SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs835647 | snp | A/G | 0.41507 | 0.187755 | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136950237 | TAAGGAAGACTGGGG[A/G]AAAACCCAGAAACAT | 4690 |
rs856662 | snp | C/T | 0.415399 | 0.187465 | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136949783 | CTTTGCTGTTATAAA[C/T]AGATATCTAATACGC | 4690 |
rs938525 | snp | A/G | 0.417521 | 0.185571 | intron-variant, upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136863111 | TCAGTTTGACACCGA[A/G]AGCGTTCCTACGGTT | 4690 |
rs1048145 | snp | C/T | 0.128288 | 0.218372 | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136948563 | TGTTGTTTCTAAATC[C/T]ATATGAGAATTGACA | 4690 |
rs1298139 | snp | A/G | 0 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136897157 | aggttgcagtgagct[A/G]agatcacaccactgc | 4690 |
rs1299289 | snp | A/G | 0 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136888837 | ttgaactaagtgaaa[A/G]aaagcggttacaaag | 4690 |
rs1344790 | snp | A/C | 0.425586 | 0.17796 | intron-variant | NCK1 | GRCh38.p7 | 3:136933122 | TTACATGAGTAAAAA[A/C]CTTAGTAAGAGCTGC | 4690 |
rs1347209 | snp | G/T | 0.436834 | 0.166111 | intron-variant | NCK1 | GRCh38.p7 | 3:136907855 | TACCTATTGTCCTCA[G/T]TGCTACAGGTATTAT | 4690 |
rs1385305 | snp | C/T | 0.0150606 | 0.0854603 | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136948826 | CACCCTGTTCTGTTA[C/T]GGTTTTTCATTATAT | 4690 |
rs1400265 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136922808 | aatcatagaagaatg[C/T]tgagttacagctaaa | 4690 |
rs1433318 | snp | C/T | 0.416871 | 0.186156 | intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136947612 | ACCAACATTGAGACC[C/T]GGTTCCTGCAAGGCA | 4690 |
rs1433319 | snp | A/G | 0.415235 | 0.18761 | intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136947757 | GGCATTTGAGTTTGT[A/G]GCCTCTCCTTAAAGT | 4690 |
rs1609391 | snp | A/G | 0.486332 | 0.08153 | intron-variant | NCK1 | GRCh38.p7 | 3:136896426 | atttcacttaacata[A/G]tgacctccaggtcca | 4690 |
rs1819095 | snp | C/T | 0.437683 | 0.165152 | intron-variant | NCK1 | GRCh38.p7 | 3:136905202 | tttttttgtattctt[C/T]gcagagacagggttt | 4690 |
rs1865149 | snp | C/T | 0.414905 | 0.187899 | intron-variant | NCK1 | GRCh38.p7 | 3:136876768 | ATTCGTAAATTCTCA[C/T]TGTAGCCTTACAGCT | 4690 |
rs1965106 | snp | C/T | 0.415563 | 0.18732 | upstream-variant-2KB, intron-variant | NCK1 | GRCh38.p7 | 3:136929765 | TGGGATTAGAGTGAA[C/T]GTGACAGTAATTAAC | 4690 |
rs1965107 | snp | A/T | 0.340333 | 0.233109 | upstream-variant-2KB, intron-variant | NCK1 | GRCh38.p7 | 3:136929801 | ATAGTGAAAAAACTA[A/T]TATCATAGAGCAAAG | 4690 |
rs1965108 | snp | A/G | 0.410737 | 0.191478 | upstream-variant-2KB, intron-variant | NCK1 | GRCh38.p7 | 3:136929851 | TAGGTATTACTGTAT[A/G]TAAATCTAAAATCCC | 4690 |
rs1965109 | snp | C/G | 0.416218 | 0.186739 | intron-variant | NCK1 | GRCh38.p7 | 3:136932675 | GTTCCTTGTAAAAGA[C/G]AGAGTTGGGCAAGAC | 4690 |
rs1971788 | snp | G/T | 0.410905 | 0.191336 | intron-variant | NCK1 | GRCh38.p7 | 3:136926967 | gccttaataatgttt[G/T]tatttatttatttat | 4690 |
rs2031029 | snp | A/T | 0.415891 | 0.18703 | intron-variant | NCK1 | GRCh38.p7 | 3:136880972 | TTCTGCGCtctaccc[A/T]acatttgttcattcc | 4690 |
rs2043365 | snp | C/T | 0.343701 | 0.231776 | intron-variant | NCK1 | GRCh38.p7 | 3:136932085 | gattgtgccactgca[C/T]gccagcctgggcaac | 4690 |
rs2117009 | snp | A/T | 0.437401 | 0.165472 | intron-variant | NCK1 | GRCh38.p7 | 3:136914729 | TTCCAGCCAGAAGAT[A/T]TTGGGACTTGAAATT | 4690 |
rs2117010 | snp | A/T | 0.414741 | 0.188044 | intron-variant | NCK1 | GRCh38.p7 | 3:136872741 | AGGGACTTGGTACCC[A/T]GCATTCCAGCTGCTC | 4690 |
rs2138540 | snp | C/T | 0.415399 | 0.187465 | intron-variant | NCK1 | GRCh38.p7 | 3:136902483 | tacaggcgcgagcta[C/T]cccacctggcctatt | 4690 |
rs2138541 | snp | A/T | 0.415399 | 0.187465 | intron-variant | NCK1 | GRCh38.p7 | 3:136902596 | gttttgtgtcctaac[A/T]tgatctatcctggag | 4690 |
rs2176270 | snp | C/T | 0.313082 | 0.241911 | intron-variant | NCK1 | GRCh38.p7 | 3:136902346 | gggactacaggtgca[C/T]gccaccatgcctggc | 4690 |
rs2196012 | snp | A/G | | | intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136947642 | aacaatcacagctga[A/G]aagtcaccacttgtt | 4690 |
rs2343661 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136910482 | ctctgaggtttattc[A/G]gtttgtaatttttta | 4690 |
rs2343662 | snp | A/T | 0.425432 | 0.178112 | intron-variant | NCK1 | GRCh38.p7 | 3:136882204 | ATAGCTACTATTTTT[A/T]AAAAAACATGCAGGA | 4690 |
rs2343663 | snp | C/T | 0.410905 | 0.191336 | intron-variant | NCK1 | GRCh38.p7 | 3:136882103 | agctgctatggaaaa[C/T]ggtatggtggttcct | 4690 |
rs2343664 | snp | A/C | 0 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136879541 | aagtactagggatta[A/C]gaattcaaaatatct | 4690 |
rs3076203 | in-del | -/AA | 0.415563 | 0.18732 | intron-variant, upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136863073 | CACCCCTGAACAAAA[-/AA]CCCAGCTTCCTGAGC | 4690 |
rs3076204 | in-del | -/A | | | intron-variant, upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136863020 | ATGTTAATACAGAAG[-/A]AAGGTTACAAAACCT | 4690 |
rs3223117 | microsatellite | (CA)20/21/22/23/24/26 | 0.711288 | 0.122643 | intron-variant | NCK1 | GRCh38.p7 | 3:136882550 | AAAGGTGCCCCTNAA[(CA)20/21/22/23/24/26]AGTGATGTGGGAAAG | 4690 |
rs3772386 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | NCK1 | GRCh38.p7 | 3:136928667 | AATGTACAGTAATGA[C/T]CCACAGTTCTCTTAT | 4690 |
rs3772387 | snp | C/T | 0.40853 | 0.193309 | upstream-variant-2KB, intron-variant | NCK1 | GRCh38.p7 | 3:136928639 | TATCAAATAGAAAAA[C/T]AAAATGGAGGGTTTT | 4690 |
rs3772388 | snp | C/T | 0.416055 | 0.186885 | intron-variant | NCK1 | GRCh38.p7 | 3:136928404 | TTTACAGAAACTGCA[C/T]GTTAACACTTATGAC | 4690 |
rs3845925 | snp | C/T | 0.415235 | 0.18761 | intron-variant | NCK1 | GRCh38.p7 | 3:136943220 | tgtccctgcaaaaag[C/T]aatgaatgcaattaa | 4690 |
rs3845926 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NCK1 | GRCh38.p7 | 3:136943298 | ATGTAGGGATTTCTC[C/T]GAAGgctatcattaa | 4690 |
rs3856623 | snp | C/T | 0.415235 | 0.18761 | upstream-variant-2KB, intron-variant | NCK1 | GRCh38.p7 | 3:136928965 | CAAACATGCTATTTG[C/T]GTAATTGTTCTTTGT | 4690 |
rs3915455 | snp | A/G | 0.415399 | 0.187465 | upstream-variant-2KB, intron-variant | NCK1 | GRCh38.p7 | 3:136929062 | AAGTAGTGAGTCAAC[A/G]GTATTTCATATTTGT | 4690 |
rs3963921 | snp | A/G | 0.415235 | 0.18761 | intron-variant | NCK1 | GRCh38.p7 | 3:136935842 | ggactgattgagagt[A/G]actatttttggggtg | 4690 |
rs4147503 | snp | A/G | 0.114387 | 0.210022 | intron-variant | NCK1 | GRCh38.p7 | 3:136908624 | AATCAGTCGCAGTTC[A/G]CCTCCTTTAACAGGT | 4690 |
rs4586757 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136943094 | ACTCTCTTTACCACA[A/G]AGCAGCAACTTCTTT | 4690 |
rs4594566 | snp | C/T | 0.415235 | 0.18761 | intron-variant | NCK1 | GRCh38.p7 | 3:136927226 | ATCCACCAGCCTCGG[C/T]CTCCCGAAGTGCTGG | 4690 |
rs4678272 | snp | G/T | 0.414905 | 0.187899 | intron-variant | NCK1 | GRCh38.p7 | 3:136891788 | tttggatttttctaa[G/T]ggatggtgatatgat | 4690 |
rs4678273 | snp | A/C | 0.414905 | 0.187899 | intron-variant | NCK1 | GRCh38.p7 | 3:136891791 | ggatttttctaaggg[A/C]tggtgatatgatcat | 4690 |
rs4678274 | snp | G/T | 0.418007 | 0.185132 | intron-variant | NCK1 | GRCh38.p7 | 3:136920395 | GCACAATTCATTCAC[G/T]TATTCACTCAACAAA | 4690 |
rs4678275 | snp | A/G | 0.340784 | 0.232934 | intron-variant | NCK1 | GRCh38.p7 | 3:136934841 | TAGAGAATTGGAGTC[A/G]GTTAAGCAATGGGTT | 4690 |
rs4678276 | snp | G/T | 0.415235 | 0.18761 | intron-variant | NCK1 | GRCh38.p7 | 3:136942088 | cgtgatccacccacc[G/T]ctgtctcccaaagtg | 4690 |
rs4678450 | snp | A/G | 0.415891 | 0.18703 | intron-variant | NCK1 | GRCh38.p7 | 3:136892103 | atgttgcccaagcag[A/G]tcttgaacttttagc | 4690 |
rs4678451 | snp | C/T | 0.415399 | 0.187465 | intron-variant | NCK1 | GRCh38.p7 | 3:136892154 | cagcctcccaaagtg[C/T]tgggattataggtgt | 4690 |
rs4678452 | snp | A/C | 0.415891 | 0.18703 | intron-variant | NCK1 | GRCh38.p7 | 3:136902875 | ttgcaggacaaaatc[A/C]acacacataaatcaa | 4690 |
rs5852852 | in-del | -/CTTT | 0.415727 | 0.187175 | intron-variant, upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136863017 | GATAGGTTTTGTAAC[-/CTTT]CTTCTGTATTAACAT | 4690 |
rs5852853 | in-del | -/T | 0.415563 | 0.18732 | intron-variant | NCK1 | GRCh38.p7 | 3:136931569 | TTTCAGATCTTTGCA[-/T]TTTTCATTTTTTGGG | 4690 |
rs5852856 | in-del | -/T | 0.415399 | 0.187465 | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136949841 | TGTGTAACTTGTGAA[-/T]TTTTTTTATCAATGT | 4690 |
rs6148085 | in-del | -/CCCGTGCGAGCCTGGGAGGTCG | | | intron-variant, upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136862647 | GAGCCCGGGCGGCCG[-/CCCGTGCGAGCCTGGGAGGTCG]AGTGTGCGGCGCGCT | 4690 |
rs6414337 | snp | A/G | 0.344147 | 0.231595 | intron-variant | NCK1 | GRCh38.p7 | 3:136913695 | tttttttgagacgga[A/G]tctcactctttcgcc | 4690 |
rs6439672 | snp | A/C | 0.417845 | 0.185278 | upstream-variant-2KB, intron-variant | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136860357 | ATAGAGTAGCTGTTG[A/C]CCAGTTTCATGGTCT | 4690 |
rs6439673 | snp | A/G | 0.414905 | 0.187899 | intron-variant | NCK1 | GRCh38.p7 | 3:136874114 | aaaattggacatttg[A/G]ttttcagttttttgg | 4690 |
rs6439674 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136878243 | gtgaaaccccatctc[A/G]actataaacacacaa | 4690 |
rs6439675 | snp | A/G | 0.438666 | 0.164028 | intron-variant | NCK1 | GRCh38.p7 | 3:136906594 | ttgggtaccaggagt[A/G]gcacaggtgagccag | 4690 |
rs6439676 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NCK1 | GRCh38.p7 | 3:136938521 | tgcagtctatttagt[A/G]ccacattttttgcat | 4690 |
rs6761993 | snp | C/T | 0.436834 | 0.166111 | intron-variant | NCK1 | GRCh38.p7 | 3:136907060 | ctgtggccttgttac[C/T]gggaagggtggggtt | 4690 |
rs6768002 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136905024 | ttttttttttttttt[C/T]ctttttgagatggag | 4690 |
rs6771717 | snp | C/T | 0.417359 | 0.185718 | intron-variant | NCK1 | GRCh38.p7 | 3:136936471 | attcatgtacagtta[C/T]tgtttgaatatctat | 4690 |
rs6775389 | snp | C/T | 0.415235 | 0.18761 | intron-variant | NCK1 | GRCh38.p7 | 3:136940882 | gccaccccactctct[C/T]agttatcctttacat | 4690 |
rs6777816 | snp | C/T | 0.415235 | 0.18761 | intron-variant | NCK1 | GRCh38.p7 | 3:136864144 | TTTCTAGGCATTATC[C/T]TTTGTCCAGGTTTCT | 4690 |
rs6777873 | snp | A/G | 0.417521 | 0.185571 | intron-variant, upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136864030 | ggcgtgaacccggga[A/G]gcggagcttgcagtg | 4690 |
rs6782716 | snp | A/G | 0.415235 | 0.18761 | intron-variant | NCK1 | GRCh38.p7 | 3:136936110 | cagtgacgtgatctc[A/G]gctcactgcaacctc | 4690 |
rs6783508 | snp | A/G | 0.415235 | 0.18761 | intron-variant | NCK1 | GRCh38.p7 | 3:136900724 | tttttaacactccct[A/G]cttcacagatggatg | 4690 |
rs6783999 | snp | C/T | 0.415235 | 0.18761 | intron-variant | NCK1 | GRCh38.p7 | 3:136923981 | AATAAGCAAAATTTT[C/T]CTTTGAGAATAATCA | 4690 |
rs6784005 | snp | C/G | 0.415399 | 0.187465 | intron-variant | NCK1 | GRCh38.p7 | 3:136893919 | TGGTTTAAGTTGCTT[C/G]TGTCCTTTCGGCTTT | 4690 |
rs6784074 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136893928 | TTGCTTCTGTCCTTT[A/C]GGCTTTCATCCTTGT | 4690 |
rs6786302 | snp | A/G | 0.415235 | 0.18761 | intron-variant | NCK1 | GRCh38.p7 | 3:136937187 | tgtttatagatatcc[A/G]tttgttccagtaccc | 4690 |
rs6786648 | snp | C/T | 0.40853 | 0.193309 | intron-variant | NCK1 | GRCh38.p7 | 3:136871628 | ctctatcgccataaa[C/T]tatttttgcctgttt | 4690 |
rs6796458 | snp | A/T | 0 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136939863 | ttttttttttttttt[A/T]aaatagagacagggt | 4690 |
rs6797509 | snp | C/T | 0.40853 | 0.193309 | intron-variant | NCK1 | GRCh38.p7 | 3:136865930 | TTTTATCTCTATGCG[C/T]GTAACAATATTGGCT | 4690 |
rs6800032 | snp | C/T | 0.4087 | 0.193169 | intron-variant | NCK1 | GRCh38.p7 | 3:136903718 | gtgagagccacaccg[C/T]gcctggccAAATTag | 4690 |
rs6800690 | snp | A/G | 0.437259 | 0.165632 | intron-variant | NCK1 | GRCh38.p7 | 3:136904184 | tttttagacagtctc[A/G]ctctgccacctaggc | 4690 |
rs6801341 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136919982 | GAAGTTTGGTTGGGG[G/T]ACAGATCTCACAGTA | 4690 |
rs6803618 | snp | C/T | 0.436834 | 0.166111 | intron-variant | NCK1 | GRCh38.p7 | 3:136904949 | gttgacactttccaa[C/T]gtagtttgtatttca | 4690 |
rs6807626 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136878179 | tttgggaggccaaga[C/T]gggcagatcacttga | 4690 |
rs6809885 | snp | A/T | 0.0271762 | 0.113356 | intron-variant | NCK1 | GRCh38.p7 | 3:136903400 | gctttaaAAAcattt[A/T]aaaaaatctattcaa | 4690 |
rs6810086 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136903545 | ttctcctgcctcagc[C/T]tcctgagtagctggg | 4690 |
rs7427391 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136904991 | cttcagttctggaat[C/T]cctgtttggtttttc | 4690 |
rs7429516 | snp | C/T | 0.415235 | 0.18761 | intron-variant | NCK1 | GRCh38.p7 | 3:136864845 | tcactgcaacctctg[C/T]ctcccgggttcaatc | 4690 |
rs7431100 | snp | A/G | 0.415235 | 0.18761 | intron-variant | NCK1 | GRCh38.p7 | 3:136926045 | tgtagtgacatctca[A/G]tgtggttttaatttg | 4690 |
rs7433160 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | NCK1 | GRCh38.p7 | 3:136905075 | tagagtgctatggca[C/T]gatctcagctaactg | 4690 |
rs7434143 | snp | G/T | 0.417845 | 0.185278 | intron-variant | NCK1 | GRCh38.p7 | 3:136881825 | cttaatgtcttgaag[G/T]ttcatccgttttgta | 4690 |
rs7611847 | snp | G/T | 0.415399 | 0.187465 | intron-variant | NCK1 | GRCh38.p7 | 3:136934039 | GAAAATTAAACACCA[G/T]AAGCACTAGAAGGTA | 4690 |
rs7617932 | snp | A/G | 0.40853 | 0.193309 | intron-variant | NCK1 | GRCh38.p7 | 3:136884757 | agggagtctcactct[A/G]ttgcccaggttggag | 4690 |
rs7627298 | snp | C/T | 0.41507 | 0.187755 | intron-variant | NCK1 | GRCh38.p7 | 3:136865374 | acaggtgtgcgccac[C/T]gtggctggccTATAT | 4690 |
rs7627443 | snp | C/G | 0.409212 | 0.192748 | intron-variant | NCK1 | GRCh38.p7 | 3:136865378 | gtgtgcgccaccgtg[C/G]ctggccTATATTCAT | 4690 |
rs7629659 | snp | C/T | 0.40853 | 0.193309 | intron-variant | NCK1 | GRCh38.p7 | 3:136884928 | ttttcaccacgttgg[C/T]caggctggtcttgaa | 4690 |
rs7629882 | snp | C/T | 0.417521 | 0.185571 | intron-variant | NCK1 | GRCh38.p7 | 3:136885198 | gtgagaatatggata[C/T]tgtggccgtggacaa | 4690 |
rs7631017 | snp | C/G | 0.409212 | 0.192748 | intron-variant | NCK1 | GRCh38.p7 | 3:136889540 | gtgtggaaggggacc[C/G]gagcgggttgccact | 4690 |
rs7636956 | snp | A/G | 0.415563 | 0.18732 | intron-variant | NCK1 | GRCh38.p7 | 3:136944199 | TCTTGGCTCACTGCA[A/G]CCTCCGCCTGCCAGG | 4690 |
rs7642679 | snp | C/T | 0.161596 | 0.233848 | intron-variant | NCK1 | GRCh38.p7 | 3:136889526 | acaaagcttccacag[C/T]gtggaaggggacccg | 4690 |
rs7645773 | snp | A/G | 0.415399 | 0.187465 | intron-variant | NCK1 | GRCh38.p7 | 3:136899372 | TACATTTGGATTTAG[A/G]TTCCTTCTCTTTCTT | 4690 |
rs7647451 | snp | C/G | 0.415235 | 0.18761 | intron-variant | NCK1 | GRCh38.p7 | 3:136935086 | TTTGTATTTTTAGTA[C/G]TGACAGGGTTTCGCA | 4690 |
rs7648817 | snp | C/T | 0.399025 | 0.200727 | intron-variant | NCK1 | GRCh38.p7 | 3:136930621 | TGTTTATTAAATCCA[C/T]TGTTTTCTTGAAGTT | 4690 |
rs7649211 | snp | A/C | 0.41507 | 0.187755 | intron-variant | NCK1 | GRCh38.p7 | 3:136865319 | cgaactcctgacctc[A/C]agcaatctgcccacc | 4690 |
rs7651059 | snp | C/G | 0.161596 | 0.233848 | intron-variant | NCK1 | GRCh38.p7 | 3:136906312 | AAgaggtctcactct[C/G]ttgcccaggctggtc | 4690 |
rs7651085 | snp | C/G | 0.437259 | 0.165632 | intron-variant | NCK1 | GRCh38.p7 | 3:136906497 | gttgaaattgcctgt[C/G]cttgggcttcagggc | 4690 |
rs7651644 | snp | A/G | 0.4087 | 0.193169 | intron-variant | NCK1 | GRCh38.p7 | 3:136931004 | TTTTAACTACTTTTT[A/G]CTTACTTTTTTTTTA | 4690 |
rs9289523 | snp | C/G | 0.437824 | 0.164991 | intron-variant | NCK1 | GRCh38.p7 | 3:136916747 | ACTTAGAAAATAAAA[C/G]AGTTTGTTTAGTTCA | 4690 |
rs9681238 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136905556 | cagtgtctggcCTCA[A/G]AAttctcttgtatct | 4690 |
rs9811169 | snp | A/G | 0.415399 | 0.187465 | intron-variant | NCK1 | GRCh38.p7 | 3:136881241 | TTAAttttttttgag[A/G]tggagtctcactctg | 4690 |
rs9815771 | snp | C/T | 0.415235 | 0.18761 | intron-variant | NCK1 | GRCh38.p7 | 3:136885855 | CTTTCATAAGAGATA[C/T]GTTCTTTTTAGAATG | 4690 |
rs9817967 | snp | A/G | 0.431029 | 0.17242 | intron-variant | NCK1 | GRCh38.p7 | 3:136910648 | AGTTTTAAATTTAAt[A/G]ttgttaattgacaaa | 4690 |
rs9818792 | snp | C/T | 0.410737 | 0.191478 | intron-variant | NCK1 | GRCh38.p7 | 3:136870478 | TTATTCCAGCTGTAT[C/T]GCAGAAATATTTTAT | 4690 |
rs9819804 | snp | C/T | 0.417196 | 0.185864 | intron-variant | NCK1 | GRCh38.p7 | 3:136865114 | AGGCGCCTGCCACCA[C/T]GCCTGACTAATTTTT | 4690 |
rs9824147 | snp | A/T | 0.105924 | 0.204309 | intron-variant | NCK1 | GRCh38.p7 | 3:136899156 | TTGGAGACTTCATGG[A/T]CACTCCTGCCAGTGC | 4690 |
rs9828009 | snp | C/T | 0.432944 | 0.170387 | intron-variant | NCK1 | GRCh38.p7 | 3:136912433 | cttttggcattccca[C/T]aatgtgtgtgttcgt | 4690 |
rs9833022 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | NCK1 | GRCh38.p7 | 3:136913280 | gggtttttgtgtgtg[C/T]ttgtttttctttttg | 4690 |
rs9833952 | snp | A/G | 0.417196 | 0.185864 | intron-variant | NCK1 | GRCh38.p7 | 3:136943761 | GAGGAAGACAGACAA[A/G]TAAACAAGTACAATG | 4690 |
rs9834861 | snp | A/G | 0.415399 | 0.187465 | intron-variant | NCK1 | GRCh38.p7 | 3:136873375 | aatttctcccatttg[A/G]aatggctgtatttac | 4690 |
rs9836807 | snp | A/C | 0.415399 | 0.187465 | upstream-variant-2KB, intron-variant, nc-transcript-variant | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136861682 | CCCAAGCACGAGGAC[A/C]CTTTTAGAGGGCCCT | 4690 |
rs9837990 | snp | C/G | 0.436976 | 0.165952 | intron-variant | NCK1 | GRCh38.p7 | 3:136914094 | ggtcttttaaatccc[C/G]tttagcctgactgcg | 4690 |
rs9838022 | snp | C/T | 0.425277 | 0.178263 | intron-variant | NCK1 | GRCh38.p7 | 3:136889999 | cctgcgctgtgtgcc[C/T]gcactcctgagccct | 4690 |
rs9840500 | snp | A/G | 0.170084 | 0.236883 | intron-variant | NCK1 | GRCh38.p7 | 3:136902496 | tatcccacctggcct[A/G]ttattcttgatttct | 4690 |
rs9841985 | snp | C/G | 0.4087 | 0.193169 | intron-variant | NCK1 | GRCh38.p7 | 3:136890057 | ggagcagagggtggt[C/G]cttgttggggaggct | 4690 |
rs9842145 | snp | C/T | 0.415399 | 0.187465 | intron-variant | NCK1 | GRCh38.p7 | 3:136890130 | gcgggctgcaggtcc[C/T]gagccctgccccacg | 4690 |
rs9842400 | snp | C/T | 0.41507 | 0.187755 | intron-variant | NCK1 | GRCh38.p7 | 3:136941381 | gtgatccgcccacct[C/T]ggcctcccaaagtgc | 4690 |
rs9842436 | snp | A/G | 0.417359 | 0.185718 | intron-variant | NCK1 | GRCh38.p7 | 3:136890175 | gcccggcaagaaatc[A/G]agcgcagcgctggtg | 4690 |
rs9843733 | snp | C/G | 0.444444 | 0.157135 | intron-variant | NCK1 | GRCh38.p7 | 3:136880370 | ttattagggtggacc[C/G]taatccaccatgact | 4690 |
rs9845460 | snp | A/G | 0.340108 | 0.233197 | intron-variant | NCK1 | GRCh38.p7 | 3:136868275 | GTTTCTTTCCCCTAT[A/G]CTTGTTAGGTGTATT | 4690 |
rs9846334 | snp | C/T | 0.415399 | 0.187465 | intron-variant | NCK1 | GRCh38.p7 | 3:136896384 | atgagttagaacata[C/T]tatatttgtctttct | 4690 |
rs9846691 | snp | C/T | 0.425432 | 0.178112 | intron-variant | NCK1 | GRCh38.p7 | 3:136887429 | GTTTGGAATAAAGGA[C/T]AAGTTAAAAGGGCAG | 4690 |
rs9846754 | snp | A/G | 0.415235 | 0.18761 | intron-variant | NCK1 | GRCh38.p7 | 3:136926571 | tgagccaccgcgccc[A/G]gccACTCtttttgtt | 4690 |
rs9848867 | snp | C/T | 0.415891 | 0.18703 | intron-variant | NCK1 | GRCh38.p7 | 3:136881206 | atctcttcacttaca[C/T]tattggcctcttaTT | 4690 |
rs9851726 | snp | C/G | 0.415235 | 0.18761 | intron-variant | NCK1 | GRCh38.p7 | 3:136927545 | ATTGATTGATTGAGA[C/G]AGATTCTCCCTCTGT | 4690 |
rs9853404 | snp | A/T | 0.0228947 | 0.104514 | intron-variant | NCK1 | GRCh38.p7 | 3:136864944 | tttgtatatatatat[A/T]tttttctttttcttt | 4690 |
rs9853417 | snp | A/G | 0.415891 | 0.18703 | intron-variant | NCK1 | GRCh38.p7 | 3:136892388 | agtttgactcttttc[A/G]gttgcctgtgctACT | 4690 |
rs9855314 | snp | A/G | 0.415727 | 0.187175 | intron-variant | NCK1 | GRCh38.p7 | 3:136882803 | TCTTATCTAATTGCA[A/G]GGGTGGCTGGGAAGT | 4690 |
rs9856828 | snp | C/T | 0.415399 | 0.187465 | intron-variant | NCK1 | GRCh38.p7 | 3:136889140 | caagtgatcttccca[C/T]ctctgcctcccaaag | 4690 |
rs9859665 | snp | C/T | 0.415235 | 0.18761 | intron-variant | NCK1 | GRCh38.p7 | 3:136883319 | ACATCTCTAGCCATA[C/T]GGTCATTTTCTGTAA | 4690 |
rs9859810 | snp | A/G | 0.43598 | 0.167067 | intron-variant | NCK1 | GRCh38.p7 | 3:136911144 | ccacattttttcttc[A/G]ttaatccattgatgg | 4690 |
rs9863551 | snp | A/G | 0.425123 | 0.178415 | intron-variant | NCK1 | GRCh38.p7 | 3:136887009 | CCACCATGCCCGGCT[A/G]ATTTTTGTGTTATTA | 4690 |
rs9864941 | snp | A/G | 0.415727 | 0.187175 | intron-variant | NCK1 | GRCh38.p7 | 3:136894945 | TGGCACTACTATCTC[A/G]GCTCACTGCAACCTC | 4690 |
rs9867325 | snp | C/G | 0.170084 | 0.236883 | intron-variant | NCK1 | GRCh38.p7 | 3:136900067 | TCTTACATCTCACAG[C/G]CTGCACCATGGTCCC | 4690 |
rs9870377 | snp | A/G | 0.456332 | 0.141164 | intron-variant | NCK1 | GRCh38.p7 | 3:136878278 | gccggatgtggtggc[A/G]ggcacctataatccc | 4690 |
rs9874887 | snp | A/T | 0.415727 | 0.187175 | intron-variant | NCK1 | GRCh38.p7 | 3:136882720 | AGAAAGATTTTAGGG[A/T]CCAGGCTAGAAGTGG | 4690 |
rs9875196 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136882933 | CCTTATTACATGACt[G/T]ttttaaagacagtct | 4690 |
rs9877089 | snp | C/T | 0.148996 | 0.228688 | intron-variant | NCK1 | GRCh38.p7 | 3:136937751 | attgttcattgttaa[C/T]gtatagaaatacaac | 4690 |
rs9878117 | snp | A/G | 0.415399 | 0.187465 | intron-variant | NCK1 | GRCh38.p7 | 3:136902165 | tttatatagtttcca[A/G]agttcttcttaactc | 4690 |
rs9878367 | snp | C/T | 0.415399 | 0.187465 | intron-variant | NCK1 | GRCh38.p7 | 3:136893307 | tctGCGCcatccacg[C/T]caacatctatttttt | 4690 |
rs9878464 | snp | C/G | 0.424968 | 0.178567 | intron-variant | NCK1 | GRCh38.p7 | 3:136867664 | atgttggaatccaac[C/G]ttgtgttttacagat | 4690 |
rs9879531 | snp | A/G | 0.19459 | 0.243782 | intron-variant | NCK1 | GRCh38.p7 | 3:136920133 | CATCAAGTAATTTTA[A/G]TTGGTAAATACTCTT | 4690 |
rs9881139 | snp | A/G | 0.436692 | 0.166271 | intron-variant | NCK1 | GRCh38.p7 | 3:136915198 | TTCATCAAGTAGATC[A/G]CATTACTACTAAGGG | 4690 |
rs9883108 | snp | C/G | 0.41507 | 0.187755 | intron-variant | NCK1 | GRCh38.p7 | 3:136868011 | CAACCTCCGCCTCTC[C/G]GGTTCAAGCAATTCT | 4690 |
rs9883131 | snp | A/G | 0.415399 | 0.187465 | intron-variant | NCK1 | GRCh38.p7 | 3:136875505 | agggattgcaatcct[A/G]gtctctgataaaaca | 4690 |
rs9883979 | snp | A/G | 0.41507 | 0.187755 | intron-variant | NCK1 | GRCh38.p7 | 3:136926575 | ccaccgcgcccggcc[A/G]CTCtttttgtttttt | 4690 |
rs10804645 | snp | A/G | 0.340559 | 0.233022 | intron-variant | NCK1 | GRCh38.p7 | 3:136924892 | TATATGGGTTAAAAA[A/G]GGGAAAAGGTCAGGA | 4690 |
rs10935209 | snp | A/T | 0.409212 | 0.192748 | intron-variant | NCK1 | GRCh38.p7 | 3:136920257 | TTCTTCTTTTTTTTT[A/T]AAAAATAGTGTAGGT | 4690 |
rs10935210 | snp | A/G | 0.425277 | 0.178263 | intron-variant | NCK1 | GRCh38.p7 | 3:136932311 | CCTGCAGCAACCCCA[A/G]ATTTTTATTTATTTT | 4690 |
rs10935211 | snp | C/T | 0 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136944112 | AAAAGGAAAAACAAC[C/T]TTTTTTTTTTTTTTT | 4690 |
rs11294236 | in-del | -/T | 0.415563 | 0.18732 | intron-variant | NCK1 | GRCh38.p7 | 3:136866933 | GCCTAGTCTTTAAAA[-/T]TTTTTTTTTCTCCTA | 4690 |
rs11316539 | in-del | -/T | 0.418007 | 0.185132 | intron-variant | NCK1 | GRCh38.p7 | 3:136933711 | AAGATTTAAGTAATC[-/T]TTTTTTTTTTCTTGA | 4690 |
rs11332327 | in-del | -/A | 0.35574 | 0.226537 | intron-variant | NCK1 | GRCh38.p7 | 3:136870688 | TTAGCTATAGTCTTT[-/A]AAAAAAAAAAAAAAA | 4690 |
rs11360865 | in-del | -/A | 0.415891 | 0.18703 | intron-variant | NCK1 | GRCh38.p7 | 3:136893355 | CATTCTTGCAGGAGT[-/A]AGGTGGTACTGCATT | 4690 |
rs11370944 | in-del | -/T/TT | 0 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136917247 | TTTTTTTTTTTTTTT[-/T/TT]GCTTAATCAGCTATC | 4690 |
rs11433927 | in-del | -/A | 0.417196 | 0.185864 | intron-variant | NCK1 | GRCh38.p7 | 3:136923316 | TCCCAGCACTTTGGG[-/A]AGGCCGAGGCAGGCG | 4690 |
rs11455373 | in-del | -/T/TT/TTT | 0.272511 | 0.248984 | intron-variant | NCK1 | GRCh38.p7 | 3:136917232 | TTTTTTTTTTTTTTT[-/T/TT/TTT]GCTTAATCAGCTATC | 4690 |
rs11547829 | snp | A/C/T | 0.00527406 | 0.0510805 | missense, downstream-variant-500B | NCK1, LOC107986136 | GRCh38.p7 | 3:136945867 | AGTCCTTTGGGTGAC[A/C/T]ATGTGGGTTCTCTGT | 4690 |
rs11547830 | snp | A/C | 0 | 0 | missense, downstream-variant-500B | NCK1, LOC107986136 | GRCh38.p7 | 3:136945823 | AAGTTGGATGGTTCC[A/C]TTCAAACTATGTAAC | 4690 |
rs11715604 | snp | A/T | 0.18134 | 0.240387 | intron-variant | NCK1 | GRCh38.p7 | 3:136870707 | AAAAAAAAAAAAAAA[A/T]GGCCTGTGAGGTCTT | 4690 |
rs11720293 | snp | A/C | 0 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136932936 | AACAACATGCTTAAA[A/C]TAAAGAATACTGAAA | 4690 |
rs11917123 | snp | G/T | 0.42 | 0.183303 | intron-variant | NCK1 | GRCh38.p7 | 3:136902197 | ttgtttttttttttt[G/T]tttttgtttttgttt | 4690 |
rs11921170 | snp | C/T | 0.415235 | 0.18761 | intron-variant | NCK1 | GRCh38.p7 | 3:136886955 | TTCAAGCGATTCTTA[C/T]GCCTCAGCCTCCCAA | 4690 |
rs11925491 | snp | G/T | 0 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136915043 | ggaagcatactgagg[G/T]tctcaccagatgaag | 4690 |
rs11925803 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136925000 | CCCCACCAAAAATTA[A/G]GGGGatagctgaacc | 4690 |
rs12330283 | snp | C/T | 0.414905 | 0.187899 | intron-variant | NCK1 | GRCh38.p7 | 3:136871569 | ctcttgcgccccctc[C/T]aatcagtgtctcttt | 4690 |
rs12487901 | snp | A/C | 0.417359 | 0.185718 | intron-variant | NCK1 | GRCh38.p7 | 3:136871460 | TTATTGAaaactgca[A/C]aaatttaaatgtata | 4690 |
rs12488365 | snp | A/C | 0.415235 | 0.18761 | intron-variant | NCK1 | GRCh38.p7 | 3:136887636 | AACTTCTTTAGCATA[A/C]AATTCAGATACAACT | 4690 |
rs12489085 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136895283 | GCAAACTGATGATAG[A/G]TGTGTATAAGGCTTT | 4690 |
rs12491278 | snp | A/G | 0.414741 | 0.188044 | intron-variant | NCK1 | GRCh38.p7 | 3:136880210 | gaatggcgtgaaccc[A/G]ggaggtggagcttgc | 4690 |
rs12493179 | snp | A/G | 0.5 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136940700 | caggcacctgacatc[A/G]tgcctaactaatttt | 4690 |
rs12629000 | snp | A/T | 0.34303 | 0.232046 | intron-variant | NCK1 | GRCh38.p7 | 3:136924729 | TCACCACACTGCCAT[A/T]AGGCAGGAGGAGGGG | 4690 |
rs12630955 | snp | C/T | 0.40853 | 0.193309 | intron-variant | NCK1 | GRCh38.p7 | 3:136867312 | atctcgctctgttgc[C/T]caggctggagtacag | 4690 |
rs12633003 | snp | A/C | 0.415563 | 0.18732 | intron-variant | NCK1 | GRCh38.p7 | 3:136889764 | caccagagtagctag[A/C]tacggagtgtcgatt | 4690 |
rs12633073 | snp | A/G | 0.411242 | 0.191052 | intron-variant | NCK1 | GRCh38.p7 | 3:136889807 | aaccctgagctagac[A/G]cagggtgctgattgg | 4690 |
rs12637237 | snp | G/T | 0.0637235 | 0.166737 | intron-variant | NCK1 | GRCh38.p7 | 3:136926985 | TTTATTTATTTATTT[G/T]TTTGAGACCAAGTCT | 4690 |
rs12637949 | snp | A/C | 0.414741 | 0.188044 | intron-variant | NCK1 | GRCh38.p7 | 3:136873345 | ctagaggcctttaac[A/C]cctttgttctgggca | 4690 |
rs13066545 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136864782 | tttttttttttttga[A/G]acagagtctctgttg | 4690 |
rs13066555 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136864788 | tttttttgagacaga[A/G]tctctgttgcccagg | 4690 |
rs13073883 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136867109 | ttctttctttctttc[C/T]ttctttctttgtttc | 4690 |
rs13077864 | snp | C/T | 0.268452 | 0.249318 | intron-variant | NCK1 | GRCh38.p7 | 3:136890996 | atacaatatttgtcc[C/T]ttatgactggcttat | 4690 |
rs13091654 | snp | A/G | 0.0023933 | 0.0345097 | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136949838 | AGTTGTGTAACTTGT[A/G]AATTTTTTTTATCAA | 4690 |
rs13099529 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136908764 | AGATATTAAAAGTAG[A/G]CAGCTAATGGTTTCT | 4690 |
rs13314118 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136884732 | GCttttttttttttc[C/T]ttttttgagagggag | 4690 |
rs13315318 | snp | C/T | 0.415727 | 0.187175 | intron-variant | NCK1 | GRCh38.p7 | 3:136936830 | ttgaagtagttgttt[C/T]tgttgttgggttcta | 4690 |
rs13320485 | snp | C/T | 0.0231025 | 0.104964 | missense, downstream-variant-500B | NCK1, LOC107986136 | GRCh38.p7 | 3:136945895 | TGTCAGAGAAATTAG[C/T]AGCAGTCGTCAATAA | 4690 |
rs13324011 | snp | A/T | 0 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136920882 | TAAATGGCCTTATAG[A/T]TGATTGTAATCATAT | 4690 |
rs16844164 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | NCK1 | GRCh38.p7 | 3:136878847 | ACACAATTGGAGGTC[A/G]AGCGTTCTACAGAAA | 4690 |
rs16844167 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NCK1 | GRCh38.p7 | 3:136880959 | CTCCAGGTCTGCTTT[C/T]TGCGCTCTACCCTAC | 4690 |
rs16844241 | snp | A/G | 0.286303 | 0.24735 | intron-variant | NCK1 | GRCh38.p7 | 3:136916329 | TTCTCAAATGTTATG[A/G]TTAGTCATAAGTTAA | 4690 |
rs17300553 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136870747 | GGCTTTTGTCTACGT[C/T]TCACTTCATCTCTTG | 4690 |
rs17301365 | snp | C/T | 0.126909 | 0.217598 | intron-variant | NCK1 | GRCh38.p7 | 3:136943687 | GTATGTACTGCTAAG[C/T]GTTGGAGACAGAAAC | 4690 |
rs17366890 | snp | A/C | 0.173643 | 0.238054 | intron-variant | NCK1 | GRCh38.p7 | 3:136917741 | ATAACAGTTCTTTCC[A/C]ACAGCACTTACGAGT | 4690 |
rs28370972 | snp | C/T | 0.124491 | 0.216211 | intron-variant | NCK1 | GRCh38.p7 | 3:136917843 | TGGATGACAAATACA[C/T]CAGTAAGCTCTCACC | 4690 |
rs28411139 | snp | A/C | | | intron-variant | NCK1 | GRCh38.p7 | 3:136864499 | TCACACACACACAAA[A/C]AAAAAACAGAAACAA | 4690 |
rs28489326 | snp | C/T | 0.150667 | 0.229419 | intron-variant | NCK1 | GRCh38.p7 | 3:136915704 | GGAAGAGAGTGAAGG[C/T]GAAGGTGCCAAACAC | 4690 |
rs28517333 | snp | G/T | 0.0244538 | 0.107838 | intron-variant | NCK1 | GRCh38.p7 | 3:136894884 | GTTTTGTTTTGTTTT[G/T]TTTTTGAGATGGAGT | 4690 |
rs28564581 | snp | C/G | 0.410737 | 0.191478 | intron-variant | NCK1 | GRCh38.p7 | 3:136864318 | CAACACGGTGAAACC[C/G]CGTCTCTACTGAAAA | 4690 |
rs28603173 | snp | A/G | | | upstream-variant-2KB, intron-variant | NCK1 | GRCh38.p7 | 3:136929975 | TCTATTTAAGTCTTA[A/G]GAAATCTCTGTTAAC | 4690 |
rs28672119 | snp | C/G | 0.415727 | 0.187175 | intron-variant | NCK1 | GRCh38.p7 | 3:136864423 | ATGAACCCGGGAGTC[C/G]GAGGTTGCAGTGAGC | 4690 |
rs28689774 | snp | A/C | 0.32 | 0.24 | intron-variant | NCK1 | GRCh38.p7 | 3:136864497 | CGTCACACACACACA[A/C]AAAAAAAACAGAAAC | 4690 |
rs34046138 | in-del | -/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136906690 | TGGGATAACCTTTAG[-/G]ACCCAAGCTGTCTGT | 4690 |
rs34072779 | in-del | -/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136918829 | ATTCATGTAACCTTT[-/G]CTTGGCCTCATTGTC | 4690 |
rs34084410 | in-del | -/C | | | intron-variant | NCK1 | GRCh38.p7 | 3:136919883 | TTCAGTTTTAGATTC[-/C]TGTTGTACTTTAACA | 4690 |
rs34099273 | in-del | -/C | | | intron-variant | NCK1 | GRCh38.p7 | 3:136938641 | TGAATTTGCTTATGG[-/C]AAAAAATGTGTGTTA | 4690 |
rs34144951 | in-del | -/A | 0.449599 | 0.150533 | intron-variant | NCK1 | GRCh38.p7 | 3:136870341 | TCAAAAAAAAAAAAA[-/A]TTCATCCTTTTCTTC | 4690 |
rs34177184 | in-del | -/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136910701 | GTACAATGGGATGTT[-/G]CTGACACATGTATAC | 4690 |
rs34192022 | in-del | -/G | | | upstream-variant-2KB, intron-variant | NCK1 | GRCh38.p7 | 3:136929566 | CAGAAGAGACCAGGG[-/G]TTAGAATCAGCAATA | 4690 |
rs34322362 | in-del | -/TT | | | intron-variant | NCK1 | GRCh38.p7 | 3:136867426 | TTTTTTTTTTTTTTT[-/TT]GTAGAGATAGGGTCT | 4690 |
rs34349896 | in-del | -/TC | | | intron-variant | NCK1 | GRCh38.p7 | 3:136867265 | CTGTCTCTCTCTCTC[-/TC]TTTCTTTCTTTCTTC | 4690 |
rs34484068 | in-del | -/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136897692 | TCTTCACCCTTTTTT[-/T]AGACAAATGCTCACT | 4690 |
rs34495274 | in-del | -/A | | | intron-variant | NCK1 | GRCh38.p7 | 3:136917555 | GCCCATGTAACCAAA[-/A]TATGAAAGCAATTTA | 4690 |
rs34516637 | in-del | -/A | | | intron-variant | NCK1 | GRCh38.p7 | 3:136883815 | AAATGGAACAGAAAA[-/A]GGATGGATGAGAGAC | 4690 |
rs34535819 | in-del | -/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136926182 | TTGTTTTTCTAATGT[-/G]TTCTTTAACTTTTCT | 4690 |
rs34553311 | in-del | -/TG | 0.5 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136923121 | GTGTGTGTGTGTGTG[-/TG]CGCGCCTGTGTGCAT | 4690 |
rs34682748 | in-del | -/T | 0.416218 | 0.186739 | intron-variant | NCK1 | GRCh38.p7 | 3:136930981 | AACTTTGGAATTAAC[-/T]TTTTTTTTTTTAACT | 4690 |
rs34688121 | in-del | -/AA | 0.415563 | 0.18732 | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136949419 | CCTCTTTTCAGCTTT[-/AA]GTTTTGTTGATTGGG | 4690 |
rs34746192 | in-del | -/G | 0.415399 | 0.187465 | intron-variant | NCK1 | GRCh38.p7 | 3:136894883 | GTTTTGTTTTGTTTT[-/G]TTTTTTGAGATGGAG | 4690 |
rs34747213 | in-del | -/C | | | intron-variant | NCK1 | GRCh38.p7 | 3:136872910 | CCACCTGCATTTCAG[-/C]AAGATGTATGGAAAT | 4690 |
rs34767461 | in-del | -/A | 0.422 | 0.181428 | intron-variant | NCK1 | GRCh38.p7 | 3:136941713 | ATTTACAAAAAAAAA[-/A]CTGCAATACTACTGA | 4690 |
rs34776608 | in-del | -/TT | 0 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136941133 | TTTTTTTTTTTTTTT[-/TT]GGAGGGTGGGGGTCA | 4690 |
rs34799319 | snp | A/G | 0.48546 | 0.0840147 | intron-variant | NCK1 | GRCh38.p7 | 3:136867776 | GATCTTCTGACGCAA[A/G]TTCTGTGTGTTTATG | 4690 |
rs34813529 | in-del | -/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136887593 | TAATTGGTGACTTTT[-/T]AAGTTATTTGTCACC | 4690 |
rs34828302 | in-del | -/A/T | 0.131723 | 0.220251 | intron-variant | NCK1 | GRCh38.p7 | 3:136899433 | CTTTTTTTTTTTTTT[-/A/T]AAATTTCTTTAACTT | 4690 |
rs34864054 | in-del | -/A | | | intron-variant | NCK1 | GRCh38.p7 | 3:136884565 | GTGCCTCAGCCTCCA[-/A]GAGTAGCTGGGATTA | 4690 |
rs34890260 | in-del | -/C | | | intron-variant | NCK1 | GRCh38.p7 | 3:136881677 | TACTAACAACTCCCC[-/C]AAGTCTTCCCTCCTC | 4690 |
rs34923852 | in-del | -/A | | | intron-variant | NCK1 | GRCh38.p7 | 3:136869416 | GAGTGTGATGGCGAA[-/A]TGCCTGTAATCTCAG | 4690 |
rs34994998 | snp | G/T | 0.5 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136887160 | CTATCTTTTATATTG[G/T]GTTTTATTTCTTTAG | 4690 |
rs35039322 | snp | C/T | 0.5 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136887342 | TCAGCATTTTTTTTC[C/T]ATCTTAACATAAAAT | 4690 |
rs35087010 | in-del | -/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136872428 | ATTCAAGAAGTGACT[-/T]GGGTGCTGTTAAAGG | 4690 |
rs35127615 | snp | A/G | 0.151334 | 0.229706 | intron-variant | NCK1 | GRCh38.p7 | 3:136906427 | TGATAAGGTTTTGCT[A/G]AGGTCTGGGTTGCCA | 4690 |
rs35133420 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136883220 | GCCCCCATGCCCAGC[C/T]TACTTCTTATTACAT | 4690 |
rs35150598 | snp | G/T | 0.5 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136870546 | TTGATCATTTGCAAG[G/T]ACTACATGCTCTTGA | 4690 |
rs35187579 | in-del | -/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136895407 | CCATACCACCTTTTT[-/T]AAAAAATTGCCATAC | 4690 |
rs35197703 | in-del | -/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136866325 | TCTTTTTTTTTTTTT[-/T]GAGACAGAGTCTCGC | 4690 |
rs35254283 | in-del | -/T | 0.450231 | 0.149691 | intron-variant | NCK1 | GRCh38.p7 | 3:136936056 | TTTTTTTTTTTTTTT[-/T]CTGAGACAGAGTCTC | 4690 |
rs35310696 | in-del | -/G | | | frameshift-variant, downstream-variant-500B | NCK1, LOC107986136 | GRCh38.p7 | 3:136945660 | TTGTTGACCCAGGGG[-/G]AACGTCTCTATGACC | 4690 |
rs35320281 | in-del | -/A/AA | 0.42574 | 0.177808 | intron-variant | NCK1 | GRCh38.p7 | 3:136879131 | AACAATCAGAACAAC[-/A/AA]AAAAAAAAAGGCTCA | 4690 |
rs35336033 | in-del | -/G | 0.40853 | 0.193309 | intron-variant | NCK1 | GRCh38.p7 | 3:136937953 | ATAAAAGTGGTGGAA[-/G]GAGAGCATCCTTGTT | 4690 |
rs35339486 | snp | C/T | 0.415563 | 0.18732 | intron-variant | NCK1 | GRCh38.p7 | 3:136895397 | ATTAAAATTGCCATA[C/T]CACCTTTTTTAAAAA | 4690 |
rs35414832 | in-del | -/TT | 0.417034 | 0.18601 | intron-variant | NCK1 | GRCh38.p7 | 3:136874810 | TGCATTAATGAAAAC[-/TT]TTTTTCATGTTCATG | 4690 |
rs35418026 | in-del | -/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136870319 | GCACTCCAGCCTGGG[-/G]TGACAAGGAGAGACT | 4690 |
rs35463509 | in-del | -/GT | | | intron-variant | NCK1 | GRCh38.p7 | 3:136882589 | TGTGTGTGTGTGTGT[-/GT]TGAGGGGCACCTTTG | 4690 |
rs35467327 | in-del | -/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136942398 | CTCTATATTCCTGGT[-/G]CATGTGGGGCCGCTG | 4690 |
rs35487850 | in-del | -/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136877236 | GCCTATGAAAGTTTT[-/T]CCCAAATTGACACAT | 4690 |
rs35510756 | in-del | -/C | | | intron-variant | NCK1 | GRCh38.p7 | 3:136909501 | ATTATTTAAACAACC[-/C]AATTTCAATGGCAGA | 4690 |
rs35543716 | in-del | -/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136884434 | ATAGAGTACAGCTTT[-/T]GAGTTCTTGTCTTTT | 4690 |
rs35575275 | in-del | -/C | | | intron-variant | NCK1 | GRCh38.p7 | 3:136911762 | CTTGCACAGAAGTTC[-/C]TAGTGGTAATGAATT | 4690 |
rs35604872 | in-del | -/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136882715 | TGTGGAGAAAGATTT[-/T]AGGGTCCAGGCTAGA | 4690 |
rs35688993 | in-del | -/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136945116 | ACATAACTGCAATTT[-/T]ATATTGCATATCATA | 4690 |
rs35708231 | in-del | -/TCT | | | intron-variant, upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136863023 | TTTTGTAACCTTTCT[-/TCT]GTATTAACATACAAG | 4690 |
rs35719347 | snp | A/G | 0.444444 | 0.157135 | intron-variant | NCK1 | GRCh38.p7 | 3:136906844 | TGGGAGGAGTGCTTA[A/G]GTGCCAACAGTGGTG | 4690 |
rs35720315 | in-del | -/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136879309 | AAAAGAAGGAATTAT[-/T]CAGTAAAATATTCAA | 4690 |
rs35721418 | in-del | -/C | | | intron-variant | NCK1 | GRCh38.p7 | 3:136924384 | GAAATGCTACAGGAC[-/C]AAGTGAAGCCAGCTT | 4690 |
rs35760633 | snp | C/T | 0.40853 | 0.193309 | intron-variant | NCK1 | GRCh38.p7 | 3:136870084 | CAGCGCAGTGGCTCA[C/T]GCCTGTAATCCCATT | 4690 |
rs35773748 | in-del | -/A | | | intron-variant | NCK1 | GRCh38.p7 | 3:136897932 | TAAAAAGCTGTATTA[-/A]TCTAATATCATAATA | 4690 |
rs35806195 | in-del | -/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136899878 | CCATCCTTTTTTTTT[-/T]AGGGGTTTTCTCTTC | 4690 |
rs35833141 | in-del | -/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136897184 | ACCTCTGCCTCCCAG[-/G]TTCAAGTGATTCTCC | 4690 |
rs35845754 | in-del | -/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136895805 | CTGACCTCAGGTGAT[-/G]CCTCCCACCTTGGCC | 4690 |
rs35858169 | in-del | -/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136881237 | TTATTTAATTTTTTT[-/T]GAGATGGAGTCTCAC | 4690 |
rs35976394 | in-del | -/TTT | | | intron-variant | NCK1 | GRCh38.p7 | 3:136886818 | GTTACATGATCAGTC[-/TTT]TTTTTTTTTTTTTTT | 4690 |
rs35988747 | in-del | -/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136895736 | CACCCCGCTAATTTT[-/T]GCATTTTTAGTAGAG | 4690 |
rs36033316 | in-del | -/A | | | intron-variant | NCK1 | GRCh38.p7 | 3:136898404 | AAAAAAAAAAAAAAA[-/A]GGTGGATGCAGTGGT | 4690 |
rs36043323 | in-del | -/AG | 0.417845 | 0.185278 | intron-variant | NCK1 | GRCh38.p7 | 3:136903774 | GATCAGTTTACATTC[-/AG]AGTTATTGATGTGTG | 4690 |
rs36120048 | in-del | -/C | | | intron-variant | NCK1 | GRCh38.p7 | 3:136921684 | TAGGGAAGAGTGTCC[-/C]AGTGTGAACTCAACT | 4690 |
rs55650043 | snp | A/T | 0.499958 | 0.00459246 | intron-variant | NCK1 | GRCh38.p7 | 3:136870051 | TTTTTTTTTTTTTTT[A/T]AAAGAATCATCCTGG | 4690 |
rs55659307 | in-del | -/CT | | | intron-variant | NCK1 | GRCh38.p7 | 3:136867180 | CTTCCTTCCTTCCTT[-/CT]TTCTTTCTTTTCTTT | 4690 |
rs55815126 | in-del | -/T | 0.458775 | 0.137524 | intron-variant | NCK1 | GRCh38.p7 | 3:136904834 | CATTTTTTTTTTTTT[-/T]AATTATTACTTTTTG | 4690 |
rs55857042 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136867050 | CTATGTTGCTTGCTT[G/T]TCTTTCTTTCTTTCT | 4690 |
rs55964045 | snp | A/G | 0.0314385 | 0.121371 | intron-variant | NCK1 | GRCh38.p7 | 3:136913635 | CCTTTTCCTGGACAT[A/G]CACAGTGATTTTCTT | 4690 |
rs55964348 | in-del | -/GTCTTG | | | intron-variant | NCK1 | GRCh38.p7 | 3:136912873 | CCCAAACTGGTCTTG[-/GTCTTG]ATATCCTGGACTCAA | 4690 |
rs56028023 | in-del | -/TTTGTTTCTTTCTTTC | | | intron-variant | NCK1 | GRCh38.p7 | 3:136867117 | TTCTTTCTTTCTTTC[-/TTTGTTTCTTTCTTTC]CTTCCTTCCTTCCTT | 4690 |
rs56050231 | snp | A/G | 0.0205511 | 0.0992634 | upstream-variant-2KB, intron-variant, nc-transcript-variant | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136861636 | CCGAAGGTCCTCTTC[A/G]TAACACTACTGCCGC | 4690 |
rs56143028 | in-del | -/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136867051 | TATGTTGCTTGCTTT[-/T]CTTTCTTTCTTTCTT | 4690 |
rs56152232 | in-del | -/AAAAAAA/AAAAAAAA/AAAAAAAAA | | | upstream-variant-2KB, intron-variant | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136861504 | AAAAAAAAAAAAAAA[-/AAAAAAA/AAAAAAAA/AAAAAAAAA]GAGGCAGGTTACGGC | 4690 |
rs56207021 | snp | G/T | 0.093777 | 0.195178 | intron-variant | NCK1 | GRCh38.p7 | 3:136885461 | AGGTGCATGCCACCA[G/T]GGCTGGTTAATTTTT | 4690 |
rs56243004 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | NCK1 | GRCh38.p7 | 3:136865619 | TATAGAAAAATACCA[A/G]ATGTTCTTTATCTGC | 4690 |
rs56280070 | in-del | -/CT/TC | | | intron-variant | NCK1 | GRCh38.p7 | 3:136867254 | TGTCTCTCTCTCTCT[-/CT/TC]TTCTTTCTTTCTTCT | 4690 |
rs56308712 | snp | G/T | 0.128288 | 0.218372 | intron-variant, upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136863195 | CTAGAAATTAGGAAA[G/T]AATTAGGTTAAAGAG | 4690 |
rs56346960 | in-del | -/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136867059 | TTGCTTTTCTTTCTT[-/T]CTTTCTTTCTTTCTT | 4690 |
rs56752324 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | NCK1 | GRCh38.p7 | 3:136866287 | TTTTTGTACCTTCGT[A/G]TCATTCCTTTTTCTT | 4690 |
rs56853411 | in-del | -/C | 0.434831 | 0.168337 | intron-variant | NCK1 | GRCh38.p7 | 3:136864496 | CGTCACACACACACA[-/C]AAAAAAAAACAGAAA | 4690 |
rs56924222 | in-del | -/T | 0.0174175 | 0.0916809 | intron-variant | NCK1 | GRCh38.p7 | 3:136915651 | TTAAAAGGTTCACAG[-/T]TTCCTCAGGCTGTAT | 4690 |
rs56959241 | in-del | -/GTGT/GTGTGTGT | 0 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136893179 | TGTGTGTGTGTGTGT[-/GTGT/GTGTGTGT]ATATATATATATACA | 4690 |
rs57065412 | in-del | -/GTT | 0 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136902200 | TTTTTTTTTTTTTTT[-/GTT]TTGTTTTTGTTTTTT | 4690 |
rs57504725 | in-del | -/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136939863 | TTTTTTTTTTTTTTA[-/T]AAATAGAGACAGGGT | 4690 |
rs57546375 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | NCK1 | GRCh38.p7 | 3:136878129 | AACATGCTAAGTAGG[C/T]CGGACATGGTGGCTC | 4690 |
rs57596314 | in-del | -/T/TT | 0 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136912180 | TTTTTTTTTTTTTTT[-/T/TT]GAGACCGAGTCTCGC | 4690 |
rs57808674 | in-del | -/AA/C | 0.434831 | 0.168337 | intron-variant | NCK1 | GRCh38.p7 | 3:136864497 | GTCACACACACACAA[-/AA/C]AAAAAAAACAGAAAC | 4690 |
rs58317894 | in-del | -/AAAAAAAAAA | 0 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136880002 | TTAAAAAAAAAAAAA[-/AAAAAAAAAA]GGCTGGGCACAGTGG | 4690 |
rs58385753 | in-del | -/TTTTTTTTTTTTT | | | intron-variant | NCK1 | GRCh38.p7 | 3:136889062 | TTTTTTTTTTTTTTT[-/TTTTTTTTTTTTT]GTAGAGACAGTCTCA | 4690 |
rs58850362 | snp | A/G | 0.0402882 | 0.136092 | intron-variant | NCK1 | GRCh38.p7 | 3:136873990 | TTTTTGTGGATGGCT[A/G]CTTTTGCTTAACATT | 4690 |
rs59203615 | in-del | -/GT/TT/TTA | | | intron-variant | NCK1 | GRCh38.p7 | 3:136902195 | TTTGTTTTTTTTTTT[-/GT/TT/TTA]TTTTTTTGTTTTTGT | 4690 |
rs59338334 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136921628 | ATAAACTGGACACTA[A/G]TTAAAATGGTAAGGA | 4690 |
rs59381434 | snp | G/T | 0.0119091 | 0.0762411 | intron-variant | NCK1 | GRCh38.p7 | 3:136897232 | TAGCTGGGATTACAG[G/T]TATGTGCCACCATGC | 4690 |
rs60491982 | in-del | -/T | 0.437259 | 0.165632 | intron-variant | NCK1 | GRCh38.p7 | 3:136905985 | TTTGGCGGTGTCATA[-/T]TTCCTTGCTTTTTCA | 4690 |
rs60498879 | in-del | -/TTTA | | | intron-variant | NCK1 | GRCh38.p7 | 3:136939860 | TTTTTTTTTTTTTTT[-/TTTA]AAATAGAGACAGGGT | 4690 |
rs61123867 | snp | C/T | 0.415891 | 0.18703 | intron-variant | NCK1 | GRCh38.p7 | 3:136880006 | AAAAAAAAAAAAGGC[C/T]GGGCACAGTGGCTCA | 4690 |
rs61135304 | snp | A/T | 0.183886 | 0.241099 | intron-variant | NCK1 | GRCh38.p7 | 3:136899434 | CTTTTTTTTTTTTTT[A/T]AATTTCTTTAACTTT | 4690 |
rs61731511 | snp | A/T | 0.0104239 | 0.0714373 | synonymous-codon, downstream-variant-500B | NCK1, LOC107986136 | GRCh38.p7 | 3:136945965 | TTACCCATTCAGCTC[A/T]TCTAATGATGAAGAA | 4690 |
rs62408865 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136919229 | AATTTTTTTTTTTCT[G/T]GAGGGGGAGTGATAG | 4690 |
rs62408866 | snp | A/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136939866 | TTTTTTTTTTTTAAA[A/T]TAGAGACAGGGTCTC | 4690 |
rs62408867 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136941136 | TTTTTTTTTTTTTTG[G/T]AGGGTGGGGGTCAGG | 4690 |
rs62408868 | snp | C/T | 0.0850919 | 0.187897 | intron-variant | NCK1 | GRCh38.p7 | 3:136944793 | GAGCATAAAATCACA[C/T]GCTAAGAAATGGGCA | 4690 |
rs62408869 | snp | A/G | 0.5 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136944894 | CATTTCTTTCAACAC[A/G]TATGTGTTAAGCATT | 4690 |
rs62410394 | snp | C/T | | | intron-variant, upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136862659 | CCGCCCGTGCGAGCC[C/T]GGGAGGTCGAGTGTG | 4690 |
rs62410395 | snp | A/C | | | intron-variant, upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136862663 | CCGTGCGAGCCTGGG[A/C]GGTCGAGTGTGCGGC | 4690 |
rs62410396 | snp | C/T | | | intron-variant, upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136862666 | TGCGAGCCTGGGAGG[C/T]CGAGTGTGCGGCGCG | 4690 |
rs62410397 | snp | A/G | | | intron-variant, upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136863921 | CCTAGCAGACACGGT[A/G]AAACCCCGTCTCTAC | 4690 |
rs62410398 | snp | A/C | 0.5 | 0 | intron-variant, upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136863925 | GCAGACACGGTGAAA[A/C]CCCGTCTCTACTAAA | 4690 |
rs62410399 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | NCK1 | GRCh38.p7 | 3:136870024 | GAATGGATGTTTCTC[A/G]AAAGTTTTTTTTTTT | 4690 |
rs62410400 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136870055 | TTTTTTTTTTTAAAA[G/T]AATCATCCTGGCCCA | 4690 |
rs62410402 | snp | A/G | 0.0456336 | 0.143994 | intron-variant | NCK1 | GRCh38.p7 | 3:136871751 | TTGGCAGAACCTGGT[A/G]GGAGGTAATTGAACC | 4690 |
rs62410436 | snp | A/C | 0.426047 | 0.177503 | intron-variant | NCK1 | GRCh38.p7 | 3:136878707 | TGTATCTCAATAAAG[A/C]TATTTTTTTTTAAGA | 4690 |
rs62410437 | snp | C/T | 0 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136886837 | TTTTTTTTTTTTTTC[C/T]TATCTTTCTTTTTCT | 4690 |
rs62410438 | snp | A/G | 0.285257 | 0.247501 | intron-variant | NCK1 | GRCh38.p7 | 3:136889603 | TCTGGCCCCACCCAC[A/G]TGCTGCTGATTGGTA | 4690 |
rs62410439 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136901377 | TCTTTTTTTTTTTAA[A/T]TATTTTTTATTGCAT | 4690 |
rs66507915 | in-del | -/A | 0.415399 | 0.187465 | intron-variant | NCK1 | GRCh38.p7 | 3:136878703 | GAGTTGTATCTCAAT[-/A]AAGCTATTTTTTTTT | 4690 |
rs66522557 | in-del | -/TG | | | intron-variant | NCK1 | GRCh38.p7 | 3:136882548 | ACTTTCCCACATCAC[-/TG]TGTGTGTGTGTGTGT | 4690 |
rs66808197 | snp | A/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136866933 | GCCTAGTCTTTAAAA[A/T]TTTTTTTTTCTCCTA | 4690 |
rs66900682 | in-del | -/G | 0.00517822 | 0.0506191 | intron-variant | NCK1 | GRCh38.p7 | 3:136944111 | AAAAAAAAAAAAAAG[-/G]TTGTTTTTCCTTTTC | 4690 |
rs66911059 | in-del | -/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136894884 | TTTTGTTTTGTTTTT[-/G]TTTTTGAGATGGAGT | 4690 |
rs71134421 | in-del | -/ATTTATTTATTTATTT | 0 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136923595 | CCCCACTGGACAGCC[-/ATTTATTTATTTATTT]ATTTATTTATTTATT | 4690 |
rs71304270 | in-del | -/A | 0.5 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136905024 | CTCCATCTCAAAAAG[-/A]AAAAAAAAAAAAAAA | 4690 |
rs71304271 | in-del | AGCC/GGCCTTTTTTTTTT | 0.5 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136880003 | TGAGCCACTGTGCCC[AGCC/GGCCTTTTTTTTTT]TTTTTTTTTTTTTAA | 4690 |
rs71336084 | snp | C/T | 0.5 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136936129 | CACTGCAACCTCTGC[C/T]TCTTGGGTTCAAGTG | 4690 |
rs71626031 | in-del | -/T | 0.5 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136916501 | TTTCAACATGAGATT[-/T]GGAGAGAACCTTCAA | 4690 |
rs71626032 | in-del | -/A | 0.17654 | 0.238964 | intron-variant | NCK1 | GRCh38.p7 | 3:136918342 | AAAATATTCTGGAAA[-/A]AAAAAATACACTAAT | 4690 |
rs71626034 | in-del | -/C | 0.5 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136944204 | GCTCACTGCAACCTC[-/C]GCCTGCCAGGTTCAA | 4690 |
rs71626035 | in-del | -/C | 0.5 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136944229 | GTTCAAACGATTCTC[-/C]TGCCTCAGCCTCCTG | 4690 |
rs71630059 | snp | A/G | 0.228842 | 0.249103 | intron-variant, upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136862769 | AGGGACGTGGTAGGA[A/G]GAAGGGCGCTCTCAC | 4690 |
rs71630060 | snp | C/G | 0 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136867088 | TTTCTTTCTTTCTTT[C/G]TTTCTTTCTTTCTTT | 4690 |
rs71630061 | snp | C/T | 0 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136867137 | TTCTTTCTTTCTTTC[C/T]TTCTTTCCTTCCTTC | 4690 |
rs71630062 | snp | C/T | 0 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136867141 | TTCTTTCTTTCTTTC[C/T]TTCCTTCCTTCCTTC | 4690 |
rs71637093 | in-del | AAAAAAATAGCT/GAGGTTGTATC | 0.5 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136878705 | CTCAACCTTTCTTAA[AAAAAAATAGCT/GAGGTTGTATC]TTATTGAGATACAAC | 4690 |
rs72234296 | in-del | -/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136884725 | GCCTGAGCTTTTTTT[-/T]TTTTTCTTTTTTTGA | 4690 |
rs72327296 | in-del | -/TTT | | | intron-variant | NCK1 | GRCh38.p7 | 3:136944130 | TTTTTTTTTTTTTTT[-/TTT]TTTTTTGAGACAGAG | 4690 |
rs72448103 | in-del | -/A | | | intron-variant | NCK1 | GRCh38.p7 | 3:136870051 | TTTTTTTTTTTTTTT[-/A]AAAGAATCATCCTGG | 4690 |
rs72630187 | snp | C/T | | | intron-variant, upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136863020 | AGGTTTTGTAACCTT[C/T]CTTCTGTATTAACAT | 4690 |
rs72978714 | snp | C/G | 0.0134174 | 0.0808001 | missense, nc-transcript-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136946128 | AATCCATTAACTTCA[C/G]GTTTGGAACCATCAC | 4690 |
rs72989152 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | NCK1 | GRCh38.p7 | 3:136866097 | ACCAGTGATAACTCT[C/G]TGTTATCTTCAGAGT | 4690 |
rs72989160 | snp | A/G | 0.0460142 | 0.144533 | intron-variant | NCK1 | GRCh38.p7 | 3:136872673 | CGTGGAAGCCTTGGA[A/G]GAAAAAGTGGTTTTG | 4690 |
rs73231937 | snp | A/G | 0.105214 | 0.203807 | intron-variant | NCK1 | GRCh38.p7 | 3:136888356 | CATTAAAAGTATACA[A/G]TTCAGCTTTTAGTAT | 4690 |
rs73231943 | snp | C/T | 0.136506 | 0.222754 | intron-variant | NCK1 | GRCh38.p7 | 3:136902776 | GAAGTCAAACTGTCC[C/T]CCTTTGCTGATGATA | 4690 |
rs73231944 | snp | A/C | 0.127254 | 0.217792 | intron-variant | NCK1 | GRCh38.p7 | 3:136903166 | TTGGAATTGTTAAAT[A/C]CTCCTCCTGAATTTT | 4690 |
rs73231949 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NCK1 | GRCh38.p7 | 3:136913437 | CTATGCCTGCCTAAT[A/G]TTTTATTTTTTGTAG | 4690 |
rs73231951 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136914109 | CTTTAGCCTGACTGC[G/T]GGGAGCAGTGGCCTC | 4690 |
rs73231953 | snp | A/G | 0.128288 | 0.218372 | intron-variant | NCK1 | GRCh38.p7 | 3:136920673 | TCTGAAGATTATTAC[A/G]TTTTATCTAAAGAAA | 4690 |
rs73231958 | snp | A/G | 0.137187 | 0.223099 | intron-variant | NCK1 | GRCh38.p7 | 3:136925436 | CTCCAGTGGCAATAC[A/G]TCTGGCAGAAGTATA | 4690 |
rs73231964 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136932907 | CACTTACTCAGTGAT[A/G]CAGGTGAAGGAAAAA | 4690 |
rs73231966 | snp | A/G | 0.128288 | 0.218372 | intron-variant | NCK1 | GRCh38.p7 | 3:136933292 | AGATATTCTTTAACA[A/G]TGGTATTGAGAAACT | 4690 |
rs73231972 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | NCK1 | GRCh38.p7 | 3:136937379 | GGCTTTGTAGTAAGT[A/T]TTGAAATCAGAAAGG | 4690 |
rs73231973 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | NCK1 | GRCh38.p7 | 3:136938016 | TTTGTCTTTCACCAT[G/T]GAGTGTGATGTCAGC | 4690 |
rs73231974 | snp | A/G | 0.103438 | 0.202533 | intron-variant | NCK1 | GRCh38.p7 | 3:136940999 | ATCATGTTATTTTTA[A/G]TCTATTTACATTTAA | 4690 |
rs73231975 | snp | C/T | 0.136847 | 0.222927 | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136949570 | AAGAGGCCAATCTGC[C/T]TCTGTAGGCTATAGA | 4690 |
rs73864638 | snp | C/G | 0.02016 | 0.0983543 | intron-variant | NCK1 | GRCh38.p7 | 3:136904900 | GCCTTTCTTAATGTT[C/G]TGAGAATCTTTTATC | 4690 |
rs73864640 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | NCK1 | GRCh38.p7 | 3:136928316 | TGGCAGCAGTGTGCA[C/T]AATTGACTTGAAAAG | 4690 |
rs73864641 | snp | G/T | 0.0123036 | 0.0774623 | intron-variant | NCK1 | GRCh38.p7 | 3:136932757 | AACAACTAAGCAGTC[G/T]TAGGTGTGTCATAGG | 4690 |
rs73864642 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136947055 | CTTGGCTTTGCGTGA[A/G]TATATTTGTACAAAA | 4690 |
rs73864644 | snp | A/G | 0.0209421 | 0.100162 | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136950602 | ATAATACTTGAAGTA[A/G]CTTTAAGAACTGAAA | 4690 |
rs74282431 | snp | C/G/T | 0.00755907 | 0.0610114 | intron-variant | NCK1 | GRCh38.p7 | 3:136937300 | TTATTTTAGGACTCT[C/G/T]GATTCTATTTCATTG | 4690 |
rs74499386 | snp | C/G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136867257 | TCCGTCCGTCTGTCT[C/G/T]TCTCTCTCTTTCTTT | 4690 |
rs74593146 | snp | A/G | 0.0165278 | 0.0893908 | intron-variant | NCK1 | GRCh38.p7 | 3:136921028 | GGATATAGTGTCTTT[A/G]AAGAGGTAACTGAGG | 4690 |
rs74736071 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | NCK1 | GRCh38.p7 | 3:136885845 | TTATAGCAACCTTTC[A/G]TAAGAGATATGTTCT | 4690 |
rs74910449 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136910692 | CTTTTCTGGGGTACA[A/G]TGGGATGTTCTGACA | 4690 |
rs75117715 | snp | G/T | 0.5 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136905030 | TTTTTTTTTTCTTTT[G/T]GAGATGGAGTCTCGC | 4690 |
rs75233200 | snp | A/C | 0.5 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136897433 | TTTAACTTGGCTGAA[A/C]TGATATTTCATGTGG | 4690 |
rs75286129 | snp | C/T | 0 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136939842 | ATTTATTGAGGCCTT[C/T]TTTTTTTTTTTTTTT | 4690 |
rs75325304 | snp | C/G | 0.0115144 | 0.0749975 | intron-variant | NCK1 | GRCh38.p7 | 3:136912842 | TTTTTTTTGTAGAAG[C/G]AGGGTCTTGCTGTTT | 4690 |
rs75534883 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | NCK1 | GRCh38.p7 | 3:136916553 | GAATATGCTTACTAG[A/C]AGAGATGACACAATC | 4690 |
rs75535969 | snp | A/T | 0.426047 | 0.177503 | intron-variant | NCK1 | GRCh38.p7 | 3:136878711 | TCTCAATAAAGCTAT[A/T]TTTTTTTAAGAAAGG | 4690 |
rs75608933 | snp | C/T | 0.426047 | 0.177503 | intron-variant | NCK1 | GRCh38.p7 | 3:136878716 | ATAAAGCTATTTTTT[C/T]TTAAGAAAGGTTGAG | 4690 |
rs75645094 | snp | C/T | 0.0341408 | 0.126114 | intron-variant | NCK1 | GRCh38.p7 | 3:136896797 | TAGCACTGTGCCTGG[C/T]CCCATACATCTGTTG | 4690 |
rs75698185 | snp | A/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136931569 | TTTCAGATCTTTGCA[A/T]TTTTCATTTTTTGGG | 4690 |
rs75725949 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | NCK1 | GRCh38.p7 | 3:136906960 | GGCTCCCCACTGGTA[C/T]GTGCAGGTACTGGCT | 4690 |
rs75755018 | in-del | -/TTT | | | intron-variant | NCK1 | GRCh38.p7 | 3:136912504 | AGTCTTTTTTTTTTT[-/TTT]ATGTTGCCCTATCAT | 4690 |
rs75774739 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | NCK1 | GRCh38.p7 | 3:136913510 | TAGGCTCAAGCAGTC[C/G]TCCCGCTTTGGCCTC | 4690 |
rs75865690 | snp | C/T | 0 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136939843 | TTTATTGAGGCCTTT[C/T]TTTTTTTTTTTTTTT | 4690 |
rs75887337 | snp | G/T | 0 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136907293 | GTGGAGAATGTCAAT[G/T]GGGTCTCCAGGGATG | 4690 |
rs75895552 | snp | C/T | 0.426047 | 0.177503 | intron-variant | NCK1 | GRCh38.p7 | 3:136878714 | CAATAAAGCTATTTT[C/T]TTTTAAGAAAGGTTG | 4690 |
rs75981857 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NCK1 | GRCh38.p7 | 3:136907335 | GGTCTGTTGGGTTCC[C/T]GGGCATGACAAAGTC | 4690 |
rs76028950 | snp | A/G | 0.5 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136897271 | TTTTTTGTATTTTTA[A/G]TAGAGATGGGGTTTT | 4690 |
rs76136200 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136912873 | CCCAAACTGGTCTTG[A/G]TCTTGATATCCTGGA | 4690 |
rs76148091 | snp | A/T | 0.0941369 | 0.195465 | intron-variant | NCK1 | GRCh38.p7 | 3:136869082 | ATCTCTACTAAAGAT[A/T]TAAAAAAATGAGCCC | 4690 |
rs76228243 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | NCK1 | GRCh38.p7 | 3:136898461 | TTCCACTTTTATTAA[A/G]GGTTTTGACAATGAA | 4690 |
rs76304742 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | NCK1 | GRCh38.p7 | 3:136925919 | TGTCAGACAATTTTG[C/T]GGAGTATCTGTACCA | 4690 |
rs76316086 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | NCK1 | GRCh38.p7 | 3:136938110 | TGAGCATTGTTATCA[A/T]GAAACGGTTTTGGAT | 4690 |
rs76411022 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | NCK1 | GRCh38.p7 | 3:136910427 | TTACAATTATTCTAG[C/T]TTTTAGAGTAATGTT | 4690 |
rs76435291 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136888796 | TCTGAACCTTTCATA[C/T]ACATGGAATCATATA | 4690 |
rs76435680 | snp | C/T | 0.5 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136899420 | CCTTCATTTCTTTTC[C/T]TTTTTTTTTTTTTAA | 4690 |
rs76489751 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | NCK1 | GRCh38.p7 | 3:136883997 | ATTGATGCATATTCA[A/G]TTTGAGGTGATAGCA | 4690 |
rs76501504 | snp | A/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136912920 | GCCTCAGCCTCCTAA[A/T]ATACAAGGATTACAG | 4690 |
rs76657771 | in-del | -/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136905429 | GAATTCTCTTGTATC[-/T]TTTTTTTTTTGAGAC | 4690 |
rs76674445 | snp | A/C | 0.02016 | 0.0983543 | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136949227 | GTTATTTATTTTTTT[A/C]ATCCCACTTGTATTA | 4690 |
rs77024879 | snp | A/T | 0 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136912504 | AGTCTTTTTTTTTTT[A/T]TTATGTTGCCCTATC | 4690 |
rs77037303 | snp | A/T | 0 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136871250 | AAGTAAAAAAAAAAA[A/T]TTAGCCAGGTTTGGC | 4690 |
rs77203258 | snp | C/T | 0.0554779 | 0.157039 | intron-variant | NCK1 | GRCh38.p7 | 3:136938517 | TTTGTGCAGTCTATT[C/T]AGTACCACATTTTTT | 4690 |
rs77230467 | snp | C/T | 0.5 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136903250 | TAAAGTTTGTTTTGT[C/T]TGATACAAGTATAGC | 4690 |
rs77239893 | snp | A/G | 0.5 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136931019 | GCTTACTTTTTTTTT[A/G]GCGGAACAGTGTAAA | 4690 |
rs77277219 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | NCK1 | GRCh38.p7 | 3:136940126 | CCTTGGACTCCCAAA[A/G]TGTTGGAATTACAGG | 4690 |
rs77366837 | snp | G/T | 0.0154538 | 0.0865337 | intron-variant | NCK1 | GRCh38.p7 | 3:136881990 | TTTCCATGAACATGG[G/T]TGTAGAAATATCTGT | 4690 |
rs77385657 | snp | A/C | 0.00398564 | 0.0444627 | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136951324 | TTGTTGCTGGGGTAC[A/C]TTCTTCAGGGTACAT | 4690 |
rs77618629 | snp | C/T | 0.0221141 | 0.102801 | upstream-variant-2KB, intron-variant | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136860881 | CACAGGCCAACCACA[C/T]GCATGCATTACCAAT | 4690 |
rs77761631 | snp | G/T | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136951999 | GATTTGGTTGGGTAT[G/T]ACAATAATTACCCAA | 4690 |
rs77794689 | snp | C/T | 0 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136905022 | CTTTTTTTTTTTTTT[C/T]TTCTTTTTGAGATGG | 4690 |
rs77846786 | snp | A/C | 0.0232847 | 0.105357 | intron-variant | NCK1 | GRCh38.p7 | 3:136878848 | CACAATTGGAGGTCA[A/C]GCGTTCTACAGAAAA | 4690 |
rs77980724 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136946787 | ATTGGAATGCACTTT[C/T]ATTATAACCTCAAAA | 4690 |
rs77994069 | snp | A/G | 0.0165278 | 0.0893908 | intron-variant | NCK1 | GRCh38.p7 | 3:136933257 | CAAATAAAACATGAT[A/G]TAATTAATCCACTTT | 4690 |
rs78047947 | in-del | -/TTCTT | | | intron-variant | NCK1 | GRCh38.p7 | 3:136870364 | AAAAAATTCATCCTT[-/TTCTT]CCAAAAATTTTAGCA | 4690 |
rs78078379 | snp | G/T | 0.0391387 | 0.134304 | intron-variant | NCK1 | GRCh38.p7 | 3:136871063 | CTTTTGATTAATTCC[G/T]GTTGTGGATCCAACT | 4690 |
rs78255371 | snp | A/T | 0.426047 | 0.177503 | intron-variant | NCK1 | GRCh38.p7 | 3:136878712 | CTCAATAAAGCTATT[A/T]TTTTTTAAGAAAGGT | 4690 |
rs78389625 | snp | G/T | 0.5 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136907292 | GGTGGAGAATGTCAA[G/T]GGGGTCTCCAGGGAT | 4690 |
rs78399442 | snp | C/T | 0.5 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136917232 | TTAAAACATTATGAG[C/T]TTTTTTTTTTTTTTT | 4690 |
rs78400334 | in-del | -/TTT | | | intron-variant | NCK1 | GRCh38.p7 | 3:136921526 | CTTAGTGCCTTTGTG[-/TTT]ATGCTTCTTTGGATA | 4690 |
rs78540600 | snp | C/T | 0.5 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136869444 | CAGCTACTCAAGAGG[C/T]TGAGACAGGAGAATC | 4690 |
rs78568074 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | NCK1 | GRCh38.p7 | 3:136881467 | TCATGATCTGCCCGC[C/T]TCGGCCTCCCAAGTG | 4690 |
rs78590282 | snp | A/C | 0.5 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136880284 | AGCGAGACTCCGTCT[A/C]AAAAAAAAAAAAAGA | 4690 |
rs78597065 | snp | C/G | 0.0329836 | 0.124112 | intron-variant | NCK1 | GRCh38.p7 | 3:136877476 | GTGTATAGAGCCATG[C/G]TTAGAGGAAGAGTTA | 4690 |
rs78671869 | snp | A/C | | | intron-variant | NCK1 | GRCh38.p7 | 3:136879131 | GAACAATCAGAACAA[A/C]AAAAAAAAAGGCTCA | 4690 |
rs78676139 | snp | G/T | 0.0146672 | 0.084371 | intron-variant | NCK1 | GRCh38.p7 | 3:136898120 | GTGGCTGTTGGTGGG[G/T]TGCAGTGGCTCACAC | 4690 |
rs78772556 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136909479 | CTAAGAGCTTGCTCT[C/G/T]AGAGACAATTATTTA | 4690 |
rs78856468 | snp | A/C | 0.5 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136880285 | GCGAGACTCCGTCTC[A/C]AAAAAAAAAAAAGAA | 4690 |
rs78938153 | snp | C/G | 0.0165278 | 0.0893908 | intron-variant | NCK1 | GRCh38.p7 | 3:136896367 | TCTTTTAAACCCACT[C/G]AATGAGTTAGAACAT | 4690 |
rs79151895 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | NCK1 | GRCh38.p7 | 3:136910365 | TTTGGTTATTTTATG[C/T]ATTTGTCTCTTATGT | 4690 |
rs79249447 | snp | C/T | 0 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136886835 | TTTTTTTTTTTTTTT[C/T]CCTATCTTTCTTTTT | 4690 |
rs79250161 | snp | A/G | 0.5 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136903225 | TTGTCTCTTTTTACT[A/G]TTTTTGACTTAAAGT | 4690 |
rs79263981 | snp | C/T | 0.426047 | 0.177503 | intron-variant | NCK1 | GRCh38.p7 | 3:136878713 | TCAATAAAGCTATTT[C/T]TTTTTAAGAAAGGTT | 4690 |
rs79380768 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136922139 | GGCCATCTGGGTTTG[C/T]TATTGGCATTTATCT | 4690 |
rs79427190 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | NCK1 | GRCh38.p7 | 3:136903368 | AGTTTATTGTAGGTA[A/G]TATATAGGTGGGTCA | 4690 |
rs79440984 | snp | C/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136892125 | ACTTTTAGCCTCAAG[C/G]GATCCTCCTGTCTCA | 4690 |
rs79462568 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | NCK1 | GRCh38.p7 | 3:136893655 | AGTCCCATCTCTTTA[C/T]CTTTGTTTTTGAGGC | 4690 |
rs79593743 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | NCK1 | GRCh38.p7 | 3:136921042 | TAAAGAGGTAACTGA[A/G]GTAAAATGAGGTCGT | 4690 |
rs79668617 | in-del | -/TGGTCT | 0.436834 | 0.166111 | intron-variant | NCK1 | GRCh38.p7 | 3:136912865 | TGCTGTTTCCCAAAC[-/TGGTCT]TGGTCTTGATATCCT | 4690 |
rs79750596 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | NCK1 | GRCh38.p7 | 3:136930768 | AAATTGTAGTTTCGA[C/T]TTGGTAAGTAAAATA | 4690 |
rs79906627 | in-del | -/TT | | | intron-variant | NCK1 | GRCh38.p7 | 3:136930991 | TTAACTTTTTTTTTT[-/TT]AACTACTTTTTGCTT | 4690 |
rs79929954 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | NCK1 | GRCh38.p7 | 3:136904906 | CTTAATGTTCTGAGA[A/G]TCTTTTATCTGCTTA | 4690 |
rs79989361 | snp | A/T | 0.0752113 | 0.178743 | intron-variant | NCK1 | GRCh38.p7 | 3:136864708 | TTAAAAAGGAAAATA[A/T]TAAAGAAAAGAGATA | 4690 |
rs80135728 | snp | A/T | 0 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136871252 | GTAAAAAAAAAAAAT[A/T]AGCCAGGTTTGGCTG | 4690 |
rs80201571 | snp | G/T | 0.241914 | 0.249869 | intron-variant | NCK1 | GRCh38.p7 | 3:136940937 | TTTTCAAACCTATTT[G/T]CATCTTTGTTTGGAT | 4690 |
rs80346532 | snp | C/G | 0.5 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136916087 | GAACAACAGCTATCA[C/G]AGAACAACAAGGGGG | 4690 |
rs111257889 | snp | C/T | 0.5 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136916092 | ACAGCTATCACAGAA[C/T]AACAAGGGGGGAAAT | 4690 |
rs111267708 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136875043 | CGTCTATTTTTAACA[A/C]TTTTTCTTGGATATT | 4690 |
rs111280881 | snp | C/G | 0.5 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136940495 | ACTTCTTGATGGACT[C/G]ATTCTTTTATCAATA | 4690 |
rs111286586 | snp | G/T | 0.5 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136902198 | TGTTTTTTTTTTTTT[G/T]TTTTGTTTTTGTTTT | 4690 |
rs111290259 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136908233 | CCGTATCACTTCGTC[A/G]TATTAACATTCCTTC | 4690 |
rs111356566 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | NCK1 | GRCh38.p7 | 3:136871882 | TCTTATCTGCCGCCA[C/T]GTGAGAAGACATGCC | 4690 |
rs111361438 | in-del | -/G | 0 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136912181 | TTTTTTTTTTTTTTT[-/G]AGACCGAGTCTCGCT | 4690 |
rs111393181 | in-del | -/A | 0.5 | 0 | intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136947315 | GCTTTGGGGGTTGAT[-/A]ATAGACTGTAACAAC | 4690 |
rs111420281 | snp | A/T | 0.5 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136878023 | CATGTTATAACATGA[A/T]GAACCTTGAAAGCAT | 4690 |
rs111443780 | snp | A/G | 0.5 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136908030 | ATCTTAGTAGTGATG[A/G]TGTTTCTGAAAGTCC | 4690 |
rs111457267 | snp | C/G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136862024 | TCTCACCCTCTAGCT[C/G/T]TCTACTCTCCGCCGC | 4690 |
rs111530852 | snp | A/C/G | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136862760 | CGGGAAGGTAGGGAC[A/C/G]TGGTAGGAGGAAGGG | 4690 |
rs111575333 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136866617 | TGGCCTCTTTCTTTC[C/T]TCTTTTTTTTTTTCT | 4690 |
rs111616017 | snp | A/G | 0.5 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136889335 | AAGGTGGCGCGTCTG[A/G]AGTTTGCTCCTTCTG | 4690 |
rs111695432 | in-del | -/T | 0 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136919215 | CAAAGCATAAAGCAA[-/T]TTTTTTTTTTTCTTG | 4690 |
rs111705120 | snp | C/T | 0.5 | 0 | missense, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136948271 | TAGCCAAATGATTTC[C/T]CAGTATCACTAAAAG | 4690 |
rs111780498 | snp | C/T | 0.5 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136867911 | GGGAACCTTCATATT[C/T]ACATTGTAAATTTTT | 4690 |
rs111805981 | snp | A/C | 0.5 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136896785 | GGATTACAGACCTAG[A/C]ACTGTGCCTGGCCCC | 4690 |
rs111822124 | snp | C/T | 0.5 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136894395 | CATTGGTTCAGTGCA[C/T]ATGCTGCATCCCAAA | 4690 |
rs111827556 | snp | A/C | 0.5 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136884565 | TGTGCCTCAGCCTCC[A/C]GAGTAGCTGGGATTA | 4690 |
rs111836974 | in-del | -/T | 0.5 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136888408 | ACCACAATATCAGAA[-/T]TTTTTTTTTTTTTGA | 4690 |
rs112010439 | snp | A/G | 0.5 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136917062 | TTATCAAATGTATTC[A/G]TATGTAATATGTAAA | 4690 |
rs112070687 | snp | C/T | 0.5 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136867206 | TTCTTTCTTTTCCCT[C/T]CCTTCCTTCCTTCCT | 4690 |
rs112071500 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136944308 | ATTTTTAGTAGAGAC[A/G]GGGTTTCACCATGTT | 4690 |
rs112127394 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136866594 | TTACAGGTGTGAGCC[A/G]CTGTGCCTGGCCTCT | 4690 |
rs112152180 | in-del | -/G | 0.5 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136902191 | ACTCTTTGTTTTTTT[-/G]TTTTTTTTTTTGTTT | 4690 |
rs112238516 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136872730 | TGTGCAGCCTAGGGA[-/C]CTTGGTACCCAGCAT | 4690 |
rs112274928 | snp | A/C | 0.5 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136879735 | TGAAGCTGGAAGCCA[A/C]CATTCTCAGCAAAAT | 4690 |
rs112302738 | snp | C/T | 0.5 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136910772 | ACCTTGTTTACATAT[C/T]ATTTTCATAACGAGA | 4690 |
rs112330514 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136862933 | TGCTTCAGATTCGTA[C/G]GCGAGTTGCTGGGGC | 4690 |
rs112373633 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136861186 | GGAGCGATCCTAAAC[C/T]GTGCCACAAAGATGG | 4690 |
rs112398153 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136947247 | ATCCATTTTCTGTTA[A/G]TTGCCTGATCTGGCT | 4690 |
rs112400015 | snp | C/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | NCK1 | GRCh38.p7 | 3:136929496 | TTTTGTGATTAAGAC[C/T]ATTATTTTTAGTTTT | 4690 |
rs112404238 | snp | A/G | 0.5 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136895708 | TAGCTGGGATTACAG[A/G]TGCGTACCACCACAC | 4690 |
rs112489940 | snp | C/T | 0.5 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136899733 | CTCACTGTTTCTGTT[C/T]TACTATTGCCATGTT | 4690 |
rs112492704 | in-del | -/T | 0.5 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136888120 | TGGCTAATTTTTGTA[-/T]TTTTAGTAGAGACAG | 4690 |
rs112504828 | snp | C/T | 0.5 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136888653 | GCGAGCCACCGCACC[C/T]AGCCATATTGGAACA | 4690 |
rs112515324 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | NCK1 | GRCh38.p7 | 3:136867865 | ATTTTGTGTATTTAT[A/G]CCTTCTCATAGATTG | 4690 |
rs112564204 | snp | C/T | 0.5 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136867205 | TTTCTTTCTTTTCCC[C/T]TCCTTCCTTCCTTCC | 4690 |
rs112579751 | snp | A/G | 0.5 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136908974 | CTCATGAATGAATTA[A/G]TGCTGTTATTTTAGG | 4690 |
rs112598686 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NCK1 | GRCh38.p7 | 3:136924791 | GTTCCATTATTGGAA[C/T]GCTAAGCTTGTGAGA | 4690 |
rs112614905 | snp | A/G | 0.5 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136940461 | TCTTGTTAGGTATGC[A/G]TATATTTGTAACTGT | 4690 |
rs112650061 | snp | C/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136944231 | TCAAACGATTCTCCT[C/G]CCTCAGCCTCCTGAG | 4690 |
rs112652285 | snp | A/T | 0.5 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136878022 | ACATGTTATAACATG[A/T]TGAACCTTGAAAGCA | 4690 |
rs112690301 | snp | A/G | 0.5 | 0 | upstream-variant-2KB, intron-variant | NCK1 | GRCh38.p7 | 3:136928966 | AAACATGCTATTTGC[A/G]TAATTGTTCTTTGTC | 4690 |
rs112771971 | snp | C/G | 0.5 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136913491 | CAAGCTTGTCTAGAA[C/G]TCCTAGGCTCAAGCA | 4690 |
rs112802242 | in-del | -/TT | 0.434543 | 0.168653 | intron-variant | NCK1 | GRCh38.p7 | 3:136912493 | GACTTTTCTTCAGTC[-/TT]TTTTTTTTTTTTATG | 4690 |
rs112802263 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136913761 | GCAAGCTCCGCCTCC[C/T]GGGTTCACGCCATTC | 4690 |
rs112821333 | snp | A/C/G | 0.5 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136867948 | TTGAGACAGAGTTTC[A/C/G]CAGTTTTTGCCCTGG | 4690 |
rs112842166 | in-del | -/T | 0.5 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136901363 | CTGTAGTTTTCTTTC[-/T]TTTTTTTTTTTAAAT | 4690 |
rs112842913 | snp | A/C | 0.5 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136904257 | TCCTGGGTTCAAGTG[A/C]TTCTTCTACTTTGGC | 4690 |
rs112861326 | snp | A/C | 0.5 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136898015 | TTACTATTTGAAGAA[A/C]CAGCTTTCCCTTGTT | 4690 |
rs112872475 | snp | G/T | 0.5 | 0 | downstream-variant-500B, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136951831 | AGGTAAAACCAGTCT[G/T]AGAGTCACAGCAGGT | 4690 |
rs112873040 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NCK1 | GRCh38.p7 | 3:136942463 | TTTTAACAGAGTTTC[A/G]TTAAACACCTGGAGC | 4690 |
rs112938881 | snp | A/C | 0.5 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136875145 | ATTAGTCTTTGAGGA[A/C]TGTCATAACAATACC | 4690 |
rs112945974 | snp | A/T | 0.5 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136937862 | TTTAGGATTTTCTAT[A/T]TATAAGATCATGTCA | 4690 |
rs112950440 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136937953 | ATAAAAGTGGTGGAA[A/G]GAGAGCATCCTTGTT | 4690 |
rs113020982 | snp | C/T | 0.5 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136890297 | TGCTCTGAGTGCGTG[C/T]GGGGCCTGCCAAGCC | 4690 |
rs113064503 | snp | C/T | 0.5 | 0 | intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136947895 | AGACTTTCTCATGTG[C/T]TTCTCTGACTGGAGA | 4690 |
rs113119341 | snp | C/T | 0.5 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136926337 | TGGAGTGCAGTGGCG[C/T]GATCTCGGCTCACTG | 4690 |
rs113123946 | snp | A/G | 0.5 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136903039 | CATTTAATGCTCACA[A/G]TGGGGTGCTGGTGTC | 4690 |
rs113125796 | snp | A/G | 0.5 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136868648 | TTACCATTGAATTCT[A/G]TCATCTGCTAAAAAA | 4690 |
rs113175028 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136861305 | AGAGATCGAGACCAT[C/T]CTGGTGAAACCCCGT | 4690 |
rs113179802 | snp | C/T | 0.5 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136896758 | CTCCTGCCTCGGCCT[C/T]CCAGAGTGCTAGGAT | 4690 |
rs113224918 | snp | A/C | 0.00557542 | 0.0525036 | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136949399 | GGTATTACCTATTTT[A/C]ATTTCCTCTTTTCAG | 4690 |
rs113253727 | snp | A/G | 0.5 | 0 | synonymous-codon, downstream-variant-500B | NCK1, LOC107986136 | GRCh38.p7 | 3:136945599 | CATTGGAAAAGTGAA[A/G]AGAAAACCTAGTGTG | 4690 |
rs113257107 | snp | C/G | 0.5 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136932627 | TACAAGCCATGTGGC[C/G]TGCAAAATATAACTG | 4690 |
rs113257941 | snp | A/G | 0.5 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136908846 | AGTGGGATATATACA[A/G]TATAGTGCTGTGGTT | 4690 |
rs113286574 | snp | C/T | 0.5 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136876779 | TACAGTGAGAATTTA[C/T]GAATCAGTGTAACTG | 4690 |
rs113292224 | snp | C/T | 0.5 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136887943 | TTTCTTTCTTTCTTT[C/T]TTTTTTTTTTTTTCT | 4690 |
rs113314410 | snp | A/C/G | 0.00398564 | 0.0444627 | intron-variant | NCK1 | GRCh38.p7 | 3:136906468 | CTCTCAGGCCCCAGT[A/C/G]GTGGCACCAGTGGGT | 4690 |
rs113326489 | in-del | -/A | 0.5 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136896487 | TATTTTTTAATGGCC[-/A]AATAGTATCCCATTG | 4690 |
rs113401275 | in-del | -/T | 0.5 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136878710 | ATCTCAATAAAGCTA[-/T]TTTTTTTTAAGAAAG | 4690 |
rs113437274 | snp | A/C | 0.5 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136910963 | AAGCATCATTCTACT[A/C]TCTACTTCTATGAGT | 4690 |
rs113439661 | snp | G/T | 0.5 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136943041 | TCACTGACTTGGGGT[G/T]TGGGGGATGGTGGGC | 4690 |
rs113450427 | snp | A/T | | | intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136946682 | TGGATGCAATGTGTA[A/T]GAAGGTAGTCACTGT | 4690 |
rs113455044 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136873267 | CCTGGATGTGAGACA[C/T]GGAGTCAAAGGAGAT | 4690 |
rs113456817 | snp | C/G | | | intron-variant, upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136862661 | GCCCGTGCGAGCCTG[C/G]GAGGTCGAGTGTGCG | 4690 |
rs113547894 | in-del | -/TTTA | 0.5 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136893722 | AGATTGGCTTAAACC[-/TTTA]CTACATTGATTCTAA | 4690 |
rs113576894 | snp | C/T | 0.5 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136870202 | CAAAATTTAGCTGGG[C/T]GTGGTGGTGCATGCC | 4690 |
rs113617983 | snp | C/G | 0.5 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136925430 | GCTTTCCTCCAGTGG[C/G]AATACATCTGGCAGA | 4690 |
rs113688514 | snp | A/G | 0.5 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136898934 | AATCATAAAATGGCT[A/G]GAGATCATTTATAGG | 4690 |
rs113712094 | snp | A/G | 0.5 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136905056 | CTCGCTCTGTTTCCC[A/G]GGCTAGAGTGCTATG | 4690 |
rs113770851 | snp | C/T | 0.5 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136913066 | CACCTTTAAGGTAGC[C/T]TTTTAAAAGTCTTTG | 4690 |
rs113803413 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136894883 | TGTTTTGTTTTGTTT[G/T]TTTTTTGAGATGGAG | 4690 |
rs113828837 | snp | A/G | 0.5 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136864649 | AGATCAGCCTAAGCA[A/G]TGTAGTGATACCCTG | 4690 |
rs113839511 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136920493 | AAAAGTTTGCTCTTA[A/G]AAAAACCTCAACTAT | 4690 |
rs113846374 | in-del | -/T/TT | 0.346368 | 0.23068 | intron-variant | NCK1 | GRCh38.p7 | 3:136884718 | AGCTTTTTTTTTTTT[-/T/TT]CTTTTTTTGAGAGGG | 4690 |
rs113863392 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | NCK1 | GRCh38.p7 | 3:136916587 | ACCTTATTAATAATG[C/T]AAAGCATGGGGAAAT | 4690 |
rs113910009 | snp | A/T | 0.5 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136867906 | GGCAGGGGAACCTTC[A/T]TATTTACATTGTAAA | 4690 |
rs113934076 | in-del | -/T | 0.5 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136921785 | GGGAAAGAAAGATGG[-/T]TTTTTTTGTTTTGTT | 4690 |
rs114008348 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | NCK1 | GRCh38.p7 | 3:136864668 | AGTGATACCCTGTCT[C/T]TAAATTAAGAAAATA | 4690 |
rs114010848 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | NCK1 | GRCh38.p7 | 3:136945216 | GACAAGAAGAGTATG[A/G]GTGTGGTGGAGCCTT | 4690 |
rs114031271 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | NCK1 | GRCh38.p7 | 3:136887319 | ACTACAGGAGTGCAC[C/T]GCCATGCTCAGCATT | 4690 |
rs114074681 | snp | C/T | 0.0379877 | 0.132479 | intron-variant | NCK1 | GRCh38.p7 | 3:136904481 | TTGAATATATCATTT[C/T]ATTCTCTACTGGCCT | 4690 |
rs114081694 | snp | C/G | 0.0115144 | 0.0749975 | intron-variant | NCK1 | GRCh38.p7 | 3:136876513 | ACCATACTTTGTTTT[C/G]TAGCTTGGCTTTTAT | 4690 |
rs114163297 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | NCK1 | GRCh38.p7 | 3:136884117 | AAGTCATAATAATGA[A/G]CGAGCTATCTAGAGA | 4690 |
rs114214625 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136919955 | GTAACAATACCCAAG[C/T]GACTAAGTCCGGAAG | 4690 |
rs114235856 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | NCK1 | GRCh38.p7 | 3:136895215 | TGTGATAAACAGTTT[C/T]CACTTTAACGTAGTC | 4690 |
rs114273910 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | NCK1 | GRCh38.p7 | 3:136902627 | AATGTTCTATATGCT[A/G]ATGAAAAGAATGTGT | 4690 |
rs114283829 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | NCK1 | GRCh38.p7 | 3:136936774 | TTGGCCATTCGTATA[C/T]CGTAGTTGGAACAAT | 4690 |
rs114284347 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | NCK1 | GRCh38.p7 | 3:136869502 | GGGTTGTGAGATCCC[A/G]CCACTGCACTTTAGC | 4690 |
rs114289796 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | NCK1 | GRCh38.p7 | 3:136907373 | GGCTGGGCTCTCAAA[A/G]TGAAGGTACACTGTA | 4690 |
rs114383431 | snp | C/T | 0.0429648 | 0.14013 | intron-variant | NCK1 | GRCh38.p7 | 3:136903624 | GAGATGGGGTTTCAC[C/T]GTGTAGGCCAGCCTG | 4690 |
rs114535131 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | NCK1 | GRCh38.p7 | 3:136944448 | TAAAAGAGTGGTATA[A/G]TTTATTCTATAGGAA | 4690 |
rs114585067 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NCK1 | GRCh38.p7 | 3:136900397 | TTGCTTAAGATTGTT[C/T]TGGTTGTTTGGGCTC | 4690 |
rs114598567 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | NCK1 | GRCh38.p7 | 3:136869019 | GAGGCATGCGGAGCC[C/T]CTGAGTCCAGGAGTT | 4690 |
rs114626378 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | NCK1 | GRCh38.p7 | 3:136899718 | ATACGAGGAGACTTA[C/T]TCACTGTTTCTGTTC | 4690 |
rs114689665 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | NCK1 | GRCh38.p7 | 3:136884555 | AGGCGATTCTTGTGC[C/T]TCAGCCTCCAGAGTA | 4690 |
rs114728626 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | NCK1 | GRCh38.p7 | 3:136905952 | TTGGGATGTATTGCC[C/T]GTGAATTATTGTGGT | 4690 |
rs114839326 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | NCK1 | GRCh38.p7 | 3:136922234 | TGGCCCTTACCCTCT[C/T]GCCAGGGACTGGGAA | 4690 |
rs114877229 | snp | C/T | 0.039522 | 0.134904 | intron-variant | NCK1 | GRCh38.p7 | 3:136894944 | GTGGCACTACTATCT[C/T]GGCTCACTGCAACCT | 4690 |
rs114937038 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | NCK1 | GRCh38.p7 | 3:136891087 | CCCGACCAAAGGCTG[A/G]TACTGTTCCGTTGAA | 4690 |
rs115102371 | snp | C/T | 0.0341408 | 0.126114 | intron-variant | NCK1 | GRCh38.p7 | 3:136871823 | TAGGTCTTGTGGGAT[C/T]TGATGGTTTTAAAAA | 4690 |
rs115181303 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | NCK1 | GRCh38.p7 | 3:136877646 | TAGAAGATTTGAACT[A/G]CACAGGTAAAGAGAA | 4690 |
rs115192548 | snp | C/G | 0.0193772 | 0.0965046 | intron-variant | NCK1 | GRCh38.p7 | 3:136869675 | AACCATGTATGGTTG[C/G]TTTCGTATTTTTCTT | 4690 |
rs115290401 | snp | A/G | 0.0460142 | 0.144533 | intron-variant | NCK1 | GRCh38.p7 | 3:136893130 | TTGTTTCTTTTTATG[A/G]CTAAGTAATATTCCA | 4690 |
rs115318335 | snp | A/G | 0.00438332 | 0.0466095 | downstream-variant-500B, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136951914 | TAAGTAGCTGGGCTT[A/G]TGGAAAACTGAGTTC | 4690 |
rs115430495 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | NCK1 | GRCh38.p7 | 3:136912717 | TGGCTGTGTGATCAC[A/G]GTTCATGGGCTCACT | 4690 |
rs115432423 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136882865 | CAGTCATTAGTGAAT[A/G]CTAGCAGTCTCTTTC | 4690 |
rs115512642 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NCK1 | GRCh38.p7 | 3:136922388 | TTCAAGCTTTCTAAG[A/G]TAACTGCTCTAAATG | 4690 |
rs115565006 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | NCK1 | GRCh38.p7 | 3:136920459 | AGAGCAAAGGAATGA[A/G]AATAAAGAAAGATAA | 4690 |
rs115624759 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | NCK1 | GRCh38.p7 | 3:136927320 | ATGTTAAAAATTGTC[C/T]TCTGTGGTAATGGGT | 4690 |
rs115633136 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NCK1 | GRCh38.p7 | 3:136865725 | ATTCTCTATAAATAC[C/T]GTGATGTTAGGAAGA | 4690 |
rs115751655 | snp | G/T | 0.0150606 | 0.0854603 | upstream-variant-2KB, nc-transcript-variant | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136862055 | GCAGCCTCCGCTCCC[G/T]CCACATCAGGCACGG | 4690 |
rs115807813 | snp | A/G/T | 0.00438476 | 0.0466401 | intron-variant | NCK1 | GRCh38.p7 | 3:136880321 | CCTTATTTCGAAGTG[A/G/T]GGTCTTTACAGAGGT | 4690 |
rs115812509 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | NCK1 | GRCh38.p7 | 3:136918885 | TTTTCACTAATGACC[A/G]TGTAACCATGTGAGT | 4690 |
rs115872662 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | NCK1 | GRCh38.p7 | 3:136939012 | GAGTTAATAAGTATT[C/G]TCTCCTTTTTTCTTT | 4690 |
rs115975228 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | NCK1 | GRCh38.p7 | 3:136865778 | TAAAGATTTAAGGAA[A/G]CTTTATGTCTGGCTG | 4690 |
rs115994441 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant, upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136863817 | TTGTTCGATACTGAG[A/G]GAGTCCAGGCGGGGT | 4690 |
rs115995074 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | NCK1 | GRCh38.p7 | 3:136898448 | CATTTCAAAACATTT[C/T]CACTTTTATTAAAGG | 4690 |
rs116048087 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136865877 | ACTTTGTTTTGGTGA[C/T]ATTACCATGCTTTCA | 4690 |
rs116092875 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | NCK1 | GRCh38.p7 | 3:136899600 | TTTCCTCTGTTGTAC[C/T]GCAGCTTTAGATGCT | 4690 |
rs116168197 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NCK1 | GRCh38.p7 | 3:136915458 | CTTTTATACCCAGGA[C/T]TTTTAAGTAAGAATG | 4690 |
rs116225681 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | NCK1 | GRCh38.p7 | 3:136899035 | TTGTAAAGCTGTGCT[G/T]CTTTCAGCCAAACAT | 4690 |
rs116308064 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NCK1 | GRCh38.p7 | 3:136914752 | TTGAAATTGGGAGAT[C/T]GCTTGCTATGGTTTG | 4690 |
rs116368693 | snp | C/T | 0.00676609 | 0.0577691 | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136951353 | ATCTAAACACAGTGG[C/T]CTTATACAGAAATGT | 4690 |
rs116508331 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | NCK1 | GRCh38.p7 | 3:136938578 | TTTAAAATGGCCCCC[A/G]AGCATAGTGATGAAG | 4690 |
rs116600436 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | NCK1 | GRCh38.p7 | 3:136874942 | GTCTGAAGACATTCT[C/G]ATTCTTGATTGTAAA | 4690 |
rs116612179 | snp | A/G | 0.0165278 | 0.0893908 | intron-variant | NCK1 | GRCh38.p7 | 3:136934850 | GGAGTCGGTTAAGCA[A/G]TGGGTTAGAAGGGTT | 4690 |
rs116716680 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | NCK1 | GRCh38.p7 | 3:136907128 | GGGTCACATACTTTG[C/T]TTGTGCCTTGCTCCT | 4690 |
rs116762761 | snp | A/C | 0.0162398 | 0.0886349 | intron-variant | NCK1 | GRCh38.p7 | 3:136894429 | CCAGCAGAATGACTT[A/C]TTAATCGAGCTTTTA | 4690 |
rs116805887 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136934229 | GGGTTGGGGGTACAT[A/G]TGAAGGTTTGTTACA | 4690 |
rs117046628 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136910347 | GCTCCATCCCTACCC[C/G/T]CTTTTGGTTATTTTA | 4690 |
rs117129740 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | NCK1 | GRCh38.p7 | 3:136892314 | CCTTTTCACTGTATT[A/G]ATTTAGTGTCCTTTC | 4690 |
rs117617505 | snp | G/T | 0.0154538 | 0.0865337 | intron-variant | NCK1 | GRCh38.p7 | 3:136865482 | CATGTGTTTTTCAAA[G/T]CTGAAGGTATATTTG | 4690 |
rs117828563 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | NCK1 | GRCh38.p7 | 3:136892917 | CAACCATCACCCAAC[A/G]GCAATGTACACTGTA | 4690 |
rs117980379 | snp | A/G | 0.0165278 | 0.0893908 | intron-variant | NCK1 | GRCh38.p7 | 3:136870864 | GGCTCCTTTAGGTTA[A/G]TCAGCATTAAGTTTG | 4690 |
rs137869556 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136865841 | TTATAGTCTTCCCTT[C/G]AAAACTGATTCCATA | 4690 |
rs137906345 | snp | C/G | 0.0115144 | 0.0749975 | upstream-variant-2KB, nc-transcript-variant | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136862035 | AGCTCTCTACTCTCC[C/G]CCGCGCAGCCTCCGC | 4690 |
rs137919410 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NCK1 | GRCh38.p7 | 3:136910344 | ACAGCTCCATCCCTA[C/T]CCCCTTTTGGTTATT | 4690 |
rs137920757 | snp | C/T | 0.00126377 | 0.0251056 | intron-variant, downstream-variant-500B | NCK1, LOC107986136 | GRCh38.p7 | 3:136945561 | TATATTCTCCTCTCA[C/T]GGCCCTTTTTAATTT | 4690 |
rs137935360 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136898824 | TCCATGTCAAACTGA[C/T]AGGAAAATAGAATAT | 4690 |
rs138044302 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NCK1 | GRCh38.p7 | 3:136940320 | CTGCTCAAGGCCTCT[A/G]TTTCCTTAATGATTT | 4690 |
rs138123477 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | NCK1 | GRCh38.p7 | 3:136885309 | CATAATAGAAATTAT[A/G]AAAGGAGGGAATTGT | 4690 |
rs138201494 | snp | G/T | | | upstream-variant-2KB, intron-variant | NCK1 | GRCh38.p7 | 3:136929564 | TAGCAGAAGAGACCA[G/T]GGTTAGAATCAGCAA | 4690 |
rs138305702 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | NCK1 | GRCh38.p7 | 3:136935631 | GGCCTGAAGAAGAGT[C/G]ACCATAGTGAGAAGG | 4690 |
rs138322730 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NCK1 | GRCh38.p7 | 3:136917792 | TAAAATCTCTGCTTC[C/T]ATGTCTCAGGAAGAT | 4690 |
rs138328323 | in-del | -/GT/TTG | | | intron-variant | NCK1 | GRCh38.p7 | 3:136902199 | TTTTTTTTTTTTTTT[-/GT/TTG]TTTGTTTTTGTTTTT | 4690 |
rs138345774 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | NCK1 | GRCh38.p7 | 3:136919011 | TGGTTCGTCCGTACA[A/G]TGGACTACTCAGCAC | 4690 |
rs138384799 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | NCK1 | GRCh38.p7 | 3:136879810 | GAACACATGGACACA[A/G]GGAGGGGAACATCAC | 4690 |
rs138384847 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NCK1 | GRCh38.p7 | 3:136899962 | GTTTTAACTCCTTTG[A/G]TGTTCTGGATTGCTT | 4690 |
rs138409262 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136917248 | TTTTTTTTTTTTTTT[G/T]CTTAATCAGCTATCG | 4690 |
rs138413549 | in-del | -/TGGATGCAATGTGTAA | 0.415727 | 0.187175 | intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136946667 | TTAAAAAATTGCTAT[-/TGGATGCAATGTGTAA]GAAGGTAGTCACTGT | 4690 |
rs138413760 | snp | A/T | 0.0174175 | 0.0916809 | intron-variant | NCK1 | GRCh38.p7 | 3:136877226 | GTTTTTAAGTGCCTA[A/T]GAAAGTTTTTCCCAA | 4690 |
rs138444973 | in-del | -/AAAATT | 0.0221141 | 0.102801 | intron-variant | NCK1 | GRCh38.p7 | 3:136871406 | CTGTCTAAAAAAAAC[-/AAAATT]AAAAATTTGTTTAGA | 4690 |
rs138537441 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136951025 | CAGTTAACACATGCA[C/T]CTTGCACTATTAGTG | 4690 |
rs138538279 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | NCK1 | GRCh38.p7 | 3:136866861 | CAGGTGATCCACATG[C/T]GTCGGCTTCCCAAAG | 4690 |
rs138588673 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NCK1 | GRCh38.p7 | 3:136944428 | CAGCCGGGAAAGACA[A/G]CTTTTAAAAGAGTGG | 4690 |
rs138643508 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NCK1 | GRCh38.p7 | 3:136897936 | AAAGCTGTATTATCT[A/G]ATATCATAATAGGGA | 4690 |
rs138662831 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NCK1 | GRCh38.p7 | 3:136936293 | TCATCTGCCCGCCTC[A/G]GCCTCCCAAAGTGCT | 4690 |
rs138670645 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136870929 | TCTCTCACACCAGAG[A/G]AATCCAGGGTTGGCA | 4690 |
rs138671525 | in-del | -/CGCCCGTGCGAGCCTGGGAGGT | 0.41141 | 0.19091 | intron-variant, upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136862645 | GAGAGCCCGGGCGGC[-/CGCCCGTGCGAGCCTGGGAGGT]CGAGTGTGCGGCGCG | 4690 |
rs138673645 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | NCK1 | GRCh38.p7 | 3:136893533 | TCCTTGTAGATTCTG[C/G]ATATTAGTCCTTTGT | 4690 |
rs138820444 | in-del | -/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136899426 | TTCTTTTCTTTTTTT[-/T]TTTTTTTAAATTTCT | 4690 |
rs138836592 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | NCK1 | GRCh38.p7 | 3:136928608 | ATCTAATGACCTTAT[A/G]TTTTGAACTTCACTT | 4690 |
rs138927326 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | NCK1 | GRCh38.p7 | 3:136886383 | TTGTGTAAAATGGGG[G/T]ACTATTTACATATAA | 4690 |
rs138933789 | snp | A/T | 0.0158469 | 0.0875917 | intron-variant | NCK1 | GRCh38.p7 | 3:136876909 | GTTTATTTAAAATGT[A/T]GCTGACTGTTGCCAA | 4690 |
rs138967788 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NCK1 | GRCh38.p7 | 3:136918399 | AATACAGTGAAACAA[C/T]TATTCACATTTTATT | 4690 |
rs139049312 | snp | G/T | 0.093777 | 0.195178 | intron-variant | NCK1 | GRCh38.p7 | 3:136889635 | AGCTGAGTGGTCTGT[G/T]TTGACAGGGCACTGA | 4690 |
rs139089428 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136882125 | ATAGCAGCTGCACCA[C/T]TTTACATTACCACCA | 4690 |
rs139109793 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | NCK1 | GRCh38.p7 | 3:136932597 | TTTCTTAGTTCTGTT[C/G]CCAGACATATCACTT | 4690 |
rs139111097 | in-del | -/T | 0.113685 | 0.209567 | intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136946981 | TTAAAAATGGCCTTT[-/T]CTTTTTCCTTGATGA | 4690 |
rs139116821 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | NCK1 | GRCh38.p7 | 3:136890448 | CAGAAAGGGGCTCCC[A/G]CAGTGCAGTGGTGGG | 4690 |
rs139194697 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136877690 | GCAACAATAAAATCT[G/T]GAAACTGGAAAGCGA | 4690 |
rs139239828 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136902203 | TTTTTTTTTTTTTTT[G/T]TTTTTGTTTTTTGAG | 4690 |
rs139242747 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136947467 | TTTTTAAGGTTAGAG[A/G]TCTCAAGTAGGCATA | 4690 |
rs139349144 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136906124 | TGTGGTGTTGGTTGA[A/G]TATGGCACTTTGGCT | 4690 |
rs139358240 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NCK1 | GRCh38.p7 | 3:136907888 | CCTTATATATGTGGC[A/G]TCAGCCTCAGTCCCC | 4690 |
rs139549861 | in-del | -/TTTC | 0.195837 | 0.244062 | intron-variant | NCK1 | GRCh38.p7 | 3:136887924 | GCCTTTATTGTTTCT[-/TTTC]TTTCTTTCTTTCTTT | 4690 |
rs139598839 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | NCK1 | GRCh38.p7 | 3:136919658 | ACTTTTATAAATTCT[A/G]TAGGTATAGCTATAT | 4690 |
rs139621009 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136871936 | AGGCCTCTCCTGCCA[C/T]GTGGAACTGTAAGCC | 4690 |
rs139703541 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136902475 | GCTAAGATTACAGGC[A/G]CGAGCTATCCCACCT | 4690 |
rs139738732 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NCK1 | GRCh38.p7 | 3:136933354 | TCAAGGATTTGCAAA[C/T]CAGGTCACATAAGGA | 4690 |
rs139803591 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136926574 | GCCACCGCGCCCGGC[C/T]ACTCTTTTTGTTTTT | 4690 |
rs139819562 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136882669 | CATAATCAGCTTTGG[C/T]TTCTCAGATTGTTTT | 4690 |
rs139825515 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136937380 | GCTTTGTAGTAAGTT[C/T]TGAAATCAGAAAGGG | 4690 |
rs139879712 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136888170 | GGCTGGTCTCAAACT[C/G]CTGACCTCGTGATCT | 4690 |
rs139886560 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | NCK1 | GRCh38.p7 | 3:136867621 | TGTGTGGACTTGAAT[C/T]ATAGAATTATAGAGC | 4690 |
rs139949181 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | NCK1 | GRCh38.p7 | 3:136868481 | TACAGGTGCCTGCCA[C/T]CATGCCTGGCTAATT | 4690 |
rs140020695 | snp | A/G | 4.94328e-05 | 0.00497131 | missense, downstream-variant-500B | NCK1, LOC107986136 | GRCh38.p7 | 3:136945762 | ACAAAGGTGATCGTC[A/G]TGGAGAAATGCAGTG | 4690 |
rs140160518 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | NCK1 | GRCh38.p7 | 3:136888273 | TATGATTCCATTCAG[A/T]CATTAGTCTTGTCGG | 4690 |
rs140225787 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136946436 | AGCATAAATGTTCCA[A/G]AGCTAAAGTCCGCAT | 4690 |
rs140227533 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant, upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136862451 | GTCGCTTCCTCTTCT[C/T]GCGCTGAGTTAGCCC | 4690 |
rs140311358 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | NCK1 | GRCh38.p7 | 3:136869321 | GGAGGCTGAGGTGGG[C/T]GGATAACTTGATCCC | 4690 |
rs140416859 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | NCK1 | GRCh38.p7 | 3:136940074 | CACCATCTTGCCCAG[C/G]CTGCCGTCAGACTCC | 4690 |
rs140446637 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | NCK1 | GRCh38.p7 | 3:136903082 | CGTAGTGGAATCTAT[C/G]TCTCCTTACAGATCT | 4690 |
rs140522151 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NCK1 | GRCh38.p7 | 3:136896657 | ACCCCACCACACCTG[A/G]CTAATTAAAAAAGAA | 4690 |
rs140523314 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136934760 | CACACAACCAGTAGC[A/G]GAACTAAAATTTAAA | 4690 |
rs140529634 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136878102 | CATGCTATAACACAG[A/G]TAAACCTTTAAAACA | 4690 |
rs140577754 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | NCK1 | GRCh38.p7 | 3:136879148 | AAAAAAAAGGCTCAG[G/T]AGAACAGTCAATAGA | 4690 |
rs140646437 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136881373 | TACAGGTGCACGCCA[C/G]TACGCCCGGCTAATT | 4690 |
rs140651058 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136923521 | GGTCGCTCCACTGCA[C/T]TCCAGCCTGGGTGAC | 4690 |
rs140737746 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136927898 | TCATCTTTATGTCTT[C/T]AGATTTTTAGGTGTG | 4690 |
rs140764766 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136946752 | GATATTAAGTTTCTT[C/T]ATAAATTGGTTACTT | 4690 |
rs140840337 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136909006 | ATGGGATCCATGACT[C/T]TTCCCCCACTCACCC | 4690 |
rs140857300 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | NCK1 | GRCh38.p7 | 3:136942901 | GGCAAAGCCAAGGCA[A/C]GCCATTGCTCAGGTC | 4690 |
rs140904246 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136893180 | TGTGTGTGTGTGTGT[A/G]TATATATATATACAC | 4690 |
rs140942054 | snp | A/C | 1.64738e-05 | 0.00286995 | synonymous-codon, nc-transcript-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136946127 | TAATCCATTAACTTC[A/C]GGTTTGGAACCATCA | 4690 |
rs141005402 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136860404 | CTGAGGATAGTACAG[C/T]ATAAATAGGTAAATT | 4690 |
rs141075501 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136923167 | TTGTTGTGGGGGTAG[A/T]TAAAAATTAGAATTT | 4690 |
rs141115464 | in-del | -/G/GCTC/GCTCT | | | intron-variant | NCK1 | GRCh38.p7 | 3:136867049 | CTATGTTGCTTGCTT[-/G/GCTC/GCTCT]TTCTTTCTTTCTTTC | 4690 |
rs141163554 | snp | C/T | | | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136948813 | TTCCTTGTAAAGGCA[C/T]CCTGTTCTGTTATGG | 4690 |
rs141188848 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | NCK1 | GRCh38.p7 | 3:136915959 | TCGAACTCCTGAGCC[C/T]GGGTGATCTGCCCAC | 4690 |
rs141224292 | snp | C/T | 0.00398564 | 0.0444627 | upstream-variant-2KB, nc-transcript-variant | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136861916 | TTTTTGCTGTTAAGT[C/T]TCTCCTGCGGCGCTG | 4690 |
rs141237599 | in-del | -/TTTTTTTTT | | | intron-variant | NCK1 | GRCh38.p7 | 3:136912163 | AGCTATTATTTTTTC[-/TTTTTTTTT]TTTTTTTTTGAGACC | 4690 |
rs141279605 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136909455 | CAAAATGAAACAAGG[C/G]TGTTTCCTCTAAGAG | 4690 |
rs141320863 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136926198 | TTCTTTAACTTTTCT[A/G]ACTGCTTAAGATAGA | 4690 |
rs141402818 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136877562 | TTCTAAATAAAGATG[A/G]CTGAGTGAAAGACAC | 4690 |
rs141442402 | snp | A/G | 0.000153988 | 0.00877328 | missense, downstream-variant-500B | NCK1, LOC107986136 | GRCh38.p7 | 3:136945702 | GCTTATGTGAAATTT[A/G]ACTACATGGCTGAGA | 4690 |
rs141473731 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136883679 | GTCATTCAGTAGATA[C/T]GTTGTTGGAGGGAAT | 4690 |
rs141514084 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136871425 | TTAAAAATTTGTTTA[C/G]AGAAAGTATCTTTAA | 4690 |
rs141521782 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136941575 | GTTTCAGTACTATGC[A/G]TAACTCTGCTCCTTT | 4690 |
rs141606899 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NCK1 | GRCh38.p7 | 3:136938134 | TTTGGATTTTGTCCA[A/G]TACTTTTTCTGCATC | 4690 |
rs141620641 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136950172 | ATGACTAGTAGTAAA[C/T]ATCATCTTAATTTTT | 4690 |
rs141641421 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NCK1 | GRCh38.p7 | 3:136944509 | ATTACCAAAATGTTA[C/T]GGTTTAAAAGTTGTA | 4690 |
rs141647317 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | NCK1 | GRCh38.p7 | 3:136890163 | GAGGCAGCTGAGGCC[C/T]GGCAAGAAATCGAGC | 4690 |
rs141663091 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136887716 | AGGTAGGAGAAGAGG[A/G]CAGGGAAAGACAGCT | 4690 |
rs141704854 | snp | G/T | 0.0130921 | 0.0798413 | intron-variant | NCK1 | GRCh38.p7 | 3:136899023 | ATATAAACACCCTTG[G/T]AAAGCTGTGCTTCTT | 4690 |
rs141822181 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | NCK1 | GRCh38.p7 | 3:136910483 | AAAAAATTACAAACT[A/G]AATAAACCTCAGAGT | 4690 |
rs141937484 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NCK1 | GRCh38.p7 | 3:136912773 | CAGTCCCCCTGCTTC[A/G]GCTTCCTGAGTAGCT | 4690 |
rs142002680 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136918452 | TAGAGATGACTTAAC[A/G]TATACAGGAGGTTGT | 4690 |
rs142021789 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136875158 | GACTGTCATAACAAT[A/G]CCACAGTCTGCTCTC | 4690 |
rs142043199 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | NCK1 | GRCh38.p7 | 3:136913413 | AGCTGGGACTGCAAG[C/T]GTGCACCACTATGCC | 4690 |
rs142059207 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | NCK1 | GRCh38.p7 | 3:136921991 | GGTTTCACCATGTTG[G/T]CCAGGATGGTCTTAG | 4690 |
rs142106887 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136921664 | TTTATTCAGTAACTA[C/T]TGCAGTAGGGAAGAG | 4690 |
rs142114705 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | NCK1 | GRCh38.p7 | 3:136869427 | GCGAATGCCTGTAAT[C/G]TCAGCTACTCAAGAG | 4690 |
rs142166305 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | NCK1 | GRCh38.p7 | 3:136915197 | CTTCATCAAGTAGAT[C/T]ACATTACTACTAAGG | 4690 |
rs142220559 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NCK1 | GRCh38.p7 | 3:136868755 | AGGCCTTGAATGTGG[A/G]TACAGAACAATGTAA | 4690 |
rs142293608 | in-del | -/TT | 0.0622301 | 0.165053 | intron-variant | NCK1 | GRCh38.p7 | 3:136941117 | TGTGATTTCTTTTTC[-/TT]TTTTTTTTTTTTTTT | 4690 |
rs142329952 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136938674 | TAAGCTTCATTTAGG[C/T]ATGAGTTATAGTGAT | 4690 |
rs142352623 | in-del | -/AG | 0.00478085 | 0.0486577 | downstream-variant-500B, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136951672 | GGCATATACACAGAC[-/AG]TAGTTTTTGGTATGT | 4690 |
rs142355123 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136863107 | ACGTAACCGTAGGAA[C/G]GCTCTCGGTGTCAAA | 4690 |
rs142360513 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136947153 | TTAATTGAACTTCCT[C/G]ATGTGAAGTTCAGGA | 4690 |
rs142391029 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136891565 | TCCATAAGTGAAATT[A/G]CTGGATTGTATGGTA | 4690 |
rs142422992 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136934576 | CAGGTGTGCACCACC[A/G]CGCCTGTCCTGTTGT | 4690 |
rs142429549 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | NCK1 | GRCh38.p7 | 3:136940810 | TCGGCTTCCTAAAGT[G/T]CAGGGATTACAGGCA | 4690 |
rs142439304 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NCK1 | GRCh38.p7 | 3:136890937 | CTACTTTCTATCTCT[A/G]TGAATTTGACAACTC | 4690 |
rs142462007 | snp | C/G | 0.0221141 | 0.102801 | intron-variant | NCK1 | GRCh38.p7 | 3:136941912 | GGTGCGGTCTTGGCT[C/G]ACTACAACCTCCACC | 4690 |
rs142469379 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | NCK1 | GRCh38.p7 | 3:136937107 | TATAGTTTTAGCTCT[C/G]ACATTTGGTCATTTC | 4690 |
rs142510498 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136878833 | AGGGTGGGCCCTAGA[C/G]ACAATTGGAGGTCAA | 4690 |
rs142524494 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136927719 | ACAGATGGGGTTTCA[A/C]CATGTTGGCCAAGCT | 4690 |
rs142614821 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NCK1 | GRCh38.p7 | 3:136874639 | ATTTCTTCCTTTCTG[A/G]TAAAACTAGCGACTC | 4690 |
rs142691135 | snp | C/G | 0.0193772 | 0.0965046 | intron-variant | NCK1 | GRCh38.p7 | 3:136905183 | ACACCTGGTGTGGCG[C/G]CAATTTTTTTGTATT | 4690 |
rs142830753 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | NCK1 | GRCh38.p7 | 3:136877280 | AAAGATCAAAATAAT[A/C]AATTCTTGAGTGTTT | 4690 |
rs142860288 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | NCK1 | GRCh38.p7 | 3:136872018 | AGCAGCATGAAAACA[G/T]ATTAATACAGTAAAT | 4690 |
rs142883729 | in-del | -/GTGTGT/GTGTGTGTGT | | | intron-variant | NCK1 | GRCh38.p7 | 3:136893147 | AAGTAATATTCCATA[-/GTGTGT/GTGTGTGTGT]GTGTGTGTGTGTGTG | 4690 |
rs142937630 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | NCK1 | GRCh38.p7 | 3:136886544 | TACAGGTGCTTTTTT[C/T]TTTCCTGAATGTTTT | 4690 |
rs142963209 | in-del | -/G | 0.0248432 | 0.108648 | intron-variant | NCK1 | GRCh38.p7 | 3:136887725 | AAGAGGACAGGGAAA[-/G]ACAGCTGTGTCTCAG | 4690 |
rs142981033 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NCK1 | GRCh38.p7 | 3:136894808 | ATCCTAAATTTTGCT[A/G]GATTTTTTAAATCTT | 4690 |
rs143086280 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136904106 | ATGAAGGATAACTTT[G/T]CTGGGTATAGTATCC | 4690 |
rs143151508 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant, nc-transcript-variant | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136861676 | AAGCTGCCCAAGCAC[A/G]AGGACACTTTTAGAG | 4690 |
rs143160760 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | NCK1 | GRCh38.p7 | 3:136888232 | ACAGGTGTGAGCCAC[C/T]GTGCCTGGCCCTCCT | 4690 |
rs143199030 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | NCK1 | GRCh38.p7 | 3:136937571 | GGATACTGTTGCCAT[C/T]TTACACAGAATATCT | 4690 |
rs143201082 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NCK1 | GRCh38.p7 | 3:136883168 | TCATGTGATCTGTCC[A/G]CCTTGGCCTCCCAAA | 4690 |
rs143204471 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136900816 | AAGTTTTTTGGTGGA[G/T]TCTAGGTTTCTCTAG | 4690 |
rs143217976 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136925358 | TTATTTTGAGATCAT[C/T]ATAGATCCACATGCA | 4690 |
rs143284276 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136862265 | GGCGGAGCGCAGGCC[A/T]CGTGCCGTTACGGCC | 4690 |
rs143317070 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136918223 | ATACATATCTAAATA[A/G]TATATACATATTATC | 4690 |
rs143321080 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136906448 | TGGGTTGCCAAGTAG[G/T]CCAGCTCTCAGGCCC | 4690 |
rs143402422 | snp | A/C | 0.0111196 | 0.0737302 | intron-variant | NCK1 | GRCh38.p7 | 3:136865975 | ATTTTTATCTTTGAA[A/C]TACTCACTAGCCTTT | 4690 |
rs143405427 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136871241 | CCTTTACAAAAGTAA[A/G]AAAAAAAAATTAGCC | 4690 |
rs143505746 | in-del | -/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136900132 | GTTGGCTGTAGTGGT[-/G]GGTTTCAGTTCCCAC | 4690 |
rs143615866 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NCK1 | GRCh38.p7 | 3:136943437 | GGTGTCTAGTGACAG[C/T]TGGAATTGTAATGCC | 4690 |
rs143619338 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136902683 | TTAATCACTCCTATT[C/T]AACACAGTACTGCAA | 4690 |
rs143620020 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | NCK1 | GRCh38.p7 | 3:136927117 | GCTGGGATTCCAAGT[A/G]TGCGCCACCATACCT | 4690 |
rs143669833 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136892734 | TGTTTTAAGCCACTA[C/T]TGTTACACAGCATTA | 4690 |
rs143732943 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | NCK1 | GRCh38.p7 | 3:136929787 | GTAATTAACAAAATA[G/T]AGTGAAAAAACTATT | 4690 |
rs143820099 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NCK1 | GRCh38.p7 | 3:136886305 | TACTTGTCCTTTGGT[A/G]TCCATGAGGTGTTGG | 4690 |
rs143830786 | snp | C/G | 0.02016 | 0.0983543 | intron-variant | NCK1 | GRCh38.p7 | 3:136910685 | TTTTATACTTTTCTG[C/G]GGTACAATGGGATGT | 4690 |
rs143909257 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | NCK1 | GRCh38.p7 | 3:136894414 | CTGCATCCCAAATGA[A/C]CAGCAGAATGACTTC | 4690 |
rs143982667 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NCK1 | GRCh38.p7 | 3:136932881 | AAAACTTTCTTTGGC[C/T]CCATTCTCAACACTT | 4690 |
rs144096311 | snp | A/T | 0.0240643 | 0.107019 | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136951443 | TCACATAAAATTCAG[A/T]CTTCTTGTTTCCCTT | 4690 |
rs144116830 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136914977 | TCTTGCTTCATCTCT[C/T]GTCATGTGATCTGTG | 4690 |
rs144132680 | snp | C/G | 0.0248432 | 0.108648 | intron-variant | NCK1 | GRCh38.p7 | 3:136864362 | CGGGCGTGGTGGCAC[C/G]CACCTGTAATCCCAG | 4690 |
rs144133695 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136914946 | TAAAAAGAGCCTGAC[A/G]CCTCCCCATTCTCTC | 4690 |
rs144153967 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136908137 | AAACAATGATAAATA[C/T]GATTTTCAGGGAGGA | 4690 |
rs144165056 | in-del | -/TGTC | 0.00795532 | 0.062565 | intron-variant | NCK1 | GRCh38.p7 | 3:136882324 | ATATATTTCGAGAAA[-/TGTC]TGTCTATTTTGTTCG | 4690 |
rs144192229 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | NCK1 | GRCh38.p7 | 3:136868040 | CTCTTGCCTCAGCCT[C/G]CTGAGGAGCTGGGAT | 4690 |
rs144271514 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | NCK1 | GRCh38.p7 | 3:136878131 | CATGCTAAGTAGGCC[A/G]GACATGGTGGCTCAC | 4690 |
rs144362159 | snp | A/T | 0.0123036 | 0.0774623 | intron-variant, upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136862856 | TCGGGACGCGCCCTC[A/T]CCCCTCCCCCCACCC | 4690 |
rs144467430 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136941624 | ATTACATCTTTACAC[A/G]TTAAAATATATGCCC | 4690 |
rs144526232 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | NCK1 | GRCh38.p7 | 3:136933355 | CAAGGATTTGCAAAC[C/T]AGGTCACATAAGGAA | 4690 |
rs144529999 | snp | A/C | 0.0103295 | 0.0711199 | intron-variant | NCK1 | GRCh38.p7 | 3:136920607 | GAATATTACTTATTA[A/C]CCCTCTGAACTATAA | 4690 |
rs144568247 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | NCK1 | GRCh38.p7 | 3:136936443 | GGTTATTGTGAACAG[C/T]GTTGTGATAAACATT | 4690 |
rs144592589 | snp | A/C | 0.0260105 | 0.111035 | intron-variant | NCK1 | GRCh38.p7 | 3:136874422 | TGACCTCAGGTGACC[A/C]GCCCACCTTGGCCAC | 4690 |
rs144656865 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136880767 | GTGTGTGCCACCATA[C/T]TAGCTAATTTTTTGA | 4690 |
rs144725818 | snp | G/T | 0.00914312 | 0.0669923 | intron-variant | NCK1 | GRCh38.p7 | 3:136892033 | AGCTAGGACTATAGG[G/T]GCATGCCACTGCTTG | 4690 |
rs144728514 | snp | A/G | | | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136948886 | CTAAAATTTCTTGGA[A/G]AGTGTTAATCTTTTC | 4690 |
rs144850520 | in-del | -/A | | | intron-variant | NCK1 | GRCh38.p7 | 3:136919359 | TGTAAAATAAACAGC[-/A]AAAAAAATATATGGC | 4690 |
rs144856134 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant | NCK1 | GRCh38.p7 | 3:136896571 | AAGGCAGGGTCTCAC[A/T]CTGTCACCCAGGCTG | 4690 |
rs144876497 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | NCK1 | GRCh38.p7 | 3:136882339 | ATGTCTATTTTGTTC[A/G]TTTGCCCATTTTTCA | 4690 |
rs145103642 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | NCK1 | GRCh38.p7 | 3:136883913 | ATGATTTACAATTAT[A/T]ATTAATAGATTGGTA | 4690 |
rs145123315 | snp | A/G | 0.0501905 | 0.150254 | intron-variant | NCK1 | GRCh38.p7 | 3:136880181 | TCCCAGCTAGTTAGG[A/G]GGCTGAGGCAGGAGA | 4690 |
rs145150020 | snp | C/T | 0.0310518 | 0.120672 | intron-variant | NCK1 | GRCh38.p7 | 3:136916451 | CACAACCCAAACACC[C/T]CCCATTAGGCCCCAT | 4690 |
rs145198756 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | NCK1 | GRCh38.p7 | 3:136897053 | GTTCCCTTTTTTTCT[A/G]CATCCTTACCAGTGT | 4690 |
rs145260273 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136921317 | TTTTTAACTCAGGAA[A/G]CAACTAGAGGACGTG | 4690 |
rs145301847 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NCK1 | GRCh38.p7 | 3:136877693 | ACAATAAAATCTGGA[A/G]ACTGGAAAGCGAGTG | 4690 |
rs145321685 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | NCK1 | GRCh38.p7 | 3:136934234 | GGGGGTACATGTGAA[A/G]GTTTGTTACATAGGT | 4690 |
rs145340736 | snp | C/T | 3.29473e-05 | 0.00405864 | synonymous-codon, downstream-variant-500B | NCK1, LOC107986136 | GRCh38.p7 | 3:136945866 | CAGTCCTTTGGGTGA[C/T]CATGTGGGTTCTCTG | 4690 |
rs145447348 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136903419 | AAATCTATTCAATCA[A/G]TATCTATCTTATTTA | 4690 |
rs145463012 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NCK1 | GRCh38.p7 | 3:136938329 | TTTCACAGATTCTGT[A/G]TTTGTGAATTCACTT | 4690 |
rs145484645 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136898802 | ACGGCATGTGATGTG[G/T]ACTTCCTCCATGTCA | 4690 |
rs145509298 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NCK1 | GRCh38.p7 | 3:136909274 | TATCTAGGCAAATGG[C/T]GCAAAGAAAATATGT | 4690 |
rs145530507 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136862548 | ACTTCTGCACCGGGA[A/T]TCCGCGAGACCCTCG | 4690 |
rs145545353 | snp | A/G | 0.00108667 | 0.0232842 | missense, downstream-variant-500B | NCK1, LOC107986136 | GRCh38.p7 | 3:136945907 | TAGCAGCAGTCGTCA[A/G]TAACCTAAATACTGG | 4690 |
rs145557340 | in-del | -/C | | | intron-variant | NCK1 | GRCh38.p7 | 3:136938573 | TGCTGTTTAAAATGG[-/C]CCCCAAGCATAGTGA | 4690 |
rs145568350 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | NCK1 | GRCh38.p7 | 3:136865039 | TCTTGGCTCACTGCA[A/G]CCTCTGCCTGCCGGG | 4690 |
rs145584114 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136942125 | TTACAGGTGTGAGCC[A/C]CTGTGCCCAGCCTCT | 4690 |
rs145709700 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136943072 | AGGCAACTTAGGATG[C/T]GATAGCACTCTCTTT | 4690 |
rs145730341 | snp | A/C | 0.0103295 | 0.0711199 | upstream-variant-2KB, intron-variant | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136861315 | ACCATCCTGGTGAAA[A/C]CCCGTCACTGCTAAA | 4690 |
rs145757294 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | NCK1 | GRCh38.p7 | 3:136869664 | TCTGTAACAGAAACC[A/G]TGTATGGTTGCTTTC | 4690 |
rs145788944 | snp | A/C | | | intron-variant | NCK1 | GRCh38.p7 | 3:136877201 | ACCTAATACCTACAG[A/C]ATGCAGATTGTTTTT | 4690 |
rs145814859 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | NCK1 | GRCh38.p7 | 3:136938115 | ATTGTTATCATGAAA[C/T]GGTTTTGGATTTTGT | 4690 |
rs145829518 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136924762 | GTCCATGGCTTAACC[C/T]ATTTGTGCCTAGTGT | 4690 |
rs145905741 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136879580 | GACCTTATGTGCACT[A/G]TTCACAATAGCAAAG | 4690 |
rs146045236 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136872256 | GGTTTCAGATGGAGA[C/T]GGGGAACTTGTTGGG | 4690 |
rs146095656 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136877456 | TATAGTATAACTTAA[A/G]GGATGTGTATAGAGC | 4690 |
rs146137038 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136893195 | ATATATATATATACA[C/T]ACATGTGCAAGTATC | 4690 |
rs146168699 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | NCK1 | GRCh38.p7 | 3:136890353 | CCCGCCAGCGTTGCA[C/T]GCAGCCCCAGTTCCC | 4690 |
rs146203926 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | NCK1 | GRCh38.p7 | 3:136936260 | TGGCCAGGCTGGTCA[C/T]GAACTCCTTACCTCA | 4690 |
rs146218156 | snp | G/T | 0.0209421 | 0.100162 | intron-variant | NCK1 | GRCh38.p7 | 3:136893946 | CTTTCATCCTTGTGG[G/T]ACTTGAGCCTTTAGT | 4690 |
rs146290173 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136913418 | GGACTGCAAGTGTGC[A/G]CCACTATGCCTGCCT | 4690 |
rs146338869 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | NCK1 | GRCh38.p7 | 3:136918988 | TAAAGTTCTCATTAA[A/G]TAAATGATGGTTCGT | 4690 |
rs146373878 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136871448 | ATCTTTAAATGTTTA[C/T]TGAAAACTGCACAAA | 4690 |
rs146375859 | in-del | -/TT | | | intron-variant | NCK1 | GRCh38.p7 | 3:136912179 | TTTTTTTTTTTTTTT[-/TT]TGAGACCGAGTCTCG | 4690 |
rs146424978 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136933190 | ATGGTGACATTGATT[C/T]GAGTCTGAGAGGTGC | 4690 |
rs146427056 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | NCK1 | GRCh38.p7 | 3:136886378 | GTCTCTTGTGTAAAA[A/T]GGGGTACTATTTACA | 4690 |
rs146432580 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | NCK1 | GRCh38.p7 | 3:136938765 | AAAACAGGGTTGTGT[A/C]GTGATTGGTTAACAA | 4690 |
rs146451247 | snp | C/T | 3.29484e-05 | 0.00405871 | synonymous-codon, nc-transcript-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136946100 | AAAAAACTATGTTAC[C/T]GTTATGCAGAATAAT | 4690 |
rs146514672 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136948042 | GTTAACTAGATGGAT[A/G]ATATTGGCCAAGTTA | 4690 |
rs146526350 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | NCK1 | GRCh38.p7 | 3:136943532 | AAATGAAAGTGTATG[A/T]TTTCCTTGGAATAGA | 4690 |
rs146562057 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | NCK1 | GRCh38.p7 | 3:136868350 | TTTTTTTTCTTGAGA[C/T]GGAGTCCTGCTCTGT | 4690 |
rs146610316 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | NCK1 | GRCh38.p7 | 3:136928294 | CTTAGTTCTTTGTAC[A/G]TAATTCTGGCAGCAG | 4690 |
rs146628950 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NCK1 | GRCh38.p7 | 3:136883300 | TTGCCCTTGTTCTCT[A/G]GCCACATCTCTAGCC | 4690 |
rs146677321 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136888265 | CTTTATTTTATGATT[C/T]CATTCAGTCATTAGT | 4690 |
rs146728400 | snp | A/G | 0.0146672 | 0.084371 | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136949079 | AAAACATGTTGTACA[A/G]TTTTAATTTACAACT | 4690 |
rs146801079 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136907495 | CTGCAGCACTTGAGG[G/T]CTTCTCCCATGGCTA | 4690 |
rs146872893 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NCK1 | GRCh38.p7 | 3:136927797 | GTGCTGGGATTACAG[A/G]CATGAGCCACTGCGC | 4690 |
rs146919119 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | NCK1 | GRCh38.p7 | 3:136909507 | TTAAACAACCAATTT[A/C]AATGGCAGAATGTCG | 4690 |
rs146942254 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | NCK1 | GRCh38.p7 | 3:136905280 | GCCTTCCTTGGCCTC[C/T]CAAAGTGCTGGGATT | 4690 |
rs147023876 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136934829 | ATTACTAAAGAGTAG[A/T]GAATTGGAGTCGGTT | 4690 |
rs147047055 | snp | C/T | 0.0107246 | 0.0724382 | upstream-variant-2KB, intron-variant | NCK1 | GRCh38.p7 | 3:136929178 | GCTCAAGCAACCCTC[C/T]CACCTCAGCTTCCTG | 4690 |
rs147056339 | in-del | -/GTT/TTG | 0.44651 | 0.154543 | intron-variant | NCK1 | GRCh38.p7 | 3:136902198 | GTTTTTTTTTTTTTT[-/GTT/TTG]TTTTGTTTTTGTTTT | 4690 |
rs147180625 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | NCK1 | GRCh38.p7 | 3:136877850 | GGTGGTGCTAAAAAC[A/C]GGAGGATTTCTTGAA | 4690 |
rs147181784 | snp | A/G | 0.0103295 | 0.0711199 | upstream-variant-2KB, intron-variant | NCK1 | GRCh38.p7 | 3:136929913 | CAGGATGCATTCCGT[A/G]CTACAGTATTCTGAT | 4690 |
rs147204914 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136927128 | AAGTGTGCGCCACCA[C/T]ACCTAGCTAATTTTT | 4690 |
rs147223272 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136881311 | TGCAACCTCTGCCTC[C/T]TGGGTTCAAGCAGTT | 4690 |
rs147287309 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NCK1 | GRCh38.p7 | 3:136895765 | AGACAGGGTTTTGCT[A/G]TGTTGACCAGGCTGA | 4690 |
rs147310821 | snp | A/T | 0.0103295 | 0.0711199 | intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136946744 | AAAAAATTGATATTA[A/T]GTTTCTTCATAAATT | 4690 |
rs147330914 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136900469 | TCTGTGAAAAAAGAC[A/G]TTGGTATTTTGATAG | 4690 |
rs147481903 | snp | A/G | 6.58979e-05 | 0.00573974 | missense, downstream-variant-500B | NCK1, LOC107986136 | GRCh38.p7 | 3:136945740 | TGAATTATCATTGAT[A/G]AAGGGGACAAAGGTG | 4690 |
rs147520411 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | NCK1 | GRCh38.p7 | 3:136901842 | TGTTGTTCTTTTGTG[C/G]TTTTTAAAAAAGTCG | 4690 |
rs147540017 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136862390 | GCAGACACACACACA[C/T]CCCCCTTCAGTCCGC | 4690 |
rs147555254 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136916489 | ATGGGGATCAAATTT[C/T]AACATGAGATTTGGA | 4690 |
rs147582566 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | NCK1 | GRCh38.p7 | 3:136869345 | TGATCCCAGGAGTTC[C/G]AGACCAGCTTGGCCA | 4690 |
rs147584657 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NCK1 | GRCh38.p7 | 3:136921329 | GAAACAACTAGAGGA[C/T]GTGCTCCAGCAAAAT | 4690 |
rs147625548 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NCK1 | GRCh38.p7 | 3:136874825 | TTTTTTTCATGTTCA[C/T]GCTTGATTTGGTTGG | 4690 |
rs147659917 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136938456 | TTCCCAGTTGAGGCA[A/G]TGTTCTTCCTTCTTA | 4690 |
rs147688924 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136942887 | AATGATTCAAGTCAG[A/G]CAAAGCCAAGGCAAG | 4690 |
rs147730403 | snp | A/T | 0.0209421 | 0.100162 | intron-variant | NCK1 | GRCh38.p7 | 3:136891311 | GGTTAATTTTGTATT[A/T]TTAATAGAGATGGGG | 4690 |
rs147764400 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | NCK1 | GRCh38.p7 | 3:136876392 | AAAGGATCAACAAAA[C/T]TGATAGACCGCTAGC | 4690 |
rs147794062 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136878253 | ATCTCAACTATAAAC[A/C]CACAAATTAGCCGGA | 4690 |
rs147866840 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136892352 | AAGTATGTTAAAAAG[A/C]TCTTAATTTTGATGA | 4690 |
rs147952446 | in-del | -/T | 0.0185938 | 0.0946107 | intron-variant | NCK1 | GRCh38.p7 | 3:136871092 | TAAAAAGCTTACTAA[-/T]TTTTTTTTTAAAAAA | 4690 |
rs148006126 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | NCK1 | GRCh38.p7 | 3:136936527 | TGGAATTGCTGGATC[C/G]TATGGTAATTCTTTG | 4690 |
rs148014783 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136949712 | ACTGAGTAGGATGTC[A/G]TATGATACTTTCAAC | 4690 |
rs148059081 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | NCK1 | GRCh38.p7 | 3:136892928 | CAACAGCAATGTACA[C/G]TGTACCCAATGTGTA | 4690 |
rs148174553 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | NCK1 | GRCh38.p7 | 3:136912230 | TGCAGTGGTGTGATC[C/T]TGGCTCACTGCAACC | 4690 |
rs148185441 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136904420 | AGCCTCCCAAAGTGC[C/T]AGGATTACAGGCGTG | 4690 |
rs148197442 | snp | A/G/T | 0.0002187 | 0.0104549 | missense, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136948274 | CCAAATGATTTCTCA[A/G/T]TATCACTAAAAGCAC | 4690 |
rs148203247 | snp | A/C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136893191 | GTGTATATATATATA[A/C/T]ACACACATGTGCAAG | 4690 |
rs148215094 | snp | C/T | 0.0107246 | 0.0724382 | upstream-variant-2KB, nc-transcript-variant | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136861867 | CCAGGGGGAAGCTCC[C/T]AGAGCAGTGGGGGCT | 4690 |
rs148269729 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | NCK1 | GRCh38.p7 | 3:136939098 | CCACCAGTGAAACCA[C/T]CTGGTCCAGAGCACA | 4690 |
rs148303547 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | NCK1 | GRCh38.p7 | 3:136925367 | GATCATTATAGATCC[A/C]CATGCAATTCTGAGA | 4690 |
rs148317015 | in-del | -/CTT | | | intron-variant | NCK1 | GRCh38.p7 | 3:136944112 | AAAAGGAAAAACAAC[-/CTT]TTTTTTTTTTTTTTT | 4690 |
rs148333368 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136877493 | TAGAGGAAGAGTTAT[A/G]GCCTTCAAATCTATA | 4690 |
rs148488813 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | NCK1 | GRCh38.p7 | 3:136874475 | GTGAGCCACCACGCC[C/T]GGCCCGTTTACAGGT | 4690 |
rs148526248 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136893196 | TATATATATATACAC[A/G]CATGTGCAAGTATCT | 4690 |
rs148583848 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136894756 | TGCCACCTGCTCAGT[C/T]CTGTGTCTGATAAGT | 4690 |
rs148668264 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136931833 | ACATAAAAAGAATCC[A/G]TTGTGGCTAGGCGTG | 4690 |
rs148741436 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant, upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136862907 | GGGCTGTGACTTTAA[C/T]GGTCTGGACCTGCTT | 4690 |
rs148752813 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NCK1 | GRCh38.p7 | 3:136907268 | CTTGGACCCTGTGGA[A/G]CAGCTATAGGTGGAG | 4690 |
rs148772850 | snp | A/C | 0.00034656 | 0.013159 | missense | NCK1 | GRCh38.p7 | 3:136928186 | AAAGGAAAAACAGTG[A/C]TCGGAAAGCATCTAT | 4690 |
rs148784863 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136941768 | ATGTAGCTACCTTTA[C/T]CATTGTTCTTTATTT | 4690 |
rs148841281 | snp | A/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136949161 | TTATTCAAGAAAACA[A/T]AACAGTCTCTGAGAT | 4690 |
rs148858387 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136878586 | GTTTCTTTTTGGGGT[G/T]ACAAAAATTTTCTAA | 4690 |
rs148877744 | snp | A/G | 3.29495e-05 | 0.00405877 | synonymous-codon, downstream-variant-500B | NCK1, LOC107986136 | GRCh38.p7 | 3:136945938 | GCAAGTGTTGCATGT[A/G]GTACAGGCTCTTTAC | 4690 |
rs148894667 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | NCK1 | GRCh38.p7 | 3:136943316 | AGGCTATCATTAACC[A/G]GAAGTAAGAAAATTA | 4690 |
rs148924316 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NCK1 | GRCh38.p7 | 3:136892679 | TAAGACCTGTTTTAG[A/G]CTTAATGACCTCTAG | 4690 |
rs148985266 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NCK1 | GRCh38.p7 | 3:136888831 | GTGGTCCTTTGTAAC[C/T]GCTTTCTTTCACTTA | 4690 |
rs149019959 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136877157 | CTATAATTATCAAAT[A/G]AATCTAATTGACATG | 4690 |
rs149020287 | in-del | -/CTTTT | | | intron-variant | NCK1 | GRCh38.p7 | 3:136870361 | AAAAAAAAATTCATC[-/CTTTT]CTTCCAAAAATTTTA | 4690 |
rs149047952 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | NCK1 | GRCh38.p7 | 3:136903722 | GAGCCACACCGCGCC[C/T]GGCCAAATTAGTCTG | 4690 |
rs149099281 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NCK1 | GRCh38.p7 | 3:136897114 | TATTTTGAGACAGAA[C/T]CTCACTCCCTGTCAC | 4690 |
rs149185990 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | NCK1 | GRCh38.p7 | 3:136934442 | AGGTGCCTGCCACCA[C/T]GCCTGGCTAATTTTT | 4690 |
rs149230834 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | NCK1 | GRCh38.p7 | 3:136917970 | TGTGTTGCTTCTCTG[C/G]ATCTGTCCTGTTTTA | 4690 |
rs149293084 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136936299 | GCCCGCCTCGGCCTC[C/T]CAAAGTGCTGGGATT | 4690 |
rs149346478 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | NCK1 | GRCh38.p7 | 3:136929064 | AAATATGAAATACTG[C/T]TGACTCACTACTTTA | 4690 |
rs149369997 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136867790 | AGTTCTGTGTGTTTA[G/T]GAAACCATACTACTT | 4690 |
rs149452067 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | NCK1 | GRCh38.p7 | 3:136894076 | CATTGTGTACAACAG[G/T]TCCTAATAATCAGGG | 4690 |
rs149503827 | snp | C/T | 0.161596 | 0.233848 | intron-variant | NCK1 | GRCh38.p7 | 3:136889836 | GGTGTGTTTACAAAC[C/T]TTGAGCTAGAGACAG | 4690 |
rs149581365 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136906881 | GCTAGGTGATCGCCA[C/G]GCCCACGGATTGCAT | 4690 |
rs149633881 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | NCK1 | GRCh38.p7 | 3:136900343 | TTTTGGTTACTGTAA[A/C]CTTGTAATGTATTTT | 4690 |
rs149694964 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | NCK1 | GRCh38.p7 | 3:136927196 | AGGCTGGTCTTGCAT[G/T]CCTGACCTCAGGTGA | 4690 |
rs149735765 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | NCK1 | GRCh38.p7 | 3:136874251 | TGCGATCTCAGCTCA[C/T]TGCAACTTCTGCCTC | 4690 |
rs149748350 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136920556 | TTAGGTATATAAGAC[A/G]TTACTGTCTATATGA | 4690 |
rs149750260 | snp | A/G | 0.000362343 | 0.0134551 | missense, downstream-variant-500B | NCK1, LOC107986136 | GRCh38.p7 | 3:136945903 | AAATTAGCAGCAGTC[A/G]TCAATAACCTAAATA | 4690 |
rs149770302 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136942942 | CTGCCAGACAAGTTG[A/T]AACCCACAATCACAA | 4690 |
rs149771247 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136860781 | AACCACCTCCATGAC[C/T]CAACACTGCCCATTA | 4690 |
rs149824392 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136938104 | GTTTGCTGAGCATTG[C/T]TATCATGAAACGGTT | 4690 |
rs149832286 | in-del | -/TG | | | intron-variant | NCK1 | GRCh38.p7 | 3:136923105 | CTATGCCTATGTGTA[-/TG]TGTGTGTGTGTGTGT | 4690 |
rs149852633 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NCK1 | GRCh38.p7 | 3:136888564 | CTTGCCACCATGCCC[A/G]GCTAATTTTTTGTAT | 4690 |
rs149908030 | snp | A/T | 0.0107246 | 0.0724382 | intron-variant | NCK1 | GRCh38.p7 | 3:136882253 | GTGGTTTTGATTTGC[A/T]TTTCCATAATGGCTA | 4690 |
rs149980575 | snp | A/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136896672 | GCTAATTAAAAAAGA[A/T]TTTTTTTTGTAGAAA | 4690 |
rs149992947 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136947530 | TTTAAATTCATTGCC[A/G]ATATTTAAATATTAG | 4690 |
rs150035376 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | NCK1 | GRCh38.p7 | 3:136891183 | TTGTTGCCCAGGCTG[C/G]AGTGCAGTGGCACGA | 4690 |
rs150077637 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | NCK1 | GRCh38.p7 | 3:136899224 | ACCATTTAGGTCTCT[A/T]GCTTTCAGCTGAAGG | 4690 |
rs150096864 | in-del | -/A | | | intron-variant | NCK1 | GRCh38.p7 | 3:136901375 | TTTCTTTTTTTTTTT[-/A]AAATATTTTTTATTG | 4690 |
rs150097118 | snp | C/T | 0 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136917610 | AGGATAGTTCATATC[C/T]TACACTTTTCCTGTC | 4690 |
rs150129538 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | NCK1 | GRCh38.p7 | 3:136893408 | TGGTAATTAGTGATG[C/T]TGAACATTTTTTCAT | 4690 |
rs150147149 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136909261 | GACTACTCAGAGATA[C/T]CTAGGCAAATGGTGC | 4690 |
rs150225257 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | NCK1 | GRCh38.p7 | 3:136928326 | GTGCATAATTGACTT[C/G]AAAAGGCAAGGGCTA | 4690 |
rs150271859 | snp | A/T | 1.66186e-05 | 0.00288254 | stop-gained, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136948432 | AGGAGAAAAATTATA[A/T]CTTGTCAAGCATTTA | 4690 |
rs150274722 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | NCK1 | GRCh38.p7 | 3:136923294 | GGCGCGGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 4690 |
rs150286331 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136945416 | AAAAAGAAAATTTGC[A/G]TCTTATTTCCAAAAA | 4690 |
rs150306732 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NCK1 | GRCh38.p7 | 3:136876786 | AGAATTTACGAATCA[A/G]TGTAACTGCTAAGCA | 4690 |
rs150358743 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | NCK1 | GRCh38.p7 | 3:136869341 | AACTTGATCCCAGGA[A/G]TTCGAGACCAGCTTG | 4690 |
rs150531476 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136888001 | CCAGGCTGGAGTGCA[A/G]TGGCATGATCTCTGC | 4690 |
rs150628062 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136919534 | AATAGTTTTGGCTCC[A/G]TAGACCCCTTAAGAG | 4690 |
rs150677401 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136912959 | CACTGCACCCAGCCT[C/T]CTTTGAGGTTTTCTA | 4690 |
rs150689193 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | NCK1 | GRCh38.p7 | 3:136937849 | TGTGTGTGTATTCTT[G/T]AGGATTTTCTATTTA | 4690 |
rs150836795 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136877576 | GGCTGAGTGAAAGAC[A/G]CATTTACTTTTACTC | 4690 |
rs150868767 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | NCK1 | GRCh38.p7 | 3:136941943 | TCCCGGGTTCAAGCA[A/G]TTCTCCTGCCTCAGC | 4690 |
rs150900729 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NCK1 | GRCh38.p7 | 3:136890960 | GACAACTCCTGGAAC[C/T]ATGTGTAAGTGAAAT | 4690 |
rs151058615 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136860345 | CAGAATGTAGACATA[C/G]AGTAGCTGTTGCCCA | 4690 |
rs151187750 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136869256 | AAAAAAAAAAAATTT[G/T]ATTTGTTCCGCTAGG | 4690 |
rs151196955 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NCK1 | GRCh38.p7 | 3:136915683 | GGAAGCATGGCCAGA[A/G]CAGAAGGAAGAGAGT | 4690 |
rs151271895 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NCK1 | GRCh38.p7 | 3:136934615 | TTTCATCACCCAGGT[A/G]TTAAGCCCAGTATCC | 4690 |
rs151302506 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136884536 | ACCTCCGCTTCCTGG[A/G]TTCAGGCGATTCTTG | 4690 |
rs180732675 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136940463 | TTGTTAGGTATGCAT[A/G]TATTTGTAACTGTTA | 4690 |
rs180740671 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NCK1 | GRCh38.p7 | 3:136918694 | GTGATTATTTTAAGC[C/T]CATCAGCTATCGTTA | 4690 |
rs180748591 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136896862 | TGTGAATAGTGCTAC[A/G]GTAAACATGCAAGTG | 4690 |
rs180751399 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136949549 | TAGGAATTTGGGTGT[A/G]TGGATAAGAGGCCAA | 4690 |
rs180881629 | snp | C/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136944976 | ACAAAACTCCCTGTC[C/G]TTTTGGAGGTTACAT | 4690 |
rs180895156 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136923363 | GATCGAAACCATCCT[G/T]GCTAACACAGTGAAA | 4690 |
rs180895810 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136933895 | GTATTTTTAGTAGAG[A/G]TGGGGTTTCCCCATG | 4690 |
rs180899894 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136901901 | TATTTCTTTCCTTCT[A/G]CTAATTTGGGGTTTG | 4690 |
rs180934122 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136879204 | TCTTTCATAAAGTAG[A/T]GGAAAAGATGGAAAA | 4690 |
rs180954621 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NCK1 | GRCh38.p7 | 3:136912804 | GGAACTACTTGCGCT[A/G]CTGTGCTTGGCTAAT | 4690 |
rs181104828 | snp | A/G | 0.00279162 | 0.0372561 | upstream-variant-2KB, intron-variant | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136860944 | ACTGCAAACTTTTGA[A/G]GCTGATATCCAGGGC | 4690 |
rs181271377 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NCK1 | GRCh38.p7 | 3:136873041 | ACAGAGTTCCTACTC[A/G]GGTACCGCCTAGTGG | 4690 |
rs181272024 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136918059 | AGTTCAAGGCAGGCC[A/G]TTTGTTTTTATATTA | 4690 |
rs181336413 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136939377 | TGGTCTAGCTAAAGA[A/G]TTTTCAATTTTACTG | 4690 |
rs181357929 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136901234 | TGTAACCATCCTTGC[C/T]TCTCTGGGATAAATC | 4690 |
rs181363455 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136869326 | CTGAGGTGGGCGGAT[A/G]ACTTGATCCCAGGAG | 4690 |
rs181365082 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136895500 | TTTCATCTTTTCTCT[A/G]TTAATGTTTTAGTTC | 4690 |
rs181385637 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | NCK1 | GRCh38.p7 | 3:136877832 | TGGCAGGGAGGAGGT[A/G]AGGGTGGTGCTAAAA | 4690 |
rs181402132 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NCK1 | GRCh38.p7 | 3:136912187 | TTTTTTTTTGAGACC[A/G]AGTCTCGCTCTGTCA | 4690 |
rs181421607 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NCK1 | GRCh38.p7 | 3:136933502 | GGTTAAGAAACAGTG[C/T]TATAGGAAAAGAGAA | 4690 |
rs181515886 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NCK1 | GRCh38.p7 | 3:136890827 | TCACCACCACCTGTT[C/T]GCATAAGTTTTTCAT | 4690 |
rs181541294 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136922633 | AAATTACAACTCTGA[A/G]ATACTATTTCTCCCC | 4690 |
rs181555680 | snp | G/T | 0.0517044 | 0.152246 | upstream-variant-2KB, intron-variant | NCK1 | GRCh38.p7 | 3:136928796 | GACAGTGGAGCCCAC[G/T]TCACACTGGACTTGG | 4690 |
rs181561779 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136906413 | CCATGCCTGGCCTGT[C/G]ATAAGGTTTTGCTGA | 4690 |
rs181565734 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | NCK1 | GRCh38.p7 | 3:136937418 | TCCCACTTGATTTTC[C/T]TTTTTCAAGATTGTT | 4690 |
rs181573136 | snp | A/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136886653 | AGTCTGTAGATGTCA[A/T]ACAGTTTTGTCTCCA | 4690 |
rs181598029 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136863126 | CTCGGTGTCAAACTG[A/G]TGGACCCGGAGTCAC | 4690 |
rs181791237 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136894902 | TTTGAGATGGAGTTT[C/T]ACTCTTGTTGCCCAG | 4690 |
rs181844554 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136911598 | TTGCTTTCTTGCTAC[C/T]GAATTGTCTGGAGTT | 4690 |
rs181856594 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136868255 | TGATATAAAGTCTAT[A/G]TACAGTTTCTTTCCC | 4690 |
rs181861789 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136890554 | GACTGCCAGCACGCT[C/G]TCACCTCTCAGTACT | 4690 |
rs181873731 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136933059 | AACTCTACATTAAAA[C/T]TTTAAAAGGAATTGT | 4690 |
rs181963150 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136916688 | AAATATAATAATTAG[A/T]TTAGAAGGGTAAGGA | 4690 |
rs182010746 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136950459 | GATAACCCATGTGTG[C/T]TAGTAATATCTATTG | 4690 |
rs182013832 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | NCK1 | GRCh38.p7 | 3:136874074 | GATAGTAGTATTCCA[C/T]TGGATGAATATAATG | 4690 |
rs182036094 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136872289 | CTGGAGCAAAGGTGA[C/T]TCTTGTTATGTTTTA | 4690 |
rs182086706 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136924579 | ATAAGTGTTGCAGGA[A/G]TTCTTAATAAAGGAA | 4690 |
rs182121777 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136879888 | AGGAGAAATACTTAA[C/T]GTAAATGACAAGTTG | 4690 |
rs182228802 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136903866 | CTCTGTCTCTTATTA[A/G]TTATTATTTTGGCTT | 4690 |
rs182255010 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136906008 | CTTTTTCATGTTTCC[C/T]GTGTCCTTACACTGG | 4690 |
rs182258053 | snp | G/T | 0.00358779 | 0.0422022 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136862328 | TCCTCAGGTGAGCTG[G/T]AGCTGCCCGGCTCGG | 4690 |
rs182305378 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136945265 | CTATGAAAGAAATCT[A/G]TATTTACATTTAAGA | 4690 |
rs182331952 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | NCK1 | GRCh38.p7 | 3:136869716 | AACAATAGTTGAATG[A/C]TGTAAGACAGCATAG | 4690 |
rs182338746 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136947019 | TATCACTACTTTTCC[A/G]TTTATTAAATCATGG | 4690 |
rs182391278 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NCK1 | GRCh38.p7 | 3:136902542 | TTATCTGAGGAGATA[C/T]TTGATACGATTTCAA | 4690 |
rs182452214 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136950876 | AACTTCCCCAAAATC[G/T]TAGAAGGTTTTTTAG | 4690 |
rs182454148 | snp | C/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136864214 | ACGTGTAATGTTGGC[C/G]GGGCTCGGTGGCTCA | 4690 |
rs182455401 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136898238 | CTGTCTCTACTAAAA[A/T]TACAAAAACTAGCTG | 4690 |
rs182456682 | snp | C/T | 0.0174175 | 0.0916809 | downstream-variant-500B, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136951674 | CATATACACAGACAG[C/T]AGTTTTTGGTATGTC | 4690 |
rs182459225 | snp | A/G/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | NCK1 | GRCh38.p7 | 3:136929683 | GCCTCATAGTGATAC[A/G/T]TGCACAGGGTACTAA | 4690 |
rs182466913 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136875565 | CAAAGAAGGCCATTA[G/T]GTAATGGTAAAGGGA | 4690 |
rs182467561 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NCK1 | GRCh38.p7 | 3:136907320 | GATGTGGAGATGCAG[A/G]GTCTGTTGGGTTCCC | 4690 |
rs182488011 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136886033 | ACTGAATGTTATTCC[A/G]GAAGCATTTATAAGG | 4690 |
rs182509341 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136906843 | CTGGGAGGAGTGCTT[A/G]GGTGCCAACAGTGGT | 4690 |
rs182516265 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136928355 | TAGGTAAGTTTGAGT[C/T]ATAGCAGGTGGTCAA | 4690 |
rs182617373 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | NCK1 | GRCh38.p7 | 3:136891064 | GTAGCATGTGTCTAA[A/G]GTTCCTCCCCGACCA | 4690 |
rs182709079 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136887614 | ATTTGTCACCTGGAA[C/T]AGACATAACTTCTTT | 4690 |
rs182709243 | snp | A/G | | | upstream-variant-2KB, intron-variant | NCK1 | GRCh38.p7 | 3:136930204 | AATGGTTGTGCTGGT[A/G]GAGACATTGTTTGAA | 4690 |
rs182754027 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NCK1 | GRCh38.p7 | 3:136925706 | CAATTGTTCTTTTTG[A/G]TATGAACGTACCAGT | 4690 |
rs182765342 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136903257 | TGTTTTGTTTGATAC[A/G]AGTATAGCTACTTCT | 4690 |
rs182777962 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136880543 | CTTGATTTCAGACTT[C/G]TGGCCTCCAGAACAG | 4690 |
rs182859945 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136882337 | AAATGTCTATTTTGT[G/T]CGTTTGCCCATTTTT | 4690 |
rs182876530 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136919981 | GGAAGTTTGGTTGGG[G/T]TACAGATCTCACAGT | 4690 |
rs182954652 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NCK1 | GRCh38.p7 | 3:136887270 | ACTCTTGGCCTCAAA[C/T]GATCTTCCCACCTTA | 4690 |
rs183050462 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136865992 | ACTCACTAGCCTTTA[A/G]TTGGGTTTTTTGCTT | 4690 |
rs183055390 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136888293 | AGTCTTGTCGGTTTT[A/T]AAAAAAAGGTTTTAT | 4690 |
rs183175445 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | NCK1 | GRCh38.p7 | 3:136931022 | TACTTTTTTTTTAGC[A/G]GAACAGTGTAAAGAT | 4690 |
rs183183289 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136907871 | TGCTACAGGTATTAT[A/T]TCCTTATATATGTGG | 4690 |
rs183219109 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136940974 | TGAGTGTCTTGCAGA[C/T]AACAGTTGCATCATG | 4690 |
rs183226071 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136863372 | CAGTGTGCCTAGACT[C/G]TCAGCCTTCGGCGAG | 4690 |
rs183296075 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136934339 | TGCCCAGGTTGGAGT[A/G]CAGTGGTGTGATCTC | 4690 |
rs183303893 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136913100 | ATTAGGCCCGTCTTC[G/T]GATCTTTCTCTGGGA | 4690 |
rs183319600 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NCK1 | GRCh38.p7 | 3:136914488 | TACTCTGCTTTCTCC[C/T]CAGAATCCTCTAATG | 4690 |
rs183325031 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | NCK1 | GRCh38.p7 | 3:136871212 | ATCAGCCTGGGCAAT[A/G]TAGCAAGAGCCGGCC | 4690 |
rs183326283 | snp | C/G/T | 0.00164801 | 0.0286585 | synonymous-codon, missense, downstream-variant-500B | NCK1, LOC107986136 | GRCh38.p7 | 3:136945611 | GAAAAGAAAACCTAG[C/G/T]GTGCCAGATTCTGCA | 4690 |
rs183338637 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NCK1 | GRCh38.p7 | 3:136870511 | ATTTAATAGGGCTGG[A/G]CAGTTTTTTTTGGAA | 4690 |
rs183345748 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136892304 | CTGTGGGTTACCTTT[C/T]CACTGTATTAATTTA | 4690 |
rs183458787 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | NCK1 | GRCh38.p7 | 3:136940499 | CTTGATGGACTGATT[C/G]TTTTATCAATATATG | 4690 |
rs183469903 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136941318 | TTTTTTTGGTAGAGA[C/T]GAGGTCTCAGCATGT | 4690 |
rs183480895 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136897534 | GCCTTTCTTTGAAAA[A/G]TATCTATTCATGTCC | 4690 |
rs183504202 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136876887 | AACTGGTTTCAAAGA[C/T]ACAGATGTTTATTTA | 4690 |
rs183510026 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136893424 | TGAACATTTTTTCAT[A/G]TGTTGGCCATTTGTG | 4690 |
rs183516034 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136867105 | TTCTTTCTTTCTTTC[C/T]TTCTTTCTTTCTTTG | 4690 |
rs183517766 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136920752 | ATGAGCAATTAGATA[C/T]AAACCACCAATTATG | 4690 |
rs183523615 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136899780 | TTGAGACTTCTGCAC[A/G]TTAGTGGTGACTGTT | 4690 |
rs183550352 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136935837 | TCCATCACCCCAAAA[A/T]TAGTCACTCTCAATC | 4690 |
rs183638648 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NCK1 | GRCh38.p7 | 3:136871714 | CATCTTGAATTGTTA[C/T]TCCCACAATTCCCAC | 4690 |
rs183710245 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136919290 | GCAGTGATTACATAA[C/T]TCTTAAATGTTTGTC | 4690 |
rs183723166 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | NCK1 | GRCh38.p7 | 3:136874290 | AAGTGATTGTCCTGC[C/G]TCAGCCTCCCAAGTA | 4690 |
rs183790699 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136894079 | TGTGTACAACAGGTC[A/C]TAATAATCAGGGTCA | 4690 |
rs183807988 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | NCK1 | GRCh38.p7 | 3:136882863 | CACAGTCATTAGTGA[A/T]TACTAGCAGTCTCTT | 4690 |