GRCh38.p7 | 12:56714695 | TCCAGACCCTAAGAT[A/G]AGAAACAACTTTTAC | 4666 |
rs769427550 | snp | C/G | 1.91155e-05 | 0.0030915 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717176 | CTGGGCCTCCTTTGG[C/G]GGCTGAAGTTGCTGG | 4666 |
rs769475126 | snp | A/G | 1.96381e-05 | 0.00313347 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56718548 | ACCTCCTTTGGGGGA[A/G]GGAGGAGTTGCAGCT | 4666 |
rs769515621 | snp | G/T | 1.68258e-05 | 0.00290045 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716107 | TTAGGAGGCAGAGTG[G/T]GAACTGGGGAGGGAG | 4666 |
rs769570937 | in-del | -/A | 3.32878e-05 | 0.00407956 | intron-variant, frameshift-variant | NACA | GRCh38.p7 | 12:56719709 | CAGAGGGGAGGTCAT[-/A]CTGCTGGCTGGCTTA | 4666 |
rs769601907 | in-del | -/CCTTTGGGGGATGGAGTAGCTGGACCT | 1.95785e-05 | 0.00312871 | intron-variant, cds-indel | NACA | GRCh38.p7 | 12:56718510 | GGGGGTGTGGGGGCC[-/CCTTTGGGGGATGGAGTAGCTGGACCT]CCTTTGGGGGAGGGA | 4666 |
rs769608305 | snp | A/G | 5.52756e-05 | 0.00525688 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56721383 | TTGTGGGGCAGGAGA[A/G]CAAGGAGGGGGGAGG | 4666 |
rs769664131 | snp | A/G | 3.45393e-05 | 0.00415554 | intron-variant, missense | NACA | GRCh38.p7 | 12:56719101 | GCAGAACCCTTCTTG[A/G]TTGGAGGTCTTTTAG | 4666 |
rs769697215 | snp | C/T | 1.66824e-05 | 0.00288806 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716252 | GAGGAGCCAAGGGGC[C/T]CTTTGGGGAATGAGA | 4666 |
rs769745743 | snp | A/C/G | 4.14072e-05 | 0.00454997 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717800 | GAGGAGTTGCAGCTG[A/C/G]GGTTGTGGGGGCCCC | 4666 |
rs769804619 | snp | A/G | 0.000127076 | 0.00797005 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717740 | CAGCTGGGGGAGTGG[A/G]GGCCCCTTTGGGGGG | 4666 |
rs769844520 | snp | A/G | 1.97182e-05 | 0.00313986 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716845 | GGGGTTGGAATTGCT[A/G]GGGTCTTTTTAGGGG | 4666 |
rs769884631 | in-del | -/C | 3.30404e-05 | 0.00406437 | intron-variant | NACA | GRCh38.p7 | 12:56714338 | GGTGCTTCATAAGAT[-/C]CTGAAATCCTTTTCA | 4666 |
rs769903186 | snp | A/T | 1.66665e-05 | 0.00288669 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56719544 | TGAGGTACCTTTGGC[A/T]GTTGTGGGAGCCACC | 4666 |
rs769935805 | snp | A/G | 3.90016e-05 | 0.0044158 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716908 | TCTTTGGGGGCTAGA[A/G]TTGCTGGGGTCTTTT | 4666 |
rs769979002 | snp | A/C | | | intron-variant | NACA | GRCh38.p7 | 12:56713298 | GGTAACTTATTGTAC[A/C]GCTTTAAACTGCTTG | 4666 |
rs770025764 | snp | A/G | 1.83424e-05 | 0.00302834 | intron-variant, missense | NACA | GRCh38.p7 | 12:56715919 | AGGGGGTTGGGACAG[A/G]GATTCCAGCAGATTT | 4666 |
rs770136092 | snp | C/T | 3.32602e-05 | 0.00407786 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720743 | CCTTCAGGCTGAGGC[C/T]TCCTGGGTTTTGTGG | 4666 |
rs770183522 | snp | A/G | 5.90685e-05 | 0.00543422 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56718290 | CGCAGCTGGGGGAGT[A/G]GGGGCCCCCTTGAGG | 4666 |
rs770216173 | snp | C/T | | | intron-variant | NACA | GRCh38.p7 | 12:56723859 | TTTCGACGCTGAGGA[C/T]AAAAGGATTTATTTC | 4666 |
rs770224189 | snp | A/T | 1.66843e-05 | 0.00288823 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720671 | TCTTTTGAGAAGAGG[A/T]CACCACAGGAAGAGA | 4666 |
rs770273340 | snp | A/G | 0.000273796 | 0.0116971 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718342 | TTTGGGGAGGGAAGA[A/G]TTGCAGCTGGGGTTG | 4666 |
rs770273475 | snp | C/T | 2.12443e-05 | 0.00325909 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717388 | GGAGTCATAGCGGGA[C/T]CTCCTTTGTGGGAGG | 4666 |
rs770288100 | snp | A/G | 1.81171e-05 | 0.00300969 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718889 | GGGTCTCTTTGGGGG[A/G]TAGTGTTACTCCTTT | 4666 |
rs770338808 | snp | A/T | | | intron-variant | NACA | GRCh38.p7 | 12:56724731 | GCCAGCAATTCCCAC[A/T]GCATTCTCAACCCGA | 4666 |
rs770361109 | snp | C/G | 1.98332e-05 | 0.003149 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717518 | GGGAGGGAGGAGTTA[C/G]AGCTGGGGGAGTGGG | 4666 |
rs770384499 | snp | A/G | 1.67164e-05 | 0.00289101 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56721107 | TGAGTGGGGAGCCAG[A/G]GCAACCAGAGCTAAG | 4666 |
rs770404259 | snp | A/C | 4.57928e-05 | 0.0047848 | utr-variant-5-prime, intron-variant | NACA | GRCh38.p7 | 12:56724527 | CGCCGGGCATTTCTG[A/C]AGGAAGGGAATAAAA | 4666 |
rs770449187 | snp | C/T | 1.97967e-05 | 0.0031461 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717568 | GTACCTGGGCTTCCT[C/T]TTGGGGAGGGAGGAG | 4666 |
rs770450647 | snp | A/G | 3.35312e-05 | 0.00409444 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716534 | CTTTAGATGCTTGAG[A/G]AACAGTGGCCCCCAT | 4666 |
rs770459558 | in-del | -/AGA | | | intron-variant | NACA | GRCh38.p7 | 12:56721888 | AACAGAATTCCCACG[-/AGA]AGAACAGCTGTGCTA | 4666 |
rs770466042 | snp | G/T | 0.0115353 | 0.075064 | intron-variant, missense | NACA | GRCh38.p7 | 12:56719938 | GGTACAGTTTGGAGG[G/T]CTTTTTGTGTTGGAA | 4666 |
rs770523755 | snp | A/G | 1.95785e-05 | 0.00312871 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717988 | AGACCTCCTTTTGGG[A/G]AAGGAGGAGTTGCAG | 4666 |
rs770540571 | snp | G/T | 1.65488e-05 | 0.00287647 | intron-variant | NACA | GRCh38.p7 | 12:56714487 | AATCTAAGATCTGGA[G/T]AGCACAATCTCCTTG | 4666 |
rs770559527 | in-del | -/GTT | 1.95764e-05 | 0.00312855 | intron-variant, cds-indel | NACA | GRCh38.p7 | 12:56717940 | GGAGTTGCAGCTGGG[-/GTT]GTGGGGGCCCCTTTG | 4666 |
rs770601698 | snp | G/T | 1.66454e-05 | 0.00288486 | intron-variant, stop-gained | NACA | GRCh38.p7 | 12:56721018 | GACAGAGTTATCACT[G/T]ACCCTGACTCAGCTA | 4666 |
rs770613687 | snp | C/G | 3.84187e-05 | 0.00438268 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56717150 | GGGATCCCCTTTGGA[C/G]GATGGGGTAGCTGGG | 4666 |
rs770645381 | in-del | -/T | | | intron-variant, frameshift-variant | NACA | GRCh38.p7 | 12:56718119 | GGTAGCTAGACCTCC[-/T]TTTGGGGAGGGAGGA | 4666 |
rs770648692 | snp | C/T | 9.66268e-05 | 0.00695011 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717055 | GGAGTTGCTGGGGCC[C/T]TTTTGGGAGAGGAAG | 4666 |
rs770677168 | snp | A/C | 1.76911e-05 | 0.0029741 | intron-variant, missense | NACA | GRCh38.p7 | 12:56719243 | TGGGAGAGGAAGCAA[A/C]AGGTGCCAATGCTGA | 4666 |
rs770716128 | snp | C/T | 1.77644e-05 | 0.00298025 | intron-variant, missense | NACA | GRCh38.p7 | 12:56719345 | CAGACTTTGGGATTT[C/T]AGGGGCCAGCACTAA | 4666 |
rs770725935 | snp | A/G | 0.00033331 | 0.0129052 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718447 | GATGCCCCTTTGGGG[A/G]ATGGGGTAGCTGCTG | 4666 |
rs770764998 | snp | A/C | 1.67245e-05 | 0.00289171 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720389 | AGGGACCTTTGTCAA[A/C]AGATGGAGCCACCAC | 4666 |
rs770904079 | snp | A/G | 1.96965e-05 | 0.00313813 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718624 | TTTGGGGAGGGAGGA[A/G]TTGCAGCTGGGGGTG | 4666 |
rs770917035 | snp | G/T | 1.68616e-05 | 0.00290353 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716089 | GACGGCAGAAATTGC[G/T]GTTTAGGAGGCAGAG | 4666 |
rs770943126 | snp | C/G | 1.96061e-05 | 0.00313092 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718531 | GGGGATGGAGTAGCT[C/G]GACCTCCTTTGGGGG | 4666 |
rs771007076 | snp | A/C/T | 3.29735e-05 | 0.00406028 | intron-variant | NACA | GRCh38.p7 | 12:56713025 | GAACACAATGCTATA[A/C/T]GGCGAGAGTTAAATT | 4666 |
rs771027849 | in-del | -/CTCTTTGGGGGAAGGAGAAGTCACAGCTGGTGGAATGAGGAG | 9.48524e-05 | 0.00688601 | intron-variant, cds-indel | NACA | GRCh38.p7 | 12:56716694 | TGGAGGAGTAGGTGC[lengthTooLong]CTCTTTGGGGGATGG | 4666 |
rs771094961 | snp | C/T | 3.58944e-05 | 0.00423626 | intron-variant | NACA | GRCh38.p7 | 12:56713199 | CTTCGATCTACAGGG[C/T]AGAAAATACAGATCC | 4666 |
rs771114635 | in-del | -/TACAGTTT | 1.66693e-05 | 0.00288693 | intron-variant, frameshift-variant | NACA | GRCh38.p7 | 12:56719925 | TTCAAGAGAGGCAGG[-/TACAGTTT]GGAGGTCTTTTTGTG | 4666 |
rs771161053 | snp | C/T | | | upstream-variant-2KB | NACA | GRCh38.p7 | 12:56727576 | CATACCTGGTGTGGC[C/T]GCCTTTTAAGGGAAG | 4666 |
rs771164904 | snp | C/T | 1.98285e-05 | 0.00314863 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716834 | GGGCTTCTTTGGGGG[C/T]TGGAATTGCTGGGGT | 4666 |
rs771257648 | snp | A/G/T | 3.66866e-05 | 0.00428278 | intron-variant, missense | NACA | GRCh38.p7 | 12:56715909 | TGCTTGGCAGAGGGG[A/G/T]TTGGGACAGGGATTC | 4666 |
rs771279016 | snp | A/T | 3.32895e-05 | 0.00407966 | intron-variant, missense | NACA | GRCh38.p7 | 12:56719761 | AGGCTTTTCTTTGCT[A/T]GGGTGGCTTCAGGAG | 4666 |
rs771367088 | in-del | -/CAAC | | | intron-variant | NACA | GRCh38.p7 | 12:56714554 | AAAAGTTGCCCTGAT[-/CAAC]CAACCCTGCTTCTTT | 4666 |
rs771369888 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB | NACA | GRCh38.p7 | 12:56725282 | CAGGGAACGCGGAAC[C/T]AAGATGGCGGCAGAA | 4666 |
rs771370782 | snp | C/T | 1.66275e-05 | 0.00288331 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720872 | ATTGAATAGAGGCCA[C/T]GGGAGTCACACAGTG | 4666 |
rs771370826 | snp | A/G | 3.32923e-05 | 0.00407983 | intron-variant, missense | NACA | GRCh38.p7 | 12:56719629 | GAACTTTTGAGAAGC[A/G]GACCAGCAGAGTCTG | 4666 |
rs771374065 | snp | C/T | 4.25125e-05 | 0.00461025 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717380 | GGGAGGGAGGAGTCA[C/T]AGCGGGACCTCCTTT | 4666 |
rs771453766 | in-del | -/C | 1.96872e-05 | 0.00313739 | intron-variant, frameshift-variant | NACA | GRCh38.p7 | 12:56718294 | CTGGGGGAGTGGGGG[-/C]CCCCCTTGAGGGATG | 4666 |
rs771458748 | snp | G/T | 1.66288e-05 | 0.00288343 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720752 | TGAGGCTTCCTGGGT[G/T]TTGTGGAGAAATCAG | 4666 |
rs771507750 | snp | A/G | 3.93988e-05 | 0.00443822 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718283 | GAGGAGTCGCAGCTG[A/G]GGGAGTGGGGGCCCC | 4666 |
rs771589324 | snp | C/T | 3.96087e-05 | 0.00445003 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717499 | AGAGTAGGGGTCCCT[C/T]TAGGGGAGGGAGGAG | 4666 |
rs771632219 | in-del | -/GGGGAGGGAGGA | | | intron-variant, cds-indel | NACA | GRCh38.p7 | 12:56718123 | GCTAGACCTCCTTTT[-/GGGGAGGGAGGA]GTTGCAGCTGGGGTT | 4666 |
rs771639337 | snp | C/T | 1.64808e-05 | 0.00287057 | missense | NACA | GRCh38.p7 | 12:56713583 | GAAGCAGGGCTCTTG[C/T]AGACATCTGGTTTTG | 4666 |
rs771667951 | in-del | -/AT | | | intron-variant | NACA | GRCh38.p7 | 12:56713250 | TTTGAAAAATAAATC[-/AT]ATAGTTTCACAACTC | 4666 |
rs771683289 | snp | A/G | 1.66305e-05 | 0.00288357 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716420 | TCTTTTTGGTCTGTG[A/G]ACCTTTCCGAGTGGG | 4666 |
rs771690601 | in-del | -/T | | | intron-variant | NACA | GRCh38.p7 | 12:56724374 | CTCCTAAAAAGTGTA[-/T]TTCCCCTTGGTCATT | 4666 |
rs771729008 | snp | A/G | 1.65329e-05 | 0.0028751 | intron-variant | NACA | GRCh38.p7 | 12:56714333 | ATAAAGGTGCTTCAT[A/G]AGATCCTGAAATCCT | 4666 |
rs771748726 | snp | A/C/T | 3.32581e-05 | 0.00407776 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720032 | CTGGTATCCTCAGAG[A/C/T]GGTTGCTACTTGAGT | 4666 |
rs771844906 | snp | A/G | 1.67091e-05 | 0.00289038 | intron-variant, missense | NACA | GRCh38.p7 | 12:56721241 | AGGTTGGGGCTTCAG[A/G]GGCAGTTCCCAAAGG | 4666 |
rs771906739 | snp | C/T | 3.337e-05 | 0.00408459 | intron-variant, missense | NACA | GRCh38.p7 | 12:56719489 | TAGGAGCTAAAGAGA[C/T]AGTTCCTTCTAGAAA | 4666 |
rs771980112 | snp | G/T | 3.92211e-05 | 0.0044282 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56717891 | GGGGGCCCCTTTGGG[G/T]GATGGGGTAGCTAGA | 4666 |
rs771982948 | snp | C/T | | | utr-variant-5-prime, intron-variant | NACA | GRCh38.p7 | 12:56724968 | ACCCCTTACCCTTTT[C/T]TGGATCCTGTGAAGC | 4666 |
rs772069946 | snp | C/G | 1.76777e-05 | 0.00297297 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717043 | CCCATGGGGGCTGGA[C/G]TTGCTGGGGCCTTTT | 4666 |
rs772071588 | snp | A/G | 1.79586e-05 | 0.0029965 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56716004 | TTCCGGGGGAATCAG[A/G]GGCAGCAGCTCATCC | 4666 |
rs772126102 | snp | G/T | 5.91162e-05 | 0.00543642 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717604 | GCTGGAGGAGTGGGG[G/T]CCCCTTTGGGGGGTG | 4666 |
rs772133727 | snp | G/T | 0.000349902 | 0.0132223 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56718434 | AGCTGGGGGTGTGGA[G/T]GCCCCTTTGGGGAAT | 4666 |
rs772159678 | snp | C/G | 1.92273e-05 | 0.00310053 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717143 | GGAGGGTGGGATCCC[C/G]TTTGGAGGATGGGGT | 4666 |
rs772163703 | snp | G/T | 1.64738e-05 | 0.00286995 | intron-variant, missense | NACA | GRCh38.p7 | 12:56712774 | TCAAGGAACAAAGGC[G/T]TGAACACTTACCATA | 4666 |
rs772169292 | snp | G/T | 2.18434e-05 | 0.00330472 | intron-variant | NACA | GRCh38.p7 | 12:56721476 | TGGAGAAAGGCAAAA[G/T]GAGATAAAGAAAGGG | 4666 |
rs772223765 | snp | A/G | 1.95785e-05 | 0.00312871 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718507 | GCTGGGGGTGTGGGG[A/G]CCCCTTTGGGGGATG | 4666 |
rs772226688 | snp | A/G | 2.29613e-05 | 0.00338823 | missense | NACA | GRCh38.p7 | 12:56724466 | CCTGTCTCAGCCTGG[A/G]GCTGCGGCAACTCCT | 4666 |
rs772283432 | snp | A/C | | | intron-variant, utr-variant-3-prime | NACA | GRCh38.p7 | 12:56712736 | AAAATAAAGTCACTC[A/C]TAATTGGTCAGGGCA | 4666 |
rs772349037 | in-del | -/AG | 5.40584e-05 | 0.00519868 | intron-variant, frameshift-variant | NACA | GRCh38.p7 | 12:56718912 | ACTCCTTTGGGAGAC[-/AG]AGGAGTCACAGCTGA | 4666 |
rs772369731 | snp | A/G | 0.000254455 | 0.0112767 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717649 | CCTTTTGGAGAGGGA[A/G]GAGTTACAACTGCGG | 4666 |
rs772398850 | in-del | -/GGA | 1.97182e-05 | 0.00313986 | intron-variant, cds-indel | NACA | GRCh38.p7 | 12:56716802 | ACTGGAGGCCTCTTT[-/GGA]GGATGGGGTAGCTGG | 4666 |
rs772450336 | in-del | -/AAAG | 1.65605e-05 | 0.0028775 | intron-variant | NACA | GRCh38.p7 | 12:56714709 | GAGAAACAACTTTTA[-/AAAG]CTGCTTTATAGTAGA | 4666 |
rs772455135 | snp | C/T | | | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56718275 | TGGGGAGGGAGGAGT[C/T]GCAGCTGGGGGAGTG | 4666 |
rs772457858 | snp | A/C | 1.66125e-05 | 0.00288201 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716678 | ATGGAGGAGTCACAG[A/C]TGGAGGAGTAGGTGC | 4666 |
rs772528945 | snp | C/G | 1.66407e-05 | 0.00288446 | intron-variant, missense | NACA | GRCh38.p7 | 12:56719794 | AGAGGTATCTCTGGA[C/G]AAGAGGATGTACTTT | 4666 |
rs772601582 | snp | C/T | 1.66305e-05 | 0.00288357 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716423 | TTTTGGTCTGTGGAC[C/T]TTTCCGAGTGGGAGC | 4666 |
rs772622762 | snp | A/C/T | 3.32553e-05 | 0.00407759 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720889 | GGAGTCACACAGTGG[A/C/T]AAGGAACAGTACTGA | 4666 |
rs772634815 | snp | C/G/T | 6.61512e-05 | 0.00575083 | intron-variant | NACA | GRCh38.p7 | 12:56714704 | TAAGATGAGAAACAA[C/G/T]TTTTACTGCTTTATA | 4666 |
rs772713395 | snp | G/T | 1.66366e-05 | 0.0028841 | intron-variant, missense | NACA | GRCh38.p7 | 12:56719821 | CTTTGGAAAGAAGGG[G/T]AATTTTTAGGGGCTG | 4666 |
rs772715468 | snp | A/C | 1.64784e-05 | 0.00287035 | missense | NACA | GRCh38.p7 | 12:56713586 | GCAGGGCTCTTGTAG[A/C]CATCTGGTTTTGTGA | 4666 |
rs772715490 | snp | C/G | 3.32773e-05 | 0.00407892 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720998 | CTGAGGGAGCAATGG[C/G]AGCTGACAGAGTTAT | 4666 |
rs772715755 | in-del | -/TT | 2.07458e-05 | 0.00322063 | intron-variant, frameshift-variant | NACA | GRCh38.p7 | 12:56717803 | GAGTTGCAGCTGGGG[-/TT]GTGGGGGCCCCTTTG | 4666 |
rs772718037 | snp | A/G | 1.96856e-05 | 0.00313726 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717823 | GGGGCCCCTTTGGGG[A/G]ATGGGGTAGCCAGAC | 4666 |
rs772719142 | snp | C/T | 3.89727e-05 | 0.00441416 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718673 | ATGGGGTAGCTGGGC[C/T]TCCTTTAGGGGAGGG | 4666 |
rs772724435 | snp | A/G | 9.22892e-05 | 0.00679236 | intron-variant | NACA | GRCh38.p7 | 12:56715832 | AAGAGGGGTGTGGAC[A/G]ACAGACACACCATGC | 4666 |
rs772803436 | snp | C/G/T | 0.000445883 | 0.0149247 | intron-variant | NACA | GRCh38.p7 | 12:56714339 | GTGCTTCATAAGATC[C/G/T]TGAAATCCTTTTCAA | 4666 |
rs772924203 | in-del | -/GAA | 1.93004e-05 | 0.00310641 | intron-variant, cds-indel | NACA | GRCh38.p7 | 12:56717067 | GCCTTTTTGGGAGAG[-/GAA]GAAGTGGCAACTTGT | 4666 |
rs772985409 | snp | G/T | 1.96034e-05 | 0.00313071 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717892 | GGGGCCCCTTTGGGG[G/T]ATGGGGTAGCTAGAC | 4666 |
rs773045586 | in-del | -/T | 1.66681e-05 | 0.00288682 | intron-variant, frameshift-variant | NACA | GRCh38.p7 | 12:56719783 | TTCAGGAGAAAGAGG[-/T]TATCTCTGGAGAAGA | 4666 |
rs773064419 | snp | C/T | 7.04734e-05 | 0.00593563 | intron-variant, missense | NACA | GRCh38.p7 | 12:56719216 | CACCAGAGTCCTCAG[C/T]TGGGCACTCTTTGGG | 4666 |
rs773075256 | snp | C/T | 1.64738e-05 | 0.00286995 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56712783 | AAAGGCTTGAACACT[C/T]ACCATAATCGCATTT | 4666 |
rs773154234 | snp | A/G | 1.72794e-05 | 0.00293928 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56719106 | ACCCTTCTTGGTTGG[A/G]GGTCTTTTAGTCTGA | 4666 |
rs773156145 | snp | C/G | 1.93339e-05 | 0.00310912 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717050 | GGGCTGGAGTTGCTG[C/G]GGCCTTTTTGGGAGA | 4666 |
rs773163134 | snp | A/C/G | 5.04641e-05 | 0.00502294 | intron-variant, missense | NACA | GRCh38.p7 | 12:56721282 | CCAGAGGATGACTGG[A/C/G]GAAAAGGAACTTCTA | 4666 |
rs773183766 | in-del | -/CAC | | | intron-variant | NACA | GRCh38.p7 | 12:56714238 | CAAAATCTCAAAAAT[-/CAC]CACTAGAGAACTTAC | 4666 |
rs773208902 | snp | C/T | 1.94098e-05 | 0.0031152 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718438 | GGGGGTGTGGATGCC[C/T]CTTTGGGGAATGGGG | 4666 |
rs773248329 | snp | C/T | 8.96258e-05 | 0.00669364 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56716007 | CGGGGGAATCAGAGG[C/T]AGCAGCTCATCCTCA | 4666 |
rs773300992 | snp | A/C | 3.9419e-05 | 0.00443936 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717605 | CTGGAGGAGTGGGGG[A/C]CCCTTTGGGGGGTGA | 4666 |
rs773334779 | snp | A/C | 1.68869e-05 | 0.00290571 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716080 | CCAGGAGAGGACGGC[A/C]GAAATTGCTGTTTAG | 4666 |
rs773367731 | snp | A/G | 1.88067e-05 | 0.00306643 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716689 | ACAGCTGGAGGAGTA[A/G]GTGCCTCTTTGGGGG | 4666 |
rs773393477 | snp | A/C | 3.91466e-05 | 0.004424 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56717657 | AGAGGGAGGAGTTAC[A/C]ACTGCGGGATTGGGG | 4666 |
rs773403562 | in-del | -/T | 1.9625e-05 | 0.00313243 | intron-variant, frameshift-variant | NACA | GRCh38.p7 | 12:56718538 | AGTAGCTGGACCTCC[-/T]TTTGGGGGAGGGAGG | 4666 |
rs773478456 | snp | C/T | 1.96404e-05 | 0.00313366 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718048 | GGGGTAGCTAGACCT[C/T]CTTTTGGGGAAGGAG | 4666 |
rs773540278 | snp | C/T | 1.66687e-05 | 0.00288688 | intron-variant, missense | NACA | GRCh38.p7 | 12:56719549 | TACCTTTGGCAGTTG[C/T]GGGAGCCACCCCGGC | 4666 |
rs773678556 | in-del | -/T | | | upstream-variant-2KB | NACA | GRCh38.p7 | 12:56726288 | GGCACTTCTTGGATT[-/T]TTTTTTTTTTTTTTT | 4666 |
rs773687537 | snp | A/G | 3.8141e-05 | 0.00436681 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717184 | CCTTTGGGGGCTGAA[A/G]TTGCTGGGGCCTTTT | 4666 |
rs773714939 | snp | C/T | 1.66829e-05 | 0.00288811 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720674 | TTTGAGAAGAGGTCA[C/T]CACAGGAAGAGACTG | 4666 |
rs773746556 | snp | C/T | 0.000530199 | 0.0162732 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718159 | GGGGTTGTGGGTGCC[C/T]CTTTGTGGGGTGGGG | 4666 |
rs773773690 | snp | A/G | 3.35683e-05 | 0.00409671 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56717285 | GACTGGAGTTGCTGG[A/G]GCCTTTTTGGGGGAG | 4666 |
rs773804766 | snp | A/C/G | 1.66743e-05 | 0.00288736 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720599 | AACTCTGATGTAAAG[A/C/G]TGCAAGATGAGAGCC | 4666 |
rs773831918 | snp | A/G | 1.92199e-05 | 0.00309993 | intron-variant | NACA | GRCh38.p7 | 12:56713225 | GATCCATGTGAGTAG[A/G]TTAGCAGTCTTTGAA | 4666 |
rs773845794 | snp | A/G | | | intron-variant | NACA | GRCh38.p7 | 12:56723203 | TATCATTACAGATAA[A/G]ACCTTGTGTATTTAT | 4666 |
rs773861433 | snp | C/T | 1.66297e-05 | 0.0028835 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56720027 | AGAGACTGGTATCCT[C/T]AGAGTGGTTGCTACT | 4666 |
rs773861647 | snp | C/G | 3.34482e-05 | 0.00408937 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716213 | AGGCAGCTGCTGTTA[C/G]AGGGGTGGACGCCTT | 4666 |
rs773898867 | snp | A/G | 2.30205e-05 | 0.0033926 | utr-variant-5-prime, intron-variant | NACA | GRCh38.p7 | 12:56724529 | CCGGGCATTTCTGAA[A/G]GAAGGGAATAAAAAG | 4666 |
rs773921557 | snp | A/C | 1.66535e-05 | 0.00288556 | intron-variant, missense | NACA | GRCh38.p7 | 12:56721034 | ACCCTGACTCAGCTA[A/C]AGCCACTGAAGGAGG | 4666 |
rs773945190 | snp | C/T | | | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56721191 | TAGAGCTAAGGCAGC[C/T]GGGGAGATGGGAGGC | 4666 |
rs773949570 | snp | A/G | 3.32906e-05 | 0.00407973 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56716298 | TGCTGTCTTTGAAGA[A/G]TCTTTCTGAACAGGG | 4666 |
rs773951664 | snp | C/T | 1.66335e-05 | 0.00288383 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56719943 | AGTTTGGAGGTCTTT[C/T]TGTGTTGGAAATTTA | 4666 |
rs773999938 | snp | C/T | | | intron-variant | NACA | GRCh38.p7 | 12:56722447 | GTAATCCCAGCACTT[C/T]GGGATGCCTGGGAGG | 4666 |
rs774013609 | snp | C/T | | | intron-variant | NACA | GRCh38.p7 | 12:56715180 | AAAAGCAGACACGTA[C/T]ACATATTCAGCCTCA | 4666 |
rs774015233 | snp | A/G | 1.67262e-05 | 0.00289185 | intron-variant, missense | NACA | GRCh38.p7 | 12:56721111 | TGGGGAGCCAGGGCA[A/G]CCAGAGCTAAGGGAG | 4666 |
rs774061953 | in-del | -/TT | 0.000137031 | 0.00827626 | intron-variant, frameshift-variant | NACA | GRCh38.p7 | 12:56717941 | GAGTTGCAGCTGGGG[-/TT]GTGGGGGCCCCTTTG | 4666 |
rs774124204 | snp | C/G | 3.88908e-05 | 0.00440952 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716935 | TTTTTAGAGAGAAGA[C/G]TCGCTGTTGGGGCAA | 4666 |
rs774151575 | in-del | -/TTTTGGGGAGGGAGGAGTTG | 1.98228e-05 | 0.00314817 | intron-variant, frameshift-variant | NACA | GRCh38.p7 | 12:56718119 | GGTAGCTAGACCTCC[-/TTTTGGGGAGGGAGGAGTTG]CAGCTGGGGTTGTGG | 4666 |
rs774210174 | snp | C/T | 1.72677e-05 | 0.00293829 | intron-variant, missense | NACA | GRCh38.p7 | 12:56719114 | TGGTTGGAGGTCTTT[C/T]AGTCTGAGGAGACAC | 4666 |
rs774210206 | snp | A/G | 3.66737e-05 | 0.004282 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56715941 | AGCAGATTTAGGGGT[A/G]GGCATGTTGACGAGG | 4666 |
rs774217855 | snp | C/T | 3.9374e-05 | 0.00443683 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56716853 | AATTGCTGGGGTCTT[C/T]TTAGGGGAGGGAACA | 4666 |
rs774219322 | snp | C/G | 6.34981e-05 | 0.00563427 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717757 | GCCCCTTTGGGGGGT[C/G]GGGTAGCTGGGCCTC | 4666 |
rs774298133 | snp | A/G | 1.66308e-05 | 0.00288359 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56720285 | ATTAGGAGAGCTTTT[A/G]AGAATGAGAGAGGTT | 4666 |
rs774307851 | snp | G/T | 3.93988e-05 | 0.00443822 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717811 | GCTGGGGTTGTGGGG[G/T]CCCCTTTGGGGGATG | 4666 |
rs774311260 | snp | A/G | 1.77241e-05 | 0.00297686 | intron-variant, missense | NACA | GRCh38.p7 | 12:56719248 | GAGGAAGCAACAGGT[A/G]CCAATGCTGAAGTAT | 4666 |
rs774326993 | snp | C/T | 3.34975e-05 | 0.00409238 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56720393 | ACCTTTGTCAACAGA[C/T]GGAGCCACCACTGGA | 4666 |
rs774412255 | snp | G/T | 5.82677e-05 | 0.00539726 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718430 | TTGCAGCTGGGGGTG[G/T]GGATGCCCCTTTGGG | 4666 |
rs774419005 | snp | C/T | 4.05014e-05 | 0.0044999 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56721455 | TGAAGACATAGGTAG[C/T]ACAGCTGGAGAAAGG | 4666 |
rs774468008 | in-del | -/GAG | 1.66288e-05 | 0.00288343 | intron-variant, cds-indel | NACA | GRCh38.p7 | 12:56720005 | CTTCAGGGTCTGGCA[-/GAG]GAGGAGAGACTGGTA | 4666 |
rs774490674 | snp | A/G | 1.80504e-05 | 0.00300414 | intron-variant, missense | NACA | GRCh38.p7 | 12:56715996 | GAGATTGGTTCCGGG[A/G]GAATCAGAGGCAGCA | 4666 |
rs774503284 | snp | A/G | 1.97225e-05 | 0.0031402 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717595 | GGAGTTGCAGCTGGA[A/G]GAGTGGGGGCCCCTT | 4666 |
rs774517301 | snp | A/C/G | 1.95307e-05 | 0.00312489 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718361 | CAGCTGGGGTTGTGG[A/C/G]GGCCCCTTTGGGGAG | 4666 |
rs774542813 | snp | C/G | | | intron-variant | NACA | GRCh38.p7 | 12:56724056 | GCCAAGCTCTGCTAA[C/G]TAAAACCTTGATGCA | 4666 |
rs774606822 | snp | C/T | 1.98584e-05 | 0.003151 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717541 | GGAGTGGGGGCCCCT[C/T]TGGGGGGTGGGGTAC | 4666 |
rs774672813 | snp | A/G | | | intron-variant | NACA | GRCh38.p7 | 12:56724833 | ATACTCACACTGGCT[A/G]GGCTGGGGCCTCCTG | 4666 |
rs774677183 | snp | A/G | 1.66275e-05 | 0.00288331 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720775 | GAAATCAGAACTGAG[A/G]AAATGGTGGTATCTT | 4666 |
rs774751792 | in-del | -/GA | 1.64765e-05 | 0.00287019 | intron-variant | NACA | GRCh38.p7 | 12:56712918 | ATCGACCTGAGAGAT[-/GA]GAGGGAAAAAGCAGT | 4666 |
rs774779922 | snp | C/T | 1.66319e-05 | 0.00288369 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56716448 | GGGAGCTGTGATGAT[C/T]GGCGTGCTTTCTGGA | 4666 |
rs774821159 | snp | C/T | 1.95758e-05 | 0.0031285 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56717930 | TGGGGAGGGAGGAGT[C/T]GCAGCTGGGGTTGTG | 4666 |
rs774841395 | in-del | -/A | 3.2956e-05 | 0.00405918 | splice-donor-variant | NACA | GRCh38.p7 | 12:56714599 | AGTAAGAGAATACCC[-/A]ACCTGGGCTTGTTGT | 4666 |
rs774865593 | snp | A/G | | | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56716577 | AGAAGCTGGGGAAGT[A/G]GGGGAGTCTTTGAGG | 4666 |
rs774909251 | snp | G/T | 1.96358e-05 | 0.00313329 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718024 | GTTGTGGGGGCCCCT[G/T]TTGGGGGTGGGGTAG | 4666 |
rs774966977 | snp | A/G | 1.6679e-05 | 0.00288777 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720679 | GAAGAGGTCACCACA[A/G]GAAGAGACTGAGTTG | 4666 |
rs774971155 | snp | A/C | 1.7828e-05 | 0.00298558 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56718923 | AGACAGAGGAGTCAC[A/C]GCTGAGGGAGTAGGG | 4666 |
rs774973294 | snp | A/G | 1.68168e-05 | 0.00289967 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716108 | TAGGAGGCAGAGTGG[A/G]AACTGGGGAGGGAGC | 4666 |
rs775022264 | snp | A/G | 1.66382e-05 | 0.00288424 | intron-variant, missense | NACA | GRCh38.p7 | 12:56719848 | GCTGCCTGGACTAAC[A/G]GTAATACAGTAGGGT | 4666 |
rs775045324 | snp | G/T | 1.65002e-05 | 0.00287225 | intron-variant | NACA | GRCh38.p7 | 12:56714697 | CAGACCCTAAGATGA[G/T]AAACAACTTTTACTG | 4666 |
rs775264285 | snp | C/T | | | intron-variant, missense | NACA | GRCh38.p7 | 12:56717749 | GAGTGGGGGCCCCTT[C/T]GGGGGGTGGGGTAGC | 4666 |
rs775266060 | in-del | -/GGGGAGGGAGGAG | 3.96959e-05 | 0.00445493 | intron-variant, frameshift-variant | NACA | GRCh38.p7 | 12:56718123 | GCTAGACCTCCTTTT[-/GGGGAGGGAGGAG]TTGCAGCTGGGGTTG | 4666 |
rs775269882 | snp | C/T | 1.6757e-05 | 0.00289452 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716189 | CAGGTTTAGGAAGGA[C/T]CTTCTCAAAGGCAGC | 4666 |
rs775354326 | snp | C/G | 3.94376e-05 | 0.00444041 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56716847 | GGTTGGAATTGCTGG[C/G]GTCTTTTTAGGGGAG | 4666 |
rs775362663 | snp | A/G | 3.92773e-05 | 0.00443138 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718552 | CCTTTGGGGGAGGGA[A/G]GAGTTGCAGCTGGGG | 4666 |
rs775380230 | snp | G/T | 3.91321e-05 | 0.00442318 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717671 | CAACTGCGGGATTGG[G/T]GGCCCCTTTGTGGGG | 4666 |
rs775428247 | snp | A/C/G | 5.01839e-05 | 0.00500898 | intron-variant, missense | NACA | GRCh38.p7 | 12:56721139 | GAGCTGAAGAGGAAG[A/C/G]GGTCCCTTTCAGAGT | 4666 |
rs775434098 | snp | C/T | | | intron-variant | NACA | GRCh38.p7 | 12:56722247 | CTCTATAAACCTTCC[C/T]AGGTGATGTTAATTC | 4666 |
rs775452750 | snp | A/G | 1.96817e-05 | 0.00313695 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718645 | GCTGGGGGTGTGGGG[A/G]CCCATTTCGGGGATG | 4666 |
rs775525494 | in-del | -/G | 3.92565e-05 | 0.0044302 | intron-variant, frameshift-variant | NACA | GRCh38.p7 | 12:56718014 | TGCAGCTGGGGTTGT[-/G]GGGGCCCCTTTTGGG | 4666 |
rs775527927 | snp | A/G/T | 0.000148645 | 0.00861988 | synonymous-codon | NACA | GRCh38.p7 | 12:56724495 | CTGCTCTGTAGCAGG[A/G/T]ACGGTTTCTGTGGCT | 4666 |
rs775555316 | snp | C/T | 1.66507e-05 | 0.00288532 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56720552 | CAAAGCACTAGGACC[C/T]GTTTGACCTAAAAGT | 4666 |
rs775559747 | snp | A/G | 5.53011e-05 | 0.00525809 | intron-variant | NACA | GRCh38.p7 | 12:56715852 | ACACACCATGCACAC[A/G]GCAAACCAAGGCAAA | 4666 |
rs775637419 | snp | C/T | | | intron-variant | NACA | GRCh38.p7 | 12:56713307 | TTGTACAGCTTTAAA[C/T]TGCTTGCCCTCACAG | 4666 |
rs775643455 | snp | C/T | 1.67618e-05 | 0.00289493 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56720405 | AGATGGAGCCACCAC[C/T]GGAAAGGCAGCCACA | 4666 |
rs775646284 | snp | C/T | 1.95467e-05 | 0.00312618 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718349 | AGGGAAGAGTTGCAG[C/T]TGGGGTTGTGGGGGC | 4666 |
rs775647569 | snp | A/G | 1.83437e-05 | 0.00302845 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56715929 | GACAGGGATTCCAGC[A/G]GATTTAGGGGTGGGC | 4666 |
rs775652034 | snp | C/T | 1.94949e-05 | 0.00312203 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716912 | TGGGGGCTAGAGTTG[C/T]TGGGGTCTTTTTAGA | 4666 |
rs775696720 | snp | A/G | | | intron-variant | NACA | GRCh38.p7 | 12:56714914 | CAGAAATGAGGACTA[A/G]TCACTAGAAATAGCT | 4666 |
rs775711939 | snp | C/G | 5.60229e-05 | 0.00529229 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56721392 | AGGAGAGCAAGGAGG[C/G]GGGAGGGTAGGTCCA | 4666 |
rs775768350 | snp | A/G | | | intron-variant, missense | NACA | GRCh38.p7 | 12:56719833 | GGGGAATTTTTAGGG[A/G]CTGCCTGGACTAACG | 4666 |
rs775789377 | in-del | -/G | 1.97619e-05 | 0.00314333 | intron-variant, frameshift-variant | NACA | GRCh38.p7 | 12:56716808 | GCCTCTTTGGAGGAT[-/G]GGGGTAGCTGGGGCT | 4666 |
rs775806463 | snp | A/G | 5.91302e-05 | 0.00543706 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718303 | GTGGGGGCCCCCTTG[A/G]GGGATGGGGTAGCTG | 4666 |
rs775922980 | snp | A/C/T | 7.02266e-05 | 0.00592531 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718769 | CTGGAGTTGCTCGGG[A/C/T]CTTTTTGGGGGAGGA | 4666 |
rs775925041 | snp | C/G | 2.09853e-05 | 0.00323916 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717404 | CTCCTTTGTGGGAGG[C/G]GGTTGCAGCTGGGGG | 4666 |
rs775973308 | snp | A/G | | | intron-variant, missense | NACA | GRCh38.p7 | 12:56716386 | GGATCTGGGCATATA[A/G]GAGGTGAAGTAGCAG | 4666 |
rs776010027 | snp | A/G | 1.64833e-05 | 0.00287078 | intron-variant | NACA | GRCh38.p7 | 12:56714553 | ACAAAAGTTGCCCTG[A/G]TCAACCCTGCTTCTT | 4666 |
rs776013059 | snp | A/T | 0.000496736 | 0.0157519 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717530 | TTACAGCTGGGGGAG[A/T]GGGGGCCCCTTTGGG | 4666 |
rs776106973 | in-del | -/CAC | 1.66283e-05 | 0.00288338 | intron-variant, cds-indel | NACA | GRCh38.p7 | 12:56720201 | TGTACAGGGGTTAGT[-/CAC]CACAAGTGGGGTGGT | 4666 |
rs776114193 | snp | C/G | 1.65042e-05 | 0.0028726 | intron-variant | NACA | GRCh38.p7 | 12:56714346 | ATAAGATCCTGAAAT[C/G]CTTTTCAAATCTTAC | 4666 |
rs776118153 | snp | A/G | 1.6646e-05 | 0.00288491 | intron-variant, missense | NACA | GRCh38.p7 | 12:56719645 | GACCAGCAGAGTCTG[A/G]GCCTGCATAAGAATC | 4666 |
rs776120629 | snp | C/G | 1.93175e-05 | 0.00310779 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56717060 | TGCTGGGGCCTTTTT[C/G]GGAGAGGAAGAAGTG | 4666 |
rs776153660 | snp | A/C | | | intron-variant | NACA | GRCh38.p7 | 12:56723861 | TCGACGCTGAGGATA[A/C]AAGGATTTATTTCAA | 4666 |
rs776206883 | snp | A/G | 0.000103752 | 0.00720177 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718985 | GCGTCGTGGCTGGTG[A/G]GTCTTTAGAGCCTTG | 4666 |
rs776320396 | snp | A/G | 1.95884e-05 | 0.00312951 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717991 | CCTCCTTTTGGGGAA[A/G]GAGGAGTTGCAGCTG | 4666 |
rs776394304 | snp | C/G | 1.72662e-05 | 0.00293817 | intron-variant, missense | NACA | GRCh38.p7 | 12:56719089 | GTATCAGGGCCAGCA[C/G]AACCCTTCTTGGTTG | 4666 |
rs776412450 | snp | A/G | 1.96493e-05 | 0.00313436 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56718533 | GGATGGAGTAGCTGG[A/G]CCTCCTTTGGGGGAG | 4666 |
rs776469052 | in-del | -/GGAGGA | 6.03173e-05 | 0.00549136 | intron-variant, cds-indel | NACA | GRCh38.p7 | 12:56718129 | CCTCCTTTTGGGGAG[-/GGAGGA]GTTGCAGCTGGGGTT | 4666 |
rs776484125 | snp | C/T | 4.98873e-05 | 0.00499411 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720262 | ACTAAAGGATAATGA[C/T]AAGTGGCATTAGGAG | 4666 |
rs776484177 | snp | G/T | 0.0001031 | 0.00717909 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716014 | ATCAGAGGCAGCAGC[G/T]CATCCTCATCAGCAG | 4666 |
rs776522692 | snp | A/G | 1.94411e-05 | 0.00311772 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718448 | ATGCCCCTTTGGGGA[A/G]TGGGGTAGCTGCTGG | 4666 |
rs776558536 | in-del | -/TGGGGAA | 1.94064e-05 | 0.00311493 | intron-variant, frameshift-variant | NACA | GRCh38.p7 | 12:56718442 | GTGTGGATGCCCCTT[-/TGGGGAA]TGGGGTAGCTGCTGG | 4666 |
rs776572525 | snp | C/T | 3.32557e-05 | 0.00407759 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720143 | ACATTGGAGGAGAAA[C/T]ACAAGTAGCTACCTC | 4666 |
rs776662204 | snp | A/G | 1.67705e-05 | 0.00289568 | intron-variant, missense | NACA | GRCh38.p7 | 12:56721270 | GGTAGGGCTGTTCCA[A/G]AGGATGACTGGGGAA | 4666 |
rs776664587 | snp | C/G | 1.66294e-05 | 0.00288347 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720041 | TCAGAGTGGTTGCTA[C/G]TTGAGTAGAAGGCTC | 4666 |
rs776677872 | snp | A/G | 1.6684e-05 | 0.00288821 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56720669 | AGTCTTTTGAGAAGA[A/G]GTCACCACAGGAAGA | 4666 |
rs776709775 | snp | A/C | 3.84084e-05 | 0.00438209 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716720 | AAGGAGAAGTCACAG[A/C]TGGTGGAATGAGGAG | 4666 |
rs776751518 | snp | C/G | 1.67164e-05 | 0.00289101 | intron-variant, missense | NACA | GRCh38.p7 | 12:56721159 | CCTTTCAGAGTTGGA[C/G]CTATCATGGGAGAGG | 4666 |
rs776757899 | snp | C/T | 1.8272e-05 | 0.00302253 | intron-variant | NACA | GRCh38.p7 | 12:56713206 | CTACAGGGTAGAAAA[C/T]ACAGATCCATGTGAG | 4666 |
rs776789795 | snp | A/G | | | upstream-variant-2KB | NACA | GRCh38.p7 | 12:56727768 | GTGGAGTCATTAAAG[A/G]CAGACTCTGAAATAA | 4666 |
rs776875298 | snp | A/G | 1.75443e-05 | 0.00296173 | intron-variant, missense | NACA | GRCh38.p7 | 12:56719371 | ACTAAGGTAGCCAGA[A/G]GAGCACAGGTATTCT | 4666 |
rs777020356 | snp | C/T | | | intron-variant | NACA | GRCh38.p7 | 12:56722505 | CCGACCTGACCAACA[C/T]GGTGAAACCCCGTCT | 4666 |
rs777132140 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime | NACA | GRCh38.p7 | 12:56725391 | GGGTCAAGAGCTGCC[A/G]GCAGCCACTTCCTTT | 4666 |
rs777134528 | snp | C/T | 0.000108988 | 0.00738121 | missense | NACA | GRCh38.p7 | 12:56724512 | CGGTTTCTGTGGCTT[C/T]GCCGGGCATTTCTGA | 4666 |
rs777160812 | snp | A/C | 1.9714e-05 | 0.00313952 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56718287 | AGTCGCAGCTGGGGG[A/C]GTGGGGGCCCCCTTG | 4666 |
rs777165665 | snp | A/C/T | 6.3952e-05 | 0.00565443 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717383 | AGGGAGGAGTCATAG[A/C/T]GGGACCTCCTTTGTG | 4666 |
rs777232991 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime | NACA | GRCh38.p7 | 12:56725294 | AACCAAGATGGCGGC[A/G]GAAAGACCGAGCGAG | 4666 |
rs777322987 | snp | C/T | 1.64732e-05 | 0.0028699 | missense | NACA | GRCh38.p7 | 12:56712893 | TGTCCTTAACTTCTA[C/T]ACCTGTTTCATCGAC | 4666 |
rs777345549 | snp | C/T | 0.000198291 | 0.0099552 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717563 | GTGGGGTACCTGGGC[C/T]TCCTTTTGGGGAGGG | 4666 |
rs777443409 | snp | C/T | 3.30338e-05 | 0.00406397 | intron-variant | NACA | GRCh38.p7 | 12:56714461 | AGATAAAACAGCTAT[C/T]AGTTAACCAGAATCT | 4666 |
rs777444159 | snp | C/G | 1.95735e-05 | 0.00312832 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717985 | GCTAGACCTCCTTTT[C/G]GGGAAGGAGGAGTTG | 4666 |
rs777453491 | snp | A/C | 1.6985e-05 | 0.00291414 | intron-variant, missense | NACA | GRCh38.p7 | 12:56719432 | AAGCTGTAGGAACCA[A/C]GGGTAAAGTAGTAAG | 4666 |
rs777531581 | snp | G/T | 1.64779e-05 | 0.00287031 | missense | NACA | GRCh38.p7 | 12:56714672 | GATTCATCACTGTCA[G/T]ATTCTGTTCCAGACC | 4666 |
rs777543467 | snp | C/G | 1.77584e-05 | 0.00297974 | intron-variant, missense | NACA | GRCh38.p7 | 12:56719332 | GAGGGTGAGGGCACA[C/G]ACTTTGGGATTTCAG | 4666 |
rs777548762 | snp | C/T | 3.36632e-05 | 0.0041025 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720502 | GCCCCTGTGGAAGAA[C/T]GATCTACAGAAATGG | 4666 |
rs777554553 | snp | A/G | 1.80817e-05 | 0.00300675 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718732 | CCTTTGGGGGATGGG[A/G]AAGCTGGGATTCCTT | 4666 |
rs777572906 | in-del | -/AAAG | 2.51601e-05 | 0.00354675 | intron-variant | NACA | GRCh38.p7 | 12:56721482 | AAGGCAAAAGGAGAT[-/AAAG]AAAGGGGGAGGGGGA | 4666 |
rs777634557 | snp | A/G | 3.19402e-05 | 0.00399613 | intron-variant | NACA | GRCh38.p7 | 12:56724437 | ATTAATGGCAAGGAG[A/G]GTAGGGAAACCTACC | 4666 |
rs777704916 | snp | A/G | | | intron-variant, missense | NACA | GRCh38.p7 | 12:56719485 | TTTTTAGGAGCTAAA[A/G]AGACAGTTCCTTCTA | 4666 |
rs777728884 | snp | A/G | 1.96961e-05 | 0.0031381 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56718083 | TGCAGCTGGGGTTGT[A/G]GGGGCCCCTTTTGGG | 4666 |
rs777801740 | snp | A/C/G | 3.57144e-05 | 0.00422566 | intron-variant | NACA | GRCh38.p7 | 12:56713197 | ATCTTCGATCTACAG[A/C/G]GTAGAAAATACAGAT | 4666 |
rs777813289 | snp | C/T | 5.76884e-05 | 0.00537037 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717145 | AGGGTGGGATCCCCT[C/T]TGGAGGATGGGGTAG | 4666 |
rs777852632 | snp | G/T | 1.96057e-05 | 0.00313089 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718526 | CTTTGGGGGATGGAG[G/T]AGCTGGACCTCCTTT | 4666 |
rs777911115 | snp | C/G | 3.81534e-05 | 0.00436752 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717229 | GTCACTGCTGGGGGA[C/G]TGAGATCTCCTTTGG | 4666 |
rs777928058 | snp | A/C | 1.6643e-05 | 0.00288465 | intron-variant, missense | NACA | GRCh38.p7 | 12:56719739 | ACCTATAGGGAGAGG[A/C]TCCCCAAGGCTTTTC | 4666 |
rs777931483 | snp | C/G | 1.66391e-05 | 0.00288431 | intron-variant, missense | NACA | GRCh38.p7 | 12:56719879 | CTTTCTTGGTGGTGA[C/G]TCCTGCTTGGGCTGG | 4666 |
rs777942658 | snp | A/G | 3.93957e-05 | 0.00443805 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718621 | CCTTTTGGGGAGGGA[A/G]GAGTTGCAGCTGGGG | 4666 |
rs778066811 | in-del | -/G | 1.72259e-05 | 0.00293474 | intron-variant, frameshift-variant | NACA | GRCh38.p7 | 12:56716599 | TCTTTGAGGGAGGAA[-/G]GAGTCACAGGTGGGG | 4666 |
rs778085879 | snp | C/T | 1.67066e-05 | 0.00289016 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56716232 | GGTGGACGCCTTAGA[C/T]TCAGGAGGAGCCAAG | 4666 |
rs778087725 | snp | A/C | 1.66749e-05 | 0.00288741 | intron-variant | NACA | GRCh38.p7 | 12:56713512 | AACCCTGGTCTGGAA[A/C]AATGCCCAAGAAAAG | 4666 |
rs778097307 | snp | A/G | 1.95528e-05 | 0.00312666 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56716889 | AGCTGGGGGAATGAG[A/G]GCCTCTTTGGGGGCT | 4666 |
rs778106392 | snp | C/G | 1.66272e-05 | 0.00288328 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720856 | AGGGAGGCCACTCCA[C/G]ATTGAATAGAGGCCA | 4666 |
rs778116945 | snp | A/G | 4.16043e-05 | 0.00456075 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717787 | CCTTTTGGGGAGGGA[A/G]GAGTTGCAGCTGGGG | 4666 |
rs778137678 | snp | G/T | 1.72397e-05 | 0.00293591 | intron-variant, missense | NACA | GRCh38.p7 | 12:56719060 | AAACAGGGGATGAGA[G/T]ATTTCCAATAGGAGT | 4666 |
rs778185050 | snp | G/T | 1.83451e-05 | 0.00302857 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56715905 | AGGTTGCTTGGCAGA[G/T]GGGGTTGGGACAGGG | 4666 |
rs778198426 | snp | C/T | 3.32585e-05 | 0.00407776 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56720747 | CAGGCTGAGGCTTCC[C/T]GGGTTTTGTGGAGAA | 4666 |
rs778207988 | snp | A/G | 1.97638e-05 | 0.00314349 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56716820 | GGATGGGGTAGCTGG[A/G]GCTTCTTTGGGGGTT | 4666 |
rs778209666 | snp | A/G | 3.94228e-05 | 0.00443958 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718276 | GGGGAGGGAGGAGTC[A/G]CAGCTGGGGGAGTGG | 4666 |
rs778296181 | snp | A/C | 7.38225e-05 | 0.00607502 | intron-variant | NACA | GRCh38.p7 | 12:56715834 | GAGGGGTGTGGACGA[A/C]AGACACACCATGCAC | 4666 |
rs778320884 | in-del | -/GACAGAGGAGTCACAGCTGAGGGAGTAGGGGCCCCTTTGGGG | 3.60305e-05 | 0.00424429 | intron-variant, cds-indel | NACA | GRCh38.p7 | 12:56718909 | GTTACTCCTTTGGGA[lengthTooLong]GATGGAGGAGTGGGA | 4666 |
rs778387182 | snp | A/G | | | intron-variant | NACA | GRCh38.p7 | 12:56723657 | AATTGCCCTTAAATA[A/G]CAAATGAAATTTAAA | 4666 |
rs778408573 | snp | A/G | 1.71067e-05 | 0.00292456 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56721320 | CGAGGCAATAGTAGA[A/G]GGGGAAGGGAATGGG | 4666 |
rs778479437 | snp | C/T | 0.000178326 | 0.00944092 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56717558 | GGGGGGTGGGGTACC[C/T]GGGCTTCCTTTTGGG | 4666 |
rs778500309 | snp | C/G | 5.87446e-05 | 0.0054193 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718331 | CTGGACCTCCTTTTG[C/G]GGAGGGAAGAGTTGC | 4666 |
rs778589210 | snp | C/G | 6.6517e-05 | 0.00576663 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716395 | CATATAGGAGGTGAA[C/G]TAGCAGAACTCTTTT | 4666 |
rs778590276 | snp | A/G | 0.000138571 | 0.00832265 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717490 | GTAGCTGGGAGAGTA[A/G]GGGTCCCTTTAGGGG | 4666 |
rs778591830 | snp | A/G | 3.54283e-05 | 0.00420867 | intron-variant, missense | NACA | GRCh38.p7 | 12:56719350 | TTTGGGATTTCAGGG[A/G]CCAGCACTAAGGTAG | 4666 |
rs778643746 | snp | G/T | 1.65323e-05 | 0.00287505 | intron-variant, utr-variant-3-prime | NACA | GRCh38.p7 | 12:56712579 | AAAAGATAATTAGCG[G/T]TTCTTATAGGCAAAT | 4666 |
rs778658412 | in-del | -/TTGCAGCTGGGGGCA | 1.98466e-05 | 0.00315006 | intron-variant, cds-indel | NACA | GRCh38.p7 | 12:56718205 | TTGGGGAGGGAGGAG[-/TTGCAGCTGGGGGCA]TGGGGGCCCCTTTGG | 4666 |
rs778679071 | snp | A/C | 1.66607e-05 | 0.00288619 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716492 | GTACTTCTTTCAGAG[A/C]TGTGGGGCCTTTCTT | 4666 |
rs778679237 | snp | C/T | 3.34119e-05 | 0.00408715 | intron-variant | NACA | GRCh38.p7 | 12:56713732 | CTCTTTAGAAGCAGC[C/T]TAAAGAAGCAAGGAA | 4666 |
rs778696789 | snp | C/G | 3.3475e-05 | 0.00409101 | intron-variant, missense | NACA | GRCh38.p7 | 12:56719465 | TACCTTCCTTAACTG[C/G]GTGGTTTTTAGGAGC | 4666 |
rs778783563 | snp | A/C | 3.05516e-05 | 0.00390831 | intron-variant | NACA | GRCh38.p7 | 12:56724573 | ATTGGGATACATTCA[A/C]TTGCCCAACCCGGAG | 4666 |
rs778787645 | snp | A/C | 1.6784e-05 | 0.00289685 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720519 | ATCTACAGAAATGGT[A/C]TTCACTGTAGGGTCT | 4666 |
rs778877531 | snp | A/T | 2.92744e-05 | 0.00382575 | intron-variant | NACA | GRCh38.p7 | 12:56724444 | GCAAGGAGGGTAGGG[A/T]AACCTACCTGTCTCA | 4666 |
rs778957583 | snp | C/T | 1.70069e-05 | 0.00291602 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716066 | ATTCCAACACCAGCC[C/T]AGGAGAGGACGGCAG | 4666 |
rs778962832 | snp | A/G | 0.000274779 | 0.0117181 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56717879 | AGCTGGGGTTGTGGG[A/G]GCCCCTTTGGGGGAT | 4666 |
rs778966243 | snp | C/T | 1.93688e-05 | 0.00311191 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717032 | GAGTGGGGGCCCCCA[C/T]GGGGGCTGGAGTTGC | 4666 |
rs779008192 | in-del | -/GGA | 1.97478e-05 | 0.00314222 | intron-variant, cds-indel | NACA | GRCh38.p7 | 12:56717592 | GGAGGAGTTGCAGCT[-/GGA]GGAGTGGGGGCCCCT | 4666 |
rs779035786 | snp | C/T | 1.68354e-05 | 0.00290128 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720434 | CAGTAGCAGGAACTA[C/T]CTCATTTCTGGAAGG | 4666 |
rs779037283 | snp | A/G | | | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56719196 | GGAAGATGCAGTAGC[A/G]GAAGCACCAGAGTCC | 4666 |
rs779052728 | snp | C/G | 1.95658e-05 | 0.0031277 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717965 | CCCCTTTGGGGGATG[C/G]GGTAGCTAGACCTCC | 4666 |
rs779063871 | snp | C/T | 1.66338e-05 | 0.00288386 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720962 | CCTCAGAGGGAACTT[C/T]ATTAAGATTAGTCTT | 4666 |
rs779150027 | snp | A/C/G | 3.29686e-05 | 0.00405998 | intron-variant | NACA | GRCh38.p7 | 12:56712948 | GTAAATTAAAGGCAA[A/C/G]AACAATTTCAGCAGT | 4666 |
rs779158501 | snp | A/G | 1.96682e-05 | 0.00313588 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718600 | GGGGATGGAGTAGCT[A/G]GACCTCCTTTTGGGG | 4666 |
rs779239441 | snp | A/T | 1.68136e-05 | 0.0028994 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716135 | GAGCAAGAGGCAGAG[A/T]GACTGGTGGGGAGGG | 4666 |
rs779248908 | snp | C/G | 6.65458e-05 | 0.00576788 | intron-variant, missense | NACA | GRCh38.p7 | 12:56719896 | CCTGCTTGGGCTGGA[C/G]AGAAAGGGGCTCCTT | 4666 |
rs779255274 | snp | C/T | | | intron-variant | NACA | GRCh38.p7 | 12:56724803 | AGACGCTACTGTGAA[C/T]CCCCTCCACTCCTAA | 4666 |
rs779259890 | snp | C/G | 1.95605e-05 | 0.00312728 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718496 | GAGGAGTCACAGCTG[C/G]GGGTGTGGGGGCCCC | 4666 |
rs779325302 | snp | A/G | 1.64787e-05 | 0.00287038 | missense | NACA | GRCh38.p7 | 12:56713096 | TCTTGTACAGTTGGA[A/G]TCTGTGTGTTTTCTT | 4666 |
rs779345811 | snp | A/C | 8.31414e-05 | 0.006447 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720881 | AGGCCATGGGAGTCA[A/C]ACAGTGGTAAGGAAC | 4666 |
rs779349479 | snp | A/G | 1.9598e-05 | 0.00313028 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56717642 | TGGGCCTCCTTTTGG[A/G]GAGGGAGGAGTTACA | 4666 |
rs779358866 | snp | C/T | 3.45e-05 | 0.00415317 | intron-variant, missense | NACA | GRCh38.p7 | 12:56719069 | ATGAGAGATTTCCAA[C/T]AGGAGTATCAGGGCC | 4666 |
rs779447473 | snp | A/G | 4.98848e-05 | 0.00499399 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720244 | GAAACGGGCATTTGG[A/G]CCACTAAAGGATAAT | 4666 |
rs779454952 | snp | C/G | 1.7309e-05 | 0.0029418 | intron-variant, missense | NACA | GRCh38.p7 | 12:56719146 | CTAACCCCTAAAGGA[C/G]ATGGGGAATCAGCTA | 4666 |
rs779462506 | snp | A/G | | | intron-variant, utr-variant-3-prime | NACA | GRCh38.p7 | 12:56712723 | TATTTAGCAAGACAA[A/G]ATAAAGTCACTCATA | 4666 |
rs779484536 | in-del | -/TTT | | | upstream-variant-2KB | NACA | GRCh38.p7 | 12:56726286 | TGGGCACTTCTTGGA[-/TTT]TTTTTTTTTTTTTTT | 4666 |
rs779588777 | snp | C/T | | | intron-variant | NACA | GRCh38.p7 | 12:56722211 | AAACAAGAAAACCAA[C/T]CACAAAAGGACTGTA | 4666 |
rs779609773 | snp | A/G | 1.96763e-05 | 0.00313652 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56716784 | AGGAGTCACTGCTGG[A/G]GGACTGGAGGCCTCT | 4666 |
rs779648535 | snp | C/T | 3.94042e-05 | 0.00443853 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718247 | TGGGGGATGGGGTAG[C/T]TGGGCCTCCTTTTGG | 4666 |
rs779655054 | snp | G/T | | | intron-variant, missense | NACA | GRCh38.p7 | 12:56715882 | ATACCCTTGTTGTTC[G/T]TCGTAACAGGTTGCT | 4666 |
rs779684137 | in-del | -/GCT | 1.94846e-05 | 0.00312121 | intron-variant, cds-indel | NACA | GRCh38.p7 | 12:56718384 | TTGGGGAGTGGGGTA[-/GCT]GCTGGACTTCCTTTG | 4666 |
rs779705695 | snp | G/T | | | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56718401 | TGCTGGACTTCCTTT[G/T]GGGGAGGGAGGAGTT | 4666 |
rs779738762 | snp | A/G | 2.05109e-05 | 0.00320235 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717344 | CCCCTTTGGGAGATG[A/G]GATAGCTGGTCCTCT | 4666 |
rs779798540 | snp | A/G | 1.83677e-05 | 0.00303043 | intron-variant, missense | NACA | GRCh38.p7 | 12:56715888 | TTGTTGTTCTTCGTA[A/G]CAGGTTGCTTGGCAG | 4666 |
rs779803510 | snp | C/T | 1.6577e-05 | 0.00287893 | intron-variant | NACA | GRCh38.p7 | 12:56713530 | TGCCCAAGAAAAGTT[C/T]ACTCACCTTGGCTTC | 4666 |
rs779827711 | snp | A/C | | | upstream-variant-2KB | NACA | GRCh38.p7 | 12:56727937 | TATATATACACACAC[A/C]CACTCACACTCTAAT | 4666 |
rs779904430 | snp | C/T | 1.67321e-05 | 0.00289236 | intron-variant, missense | NACA | GRCh38.p7 | 12:56721249 | GCTTCAGGGGCAGTT[C/T]CCAAAGGTAGGGCTG | 4666 |
rs779936716 | snp | C/G | 1.66582e-05 | 0.00288597 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720710 | AAAGAGATAAGGCAG[C/G]AGGTGGACTAACAGG | 4666 |
rs779989127 | snp | C/T | 3.32613e-05 | 0.00407793 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716382 | TGAGGGATCTGGGCA[C/T]ATAGGAGGTGAAGTA | 4666 |
rs780002147 | snp | A/G | | | intron-variant | NACA | GRCh38.p7 | 12:56723413 | AATCTCTAAAATCTC[A/G]TTTTGTACTGAAATT | 4666 |
rs780007994 | snp | A/G | 1.9645e-05 | 0.00313403 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717853 | CCTCCTTTTGGGGAG[A/G]GAGGAGTTGCAGCTG | 4666 |
rs780028625 | snp | A/G | 1.66874e-05 | 0.0028885 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56720648 | TGGGGGGGTGTTGGG[A/G]CCCGCAGTCTTTTGA | 4666 |
rs780094833 | snp | C/T | 5.81018e-05 | 0.00538958 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717029 | GCAGAGTGGGGGCCC[C/T]CATGGGGGCTGGAGT | 4666 |
rs780097804 | snp | C/T | 1.8331e-05 | 0.0030274 | intron-variant, missense | NACA | GRCh38.p7 | 12:56715952 | GGGTGGGCATGTTGA[C/T]GAGGACCGACTGGAA | 4666 |
rs780117383 | snp | A/G | 7.20734e-05 | 0.00600262 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718870 | TTCACCACTGAAGGA[A/G]TGGGGGTCTCTTTGG | 4666 |
rs780134858 | snp | A/C | | | intron-variant | NACA | GRCh38.p7 | 12:56724592 | CCCAACCCGGAGATA[A/C]GTATTCTTAAAAACT | 4666 |
rs780210038 | snp | C/G | 1.66294e-05 | 0.00288347 | intron-variant, missense | NACA | GRCh38.p7 | 12:56719997 | TTTGAGGTCTTCAGG[C/G]TCTGGCAGAGGAGGA | 4666 |
rs780214649 | snp | C/T | 3.48426e-05 | 0.00417374 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56718953 | GGCCCCTTTGGGGGA[C/T]GGAGGAGTGGGAGAA | 4666 |
rs780303021 | snp | G/T | 3.63227e-05 | 0.00426146 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56715986 | CACTCCCCCAGAGAT[G/T]GGTTCCGGGGGAATC | 4666 |
rs780388132 | in-del | -/TA | 1.97986e-05 | 0.00314626 | intron-variant, frameshift-variant | NACA | GRCh38.p7 | 12:56718106 | CTTTTGGGGGTGGGG[-/TA]GCTAGACCTCCTTTT | 4666 |
rs780390297 | snp | C/T | 1.95597e-05 | 0.00312721 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56718488 | GGGGGAGGGAGGAGT[C/T]ACAGCTGGGGGTGTG | 4666 |
rs780390926 | snp | C/T | 1.64768e-05 | 0.00287021 | intron-variant, utr-variant-3-prime | NACA | GRCh38.p7 | 12:56712735 | CAAAATAAAGTCACT[C/T]ATAATTGGTCAGGGC | 4666 |
rs780413501 | snp | G/T | 3.34185e-05 | 0.00408756 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56721092 | AGAACTCTTCTGAAC[G/T]GAGTGGGGAGCCAGG | 4666 |
rs780484803 | snp | C/T | 1.94445e-05 | 0.00311799 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56718416 | GGGGGAGGGAGGAGT[C/T]GCAGCTGGGGGTGTG | 4666 |
rs780514499 | snp | A/G | | | utr-variant-3-prime | NACA | GRCh38.p7 | 12:56712489 | TACAAATTTCAAACC[A/G]AGCTGCAGTTACTCC | 4666 |
rs780574561 | snp | C/T | 3.32701e-05 | 0.00407847 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56720975 | TTTATTAAGATTAGT[C/T]TTTGGTTCTGAGGGA | 4666 |
rs780625518 | in-del | -/G | 1.95708e-05 | 0.0031281 | intron-variant, frameshift-variant | NACA | GRCh38.p7 | 12:56717681 | ATTGGGGGCCCCTTT[-/G]TGGGGTGGGGTAGCT | 4666 |
rs780724028 | in-del | -/G | 1.70845e-05 | 0.00292267 | intron-variant, frameshift-variant | NACA | GRCh38.p7 | 12:56721318 | GTCGAGGCAATAGTA[-/G]AGGGGGAAGGGAATG | 4666 |
rs780731464 | in-del | -/CTT | | | upstream-variant-2KB | NACA | GRCh38.p7 | 12:56727456 | TCTCCTGCCACAAAA[-/CTT]CTCCTGTTTCACCGT | 4666 |
rs780745503 | snp | C/G | 1.84636e-05 | 0.00303833 | intron-variant | NACA | GRCh38.p7 | 12:56715821 | GGGTAGCGCCCAAGA[C/G]GGGTGTGGACGACAG | 4666 |
rs780761309 | snp | A/T | 3.9268e-05 | 0.00443086 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717623 | CTTTGGGGGGTGAGG[A/T]AGCTGGGCCTCCTTT | 4666 |
rs780763493 | snp | A/T | 1.68111e-05 | 0.00289918 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716548 | GGAACAGTGGCCCCC[A/T]TTTTACATGTGACAG | 4666 |
rs780781848 | snp | A/C | 1.78086e-05 | 0.00298396 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56719328 | AAGAGAGGGTGAGGG[A/C]ACAGACTTTGGGATT | 4666 |
rs780846428 | snp | C/T | 1.6483e-05 | 0.00287076 | missense | NACA | GRCh38.p7 | 12:56714682 | TGTCAGATTCTGTTC[C/T]AGACCCTAAGATGAG | 4666 |
rs780853391 | snp | C/T | 9.2182e-05 | 0.00678841 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716657 | TTGCTGGGCCCTTTT[C/T]GGGGGATGGAGGAGT | 4666 |
rs780857941 | snp | G/T | 3.55619e-05 | 0.0042166 | intron-variant, stop-gained | NACA | GRCh38.p7 | 12:56721362 | AGCAGCTGAGAGAGG[G/T]CACTGTTGTGGGGCA | 4666 |
rs780860127 | snp | A/G | 0.000115002 | 0.00758207 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717247 | AGATCTCCTTTGGAT[A/G]GGGTGGCTGCGCCTT | 4666 |
rs780869837 | snp | A/T | 5.06291e-05 | 0.0050311 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720485 | TCTGAGAAGGATAAG[A/T]GGCCCCTGTGGAAGA | 4666 |
rs780871894 | snp | C/T | 3.49266e-05 | 0.00417876 | intron-variant, missense | NACA | GRCh38.p7 | 12:56719176 | AGGTAAGTCAGAGTT[C/T]CTTTGGAAGATGCAG | 4666 |
rs780883822 | snp | A/G | 0.000197025 | 0.00992339 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718087 | GCTGGGGTTGTGGGG[A/G]CCCCTTTTGGGGGTG | 4666 |
rs780950107 | snp | C/T | 1.67854e-05 | 0.00289697 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56716166 | TGCTGCAGAGACAGA[C/T]GCTGATTCAGGTTTA | 4666 |
rs780958638 | snp | C/G | 1.965e-05 | 0.00313443 | intron-variant, stop-gained | NACA | GRCh38.p7 | 12:56721441 | GTGACACTCAAGGCT[C/G]AAGACATAGGTAGCA | 4666 |
rs780970306 | snp | C/G | 1.66463e-05 | 0.00288494 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56719694 | CGAGGAGTTAACACC[C/G]AGAGGGGAGGTCATA | 4666 |
rs780975438 | snp | C/T | 3.93879e-05 | 0.00443761 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56718239 | GGCCCCTTTGGGGGA[C/T]GGGGTAGCTGGGCCT | 4666 |
rs780993125 | snp | C/T | 4.98815e-05 | 0.00499382 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720854 | GAAGGGAGGCCACTC[C/T]AGATTGAATAGAGGC | 4666 |
rs781030172 | snp | C/G | | | intron-variant | NACA | GRCh38.p7 | 12:56722193 | TACTTACTCACAAAA[C/G]CCAAACAAGAAAACC | 4666 |
rs781056521 | snp | A/G | 1.66272e-05 | 0.00288328 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720829 | AGGGTAGTTGTGGGT[A/G]TTGTCTGAGGAAGGG | 4666 |
rs781061730 | in-del | -/TTGTAT | 1.66707e-05 | 0.00288705 | intron-variant, cds-indel | NACA | GRCh38.p7 | 12:56719519 | AAGGGCTGGCTGTAG[-/TTGTAT]AAGTTGAGGTACCTT | 4666 |
rs781081871 | snp | A/G | | | intron-variant | NACA | GRCh38.p7 | 12:56721997 | TGGGGAATCTGAACT[A/G]AATAAGAAAACACAG | 4666 |
rs781172702 | in-del | -/A | 1.67764e-05 | 0.00289619 | intron-variant, frameshift-variant | NACA | GRCh38.p7 | 12:56716537 | AGATGCTTGAGGAAC[-/A]AGTGGCCCCCATTTT | 4666 |
rs781237360 | snp | A/G | 1.66902e-05 | 0.00288874 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56716246 | ACTCAGGAGGAGCCA[A/G]GGGGCCCTTTGGGGA | 4666 |
rs781259933 | snp | A/G | 1.96973e-05 | 0.00313819 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718634 | GAGGAGTTGCAGCTG[A/G]GGGTGTGGGGGCCCA | 4666 |
rs781294084 | snp | A/G | | | intron-variant | NACA | GRCh38.p7 | 12:56714738 | GAAATTATAAGAGAA[A/G]GTACTTCACCACAGC | 4666 |
rs781344393 | snp | A/T | 1.66446e-05 | 0.00288479 | intron-variant, missense | NACA | GRCh38.p7 | 12:56720719 | AGGCAGCAGGTGGAC[A/T]AACAGGCCCCTTCAG | 4666 |
rs781355203 | snp | C/G | 2.0782e-05 | 0.00322344 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717797 | AGGGAGGAGTTGCAG[C/G]TGGGGTTGTGGGGGC | 4666 |
rs781443338 | snp | A/G | 5.85875e-05 | 0.00541205 | intron-variant, missense | NACA | GRCh38.p7 | 12:56716899 | ATGAGGGCCTCTTTG[A/G]GGGCTAGAGTTGCTG | 4666 |
rs781461023 | snp | A/G | 1.72074e-05 | 0.00293316 | intron-variant, missense | NACA | GRCh38.p7 | 12:56719038 | AGAAATGAAGCTTCA[A/G]CTGGAGAAACAGGGG | 4666 |
rs781505432 | snp | C/T | 1.65655e-05 | 0.00287793 | intron-variant | NACA | GRCh38.p7 | 12:56713699 | CTAAAGAAGAGAAAA[C/T]AGTATCAGGTTTTCA | 4666 |
rs781513748 | in-del | -/TG | 1.65712e-05 | 0.00287843 | intron-variant | NACA | GRCh38.p7 | 12:56714315 | TAAACAGTTCCACTC[-/TG]TATAAAGGTGCTTCA | 4666 |
rs781588996 | snp | A/G | 1.65477e-05 | 0.00287638 | intron-variant, utr-variant-3-prime | NACA | GRCh38.p7 | 12:56712592 | CGGTTCTTATAGGCA[A/G]ATCAGGAGAATTCAG | 4666 |
rs781611266 | snp | C/G | 1.98057e-05 | 0.00314682 | intron-variant, missense | NACA | GRCh38.p7 | 12:56717509 | TCCCTTTAGGGGAGG[C/G]AGGAGTTACAGCTGG | 4666 |
rs781626725 | snp | C/T | 3.64266e-05 | 0.00426755 | intron-variant, missense | NACA | GRCh38.p7 | 12:56715978 | TGGAAAGGCACTCCC[C/T]CAGAGATTGGTTCCG | 4666 |
rs781636807 | snp | G/T | 1.80876e-05 | 0.00300724 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718876 | ACTGAAGGAGTGGGG[G/T]TCTCTTTGGGGGGTA | 4666 |
rs781638982 | snp | A/G | 1.67016e-05 | 0.00288973 | intron-variant, missense | NACA | GRCh38.p7 | 12:56721204 | GCTGGGGAGATGGGA[A/G]GCCCTATTAGGTTTG | 4666 |
rs781640452 | snp | C/G | 1.66286e-05 | 0.0028834 | intron-variant, synonymous-codon | NACA | GRCh38.p7 | 12:56720015 | TGGCAGAGGAGGAGA[C/G]ACTGGTATCCTCAGA | 4666 |
rs781666185 | in-del | -/A | 1.98077e-05 | 0.00314697 | intron-variant, frameshift-variant | NACA | GRCh38.p7 | 12:56718111 | GGGGGTGGGGTAGCT[-/A]GACCTCCTTTTGGGG | 4666 |
rs781684998 | snp | A/T | | | intron-variant | NACA | GRCh38.p7 | 12:56715664 | ATACACAATGTACTA[A/T]GTATCTATCTGAAGT | 4666 |
rs781756506 | snp | G/T | 1.95628e-05 | 0.00312746 | intron-variant, missense | NACA | GRCh38.p7 | 12:56718340 | CTTTTGGGGAGGGAA[G/T]AGTTGCAGCTGGGGT | 4666 |
rs781766977 | in-del | -/GCA | | | intron-variant, cds-indel | NACA | GRCh38.p7 | 12:56718147 | GAGTTGCAGCTGGGG[-/GCA]TTGTGGGTGCCCCTT | 4666 |
rs796160399 | snp | C/T | | | upstream-variant-2KB | NACA | GRCh38.p7 | 12:56727061 | AATTAGCTAAACCAG[C/T]CAACATTTATTTATT | 4666 |
rs796334630 | snp | C/T | | | intron-variant | NACA | GRCh38.p7 | 12:56714163 | TTCTGTTACTTTCAA[C/T]GGGATTCTACCACTA | 4666 |
rs796394751 | snp | C/G | | | upstream-variant-2KB | NACA | GRCh38.p7 | 12:56726655 | CTCGGCTCACTGCAA[C/G]CTCCCCTTCCCGGGT | 4666 |
rs796411807 | multinucleotide-polymorphism | AC/CT | | | downstream-variant-500B | NACA | GRCh38.p7 | 12:56712154 | GAGACGGGGTTTCAA[AC/CT]TGTTAGCCAGGATGG | 4666 |