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 |