SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs15139 | snp | G/T | 0 | 0 | utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105894119 | AAGGAAAAAGAAAAT[G/T]CAATTTCTTCATAAA | 8440 |
rs714068 | snp | C/T | 0.297382 | 0.245469 | intron-variant | NCK2 | GRCh38.p7 | 2:105791468 | GCACCCTCGCCCCGT[C/T]GCCGTGCTTACCGGC | 8440 |
rs714355 | snp | C/T | 0.370772 | 0.218893 | intron-variant | NCK2 | GRCh38.p7 | 2:105791252 | GAATGTTGATTCATC[C/T]AGAGAAACCTGAGGC | 8440 |
rs717730 | snp | A/G | 0.123452 | 0.215605 | intron-variant | NCK2 | GRCh38.p7 | 2:105750900 | ACGATCACAGAGATG[A/G]CAGGCTCAGAGGAGA | 8440 |
rs746436 | snp | C/G | 0.394372 | 0.233857 | intron-variant | NCK2 | GRCh38.p7 | 2:105789999 | GAGTCCAACACTAGC[C/G]TGTTCATGTATTGAG | 8440 |
rs746437 | snp | A/G | 0.419296 | 0.183954 | intron-variant | NCK2 | GRCh38.p7 | 2:105790216 | CCTAATGACATGCAC[A/G]CTATTTCTAACGGTT | 8440 |
rs768003 | snp | G/T | 0 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105868384 | GGCAACTGTTCATAA[G/T]TTAAAGGCTGGGGTG | 8440 |
rs879900 | snp | C/T | 0.433527 | 0.169758 | intron-variant | NCK2 | GRCh38.p7 | 2:105877891 | GGGCAACTTCTTAAT[C/T]TGTGGAAATAAGGAA | 8440 |
rs905084 | snp | C/T | 0.491885 | 0.0631791 | intron-variant | NCK2 | GRCh38.p7 | 2:105768278 | GCCACCGGCCACACG[C/T]GGCCACTGAGCACTC | 8440 |
rs934305 | snp | A/G | 0.0337553 | 0.125452 | intron-variant | NCK2 | GRCh38.p7 | 2:105845463 | gaggatgcagtgagt[A/G]aagatcagtcactgc | 8440 |
rs934306 | snp | G/T | 0.408359 | 0.193449 | intron-variant | NCK2 | GRCh38.p7 | 2:105843198 | TGAAACATAAATAAG[G/T]TATATATGAAACATA | 8440 |
rs934307 | snp | A/C | 0.26271 | 0.249677 | intron-variant | NCK2 | GRCh38.p7 | 2:105809340 | AATTGCTGTGTAAGC[A/C]CCTCAGTCTGTGGTA | 8440 |
rs997136 | snp | C/T | 0.499992 | 0.00199679 | intron-variant | NCK2 | GRCh38.p7 | 2:105749565 | TCCTTCTGCAGGCCA[C/T]ACATGAGGAACACCA | 8440 |
rs997522 | snp | A/G | 0.499933 | 0.00579035 | intron-variant | NCK2 | GRCh38.p7 | 2:105749775 | TGTCCCCACATCCTG[A/G]TTATGGGCCAGGGTT | 8440 |
rs1012028 | snp | C/G | 0 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105760706 | ACCAGTTACAGCTGA[C/G]AACCCTATTGTGGAA | 8440 |
rs1052624 | snp | G/T | 0 | 0 | utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105893800 | GAAAGACAGATGTTT[G/T]GGTAATTTACCCCAA | 8440 |
rs1076069 | snp | A/G | 0.25634 | 0.24992 | intron-variant | NCK2 | GRCh38.p7 | 2:105812545 | CTGAACGGGAGATCC[A/G]CTTGCAGGCCTCTGC | 8440 |
rs1114475 | snp | G/T | 0.489083 | 0.0730708 | intron-variant | NCK2 | GRCh38.p7 | 2:105759776 | TTTCTTAGACTCGCC[G/T]TGTTTTTAATGGCTT | 8440 |
rs1114882 | snp | A/G | 0.488424 | 0.0751925 | intron-variant | NCK2 | GRCh38.p7 | 2:105760112 | aggaagagggagttc[A/G]gctgtacctcctgta | 8440 |
rs1367404 | snp | G/T | 0.499816 | 0.0095829 | intron-variant | NCK2 | GRCh38.p7 | 2:105770408 | ATCTTTTGAGAGGTA[G/T]ATTTATGTGTCCTGA | 8440 |
rs1367405 | snp | A/G | 0.499809 | 0.00978247 | intron-variant | NCK2 | GRCh38.p7 | 2:105770684 | TATTGCCTAGGATAT[A/G]GATATCGATATTTAG | 8440 |
rs1367406 | snp | A/G | 0.0887219 | 0.191022 | intron-variant | NCK2 | GRCh38.p7 | 2:105803946 | ACTCACAAGGCACAT[A/G]GTATCCTCAGCTTTC | 8440 |
rs1465639 | snp | A/G | 0.433818 | 0.169443 | intron-variant | NCK2 | GRCh38.p7 | 2:105822725 | AATGGAATGTTATGT[A/G]TTCAGTTTCTATCTA | 8440 |
rs1465640 | snp | A/G | 0.425123 | 0.178415 | intron-variant | NCK2 | GRCh38.p7 | 2:105822647 | TCTTCAGCTTTCTAG[A/G]AAGCCACACTGCTAG | 8440 |
rs1465641 | snp | A/G | 0.433818 | 0.169443 | intron-variant | NCK2 | GRCh38.p7 | 2:105822480 | GGCGCTGTGGGAAGC[A/G]TCAGGGACCTTAGAG | 8440 |
rs1549768 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105819343 | TCTACCCCAATGACT[C/T]TTTTTTTTTTTTTTT | 8440 |
rs1549769 | snp | G/T | 0.256897 | 0.249905 | intron-variant | NCK2 | GRCh38.p7 | 2:105812862 | AGTTTGTTTTCAACG[G/T]TACTGCTTCTCTTAG | 8440 |
rs1549770 | snp | G/T | 0.402982 | 0.197728 | intron-variant | NCK2 | GRCh38.p7 | 2:105812811 | AAAAAAAAAAAGCCT[G/T]GTTGAATAGTGTCAC | 8440 |
rs1549771 | snp | A/G | 0.0865458 | 0.189163 | intron-variant | NCK2 | GRCh38.p7 | 2:105784039 | ATGGTGTTGAGGCCA[A/G]CCAGGTGCCACAGAA | 8440 |
rs1594403 | snp | C/G | 0.0785177 | 0.181917 | intron-variant | NCK2 | GRCh38.p7 | 2:105833928 | atgcaaattaaacaa[C/G]ttgctcttgaatgaa | 8440 |
rs1864555 | snp | C/T | 0.0883596 | 0.190715 | intron-variant | NCK2 | GRCh38.p7 | 2:105804449 | TTAGCTGTGTAAGCA[C/T]TTCCAAAGCCAAAAC | 8440 |
rs1897169 | snp | C/T | 0.499722 | 0.0117779 | | | GRCh38.p7 | 2:105781167 | ACACAAAGGCACCTC[C/T]AGGAAATGGGAAGCT | 8440 |
rs1986014 | snp | A/G | 0.338976 | 0.23363 | intron-variant | NCK2 | GRCh38.p7 | 2:105760506 | ACCTCCATCCTTGCC[A/G]TTCACACCTCTTCCC | 8440 |
rs1986015 | snp | A/G | 0.338523 | 0.233803 | intron-variant | NCK2 | GRCh38.p7 | 2:105760625 | CTTTGTATCAACCAA[A/G]GGTCTTTGCTTTCTG | 8440 |
rs2033008 | snp | A/T | 0.436834 | 0.166111 | intron-variant | NCK2 | GRCh38.p7 | 2:105886129 | GTGCCTGTAGGCATC[A/T]TTCCAGTTTCAAAGA | 8440 |
rs2047699 | snp | A/G | 0.420255 | 0.183066 | intron-variant | NCK2 | GRCh38.p7 | 2:105796620 | CAAATGCAAAAGGAA[A/G]AAAAGCACCATCTCC | 8440 |
rs2060036 | snp | C/T | 0.40086 | 0.199352 | intron-variant | NCK2 | GRCh38.p7 | 2:105819644 | TGTCTACGTGGCACC[C/T]GTGTGTTGGGAGCTC | 8440 |
rs2060037 | snp | C/G | 0.0607341 | 0.163335 | intron-variant | NCK2 | GRCh38.p7 | 2:105811848 | GGTCAATCGATGGGC[C/G]AAACCCCTATTAACT | 8440 |
rs2062657 | snp | C/T | 0.300673 | 0.244811 | intron-variant | NCK2 | GRCh38.p7 | 2:105777201 | TTCCTAAAGCAGCAG[C/T]GACGAGAGTAGAAGG | 8440 |
rs2082183 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | NCK2 | GRCh38.p7 | 2:105843864 | ggaagtctccaggaa[C/T]agcccacgcttaagg | 8440 |
rs2082184 | snp | A/G | 0.077417 | 0.180873 | intron-variant | NCK2 | GRCh38.p7 | 2:105840531 | gtcaacagtgtcaga[A/G]ctgaattaaattagc | 8440 |
rs2099211 | snp | A/G | 0.0807149 | 0.183963 | intron-variant | NCK2 | GRCh38.p7 | 2:105843673 | atattgctttttctt[A/G]aattgttccagcttt | 8440 |
rs2134082 | snp | C/G | 0.338976 | 0.23363 | intron-variant | NCK2 | GRCh38.p7 | 2:105760626 | CCAGAAAGCAAAGAC[C/G]CTTGGTTGATACAAA | 8440 |
rs2163349 | snp | C/T | 0.427727 | 0.175821 | intron-variant | NCK2 | GRCh38.p7 | 2:105841192 | AAAAGGTTACATGCC[C/T]GTGAGACTTTGGTTA | 8440 |
rs2163350 | snp | C/T | 0.238749 | 0.249747 | intron-variant | NCK2 | GRCh38.p7 | 2:105828825 | GGCCACTGGGTACAG[C/T]TGAAAAGATGAGTGA | 8440 |
rs2173883 | snp | C/G | 0.373397 | 0.217424 | intron-variant | NCK2 | GRCh38.p7 | 2:105760504 | GAAGAGGTGTGAACG[C/G]CAAGGATGGAGGTGA | 8440 |
rs2376977 | snp | A/G | 0.0905309 | 0.192535 | intron-variant | NCK2 | GRCh38.p7 | 2:105791634 | TTTCGAACTGACTCC[A/G]TAATAGATCTGATCA | 8440 |
rs2377338 | snp | A/G | 0.112631 | 0.208878 | intron-variant | NCK2 | GRCh38.p7 | 2:105834818 | tgggcctacaggtag[A/G]tgtgtgctaccatgt | 8440 |
rs2377339 | snp | A/G | 0.0685596 | 0.171987 | intron-variant | NCK2 | GRCh38.p7 | 2:105840835 | gaggctgaatcttgc[A/G]tcccccttttcctaa | 8440 |
rs2377340 | snp | A/G | 0.310632 | 0.242536 | intron-variant | NCK2 | GRCh38.p7 | 2:105844270 | gtagtgtgggatcct[A/G]ggtgggatcttggga | 8440 |
rs2553069 | snp | C/T | 0.0799831 | 0.183287 | | | GRCh38.p7 | 2:105873081 | CCCAGTTCCATGATC[C/T]TTGGCCAGCAGTCAG | 8440 |
rs2889526 | snp | A/T | 0 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105755410 | ATTTGTTGCTTCTTA[A/T]CTTGATTGTGCCGAG | 8440 |
rs2889602 | snp | C/G | 0.397633 | 0.201754 | intron-variant | NCK2 | GRCh38.p7 | 2:105812620 | GCATTTGAGAGCTCT[C/G]AGGCCTATGCTAATC | 8440 |
rs2889603 | snp | A/G | 0.132751 | 0.2208 | intron-variant | NCK2 | GRCh38.p7 | 2:105831217 | tacctaaagtgatct[A/G]tacattcagtgcaat | 8440 |
rs2889604 | snp | C/T | 0.40263 | 0.198 | intron-variant | NCK2 | GRCh38.p7 | 2:105832076 | aatgtagacatcttt[C/T]actttcttggttaaa | 8440 |
rs3047649 | in-del | -/CCC | 0 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105812789 | TCTGCTCATTACTGA[-/CCC]AGCCAGGTGACACTA | 8440 |
rs3047655 | in-del | -/AT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105844769 | TATATATATATATAT[-/AT]GTATGTATGTATATA | 8440 |
rs3047674 | in-del | -/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105845398 | CATTTATATTTTGAA[-/T]TTTTTTTTTTTTTTT | 8440 |
rs3073520 | in-del | -/TGAA | 0.420344 | 0.182983 | intron-variant | NCK2 | GRCh38.p7 | 2:105757955 | CACAGCTGGGGTGAA[-/TGAA]GCACCTCTATTCTCT | 8440 |
rs3073523 | in-del | -/A/AA/AAA | 0.5 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105779324 | AAAAAAAAAAAAAAA[-/A/AA/AAA]GAATCCGTCATAAAA | 8440 |
rs3073525 | in-del | -/CTTAGGC | 0 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105786865 | ACCCTAGCCTTAGGC[-/CTTAGGC]TGACTCCCTTACCTC | 8440 |
rs3739131 | snp | C/G | 0.1652 | 0.235179 | intron-variant | NCK2 | GRCh38.p7 | 2:105882203 | TGTTTGCTACTCCGT[C/G]ATTTACTTGCATCTG | 8440 |
rs3754801 | snp | C/T | 0.303688 | 0.244167 | intron-variant | NCK2 | GRCh38.p7 | 2:105876735 | TCATTAAAGTAAAAC[C/T]ACCTACTGCTTCCAG | 8440 |
rs3754802 | snp | C/T | 0.335101 | 0.23507 | intron-variant | NCK2 | GRCh38.p7 | 2:105872939 | GACAGGCGCTGCTAA[C/T]GTCCACTTCCGGGAA | 8440 |
rs3754803 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105871340 | TGATCAGTAACCAGC[A/C]CTACAATAACGTGGC | 8440 |
rs3754804 | snp | A/G | 0.16618 | 0.23553 | intron-variant | NCK2 | GRCh38.p7 | 2:105871324 | CTACAATAACGTGGC[A/G]CAGCGCCTGACAGCA | 8440 |
rs3754805 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105871090 | TTCACACGCACTCAT[C/T]GACCCTCCAGGCCTG | 8440 |
rs3754806 | snp | C/T | 0.305685 | 0.24372 | intron-variant | NCK2 | GRCh38.p7 | 2:105870926 | ACCAAGATCCTACGA[C/T]GTGCTGGGCACTCAC | 8440 |
rs3754807 | snp | A/T | 0.304188 | 0.244057 | intron-variant | NCK2 | GRCh38.p7 | 2:105852877 | AGGATAAAGTTTACA[A/T]GAAGCTCCTATCAGA | 8440 |
rs3754808 | snp | C/T | 0 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105852454 | ACTGCAAGCCAATTA[C/T]ATCAGTATCTTTATG | 8440 |
rs3769485 | snp | C/T | 0.420574 | 0.182769 | intron-variant | NCK2 | GRCh38.p7 | 2:105763648 | GGGTTGGGTTGTGCA[C/T]TGGGAACTTAGGGGT | 8440 |
rs3769486 | snp | C/G | 0.439918 | 0.162576 | intron-variant | NCK2 | GRCh38.p7 | 2:105763744 | CTTTCTGATTCTCAG[C/G]CGTGTTGTGGCAAAA | 8440 |
rs3769487 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | NCK2 | GRCh38.p7 | 2:105891172 | GGGAGTATGTGAGTA[C/T]TGAGAGTGTGTGAGA | 8440 |
rs3769488 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105891083 | AGCCCTCTGGACAAT[A/G]TGGAGCTGAGCATGT | 8440 |
rs3769489 | snp | C/T | 0.335788 | 0.23482 | intron-variant | NCK2 | GRCh38.p7 | 2:105890968 | CCCAGACCAGTTTTC[C/T]GCTTTTCTCAAAGCC | 8440 |
rs3769490 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | NCK2 | GRCh38.p7 | 2:105890729 | GAGAAGACTCAAATT[A/G]TGCAAGGCAGCTGGG | 8440 |
rs3769491 | snp | A/G | 0.335788 | 0.23482 | intron-variant | NCK2 | GRCh38.p7 | 2:105890197 | AGCAATAAAATTTTC[A/G]CAGCAGAAGAGGTAA | 8440 |
rs3769492 | snp | C/T | 0.336017 | 0.234736 | intron-variant | NCK2 | GRCh38.p7 | 2:105890171 | GGTAATTTTTAATTT[C/T]GTGGGCTCCTGAGCA | 8440 |
rs3769493 | snp | C/G | 0.230017 | 0.2492 | intron-variant | NCK2 | GRCh38.p7 | 2:105890151 | CCTTAACTTTTAAAG[C/G]TTTCTGCTCAGGAGC | 8440 |
rs3769494 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NCK2 | GRCh38.p7 | 2:105888003 | TGGTGTTCAACAAAC[A/G]TGCAGACTTAAAAAT | 8440 |
rs3769495 | snp | C/G | 0.317933 | 0.240593 | intron-variant | NCK2 | GRCh38.p7 | 2:105887720 | TGTTTTCTCATAGAA[C/G]GAAAAAAATGAATGC | 8440 |
rs3769496 | snp | C/T | 0.165853 | 0.235413 | intron-variant | NCK2 | GRCh38.p7 | 2:105879420 | GCAGGATGGTTCAAC[C/T]ACACAATGAAAGCAC | 8440 |
rs3769497 | snp | G/T | 0.0995161 | 0.199636 | intron-variant | NCK2 | GRCh38.p7 | 2:105873565 | AAACGTGGTAAATAT[G/T]GGTGAGCTGAAAAGA | 8440 |
rs3769498 | snp | C/T | 0.304438 | 0.244001 | intron-variant | NCK2 | GRCh38.p7 | 2:105871955 | CACCAATTTCCCTTG[C/T]ACGAAATCTCAGCCC | 8440 |
rs3769499 | snp | C/T | 0.0850919 | 0.187897 | intron-variant | NCK2 | GRCh38.p7 | 2:105864989 | GAGGGCTCTGGTGAC[C/T]GCTTTTTAGTTGAAG | 8440 |
rs3769500 | snp | C/T | 0.303688 | 0.244167 | intron-variant | NCK2 | GRCh38.p7 | 2:105864968 | TTAGTTGAAGGTACT[C/T]GTGTTATTTGGATGG | 8440 |
rs3769501 | snp | C/G | 0.108402 | 0.206034 | intron-variant | NCK2 | GRCh38.p7 | 2:105863350 | GACAACTGAAGCTTA[C/G]ACTCGGCTTCCACGA | 8440 |
rs3769502 | snp | C/T | 0.470521 | 0.117772 | intron-variant | NCK2 | GRCh38.p7 | 2:105862295 | CTAACCTGGGTCTTT[C/T]GATCTAAGTAAAATC | 8440 |
rs3769503 | snp | A/G | 0.0788843 | 0.182262 | intron-variant | NCK2 | GRCh38.p7 | 2:105860829 | GGAATGGTTAATCCA[A/G]GCATGAGAGGCAATC | 8440 |
rs3769504 | snp | C/T | 0.478603 | 0.101197 | intron-variant | NCK2 | GRCh38.p7 | 2:105860636 | ATGCCCCTGCTCAAA[C/T]CTTCAACTGTTTGTG | 8440 |
rs3820890 | snp | C/T | 0.429987 | 0.173507 | intron-variant | NCK2 | GRCh38.p7 | 2:105879837 | CTTTCTCCTTTTCTT[C/T]CTTAAACTAGAGTAA | 8440 |
rs3832068 | in-del | -/T/TT/TTT | 0.561358 | 0.185895 | intron-variant | NCK2 | GRCh38.p7 | 2:105855369 | ACTTTTAAAACAGAC[-/T/TT/TTT]TTTTTTTTTTTTGAA | 8440 |
rs3834120 | in-del | -/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105884241 | GCAGTGGATGGTGGG[-/G]AAAAAAACAAGCAAA | 8440 |
rs3835868 | in-del | -/TG | 0.439918 | 0.162576 | intron-variant | NCK2 | GRCh38.p7 | 2:105763601 | TTGTGTTCTGGGATC[-/TG]TGATTATTTACTGTT | 8440 |
rs3835869 | in-del | -/T | 0.0898077 | 0.191933 | intron-variant | NCK2 | GRCh38.p7 | 2:105888309 | GACCACTTCTTCCTG[-/T]TATGTCCTTCTATGA | 8440 |
rs3835871 | in-del | -/AAT | 0.0792508 | 0.182605 | intron-variant | NCK2 | GRCh38.p7 | 2:105856332 | TAAGAAGGTAACAAC[-/AAT]GTTTTAAATGTCAGC | 8440 |
rs3929435 | snp | A/C/T | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105761542 | actgtcccag[A/C/T] | 8440 |
rs3954042 | snp | C/T | 0.112983 | 0.209108 | intron-variant | NCK2 | GRCh38.p7 | 2:105836891 | gctacccagcatgaa[C/T]ggtctttctagagta | 8440 |
rs4012805 | in-del | -/AC/ACAA/ACAC/ACACACTA/ACACTA | | | utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105894020 | CACACACACACACAC[-/AC/ACAA/ACAC/ACACACTA/ACACTA]TATATATATATATAT | 8440 |
rs4316956 | snp | C/G | 0.417196 | 0.185864 | intron-variant | NCK2 | GRCh38.p7 | 2:105789768 | GCTTTTTCTGACACA[C/G]ACTGCTGCCCCACAC | 8440 |