SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs114537458 | snp | A/G | 0.031825 | 0.122064 | intron-variant | NCK2 | GRCh38.p7 | 2:105841907 | TTCAGAGAGGGGAAG[A/G]GAGCTCGCTTAGAAA | 8440 |
rs114544799 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | NCK2 | GRCh38.p7 | 2:105844222 | GAGAACTGCCACAGT[C/G]AAGAGGCGCCTAAGC | 8440 |
rs114569174 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | NCK2 | GRCh38.p7 | 2:105837767 | CTAACACATTATCAA[C/T]CTTTTTCATTTTTAC | 8440 |
rs114569461 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | NCK2 | GRCh38.p7 | 2:105817050 | GCATGGTGGCGTGCA[C/T]ATGTAGTCTCAGCTA | 8440 |
rs114572893 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105751411 | CCCTGACAGTCAGGT[C/T]TGGCCATGACCTGCA | 8440 |
rs114590468 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | NCK2 | GRCh38.p7 | 2:105842855 | TTTCAGGGGGGTGGA[C/T]GCTGTGAGAAATATG | 8440 |
rs114597171 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105880108 | ATTTTTACCTTAGGG[C/T]TTTTCTAGCATTTTT | 8440 |
rs114649076 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | NCK2 | GRCh38.p7 | 2:105781790 | CGAAAATTTGTAGAC[A/G]TGTCTGTTTCTCCAG | 8440 |
rs114656899 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | NCK2 | GRCh38.p7 | 2:105813932 | CGTAGTGCTAGTGAA[C/G]TACTTTTAGAGAAAA | 8440 |
rs114663145 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | NCK2 | GRCh38.p7 | 2:105827419 | TGAAGATCTCCATAC[C/T]CTTCTCAACAGTTGA | 8440 |
rs114686790 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | NCK2 | GRCh38.p7 | 2:105780152 | AAAATTTCTGGTTGC[A/G]AGATTAATCAAGAAT | 8440 |
rs114692829 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | NCK2 | GRCh38.p7 | 2:105860293 | CCTGTCTCAAAAAAT[G/T]AGCCATAAAAAAACA | 8440 |
rs114693785 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | NCK2 | GRCh38.p7 | 2:105891223 | ACACACTTAGAGCTG[C/T]GGTATCTCATGCTCC | 8440 |
rs114700151 | snp | G/T | 0.0162398 | 0.0886349 | intron-variant | NCK2 | GRCh38.p7 | 2:105781609 | TGGCAGAGGTCTTTG[G/T]GCATCAGTTTTATTA | 8440 |
rs114708097 | snp | C/T | 0.0322114 | 0.122752 | intron-variant | NCK2 | GRCh38.p7 | 2:105846823 | TTTCACTTCTAGGTA[C/T]ACACCCAATGGACTG | 8440 |
rs114716247 | snp | G/T | 0.0150606 | 0.0854603 | intron-variant | NCK2 | GRCh38.p7 | 2:105748610 | TTTTGTAGAGACAGG[G/T]TCTTGCTGCTTTGCC | 8440 |
rs114725966 | snp | A/T | 0.0107246 | 0.0724382 | intron-variant | NCK2 | GRCh38.p7 | 2:105817194 | AAAAAAAAAAAACCT[A/T]CATCAAATGAGATGC | 8440 |
rs114767518 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | NCK2 | GRCh38.p7 | 2:105856262 | TACAGTATTTACTGC[C/T]TCAGATTACCTGAGA | 8440 |
rs114777940 | snp | A/C | 0.0236746 | 0.106192 | intron-variant | NCK2 | GRCh38.p7 | 2:105882983 | CTGGCACAATGAATA[A/C]GTGCTCATTCAAGGG | 8440 |
rs114780078 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | NCK2 | GRCh38.p7 | 2:105783048 | CCTTTTTGGGTACCT[A/G]GGATATAACCGTGGA | 8440 |
rs114782847 | snp | C/G | 0.0134861 | 0.0810011 | intron-variant | NCK2 | GRCh38.p7 | 2:105801365 | TCGGCTTGCCTCCCC[C/G]CTTCCCCATGTCATC | 8440 |
rs114807783 | snp | C/G | 0.0228947 | 0.104514 | utr-variant-5-prime | NCK2 | GRCh38.p7 | 2:105816541 | TGTAACTTCAGAGGT[C/G]TAATTAGCTGAAAAC | 8440 |
rs114829912 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NCK2 | GRCh38.p7 | 2:105755004 | GACTCCCCTCACCCC[A/G]TCTCTCCCGCCCTGA | 8440 |
rs114837130 | snp | G/T | 0.0225045 | 0.103662 | intron-variant | NCK2 | GRCh38.p7 | 2:105778053 | TCAGCTGTGCTTGGA[G/T]GAGCTGCCAAAGTGG | 8440 |
rs114850077 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | NCK2 | GRCh38.p7 | 2:105844432 | TATTTTAGTCTAAAA[A/G]ATATTTTTGGGCCAG | 8440 |
rs114852375 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | NCK2 | GRCh38.p7 | 2:105811280 | TATGTCCCAAAGATA[C/T]AGGATTGGAGTTGAG | 8440 |
rs114862238 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | NCK2 | GRCh38.p7 | 2:105776894 | GTTCTTCCTGACCCC[C/T]TGGAGCCTCTCTCAG | 8440 |
rs114886153 | snp | G/T | 0.031825 | 0.122064 | intron-variant | NCK2 | GRCh38.p7 | 2:105854766 | CATTTAATTATAATG[G/T]TATTTAGAATTTTTT | 8440 |
rs114903315 | snp | A/C | 0.0322114 | 0.122752 | intron-variant | NCK2 | GRCh38.p7 | 2:105846513 | GGGTGTAGCAGAAAA[A/C]TGTAGATGATCTTTA | 8440 |
rs114905728 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | NCK2 | GRCh38.p7 | 2:105855006 | AAGGATGAAGTGTCC[A/G]GGTAGTTCTCTAATG | 8440 |
rs114913318 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | NCK2 | GRCh38.p7 | 2:105873260 | CACTCTCAGGATGTT[C/T]TCTGACCACTGTGCC | 8440 |
rs114915500 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | NCK2 | GRCh38.p7 | 2:105790395 | GCAAGTAGCCTGACT[C/T]CTAGGATGGGTAGCA | 8440 |
rs114933795 | snp | G/T | 0.0399052 | 0.1355 | intron-variant | NCK2 | GRCh38.p7 | 2:105765788 | GCTTAGAATAGGGGG[G/T]GTGTGTGTGTGTGTG | 8440 |
rs114974796 | snp | A/G | 0.031825 | 0.122064 | intron-variant | NCK2 | GRCh38.p7 | 2:105792848 | GCCTCCACCTGTAAT[A/G]CACAGGGGTTGCAAA | 8440 |
rs114995510 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | NCK2 | GRCh38.p7 | 2:105766075 | TGACATTGCTACCAT[A/G]GATAGTAGAAATCGC | 8440 |
rs115009775 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | NCK2 | GRCh38.p7 | 2:105793265 | CCAGAGTGCTGCCTG[C/T]TTTTTTGTCCCCTTA | 8440 |
rs115015699 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | NCK2 | GRCh38.p7 | 2:105764393 | CCACATGTTTATCGC[C/T]GGCCACCCTCCTAGG | 8440 |
rs115021586 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | NCK2 | GRCh38.p7 | 2:105884425 | AGCCTCCCTGCAGGA[A/C]TCAGTCAGGCATCTT | 8440 |
rs115027465 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | NCK2 | GRCh38.p7 | 2:105859745 | GCTGTAGGATTGTTA[C/T]GTAAGATCCAAAAGC | 8440 |
rs115032882 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | NCK2 | GRCh38.p7 | 2:105755508 | TTCATGAGTGCCTCC[A/G]GTTGGTGAGGGTTCC | 8440 |
rs115041340 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | NCK2 | GRCh38.p7 | 2:105890775 | TGAGTTGTCATTGGT[A/C]GAAATGGAGTGATTC | 8440 |
rs115064093 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NCK2 | GRCh38.p7 | 2:105752722 | AAGTCTCTGGTTCCG[C/T]CTGGATAATGGCCTC | 8440 |
rs115087400 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | NCK2 | GRCh38.p7 | 2:105782882 | CGCTCCCAACTGGAG[A/G]GGCGTAGGGGGCAGT | 8440 |
rs115088539 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | NCK2 | GRCh38.p7 | 2:105843857 | TCCCCACCCTTAAGC[A/G]TGGGCTGTTCCTGGA | 8440 |
rs115092001 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | NCK2 | GRCh38.p7 | 2:105870011 | AAAGTCAGGTTCAGA[A/G]CCCTGGACACAAGGA | 8440 |
rs115095346 | snp | A/G | 0.0209541 | 0.100278 | intron-variant | NCK2 | GRCh38.p7 | 2:105892613 | GGCTGAGGCTGGGAG[A/G]GGGGTGGGGATCACC | 8440 |
rs115096159 | snp | C/T | 0.0263992 | 0.111815 | intron-variant, utr-variant-5-prime | NCK2 | GRCh38.p7 | 2:105773323 | TGTCCCTCTCCTTTC[C/T]AGCCACCCGCTTGAG | 8440 |
rs115142546 | snp | G/T | 0.0115144 | 0.0749975 | intron-variant | NCK2 | GRCh38.p7 | 2:105777871 | TTGAAGAGAGGATCG[G/T]TACTGGGGTGACAGC | 8440 |
rs115151868 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | NCK2 | GRCh38.p7 | 2:105860571 | GTCAGAACCGCATGG[A/G]GAGGCCTTACTGGGC | 8440 |
rs115170271 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | NCK2 | GRCh38.p7 | 2:105828758 | AAATAGGATGCTGCT[A/G]TGTTGACCTCTTAGT | 8440 |
rs115172556 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | NCK2 | GRCh38.p7 | 2:105883422 | GGGCTAAGTATAATG[C/T]ACAAAATATGATCTT | 8440 |
rs115180012 | snp | A/G | 0.0379877 | 0.132479 | intron-variant | NCK2 | GRCh38.p7 | 2:105802277 | AAATGTGGTGTGGGA[A/G]GCTGGGCCCACTGTG | 8440 |
rs115240904 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | NCK2 | GRCh38.p7 | 2:105888033 | AGATACTCTGAGCCC[A/G]GTGTGGGGATGTGGA | 8440 |
rs115265456 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | NCK2 | GRCh38.p7 | 2:105868127 | CTCCTGCATGGCCCA[C/T]GTGCTGCCTTGGTGT | 8440 |
rs115270471 | snp | G/T | 0.0260105 | 0.111035 | intron-variant | NCK2 | GRCh38.p7 | 2:105789794 | CACACACCCCCAGTT[G/T]CTGCCTCAGTGGTCT | 8440 |
rs115281595 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | NCK2 | GRCh38.p7 | 2:105782118 | TACTATGACTGCGGG[A/G]AGTTGCTTTTGGGCT | 8440 |
rs115284204 | snp | A/T | 0.0228947 | 0.104514 | intron-variant | NCK2 | GRCh38.p7 | 2:105830749 | TTCTCATTGAGATGA[A/T]ACCTTATTGTGGCTT | 8440 |
rs115290788 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | NCK2 | GRCh38.p7 | 2:105793655 | CTCTGATTTAAGATA[C/T]TTTGTGTGTATTTTT | 8440 |
rs115295616 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | NCK2 | GRCh38.p7 | 2:105840323 | TCACCCCTGTAACAC[A/G]TGGGACACATGGAGA | 8440 |
rs115296094 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | NCK2 | GRCh38.p7 | 2:105833508 | TATTAGTCTCTAATG[A/G]TCTTTTATATTTCTG | 8440 |
rs115308684 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | NCK2 | GRCh38.p7 | 2:105824881 | GCTCAGCATTTGTGG[A/G]ACACCAGTGTCACCC | 8440 |
rs115312856 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | NCK2 | GRCh38.p7 | 2:105748258 | CTCATCCCAAGGGTC[A/G]TCTCTTACTTCTTTT | 8440 |
rs115436337 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | NCK2 | GRCh38.p7 | 2:105816898 | CTCTTGAATCCATAA[C/T]GAATCCTGGTCCCTG | 8440 |
rs115487386 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | NCK2 | GRCh38.p7 | 2:105774867 | TGTGGCTTAATGAGC[C/T]GTGTAGATGTACAGC | 8440 |
rs115498953 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | NCK2 | GRCh38.p7 | 2:105847870 | GCTAGATACAAGCTG[A/G]TAGCATTAGCATTAG | 8440 |
rs115500801 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | NCK2 | GRCh38.p7 | 2:105827662 | TACAGAGTGTCTTCT[A/G]TCTTTTAATAGAATT | 8440 |
rs115510359 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | NCK2 | GRCh38.p7 | 2:105789482 | GCATGAGCCACCTTG[C/T]CTGGCCTCACAACCT | 8440 |
rs115511870 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | NCK2 | GRCh38.p7 | 2:105791816 | TTGATAGGCCACTCA[A/G]TATTTTCATATCTGT | 8440 |
rs115515826 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | NCK2 | GRCh38.p7 | 2:105816123 | GCAGCTTTAATCTGG[A/G]ATATATTTAAAACAT | 8440 |
rs115532462 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | NCK2 | GRCh38.p7 | 2:105863709 | TGAGTTATGCAGCTC[A/G]GGCACCTGTGCTTTC | 8440 |
rs115563450 | snp | C/G | 0.0329836 | 0.124112 | intron-variant | NCK2 | GRCh38.p7 | 2:105889772 | TAAATTTTATGTAGA[C/G]ATAGGGTCCCACTAT | 8440 |
rs115564969 | snp | C/T | 0.125182 | 0.216612 | intron-variant | NCK2 | GRCh38.p7 | 2:105873467 | CTTAGGAAACATGCA[C/T]GCCACCCAGCTATGA | 8440 |
rs115570913 | snp | A/T | 0.0260105 | 0.111035 | intron-variant | NCK2 | GRCh38.p7 | 2:105792732 | AAACTGCACATCAGA[A/T]CCAGAGCCAGTCTGG | 8440 |
rs115585075 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | NCK2 | GRCh38.p7 | 2:105880070 | ATGTTCCGGAATTCC[A/G]TGCATTTTAACACAG | 8440 |
rs115587318 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | NCK2 | GRCh38.p7 | 2:105768449 | CGTCACCAGTTGCAT[A/G]TCCTAAGCCACCTGT | 8440 |
rs115609328 | snp | A/G | 0.00597247 | 0.0543191 | upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105743649 | ATCTCCCCATATGAC[A/G]GATTTTAGAAAGGCT | 8440 |
rs115618238 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105759610 | ATTCACATCTTACGT[A/T]ACTATAGTACATTGG | 8440 |
rs115621302 | snp | A/T | 0.0260105 | 0.111035 | intron-variant | NCK2 | GRCh38.p7 | 2:105789562 | TCTTTCTAGTTGAAG[A/T]GATGTTTCCCTGAGT | 8440 |
rs115641980 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105843645 | GTAGCCAGCTGAAAA[C/T]GCTCCCATACACAAA | 8440 |
rs115658569 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | NCK2 | GRCh38.p7 | 2:105867900 | TATGCCAGGGAATTA[A/G]AGAACCATCTTCCTA | 8440 |
rs115663749 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | NCK2 | GRCh38.p7 | 2:105793530 | TAGGCATTGCACTGG[C/T]TAACAAGTTTATTTG | 8440 |
rs115664534 | snp | C/G | 0.0228947 | 0.104514 | intron-variant | NCK2 | GRCh38.p7 | 2:105838763 | ACTGATGGAGGCCGA[C/G]CGTAGGCCTTTCATC | 8440 |
rs115672278 | snp | C/T | 0.0101545 | 0.0705277 | intron-variant | NCK2 | GRCh38.p7 | 2:105882074 | CTGCGCCCACAGCTC[C/T]GGCTGCAGGCAGTAA | 8440 |
rs115688875 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | NCK2 | GRCh38.p7 | 2:105748010 | GTATGTTTATTTCTA[A/C]AGGTAAATGAACGTT | 8440 |
rs115708103 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105781388 | TCCCTTCCCACACTG[C/T]AAGACTTGACTAAAT | 8440 |
rs115725304 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | NCK2 | GRCh38.p7 | 2:105793237 | CTGGGAATGGGTGGA[A/G]AACTTCTGGAAACCA | 8440 |
rs115730988 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | NCK2 | GRCh38.p7 | 2:105763745 | TTTCTGATTCTCAGC[C/T]GTGTTGTGGCAAAAT | 8440 |
rs115737474 | snp | G/T | 0.0267878 | 0.112589 | intron-variant | NCK2 | GRCh38.p7 | 2:105832938 | GTGTTAGTTTGTCTT[G/T]ATAAGTTTGGAAAAA | 8440 |
rs115738500 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | NCK2 | GRCh38.p7 | 2:105875799 | TTACAGTATTTTGTT[A/G]TAGGCGCCTGAACCA | 8440 |
rs115741510 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | NCK2 | GRCh38.p7 | 2:105883408 | TCCAGAGTCCTTAAG[G/T]GCTAAGTATAATGCA | 8440 |
rs115812554 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | NCK2 | GRCh38.p7 | 2:105814952 | ATAATAGCCCCTGAA[A/G]ATGACACATACAGAG | 8440 |
rs115831561 | snp | C/G | 0.0387552 | 0.1337 | intron-variant | NCK2 | GRCh38.p7 | 2:105820784 | TTGACTTTTGAAAAG[C/G]TTTTGGAGGCTTTTT | 8440 |
rs115850662 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | NCK2 | GRCh38.p7 | 2:105871821 | TTCTAAAGCTAAACT[A/G]CTAGAGGTAAAAAGT | 8440 |
rs115870039 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | NCK2 | GRCh38.p7 | 2:105787253 | TCTCAGCTCTGACAT[A/G]GTCATATCTGTAGGC | 8440 |
rs115871080 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | NCK2 | GRCh38.p7 | 2:105830385 | GGCTTATCCATGTTG[C/T]CATGAGTGACAAGTG | 8440 |
rs115879947 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | NCK2 | GRCh38.p7 | 2:105773601 | CCCAATACCATAGTA[C/T]CCCTTTGACACTATG | 8440 |
rs115897328 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | NCK2 | GRCh38.p7 | 2:105778692 | GGTTATGTGTATCAA[C/T]TGAGATAATGGTTAT | 8440 |
rs115904469 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | NCK2 | GRCh38.p7 | 2:105747815 | AATGTGATTTCGTGT[A/G]TCTTGTTCCATGCCT | 8440 |
rs115907432 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | NCK2 | GRCh38.p7 | 2:105768991 | CAGAGGTTGGGGTGT[A/G]GGGGGTGCAGAAAGT | 8440 |
rs115915230 | snp | A/G | 0.0322114 | 0.122752 | intron-variant | NCK2 | GRCh38.p7 | 2:105823432 | CCAAAAGCATTTTGA[A/G]TTTGAGATTTCTGCC | 8440 |
rs115950492 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | NCK2 | GRCh38.p7 | 2:105766803 | GCATGCAGGATTTTC[A/G]TTCCCTCCAAACTAT | 8440 |
rs116020455 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | NCK2 | GRCh38.p7 | 2:105864602 | TATGACATACTTCTT[G/T]ATGTCAGTGAATTTT | 8440 |
rs116022521 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | NCK2 | GRCh38.p7 | 2:105826623 | TTCCCAATGGATTGC[A/T]TGGTAAAGGGCTCTG | 8440 |
rs116022781 | snp | C/T | 0.040671 | 0.13668 | intron-variant | NCK2 | GRCh38.p7 | 2:105784260 | AGGCATGAGACACCA[C/T]GCCCGGCTGTTATTT | 8440 |
rs116025549 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | NCK2 | GRCh38.p7 | 2:105781010 | TCTTTTCTCATTGCC[C/T]GAATCTAGATTTTGT | 8440 |
rs116032203 | snp | A/G | 0.0168055 | 0.0901129 | intron-variant | NCK2 | GRCh38.p7 | 2:105874564 | TAGCAAAAATTAAAT[A/G]ATTTTGCCATAGAGC | 8440 |
rs116033386 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | NCK2 | GRCh38.p7 | 2:105793081 | GTGCAGGCTTTATAT[A/G]ATGGCCGTGGAATTG | 8440 |
rs116034741 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | NCK2 | GRCh38.p7 | 2:105888795 | GAGAGTACATTCAGG[C/T]AGCCCTACAGAGCCC | 8440 |
rs116037222 | snp | A/C | 0.0260105 | 0.111035 | intron-variant | NCK2 | GRCh38.p7 | 2:105784649 | TGTGGTTAGGCAGGC[A/C]GTTACAAATGCTTGC | 8440 |
rs116038905 | snp | C/T | 0.0270757 | 0.113158 | intron-variant | NCK2 | GRCh38.p7 | 2:105805908 | ATATTTGCATAAACA[C/T]AACGAGAGGTTTTGG | 8440 |
rs116044467 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | NCK2 | GRCh38.p7 | 2:105827697 | CTTTTTGCTTTAAAA[C/T]GAGTCTCAAATGGTC | 8440 |
rs116085778 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | NCK2 | GRCh38.p7 | 2:105797551 | GGCTGCTCTCTTGAC[A/G]GCGTCTTAGGGTCAG | 8440 |
rs116098659 | snp | C/T | 0.0850919 | 0.187897 | intron-variant | NCK2 | GRCh38.p7 | 2:105853255 | TTGGTTCATCTTCTA[C/T]CTAAGAAGTAGAGAG | 8440 |
rs116100590 | snp | A/C | 0.00597247 | 0.0543191 | upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105743877 | CCAGGAGCCTAAGAA[A/C]GAATCTCATTAACAT | 8440 |
rs116129698 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | NCK2 | GRCh38.p7 | 2:105795512 | CAAAAGAGTTAGAAA[A/G]TACATGGATATTCCT | 8440 |
rs116143750 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | NCK2 | GRCh38.p7 | 2:105759737 | GTTTCCTTTAGTCTC[C/T]GTAGCGCCTCTGATC | 8440 |
rs116168125 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | NCK2 | GRCh38.p7 | 2:105781455 | CCAGAACTAGTGACC[C/T]TCCTTGGCCTTCTAG | 8440 |
rs116188069 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | NCK2 | GRCh38.p7 | 2:105867747 | GCAGAGCATTTCCCA[A/G]GAACTGGCATCTTGG | 8440 |
rs116197604 | snp | G/T | 0.0174175 | 0.0916809 | intron-variant | NCK2 | GRCh38.p7 | 2:105839241 | GCAGCTTTGGATTTG[G/T]TTCTGTTTGGGTGGG | 8440 |
rs116223469 | snp | A/G | 0.031825 | 0.122064 | intron-variant | NCK2 | GRCh38.p7 | 2:105840692 | ATGTTGCCTTCCTCA[A/G]GTTCAATTAATTTGC | 8440 |
rs116241233 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | NCK2 | GRCh38.p7 | 2:105825540 | ATTTCTTCCCACACC[C/T]GGTGTTTTCCACTTT | 8440 |
rs116244879 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | NCK2 | GRCh38.p7 | 2:105783838 | ACAAGGGCATTTCTT[C/T]CCAGAAAGTGGGAGT | 8440 |
rs116254108 | snp | A/C/G | 0.0189856 | 0.0955633 | intron-variant | NCK2 | GRCh38.p7 | 2:105762703 | CTATTTTCCTGTTAC[A/C/G]TAATAGTGATGCACG | 8440 |
rs116258224 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | NCK2 | GRCh38.p7 | 2:105748016 | TTATTTCTAAAGGTA[A/C]ATGAACGTTAGCAAG | 8440 |
rs116277788 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | NCK2 | GRCh38.p7 | 2:105784965 | TTTGTGTGTTTTTTC[A/G]TTTTTGTTTTGTTTT | 8440 |
rs116299309 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | NCK2 | GRCh38.p7 | 2:105804420 | AGGCATGTAGGTTTT[C/T]ATGCTCTTGTCTGGT | 8440 |
rs116325439 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105793154 | AGAGGTGGGAAGCCA[C/G]AGATGTAGGACATCT | 8440 |
rs116331553 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | NCK2 | GRCh38.p7 | 2:105858681 | CTCTCCTGCTTTCTT[G/T]TACTCATTTGCTGTC | 8440 |
rs116332019 | snp | G/T | 0.0185938 | 0.0946107 | intron-variant | NCK2 | GRCh38.p7 | 2:105812188 | TCTAATTGCAGTGAG[G/T]CTTTTTGAAGCTGCT | 8440 |
rs116333350 | snp | C/T | 0.031825 | 0.122064 | utr-variant-5-prime | NCK2 | GRCh38.p7 | 2:105816436 | TCTTTTTAGATTTCA[C/T]GTGTTCTTTGTATAC | 8440 |
rs116368977 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | NCK2 | GRCh38.p7 | 2:105832855 | TCTTCTCTTTTTTTT[C/T]TTTATTTTGTTTCGT | 8440 |
rs116384858 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | NCK2 | GRCh38.p7 | 2:105890497 | AATATTAATCATCTA[C/T]AGGCTGAGGCCTAAT | 8440 |
rs116427876 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | NCK2 | GRCh38.p7 | 2:105823655 | TTTGGATGGAAACGA[A/G]TAACCCTTAGTGCTT | 8440 |
rs116428598 | snp | A/G | 0.081446 | 0.184634 | intron-variant | NCK2 | GRCh38.p7 | 2:105818524 | ATATATATTTCCAAC[A/G]TGGTATATTTAACAG | 8440 |
rs116444924 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | NCK2 | GRCh38.p7 | 2:105879066 | ATTGTGATGGCCACT[A/G]TCAAATGTCTTTTTT | 8440 |
rs116454656 | snp | A/G | 0.0729998 | 0.176553 | intron-variant | NCK2 | GRCh38.p7 | 2:105829170 | ATAGGTACAAAATAC[A/G]TAGGTGTCATTTATG | 8440 |
rs116474055 | snp | C/T | 0.0322114 | 0.122752 | intron-variant | NCK2 | GRCh38.p7 | 2:105848579 | CTTTGCTCCCGAGAA[C/T]AGCAGTGCACACGGC | 8440 |
rs116475354 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NCK2 | GRCh38.p7 | 2:105747682 | AGCTCACTTCAGATG[C/T]TTAGGAAATTAGTTT | 8440 |
rs116478131 | snp | A/T | 0.0821764 | 0.185298 | intron-variant | NCK2 | GRCh38.p7 | 2:105843522 | GGACTGGGGTAGAAA[A/T]TATGCAAGAAAAGCC | 8440 |
rs116483251 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | NCK2 | GRCh38.p7 | 2:105819710 | TACAAAAATATCTAC[C/T]CATGTAATTTTAAAG | 8440 |
rs116540218 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | NCK2 | GRCh38.p7 | 2:105788441 | GTTTGTATATTTATA[A/G]TCATACTCTATCCAA | 8440 |
rs116547789 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | NCK2 | GRCh38.p7 | 2:105751975 | CATCCTATATTTTGC[C/T]CAATATATATATAAA | 8440 |
rs116555277 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | NCK2 | GRCh38.p7 | 2:105822599 | TCAAGGTTATGCCAA[A/G]CATTTTTTCTTTTCT | 8440 |
rs116556413 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | NCK2 | GRCh38.p7 | 2:105874296 | CAAAAACTTGTAGAA[A/G]CTGAGCTGAACGTTA | 8440 |
rs116568380 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NCK2 | GRCh38.p7 | 2:105750509 | TGGTGCTCCCATCAT[C/T]CAGATCTGGGATCTC | 8440 |
rs116611022 | snp | C/G | 0.0197687 | 0.0974348 | upstream-variant-2KB, intron-variant | NCK2 | GRCh38.p7 | 2:105850479 | AGAGCTGTTTTTCCA[C/G]CATAACTTGGGGGTC | 8440 |
rs116627306 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | NCK2 | GRCh38.p7 | 2:105801085 | GGGCGTGCTGAGCCC[A/G]TCAGCATTTGTTCTC | 8440 |
rs116650359 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105880438 | AGGATTGTAAGAAGA[A/G]AAGAAAGGTGAAGAT | 8440 |
rs116684482 | snp | G/T | 0.0205511 | 0.0992634 | intron-variant | NCK2 | GRCh38.p7 | 2:105878130 | AAGTGTTTTTAAAGA[G/T]GACTTTGGCCCTCTT | 8440 |
rs116697117 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | NCK2 | GRCh38.p7 | 2:105811264 | ATAATGTCCATTCCC[A/G]TATGTCCCAAAGATA | 8440 |
rs116735657 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | NCK2 | GRCh38.p7 | 2:105826230 | CAAAGCGGGAAGAGC[A/G]GCTTATAAAACCATC | 8440 |
rs116794386 | snp | G/T | 0.0228947 | 0.104514 | intron-variant | NCK2 | GRCh38.p7 | 2:105812623 | TTTGAGAGCTCTGAG[G/T]CCTATGCTAATCCAT | 8440 |
rs116825351 | snp | C/G | 0.0314385 | 0.121371 | intron-variant | NCK2 | GRCh38.p7 | 2:105859385 | CCGTGGCTCACCCTG[C/G]CACCCTACCTACCTG | 8440 |
rs116828374 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | NCK2 | GRCh38.p7 | 2:105762914 | TAAAAGCAACCTGAG[A/G]CCAGGCGCAGTGGCT | 8440 |
rs116829275 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | NCK2 | GRCh38.p7 | 2:105863433 | AGTGACCTTTGAGAA[C/G]AGTAACCAAAGGCTT | 8440 |
rs116920222 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | NCK2 | GRCh38.p7 | 2:105842129 | TTTCTCTCGTTTCCC[A/G]GGCTGGAGTGCAATG | 8440 |
rs117046125 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | NCK2 | GRCh38.p7 | 2:105808642 | CTGCAGGGTGGATCA[C/T]CCAGCGTCTTCAGTG | 8440 |
rs117189716 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | NCK2 | GRCh38.p7 | 2:105798308 | AGCCCGGATAGCCTC[A/G]CTGTGGCCTCTTGTT | 8440 |
rs117343449 | snp | A/C/T | 0.00835572 | 0.0641442 | intron-variant | NCK2 | GRCh38.p7 | 2:105799315 | TAAAGGGTGTTTTCC[A/C/T]TATGTCCTTCTATAC | 8440 |
rs117464963 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105813831 | TTTTGTAGTATTAAG[A/G]ATCCACATTAAAATG | 8440 |
rs117501762 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | NCK2 | GRCh38.p7 | 2:105881174 | GCTGCCAGCAACCGT[A/C]TTTTTCTCATGGTAA | 8440 |
rs117803435 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | NCK2 | GRCh38.p7 | 2:105766579 | CCTCCCACCTCAGCC[C/T]CCCAAAATGTAGGGA | 8440 |
rs117813704 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | NCK2 | GRCh38.p7 | 2:105868119 | CTGTAGGGCTCCTGC[A/G]TGGCCCACGTGCTGC | 8440 |
rs117865776 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105785735 | TTGTGCTTTATAAGC[C/T]GAAGCTTGGGAGAAC | 8440 |
rs117933494 | snp | A/C | 0.0182019 | 0.0936463 | intron-variant | NCK2 | GRCh38.p7 | 2:105862302 | CTTAGATCAAAAGAC[A/C]CAGGTTAGTCGAGTA | 8440 |
rs117970405 | snp | C/T | 0.000683114 | 0.0184686 | synonymous-codon, intron-variant | NCK2 | GRCh38.p7 | 2:105881374 | GCGGGATGCGTCCCC[C/T]ACGCCCAGCACGGAC | 8440 |
rs117971646 | snp | G/T | 0.0126979 | 0.078662 | intron-variant | NCK2 | GRCh38.p7 | 2:105869635 | TCCTGAGCAGGTGTG[G/T]TCCTGCAGAACAGCA | 8440 |
rs118026024 | snp | C/T | 0.00148003 | 0.0271629 | intron-variant | NCK2 | GRCh38.p7 | 2:105855340 | CATTTCAAGGGACAC[C/T]GTTCGTCTTTCTAGT | 8440 |
rs118042316 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | NCK2 | GRCh38.p7 | 2:105781235 | TTCTACCATTCAGCC[C/T]TTGTGAATTTTATGA | 8440 |
rs118079753 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NCK2 | GRCh38.p7 | 2:105790677 | AGGCCCTTAGTGCCT[C/T]CTTCCTCTGTTCTGG | 8440 |
rs118106287 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105811625 | GCCCTGAGTTTTGGG[G/T]TGCATGAAGGATGCC | 8440 |
rs118139708 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | NCK2 | GRCh38.p7 | 2:105813016 | CGATTTGCAGAATGC[A/G]ACTGTCAAGGTTCTA | 8440 |
rs118166410 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | NCK2 | GRCh38.p7 | 2:105783601 | GTTCGCGGAGAATAA[C/T]GGTGTGTTTTTTCCA | 8440 |
rs137864448 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105815985 | CACCCCATCACCTCC[G/T]TCCACCTGCTGTTCA | 8440 |
rs137868721 | snp | C/T | 0.000215591 | 0.0103802 | missense, intron-variant | NCK2 | GRCh38.p7 | 2:105881877 | TCCTCAGTGACGGGC[C/T]TGCCCTGCACCCTGC | 8440 |
rs137875252 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | NCK2 | GRCh38.p7 | 2:105777236 | CTGTCCCCATAGCCA[C/T]GAGCCGGGGTGTTGC | 8440 |
rs137914261 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | NCK2 | GRCh38.p7 | 2:105850623 | TAGCTGTAGTAATGA[A/G]GCCAAAAATTAGGTT | 8440 |
rs137933119 | in-del | -/TTTA | 0.317933 | 0.240593 | intron-variant | NCK2 | GRCh38.p7 | 2:105794696 | TTAATAGTTTATTAT[-/TTTA]TTTATTTATTTATTT | 8440 |
rs137953799 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | NCK2 | GRCh38.p7 | 2:105879006 | TTGAAAGAAGTCACT[A/G]AAGTAGAATATTCGT | 8440 |
rs137969463 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105813048 | CCCTTTCGTGGTGAT[A/C]TTTGTCAGGAGAAGG | 8440 |
rs137975619 | snp | C/T | 0.000100531 | 0.00708911 | synonymous-codon, intron-variant | NCK2 | GRCh38.p7 | 2:105881791 | TGAGAAGCCGGAGAA[C/T]GACCCCGAGTGGTGG | 8440 |
rs138080475 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NCK2 | GRCh38.p7 | 2:105841457 | ACAGGGGAAGGGGCA[C/T]GGAGCTTCCATGCCT | 8440 |
rs138111777 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NCK2 | GRCh38.p7 | 2:105808593 | AGGGCTGGGGAGCAC[A/G]TGAAAAACACCAGAG | 8440 |
rs138116436 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105890272 | ATTAAGGAGCTTGAA[C/T]TAAAAGCAAATTTCC | 8440 |
rs138120731 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105844595 | AAAAAAAAAACAGCT[A/G/T]GGCATGGAGGCTCTT | 8440 |
rs138126201 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105825503 | AGCGCTTTGGAACAT[A/G]GCAGATATGGGAACG | 8440 |
rs138136516 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | NCK2 | GRCh38.p7 | 2:105776029 | ATAATTTGAAAAAAT[G/T]TCCCCCTTGTATTTT | 8440 |
rs138152652 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | NCK2 | GRCh38.p7 | 2:105790300 | CGTCATTGCCCACCA[C/T]CTATTTTTAGCAGAT | 8440 |
rs138187761 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | NCK2 | GRCh38.p7 | 2:105870863 | CCAGACACAGCCAGT[A/G]ACAGCGGTGCTTTCA | 8440 |
rs138197393 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105755716 | AACCCATGCCTATAA[A/G]TTCGTGGTTCTCAGC | 8440 |
rs138200637 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105800021 | ATCTGTCATTTGGAA[A/G]CACCATCTTTGTTCA | 8440 |
rs138223401 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | NCK2 | GRCh38.p7 | 2:105874632 | CTTGAATATGTTTCC[A/G]AAGTACCAAGTTTGT | 8440 |
rs138235431 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | NCK2 | GRCh38.p7 | 2:105760336 | GAAATGCAAATTCCG[A/G]GGAACTGCCTGACTT | 8440 |
rs138245352 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105840983 | CCAGAAACAAGGACA[A/G]ACCAGTTGTAACTTT | 8440 |
rs138258282 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | NCK2 | GRCh38.p7 | 2:105885188 | GGAAAAGGTGCAGAG[C/T]TGGCCTGCAAGTGCG | 8440 |
rs138278396 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105857933 | TCTGTGCAAAGCTTA[C/T]AGATGTGGCGTTGCC | 8440 |
rs138310754 | in-del | -/CTTGA | 0.00318978 | 0.0398085 | intron-variant | NCK2 | GRCh38.p7 | 2:105842640 | TAAGTGCTCTTGACT[-/CTTGA]CTTGTGTCATTATGT | 8440 |
rs138350009 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | NCK2 | GRCh38.p7 | 2:105868043 | AGGTATGAGGCTACT[A/G]AGAGAGCGCTCGTTT | 8440 |
rs138371502 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NCK2 | GRCh38.p7 | 2:105798282 | AAGGGAAGCCTCCCT[C/T]CTATCCTGGGAGCCC | 8440 |
rs138383955 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105812486 | ATTCCCTCAGACAGC[C/G]CTGACCCCGTGCTGT | 8440 |
rs138451161 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105820910 | GGGATTTCACAAACC[A/G]AGTCAGTTGGTGATG | 8440 |
rs138481438 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105824372 | GCCTTCCGGAATATG[C/T]CACTTATGATCTTAC | 8440 |
rs138493683 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NCK2 | GRCh38.p7 | 2:105755026 | CCGCCCTGAACACCA[C/T]TTATCTTAATAGTGT | 8440 |
rs138508918 | snp | C/G | 1.78029e-05 | 0.00298348 | synonymous-codon, intron-variant | NCK2 | GRCh38.p7 | 2:105881362 | GAAGACCAGCGCGCG[C/G]GATGCGTCCCCCACG | 8440 |
rs138533444 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105863245 | TGTGGGTCTGTCATC[A/G]TGATTATAAATATTC | 8440 |
rs138573902 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | NCK2 | GRCh38.p7 | 2:105865145 | GCAGTAGAAAAGCCT[A/G]AACCAAGTCCCCCAA | 8440 |
rs138584857 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105882181 | AGATGAATGCAATTT[A/G]GTATAATGTTTGCTA | 8440 |
rs138611361 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | NCK2 | GRCh38.p7 | 2:105851914 | TTCGGTTTTGTTTTG[G/T]TTTGGTTTGGTTTAA | 8440 |
rs138625512 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105782574 | GAACTCCATGCATAG[A/G]TAGTATGTGGTTTTA | 8440 |
rs138638216 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | NCK2 | GRCh38.p7 | 2:105878606 | TGTGAGGAAATAAAT[A/G]TCTGTTGTTTAAGCC | 8440 |
rs138643267 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105770143 | AAAAAAAAAAAAAAA[A/G]AAAAAGGTATATTGC | 8440 |
rs138666302 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | NCK2 | GRCh38.p7 | 2:105871266 | CTGAGCACCAGTGAG[C/T]GCTCCCACAGCCTGC | 8440 |
rs138671182 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | NCK2 | GRCh38.p7 | 2:105776586 | CTATGACATTTTGAG[C/T]ATGATCAGAAAAAGG | 8440 |
rs138693851 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105865511 | CTGGCGACTCCCACC[C/T]ACACGACTGTTGAGG | 8440 |
rs138700038 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | NCK2 | GRCh38.p7 | 2:105764815 | ATTTATAACTTTTGT[A/G]TAATTTTCTATTCTT | 8440 |
rs138700311 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105749632 | GTTTACAGAACACAG[C/T]GTCCTTGGGTATCTG | 8440 |
rs138727698 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | NCK2 | GRCh38.p7 | 2:105821314 | TCATTAAGATTTTAG[A/G]GCTAAAGCTTCTGTT | 8440 |
rs138786837 | in-del | -/AC | | | intron-variant | NCK2 | GRCh38.p7 | 2:105752912 | CCCACACGGACACAG[-/AC]ACACACACACACATT | 8440 |
rs138791803 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105804682 | CTTCATTGACTGCTT[G/T]CAAATTTATTTATTG | 8440 |
rs138793077 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105793069 | GAGCATCAAGCAGTG[A/C]AGGCTTTATATAATG | 8440 |
rs138793084 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105835355 | GGGTATAGTATTCTT[A/G]GCTGGTTTTATATAT | 8440 |
rs138813131 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105797483 | AGCAGGCTGCCAGGC[C/T]GTGCGGGCTAGCAGA | 8440 |
rs138828831 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | NCK2 | GRCh38.p7 | 2:105808054 | ACTACAGGTGTGTAC[C/T]GCTATGCCCAGCTAG | 8440 |
rs138833244 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | NCK2 | GRCh38.p7 | 2:105872492 | TCCCTGACCTCCTCC[C/T]CTTTATTGCGATTGT | 8440 |
rs138850961 | in-del | -/T | 0.031825 | 0.122064 | intron-variant | NCK2 | GRCh38.p7 | 2:105842441 | GGAAAGTTTGTAACA[-/T]TTTTTTCCTATATAC | 8440 |
rs138879032 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105759722 | TCCCATCCAGGGCAC[A/G]TTTCCTTTAGTCTCC | 8440 |
rs138888288 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105829405 | TGATGAACTAAAATT[G/T]GTCCATTATTAAGTA | 8440 |
rs138897508 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | NCK2 | GRCh38.p7 | 2:105816260 | GCCGTGAAGTAAGAT[C/T]GTACAACCACACTCC | 8440 |
rs138916901 | in-del | -/GTTT | 0.434398 | 0.168811 | intron-variant | NCK2 | GRCh38.p7 | 2:105867439 | CCAAAATAAATGTGG[-/GTTT]GTTTTTGTGTATCTT | 8440 |
rs138917280 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105841787 | AGGAAATGGGAAGAT[A/G]ACCAAATGTGTTTTA | 8440 |
rs138919973 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | NCK2 | GRCh38.p7 | 2:105879221 | GTTCAATGTTATTTC[G/T]TGACATCATTGTTGC | 8440 |
rs138955394 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | NCK2 | GRCh38.p7 | 2:105845437 | TCTTACTCTGTCACC[C/T]AGGTTGGAGTGCAGT | 8440 |
rs138997516 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | NCK2 | GRCh38.p7 | 2:105892699 | AAAAATACAAATATT[A/G]GCCGGGCATGGTGGC | 8440 |
rs139005239 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | NCK2 | GRCh38.p7 | 2:105801524 | AGAGACCTTTGTCAC[A/G]TGCTGGCTGTAGCAG | 8440 |
rs139065433 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105879700 | CCAGGGTAGTGGCAG[G/T]GGGAGGGGGGCAGCA | 8440 |
rs139120383 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105868318 | CACAGATTTTGGGCA[C/T]GCACTCAGGTTGTCC | 8440 |
rs139126086 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105887686 | AGGAGGAAATAAAGG[A/G]TATTAAAGTCTGTCC | 8440 |
rs139129964 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105799104 | TAAGAAGCTCTCGCT[A/G]TGTCCTGTCTGTCCT | 8440 |
rs139213765 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | NCK2 | GRCh38.p7 | 2:105862400 | AATAGCACCCCAGGC[A/C]AGCCTCAGTAGTGTT | 8440 |
rs139228461 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105789739 | ACTTAGGCTTGCTCC[C/T]GGTTAACGGGAGGGC | 8440 |
rs139250663 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105773037 | GCTGGGACTACAGGT[A/G]TGTAGCACCCCACTC | 8440 |
rs139254828 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | NCK2 | GRCh38.p7 | 2:105822654 | TGTGGCTTCCTAGAA[A/C]GCTGAAGAAACAAAA | 8440 |
rs139265895 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | NCK2 | GRCh38.p7 | 2:105746233 | GATGAGCAGGCCCCA[C/G]TGTGGGCAGGAGGGG | 8440 |
rs139267126 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NCK2 | GRCh38.p7 | 2:105752555 | GGTAAAAAACAACAT[C/T]GTATACAGTGATGGG | 8440 |
rs139293847 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105883294 | CTTTTAGATCGTGTT[G/T]GAAGCCTTAAGCAAA | 8440 |
rs139321999 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | NCK2 | GRCh38.p7 | 2:105784230 | CGCCTCAGCCTCCCA[A/G]AATGCTGGGACTACA | 8440 |
rs139343203 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105885855 | CTTTTGTTGAGTGGG[A/C]TTTATCTCTTGAAGT | 8440 |
rs139383081 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NCK2 | GRCh38.p7 | 2:105890015 | AGTGGTCATATGTAA[C/T]GGTGTATGTTAGTAT | 8440 |
rs139405514 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | NCK2 | GRCh38.p7 | 2:105871953 | ATGGGCTGAGATTTC[A/G]TGCAAGGGAAATTGG | 8440 |
rs139408845 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | NCK2 | GRCh38.p7 | 2:105864409 | ACACCTCGGAGAAGT[A/G]TTAGAATGACTCAAG | 8440 |
rs139409205 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | NCK2 | GRCh38.p7 | 2:105879650 | TGAAACGTACGTGGC[C/G]TCACATGCCTCCTGG | 8440 |
rs139424037 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | NCK2 | GRCh38.p7 | 2:105778424 | GACCATCCTCTGTGG[C/T]GTGGGAAGTGGTGGT | 8440 |
rs139424488 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | NCK2 | GRCh38.p7 | 2:105866500 | GGCAGGAGGTGGGGG[C/T]GATGGTTTCGGGATG | 8440 |
rs139428279 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105848082 | GAACCTTATGTTCAA[A/C/G]CCATTGAGCCTAGTG | 8440 |
rs139441260 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105866863 | ATATGCTTCCTGGGT[A/G]TTGAGTGCTTGGGAT | 8440 |
rs139446282 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NCK2 | GRCh38.p7 | 2:105766170 | TGAGTGGGGAAGTGG[A/G]GCCTAGGAAGCACAT | 8440 |
rs139467405 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | NCK2 | GRCh38.p7 | 2:105762992 | CTGAGCTCAGGAGTT[C/T]GAAACCAGCCTGGGC | 8440 |
rs139532408 | snp | G/T | 0.0418186 | 0.138422 | intron-variant | NCK2 | GRCh38.p7 | 2:105806324 | CTCACTGCAAGCTCC[G/T]CCTCCCGGGTTCACG | 8440 |
rs139536126 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | NCK2 | GRCh38.p7 | 2:105873468 | TTAGGAAACATGCAC[A/G]CCACCCAGCTATGAA | 8440 |
rs139539814 | in-del | -/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105762418 | GGGGTTCAGTCTGTC[-/T]CTTCTGTAGTCTGGA | 8440 |
rs139551636 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105762533 | TCCTGAACCATGGGC[A/C]TGTGGTGGTGAGTGC | 8440 |
rs139553691 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | NCK2 | GRCh38.p7 | 2:105830250 | CTTCCCCACCTCTAG[C/T]AACCTCTATTCTATT | 8440 |
rs139575949 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105869087 | CCTTACCTGGGAAAC[A/G]GGGCTCCTCTCATAG | 8440 |
rs139612532 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105866379 | CAGATGGCTTCTTGC[G/T]GTTGTCAGTACTAGC | 8440 |
rs139648717 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105752008 | CTATGTGTAATCAAC[A/C]TAAAATGTAATTAAT | 8440 |
rs139655071 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | NCK2 | GRCh38.p7 | 2:105873699 | AGAGACTGAAAGTCA[A/G]CTCAAAAGTAACTGA | 8440 |
rs139664702 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | NCK2 | GRCh38.p7 | 2:105806773 | GCAGTGCGGTATTTT[C/T]AGTTTCTTAGAAGCA | 8440 |
rs139695088 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105750700 | AGAGAAAAATCTTGA[C/T]TTGATTTCATTTATG | 8440 |
rs139704719 | snp | A/T | 0.00993419 | 0.0697739 | intron-variant | NCK2 | GRCh38.p7 | 2:105809980 | TAGTGGAGGGCTGTG[A/T]TGTCAGAATGGGCCT | 8440 |
rs139706629 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | NCK2 | GRCh38.p7 | 2:105766718 | GGGCGGGGTCTGCAG[C/G]TGAACATCGAACCAG | 8440 |
rs139760374 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105831452 | ATATCATTCTATGCT[A/G]TAAAATCTTTGCCCA | 8440 |
rs139774383 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105859224 | TACTTTATGACACCA[C/G]CTGGAGCCTTGCAAA | 8440 |
rs139820978 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105810883 | TTTATATTAATATTT[G/T]CCCGGCTATGGGCCA | 8440 |
rs139820986 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105858947 | CTTTGCCACAGATAA[C/T]AGGGAACAATGATCA | 8440 |
rs139861375 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105846679 | GTAGACAATAACAGG[C/T]GTTGACAAGGATGTA | 8440 |
rs139895554 | snp | C/G/T | 0.0166638 | 0.0900038 | intron-variant | NCK2 | GRCh38.p7 | 2:105863973 | TTGAGACTTGGCGAG[C/G/T]GGGGGTGGGGTCTCA | 8440 |
rs139902539 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105790934 | AGCCAGAGTCCAACC[C/T]CTCCCCTTTATATCA | 8440 |
rs139922717 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NCK2 | GRCh38.p7 | 2:105793364 | AAATTAGATGATAAT[A/G]AAGTTAAAGGTTCTT | 8440 |
rs139925588 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105747943 | TTTAGTAGCACAATT[A/T]AAAAATTAGACTCTT | 8440 |
rs139960621 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105888047 | CGGTGTGGGGATGTG[A/G]AGCTAAATAGGGTTC | 8440 |
rs139980979 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105891199 | TCCCTCTCACATCTG[C/T]GCACGCTCACACACT | 8440 |
rs139982351 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | NCK2 | GRCh38.p7 | 2:105855397 | GTCTGTTTTAAAAGT[G/T]AATATCTTCCTAGTT | 8440 |
rs139991744 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | NCK2 | GRCh38.p7 | 2:105855820 | CAGCCATACTGTTGT[C/T]CCCATGTGCCTCTTT | 8440 |
rs140072484 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | NCK2 | GRCh38.p7 | 2:105825784 | CAGTAAATATACACT[C/G]TGCTCTGTCAGTTAC | 8440 |
rs140104514 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | NCK2 | GRCh38.p7 | 2:105842936 | GCTTAGCAGGAGGGA[C/T]AGTCTAGTGGAGATA | 8440 |
rs140114951 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | NCK2 | GRCh38.p7 | 2:105773425 | TTTTTCATCCCTGGA[A/G]TGCCTCCTTGTTTCC | 8440 |
rs140134214 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NCK2 | GRCh38.p7 | 2:105777667 | AGTCTGTGGACACCA[A/G]TGCGCACAATTCCTA | 8440 |
rs140170047 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | NCK2 | GRCh38.p7 | 2:105873752 | AGTTGGCTCAGATGA[G/T]TGGGAAGTACGATTG | 8440 |
rs140171381 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | NCK2 | GRCh38.p7 | 2:105820749 | TGCAAAGGGCCTTGT[C/G]TGCTATGCTGCAGAT | 8440 |
rs140177578 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105814024 | TGGTGAGGGCCTTCT[A/G]CAGTCCAAGTGACCG | 8440 |
rs140182700 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | NCK2 | GRCh38.p7 | 2:105884737 | AACCAACAAACGAAC[A/G]AACCTCTTGGACCCT | 8440 |
rs140213675 | snp | C/T | 0.079617 | 0.182947 | intron-variant | NCK2 | GRCh38.p7 | 2:105861781 | CAGCCTCCCAAAGTC[C/T]TGGGATTATAGGCAT | 8440 |
rs140218688 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105816713 | TCAGTCAGTGTAGCC[G/T]TGATTTGTTGAATCA | 8440 |
rs140242023 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105746811 | GTAGTTTTGATTGGA[C/G]AAGGTGGCGGAATCT | 8440 |
rs140270476 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NCK2 | GRCh38.p7 | 2:105837952 | TTGTAGGAGTTCTTA[C/T]ATATTCAACACCAGT | 8440 |
rs140302015 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105857387 | CTGGAGCGCAGCGTC[A/G]GTTCGAGTAGGCCAA | 8440 |
rs140308288 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | NCK2 | GRCh38.p7 | 2:105799318 | AGGGTGTTTTCCATA[A/T]GTCCTTCTATACTTT | 8440 |
rs140367761 | snp | A/C/G | 3.307e-05 | 0.00406622 | synonymous-codon, intron-variant | NCK2 | GRCh38.p7 | 2:105881764 | CGAGAAGGGGGAGAC[A/C/G]ATGGAGGTGATTGAG | 8440 |
rs140384294 | snp | A/G | 1.94505e-05 | 0.00311847 | intron-variant | NCK2 | GRCh38.p7 | 2:105881298 | GTGCCCAAGTGCCCT[A/G]CGCCACTGAGCCTTG | 8440 |
rs140390014 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | NCK2 | GRCh38.p7 | 2:105791437 | GTGTAAAGTGCCTAA[C/T]AACAATGTAGGGAGT | 8440 |
rs140403010 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | NCK2 | GRCh38.p7 | 2:105815564 | AGGACTGAAAATACT[G/T]ACCAAGTGCAGTGAA | 8440 |
rs140404554 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | NCK2 | GRCh38.p7 | 2:105850171 | CTCAGACCCTTAACT[C/T]CTTTCTTCTGTAATA | 8440 |
rs140411730 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NCK2 | GRCh38.p7 | 2:105780749 | GATTAATTTCCTTAC[A/G]GAAGACACCCCAGAG | 8440 |
rs140419541 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NCK2 | GRCh38.p7 | 2:105819507 | TCAGAGTCTGTCACT[A/G]CTTCTTTAGAAAGGT | 8440 |
rs140420866 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105768668 | TTAAAACATGATGAG[C/T]TTTTTTTGAAATTTT | 8440 |
rs140432202 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105748346 | ACAGCACTTTCTTTG[A/T]GTCCCTGATTTGTCA | 8440 |
rs140437208 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NCK2 | GRCh38.p7 | 2:105832306 | TCTTTTCCAGTATGA[C/T]TGCTTTTTCTTTTTC | 8440 |
rs140510324 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | NCK2 | GRCh38.p7 | 2:105874256 | CTAAAAAAGTAGATG[C/T]AAATTAAATGAATAT | 8440 |
rs140529216 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | NCK2 | GRCh38.p7 | 2:105833170 | CGTGATCTCTGCTCA[C/T]TGCAACTTCCATCTC | 8440 |
rs140535294 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105763746 | TTCTGATTCTCAGCC[A/G]TGTTGTGGCAAAATG | 8440 |
rs140622687 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | NCK2 | GRCh38.p7 | 2:105872190 | CAGCTGGAGAGCTCT[A/G]TGCTCCTGCCCTGCC | 8440 |
rs140637850 | in-del | -/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105826289 | ACAGCATGGGGGAAA[-/C]CCGCCCCCATGACTC | 8440 |
rs140638227 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105800980 | TGTCAGAAGATTGGA[A/G]ACAGGCAAATGTTCT | 8440 |
rs140668781 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105883072 | GCTCTCTTTGAGGAC[A/G]GAGCATCGTGGTGGT | 8440 |
rs140687065 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105817492 | CTTTATGAGAAGACA[C/T]ATTTTCACCTCCAGA | 8440 |
rs140718075 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | NCK2 | GRCh38.p7 | 2:105753609 | CTTGTCTCCTCCACA[C/T]TGGGGGCTGAGAAAA | 8440 |
rs140724986 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105783683 | ATATTCTGGGTAATA[A/G]CCCTACATAAATGTA | 8440 |
rs140736760 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | NCK2 | GRCh38.p7 | 2:105802819 | TGTCACATACATGGG[C/T]CATGGATGATGACTG | 8440 |
rs140767608 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NCK2 | GRCh38.p7 | 2:105862259 | GTCGGTCTTGAGCCT[A/G]TGCTTCATACTAAGC | 8440 |
rs140773566 | snp | A/T | 0.0193772 | 0.0965046 | intron-variant | NCK2 | GRCh38.p7 | 2:105759418 | TTTCCAAAGTGTAAT[A/T]TGTTATTGTTGAAAG | 8440 |
rs140836660 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | NCK2 | GRCh38.p7 | 2:105880143 | ATGCACAGGAAGAAA[C/T]GTTTCTCAATCTGAT | 8440 |
rs140853322 | in-del | -/CA/CACA | | | utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105893999 | ACACACACACACGTG[-/CA/CACA]CACACACACACACAC | 8440 |
rs140855100 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | NCK2 | GRCh38.p7 | 2:105814818 | GCACACAGGGGGGAG[A/G]CCTGTATTTGGACAG | 8440 |
rs140892917 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105812064 | TCATTAATCAGCTTC[C/T]AATTAACCTACTAAC | 8440 |
rs140950068 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105820068 | ATCAACTGACCCTTT[A/G]GGGACAGTATGGAAA | 8440 |
rs140961953 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B | NCK2 | GRCh38.p7 | 2:105894552 | CTCTTGGCAGCCAGC[A/G]CTCTCACACCATGTG | 8440 |
rs140999194 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | NCK2 | GRCh38.p7 | 2:105844448 | ATATTTTTGGGCCAG[A/G]CATGGTGGCTCACGC | 8440 |
rs141017840 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NCK2 | GRCh38.p7 | 2:105799748 | TGGAGGGATGCTTCC[C/T]TCTACCTCAAGCCTA | 8440 |
rs141023741 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105869448 | TGTAGATGCAGAGAG[A/G]TGTTACAGAAAGTGC | 8440 |
rs141096214 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105759141 | GGTTGATCGAATACC[G/T]AGATTCCTGGTTCTT | 8440 |
rs141108869 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105784752 | TGTTGAGGTCCATCC[A/G]TTCCTCAGCAGCCAC | 8440 |
rs141130115 | snp | C/G | 0.0263992 | 0.111815 | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105771426 | ATAAAAATTAGCTGG[C/G]TGTGGTGAGGGCGCC | 8440 |
rs141130496 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | NCK2 | GRCh38.p7 | 2:105860057 | TGGGAGGCTGAGGTA[A/G]AAGGATCAGTTGAGG | 8440 |
rs141147125 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | NCK2 | GRCh38.p7 | 2:105787880 | ATGATCTCATTCTGT[C/T]AGAAACACATGCGTA | 8440 |
rs141175090 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105841914 | AGGGGAAGGGAGCTC[A/G]CTTAGAAAATGGAGT | 8440 |
rs141205831 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | NCK2 | GRCh38.p7 | 2:105866922 | TCATGTAAAAGGAGA[A/C]GCTGATTCTTTATGG | 8440 |
rs141208664 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | NCK2 | GRCh38.p7 | 2:105874991 | ACTTAAAATTATACT[A/T]TCTGTCTGCTCACTG | 8440 |
rs141225838 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NCK2 | GRCh38.p7 | 2:105795843 | ACTTCCTTCCTTCGC[C/T]GCTTCCTCTCATCTT | 8440 |
rs141256020 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | NCK2 | GRCh38.p7 | 2:105872376 | AGTCCTTCTGCTCAC[A/C]GCCGTGGTGTAGCCT | 8440 |
rs141265150 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105753946 | AGGTCCTGATGGGAA[C/T]TCTGACACTGGCTGC | 8440 |
rs141287721 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | NCK2 | GRCh38.p7 | 2:105808115 | ACCATGTTGGCCAGG[A/C]TGGTCTTGATCTGAC | 8440 |
rs141298358 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105870914 | ACATACGGGTGTGTG[A/C]GTGCCCAGCACATCG | 8440 |
rs141377053 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105874458 | GGGGGAAACCCCCAC[A/G]GATCAATAATCTCGA | 8440 |
rs141402295 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105834867 | TATTTTTGTAGAGAT[A/G]GGGTCTCATTGTATT | 8440 |
rs141438389 | snp | A/C | 0.0111196 | 0.0737302 | intron-variant | NCK2 | GRCh38.p7 | 2:105867611 | AAGGTGGGGTCCGTA[A/C]CCTTGGAATACTAAG | 8440 |
rs141440858 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | NCK2 | GRCh38.p7 | 2:105840033 | TAGGGACAAAAGCCA[A/G]TTAGTGGAGGCTCAA | 8440 |
rs141457072 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | NCK2 | GRCh38.p7 | 2:105767753 | GTCCCTTTATTGGCG[C/G]GAGGTTTGAGGTTTC | 8440 |
rs141466827 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | NCK2 | GRCh38.p7 | 2:105762097 | GAAAACAAGGACTTT[C/T]GCTTTGCTAGAAAAT | 8440 |
rs141488640 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105812671 | TTTAAATAAAAGGAA[A/G]AGGACAATTGCCTTA | 8440 |
rs141509486 | snp | C/T | 1.82677e-05 | 0.00302217 | synonymous-codon, intron-variant | NCK2 | GRCh38.p7 | 2:105881917 | ACAGATAAGCTACAC[C/T]GGGCCCTCGTCCAGC | 8440 |
rs141553190 | in-del | -/TTTTTGT | 0.296109 | 0.245711 | intron-variant | NCK2 | GRCh38.p7 | 2:105829920 | TAGTCATTCATTCTC[-/TTTTTGT]TTTTTTGAGTTGATA | 8440 |
rs141564651 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105825330 | CATGTATTCACACCT[A/G]AGATAATTCATCATA | 8440 |
rs141575856 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | NCK2 | GRCh38.p7 | 2:105755631 | ATTGGGAAGTAGAAA[C/G]AATTTACTTGTGCAG | 8440 |
rs141577017 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105813456 | TCATAACTCCCTTCT[C/T]AACCCTGAACTGCTC | 8440 |
rs141620162 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105852123 | GGGTCGGGGAGGGGA[A/G]GTCCACAGGCCTGGG | 8440 |
rs141623514 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105849436 | GGTCTTCTCTGTGGC[C/G]GGATAAATTGGTTAG | 8440 |
rs141649990 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105805874 | ATGTTTCAGGGTTTG[A/G]ATTTTTCCAGATTTT | 8440 |
rs141662781 | snp | C/T | 0.259397 | 0.249823 | intron-variant | NCK2 | GRCh38.p7 | 2:105807741 | CTTCTTTCCTTCCTT[C/T]CTTCCTTCCCTCCCT | 8440 |
rs141663760 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NCK2 | GRCh38.p7 | 2:105809880 | CCACTGAGCACTGCT[A/G]GAAGAAGAGGGAGTG | 8440 |
rs141683608 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105846238 | TTCTAGTTGAAGCGA[C/T]AGTGCCACCACTTCT | 8440 |
rs141693560 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105816037 | CCCAACCCGAGTGTC[A/G]GAGCTTGCCCAGGGA | 8440 |
rs141699812 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant, utr-variant-5-prime | NCK2 | GRCh38.p7 | 2:105745943 | AGTTAGCTTGGCATT[A/G]TGTGGAGGGGTTTAA | 8440 |
rs141702555 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105792104 | ATGGATGAGATTTTG[A/G]AGACCCCTCCTGCTC | 8440 |
rs141714567 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105800308 | TTCTCTGCTGTGAAC[A/G]GGGTAATGAGGTGTT | 8440 |
rs141731038 | in-del | -/C | 0.00478085 | 0.0486577 | intron-variant | NCK2 | GRCh38.p7 | 2:105748276 | CTTACTTCTTTTCTT[-/C]CCCCACATCTTATCA | 8440 |
rs141758759 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | NCK2 | GRCh38.p7 | 2:105871125 | GGGTGATGAGACAGC[A/G]AGTGAGGTTTATTAA | 8440 |
rs141759231 | in-del | -/TACTC | 0.0240643 | 0.107019 | intron-variant | NCK2 | GRCh38.p7 | 2:105888954 | AGCTTAAATGTAGAG[-/TACTC]TACCATACTATCAGT | 8440 |
rs141793003 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | NCK2 | GRCh38.p7 | 2:105864817 | TGTAACCTCTAGCTC[A/G]CATGTGCATGTACAC | 8440 |
rs141797192 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | NCK2 | GRCh38.p7 | 2:105866457 | ACCAGGAACTGGTTT[C/T]GTGGAAGACAGTTTT | 8440 |
rs141822584 | in-del | -/TT | 0.0988009 | 0.199095 | intron-variant | NCK2 | GRCh38.p7 | 2:105845398 | CATTTATATTTTGAA[-/TT]TTTTTTTTTTTTTTG | 8440 |
rs141834381 | in-del | -/CCC | | | intron-variant | NCK2 | GRCh38.p7 | 2:105812787 | CATCTGCTCATTACT[-/CCC]GAAGCCAGGTGACAC | 8440 |
rs141859585 | snp | A/C | 0.00398564 | 0.0444627 | utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105893708 | CAGTGAGGAGACTGC[A/C]CAGTGCCTTTGGGGC | 8440 |
rs141877149 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | NCK2 | GRCh38.p7 | 2:105887043 | CTCTTCACACTTGGG[A/G]CAAGGAAGAGATAAT | 8440 |
rs141912922 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | NCK2 | GRCh38.p7 | 2:105797487 | GGCTGCCAGGCTGTG[C/T]GGGCTAGCAGAAGGG | 8440 |
rs141932875 | snp | C/T | 0.349671 | 0.229272 | intron-variant | NCK2 | GRCh38.p7 | 2:105794733 | TATTTATTTTTGAGA[C/T]GGAGTCTTGCTCTGT | 8440 |
rs141984509 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NCK2 | GRCh38.p7 | 2:105882577 | TTTTAAAGCACTTAC[A/G]AGATAAATTGAAAAG | 8440 |
rs141984711 | snp | A/C/G | 0.000611139 | 0.0174699 | synonymous-codon, intron-variant | NCK2 | GRCh38.p7 | 2:105881944 | CAGCGGGCGCTTCGC[A/C/G]GGCAGAGAGTGGTAC | 8440 |
rs141992820 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NCK2 | GRCh38.p7 | 2:105792735 | CTGCACATCAGAACC[A/G]GAGCCAGTCTGGTGC | 8440 |
rs142001130 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | NCK2 | GRCh38.p7 | 2:105865322 | TCATTTTGCATGTGA[A/G]AAAACTGATACTCAG | 8440 |
rs142011951 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | NCK2 | GRCh38.p7 | 2:105854370 | TGGGGAATAATTTTA[C/T]ATTTATAAAAAAGTT | 8440 |
rs142017493 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | NCK2 | GRCh38.p7 | 2:105750153 | GTCCATGACCCCGGG[A/G]CCGGCAGGGCTGGTT | 8440 |
rs142021499 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105783164 | GCTTTGCTTTCTGCC[A/G]CAGCAGCTGAGGAAG | 8440 |
rs142022688 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | NCK2 | GRCh38.p7 | 2:105829584 | GTTGACCTTGACAGT[C/T]TTGAGGAGTCGGGTA | 8440 |
rs142061682 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105793153 | GAGAGGTGGGAAGCC[A/G]CAGATGTAGGACATC | 8440 |
rs142102474 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | NCK2 | GRCh38.p7 | 2:105791730 | TGGTATACATTCTTC[A/G]TAGAGCTTGTGAGTT | 8440 |
rs142104933 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | NCK2 | GRCh38.p7 | 2:105763161 | CGAGATCATGCCACC[A/G]CACTCCAGCCTGGGC | 8440 |
rs142123150 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105776354 | TCTGGAAGCAGCCAA[A/G]GCACGTTTGGGGGAG | 8440 |
rs142163574 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105880746 | GAAGGAAACCACCTA[C/G]TCTTGTTATCTTTTG | 8440 |
rs142193522 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | NCK2 | GRCh38.p7 | 2:105796987 | GCTGGGGTGAGTGTT[C/T]GCTGTGATGATGGTT | 8440 |
rs142193798 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105847242 | GATAGATGATGTTGA[C/T]GTTTGCACAACAGGG | 8440 |
rs142200204 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105826743 | AGTATCCTTTCCTCT[G/T]AGCAGCTTCCCTAGC | 8440 |
rs142244335 | snp | C/T | 3.30453e-05 | 0.00406467 | synonymous-codon, intron-variant | NCK2 | GRCh38.p7 | 2:105881749 | GGAGGAGCTCAACTT[C/T]GAGAAGGGGGAGACC | 8440 |
rs142266692 | in-del | -/GA | | | intron-variant | NCK2 | GRCh38.p7 | 2:105760792 | GGTTTTGTCACATGT[-/GA]GAGAGAGAGAGAGGC | 8440 |
rs142275310 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105877960 | AGTAAAGTCAGGTCC[C/T]TCTCCATCTCCAGAC | 8440 |
rs142276939 | snp | C/T | 0.00122034 | 0.0246714 | synonymous-codon | NCK2 | GRCh38.p7 | 2:105855162 | GCTGTGGTTGCTGGA[C/T]GACTCCAAGACGTGG | 8440 |
rs142287310 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105807369 | GATTAATTCTGGGCT[A/G]TGGGAAAGCCCTCCG | 8440 |
rs142309361 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NCK2 | GRCh38.p7 | 2:105781761 | TGTGACAGAGCTGTC[A/G]CCTCTCCGCAGTACG | 8440 |
rs142329131 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | NCK2 | GRCh38.p7 | 2:105779899 | GAATGCCATAGCCTA[C/T]GAGACCGCCTTCACC | 8440 |
rs142362991 | snp | A/G | 4.94466e-05 | 0.00497201 | synonymous-codon | NCK2 | GRCh38.p7 | 2:105855135 | GGAGCTGGACATCAA[A/G]AAGAACGAGCGGCTG | 8440 |
rs142363486 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | NCK2 | GRCh38.p7 | 2:105747789 | GCACGTTTTCAAAGG[G/T]CCTAAGCTAAAATGT | 8440 |
rs142365548 | in-del | -/T/TT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105831417 | ATAAGCATGATATCT[-/T/TT]TTTTTTTTTTTTTGT | 8440 |
rs142411203 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | NCK2 | GRCh38.p7 | 2:105877061 | CAAGAGGAGAAGGAC[A/G]AGGGATCGCTGAGTC | 8440 |
rs142419945 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105872114 | CTGCCAGCAGGACAC[C/T]TAGAAGAGAAAGGTC | 8440 |
rs142421290 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | NCK2 | GRCh38.p7 | 2:105879049 | AAGTGTCTTTATAAC[A/G]TATTGTGATGGCCAC | 8440 |
rs142424998 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105777877 | AGAGGATCGGTACTG[C/G]GGTGACAGCTCACAG | 8440 |
rs142427776 | snp | A/G | 1.79693e-05 | 0.00299739 | synonymous-codon, intron-variant | NCK2 | GRCh38.p7 | 2:105881359 | CAGGAAGACCAGCGC[A/G]CGGGATGCGTCCCCC | 8440 |
rs142428463 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105811534 | ATCCAGAAGTTGCCA[A/G]CCTGGAGATTCAGTC | 8440 |
rs142439886 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105813096 | ATCAGACAAGTGTGC[A/G]TTCAAATTCTGGTTG | 8440 |
rs142466689 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105775421 | TAATTATTTTTAACC[A/G]AAATTTAGTTTTTAA | 8440 |
rs142479667 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | NCK2 | GRCh38.p7 | 2:105777299 | TTTAATGTTGCACCT[G/T]GTTGTGTCTTTGACA | 8440 |
rs142498577 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105824576 | AGAGCTCATTTAGTA[A/G]CGTTTTTGTAATACA | 8440 |
rs142544758 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NCK2 | GRCh38.p7 | 2:105799517 | CTGAATTCCCAGAGG[C/T]CTCTGGGTCTGTTTC | 8440 |
rs142581278 | in-del | -/T | 0.0260105 | 0.111035 | intron-variant | NCK2 | GRCh38.p7 | 2:105789244 | CAGGCTGGAGTGTAG[-/T]TGGCGCGATCTTGGC | 8440 |
rs142593193 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105890793 | AATGGAGTGATTCCT[C/T]GTTTTGCAAGGGTTG | 8440 |
rs142608765 | snp | C/G | 0.031825 | 0.122064 | intron-variant | NCK2 | GRCh38.p7 | 2:105825923 | TTGGAGTTCCTGGCT[C/G]CATTAGATCTTGATG | 8440 |
rs142611354 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | NCK2 | GRCh38.p7 | 2:105856344 | AAACGTTGTTACCTT[C/T]TTATGAGTATAATGT | 8440 |
rs142658729 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | NCK2 | GRCh38.p7 | 2:105866589 | TAGATCCCTCACAGG[C/T]GTAGTTCACAATAGT | 8440 |
rs142676809 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NCK2 | GRCh38.p7 | 2:105794109 | GCTGGAGTGCAGTGG[C/T]GCCATTTTGGCTCAC | 8440 |
rs142712227 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | NCK2 | GRCh38.p7 | 2:105752763 | TGTGTTGCTGCAAAA[G/T]ATATGATTTCATTGT | 8440 |
rs142715187 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105761294 | TCATTTTAACTCCTG[A/G]CTGACTGACTTCCAG | 8440 |
rs142746919 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105749640 | AACACAGTGTCCTTG[A/G]GTATCTGCCTTTGCC | 8440 |
rs142774715 | in-del | -/T | 0.314579 | 0.274487 | intron-variant | NCK2 | GRCh38.p7 | 2:105833666 | ATTGATTTTTTGCAT[-/T]TTTTTTGGCCTCTTT | 8440 |
rs142784410 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | NCK2 | GRCh38.p7 | 2:105765429 | GGTCATCCTGAGGCC[A/G]GCCCCACGGCCAGTT | 8440 |
rs142786930 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | NCK2 | GRCh38.p7 | 2:105876768 | GATGAGGCGATGAAG[C/T]GGAGATGTGTAGAAA | 8440 |
rs142806122 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | NCK2 | GRCh38.p7 | 2:105828780 | CCTCTTAGTAAATTA[A/G]GCATGCTCTCTACAG | 8440 |
rs142826005 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NCK2 | GRCh38.p7 | 2:105844148 | TCAGACAAATCCTAA[C/T]GGGTGGGGGGACATT | 8440 |
rs142827715 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | NCK2 | GRCh38.p7 | 2:105868200 | TCTGCACATCAGCCT[A/G]CATTGACTCATGTCA | 8440 |
rs142840415 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NCK2 | GRCh38.p7 | 2:105774598 | GTCCACTGCAGGTCT[A/G]GTCATGTGGCTGGGG | 8440 |
rs142854467 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NCK2 | GRCh38.p7 | 2:105825574 | GATTCTGGCTTGGGG[A/G]ATGGTGGGTTCCTGA | 8440 |
rs142857338 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NCK2 | GRCh38.p7 | 2:105871526 | TTTGAGACAGAGTCT[C/T]CCTCTGTCGCCCAGG | 8440 |
rs142863192 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105822467 | GTGCTGAGGCCATCT[C/G]TAAGGTCCCTGACGC | 8440 |
rs142866636 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | NCK2 | GRCh38.p7 | 2:105756451 | TTGCAACTTTGGAAC[C/G]ATGTGTGTTTCTCTT | 8440 |
rs142873920 | snp | A/G/T | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105801074 | AGGTGAAAGCTGGGC[A/G/T]TGCTGAGCCCGTCAG | 8440 |
rs142882504 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105786382 | GGGGACAGGATGGGA[A/G]TTCGGGAAGGCTGGG | 8440 |
rs142896657 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | NCK2 | GRCh38.p7 | 2:105872880 | TCCCCTTTCTCCTTC[A/T]TCCGGGGACACCTCT | 8440 |
rs142917041 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | NCK2 | GRCh38.p7 | 2:105762579 | GAACTTTGGGGTGGG[A/G]AAAAACATCCTTATT | 8440 |
rs142938033 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105839714 | GGGTGCAGGAGTCTG[A/G]CATTTGGGGATAGAG | 8440 |
rs142985558 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | NCK2 | GRCh38.p7 | 2:105875131 | AGCTTGGTTAAGGAG[C/T]TTGTTCACACTCCTT | 8440 |
rs143020992 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105820315 | TCAGCCATACACTTC[A/G]GCATGTCAGAAAGAA | 8440 |
rs143028427 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105885937 | TTTTTACTGTTTAGA[C/G]TTTGAAAATAAACGT | 8440 |
rs143037116 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | NCK2 | GRCh38.p7 | 2:105874671 | TCAGCTTAAATCTCC[C/T]GAACTCCAGCTGGAA | 8440 |
rs143054485 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | NCK2 | GRCh38.p7 | 2:105864729 | TTTCTCTCATGTTAA[A/G]GACTGGACCTGGCCT | 8440 |
rs143080277 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NCK2 | GRCh38.p7 | 2:105749599 | TGTTGCTGGGTAGAG[C/T]TGTTTTTTTGTGAGG | 8440 |
rs143140463 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105872640 | CAAATGAGCAAAGAA[C/T]CCTTCTTGAGAACTC | 8440 |
rs143157456 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NCK2 | GRCh38.p7 | 2:105780474 | TCCTGCTTCTCGCTC[A/G]TGTCCTGTGTCACAT | 8440 |
rs143200577 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | NCK2 | GRCh38.p7 | 2:105814983 | GTGGTGTTTGGGGCA[G/T]GGTACCCAGCACATT | 8440 |
rs143205233 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | NCK2 | GRCh38.p7 | 2:105888203 | CTTCTGAAAAGAAGG[A/G]TCAAATGAATGGGTT | 8440 |
rs143254526 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | NCK2 | GRCh38.p7 | 2:105806395 | GGCACCCACCACCAC[A/G]TCCGGCTAACTTTTT | 8440 |
rs143277911 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105858516 | ACCACCCACATTTGC[C/T]ATTTTTACTGCTTTG | 8440 |
rs143279923 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105890095 | TTAAAGAACACTCCC[C/G]AACTTTTAGCACTCC | 8440 |
rs143320625 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105862801 | AATAATGTTTTTTGC[A/G]CCGTTTTTGTAATTT | 8440 |
rs143332121 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105790012 | GCGTGTTCATGTATT[C/G]AGTGCAAGGGAGCAG | 8440 |
rs143369924 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | NCK2 | GRCh38.p7 | 2:105867249 | CAGAGATGCATTTAA[C/T]ACTTCACGTTTACTT | 8440 |
rs143376105 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105767902 | ATTCCTTCCCTCTCT[A/G]TTACTCACATCCCCG | 8440 |
rs143399813 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105755166 | CCTTAAATTAAGCCA[A/T]CTGTCTTGCTTCAGT | 8440 |
rs143424852 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105748064 | GACACACATCCACAT[G/T]TGTACTGGCACATAC | 8440 |
rs143433754 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | NCK2 | GRCh38.p7 | 2:105878734 | AATTTGACTAAGAGC[A/C]TGCAGCTCTCTGTCA | 8440 |
rs143439867 | in-del | -/AG | 0.0138799 | 0.0821421 | intron-variant | NCK2 | GRCh38.p7 | 2:105767813 | GATACCCATTGTCTC[-/AG]GGGATTGCTAGCATG | 8440 |
rs143441756 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105862148 | TTGCAATTTACCAGG[C/T]GGCTTAACACTTACA | 8440 |
rs143453977 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NCK2 | GRCh38.p7 | 2:105845739 | CAAAATTTACAAGTA[C/T]CTTACAGCTGTGAAA | 8440 |
rs143455789 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | NCK2 | GRCh38.p7 | 2:105891270 | TTTTTTTGTTTGTTT[C/T]CTTTTTTTTTTTCAT | 8440 |
rs143469394 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant, utr-variant-5-prime | NCK2 | GRCh38.p7 | 2:105745830 | TCACAATCGCTCGGC[C/T]CTCTCGGTTTTTTTC | 8440 |
rs143475451 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NCK2 | GRCh38.p7 | 2:105889406 | GGCTCCAGCACTGCC[A/G]ATGTTTGTTCCAGAT | 8440 |
rs143478240 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105750030 | GACCCTGTCTCAAAA[A/G]CAAACAAACACACAC | 8440 |
rs143485808 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NCK2 | GRCh38.p7 | 2:105791185 | TGAAGAGGTGACAGC[A/G]GAAGATCTCTAATCC | 8440 |
rs143497998 | snp | A/T | 0.0115144 | 0.0749975 | intron-variant | NCK2 | GRCh38.p7 | 2:105864021 | GCAAGTGAGGATGTG[A/T]AGACGGAAACCCATA | 8440 |
rs143564676 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NCK2 | GRCh38.p7 | 2:105811535 | TCCAGAAGTTGCCAG[C/T]CTGGAGATTCAGTCC | 8440 |
rs143569568 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105841163 | CTGATGTAAAATGTA[A/G]ATTTACTGGGCACTA | 8440 |
rs143625326 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | NCK2 | GRCh38.p7 | 2:105873918 | CGGTATTTCCCCCAT[A/G]ACTGTAGCAAGGGTC | 8440 |
rs143676949 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105790626 | TCTTACTGCATCCCC[C/T]GCACCTGTCCTCATC | 8440 |
rs143685767 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NCK2 | GRCh38.p7 | 2:105835881 | ACCTGTCTCTATGTT[C/T]AGAAATTCTTTCTTC | 8440 |
rs143695122 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105764918 | GAGTTGAAAGCGCCA[C/T]ACTTGCATAAGTAGT | 8440 |
rs143706220 | snp | C/G | 0.1652 | 0.235179 | intron-variant | NCK2 | GRCh38.p7 | 2:105765805 | TGTGTGTGTGTGTGT[C/G]TGTGTGTGTGTCTGT | 8440 |
rs143715835 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105836870 | CCTGGGACTCAGGGA[G/T]TAGGGGCTACCCAGC | 8440 |
rs143717752 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NCK2 | GRCh38.p7 | 2:105874658 | TTTGTTTGACGCTTC[A/G]GCTTAAATCTCCCGA | 8440 |
rs143758572 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105792532 | TTATTTACAACTGGT[G/T]GTTAAAGTCAGAATC | 8440 |
rs143792408 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105828488 | ACCGCAGATCAGTGT[G/T]GAGTGCAGAATTTAA | 8440 |
rs143796517 | snp | C/T | 0.00119737 | 0.0244387 | downstream-variant-500B | NCK2 | GRCh38.p7 | 2:105894308 | TTGGGAAAACTCAGA[C/T]TCAATCATGGGAGAG | 8440 |
rs143851031 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105802241 | ACACACCCTCTACCT[A/G]TACTCAGAAATCACT | 8440 |
rs143871157 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | NCK2 | GRCh38.p7 | 2:105840309 | GGCACCCAGACAGCT[C/T]ACCCCTGTAACACGT | 8440 |
rs143896992 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105808786 | CAGGAAAATCGGGAC[A/G]CTAATGAGATATGAG | 8440 |
rs143911032 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105770152 | AAAAAAGAAAAAGGT[A/G]TATTGCAACAAGAAA | 8440 |
rs143912461 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105843304 | GGAATTTTTCACTTG[C/T]AGTGCTCAAGTTTTG | 8440 |
rs143952945 | snp | C/T | 0.021333 | 0.101051 | intron-variant | NCK2 | GRCh38.p7 | 2:105785220 | CCTGACCTCATGATC[C/T]GCCCATCTCGGCCTC | 8440 |
rs143959488 | in-del | -/GGGG | | | intron-variant | NCK2 | GRCh38.p7 | 2:105858044 | TGTTCTTTGTTTTTT[-/GGGG]TTTTTTTTTTGTTTT | 8440 |
rs144028098 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | NCK2 | GRCh38.p7 | 2:105758441 | TTTGAGACAGAGTCT[C/T]GCTCTGTCACCCATG | 8440 |
rs144030749 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | NCK2 | GRCh38.p7 | 2:105773365 | TTCTCGCCGTCTGGT[A/G]CACGTGCCGGCCTCC | 8440 |
rs144072118 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105747048 | TAACCCCCTCTGTCC[A/T]CTTGTGGAGAAACTG | 8440 |
rs144076108 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NCK2 | GRCh38.p7 | 2:105816781 | TTATCTCTGTTCCTG[C/T]TTTAGTGTGTGATGG | 8440 |
rs144092164 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105887850 | AAGCTGGCAAAGCCA[C/T]AGAGATGGGATCAAA | 8440 |
rs144121024 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105821070 | TACATCCATAAAAAC[G/T]CTATCCAGTAATATT | 8440 |
rs144121503 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105786880 | CTGACTCCCTTACCT[C/T]TGCTGCTCAGGCACC | 8440 |
rs144124674 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | NCK2 | GRCh38.p7 | 2:105883664 | TGAATTCAGGGACCA[A/G]GTCCCTTTGGATAAG | 8440 |
rs144136010 | in-del | -/ATTACACATA | 0.0726307 | 0.176182 | intron-variant | NCK2 | GRCh38.p7 | 2:105759472 | AGGCTTTTATATAAT[-/ATTACACATA]AAAACATATGGTATA | 8440 |
rs144154777 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | NCK2 | GRCh38.p7 | 2:105823044 | GAGCTTGAAATGAGC[A/G]CATTGCTGCAGTTGA | 8440 |
rs144187288 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | NCK2 | GRCh38.p7 | 2:105868409 | GGGGTGGCCTGCGTT[C/T]CTTCCTGGAAGCAGG | 8440 |
rs144223041 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | NCK2 | GRCh38.p7 | 2:105863701 | ACTAGGGCTGAGTTA[C/T]GCAGCTCGGGCACCT | 8440 |
rs144231814 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | NCK2 | GRCh38.p7 | 2:105790443 | AGGAGAGTCTGTGCC[C/T]GTGAGGAGACCCCTC | 8440 |
rs144250725 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | NCK2 | GRCh38.p7 | 2:105799329 | CATATGTCCTTCTAT[A/G]CTTTTACTTTTTCAT | 8440 |
rs144268010 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NCK2 | GRCh38.p7 | 2:105752050 | TATTCTTTTATTTGC[A/G]TGAGGGCTTTGAAAT | 8440 |
rs144271477 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | NCK2 | GRCh38.p7 | 2:105832371 | ACATTGAATAAGAGT[C/T]GTGAAGGAATAGGCA | 8440 |
rs144309744 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | NCK2 | GRCh38.p7 | 2:105795086 | TTTCTCATATATCCA[A/G]TTCCCCCACATGAAC | 8440 |
rs144325522 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105858449 | AGACAGGATTTTGCC[A/G]TGTTGCCTGGGCTGA | 8440 |
rs144345649 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | NCK2 | GRCh38.p7 | 2:105813137 | GGTCATTTGGTTCCT[C/G]GGCTGAATGATAAGA | 8440 |
rs144388887 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | NCK2 | GRCh38.p7 | 2:105873727 | TGAAGGGGAAAAAAA[G/T]AAAACGAAAAGTTGG | 8440 |
rs144444624 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | NCK2 | GRCh38.p7 | 2:105766933 | TGCTGCCTGTGCAGT[A/G]TTGGTGAAACTCAGG | 8440 |
rs144444679 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NCK2 | GRCh38.p7 | 2:105810015 | GGAGAGTGGGTGCTG[A/G]GGTCTCATTCAGTGG | 8440 |
rs144454949 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | NCK2 | GRCh38.p7 | 2:105872201 | CTCTATGCTCCTGCC[C/T]TGCCCAGATCCCTCT | 8440 |
rs144459854 | in-del | -/TAGCCCTATTTGAATTATCTTCT | 0.00914312 | 0.0669923 | intron-variant | NCK2 | GRCh38.p7 | 2:105815323 | ATAACATTTTTATGA[-/TAGCCCTATTTGAATTATCTTCT]TATCTTTGACTAAAA | 8440 |
rs144473130 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105803135 | GGGAAAGCAAGGTTA[A/G]GCTTATTTTCTACTG | 8440 |
rs144511766 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NCK2 | GRCh38.p7 | 2:105807083 | AGGTAGAGTCTGAGT[A/G]ACACTTGGAATCCCT | 8440 |
rs144515681 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105839323 | AAAGTTCCCCAAAGC[A/G]AGTGCCAGGAGGGTA | 8440 |
rs144546963 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | NCK2 | GRCh38.p7 | 2:105793902 | GTTTATGGGTTGCTT[C/T]TGGTTTGGTCATTGT | 8440 |
rs144599082 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105782234 | GGCAGGCGGGGTGGC[C/T]GGGCCCAGGGACTCA | 8440 |
rs144603831 | snp | C/T | 0.00318978 | 0.0398085 | utr-variant-5-prime, intron-variant | NCK2 | GRCh38.p7 | 2:105851867 | AGTAAGTGAGCGAGC[C/T]GGACGTCGATTGACT | 8440 |
rs144603845 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | NCK2 | GRCh38.p7 | 2:105884466 | CCTTTTTTTCTTGCA[A/G]TCTTTGGGCCTGGGC | 8440 |
rs144618431 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | NCK2 | GRCh38.p7 | 2:105784806 | ACTTCCCATTTCAAC[A/G]TTCTTAGAATATGCA | 8440 |
rs144623748 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | NCK2 | GRCh38.p7 | 2:105856798 | TCCTTCTCCACTGAG[C/G]TGCCTCCCTTTCATC | 8440 |
rs144636993 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | NCK2 | GRCh38.p7 | 2:105882132 | CCGCGCCCTTTTCAC[A/G]TTGTGTGAGTACACT | 8440 |
rs144644286 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105855619 | AGCTCTGCCAGTGTC[A/G]TGACATGAAGTTCTT | 8440 |
rs144660773 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | NCK2 | GRCh38.p7 | 2:105784040 | TCTGTGGCACCTGGT[G/T]GGCCTCAACACCATG | 8440 |
rs144677137 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | NCK2 | GRCh38.p7 | 2:105821979 | GTAACGACCCATTCT[C/G]CAAGTGCTTACCTTA | 8440 |
rs144694136 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105880404 | GTGGGAAATTAGTCT[A/G]CTGTTTTGAAAGAAG | 8440 |
rs144731858 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NCK2 | GRCh38.p7 | 2:105848480 | CTCCAAAATAACATA[C/T]TGAGCAAAGGTCTTA | 8440 |
rs144762403 | snp | A/G | 2.87584e-05 | 0.00379188 | missense, utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105893154 | ACGGGGAGAAGCTCT[A/G]CCTCGTCAGGGCCCT | 8440 |
rs144775964 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105882526 | CCAAGGTCATTGCCA[A/C]GGCAGGCAGCGCCAC | 8440 |
rs144783153 | snp | A/G | 0.0267878 | 0.112589 | utr-variant-5-prime | NCK2 | GRCh38.p7 | 2:105816551 | GAGGTGTAATTAGCT[A/G]AAAACATCATCGTTT | 8440 |
rs144786614 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | NCK2 | GRCh38.p7 | 2:105873569 | TTCAGCTCACCCATA[A/T]TTACCACGTTTTCAG | 8440 |
rs144803647 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | NCK2 | GRCh38.p7 | 2:105782947 | GAGGGTGGCAGCCTC[A/G]CCTTTATTTCCGGTG | 8440 |
rs144805750 | in-del | -/TCTTT | 0.0126979 | 0.078662 | intron-variant | NCK2 | GRCh38.p7 | 2:105747955 | ATTAAAAAATTAGAC[-/TCTTT]TCTTTTCCTGCATTT | 8440 |
rs144845328 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | NCK2 | GRCh38.p7 | 2:105787909 | TATACCGCCCCCCAC[C/T]GCCCCCGACTTGTAG | 8440 |
rs144874096 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | NCK2 | GRCh38.p7 | 2:105864578 | GCTTGGGAGGTACAC[A/G]GTTATCCTTATGACA | 8440 |
rs144882542 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105791480 | CGTTGCCGTGCTTAC[C/T]GGCCAGAGTGCTGCT | 8440 |
rs144892712 | snp | C/T | 0.0345262 | 0.126772 | intron-variant | NCK2 | GRCh38.p7 | 2:105763082 | ATGTGCCTGTAGTCC[C/T]AGCTACTCAGGAGGC | 8440 |
rs144900059 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | NCK2 | GRCh38.p7 | 2:105748527 | CCCACCTCAGCCTCC[C/G]AGTAGCTGGGACTAC | 8440 |
rs144924545 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105802029 | TGCTCCTCCAGGAAG[A/G]CCTCAACTGCCTACT | 8440 |
rs144983642 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | NCK2 | GRCh38.p7 | 2:105828798 | ATGCTCTCTACAGGG[A/T]AGGACCATCACTCAC | 8440 |
rs144983673 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NCK2 | GRCh38.p7 | 2:105872462 | GGACCGAAAGAGACA[C/T]GCTCAGGGAGGTCCT | 8440 |
rs144992537 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NCK2 | GRCh38.p7 | 2:105860012 | AATCAGGGCTGGGCA[C/T]GATGGTTTATGCCTG | 8440 |
rs145018010 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105835225 | TTTGCTTCCAAATGT[A/G]GGGTTTCCTTAAGCA | 8440 |
rs145026095 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105764271 | AGCACCTTTGCATCC[A/G]CACCCTGCAGGTTAA | 8440 |
rs145032028 | snp | G/T | 0.0115144 | 0.0749975 | intron-variant | NCK2 | GRCh38.p7 | 2:105870986 | AGCAGGGTCAGCGTG[G/T]TGTGTGCTTGGGAGG | 8440 |
rs145073355 | snp | A/C | 0.0260105 | 0.111035 | intron-variant | NCK2 | GRCh38.p7 | 2:105763013 | CAGCCTGGGCAACAC[A/C]GTGAAACCCCGTCTC | 8440 |
rs145102949 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105869253 | GAGAAAGTGCCACAC[C/T]GGATCCTGCATGTGT | 8440 |
rs145136070 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NCK2 | GRCh38.p7 | 2:105759214 | TGGTCTTATTCAAGG[A/G]AGCAAGATTTTTTGT | 8440 |
rs145141990 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NCK2 | GRCh38.p7 | 2:105872011 | GAAGCTGTCAAGAAT[A/G]CATTTACTGCTTTTT | 8440 |
rs145171098 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105750072 | CACACACACACAAAA[A/C]AACAACAACAGAATG | 8440 |
rs145207648 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105848196 | AGACTGGCTCATTTA[A/G]TCCTCACCGAAGCTC | 8440 |
rs145233851 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | NCK2 | GRCh38.p7 | 2:105812764 | GTTATGATACACACC[C/T]GAGTCCAACATCTGC | 8440 |
rs145258554 | snp | A/G | 1.65671e-05 | 0.00287807 | synonymous-codon, intron-variant | NCK2 | GRCh38.p7 | 2:105881773 | GGAGACCATGGAGGT[A/G]ATTGAGAAGCCGGAG | 8440 |
rs145276353 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | NCK2 | GRCh38.p7 | 2:105815693 | TCAGAAGTCTTGAAA[C/G]TAGGGGTGCTTTTTA | 8440 |
rs145301645 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105857790 | TCATGCTCACCTGGA[G/T]GTTTTTGTTGGACAA | 8440 |
rs145332932 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NCK2 | GRCh38.p7 | 2:105796948 | AAGTGTCAGCACTTA[C/T]CTGTGGTTGGTTCAG | 8440 |
rs145379827 | in-del | -/CCCCC | | | intron-variant | NCK2 | GRCh38.p7 | 2:105822437 | GGACTTTGTATTTAA[-/CCCCC]CAGCCACTTCCTGTG | 8440 |
rs145386354 | snp | C/T | 0 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105807189 | AACCTGGGCCCTGAC[C/T]GGAACAGCTCACTCT | 8440 |
rs145391872 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NCK2 | GRCh38.p7 | 2:105814368 | CACTGGCACCTTTCA[A/G]TGGATTTTCAGTAGC | 8440 |
rs145432883 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NCK2 | GRCh38.p7 | 2:105834641 | AAATTTAATTCATTT[A/G]CATTAAAGGGTTTTT | 8440 |
rs145443472 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105888252 | CCAGAACCATTGATT[C/G]AAAAACTATGAGAAT | 8440 |
rs145456368 | snp | A/G | 0.0887219 | 0.191022 | intron-variant | NCK2 | GRCh38.p7 | 2:105810918 | CAGTGGCTCACACCT[A/G]TAATCTCAGCACTTT | 8440 |
rs145457791 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105859041 | AGCTCAGTGGAGAGC[A/G]GTCCTGGGCTGAGGT | 8440 |
rs145470764 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | NCK2 | GRCh38.p7 | 2:105787993 | CTCCACGTGCCACCA[A/G]CCAAGGACAAATCAG | 8440 |
rs145488943 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105766713 | GGCGGGGGCGGGGTC[A/T]GCAGGTGAACATCGA | 8440 |
rs145522105 | in-del | -/AGAA/GAAG | | | utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105893738 | TGTGCTTGCAATAAA[-/AGAA/GAAG]GAATTTCCTGGAAAG | 8440 |
rs145523444 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105780808 | ACACAGCAAGAAGCC[A/G]CCGTGTAGGAACCAG | 8440 |
rs145547076 | snp | C/G/T | 0.00676609 | 0.0577691 | intron-variant | NCK2 | GRCh38.p7 | 2:105883397 | TAAGTGCTTGGTCCA[C/G/T]AGTCCTTAAGGGCTA | 8440 |
rs145570181 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NCK2 | GRCh38.p7 | 2:105874438 | TAATAGGTTCTGACT[C/T]TAGTGGGGGAAACCC | 8440 |
rs145570678 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105784570 | ATTCAGGTCTTTACA[A/G]TGTAGGTGAGCATAA | 8440 |
rs145573371 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105784347 | TTCCCACCTGCTGAT[C/T]GGACTCCTTGTGGTG | 8440 |
rs145634697 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105797689 | TGTGTGGAGCCTCCC[C/T]GTTTAGGCTTAGTGA | 8440 |
rs145637675 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105867659 | TTCACAGTGGGGTGT[G/T]TGGGATTCACATTGC | 8440 |
rs145645674 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | NCK2 | GRCh38.p7 | 2:105870689 | GAACCTGGGAGGCGG[A/G]GGTTGCAGCCAAGAT | 8440 |
rs145654575 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105799918 | TTTTTAACAGTGAGA[C/G]AAACACTCAAACACT | 8440 |
rs145711685 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | NCK2 | GRCh38.p7 | 2:105876165 | GATTTATCCAAAGCA[C/T]GCTGCTGTGACACCT | 8440 |
rs145720219 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105810337 | GAGAGAGAGAGCGAG[C/T]GAGCAAGCACACAAG | 8440 |
rs145837390 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | NCK2 | GRCh38.p7 | 2:105791963 | TTTTTTAAGCATAAT[C/T]AGAAACAAAAAGAAG | 8440 |
rs145844222 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105773796 | GCTCCCCTGAGCTTG[A/T]GTCTGGCAGGCTGCC | 8440 |
rs145862828 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | NCK2 | GRCh38.p7 | 2:105760334 | GAGAAATGCAAATTC[C/G]GGGGAACTGCCTGAC | 8440 |
rs145891141 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105870124 | AAAGGGACTACCTGC[A/G]CATAGAGATGTTGGA | 8440 |
rs145896730 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105763844 | AATTGGCTCAGACAT[A/T]ACTTTCATTGTGCCT | 8440 |
rs145955210 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105777540 | ATAATCATGCGGATT[A/G]TACCCACACACCAAA | 8440 |
rs145956639 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | NCK2 | GRCh38.p7 | 2:105846601 | TGAGGATGCAGTACA[A/G]ATACTGTTCAGTTAA | 8440 |
rs145992316 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105826031 | TTAGAAGGCTGATAC[C/T]GTGTATTAGTCTGTT | 8440 |
rs145995306 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105891101 | TGTCCAGAGGGCTCT[C/T]CTGCCCCCACACGCA | 8440 |
rs146003890 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105790631 | CTGCATCCCCCGCAC[C/G]TGTCCTCATCTTAGG | 8440 |
rs146012572 | in-del | -/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105770143 | AAAAAAAAAAAAAAA[-/G]AAAAAGGTATATTGC | 8440 |
rs146018354 | snp | A/C/T | 0.00159649 | 0.0282165 | upstream-variant-2KB, intron-variant | NCK2 | GRCh38.p7 | 2:105849759 | TTACTCTGCAAGGAA[A/C/T]CTGGTGCTTAGAAAA | 8440 |
rs146022121 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105804648 | TTAGAATTTAGAATT[A/T]CTCTTTGATTCTGTC | 8440 |
rs146079434 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | NCK2 | GRCh38.p7 | 2:105825639 | CATGTTATCACATAG[C/T]AGAGAATGATAATTT | 8440 |
rs146082910 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | NCK2 | GRCh38.p7 | 2:105756893 | CATCACAACCTCCCC[C/G]CTCCTGGGTTCAAGT | 8440 |
rs146094118 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | NCK2 | GRCh38.p7 | 2:105761479 | GGGGACACTACTTCC[G/T]GCTCCACCCTTCCCA | 8440 |
rs146098736 | in-del | -/AAAG | 0.434543 | 0.168653 | intron-variant | NCK2 | GRCh38.p7 | 2:105870754 | AGACCCTGTCTCAAA[-/AAAG]AAAGAAAGAAAGAAT | 8440 |
rs146129308 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NCK2 | GRCh38.p7 | 2:105879191 | ATGTTTGCAAAGGTC[C/T]ATTAAAAGTTTATTG | 8440 |
rs146133931 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant, utr-variant-5-prime | NCK2 | GRCh38.p7 | 2:105773422 | TGGTTTTTCATCCCT[C/G]GAATGCCTCCTTGTT | 8440 |
rs146147970 | in-del | -/GAGA | 0.0228947 | 0.104514 | intron-variant | NCK2 | GRCh38.p7 | 2:105810374 | GGCAGTAGAGGGAGG[-/GAGA]GAGAGAAAAACAGGA | 8440 |
rs146237740 | snp | A/C | 0.0115144 | 0.0749975 | intron-variant | NCK2 | GRCh38.p7 | 2:105866474 | TGGAAGACAGTTTTT[A/C]CATGGATGGTGGCAG | 8440 |
rs146249486 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105822554 | TGCATAGTCAATAAC[A/G]TAATTATTTTCTCTT | 8440 |
rs146317213 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105793328 | CTGTCATGGTCCTAG[C/T]GGGAGTGTCATTTAG | 8440 |
rs146321217 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | NCK2 | GRCh38.p7 | 2:105866189 | AAAGTGCCGGGATTA[C/T]AGGCGTGAGCCACCG | 8440 |
rs146358226 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105847364 | AAACTTTGTTAAATA[C/T]ATTTTATCACAACTT | 8440 |
rs146370067 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | NCK2 | GRCh38.p7 | 2:105806438 | GAGACGGGGTTTCAC[C/T]GTGTTACCCAGGATG | 8440 |
rs146370163 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NCK2 | GRCh38.p7 | 2:105853182 | CATTTCTCCCTAGTT[C/T]GGAGAAATGTCTAGT | 8440 |
rs146424123 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105819652 | AACACACGGGTGCCA[C/T]GTAGACAAGACGGTA | 8440 |
rs146426064 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | NCK2 | GRCh38.p7 | 2:105883960 | TAGCAGCACCGTCTT[C/T]GTCTGAGGTTCCACG | 8440 |
rs146479771 | snp | A/T | 0.0170251 | 0.090679 | intron-variant | NCK2 | GRCh38.p7 | 2:105787389 | AGCCCTCTGAGGAAA[A/T]AGGGTTGAGAGTAGG | 8440 |
rs146492224 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105775469 | ATCTTGTTTGAACTT[A/G]ATCATTTTTCCTCTG | 8440 |
rs146529405 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | NCK2 | GRCh38.p7 | 2:105784710 | ACTATAACACCATCA[A/G]ACTTGCCCCTGGAGG | 8440 |
rs146529595 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105823054 | TGAGCGCATTGCTGC[A/G]GTTGAGGTTCTCAAA | 8440 |
rs146553681 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105803182 | TTATCTAAGATAGTT[A/G]TTAATATAAACATTT | 8440 |
rs146606090 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NCK2 | GRCh38.p7 | 2:105767368 | TATTCCCTTGTTTCC[A/G]CAATAACCTAGTTAG | 8440 |
rs146623754 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NCK2 | GRCh38.p7 | 2:105764151 | CTTTCACGTGGGTGC[A/G]TGCTGTTTGCACGCC | 8440 |
rs146648921 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105873738 | AAAAGAAAACGAAAA[A/G]TTGGCTCAGATGATT | 8440 |
rs146654576 | in-del | -/T | 0.00716266 | 0.059414 | intron-variant | NCK2 | GRCh38.p7 | 2:105766656 | ACTGCTTTGTATCTG[-/T]TGACTTGTCACCTTT | 8440 |
rs146714011 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | NCK2 | GRCh38.p7 | 2:105889665 | CATACCTCACTGTTG[A/C]CTTGACCTCCCGGGC | 8440 |
rs146719702 | snp | G/T | 0.198014 | 0.244535 | intron-variant | NCK2 | GRCh38.p7 | 2:105818394 | TAACAAACCTGCACG[G/T]TTTGCACATGTACCC | 8440 |
rs146724183 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | NCK2 | GRCh38.p7 | 2:105748227 | GGCTCAGTCTCCTCC[G/T]TGTCCTGAGTTCTTA | 8440 |
rs146735851 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105752274 | AATAATTATAATGGT[C/T]ATTATTATTATGCTT | 8440 |
rs146751625 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105786856 | CCCTGCTCCCACCCT[A/G]GCCTTAGGCTGACTC | 8440 |
rs146769659 | snp | G/T | 0.0107246 | 0.0724382 | intron-variant | NCK2 | GRCh38.p7 | 2:105864090 | GTGAGCAAGAGGGCT[G/T]GGGCAGCCTCTGGGG | 8440 |
rs146787727 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105840702 | CCTCAGGTTCAATTA[A/G]TTTGCTAGAGCAGCA | 8440 |
rs146792010 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | NCK2 | GRCh38.p7 | 2:105892775 | CGCTTGAACCCGTGA[A/G]GCGGAGGTTGCAGTG | 8440 |
rs146828302 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | NCK2 | GRCh38.p7 | 2:105827290 | AGGCGTGAGCCACCG[C/T]GCCTGGCTGACATAG | 8440 |
rs146828402 | snp | C/T | 0.084728 | 0.187577 | intron-variant | NCK2 | GRCh38.p7 | 2:105789302 | AAGCAATTCTCCTGC[C/T]TCAGCCTCCTGAGTA | 8440 |
rs146841228 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105802413 | TACTTGAGGCTGGGT[C/T]ATTTATAAAGAAAAG | 8440 |
rs146889586 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NCK2 | GRCh38.p7 | 2:105799824 | CTGGCCTTCCCCTCC[A/G]CCATCTTGCCACTAT | 8440 |
rs146891312 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105844017 | TTTGATATGGTAAGA[C/T]GAGAATAGCATGTTG | 8440 |
rs146948579 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105754159 | TTTGGGCAGTTTCTT[C/T]CAACTCACAGGTTTA | 8440 |
rs146950324 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | NCK2 | GRCh38.p7 | 2:105824273 | CTTGGGCCCCTGACG[A/G]TGCTCACAGGGAATG | 8440 |
rs146980729 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | NCK2 | GRCh38.p7 | 2:105808220 | TTGTTTCTTAAGAAA[A/C]GAACATTACATCATT | 8440 |
rs146983530 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105874602 | ACTTGAGCACACCGC[A/G]TCTAAACGAATTGGC | 8440 |
rs146990418 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | NCK2 | GRCh38.p7 | 2:105770550 | TCTTAGAAGTAGAAG[A/G]CTATAGAATATCTGT | 8440 |
rs146993597 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | NCK2 | GRCh38.p7 | 2:105877258 | GGCCACAGCTTTCTT[G/T]CTCTGGTATCCTTAG | 8440 |
rs147067591 | in-del | -/C | 0.0103295 | 0.0711199 | intron-variant | NCK2 | GRCh38.p7 | 2:105860285 | AGTGAGACCCTGTCT[-/C]AAAAAATGAGCCATA | 8440 |
rs147087041 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | NCK2 | GRCh38.p7 | 2:105865052 | GGGCCGCAGGCTCCC[C/T]CAGCCAGCATCAGTG | 8440 |
rs147095555 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | NCK2 | GRCh38.p7 | 2:105749736 | GTGTGAGGGGAGGCC[A/G]GCAGGAGCAATGTCA | 8440 |
rs147096563 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105820751 | CAAAGGGCCTTGTCT[G/T]CTATGCTGCAGATTC | 8440 |
rs147097370 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105866976 | GTTTTTCTGAGTTGA[A/G]TGTTCTTCAGGAATG | 8440 |
rs147138381 | in-del | -/ACA | 0.0325976 | 0.123435 | upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105743073 | TTACAGGGTGGGAAG[-/ACA]ACAACCTCTCTAGAG | 8440 |
rs147144518 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NCK2 | GRCh38.p7 | 2:105837643 | GCTGCTGCCTTGTAC[A/G]TATGTCAGTATTCTG | 8440 |
rs147191706 | snp | A/C | 0.0221141 | 0.102801 | intron-variant | NCK2 | GRCh38.p7 | 2:105800465 | AAATTCTGAGGTGCA[A/C]AGTTCCTGAGCTTTA | 8440 |
rs147206668 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105799186 | ATCTATCTGTGGTAT[A/G]TTTTATCATGTAAGA | 8440 |
rs147207862 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | NCK2 | GRCh38.p7 | 2:105841540 | CTTTTTGGGTTTTTA[C/T]GGAAGCTTCATTGCA | 8440 |
rs147241788 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | NCK2 | GRCh38.p7 | 2:105879678 | TGGCGCCGCGTGGGC[A/G]CATGTCCCAGGGTAG | 8440 |
rs147252008 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | NCK2 | GRCh38.p7 | 2:105883071 | TGCTCTCTTTGAGGA[C/T]GGAGCATCGTGGTGG | 8440 |
rs147292635 | in-del | -/CACA | | | utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105894010 | CGTGCACACACACAC[-/CACA]ACACACACACTATAT | 8440 |
rs147297171 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105785798 | AGCAGGAGGTTGGGC[G/T]CAGGACTCCTAGTAA | 8440 |
rs147313990 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105783386 | GCATTAAATTGTGCC[C/T]GTGTTCTGGGGTAGC | 8440 |
rs147314115 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | NCK2 | GRCh38.p7 | 2:105821281 | AAAGATTTTTTACAC[A/G]CAAAGCCCAGTGCTC | 8440 |
rs147348581 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105869062 | CATACGATCCAGCCC[C/T]GCTGCCCACCCTTAC | 8440 |
rs147357939 | in-del | -/A | | | intron-variant | NCK2 | GRCh38.p7 | 2:105779307 | CGAGACTCCGTCTCA[-/A]AAAAAAAAAAAAAAA | 8440 |
rs147402886 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105765629 | TATCGTATTTTTGGT[C/T]GCTGGCTAAAACAGA | 8440 |
rs147418165 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NCK2 | GRCh38.p7 | 2:105805160 | ATGGGCACGGAGGCC[A/G]GTCTCCTAGAAGAGA | 8440 |
rs147419183 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105762855 | GTTTTTAAGTAATAT[A/G]TTAATAACTGTGTTC | 8440 |
rs147420646 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105872941 | CCCGGAAGTGGACAT[A/T]AGCAGCGCCTGTCCT | 8440 |
rs147452621 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105886134 | TGTAGGCATCTTTCC[A/G]GTTTCAAAGATAACA | 8440 |
rs147462926 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105858570 | CATGGTAAGATTCCT[G/T]CCTGCTTTGGAATAA | 8440 |
rs147466543 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | NCK2 | GRCh38.p7 | 2:105785874 | AAAATAAATACGATA[A/T]CTAGTAGCAGTGCAA | 8440 |
rs147495198 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | NCK2 | GRCh38.p7 | 2:105883122 | GGTGTCATCAATTTT[A/G]CGGAGCCTTACATGT | 8440 |
rs147525703 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105863023 | TAATACCAGATGTCA[A/T]CGTGCCCAGCTGATG | 8440 |
rs147556683 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105832197 | TTGGTATATAGAAGA[A/G]ACACTACTGATTTTT | 8440 |
rs147578557 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | NCK2 | GRCh38.p7 | 2:105759391 | CCTTTTGTTGAGCAC[A/G]GTGTTTTAACGTTTC | 8440 |
rs147606587 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105877641 | GCATGCAAGCAGGCA[C/G]GGAGGGAGTGGAGTA | 8440 |
rs147616753 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | NCK2 | GRCh38.p7 | 2:105880575 | AGGTTATACAGGCTG[C/T]GTTCCCTAAGACTGG | 8440 |
rs147661118 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105774733 | ATCTGTGTTCCACAA[A/G]TACACTCAATTTTTA | 8440 |
rs147661179 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105814583 | TTTTGGTTTGCTGTT[A/G]GCATAAGGAGTCTCT | 8440 |
rs147670809 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | NCK2 | GRCh38.p7 | 2:105779230 | GAGAATCGCTAGAAA[C/T]TGGGAGACAGAGGTT | 8440 |
rs147706392 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NCK2 | GRCh38.p7 | 2:105877017 | CCGGCTGCCACCTGG[C/T]GGGGTCACAGCTCCA | 8440 |
rs147710955 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | NCK2 | GRCh38.p7 | 2:105867050 | TTCTAAACTAAGCCG[C/T]TCTCCAAGGAACCAC | 8440 |
rs147720430 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105869274 | CTGCATGTGTCCCTA[A/G]CCATAACAGCGAACT | 8440 |
rs147735624 | in-del | -/ATT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105856330 | GAGCTGACATTTAAA[-/ATT]ACGTTGTTACCTTCT | 8440 |
rs147765714 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | NCK2 | GRCh38.p7 | 2:105799337 | CTTCTATACTTTTAC[A/T]TTTTCATTGTAAATC | 8440 |
rs147765848 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | NCK2 | GRCh38.p7 | 2:105753911 | AGTCCAAATGTAGAT[C/T]CTTGGGAGACTGCTG | 8440 |
rs147775802 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105759014 | AAGTAAAATGGTTTT[A/G]GTGATTTACTATAGT | 8440 |
rs147809845 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105866875 | GGTGTTGAGTGCTTG[C/G]GATGCTCAGTGTGGC | 8440 |
rs147871858 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NCK2 | GRCh38.p7 | 2:105855668 | GTCCATTTGGCCTAC[A/G]TGCCTAGAGCAGGGG | 8440 |
rs147876257 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NCK2 | GRCh38.p7 | 2:105784052 | GGTTGGCCTCAACAC[C/T]ATGCGTGGCATTGGC | 8440 |
rs147879012 | snp | A/G/T | 8.3095e-05 | 0.00644526 | missense, stop-gained, intron-variant | NCK2 | GRCh38.p7 | 2:105881474 | TTCGCCTATGTGGCC[A/G/T]AGCGGGAGGATGAGT | 8440 |
rs147915352 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105849240 | TATCTACAAAAAGTA[A/G]AAAACTAGCAGGGCG | 8440 |
rs147922486 | snp | A/G | 0.00128894 | 0.0253536 | missense, utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105893045 | TTCAAGGTGCAGCTC[A/G]TGGACAATGTCTACT | 8440 |
rs147932552 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | NCK2 | GRCh38.p7 | 2:105864783 | ATGAGTTTGGCCCTC[C/T]GAACCCACGGGAAAG | 8440 |
rs147973485 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105846036 | TTAACATCATGTAAG[A/C]AAATTGGCTTATTAA | 8440 |
rs147974733 | snp | C/G | 0.00716266 | 0.059414 | intron-variant, utr-variant-5-prime | NCK2 | GRCh38.p7 | 2:105745907 | GTTTTAAGGCATGGA[C/G]GGTAACTGCCTTATG | 8440 |
rs147983062 | snp | A/G/T | 0.00199481 | 0.0315187 | intron-variant | NCK2 | GRCh38.p7 | 2:105805550 | TAAATTAAATTTCCC[A/G/T]AACTTACTCATAACC | 8440 |
rs148018944 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105788727 | CCATAGAATGCATAA[A/T]TTTTTTTGTTTGTTC | 8440 |
rs148035007 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105800258 | GGTTCCAACTGCACA[C/G]CTTGTTCTCTGTCCT | 8440 |
rs148089094 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105828489 | CCGCAGATCAGTGTG[C/G]AGTGCAGAATTTAAG | 8440 |
rs148164355 | snp | C/G | 0.00119737 | 0.0244387 | downstream-variant-500B | NCK2 | GRCh38.p7 | 2:105894491 | TCTCAAGCTTGGTCT[C/G]AACTTTGCTCTTTGG | 8440 |
rs148179499 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NCK2 | GRCh38.p7 | 2:105792629 | TCCACCTTCCCCATG[C/T]CAGTTGATTTGTTGG | 8440 |
rs148185353 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | NCK2 | GRCh38.p7 | 2:105809597 | TTTCACTGTCACATT[A/G]TGAAGTACTGGGTGT | 8440 |
rs148188915 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NCK2 | GRCh38.p7 | 2:105784879 | GTAAAGTTAGGAACA[C/T]GTGCATGCACTTAGG | 8440 |
rs148195028 | snp | C/T | 0.0263992 | 0.111815 | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105771419 | TAAAAATATAAAAAT[C/T]AGCTGGGTGTGGTGA | 8440 |
rs148227888 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105884489 | GCCTGGGCCTTTAAT[C/T]GAGGTTATCACATGA | 8440 |
rs148231762 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105820345 | AGTGAAATAAATGCT[A/G]GCCTGGTAGAACAGT | 8440 |
rs148239532 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | NCK2 | GRCh38.p7 | 2:105872856 | GAAATCTCTGAAAAA[C/G]TAACTGAGTCCCCTT | 8440 |
rs148241141 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105780628 | TCACTGATGTGGTCT[C/G]AATGTGTCCCTCATA | 8440 |
rs148247719 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105765299 | TTGAAAACAAATTGA[C/G/T]GAGAATTTGTACATA | 8440 |
rs148253811 | in-del | -/AAATA | 0.0119091 | 0.0762411 | intron-variant | NCK2 | GRCh38.p7 | 2:105885406 | AAGTATTTGGCTGGG[-/AAATA]AAATAGAATAGCTCC | 8440 |
rs148302055 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | NCK2 | GRCh38.p7 | 2:105867318 | TGAATTAAATATAAT[A/G]TATCAGAATTTAGAA | 8440 |
rs148322287 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105871108 | GAGTGCGTGTGAAAT[C/T]GGGGTGATGAGACAG | 8440 |
rs148335434 | snp | G/T | 0.0260105 | 0.111035 | intron-variant | NCK2 | GRCh38.p7 | 2:105761610 | GAGTGGCTCATAGTG[G/T]CTCATGCCTGTAATC | 8440 |
rs148384972 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | NCK2 | GRCh38.p7 | 2:105858489 | CCTGGGATCAATCTA[A/G]TAACTCATGGCACCA | 8440 |
rs148387992 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105755190 | CTTCAGTTCCCTTTT[C/T]GTAGTTTCCTTACTA | 8440 |
rs148428268 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105839351 | GTAGAACAGAGAGAC[G/T]GGTAGACTGGAGAGG | 8440 |
rs148470991 | in-del | -/TGCA | 0.0103295 | 0.0711199 | intron-variant | NCK2 | GRCh38.p7 | 2:105849349 | CTGTGATTGTGCCAC[-/TGCA]TGCACTCCAGCCTCA | 8440 |
rs148480895 | in-del | -/TAAT | 0.021333 | 0.101051 | intron-variant | NCK2 | GRCh38.p7 | 2:105820693 | CTTGAAAAGTGACTG[-/TAAT]TGATTGTTGGAGGCT | 8440 |
rs148489770 | snp | G/T | 0.0263992 | 0.111815 | intron-variant | NCK2 | GRCh38.p7 | 2:105793999 | TTATAAATTCACATT[G/T]ATACTTATAACTCAA | 8440 |
rs148499219 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105786150 | TCTGTTGTGTCTAGG[A/G]CAGCATGATTAGCGT | 8440 |
rs148537946 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105886322 | ATCACCTGATTCTGA[C/T]TCTCAAATGGGCCAG | 8440 |
rs148541757 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105822400 | CAGACCTGCCAAAAG[A/T]GAAGTTCTCTGTACA | 8440 |
rs148550295 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105783100 | CCTTAGAATAAGAGT[A/T]GCAGAAGGCCAGAGC | 8440 |
rs148553401 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105853965 | GGATTCCAGCTAGAG[C/T]ACCTTAGCAGGAGAG | 8440 |
rs148565041 | in-del | -/CTT | 0.00795532 | 0.062565 | intron-variant | NCK2 | GRCh38.p7 | 2:105749552 | AATTTAGGTTAAGTC[-/CTT]CTGCAGGCCATACAT | 8440 |
rs148634889 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105802067 | ACCATGATTTGTACA[C/G]CAGCTTGGATGAAGA | 8440 |
rs148635628 | in-del | -/AATA | 0.0263992 | 0.111815 | intron-variant | NCK2 | GRCh38.p7 | 2:105830559 | TGCAGCTGTCACATC[-/AATA]TACTCATTTCCTTTT | 8440 |
rs148638031 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105872031 | TACTGCTTTTTCTCC[A/G]TGGTGGTCAGGAATT | 8440 |
rs148651991 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | NCK2 | GRCh38.p7 | 2:105810294 | CTTCTTAAGATGCTA[C/T]TTGAAAAAAACAAAA | 8440 |
rs148689518 | snp | G/T | 0.0115144 | 0.0749975 | intron-variant | NCK2 | GRCh38.p7 | 2:105868444 | GCTGAGGCAGCTGTT[G/T]ATGGGGAATCTTGCT | 8440 |
rs148699228 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | NCK2 | GRCh38.p7 | 2:105826693 | AGTTATCCTCACAGT[A/G]TCCTTCTCTCTCAAT | 8440 |
rs148703117 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | NCK2 | GRCh38.p7 | 2:105758624 | CATATTGGCCAGGCT[A/G]GTCTTGAACTCCTGA | 8440 |
rs148705374 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105848351 | TCACAAAAGTGGTCC[C/T]ATCAGTGTCCACAGA | 8440 |
rs148743040 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105890664 | TACAAACTATACTTA[C/T]AATTGTTCCTTTCAT | 8440 |
rs148750976 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | NCK2 | GRCh38.p7 | 2:105790604 | AGTGTCATCACTTGA[C/T]GTGACATCTTACTGC | 8440 |
rs148762813 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | NCK2 | GRCh38.p7 | 2:105813211 | AAGGTGAAGCCACGG[C/T]GAGTGTCTCACTGGA | 8440 |
rs148812245 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | NCK2 | GRCh38.p7 | 2:105788188 | GATAAGTTTTTTCAT[C/T]AGCTATGTGAATTGG | 8440 |
rs148839655 | in-del | -/CCTCCCTCCCTCCCTC | | | intron-variant | NCK2 | GRCh38.p7 | 2:105861904 | GGCCTGGAATTCTTT[-/CCTCCCTCCCTCCCTC]CCTCCCTCCCTCCCT | 8440 |
rs148854090 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | NCK2 | GRCh38.p7 | 2:105824039 | GTCCTCAGGTAGGCT[C/T]TCCCTTACAGGGATG | 8440 |
rs148856941 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | NCK2 | GRCh38.p7 | 2:105888708 | TGGAGGGCAGCTTCC[A/G]AGATGGGCATTGTGG | 8440 |
rs148864210 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NCK2 | GRCh38.p7 | 2:105784386 | GGCTTGGGGTGAATC[A/G]GGAGGGGAGAGTTTA | 8440 |
rs148908691 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105883581 | GAAAAAGGTGTTCTC[C/T]GGGGTTGCTGGCCTT | 8440 |
rs148949240 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105804269 | ATGTGTGTAAATGAA[C/T]GGACCAGCGCTTTTC | 8440 |
rs148950735 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105872502 | CCTCCTCTTTATTGC[A/G]ATTGTCACCGTTGGT | 8440 |
rs148953102 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NCK2 | GRCh38.p7 | 2:105780419 | GGCTCTCTCATTTTC[A/G]TTTGGTATCTGGGTT | 8440 |
rs149002042 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | NCK2 | GRCh38.p7 | 2:105870444 | ATGTTTCATTATGGG[G/T]TATGCATGCCTAGAA | 8440 |
rs149004253 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105774278 | TCCTCTAAAGTGCTG[C/G]GATTACAGGTGTGAG | 8440 |
rs149015278 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105760091 | TCTTTGGAAGGAGGT[A/C]ATTTAAGGAAGAGGG | 8440 |
rs149022188 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NCK2 | GRCh38.p7 | 2:105819944 | AGATAAAATATAGTC[C/T]CAGCCACCTTTCCCC | 8440 |
rs149025305 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | NCK2 | GRCh38.p7 | 2:105749179 | AACCTGAATTCAAAA[C/T]GCTGGGCAGACCGTT | 8440 |
rs149064279 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | NCK2 | GRCh38.p7 | 2:105864719 | AGGCATTCAATTTCT[C/T]TCATGTTAAAGACTG | 8440 |
rs149095527 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | NCK2 | GRCh38.p7 | 2:105880686 | TCTGCATTTATACTT[G/T]ATTTTTCTGAGAGGC | 8440 |
rs149159879 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105841005 | TGTAACTTTAGGTCA[C/G]TAATTGAGGTCTACC | 8440 |
rs149216193 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105807314 | CCCAGGTGCTCTCCT[C/T]GAAGGGCAGGGGAAA | 8440 |
rs149216913 | in-del | -/TGA | 0.00279162 | 0.0372561 | intron-variant | NCK2 | GRCh38.p7 | 2:105858118 | TCCTATTACTGTTGG[-/TGA]TGATAATTAAACAGG | 8440 |
rs149221985 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105796970 | TTGGTTCAGTACCCC[C/T]AGCTGGGGTGAGTGT | 8440 |
rs149224339 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | NCK2 | GRCh38.p7 | 2:105867135 | GTAACATAAGGGGAA[A/G]AAAATTCAGCTATCT | 8440 |
rs149256695 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NCK2 | GRCh38.p7 | 2:105878703 | AAACCAGTACACAGA[A/G]AGACATTTATTAAGT | 8440 |
rs149263311 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | NCK2 | GRCh38.p7 | 2:105873538 | CACACCCAAAACCCT[C/T]GGTCACTGTGTTCTT | 8440 |
rs149265123 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NCK2 | GRCh38.p7 | 2:105782891 | CTGGAGAGGCGTAGG[A/G]GGCAGTTACTCCAGA | 8440 |
rs149323469 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105776789 | CCACACGTGACTATT[C/T]GAGGGTACCATAGCC | 8440 |
rs149325301 | snp | C/T | 0.0295035 | 0.117819 | intron-variant | NCK2 | GRCh38.p7 | 2:105830572 | TCAATATACTCATTT[C/T]CTTTTCTGTGGGTAA | 8440 |
rs149340449 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105751157 | TTAGTGGTCATTTCC[A/G]CCATCCCAAACCATT | 8440 |
rs149378789 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | NCK2 | GRCh38.p7 | 2:105866022 | CAGGTTCGAGCAATT[C/T]TCCTGACTCAGCTTC | 8440 |
rs149414240 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime | NCK2 | GRCh38.p7 | 2:105816458 | TTTGTATACAAGCGA[C/T]GTCCCAGATTATAAT | 8440 |
rs149416859 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | NCK2 | GRCh38.p7 | 2:105882291 | TTAGCTCACAGAGGT[A/G]GTTCTGCTTCTCTCC | 8440 |
rs149531099 | in-del | -/C | 0.0119091 | 0.0762411 | intron-variant | NCK2 | GRCh38.p7 | 2:105862947 | TAAGTTTGGCATAAG[-/C]CTTTAAGAGGCCAGA | 8440 |
rs149531372 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105808780 | ATGAGACAGGAAAAT[C/T]GGGACACTAATGAGA | 8440 |
rs149538870 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | NCK2 | GRCh38.p7 | 2:105868405 | GGCTGGGGTGGCCTG[C/T]GTTCCTTCCTGGAAG | 8440 |
rs149542632 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105799121 | GTCCTGTCTGTCCTT[C/T]GTGTCCTAAGTTGCA | 8440 |
rs149590874 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105890417 | TAAATTGAGCCTGGC[A/T]TATAGTAAACTCTAT | 8440 |
rs149592868 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | NCK2 | GRCh38.p7 | 2:105800050 | CATGTGGTATCATTA[G/T]ATGTGTCTTTGCACC | 8440 |
rs149625626 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | NCK2 | GRCh38.p7 | 2:105858298 | GGGCCTCACTCTGTT[A/G]CCTAGGCTGGAGTGC | 8440 |
rs149641907 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105885247 | GTTCCCGAAGATATC[A/T]TGTATTTATTATGTC | 8440 |
rs149664097 | snp | C/G | 0.0130921 | 0.0798413 | intron-variant | NCK2 | GRCh38.p7 | 2:105866871 | CCTGGGTGTTGAGTG[C/G]TTGGGATGCTCAGTG | 8440 |
rs149673311 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NCK2 | GRCh38.p7 | 2:105823371 | GAGTGTGTCCCAGTG[C/T]CCTTGTGCTCCCCAT | 8440 |
rs149677120 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105753864 | AGGTGGCTTTGAAAT[C/T]TGCTTCTGAGGTTGT | 8440 |
rs149719535 | in-del | -/CTTAGGC | | | intron-variant | NCK2 | GRCh38.p7 | 2:105786859 | GCTCCCACCCTAGCC[-/CTTAGGC]TTAGGCTGACTCCCT | 8440 |
rs149727980 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | NCK2 | GRCh38.p7 | 2:105883299 | AGATCGTGTTTGAAG[C/T]CTTAAGCAAATTAAG | 8440 |
rs149730605 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105793456 | GAACTTCTGACCTCG[A/G]GCATCCTGTTTCTGA | 8440 |
rs149823358 | snp | C/T | 0 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105869605 | CTCTTTTTGTGTATT[C/T]GTCACATTTCACTTT | 8440 |
rs149842148 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105810321 | AAAAGTGTGTGTGTG[A/T]GAGAGAGAGAGCGAG | 8440 |
rs149844441 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105875835 | GATACCATCAGATCT[C/T]TAAGGTTTCTTCTAG | 8440 |
rs149852462 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NCK2 | GRCh38.p7 | 2:105773732 | TCTGAGCCAGGTGCT[A/G]TTTCAGGCCCTGGTG | 8440 |
rs149887069 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105864573 | CTCAGGCTTGGGAGG[C/T]ACACAGTTATCCTTA | 8440 |
rs149891225 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NCK2 | GRCh38.p7 | 2:105791472 | CCTCGCCCCGTTGCC[A/G]TGCTTACCGGCCAGA | 8440 |
rs149895052 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105842418 | AAGTGTAGAAATCCT[A/G]AACACTGAGGAAAGT | 8440 |
rs149905221 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105801946 | TGCAGGCCCATCTCC[C/T]TGCATGGAGAACTGT | 8440 |
rs149920128 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | NCK2 | GRCh38.p7 | 2:105758107 | TTGCTTGAGAGCTTT[A/C]TCTCTTAAAAATGAG | 8440 |
rs149991314 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | NCK2 | GRCh38.p7 | 2:105879670 | ATGCCTCCTGGCGCC[A/G]CGTGGGCACATGTCC | 8440 |
rs150005668 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | NCK2 | GRCh38.p7 | 2:105784269 | ACACCACGCCCGGCT[A/G]TTATTTCTAATAGGA | 8440 |
rs150031257 | snp | C/T | 1.70461e-05 | 0.00291938 | synonymous-codon, intron-variant | NCK2 | GRCh38.p7 | 2:105881416 | CGCCAATGGCAGCGG[C/T]GCCGACCGCATCTAC | 8440 |
rs150057082 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105778697 | TGTGTATCAATTGAG[A/T]TAATGGTTATTTTTT | 8440 |
rs150101967 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105816214 | GGGAGACTTAGGCAG[C/G]AGGATCACTTGAGCT | 8440 |
rs150104910 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | NCK2 | GRCh38.p7 | 2:105746107 | AGCGTGCGTGGAGTC[A/G]GCCTTGGCCACTTCA | 8440 |
rs150155525 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | NCK2 | GRCh38.p7 | 2:105878433 | ATAAGAAAAGGAGAT[G/T]GGAACACAAAGAAAA | 8440 |
rs150156150 | snp | A/G | 8.76432e-05 | 0.00661921 | synonymous-codon | NCK2 | GRCh38.p7 | 2:105855219 | GACGGGCTATGTACC[A/G]TCCAACTACGTGGAG | 8440 |
rs150160335 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105812139 | AAAACTTGATACTTT[G/T]ACTTTTCAGGACAGC | 8440 |
rs150164135 | in-del | -/G | 0.0256215 | 0.110247 | intron-variant | NCK2 | GRCh38.p7 | 2:105762296 | CAGAGCATCAAACCA[-/G]GGGGGGTCTAGGTCC | 8440 |
rs150169923 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105776391 | CAGAACCCCTGTCAC[C/T]ATGCATATACCAGGT | 8440 |
rs150197372 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | NCK2 | GRCh38.p7 | 2:105865410 | AGTGTGGCCTGACTC[C/T]GCCTCTTGTGATTGC | 8440 |
rs150221753 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | NCK2 | GRCh38.p7 | 2:105803551 | GAGGTTAATTAGCAG[C/T]CTTCAATTTCTACAG | 8440 |
rs150248703 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | NCK2 | GRCh38.p7 | 2:105862294 | TGATTTTACTTAGAT[C/G]AAAAGACCCAGGTTA | 8440 |
rs150258063 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | NCK2 | GRCh38.p7 | 2:105759701 | CATCCTTTTTCTGTC[C/T]CAGGATCCCATCCAG | 8440 |
rs150363707 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NCK2 | GRCh38.p7 | 2:105850293 | TAACCCAGCAAGATA[C/T]GGTTCATAGGATTGT | 8440 |
rs150371533 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | NCK2 | GRCh38.p7 | 2:105748526 | TCCCACCTCAGCCTC[C/T]GAGTAGCTGGGACTA | 8440 |
rs150400835 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105840909 | GAAAGGTAAAAGGCC[A/G]TGGGCATCTGAAAGG | 8440 |
rs150408129 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NCK2 | GRCh38.p7 | 2:105890166 | GTTTCTGCTCAGGAG[C/T]CCACGAAATTAAAAA | 8440 |
rs150417103 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NCK2 | GRCh38.p7 | 2:105874283 | ATATACAGCAACACA[A/G]AAACTTGTAGAAGCT | 8440 |
rs150431388 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105769623 | CCTACTGCACTGCCC[A/T]CTGCCCTCTGGAGGG | 8440 |
rs150453347 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105833323 | GCTGATCTCGAACTC[C/T]GGGCCTCAGGTGATC | 8440 |
rs150460825 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105884801 | GTCCTTCCATTTCTT[C/T]CTCCTCCCTCGCTCT | 8440 |
rs150463318 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | NCK2 | GRCh38.p7 | 2:105796591 | TCTGGACTGAGCCTG[C/G]GAGCTGGAAGGCTGG | 8440 |
rs150504236 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | NCK2 | GRCh38.p7 | 2:105873330 | AAGTCAACTCTGAGA[C/G]CCCCCAGAAAATCGA | 8440 |
rs150508099 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NCK2 | GRCh38.p7 | 2:105805912 | TTGCATAAACATAAC[A/G]AGAGGTTTTGGGGAT | 8440 |
rs150519692 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105766136 | GAAACAAAAGAATGA[A/G]GGGAGGCGCAGGTGG | 8440 |
rs150556124 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105871213 | TTTGTTTGTCCTTCC[C/T]AAGGAGATAAATACA | 8440 |
rs150565996 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NCK2 | GRCh38.p7 | 2:105829619 | TTACAAAGTCCCCCA[A/G]TTGAGAGTTGTCTGA | 8440 |
rs150571648 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NCK2 | GRCh38.p7 | 2:105762455 | AATCTAGAGATTCGC[C/T]GAAGCTCATGTCCCA | 8440 |
rs150623713 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NCK2 | GRCh38.p7 | 2:105792897 | AGTCACTCCTTCTGC[A/G]CTTGCTAGCCAGGTG | 8440 |
rs150651319 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105859128 | GCACTATGCTACATC[C/T]TTTGAGATGGGGAAG | 8440 |
rs150666362 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105810036 | CATTCAGTGGCAGGG[C/T]CAGGGCTGAGAGGGA | 8440 |
rs150682861 | snp | A/C | 0.0103295 | 0.0711199 | intron-variant | NCK2 | GRCh38.p7 | 2:105854412 | ACAGAACTTTCCCTT[A/C]TACCCTTTACCTGGT | 8440 |
rs150686079 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NCK2 | GRCh38.p7 | 2:105750229 | ACGTAGCCTTCCTTC[C/T]GTGAGTGCACTGAGA | 8440 |
rs150713111 | snp | A/G | 0.195214 | 0.243923 | intron-variant | NCK2 | GRCh38.p7 | 2:105842179 | CAACCTCTGCCTCCC[A/G]GTTTCAAGTGATTCT | 8440 |
rs150720976 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105820067 | GATCAACTGACCCTT[A/T]AGGGACAGTATGGAA | 8440 |
rs150755273 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | NCK2 | GRCh38.p7 | 2:105875005 | TTTCTGTCTGCTCAC[C/T]GAGTGACAAATGTTA | 8440 |
rs150771572 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | NCK2 | GRCh38.p7 | 2:105836311 | CTATAGTATCATTTG[G/T]GTAGGATGCTTTGGG | 8440 |
rs150772481 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105887438 | GTAGATTATTGATGC[C/T]TGGAGACTTCAGCGT | 8440 |
rs150781274 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | NCK2 | GRCh38.p7 | 2:105798981 | TATCATTTTAGTGAA[A/G]TTCAGATGTCCCTTT | 8440 |
rs150834184 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105825489 | GCACTGGGCACTGCA[G/T]CGCTTTGGAACATAG | 8440 |
rs150876690 | snp | G/T | 0.0263992 | 0.111815 | intron-variant | NCK2 | GRCh38.p7 | 2:105777954 | CCTGTCTTCTTGTCA[G/T]GGAAAGTTCTTTTGT | 8440 |
rs150893185 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105813621 | CACGACTGCTTGCAG[A/G]GGGGCATCTCACTGC | 8440 |
rs150897408 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105790139 | GTGAGCTAAAAATAC[A/G]GGCAGCCGTTTCTTC | 8440 |
rs150904549 | snp | C/T | 0.000104035 | 0.00721156 | synonymous-codon, intron-variant | NCK2 | GRCh38.p7 | 2:105881389 | CACGCCCAGCACGGA[C/T]GCCGAGTACCCCGCC | 8440 |
rs150916081 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NCK2 | GRCh38.p7 | 2:105879627 | TAAATGAATCAGTGT[A/G]TTTGCTCTGAAACGT | 8440 |
rs150931452 | snp | G/T | 0.0115144 | 0.0749975 | intron-variant | NCK2 | GRCh38.p7 | 2:105866604 | CGTAGTTCACAATAG[G/T]GTTTGCGCTCCTGTG | 8440 |
rs150954352 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105889482 | CTTATTAAAACACAC[A/G]GTGCTGGAGGTTAAA | 8440 |
rs150980328 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105811594 | CAGCTTGTCTCGTGG[A/G]ACAGGTGTGATTGAG | 8440 |
rs150997503 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | NCK2 | GRCh38.p7 | 2:105753237 | CGCCTTATCAGCCAA[C/G]TGGTTGGGGAAGGCC | 8440 |
rs151022772 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | NCK2 | GRCh38.p7 | 2:105856495 | TCTTTTGGGGAATGG[A/G]GAATGAGGAATACGT | 8440 |
rs151032424 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | NCK2 | GRCh38.p7 | 2:105844329 | GGACATCTGAATAAA[C/T]CATGAACTTTAGTTA | 8440 |
rs151052305 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105786548 | GCTCAGACTCATCCA[C/T]ACCTTTAGGAAAAGG | 8440 |
rs151084917 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | NCK2 | GRCh38.p7 | 2:105839917 | GGCTGTGTGATCTCC[A/G]CGCAGCTGGTGGACG | 8440 |
rs151095165 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105799646 | AACAAAACGGAATAC[C/T]ACTATATGAAAGCCT | 8440 |
rs151139765 | in-del | -/A | | | intron-variant | NCK2 | GRCh38.p7 | 2:105857048 | TTTTTTTTTTTTTTT[-/A]TGTATTTACAAGATT | 8440 |
rs151144760 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105891927 | TCACAGAATTTAAAT[A/G]TTTTTCAATAAAATC | 8440 |
rs151211966 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105791343 | ACCTCTGTGCCTTCA[C/T]GTTTTTCTCTTCACT | 8440 |
rs151233661 | in-del | -/TTACACATAA | | | intron-variant | NCK2 | GRCh38.p7 | 2:105759464 | ATGCATACAGGCTTT[-/TTACACATAA]TATATAATAAAACAT | 8440 |
rs151238863 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | NCK2 | GRCh38.p7 | 2:105874014 | GAAGGCTCGGGGTGA[A/G]ATGGGGCCCTTCACA | 8440 |
rs151243673 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105807484 | TACAGCTGATATCTA[C/T]GTAATTTGAGAAGTG | 8440 |
rs151260592 | in-del | -/CTTG | | | intron-variant | NCK2 | GRCh38.p7 | 2:105836176 | AGGTTTTATTGTTTC[-/CTTG]CTTTTTCGTGTTTCT | 8440 |
rs151262573 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | NCK2 | GRCh38.p7 | 2:105747857 | ACTCAGAAGAAGGTC[A/G]TGACGGCCTTTTAAC | 8440 |
rs151296887 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NCK2 | GRCh38.p7 | 2:105872155 | TATTTTTGCTTTGCT[C/T]GACACGTTTCTGCCA | 8440 |
rs151300734 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105832741 | TTTGCATCTATGTTC[A/C]TCAGGCACATTGGCC | 8440 |
rs151303688 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NCK2 | GRCh38.p7 | 2:105763560 | AGTGGGAAATATTCA[A/G]TTTGTTAGTTGAAAA | 8440 |
rs180672407 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105808895 | GTTTGTGGGCAAACT[A/G]ATTTTTGCTTGTGAT | 8440 |
rs180687236 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105826292 | AGCATGGGGGAAACC[A/G]CCCCCATGACTCAAT | 8440 |
rs180697882 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105757773 | GAAGTCCCCCTCTAA[C/T]CTCTAACCCAACCCC | 8440 |
rs180698840 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105845202 | AGTAGCCTAATAATA[C/T]TTTAACATTATGAGA | 8440 |
rs180710763 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105773993 | CCTCAGGTGGAAGAT[A/G]TGGATTTTTCCAGCT | 8440 |
rs180915620 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105807747 | TCCTTCCTTCCTTCC[C/T]TCCCTCCCTCCCTCC | 8440 |
rs180927844 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105849443 | TCTGTGGCGGGATAA[A/G]TTGGTTAGTCAGTGG | 8440 |
rs180928879 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | NCK2 | GRCh38.p7 | 2:105859417 | GACTTCTGCATCCAG[C/T]GTCACCTGCCCCAGG | 8440 |
rs180929484 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105871103 | TCGATGAGTGCGTGT[A/G]AAATCGGGGTGATGA | 8440 |
rs180938512 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105888379 | CACAGAGAAATTACT[A/G]TATACCAAGTAAGTA | 8440 |
rs180941067 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105840188 | TAGCATGTCTTATGC[A/T]AAATGAGATGATCCA | 8440 |
rs180947118 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NCK2 | GRCh38.p7 | 2:105798677 | GTTGCTGGTGATTAA[A/G]TTTATGTGGACGGTG | 8440 |
rs180955218 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105813955 | AGAGAAAAGCACACA[C/G]TCCTTCTGTATATTC | 8440 |
rs180955382 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105830367 | ATATAATAACATTAT[C/T]CAGGCTTATCCATGT | 8440 |
rs180974765 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105822978 | GGCCCTGGGCCGGCC[A/G]TGTGGCGGATGTGTA | 8440 |
rs180980472 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105779277 | GTGCCACTGCACTCC[A/G]GCCTGGGCAACAGGG | 8440 |
rs180981425 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105743816 | ATCAAATAATACAGC[C/T]TTGTAACCTTGGGTA | 8440 |
rs180990544 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105791396 | TGGTGGAAGGCTCGG[C/T]GGCTTTCACGATGGG | 8440 |
rs181018573 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105761344 | GAGAAGAGTGGCTCA[C/T]CTTTCTCTTGGGTAC | 8440 |
rs181103607 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105857714 | CTTGGGGATCAGTAT[C/T]CCCGTCATGAGGGAG | 8440 |
rs181106674 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105880083 | CCGTGCATTTTAACA[C/T]AGTTAAAACATTTTT | 8440 |
rs181139176 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105822494 | ACGCTTCCCACAGCG[C/T]CCCTGTTCAGGGCGA | 8440 |
rs181141144 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105839584 | GCACAGGAGGTAGTT[G/T]GTTTATTTGATTGGT | 8440 |
rs181173918 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105891185 | CAATACTCACATACT[C/T]CCTCTCACATCTGCG | 8440 |
rs181250613 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105791098 | GGGTAGGTACTGTAT[A/G]TGGGAGCCACTTGGA | 8440 |
rs181262323 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NCK2 | GRCh38.p7 | 2:105760650 | TTTCTGGATAACTTC[A/G]TCCTTCTTTTGGTGG | 8440 |
rs181262773 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | NCK2 | GRCh38.p7 | 2:105769769 | GGAATGCATGTGTCA[C/G]TGTGTCAGGCGTGGT | 8440 |
rs181270078 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105753826 | TGCTTTTATGACATC[C/T]GGGAAGGTCTTGAAG | 8440 |
rs181276901 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105778380 | CTTTGGCCCAGTTTG[G/T]TCAGCTGCCCACTCT | 8440 |
rs181290967 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105807581 | TGTGAGGGTGACCAT[C/G]AGTGACACCAGCCTC | 8440 |
rs181322274 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105876972 | GAATCCCTGCTTGTT[C/T]TGCAGCAGAAACCGT | 8440 |
rs181355960 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NCK2 | GRCh38.p7 | 2:105836838 | TCCAGTCTCCAAATG[A/G]TGCCTTGCTGCAGCA | 8440 |
rs181359048 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105854114 | ACACAGTGTGTAGCC[C/T]TTTCAGATTGGCTTC | 8440 |
rs181364505 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | NCK2 | GRCh38.p7 | 2:105821928 | TTCCTTCTGCTTCCC[A/G]GGCTGCTGTCTCTGA | 8440 |
rs181369989 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105839008 | TTTTATATGAGGTGG[C/G]GCAGGTTTGGCTTGG | 8440 |
rs181385097 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105790349 | AGTGGGAACAGTTGC[C/T]GAGCCCTGGGCTTCT | 8440 |
rs181395997 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105769152 | TATGAATCACTAAGG[A/G]CACTCTTGTTGCTCA | 8440 |
rs181397354 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105807315 | CCAGGTGCTCTCCTC[A/G]AAGGGCAGGGGAAAT | 8440 |
rs181428147 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105753553 | TGTAAATGCCTGTGT[A/G]ATGTGCCTCTTCATC | 8440 |
rs181453563 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105863880 | CGTCGTCTGTATAAC[A/G]GGATACGTGACTGCT | 8440 |
rs181490145 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NCK2 | GRCh38.p7 | 2:105857373 | GCCATCCAGCCCTGC[C/T]GGAGCGCAGCGTCGG | 8440 |
rs181508591 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105762147 | ATGCACTGCTCTTGG[A/G]TTTTCCTTAGAAGAA | 8440 |
rs181586083 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105818494 | CCTGTACATCTTACT[A/G]TCAGCTTATAAGAAA | 8440 |
rs181587327 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | NCK2 | GRCh38.p7 | 2:105836035 | TTTTCTGATTTCGTT[G/T]AATTTTCCATGTTCC | 8440 |
rs181596715 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NCK2 | GRCh38.p7 | 2:105885238 | AAGATTTTAGTTCCC[A/G]AAGATATCATGTATT | 8440 |
rs181599403 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105788107 | TTCTCAATTTGACTT[G/T]CCTTTCACTTCCGTA | 8440 |
rs181611110 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105781653 | GAAAATAGCAGTCTT[A/G]TAAGGTAGTTGTTAG | 8440 |
rs181614801 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NCK2 | GRCh38.p7 | 2:105804533 | TATTCAGACAGAAAT[A/G]GCTTAATTGGATTTC | 8440 |
rs181615672 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | NCK2 | GRCh38.p7 | 2:105843945 | CCTGACAAACACCGC[C/T]TCAGCCAGGTGATCA | 8440 |
rs181622216 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105814647 | GCAAAGCCCACTCAT[C/T]CGGAGTCCAAGGCCT | 8440 |
rs181626366 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105744271 | CAGGGATGATGGACT[A/G]AAAATGTGTCTGGTT | 8440 |
rs181632341 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | NCK2 | GRCh38.p7 | 2:105765096 | ATCTTTATGGCTCTT[C/G]ATGCATCTTGCCATA | 8440 |
rs181637142 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105749416 | GTACTAATGCATGCA[C/T]GCTCATTCATTGTTT | 8440 |
rs181743723 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105876118 | GGAAGGGTTTTGTAA[C/T]GGTCACATTCTAGAT | 8440 |
rs181803772 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105808561 | CCAGGAGTAACCACC[A/C]GTTTACTACAAATGC | 8440 |
rs181830097 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105772858 | CTTCCTTCACAGTGT[A/G]TTCCTGGCGACCTCC | 8440 |
rs181841270 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105845857 | ACCTCACTTGTGTTT[C/T]CTAAGAAGCCAAGTT | 8440 |
rs181860096 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NCK2 | GRCh38.p7 | 2:105864792 | GCCCTCCGAACCCAC[A/G]GGAAAGATCTGTAAC | 8440 |
rs181867103 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105885571 | AATTGCCTTGAAGCT[C/T]GTTAAAACAAATTGC | 8440 |
rs181873411 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105809748 | AATAATGAGTACTGT[C/T]TAAGATGCTAAGGGA | 8440 |
rs181876092 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105795545 | CTTATTTTTGCTTTA[A/C]CAAACTTGGTCTATT | 8440 |
rs181888877 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | NCK2 | GRCh38.p7 | 2:105827156 | AGGTGCCTACCACCA[C/G]GCCCGGCTAATTTTT | 8440 |
rs181890758 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105758830 | AGTTGTTACAAAACT[A/G]TTTTCCAAAGGTTGG | 8440 |
rs181901733 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105774398 | TAACTTGGCTGTGTG[A/T]TGATGGTCTGACTGG | 8440 |
rs182039695 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105853543 | CCCTTGCATCCCTCC[C/T]TTCCCTCTTGCCCCA | 8440 |
rs182044387 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105853824 | TAAGAGGAAACATCA[C/G]GGGTGGAGCGTGGGG | 8440 |
rs182046756 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | NCK2 | GRCh38.p7 | 2:105890365 | ACCATGATTCACTCC[C/G]ATACTGCCTCCACTA | 8440 |
rs182057287 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105759590 | TGTGTCTACTTTCCC[C/T]TGTGATTCACATCTT | 8440 |
rs182059906 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105786981 | GCGTGGTGCCGCACA[A/G]GTGCTCCCTGGCCTT | 8440 |
rs182064166 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105825435 | AGACTTGTCTTATGC[C/T]CAGAAATTTAACAAA | 8440 |
rs182079719 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NCK2 | GRCh38.p7 | 2:105748361 | TGTCCCTGATTTGTC[A/G]TCTGTGACATTCTTT | 8440 |
rs182088448 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105756828 | TTATTTTTTGAGACG[A/G]AGTTTCGCTCTTGTC | 8440 |
rs182089139 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105871282 | GCTCCCACAGCCTGC[A/G]GGAGACAGGCCTTTA | 8440 |
rs182105356 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NCK2 | GRCh38.p7 | 2:105794354 | ACCATGCCTGGCTGA[A/G]TCCTTTGATTTTATA | 8440 |
rs182208474 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NCK2 | GRCh38.p7 | 2:105871893 | GCGGGGAGGAAACTA[C/T]ATGACACCTGACAAC | 8440 |
rs182214630 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NCK2 | GRCh38.p7 | 2:105892003 | TGTTTAAAATGCGAC[C/T]GGAATTTTCCACTGC | 8440 |
rs182229092 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105832194 | TTATTGGTATATAGA[A/G]GAAACACTACTGATT | 8440 |
rs182230586 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | NCK2 | GRCh38.p7 | 2:105815989 | CCATCACCTCCTTCC[A/C]CCTGCTGTTCACCGG | 8440 |
rs182243679 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | NCK2 | GRCh38.p7 | 2:105851745 | GTTGATTGGCTGGCC[A/G]TCTGGTGTGACTTAG | 8440 |
rs182256835 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105800909 | TACATGCCTGTCCAG[C/G]TGGTTGGCAGAAGCC | 8440 |
rs182309463 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NCK2 | GRCh38.p7 | 2:105835374 | GGTTTTATATATATA[C/T]ACATATATATACACA | 8440 |
rs182317953 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | NCK2 | GRCh38.p7 | 2:105831310 | AAACCGCAAAAGAAC[C/G]CTGAATAGCCAAAGC | 8440 |
rs182332748 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105875442 | GCCTGAGAACAACTG[G/T]CCAAGCTGCTGCAGA | 8440 |
rs182349051 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105804066 | TGGCTTTGCTTGCCC[A/G]TTTTTTACGGGGCAA | 8440 |
rs182353466 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105765891 | AAAATTAAGAGTCTA[G/T]GTAAGCCACACCCAA | 8440 |
rs182362323 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105770040 | CAGAGTACAGTGAGT[C/T]AAACCATTGAGAGTG | 8440 |
rs182365106 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105805780 | ATGGCAGGATTTCCC[G/T]TTTTAGGATTGAATA | 8440 |
rs182370222 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NCK2 | GRCh38.p7 | 2:105754223 | TTCTACACGTAGCAG[A/G]TTCCAGGATATGTGG | 8440 |
rs182391192 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105764708 | GATAATATACTGACT[C/T]TTAAGCATAGTTTTT | 8440 |
rs182473712 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105782603 | TAGTACTTTTTATTT[A/T]GTTAGAGCAGTTTTG | 8440 |
rs182478880 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105815293 | TTTTTAAATCAAAAT[A/T]TATGAACTTGCCTTA | 8440 |
rs182480289 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105800242 | TGAGTCCCCAGGCTC[C/T]GGTTCCAACTGCACA | 8440 |
rs182494794 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | NCK2 | GRCh38.p7 | 2:105762469 | CTGAAGCTCATGTCC[C/T]AGGGTCTTGACGTAG | 8440 |
rs182505075 | snp | C/G | 0.358303 | 0.225323 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | NCK2 | GRCh38.p7 | 2:105745014 | CGCCCGGGCCGGCAG[C/G]GTCCGCCCGGCGGCG | 8440 |
rs182553315 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105884309 | TTCTCAGGTTAGAGC[G/T]GGCTTTCGCAGCCAC | 8440 |
rs182572682 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105841567 | TGCATAGGCATGACT[C/G]GTTAAACCCTTGGCC | 8440 |
rs182574261 | snp | A/C/G | 0.0158775 | 0.087933 | intron-variant | NCK2 | GRCh38.p7 | 2:105861618 | CTCCCAGGTTCAAGC[A/C/G]ATTCTCCTGCTTCAG | 8440 |
rs182580622 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105883789 | AAAGAACTAAAGCAC[A/G]AATTGTTTGTATTTC | 8440 |
rs182585168 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105879569 | GTTTCCCATGCACAT[A/G]CATAAAATGTGGTAC | 8440 |
rs182587239 | snp | C/G | | | upstream-variant-2KB, intron-variant | NCK2 | GRCh38.p7 | 2:105850163 | GCTTGAATCTCAGAC[C/G]CTTAACTCCTTTCTT | 8440 |
rs182623745 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105783710 | TGTATTCAGATTATG[G/T]TTTTTTTTCGCTAAT | 8440 |
rs182630337 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105788401 | TTCAGTCTTTTTTCC[A/G]TGCTTAGGTTTCCTT | 8440 |
rs182649665 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105750413 | TTAGGGCTTTACCAT[A/T]TGAATTTAGGGTGGA | 8440 |
rs182664013 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant, utr-variant-5-prime | NCK2 | GRCh38.p7 | 2:105745680 | AACTATTTATGTTCG[C/T]GCACAAAGCTGCTGT | 8440 |
rs182692595 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105796575 | GTTCAGATCGGCAGC[A/G]TCTGGACTGAGCCTG | 8440 |
rs182695811 | snp | C/G | 0.0162398 | 0.0886349 | intron-variant | NCK2 | GRCh38.p7 | 2:105776511 | TGCTAGCCTACCCAC[C/G]CGTGGAGGGCTCCTG | 8440 |
rs182700115 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105818884 | ATGTTCTTTCTCTTC[A/G]ACCACCTTAAAAGAA | 8440 |
rs182701700 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105810594 | AACCTGTTAAAAAGG[C/T]AATATGTAATTAAAT | 8440 |
rs182858965 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105754587 | TTCATTTTAAGGACA[A/G]TCACTTTAAAAGCTT | 8440 |
rs182870524 | snp | A/G | 0.0391387 | 0.134304 | intron-variant | NCK2 | GRCh38.p7 | 2:105771072 | GGACTACAGGCGCCC[A/G]CCACCATGCCCAGCT | 8440 |
rs182895681 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105792542 | CTGGTTGTTAAAGTC[A/C]GAATCCACGTAAGGT | 8440 |
rs182897847 | snp | G/T | 0.00279162 | 0.0372561 | upstream-variant-2KB, intron-variant | NCK2 | GRCh38.p7 | 2:105851003 | AAGACCCTCCAGATG[G/T]GCTTCCAGCCAGCCT | 8440 |
rs182906052 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105824267 | TTTCCACTTGGGCCC[C/T]TGACGGTGCTCACAG | 8440 |
rs182910526 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | NCK2 | GRCh38.p7 | 2:105762932 | AGGCGCAGTGGCTCA[C/T]GCCTGTAATCCTAGC | 8440 |
rs182937793 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105754888 | GAAACAACCTTGGTT[G/T]CAGAATCTAGCAAGA | 8440 |
rs183039233 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NCK2 | GRCh38.p7 | 2:105886780 | ATTTGGGGATAGGGA[A/G]GGCTAACCACACACA | 8440 |
rs183047548 | snp | C/G | 0.0174175 | 0.0916809 | intron-variant | NCK2 | GRCh38.p7 | 2:105855917 | TTGCCTCACTGCAAG[C/G]TCCACCTCCTGGGTT | 8440 |
rs183058609 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | NCK2 | GRCh38.p7 | 2:105806399 | CCCACCACCACGTCC[A/G]GCTAACTTTTTGTAT | 8440 |
rs183070307 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105820004 | TTGGGACTGTGCTAA[C/T]TGCTGTAGTGGAGGT | 8440 |
rs183070458 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | NCK2 | GRCh38.p7 | 2:105867356 | AAATTCTGTCTTGCA[A/C]GATTGTTCATAATAG | 8440 |
rs183072161 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105837464 | TCTTGGTTTTCACTT[C/T]CTTGGTATGATAGTG | 8440 |
rs183084572 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105750914 | GCCATCTCTGTGATC[A/G]TGCAGTCTTTGCCAC | 8440 |
rs183091589 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NCK2 | GRCh38.p7 | 2:105789385 | TAGAGATGGGGTTTC[A/G]CCATGTTGGCCAGGC | 8440 |
rs183096729 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105767225 | TTCATGTCACACATA[C/T]ATGTCATGTCATTGA | 8440 |
rs183104184 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105869134 | CTAGCCTGTTCATAC[A/G]TGCCCTCACATCTGA | 8440 |
rs183112871 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NCK2 | GRCh38.p7 | 2:105887595 | AAGTACCTGGAGCAA[A/G]GCCCCTCCCTCCCGT | 8440 |
rs183138957 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | NCK2 | GRCh38.p7 | 2:105811233 | TACATTTTTGGCACC[A/G]CATCATCAATTTTTG | 8440 |
rs183139102 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105828537 | CTTTGTCTCGACTCT[A/G]AAGTCTAAGAAACAA | 8440 |
rs183147279 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105847635 | GGCCTGGTGGGACAC[A/G]CAGGGTACATCAGGG | 8440 |
rs183156788 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105827971 | TCAGTTTCCTGGTTT[C/T]GATATTTTACTGCAG | 8440 |
rs183184299 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105831793 | CTGTTTTGATTACTA[A/T]AGCTTGTAGTATATT | 8440 |
rs183191874 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105871586 | CTGCAACCTCCGACT[C/T]CCAGGTTCAAGCAAT | 8440 |
rs183202083 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105868853 | GAAGCAGTCGAGGCC[C/T]GGGGCAGCCAAGCGA | 8440 |
rs183219059 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105771479 | GCTGAGTCAGGAGAA[A/T]CACTTGACCCGAGAG | 8440 |
rs183289021 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105808444 | CACCTCTAACTTGTT[C/T]CATTTACTAAATCAC | 8440 |
rs183317355 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105750762 | CTTATTTGGGGGTTG[A/G]TTTGTCTTTAATTGA | 8440 |
rs183398320 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | NCK2 | GRCh38.p7 | 2:105887229 | AGAGAAACTATTAAT[A/C]AGTGGATCACGATTT | 8440 |
rs183409858 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105893680 | GCAATACTGGAACCA[C/T]CGGGTGCGATGGCAG | 8440 |
rs183431750 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105847421 | TGTGTGCTTGAACTT[A/T]TGCTGAATAATATGT | 8440 |
rs183446971 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105878139 | TAAAGAGGACTTTGG[C/T]CCTCTTTTGGTAAAG | 8440 |
rs183469777 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105846671 | GTCAAAAAGTAGACA[A/G]TAACAGGCGTTGACA | 8440 |
rs183516493 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105810133 | TAGAAACAGGGAAAG[A/G]AGTGTGGAATTTTAT | 8440 |
rs183529055 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105775248 | GAGAATTTGCCTGTT[C/T]CTTTGTGGATTTTTA | 8440 |
rs183532696 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | NCK2 | GRCh38.p7 | 2:105840994 | GACAGACCAGTTGTA[A/G]CTTTAGGTCAGTAAT | 8440 |
rs183540376 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105861056 | CCAGGCAGCAGTGAA[G/T]GTAACAATTGTTTAC | 8440 |
rs183550834 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105807822 | TCTATCTCTCCCTCC[C/T]TCCCTCCCTTCTATC | 8440 |
rs183554534 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105791684 | TTGATACAGGGTTTC[A/G]TTTTTCTACTTGACA | 8440 |
rs183557185 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | NCK2 | GRCh38.p7 | 2:105823823 | TTGGTGAGATTTGAG[C/T]TTGATTGCTGCCTGC | 8440 |
rs183644161 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105793088 | CTTTATATAATGGCC[C/G]TGGAATTGAGAAGTG | 8440 |
rs183647293 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105772253 | ATTTAGACTGTTGAT[G/T]TTTAACTTTCTCAAG | 8440 |
rs183675126 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | NCK2 | GRCh38.p7 | 2:105755786 | GCTCAGAAGCCTTAC[A/G]TTGGTGATTGTCTAC | 8440 |
rs183722236 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105855448 | AATTAAGAGATGAAG[A/G]TGGAGAAAGAGGATG | 8440 |
rs183727209 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105795990 | CTTGTAAAAAGAGCA[A/C]AACAGTTTAGCATTT | 8440 |
rs183739876 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B | NCK2 | GRCh38.p7 | 2:105894469 | GAAACCCCAAGGGAA[C/T]CCAGAATCTCAAGCT | 8440 |
rs183742740 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105827729 | CACATATTGTATGAT[G/T]CCATTTATATAACAT | 8440 |
rs183764164 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105834410 | TTTGCCACTTTATGT[G/T]TTTTGACTTAAAGTC | 8440 |
rs183765612 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NCK2 | GRCh38.p7 | 2:105853455 | ATAGATTTTAACAAA[C/T]GTATAATGACAGGTG | 8440 |
rs183766597 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105759268 | ATCGTTTTACGTATT[C/T]AAGTACACATAGTAC | 8440 |
rs183773942 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105874964 | CCTTTAAATCCAAGT[C/T]AGCTATTTGCCACTT | 8440 |
rs183781681 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105819458 | GACAGATCTTCTGAT[C/T]GGATCATCAGAACTC | 8440 |
rs183794264 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105817164 | CTGGGCAACACGGCA[A/G]GACTTGGTCTCAAAA | 8440 |
rs183813799 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105788724 | TATCCATAGAATGCA[C/T]AATTTTTTTTGTTTG | 8440 |
rs183828200 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105863337 | AGCAGCCTGGTTCTC[A/G]TGGAAGCCGAGTCTA | 8440 |
rs183835358 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105885053 | TAAAATGAACAGTAA[C/T]CCTTTACTGGGTTTC | 8440 |
rs183939125 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105877698 | CTAGTTTCATTTCCT[A/G]TAGAAATCATATTAC | 8440 |
rs183965309 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105806034 | CTGGGTAAACTGTGT[C/T]GTGTGCCTGCGTTTT | 8440 |
rs183980757 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105837278 | CTCCTTGATTTTTAA[C/T]GTTAGTTTTACCACA | 8440 |
rs183985861 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105766384 | GCTGGAGTGCAGTGC[C/T]GCCATCATGGCTCAC | 8440 |
rs184034762 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105873224 | GATTTGTACCCAAAA[A/G]TCTGTCCCACTCTCA | 8440 |
rs184051449 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105803190 | GATAGTTGTTAATAT[A/G]AACATTTATTCTGCT | 8440 |
rs184059405 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105816748 | AAATTTAAGCTTTCA[A/G]TGAGGGAGAAAATTA | 8440 |
rs184064917 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105832874 | ATTTTGTTTCGTTTC[A/G]TTTTTGTTTCGTTTT | 8440 |
rs184069451 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105832434 | TTTTCAGCTTTTGCC[C/T]ATTCAGTATGATGTT | 8440 |
rs184073551 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105763906 | TAGAAGTTCCCTTAC[A/G]ATGATGGACTGTGTG | 8440 |
rs184079065 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105763185 | CCTGGGCGACAGAAC[A/G]AGACTCTTGTCTCCA | 8440 |
rs184080057 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105747940 | CCATTTAGTAGCACA[A/G]TTAAAAAATTAGACT | 8440 |
rs184083187 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105785797 | CAGCAGGAGGTTGGG[C/T]GCAGGACTCCTAGTA | 8440 |
rs184088755 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | NCK2 | GRCh38.p7 | 2:105801509 | GGGACAAAGCATGAC[A/G]GAGACCTTTGTCACG | 8440 |
rs184176902 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105852038 | TTTAATTTTCACGTG[C/T]CCTAGAATCTTAGAA | 8440 |
rs184197468 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105816330 | ATAAATAACAAAAAA[A/C]CCCATTAGTTTTAGG | 8440 |
rs184219419 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NCK2 | GRCh38.p7 | 2:105883490 | AGGAAGTCCTGCAGT[A/G]TGGAGACATTGGTCC | 8440 |
rs184248679 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105784777 | AGCCACTGTTCCAGG[C/T]CCGTGTTTCCCACAC | 8440 |
rs184287533 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105837752 | TGATTTTCAACCTTC[C/G]TAACACATTATCAAC | 8440 |
rs184287937 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105812983 | GCAGATACCCCAGAC[A/T]GATGGCATCAGCAGA | 8440 |
rs184290555 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105798355 | TCTTGAAACTGGGTT[A/G]GCTGAGTCATTTTTT | 8440 |
rs184294416 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105879667 | CACATGCCTCCTGGC[A/G]CCGCGTGGGCACATG | 8440 |
rs184297447 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105856705 | GAGACATGGAACTTC[A/G]TATGAATCATACCAG | 8440 |
rs184300941 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105878468 | ATTGGAACACAGACA[C/T]ACTCAGAGGGAAGAC | 8440 |
rs184305594 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105830208 | ATCCAGTTAACCAAC[C/T]TTTTCCTATTCCTCC | 8440 |
rs184311031 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NCK2 | GRCh38.p7 | 2:105822233 | GAGGTTTGAGAAGGG[A/G]GCACCAGCTGGGAAC | 8440 |
rs184312096 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105760904 | TGTGTCATGCCTTGC[A/G]CTTTGGGACACCCCT | 8440 |
rs184316938 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105743102 | AGAGGAGGCAGATGG[A/G]CAGGTCAGAAAGGTA | 8440 |
rs184323882 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105778796 | GGTGTGATCATAGCT[C/T]GCTGCAGCCTCAAAC | 8440 |
rs184325956 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105839080 | AGGGAGAGCAAGGGA[A/G]GGGACATTTGAATGG | 8440 |
rs184326135 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105887763 | TGAGAGAGGGAGAGG[C/T]GTATCTGATCAGGAC | 8440 |
rs184327736 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | NCK2 | GRCh38.p7 | 2:105857391 | AGCGCAGCGTCGGTT[C/G]GAGTAGGCCAATCCC | 8440 |
rs184336722 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105790629 | TACTGCATCCCCCGC[A/G]CCTGTCCTCATCTTA | 8440 |
rs184347539 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NCK2 | GRCh38.p7 | 2:105807383 | TATGGGAAAGCCCTC[C/T]GATTTATATATGACA | 8440 |
rs184359649 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105786273 | ATCTATGTAATAACC[A/G]TAGTGATCATTAGCT | 8440 |
rs184360087 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | NCK2 | GRCh38.p7 | 2:105747099 | TGCTGAAGGTGCCTT[A/G]CAGGTGGCTGTGCTC | 8440 |
rs184379975 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NCK2 | GRCh38.p7 | 2:105748283 | TCTTTTCTTCCCCAC[A/G]TCTTATCAACTCCAA | 8440 |
rs184397616 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105808149 | ATGATCCACCCACCT[C/T]GGCCTCCCAAAGTGC | 8440 |
rs184478181 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105803621 | AGCAAGTCCTCATGC[C/T]CCTGCATCATGTGCA | 8440 |
rs184480192 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105824630 | GTACCACGTCTCGGC[A/G]GCGTGTGCTTAGAAC | 8440 |
rs184496864 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105862403 | AGCACCCCAGGCCAG[A/C]CTCAGTAGTGTTACT | 8440 |
rs184520490 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105764028 | AATTTAGTCCTCTCT[A/G]CAACCCCACGAGGCT | 8440 |
rs184590123 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105790101 | TTCCTATTTGTAGAA[C/T]GAGAAGAATTAAAAG | 8440 |
rs184598961 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105853047 | TTTAAAAATGGTATT[C/T]ATGCTTCCATGGAGT | 8440 |
rs184603624 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105825518 | AGCAGATATGGGAAC[A/G]CTAATAATTTCTTCC | 8440 |
rs184620758 | snp | C/T | 0.0126979 | 0.078662 | utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105893996 | TTATACACACACACA[C/T]GTGCACACACACACA | 8440 |
rs184625057 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NCK2 | GRCh38.p7 | 2:105768907 | CCAATGAGTTCATGA[C/T]GTGGAGGCTCCCCAC | 8440 |
rs184631929 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105752849 | TTCTGATAACATGTT[A/G]AGTACAAGCTAAAAT | 8440 |
rs184633019 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105757381 | TTTTCTTCAAAGTGG[C/G]ATGGGATGAACTGAT | 8440 |
rs184634561 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105796830 | GGAAAGGAAATATAT[A/G]TAATTAGAACACTTA | 8440 |
rs184639601 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | NCK2 | GRCh38.p7 | 2:105794389 | CTTTATGCTGAAAAT[A/C]TTTGTCCCTAGGATC | 8440 |
rs184743087 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105808606 | ACGTGAAAAACACCA[C/G]AGGGATGGAGTGCCA | 8440 |
rs184746844 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105873784 | ATCCAGGGGTGCAAC[C/T]CTTGGTTGGGGCCTG | 8440 |
rs184757881 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | NCK2 | GRCh38.p7 | 2:105845041 | TCCCTGCTGGCAGGT[A/G]GGTACAGGTTCTTGT | 8440 |
rs184758683 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | NCK2 | GRCh38.p7 | 2:105773312 | TTAGTCCCCCTTGTC[C/T]CTCTCCTTTCCAGCC | 8440 |
rs184798562 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105884736 | GAACCAACAAACGAA[C/T]GAACCTCTTGGACCC | 8440 |
rs184819607 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NCK2 | GRCh38.p7 | 2:105825280 | ATCTTCCCTAAAGGG[A/G]CCTTCTACTCTAAGG | 8440 |
rs184821868 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105843303 | TGGAATTTTTCACTT[C/G]TAGTGCTCAAGTTTT | 8440 |
rs184828961 | snp | A/C/T | 0.0023933 | 0.0345097 | intron-variant | NCK2 | GRCh38.p7 | 2:105862841 | CTAAAAGAAGCAGAC[A/C/T]TATCAGCAGTGGTTT | 8440 |
rs184842642 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105772568 | ATGTTACTGATGCTG[A/G]GTTAAACATTGAGCC | 8440 |
rs184849502 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105808423 | CTGGACTCCCTGATA[C/T]ATTAGCACCTCTAAC | 8440 |
rs184850698 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NCK2 | GRCh38.p7 | 2:105794087 | GGAATCTTGCTCTGT[C/T]GCCCAGGCTGGAGTG | 8440 |
rs184885197 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105870654 | CAGCTACTTGGGAGA[C/T]GGAGGCACAAGAATC | 8440 |
rs184932336 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105806517 | TGCTGGGATTACAGG[C/T]GTGAGCCACCACTCC | 8440 |
rs184966193 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | NCK2 | GRCh38.p7 | 2:105768256 | ATAGCTGGACTCACC[A/C]CCCCTTGAGTGCTCA | 8440 |
rs184989037 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105848608 | GCCTGCCTCCAACAC[A/G]CTGCAAGAGAGAGGG | 8440 |
rs185005728 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105888093 | TTCAAACACAGAATC[G/T]AAAGCCTAAACAAAA | 8440 |
rs185014108 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105877331 | TTCAGGATCTCCCAT[C/G]CCTTCTGTTCTAGAT | 8440 |
rs185039399 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NCK2 | GRCh38.p7 | 2:105789746 | CTTGCTCCCGGTTAA[C/T]GGGAGGGCTTTTTCT | 8440 |
rs185045234 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105837069 | CTCTGAGTCAGTCCT[A/G]GCTGGCTGCTTTTCT | 8440 |
rs185052576 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105854492 | TGTTGTCCAAACTAA[G/T]AGATTGACAATTATT | 8440 |
rs185056899 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105821420 | TCAGCCTCCTTCTGC[C/T]GCACTCTGGACCCCT | 8440 |
rs185060709 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105751564 | CACACATGCTGAGCT[A/G]CAAGTCATCTGTGGC | 8440 |
rs185182178 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | NCK2 | GRCh38.p7 | 2:105811856 | GGGGTTTCGCCCATC[A/G]ATTGACCTACTGCTT | 8440 |
rs185190024 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NCK2 | GRCh38.p7 | 2:105848065 | CGTTTTTGAGTCCCC[A/G]TGAACCTTATGTTCA | 8440 |
rs185217927 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105778182 | GTCCCGGGCTTAGAG[C/G]GGGACTGGGGACCTA | 8440 |
rs185268777 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NCK2 | GRCh38.p7 | 2:105869721 | GTGTCTCATCCTTGC[C/T]GCGTCTTGTACACTC | 8440 |
rs185291261 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105809192 | CCTGGTGGTTTTGAC[C/T]TCGAGTTCTTTCAAT | 8440 |
rs185300070 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105828717 | GAGCAGGTCACCACT[C/T]CCCCCTTGGGGCTGC | 8440 |
rs185300588 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105836226 | TATCTGCACTGTTAG[C/T]GAAATAGTTTCTTTT | 8440 |
rs185302755 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NCK2 | GRCh38.p7 | 2:105818547 | TTTAACAGAACAAAA[C/T]AGAAAAGATTGTTAA | 8440 |
rs185317422 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105757781 | CCTCTAACCTCTAAC[A/C]CAACCCCCAAGGCCA | 8440 |
rs185318434 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105760593 | ACCACCTCTTGGATC[A/T]CTCCATCTGAGGCTC | 8440 |
rs185318665 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105853987 | GCAGGAGAGTCTTGC[A/C]AAAATTGGGCAATGC | 8440 |
rs185325085 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | NCK2 | GRCh38.p7 | 2:105788190 | TAAGTTTTTTCATCA[C/G]CTATGTGAATTGGAG | 8440 |
rs185326644 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | NCK2 | GRCh38.p7 | 2:105798004 | TTGGTTCATTTCCTA[G/T]GAGAAGAAAATTATA | 8440 |
rs185329573 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105765145 | ATGCCAGTTTTCAGT[A/T]GTGTGGAAGTATCAA | 8440 |
rs185331230 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105774054 | CGCCCTGTTGCCCAG[C/G]CTGGAGTGCAGTGGC | 8440 |
rs185342785 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105805280 | GGAGGAAATAGCAGA[C/T]GCGAGGGCAAAGAGT | 8440 |
rs185362300 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105749472 | CATATTTAATAGTCG[A/C]ATAACATGGTGCACT | 8440 |
rs185417044 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105821681 | TTGGCAGGTGCCCGG[C/T]ACAGGGCTTGTCACT | 8440 |
rs185422126 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105857261 | TTTTTCATGAGCTGT[A/G]ATCGGTTCAGCCAAT | 8440 |
rs185496595 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105760111 | AAGGAAGAGGGAGTT[A/C/T]AGCTGTACCTCCTGT | 8440 |
rs185517497 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105879270 | GCGTAGCCCTCACGC[C/T]CCGGCTTGCTAGCTG | 8440 |
rs185549783 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105838957 | CATGGAAAAAGAGAA[A/G]ACAGAAGAAAGGAAT | 8440 |
rs185552710 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NCK2 | GRCh38.p7 | 2:105858538 | ACTGCTTTGGGAGTC[C/T]ACCTAATTCATAAAT | 8440 |
rs185553032 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | NCK2 | GRCh38.p7 | 2:105815727 | CAAGGCTATGGGTCC[A/G]GTTGGTGGCTTCTCA | 8440 |
rs185557145 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105832070 | GTTTTTAATGTAGAC[A/G]TCTTTCACTTTCTTG | 8440 |
rs185559023 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105880633 | GAATTCATTTAGTCT[A/G]ACTTCCCACCCATTC | 8440 |
rs185561129 | snp | G/T | | | upstream-variant-2KB, intron-variant | NCK2 | GRCh38.p7 | 2:105851061 | AAGACCGAAGCCTGT[G/T]AGGATACAGGGTGAT | 8440 |
rs185575957 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105783282 | GTAGCCTCGCTAGAG[C/T]TTGGGTGGGCCCCCA | 8440 |
rs185585260 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105807068 | TGTAATGTGGAATGA[A/G]GGTAGAGTCTGAGTA | 8440 |
rs185593203 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105777055 | CCCTAGGTCTGAAGG[C/G]CAAAATGAGGCCTTG | 8440 |
rs185594560 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105800590 | CCCAGCTGACATGGG[A/G]TTAGTCTCAAAGTTC | 8440 |
rs185673697 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105875484 | CTGGCCAAGCTGCCT[C/T]AGATCGTGTTCCCCC | 8440 |
rs185804771 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105853580 | CACTTATTTTCTTAC[C/T]GTCTCCATAGATTTG | 8440 |
rs185868735 | snp | A/C | 0.0134861 | 0.0810011 | upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105744545 | GTCTGTGTTTTCACT[A/C]TCCTCCCCACCCACC | 8440 |
rs185874619 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105769171 | TCTTGTTGCTCAGTA[A/G]ATACCAAGGGCTTTA | 8440 |
rs185876378 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105756369 | CAGTCATCCTATCTC[A/G]TATGGACTGAGAAAG | 8440 |
rs185883169 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105762163 | TTTTCCTTAGAAGAA[G/T]CTTGTGAGAAGCACA | 8440 |
rs185905111 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105819059 | ATGCCATATTGTCCC[A/G]TTGATTTAGGGTGTT | 8440 |
rs185910006 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105845475 | CTTTACTCACTGCAT[C/T]CTCCGCCTCTTGAGC | 8440 |
rs185923002 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105885492 | CCAAAACTCTATTTT[C/T]AGGCAATTTCATCAT | 8440 |
rs185949581 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | NCK2 | GRCh38.p7 | 2:105788647 | GGCCAGTGCAGAACT[C/T]CCTCATCTCTAAGTG | 8440 |
rs185970497 | snp | A/C | 0.0134861 | 0.0810011 | intron-variant | NCK2 | GRCh38.p7 | 2:105750642 | AAGCCTTGGTGCTGG[A/C]CTTCCAAAGGCTGGA | 8440 |
rs186039055 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105883646 | CAGGTGGTCATTGCT[C/G]TCTGAATTCAGGGAC | 8440 |
rs186047340 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NCK2 | GRCh38.p7 | 2:105864025 | GTGAGGATGTGAAGA[C/T]GGAAACCCATAGGTG | 8440 |
rs186068389 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | NCK2 | GRCh38.p7 | 2:105765913 | CACACCCAAACTCCA[G/T]ACCCACAGAGACAAT | 8440 |
rs186074463 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | NCK2 | GRCh38.p7 | 2:105826806 | ATTTTATATATGTGT[A/G]TATATATATATGTAT | 8440 |
rs186078595 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105805818 | TGTGTGTGTATATAT[A/G]TAGGGTAAGAATTCC | 8440 |
rs186156515 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105827790 | AGCAGGTTAGTGTTT[A/T]CAAGGGGTTGGTGAT | 8440 |
rs186173013 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NCK2 | GRCh38.p7 | 2:105868382 | AGGGCAACTGTTCAT[A/G]AGTTAAAGGCTGGGG | 8440 |
rs186263966 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105886825 | AAAGTGGACAGGGAA[C/T]GCTCCGTTTGCCTAG | 8440 |
rs186285813 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | NCK2 | GRCh38.p7 | 2:105889037 | AATTTCTTGAAATCT[C/G]TTCTAGAAAGCCAAC | 8440 |
rs186298695 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105876216 | CAGGTAAATTCTGTG[C/T]AGTAGGATTTTATGA | 8440 |
rs186301691 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105846726 | TGTGTACTGTTGGTG[A/G]AATTGTAGATGCAGC | 8440 |
rs186302145 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105807810 | CCCTCCCTCCCTTCT[A/C]TCTCTCCCTCCCTCC | 8440 |
rs186302289 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105849453 | GATAAATTGGTTAGT[C/T]AGTGGAAAGGTGAAT | 8440 |
rs186308359 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105871242 | CAGAGAGATGAGGAG[A/G]ATGGTGAGCTGAGCA | 8440 |
rs186320950 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | NCK2 | GRCh38.p7 | 2:105754380 | TGCCCATCTTAGAGG[A/G]CAAAGTCCATCAATG | 8440 |
rs186327824 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105791460 | TAGGGAGTGCACCCT[C/T]GCCCCGTTGCCGTGC | 8440 |
rs186329051 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105830985 | GATAATAAATAGTCC[C/T]TTATTGGATGAATAG | 8440 |
rs186330640 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105814278 | TTAACACATTGACAG[C/T]TTGTCAGTGGAATGC | 8440 |
rs186330805 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | NCK2 | GRCh38.p7 | 2:105770185 | GGATGGTGCTGTGGA[C/T]ATGGGGTGTGGTTGC | 8440 |
rs186395513 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105871653 | ATATGCCACCACACC[C/T]AGCTAATTTTTTTGT | 8440 |
rs186429797 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | NCK2 | GRCh38.p7 | 2:105764825 | TTTGTATAATTTTCT[A/G]TTCTTCTCACTCTGA | 8440 |
rs186434488 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | NCK2 | GRCh38.p7 | 2:105748775 | ACCGCTTGGGGGCAG[A/T]CTGGTCTTGCCACTT | 8440 |
rs186474845 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105807669 | ACAAGGTAGTTGTTT[A/T]TTTCAACCTCTCTCC | 8440 |
rs186480867 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105839648 | TTAGTTTTAGACGTG[A/G]GATTTGAAGTGCATG | 8440 |
rs186491661 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105769770 | GAATGCATGTGTCAG[C/T]GTGTCAGGCGTGGTC | 8440 |
rs186497886 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105845961 | ACCATGCTGTCTTCT[C/G]GCTTGGCAGAAGGCA | 8440 |
rs186507480 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105866637 | AATCTAATGCTGCAC[C/T]GCCTGACAGGAGGCA | 8440 |
rs186513705 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | NCK2 | GRCh38.p7 | 2:105885834 | GAACTTCATTTAGAA[C/G]TGAAGCTTTTGTTGA | 8440 |
rs186525036 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105795645 | GGCAGTGTCTGCAGG[C/T]GTTGTTGATTGTCAC | 8440 |
rs186529783 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105809846 | TGAAGAGCTTCTTGA[A/G]TGAGAGATCTTACCT | 8440 |
rs186532190 | snp | A/G/T | 0.00716266 | 0.059414 | intron-variant | NCK2 | GRCh38.p7 | 2:105827246 | CCTCGTGATCTACCC[A/G/T]CCTTGGCCTCCCAAA | 8440 |
rs186606918 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105828471 | TGACAGCACACTCAC[C/T]CACCGCAGATCAGTG | 8440 |
rs186618821 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105891630 | CTCAGCTTACAACTT[C/G]CACCTCCCAGGTTCA | 8440 |
rs186619893 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105776732 | ACTTAGTCCAGGCTC[C/T]GGGCTCCCAGCTCCT | 8440 |
rs186626082 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105810776 | ATATATCAAGAAAAC[C/T]CTTTACAAACCTTGT | 8440 |
rs186629196 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105796652 | CAAGGAAGAGTATCC[C/T]GTAGTTTAGTGTTAT | 8440 |
rs186644407 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105759680 | TCCATAGTTTATTTG[C/T]CCTGACATCCTTTTT | 8440 |
rs186674284 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105822561 | TCAATAACATAATTA[G/T]TTTCTCTTAGTTGTG | 8440 |
rs186680960 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105891087 | GCTCAGCTCCACATT[G/T]TCCAGAGGGCTCTCC | 8440 |
rs186707990 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105856834 | TTCCCCCACATAAGC[A/G]TGCCACTTGAAAGAA | 8440 |
rs186714456 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105791147 | CTCAGCCACTCTGCA[C/T]CCTCATTTTCTCATT | 8440 |
rs186717214 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | NCK2 | GRCh38.p7 | 2:105850185 | TCCTTTCTTCTGTAA[C/T]ATTTGGTTCACCTTG | 8440 |
rs186721401 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NCK2 | GRCh38.p7 | 2:105878774 | GACCCTCTGAGTTGC[A/G]CCAAAGACTATTTAG | 8440 |
rs186728517 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105753945 | CAGGTCCTGATGGGA[A/G]CTCTGACACTGGCTG | 8440 |
rs186745415 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105782025 | GCGGCCCATCAGGTC[C/T]CTCAAGCTGAGGGAG | 8440 |
rs186745813 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105814801 | TACTCATGAGACACA[A/G]GGCACACAGGGGGGA | 8440 |
rs186799191 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105753702 | TTGCACAAGGCCATT[C/T]TTGCTGCTTCTGTTT | 8440 |
rs186808937 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105825051 | AGATGAGTGGGCACT[C/G]GAGGTGCTTGGGGAC | 8440 |
rs186811014 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105871975 | GGAAATTGGTGCCCA[A/G]AAGGGACATGGAAGA | 8440 |
rs186821670 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NCK2 | GRCh38.p7 | 2:105892203 | AAAAAAAAGAATTAG[A/G]AAAATTTTGATGTCT | 8440 |
rs186918844 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NCK2 | GRCh38.p7 | 2:105831472 | ATCTTTGCCCAGACC[A/G]ATGTCCTAATGTATT | 8440 |
rs186937123 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105871364 | CTGATCAAGGTGCTC[C/T]GCACGCTTTGGGATC | 8440 |
rs186945663 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105799423 | TTTCAGATGGCCAAC[C/G]AGAGTACCCCATGGC | 8440 |
rs186983838 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NCK2 | GRCh38.p7 | 2:105806428 | ATTTTTAGTAGAGAC[A/G]GGGTTTCACCGTGTT | 8440 |
rs186990178 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105860725 | GAGAGGAGAACACAC[C/T]GGTCCATAGAGAGCC | 8440 |
rs186994322 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105820694 | TTGAAAAGTGACTGT[A/T]ATTGATTGTTGGAGG | 8440 |
rs187018265 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105823345 | CGTGTCTGGTGGAGG[A/G]TGTGGGAGGGGAGTG | 8440 |
rs187020989 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105789464 | AAGGTGCTGGGCTTA[C/G]AGGCATGAGCCACCT | 8440 |
rs187024438 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105767396 | TAGTATTTTGTGAAA[C/G]GTGTTCTTTATAAGT | 8440 |
rs187034178 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105798802 | CATTTAGGGAAATTA[A/G]TACAAAATGTTCTTA | 8440 |
rs187087145 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105761473 | AGGTGGGGGGACACT[A/G]CTTCCTGCTCCACCC | 8440 |
rs187149882 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105762556 | GTGAGTGCATGGAGG[A/T]TATCTGTGAACTTTG | 8440 |
rs187197212 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105884038 | ACACGGGCCATTTTC[A/G]GCTGTTAGTGTGCAT | 8440 |
rs187205335 | snp | A/G | 1.65479e-05 | 0.0028764 | synonymous-codon, intron-variant | NCK2 | GRCh38.p7 | 2:105881770 | GGGGGAGACCATGGA[A/G]GTGATTGAGAAGCCG | 8440 |
rs187207796 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105874700 | AAGATGACAGGCAGA[A/G]CATGTTTTAAAGTCA | 8440 |
rs187225244 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105840425 | CTACTCTACTCTACT[C/G]TCACAACACACTTCT | 8440 |
rs187258179 | snp | C/T | | | upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105743896 | TCTCATTAACATGGA[C/T]GCAGGCTATCCTGCC | 8440 |
rs187262390 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105779906 | ATAGCCTACGAGACC[A/G]CCTTCACCCTCTCAT | 8440 |
rs187321928 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105835479 | TCTCCTGGCCTGTAA[A/G]GTTTCTGCTGAGAAA | 8440 |
rs187359384 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105774565 | GAGTCAGATTTGATC[A/G]TCTCAATTTGGGCAG | 8440 |
rs187459415 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105841133 | CATAATTGTCTCTTC[C/T]GACATTCACTTTATC | 8440 |
rs187463767 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | NCK2 | GRCh38.p7 | 2:105861537 | TTTTTTTTTTTGAGA[C/T]GGTGTCTTGCTCTGT | 8440 |
rs187480136 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105807962 | AGGCTGGAGTGCAGT[C/G]TGCGATCTCAGCTCA | 8440 |
rs187482636 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105763193 | ACAGAACGAGACTCT[G/T]GTCTCCAAAAAAAAC | 8440 |
rs187484076 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105791729 | GTGGTATACATTCTT[C/T]GTAGAGCTTGTGAGT | 8440 |
rs187497253 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105784880 | TAAAGTTAGGAACAC[A/G]TGCATGCACTTAGGC | 8440 |
rs187497510 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105823843 | TTGCTGCCTGCAAGC[A/T]GTAAGGATGATCCTA | 8440 |
rs187507436 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105747128 | TCAGTTTTCATGCTT[G/T]GTGTTTTGCTTAGGA | 8440 |
rs187524956 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105887444 | TATTGATGCTTGGAG[A/G]CTTCAGCGTGGCTGG | 8440 |
rs187542661 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | NCK2 | GRCh38.p7 | 2:105793109 | TTGAGAAGTGGCAGT[G/T]TGGCTCGCAAATTGG | 8440 |
rs187547497 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105772408 | CCTTTCTTTGTTCCC[A/G]GGGAATGTGGGCATA | 8440 |
rs187548829 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | NCK2 | GRCh38.p7 | 2:105808163 | TTGGCCTCCCAAAGT[G/T]CTGGGATTACAGGCG | 8440 |
rs187551196 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NCK2 | GRCh38.p7 | 2:105847524 | AATGCAGGTGTGCAG[C/T]GGAACTGGCCTCCCT | 8440 |
rs187553259 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | NCK2 | GRCh38.p7 | 2:105832244 | ATCCTGCAATTTCAC[C/T]GGATCTGTTTACCAA | 8440 |
rs187553355 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant | NCK2 | GRCh38.p7 | 2:105851885 | ACGTCGATTGACTGG[C/T]CTTCAGAAGCAGGTT | 8440 |
rs187555401 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105821532 | AGCCTTTAATGCTGC[A/G]GATAAATCTGTGGTA | 8440 |
rs187570508 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105755796 | CTTACGTTGGTGATT[A/G]TCTACAGAAGAAAAT | 8440 |
rs187598083 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | NCK2 | GRCh38.p7 | 2:105759116 | GATCTGAGTTTGATA[A/C]AATTTTAAAGGTTGA | 8440 |
rs187612619 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105787910 | ATACCGCCCCCCACC[A/G]CCCCCGACTTGTAGA | 8440 |
rs187617645 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105818271 | CACCACACACTGGGG[A/C]CTGTTTTGGGGTGGG | 8440 |
rs187669293 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105837522 | CTTCCCTCCATCAGG[G/T]TTATTTTCTCTTCTT | 8440 |
rs187669554 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105856584 | TTTTCTTTTCTGCCA[C/T]GTTGAAAAGTCTAAA | 8440 |
rs187676127 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105878176 | TCAGAGCAACAAGAA[A/T]GCCACAGCTTAGTTA | 8440 |
rs187770454 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105838145 | ACCACTATTTATAAA[C/T]CTTAGCATTTTCAAG | 8440 |
rs187778351 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | NCK2 | GRCh38.p7 | 2:105862545 | GATTTAGTGGTAGGC[C/T]GCTTTGTACGTTTGG | 8440 |
rs187785702 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105869171 | CCTGACCCTGAGAGC[C/T]GAAGTGAGCTGAGAC | 8440 |
rs187792137 | snp | A/G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105887643 | GCTTAGAAGAAAATC[A/G/T]CATTAATACATAAGC | 8440 |
rs187809781 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105796015 | GCATTTGAAAGCTCT[A/G]TTGTAGTTTGCTCTG | 8440 |
rs187812513 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | NCK2 | GRCh38.p7 | 2:105828660 | GGGGTCAAGAGACCC[A/C]GGAAGAGGTCTCAGC | 8440 |
rs187812947 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105806614 | TTTTAAATGGAAAAT[A/T]TTAAATTTCCTTTTT | 8440 |
rs187814699 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105811236 | ATTTTTGGCACCACA[G/T]CATCAATTTTTGATA | 8440 |
rs187816932 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | NCK2 | GRCh38.p7 | 2:105868863 | AGGCCCGGGGCAGCC[A/G]AGCGACTTGGCCAGG | 8440 |
rs187826609 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NCK2 | GRCh38.p7 | 2:105847934 | ACCCAAGACTTATTG[A/G]GATCTCTTCGTAAAA | 8440 |
rs187854144 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105759343 | AATACCCTCACGTTC[C/G]TGTATTAAGCTGATC | 8440 |
rs187993027 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105767013 | TGAGGACACCTGCCC[A/T]GGTGTGTCACACCTA | 8440 |
rs188002773 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105750780 | TGTCTTTAATTGAGA[A/C]CATGATAAAATATCA | 8440 |
rs188006771 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NCK2 | GRCh38.p7 | 2:105788769 | TTTTCTTCATTCTTA[C/T]ATAGCTTAAATCAGT | 8440 |
rs188021914 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105884418 | GGGGTTCAGCCTCCC[G/T]GCAGGACTCAGTCAG | 8440 |
rs188041214 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105841568 | GCATAGGCATGACTG[G/T]TTAAACCCTTGGCCA | 8440 |
rs188075605 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105808046 | TAGCCGGGACTACAG[A/G]TGTGTACCGCTATGC | 8440 |
rs188092802 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105771894 | TCTCCGCAGCTGTTC[C/G]CAGAAGCTTCCTCAG | 8440 |
rs188094225 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105750963 | GCAGAATGTGCATGA[C/T]GGTGGTGAGGTGCAC | 8440 |
rs188098247 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | NCK2 | GRCh38.p7 | 2:105775961 | AAAAAACAGTGCGAG[C/G]GATAATTGTTGACCG | 8440 |
rs188113326 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105810227 | ACCCTTCTCACCCCC[A/G]ATTCTACTCCCTAAA | 8440 |
rs188162320 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105848778 | TGAATGAGTTTCCAT[A/T]AATTGATCAGTTGCA | 8440 |
rs188176445 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105870735 | CAGCCTGGGTGACAC[A/G]GTGAGACCCTGTCTC | 8440 |
rs188193333 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | NCK2 | GRCh38.p7 | 2:105813811 | TGGATTTTGCAGTGG[A/T]AAAATTTTGTAGTAT | 8440 |
rs188199317 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105798676 | GGTTGCTGGTGATTA[A/C]GTTTATGTGGACGGT | 8440 |
rs188209732 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105830316 | GTGAGTGAGAACTCT[C/G]GTATTTATCTTTCTT | 8440 |
rs188214621 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NCK2 | GRCh38.p7 | 2:105761014 | CCTCATCCTGCTTCC[A/G]CCTGAGGAAGCCCTG | 8440 |
rs188223778 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105743343 | ACAAGCTACAAACTG[A/G]GTCAATATTGCTATA | 8440 |
rs188229965 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105778842 | ATCCTCCTGCCTCAG[C/T]TTCCCAAGTAGCTAG | 8440 |
rs188283550 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105852051 | TGTCCTAGAATCTTA[A/G]AATTCTGAGTTGGAA | 8440 |
rs188296154 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105893688 | GGAACCACCGGGTGC[A/G]ATGGCAGTGAGGAGA | 8440 |
rs188305622 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime | NCK2 | GRCh38.p7 | 2:105816576 | TCGTTTTGAAGAGTT[C/G]TGCGTTTTGCCAGTC | 8440 |
rs188311416 | snp | A/G | | | downstream-variant-500B | NCK2 | GRCh38.p7 | 2:105894289 | GCTCTGTGTGTATTT[A/G]TCTTTGGGAAAACTC | 8440 |
rs188328889 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | NCK2 | GRCh38.p7 | 2:105862054 | CCCTGCCCCGGGTAA[C/T]TAAAGGCCCTTTAGT | 8440 |
rs188339064 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105792847 | GGCCTCCACCTGTAA[C/T]GCACAGGGGTTGCAA | 8440 |
rs188354987 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105754644 | GAGGTTGGGGGGAGC[A/T]GCTGCATTGGTAAGA | 8440 |
rs188357586 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105824328 | AGTGAGAGCCCAGTC[A/G]CTCCTCAGTCAGACT | 8440 |
rs188386304 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105755080 | TACTGCCCTCATATG[A/G]CTTTTCTTTTATGTG | 8440 |
rs188412215 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105845803 | TGGTGACTGTTATCC[A/G]TCTACTTTGGGAGCA | 8440 |
rs188439083 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | NCK2 | GRCh38.p7 | 2:105853456 | TAGATTTTAACAAAT[A/G]TATAATGACAGGTGT | 8440 |
rs188449268 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105874989 | CCACTTAAAATTATA[C/T]TTTCTGTCTGCTCAC | 8440 |
rs188488470 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105760616 | TGAGGCTCCCTTTGT[A/T]TCAACCAAGGGTCTT | 8440 |
rs188572236 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105873475 | ACATGCACGCCACCC[A/G]GCTATGAATTATGTC | 8440 |
rs188594429 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105801816 | CACCAAAAGCACATG[A/G]GACTTTACAGGGCGC | 8440 |
rs188598577 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105832469 | GTGCATCTGTCGTTA[A/G]GGCTCGTATTACCTA | 8440 |
rs188610069 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105763059 | AAGAATTAGCCAGGC[A/G/T]TGGTGGTATGTGCCT | 8440 |
rs188616166 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | NCK2 | GRCh38.p7 | 2:105800983 | CAGAAGATTGGAGAC[A/G]GGCAAATGTTCTAAT | 8440 |
rs188656390 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105771201 | TGCTGGGATTACAGG[C/G]GTGAGCCACCGCGCC | 8440 |
rs188712762 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105853342 | TACTTCCAAAATTGA[C/T]TTTACTGGATATATA | 8440 |
rs188733534 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105757748 | CTCTGGGTGGGGGAA[A/G]CACATATGGGAAGTC | 8440 |
rs188735654 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105803512 | CAAGGTGACTGCTAT[C/T]GTCTCCAAGGAAACC | 8440 |
rs188747490 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NCK2 | GRCh38.p7 | 2:105817009 | TTTGATGCTGAGAAG[A/G]TAAATCTGTGTCAAA | 8440 |
rs188747625 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant | NCK2 | GRCh38.p7 | 2:105833279 | CTTTTGTACTTTTAC[G/T]AGAGATGAGCTTTCA | 8440 |
rs188768365 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105785842 | TTATTTAGCTGTTCT[C/T]ATTTGATGTGCTGAA | 8440 |
rs188772375 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | NCK2 | GRCh38.p7 | 2:105764010 | ATTTCATATGTGTTG[C/G]CTAATTTAGTCCTCT | 8440 |
rs188818545 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105863024 | AATACCAGATGTCAA[C/T]GTGCCCAGCTGATGC | 8440 |
rs188826824 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105884826 | CGCTCTCCTCTCTCA[C/T]CTACAATTGTCATTT | 8440 |
rs188840352 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105877756 | TTCTGGACACCAGCC[A/G]CTATCAGAACTATGC | 8440 |
rs188843503 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105787925 | GCCCCCGACTTGTAG[A/G]TCCCTGGCCCATTGG | 8440 |
rs188848162 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NCK2 | GRCh38.p7 | 2:105808515 | TGCTGGATCCCTGCT[C/T]TTGAGAAAGGATCTT | 8440 |
rs188850309 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105825371 | TCCCATTCCGTTACT[A/G]GTGTTTAGTTCTGAT | 8440 |
rs188851599 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NCK2 | GRCh38.p7 | 2:105777402 | GGAGGCCACATCTTG[C/T]ACACAGACTCCTGAG | 8440 |
rs188856300 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | NCK2 | GRCh38.p7 | 2:105843592 | AAGAAACAAACGAAC[A/G]AACACTCGCAGTGAT | 8440 |
rs188861271 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105804302 | TGATGTTTGCACTGG[A/G]TGAGGATTATCTGAG | 8440 |
rs188862260 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NCK2 | GRCh38.p7 | 2:105806081 | ATGAAGTTAGGTGTC[A/G]AATTTTTTACTTGCA | 8440 |
rs188868277 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105816035 | TCCCCAACCCGAGTG[C/T]CGGAGCTTGCCCAGG | 8440 |
rs188872797 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105837279 | TCCTTGATTTTTAAC[A/G]TTAGTTTTACCACAT | 8440 |
rs188878945 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NCK2 | GRCh38.p7 | 2:105765075 | GCAGAGTTACATGGT[A/G]TGGACATCTTTATGG | 8440 |
rs188884719 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105784010 | GGACCTGCTTCAGCT[C/G]GACGGCAGGTCCCTT | 8440 |
rs188886903 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105749308 | AATTTTAAGTATTGC[A/G]GTTGCTTCTTTTGAG | 8440 |
rs188923064 | snp | C/T | | | intron-variant, utr-variant-5-prime | NCK2 | GRCh38.p7 | 2:105745862 | GGGCGATTTAATCAC[C/T]GAGTGCTTTTGGAAA | 8440 |
rs189068509 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105879938 | CACTGATTAAGGTAG[A/G]GGTCGAAGCAGAGCT | 8440 |
rs189071006 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NCK2 | GRCh38.p7 | 2:105888246 | CATTCTCCAGAACCA[C/T]TGATTCAAAAACTAT | 8440 |
rs189095404 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | NCK2 | GRCh38.p7 | 2:105822407 | GCCAAAAGAGAAGTT[A/C]TCTGTACAGGCCAGG | 8440 |
rs189101276 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105839345 | AGGAGGGTAGAACAG[A/G]GAGACTGGTAGACTG | 8440 |
rs189103595 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105857595 | AGGCAAGCAGTTCTT[A/G]GGAAACATTCCTGTT | 8440 |
rs189106322 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105855482 | TTCATTTCCTGGAGA[C/T]TCTGGAGTTTGGGGT | 8440 |
rs189109177 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105789747 | TTGCTCCCGGTTAAC[A/G]GGAGGGCTTTTTCTG | 8440 |
rs189122702 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | NCK2 | GRCh38.p7 | 2:105752342 | AATGTCATCCTTCAG[A/G]CACTCAGCACATGAT | 8440 |
rs189123905 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105807562 | TGCCTCCTTCCTAGG[G/T]TGGTGTGAGGGTGAC | 8440 |
rs189129203 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | NCK2 | GRCh38.p7 | 2:105791032 | AGGTTGTCCGCTCCC[A/C]CTCAGGAAACTTTGG | 8440 |
rs189136837 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105819790 | ACCTATTAAAATTTA[C/T]TTTTGTGGTTTAGAA | 8440 |
rs189142840 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NCK2 | GRCh38.p7 | 2:105760183 | AGATTTATCTATTCT[C/T]CCAAAAGGGACCAAG | 8440 |
rs189144916 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | NCK2 | GRCh38.p7 | 2:105797149 | TTTCAGCATCTCCCC[A/C]ACCCACAAGAAAAAA | 8440 |
rs189307416 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105864495 | ACTGAGCCACGGTGC[A/G]TAGTGGAGTTTGAGG | 8440 |
rs189324798 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105834568 | TGTTTTTTGTAAGCA[G/T]CATATAGTTAGGTGG | 8440 |
rs189354436 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105803661 | CCAGCTTCACACCCA[A/G]GTTAGTCGTCTTTCA | 8440 |
rs189373987 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | NCK2 | GRCh38.p7 | 2:105790304 | ATTGCCCACCATCTA[G/T]TTTTAGCAGATCTTG | 8440 |
rs189382574 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | NCK2 | GRCh38.p7 | 2:105768993 | GAGGTTGGGGTGTAG[C/G]GGGTGCAGAAAGTTC | 8440 |
rs189388056 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105798040 | ATTTTTATTAATTTA[C/T]GGTTTTGATCCATCT | 8440 |
rs189397288 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105807303 | CTAAAATCACACCCA[A/G]GTGCTCTCCTCGAAG | 8440 |
rs189417783 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105753340 | GACCATTGGCCTGGC[G/T]GCTCCTCTCCCCCAG | 8440 |
rs189424712 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105768380 | TAGCTTTTCAGGGTT[C/T]GTGCCGGCCTCACAA | 8440 |
rs189446007 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105889769 | TTTTAAATTTTATGT[A/T]GAGATAGGGTCCCAC | 8440 |
rs189472582 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105831299 | AGATTTGTAGGAAAC[C/T]GCAAAAGAACCCTGA | 8440 |
rs189474144 | snp | A/C | | | upstream-variant-2KB, intron-variant | NCK2 | GRCh38.p7 | 2:105849860 | TATTCAGAGGGTATT[A/C]ATTATGACTGTAGTT | 8440 |
rs189482507 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105871258 | ATGGTGAGCTGAGCA[A/C]CAGTGAGCGCTCCCA | 8440 |
rs189545480 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105871885 | CTTAGAGAGCGGGGA[A/G]GAAACTACATGACAC | 8440 |
rs189556966 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105891999 | ACTATGTTTAAAATG[C/T]GACCGGAATTTTCCA | 8440 |
rs189575870 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | NCK2 | GRCh38.p7 | 2:105815746 | GGTGGCTTCTCAACA[A/C]ATGGCTGGTGCAACA | 8440 |
rs189576204 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105832181 | TTCAGCTAGTTTGTT[A/T]TTGGTATATAGAAGA | 8440 |
rs189585858 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105885091 | CTGTACAAGTTGTCA[A/G]TATTTTATTTTCTTA | 8440 |
rs189589576 | snp | C/T | 0.0023933 | 0.0345097 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | NCK2 | GRCh38.p7 | 2:105851706 | GCTGTCCCTCTGAAG[C/T]AGTCTCACTGCAGTG | 8440 |
rs189599448 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105783541 | CAAGGCACAGGTTAA[C/T]GTGCAGTATTTGCCA | 8440 |
rs189599896 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105885542 | ATTCTCTAACTGTAT[A/G]TAGTGTGTATCAGAA | 8440 |
rs189602586 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105762913 | TTAAAAGCAACCTGA[A/G]GCCAGGCGCAGTGGC | 8440 |
rs189609239 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105808624 | GGATGGAGTGCCACG[C/T]GACTGCAGGGTGGAT | 8440 |
rs189615206 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105800847 | GGAAAAAGTGAGTGG[A/G]AGAGCACCTTGCTGC | 8440 |
rs189627100 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105845147 | CATGCTTAGGAATGT[A/G/T]GGCATAAACCATATA | 8440 |
rs189633518 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105773893 | GTCTTTTCTTTAACT[A/G]TTTTTATTTGCCTTA | 8440 |
rs189638976 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | NCK2 | GRCh38.p7 | 2:105786697 | GGGTCCCCGGGCAGG[C/G]CTTCCTGTCTCCATC | 8440 |
rs189644500 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105817456 | TCCGGTGTTCTCTTT[C/G]TGGCTGGGCAGTAAG | 8440 |
rs189665129 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105748022 | CTAAAGGTAAATGAA[C/T]GTTAGCAAGTATTAC | 8440 |
rs189671443 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105753783 | GCTGAAAACCTTGTA[A/G]CAGGACATACCAAAT | 8440 |
rs189677947 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105778275 | GCACATGTGGTAGTG[A/G]CCTTTGCCAACATCC | 8440 |
rs189823255 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105877655 | AGGGAGGGAGTGGAG[C/T]AGATTCTTGGCACCC | 8440 |
rs189847904 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105863505 | TAATAGGGTGTGTTC[C/T]GATCAGAAGGGGGAG | 8440 |
rs189879454 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105853586 | TTTTCTTACTGTCTC[C/T]ATAGATTTGTCTTTT | 8440 |
rs189886814 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105825901 | GTGTCCTGGTGATCC[A/G]TCAGGTTTGGAGTTC | 8440 |
rs189907322 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105794930 | CTACTCTCTCTATCT[C/T]CTTTTTTCCCTACTC | 8440 |
rs189907512 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | NCK2 | GRCh38.p7 | 2:105818446 | AAATATATATATATA[A/T]AAAGATTTTATTCCT | 8440 |
rs189934993 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105794335 | AGGATTACAGGCATG[C/T]GCCACCATGCCTGGC | 8440 |
rs189948596 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105756817 | TTCTGAACTTTTTAT[G/T]TTTTGAGACGGAGTT | 8440 |
rs190000694 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NCK2 | GRCh38.p7 | 2:105809267 | GTTGCGTGTGTCATA[C/T]GTCGTGACACATATG | 8440 |
rs190004915 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105795468 | CGGGTAATTATAAAA[A/G]CTGCTGCATAAATAT | 8440 |
rs190008949 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105827054 | GCCCAGGCTGGAGTG[A/C]AGTGGCACGATCTCG | 8440 |
rs190025108 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105758032 | TTAGTTTGCTTAGGA[G/T]GAACACATGATTTGT | 8440 |
rs190042139 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | NCK2 | GRCh38.p7 | 2:105774212 | CAGGTTTTCACCATG[C/T]TGGCCAGGCTGGTCT | 8440 |
rs190085327 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105876295 | AGTCTTGCTAAAACA[C/G]ATGACCGCACACCAT | 8440 |
rs190095326 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105875587 | TCATGAATGGGATTC[A/G]TGCCCTTATAAAAGA | 8440 |
rs190115686 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105818681 | GAGAATATTACAGTG[G/T]ACATTTGTATAAAAA | 8440 |
rs190122038 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NCK2 | GRCh38.p7 | 2:105836324 | TGGGTAGGATGCTTT[A/G]GGTTTGATTCTGGGT | 8440 |
rs190127499 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105836032 | TGTTTTTCTGATTTC[A/G]TTGAATTTTCCATGT | 8440 |
rs190129039 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105854105 | GTCAGAATCACACAG[C/T]GTGTAGCCTTTTCAG | 8440 |
rs190132655 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NCK2 | GRCh38.p7 | 2:105788308 | TTTCATGGAGTTAAA[A/G]CCATTGCTTAAAAGT | 8440 |
rs190144667 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105805755 | TCCCAGTTCATCTGC[A/G]TTATTGCAAATGGCA | 8440 |
rs190146125 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105869758 | ATATTCAAAAACGCT[C/T]GGGCTCATGGATCTG | 8440 |
rs190148715 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105759406 | AGTGTTTTAACGTTT[C/T]CAAAGTGTAATTTGT | 8440 |
rs190170568 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105772842 | TCTAGGTCTCCTGGT[A/C]CTTCCTTCACAGTGT | 8440 |
rs190171053 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NCK2 | GRCh38.p7 | 2:105769406 | ACTCTCACTGTGCTG[A/G]TAACTCCCCCGTTCT | 8440 |
rs190176931 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | NCK2 | GRCh38.p7 | 2:105829235 | TGAACCTACCTCCCA[A/T]CTTAAAAACTAGAAT | 8440 |
rs190207735 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105764114 | GTCCGAGTGCTAGTC[C/T]TGGCAGCTTCGCTTT | 8440 |
rs190386194 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105879556 | GGCTTACTCTTGTGT[C/T]TCCCATGCACATGCA | 8440 |
rs190405416 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105888004 | TTTTTAAGTCTGCAC[A/G]TTTGTTGAACACCAG | 8440 |
rs190413076 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105812189 | CTAATTGCAGTGAGG[C/T]TTTTTGAAGCTGCTT | 8440 |
rs190417683 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NCK2 | GRCh38.p7 | 2:105838985 | AATGGAGAGTGGTGC[A/G]GCAGCTATTTTATAT | 8440 |
rs190429616 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105848085 | CCTTATGTTCAAGCC[A/G]TTGAGCCTAGTGATG | 8440 |
rs190435927 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105814548 | TCTTTTGCGGGGTCT[A/G]GTAGAGAAGCTGCTC | 8440 |
rs190437409 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105748356 | CTTTGTGTCCCTGAT[A/T]TGTCATCTGTGACAT | 8440 |
rs190451923 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | NCK2 | GRCh38.p7 | 2:105780845 | GGCCCTTACCAGACA[C/T]TGAATTTCCTGGTAC | 8440 |
rs190499364 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105846308 | TTGACTTAGAGTCTA[A/G]TCTGCAGAACGCTAG | 8440 |
rs190507443 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105819939 | AAAATAGATAAAATA[C/T]AGTCCCAGCCACCTT | 8440 |
rs190507715 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105867090 | TCAAATCAGTACAAA[G/T]CCAAACTGTTCCCCT | 8440 |
rs190513675 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105885927 | GTTTGTTTGTTTTTT[A/T]CTGTTTAGAGTTTGA | 8440 |
rs190533360 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105827491 | TATAGGAACACTCAC[C/T]ACCATCAATTAATAT | 8440 |
rs190635145 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105859170 | GAGGTATTTTTCAAA[G/T]ATTTTCCCTCAAGCT | 8440 |
rs190655067 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105782107 | TACTCTGTTCTTACT[A/G]TGACTGCGGGAAGTT | 8440 |
rs190662739 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105799122 | TCCTGTCTGTCCTTC[A/G]TGTCCTAAGTTGCAA | 8440 |
rs190665193 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | NCK2 | GRCh38.p7 | 2:105821905 | GGTCTGTTGCTTACC[A/G]GCCCACGTTCCTTCT | 8440 |
rs190666039 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | NCK2 | GRCh38.p7 | 2:105822800 | GAATTTTCGTGAATT[A/C]TCTTTAATGCCAGGT | 8440 |
rs190682781 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NCK2 | GRCh38.p7 | 2:105857264 | TTCATGAGCTGTGAT[C/T]GGTTCAGCCAATGCG | 8440 |
rs190690494 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105762259 | GAAAGAGGCCTTGCC[A/G]AGGAAACAGGCAGCT | 8440 |
rs190694272 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105754117 | GGGAGAAGCTCCTGC[A/G]TGTTCCAAGTTTCAG | 8440 |
rs190698195 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105791393 | GTGTGGTGGAAGGCT[C/T]GGTGGCTTTCACGAT | 8440 |
rs190737165 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105841550 | TTTTATGGAAGCTTC[A/C]TTGCATAGGCATGAC | 8440 |
rs190750257 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105861595 | TCTCGGCTCACTGCA[A/G]CCTCCACCTCCCAGG | 8440 |
rs190758578 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105883666 | AATTCAGGGACCAAG[G/T]CCCTTTGGATAAGGA | 8440 |
rs190764866 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105807966 | TGGAGTGCAGTGTGC[A/G]ATCTCAGCTCACTTT | 8440 |
rs190782994 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105823969 | GGTCCGGAGCAGTCC[C/G]TGGCCGGCGTGAACT | 8440 |
rs190851904 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105872026 | ACATTTACTGCTTTT[C/T]CTCCATGGTGGTCAG | 8440 |
rs190858251 | snp | A/C/G | 0.000350041 | 0.0132252 | intron-variant | NCK2 | GRCh38.p7 | 2:105892951 | CTCCCCGCTGTGGCC[A/C/G]GGCTGTAACTGTGTT | 8440 |
rs190900351 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | NCK2 | GRCh38.p7 | 2:105880801 | TGGTTTTAGAGACAG[G/T]GCCTCACTCTGTTGC | 8440 |
rs190912175 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105805925 | ACGAGAGGTTTTGGG[A/G]ATGGAGCCAAGTCCA | 8440 |
rs190916552 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105837120 | GAGCTTCTGTCCCTC[A/G]GAGGGTCTTGTTGCT | 8440 |
rs190919246 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105807690 | ACCTCTCTCCTTTTT[A/T]TTTTCTCTTTTCTTT | 8440 |
rs190930431 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | NCK2 | GRCh38.p7 | 2:105839678 | GTTAGACATCCAGAT[A/G]CAGATGTTCACCAGG | 8440 |
rs190934302 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | NCK2 | GRCh38.p7 | 2:105765959 | AGCTGCTGAATTTGC[A/G]GTGACTTGTTACATG | 8440 |
rs190934653 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105769840 | AGATTTTAATCCCTC[A/G]GAGTAATCTTTGGCC | 8440 |
rs190956794 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105745434 | CGCGGGCGAGGATCA[G/T]GGCAGGGGGCCCGGC | 8440 |
rs191036792 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105807813 | TCCCTCCCTTCTATC[C/T]CTCCCTCCCTCCCTC | 8440 |
rs191050694 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105823621 | ATGTTAACAAAGAGT[A/G]TATTAACAAGATGCC | 8440 |
rs191054578 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105840784 | ATCTCAGGACCTCCT[A/G]CTAAACTGCTTATGC | 8440 |
rs191066667 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105754557 | TCTTTCATGCTTTCC[C/T]TCTCATCAGCTGTCT | 8440 |
rs191077229 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105791622 | GAGCAAAGAGCATTT[C/T]GAACTGACTCCATAA | 8440 |
rs191081939 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105770800 | CCTTTAAAGTATTTC[A/G]GATCCAGGAAGTCAT | 8440 |
rs191132885 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105854911 | GGTCATTTTAAAGTT[A/G]AGCATTTCAAGACCC | 8440 |
rs191134593 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | NCK2 | GRCh38.p7 | 2:105886829 | TGGACAGGGAACGCT[C/T]CGTTTGCCTAGATTA | 8440 |
rs191153918 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105819393 | TGCAAATGCAGTCAT[G/T]TATCAATCCACTTGT | 8440 |
rs191164327 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105846925 | AGCAACACAAATGTC[A/G]AGTGATGGATGAACG | 8440 |
rs191177146 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105755652 | ACTTGTGCAGGTACA[C/T]GAATACCTTTTTAAA | 8440 |
rs191194146 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NCK2 | GRCh38.p7 | 2:105810435 | CTCCCTCTTTCCTTC[C/T]TTCAGAAAAAGGGGG | 8440 |
rs191200518 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105788722 | TTTATCCATAGAATG[C/T]ATAATTTTTTTTGTT | 8440 |
rs191215523 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | NCK2 | GRCh38.p7 | 2:105750754 | GGTAGACACTTATTT[A/G]GGGGTTGGTTTGTCT | 8440 |
rs191240349 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105853357 | CTTTACTGGATATAT[A/G]ATACACGCATCTATT | 8440 |
rs191252350 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | NCK2 | GRCh38.p7 | 2:105749937 | CGGGAGGCTGAGTCA[C/T]GCGAATTGCTTGAAC | 8440 |
rs191254682 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105803586 | GAAAGTGCGGAACTG[A/G]CATTAGCATCCAGTT | 8440 |
rs191271237 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105834324 | GTGGGTGCCCTGTTC[G/T]TGGGTACATATATAT | 8440 |
rs191274967 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105817015 | GCTGAGAAGATAAAT[A/C]TGTGTCAAAGGATAG | 8440 |
rs191293180 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105786163 | GGGCAGCATGATTAG[C/T]GTTGTGGACTGAACA | 8440 |
rs191357483 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105869052 | TCCAAAGCAGCATAC[A/G]ATCCAGCCCCGCTGC | 8440 |
rs191390474 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105828530 | GTAATGACTTTGTCT[C/G]GACTCTGAAGTCTAA | 8440 |
rs191393073 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105847634 | GGGCCTGGTGGGACA[C/T]GCAGGGTACATCAGG | 8440 |
rs191398951 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105827837 | GGTGGGTGTGACTGT[A/G]CAAGGGATAATGTCA | 8440 |
rs191408733 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105776780 | GCAGTCGGACCACAC[A/G]TGACTATTCGAGGGT | 8440 |
rs191409769 | snp | A/C | 0.0228947 | 0.104514 | intron-variant | NCK2 | GRCh38.p7 | 2:105855778 | GCTTTGTGACATCAG[A/C]GGCCGCTCCATGGTG | 8440 |
rs191416964 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105868750 | GCTATACACAGTTAC[A/G]TTTAAAAAGTGAAGT | 8440 |
rs191424677 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105811009 | TGAAACCCCGTCTCT[A/C]CTAAAAATACAAAAA | 8440 |
rs191424966 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105796775 | AATAACTAAGCATTT[C/G]TCTTTGACGCAGGTA | 8440 |
rs191427338 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105796183 | AGTCTCTGTATTGGC[C/T]GCCCTCTGGGCACTG | 8440 |
rs191428455 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105752740 | GGATAATGGCCTCCA[C/G]TTCCATCTGTGTTGC | 8440 |
rs191444438 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105759801 | TGGCTTGACAGCTTT[A/G]AGGAGCAAAACTGCT | 8440 |
rs191456847 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | NCK2 | GRCh38.p7 | 2:105765685 | TTTTTTTAATTACTA[A/T]TATGTTCCTTAAAGA | 8440 |
rs191466836 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105795811 | ATTCCTCCCTCTAGA[C/T]CTCTCCCTCCTCCCT | 8440 |
rs191504570 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | NCK2 | GRCh38.p7 | 2:105759256 | CACATGCAGTATATC[A/G]TTTTACGTATTCAAG | 8440 |
rs191669344 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NCK2 | GRCh38.p7 | 2:105878088 | TTTCTATTTTGATGG[C/T]CATCCAACACTGGTA | 8440 |
rs191705417 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105837296 | TAGTTTTACCACATA[C/T]GTAAGTCTAAACTAC | 8440 |
rs191715824 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105831770 | TCTGTTTTTATGCCA[A/G]TACGATGCTGTTTTG | 8440 |
rs191730882 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105809939 | GAGAGGGCAGGCAGG[G/T]AAGGGAGCGAGCGGG | 8440 |
rs191734722 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | NCK2 | GRCh38.p7 | 2:105871571 | CGCGATCTCGGCTCA[C/T]TGCAACCTCCGACTC | 8440 |
rs191739277 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105837614 | TTTCTGTACTGCATA[G/T]AAGTAGAAGTGGAGC | 8440 |
rs191743392 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105856619 | CTCTGCAAAATCATC[A/G]AAAGCCTTCATGTAT | 8440 |
rs191745000 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105798324 | CTGTGGCCTCTTGTT[G/T]GTACATCCAGAATAT | 8440 |
rs191748498 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105774678 | TCTGTGGTGCGGTAG[A/G]GAGAGGAGGTGTCAA | 8440 |
rs191753503 | snp | C/T | 0.0263992 | 0.111815 | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105771292 | AAACATGAGGGCTGG[C/T]GGGGTGGCTCACGTG | 8440 |
rs191756952 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105799803 | CAAGAAGCCATTGGT[C/T]CTTACCTGGCCTTCC | 8440 |
rs191757418 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105878393 | TCACTGGGGTGGGCC[C/T]TCATCCAGTCTAACT | 8440 |
rs191764460 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105806486 | TCGTGATCCACCCCG[C/T]GTTGGCCTCCCAAAG | 8440 |
rs191771689 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105820938 | ATGTGCATGTCCAGC[A/G]TGTAAATGTCAGCAG | 8440 |
rs191879871 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105869572 | TGCCACCTGCGTGTT[A/C]CCCCGTGAATGTGCT | 8440 |
rs191893849 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105801420 | GATGTGCTTTTTTCT[C/T]TTTTTTTTTTTCTCC | 8440 |
rs191896781 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105887679 | GGAATGGAGGAGGAA[A/G]TAAAGGATATTAAAG | 8440 |
rs191927327 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B | NCK2 | GRCh38.p7 | 2:105894349 | AGCATTCACTCATTG[C/T]GGAGTGGAAATCATT | 8440 |
rs191930537 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NCK2 | GRCh38.p7 | 2:105847988 | ATTTTACTACCTTTG[A/G]GTGTTGGCACATCTT | 8440 |
rs191957981 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105883393 | ATATTAAGTGCTTGG[C/T]CCAGAGTCCTTAAGG | 8440 |
rs191987131 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105891146 | CAGATGAACTCACAC[A/G]CTACGCATACTCTCA | 8440 |
rs192008663 | snp | G/T | | | upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105744238 | CGAGTTTCTTCTTCT[G/T]TTAGGAAGTGCCTCG | 8440 |
rs192018934 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | NCK2 | GRCh38.p7 | 2:105806131 | AAATTATCAGATTTT[C/G]GAGCAATTTGTATTT | 8440 |
rs192020412 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105792454 | TATTACGGAATTTCA[A/G]TAACAATAACTACTT | 8440 |
rs192025432 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NCK2 | GRCh38.p7 | 2:105850473 | GTTCTGAGAGCTGTT[C/T]TTCCAGCATAACTTG | 8440 |
rs192041520 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105750880 | CAGCCAGGGTGGAGA[A/G]GCCGTCTCCTCTGAG | 8440 |
rs192045003 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105789250 | TGGAGTGTAGTGGCG[C/T]GATCTTGGCTTACTG | 8440 |
rs192050854 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105815042 | CATGAGAAACAAGAA[C/G]TCTTGGTCAAGAACT | 8440 |
rs192054660 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NCK2 | GRCh38.p7 | 2:105767060 | CTCGTATGGTCAGCC[A/G]GGTTCAGGCCCACAC | 8440 |
rs192145082 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105863201 | TGATTGCTGGGAAAT[C/G]GGAAATTCTCATTTC | 8440 |
rs192159118 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105884862 | TAGCAGCTAAAGGTG[A/T]TGCATTGTTGTTGCT | 8440 |
rs192164733 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105824543 | GAGAAGCTAAATGTA[A/G]CCGTATCTTCCAACC | 8440 |
rs192174567 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105862126 | AGCTTGCAATTTATA[C/T]AGCACTTTGCAATTT | 8440 |
rs192183271 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105792957 | CGTGCAGTTTAGATG[C/G]GAGTCTTTCCCTTTC | 8440 |
rs192200067 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105764021 | GTTGCCTAATTTAGT[C/T]CTCTCTACAACCCCA | 8440 |
rs192266729 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime | NCK2 | GRCh38.p7 | 2:105816580 | TTTGAAGAGTTCTGC[C/G]TTTTGCCAGTCACCT | 8440 |
rs192268784 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105802742 | CAACACTGGGGATCA[C/G]ATTTCAACATGAGAA | 8440 |
rs192272511 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105860870 | AACTTGTGGGGCACA[C/T]GAGATGGGGAATTTT | 8440 |
rs192284513 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105763792 | GACCCTGTGTTTAAA[G/T]AAATATGCTATAAAA | 8440 |
rs192293657 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105747772 | GATGGAAATACTTCA[C/T]GGCACGTTTTCAAAG | 8440 |
rs192296775 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105785490 | CAAAGTGACACGACC[A/C]AAAGACCGCCAATAC | 8440 |
rs192367447 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105761953 | CTGTGTTACAGTTTA[C/T]GTTTTCTCTTTTGTC | 8440 |
rs192404907 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105838760 | CCTACTGATGGAGGC[C/T]GACCGTAGGCCTTTC | 8440 |
rs192420045 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105879020 | TAAAGTAGAATATTC[A/G]TCTATCAGTTATAAA | 8440 |
rs192442567 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NCK2 | GRCh38.p7 | 2:105806619 | AATGGAAAATTTTAA[A/G]TTTCCTTTTTATTCC | 8440 |
rs192444546 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105825127 | CCAGGCTTTGGAGCT[C/G]TGTGAGTCCATGCCT | 8440 |
rs192460024 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105768736 | TATGTATGGCCCAAG[A/C]TGATTCTTACAGTGT | 8440 |
rs192460740 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | NCK2 | GRCh38.p7 | 2:105842896 | AGTGGGTGGTGGGGT[C/G]GGGGGGTTCTTACTG | 8440 |
rs192467612 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NCK2 | GRCh38.p7 | 2:105862632 | ACCTCGGGAGTAACT[A/G]GCAAGCCTTGAAGGG | 8440 |
rs192477456 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105772543 | CCTCCGCAGCACTGG[A/G]GTCAGCCGCATGTTA | 8440 |
rs192484828 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105808288 | TTTTCATATACCTTA[C/T]TCCAGTTGGAAAAGT | 8440 |
rs192490703 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105793221 | AATATTCATGTATTT[C/T]CTGGGAATGGGTGGA | 8440 |
rs192512375 | snp | A/C/G/T | 0.00557542 | 0.0525036 | intron-variant | NCK2 | GRCh38.p7 | 2:105755976 | CAAATTAGACCTTAC[A/C/G/T]AAGGGAAAAGGAAAG | 8440 |
rs192513981 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105884164 | GTTCATAACCAAGGC[A/G]TTCTCAGCTGTCATC | 8440 |
rs192552589 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105842149 | GGAGTGCAATGGCGC[A/G]ACCTCGGCTCACTGC | 8440 |
rs192580960 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105748166 | ACAGTGATGTCATAC[A/G]GTGTCACTGTCCCTG | 8440 |
rs192599699 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | NCK2 | GRCh38.p7 | 2:105808108 | GGGTTTCACCATGTT[A/G]GCCAGGATGGTCTTG | 8440 |
rs192621462 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105772187 | ACAGCCTCTCGGAGC[C/T]TCCTGGGAACTCTTG | 8440 |
rs192648512 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105848236 | TGCAAACACAGAAAT[C/G]GGGGGCAGAGTGGTC | 8440 |
rs192662626 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105888032 | CAGATACTCTGAGCC[C/T]GGTGTGGGGATGTGG | 8440 |
rs192669791 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105812853 | TGCTAACATCTAAGA[A/G]AAGCAGTAACGTTGA | 8440 |
rs192694690 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105789566 | TCTAGTTGAAGAGAT[A/G]TTTCCCTGAGTCTTT | 8440 |
rs192708256 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105751535 | CAGCATCTAAATATC[C/G]CCTTCCCCATATACA | 8440 |
rs192757072 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105887539 | ATTTCATAAAGTCCA[A/C]AGTGAAAGATAAGGA | 8440 |
rs192759280 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105857186 | CAGTTTTCTAGAAGC[A/T]GAAAAGACAAAGCCA | 8440 |
rs192770376 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105789941 | ATGTTCACGAATGGA[C/T]GTTGTGTTTTGCCAT | 8440 |
rs192775452 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105821614 | CCACATTGATTCCAC[A/G]GTGCCCCGGTGGTGC | 8440 |
rs192825054 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105828678 | AAGAGGTCTCAGCTT[G/T]TCTTTGATCACCTAT | 8440 |
rs192834197 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | NCK2 | GRCh38.p7 | 2:105760580 | TCCCACAGTTTTGAC[C/T]ACCTCTTGGATCTCT | 8440 |
rs192835263 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | NCK2 | GRCh38.p7 | 2:105798003 | TTTGGTTCATTTCCT[A/C]GGAGAAGAAAATTAT | 8440 |
rs192881365 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105870504 | TCACACCTGTAATTC[C/T]CAGCACAGTGGGAGG | 8440 |
rs192895082 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105829338 | AGATTTACAGAAGGC[C/T]TATGAAGATAGCCTA | 8440 |
rs192923333 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NCK2 | GRCh38.p7 | 2:105767787 | GCCCGCACCTGGGAA[A/G]GGAGGAGGAGGATAC | 8440 |
rs192947412 | snp | C/G/T | 0.00162866 | 0.02849 | intron-variant | NCK2 | GRCh38.p7 | 2:105873667 | GGTGGTTTTATTTTT[C/G/T]GGGGGCTCTTAATTG | 8440 |
rs192964688 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105832746 | ATCTATGTTCATCAG[A/G]CACATTGGCCTGTAG | 8440 |
rs193028763 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105811395 | CTTCCTTTTCTGGCT[C/G]TAATTTGCTTCTCAT | 8440 |
rs193036946 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105777412 | TCTTGCACACAGACT[C/G]CTGAGAGTGTGGGTG | 8440 |
rs193068046 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | NCK2 | GRCh38.p7 | 2:105884554 | TGGAATGGATCTTCA[A/G]TAAAATATCCTGAGT | 8440 |
rs193089338 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NCK2 | GRCh38.p7 | 2:105816213 | GGGGAGACTTAGGCA[A/G]GAGGATCACTTGAGC | 8440 |
rs193103300 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105784500 | TTAAATTCAAGATAC[A/G]TTTGTGTTTCCACTA | 8440 |
rs193109189 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | NCK2 | GRCh38.p7 | 2:105746098 | ACAAAGCCGAGCGTG[C/T]GTGGAGTCGGCCTTG | 8440 |
rs193178390 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105893758 | TTCCTGGAAAGGCAG[C/T]CTGCAAAAGAGGGAA | 8440 |
rs193192073 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105754858 | TGAATTTTCATCAAA[C/T]GATTAAAAAAAAGTG | 8440 |
rs193251377 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105832287 | TTGCTGGAATTTTCC[A/G]TTTTCTTTTCCAGTA | 8440 |
rs193255642 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NCK2 | GRCh38.p7 | 2:105763160 | CCGAGATCATGCCAC[C/T]GCACTCCAGCCTGGG | 8440 |
rs193257966 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105801250 | GAGGCCTGCCGGGCT[C/G]TCATCTCCTTGGGGA | 8440 |
rs199507013 | in-del | -/T | 0.00835141 | 0.0640778 | intron-variant | NCK2 | GRCh38.p7 | 2:105757360 | CTTGATTATTAGGGA[-/T]TTTTTTTTTCTTCAA | 8440 |
rs199616472 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105811402 | TTCTGGCTGTAATTT[G/T]CTTCTCATTATATAT | 8440 |
rs199651774 | in-del | -/A | | | intron-variant | NCK2 | GRCh38.p7 | 2:105835423 | TGTATATATATATAT[-/A]TTTTTTTTTTGGTCA | 8440 |
rs199651832 | snp | A/G | 0.00199794 | 0.0315433 | missense, intron-variant | NCK2 | GRCh38.p7 | 2:105881969 | TGGTACTACGGGAAC[A/G]TGACGCGGCACCAGG | 8440 |
rs199660669 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105758413 | GTTTTTGTTGTTTTT[G/T]TTTTTTTTTTTTTTT | 8440 |
rs199684573 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105891569 | TTTTTTTTTTTTTTT[G/T]AGATTTTTCGCTCTT | 8440 |
rs199727155 | snp | C/G/T | 1.66624e-05 | 0.00288633 | missense, synonymous-codon, intron-variant | NCK2 | GRCh38.p7 | 2:105881461 | GGCCTTCGTCAAGTT[C/G/T]GCCTATGTGGCCGAG | 8440 |
rs199727312 | in-del | -/C | | | upstream-variant-2KB, intron-variant | NCK2 | GRCh38.p7 | 2:105850576 | TTGTAGCCCTTCTCT[-/C]CTTTGGGCTAGACCT | 8440 |
rs199739176 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105752162 | TGGCAGCCTTGTTGC[A/G]GAGTGTGAGTCTATA | 8440 |
rs199762484 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105824271 | CACTTGGGCCCCTGA[C/T]GGTGCTCACAGGGAA | 8440 |
rs199798899 | in-del | -/AC | | | intron-variant | NCK2 | GRCh38.p7 | 2:105844576 | AGTAGAAAAAAACAA[-/AC]AAAAAAAAAAAAACA | 8440 |
rs199843222 | in-del | -/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105770137 | GTAAAAAAAAAAAAA[-/G]AAAAAGAAAAAGGTA | 8440 |
rs199930056 | snp | C/T | 8.32924e-05 | 0.00645285 | synonymous-codon | NCK2 | GRCh38.p7 | 2:105855192 | GTGGCGGGTGAGGAA[C/T]GCGGCCAACAGGACG | 8440 |
rs199952764 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105855438 | ATAATCTAAGAATTA[A/G]GAGATGAAGATGGAG | 8440 |
rs199964559 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105887730 | TTTTCCTTCTATGAG[A/T]AAACAATGATTAAAT | 8440 |
rs199969411 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105819918 | ACTGTTGTAGCAGTT[A/T]AAAAAAAAATAGATA | 8440 |
rs199991417 | in-del | -/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105883064 | GGGATGTGCTCTCTT[-/C]TGAGGACGGAGCATC | 8440 |
rs200007047 | snp | C/T | 0.288906 | 0.246954 | intron-variant | NCK2 | GRCh38.p7 | 2:105780335 | ATATATACACACACA[C/T]ACACACACACACACA | 8440 |
rs200027888 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105889571 | TGAGAATTTGCATTT[C/T]TTTTTTTTTTTTTTT | 8440 |
rs200055673 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105784114 | GTCACTGGGAGCTTT[C/T]CTTTTTTGAGAGAGG | 8440 |
rs200094183 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105838278 | TGATAAAGATAAATG[C/G]AAATTTTTAAATGCT | 8440 |
rs200102865 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105759471 | ACAGGCTTTTATATA[A/T]TAAAACATATGGTAT | 8440 |
rs200123040 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105821621 | GATTCCACAGTGCCC[C/T]GGTGGTGCAGTCAGT | 8440 |
rs200124168 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105819323 | TGGTAACTCCGTTTT[C/T]TTTAAAAAAAAAAAA | 8440 |
rs200140158 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105807788 | TCCCTCCCTCCCTTC[C/T]CTCTCTCCCTCCCTC | 8440 |
rs200150936 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105839878 | AAAACTAAGAAGGAA[C/G]GGTCAGCAAGGGACA | 8440 |
rs200169103 | in-del | -/TG | 0.0260105 | 0.111035 | intron-variant | NCK2 | GRCh38.p7 | 2:105792387 | AGCCCCTATAGACTC[-/TG]TAACAGATTATTTCT | 8440 |
rs200184577 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105890314 | AGTCATCTGTTGATC[A/C]TTTGGCTTAATTAAA | 8440 |
rs200185858 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105846490 | CTGAAAAAAAAAAAA[A/T]AATAGGAGGGTGTAG | 8440 |
rs200222338 | in-del | -/T | 0.00438332 | 0.0466095 | intron-variant | NCK2 | GRCh38.p7 | 2:105891253 | TCTTTCATGCAACTC[-/T]TTTTTTTTGTTTGTT | 8440 |
rs200229213 | in-del | -/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105834503 | CATTTCTGTGGAAGA[-/T]TTTTTTTTTCATCCT | 8440 |
rs200231173 | in-del | -/T | 0.0115144 | 0.0749975 | intron-variant | NCK2 | GRCh38.p7 | 2:105868715 | CTACTGTGGGTTTTC[-/T]TTTTTCTTCTTCAAA | 8440 |
rs200266130 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105835393 | TATATATACACATAT[A/G]TATATATATATACGT | 8440 |
rs200271316 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105806243 | CATTTTCTTTCTTTT[C/T]TTTTTTTTTTTTGAG | 8440 |
rs200294110 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105750037 | TCTCAAAAGCAAACA[A/C]ACACACACACACACA | 8440 |
rs200414964 | in-del | -/TTTTTTTTT | 0.39009 | 0.207062 | intron-variant | NCK2 | GRCh38.p7 | 2:105806239 | ATCACATTTTCTTTC[-/TTTTTTTTT]TTTTTTTTGAGACAG | 8440 |
rs200434042 | in-del | -/AAAAA | | | intron-variant | NCK2 | GRCh38.p7 | 2:105770125 | AAAGCACTAATAAGT[-/AAAAA]AAAAAAAAAAAAAGA | 8440 |
rs200477344 | in-del | -/GG | | | intron-variant | NCK2 | GRCh38.p7 | 2:105830669 | CCTTGCCAGGAATTT[-/GG]GGTGTGTGTGTGTGT | 8440 |
rs200482430 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105891567 | TTTTTTTTTTTTTTT[G/T]TGAGATTTTTCGCTC | 8440 |
rs200484655 | in-del | -/AC | | | intron-variant | NCK2 | GRCh38.p7 | 2:105760624 | CTTTGTATCAACCAA[-/AC]GGGTCTTTGCTTTCT | 8440 |
rs200508739 | in-del | -/A | 0.02016 | 0.0983543 | intron-variant | NCK2 | GRCh38.p7 | 2:105763199 | GAGACTCTTGTCTCC[-/A]AAAAAAAACAAAACA | 8440 |
rs200548114 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105884231 | ACAAGTCCTTTGCTT[G/T]TTTTTTTCCCACCAT | 8440 |
rs200549046 | in-del | -/A | 0.0217236 | 0.101931 | intron-variant | NCK2 | GRCh38.p7 | 2:105796531 | AGAGAGGGCCTGGGG[-/A]ACATGAGTGTGTGGC | 8440 |
rs200550213 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105841716 | CTGCCTAGGGGCTGC[A/C]AGCCACCAGTCACCT | 8440 |
rs200591707 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105795303 | GTGATATATTTTTAA[A/T]TTTTTTTTTCCTCAA | 8440 |
rs200594599 | snp | A/G | 9.98851e-05 | 0.0070663 | missense | NCK2 | GRCh38.p7 | 2:105892997 | CCCAGCGACTTCTCC[A/G]TGTCCCTTAAAGCGT | 8440 |
rs200601192 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105774011 | GATTTTTCCAGCTAT[C/T]TTTTTTTTTTTTTTT | 8440 |
rs200603433 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105759467 | GCATACAGGCTTTTA[C/T]ATAATAAAACATATG | 8440 |
rs200636557 | snp | A/G | 1.65999e-05 | 0.00288091 | missense, intron-variant | NCK2 | GRCh38.p7 | 2:105881481 | ATGTGGCCGAGCGGG[A/G]GGATGAGTTGTCCCT | 8440 |
rs200637559 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105759472 | CAGGCTTTTATATAA[A/T]AAAACATATGGTATA | 8440 |
rs200650044 | in-del | -/C | 0.00993419 | 0.0697739 | intron-variant | NCK2 | GRCh38.p7 | 2:105754677 | CAGCTCCCCCAACAA[-/C]CTTTTTTTTTTTTTT | 8440 |
rs200692351 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105786855 | GCCCTGCTCCCACCC[G/T]AGCCTTAGGCTGACT | 8440 |
rs200741542 | in-del | -/ACACACTA | | | utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105894015 | CACACACACACACAC[-/ACACACTA]TATATATATATATTA | 8440 |
rs200765500 | in-del | -/GG | | | intron-variant | NCK2 | GRCh38.p7 | 2:105765783 | ATACAGCTTAGAATA[-/GG]GGGTGTGTGTGTGTG | 8440 |
rs200819431 | in-del | -/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105815449 | CTGTGAGTGAACTGT[-/C]AAGACAGATCCCCAT | 8440 |
rs200828017 | snp | G/T | | | utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105893735 | GGGCTGTGCTTGCAA[G/T]AAAGAATTTCCTGGA | 8440 |
rs200867156 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105892500 | TCAGAATCGTGGACT[A/C]CCTCCAGGTCTTTCT | 8440 |
rs200909126 | in-del | -/AT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105846489 | ACTGAAAAAAAAAAA[-/AT]AATAGGAGGGTGTAG | 8440 |
rs200948465 | snp | C/G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105765817 | TGTGTGTGTGTGTGT[C/G/T]TGTGTGTGTGTGTGT | 8440 |
rs200950807 | snp | C/T | 0.0004442 | 0.0148964 | intron-variant | NCK2 | GRCh38.p7 | 2:105882084 | AGCTCCGGCTGCAGG[C/T]AGTAAATGCGCCTTG | 8440 |
rs201031320 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105834652 | ATTTACATTAAAGGG[G/T]TTTTTTTTCAATTTT | 8440 |
rs201064545 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105846491 | TGAAAAAAAAAAAAT[A/T]ATAGGAGGGTGTAGC | 8440 |
rs201081835 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105822179 | GTGCAGTTTGGAGAG[A/G]TCTTTGGAAACGTAA | 8440 |
rs201083796 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105778915 | GGTTATTTTTTTTTT[A/G]AAGAGCTTTAAGAAT | 8440 |
rs201141545 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105867441 | AAAATAAATGTGGGT[G/T]TGTTTTTGTGTATCT | 8440 |
rs201216509 | in-del | -/TTAT | 0.00953873 | 0.0683987 | intron-variant | NCK2 | GRCh38.p7 | 2:105833573 | TTTGATATTCTGATA[-/TTAT]TTATTTGGCTTTTCT | 8440 |
rs201262001 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105875083 | GTCATGGCACAGTTG[A/G]TGGCTGGTCTTTAAT | 8440 |
rs201271223 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105822178 | AGTGCAGTTTGGAGA[C/G]TTCTTTGGAAACGTA | 8440 |
rs201291166 | in-del | -/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105792614 | TTTGTTTTTTTTTTT[-/T]CCACCTTCCCCATGC | 8440 |
rs201294726 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105807793 | CCCTCCCTTCTCTCT[A/C]TCCCTCCCTCCCTTC | 8440 |
rs201337770 | in-del | -/TG | 0.00438332 | 0.0466095 | intron-variant | NCK2 | GRCh38.p7 | 2:105848942 | TTTTTTTCTACTAAC[-/TG]AACTCTAAACCAATT | 8440 |
rs201371399 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105891565 | TTTTTTTTTTTTTTT[G/T]TTTGAGATTTTTCGC | 8440 |
rs201405537 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105891568 | TTTTTTTTTTTTTTT[A/T]GAGATTTTTCGCTCT | 8440 |
rs201406196 | snp | A/G | 0.00199797 | 0.0315435 | missense, intron-variant | NCK2 | GRCh38.p7 | 2:105881388 | CCACGCCCAGCACGG[A/G]CGCCGAGTACCCCGC | 8440 |
rs201418674 | snp | C/T | 9.89201e-05 | 0.00703209 | missense | NCK2 | GRCh38.p7 | 2:105855080 | TGACAGAAGAAGTTA[C/T]TGTGATAGCCAAGTG | 8440 |
rs201469508 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105846478 | GGTAGATACTCACTG[A/G]AAAAAAAAAAATAAT | 8440 |
rs201469520 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105806845 | CAAAATTAAAAAAAA[A/C]CCCAACCAACCATCC | 8440 |
rs201506024 | in-del | -/A | 0.0216234 | 0.101706 | intron-variant | NCK2 | GRCh38.p7 | 2:105805908 | TATTTGCATAAACAT[-/A]AACGAGAGGTTTTGG | 8440 |
rs201532464 | in-del | -/C | 0.0217236 | 0.101931 | intron-variant | NCK2 | GRCh38.p7 | 2:105803620 | AAGCAAGTCCTCATG[-/C]CCCTGCATCATGTGC | 8440 |
rs201535720 | in-del | -/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105756348 | CAATCAATCTTTCCC[-/T]TTCTTCAGTCATCCT | 8440 |
rs201544529 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105812790 | TCTGCTCATTACTGA[A/C]GCCAGGTGACACTAT | 8440 |
rs201698859 | in-del | -/T | 0.00716266 | 0.059414 | upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105742991 | ACAATCAACTCTCTC[-/T]TTAAAAAAAAAAGGT | 8440 |
rs201705591 | in-del | -/T/TTA | | | intron-variant | NCK2 | GRCh38.p7 | 2:105832718 | ATTTTTTTTTTTTTT[-/T/TTA]GAGGATTTTTGCATC | 8440 |
rs201769136 | in-del | -/CATAGGCATAT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105871631 | CTCCCCAGTGGCTAT[-/CATAGGCATAT]GCCACCACACCCAGC | 8440 |
rs201775086 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105759469 | ATACAGGCTTTTATA[C/T]AATAAAACATATGGT | 8440 |
rs201795527 | in-del | -/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105748386 | TCTTTCCTGCAGTTG[-/T]TTTTTTTTCTTTTTT | 8440 |
rs201833577 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105777908 | GATTCCAGCAGCAGC[A/C]CCTTGGTTTCGCCTA | 8440 |
rs201862932 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105875973 | CTTGCTTTTTTTTTA[A/C]TTACTTTCATTCTTT | 8440 |
rs201874532 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105846488 | CACTGAAAAAAAAAA[A/T]ATAATAGGAGGGTGT | 8440 |
rs201881094 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105819916 | TGACTGTTGTAGCAG[G/T]TAAAAAAAAAATAGA | 8440 |
rs201886320 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105858057 | TTGGGGTTTTTTTTT[G/T]GTTTTTTTTTTTGCT | 8440 |
rs201888318 | snp | A/C/G | 0.000116069 | 0.00761723 | synonymous-codon, missense, intron-variant | NCK2 | GRCh38.p7 | 2:105881677 | GCTGAGCAATGGCCA[A/C/G]GGCTCCCGCGTGCTG | 8440 |
rs201933563 | in-del | -/ATAT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105844748 | TTGGGGCGGGGGGGG[-/ATAT]ATATATATATATATA | 8440 |
rs201989033 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105785011 | TGAGACGGAGTCTCG[C/G]TCTGTCGCCCAGGCT | 8440 |
rs201992587 | in-del | -/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105765988 | GGCAGCAGGTGACGC[-/T]TTACACTGCACAGGT | 8440 |
rs201994637 | in-del | -/G | 0.0263992 | 0.111815 | intron-variant | NCK2 | GRCh38.p7 | 2:105762912 | TTAAAAGCAACCTGA[-/G]GGCCAGGCGCAGTGG | 8440 |
rs202070326 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105763604 | TGTTCTGGGATCTGT[A/G]ATTATTTACTGTTAC | 8440 |
rs202096647 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105891566 | TTTTTTTTTTTTTTT[A/T]TTGAGATTTTTCGCT | 8440 |
rs202112973 | in-del | -/TCTC | 0.0146672 | 0.084371 | intron-variant | NCK2 | GRCh38.p7 | 2:105834272 | TTCTATTGGGGTCTA[-/TCTC]TCTCTTTAGCTCTAA | 8440 |
rs202137036 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105877803 | ATTGAATGGGAATTT[A/G]CTGGGAGTACAGTCT | 8440 |
rs202144192 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105750830 | TTTTTCTGAACCCTG[A/G]ATGAAGAGAGCAAAG | 8440 |
rs202148354 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105822180 | TGCAGTTTGGAGAGT[C/T]CTTTGGAAACGTAAG | 8440 |
rs202208091 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105755409 | AATTTGTTGCTTCTT[A/G]ACTTGATTGTGCCGA | 8440 |
rs367630081 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105890054 | TTCTTTTTCAGATTT[C/T]CTACAGAAAATCTAC | 8440 |
rs367648514 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105853303 | TATTTATTTTATTTA[G/T]TCAGCCACACTTTTG | 8440 |
rs367649163 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105799010 | TTTCATCAGTTTGAA[A/G]GCCTTATATTTTCTT | 8440 |
rs367654743 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | NCK2 | GRCh38.p7 | 2:105818162 | AAACCATCATTCTCA[A/G]CAAACTATCGCAAGG | 8440 |
rs367655106 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105783058 | TACCTGGGATATAAC[A/C]GTGGAACAAGATAGA | 8440 |
rs367667536 | snp | A/G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105810939 | TCAGCACTTTGGGAG[A/G/T]CCCAGGTGGGCGGAT | 8440 |
rs367670284 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105756406 | GAGAAATTAATAGTA[A/C]TTCTTTGCACAGACT | 8440 |
rs367698038 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105764363 | AATGCTTCCTTCTGC[A/G]GGGCTGTCTGAGCTC | 8440 |
rs367702463 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105814933 | ACAACACAACTTAAC[A/G]TTTATAATAGCCCCT | 8440 |
rs367714427 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105778667 | GAAATCATGCCCTTG[C/T]TACTGCACTGGTTAT | 8440 |
rs367720669 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105827443 | CAGTTGATAGAACAA[C/T]CACACAGAAAGTACA | 8440 |
rs367723398 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105760524 | CACACCTCTTCCCTG[A/C]TGGTGGCACCTAGCT | 8440 |
rs367723702 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105822787 | AGAATTTACAAAGGA[A/T]TTTTCGTGAATTCTC | 8440 |
rs367740675 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105804075 | TTGCCCATTTTTTAC[C/G]GGGCAAATTATATAC | 8440 |
rs367751146 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NCK2 | GRCh38.p7 | 2:105769067 | TCCCCTCCAGGCTAT[C/T]TAGGGGCACCCCCCA | 8440 |
rs367757764 | in-del | -/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105773691 | GAAGCAGCAGTCACC[-/C]ACTCAACAACTATTT | 8440 |
rs367761173 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105813099 | AGACAAGTGTGCATT[C/G]AAATTCTGGTTGTGA | 8440 |
rs367795598 | in-del | -/CCTT | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105836625 | TTGTTCTAGGGGAAG[-/CCTT]CCTTCTGTGCTGGAC | 8440 |
rs367826631 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105884943 | AAATCCAGAAAACTC[A/G]GAAATCCTACTCACC | 8440 |
rs367841392 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105838293 | CAAATTTTTAAATGC[C/T]GGAATTTTATTAAAA | 8440 |
rs367845810 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105822256 | CTGGGAACCTGAATC[C/T]CCCGAGGGCCTCTGC | 8440 |
rs367890932 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105873045 | GCCAGGAAAGGTCAC[C/T]GTCCTTCCATATCCC | 8440 |
rs367905129 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105792921 | CCAGGTGAGGAGAGT[A/G]CTTGTCAGCTATTAC | 8440 |
rs367926950 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105857832 | TATCTCAGCATGAGT[G/T]TTCCCTTGCCCTGTT | 8440 |
rs367931132 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105806800 | AGCAAATCCCATTCC[A/G]TAGGGGGCTTCGCAG | 8440 |
rs368092882 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105879554 | CTGGCTTACTCTTGT[A/G]TTTCCCATGCACATG | 8440 |
rs368104323 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105852100 | GACCACGCATCGGAC[A/G]GTTGGGCGGGTCGGG | 8440 |
rs368158634 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105783807 | CTTCCCCACAGAGAG[A/G]GTTTTGCAGCTGGAA | 8440 |
rs368161463 | snp | A/G | 1.65696e-05 | 0.00287828 | missense | NCK2 | GRCh38.p7 | 2:105855182 | CCAAGACGTGGTGGC[A/G]GGTGAGGAACGCGGC | 8440 |
rs368174126 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105825278 | TGATCTTCCCTAAAG[G/T]GGCCTTCTACTCTAA | 8440 |
rs368180084 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105834134 | TTAGATGAAATTTTC[G/T]GTAAATGTCTGTTAG | 8440 |
rs368197614 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105861735 | GGCCAGGCTGGTCTC[A/G]AACTCCTGACCTCAA | 8440 |
rs368237045 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105846610 | AGTACAAATACTGTT[C/G]AGTTAAGAAATTGAT | 8440 |
rs368248740 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105792623 | TTTTTTTCCACCTTC[C/T]CCATGCCAGTTGATT | 8440 |
rs368250747 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105815616 | CCACAACCAGGAGGG[C/T]GCTGGTCACCTTTGT | 8440 |
rs368285147 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | NCK2 | GRCh38.p7 | 2:105789701 | GAGGACCTTGCTCCC[C/T]GGCTTGTGATTCTCA | 8440 |
rs368295909 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105833460 | TTACTTGTTTTCCTT[C/G]GGTTTTCTAAGTTAT | 8440 |
rs368300274 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105838767 | ATGGAGGCCGACCGT[A/G]GGCCTTTCATCCACT | 8440 |
rs368302246 | snp | A/G | | | upstream-variant-2KB, intron-variant | NCK2 | GRCh38.p7 | 2:105851388 | CCTGCCTCAGCCTCC[A/G]GAGTAGCTGGGACTA | 8440 |
rs368379013 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105797843 | GCACAGAAAAAAAAC[C/T]CTTTCAGCAATTTGG | 8440 |
rs368380822 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105842071 | AAGGGAAAGTAGTAA[C/T]AGTATTTGTGGGGGT | 8440 |
rs368384991 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | NCK2 | GRCh38.p7 | 2:105891062 | ACCAGCCCTGCCTCG[C/G]AGAGCACATGCTCAG | 8440 |
rs368388967 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105824718 | GCTGGGTTTTAACTT[A/C]CGGCCTTGGTTCCTT | 8440 |
rs368417738 | snp | A/C/G | 6.05851e-05 | 0.00550359 | missense, intron-variant | NCK2 | GRCh38.p7 | 2:105882035 | GACTTCCTCATTAGG[A/C/G]ACAGCGAGTCCTCGG | 8440 |
rs368419113 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105750601 | AGCTCTTTATATATT[A/G]GTTGTAGCACCCCAT | 8440 |
rs368435827 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105824920 | ACTGCAGTAAGATCA[A/G]GAGCCCATCTCCCAC | 8440 |
rs368455427 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105789430 | CTGGCCTCAAGTGAT[A/C]CACCCGCCTCGGCCT | 8440 |
rs368474261 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105817862 | CAACCATTGTGGAAG[A/T]CAGTGTGGCGATTCC | 8440 |
rs368480173 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105863886 | CTGTATAACGGGATA[C/T]GTGACTGCTTGTCTC | 8440 |
rs368606023 | in-del | -/TTCC | | | intron-variant | NCK2 | GRCh38.p7 | 2:105807731 | TCCTTCCTTCCTTCT[-/TTCC]TTCCTTCCTTCCTTC | 8440 |
rs368661979 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105886516 | CCCTCTGAGTCCTTT[C/T]TTTGTTCCAAATCCT | 8440 |
rs368662562 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105822442 | TTTGTATTTAACAGC[C/T]ACTTCCTGTGTGCTG | 8440 |
rs368706967 | in-del | -/AT/ATAT | 0.49998 | 0.00319482 | intron-variant | NCK2 | GRCh38.p7 | 2:105844747 | TTGGGGCGGGGGGGG[-/AT/ATAT]ATATATATATATATA | 8440 |
rs368732142 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105858999 | ATCCAGTTGATGTTT[C/T]TGAAGGGCTCAGACT | 8440 |
rs368732656 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105835377 | TTTATATATATATAC[A/G]TATATATACACATAT | 8440 |
rs368734249 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105824592 | CGTTTTTGTAATACA[C/T]TGGTCATTTTCCCAG | 8440 |
rs368760868 | in-del | -/T | | | utr-variant-5-prime, intron-variant | NCK2 | GRCh38.p7 | 2:105851854 | GGGCGTCAGTGCAGT[-/T]AAGTGAGCGAGCCGG | 8440 |
rs368813139 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105871980 | TTGGTGCCCAAAAGG[A/G]ACATGGAAGACTGGG | 8440 |
rs368821936 | snp | C/T | 0.000696837 | 0.018653 | intron-variant | NCK2 | GRCh38.p7 | 2:105882093 | TGCAGGCAGTAAATG[C/T]GCCTTGCGCGGTGGG | 8440 |
rs368822962 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105830280 | TCTCTACTTTTATGC[A/G]TCAGCTTTTGTAGCT | 8440 |
rs368920012 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105768439 | TCCCCATTTCCGTCA[C/T]CAGTTGCATGTCCTA | 8440 |
rs368926554 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105826581 | ACTAATAAAGCAAGA[A/G]TTTCTTATTCCCAAA | 8440 |
rs368936828 | snp | C/T | 3.31312e-05 | 0.00406995 | synonymous-codon, intron-variant | NCK2 | GRCh38.p7 | 2:105881518 | GGGGTCGCGCGTCAC[C/T]GTCATGGAGAAGTGC | 8440 |
rs368955011 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105751915 | AATCATAATGTTCTG[G/T]TAGCCACATTAAAAA | 8440 |
rs368999483 | snp | C/G/T | 0.000201111 | 0.010026 | intron-variant | NCK2 | GRCh38.p7 | 2:105855306 | TGAGTGTTTCACCCT[C/G/T]GAGAGAGGAAGCCTT | 8440 |
rs369016881 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105776998 | GCTGGACAGCCAAAG[A/G]CATCTTCCCCAGAGA | 8440 |
rs369023378 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105860062 | GGCTGAGGTAGAAGG[A/T]TCAGTTGAGGCCACG | 8440 |
rs369061866 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105829297 | GCCATTGCCTTTTCC[C/T]CCAGAAGTTATTTTA | 8440 |
rs369065415 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105812491 | CTCAGACAGCGCTGA[A/C]CCCGTGCTGTGTTGG | 8440 |
rs369122268 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105794007 | TCACATTGATACTTA[C/T]AACTCAAAATTAGGA | 8440 |
rs369160291 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NCK2 | GRCh38.p7 | 2:105831380 | CTTGACTGGAAAATA[C/T]GCTACAAAGCTACCA | 8440 |
rs369171347 | in-del | -/ACACACAC | | | intron-variant | NCK2 | GRCh38.p7 | 2:105864829 | CTCACATGTGCATGT[-/ACACACAC]ACACACACACACACA | 8440 |
rs369174350 | in-del | -/GTTTTTT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105829925 | ATTCATTCTCTTTTT[-/GTTTTTT]TGAGTTGATACATTT | 8440 |
rs369177334 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105795520 | TTAGAAAATACATGG[A/C]TATTCCTGTCTTATT | 8440 |
rs369185371 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105859089 | ACTCCACTTAGAAAA[C/T]TGTGCAGGCGAGGTG | 8440 |
rs369245379 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105855541 | GGGACCCCTGCACAG[G/T]TATCTCCTTGTATCA | 8440 |
rs369271463 | snp | A/C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105892000 | CTATGTTTAAAATGC[A/C/G]ACCGGAATTTTCCAC | 8440 |
rs369277997 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105823391 | GTGCTCCCCATTCCC[A/G]TGCTGCAGGTGCCTC | 8440 |
rs369281801 | snp | A/C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105818636 | TCCAACTTTTAGGTG[A/C/G]TATGTCTTCTGGTTG | 8440 |
rs369281842 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105865042 | GCTGGTGTCAGGGCC[A/G]CAGGCTCCCTCAGCC | 8440 |
rs369295762 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105865724 | TTGAGTTTAATCTGG[A/G]AGCAGTTTTGTCAGC | 8440 |
rs369311014 | snp | A/G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105831981 | GTAGATTGCTTTGGA[A/G/T]GTAATGGTCATTAAC | 8440 |
rs369332771 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105889418 | GCCGATGTTTGTTCC[A/G]GATTTTCTTTCTTCC | 8440 |
rs369355729 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105882663 | ATGAGGCCACTCGAC[G/T]GGGGCAGCAGACCCA | 8440 |
rs369374583 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105769868 | GCCTCTCCTCCTTCC[A/G]TGTGTGATGTTTCTT | 8440 |
rs369376720 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, utr-variant-5-prime | NCK2 | GRCh38.p7 | 2:105773279 | TTGCAGTTGTTTCTC[A/G]AATCCTCTAACACTG | 8440 |
rs369379486 | snp | A/C | 1.66261e-05 | 0.00288319 | missense, intron-variant | NCK2 | GRCh38.p7 | 2:105881628 | AGGCGGCTGCGGAGT[A/C]CCCAAGCTTCCTGAG | 8440 |
rs369402269 | snp | A/C | | | intron-variant, utr-variant-5-prime | NCK2 | GRCh38.p7 | 2:105746057 | CCAGGCACCTGACTT[A/C]AACTAGTATTGTAAC | 8440 |
rs369458008 | in-del | -/AAAA | 0.0228947 | 0.104514 | intron-variant | NCK2 | GRCh38.p7 | 2:105842488 | GAAAATATATACATT[-/AAAA]AAATAAAAATCTGAA | 8440 |
rs369519405 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105786343 | CTTGTTCCATTAGCC[C/G]TGGGAACGGCCAGTG | 8440 |
rs369524150 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105867533 | TACTTCGAGAGAAAA[C/T]AGACACGGATTGTCT | 8440 |
rs369533398 | snp | A/C | | | utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105893484 | CCCTCTTTAAAAAGA[A/C]GCAGGGCACCTGTGA | 8440 |
rs369542033 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105767885 | GCACTTAATAAATAC[C/T]AATTCCTTCCCTCTC | 8440 |
rs369612450 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105892921 | CACAAGAGATGTGGA[C/T]GGATTTAGACACAGC | 8440 |
rs369625436 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105752356 | GACACTCAGCACATG[A/G]TGTTTTAGAGCACTA | 8440 |
rs369678676 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105841490 | TCCAGGAACCTCCCC[A/G]TGTTCAGATATCTGG | 8440 |
rs369694991 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105879273 | TAGCCCTCACGCCCC[A/G]GCTTGCTAGCTGTTT | 8440 |
rs369710983 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | NCK2 | GRCh38.p7 | 2:105808035 | AGCCTCTTGAGTAGC[C/T]GGGACTACAGGTGTG | 8440 |
rs369714581 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105835455 | CATTTTGAATATATC[A/G]TAGTGAACTCTCCTG | 8440 |
rs369718903 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105776196 | CACTTCCTGTACGTT[A/G]CTACAGTGTCCTGGG | 8440 |
rs369723130 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105791008 | CAAGAGTTGGAAGGC[A/G]CTGCTTAGAGGTTGT | 8440 |
rs369724788 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105834917 | TCCTGGGCTCAAGCA[A/G]TCCTCCCATCCCAGC | 8440 |
rs369761479 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105829925 | ATTCATTCTCTTTTT[G/T]TTTTTTTGAGTTGAT | 8440 |
rs369767811 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105780688 | TATTTGGAGGTGGGG[A/C]CTTTGGGAGGTGATT | 8440 |
rs369783048 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105751430 | CCATGACCTGCACAC[A/G]GTGGCTCTCCATCGT | 8440 |
rs369796107 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105852844 | TTTCTGAAAGTGGAT[A/T]ACAAAATTGTCTCCA | 8440 |
rs369797825 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105783138 | GGTGGTTTAACTTTC[A/T]CTGCAGCACTGCTTT | 8440 |
rs369924010 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105783460 | AACAGCTCGATGCAG[C/T]GTTGCCTGTCTGAGC | 8440 |
rs369952542 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105826734 | GGCCAAGTAAGTATC[C/G]TTTCCTCTGAGCAGC | 8440 |
rs369955878 | snp | A/G | 0.000254814 | 0.0112846 | synonymous-codon, utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105893101 | CATGGACGAGCTGGT[A/G]GAACACTACAAAAAG | 8440 |
rs369958193 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105865688 | AGCTGAGTGTCATAG[G/T]AGTATACTCCTTTTC | 8440 |
rs369959872 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105853002 | TTATTTATAAAAAAA[A/T]TTTTTTAGCATCTAG | 8440 |
rs369974014 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105746771 | ATCCTACCTCAGTAT[A/G]TTCTGCCCTGGAGGT | 8440 |
rs369980011 | in-del | -/T/TT/TTT | 0.00953873 | 0.0683987 | intron-variant | NCK2 | GRCh38.p7 | 2:105871503 | GGTTTTTCTTTTTTC[-/T/TT/TTT]TTTTTTTTTTGAGAC | 8440 |
rs370096765 | in-del | -/AAC | | | upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105743078 | GGGTGGGAAGACAAC[-/AAC]CTCTCTAGAGGAGGC | 8440 |
rs370105583 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105859584 | TAATGCTAACTGTGA[A/G]ACAGCCTTTGCACTG | 8440 |
rs370214981 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105785107 | CCTCAGCCTCCTGAG[C/T]ACATGGGACTACAGG | 8440 |
rs370226892 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105759170 | TTGGGCCTTCAGAAG[A/G]AGAGAATTTCACGTG | 8440 |
rs370241867 | snp | C/T | 0.000153988 | 0.00877328 | missense, intron-variant | NCK2 | GRCh38.p7 | 2:105881973 | ACTACGGGAACGTGA[C/T]GCGGCACCAGGCCGA | 8440 |
rs370269248 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105771016 | CAAGCTCTGCCTCCC[A/G]GGTTCACGCCATTCT | 8440 |
rs370283780 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105873680 | TTTGGGGGCTCTTAA[C/T]TGAAGAGACTGAAAG | 8440 |
rs370307444 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | NCK2 | GRCh38.p7 | 2:105810323 | AAGTGTGTGTGTGTG[A/T]GAGAGAGAGCGAGCG | 8440 |
rs370323661 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105875385 | CCCAGTCCCCTGGGC[C/T]GTACACACATGGAAT | 8440 |
rs370389100 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105781392 | TTCCCACACTGCAAG[A/G]CTTGACTAAATGCAA | 8440 |
rs370410105 | snp | C/T | 0.0325976 | 0.123435 | intron-variant | NCK2 | GRCh38.p7 | 2:105832464 | TAGCTGTGCATCTGT[C/T]GTTAAGGCTCGTATT | 8440 |
rs370419530 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105796492 | TGGAGCAGGGAGCAC[A/T]TGGGGTATTATTGGC | 8440 |
rs370420780 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105889341 | ATCATGGGCTGCTTT[G/T]CCCATAAATGGCATT | 8440 |
rs370439183 | in-del | -/GA | | | utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105894099 | AGTAAGAGACACACA[-/GA]ATGTTTATGAAGAAA | 8440 |
rs370446000 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105824010 | AGTCTGCAGTGGTGA[C/T]GTCCCTCTTGAGTGT | 8440 |
rs370459853 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105884027 | ATCTTGCCGTGACAC[A/G]GGCCATTTTCAGCTG | 8440 |
rs370479422 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105857855 | GCCCTGTTGAGCTGC[A/G]TCCAGTGGAAGAGGA | 8440 |
rs370482158 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105837898 | GACTGTGTATTTTGC[C/T]TGCTGCCTAATTGAG | 8440 |
rs370529360 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105792355 | GCAGTTATCAATTAA[A/T]GGCCAATCCTTTATC | 8440 |
rs370530184 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105868572 | GTAAACATGCAGTTC[A/G]TTCTAATGCTGCTAA | 8440 |
rs370557834 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105827234 | TCGATCTCCTGACCT[C/T]GTGATCTACCCGCCT | 8440 |
rs370610520 | snp | A/C | | | upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105743931 | AATCAGAATCATTTG[A/C]ATATTAGGATTTCCT | 8440 |
rs370653325 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NCK2 | GRCh38.p7 | 2:105748769 | TTCTGAACCGCTTGG[A/G]GGCAGACTGGTCTTG | 8440 |
rs370785605 | snp | A/G | | | utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105893818 | TAATTTACCCCAAAT[A/G]TGCCATCCACATAGT | 8440 |
rs370835032 | in-del | -/GT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105835376 | TTTATATATATATAC[-/GT]ATATATATACACATA | 8440 |
rs370856689 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105875954 | CATGTCTATGAAACA[A/G]CATCTTGCTTTTTTT | 8440 |
rs370889529 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105883296 | TTTAGATCGTGTTTG[A/C]AGCCTTAAGCAAATT | 8440 |
rs370891315 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105836759 | GTGGATACGGTGAGA[C/T]GTTGACAGGACCCCA | 8440 |
rs370892024 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105871685 | TTTTTAGTAGAGACG[A/G]GGTTTCACCATTTTG | 8440 |
rs370900779 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105806333 | AGCTCCGCCTCCCGG[A/G]TTCACGCCATTCTCC | 8440 |
rs370923694 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105885877 | TCTTGAAGTATATTT[C/G]TGTTGAGTTTTTTGG | 8440 |
rs370944534 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105837586 | TGCATGTCCCTGAGG[C/T]ACAGTGCAAGAGTTT | 8440 |
rs370986212 | in-del | -/ACAC/ACACACAC | | | intron-variant | NCK2 | GRCh38.p7 | 2:105750037 | CTCAAAAGCAAACAA[-/ACAC/ACACACAC]ACACACACACACACA | 8440 |
rs370997190 | in-del | -/AACTT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105755409 | AATTTGTTGCTTCTT[-/AACTT]GATTGTGCCGAGCAC | 8440 |
rs371017821 | snp | C/G | 0.000275665 | 0.011737 | synonymous-codon, utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105893143 | CACCAGCGAGCACGG[C/G]GAGAAGCTCTACCTC | 8440 |
rs371053834 | in-del | -/AAAG | 0.00398564 | 0.0444627 | intron-variant | NCK2 | GRCh38.p7 | 2:105784823 | TCTTAGAATATGCAC[-/AAAG]AGTGTGTCCTCAGAT | 8440 |
rs371092152 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105788271 | TTTGTGCCCTTGAAA[C/G]TTCTACACCCATAAA | 8440 |
rs371117371 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105778884 | CACACCACTATACCA[A/G]GCTAATTGAGATAAT | 8440 |
rs371130735 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105766930 | TCCTGCTGCCTGTGC[A/G]GTGTTGGTGAAACTC | 8440 |
rs371161239 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105823645 | AGATGCCAGTTTTGG[A/G]TGGAAACGAATAACC | 8440 |
rs371201340 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105770740 | TAAACTTAAAGATCT[C/T]TAACAGGTCAAGAAA | 8440 |
rs371236589 | snp | C/T | 0.000153988 | 0.00877328 | missense, intron-variant | NCK2 | GRCh38.p7 | 2:105881864 | AACTACGTGGTGGTC[C/T]TCAGTGACGGGCCTG | 8440 |
rs371240087 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105857089 | ATGAAGTGCTTAGAG[A/G]CTTGTAGGAAGTAGA | 8440 |
rs371262662 | snp | A/C/G | 4.03749e-05 | 0.0044929 | synonymous-codon, utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105893119 | ACACTACAAAAAGGC[A/C/G]CCCATCTTCACCAGC | 8440 |
rs371283355 | snp | C/T | | | utr-variant-5-prime, intron-variant | NCK2 | GRCh38.p7 | 2:105851862 | AGTGCAGTAAGTGAG[C/T]GAGCCGGACGTCGAT | 8440 |
rs371293966 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105875599 | TTCGTGCCCTTATAA[A/G]AGAGACCTCAGAGAG | 8440 |
rs371296417 | in-del | -/TC | | | intron-variant | NCK2 | GRCh38.p7 | 2:105765803 | GTGTGTGTGTGTGTG[-/TC]TGTGTGTGTGTGTCT | 8440 |
rs371297586 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105809437 | GGGCCTTTCTCCAGC[G/T]CTTGCAGACAGATGC | 8440 |
rs371308444 | snp | C/G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105820670 | GCACTTAATTCTTCC[C/G/T]GTGTGTACTTGAAAA | 8440 |
rs371324351 | in-del | -/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105790557 | CTGGTTTCCTAGGCC[-/C]TTTGAGAAGTGTGCC | 8440 |
rs371354872 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105840667 | ATTCTGGCTATAAAC[G/T]GGGGTTCCCATGTTG | 8440 |
rs371364187 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105883879 | AAAGTCAAGGAACAA[C/T]ATATATGATTCTAGG | 8440 |
rs371374737 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105829926 | TTCATTCTCTTTTTG[C/T]TTTTTTGAGTTGATA | 8440 |
rs371375679 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105845652 | ACCCACCTCAGCCTC[C/T]CAAAGTGCCAGGATT | 8440 |
rs371416082 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105783074 | GTGGAACAAGATAGA[C/T]GGGGAAGCTGCCTTA | 8440 |
rs371424815 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105835387 | TATACATATATATAC[A/G]CATATATATATATAT | 8440 |
rs371468157 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105869206 | CCCTCTGGAGCTTTT[C/T]AGGGAGGATAGAGGT | 8440 |
rs371505263 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105756513 | AACTTTGTCAGGTAG[A/C]GGGAGGCCAGTGTTG | 8440 |
rs371518634 | in-del | -/TATATATATATATATATATATATATATATAT/TATG/TGTGTG | | | intron-variant | NCK2 | GRCh38.p7 | 2:105835393 | ATATATACACATATA[lengthTooLong]TATATATATATACGT | 8440 |
rs371525998 | in-del | -/TA | | | intron-variant | NCK2 | GRCh38.p7 | 2:105826805 | CATTTTATATATGTG[-/TA]TATATATATATGTAT | 8440 |
rs371565138 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105782284 | TGTAGATGGATGGAT[G/T]ATCAGGCACATCCTG | 8440 |
rs371594928 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105786677 | TGGCCTGGCCTGACT[C/G]TCCTGGGTCCCCGGG | 8440 |
rs371601149 | in-del | -/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105840865 | ATGAACAGCTGTTAC[-/C]ACCATTATGCATCAG | 8440 |
rs371620065 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105782728 | GCAAAATGGGCTGCA[A/G]CTGCCTGTAGAGGCG | 8440 |
rs371664451 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105807280 | CTCTCTAAGATTCAT[A/G]GGTGGTTCTAAAATC | 8440 |
rs371679145 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105770458 | TCTTACAACTAAGAA[C/G]GCCTGAAACTTACTG | 8440 |
rs371695948 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105765702 | ATGTTCCTTAAAGAC[A/G]TTTTCAGAAACAGTT | 8440 |
rs371772351 | multinucleotide-polymorphism | AC/GG | | | intron-variant | NCK2 | GRCh38.p7 | 2:105760625 | CTTTGTATCAACCAA[AC/GG]GTCTTTGCTTTCTGG | 8440 |
rs371902771 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105887911 | GTACCCACTTATCGC[A/G]AGCACAAATTGCAAA | 8440 |
rs371908198 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105838783 | GGCCTTTCATCCACT[C/G]TCTCTTTCACATGTT | 8440 |
rs371941795 | snp | A/G | | | upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105744303 | GGAAAGTAAATAGAT[A/G]CAAAGCAAATAAATA | 8440 |
rs371945251 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105810928 | CACCTGTAATCTCAG[C/T]ACTTTGGGAGGCCCA | 8440 |
rs372008521 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105891115 | TCCTGCCCCCACACG[C/T]ACTTATACATTCACA | 8440 |
rs372072439 | snp | A/G | 4.96504e-05 | 0.00498224 | synonymous-codon, utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105893011 | CGTGTCCCTTAAAGC[A/G]TCAGGGAAGAACAAA | 8440 |
rs372077930 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105876375 | CATGGGTGAGGACCC[A/C]CCTACCTCACGTCTC | 8440 |
rs372122827 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105848392 | GTAATTTCAACGGTC[C/G]GAAGAGAGTTTACCG | 8440 |
rs372185882 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105829753 | TGACTCCCTCTCCCC[C/G]TTTCCCTATGTACTC | 8440 |
rs372186694 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105835419 | TACGTGTATATATAT[A/G]TATATTTTTTTTTTG | 8440 |
rs372253437 | snp | A/C | 0.0119091 | 0.0762411 | intron-variant | NCK2 | GRCh38.p7 | 2:105892796 | GGTTGCAGTGAGCCG[A/C]GATTGGGCCACTACA | 8440 |
rs372300211 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NCK2 | GRCh38.p7 | 2:105835159 | TTATGTTTTCGCACT[A/G]CCAGTGAGTTTTATA | 8440 |
rs372304560 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105864523 | AGGTTAGGGTGGGAC[A/G]TCAGTAGGATGCAGA | 8440 |
rs372358059 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105810277 | TCTCACCTTCTGGCC[C/T]GCTTCTTAAGATGCT | 8440 |
rs372366423 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105878250 | ATAGCATCAGCTGAA[C/T]GCTGGTGCCTGTCAT | 8440 |
rs372369152 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105872308 | GCCTGCCCTGTGCCC[C/T]TGCTGTTCACAGTGT | 8440 |
rs372379191 | snp | C/T | | | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105771654 | GAAAGTAATGTTCTT[C/T]TCTTATCAATAGAAG | 8440 |
rs372379552 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105833084 | CCTCCCCTCTTTTTT[C/T]TTTTCTTTTTCTTCT | 8440 |
rs372486577 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105786411 | GGAGTGTTGTCTTGG[A/G]CCTGTCTGGAAAGGT | 8440 |
rs372490645 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105770954 | TTGAGACGGAGTCTC[C/G]CTCTGTCGCCCAGGC | 8440 |
rs372525810 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105820789 | TTTTGAAAAGCTTTT[A/G]GAGGCTTTTTCATGA | 8440 |
rs372544766 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105783023 | CAACAGGTAAGCCTT[A/G]AGGCCAGAGCCTTTT | 8440 |
rs372559095 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105878927 | CCTCACCAAAGTCTA[A/G]TTTGCTGCCTGGTAT | 8440 |
rs372614133 | snp | C/T | 0.000360315 | 0.0134174 | intron-variant | NCK2 | GRCh38.p7 | 2:105882100 | AGTAAATGCGCCTTG[C/T]GCGGTGGGTCTGTGT | 8440 |
rs372642089 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105814648 | CAAAGCCCACTCATC[C/T]GGAGTCCAAGGCCTA | 8440 |
rs372650540 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105776098 | TACTGCAGGCCACCT[C/T]TGGGGGTGTGGGTGC | 8440 |
rs372651078 | snp | A/G | 3.32082e-05 | 0.00407468 | missense, intron-variant | NCK2 | GRCh38.p7 | 2:105881594 | TTCCCCTCCAACTAC[A/G]TCTTGGAGGAGGTGG | 8440 |
rs372656944 | in-del | -/TGTGTGTG | | | intron-variant | NCK2 | GRCh38.p7 | 2:105823133 | AAAGTCCTCTCATGC[-/TGTGTGTG]TGTGTGTGTGTGTGT | 8440 |
rs372666253 | snp | G/T | | | upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105744453 | CCCAGCAACTAGAGC[G/T]TCGTGATAAGAACAA | 8440 |
rs372706152 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105873805 | TTGGGGCCTGTCTCT[C/T]TGAGCCTCTCCCTGC | 8440 |
rs372773322 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105824626 | TTAAGTACCACGTCT[C/T]GGCGGCGTGTGCTTA | 8440 |
rs372821003 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105841359 | CTTCTGTGATTGAAT[A/G]TCTACCTCAGTCACT | 8440 |
rs372857911 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105849016 | ACATATGTATTTTTG[A/G]AATTTCAAGTTAATA | 8440 |
rs372870254 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NCK2 | GRCh38.p7 | 2:105749853 | CGTGTATTAGTCAGC[C/T]CCAGCTGCCTTAAGA | 8440 |
rs372901686 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105839629 | CATGGGGAGAATGAA[A/G]AGCTTAGTTTTAGAC | 8440 |
rs372931950 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105867579 | GGAGGACAAGGCAGG[A/T]GAGACCCTGGGAAGT | 8440 |
rs372983218 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105865200 | GCAAATGGGCCGTGA[C/T]AATTATTTCTCCTCG | 8440 |
rs372995719 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105826613 | TAGAGCCAAATTCCC[A/G]ATGGATTGCATGGTA | 8440 |
rs373017071 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105839896 | TCAGCAAGGGACAGG[C/T]AGCAGGGCTGTGTGA | 8440 |
rs373025110 | in-del | -/A | | | utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105894260 | TTGTAATAAAAAAAA[-/A]GTATTATGACAAGGC | 8440 |
rs373034023 | snp | C/T | | | upstream-variant-2KB, intron-variant | NCK2 | GRCh38.p7 | 2:105849839 | TCCTGACAGGTATGA[C/T]ATAAATATTCAGAGG | 8440 |
rs373049830 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105816728 | TTGATTTGTTGAATC[A/G]CATTAAATTTAAGCT | 8440 |
rs373062325 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105818942 | GTTATGCCCCTTTGA[A/T]GTGTGGTATTTAGAA | 8440 |
rs373072982 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105803388 | AATTAGGCTGAGCTC[C/T]TTAAGAAGGGCCACT | 8440 |
rs373090752 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105747334 | CCTTGCATGTGCACA[A/G]ACTGGATAACCTTTT | 8440 |
rs373108494 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105866432 | AACAGCAGTCCCCAA[A/G]CTTTTTGGCACCAGG | 8440 |
rs373152665 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105827279 | GCTGGGTTTACAGGC[A/G]TGAGCCACCGCGCCT | 8440 |
rs373181639 | in-del | -/CGTG | | | intron-variant | NCK2 | GRCh38.p7 | 2:105835406 | ATATATATATATATA[-/CGTG]TATATATATATATAT | 8440 |
rs373188176 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105847944 | TATTGGGATCTCTTC[A/G]TAAAACCTCACAGAA | 8440 |
rs373193516 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105867705 | GGGTGAGAGCCAGTC[A/G]TGTCCTGGTGAAAGG | 8440 |
rs373215267 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | NCK2 | GRCh38.p7 | 2:105815369 | ACTAAAATAGAATTC[A/G]ATTTTTCTATGGGGT | 8440 |
rs373232152 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105870521 | AGCACAGTGGGAGGC[C/T]GAGGTGGGCAGATCA | 8440 |
rs373241447 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105854748 | TACTTAATGAAATGG[A/G]CTCATTTAATTATAA | 8440 |
rs373267496 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105820261 | TTTGCCATTTGGTCG[A/G]TGGTCCTTGAAGTGC | 8440 |
rs373306339 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105813948 | TACTTTTAGAGAAAA[G/T]CACACACTCCTTCTG | 8440 |
rs373327851 | in-del | -/AA | | | intron-variant | NCK2 | GRCh38.p7 | 2:105770125 | AAAGCACTAATAAGT[-/AA]AAAAAAAAAAAAAAA | 8440 |
rs373338485 | in-del | -/TTC | 0.00636936 | 0.0560724 | upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105743407 | GACTGATGACTAGAA[-/TTC]TTCTTTTCTTATTGT | 8440 |
rs373385920 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105762481 | TCCCAGGGTCTTGAC[A/G]TAGTGTGAAGTTCTG | 8440 |
rs373405658 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105762941 | GGCTCACGCCTGTAA[C/T]CCTAGCACTTTGGGA | 8440 |
rs373409605 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105816003 | CACCTGCTGTTCACC[A/G]GGTGTGTGGTTGGCC | 8440 |
rs373410068 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105780786 | CTCACCCCTTCAGCA[C/T]GTGAGGACACAGCAA | 8440 |
rs373413217 | snp | A/G | 0.000153988 | 0.00877328 | missense, intron-variant | NCK2 | GRCh38.p7 | 2:105881654 | CTGAGCCTGCGCAAG[A/G]GCGCCTCGCTGAGCA | 8440 |
rs373419457 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105855345 | CAAGGGACACTGTTC[A/G]TCTTTCTAGTTAGTT | 8440 |
rs373421143 | in-del | -/TAT/TATTATTAT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105865902 | TCTTAAAGACAGAGA[-/TAT/TATTATTAT]TATTATTATTATTAT | 8440 |
rs373421358 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105767678 | CCAGAAGAAGAACCG[C/T]AGCCCCTAGTGTGCA | 8440 |
rs373430649 | in-del | -/TA | | | upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105742993 | AATCAACTCTCTCTT[-/TA]AAAAAAAAAGGTGCG | 8440 |
rs373451037 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105776230 | GGACACCCCAACTTC[A/C]GTCCCAGCGACAGAA | 8440 |
rs373471108 | snp | C/G | | | intron-variant, utr-variant-5-prime | NCK2 | GRCh38.p7 | 2:105746304 | GAAAGAAACAACCCT[C/G]AGAGGCCGGTGGGCG | 8440 |
rs373475850 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105819774 | CACAAAACCTTGATT[C/T]ACCTATTAAAATTTA | 8440 |
rs373481456 | snp | A/G | | | upstream-variant-2KB, intron-variant | NCK2 | GRCh38.p7 | 2:105850756 | AAATTTCAGTAGTCA[A/G]TTAGCTGGAATGCAT | 8440 |
rs373529013 | in-del | -/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105858047 | CTTTGTTTTTTGGGG[-/T]TTTTTTTTTTGTTTT | 8440 |
rs373543976 | in-del | -/A | | | intron-variant | NCK2 | GRCh38.p7 | 2:105847330 | GGGTGAAAAAAAAAA[-/A]GAATATGGTTAAAAT | 8440 |
rs373546010 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105866007 | GCAACCTCCGCCTAC[C/T]AGGTTCGAGCAATTT | 8440 |
rs373557822 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105844770 | TATATATATATATAT[A/G]TATGTATGTATATAT | 8440 |
rs373564375 | snp | A/G | | | utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105893854 | TTCCTCTTGCCCTTC[A/G]GCTTGTTTGAATCTC | 8440 |
rs373599940 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105857994 | CCCTCCTGCCTCTCA[G/T]TAGTTGCATTTGTGT | 8440 |
rs373600137 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105821871 | TCCCCATCTATTAAC[A/G]GCAGCCCGGGAAGCA | 8440 |
rs373606612 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105769829 | GAGAAAAACTCAGAT[A/T]TTAATCCCTCGGAGT | 8440 |
rs373629423 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105871325 | GCTGTCAGGCGCTGC[A/G]CCACGTTATTGTAGT | 8440 |
rs373672266 | snp | A/G | 0.000144082 | 0.00848647 | utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105893227 | ACGGTGGAGCTGCCC[A/G]CCCGGCCTTGTGGCA | 8440 |
rs373717589 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105884097 | CCCTGAGGTGTGTGT[C/G]TGGCTTCTTTTCTCC | 8440 |
rs373730963 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105864425 | TTAGAATGACTCAAG[A/C]GTTTCCAGCCTGAAG | 8440 |
rs373731108 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105844405 | ATGTAATATGTTAAT[A/G]ATAAAGGAACCTATT | 8440 |
rs373771333 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105781480 | TTCTAGTCCATGTAC[A/G]TCTGTTTCGTAATAT | 8440 |
rs373783713 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105877068 | AGAAGGACAAGGGAT[C/G]GCTGAGTCCCCTAAG | 8440 |
rs373790029 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105746534 | GCGTGTGAACACTCC[C/T]TCAATTCACTTTGCA | 8440 |
rs373793071 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105808828 | GGAATTGGTAATGAT[A/G]TGGGGTGTGATACTG | 8440 |
rs373804908 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105786848 | TCTACCAGCCCTGCT[C/G]CCACCCTAGCCTTAG | 8440 |
rs373817458 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105766975 | GATGTGAAGAGACAC[A/G]CTTGGGAGGAACTCT | 8440 |
rs373828898 | in-del | -/AAGG | | | intron-variant | NCK2 | GRCh38.p7 | 2:105879834 | CCTTTACTCTAGTTT[-/AAGG]AAGAAAAGGAGAAAG | 8440 |
rs373848095 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105889054 | TCTAGAAAGCCAACC[A/G]TGGAAGGACTGCAAC | 8440 |
rs373850480 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105839096 | GGGACATTTGAATGG[A/C]GGCTTGAACAAAGTA | 8440 |
rs373866168 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105757397 | ATGGGATGAACTGAT[C/T]TATGTGTAAATTGAT | 8440 |
rs373945727 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105806550 | GCCACATATATTCTC[A/T]TCATTCATCAGTGGA | 8440 |
rs373961795 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105760293 | TGCCCCAGCATGGGG[G/T]TTCCAGAATGTGGTC | 8440 |
rs373976163 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105840948 | ACAGATCATTCTTAA[A/G]TAAATCCTTTCCTGG | 8440 |
rs373985890 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105801640 | CCTCCTGCTTGGCTT[C/T]TTACCTACCCTGTGA | 8440 |
rs374042914 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105857145 | GACCTGGAAATTCCC[C/T]TGAAAACCTTGTCAG | 8440 |
rs374086685 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105876639 | CTGTCTTGTTGAGAA[A/G]ATATGTTAAAATTCT | 8440 |
rs374108600 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105868642 | TAAGAAACTTCATTC[A/C/G]GTGGCGAGAAAGGTT | 8440 |
rs374110195 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105818142 | AGGGACATGGATGAA[A/G]CTGGAAACCATCATT | 8440 |
rs374113574 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105782798 | TAGGCTTGTGCTCAG[C/G]TCTGGCAGCCACAGC | 8440 |
rs374124949 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-5-prime | NCK2 | GRCh38.p7 | 2:105773358 | ACCTGTCTTCTCGCC[A/G]TCTGGTACACGTGCC | 8440 |
rs374160036 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105779306 | GGCGAGACTCCGTCT[A/C]AAAAAAAAAAAAAAA | 8440 |
rs374177160 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105782312 | CTGCTGATGGCTTCC[A/G]CCAGCCCATGGGGAT | 8440 |
rs374181605 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105791643 | GACTCCATAATAGAT[C/T]TGATCATAGTGACCT | 8440 |
rs374190910 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105788456 | GTCATACTCTATCCA[A/G]ATGAACTTTTCTCAT | 8440 |
rs374192310 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105780321 | AATATGGGAGAGAGA[G/T]ATATACACACACACA | 8440 |
rs374196830 | snp | A/G | | | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105772739 | AAACTCTTCTTTCTG[A/G]AATTGACTTCTTCTC | 8440 |
rs374284772 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105758753 | AAATTCTTGACTTCT[A/G]CACAGTAGTCAAGAC | 8440 |
rs374321547 | snp | C/T | 0.000153988 | 0.00877327 | utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105893183 | CTGCAGTGACGGCGC[C/T]CCGGCCCCACACTCG | 8440 |
rs374337476 | in-del | -/CCTC | | | intron-variant | NCK2 | GRCh38.p7 | 2:105861904 | GGCCTGGAATTCTTT[-/CCTC]CCTCCCTCCCTCCCT | 8440 |
rs374403213 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105791824 | CCACTCAATATTTTC[A/G]TATCTGTTGTATATT | 8440 |
rs374410946 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105841114 | ACCTACCCAGAGATG[A/C]CTGCATAATTGTCTC | 8440 |
rs374498098 | in-del | -/C | 0.00676609 | 0.0577691 | intron-variant | NCK2 | GRCh38.p7 | 2:105890632 | TTGGTCTATTTGAGA[-/C]CAGAGGCATGCATAA | 8440 |
rs374502484 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NCK2 | GRCh38.p7 | 2:105779052 | TGGCTCACACCTGTA[A/G]TCCCAGCACTTTGGG | 8440 |
rs374504585 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105789384 | GTAGAGATGGGGTTT[C/T]GCCATGTTGGCCAGG | 8440 |
rs374552067 | snp | C/G | 1.84954e-05 | 0.00304095 | missense, intron-variant | NCK2 | GRCh38.p7 | 2:105881941 | GTCCAGCGGGCGCTT[C/G]GCGGGCAGAGAGTGG | 8440 |
rs374605465 | in-del | -/A | 0.00279162 | 0.0372561 | intron-variant | NCK2 | GRCh38.p7 | 2:105805515 | TTTAAAATTTCATTT[-/A]TTTTTAAAATTAAAC | 8440 |
rs374645392 | in-del | -/CCAG | 0.00874735 | 0.0655527 | intron-variant | NCK2 | GRCh38.p7 | 2:105749997 | TCACACCACTGCACT[-/CCAG]CCTGGGTGACAGCGT | 8440 |
rs374650580 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105793234 | TTTCTGGGAATGGGT[A/G]GAGAACTTCTGGAAA | 8440 |
rs374659020 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105767500 | GTTGGCAAAGTGGCC[C/T]ATGGACCAAATCCAG | 8440 |
rs374672675 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105833089 | CCTCTTTTTTCTTTT[C/T]TTTTTCTTCTTTTCT | 8440 |
rs374680074 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105784778 | GCCACTGTTCCAGGC[C/T]CGTGTTTCCCACACT | 8440 |
rs374692316 | snp | C/T | 3.26089e-05 | 0.00403774 | intron-variant | NCK2 | GRCh38.p7 | 2:105855304 | GGTGAGTGTTTCACC[C/T]TCGAGAGAGGAAGCC | 8440 |
rs374708207 | multinucleotide-polymorphism | AT/CC | | | intron-variant | NCK2 | GRCh38.p7 | 2:105779920 | CGCCTTCACCCTCTC[AT/CC]TCAGGATAGCGTGTA | 8440 |
rs374749844 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105861593 | AATCTCGGCTCACTG[C/T]AACCTCCACCTCCCA | 8440 |
rs374774441 | snp | A/G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105818283 | GGGCCTGTTTTGGGG[A/G/T]GGGGGGAGGGGGGAG | 8440 |
rs374776374 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105854160 | TGCGTTTAAGGTTCC[A/G]CTATGTCTTTTCATG | 8440 |
rs374778581 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105790678 | GGCCCTTAGTGCCTC[C/T]TTCCTCTGTTCTGGG | 8440 |
rs374786417 | snp | C/G | 0.000153988 | 0.00877328 | intron-variant | NCK2 | GRCh38.p7 | 2:105892978 | TGTTCTGTTTCCTCC[C/G]CAGCCCAGCGACTTC | 8440 |
rs374938275 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105848403 | GGTCGGAAGAGAGTT[C/G/T]ACCGGCAGCAGATTT | 8440 |
rs374941662 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105874102 | ATAGAACCATGACAT[G/T]AATCTCATGTGGCCG | 8440 |
rs374952006 | snp | C/T | 3.52137e-05 | 0.00419591 | intron-variant | NCK2 | GRCh38.p7 | 2:105892936 | TGGATTTAGACACAG[C/T]TCCCCGCTGTGGCCC | 8440 |
rs374968274 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105789038 | ATCTCCCCCTCCTCC[C/T]GATGCCCGCAGCCTC | 8440 |
rs374976479 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105865206 | GGGCCGTGATAATTA[C/T]TTCTCCTCGAGTGCC | 8440 |
rs375017425 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105749661 | TGCCTTTGCCGTGTC[A/G]CAGCTGTGTGTAGAT | 8440 |
rs375023073 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105885997 | TTAGGAGGAGGTAGA[C/T]TGTCAGAGCAATGTG | 8440 |
rs375031072 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105833156 | CTGGAGTGTAGTGGC[A/G]TGATCTCTGCTCACT | 8440 |
rs375062581 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105882297 | CACAGAGGTGGTTCT[C/G]CTTCTCTCCCAAGAT | 8440 |
rs375073356 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105808460 | CATTTACTAAATCAC[A/G]GATTAATCGGGTGGT | 8440 |
rs375097045 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105799985 | TTTCCTTTGGTCAGC[A/G]TAGCTTCTGGTAATA | 8440 |
rs375129659 | in-del | -/TT | 0.00557542 | 0.0525036 | intron-variant | NCK2 | GRCh38.p7 | 2:105760049 | ACTGTCAAGTGACTC[-/TT]TTCCCTTCTTTCCAT | 8440 |
rs375200499 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105767188 | ACCATTCCATATTCC[C/T]AGGTATATGCTTGTA | 8440 |
rs375239852 | in-del | -/TGTG | | | intron-variant | NCK2 | GRCh38.p7 | 2:105835417 | ATACGTGTATATATA[-/TGTG]TATATATTTTTTTTT | 8440 |
rs375247351 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105879048 | AAAGTGTCTTTATAA[C/T]GTATTGTGATGGCCA | 8440 |
rs375253240 | in-del | -/GT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105884088 | TGCAAGAGCCCTGAG[-/GT]GTGTGTGTGTGGCTT | 8440 |
rs375262738 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105883584 | AAAGGTGTTCTCCGG[A/G]GTTGCTGGCCTTAGG | 8440 |
rs375284076 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105750776 | GGTTTGTCTTTAATT[G/T]AGACCATGATAAAAT | 8440 |
rs375321440 | in-del | -/AG | | | intron-variant | NCK2 | GRCh38.p7 | 2:105854092 | TAAGGATAAACTGTC[-/AG]AGAATCACACAGTGT | 8440 |
rs375368741 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105812282 | TCATCTCCTTGGACA[C/T]CTTTGAGTTTCGGAT | 8440 |
rs375379779 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105774708 | AGTTGTCTGGGGCCT[C/G]GATGACGAAATCTGT | 8440 |
rs375395174 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105839069 | ATGAGAGAGGCAGGG[A/G]GAGCAAGGGAGGGGA | 8440 |
rs375398048 | snp | A/G | 9.93493e-05 | 0.00704732 | missense, utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105893054 | CAGCTCGTGGACAAT[A/G]TCTACTGCATTGGGC | 8440 |
rs375408325 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105822984 | GGGCCGGCCGTGTGG[C/T]GGATGTGTATGTAAG | 8440 |
rs375413276 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105783350 | GAGGAGACTTCCCTG[A/G]GCTTCCTTCCTCGGA | 8440 |
rs375415874 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105804549 | GCTTAATTGGATTTC[A/G]GCCCAGACACAGTAT | 8440 |
rs375422663 | snp | A/G | 3.32154e-05 | 0.00407512 | missense, intron-variant | NCK2 | GRCh38.p7 | 2:105881478 | CCTATGTGGCCGAGC[A/G]GGAGGATGAGTTGTC | 8440 |
rs375426212 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105758327 | TTTACAGGTTTGTTT[C/T]ATCCTATTGATGGTT | 8440 |
rs375461757 | snp | A/C | 1.7978e-05 | 0.00299811 | missense | NCK2 | GRCh38.p7 | 2:105855227 | ATGTACCGTCCAACT[A/C]CGTGGAGCGGAAGAA | 8440 |
rs375467746 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105761746 | TGAGCTGGGTATGGT[A/G]GCAAGTGCCTGTAGT | 8440 |
rs375508358 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105871684 | ATTTTTAGTAGAGAC[C/G]GGGTTTCACCATTTT | 8440 |
rs375512251 | snp | A/G | 0.000153988 | 0.00877327 | synonymous-codon, intron-variant | NCK2 | GRCh38.p7 | 2:105882013 | CAACGAGCGGGGCGT[A/G]GAGGGCGACTTCCTC | 8440 |
rs375512483 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105849303 | TGAGGCAGATGGATC[A/G]CTTGAGCCCAGGAGT | 8440 |
rs375525992 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105780810 | ACAGCAAGAAGCCGC[C/T]GTGTAGGAACCAGGA | 8440 |
rs375532933 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105833419 | CTTTCTGCTTCATTG[G/T]CAGCAAGTTATGTGT | 8440 |
rs375533115 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | NCK2 | GRCh38.p7 | 2:105891708 | ACTACCACCATGCCT[C/G]GCTAATTTTGTATTT | 8440 |
rs375598903 | in-del | -/TCTAC | | | intron-variant | NCK2 | GRCh38.p7 | 2:105888957 | TTAAATGTAGAGTAC[-/TCTAC]CATACTATCAGTACT | 8440 |
rs375611334 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105792745 | GAACCAGAGCCAGTC[C/T]GGTGCGATTTTCTGG | 8440 |
rs375693942 | in-del | -/TTCT | 0.00557542 | 0.0525036 | intron-variant | NCK2 | GRCh38.p7 | 2:105798375 | AGTCATTTTTTTTTC[-/TTCT]TTCAGTGTTCTCCTT | 8440 |
rs375726594 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105870985 | GAGCAGGGTCAGCGT[A/G]TTGTGTGCTTGGGAG | 8440 |
rs375745324 | snp | C/G | | | intron-variant, utr-variant-5-prime | NCK2 | GRCh38.p7 | 2:105746248 | GTGTGGGCAGGAGGG[C/G]GCCTAAAATATCGCA | 8440 |
rs375746848 | in-del | -/AG | | | intron-variant | NCK2 | GRCh38.p7 | 2:105770142 | AAAAAAAAAAAAAAA[-/AG]AAAAAGGTATATTGC | 8440 |
rs375753068 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105776970 | GGGGAGTGGCTTCAC[A/G]AGAGTGTGAAGGGCT | 8440 |
rs375754428 | in-del | -/CTC | | | intron-variant | NCK2 | GRCh38.p7 | 2:105861511 | GCCGTTGAGGTTTTT[-/CTC]TTTTTTTTTTTTTTT | 8440 |
rs375769001 | snp | A/T | | | intron-variant, utr-variant-5-prime | NCK2 | GRCh38.p7 | 2:105746143 | TTCAGGTTGGCAGAT[A/T]CCTCTTTATTTGGCT | 8440 |
rs375773927 | in-del | -/TACT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105853577 | AAGCACTTATTTTCT[-/TACT]GTCTCCATAGATTTG | 8440 |
rs375799675 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105857050 | TTTTTTTTTTTTTTT[G/T]TATTTACAAGATTCT | 8440 |
rs375814417 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105848204 | TCATTTAATCCTCAC[A/C]GAAGCTCTGACCCAT | 8440 |
rs375848411 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105871534 | AGAGTCTCCCTCTGT[C/T]GCCCAGGCTGGAGTG | 8440 |
rs375869622 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105868128 | TCCTGCATGGCCCAC[A/C/G]TGCTGCCTTGGTGTA | 8440 |
rs375882680 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105842902 | TGGTGGGGTGGGGGG[A/G]TTCTTACTGCTTGCC | 8440 |
rs375886135 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105852091 | CAAAATGCAGACCAC[A/G]CATCGGACGGTTGGG | 8440 |
rs375890921 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105871740 | CCTCAAGTGATCTGC[C/T]CACCTTGGCCTCCCA | 8440 |
rs375912698 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105783095 | AGCTGCCTTAGAATA[A/C]GAGTTGCAGAAGGCC | 8440 |
rs375918219 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105819595 | TGGTGAGGCAGGGGA[G/T]TGTGGCATGCTCACC | 8440 |
rs375926977 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105792352 | TCAGCAGTTATCAAT[A/T]AATGGCCAATCCTTT | 8440 |
rs375933987 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105886308 | GAAGTTTAGTGCTCA[C/T]CACCTGATTCTGATT | 8440 |
rs375939155 | in-del | -/A | | | intron-variant | NCK2 | GRCh38.p7 | 2:105752548 | CACCATAGGAAAGGT[-/A]AAAAAACAACATTGT | 8440 |
rs375984517 | in-del | -/A | | | intron-variant | NCK2 | GRCh38.p7 | 2:105845751 | TACCTTACAGCTGTG[-/A]AAAAAAAAATAGGAA | 8440 |
rs375989559 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105770888 | GCAATTCTGATGTTA[A/G]TATCATGATTTCTTT | 8440 |
rs376058366 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105751444 | CGGTGGCTCTCCATC[A/G/T]TACTTGGGTCAGTGA | 8440 |
rs376100088 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon, intron-variant | NCK2 | GRCh38.p7 | 2:105881866 | CTACGTGGTGGTCCT[C/T]AGTGACGGGCCTGCC | 8440 |
rs376115152 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105836904 | AATGGTCTTTCTAGA[A/G]TAAAACAACTGCATG | 8440 |
rs376130161 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105763605 | GTTCTGGGATCTGTG[A/C]TTATTTACTGTTACA | 8440 |
rs376132771 | in-del | -/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105795302 | GTGATATATTTTTAA[-/T]TTTTTTTTTTCCTCA | 8440 |
rs376146858 | in-del | -/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105797743 | CATGATCAGTTAAAA[-/C]AAAACACCTGATGTT | 8440 |
rs376168586 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105768700 | TTTTTCTCATCAGCT[A/G]CAGTTAATGTTAGTG | 8440 |
rs376202499 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105867048 | CTTTCTAAACTAAGC[C/T]GCTCTCCAAGGAACC | 8440 |
rs376217525 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105759917 | AAGGCCACCGAGGTA[A/G]TGTGCCATTTTGTAT | 8440 |
rs376244103 | snp | C/G | | | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105772948 | CCAGGCTGGAGTGCA[C/G]TGGTGTGATCATGGC | 8440 |
rs376270850 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105765747 | TTTTCACACCCGTAA[A/C]AGGCAGATAGCCTCC | 8440 |
rs376276729 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105777460 | GCTCACCACCTGGCA[C/T]GGCGTGGGTGGAGAG | 8440 |
rs376311265 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105792583 | AGCTGAATGATCTAT[A/T]GATTTGTCCAAACTC | 8440 |
rs376323437 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105779420 | TTAATTAACTAAAGG[A/G]GATACTTTAAGTTGA | 8440 |
rs376324909 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | NCK2 | GRCh38.p7 | 2:105869115 | TAGACCCACAGTGCT[C/G]CCCCTAGCCTGTTCA | 8440 |
rs376355291 | snp | C/T | | | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105771993 | ATTGGATATTGTCGT[C/T]AAAGTGTCCAGGAAC | 8440 |
rs376363279 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105835391 | CATATATATACACAT[A/G]TATATATATATATAC | 8440 |
rs376393379 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105831352 | AAAAGAACAAAGCTG[C/G]AGGCACATGGTGCTT | 8440 |
rs376486099 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105782699 | TGGGGGATCCGGCCC[A/G]TTGAAATCATTTGGC | 8440 |
rs376506243 | snp | A/G | | | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105772655 | AATAAGTCAATGACA[A/G]AAACACTGTGCTTCT | 8440 |
rs376509863 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105763038 | CGTCTCTACTAAAGA[A/T]TACAAAAGAATTAGC | 8440 |
rs376540806 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105839081 | GGGAGAGCAAGGGAG[G/T]GGACATTTGAATGGC | 8440 |
rs376546247 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105815685 | TGTTCGTCTCAGAAG[C/T]CTTGAAACTAGGGGT | 8440 |
rs376597870 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105749626 | GAGGCAGTTTACAGA[A/G]CACAGTGTCCTTGGG | 8440 |
rs376617707 | in-del | -/TT/TTT | 0.480618 | 0.0965156 | intron-variant | NCK2 | GRCh38.p7 | 2:105774011 | ATTTTTCCAGCTATC[-/TT/TTT]TTTTTTTTTTTTTTT | 8440 |
rs376669820 | snp | A/G | 3.31587e-05 | 0.00407164 | missense, intron-variant | NCK2 | GRCh38.p7 | 2:105881678 | CTGAGCAATGGCCAG[A/G]GCTCCCGCGTGCTGC | 8440 |
rs376701003 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105831878 | TTGGCTATTTGAGGT[A/C]TTTTGTGGTTGCATA | 8440 |
rs376766738 | in-del | -/A | 0.00279162 | 0.0372561 | intron-variant | NCK2 | GRCh38.p7 | 2:105761614 | GGCTCATAGTGGCTC[-/A]TGCCTGTAATCCCAG | 8440 |
rs376800241 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105835425 | TATATATATATATAT[A/T]TTTTTTTTGGTCAGC | 8440 |
rs376823104 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105767769 | GAGGTTTGAGGTTTC[C/T]GTGCCCGCACCTGGG | 8440 |
rs376825604 | in-del | -/CCTGGCCC | | | intron-variant | NCK2 | GRCh38.p7 | 2:105787935 | GTAGATCCCTGGCCC[-/CCTGGCCC]ATTGGCAGAAGTGAG | 8440 |
rs376845878 | in-del | -/CTCC | 0.382666 | 0.211895 | intron-variant | NCK2 | GRCh38.p7 | 2:105807839 | CCCTCCCTTCTATCT[-/CTCC]CTCCCTCCCTCCCTC | 8440 |
rs376855136 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105839693 | GCAGATGTTCACCAG[A/G]TAGCTGGGTGCAGGA | 8440 |
rs376914151 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105891484 | AGAACATTTATCGTT[A/C]AGTATCTTCTTTCCT | 8440 |
rs376957526 | in-del | -/AGAA | | | intron-variant | NCK2 | GRCh38.p7 | 2:105870768 | AAAAGAAAGAAAGAA[-/AGAA]TAAAGGTAAATATCC | 8440 |
rs376969452 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105841777 | AGGCTAAGCCAGGAA[A/G]TGGGAAGATGACCAA | 8440 |
rs376982580 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105809210 | GAGTTCTTTCAATTC[A/T]CTCATCCTTGCATTT | 8440 |
rs376994256 | snp | C/T | | | upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105743641 | TAAATATTATCTCCC[C/T]ATATGACAGATTTTA | 8440 |
rs376999470 | in-del | -/GG | | | intron-variant | NCK2 | GRCh38.p7 | 2:105778070 | GCTGCCAAAGTGGCA[-/GG]GTAAAAGAAACCCCA | 8440 |
rs377069887 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NCK2 | GRCh38.p7 | 2:105864914 | AGATGCAGTTAACAC[C/T]ATCCAAATAATACTA | 8440 |
rs377077909 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105869717 | TGCCGTGTCTCATCC[A/T]TGCCGCGTCTTGTAC | 8440 |
rs377093240 | snp | A/G | | | utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105893944 | ACAGATGATTAAGGA[A/G]AACAGCTGATCTTTG | 8440 |
rs377104409 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105838827 | TATGCATGCTAGGCA[C/T]CCATCTAAGTCTTGG | 8440 |
rs377118531 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105771052 | CTCAGCCTCCCGAGT[A/T]GCTGGGACTACAGGC | 8440 |
rs377130014 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105855511 | GTCCTGTGTATGGAG[A/G]CACTTTGTGTGCTTG | 8440 |
rs377136548 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105776369 | AGCACGTTTGGGGGA[A/G]GGAGTTCAGAACCCC | 8440 |
rs377143797 | snp | A/G | | | intron-variant, utr-variant-5-prime | NCK2 | GRCh38.p7 | 2:105746002 | TGGGGATCTCTGTGA[A/G]GGTCTGCGGTGGATG | 8440 |
rs377155191 | snp | C/T | 1.66255e-05 | 0.00288314 | synonymous-codon, intron-variant | NCK2 | GRCh38.p7 | 2:105881611 | CTTGGAGGAGGTGGA[C/T]GAGGCGGCTGCGGAG | 8440 |
rs377263352 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NCK2 | GRCh38.p7 | 2:105747258 | AAACAGCAGATCTTA[C/T]GTACACAGTACTATA | 8440 |
rs377275751 | in-del | -/ACC | | | intron-variant | NCK2 | GRCh38.p7 | 2:105777910 | TCCAGCAGCAGCACC[-/ACC]TTGGTTTCGCCTAGC | 8440 |
rs377325339 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105806028 | GGGGTGCTGGGTAAA[C/T]TGTGTTGTGTGCCTG | 8440 |
rs377333180 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105806997 | TTGCTGTAAGACATC[C/T]TATCCCACACCCTCA | 8440 |
rs377340485 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105757752 | GGGTGGGGGAAGCAC[A/G]TATGGGAAGTCCCCC | 8440 |
rs377353320 | snp | C/T | | | upstream-variant-2KB, intron-variant | NCK2 | GRCh38.p7 | 2:105849904 | CTCTCTTAATGCTGG[C/T]ACATCCGGCCTCAGG | 8440 |
rs377354223 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105816763 | ATGAGGGAGAAAATT[A/G]GATTATCTCTGTTCC | 8440 |
rs377368952 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105787252 | GTCTCAGCTCTGACA[C/T]GGTCATATCTGTAGG | 8440 |
rs377385857 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105817271 | AACCTACTTGTGTAT[C/G]TTACAATAAAATCAT | 8440 |
rs377390946 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105796187 | TCTGTATTGGCCGCC[C/T]TCTGGGCACTGTGGC | 8440 |
rs377405377 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105880983 | TGCAGACACGGTCTC[A/G]CTATGTTGCTTAGGC | 8440 |
rs377410806 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105889228 | CAGCAGTGTCCCAGC[C/T]GTCCCTTCAGGGGAA | 8440 |
rs377412528 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105835968 | ATTCAGTTCCAAGAC[G/T]TTTTGTGATAAATAT | 8440 |
rs377434001 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105783027 | AGGTAAGCCTTAAGG[C/T]CAGAGCCTTTTTGGG | 8440 |
rs377463569 | in-del | -/A | | | intron-variant | NCK2 | GRCh38.p7 | 2:105807525 | TTATGTTTCTCAATA[-/A]GGGTCACTTGGGGAC | 8440 |
rs377500723 | in-del | -/TTAAA | 0.0023933 | 0.0345097 | intron-variant | NCK2 | GRCh38.p7 | 2:105878119 | GATCATGGCCAAGTG[-/TTAAA]TTTTTAAAGAGGACT | 8440 |
rs377563718 | in-del | -/TGTGTGTGTGT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105830670 | CTTGCCAGGAATTTG[-/TGTGTGTGTGT]GTGTGTGTGTGTGTG | 8440 |
rs377588899 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105835872 | TTTCAAAAGACCTGT[C/T]TCTATGTTCAGAAAT | 8440 |
rs377592680 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105783868 | TTGTTTCGCTTCTCC[C/G]TTTATAGTACTGCCT | 8440 |
rs377594931 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NCK2 | GRCh38.p7 | 2:105829258 | AGGTAGAGAACAGTA[C/T]TGAGAATATTCTAGT | 8440 |
rs377595425 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105769505 | TTTAAATGTAGCACA[A/C/G]AAATTGTGACTCTAC | 8440 |
rs377596558 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105758774 | TAGTCAAGACTGATA[C/T]TTCTACCCAGTACCC | 8440 |
rs377630103 | in-del | -/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105869252 | TGAGAAAGTGCCACA[-/C]CGGATCCTGCATGTG | 8440 |
rs377702250 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105875320 | CTGTGTAGAGCAAAC[A/G]GAACATTGCAGCTGC | 8440 |
rs377730513 | snp | A/C/T | 0.000467535 | 0.0152837 | utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105893213 | GCCTCCCGGGCCCCA[A/C/T]GGTGGAGCTGCCCGC | 8440 |
rs377758060 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105884179 | GTTCTCAGCTGTCAT[C/T]TGTGACTACCAGGGA | 8440 |
rs377759138 | snp | C/G | 1.81099e-05 | 0.00300909 | missense, intron-variant | NCK2 | GRCh38.p7 | 2:105881896 | CCTGCACCCTGCGCA[C/G]GCCCCACAGATAAGC | 8440 |
rs377763489 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105837485 | TATGATAGTGAATCA[C/T]GTGACTATACCACCT | 8440 |
rs386390815 | in-del | -/TT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105774012 | TTTTTCCAGCTATCT[-/TT]TTTTTTTTTTTTTTG | 8440 |
rs386390816 | in-del | -/TT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105774025 | CTTTTTTTTTTTTTT[-/TT]TGAGACGGAGTCTCG | 8440 |
rs386648887 | in-del | ATC/GAGTGCAG | | | intron-variant | NCK2 | GRCh38.p7 | 2:105758460 | CTGTCACCCATGCTG[ATC/GAGTGCAG]TCGCTTGATCTCGGC | 8440 |
rs386648889 | in-del | ACTTAATCA/CTTGCTTATT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105775465 | ATTGATCTTGTTTGA[ACTTAATCA/CTTGCTTATT]TTTTTCCTCTGACTT | 8440 |
rs386648891 | multinucleotide-polymorphism | CC/TG | | | intron-variant | NCK2 | GRCh38.p7 | 2:105812619 | GGCATTTGAGAGCTC[CC/TG]AGGCCTATGCTAATC | 8440 |
rs386648892 | multinucleotide-polymorphism | CTG/TTC | | | intron-variant | NCK2 | GRCh38.p7 | 2:105852268 | GGCAGGTGCGCATCA[CTG/TTC]CTCAACATTTACTTC | 8440 |
rs386648893 | multinucleotide-polymorphism | ATC/GTT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105852944 | CTTCCCAAAAGGTTT[ATC/GTT]ATCTTTAAATTTGGA | 8440 |
rs386648894 | multinucleotide-polymorphism | AC/GT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105875782 | TTTATAAGTCAGTTG[AC/GT]TTACAGTATTTTGTT | 8440 |
rs397694985 | in-del | -/AA | 0 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105817190 | AAAAAAAAAAAAAAA[-/AA]CCTACATCAAATGAG | 8440 |
rs397695592 | in-del | -/T | 0 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105765034 | CCATTTTTTTTTTTT[-/T]AGTGTAAATTCCTTG | 8440 |
rs397703427 | in-del | -/A | 0 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105806717 | AATGAGGGAAAAAAA[-/A]TCACGTTGATTCAGT | 8440 |
rs397703585 | in-del | -/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105833674 | TTTTGCATTTTTTTG[-/G]GCCTCTTTTGTTCAG | 8440 |
rs397716434 | in-del | -/TG | | | intron-variant | NCK2 | GRCh38.p7 | 2:105763603 | GTGTTCTGGGATCTG[-/TG]ATTATTTACTGTTAC | 8440 |
rs397723996 | in-del | -/C | 0 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105883060 | GACTGGGATGTGCTC[-/C]TCTTTGAGGACGGAG | 8440 |
rs397725020 | in-del | -/T | 0 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105838113 | GTCCTTTTTTTTTTT[-/T]GTACCAGCAATAGAT | 8440 |
rs397732678 | in-del | -/A | 0.5 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105799281 | GTTTAAAAAAAAAAA[-/A]GTTCTTCCTTCAGGG | 8440 |
rs397753700 | in-del | -/T | 0.375 | 0.216506 | intron-variant | NCK2 | GRCh38.p7 | 2:105843411 | GAGGGGAGGGCTAGG[-/T]TTTTTTTTTTTTTTT | 8440 |
rs397754933 | in-del | -/A | 0 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105855381 | TTCAAAAAAAAAAAA[-/A]GTCTGTTTTAAAAGT | 8440 |
rs397766981 | in-del | -/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105814075 | CTGATACTGTTTTTT[-/T]GCACAAAAGTGTATA | 8440 |
rs397773825 | in-del | -/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105820072 | ACTGACCCTTTAGGG[-/G]ACAGTATGGAAAAGC | 8440 |
rs397800817 | in-del | -/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105772911 | TTTTTTTTTTTTTTT[-/T]GAGATGGTCTCCCTT | 8440 |
rs397824532 | in-del | -/T | 0.5 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105806255 | TTTTTTTTTTTTTTT[-/T]GAGACAGAGTCTCAC | 8440 |
rs397829850 | in-del | -/T | 0.5 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105769798 | GTCAGTAAAAGGAGT[-/T]GTAGAAGGTAAACCG | 8440 |
rs397869511 | in-del | -/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105833017 | TTTTTTTTTTTTTTT[-/T]AAATGGATTCAGTCT | 8440 |
rs397870319 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105819342 | AAAAAAAAAAAAAAA[A/G]AGTCATTGGGGTAGA | 8440 |
rs397872602 | in-del | -/A | | | intron-variant | NCK2 | GRCh38.p7 | 2:105841717 | GCCTAGGGGCTGCCA[-/A]GCCACCAGTCACCTC | 8440 |
rs397933946 | in-del | -/CT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105892499 | TCAGAATCGTGGACT[-/CT]ACCTCCAGGTCTTTC | 8440 |
rs398042556 | in-del | -/G | 0.5 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105863996 | GGGTCTCACTTGAGG[-/G]ATGCAGAGTGCAAGT | 8440 |
rs398090531 | in-del | -/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105834660 | TAAAGGGTTTTTTTT[-/T]CAATTTTAATTTTTT | 8440 |
rs398090532 | in-del | -/A | | | intron-variant | NCK2 | GRCh38.p7 | 2:105888310 | TCATAGAAGGACATA[-/A]CAGGAAGAAGTGGTC | 8440 |
rs398104590 | in-del | -/TT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105765676 | GTGGGTTTTTTTTTT[-/TT]AATTACTAATATGTT | 8440 |
rs527267949 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105894203 | TACGATTGAAGAAGG[A/G]GTCTTGAGATCCCCT | 8440 |
rs527273634 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105866965 | AGAAGTAGTTTGTTT[G/T]TCTGAGTTGAATGTT | 8440 |
rs527290338 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105757312 | CTTTTATAGCCCCAA[C/T]TTTCGCTGTGTTAAA | 8440 |
rs527292340 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105872248 | AGCTGAAGGTGCCTG[C/T]TGCTGCTTGCACGCT | 8440 |
rs527318150 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105786778 | CCCTTCTGCCTCCCC[C/G]ACGCATTGCTTCCTC | 8440 |
rs527389260 | in-del | -/CTCC | | | intron-variant | NCK2 | GRCh38.p7 | 2:105861933 | TCCCTCCCTCCCTCC[-/CTCC]TGCCCGCTCCCCCCT | 8440 |
rs527438761 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105838602 | TATGTAGAATAACAA[C/T]GAATATATCAAGAAG | 8440 |
rs527470034 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105754395 | ACAAAGTCCATCAAT[A/G]TCTCCTTCGATTTTC | 8440 |
rs527473561 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | NCK2 | GRCh38.p7 | 2:105752309 | GGGAAAGGTGTAACC[-/T]TTTTAAATATGAGGA | 8440 |
rs527527719 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105798303 | CTGGGAGCCCGGATA[G/T]CCTCACTGTGGCCTC | 8440 |
rs527550699 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105844653 | TGAGGCAGAATTGCT[C/T]GAACCCAGGAGGAGG | 8440 |
rs527575784 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NCK2 | GRCh38.p7 | 2:105797889 | TTAATTTATGGCTTC[A/G]CAACTTTTTTTAAGC | 8440 |
rs527593182 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105865690 | CTGAGTGTCATAGGA[A/G]TATACTCCTTTTCCG | 8440 |
rs527611821 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105892004 | GTTTAAAATGCGACC[A/G]GAATTTTCCACTGCT | 8440 |
rs527627078 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105834334 | TGTTCTTGGGTACAT[A/G]TATATTTACAATTGT | 8440 |
rs527628017 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105813689 | GTGCTCAGCACACTC[A/G]CCCAACACTGCAGCT | 8440 |
rs527637582 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105787443 | CTTCTGAAAAGAGAC[A/G]GCAGAGAGCTCTCTC | 8440 |
rs527640107 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105793631 | TTGTTTTGAGTAGCA[A/G]TTGTGGAACTCTGAT | 8440 |
rs527665318 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105832831 | CTTAGAGTGAGTTAG[A/G]AAGAATTCTCTTCTC | 8440 |
rs527667126 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105840022 | TGGCAGTATGGTAGG[A/G]ACAAAAGCCAATTAG | 8440 |
rs527668493 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105880254 | TTAAATTCAACACAT[A/G]CCTATAGGCTGGTTG | 8440 |
rs527698570 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105749408 | AATGACATGTACTAA[C/T]GCATGCACGCTCATT | 8440 |
rs527700731 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105756610 | GGGGTCCTGTGGTGA[A/G]TGGCCATGGGGGAAT | 8440 |
rs527737026 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105755710 | GACCCGAACCCATGC[C/G]TATAAATTCGTGGTT | 8440 |
rs527737423 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105763176 | GCACTCCAGCCTGGG[C/T]GACAGAACGAGACTC | 8440 |
rs527743987 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105887339 | TAAAAGGGGAAAAAC[A/G]TGTCTTTACCAAAAG | 8440 |
rs527744248 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B | NCK2 | GRCh38.p7 | 2:105894551 | ACTCTTGGCAGCCAG[C/T]GCTCTCACACCATGT | 8440 |
rs527752745 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105839496 | TTGAGGGATGAGTCT[C/G]AGATTGGGGGCTGGG | 8440 |
rs527766317 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105847608 | TTCAGGGGGCTCCCA[A/G]GGTGGGAGAGGGGCC | 8440 |
rs527827471 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105762916 | AAAGCAACCTGAGGC[C/T]AGGCGCAGTGGCTCA | 8440 |
rs527862963 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105762453 | GGAATCTAGAGATTC[A/G]CTGAAGCTCATGTCC | 8440 |
rs527891308 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105812314 | GATAAACACATCTAA[A/G]CTGCTCAGTATCAGT | 8440 |
rs527908444 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105854162 | CGTTTAAGGTTCCGC[C/T]ATGTCTTTTCATGGC | 8440 |
rs527910254 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NCK2 | GRCh38.p7 | 2:105861538 | TTTTTTTTTTGAGAC[A/G]GTGTCTTGCTCTGTC | 8440 |
rs527992429 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105773550 | GTGCTTCATACTTCA[A/T]GTCTTTCCTTCCCCT | 8440 |
rs527997493 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105869826 | TTAAAAATTATAATG[-/A]AAAAAATTTTTAATT | 8440 |
rs528009134 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105867539 | GAGAGAAAATAGACA[C/T]GGATTGTCTAAAAAG | 8440 |
rs528023093 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NCK2 | GRCh38.p7 | 2:105817979 | AAAGACACATGCACA[C/T]GTATGTTTATTGCAG | 8440 |
rs528026293 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105860748 | AGAGAGCCGTGGATG[C/T]CGGCGGCGCTGTAAT | 8440 |
rs528046499 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | NCK2 | GRCh38.p7 | 2:105796793 | TTTGACGCAGGTAAA[C/T]GCAGTATACATTTGA | 8440 |
rs528072166 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105843324 | CTCAAGTTTTGGATT[C/T]GGAGCATTTTGGATT | 8440 |
rs528076792 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105759709 | TTCTGTCCCAGGATC[C/T]CATCCAGGGCACGTT | 8440 |
rs528109413 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105824245 | TCACGTTTCCATAGA[A/G]TACTGCTTTCCACTT | 8440 |
rs528120898 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105796242 | GCAGGCGTGTGTAAG[A/T]ATATATGGCTGGTGG | 8440 |
rs528142012 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105882703 | TGGGCAGGCTGGGGG[C/T]GGTGAGTTTCAGGCA | 8440 |
rs528145429 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105842725 | GAAGTACTCACAGCA[A/G]AGACTGCAGGTGGGC | 8440 |
rs528152727 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105890239 | ATGCATACAGGCACA[C/T]ACACACCATGATGTT | 8440 |
rs528158771 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105802397 | CATTACTGTAAAGGA[A/G]TACTTGAGGCTGGGT | 8440 |
rs528167278 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105759325 | ATTGCATTTCAGCCA[C/T]GTAATACCCTCACGT | 8440 |
rs528205879 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NCK2 | GRCh38.p7 | 2:105765141 | GGTTATGCCAGTTTT[C/T]AGTAGTGTGGAAGTA | 8440 |
rs528233883 | in-del | -/AACTT | 0.00279162 | 0.0372561 | upstream-variant-2KB, intron-variant | NCK2 | GRCh38.p7 | 2:105850600 | TAGACCTGAGTAATA[-/AACTT]AACTAGCTGTAGTAA | 8440 |
rs528241444 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105808926 | TTGCTTTAGCCATCT[A/T]GTGAGGGCTGGGGTG | 8440 |
rs528257219 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105871293 | CTGCGGGAGACAGGC[A/C]TTTAGACAGGCAAGG | 8440 |
rs528279182 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105808360 | GCCATGGACCCTGTA[A/G]AAAATCCCATTTGAA | 8440 |
rs528284273 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105770834 | GGGTTAAACAGTTTG[A/G]CATTTCAGTTTGCTT | 8440 |
rs528311125 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105864057 | GGGGAAGGCCATCGG[C/T]GAGCCAGCCGGACTG | 8440 |
rs528313099 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105857240 | CTTCCGCCCAGCATG[C/G]TTAGTTTTTTCATGA | 8440 |
rs528317632 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105786473 | GGAGGTGGCCCTGGC[C/T]GCTGCTGGGATCTTG | 8440 |
rs528386284 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | NCK2 | GRCh38.p7 | 2:105821562 | AATTGGTTAAATAAT[C/T]GCCCAGTAAGTATTG | 8440 |
rs528415300 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105869864 | TTGGCATCTGTGTTC[A/C]CATTTGACTTTCATT | 8440 |
rs528424245 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105863715 | ATGCAGCTCGGGCAC[C/T]TGTGCTTTCAGAGAG | 8440 |
rs528424490 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105859627 | GCTTTTGGATGGGGA[C/T]AGGGTGGCTGGCACC | 8440 |
rs528432980 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105813911 | TTATTTCTAAAGGGA[A/G]ATGCACGTAGTGCTA | 8440 |
rs528484293 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105776895 | TTCTTCCTGACCCCT[C/T]GGAGCCTCTCTCAGT | 8440 |
rs528506282 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105810598 | TGTTAAAAAGGCAAT[A/G]TGTAATTAAATTGTC | 8440 |
rs528532078 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105822335 | TCCACCCATGGAGGC[C/G]CAGGATGGTGCTCAG | 8440 |
rs528551452 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105771929 | ACTTCCTCCCTCCCA[A/G]GGCTGTTCCAGGGCC | 8440 |
rs528555201 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105782366 | CCACCAAAAATCTCC[C/G]TAAAACTAGTTCCAC | 8440 |
rs528585623 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime | NCK2 | GRCh38.p7 | 2:105816456 | TCTTTGTATACAAGC[A/G]ACGTCCCAGATTATA | 8440 |
rs528600946 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105779090 | GGCAGGTGGATCACT[A/T]GAGGTCATGAGTTTT | 8440 |
rs528626809 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | NCK2 | GRCh38.p7 | 2:105820087 | GACAGTATGGAAAAG[C/G]CAGGAGATGTTACGT | 8440 |
rs528664195 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105839177 | GACCCCAAGGTGAGA[A/G]TCAGAGTTTGGAAAA | 8440 |
rs528669800 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105778153 | AGGAGATGTTGGCAG[G/T]CCTCTGGGACTGGGT | 8440 |
rs528686222 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105870868 | CACAGCCAGTAACAG[C/T]GGTGCTTTCACCCTA | 8440 |
rs528744387 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | NCK2 | GRCh38.p7 | 2:105746181 | TTTTGCCAACAGGTT[G/T]AAGGCTGCTTCTGCC | 8440 |
rs528744862 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105863468 | ACAGGGATGCAGACA[C/T]GATGCAGCAACCCCA | 8440 |
rs528767637 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105876688 | TACCCTGTTAAACAC[A/C]CATTGGACTTCAAAT | 8440 |
rs528797959 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105863391 | TCCCTTGGAAATCCC[A/G]TCTGAGCCACTGCAT | 8440 |
rs528805381 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NCK2 | GRCh38.p7 | 2:105836007 | AATTTCTCCATGAAT[C/T]CTCATGAATTGTTTT | 8440 |
rs528821516 | in-del | -/AA | 0.00358779 | 0.0422022 | intron-variant | NCK2 | GRCh38.p7 | 2:105864422 | GTATTAGAATGACTC[-/AA]GAGTTTCCAGCCTGA | 8440 |
rs528830422 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105791360 | TTTTTCTCTTCACTC[C/T]AGAAGAAGAGTGACC | 8440 |
rs528833124 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105745540 | TCGGGGCTAGCGTGG[G/T]ACCGTGCGGTGGCCA | 8440 |
rs528858646 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105841996 | TAAAATGGCACTAGC[C/T]GCCCTGGGGCAGGTG | 8440 |
rs528860820 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105836956 | TGGGGCTCAAGGCCT[A/G]TGATGGCTCTGGCTA | 8440 |
rs528879028 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105877446 | ATTGACGTCTTTCCC[A/G]CACAGTACCCCTCCA | 8440 |
rs528896850 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, utr-variant-5-prime | NCK2 | GRCh38.p7 | 2:105746327 | GGTGGGCGTGGCTTG[C/T]TGGGACCTACAGGTA | 8440 |
rs528905403 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105797641 | GATGAGTATGGTAAC[A/G]GTGAGGCAGGAAGTG | 8440 |
rs528931719 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105796968 | GGTTGGTTCAGTACC[C/G]CTAGCTGGGGTGAGT | 8440 |
rs528949708 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105883430 | TATAATGCACAAAAT[A/G]TGATCTTGGCTTAAA | 8440 |
rs529001811 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105843506 | AGATATACTGATTCT[A/G]GGACTGGGGTAGAAA | 8440 |
rs529041251 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105759738 | TTTCCTTTAGTCTCC[A/G]TAGCGCCTCTGATCT | 8440 |
rs529043744 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105760765 | CCCTAGATGCCAGGC[G/T]TCTCTGAAAATGGTT | 8440 |
rs529045268 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-5-prime, intron-variant | NCK2 | GRCh38.p7 | 2:105851843 | TGGTGAATTGGTGGG[C/T]GTCAGTGCAGTAAGT | 8440 |
rs529060007 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NCK2 | GRCh38.p7 | 2:105851159 | GAGGGAGCCATTGTT[C/G]TATCAGTGCATGGCC | 8440 |
rs529088603 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105809948 | GGCAGGGAAGGGAGC[A/G]AGCGGGACTCTGTTA | 8440 |
rs529089810 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105778300 | ACATCCTGGAGGCAT[A/G]TGTCTCCAGCAGAGG | 8440 |
rs529099906 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105871405 | TTACCATGGAGGGAA[A/G]GCCAGTGGTGTTTCC | 8440 |
rs529107908 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105858308 | CTGTTGCCTAGGCTG[A/G]AGTGCAGTGGCACAA | 8440 |
rs529116352 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105771258 | CTTTTATATTTTCCA[A/T]TCTGACTTTCTAGTA | 8440 |
rs529123841 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NCK2 | GRCh38.p7 | 2:105850294 | AACCCAGCAAGATAC[A/G]GTTCATAGGATTGTC | 8440 |
rs529143122 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105765160 | AGTGTGGAAGTATCA[A/G]TTTCACCCAAATAAT | 8440 |
rs529151882 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105777808 | AAGCAGGAAACAAAC[A/G]CGTGCATCTTGAAAA | 8440 |
rs529154656 | in-del | -/T | 0.00557542 | 0.0525036 | intron-variant | NCK2 | GRCh38.p7 | 2:105803149 | AGGCTTATTTTCTAC[-/T]GTATCACAAATTAGT | 8440 |
rs529187403 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105796554 | TGTGTGGCACAGAAC[A/G]CAGGTGTTCAGATCG | 8440 |
rs529222447 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NCK2 | GRCh38.p7 | 2:105864713 | TCAGCCAGGCATTCA[A/G]TTTCTCTCATGTTAA | 8440 |
rs529234592 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | NCK2 | GRCh38.p7 | 2:105805545 | CATTTTAAATTAAAT[C/T]TCCCGAACTTACTCA | 8440 |
rs529239546 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105857718 | GGGATCAGTATCCCC[A/G]TCATGAGGGAGAAAT | 8440 |
rs529239859 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105844722 | CCTGAGCAACAGAGT[A/G]AGACTCTGTCTTGGG | 8440 |
rs529252689 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105767672 | CCTTTTCCAGAAGAA[A/G]AACCGCAGCCCCTAG | 8440 |
rs529266260 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105761462 | GGTGGAAGGCCAGGT[C/G/T]GGGGGACACTACTTC | 8440 |
rs529268898 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105798316 | TAGCCTCACTGTGGC[C/T]TCTTGTTTGTACATC | 8440 |
rs529273646 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105853216 | TTTAAGGACTGAATA[C/T]TGAATTTTTCTGCTT | 8440 |
rs529292865 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105860539 | ACAGCGGGGCATGGA[A/G]GATGAGCGAGCATGT | 8440 |
rs529346644 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105892738 | GTAATCCCAGGTACT[C/T]GGGAGGCCGAGACAG | 8440 |
rs529355972 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105767021 | CCTGCCCAGGTGTGT[C/T]ACACCTACTCTTATG | 8440 |
rs529373796 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105817019 | AGAAGATAAATCTGT[A/G]TCAAAGGATAGCTGG | 8440 |
rs529376635 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | NCK2 | GRCh38.p7 | 2:105811180 | AAAAAAAAAAAAAAT[A/G]CATTATGGCTTTCTT | 8440 |
rs529426078 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | NCK2 | GRCh38.p7 | 2:105859752 | GATTGTTACGTAAGA[C/T]CCAAAAGCAGTGAAA | 8440 |
rs529445347 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105886046 | TCATGGTTAGGCTCC[A/G]TGATCCATGGTGTTT | 8440 |
rs529459627 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-5-prime | NCK2 | GRCh38.p7 | 2:105816545 | ACTTCAGAGGTGTAA[A/T]TAGCTGAAAACATCA | 8440 |
rs529474712 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105865564 | CCCCCAAAATGCTAA[C/G]GGAACAGTTCCCCAG | 8440 |
rs529487313 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105866313 | ATCACGGTTGACATT[C/G]TGTCTCTTTTCCCAG | 8440 |
rs529499858 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105780043 | ACTACTCTAATTTCC[A/G]TTTTTCCAGTTTTGC | 8440 |
rs529499913 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105772038 | TCTTTGAGAACTCAG[C/T]TTGTAAGCTGCGTCC | 8440 |
rs529501098 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105822888 | TTCCTTGCCTAGTAC[A/G]GCCCAGCGTTGGATG | 8440 |
rs529520818 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105871745 | AGTGATCTGCCCACC[C/T]TGGCCTCCCAAAGTG | 8440 |
rs529537702 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105779302 | ACAGGGCGAGACTCC[A/G]TCTCAAAAAAAAAAA | 8440 |
rs529582876 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105878232 | GAGCACTTCCTGTGC[A/T]TTATAGCATCAGCTG | 8440 |
rs529602068 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105856919 | TAGCATGAATAGAGA[A/G]AAACTTGAAGGTTGT | 8440 |
rs529635164 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105828620 | TACCTATTTTCATGA[A/G]TCTAGACACACAAGC | 8440 |
rs529645578 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105826677 | ATTTGGGTCATTACT[A/G]AGTTATCCTCACAGT | 8440 |
rs529656888 | in-del | -/G | 0.00438332 | 0.0466095 | intron-variant | NCK2 | GRCh38.p7 | 2:105810810 | AAATTTACAAAATTT[-/G]TCACTAATCGAATTC | 8440 |
rs529661357 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105856509 | GAGAATGAGGAATAC[G/T]TAGGAAAACTGAAAG | 8440 |
rs529693687 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105808887 | ACTGAAGTGTTTGTG[A/G]GCAAACTAATTTTTG | 8440 |
rs529717949 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105769311 | AGCTGGCTGCGCCCT[A/G]TTTAAAGCCCTCCTC | 8440 |
rs529744535 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105829605 | GAGTCGGGTATTTTT[C/T]ACAAAGTCCCCCAAT | 8440 |
rs529785388 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105820002 | GTTTGGGACTGTGCT[A/C]ACTGCTGTAGTGGAG | 8440 |
rs529819574 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105776045 | TCCCCCTTGTATTTT[A/G]GTTTGGCCCAATTTG | 8440 |
rs529824978 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105813040 | GGTTCTAGCCCTTTC[A/G]TGGTGATCTTTGTCA | 8440 |
rs529826074 | snp | C/G | | | upstream-variant-2KB, intron-variant | NCK2 | GRCh38.p7 | 2:105850900 | CATCCTGCACCATAG[C/G]AAATTACTCTTAACT | 8440 |
rs529843999 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105868910 | ACAGCAAGGCCAGGA[A/G]TGGGCCCCTCGCAGC | 8440 |
rs529860774 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105825958 | TTCTGATTAACCAAA[A/G]TGATTGCATTACATC | 8440 |
rs529893088 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105825442 | TCTTATGCTCAGAAA[C/T]TTAACAAAATATAAT | 8440 |
rs529899679 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105743387 | AATTAATCTAAAATT[G/T]GGCAGACTGATGACT | 8440 |
rs529902570 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105775043 | AATATAATAATAATA[A/G]TAATTACCAGATGGA | 8440 |
rs529903003 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105763686 | AACTTCCAGTATCAG[G/T]ACAGTGTAAATGACT | 8440 |
rs529913745 | snp | C/G | | | upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105744120 | GCGACACTCCTTCTA[C/G]GGGCACATTCGGGCA | 8440 |
rs529941595 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105782391 | TTCCACTCTCTCCAC[A/G]GCAGGTGTCAGAGTT | 8440 |
rs529959145 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105788024 | AGTTGGGATGTGTCT[C/G]CTTCCAAGGTTGGAT | 8440 |
rs529969030 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105749826 | GTTCAGAAAGCTTAT[G/T]CCTGTTTAGTGCGTG | 8440 |
rs529970115 | in-del | -/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105848007 | TGGCACATCTTTCTG[-/T]TTTAAGTTTTCTGTT | 8440 |
rs530024633 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105777212 | CGTCACTGCTGCTTT[A/G]GGAACCTGCTGTCCC | 8440 |
rs530041332 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105864231 | CTTGTCTTCAGGACA[C/T]GACTGGAAGGGCCTG | 8440 |
rs530085712 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105824272 | ACTTGGGCCCCTGAC[A/G]GTGCTCACAGGGAAT | 8440 |
rs530125435 | in-del | -/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105783709 | TGTATTCAGATTATG[-/T]TTTTTTTTTCGCTAA | 8440 |
rs530147479 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105783927 | GGAATTTGCACGAGA[A/C]AATGAAACACCCTTT | 8440 |
rs530162629 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | NCK2 | GRCh38.p7 | 2:105744676 | AGCCCCGCGCTATCC[C/T]GGCGCCCGTACCGGG | 8440 |
rs530167689 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105856912 | AAGAGGGTAGCATGA[A/G]TAGAGAAAAACTTGA | 8440 |
rs530186292 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105789598 | TGATGAAAATGATCC[A/T]CTTGCTACATAAAAT | 8440 |
rs530199411 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105745290 | CGGTGCTCTCGGCCC[C/T]GCCGCGGCCTGGGCG | 8440 |
rs530215013 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105875130 | TAGCTTGGTTAAGGA[A/G]TTTGTTCACACTCCT | 8440 |
rs530226468 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105790085 | CTTTGTGGAATGTTA[C/T]TTCCTATTTGTAGAA | 8440 |
rs530243823 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105806323 | GCTCACTGCAAGCTC[C/T]GCCTCCCGGGTTCAC | 8440 |
rs530247043 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105751195 | TCTCCTGCAACCTGC[A/C]CGCCTTCTCAGTTAT | 8440 |
rs530278577 | in-del | -/TTT | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105871798 | CTGTGCCCGGCCTGG[-/TTT]TTGTTTTCTAAAGCT | 8440 |
rs530279136 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105795431 | TAAACTGAATGGGCC[C/T]GTTTATTTAGTTATT | 8440 |
rs530281349 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105758341 | TTATCCTATTGATGG[G/T]TTCATTTGAACTGTG | 8440 |
rs530287070 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105889509 | TAAAACACAGATGGC[C/T]GGGCTCCACCCCAGA | 8440 |
rs530294524 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105842366 | GTTGGGATTACAGGC[A/G]TGAGCCACTGCACCC | 8440 |
rs530297374 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105841838 | TTCATCAACTGAGGC[C/T]ACAGAAAGGGGAGGA | 8440 |
rs530331436 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105802480 | AAGCATGGTGCCAGC[A/C]TCTACTTCTGGTGAG | 8440 |
rs530370324 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105824163 | CTTGTGATTGTTACC[G/T]TATTTCACATGTGTG | 8440 |
rs530371612 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105849224 | TTTGTAGATAACCCC[A/G]TATCTACAAAAAGTA | 8440 |
rs530404326 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105801553 | AGTCGAGTGAGGAGA[C/G]GGGCCCATGGCACAA | 8440 |
rs530406857 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105794911 | GAATGATTATTTTGT[A/G]TGACTACTCTCTCTA | 8440 |
rs530409273 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105758535 | CTGCCTCAGCCTCTC[A/G]AGTAGCTGGTACTAC | 8440 |
rs530426890 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105801696 | CAGGCTCATCTCAAG[A/G]GCTGGGTGTTTGGGG | 8440 |
rs530443009 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105888793 | TTGAGAGTACATTCA[G/T]GCAGCCCTACAGAGC | 8440 |
rs530485206 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105826457 | GCTTGTAGTGTGGAT[A/G]ATATGTTAGTTGGGA | 8440 |
rs530488809 | snp | A/T | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | NCK2 | GRCh38.p7 | 2:105850092 | AGGCAGGTGGCGGTG[A/T]CCCATTTTACAGAAG | 8440 |
rs530491274 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NCK2 | GRCh38.p7 | 2:105802214 | GTGATGAAGTGGAAC[A/G]GGAAGATGTGCACAC | 8440 |
rs530499008 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105849300 | GGCTGAGGCAGATGG[A/T]TCGCTTGAGCCCAGG | 8440 |
rs530510389 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105765101 | TATGGCTCTTGATGC[A/G]TCTTGCCATAACGCC | 8440 |
rs530532051 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105808794 | TCGGGACACTAATGA[C/G]ATATGAGCTTTATAT | 8440 |
rs530564577 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105874578 | TGATTTTGCCATAGA[G/T]CCCCCAAAACTTGAG | 8440 |
rs530568140 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105847753 | TCTAAAATGAACAAC[A/C]AATAGTTTAAATTTA | 8440 |
rs530571898 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105863628 | GGAAAATAATACTGG[C/G]ACAAGATGGACAGTC | 8440 |
rs530632001 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | NCK2 | GRCh38.p7 | 2:105820587 | GACCCTGCCTTCTTT[G/T]GGGGAGCGGAGACCA | 8440 |
rs530659837 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105786454 | AGACCTGGCTGCCAG[C/G]CTTGGAGGTGGCCCT | 8440 |
rs530668975 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NCK2 | GRCh38.p7 | 2:105820021 | GCTGTAGTGGAGGTT[C/T]TTACAGCCAGTCCCT | 8440 |
rs530708217 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105766174 | TGGGGAAGTGGGGCC[A/T]AGGAAGCACATTCTG | 8440 |
rs530722071 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | NCK2 | GRCh38.p7 | 2:105776686 | CCAGCCAGCCTCCCT[C/G]GTTTTAGCTCAGCCA | 8440 |
rs530723951 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105769346 | TAAAACAGCTGATGC[A/G]TGCCTATTTTACATT | 8440 |
rs530736728 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105783177 | CCGCAGCAGCTGAGG[A/G]AGCCAATTTAACCTT | 8440 |
rs530738573 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | NCK2 | GRCh38.p7 | 2:105869417 | CAGGGGTTTCCTTGT[G/T]TTACAGATGAAGACA | 8440 |
rs530745897 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105863025 | ATACCAGATGTCAAC[A/G]TGCCCAGCTGATGCT | 8440 |
rs530752377 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105826044 | ACTGTGTATTAGTCT[C/G]TTTTCCTACTGCAAT | 8440 |
rs530763244 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105776105 | GGCCACCTCTGGGGG[C/T]GTGGGTGCGGAGCAG | 8440 |
rs530764533 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105865320 | CCTCATTTTGCATGT[C/G]AGAAAACTGATACTC | 8440 |
rs530871324 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105743508 | AAAACAAGGAAAAAT[A/G]AGGCTGTTCTGATTC | 8440 |
rs530902480 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105858498 | AATCTAGTAACTCAT[A/G]GCACCACCCACATTT | 8440 |
rs530937614 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105870838 | CAGGAAATAATGTAC[C/T]ACAGAGCCACCAGAC | 8440 |
rs530943560 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, utr-variant-5-prime | NCK2 | GRCh38.p7 | 2:105746053 | GACCCCAGGCACCTG[A/G]CTTAAACTAGTATTG | 8440 |
rs530966399 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105880381 | TAATGCACTCATCAC[A/G]ATCTGTTGTGGGAAA | 8440 |
rs530987574 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105822311 | TTAACAGCTCCTGTG[C/G]CTTCCAGCTCCACCC | 8440 |
rs530996540 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105870196 | AGACCACAGTGCCAC[A/G]GGGCCAAGCAGGGGC | 8440 |
rs530999479 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105776074 | TGGTGTGGCCTGGAG[C/T]ATGTCCCTTACTGCA | 8440 |
rs531031510 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105779237 | GCTAGAAACTGGGAG[A/G]CAGAGGTTGCAGTGA | 8440 |
rs531034802 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105827291 | GGCGTGAGCCACCGC[A/G]CCTGGCTGACATAGC | 8440 |
rs531056366 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105784862 | CAGAATAGGATACAC[A/G]AGTAAAGTTAGGAAC | 8440 |
rs531067747 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105751822 | CTCCCTGCAAATGCC[A/G]TTTGAACTGATGGAT | 8440 |
rs531068210 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105799534 | TCTGGGTCTGTTTCC[C/T]ATGTTCCTGCTTCCT | 8440 |
rs531128101 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105876315 | CCGCACACCATGCCT[C/T]GGTAAGGGCAGGATG | 8440 |
rs531139169 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105883336 | AGCGCTTTTAACTCA[A/G]TCGAGCAGAAACTTA | 8440 |
rs531165314 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105779417 | TTTTTAATTAACTAA[A/T]GGGGATACTTTAAGT | 8440 |
rs531176223 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105790125 | TTAAAAGTTGATTTG[G/T]GAGCTAAAAATACGG | 8440 |
rs531192943 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105841679 | TGCCTTGGTCTTTCT[A/G]GTGACCAACCCCATC | 8440 |
rs531205154 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105868207 | ATCAGCCTGCATTGA[C/T]TCATGTCAGTTTTTG | 8440 |
rs531221807 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NCK2 | GRCh38.p7 | 2:105867671 | TGTGTGGGATTCACA[C/T]TGCTGTGTGCGCTTG | 8440 |
rs531329818 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | NCK2 | GRCh38.p7 | 2:105787352 | GAAGTTCTAACCCCC[A/C]GTGTGACTATATTTG | 8440 |
rs531333946 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105749305 | CAGAATTTTAAGTAT[C/T]GCAGTTGCTTCTTTT | 8440 |
rs531394091 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105872324 | TGCTGTTCACAGTGT[A/G]GCCCTAACACCTCCT | 8440 |
rs531411742 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105886974 | GCTTCAGGCCTGTGG[A/G]GTAAATATTTTATAG | 8440 |
rs531420329 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105748677 | CCTGCCTTGACCTCC[A/T]AAAGTACTGGGATTA | 8440 |
rs531457437 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105781002 | TGACCCTCTCTTTTC[C/T]CATTGCCCGAATCTA | 8440 |
rs531473951 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105824281 | CCTGACGGTGCTCAC[A/G]GGGAATGAGTGGGAA | 8440 |
rs531496563 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105793083 | GCAGGCTTTATATAA[C/T]GGCCGTGGAATTGAG | 8440 |
rs531543303 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105754524 | GCCTGGCTACAGGAG[A/G]GGAGAGCAGTTGCTG | 8440 |
rs531599025 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | NCK2 | GRCh38.p7 | 2:105838756 | AACACCTACTGATGG[A/C]GGCCGACCGTAGGCC | 8440 |
rs531613186 | in-del | -/A | | | intron-variant | NCK2 | GRCh38.p7 | 2:105847320 | TGCAGGGGTTGGGTG[-/A]AAAAAAAAAAGAATA | 8440 |
rs531634990 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105794445 | CTTGTGTGTTTTATT[C/T]ATATACAATATATAT | 8440 |
rs531671035 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105800952 | TTTGAGGGGTCTTGA[A/G]GGAGAGGAGAAGTGT | 8440 |
rs531678098 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105888567 | TGTCCATCTATGATG[G/T]CTTAAAAAGATGTCC | 8440 |
rs531678392 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105793748 | GCCTTAGGTGGCCTT[C/T]GTGTTCTCTTGCCAC | 8440 |
rs531678872 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105857237 | CATCTTCCGCCCAGC[A/G]TGCTTAGTTTTTTCA | 8440 |
rs531683563 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105884349 | ACCAAGAGCCCTTAG[A/G]TTCATGATCTGACAT | 8440 |
rs531729747 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105874401 | TTAATAAAAGCTTTT[C/T]GTAATATTTAGCTGA | 8440 |
rs531756075 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105800244 | AGTCCCCAGGCTCCG[C/G]TTCCAACTGCACACC | 8440 |
rs531765276 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105864758 | CTTCTCTTCTTTGTC[A/C]CTTTCACACATGAGT | 8440 |
rs531787734 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105757302 | CTTTCACAACCTTTT[A/G]TAGCCCCAACTTTCG | 8440 |
rs531794133 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105832592 | TTGTTGATGTGATGT[A/G]TCACATTTATTGATT | 8440 |
rs531795151 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105749903 | GGCGCAGTGGCTCAC[A/G]GCTGTAATCCCAGCT | 8440 |
rs531813030 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105806936 | TTCTCAGATGCCCGT[A/G]GTCATGGGGTGATCT | 8440 |
rs531818727 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | NCK2 | GRCh38.p7 | 2:105748727 | CCTGCCCTATGGTTT[G/T]TTTGCCTTCATCTTT | 8440 |
rs531827252 | snp | A/C | 0.000399281 | 0.0141238 | downstream-variant-500B | NCK2 | GRCh38.p7 | 2:105894570 | CTCACACCATGTGTC[A/C]CCCACGACTAACTCT | 8440 |
rs531834162 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105855714 | TTTCCCTCTCTGAAA[C/T]GGATGCTACATCACA | 8440 |
rs531886384 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105774731 | AAATCTGTGTTCCAC[A/G]AGTACACTCAATTTT | 8440 |
rs531899398 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105812876 | AACGTTGAAAACAAA[C/T]TTGGTGTGTGTACAT | 8440 |
rs531902610 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105847693 | AATTCACTGGATAAT[C/T]ACCCATCCCAAGTAC | 8440 |
rs531907097 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105768364 | GGTTCAGTTCTGACA[C/G]TAGCTTTTCAGGGTT | 8440 |
rs531912816 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105888062 | GAGCTAAATAGGGTT[A/C]TTGCACTTAGTTGTA | 8440 |
rs531936844 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105862647 | AGCAAGCCTTGAAGG[C/G]GTTCAAGGGTGAGGT | 8440 |
rs531943682 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105787328 | ATGTCCCCCAGAAAT[A/T]CAGGTGGTGAAGTTC | 8440 |
rs531979591 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105768865 | GTCCCCATGCCCCCT[A/G]GGGGAGACACCTCCT | 8440 |
rs532024426 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | NCK2 | GRCh38.p7 | 2:105806387 | GGACTACAGGCACCC[A/G]CCACCACGTCCGGCT | 8440 |
rs532061779 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105812543 | CTCTGAACGGGAGAT[C/G]CACTTGCAGGCCTCT | 8440 |
rs532071270 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105788141 | TGTAGGGGATTAGAA[C/G]TGAGAGTTGGGGAGG | 8440 |
rs532107263 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105819544 | CGTCAGTGACATTAG[C/G]AGACCTGAAGCTGTT | 8440 |
rs532116067 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105762011 | ATCTTGTCCTTTTTC[-/T]TAAGTTTTTGCGTTG | 8440 |
rs532116290 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | NCK2 | GRCh38.p7 | 2:105813617 | CGGCCACGACTGCTT[C/G]CAGGGGGGCATCTCA | 8440 |
rs532116665 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105807058 | TGACCCGTGATGTAA[C/T]GTGGAATGAAGGTAG | 8440 |
rs532139617 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105811232 | ATACATTTTTGGCAC[C/G]ACATCATCAATTTTT | 8440 |
rs532184116 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105761134 | GCCATGCTGGTGTGC[C/T]TGCCCGCCCACCCTA | 8440 |
rs532197287 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105832386 | CGTGAAGGAATAGGC[A/G]TTCTTATATTTTTCC | 8440 |
rs532209857 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105880167 | ATCTGATTCGATACT[C/G]GTATCTGTGACTGAA | 8440 |
rs532235293 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105831958 | TTGATAGGGATCACA[C/T]TGAAAATGTAGATTG | 8440 |
rs532265380 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105749327 | GCTTCTTTTGAGACA[A/G]TTTTGGAAGCTGGGG | 8440 |
rs532293182 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105781489 | ATGTACGTCTGTTTC[A/G]TAATATTTCTGCACT | 8440 |
rs532302594 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105787958 | GAAGTGAGTAGACCT[A/G]GGCTTCCTGCCCTCC | 8440 |
rs532337342 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105873035 | TCACCCGGCTGCCAG[A/G]AAAGGTCACTGTCCT | 8440 |
rs532348202 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105755607 | GATCGTATTAGTTAT[C/T]AGACCTAGATTGGGA | 8440 |
rs532360545 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105824888 | ATTTGTGGGACACCA[A/G]TGTCACCCTCTCCAC | 8440 |
rs532391569 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105787377 | TATTTGGAGATGAGC[C/T]CTCTGAGGAAATAGG | 8440 |
rs532401096 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | NCK2 | GRCh38.p7 | 2:105783240 | AAGATGGAAAGTAAT[G/T]GCAGTGGAATGTTCT | 8440 |
rs532401206 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105789554 | AAGAGAGTTCTTTCT[A/G]GTTGAAGAGATGTTT | 8440 |
rs532429381 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant | NCK2 | GRCh38.p7 | 2:105802209 | CTGATGTGATGAAGT[C/G]GAACGGGAAGATGTG | 8440 |
rs532443450 | snp | C/G | 0.000169159 | 0.00919515 | synonymous-codon, intron-variant | NCK2 | GRCh38.p7 | 2:105881971 | GTACTACGGGAACGT[C/G]ACGCGGCACCAGGCC | 8440 |
rs532483456 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105748715 | GAGCCACCATACCCT[A/G]CCCTATGGTTTTTTT | 8440 |
rs532488194 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105788796 | CAGTTACAAACAAGC[C/T]ACTGTAATCCAATAC | 8440 |
rs532492209 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105819663 | GCCACGTAGACAAGA[C/T]GGTACATGGAGACCA | 8440 |
rs532494519 | snp | C/G | | | upstream-variant-2KB, intron-variant | NCK2 | GRCh38.p7 | 2:105851070 | GCCTGTGAGGATACA[C/G]GGTGATGGGGCACTC | 8440 |
rs532537602 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105880927 | ACAGATGTGCACCAC[A/C]GGTGGCTAATTTTTT | 8440 |
rs532544784 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105750460 | AGTGTGTCTGTCTAG[G/T]TTCCACAACAGGGCT | 8440 |
rs532552967 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105881182 | CAACCGTATTTTTCT[C/T]ATGGTAATTACAGTT | 8440 |
rs532553089 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105889399 | TGTTGGTGGCTCCAG[C/G]ACTGCCGATGTTTGT | 8440 |
rs532554432 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105794835 | CCTGCCTCAGCCTCC[A/C]GAATAGTTTATTATC | 8440 |
rs532572465 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105744427 | GAATGCTTCCGGGAG[A/G]GGGGCGGCTGCCCAG | 8440 |
rs532582954 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105757472 | ATATGGGTGCAGAGA[C/T]GTAGAAAGGCTACGT | 8440 |
rs532596242 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105826092 | TGGGTTATTTATACA[A/G]GAAAGAGATTTAATT | 8440 |
rs532615914 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105888707 | ATGGAGGGCAGCTTC[C/T]GAGATGGGCATTGTG | 8440 |
rs532641904 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105763780 | CCTGGAGTTTTTGAC[A/C]CTGTGTTTAAAGAAA | 8440 |
rs532646951 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105766886 | ATCAAATTAGTTTAG[C/T]AACTGGCTGGAGGCT | 8440 |
rs532677697 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NCK2 | GRCh38.p7 | 2:105763267 | CTGCCAAGGGGAGAG[C/T]GGGACCTCGCCAGGG | 8440 |
rs532679877 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105888147 | AGAGGTTGGTTTTCC[A/G]CCAACCTATTAATTG | 8440 |
rs532682959 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NCK2 | GRCh38.p7 | 2:105785103 | CCTGCCTCAGCCTCC[C/T]GAGCACATGGGACTA | 8440 |
rs532699222 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105841673 | TAATCCTGCCTTGGT[C/G]TTTCTGGTGACCAAC | 8440 |
rs532734488 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105856460 | GGTTTTAAAAAAATT[C/T]CTAACAAGAGGATTT | 8440 |
rs532736339 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105826058 | TGTTTTCCTACTGCA[A/G]TAAAGAACTATGCGA | 8440 |
rs532737338 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105840908 | GGAAAGGTAAAAGGC[C/T]GTGGGCATCTGAAAG | 8440 |
rs532771307 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105784014 | CTGCTTCAGCTGGAC[A/G]GCAGGTCCCTTCTGT | 8440 |
rs532811692 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105756749 | AACATTTGCCTTCAC[G/T]CAGTGACTGCTTGGC | 8440 |
rs532822768 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105800262 | CCAACTGCACACCTT[A/G]TTCTCTGTCCTCCCT | 8440 |
rs532826472 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105884768 | CTTTCCTGTCCTGAA[C/T]TTCAGTACCTACTGC | 8440 |
rs532844332 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105754361 | ATGCCTAGAAAGACG[A/C]CCATGCCCATCTTAG | 8440 |
rs532863747 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | NCK2 | GRCh38.p7 | 2:105894662 | CACATGACTTGGCAT[C/T]TGTGCCCTCCTAGGC | 8440 |
rs532866291 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105798201 | CTGATATGATGATTT[C/T]GTTGAAAAAATGTAT | 8440 |
rs532882621 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105803000 | GAATTAACTTGAAGT[A/C]TTTCTAGAAGAGAGC | 8440 |
rs532896364 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105874179 | TTACCTATTGAAATA[C/T]TATGATGATAAATTT | 8440 |
rs532923772 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105867171 | CTATTTTAAATGTTC[C/T]GCTTCTCCAACAAAT | 8440 |
rs532934278 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105871862 | AACTTCCTAAGGTCA[A/G]TTAGGACCTTAGAGA | 8440 |
rs532942491 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105878296 | TTCCTGAAATTCATA[C/G]GAAGTCCCAATCCCC | 8440 |
rs532973794 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105750125 | TATTTTCTCACAGTT[A/C]TGGAGGCTGGAAGTC | 8440 |
rs532989101 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105795703 | TAAACATCCTACAAC[G/T]CAGGGGACAGCTCCA | 8440 |
rs533069339 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105771865 | GGCCTGCCCATCACT[C/T]AGATCTATATTTTTC | 8440 |
rs533094649 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | NCK2 | GRCh38.p7 | 2:105753751 | TTGTTGAAGTGAAGG[G/T]AGGCAGGTAGGTTCT | 8440 |
rs533108585 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | NCK2 | GRCh38.p7 | 2:105844597 | AAAAAAAACAGCTGG[A/G]CATGGAGGCTCTTAC | 8440 |
rs533110255 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105837045 | CCTATAACAGGGAGT[C/T]CCCCTTGGCTCTGAG | 8440 |
rs533115015 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NCK2 | GRCh38.p7 | 2:105851291 | TTTTCTGAGACGGAG[C/T]CTCGCTCTGTCGCCT | 8440 |
rs533117930 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105797722 | TGATGCAAAGTCTTT[C/T]GTAACCATGATCAGT | 8440 |
rs533119361 | in-del | -/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105833002 | CTTTGTTGGGAGACT[-/T]TTTTTTTTTTTTTTT | 8440 |
rs533128701 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105757636 | CAAACCAGACAAACA[C/T]CAGCCTTTGGGGAGC | 8440 |
rs533130713 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NCK2 | GRCh38.p7 | 2:105776145 | GGCTGGGGACCTCCC[C/T]TAGGAATCTCAGTGC | 8440 |
rs533157896 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105804021 | ACGTTGAGTGCATCT[C/T]TGCCATCCCTCTCCC | 8440 |
rs533168781 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105773883 | TAGTCCAGCAGTCTT[G/T]TCTTTAACTGTTTTT | 8440 |
rs533175661 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105836474 | AAAACAAGGACAGTG[G/T]GTGGGCTGGTTTTCA | 8440 |
rs533178748 | snp | A/T | 0.021333 | 0.101051 | intron-variant | NCK2 | GRCh38.p7 | 2:105806239 | ATCACATTTTCTTTC[A/T]TTTTTTTTTTTTTTT | 8440 |
rs533220693 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105867863 | GAGTCTTAAGTTTAC[A/G]AATAAAGAAACGTGA | 8440 |
rs533244550 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105854968 | ATAAAAGCTGTCAGT[G/T]CCTAATTTTTCAAGT | 8440 |
rs533252014 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105794583 | AATTATTGTATTTCA[A/G]AGTCTTTCAGGATAA | 8440 |
rs533255602 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105810401 | AACAGGATTTGCTTT[A/C]CTGACTCCTCACTCT | 8440 |
rs533295286 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105816411 | CAAGCAGACCTAATA[C/T]ATGCTTCTTTCTTTT | 8440 |
rs533320928 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105811710 | ATGATGCTTGCAGGC[A/G]GGTGCGGGTCTCCTG | 8440 |
rs533334239 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105792820 | GCCCATGTGAGCAAC[C/T]TGGATGGCCGTGGCC | 8440 |
rs533340052 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NCK2 | GRCh38.p7 | 2:105887129 | GCAGGAGTAATTTTT[A/G]TTAAAAGAAGGCTAC | 8440 |
rs533356321 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | NCK2 | GRCh38.p7 | 2:105773392 | CTCCATCAGTCCATG[C/T]ACCTTTGCTCATGCT | 8440 |
rs533359087 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105817881 | TGTGGCGATTCCTCA[A/G]GGATCTAGAACTAGA | 8440 |
rs533368368 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105799124 | CTGTCTGTCCTTCGT[A/G]TCCTAAGTTGCAAAT | 8440 |
rs533403253 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105893719 | CTGCCCAGTGCCTTT[C/G]GGGCTGTGCTTGCAA | 8440 |
rs533415673 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105893269 | CGCGGGGACGGCCCC[G/T]ACGGCTTCTCTGCGA | 8440 |
rs533437490 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105845860 | TCACTTGTGTTTCCT[A/G]AGAAGCCAAGTTCCA | 8440 |
rs533439037 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105771122 | AGAGACGGGGTTTCA[C/T]TCTGTTAGCCAGGAT | 8440 |
rs533454918 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105824160 | TTGCTTGTGATTGTT[A/C]CCTTATTTCACATGT | 8440 |
rs533458131 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105805578 | ACCAAAATTTTGTAC[C/T]CATCCACCAAAATCC | 8440 |
rs533460749 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105774875 | AATGAGCCGTGTAGA[C/T]GTACAGCTGAAAAAA | 8440 |
rs533487513 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105872164 | TTTGCTCGACACGTT[C/T]CTGCCAGCCTCAGCT | 8440 |
rs533509053 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105854042 | GTTGAGGCCTTAAAG[A/G]GAAGAAGATTCAAAG | 8440 |
rs533526161 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105809551 | TTGGATTAGGGTCCC[A/T]GATTCATTTTAACCA | 8440 |
rs533547880 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105772925 | TTGAGATGGTCTCCC[G/T]TTGTTGCCCAGGCTG | 8440 |
rs533557987 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105810888 | ATTAATATTTGCCCG[C/G]CTATGGGCCAGGTGC | 8440 |
rs533575454 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105817277 | CTTGTGTATGTTACA[A/G]TAAAATCATAACTGT | 8440 |
rs533583455 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105859830 | GAGGCAGAGCCTCAG[C/T]GAAGGTACAGGGGCT | 8440 |
rs533605693 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105772757 | TTGACTTCTTCTCCC[C/T]TCCCATTTTCACAGT | 8440 |
rs533654822 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105779631 | GGGCAGATGGAAAGG[A/G]GAGCTTGCTCTCCGC | 8440 |
rs533690464 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | NCK2 | GRCh38.p7 | 2:105778582 | ACAGAGTAATGCAGG[A/T]TGCTGGTGGCTGCGT | 8440 |
rs533697230 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105780287 | TAAATATTTAGATGT[C/G]TGTCACATTTATTTC | 8440 |
rs533697510 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105866378 | ACAGATGGCTTCTTG[A/C]TGTTGTCAGTACTAG | 8440 |
rs533716395 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105823773 | TCTCAGCTTCTCAGA[A/G]TCACACCTGACCAAC | 8440 |
rs533760112 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105861571 | CTAGGCTGGAGTGCA[A/G]TGGCACAATCTCGGC | 8440 |
rs533760761 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105747366 | AAATACCCTAAGACT[C/T]CCGGAATGGCGCAGA | 8440 |
rs533766196 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105852460 | GATACTGATATAATT[G/T]GCTTGCAGTAGGGCT | 8440 |
rs533769074 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105750849 | AAGAGAGCAAAGCAA[C/G]AGGTGGGGCCAATGG | 8440 |
rs533775420 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | NCK2 | GRCh38.p7 | 2:105766771 | TTCCTTTACTCGGCT[A/C]TCCCTCCATCTTGTG | 8440 |
rs533780510 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105859431 | GCGTCACCTGCCCCA[C/G]GGCTCACTCCTCAGC | 8440 |
rs533795331 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105871088 | CACAGGCCTGGAGGG[A/T]CGATGAGTGCGTGTG | 8440 |
rs533808959 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105772318 | GCCTTCTGCCCCATG[A/G]AATAAACAGCACTAA | 8440 |
rs533836286 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105816648 | CTTAAAACAGAAGTT[A/G]CAGCTTTTTGCTTCA | 8440 |
rs533845492 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105858552 | CCACCTAATTCATAA[A/C]TCCATGGTAAGATTC | 8440 |
rs533845606 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105891858 | GGCCAATAAAAGACA[A/C]ATTTTAATTAAAATA | 8440 |
rs533854875 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105883651 | GGTCATTGCTGTCTG[A/G]ATTCAGGGACCAAGT | 8440 |
rs533859967 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105865897 | CTTCACTCTTAAAGA[C/G]AGAGATATTATTATT | 8440 |
rs533914028 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105824443 | CAACGTCAGAAGTAC[C/T]TGGGAAAGGCAGGGA | 8440 |
rs533929430 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105823185 | GTGTCACAATGGAGG[A/G]GGTGTTGTAGGGCTT | 8440 |
rs533976223 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105871391 | GATCAACCCTCATTT[C/T]ACCATGGAGGGAAGG | 8440 |
rs533989264 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105748768 | ATTCTGAACCGCTTG[G/T]GGGCAGACTGGTCTT | 8440 |
rs534033589 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105790327 | AGATCTTGCCCTGCT[A/G]ACTCAGAGTGGGAAC | 8440 |
rs534048931 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105837160 | AATTCCAGTGTTCTC[C/T]CTTGGACATTTTACT | 8440 |
rs534062985 | snp | G/T | | | downstream-variant-500B | NCK2 | GRCh38.p7 | 2:105894587 | CCACGACTAACTCTC[G/T]ATTTGTCCTCTTGAT | 8440 |
rs534086003 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105836447 | TTTTGGAGGCGTGGT[A/G]TGGCTTTACTGAAAA | 8440 |
rs534122412 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105788615 | CTTATATGTAGGTTA[A/G]ATAAGACACTTCTGT | 8440 |
rs534135482 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105781067 | CTTCTTGCTTTCAGA[C/T]TTTTCTCCCTCCCAC | 8440 |
rs534151439 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105882172 | GGGAGACGCAGATGA[A/G]TGCAATTTAGTATAA | 8440 |
rs534160691 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105893282 | CCGACGGCTTCTCTG[C/T]GAGTCTCTCTTTATG | 8440 |
rs534161786 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105811659 | TGGAGGTCCTTTGTC[A/T]GGGAGTGTGTTCAGT | 8440 |
rs534183870 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105867156 | TCAGCTATCTTAATT[A/C]TATTTTAAATGTTCC | 8440 |
rs534220736 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105805023 | GTCATTTTATCCAGA[A/G]CCTGCCATGGGCCTC | 8440 |
rs534224227 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105787009 | CTTGGTGGCTCTCAA[C/T]GGGGTGAGCATGTGC | 8440 |
rs534225513 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105767133 | CCAGGGAGGCTCCGA[A/C]CTGGAAGCCTGGACC | 8440 |
rs534230598 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NCK2 | GRCh38.p7 | 2:105872501 | TCCTCCTCTTTATTG[C/T]GATTGTCACCGTTGG | 8440 |
rs534237045 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105879146 | TGCTCTTCCACAGGC[A/G]TTTTTTCTCAAGTAG | 8440 |
rs534245176 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105879267 | TCAGCGTAGCCCTCA[C/T]GCCCCGGCTTGCTAG | 8440 |
rs534261597 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105786574 | AAAGGAGGTAATGCC[A/G]GCCTCGCGCGGTTAT | 8440 |
rs534305914 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105855648 | TTTCTCTCTTATACA[A/G]TCCTGTCCATTTGGC | 8440 |
rs534308693 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105878763 | CAGTCTGCACTGACC[C/T]TCTGAGTTGCGCCAA | 8440 |
rs534341283 | in-del | -/TTT | 0.376592 | 0.215579 | intron-variant | NCK2 | GRCh38.p7 | 2:105855833 | GTCCCCATGTGCCTC[-/TTT]TTTTTTTTTTTTTTT | 8440 |
rs534354614 | in-del | -/GTCCGCCCGGGCCGGCAGC | 0.00199481 | 0.0315187 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | NCK2 | GRCh38.p7 | 2:105744996 | GCCCGGGCCGGCAGG[-/GTCCGCCCGGGCCGGCAGC]GTCCGCCCGGCGGCG | 8440 |
rs534365972 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105792280 | GTGATTTCTTAGTTA[G/T]CAAGATCATCATATT | 8440 |
rs534383880 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105834606 | TAATCCATCTGTCCA[C/G]TCTATATCTTTTAAT | 8440 |
rs534395162 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105744145 | CGGGCAGCTCCTCTT[C/T]GGGTTCTGCCCCCAC | 8440 |
rs534396143 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105838137 | AATAGATAACCACTA[C/T]TTATAAACCTTAGCA | 8440 |
rs534417158 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105833902 | TTCTTAATTTCTTCA[C/T]TGACTCATTGTTCAT | 8440 |
rs534489819 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105795069 | AGCAGAAGGTACAGA[A/G]TTTTCTCATATATCC | 8440 |
rs534536911 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105848538 | GTCAGCCATGCTCAG[G/T]GGGAGCAGCCACAGA | 8440 |
rs534552537 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105784075 | GCATTGGCAGTGATG[A/G]AATTCATTTTCATTC | 8440 |
rs534577651 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105868773 | AGTGAAGTTAATCGA[C/T]AGTTTGCACTATCTG | 8440 |
rs534596992 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105875863 | TAGAACTTAAACACC[A/G]TAATTTTATGATGAT | 8440 |
rs534637393 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105807233 | CTGTGACGCACCTGC[A/G]TGGGAAGGGCCGCCC | 8440 |
rs534652552 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105815537 | CCAGGGTCCCCTCGA[A/T]AACGTTAGTCAAGGA | 8440 |
rs534661535 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105798146 | TATTCTATGAAAGGA[A/G]TAGGAGCTAATGTTC | 8440 |
rs534667281 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105882148 | TTGTGTGAGTACACT[A/G]GAAAGAGCGGGAGAC | 8440 |
rs534674813 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105809195 | GGTGGTTTTGACCTC[A/G]AGTTCTTTCAATTCA | 8440 |
rs534685156 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105789330 | GTAGCTGGGATTACA[A/G]GTGTGCACCACCATG | 8440 |
rs534686906 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105752458 | GGTTTGAATTCTAGA[A/G]GTTACCAGTGTAAAA | 8440 |
rs534688456 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105751254 | CCTTGAATTCTCCCT[A/C]AGCTCCCAACTAGTT | 8440 |
rs534714473 | in-del | -/A | 0.40449 | 0.196552 | intron-variant | NCK2 | GRCh38.p7 | 2:105846479 | GTAGATACTCACTGA[-/A]AAAAAAAAAATAATA | 8440 |
rs534718889 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105758708 | CCACTGAGCCCGTCC[C/T]GTTTTTGTATTTTTT | 8440 |
rs534722466 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105842085 | ATAGTATTTGTGGGG[G/T]TTTTTTTCTTTTTTT | 8440 |
rs534727383 | snp | C/G | 1.66203e-05 | 0.00288268 | missense, intron-variant | NCK2 | GRCh38.p7 | 2:105881639 | GAGTCCCCAAGCTTC[C/G]TGAGCCTGCGCAAGG | 8440 |
rs534737908 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | NCK2 | GRCh38.p7 | 2:105842846 | GGAATGAGTTTTCAG[C/G]GGGGTGGACGCTGTG | 8440 |
rs534756936 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105759580 | TGATATAAACTGTGT[A/C]TACTTTCCCCTGTGA | 8440 |
rs534786982 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105757921 | ACATTCCACATGCCA[C/G]TTGTAAGCCAGGTCT | 8440 |
rs534788339 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105801797 | GACATTTTCTGTGAG[C/T]GTGCACCAAAAGCAC | 8440 |
rs534802060 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105890774 | CTGAGTTGTCATTGG[G/T]AGAAATGGAGTGATT | 8440 |
rs534834823 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105772050 | CAGCTTGTAAGCTGC[A/G]TCCTGCCTGTGGAAC | 8440 |
rs534881370 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105764063 | TCAGCCCCGTTTAAC[A/G]GATGAGGTAGCTGAG | 8440 |
rs534922175 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105769416 | TGCTGGTAACTCCCC[C/G]GTTCTTGCTTCTCAG | 8440 |
rs534937240 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105770494 | TTGTGTGTGTGTATG[C/T]GAATGTGTGTTTACA | 8440 |
rs534948595 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105856618 | CCTCTGCAAAATCAT[C/T]GAAAGCCTTCATGTA | 8440 |
rs534955738 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105863951 | GTGAAGAATACTCTG[A/G]GCTGGGTTGAGACTT | 8440 |
rs534990686 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105797223 | ATCTTAGAAAGGACA[C/T]CCCTATTTCAGCTCC | 8440 |
rs535025369 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105803510 | AACAAGGTGACTGCT[A/G]TTGTCTCCAAGGAAA | 8440 |
rs535037048 | snp | A/G | 0.00478085 | 0.0486577 | upstream-variant-2KB, intron-variant | NCK2 | GRCh38.p7 | 2:105851411 | TGGGACTACAGGAGC[A/G]TGCCACCACCCCCGG | 8440 |
rs535052190 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105891200 | CCCTCTCACATCTGC[G/T]CACGCTCACACACTT | 8440 |
rs535059117 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105821917 | ACCAGCCCACGTTCC[C/T]TCTGCTTCCCGGGCT | 8440 |
rs535059373 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105828088 | TACTTATCTCAAAAT[A/T]AAAAGTTTAAACTTT | 8440 |
rs535093840 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105864564 | GGTGTGAATCTCAGG[C/T]TTGGGAGGTACACAG | 8440 |
rs535109700 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105839281 | TGGGGTTTGCAGAGA[A/G]GACTGACACAAATAC | 8440 |
rs535122506 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105810068 | GGAGAAAGAGCACAC[A/G]CATCCCCACTCTTCA | 8440 |
rs535122556 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105802687 | CATGCATGAGGGATC[C/T]GCCCTCGCGATGCAG | 8440 |
rs535125362 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105806328 | CTGCAAGCTCCGCCT[-/C]CCGGGTTCACGCCAT | 8440 |
rs535142475 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105827473 | ACAGAAAGTCAGCAG[A/G]GCTATAGGAACACTC | 8440 |
rs535148607 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105866894 | GCTCAGTGTGGCTTA[G/T]ATATTCTGTGAGTCA | 8440 |
rs535178238 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NCK2 | GRCh38.p7 | 2:105827157 | GGTGCCTACCACCAC[A/G]CCCGGCTAATTTTTG | 8440 |
rs535203688 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105867846 | TTGAGTTACTCAAGC[A/G]GGAGTCTTAAGTTTA | 8440 |
rs535213223 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NCK2 | GRCh38.p7 | 2:105837551 | TTTAACTGTCATAAG[C/T]AGTACTGCCCTGAGC | 8440 |
rs535213986 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105771080 | GGCGCCCGCCACCAT[A/G]CCCAGCTACTTTTTT | 8440 |
rs535244307 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105815674 | TAGTTTTGGAGTGTT[C/T]GTCTCAGAAGTCTTG | 8440 |
rs535270011 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105802499 | ACTTCTGGTGAGGAC[C/T]TCAAGCTGCTTTCCA | 8440 |
rs535271296 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105795644 | AGGCAGTGTCTGCAG[A/G]CGTTGTTGATTGTCA | 8440 |
rs535283044 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105834672 | TTTTCAATTTTAATT[A/T]TTTTATTTTTTTAGA | 8440 |
rs535296337 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105870385 | CCTGCCATCCTGTGG[C/T]AGTCCCTTCCTGAAC | 8440 |
rs535312102 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105836261 | AGTTTCATGGAGTAT[C/G]TTTCATAGGGAACAG | 8440 |
rs535344915 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105889797 | CACTATGTTGCCCAG[G/T]CTGATCTCAAAGTCC | 8440 |
rs535369656 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105808092 | ATTTTTGGTAGAGAC[A/G]GGGTTTCACCATGTT | 8440 |
rs535387661 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105801385 | CCCATGTCATCGTGT[A/G]CACCAGCACGTGGTT | 8440 |
rs535417556 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105820766 | GCTATGCTGCAGATT[C/T]GTTTGACTTTTGAAA | 8440 |
rs535433895 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | NCK2 | GRCh38.p7 | 2:105870925 | TGTGAGTGCCCAGCA[C/T]ATCGTAGGATCTTGG | 8440 |
rs535437423 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105877870 | TTTACCTCCTGTAGC[C/G]TCAGTTTCCTTATTT | 8440 |
rs535502826 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105867682 | CACATTGCTGTGTGC[A/G]CTTGGCTGGGTGAGA | 8440 |
rs535506939 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105819164 | CCCCAGCCATTGTTG[A/G]CTCTTCTAGCTTTGG | 8440 |
rs535508987 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105875990 | TACTTTCATTCTTTC[A/T]TTCTTTTTCATGCAA | 8440 |
rs535532503 | in-del | -/TCTC | 0.0023933 | 0.0345097 | intron-variant | NCK2 | GRCh38.p7 | 2:105786084 | CCCTTCCACTGCACA[-/TCTC]TCTATCAGTTAATTA | 8440 |
rs535534424 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105883714 | TGGGTTTCATCTCAG[A/T]ACTCTGCACCCCACT | 8440 |
rs535542145 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105837786 | TTTCATTTTTACCCA[C/T]CTACTATAAAATGGG | 8440 |
rs535567144 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105843750 | TAAATGATGGAATAC[A/G]TTAATTAGTAGGGGA | 8440 |
rs535581137 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105766662 | TTGTATCTGTTGACT[G/T]GTCACCTTTCAGGGT | 8440 |
rs535584699 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105752186 | GTCTATACACTTTTC[A/T]TGATTTAAGCCTCAT | 8440 |
rs535591096 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105852081 | ATAAGCCTATCAAAA[C/T]GCAGACCACGCATCG | 8440 |
rs535592555 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105891233 | AGCTGCGGTATCTCA[C/T]GCTCCTCTTTCATGC | 8440 |
rs535601636 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105810657 | GTTTTTATGTTGATT[A/G]CAAAGACAAGTAGCA | 8440 |
rs535616547 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105882936 | AGTAAGTATGTACTA[A/C]CTGCTGCCACTGCTG | 8440 |
rs535625307 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105875393 | CCTGGGCTGTACACA[A/C]ATGGAATCCTGGGAC | 8440 |
rs535626440 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105864522 | GAGGTTAGGGTGGGA[C/T]GTCAGTAGGATGCAG | 8440 |
rs535626827 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105842738 | CAAAGACTGCAGGTG[A/G]GCTCTGGGAGGCCTG | 8440 |
rs535652698 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NCK2 | GRCh38.p7 | 2:105851491 | TTCCATCTCCTGACC[C/T]CGTGAAGCGCCTGCC | 8440 |
rs535670898 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105859312 | TTACCCAAAAAGTTA[A/C]GGTTCCATTTACAAC | 8440 |
rs535716149 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105758844 | TATTTTCCAAAGGTT[A/G]GAACTGATTTCAGGG | 8440 |
rs535744305 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105764790 | ATATTTGCAGCTCAT[C/G]CTTGTAAGTATTTAT | 8440 |
rs535747409 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105758165 | TGCAGGTCTCAGGTA[A/G]CACACTAATACTTCC | 8440 |
rs535753067 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105757985 | TCATGCCAGGGTGGG[C/T]GTTATTATTCCAGGG | 8440 |
rs535783129 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105822493 | GACGCTTCCCACAGC[A/G]CCCCTGTTCAGGGCG | 8440 |
rs535784066 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105756169 | GTTAGAAGTTCCCTT[A/G]GTCTTCTCACTGTCT | 8440 |
rs535784120 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105849657 | TCAGACAAGAGGGCT[A/G]GGAGAGTGACACTTT | 8440 |
rs535816179 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105815696 | GAAGTCTTGAAACTA[A/G]GGGTGCTTTTTAGCC | 8440 |
rs535825251 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105756826 | TTTTATTTTTTGAGA[C/T]GGAGTTTCGCTCTTG | 8440 |
rs535856300 | snp | C/G | | | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105771773 | GGGTTGACCGCTACT[C/G]GCAGCTTTTTCTAAC | 8440 |
rs535892530 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105792981 | CCCTTTCTCACCAAC[C/T]GAGTCAGCTTTTCCC | 8440 |
rs535934667 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105871080 | CTGCAGACACAGGCC[-/T]TGGAGGGTCGATGAG | 8440 |
rs535935205 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105829597 | GTTTTGAGGAGTCGG[G/T]TATTTTTTACAAAGT | 8440 |
rs535943148 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105804121 | ACTCTCAGGATTTAC[C/T]AATTTCAAGGGTGTA | 8440 |
rs535943410 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105797391 | GACTGCCAGCCATGC[A/G]GTTCCATATTGTGCA | 8440 |
rs535977253 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | NCK2 | GRCh38.p7 | 2:105855858 | TTTTTTTTTTGAGAC[A/G]GAGTCTCACACTCTT | 8440 |
rs536038510 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105766130 | TTAAAGGAAACAAAA[A/G]AATGAGGGGAGGCGC | 8440 |
rs536051163 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105768554 | ACAGAACTCAGAAAG[C/G]CACTTTGCTTATTGT | 8440 |
rs536069599 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105861702 | GTATTTTTAGTACAG[A/G]TGGGGTTTTACCATG | 8440 |
rs536090608 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105771531 | GATTGGGCCACTGTA[C/T]TCCAGCCTGGGCGAC | 8440 |
rs536115786 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105861084 | TACGGAAAACTATCA[A/G]CCATTTTCTAAATTG | 8440 |
rs536124709 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105824573 | CTGAGAGCTCATTTA[G/T]TAACGTTTTTGTAAT | 8440 |
rs536126991 | snp | A/G | | | utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105894065 | TTTTTCAGGGTTTAC[A/G]AAAGAGTATGTGATT | 8440 |
rs536151023 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105858347 | TACTGTAGTATTGAC[C/T]TCAGGTGATCCTCCC | 8440 |
rs536161504 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105845538 | AGCTGAAATTACAGG[C/T]ATGTACCAGCATGCC | 8440 |
rs536178389 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105771139 | CTGTTAGCCAGGATG[C/G]TCTCGATCTCCTGAC | 8440 |
rs536243842 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105764124 | TAGTCCTGGCAGCTT[C/T]GCTTTGCAGAGCTTT | 8440 |
rs536254253 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105800362 | GATAGTGCATAAAGA[A/G]GGCCTAGTCTGGTCT | 8440 |
rs536256969 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105793411 | TGCCATCTTGGATCC[C/T]ACTGGTTTCAGCTGG | 8440 |
rs536273354 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105839788 | CAAAGCCAAGAGGGC[A/G]GATGGAGGGGAGGCT | 8440 |
rs536312545 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105763326 | CGAGCTGCTGGGACC[A/G]AGGCTGCTGGCCAGA | 8440 |
rs536360923 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105776249 | CCAGCGACAGAAACC[A/G]TACATCCTGGGTTTT | 8440 |
rs536365840 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105894270 | AAAAAAGTATTATGA[C/T]AAGGCTCTGTGTGTA | 8440 |
rs536378812 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105806459 | ACCCAGGATGGTCTC[G/T]ATCTCTTGACCTCGT | 8440 |
rs536381482 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105762091 | TGACCTGAAAACAAG[C/G]ACTTTCGCTTTGCTA | 8440 |
rs536399237 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105783274 | TGCTGTTTGTAGCCT[C/T]GCTAGAGCTTGGGTG | 8440 |
rs536460483 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105779675 | ATGCAGGTGGAGGAG[A/G]GGAGGAAAGAGCTTT | 8440 |
rs536476607 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | NCK2 | GRCh38.p7 | 2:105774290 | CTGGGATTACAGGTG[G/T]GAGCCACTGTGCCCA | 8440 |
rs536487980 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105782694 | GAGAGTGGGGGATCC[A/G]GCCCGTTGAAATCAT | 8440 |
rs536494358 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105874629 | TGGCTTGAATATGTT[C/T]CCAAAGTACCAAGTT | 8440 |
rs536500580 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105750615 | TGGTTGTAGCACCCC[A/G]TAACAGGGAACAAGC | 8440 |
rs536506422 | snp | C/G | 5.84676e-05 | 0.00540651 | intron-variant | NCK2 | GRCh38.p7 | 2:105881279 | TAGGCTAGGGAGTGT[C/G]GTGGTGCCCAAGTGC | 8440 |
rs536506713 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105873862 | GAACCTCTGCAGCGT[A/G]GGCAGATGCTGCTGC | 8440 |
rs536511578 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105771775 | GTTGACCGCTACTGG[A/C]AGCTTTTTCTAACCA | 8440 |
rs536517653 | snp | C/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105743093 | AACCTCTCTAGAGGA[C/G]GCAGATGGGCAGGTC | 8440 |
rs536546401 | snp | C/T | 0.0322114 | 0.122752 | intron-variant | NCK2 | GRCh38.p7 | 2:105832848 | AGAATTCTCTTCTCT[C/T]TTTTTTTTTTATTTT | 8440 |
rs536563659 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105781614 | GAGGTCTTTGTGCAT[C/G]AGTTTTATTATCTGA | 8440 |
rs536589321 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105750067 | ACACACACACACACA[A/C]AAAACAACAACAACA | 8440 |
rs536618611 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105874667 | CGCTTCAGCTTAAAT[C/G]TCCCGAACTCCAGCT | 8440 |
rs536629651 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105804176 | AATTTTGAGTCTAGA[A/G]AAAGCTTGAGATGTT | 8440 |
rs536630513 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105833716 | TTATTATTTCTTTCT[A/G]CTAATTTTGGGTTTG | 8440 |
rs536637139 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105873825 | CCTCTCCCTGCTCAC[C/T]TCTGCCCTTCACTCC | 8440 |
rs536642100 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105843312 | TCACTTGTAGTGCTC[A/G]AGTTTTGGATTCGGA | 8440 |
rs536647325 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105848591 | GAATAGCAGTGCACA[C/T]GGCCTGCCTCCAACA | 8440 |
rs536647487 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105857284 | CAGCCAATGCGTGTA[C/T]TCCCAGGCTCTCAGA | 8440 |
rs536671864 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105871879 | TAGGACCTTAGAGAG[C/T]GGGGAGGAAACTACA | 8440 |
rs536719096 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | NCK2 | GRCh38.p7 | 2:105750138 | TTCTGGAGGCTGGAA[G/T]TCCATGACCCCGGGG | 8440 |
rs536722996 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105841089 | GAACAAGTCCAGACT[C/T]ATTTCTTCCACCTAC | 8440 |
rs536747909 | in-del | -/G | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105842845 | AGGAATGAGTTTTCA[-/G]GGGGGTGGACGCTGT | 8440 |
rs536759706 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105840413 | ATGCAGTTTCTCCTA[C/T]TCTACTCTACTCTCA | 8440 |
rs536777662 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105800422 | TTGCCATTAGCATTC[A/G]TCTGTTTCCTTTCCT | 8440 |
rs536786862 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105820131 | TAAAGAATGAGGAGA[C/T]GTGTACAGAGGTATA | 8440 |
rs536788703 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105848476 | CTCTCTCCAAAATAA[C/T]ATACTGAGCAAAGGT | 8440 |
rs536797395 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105824363 | TTATTTAGTGCCTTC[C/T]GGAATATGCCACTTA | 8440 |
rs536822788 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105819885 | CCACCTGTATTTTGG[C/G]CTATTTTTCTTGCAG | 8440 |
rs536847066 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105763532 | TATAAATTTTATTTA[A/T]TTAAGTTGTCACAGT | 8440 |
rs536868363 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105807201 | GACCGGAACAGCTCA[C/T]TCTGGGTGTTACTGT | 8440 |
rs536888640 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105788969 | ACTGATATAGACAAT[A/T]GTTATTTAAAACATG | 8440 |
rs536898871 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105868847 | GAAAATGAAGCAGTC[A/G]AGGCCCGGGGCAGCC | 8440 |
rs536899780 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105799812 | ATTGGTCCTTACCTG[G/T]CCTTCCCCTCCGCCA | 8440 |
rs536914305 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105825648 | ACATAGCAGAGAATG[A/T]TAATTTCTCTTGTTT | 8440 |
rs536920484 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105842571 | GTTTAAATTTCCCCT[C/T]GGTCCTTTTGGCAGT | 8440 |
rs536931922 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105821980 | TAACGACCCATTCTC[C/G]AAGTGCTTACCTTAA | 8440 |
rs537014567 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105789112 | CCTTCCTCAGCTGAG[A/G]GCCTGGGACCCTCGG | 8440 |
rs537050938 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105761698 | GCCTGGGCAACATGG[C/T]GAAACCCTGTCTCTA | 8440 |
rs537066538 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NCK2 | GRCh38.p7 | 2:105849765 | TGCAAGGAACCTGGT[A/G]CTTAGAAAACTCAGT | 8440 |
rs537085252 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105764883 | AAATCCTTTTTTTCC[A/G]TGTTGTGTGATATCC | 8440 |
rs537095761 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105888933 | ATGTGTTAAGATTCT[C/T]TGACAAGCTTAAATG | 8440 |
rs537136457 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105794194 | GCTGGGATTACAGGC[A/G]CCTGCCACCACGCTG | 8440 |
rs537142033 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105801252 | GGCCTGCCGGGCTGT[C/T]ATCTCCTTGGGGACA | 8440 |
rs537158568 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105763968 | TAATAATAGCTGATA[C/T]TTATTGAGCACTTAA | 8440 |
rs537178501 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105857326 | GCCCGTCCTGGAGCC[A/G]GCACTGGGCCCGCGC | 8440 |
rs537181047 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105807650 | GCGGAGGCTGATCTG[A/C]CCCACAAGGTAGTTG | 8440 |
rs537184447 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105777197 | GGAACCTTCTACTCT[C/T]GTCACTGCTGCTTTA | 8440 |
rs537199260 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105800379 | GCCTAGTCTGGTCTG[C/T]GGTACCCAGGATAGG | 8440 |
rs537199665 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105856582 | TCTTTTCTTTTCTGC[A/C]ATGTTGAAAAGTCTA | 8440 |
rs537240739 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105863868 | GAGCCTCAGTTGCGT[C/T]GTCTGTATAACGGGA | 8440 |
rs537253265 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105869606 | TCTTTTTGTGTATTC[A/G]TCACATTTCACTTTC | 8440 |
rs537304703 | snp | C/T | 0.0154538 | 0.0865337 | upstream-variant-2KB, utr-variant-5-prime | NCK2 | GRCh38.p7 | 2:105744707 | ACCCGGGCGCGGAGC[C/T]TGGCGACGACGGGGG | 8440 |
rs537315152 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105869172 | CTGACCCTGAGAGCC[A/G]AAGTGAGCTGAGACT | 8440 |
rs537362745 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105768628 | ATGGCTTTGAATACG[A/G]CCCAACACAAATACT | 8440 |
rs537378675 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105744104 | AACGGTCCCATCATT[A/G]GCGACACTCCTTCTA | 8440 |
rs537390702 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105826332 | TGGTCTGTCCATTAA[C/T]ACATGGGGATTATAG | 8440 |
rs537405265 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NCK2 | GRCh38.p7 | 2:105850440 | TCCAAGACTTGAAAA[G/T]GCAGCTTAGCTCATG | 8440 |
rs537436435 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105856129 | GTGAGCCACCGTGCC[C/T]GGCTCCCCATGTGCC | 8440 |
rs537443413 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105869284 | CCCTAGCCATAACAG[C/T]GAACTGGTATGGGGA | 8440 |
rs537467668 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105857799 | CCTGGAGGTTTTTGT[C/T]GGACAAAGGGATGTT | 8440 |
rs537475003 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105892884 | CCCAGTGTTTGAGCA[A/G]TGGGTGGTTTGGATT | 8440 |
rs537552156 | snp | A/G | | | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105772551 | GCACTGGGGTCAGCC[A/G]CATGTTACTGATGCT | 8440 |
rs537572127 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105773119 | ATCCAGGCTGGTCTG[C/T]AACTCCTGGCCTCAA | 8440 |
rs537610084 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105776882 | TCTGGCCTTGGGGTT[C/T]TTCCTGACCCCTTGG | 8440 |
rs537631340 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105775486 | TCATTTTTCCTCTGA[C/G]TTGCTTATTTTTTTC | 8440 |
rs537639984 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105866509 | TGGGGGCGATGGTTT[C/T]GGGATGAAACTGTTC | 8440 |
rs537643742 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105804593 | TGGATGGCATTAATT[A/G]GGCAGCTGCCATAGG | 8440 |
rs537696362 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105786419 | GTCTTGGGCCTGTCT[A/G]GAAAGGTCTCTGCCT | 8440 |
rs537697497 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105779704 | TTGATTTTTTTTTTT[C/T]CCACTAATCAGCTTT | 8440 |
rs537700267 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105786761 | AGCTTCTACTCTCTC[C/T]TCCCTTCTGCCTCCC | 8440 |
rs537701428 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105820471 | GGTGTCTGAGGGCTT[G/T]AGTAACGTCTCAGCC | 8440 |
rs537701953 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105748038 | GTTAGCAAGTATTAC[C/T]TCTGCCCAGTGACAC | 8440 |
rs537703221 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105828790 | AATTAGGCATGCTCT[C/G]TACAGGGAAGGACCA | 8440 |
rs537709019 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105795183 | CACCCAAAGTCCAGG[G/T]TTTATATTTGGGTTC | 8440 |
rs537710809 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105827042 | TCTTGCTCTGTTGCC[C/T]AGGCTGGAGTGCAGT | 8440 |
rs537712959 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105875198 | TGTGTCCTTGCCCTC[C/G]AACCTGGCTGCTGAC | 8440 |
rs537714663 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105829867 | TAAGTTATTTAGAGT[A/T]ATTCTTCCAACAAGA | 8440 |
rs537718382 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105878527 | CATCTGCAGGTCCAG[A/G]AGAGAGGCCTTGCAA | 8440 |
rs537723974 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105789668 | TAAAGCACTTATTGT[A/C]CATCATCATCTGCTG | 8440 |
rs537750821 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105837962 | TCTTATATATTCAAC[A/G]CCAGTCCTGTACGAT | 8440 |
rs537790329 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105747524 | AGACAGGGCTTGCGG[A/G]AATCATTCTCTGACA | 8440 |
rs537797013 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105834465 | CTGGTATAAGTATAG[C/G]TACTCTTGCTTACTT | 8440 |
rs537798634 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105818553 | AGAACAAAATAGAAA[A/G]GATTGTTAAATCAAG | 8440 |
rs537827817 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | NCK2 | GRCh38.p7 | 2:105819170 | CCATTGTTGGCTCTT[C/G]TAGCTTTGGGTCCCC | 8440 |
rs537842168 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105889023 | GTCCTTTTTCATCCA[A/C]TTTCTTGAAATCTGT | 8440 |
rs537853681 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105853575 | GCAAGCACTTATTTT[C/T]TTACTGTCTCCATAG | 8440 |
rs537864009 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | NCK2 | GRCh38.p7 | 2:105805152 | TGCTTTTTATGGGCA[C/T]GGAGGCCGGTCTCCT | 8440 |
rs537880842 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant | NCK2 | GRCh38.p7 | 2:105786371 | GTGGGCAGGCTGGGG[-/A]CAGGATGGGAGTTCG | 8440 |
rs537896310 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | NCK2 | GRCh38.p7 | 2:105818169 | CATTCTCAGCAAACT[A/G]TCGCAAGGACAAAAA | 8440 |
rs537902956 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NCK2 | GRCh38.p7 | 2:105811463 | AATAACTTAAGCAGA[C/T]CCTTAGAATGACCTT | 8440 |
rs537918198 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105825103 | TGGCTCCTGCCTCCT[C/T]CTCTCCCTCCAGGCT | 8440 |
rs537928642 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105859372 | CAGGCCCACCTGCCC[A/C/G]TGGCTCACCCTGCCA | 8440 |
rs537934112 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105791025 | TGCTTAGAGGTTGTC[C/T]GCTCCCACTCAGGAA | 8440 |
rs537938777 | snp | A/G | 0 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105787565 | AGCCTCCAGAGCTGC[A/G]AGAAATGAATACCTG | 8440 |
rs537970725 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105768724 | GTTAGTGTATTTTAT[A/G]TATGGCCCAAGATGA | 8440 |
rs537982170 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105817443 | GTAGTCCAGTTAATC[C/T]GGTGTTCTCTTTCTG | 8440 |
rs538014541 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105823893 | TGTTTCGTGATCAAA[C/T]GCCTTGTTCCGTGAC | 8440 |
rs538053708 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105799775 | CCTAAAAGTGGTTAA[A/G]ATAGATCCATTTCAA | 8440 |
rs538101542 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105893961 | ACAGCTGATCTTTGG[A/G]GAAGGGAGCTACCAA | 8440 |
rs538102339 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105823295 | ACAGAACTGAAGGGA[A/G]CACGTGGAACTGCAG | 8440 |
rs538128379 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105785883 | ACGATATCTAGTAGC[A/T]GTGCAATACTTTTGG | 8440 |
rs538184787 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | NCK2 | GRCh38.p7 | 2:105805901 | TTTTGGAATATTTGC[A/T]TAAACATAACGAGAG | 8440 |
rs538227097 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105861810 | ATGAGCCACCGCACC[C/T]GGCCAGTTTCTCTCA | 8440 |
rs538227504 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105799823 | CCTGGCCTTCCCCTC[C/T]GCCATCTTGCCACTA | 8440 |
rs538232115 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105868490 | GTTTTTTTAAGGAAC[A/G]TAGTTGTTGATTGTC | 8440 |
rs538244200 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105868011 | CTATTCCATTTTAGT[A/G]TCTGTTTCCTGGAAG | 8440 |
rs538244853 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105762993 | TGAGCTCAGGAGTTC[A/G]AAACCAGCCTGGGCA | 8440 |
rs538251468 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105882369 | CCTGGTTGCCCATTC[A/T]GTGTACGTAGAAGGC | 8440 |
rs538253091 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105768637 | AATACGGCCCAACAC[A/G]AATACTTAAACTTTC | 8440 |
rs538292232 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105894137 | TTTCTTTTTCCTTTA[C/T]ATTTGAACTTCTTTA | 8440 |
rs538369498 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105768184 | TTGCTAATGCCATTC[A/G]TTTGCTTTCTTTGCC | 8440 |
rs538385430 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105749490 | AACATGGTGCACTTG[A/G]TTCTGGCCCTCATTT | 8440 |
rs538386504 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | NCK2 | GRCh38.p7 | 2:105874481 | ATCTCGATTCTTAGC[-/A]AAAAATAGCATTTTC | 8440 |
rs538405007 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105787078 | TGCTGTCTTGCTCTG[C/T]CCGCTGCAGGCGTGG | 8440 |
rs538413802 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105773703 | ACCCACTCAACAACT[A/G]TTTGAGCACCTACTC | 8440 |
rs538419351 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105831437 | TTTGTCTTTTTGATA[A/G]TATCATTCTATGCTG | 8440 |
rs538422382 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105748889 | CACTGAGATTCAAGT[A/G]GTAAGAGACCTCCAG | 8440 |
rs538430245 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105839604 | ATTTGATTGGTTTCC[C/T]TTTGTTTTTCATGGG | 8440 |
rs538470479 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105879354 | TGGACAAAAAAGTTT[A/G]CTTTCATGGATGGCC | 8440 |
rs538483972 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105886538 | CCAAATCCTGAGAAC[C/G]TATGAACTCCTGAAT | 8440 |
rs538513252 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105839045 | ATTGGATGGAATCAG[A/C]GAAGGAATATGAGAG | 8440 |
rs538515831 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105807307 | AATCACACCCAGGTG[C/T]TCTCCTCGAAGGGCA | 8440 |
rs538522033 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105872405 | CTGTCTTCCTTGCCA[C/T]GGGTACTTCCTGTCC | 8440 |
rs538550887 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105846211 | ATTATGTGTAAAATA[C/G]CATTTCCCAGATTCT | 8440 |
rs538566140 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105784216 | TCAAGTAATCCGCCC[A/G]CCTCAGCCTCCCAAA | 8440 |
rs538588070 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105821421 | CAGCCTCCTTCTGCC[A/G]CACTCTGGACCCCTG | 8440 |
rs538627211 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105755415 | TTGCTTCTTAACTTG[A/T]TTGTGCCGAGCACCT | 8440 |
rs538646459 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105769019 | AGTTCCCACTCTCTA[A/T]TCACACGTTTTGTCT | 8440 |
rs538659933 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105846318 | GTCTAGTCTGCAGAA[C/T]GCTAGTGTGTCTTGG | 8440 |
rs538672423 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105813300 | GGAGGGATTCCCTGA[A/G]CCTCCTGAAGGCTGA | 8440 |
rs538696627 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105769331 | AAGCCCTCCTCTCAG[G/T]AAAACAGCTGATGCG | 8440 |
rs538715905 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105819787 | TTCACCTATTAAAAT[G/T]TACTTTTGTGGTTTA | 8440 |
rs538724646 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105893398 | GGAGGGGAGGAGCAG[A/G]GCGAGTTCACATTAT | 8440 |
rs538731815 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105812555 | GATCCACTTGCAGGC[C/T]TCTGCTGGGCCTCCT | 8440 |
rs538751095 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NCK2 | GRCh38.p7 | 2:105787039 | CCCTGCTTTCCTCTC[C/T]TCTGCCCTTTGCTGC | 8440 |
rs538764451 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105782614 | ATTTTGTTAGAGCAG[G/T]TTTGTTTTCATGGCT | 8440 |
rs538800780 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105825550 | ACACCTGGTGTTTTC[C/T]ACTTTGGAGATTCTG | 8440 |
rs538803959 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105788346 | AAGGAGAGGGAAATT[A/C]TTTTCTCCATTTCTA | 8440 |
rs538842835 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105873845 | CCCTTCACTCCTTAC[A/G]TGAACCTCTGCAGCG | 8440 |
rs538884751 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105828063 | CCCTTTGGAATTTCC[C/T]GTGAACCTATACTTA | 8440 |
rs538893757 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105880477 | TTGCCCAGTAGGGCT[A/G]TTATGCTGCCCAGGG | 8440 |
rs538903503 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105884897 | CTCCATATTTCGTTA[C/T]CATACCTTCACCTGT | 8440 |
rs538908672 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105880062 | CTCCTAGAATGTTCC[A/G]GAATTCCGTGCATTT | 8440 |
rs538908756 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105888128 | TGATGATAGAGGCCC[C/T]GAGAGAGGTTGGTTT | 8440 |
rs538917393 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105786946 | AGACTCGAAGCAGGG[A/G]ACCTGCGAAACTTCA | 8440 |
rs538943008 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105793346 | GAGTGTCATTTAGTA[C/T]GGAAATTAGATGATA | 8440 |
rs538967226 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105823908 | CGCCTTGTTCCGTGA[A/C]CTTCCCGTGTGAAGG | 8440 |
rs538968653 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105887562 | GATAAGGAGAAGTTT[C/T]AAGGTTTAAAGAACC | 8440 |
rs539020644 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105779523 | GTGGGTGGCTGCGTC[C/T]AGCTGAACTTGGCTT | 8440 |
rs539029196 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105856055 | TAGCCAGGATGATCT[C/T]GATCTCTTGACCTTG | 8440 |
rs539031993 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105871205 | ATGGTGACTTTGTTT[A/G]TCCTTCCCAAGGAGA | 8440 |
rs539043675 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105862460 | AGAACACAGCAGTCA[C/T]AGGTACGAGACCCAG | 8440 |
rs539048191 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105889688 | TCCCGGGCTCAAGTG[A/G]TCCTCCCACCCTGGC | 8440 |
rs539066659 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105816175 | TAGCCAGGGGTGGTG[G/T]CATGCCTGTGGTCCC | 8440 |
rs539102150 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105868611 | GACTAAATCTGTAAT[G/T]TTTAACCGGCTGTGC | 8440 |
rs539147746 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105874233 | GGAAGCTAATCTTAG[C/T]AGCATAACTAAAAAA | 8440 |
rs539208644 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105749940 | GAGGCTGAGTCACGC[A/G]AATTGCTTGAACCCA | 8440 |
rs539217648 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105790826 | TTGGGTGGAGGGAAC[A/G]GCCTTTGAGCTGTGC | 8440 |
rs539219499 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105832731 | TTTGAGGATTTTTGC[A/G]TCTATGTTCATCAGG | 8440 |
rs539227987 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105784739 | GGAGCAGTGTGTCTG[C/T]TGAGGTCCATCCGTT | 8440 |
rs539241274 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105752958 | AAGCACTTTCCATGT[A/G]ATAACTCATTGAGTC | 8440 |
rs539243316 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105827586 | CACAGAGCATTTGCC[A/G]TGTTAGGGCATGTCC | 8440 |
rs539262549 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NCK2 | GRCh38.p7 | 2:105793995 | TCTATTATAAATTCA[C/T]ATTGATACTTATAAC | 8440 |
rs539308656 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105832213 | ACACTACTGATTTTT[A/G]TATGTTGATTTTAGT | 8440 |
rs539330358 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105748200 | AGCCTCTGTGTTCCC[C/T]CTCAACTCCTTGGCT | 8440 |
rs539342031 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105796566 | AACGCAGGTGTTCAG[A/G]TCGGCAGCGTCTGGA | 8440 |
rs539348534 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105839649 | TAGTTTTAGACGTGA[G/T]ATTTGAAGTGCATGT | 8440 |
rs539362292 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105890513 | AGGCTGAGGCCTAAT[C/G]TGAGATTAACCTTCT | 8440 |
rs539397386 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105771569 | GAACTCCCTCTCAAA[A/G]ACAGAAAGACCTAAT | 8440 |
rs539445073 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105865013 | AGCCCTCCCCAGCAG[A/G]AGGCCTCTTGGTAGC | 8440 |
rs539478482 | in-del | -/A | 0.0142736 | 0.0832652 | intron-variant | NCK2 | GRCh38.p7 | 2:105760213 | ATTTTCAGTGGGGAT[-/A]AGAAGGCACTGTGGC | 8440 |
rs539501900 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105785157 | CTAATTTTTTGTATT[G/T]TTAGTAGAGACAGGA | 8440 |
rs539512934 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105835941 | CAATTTTTTTATTTA[A/G]TTCATTTAATTATTC | 8440 |
rs539517875 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105838052 | AAAATCAATAATTCC[A/T]ACATGAGAATTCACT | 8440 |
rs539531662 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105798385 | TTTTCTTCTTTCAGT[C/G]TTCTCCTTTTTTCTT | 8440 |
rs539546632 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105861805 | TAGGCATGAGCCACC[A/G]CACCCGGCCAGTTTC | 8440 |
rs539570289 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105828265 | GAATTGGGCACCGTT[A/C]AAGATTGCTGAAAAT | 8440 |
rs539587929 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105746611 | CGAGTTTTACGTAAA[A/G]AGAATGGCAGTCATC | 8440 |
rs539589308 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105833198 | CTCCCGGATTCAAAC[G/T]ATTTTCCTGCCTCAA | 8440 |
rs539597038 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105876848 | TACCTACAAGGTAAT[A/G]AGTTTGCCTTCGAAT | 8440 |
rs539615898 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105804939 | TGCAGGGTACTGGAT[A/G]GTCACAGCTGATCTT | 8440 |
rs539631508 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105831229 | TCTATACATTCAGTG[C/G]AATCCCTATCAAAAT | 8440 |
rs539641071 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105844425 | AGGAACCTATTTTAG[C/T]CTAAAAAATATTTTT | 8440 |
rs539717753 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105835566 | TGTTTTCAGACTTCT[C/T]ACTTTGTCTTACTTT | 8440 |
rs539751357 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105802568 | CCCATGGCGAGAACA[C/T]GGAAGCAAGAGAGAG | 8440 |
rs539753887 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105842816 | GTGGCAGGAGAGGGC[A/G]GCTGTGGTTTTGGAG | 8440 |
rs539799047 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105786522 | CATGAGATGCTGAGT[C/T]GGTTCCTTTAGCTCA | 8440 |
rs539856076 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105803793 | CTGGGCCTCATAACC[A/G]CCTAGAAGCTTTTAT | 8440 |
rs539877814 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105766287 | GGGGAGAACCTGATG[G/T]ATTTCTTTCTCCTTC | 8440 |
rs539880028 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105814526 | AGTTCTAAATCCAGC[G/T]CATTGTTCTTTTGCG | 8440 |
rs539885184 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NCK2 | GRCh38.p7 | 2:105792051 | TCTGCACAGAGCCGT[A/G]GGAACGCTTCCCCAG | 8440 |
rs539892314 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105803158 | TTCTACTGTATCACA[A/T]ATTAGTTTTTATCTA | 8440 |
rs539921007 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105791481 | GTTGCCGTGCTTACC[A/G]GCCAGAGTGCTGCTG | 8440 |
rs539931681 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105753987 | GAGTTGTCTGTGCCA[A/G]CTTCTCGAACCTACC | 8440 |
rs539953638 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105856298 | ATTGCGAGGACTTTT[C/T]TGAAGAATGACTCAT | 8440 |
rs539980092 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105809922 | TTCCCAACACTGAGG[A/G]GGAGAGGGCAGGCAG | 8440 |
rs540023741 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105760696 | GAAGGGAGAAACCAG[A/T]TACAGCTGAGAACCC | 8440 |
rs540029998 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105804275 | GTAAATGAACGGACC[A/T]GCGCTTTTCTTTGAT | 8440 |
rs540039817 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105852211 | AGGATGACACCTCCC[C/T]GAAAGGTGGGTGTTT | 8440 |
rs540062564 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105875303 | TCAAGCACCCAGGGC[C/G]CCTGTGTAGAGCAAA | 8440 |
rs540128477 | snp | A/G | | | upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105743154 | TTTGATGAATGAAAA[A/G]ATGATGGTGTTTCAG | 8440 |
rs540132786 | in-del | -/AAAG | | | intron-variant | NCK2 | GRCh38.p7 | 2:105885457 | GTTATAATATTTCTT[-/AAAG]AAATTATAACTTTTA | 8440 |
rs540134972 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105777200 | ACCTTCTACTCTCGT[C/T]ACTGCTGCTTTAGGA | 8440 |
rs540140283 | in-del | -/CT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105769012 | TGCAGAAAGTTCCCA[-/CT]CTCTAATCACACGTT | 8440 |
rs540156146 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105876204 | AATGCTCAAAACCAG[A/G]TAAATTCTGTGCAGT | 8440 |
rs540156690 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105772160 | TTAGCAGTTTCCACC[A/G]GTGTCTTCCCAACAG | 8440 |
rs540161715 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105821599 | GCTGGGAAAACATTG[A/C]CACATTGATTCCACA | 8440 |
rs540179785 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105869938 | CAGGTTTAAATATTC[C/T]ATCATTTTGTTTGCC | 8440 |
rs540196598 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant, utr-variant-5-prime | NCK2 | GRCh38.p7 | 2:105745837 | CGCTCGGCTCTCTCG[G/T]TTTTTTTCAGGGCGA | 8440 |
rs540252256 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105891502 | TATCTTCTTTCCTGC[A/C]TGCTTTTCAGCAAAT | 8440 |
rs540280050 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NCK2 | GRCh38.p7 | 2:105859646 | GTGGCTGGCACCCGT[A/G]GGTGAAATTGACAGG | 8440 |
rs540304018 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105818970 | GAACAGCATAAGATT[A/G]ATATGCAATAAGGAT | 8440 |
rs540315135 | snp | C/T | 0.00599036 | 0.0543994 | intron-variant | NCK2 | GRCh38.p7 | 2:105866744 | ACTGGTCTGTGGCCC[C/T]GGGGGGTTGGGGACC | 8440 |
rs540331916 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105823299 | AACTGAAGGGAACAC[A/G]TGGAACTGCAGAAGT | 8440 |
rs540341836 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105856441 | CTGTGTCACATTTAC[C/T]TGGGGTTTTAAAAAA | 8440 |
rs540375131 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105771219 | GAGCCACCGCGCCCC[A/G]CCCAATATCACTATT | 8440 |
rs540399337 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105815791 | GAACGAGTCTCTAAA[C/T]AATATCCATGCCCTT | 8440 |
rs540412296 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105858291 | TGAGACAGGGCCTCA[C/T]TCTGTTGCCTAGGCT | 8440 |
rs540418174 | snp | C/T | | | upstream-variant-2KB, intron-variant | NCK2 | GRCh38.p7 | 2:105851170 | TGTTGTATCAGTGCA[C/T]GGCCATAACTCAGCT | 8440 |
rs540424144 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105854197 | TAGCTCATTTCTTTT[C/T]GGTACTGAATAATAT | 8440 |
rs540455759 | in-del | -/TTTTTTTTTTTTTTTTTT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105880951 | ATTTTTTTTTTTTTT[-/TTTTTTTTTTTTTTTTTT]GCAGACACGGTCTCG | 8440 |
rs540487763 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105822105 | CCTTTCTTTCTTACT[A/G]TACCAGGAATTTCGT | 8440 |
rs540500338 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105837564 | AGCAGTACTGCCCTG[A/G]GCACTGTGCATGTCC | 8440 |
rs540537654 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105827682 | TTAATAGAATTTCTT[C/T]TTTTTGCTTTAAAAT | 8440 |
rs540570055 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105798156 | AAGGAGTAGGAGCTA[A/G]TGTTCGCTTGTTGTA | 8440 |
rs540571593 | in-del | -/C | 0.00199481 | 0.0315187 | intron-variant | NCK2 | GRCh38.p7 | 2:105786847 | TCTACCAGCCCTGCT[-/C]CCCACCCTAGCCTTA | 8440 |
rs540574245 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105766924 | CCGTCTTCCTGCTGC[C/T]TGTGCAGTGTTGGTG | 8440 |
rs540577581 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105892410 | CATAATGAGTTTGCA[C/G]TTTTCAAATAACTAA | 8440 |
rs540598868 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105811067 | GTAGTCCCAGCTACT[C/T]GGGAGGCTGAGGTAA | 8440 |
rs540607583 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105863512 | GTGTGTTCCGATCAG[A/T]AGGGGGAGCCTGGTC | 8440 |
rs540626046 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105769278 | CTGCCCCGCCCCACC[A/C]CTCCCCTCCCCATCC | 8440 |
rs540674390 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105862751 | CGGGTAATGGAACAT[C/T]GTCTTGGCAGCTTAG | 8440 |
rs540692481 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105826469 | GATGATATGTTAGTT[G/T]GGAGGCCTGTGATTG | 8440 |
rs540700145 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105785017 | GGAGTCTCGCTCTGT[C/T]GCCCAGGCTGGAGTG | 8440 |
rs540700945 | in-del | -/CCC/CCCC | 0.00159641 | 0.0282137 | intron-variant | NCK2 | GRCh38.p7 | 2:105812788 | ATCTGCTCATTACTG[-/CCC/CCCC]AAGCCAGGTGACACT | 8440 |
rs540731574 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105868871 | GGCAGCCAAGCGACT[C/T]GGCCAGGGCTATGAG | 8440 |
rs540735569 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105819957 | TCCCAGCCACCTTTC[C/T]CCATGCCCTTTCAGG | 8440 |
rs540743312 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105871656 | TGCCACCACACCCAG[C/T]TAATTTTTTTGTATT | 8440 |
rs540771868 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105758704 | TGAGCCACTGAGCCC[A/G]TCCCGTTTTTGTATT | 8440 |
rs540793677 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105786148 | CATCTGTTGTGTCTA[C/G]GGCAGCATGATTAGC | 8440 |
rs540812276 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105806339 | GCCTCCCGGGTTCAC[A/G]CCATTCTCCTGCCTC | 8440 |
rs540840811 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105785495 | TGACACGACCAAAAG[A/G]CCGCCAATACAAAAT | 8440 |
rs540849691 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105849595 | TAGACAATAAGTAAG[G/T]GACCAGGTGGTCTCT | 8440 |
rs540893891 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105754092 | GGACGGTGAGTCTGG[C/T]GTCTCTGTTGGGAGA | 8440 |
rs540921171 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105791344 | CCTCTGTGCCTTCAC[A/G]TTTTTCTCTTCACTC | 8440 |
rs540937892 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105838160 | CCTTAGCATTTTCAA[A/G]TCACAAGAAAATCTT | 8440 |
rs540944938 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105883905 | CTAGGAATATAGGGC[A/G]GAAAGAGCTTTACTG | 8440 |
rs540956423 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105793568 | TCAGAGTAAATAGTT[A/C]TGGTTCCCCAGTATC | 8440 |
rs540978051 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | NCK2 | GRCh38.p7 | 2:105776384 | GGGAGTTCAGAACCC[C/T]TGTCACCATGCATAT | 8440 |
rs541003172 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105800055 | GGTATCATTAGATGT[C/G]TCTTTGCACCAGCAT | 8440 |
rs541024599 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105761465 | GGAAGGCCAGGTGGG[C/G]GGACACTACTTCCTG | 8440 |
rs541034831 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105781120 | TCAAAGATACAGATC[C/T]AATTGTTTTACTTCT | 8440 |
rs541047255 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105777450 | ATGACCCAGTGCTCA[C/G]CACCTGGCACGGCGT | 8440 |
rs541059252 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105875697 | CCTCACCAGACACCG[A/G]ATCTCCTGGGGCCTT | 8440 |
rs541086066 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105775538 | ATGTGTTCTTTCTTA[C/T]CTCCTTTTGGGTTTT | 8440 |
rs541104606 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105782996 | GCAGCTGAGTTGGTC[A/G]ACTATCATTTGCAAC | 8440 |
rs541126284 | in-del | -/A | | | intron-variant | NCK2 | GRCh38.p7 | 2:105822082 | CCCATTTCCTGACCC[-/A]AAAAAAGCCTTTCTT | 8440 |
rs541215318 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105758250 | TAGAGATGTAAGTAA[G/T]TGAATCACATTACTT | 8440 |
rs541219986 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105841764 | ACACTTACATTTGAG[G/T]CTAAGCCAGGAAATG | 8440 |
rs541233860 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105857350 | CCCGCGCCCGTCCCC[A/G]ACAGATGGCCATCCA | 8440 |
rs541253161 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | NCK2 | GRCh38.p7 | 2:105764269 | TCAGCACCTTTGCAT[C/G]CGCACCCTGCAGGTT | 8440 |
rs541274690 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105848967 | ACCAATTATTTGCAC[A/C]TAGACAAATATATTT | 8440 |
rs541283360 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105757035 | GTCTTGAACTCCTGA[C/T]CTCGGGTGATCTGCC | 8440 |
rs541296596 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105856826 | ATCTTTTCTTCCCCC[A/G]CATAAGCATGCCACT | 8440 |
rs541326484 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105880203 | AGTACTTACTGTAAT[C/T]GTGTTTGATGCACTG | 8440 |
rs541330111 | snp | A/G | 0 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105888435 | GAAATGCGGACAGTG[A/G]GAGGTAGCACAAAGG | 8440 |
rs541392812 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105745237 | GCCGGGGTGCGCCCG[A/G]GAAGGGGCCAGGAGA | 8440 |
rs541427058 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105856945 | GTTGTCCTGAGCTTT[A/C]TTTTTCCAATTTCTA | 8440 |
rs541438424 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105808194 | TGAGCCACTGTGCCT[G/T]GCCTCTTTCTTTGTT | 8440 |
rs541509714 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105769780 | GTCAGTGTGTCAGGC[A/G]TGGTCAGTAAAAGGA | 8440 |
rs541513458 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105795739 | AAGAATTACCGAAAC[A/G]TCTGTATGCCCCTGG | 8440 |
rs541523850 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105863582 | AGGCTTAGTCCCTGA[C/G]TTTCTGAAGCTTGTA | 8440 |
rs541525296 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105820578 | TGCGGCTCTGACCCT[A/G]CCTTCTTTGGGGGAG | 8440 |
rs541609317 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NCK2 | GRCh38.p7 | 2:105849939 | TGTTTACAAGCTCCT[C/T]ATGAGGTATTACCCT | 8440 |
rs541642809 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105835448 | TGGTCAGCATTTTGA[A/T]TATATCATAGTGAAC | 8440 |
rs541653255 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105836001 | CTGTTGAATTTCTCC[A/G]TGAATTCTCATGAAT | 8440 |
rs541684743 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105862183 | TTTTTTTATATCAGT[C/G]GTAAAGACTCTAGAA | 8440 |
rs541711841 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105795180 | AATCACCCAAAGTCC[A/G]GGGTTTATATTTGGG | 8440 |
rs541715631 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105743458 | CACAAAACTTGCACA[A/C]AAGGATGAACTGAAG | 8440 |
rs541728966 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105769731 | GCAGTACAGCCAGGC[A/G]GCCACAGGAGCCACT | 8440 |
rs541756280 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NCK2 | GRCh38.p7 | 2:105788682 | CTCCTAGAGTTTTCT[A/G]TTTTTTTGTTTTCTT | 8440 |
rs541775373 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105762933 | GGCGCAGTGGCTCAC[A/G]CCTGTAATCCTAGCA | 8440 |
rs541785142 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105784383 | ATGGGCTTGGGGTGA[A/G]TCGGGAGGGGAGAGT | 8440 |
rs541802198 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105746840 | CTTAGTGGTCTTCTG[G/T]CGGCTACTTGAGGCT | 8440 |
rs541802312 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105815546 | CCTCGAAAACGTTAG[C/T]CAAGGACTGAAAATA | 8440 |
rs541807176 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105770704 | TCGATATTTAGTAAT[C/G]TGAATTATTTTTCAT | 8440 |
rs541812687 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105863975 | GAGACTTGGCGAGGG[C/G]GGGTGGGGTCTCACT | 8440 |
rs541823514 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105795421 | GATATTGAGTTAAAC[G/T]GAATGGGCCTGTTTA | 8440 |
rs541832008 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105785264 | ATTACAGGCGTGAGC[A/G]GCAGTTGGTTCTTTA | 8440 |
rs541861315 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105888456 | AGCACAAAGGTGGCA[A/G]TTAAAGAGGAGAAAT | 8440 |
rs541873271 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105857310 | TCAGACTGAGCCAGC[C/G]GCCCGTCCTGGAGCC | 8440 |
rs541913526 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105793823 | GGGGGTTTCAGGCTC[C/T]TTTAGACAGTGCCTA | 8440 |
rs541926888 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105752600 | TTGTTACATAAATTG[C/T]CTAAGGGTGAATTCA | 8440 |
rs541965114 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105745420 | ACGCCAGCCAAGGGC[A/G]CGGGCGAGGATCAGG | 8440 |
rs541991562 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105790086 | TTTGTGGAATGTTAC[A/T]TCCTATTTGTAGAAC | 8440 |
rs542002804 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105744236 | GTCGAGTTTCTTCTT[C/T]TTTTAGGAAGTGCCT | 8440 |
rs542018969 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105789433 | GCCTCAAGTGATCCA[C/G]CCGCCTCGGCCTCCC | 8440 |
rs542021679 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105869309 | TGGGGATGACAACAC[A/G]ATGGCAGCCATCACC | 8440 |
rs542033495 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105834045 | ATTTCTTATGACTTC[A/G]TTTATGACCAAACAT | 8440 |
rs542037675 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105833995 | AGTTTTATTCTATTG[C/T]GTTCTGAGATAATAC | 8440 |
rs542055251 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105842387 | CACTGCACCCAGCTT[A/G]TTTTTTTCTCATAAA | 8440 |
rs542083507 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105882535 | TTGCCACGGCAGGCA[C/G]CGCCACTGAGTTCAT | 8440 |
rs542118955 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105810602 | AAAAAGGCAATATGT[A/G]ATTAAATTGTCTAGT | 8440 |
rs542121309 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105860102 | CCAGCCTGGGGAACA[C/T]AGCAAGACTTCATCT | 8440 |
rs542142827 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NCK2 | GRCh38.p7 | 2:105850033 | CCTTGCCCTCTAAAG[C/T]ACTTTGTATTCATGT | 8440 |
rs542150690 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105750346 | TTTATGACCTTTTTT[A/T]ACCTTAATTGCCTCC | 8440 |
rs542162750 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105880880 | CTGGCTCAAGCCATC[C/T]TCCCACCTCAGCCTC | 8440 |
rs542192527 | in-del | -/GTT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105884231 | ACAAGTCCTTTGCTT[-/GTT]TTTTTCCCACCATCC | 8440 |
rs542194186 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105873360 | AGGTTACATCATGTT[A/G]GTCTGTGAGGCCTAA | 8440 |
rs542215304 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105784814 | TTTCAACATTCTTAG[A/C]ATATGCACAAAGAGT | 8440 |
rs542256822 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105872890 | CCTTCATCCGGGGAC[A/G]CCTCTGTTGAGCAGT | 8440 |
rs542268418 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105754077 | GATGGGACTGAGATA[G/T]GACGGTGAGTCTGGC | 8440 |
rs542282061 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105827750 | TATATAACATTCTCA[A/C]AATGACAAAATTACA | 8440 |
rs542303263 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105751494 | AGTCATGGGCTTGCA[C/T]GACTGGGCTGCCTCT | 8440 |
rs542334921 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105879519 | AGTAGAAATCTAAGC[A/G]TTTCACCTGTTCTAA | 8440 |
rs542357437 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105769573 | GTTAGGCATCCATGG[C/T]TGCAGGTTTTCTAAG | 8440 |
rs542386082 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105789401 | CCATGTTGGCCAGGC[C/T]GGTCTCCCAACTCCT | 8440 |
rs542407835 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105754970 | ATTCTTCTGGTTCTC[A/C]CCTCACTTTTTTGTG | 8440 |
rs542409268 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105846361 | TAAATGAGTTGCTCA[A/G]TGATGAACTCCTGAA | 8440 |
rs542433104 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105892024 | TTTCCACTGCTGTTC[A/T]TATTTTTAAATGCTT | 8440 |
rs542437496 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105780763 | CGGAAGACACCCCAG[A/G]GGGCCCCCTCACCCC | 8440 |
rs542458838 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105802776 | GTCAGATATTCAAAC[A/G]GTAGCAACATCCTTG | 8440 |
rs542479568 | in-del | -/AAGA | | | intron-variant | NCK2 | GRCh38.p7 | 2:105801482 | ACGTTAACAGATAAG[-/AAGA]AAGACTGAGGGACAA | 8440 |
rs542486863 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105893676 | GATAGCAATACTGGA[A/G]CCACCGGGTGCGATG | 8440 |
rs542487720 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105853907 | CAGCTGTCACCTGGG[G/T]GATGGTAGAGGATGA | 8440 |
rs542495299 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105802165 | AGCCAGGATTTAGGA[C/T]TCTTGAGAAGCTGAA | 8440 |
rs542518508 | in-del | -/A | 0.00318978 | 0.0398085 | intron-variant | NCK2 | GRCh38.p7 | 2:105799194 | GTGGTATATTTTATC[-/A]TGTAAGAAAATTTTT | 8440 |
rs542574903 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105767557 | TTTATTAGAACCCAG[C/T]TGGGCTCATTCATTT | 8440 |
rs542627137 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105800690 | TGGGTTTGGTGCTTG[A/G]TTTCTGATGGGACCA | 8440 |
rs542634916 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105832262 | ATCTGTTTACCAATT[A/C]TACAGTATTTTGCTG | 8440 |
rs542666511 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105764736 | TTTGAAAAGCGAGAT[A/G]CTTCCTGTAATCTCA | 8440 |
rs542669807 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105831748 | TTCTGTTCCCTTTGT[C/T]GATGTGTCTGTTTTT | 8440 |
rs542682224 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105843718 | GAGTATAAAATAGCC[A/G]TAAGATCACAGTGAT | 8440 |
rs542711820 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105748545 | TAGCTGGGACTACGG[A/G]TGTGCACCACCATGC | 8440 |
rs542754160 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105806854 | AAAAAAACCCAACCA[A/G]CCATCCTACAGAATC | 8440 |
rs542758446 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105838662 | TTTGAATCCACATGC[A/G]AGGTAGGGCCTCAGT | 8440 |
rs542769919 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105799456 | TTTATTGAGAAGGCT[G/T]TCTCTTCCCTGGGGA | 8440 |
rs542775490 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105763177 | CACTCCAGCCTGGGC[A/G]ACAGAACGAGACTCT | 8440 |
rs542855132 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105862060 | CCCGGGTAACTAAAG[A/G]CCCTTTAGTTAGGGT | 8440 |
rs542857947 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105798904 | TCAGGAAGTTATACC[A/G]GGTTGTTGTCATCAC | 8440 |
rs542896447 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105805372 | ATTTAAAAACTAATT[A/G]TACTTTAAGAACTAA | 8440 |
rs542899610 | snp | A/G | 1.92435e-05 | 0.00310184 | missense, utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105893112 | TGGTGGAACACTACA[A/G]AAAGGCGCCCATCTT | 8440 |
rs542992076 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105775317 | GAATCCTGGTGTGCC[C/T]GTCACTGGACATCAG | 8440 |
rs542993274 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105868866 | CCCGGGGCAGCCAAG[C/T]GACTTGGCCAGGGCT | 8440 |
rs543056018 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105848096 | AGCCATTGAGCCTAG[G/T]GATGACTGGGCATTA | 8440 |
rs543076504 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105756618 | GTGGTGAGTGGCCAT[C/G]GGGGAATGTCAGGCC | 8440 |
rs543117532 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105856198 | CCTCCTGGAGTTACA[C/T]AAAGTTAACAGTATC | 8440 |
rs543123630 | snp | G/T | 0.0134861 | 0.0810011 | intron-variant | NCK2 | GRCh38.p7 | 2:105760244 | ACAGACAGCCCCTTG[G/T]CACTGTTGCGGAGGA | 8440 |
rs543123765 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105749729 | TTGAGCGGTGTGAGG[A/G]GAGGCCGGCAGGAGC | 8440 |
rs543125311 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105825339 | ACACCTGAGATAATT[C/G]ATCATAAATTCAAAA | 8440 |
rs543145095 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105813413 | TGTCCACAAAGCTCA[C/T]AGCCTTGGGCTGTCA | 8440 |
rs543148256 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105787922 | ACCGCCCCCGACTTG[C/T]AGATCCCTGGCCCAT | 8440 |
rs543158862 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105866297 | TTATCACTCAGAAGT[A/T]ATCACGGTTGACATT | 8440 |
rs543167674 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105880152 | AAGAAATGTTTCTCA[A/G]TCTGATTCGATACTC | 8440 |
rs543209471 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105748974 | TGTCCAGACAATGGG[A/T]GAATTTGGTCTGTTG | 8440 |
rs543209959 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105839879 | AAACTAAGAAGGAAG[G/T]GTCAGCAAGGGACAG | 8440 |
rs543228311 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105847401 | AAAGAAATGATGTGG[G/T]ATATTGTGTGCTTGA | 8440 |
rs543288368 | snp | A/G | 0 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105755562 | TTCAACACATTGCAC[A/G]TTCATGCGTGTGGCT | 8440 |
rs543311773 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105818750 | AGTAATCTTGAAACT[A/G]TCATGTTGGACTATG | 8440 |
rs543351101 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105757182 | GGAATAGAGATGAGT[C/G]TCCTTTTCCTTTGCT | 8440 |
rs543376307 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105762827 | AATACGTAGATTACT[A/G]TGTCTCAAGTTTGTT | 8440 |
rs543379090 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105789494 | TTGCCTGGCCTCACA[A/G]CCTTTTTTCAATGAG | 8440 |
rs543381007 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105795663 | TGTTGATTGTCACCA[A/G]TTTAGGCAGGGTGTG | 8440 |
rs543384608 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105806179 | GATGCTCAGCCTTGT[A/G]TATGTATGTGTGTGT | 8440 |
rs543403257 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105838617 | TGAATATATCAAGAA[G/T]TGGGATTGTTTTAAA | 8440 |
rs543428695 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105819528 | TTAGAAAGGTCTTGA[C/T]CGTCAGTGACATTAG | 8440 |
rs543448404 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105889902 | TTGAGAATATGCTTC[C/G]TAACCAGTTCTCAGA | 8440 |
rs543455095 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105762567 | GAGGATATCTGTGAA[C/T]TTTGGGGTGGGAAAA | 8440 |
rs543509935 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105889246 | CCCTTCAGGGGAAAT[C/T]CCCTATGAGAGATGT | 8440 |
rs543533753 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105764165 | CATGCTGTTTGCACG[C/G]CTGTGCAATGATCCT | 8440 |
rs543537639 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105759271 | GTTTTACGTATTCAA[G/T]TACACATAGTACGTT | 8440 |
rs543578086 | in-del | -/TT | 0.00597247 | 0.0543191 | intron-variant | NCK2 | GRCh38.p7 | 2:105747957 | TAAAAAATTAGACTC[-/TT]TTCTTTTCCTGCATT | 8440 |
rs543584488 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105800978 | AGTGTCAGAAGATTG[C/G]AGACAGGCAAATGTT | 8440 |
rs543599996 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105756251 | TTTCTTACCCCTCTC[C/T]TCCTGTGCTGTTTCT | 8440 |
rs543624044 | in-del | -/T | 0.00557542 | 0.0525036 | intron-variant | NCK2 | GRCh38.p7 | 2:105785173 | TTAGTAGAGACAGGA[-/T]TTCACTGTGTTAGCC | 8440 |
rs543634574 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105763147 | AGGTTGCAGTGAGCC[A/G]AGATCATGCCACCGC | 8440 |
rs543656616 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105769165 | GGGCACTCTTGTTGC[C/T]CAGTAAATACCAAGG | 8440 |
rs543660411 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105754968 | CCATTCTTCTGGTTC[A/T]CCCCTCACTTTTTTG | 8440 |
rs543661324 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NCK2 | GRCh38.p7 | 2:105856329 | CTGAGCTGACATTTA[A/G]AACGTTGTTACCTTC | 8440 |
rs543665327 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105795720 | AGGGGACAGCTCCAC[A/G]ACAAAGAATTACCGA | 8440 |
rs543674737 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105862568 | ACGTTTGGGGGGACT[C/G]TGTCCCAGAGTCAGA | 8440 |
rs543691311 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105775689 | TGAAAATTAGCTTCC[C/T]TTTTGTTTGTTTGTT | 8440 |
rs543728501 | snp | G/T | 0.00119737 | 0.0244387 | downstream-variant-500B | NCK2 | GRCh38.p7 | 2:105894335 | AGAGTAATTACTGAA[G/T]CATTCACTCATTGCG | 8440 |
rs543734781 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105799558 | GCTTCCTAGTGTTTC[A/G]TTAGTCTGTCTATCT | 8440 |
rs543754938 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105771166 | TGACCTCGTGATCCG[C/T]CTGCCTTGGCCTCCC | 8440 |
rs543765707 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105804105 | CATAGAGGCAGTGGC[A/G]ACTCTCAGGATTTAC | 8440 |
rs543793485 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105829474 | TAATGTTCATTTTCT[A/G]TCCCAGGATTCCATC | 8440 |
rs543797429 | snp | C/G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105891106 | AGAGGGCTCTCCTGC[C/G/T]CCCACACGCACTTAT | 8440 |
rs543823786 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105798165 | GAGCTAATGTTCGCT[C/T]GTTGTAATGTTTGTT | 8440 |
rs543835150 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105834069 | CAAACATACTGTAAA[A/T]CCTAGAGAATGTCCC | 8440 |
rs543836591 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105758112 | TGAGAGCTTTATCTC[C/T]TAAAAATGAGTTAAA | 8440 |
rs543860292 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105797681 | GCAGCGACTGTGTGG[A/G]GCCTCCCTGTTTAGG | 8440 |
rs543860637 | in-del | -/C | 0.00398564 | 0.0444627 | intron-variant | NCK2 | GRCh38.p7 | 2:105758652 | TGACCTTGTGATCCA[-/C]CCGCCTCAGCCTCCC | 8440 |
rs543892423 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105892562 | GAGACCCGGCTGGGC[A/G]TGGTGGCTCATGCCT | 8440 |
rs543892840 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105801408 | ACGTGGTTGAGGGAT[A/G]TGCTTTTTTCTTTTT | 8440 |
rs543897348 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105761204 | GTGCTGGGAGGTTTG[G/T]GTGTGTATGGGAGCG | 8440 |
rs543924787 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105848879 | ATAATTCAGACTGCA[A/T]GTTGAAAATCAAGGT | 8440 |
rs543937644 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105860984 | GTCGTTGTGGATCCC[A/G]AAAGAAGGGACTTGG | 8440 |
rs543964465 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105772380 | GATAAGAACCTAGAA[A/G]AAGGAAAATGTTCCT | 8440 |
rs543986192 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105856777 | CATTTTTGATTAGCA[A/G]TATGCTCCTTCTCCA | 8440 |
rs544024110 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105848203 | CTCATTTAATCCTCA[C/G]CGAAGCTCTGACCCA | 8440 |
rs544026106 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105879869 | GGTACAAGCTACCCA[A/T]GGAAGTGCTTGGAGG | 8440 |
rs544051381 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105771852 | CATTCCTTTGTGAGG[C/T]CTGCCCATCACTCAG | 8440 |
rs544067186 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105859482 | ACCTAGGCCTAGCGT[G/T]GTTAGAAACTTGCAT | 8440 |
rs544083936 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105771279 | CTTTCTAGTAAAAAA[A/G]CATGAGGGCTGGCGG | 8440 |
rs544087162 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105813563 | AGGTGCAGCAGAAGA[C/G]ACTGCGCCAGCACCA | 8440 |
rs544100591 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105837137 | AGGGTCTTGTTGCTT[C/T]TTTGCTGAATTCCAG | 8440 |
rs544158326 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105785994 | TTGTGTTTTCGTAAA[C/T]GTGTGTGTGTCCACT | 8440 |
rs544224904 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | NCK2 | GRCh38.p7 | 2:105845480 | CTCACTGCATCCTCC[G/T]CCTCTTGAGCTCAAG | 8440 |
rs544283064 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105762301 | CATCAAACCAGGGGG[C/G]GTCTAGGTCCAGGCC | 8440 |
rs544285435 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105861368 | AAGGAAGTCTGGCTC[A/G]TGCACCAGGTTCTGA | 8440 |
rs544312777 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105883045 | CCCTCCAGAGAGAGG[C/G]GACTGGGATGTGCTC | 8440 |
rs544345959 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105844149 | CAGACAAATCCTAAC[A/G]GGTGGGGGGACATTC | 8440 |
rs544351793 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105766422 | TCGACCTCCTGAGCT[C/G]AAGCAATCCTCCCAC | 8440 |
rs544385737 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105824067 | ATGTGGCCAGGGACA[A/G]GGAGAGGCTCTAGAG | 8440 |
rs544459991 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105865251 | TACCTGCCAGGTGCC[C/T]GAATATGTTTTTATT | 8440 |
rs544477556 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NCK2 | GRCh38.p7 | 2:105823652 | AGTTTTGGATGGAAA[C/T]GAATAACCCTTAGTG | 8440 |
rs544521833 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105822685 | ACAAAAAAGCCAATT[A/C]TGTACCCCTCGACCT | 8440 |
rs544550680 | in-del | -/G | 0.00599036 | 0.0543994 | intron-variant | NCK2 | GRCh38.p7 | 2:105866744 | CTGGTCTGTGGCCCC[-/G]GGGGGGTTGGGGACC | 8440 |
rs544564766 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105815946 | GAGCTCAGGTCCCTT[G/T]ATTATGGGCTGGCTG | 8440 |
rs544571606 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105786712 | GCTTCCTGTCTCCAT[C/G]GCTGTCTCTTATTTC | 8440 |
rs544590586 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105838174 | AGTCACAAGAAAATC[G/T]TGTGTTCTCACAGCT | 8440 |
rs544602496 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105849677 | AGTGACACTTTGATG[C/G]GTATCTCTGAAGCAG | 8440 |
rs544640875 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105886783 | TGGGGATAGGGAGGG[C/T]TAACCACACACATGC | 8440 |
rs544640904 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105847525 | ATGCAGGTGTGCAGC[A/G]GAACTGGCCTCCCTA | 8440 |
rs544652560 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105811660 | GGAGGTCCTTTGTCA[A/G]GGAGTGTGTTCAGTG | 8440 |
rs544660346 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105860564 | GCATGTAGTCAGAAC[C/T]GCATGGGGAGGCCTT | 8440 |
rs544661256 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105773770 | GGTGGAAAAGGAGCA[C/G]CCAAGTGCTTGCTCC | 8440 |
rs544675017 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105781166 | TAGCTTCCCATTTCC[A/T]AGAGGTGCCTTTGTG | 8440 |
rs544685712 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105867251 | GAGATGCATTTAATA[C/T]TTCACGTTTACTTTT | 8440 |
rs544702445 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105885665 | AATAGCACGTTTCTT[C/G]GTGGTGATGCTGCTG | 8440 |
rs544706392 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105762023 | TTTCTAAGTTTTTGC[A/G]TTGACTACAGTTGCA | 8440 |
rs544720425 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105825148 | GTCCATGCCTACCAG[C/T]TGTAATGTAATGGGG | 8440 |
rs544724811 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105875915 | CTTTTCAGTGTAAGA[A/G]TTAAAATCCTGCTCA | 8440 |
rs544741871 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105754918 | ATGGTTATAGAAACA[G/T]ATTTTTTTTTTCCAG | 8440 |
rs544781608 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105846309 | TGACTTAGAGTCTAG[C/T]CTGCAGAACGCTAGT | 8440 |
rs544794184 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105761311 | TGACTGACTTCCAGA[A/G]AATCTTTTTTTGGGA | 8440 |
rs544795842 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105872556 | AGTGATTCTCTATTT[C/T]ACTAGTCTGTGAGGT | 8440 |
rs544810945 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105860143 | ATTTTTTAAAAAATA[G/T]AGCATGGTGTCATGT | 8440 |
rs544812304 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105805206 | TTCCTGAATGGTGAG[G/T]TGGATTTGATTGCAC | 8440 |
rs544819187 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105764890 | TTTTTTCCATGTTGT[A/G]TGATATCCCATGGAG | 8440 |
rs544857629 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | NCK2 | GRCh38.p7 | 2:105762927 | AGGCCAGGCGCAGTG[G/T]CTCACGCCTGTAATC | 8440 |
rs544871349 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105853636 | TAAAGAAAAAACTTA[C/T]TCATGACATTTGTTG | 8440 |
rs544873935 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105859515 | TCAGCCCCAGAACTC[C/T]TGCCTCTGATCCAAC | 8440 |
rs544883018 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105786173 | ATTAGCGTTGTGGAC[C/T]GAACAATAAATTACA | 8440 |
rs544903907 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105878248 | TTATAGCATCAGCTG[A/T]ACGCTGGTGCCTGTC | 8440 |
rs544949265 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105781026 | GAATCTAGATTTTGT[C/T]TCTCACCTGGTCGTG | 8440 |
rs544991355 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105772495 | CCTCACAGATGTGCT[A/T]CTCCAGAAGTGGCCG | 8440 |
rs545017994 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105830447 | TATTCCACTGTGTAT[A/T]TGTACCACATTTTCT | 8440 |
rs545022938 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105806801 | GCAAATCCCATTCCA[C/T]AGGGGGCTTCGCAGT | 8440 |
rs545025714 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105878953 | GGTATGTCTCAGGAA[C/T]TCAGTGGCTGTATTA | 8440 |
rs545043051 | in-del | -/TGAGATATCT | 0.00755907 | 0.0610114 | intron-variant | NCK2 | GRCh38.p7 | 2:105843141 | CTACATATACATAAA[-/TGAGATATCT]TGGGAATGGGACTCA | 8440 |
rs545059698 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105801970 | GAACTGTTTTGTAGA[C/T]TGGTAGCGATTGGAC | 8440 |
rs545060935 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NCK2 | GRCh38.p7 | 2:105812829 | GCTTTTTTTTTTTTT[C/T]CCCTCCTGTGCTAAC | 8440 |
rs545139195 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105838176 | TCACAAGAAAATCTT[A/G]TGTTCTCACAGCTGT | 8440 |
rs545144031 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105844631 | TAATTGCAGCTACTC[A/G]GGAGGGTGAGGCAGA | 8440 |
rs545144575 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105812285 | TCTCCTTGGACACCT[C/T]TGAGTTTCGGATTGA | 8440 |
rs545195033 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105853001 | ATTATTTATAAAAAA[A/T]TTTTTTTAGCATCTA | 8440 |
rs545275519 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105787124 | GCTGTTACTCCCACT[A/G]CCCTCACCTTTGACC | 8440 |
rs545285761 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105811000 | CCAACATGGTGAAAC[C/T]CCGTCTCTACTAAAA | 8440 |
rs545319871 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105781352 | GCCTTCTCCCATCTC[C/T]GCTTCCACCTCCACC | 8440 |
rs545338357 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105872838 | AGTCAGAAATGATTC[A/G]GAGAAATCTCTGAAA | 8440 |
rs545348190 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105824606 | ATTGGTCATTTTCCC[A/G]GTCGTTAAGTACCAC | 8440 |
rs545400217 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105879500 | TTTATATAAGTTAAC[A/T]CAAAGTAGAAATCTA | 8440 |
rs545407956 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105760561 | CTCCCCGTGTAACCA[C/T]TTCTCCCACAGTTTT | 8440 |
rs545486982 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105861942 | CCCTCCCTCCTGCCC[A/G]CTCCCCCCTTCCCTT | 8440 |
rs545530136 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105819360 | GTCATTGGGGTAGAA[C/G]TTTTTAAAACAGTCA | 8440 |
rs545531920 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105768366 | TTCAGTTCTGACACT[A/G]GCTTTTCAGGGTTCG | 8440 |
rs545548926 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105857531 | GTGCTGAGTAGGTCA[A/G]ATCCTCTTCTGTAGA | 8440 |
rs545563469 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105777464 | ACCACCTGGCACGGC[A/G]TGGGTGGAGAGTGGT | 8440 |
rs545565216 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105868051 | GGCTACTGAGAGAGC[A/G]CTCGTTTACTGGCTT | 8440 |
rs545599477 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105861498 | AGTGGCTATTGGTGC[C/T]GTTGAGGTTTTTCTC | 8440 |
rs545605073 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105818983 | TTAATATGCAATAAG[A/G]ATAGGATTAAGTGTC | 8440 |
rs545611738 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105872072 | TCTTCCTTAAACGTA[A/C/T]GCAGTTCTTAATGGT | 8440 |
rs545628985 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105821972 | TGACATGGTAACGAC[A/C]CATTCTCCAAGTGCT | 8440 |
rs545650256 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105870351 | GCAACTCCCTTCTGT[A/G]GCATGAGGCTTCTTC | 8440 |
rs545662585 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105867519 | GATTAGTGGGAGGAT[A/G]CTTCGAGAGAAAATA | 8440 |
rs545663213 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105780809 | CACAGCAAGAAGCCG[C/T]CGTGTAGGAACCAGG | 8440 |
rs545665962 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105846319 | TCTAGTCTGCAGAAC[A/G]CTAGTGTGTCTTGGC | 8440 |
rs545693536 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105824169 | ATTGTTACCTTATTT[C/T]ACATGTGTGAGTGCC | 8440 |
rs545695882 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105749024 | TTTCTGTCATGTGAG[A/T]CATTTGTAGTCCTGA | 8440 |
rs545708922 | in-del | -/GCC | | | intron-variant | NCK2 | GRCh38.p7 | 2:105840905 | ACGGAAAGGTAAAAG[-/GCC]GCCGTGGGCATCTGA | 8440 |
rs545738261 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105779120 | TTGGCCAGCCTGGCC[A/C]ACATGGTGAAACCCT | 8440 |
rs545759729 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | NCK2 | GRCh38.p7 | 2:105783720 | TTATGTTTTTTTTTC[A/G]CTAATAGGTGAAAAA | 8440 |
rs545776617 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | NCK2 | GRCh38.p7 | 2:105866149 | GAACTCCTGACCTCA[A/G]GTGATCCACCCACCT | 8440 |
rs545777513 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NCK2 | GRCh38.p7 | 2:105850867 | ATGGGTCATCTGCAG[G/T]CTCTTTCTGTTCAAA | 8440 |
rs545789704 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | NCK2 | GRCh38.p7 | 2:105858050 | TTGTTTTTTGGGGTT[G/T]TTTTTTTGTTTTTTT | 8440 |
rs545790126 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105751520 | CCTCTCTGTTTCTCC[C/T]AGCATCTAAATATCC | 8440 |
rs545831502 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105883903 | TTCTAGGAATATAGG[A/G]CGGAAAGAGCTTTAC | 8440 |
rs545833145 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105779786 | TATACATAGTAATTC[C/T]CTAGCAGAAATGTAG | 8440 |
rs545860601 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105771164 | CCTGACCTCGTGATC[C/T]GCCTGCCTTGGCCTC | 8440 |
rs545862398 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105765103 | TGGCTCTTGATGCAT[C/G]TTGCCATAACGCCCT | 8440 |
rs545881036 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105864594 | GTTATCCTTATGACA[C/T]ACTTCTTTATGTCAG | 8440 |
rs545888180 | in-del | -/TT/TTT | 0.437401 | 0.165472 | intron-variant | NCK2 | GRCh38.p7 | 2:105765666 | GTAGTGGGTAGTGGG[-/TT/TTT]TTTTTTTTTTAATTA | 8440 |
rs545892433 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105748391 | TCCTGCAGTTGTTTT[G/T]TTTCTTTTTTTAAGG | 8440 |
rs545903913 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105746923 | TGTCCCGGAGGCCTC[C/G]CCTGGATTCTGAGCT | 8440 |
rs545923838 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105833794 | TGGGCATTTATTGCT[A/G]TAAACATCCCTCTTA | 8440 |
rs545937688 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105877992 | CCTGCCTCTTGAATT[C/T]CACTGCACCAGCAGC | 8440 |
rs545952135 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105828883 | AAACCATAGCTCTTA[C/G]TATGAGCTCACACAC | 8440 |
rs545960826 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105821384 | ACTTGTGGAGTTTCC[A/G]CCCAAATAAATGGGC | 8440 |
rs546003574 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105864054 | TGTGGGGAAGGCCAT[C/T]GGCGAGCCAGCCGGA | 8440 |
rs546017897 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105832361 | TATAAACAATACATT[G/T]AATAAGAGTCGTGAA | 8440 |
rs546018905 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NCK2 | GRCh38.p7 | 2:105836003 | GTTGAATTTCTCCAT[A/G]AATTCTCATGAATTG | 8440 |
rs546020643 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105843927 | GTAACTTCAGTGGAG[A/G]ATCCTGACAAACACC | 8440 |
rs546048839 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105827189 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCATGT | 8440 |
rs546080975 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105753468 | AGGGAACTGCAGTGG[C/T]ACTGGATGAGGGGGA | 8440 |
rs546089750 | snp | A/G | | | upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105743757 | TGACTCTAGTTACCT[A/G]TCCTTGGGTACTTCC | 8440 |
rs546095736 | snp | A/G/T | 0.00358779 | 0.0422022 | intron-variant | NCK2 | GRCh38.p7 | 2:105888269 | AAAACTATGAGAATG[A/G/T]AAAAATCATTCCTTA | 8440 |
rs546102046 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105882352 | CAAACATCATTTTCT[C/T]TCCTGGTTGCCCATT | 8440 |
rs546127596 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105834758 | CTGTAGCCTTGAACT[A/G]TTGGGTTTAAGTGAC | 8440 |
rs546132919 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105771884 | TCTATATTTTTCTCC[A/G]CAGCTGTTCCCAGAA | 8440 |
rs546141769 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105827414 | ATACTTGAAGATCTC[C/T]ATACTCTTCTCAACA | 8440 |
rs546177094 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105803669 | ACACCCAGGTTAGTC[A/G]TCTTTCACACTTGTG | 8440 |
rs546205016 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105816417 | GACCTAATATATGCT[G/T]CTTTCTTTTTAGATT | 8440 |
rs546209969 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NCK2 | GRCh38.p7 | 2:105851616 | CTCCAGGAGTTTCAG[A/G]AGCGGAAGCGTTCAG | 8440 |
rs546217272 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105882055 | CGAGTCCTCGGTAAG[G/T]GCGCTGCGCCCACAG | 8440 |
rs546220034 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | NCK2 | GRCh38.p7 | 2:105779082 | GAGGCTGAGGCAGGT[A/G]GATCACTTGAGGTCA | 8440 |
rs546236651 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105871188 | CCAGATCTGAGGCCA[C/T]GATGGTGACTTTGTT | 8440 |
rs546258333 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105767305 | TTGGATGTCTGATAT[A/G]AGCTTAGAAGCCTAA | 8440 |
rs546263834 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105786067 | TTGCCTTATTCTCAC[A/G]TCCCTTCCACTGCAC | 8440 |
rs546268871 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105752800 | ATGGCTGAATAGTCT[A/G]TTTTCTTTATCCAGT | 8440 |
rs546272250 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | NCK2 | GRCh38.p7 | 2:105768288 | TGGCCGCGTGTGGCC[A/G]GTGGCTGTGTTATCA | 8440 |
rs546287610 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105828478 | ACACTCACCCACCGC[A/G]GATCAGTGTGGAGTG | 8440 |
rs546298608 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105785317 | GGCCATGCTGTGTGT[A/G]TCCAAGTGTAAAAAG | 8440 |
rs546302077 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105877106 | CCATGTAAAGGCTCT[C/T]CTGACTCTAGGGTTG | 8440 |
rs546319525 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105843453 | AAGGATTCATGTGTA[A/G]AAAGTGGACTACAGG | 8440 |
rs546371069 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105891072 | CCTCGGAGAGCACAT[A/G]CTCAGCTCCACATTG | 8440 |
rs546386576 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105791260 | ATTCATCTAGAGAAA[C/T]CTGAGGCAGTGATGT | 8440 |
rs546392671 | in-del | -/ATAG | 0.00279162 | 0.0372561 | intron-variant | NCK2 | GRCh38.p7 | 2:105844822 | TATATATACATAAAA[-/ATAG]ATATATATATTTTGA | 8440 |
rs546403935 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105862246 | TAGTGGGAAGGGGGT[C/T]GGTCTTGAGCCTGTG | 8440 |
rs546453534 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105808379 | ATCCCATTTGAAAAT[G/T]ACAGCCTGGAAAGAG | 8440 |
rs546456420 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105883794 | ACTAAAGCACGAATT[A/G]TTTGTATTTCCTTTT | 8440 |
rs546498345 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105759681 | CCATAGTTTATTTGC[C/G]CTGACATCCTTTTTC | 8440 |
rs546508578 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105803062 | GTTGTCATTTTTCAA[A/G]TTGATGGTTTTCCTT | 8440 |
rs546517453 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105891400 | CCAGGGCACCGCCTG[C/T]CTGGCATGTGTTAGT | 8440 |
rs546517782 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105770859 | TTGCTTATCATTTCA[A/G]TCTTCAGTGTTTGGC | 8440 |
rs546519438 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105883374 | CGCTGGAAAACCAAT[G/T]ACAATATTAAGTGCT | 8440 |
rs546529634 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105890942 | TGGACCCTCAGAGCA[A/G]GAAGTTTCTGGGCTT | 8440 |
rs546542316 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NCK2 | GRCh38.p7 | 2:105815365 | TTTGACTAAAATAGA[A/G]TTCGATTTTTCTATG | 8440 |
rs546567689 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105745554 | GGACCGTGCGGTGGC[C/G]AGGGTCGCCAGGGCG | 8440 |
rs546597547 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105848050 | AATCTATTGCACATA[A/C/T]GTTTTTGAGTCCCCG | 8440 |
rs546598287 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105790256 | TTGGATTAAAATGAC[A/G]GACTCGTTTCTTGGC | 8440 |
rs546606251 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105752137 | ATTGGCCTTGGCCAC[A/G]CGCGACTAGTGGCAG | 8440 |
rs546626791 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105796247 | CGTGTGTAAGTATAT[A/G]TGGCTGGTGGGCAGA | 8440 |
rs546648451 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105875877 | CGTAATTTTATGATG[A/G]TAGATTTAAAGTGCT | 8440 |
rs546652146 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105859296 | TAAGGGCTGACTCAC[A/G]TTACCCAAAAAGTTA | 8440 |
rs546709977 | in-del | -/AA | | | intron-variant | NCK2 | GRCh38.p7 | 2:105770141 | AAAAAAAAAAAAAAA[-/AA]GAAAAAGGTATATTG | 8440 |
rs546711698 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105882835 | AGACTTCCAAAACAA[A/G]CATTTAGGAGATAGA | 8440 |
rs546724324 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105766609 | ATTACAGACTTGAGC[C/T]ACTGTGCCTGGCCTA | 8440 |
rs546733678 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NCK2 | GRCh38.p7 | 2:105759342 | TAATACCCTCACGTT[C/T]GTGTATTAAGCTGAT | 8440 |
rs546745074 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105810613 | ATGTAATTAAATTGT[C/G]TAGTTATGGCACTGA | 8440 |
rs546760562 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | NCK2 | GRCh38.p7 | 2:105850253 | TTTAATGTTGTAGGG[G/T]CACTGGCTACTATCA | 8440 |
rs546763259 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105771991 | AAATTGGATATTGTC[C/G]TCAAAGTGTCCAGGA | 8440 |
rs546766087 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105858527 | TTGCCATTTTTACTG[C/T]TTTGGGAGTCCACCT | 8440 |
rs546772269 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105758806 | AATTACTGTACTGCT[C/G]TGACAGTAAGTTGTT | 8440 |
rs546778785 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105788670 | TCTAAGTGCCTTCTC[C/T]TAGAGTTTTCTATTT | 8440 |
rs546855468 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105865501 | GGCATCAATACTGGC[A/G]ACTCCCACCCACACG | 8440 |
rs546856546 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105764709 | ATAATATACTGACTC[C/T]TAAGCATAGTTTTTG | 8440 |
rs546866504 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105857670 | CCCCTTTATTGAGTA[C/T]AGCAGTTGATCTTCA | 8440 |
rs546873262 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105814797 | ATATTACTCATGAGA[A/C]ACAGGGCACACAGGG | 8440 |
rs546896343 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | NCK2 | GRCh38.p7 | 2:105883590 | GTTCTCCGGGGTTGC[C/T]GGCCTTAGGGAGGAC | 8440 |
rs546934709 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105844312 | CATTAAGGGAAAGCT[A/G]AGGACATCTGAATAA | 8440 |
rs546938420 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105892018 | CGGAATTTTCCACTG[C/T]TGTTCATATTTTTAA | 8440 |
rs546939876 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105863726 | GCACCTGTGCTTTCA[A/G]AGAGCATGTAGCATT | 8440 |
rs546940343 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105880662 | TCTAGGAATGAAAAA[G/T]ATATTTTCTCTGCAT | 8440 |
rs546945546 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105763298 | ACCAGGTGTCACTGC[A/G]TCCTCTGATGACCGA | 8440 |
rs546974486 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105856483 | GAGGATTTGTTTTCT[G/T]TTGGGGAATGGAGAA | 8440 |
rs546978748 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105876992 | GCAGAAACCGTCCCT[C/T]TGAGATGTCCCGGCT | 8440 |
rs546995877 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NCK2 | GRCh38.p7 | 2:105804074 | CTTGCCCATTTTTTA[C/T]GGGGCAAATTATATA | 8440 |
rs547063632 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105847892 | TAGCATTAGCCACAC[C/T]GGGAGCATTAAAAAA | 8440 |
rs547097144 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105751544 | AATATCCCCTTCCCC[A/G]TATACACACATGCTG | 8440 |
rs547111378 | in-del | -/G | 0.00398564 | 0.0444627 | intron-variant | NCK2 | GRCh38.p7 | 2:105767578 | TCATTCATTTCCACA[-/G]CATCTGTGGCTGCCC | 8440 |
rs547112295 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105861624 | GGTTCAAGCGATTCT[C/T]CTGCTTCAGCCTCCC | 8440 |
rs547120242 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105810109 | TCAGCTTAGCAGAGG[A/G/T]TGCAGTGATAGAAAC | 8440 |
rs547123311 | in-del | -/A | 0.00358779 | 0.0422022 | utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105894252 | TTTGGATATTGTAAT[-/A]AAAAAAAAGTATTAT | 8440 |
rs547127533 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105866013 | TCCGCCTACCAGGTT[C/T]GAGCAATTTTCCTGA | 8440 |
rs547131455 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105757317 | ATAGCCCCAACTTTC[A/G]CTGTGTTAAAATTGA | 8440 |
rs547155850 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105768513 | CATGACCTCACTTCA[A/G]GTTCCATAATTTGCC | 8440 |
rs547164458 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105816052 | GGAGCTTGCCCAGGG[A/G]ATGAAAGGTGGGAAG | 8440 |
rs547212825 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105864897 | TGCAAATGGATGACT[A/T]TAGATGCAGTTAACA | 8440 |
rs547226035 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NCK2 | GRCh38.p7 | 2:105778171 | TCTGGGACTGGGTCC[C/T]GGGCTTAGAGGGGGA | 8440 |
rs547264496 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105818976 | CATAAGATTAATATG[C/T]AATAAGGATAGGATT | 8440 |
rs547306712 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105832043 | TTCAATTTCTTTTAT[C/T]GGTATTTTGTAGTTT | 8440 |
rs547307355 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105824986 | CCCCCAAGCTGCAGG[C/G]AAGTGATGCTGCCCA | 8440 |
rs547311719 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105867784 | CTTACTAAGATGATC[A/T]CACCCTGCTTCAGCT | 8440 |
rs547313094 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105784983 | TTTGTTTTGTTTTTG[G/T]TTTTGTTTGTTTTGA | 8440 |
rs547376320 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105863545 | ATGTTATTTCATCTG[A/G]TCGGGATGTGAAGGA | 8440 |
rs547403577 | snp | A/C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105803303 | CTGCTGTTTTTTATA[A/C/G]GCACGTTTTCTTGCA | 8440 |
rs547469297 | in-del | -/TG | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105867224 | CTAAGACAAGGACTC[-/TG]TGGGTTTTCAGAGAT | 8440 |
rs547473255 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105819598 | TGAGGCAGGGGAGTG[C/T]GGCATGCTCACCCAG | 8440 |
rs547474151 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105834406 | TTTCTTTGCCACTTT[A/G]TGTTTTTTGACTTAA | 8440 |
rs547479760 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105813020 | TTGCAGAATGCGACT[A/G]TCAAGGTTCTAGCCC | 8440 |
rs547484439 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105776239 | AACTTCCGTCCCAGC[A/G]ACAGAAACCGTACAT | 8440 |
rs547484780 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105783246 | GAAAGTAATGGCAGT[A/G]GAATGTTCTGCGTGC | 8440 |
rs547494860 | snp | C/T | 1.97896e-05 | 0.00314554 | synonymous-codon, intron-variant | NCK2 | GRCh38.p7 | 2:105882022 | GGGCGTGGAGGGCGA[C/T]TTCCTCATTAGGGAC | 8440 |
rs547505200 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105857509 | TCTTATTCTGCCCTC[C/T]AGGCCTGTGCTGAGT | 8440 |
rs547511741 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105755653 | CTTGTGCAGGTACAC[A/G]AATACCTTTTTAAAT | 8440 |
rs547514834 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | NCK2 | GRCh38.p7 | 2:105820126 | AGTTTTAAAGAATGA[A/G]GAGACGTGTACAGAG | 8440 |
rs547516382 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105812616 | CAAGGCATTTGAGAG[C/T]TCTGAGGCCTATGCT | 8440 |
rs547522918 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105788883 | GACTAGTCAGGGCAG[A/C/T]GGATCTCTTATCTGC | 8440 |
rs547525972 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105869099 | AACGGGGCTCCTCTC[A/C]TAGACCCACAGTGCT | 8440 |
rs547540341 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105744530 | AGGCTGGAAGTTGCC[A/G]TCTGTGTTTTCACTC | 8440 |
rs547560819 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105871538 | TCTCCCTCTGTCGCC[C/T]AGGCTGGAGTGCAGT | 8440 |
rs547577427 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105782270 | GCCCTTCCTTCTGGT[A/G]TAGATGGATGGATTA | 8440 |
rs547591042 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105874600 | AAACTTGAGCACACC[A/G]CGTCTAAACGAATTG | 8440 |
rs547614026 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105757540 | GGCTATGTTTTCACT[C/G]AGTTGTGTACCTGCA | 8440 |
rs547671770 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105749387 | CCGAAAATGCCATGA[G/T]GAGAGAATGACATGT | 8440 |
rs547703563 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105749961 | CTTGAACCCAGGAGG[C/T]GGAGGTTGCAGTGAG | 8440 |
rs547705039 | in-del | -/CTGCTTAG | 0.00159617 | 0.0282053 | upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105744391 | TGATGGACAACAGGC[-/CTGCTTAG]CTGAGTGCCGTGGGA | 8440 |
rs547723388 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105879722 | GGGGCAGCAGCCCAG[C/T]TCTCCACCATTGAGG | 8440 |
rs547742401 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105757587 | GACCAGCCATGGGCC[A/G]GGCACTGTGCTGGGT | 8440 |
rs547749672 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105840304 | AGAGAGGCACCCAGA[C/T]AGCTCACCCCTGTAA | 8440 |
rs547763290 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105820716 | TGTTGGAGGCTGGCC[A/G]TTACTAGGGACGGAA | 8440 |
rs547784381 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105848363 | TCCTATCAGTGTCCA[C/T]AGAGGAAACCTCTGT | 8440 |
rs547837099 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105841043 | TCTCCACACTGATAG[C/T]GTGGATTACAAGCTT | 8440 |
rs547841981 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105826798 | TTAGAGACATTTTAT[A/G]TATGTGTATATATAT | 8440 |
rs547844821 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105856545 | TTATACACCAAATGT[A/G]GTGGGTGTTGCAAAA | 8440 |
rs547866011 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105875007 | TCTGTCTGCTCACTG[A/G]GTGACAAATGTTATT | 8440 |
rs547892382 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105743682 | GGACCACCTGTGCAA[C/T]GTTACACAGTTCAGG | 8440 |
rs547925680 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105826163 | AATCATGGCAGAAGA[C/T]GAAGGGGAAGCAAGG | 8440 |
rs547928131 | snp | A/T | 0 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105834200 | CTTCTTTGTTGATTT[A/T]CTGCCTGGATGATCT | 8440 |
rs547958792 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105763360 | AGTCTACACAGGCAT[C/T]GCAGAAAAGTAGCTC | 8440 |
rs547959606 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105855886 | CTTGCCCAGGCTGGA[G/T]TGCAGTGGCACGATC | 8440 |
rs547963922 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105833285 | TACTTTTACTAGAGA[G/T]GAGCTTTCACCTTGT | 8440 |
rs547984269 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105807087 | AGAGTCTGAGTAACA[C/T]TTGGAATCCCTGGAG | 8440 |
rs548021238 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105801009 | CTAATTTTCTAAACG[C/T]AGAAAAAAGCAGAAG | 8440 |
rs548041408 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105848333 | GCAGCTGAAGAGGAT[C/G]TTTCACAAAAGTGGT | 8440 |
rs548049239 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105768967 | AGTCTCCTGGCCCCC[A/C]ACCCCTCCCAGAGGT | 8440 |
rs548149014 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105807397 | CCGATTTATATATGA[C/T]AATACAAGTTGTTCT | 8440 |
rs548180124 | in-del | -/TTTTTTTTTTTTT | 0.340784 | 0.232934 | intron-variant | NCK2 | GRCh38.p7 | 2:105880937 | ACCACAGGTGGCTAA[-/TTTTTTTTTTTTT]TTTTTTTTTTTTTTT | 8440 |
rs548212401 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105763937 | AAGGTACATTCTTAA[A/G]GTATTCATGTGTCAA | 8440 |
rs548249012 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105769323 | CCTATTTAAAGCCCT[C/T]CTCTCAGTAAAACAG | 8440 |
rs548271700 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105776803 | TCGAGGGTACCATAG[C/T]CCTCTGGTTTCTTTC | 8440 |
rs548293424 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105869602 | TGTCTCTTTTTGTGT[A/G]TTCGTCACATTTCAC | 8440 |
rs548377679 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105763687 | ACTTCCAGTATCAGG[A/T]CAGTGTAAATGACTT | 8440 |
rs548378989 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105776076 | GTGTGGCCTGGAGCA[C/T]GTCCCTTACTGCAGG | 8440 |
rs548390133 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105784314 | TTCTCACCCCAGTGG[C/T]ATTTCTGGGGAGCAG | 8440 |
rs548402307 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105869019 | CCAGAGCACTTATGT[C/T]TCAGTAACGTTTGTT | 8440 |
rs548407362 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105751196 | CTCCTGCAACCTGCC[C/T]GCCTTCTCAGTTATA | 8440 |
rs548416053 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105775125 | TGTTAGCTAAACTTT[A/G]GTTTTTAAAAAATAG | 8440 |
rs548432430 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105813215 | TGAAGCCACGGCGAG[G/T]GTCTCACTGGAATCA | 8440 |
rs548498246 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105782446 | GAGAAGAAACAGTCT[A/G]TATAATGAACGCTCT | 8440 |
rs548517401 | snp | A/G/T | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105825249 | CAGGACCTGGGCATC[A/G/T]GTGCTGTTAACGCTG | 8440 |
rs548541534 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105743852 | TTATTGCCTTAATAG[G/T]AAGCAGAGACCAGGA | 8440 |
rs548542900 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105857740 | GGGAGAAATATCCCC[A/G]TGGTTAGTATATATT | 8440 |
rs548557740 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105789021 | TGCACGCTTCTCTGC[C/T]AATCTCCCCCTCCTC | 8440 |
rs548580154 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105780929 | ATAAGCCACCATTCT[G/T]TGGTATTTTGTTACA | 8440 |
rs548603941 | snp | G/T | 5.84573e-05 | 0.00540604 | intron-variant | NCK2 | GRCh38.p7 | 2:105881280 | AGGCTAGGGAGTGTG[G/T]TGGTGCCCAAGTGCC | 8440 |
rs548605014 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105855607 | CTAAGTCTACCCAGC[G/T]CTGCCAGTGTCGTGA | 8440 |
rs548606866 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105864241 | GGACACGACTGGAAG[A/G]GCCTGAGCCTGGCAG | 8440 |
rs548622548 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105872282 | ACCCGCTACCTTCCC[A/C]CCGCCACCAGGCCTG | 8440 |
rs548623053 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105833529 | TATATTTCTGTGGTA[A/G]CTTGTAAAATGTCTT | 8440 |
rs548641057 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NCK2 | GRCh38.p7 | 2:105804331 | AGAAGACCTGGTGGA[C/T]GAGAAAATGGGTTTG | 8440 |
rs548641680 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105884393 | CATGCCAGGATGGAA[A/G]GGTTTCTGAGGGGTT | 8440 |
rs548667433 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105780410 | TCCCTTTCTGGCTCT[C/G]TCATTTTCGTTTGGT | 8440 |
rs548680455 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105860825 | CCAGGATTGCCTCTC[A/G]TGCTTGGATTAACCA | 8440 |
rs548694679 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105817980 | AAGACACATGCACAC[A/G]TATGTTTATTGCAGC | 8440 |
rs548772132 | in-del | -/AAATC | 0.00438332 | 0.0466095 | intron-variant | NCK2 | GRCh38.p7 | 2:105818561 | ATAGAAAAGATTGTT[-/AAATC]AAGTATGAAAGCAAA | 8440 |
rs548785341 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105789642 | ATAAAACCTGCCTTC[A/G]GAACCAGCTGTAAAG | 8440 |
rs548794739 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105754404 | ATCAATGTCTCCTTC[A/G]ATTTTCCTTAACGGT | 8440 |
rs548797296 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105826873 | AAAAGATAGACCATG[C/T]AAATACTAATCAAAA | 8440 |
rs548840942 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105786371 | GTGGGCAGGCTGGGG[A/G]CAGGATGGGAGTTCG | 8440 |
rs548863243 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | NCK2 | GRCh38.p7 | 2:105889531 | CACCCCAGAATTTCT[G/T]CTACAGCAGGGTTGA | 8440 |
rs548928688 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105791848 | GTATATTTAACACCC[A/G]AATAACTTACCAAGA | 8440 |
rs548943502 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105801604 | AGGGATGGTCTGACC[C/T]GCATCCGCATTGTCT | 8440 |
rs548945253 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105837917 | TGCCTAATTGAGTTA[C/T]TGGTCTTTTTGTTGT | 8440 |
rs548962615 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105825066 | CGAGGTGCTTGGGGA[C/T]GGAGTGGAGGTAGAC | 8440 |
rs548975850 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105759994 | TTGATCACCTGGCCC[A/G]GGTAGTGTTTGTCAG | 8440 |
rs548982078 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105844675 | AGGAGGAGGAGGTTG[C/T]AGTGAGCTGAGATCG | 8440 |
rs548995232 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105819927 | GCAGTTAAAAAAAAA[A/G]TAGATAAAATATAGT | 8440 |
rs548995541 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105794760 | CTGTCACCCAGGCTG[C/G]AGTGCAGTGGTGCAG | 8440 |
rs549000308 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105884837 | CTCATCTACAATTGT[C/T]ATTTATCCTTAGCAG | 8440 |
rs549012767 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105776435 | TGGGACAGGGTGGCC[A/G]CCCTCCAGGGTGTAC | 8440 |
rs549080792 | in-del | -/ACCTC | 0.00478085 | 0.0486577 | intron-variant | NCK2 | GRCh38.p7 | 2:105790508 | GCCCCATTTCTTGTT[-/ACCTC]ACCCACTGAGAGGAG | 8440 |
rs549114543 | snp | C/G | | | missense, intron-variant | NCK2 | GRCh38.p7 | 2:105881931 | CCGGGCCCTCGTCCA[C/G]CGGGCGCTTCGCGGG | 8440 |
rs549115244 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105830736 | TCTGATAATACCATT[C/T]TCATTGAGATGATAC | 8440 |
rs549144651 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | NCK2 | GRCh38.p7 | 2:105806383 | GCTGGGACTACAGGC[A/G]CCCACCACCACGTCC | 8440 |
rs549145247 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105832120 | ATTTGGCTTTTTTTC[C/T]TTTATTTTTAGCTAT | 8440 |
rs549190776 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105747411 | TTTACTTGATCAGTT[C/G]CACTAGCTTAGTTTG | 8440 |
rs549212494 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105887376 | ATGATACAACTTGTG[A/G]TAAGAAACCAACAGG | 8440 |
rs549264274 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105884257 | ACCATCCACTGCCTC[C/T]CCCCGTCCCCATGTG | 8440 |
rs549275655 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105893775 | TGCAAAAGAGGGAAC[C/T]GGTGACTCAGAAAGA | 8440 |
rs549300729 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105797908 | CTTTTTTTAAGCTAC[C/T]GGCACTAACAGCAGA | 8440 |
rs549347213 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105863226 | CATTTCGGCATTATA[C/G]GATTGTGGGTCTGTC | 8440 |
rs549357983 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105832474 | TCTGTCGTTAAGGCT[C/G]GTATTACCTAATTTG | 8440 |
rs549394457 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105767917 | ATTACTCACATCCCC[A/G]GCTCTCATCCTTAAG | 8440 |
rs549424542 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105873176 | ATTTGTGCGTGAGTC[C/T]CTTCCAACTTAAATT | 8440 |
rs549424622 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105880274 | TAGGCTGGTTGCAGC[C/T]CATTAAAGTGATTTT | 8440 |
rs549446135 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105888040 | CTGAGCCCGGTGTGG[A/G]GATGTGGAGCTAAAT | 8440 |
rs549488276 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105879855 | GAAAAGGAGAAAGGG[G/T]TACAAGCTACCCATG | 8440 |
rs549491987 | snp | A/G | 0.000584214 | 0.0170812 | synonymous-codon | NCK2 | GRCh38.p7 | 2:105855195 | GCGGGTGAGGAACGC[A/G]GCCAACAGGACGGGC | 8440 |
rs549513741 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105762920 | CAACCTGAGGCCAGG[C/T]GCAGTGGCTCACGCC | 8440 |
rs549555863 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105755191 | TTCAGTTCCCTTTTC[A/G]TAGTTTCCTTACTAG | 8440 |
rs549587318 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105835358 | TATAGTATTCTTGGC[C/T]GGTTTTATATATATA | 8440 |
rs549599445 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105768435 | ACCATCCCCATTTCC[A/G]TCACCAGTTGCATGT | 8440 |
rs549599812 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105748691 | CAAAAGTACTGGGAT[G/T]ACAGGCCAGAGCCAC | 8440 |
rs549617818 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105861544 | TTTTGAGACGGTGTC[C/T]TGCTCTGTCACCTAG | 8440 |
rs549621682 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105812410 | ACCAGCCTTTTCCCA[C/T]TTGAATAAGGTTCTC | 8440 |
rs549629906 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105893292 | CTCTGCGAGTCTCTC[C/T]TTATGTTCAGGTCGC | 8440 |
rs549647684 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105846142 | TGTCTAAGACACCAA[C/T]GAGAAAGCCAAGGAA | 8440 |
rs549662045 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105854259 | TCTATAAACTGTGTC[C/G]TACTAAAGGACATTT | 8440 |
rs549687725 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105748050 | TACCTCTGCCCAGTG[A/G]CACACATCCACATGT | 8440 |
rs549704556 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105824287 | GGTGCTCACAGGGAA[G/T]GAGTGGGAAATGCAG | 8440 |
rs549708388 | in-del | -/GT | 0.00723027 | 0.0596897 | intron-variant | NCK2 | GRCh38.p7 | 2:105884089 | TGCAAGAGCCCTGAG[-/GT]GTGTGTGTGGCTTCT | 8440 |
rs549714786 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105786922 | AGCATGGTGATAACA[A/G]CACCGTCCAGACTCG | 8440 |
rs549745802 | in-del | -/TCT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105855831 | TTGTCCCCATGTGCC[-/TCT]TTTTTTTTTTTTTTT | 8440 |
rs549761161 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105819771 | CCACACAAAACCTTG[A/C]TTCACCTATTAAAAT | 8440 |
rs549785727 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105812544 | TCTGAACGGGAGATC[C/T]ACTTGCAGGCCTCTG | 8440 |
rs549807473 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105794681 | TGGACTTTAAAAAAG[G/T]TAATAGTTTATTATT | 8440 |
rs549842817 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105781468 | CCCTCCTTGGCCTTC[C/T]AGTCCATGTACGTCT | 8440 |
rs549858027 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105794731 | TTTATTTATTTTTGA[G/T]ACGGAGTCTTGCTCT | 8440 |
rs549859169 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105824843 | CTGGTTGCCATGCCC[C/T]ACAGAATTCAGTGGG | 8440 |
rs549871580 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105818921 | CTTGGAACCTTTTCA[A/G]TTTCAGTTATGCCCC | 8440 |
rs549879576 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105787361 | ACCCCCAGTGTGACT[A/G]TATTTGGAGATGAGC | 8440 |
rs549892473 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105793856 | CCAGCTGGGGTCTGC[A/G]TGCCTTCAAAGAACT | 8440 |
rs549898743 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105766194 | AGCACATTCTGGTAG[C/T]AGGAGAGCCCGGGAA | 8440 |
rs549913571 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NCK2 | GRCh38.p7 | 2:105782594 | ATGTGGTTTTAGTAC[C/T]TTTTATTTTGTTAGA | 8440 |
rs549987626 | in-del | -/TGAA | 0.337614 | 0.234145 | intron-variant | NCK2 | GRCh38.p7 | 2:105757951 | CCACCACAGCTGGGG[-/TGAA]TGAAGCACCTCTATT | 8440 |
rs550026006 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105832631 | TTGACCACATCCTTG[C/T]ATTTCTGGAATGTGT | 8440 |
rs550047358 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105768787 | AAGATTGGACACCCC[G/T]GTTTTAAAGGATGCA | 8440 |
rs550047370 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105887529 | TACCCTCATCATTTC[A/G]TAAAGTCCAAAGTGA | 8440 |
rs550047410 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | NCK2 | GRCh38.p7 | 2:105894586 | CCCACGACTAACTCT[C/T]GATTTGTCCTCTTGA | 8440 |
rs550068406 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105830141 | TTTTAAAGTCACCCT[A/T]CAGTGCTATCAAACA | 8440 |
rs550072481 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105755053 | GTGTGTGTGTTTCCC[A/G]TCTGTCTTTGTTACT | 8440 |
rs550093334 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105792750 | AGAGCCAGTCTGGTG[A/C]GATTTTCTGGCAAGG | 8440 |
rs550100419 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105752625 | AATTCAGGACCTTTA[C/T]TGTATCCATCACTCA | 8440 |
rs550130051 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105792024 | AAGCAAGCTGTTGAT[G/T]GTGTTGTGGGCTCTG | 8440 |
rs550139760 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105792887 | TTTCTGATTCAGTCA[C/T]TCCTTCTGCACTTGC | 8440 |
rs550143851 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105826063 | TCCTACTGCAATAAA[G/T]AACTATGCGAGACTG | 8440 |
rs550165777 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105799797 | CCATTTCAAGAAGCC[A/G]TTGGTCCTTACCTGG | 8440 |
rs550180386 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105791374 | CCAGAAGAAGAGTGA[C/T]CAGGTGTGGTGGAAG | 8440 |
rs550184903 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105874434 | TTAATAATAGGTTCT[G/T]ACTCTAGTGGGGGAA | 8440 |
rs550190366 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105806764 | GGATAACATGCAGTG[C/T]GGTATTTTCAGTTTC | 8440 |
rs550190803 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105827743 | TTCCATTTATATAAC[A/G]TTCTCAAAATGACAA | 8440 |
rs550192255 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105762961 | GCACTTTGGGAGGCC[A/G]ACGTAGGCGGATTGC | 8440 |
rs550230652 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105868493 | TTTTTAAGGAACATA[A/G]TTGTTGATTGTCTGA | 8440 |
rs550296748 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | NCK2 | GRCh38.p7 | 2:105888519 | AGTCTAGTTAGGTTT[A/T]AGTCCAATCATAGAA | 8440 |
rs550310827 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NCK2 | GRCh38.p7 | 2:105756725 | TATTGAAGTCCCCTC[A/G]TCCCTCAAAACATTT | 8440 |
rs550321888 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105749915 | CACGGCTGTAATCCC[A/G]GCTACTCGGGAGGCT | 8440 |
rs550325290 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105891105 | CAGAGGGCTCTCCTG[C/T]CCCCACACGCACTTA | 8440 |
rs550332535 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105877591 | AGGGGCCTCTTCATT[C/T]TGTAGAGAAAGAGAA | 8440 |
rs550340820 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105836963 | CAAGGCCTATGATGG[A/C]TCTGGCTAAGATTGT | 8440 |
rs550342484 | in-del | -/T | 0.00597247 | 0.0543191 | intron-variant | NCK2 | GRCh38.p7 | 2:105869913 | TATACTTTTAGACCA[-/T]TTTTTTTTTCAGGTT | 8440 |
rs550354801 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105840207 | TGAGATGATCCAGAA[A/G]GACACAGTAGCTCCA | 8440 |
rs550369963 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105800253 | GCTCCGGTTCCAACT[G/T]CACACCTTGTTCTCT | 8440 |
rs550380678 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105796536 | AGGGCCTGGGGACAT[A/G]AGTGTGTGGCACAGA | 8440 |
rs550382323 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105832465 | AGCTGTGCATCTGTC[A/G]TTAAGGCTCGTATTA | 8440 |
rs550393916 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105883974 | TTGTCTGAGGTTCCA[C/T]GTGGCCTGATGCTGT | 8440 |
rs550403435 | snp | C/T | 0 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105847696 | TCACTGGATAATCAC[C/T]CATCCCAAGTACTTA | 8440 |
rs550406739 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | NCK2 | GRCh38.p7 | 2:105807008 | CATCCTATCCCACAC[C/T]CTCATGCTGAAGAGT | 8440 |
rs550419306 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105802518 | AGCTGCTTTCCACTC[A/G]TGGCAGAAGGTGAAG | 8440 |
rs550440709 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105839645 | AGCTTAGTTTTAGAC[C/G]TGAGATTTGAAGTGC | 8440 |
rs550544379 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105821424 | CCTCCTTCTGCCGCA[C/T]TCTGGACCCCTGGGT | 8440 |
rs550551342 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105765895 | TTAAGAGTCTAGGTA[A/C]GCCACACCCAAACTC | 8440 |
rs550563990 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105787144 | CACCTTTGACCCTCA[A/G]CCCTGAGCACTCAGC | 8440 |
rs550567870 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105858391 | GAGTATCTGGGACTA[C/T]GGGCATGCACTACCA | 8440 |
rs550570788 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105785085 | CTGGGTTCACGCCAT[A/T]CTCCTGCCTCAGCCT | 8440 |
rs550578634 | in-del | -/C | 0.00199481 | 0.0315187 | intron-variant | NCK2 | GRCh38.p7 | 2:105852970 | ATTTGGAAGTTAATT[-/C]ATGAAAGAAACGTGT | 8440 |
rs550587088 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105828199 | CAAGCTTACATAGCA[A/G]TAGATGAATAAGTCA | 8440 |
rs550590830 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105747203 | CTGCCATATTCCCAG[C/G]CTTTGTCATTTACAT | 8440 |
rs550606224 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | NCK2 | GRCh38.p7 | 2:105844844 | TATATATTTTGAAAT[A/G]TCAAGCACAGATGCT | 8440 |
rs550607575 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105790711 | CCCCTAGGGGAGAAG[G/T]GTACATGGGTGGAGC | 8440 |
rs550629968 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105746372 | TGGCCCAGGCGCAGT[C/T]CCCGCTTCTCGGAAG | 8440 |
rs550682541 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105759263 | AGTATATCGTTTTAC[A/G]TATTCAAGTACACAT | 8440 |
rs550715557 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105752865 | AGTACAAGCTAAAAT[C/T]ATGTATTTTTAAAGT | 8440 |
rs550754637 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NCK2 | GRCh38.p7 | 2:105804853 | GCACAGTGGTGTTAG[A/G]GATTCAGTGTGTCTT | 8440 |
rs550797349 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NCK2 | GRCh38.p7 | 2:105851167 | CATTGTTGTATCAGT[A/G]CATGGCCATAACTCA | 8440 |
rs550839974 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105765231 | GCATTTTGGATTGAT[A/C]TATTCTAGAGGACCG | 8440 |
rs550841488 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105842753 | GGCTCTGGGAGGCCT[G/T]ACTGGGTTGGGGACA | 8440 |
rs550842384 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105811217 | TTTTAGTAAGCTTTG[A/C]TACATTTTTGGCACC | 8440 |
rs550859958 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NCK2 | GRCh38.p7 | 2:105850360 | TCGTATTTTAGGCGT[C/T]AGTGAAAACTGTTGA | 8440 |
rs550866096 | in-del | -/CTCCCTCCCTCCCTCC | | | intron-variant | NCK2 | GRCh38.p7 | 2:105861921 | TCCCTCCCTCCCTCC[-/CTCCCTCCCTCCCTCC]TGCCCGCTCCCCCCT | 8440 |
rs550873344 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105859769 | CAAAAGCAGTGAAAA[A/G]CAACACTTGGTGTTA | 8440 |
rs550897476 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105809253 | TTTTTCAAGTTCCTG[C/T]TGCGTGTGTCATATG | 8440 |
rs550918943 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105892675 | ACATGGCGAAACCCT[A/G]TCTCTACTAAAAATA | 8440 |
rs550963696 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NCK2 | GRCh38.p7 | 2:105786300 | AGCTGAGCATGTGCT[A/G]TGTGCCAGGCCTGGC | 8440 |
rs551022503 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105785531 | GCAGCCTGCCCAGTC[C/T]TCCTTGTAACCTGGT | 8440 |
rs551056552 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105802140 | GAGCAATGGGGACCA[C/T]CTGGGAGTGAGCCAG | 8440 |
rs551068176 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105884794 | ACTGCTTGTCCTTCC[A/G]TTTCTTCCTCCTCCC | 8440 |
rs551081537 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105823790 | CACACCTGACCAACA[G/T]TCACACTGACAAGTT | 8440 |
rs551082549 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NCK2 | GRCh38.p7 | 2:105892739 | TAATCCCAGGTACTC[A/G]GGAGGCCGAGACAGG | 8440 |
rs551088501 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105791420 | CGATGGGAGGATATA[C/T]GGTGTAAAGTGCCTA | 8440 |
rs551124863 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105824289 | TGCTCACAGGGAATG[A/T]GTGGGAAATGCAGCA | 8440 |
rs551128093 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105766700 | GAGGGAGAATCCTGG[C/T]GGGGGCGGGGTCTGC | 8440 |
rs551131153 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105884071 | CTTGTTCCATGGGGA[C/T]TCTGCAAGAGCCCTG | 8440 |
rs551136278 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105810740 | AATGGAGTACTGCTG[G/T]ATTTAAGAGGCTAGC | 8440 |
rs551198823 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105859371 | ACAGGCCCACCTGCC[C/T]GTGGCTCACCCTGCC | 8440 |
rs551222243 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105822508 | GCCCCTGTTCAGGGC[A/G]AAACATCATAAAATT | 8440 |
rs551238773 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105866329 | TGTCTCTTTTCCCAG[C/T]GTTAATATAAGTATA | 8440 |
rs551248938 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105865565 | CCCCAAAATGCTAAG[C/G]GAACAGTTCCCCAGT | 8440 |
rs551277013 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105766501 | AAGTTTTTAATTTTT[A/G]TTGTAGAGATGGAGT | 8440 |
rs551292047 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105779484 | CTGTCTGAATATGGC[G/T]GCATCTCTGCCACCT | 8440 |
rs551314100 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105820581 | GGCTCTGACCCTGCC[C/T]TCTTTGGGGGAGCGG | 8440 |
rs551317775 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105831294 | TCCTAAGATTTGTAG[A/G]AAACCGCAAAAGAAC | 8440 |
rs551330410 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105778205 | GGGACCTAGAAAGCC[C/T]CCTGCCTCTCAGCTC | 8440 |
rs551338403 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105760266 | TGCGGAGGAGGTGAT[A/G]GGATAGGATGGTGCC | 8440 |
rs551345642 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105804029 | TGCATCTCTGCCATC[C/G]CTCTCCCTCTCAGTT | 8440 |
rs551346536 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105779221 | CTGAGGCATGAGAAT[C/T]GCTAGAAACTGGGAG | 8440 |
rs551419572 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105747959 | AAAAATTAGACTCTT[C/T]TCTTTTCCTGCATTT | 8440 |
rs551424843 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105829433 | GTAAGGTCTGTACTT[C/T]ATTTGGATTTAAAAC | 8440 |
rs551434530 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105777149 | GAGCCCACGGCCCTG[C/T]GGCTGTCACTGGGCA | 8440 |
rs551470610 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105828710 | ACATCTTGAGCAGGT[C/T]ACCACTTCCCCCTTG | 8440 |
rs551476081 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105748720 | ACCATACCCTGCCCT[A/G]TGGTTTTTTTGCCTT | 8440 |
rs551501937 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105747327 | AAATCTTCCTTGCAT[A/G]TGCACAGACTGGATA | 8440 |
rs551508578 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105805704 | ATTCAGTATATGTCT[C/T]TCTGTACCTGGCTTA | 8440 |
rs551511221 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105755159 | TCTCTTCCCTTAAAT[C/T]AAGCCATCTGTCTTG | 8440 |
rs551518305 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105837792 | TTTTACCCATCTACT[A/G]TAAAATGGGATCGTA | 8440 |
rs551545743 | in-del | -/ACAC | 0.499905 | 0.00688403 | intron-variant | NCK2 | GRCh38.p7 | 2:105864829 | CTCACATGTGCATGT[-/ACAC]ACACACACACACACA | 8440 |
rs551546436 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105842180 | AACCTCTGCCTCCCG[A/G]TTTCAAGTGATTCTC | 8440 |
rs551593975 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105796847 | AATTAGAACACTTAT[A/G]GACATTAGTGGTGAC | 8440 |
rs551627491 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105893271 | CGGGGACGGCCCCGA[C/T]GGCTTCTCTGCGAGT | 8440 |
rs551641743 | snp | C/T | | | upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105743232 | ATTGATAAAGGGCCA[C/T]TGGATTTAGATAGAG | 8440 |
rs551666068 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105759953 | GTCCATGTGATCAGC[A/G]TGGCTTATGATGGTT | 8440 |
rs551681122 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105843600 | AACGAACGAACACTC[G/T]CAGTGATGGTGATAC | 8440 |
rs551682681 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105820192 | TGGACCAGCTGGGCC[A/G]TGGTTCCTGGAGACT | 8440 |
rs551710735 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105834553 | TGTCTTTATAGGTAA[C/T]GTTTTTTGTAAGCAG | 8440 |
rs551741661 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105749885 | AATAACACACAGAGG[C/T]CGGGCGCAGTGGCTC | 8440 |
rs551769789 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105879192 | TGTTTGCAAAGGTCT[A/G]TTAAAAGTTTATTGT | 8440 |
rs551798880 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | NCK2 | GRCh38.p7 | 2:105841991 | AAATGTAAAATGGCA[C/T]TAGCTGCCCTGGGGC | 8440 |
rs551858330 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105882138 | CCTTTTCACATTGTG[A/T]GAGTACACTAGAAAG | 8440 |
rs551865574 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105807007 | ACATCCTATCCCACA[C/T]CCTCATGCTGAAGAG | 8440 |
rs551888402 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105886146 | TCCAGTTTCAAAGAT[A/G]ACAAGTTATTTTTAA | 8440 |
rs551902705 | snp | A/C | | | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105771599 | TTTAGACAAATATTT[A/C]AAGAAGTTTCCCATT | 8440 |
rs551919205 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105762319 | CTAGGTCCAGGCCCG[A/G]GCGCTTCCTGCTGTC | 8440 |
rs551926707 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105805000 | TGAACCATAAATGGG[A/G]GAGAAGAGTCATTTT | 8440 |
rs551941112 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105814686 | CCTCACTCTCCAGTC[A/G]GTTGGGAAAAACCTT | 8440 |
rs551953398 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105790204 | GACATAAAAGTAAAC[C/T]GTTAGAAATAGTGTG | 8440 |
rs551998090 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105853345 | TTCCAAAATTGACTT[A/T]ACTGGATATATAATA | 8440 |
rs552022932 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105820624 | GAGCCAGAAGGCCAC[C/G]AGAGTTGTCATTTTG | 8440 |
rs552060059 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105820024 | GTAGTGGAGGTTCTT[A/C]CAGCCAGTCCCTAAT | 8440 |
rs552060434 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105866898 | AGTGTGGCTTATATA[G/T]TCTGTGAGTCATGTA | 8440 |
rs552064319 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105859917 | TTGGAGGAGTTTGCA[A/G]AGCTGACTGCTTATT | 8440 |
rs552069707 | in-del | -/TC | 0.0256215 | 0.110247 | intron-variant | NCK2 | GRCh38.p7 | 2:105882300 | AGAGGTGGTTCTGCT[-/TC]TCTCCCAAGATTCCC | 8440 |
rs552073255 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105807684 | TTTTCAACCTCTCTC[C/T]TTTTTTTTTTCTCTT | 8440 |
rs552104225 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105765966 | GAATTTGCAGTGACT[C/T]GTTACATGGCAGCAG | 8440 |
rs552112180 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105809529 | TCTTAAAAGGCCAGC[A/G]GTCCTATTGGATTAG | 8440 |
rs552123500 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105866952 | GTGCATTTGTCTTAG[A/G]AGTAGTTTGTTTTTC | 8440 |
rs552139455 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105751230 | CCCATCACCGACTCA[A/C]TCGGTTATCCTTGAA | 8440 |
rs552144447 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105866542 | CCTCAGATCATCAGC[A/G]TTAGATAGATGCTCA | 8440 |
rs552175034 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105890196 | ATTACCTCTTCTGCT[A/G]CGAAAATTTTATTGC | 8440 |
rs552196155 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105771318 | ACGTGTGTAATCCCA[C/G]CACTTTGGGAGGCTG | 8440 |
rs552210380 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105864784 | TGAGTTTGGCCCTCC[A/G]AACCCACGGGAAAGA | 8440 |
rs552273873 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105864429 | AATGACTCAAGAGTT[G/T]CCAGCCTGAAGGACC | 8440 |
rs552297656 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105808257 | TTAAGATGATTTTGT[A/T]ACTTTCAGCCTTAAA | 8440 |
rs552317168 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105764598 | GATCTCAAAGTGCAA[A/G]CCAAACACACAGCTG | 8440 |
rs552338206 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105811235 | CATTTTTGGCACCAC[A/G]TCATCAATTTTTGAT | 8440 |
rs552344970 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105892530 | TGAACATCAGATGCC[A/G]TTCTAGATATAAAAC | 8440 |
rs552354379 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105769999 | TTGGTGCCTCCATTT[C/G]CTTCACTGGAAAATG | 8440 |
rs552380458 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105827113 | CACACCATTCTCCTG[C/G]CTCAGCCTCCTGAGT | 8440 |
rs552386245 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | NCK2 | GRCh38.p7 | 2:105870257 | AGAGAGCAGCCAGCT[G/T]GAGGCTGAGGAGGCA | 8440 |
rs552390636 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105745435 | GCGGGCGAGGATCAG[A/G]GCAGGGGGCCCGGCT | 8440 |
rs552410329 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105870858 | AGCCACCAGACACAG[C/T]CAGTAACAGCGGTGC | 8440 |
rs552452242 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | NCK2 | GRCh38.p7 | 2:105744718 | GAGCCTGGCGACGAC[G/T]GGGGGCGCCCCAGGT | 8440 |
rs552459505 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105863104 | TCATCATATCTATAT[A/C]CCCAGCATGCAAGTG | 8440 |
rs552492608 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105827880 | TGATGATGAAATAGT[C/T]TTGATTGGCATGGTG | 8440 |
rs552528161 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NCK2 | GRCh38.p7 | 2:105851333 | CAGTGGCGCGATCTC[G/T]GCTCACTGCAACATC | 8440 |
rs552533409 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105876472 | CCAGGGACATGCTAG[C/T]GAATGTGCTCTTCCA | 8440 |
rs552592508 | snp | A/G | | | upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105744449 | GCTGCCCAGCAACTA[A/G]AGCTTCGTGATAAGA | 8440 |
rs552601157 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105875265 | CAAGCCTCTGTCACT[C/T]GTCTCATCTGTGGAG | 8440 |
rs552626327 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105834635 | ATTGGGAAATTTAAT[G/T]CATTTACATTAAAGG | 8440 |
rs552628320 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105826541 | AGATTACCTGATTGG[C/T]TATGTTTTTTAATGC | 8440 |
rs552659212 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105784391 | GGGGTGAATCGGGAG[A/G]GGAGAGTTTAATTTG | 8440 |
rs552705766 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105777247 | GCCACGAGCCGGGGT[A/G]TTGCGGGGGGGCAAC | 8440 |
rs552724925 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NCK2 | GRCh38.p7 | 2:105744798 | CGGCGTCACGGCGCG[A/G]CCGGGGAGGAGCGCG | 8440 |
rs552746678 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105782959 | CTCACCTTTATTTCC[A/G]GTGTCATAACAAGCC | 8440 |
rs552771419 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105827302 | CCGCGCCTGGCTGAC[A/G]TAGCATTCTTAAGTA | 8440 |
rs552790447 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | NCK2 | GRCh38.p7 | 2:105756731 | AGTCCCCTCGTCCCT[C/G]AAAACATTTGCCTTC | 8440 |
rs552812791 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105751313 | AGATCTAACATCTCA[C/G]CCCTGCTGTCCTTTT | 8440 |
rs552813876 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105801373 | CCTCCCCCCTTCCCC[A/G]TGTCATCGTGTGCAC | 8440 |
rs552823695 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105834142 | AATTTTCTGTAAATG[C/T]CTGTTAGGTGAGTTT | 8440 |
rs552835417 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105837846 | ACTTGAGTTATTTTT[A/G]TGTTTATTCACCATT | 8440 |
rs552850636 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105807915 | TCTCTTTCTGTCTCT[C/T]TCTGTCTCTGATGAA | 8440 |
rs552856011 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105842107 | TCTTTTTTTTTTTGA[A/G]CCGGAGTTTCTCTCG | 8440 |
rs552885661 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105820999 | ATAGAAGCAGCAGCA[A/G]CTGTGTTTAACTGAG | 8440 |
rs552906664 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105753154 | TTTATTATGGTGTAA[A/G]ATTTGAGAAACATTG | 8440 |
rs552915697 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105882653 | AGTCGGAGATATGAG[A/G]CCACTCGACTGGGGC | 8440 |
rs552936334 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105860750 | AGAGCCGTGGATGCC[A/G]GCGGCGCTGTAATGG | 8440 |
rs552959316 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105869647 | GTGGTCCTGCAGAAC[A/G]GCAGGCGTGCTGAAC | 8440 |
rs552994685 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105760104 | GTCATTTAAGGAAGA[C/G]GGAGTTCAGCTGTAC | 8440 |
rs553008341 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105812032 | TAGAAATTAGTTCTG[C/T]TTTTTCCCTCGTGTT | 8440 |
rs553012783 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | NCK2 | GRCh38.p7 | 2:105851459 | GAGACAGGTTTCACC[A/G]TGTTAGCCAGGATGG | 8440 |
rs553025210 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105883134 | TTTGCGGAGCCTTAC[A/G]TGTGCTTGGACGGGA | 8440 |
rs553026338 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105784099 | TTCATTCAGGAAAGC[A/G]TCACTGGGAGCTTTT | 8440 |
rs553033467 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105759587 | AACTGTGTCTACTTT[C/G]CCCTGTGATTCACAT | 8440 |
rs553054152 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105747873 | TGACGGCCTTTTAAC[A/G]GGCTATCAAAAGTGT | 8440 |
rs553064973 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105783532 | GTACACCACCAAGGC[A/G]CAGGTTAATGTGCAG | 8440 |
rs553079633 | in-del | -/GCCCTCACA | 0.00795532 | 0.062565 | intron-variant | NCK2 | GRCh38.p7 | 2:105768225 | GTCCAGTGTGTGTTT[-/GCCCTCACA]GCAAGACATAGCTGG | 8440 |
rs553095826 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105875348 | TGCTGGAGGTGCTGG[A/C]GGTACGGGGTCTCCT | 8440 |
rs553109949 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105874719 | GTTTTAAAGTCATCT[A/G]TTACAACATCTCTTC | 8440 |
rs553127233 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | NCK2 | GRCh38.p7 | 2:105850503 | GGGGGTCTTGCTAAG[A/C]TGTGTTTTAGAGTGG | 8440 |
rs553133027 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105841362 | CTGTGATTGAATGTC[C/T]ACCTCAGTCACTCAT | 8440 |
rs553168717 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105891204 | CTCACATCTGCGCAC[A/G]CTCACACACTTAGAG | 8440 |
rs553188550 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105857942 | AGCTTATAGATGTGG[C/T]GTTGCCAAGAAGGAA | 8440 |
rs553246756 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105757982 | CTCTCATGCCAGGGT[A/G]GGTGTTATTATTCCA | 8440 |
rs553255808 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105824605 | CATTGGTCATTTTCC[C/T]AGTCGTTAAGTACCA | 8440 |
rs553262549 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105765454 | CCAGTTCTTGGCTTT[C/T]CCTTTCGAGCTGGTG | 8440 |
rs553268953 | in-del | -/CCCTTCAGGGGA | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105889231 | CAGTGTCCCAGCTGT[-/CCCTTCAGGGGA]AATTCCCTATGAGAG | 8440 |
rs553283497 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105764103 | CTAAGCAATTTGTCC[A/G]AGTGCTAGTCCTGGC | 8440 |
rs553290093 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | NCK2 | GRCh38.p7 | 2:105745865 | CGATTTAATCACCGA[C/G]TGCTTTTGGAAAAAT | 8440 |
rs553301512 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105771082 | CGCCCGCCACCATGC[C/T]CAGCTACTTTTTTGT | 8440 |
rs553314779 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105790423 | GCACTCTATGCCTGG[G/T]CAGCAGGAGAGTCTG | 8440 |
rs553321809 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105815675 | AGTTTTGGAGTGTTC[C/G]TCTCAGAAGTCTTGA | 8440 |
rs553327675 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105864593 | AGTTATCCTTATGAC[A/G]TACTTCTTTATGTCA | 8440 |
rs553382314 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105835826 | CATTCTTTTTTATTC[C/T]TTTTTTCTGAATTCT | 8440 |
rs553398230 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105777242 | CCATAGCCACGAGCC[A/G]GGGTGTTGCGGGGGG | 8440 |
rs553404422 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | NCK2 | GRCh38.p7 | 2:105870418 | GGGGATTTTGAATGG[C/T]GCACAGTAGAATGTT | 8440 |
rs553405121 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105833909 | TTTCTTCATTGACTC[A/G]TTGTTCATTCAAGAG | 8440 |
rs553413459 | snp | C/T | 4.08739e-05 | 0.00452054 | intron-variant | NCK2 | GRCh38.p7 | 2:105855325 | AGAGGAAGCCTTGTG[C/T]ATTTCAAGGGACACT | 8440 |
rs553429830 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105762623 | CACTGAAATTCAGTA[C/T]TTCCTTCCTGCATGA | 8440 |
rs553429866 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105886790 | AGGGAGGGCTAACCA[C/T]ACACATGCATACTAA | 8440 |
rs553444943 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105749076 | CAGCAACAACAACAA[A/C]AAAAAAACAAAGCCA | 8440 |
rs553449232 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105835616 | TGCCTTGGAGAGGAC[G/T]TTCTTAGGTTGAATA | 8440 |
rs553473931 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105793013 | AATGGTGGGATTCTT[C/T]CCTGTCCTGTGTCAT | 8440 |
rs553507963 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105802693 | TGAGGGATCCGCCCT[C/T]GCGATGCAGACACCT | 8440 |
rs553512939 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105762139 | TTTGTGGAATGCACT[C/G]CTCTTGGGTTTTCCT | 8440 |
rs553530816 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105755423 | TAACTTGATTGTGCC[A/G]AGCACCTCATCCCTC | 8440 |
rs553539494 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105764995 | TGTGTACGTCTCTGG[G/T]TATATTTCTCTTCTT | 8440 |
rs553540138 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105803608 | CATCCAGTTTCAAAG[C/T]AAGTCCTCATGCCCC | 8440 |
rs553545887 | in-del | -/C/CC | 0.158248 | 0.232554 | intron-variant | NCK2 | GRCh38.p7 | 2:105884238 | TTTGCTTGTTTTTTT[-/C/CC]CCCACCATCCACTGC | 8440 |
rs553585316 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105861072 | GTAACAATTGTTTAC[C/G]GAAAACTATCAACCA | 8440 |
rs553597947 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105809367 | AATTTATGCCCTCAC[A/G]GTTCTGAAGGCTGGA | 8440 |
rs553628216 | snp | A/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105893412 | GGGCGAGTTCACATT[A/T]TTCCTTTTCCATCGG | 8440 |
rs553662958 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105753373 | CCCTTGCTATGTTCC[A/G]TAGGCTGGTGGTCCT | 8440 |
rs553680298 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105815142 | GGGCAATCTGCCTAG[C/T]ATACGTTTGAACTTC | 8440 |
rs553682244 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105756017 | AATCTGGCTGTTAGT[C/T]GCTGACTTCCAGTGT | 8440 |
rs553700925 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105777290 | CTCCTGCCTTTTAAT[A/G]TTGCACCTGGTTGTG | 8440 |
rs553706309 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105769345 | GTAAAACAGCTGATG[C/T]GTGCCTATTTTACAT | 8440 |
rs553739990 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105777037 | TAAGAAAGCTGCCGC[C/T]GTCCCTAGGTCTGAA | 8440 |
rs553743017 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105807245 | TGCGTGGGAAGGGCC[G/T]CCCTCGCAGACATCA | 8440 |
rs553770186 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105833555 | GTCTTCTGATATTAT[G/T]TATTTGATATTCTGA | 8440 |
rs553773090 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | NCK2 | GRCh38.p7 | 2:105773255 | TCTTTAAGAAACCAA[C/T]ATCAGCAATTGCAGT | 8440 |
rs553778388 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105847052 | TGCTAAGTGTAATTA[A/G]CCAGTCACAAATAGA | 8440 |
rs553803342 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105839097 | GGACATTTGAATGGC[C/G]GCTTGAACAAAGTAA | 8440 |
rs553809229 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105894173 | TAAATATAACGTCTT[A/G]AGATGGCACATTCCT | 8440 |
rs553842426 | in-del | -/T | 0.00398564 | 0.0444627 | intron-variant | NCK2 | GRCh38.p7 | 2:105757430 | GCTGTTGCTTTTCTC[-/T]TGAGTGTAGTTAGGA | 8440 |
rs553846735 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105769425 | CTCCCCCGTTCTTGC[C/T]TCTCAGGAAGCAAAT | 8440 |
rs553869089 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105814036 | TCTACAGTCCAAGTG[A/G]CCGTATAGGTGTTTA | 8440 |
rs553884076 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105782651 | GCTCTCCTCATGCAA[C/T]GTCAAATGATAGAAC | 8440 |
rs553907526 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105805990 | ATATACATAGCCTGC[A/G]GGTAATTTTATTTTT | 8440 |
rs553934897 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105773708 | CTCAACAACTATTTG[A/G]GCACCTACTCTGAGC | 8440 |
rs553976867 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105889166 | GAGTAACTCCATCTC[C/T]ATCAGATGCAGGGAC | 8440 |
rs554006252 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105787899 | AACACATGCGTATAC[C/T]GCCCCCCACCGCCCC | 8440 |
rs554009339 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105774630 | AGGCACACACACAAC[A/G]AACTCTAGACCTGGC | 8440 |
rs554011091 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NCK2 | GRCh38.p7 | 2:105766856 | TAGTTTGACTTACAA[A/G]TTAATATTTAAGCCA | 8440 |
rs554012085 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105887903 | TTCTAAAAGTACCCA[C/G]TTATCGCGAGCACAA | 8440 |
rs554024883 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105781049 | TGGTCGTGGTCTTCC[A/T]GTCTTCTTGCTTTCA | 8440 |
rs554053696 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105824355 | GACTTGTTTTATTTA[A/G]TGCCTTCCGGAATAT | 8440 |
rs554091969 | in-del | -/T | 0.499203 | 0.0199521 | intron-variant | NCK2 | GRCh38.p7 | 2:105794046 | TATTGTATCTTTCGA[-/T]TTTTTTTTTTTTTTT | 8440 |
rs554102472 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | NCK2 | GRCh38.p7 | 2:105750069 | ACACACACACACACA[A/C]AACAACAACAACAGA | 8440 |
rs554161199 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105873321 | GCCCACCCTAAGTCA[A/G]CTCTGAGAGCCCCCA | 8440 |
rs554179029 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NCK2 | GRCh38.p7 | 2:105763651 | TTGGGTTGTGCATTG[A/G]GAACTTAGGGGTTTA | 8440 |
rs554192041 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105749643 | ACAGTGTCCTTGGGT[A/G]TCTGCCTTTGCCGTG | 8440 |
rs554207380 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105788643 | TGTTGGCCAGTGCAG[A/G]ACTTCCTCATCTCTA | 8440 |
rs554209863 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105746362 | AGTCCCTTCCTGGCC[C/T]AGGCGCAGTCCCCGC | 8440 |
rs554237494 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105775453 | ATTTAACTTCAGATT[C/G]ATCTTGTTTGAACTT | 8440 |
rs554246510 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105856125 | AGGCGTGAGCCACCG[C/T]GCCCGGCTCCCCATG | 8440 |
rs554251284 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105750516 | CCCATCATCCAGATC[G/T]GGGATCTCTGTTTAT | 8440 |
rs554256127 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105868790 | GTTTGCACTATCTGT[A/G]GAATTCTGGAAAGGC | 8440 |
rs554260664 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105862467 | AGCAGTCACAGGTAC[A/G]AGACCCAGAGGGGAC | 8440 |
rs554324481 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105793455 | GGAACTTCTGACCTC[A/C/G]GGCATCCTGTTTCTG | 8440 |
rs554339168 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105747752 | TTCTGTTTCCTAAAA[C/T]GAGTGATGGAAATAC | 8440 |
rs554344142 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105768338 | GACACCACCTAGGTG[C/T]CCCCTAATTTGGTTC | 8440 |
rs554351399 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105839845 | CTTTAGTTCAGAAGC[A/G]CAAGTAGAGTGAGCC | 8440 |
rs554372745 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105873859 | CATGAACCTCTGCAG[A/C]GTGGGCAGATGCTGC | 8440 |
rs554384564 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105855360 | GTCTTTCTAGTTAGT[A/T]TGCTGTTTCAAAAAA | 8440 |
rs554416574 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105887703 | ATTAAAGTCTGTCCT[C/T]GGCATTCATTTTTTT | 8440 |
rs554425387 | in-del | -/AGG | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105767786 | GCCCGCACCTGGGAA[-/AGG]AGGAGGAGGAGGATA | 8440 |
rs554451866 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105819115 | TCCTGGTCGGCAGTC[A/G]GGGGTTGGCACTCAC | 8440 |
rs554497487 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105793358 | GTATGGAAATTAGAT[A/G]ATAATGAAGTTAAAG | 8440 |
rs554498107 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105788509 | GTTATCTCCATCTCC[G/T]CTTGAACAAGTAATA | 8440 |
rs554513854 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105880652 | TCCCACCCATTCTAG[A/G]AATGAAAAAGATATT | 8440 |
rs554527402 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105801393 | ATCGTGTGCACCAGC[A/G]CGTGGTTGAGGGATG | 8440 |
rs554576135 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105812193 | TTGCAGTGAGGCTTT[C/T]TGAAGCTGCTTCAGC | 8440 |
rs554585803 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105794129 | TTTTGGCTCACTGCA[A/T]CCTCCACCTGCCAGG | 8440 |
rs554586114 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105861135 | ATAGATATGCCTTTA[C/T]TAGGGAGAAGAGAGC | 8440 |
rs554597316 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105840332 | TAACACGTGGGACAC[A/G]TGGAGATGTTTTCTT | 8440 |
rs554597694 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105856173 | GGTGTTGTCAGGTTA[C/T]GGGCAGTGCCCTCCT | 8440 |
rs554627026 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105889209 | TTGAAAGGAGGAGAC[C/T]ATACAGCAGTGTCCC | 8440 |
rs554639729 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105769524 | TTGTGACTCTACTTA[C/T]AATAACGTACAGAAG | 8440 |
rs554672290 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105800374 | AGAGGGCCTAGTCTG[G/T]TCTGTGGTACCCAGG | 8440 |
rs554676829 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105776275 | GTTTTCTGTAACACT[A/C]AGTTTCTTACCTTTT | 8440 |
rs554692458 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105887162 | TAGACAACTAGGGCA[A/G]GTGACCAAATAGAAT | 8440 |
rs554708111 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105857314 | ACTGAGCCAGCCGCC[C/T]GTCCTGGAGCCGGCA | 8440 |
rs554729729 | snp | A/G | | | upstream-variant-2KB, intron-variant | NCK2 | GRCh38.p7 | 2:105850939 | CACATGGTCCTGTTG[A/G]GTTTTAAGAAACAGC | 8440 |
rs554732267 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NCK2 | GRCh38.p7 | 2:105806472 | TCGATCTCTTGACCT[C/T]GTGATCCACCCCGCG | 8440 |
rs554761025 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105768602 | CTAGGTTGTCCAACC[A/C]GCGGTCCAGGATGGC | 8440 |
rs554764403 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105775635 | TGTTTGTTTCATGCA[A/G]CCTTTCAAGTGAAGA | 8440 |
rs554772541 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105869126 | TGCTCCCCCTAGCCT[A/G]TTCATACGTGCCCTC | 8440 |
rs554817138 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105855929 | AAGCTCCACCTCCTG[A/G/T]GTTCACACCATTCTC | 8440 |
rs554824780 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105752987 | TCCTCACCAACAGAA[C/T]GTGTGGTACTTTCTG | 8440 |
rs554855895 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105825323 | GAGTTTTCATGTATT[C/T]ACACCTGAGATAATT | 8440 |
rs554856160 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105860481 | TGCTAAGCCGTAGGC[A/G]TCTCAGAATGAGGAG | 8440 |
rs554867194 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105786780 | CTTCTGCCTCCCCCA[C/T]GCATTGCTTCCTCCT | 8440 |
rs554867223 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105867912 | TTAGAGAACCATCTT[C/G]CTAGCATGTTTCTGT | 8440 |
rs554894208 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105862546 | ATTTAGTGGTAGGCC[A/G]CTTTGTACGTTTGGG | 8440 |
rs554898223 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105774338 | TAACAGATGTTTTAG[A/G]TACCTGAGTCCTCCT | 8440 |
rs554910654 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105846312 | CTTAGAGTCTAGTCT[A/G]CAGAACGCTAGTGTG | 8440 |
rs554936516 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105773716 | CTATTTGAGCACCTA[C/G]TCTGAGCCAGGTGCT | 8440 |
rs554949556 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105874652 | ACCAAGTTTGTTTGA[C/T]GCTTCAGCTTAAATC | 8440 |
rs555044497 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105828661 | GGGTCAAGAGACCCA[A/G]GAAGAGGTCTCAGCT | 8440 |
rs555076077 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | NCK2 | GRCh38.p7 | 2:105766773 | CCTTTACTCGGCTAT[A/C]CCTCCATCTTGTGGG | 8440 |
rs555079650 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105779662 | CCACGGGAGACGTAT[A/G]CAGGTGGAGGAGAGG | 8440 |
rs555098559 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105810911 | CCAGGTGCAGTGGCT[C/T]ACACCTGTAATCTCA | 8440 |
rs555108241 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105752844 | CATATTTCTGATAAC[A/G]TGTTAAGTACAAGCT | 8440 |
rs555161822 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105778654 | CTCCTTAGGCTGGGA[A/C]ATCATGCCCTTGTTA | 8440 |
rs555166904 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NCK2 | GRCh38.p7 | 2:105773627 | CTATGGTTCATTTCT[C/T]ATATGCTAGAGCATC | 8440 |
rs555184443 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105865951 | CAGAGTTTCATTCTT[A/G]TTGCCCAGGCTGAAG | 8440 |
rs555186519 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | NCK2 | GRCh38.p7 | 2:105816700 | GTTTAGTAAAATATC[A/G]GTCAGTGTAGCCTTG | 8440 |
rs555191263 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105879038 | TATCAGTTATAAAGT[A/G]TCTTTATAACGTATT | 8440 |
rs555235300 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105877759 | TGGACACCAGCCGCT[A/G]TCAGAACTATGCTCC | 8440 |
rs555238850 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105826278 | AGTATCACCAAGACA[A/G]CATGGGGGAAACCGC | 8440 |
rs555241924 | in-del | -/AAGCAGGTGAATTAGTAACAGGATTC | 0.00279162 | 0.0372561 | intron-variant | NCK2 | GRCh38.p7 | 2:105746562 | GCAAGCTTCATAGAT[-/AAGCAGGTGAATTAGTAACAGGATTC]AAGCCTTGCGAGTTT | 8440 |
rs555243229 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105876985 | TTCTGCAGCAGAAAC[C/T]GTCCCTTTGAGATGT | 8440 |
rs555257064 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105876570 | GGTTGGCTATGGTTT[-/C]CATTATGGTAGCTAA | 8440 |
rs555289137 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105788448 | TATTTATAGTCATAC[C/T]CTATCCAAATGAACT | 8440 |
rs555295346 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105892412 | TAATGAGTTTGCACT[C/T]TTCAAATAACTAAAA | 8440 |
rs555311406 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105892593 | GTAATCCGAGCAATT[C/T]GGAAGGCTGAGGCTG | 8440 |
rs555312085 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105767152 | GAAGCCTGGACCCCC[A/G]TCTGTGTTTATCTCA | 8440 |
rs555323045 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105864677 | GAGAGCTGGCACTTC[C/T]GAGGCAGCTGATTAG | 8440 |
rs555324790 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105825681 | TTAGAGATTTTTTAC[A/G]GAGCCCTTATTTTTG | 8440 |
rs555334088 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NCK2 | GRCh38.p7 | 2:105811325 | AGGGAACAGAGAGGC[A/G]TTTGGTGGCCAAGTT | 8440 |
rs555371636 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105761153 | CCGCCCACCCTACTG[A/G]GCCTCTTCTGGGCAG | 8440 |
rs555376847 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105824452 | AAGTACTTGGGAAAG[G/T]CAGGGATCCCAGGAG | 8440 |
rs555398441 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105797631 | GCCTTTTGGAGATGA[G/T]TATGGTAACAGTGAG | 8440 |
rs555435045 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105795558 | TAACAAACTTGGTCT[A/G]TTTAGTTTACATGTA | 8440 |
rs555443030 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105852578 | TTCATGCAGTAGGAA[A/C]TATTAATAAACAGCT | 8440 |
rs555453565 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | NCK2 | GRCh38.p7 | 2:105859472 | ACAGGACCACACCTA[G/T]GCCTAGCGTGGTTAG | 8440 |
rs555465161 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105824004 | GTCAGGAGTCTGCAG[C/T]GGTGACGTCCCTCTT | 8440 |
rs555470649 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105771826 | TAAAAACCCTCTGGT[A/G]TGAAAGCTGCCATTC | 8440 |
rs555502154 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105830358 | TTTCATGTAATATAA[C/T]AACATTATCCAGGCT | 8440 |
rs555503526 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105875353 | GAGGTGCTGGCGGTA[C/T]GGGGTCTCCTGCCCC | 8440 |
rs555507266 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105867208 | TCGTCTCTTTATCAC[G/T]CTAAGACAAGGACTC | 8440 |
rs555520481 | in-del | -/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105819339 | TTAAAAAAAAAAAAA[-/T]AAAAAGTCATTGGGG | 8440 |
rs555537179 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105816190 | GCATGCCTGTGGTCC[C/T]AGCTAATGGGGAGAC | 8440 |
rs555547992 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105771859 | TTGTGAGGCCTGCCC[A/G]TCACTCAGATCTATA | 8440 |
rs555553124 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105823196 | GAGGGGGTGTTGTAG[A/G]GCTTTTAGTAAACTG | 8440 |
rs555608547 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105798577 | ATATGAATAGTGAAG[C/T]TCCCCAAAGATACAT | 8440 |
rs555617735 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NCK2 | GRCh38.p7 | 2:105862203 | AGACTCTAGAATTAT[A/G]TCTAGGAAGAATTAG | 8440 |
rs555625409 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105786644 | GGCCTGATAAGCACT[C/G]TGTCCCTGTGGTGGC | 8440 |
rs555642280 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105758277 | ACTTCTCTTGGATTA[A/G]TAATGAATATTGCAC | 8440 |
rs555645645 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105805093 | TCCCAGAGGCTCTTC[C/T]TATCTGGACAGTTTT | 8440 |
rs555647315 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105798159 | GAGTAGGAGCTAATG[C/T]TCGCTTGTTGTAATG | 8440 |
rs555664309 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105792444 | GTCCTGTAAATATTA[C/T]GGAATTTCAATAACA | 8440 |
rs555699179 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105893384 | CGGCCAGCTTTAGAG[C/G]AGGGGAGGAGCAGGG | 8440 |
rs555725745 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105798688 | TTAAGTTTATGTGGA[C/T]GGTGAATCTCAACAG | 8440 |
rs555762146 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105885308 | GTCATACAGTACTTT[G/T]TTTTCCAGTAGAGAA | 8440 |
rs555806943 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105833284 | GTACTTTTACTAGAG[A/G]TGAGCTTTCACCTTG | 8440 |
rs555817583 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105767251 | ATTGAACCAAATGCA[A/G]TTTGCTGTTAATGTA | 8440 |
rs555825344 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105892807 | GCCGAGATTGGGCCA[C/G]TACACTACAGCCTGG | 8440 |
rs555857069 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105780658 | ATGTTGAGATCCTAC[A/C]CCCCAAGGTGATGGT | 8440 |
rs555874656 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105792906 | TTCTGCACTTGCTAG[C/T]CAGGTGAGGAGAGTA | 8440 |
rs555894770 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105886429 | ACCAGCAAACTTGCT[A/G]GAATGCAGATTGCCC | 8440 |
rs555904950 | in-del | -/A | | | intron-variant | NCK2 | GRCh38.p7 | 2:105796599 | GAGCCTGGGAGCTGG[-/A]AGGCTGGAGATGGTG | 8440 |
rs555907575 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | NCK2 | GRCh38.p7 | 2:105773163 | CTCAGCCTCCCAAAG[C/T]GTTGGAATTACAGGC | 8440 |
rs555926068 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105866836 | TGAGATGTACCCAGT[A/G]ATTTTTGGTATATAT | 8440 |
rs555974955 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105866510 | GGGGGCGATGGTTTC[A/G]GGATGAAACTGTTCC | 8440 |
rs555996826 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105811498 | GGCAGACGTACCTGA[A/C]TGTGTGTTCCCAGCT | 8440 |
rs556004668 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105860076 | GATCAGTTGAGGCCA[C/T]GAATTTGAGACCAGC | 8440 |
rs556036176 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105871995 | GACATGGAAGACTGG[A/G]GAAGCTGTCAAGAAT | 8440 |
rs556042936 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105754835 | GGAAATTTAATATAG[A/G]TGAAGAGTGAATTTT | 8440 |
rs556046855 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105871556 | GCTGGAGTGCAGTGG[C/T]GCGATCTCGGCTCAC | 8440 |
rs556077654 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105761653 | GAGGCTCAGGTGGGA[A/G]GATTGCTTGAGCCCA | 8440 |
rs556173101 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | NCK2 | GRCh38.p7 | 2:105819209 | TCATAGGGCATTCCC[A/T]GGTCTCTCTTCCAGA | 8440 |
rs556178409 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105779710 | TTTTTTTTTCCCACT[A/G]ATCAGCTTTTGAATT | 8440 |
rs556213271 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105786001 | TTCGTAAACGTGTGT[G/T]TGTCCACTCTTTGCC | 8440 |
rs556236807 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105837661 | TGTCAGTATTCTGCA[C/T]TACAAGATAAGCCCA | 8440 |
rs556238587 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105816907 | CCATAACGAATCCTG[A/G]TCCCTGTATTCTGTA | 8440 |
rs556252035 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | NCK2 | GRCh38.p7 | 2:105775413 | TAGATAGATAATTAT[C/T]TTTAACCGAAATTTA | 8440 |
rs556260746 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105818588 | AAAGCAAACCAAATT[G/T]TAATCAAAGCATAAC | 8440 |
rs556309378 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105790960 | TATCACAGATGCACA[C/G]TGCTAGGGGAGTGCT | 8440 |
rs556321066 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105810983 | GATTGAGACCATCCT[G/T]GCCAACATGGTGAAA | 8440 |
rs556357741 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105859483 | CCTAGGCCTAGCGTG[G/T]TTAGAAACTTGCATG | 8440 |
rs556377785 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105831302 | TTTGTAGGAAACCGC[A/C]AAAGAACCCTGAATA | 8440 |
rs556392294 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105792971 | GGGAGTCTTTCCCTT[G/T]CTCACCAACCGAGTC | 8440 |
rs556413224 | in-del | -/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105889231 | CAGTGTCCCAGCTGT[-/C]CCTTCAGGGGAAATT | 8440 |
rs556414704 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105855976 | AGTAGCTGGGACTAC[A/G]GGCACCCACCACCAC | 8440 |
rs556426158 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105823898 | CGTGATCAAACGCCT[A/T]GTTCCGTGACCTTCC | 8440 |
rs556484977 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105886591 | AACCACTACGTTGTG[A/G]AGTATGCACTTGATT | 8440 |
rs556494495 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105787090 | CTGCCCGCTGCAGGC[A/G]TGGTGGCACTGGGCA | 8440 |
rs556560990 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105768643 | GCCCAACACAAATAC[G/T]TAAACTTTCTTAAAA | 8440 |
rs556603536 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105774422 | TGACTGGTCTGACAG[A/T]TGCTCAGTATTTTCT | 8440 |
rs556626364 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105861883 | AATTTATCTTAAGAT[C/T]AGACTGGCCTGGAAT | 8440 |
rs556689294 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105868016 | CCATTTTAGTGTCTG[G/T]TTCCTGGAAGCAGGT | 8440 |
rs556692355 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105824364 | TATTTAGTGCCTTCC[A/G]GAATATGCCACTTAT | 8440 |
rs556704445 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105869567 | CCACGTGCCACCTGC[A/G]TGTTCCCCCGTGAAT | 8440 |
rs556763280 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105872629 | GCATTAAACAACAAA[C/T]GAGCAAAGAACCCTT | 8440 |
rs556817246 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105821927 | GTTCCTTCTGCTTCC[C/T]GGGCTGCTGTCTCTG | 8440 |
rs556822125 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105748944 | TGTCTACTGTGGAAG[A/G]CTTTGACCTCAGGAT | 8440 |
rs556830026 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105755278 | GCATTATCATCTTTT[A/T]TAAAAAAGGAGGAGG | 8440 |
rs556837167 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105835466 | TATCATAGTGAACTC[C/T]CCTGGCCTGTAAGGT | 8440 |
rs556875677 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105839067 | ATATGAGAGAGGCAG[A/G]GAGAGCAAGGGAGGG | 8440 |
rs556878902 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105839966 | CTGGTCAGCAGTGTC[C/T]GCTGTAGTGGACATG | 8440 |
rs556880650 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105801896 | ATGGAGCTGGCATTG[C/G]ATTCCAAAGCCAGTG | 8440 |
rs556946347 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105782698 | GTGGGGGATCCGGCC[C/T]GTTGAAATCATTTGG | 8440 |
rs556961579 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105771152 | TGCTCTCGATCTCCT[A/G]ACCTCGTGATCCGCC | 8440 |
rs556963650 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105758908 | GAATTAATGCTAGCA[G/T]TCAAAACTAGTAAAA | 8440 |
rs556984916 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105753978 | CTTCCAAGTGAGTTG[A/T]CTGTGCCAGCTTCTC | 8440 |
rs556984955 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105746893 | GGAAGCTGTGGAGGT[G/T]CCTGGCCCACTTCCT | 8440 |
rs557028405 | snp | A/C/G | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105762588 | GGTGGGAAAAAACAT[A/C/G]CTTATTTCCACCAGC | 8440 |
rs557033270 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105828820 | ATCACTCACTCATCT[C/T]TTCAACTGTACCCAG | 8440 |
rs557045999 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105760357 | TGCCTGACTTCCCGC[A/G]TGGGATAGGTTGGTC | 8440 |
rs557047064 | in-del | -/TATT | 0.00279162 | 0.0372561 | intron-variant | NCK2 | GRCh38.p7 | 2:105821082 | AACGCTATCCAGTAA[-/TATT]TATTTAACTACTAAA | 8440 |
rs557049457 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105784156 | TCACCCAGGCTGGCG[G/T]GCAGTGGCGTCATCT | 8440 |
rs557076904 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105876259 | TTGAAAGAAAAACAC[A/G]TCATTTCATCTCTTG | 8440 |
rs557083483 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105777146 | TCTGAGCCCACGGCC[C/T]TGCGGCTGTCACTGG | 8440 |
rs557089653 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105870457 | GGGTATGCATGCCTA[A/G]AAATAAGAAAAGTCA | 8440 |
rs557120763 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | NCK2 | GRCh38.p7 | 2:105837386 | CTTTGACTTCCCCAA[C/T]GCCTCCCCAATTGCA | 8440 |
rs557137505 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105789896 | ACCATCAGATAACGA[A/G]CAGGTTGGATATGAG | 8440 |
rs557153158 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, intron-variant | NCK2 | GRCh38.p7 | 2:105745104 | CCCGGGACCCGCGCC[G/T]CTGCCCTCCGGCTCC | 8440 |
rs557165009 | in-del | -/TATC | | | intron-variant | NCK2 | GRCh38.p7 | 2:105752399 | GTTAAAACTAATATC[-/TATC]ATCAAAATACCTTGT | 8440 |
rs557166346 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105834697 | TTTAGAGACAAGGTC[G/T]CGTTCTCTTACTGAA | 8440 |
rs557176756 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | NCK2 | GRCh38.p7 | 2:105851537 | GCTGGGATTACAGGC[G/T]TGAGCCACCGCACCC | 8440 |
rs557189189 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NCK2 | GRCh38.p7 | 2:105850650 | GGTTTCCTTGAACTG[C/G]TAAGCTAGAGAGAAA | 8440 |
rs557204257 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105885505 | TTCAGGCAATTTCAT[C/T]ATTCCATTTCTCTAA | 8440 |
rs557272577 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105889802 | TGTTGCCCAGGCTGA[A/T]CTCAAAGTCCTGGCC | 8440 |
rs557275718 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105842142 | CCAGGCTGGAGTGCA[A/G]TGGCGCGACCTCGGC | 8440 |
rs557290655 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105845779 | GAAGGCCTGATAAAC[C/T]GCTAAAAATGGTGAC | 8440 |
rs557300564 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105774986 | GAGCCTGAGGCCAGC[C/T]TGGGCTGTATAGCAA | 8440 |
rs557321855 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105810279 | TCACCTTCTGGCCCG[C/T]TTCTTAAGATGCTAT | 8440 |
rs557341582 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105785280 | GCAGTTGGTTCTTTA[C/T]GGTGTCACTGGGAGC | 8440 |
rs557358785 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105816177 | GCCAGGGGTGGTGGC[A/G]TGCCTGTGGTCCCAG | 8440 |
rs557371999 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | NCK2 | GRCh38.p7 | 2:105828446 | CAAGAATACTACAAT[G/T]AAAGCCCCATGACAG | 8440 |
rs557386399 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105864970 | ATCCAAATAACACGA[A/G]TACCTTCAACTAAAA | 8440 |
rs557409595 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NCK2 | GRCh38.p7 | 2:105836685 | TGCTTGGGTTCAGGT[A/G]TTGGGATTAGAGCTG | 8440 |
rs557415387 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105877018 | CGGCTGCCACCTGGC[A/G]GGGTCACAGCTCCAG | 8440 |
rs557444723 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105791203 | AGATCTCTAATCCTT[C/G]CTTCCAGGATTTAAA | 8440 |
rs557449040 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105798033 | TAACCACATTTTTAT[C/T]AATTTATGGTTTTGA | 8440 |
rs557478900 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105883759 | ATATTGTTAGAGAAT[G/T]AGCTAACTTTTTCTA | 8440 |
rs557536686 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105797449 | CTTTCTAAGGGGGAA[A/G]AAACCAGTATGGCCA | 8440 |
rs557536936 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105892157 | CCATTGCACTCTAGC[C/T]TGGGCAACAAAAGCA | 8440 |
rs557545437 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105790895 | GGGAGGAGAGTCCTC[A/T]TCTGCAGGGCTTGGT | 8440 |
rs557570686 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105759632 | GTACATTGGTTACAT[C/G]TAATGAACCAGTATT | 8440 |
rs557578267 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105870988 | CAGGGTCAGCGTGTT[A/G]TGTGCTTGGGAGGTC | 8440 |
rs557610218 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | NCK2 | GRCh38.p7 | 2:105848574 | TGCTTCTTTGCTCCC[A/G]AGAATAGCAGTGCAC | 8440 |
rs557610246 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105868976 | CCCTTCTCCAAAGCA[C/T]GGAACAGGTGGACCG | 8440 |
rs557620960 | snp | A/C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105821717 | TATATTATCTCTAGT[A/C/T]GCAAATGCAGATGTT | 8440 |
rs557623291 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | NCK2 | GRCh38.p7 | 2:105828295 | TGTTTTTGCTATCAA[C/T]GAATTTCCCTGTTCC | 8440 |
rs557639311 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105876870 | CCTTCGAATTAGAGA[A/G]AGGCAGTCGCTTAGA | 8440 |
rs557654358 | snp | G/T | 0.0271762 | 0.113356 | intron-variant | NCK2 | GRCh38.p7 | 2:105858047 | TCTTTGTTTTTTGGG[G/T]TTTTTTTTTTGTTTT | 8440 |
rs557671882 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NCK2 | GRCh38.p7 | 2:105871880 | AGGACCTTAGAGAGC[A/G]GGGAGGAAACTACAT | 8440 |
rs557675873 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105883080 | TGAGGACGGAGCATC[A/G]TGGTGGTGGAAACTG | 8440 |
rs557717863 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105868805 | AGAATTCTGGAAAGG[C/T]GATAGCCTGGCTCAG | 8440 |
rs557806754 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105838093 | ACTTTCTGTTTAACT[A/G]GAACAGTCCTTTTTT | 8440 |
rs557812197 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105777503 | TGCATTTTCTGTATG[A/G]ATCAATGGAAATGGG | 8440 |
rs557822109 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105823931 | TGTGAAGGTCTACCC[A/G]GGTCACAGTGTGAAC | 8440 |
rs557822123 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105858734 | TTTTGTCACATACAG[C/T]ACTTTGTTAAGAGTA | 8440 |
rs557824399 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105865776 | GAGTCATCTTCAGCA[A/T]CTTTGTCATCAGTTT | 8440 |
rs557885824 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105865024 | GCAGGAGGCCTCTTG[A/G]TAGCTGGTGTCAGGG | 8440 |
rs557907645 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105870585 | ACATGGTTAAACCCC[A/G]TCTCTACTAAAAATA | 8440 |
rs557929552 | snp | C/T | | | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105772206 | TGGGAACTCTTGATC[C/T]CTTTGGCCCTGAGTT | 8440 |
rs557935120 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105758655 | CCTTGTGATCCACCC[A/G]CCTCAGCCTCCCAAA | 8440 |
rs557952114 | in-del | -/TT | 0.00953873 | 0.0683987 | intron-variant | NCK2 | GRCh38.p7 | 2:105861876 | GCTCAGCAATTTATC[-/TT]AAGATCAGACTGGCC | 8440 |
rs557973627 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105746642 | GGACACGTGGAGAAG[A/G]AATTGACTTCACCTG | 8440 |
rs558016366 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105876171 | TCCAAAGCATGCTGC[C/T]GTGACACCTCCAACC | 8440 |
rs558023995 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105753994 | CTGTGCCAGCTTCTC[A/G]AACCTACCCTTTTGT | 8440 |
rs558032045 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105810835 | GAATTCCTATATGTT[A/C]GAATTTTTAGGCAGC | 8440 |
rs558044628 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105798052 | TTATGGTTTTGATCC[A/G]TCTATTTTAGACTCA | 8440 |
rs558063925 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105835704 | TCCTGCTATTACTTT[A/G]TTAAAGAGGGTTTCT | 8440 |
rs558071259 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105844426 | GGAACCTATTTTAGT[C/T]TAAAAAATATTTTTG | 8440 |
rs558117500 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105744121 | CGACACTCCTTCTAG[A/G]GGCACATTCGGGCAG | 8440 |
rs558126530 | in-del | -/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105779692 | AGGAAAGAGCTTTGA[-/T]TTTTTTTTTTTCCCA | 8440 |
rs558128501 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105852232 | GTGGGTGTTTTCCCA[A/G]GATTAAACGCCTTGG | 8440 |
rs558130576 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105804277 | AAATGAACGGACCAG[C/T]GCTTTTCTTTGATGT | 8440 |
rs558173108 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105833792 | TGTGGGCATTTATTG[C/T]TATAAACATCCCTCT | 8440 |
rs558205544 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105746939 | CCTGGATTCTGAGCT[G/T]CTTTCCTGCTTCATA | 8440 |
rs558211725 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105832885 | TTTCGTTTTTGTTTC[A/G]TTTTGTTTTGTTTTT | 8440 |
rs558235286 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105878087 | CTTTCTATTTTGATG[G/T]CCATCCAACACTGGT | 8440 |
rs558242448 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105743009 | AAAAAAAAAAGGTGC[A/G]TATCAGAATAAAAAC | 8440 |
rs558244664 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105750146 | GCTGGAAGTCCATGA[C/T]CCCGGGGCCGGCAGG | 8440 |
rs558245919 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105792056 | ACAGAGCCGTGGGAA[C/T]GCTTCCCCAGTCCTG | 8440 |
rs558249396 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105754631 | TGTGTGTCTGTGGGA[G/T]GTTGGGGGGAGCTGC | 8440 |
rs558269870 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105798404 | TCCTTTTTTCTTTTT[A/T]TAAAATGAAGAGATC | 8440 |
rs558288699 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105885191 | AAAGGTGCAGAGCTG[C/G]CCTGCAAGTGCGGGA | 8440 |
rs558297506 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105840420 | TTCTCCTACTCTACT[C/T]TACTCTCACAACACA | 8440 |
rs558298726 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105892771 | GAATCGCTTGAACCC[A/G]TGAGGCGGAGGTTGC | 8440 |
rs558310375 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105825907 | TGGTGATCCGTCAGG[A/T]TTGGAGTTCCTGGCT | 8440 |
rs558330062 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105766211 | GGAGAGCCCGGGAAT[A/G]TGGGGACTTCCCACC | 8440 |
rs558351466 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105874006 | AGGCGGGGGAAGGCT[C/T]GGGGTGAGATGGGGC | 8440 |
rs558415236 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105801347 | GTCTGTTGACCAGCT[A/C]ACTCGGCTTGCCTCC | 8440 |
rs558427938 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105803737 | AATTGGCTCTTCTTC[A/C]GTTTCTCTTATTTTC | 8440 |
rs558432857 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NCK2 | GRCh38.p7 | 2:105760740 | CCAGTCAGGGCCAGA[A/G]TAGGGAGGTCCCTAG | 8440 |
rs558439598 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105813177 | CAGGGTTGCTGTGAC[A/G]ATTCTTGCAGCTGAT | 8440 |
rs558447797 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | NCK2 | GRCh38.p7 | 2:105851680 | TACGCCAATGGAGCT[A/G]TCATTGATTGGCTGT | 8440 |
rs558469733 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105892232 | CTTAATTTCTAATAG[G/T]GTTAGACATCAGAAG | 8440 |
rs558469790 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105766738 | CATCGAACCAGCCCT[C/G]GCTCTGTCCCCAGAC | 8440 |
rs558481046 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105890719 | GCTGGGTGAGCCCAG[C/T]TGCCTTGCACAATTT | 8440 |
rs558482456 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105826397 | GGGACACAAAGCCTA[A/T]CCCCACCACCCTTCG | 8440 |
rs558511597 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105859416 | GGACTTCTGCATCCA[A/G]CGTCACCTGCCCCAG | 8440 |
rs558511971 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105756291 | ACGAAATCATCACTT[G/T]GCATAATTTTGAGCT | 8440 |
rs558524363 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105882438 | AGAGAAAGCATTCTT[C/T]GCAAGACTGGTGGCT | 8440 |
rs558531640 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105891436 | ATTGTTATTCATTTA[A/G]TGAATTGATCAAAAC | 8440 |
rs558532547 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105890630 | TATTTGGTCTATTTG[A/T]GACAGAGGCATGCAT | 8440 |
rs558547515 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105763151 | TGCAGTGAGCCGAGA[C/T]CATGCCACCGCACTC | 8440 |
rs558548517 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | NCK2 | GRCh38.p7 | 2:105889927 | CTCAGAGGATGCTCA[G/T]GCTGCTGGTCTTGAG | 8440 |
rs558566256 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105765359 | CTGACTTTAAAATGG[C/T]CCTTGAATTTCAGGG | 8440 |
rs558629844 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NCK2 | GRCh38.p7 | 2:105759450 | CAACCATGTTACCCT[A/G]TGCATACAGGCTTTT | 8440 |
rs558631865 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105805290 | GCAGACGCGAGGGCA[A/G]AGAGTTATGAAAGGG | 8440 |
rs558638349 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105788553 | TTTTTGATATTTAAC[A/G]TATCTATAGTTGTAC | 8440 |
rs558646573 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105795013 | TGCTTTTTAAAAAAA[A/G]TTTTATTTTTTAGAG | 8440 |
rs558666525 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105802600 | GGAGGGATGTGCCAG[A/G]CTCTTTTTAACCATC | 8440 |
rs558672090 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105757013 | TTTCTTCATGTTGGT[C/G]AGGTTGGTCTTGAAC | 8440 |
rs558688146 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105770414 | TGAGAGGTAGATTTA[C/T]GTGTCCTGATTAAAA | 8440 |
rs558699043 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105790336 | CCTGCTGACTCAGAG[C/T]GGGAACAGTTGCTGA | 8440 |
rs558729185 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NCK2 | GRCh38.p7 | 2:105850460 | CTTAGCTCATGAGGT[A/T]CTGAGAGCTGTTTTT | 8440 |
rs558732303 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105888983 | ATCAGTACTCTAGTA[C/G]TTGTTGAGGAGCAAG | 8440 |
rs558732344 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105777087 | GAGTTCCCAGAGCCT[C/G]AGAGCAGGTGCTCTC | 8440 |
rs558734371 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105794206 | GGCGCCTGCCACCAC[A/G]CTGGCTAATTTTTGT | 8440 |
rs558762614 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105863879 | GCGTCGTCTGTATAA[C/T]GGGATACGTGACTGC | 8440 |
rs558788210 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105807223 | TGTTACTGTCCTGTG[A/G]CGCACCTGCGTGGGA | 8440 |
rs558801108 | in-del | -/A | 0.00517822 | 0.0506191 | intron-variant | NCK2 | GRCh38.p7 | 2:105756467 | ATGTGTGTTTCTCTT[-/A]TTACTTGCACACCTT | 8440 |
rs558823090 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105863449 | AGTAACCAAAGGCTT[C/T]GAAACAGGGATGCAG | 8440 |
rs558824730 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105869620 | CGTCACATTTCACTT[A/T]CCTGAGCAGGTGTGG | 8440 |
rs558898561 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105795670 | TGTCACCAATTTAGG[C/T]AGGGTGTGGATTGTT | 8440 |
rs558927944 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105875368 | CGGGGTCTCCTGCCC[C/T]GCCCAGTCCCCTGGG | 8440 |
rs558949483 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105759067 | AATGCTTAGTGTTTT[A/G]AATGAACTTAATTTG | 8440 |
rs558968191 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NCK2 | GRCh38.p7 | 2:105849887 | AGTTGCCATTCTTAA[A/G]TCTCTCTTAATGCTG | 8440 |
rs558996423 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105842256 | TGCCAGCTAACTTTT[C/T]TGTATTTTTAGTAGA | 8440 |
rs559003718 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105827043 | CTTGCTCTGTTGCCC[A/T]GGCTGGAGTGCAGTG | 8440 |
rs559030452 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105824926 | GTAAGATCAGGAGCC[C/T]ATCTCCCACCTGAGT | 8440 |
rs559033379 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105857337 | AGCCGGCACTGGGCC[C/T]GCGCCCGTCCCCGAC | 8440 |
rs559040916 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105814472 | GCTTGGAGAGGCCGT[A/G]TTCTGACTTGCCCAC | 8440 |
rs559049010 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105781705 | ATGAAAAGTACAGAG[C/T]CTGTGGCTTGGCAAG | 8440 |
rs559067220 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105809271 | CGTGTGTCATATGTC[A/G]TGACACATATGTATG | 8440 |
rs559100335 | in-del | -/TT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105845412 | ATTTTTTTTTTTTTT[-/TT]GAGATGAATCTTACT | 8440 |
rs559111655 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105863569 | TGAAGGAAGGATAAG[C/G]CTTAGTCCCTGACTT | 8440 |
rs559125393 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105820546 | CATTGAAGTTAAGGA[A/T]CAAAGTCTTGGGACC | 8440 |
rs559153968 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105807207 | AACAGCTCACTCTGG[G/T]TGTTACTGTCCTGTG | 8440 |
rs559158514 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105780880 | ATCTTGGACTTCCAG[A/C]TTCCACAACTGTGGG | 8440 |
rs559170983 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105833076 | TCCCCTCCCCTCCCC[A/T]CTTTTTTCTTTTCTT | 8440 |
rs559186029 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105808063 | GTGTACCGCTATGCC[C/T]AGCTAGTTTTTGTAT | 8440 |
rs559186124 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105814845 | ACAGCCCAAACAACT[A/G]CATAAAACAATTCCT | 8440 |
rs559200692 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105872616 | TCCCTCAGGCTGAGC[A/G]TTAAACAACAAATGA | 8440 |
rs559223020 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105814279 | TAACACATTGACAGT[G/T]TGTCAGTGGAATGCT | 8440 |
rs559229796 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105783387 | CATTAAATTGTGCCC[A/G]TGTTCTGGGGTAGCA | 8440 |
rs559250823 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105743378 | TTTTGAGTAAATTAA[C/T]CTAAAATTGGGCAGA | 8440 |
rs559311049 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105761429 | CTCCCTCCTAGTGAT[A/G]GGACGATTCCAGGCT | 8440 |
rs559325208 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105769305 | ATCCCCAGCTGGCTG[C/T]GCCCTATTTAAAGCC | 8440 |
rs559328026 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105750249 | GTGCACTGAGAGAGA[A/G]GTCTGGTGTTTCTTC | 8440 |
rs559328223 | in-del | -/GTGT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105830671 | CTTGCCAGGAATTTG[-/GTGT]GTGTGTGTGTGTGTG | 8440 |
rs559333590 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105813785 | GGTTACAGAGAATTC[A/G]GATAATCCCTTGGAT | 8440 |
rs559351315 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | NCK2 | GRCh38.p7 | 2:105794343 | AGGCATGCGCCACCA[G/T]GCCTGGCTGAATCCT | 8440 |
rs559373993 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105840609 | TGCCCCTCCACCCCC[A/C]CTTCAGATGCCAGTT | 8440 |
rs559389420 | in-del | -/GTTT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105867443 | AATAAATGTGGGTTT[-/GTTT]TTGTGTATCTTTAGC | 8440 |
rs559398278 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105875744 | CCTCCAGAATGGTGA[A/G]AAATAAATGTCTGTA | 8440 |
rs559405736 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105868881 | CGACTTGGCCAGGGC[A/T]ATGAGTCTGCCTCAC | 8440 |
rs559420415 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105819963 | CCACCTTTCCCCATG[C/T]CCTTTCAGGATGGGA | 8440 |
rs559427598 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105888495 | AGATGTTTCAAAACC[C/T]GGGGACTGAGTCTAG | 8440 |
rs559527320 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105758255 | ATGTAAGTAATTGAA[A/T]CACATTACTTCTCTT | 8440 |
rs559533633 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105745282 | CGCCCCTCCGGTGCT[C/G]TCGGCCCTGCCGCGG | 8440 |
rs559536136 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105783000 | CTGAGTTGGTCGACT[A/G]TCATTTGCAACAGGT | 8440 |
rs559569157 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105782368 | ACCAAAAATCTCCCT[A/G]AAACTAGTTCCACTC | 8440 |
rs559571171 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105788657 | GAACTTCCTCATCTC[C/T]AAGTGCCTTCTCCTA | 8440 |
rs559577685 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105834872 | TTGTAGAGATGGGGT[C/T]TCATTGTATTGCCCA | 8440 |
rs559580831 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105749803 | GTTACCCTGGAAAGC[C/T]TCCTCAAGTTCAGAA | 8440 |
rs559595334 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | NCK2 | GRCh38.p7 | 2:105852021 | CTAGTTGTATGGGAA[C/T]TTTTAATTTTCACGT | 8440 |
rs559596991 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105795806 | TCATTATTCCTCCCT[C/T]TAGACCTCTCCCTCC | 8440 |
rs559641519 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105890016 | GTGGTCATATGTAAC[A/G]GTGTATGTTAGTATA | 8440 |
rs559658361 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | NCK2 | GRCh38.p7 | 2:105788006 | CAGCCAAGGACAAAT[C/G]AGAGTTGGGATGTGT | 8440 |
rs559662494 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105880804 | TTTTAGAGACAGGGC[A/C]TCACTCTGTTGCACA | 8440 |
rs559670442 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105789652 | CCTTCGGAACCAGCT[A/G]TAAAGCACTTATTGT | 8440 |
rs559688625 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105762178 | GCTTGTGAGAAGCAC[A/C]GTTTCTGTGCGTAAG | 8440 |
rs559703837 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105786713 | CTTCCTGTCTCCATC[A/G]CTGTCTCTTATTTCT | 8440 |
rs559721316 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105880232 | TGAAATTTTCTACTT[C/T]ATTCCCTTAAATTCA | 8440 |
rs559744499 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105822196 | CTTTGGAAACGTAAG[A/G]GTGTGTGAAGGAAGA | 8440 |
rs559783663 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105822569 | ATAATTATTTTCTCT[C/T]AGTTGTGGTGGTGAT | 8440 |
rs559796260 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105878995 | GTATTTTGTTTTTGA[A/T]AGAAGTCACTAAAGT | 8440 |
rs559857562 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105885679 | TGGTGGTGATGCTGC[C/T]GCTTTTGGGACCACA | 8440 |
rs559867536 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105751190 | CAGCTTCTCCTGCAA[C/T]CTGCCCGCCTTCTCA | 8440 |
rs559923275 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105761321 | CCAGAGAATCTTTTT[C/T]TGGGAGGGAGAAGAG | 8440 |
rs559928054 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105835792 | TTAATAGGATCCCAC[A/G]TGTCAGGTAGGCTTT | 8440 |
rs559949154 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105849028 | TTGAAATTTCAAGTT[A/G]ATATCCTGGAAGTAA | 8440 |
rs559958914 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105834290 | CTCTCTTTAGCTCTA[A/G]TAATATTTGCTTATA | 8440 |
rs559970536 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105832182 | TCAGCTAGTTTGTTA[C/T]TGGTATATAGAAGAA | 8440 |
rs559972915 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105747990 | TCCTTTGAACATTTC[C/T]CAAAGTATGTTTATT | 8440 |
rs559997462 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105866422 | GTTCATCTGTAACAG[A/C]AGTCCCCAAACTTTT | 8440 |
rs560012379 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105766892 | TTAGTTTAGTAACTG[A/G]CTGGAGGCTTCTGGC | 8440 |
rs560029886 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105859522 | CAGAACTCCTGCCTC[G/T]GATCCAACCCAGACC | 8440 |
rs560059558 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105754393 | GGACAAAGTCCATCA[A/G]TGTCTCCTTCGATTT | 8440 |
rs560081312 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105798297 | CCTATCCTGGGAGCC[C/T]GGATAGCCTCACTGT | 8440 |
rs560102293 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105844640 | CTACTCGGGAGGGTG[A/C]GGCAGAATTGCTCGA | 8440 |
rs560104428 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105892666 | GCCTGGCCAACATGG[C/T]GAAACCCTGTCTCTA | 8440 |
rs560121970 | snp | A/G | | | utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105893997 | TATACACACACACAC[A/G]TGCACACACACACAC | 8440 |
rs560142049 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105806811 | TTCCATAGGGGGCTT[C/T]GCAGTTACCAGTAAT | 8440 |
rs560149825 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105866753 | TGGCCCCGGGGGGTT[-/G]GGGACCCCTGGTCTA | 8440 |
rs560155542 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105831566 | TTTGAGTAAATTTTT[G/T]TATGTAGTGAAAGAT | 8440 |
rs560165750 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105792607 | CAAACTCGTTTGTTT[G/T]TTTTTTTCCACCTTC | 8440 |
rs560173877 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105754929 | AACAGATTTTTTTTT[C/T]CCAGCCATTTCCATT | 8440 |
rs560196401 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105798800 | TACATTTAGGGAAAT[C/T]AATACAAAATGTTCT | 8440 |
rs560231251 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105812832 | TTTTTTTTTTTTTCC[C/T]TCCTGTGCTAACATC | 8440 |
rs560247533 | in-del | -/AT | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105833942 | ACTTGTTTAATTTGC[-/AT]ATATTTATACAATTT | 8440 |
rs560266656 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105812293 | GACACCTTTGAGTTT[C/T]GGATTGATAAACACA | 8440 |
rs560318032 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105858097 | GGAGCCAAAGTGTTC[A/G]TGGCTTCCTATTACT | 8440 |
rs560332872 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105853658 | CATTTGTTGAAGAAC[A/C]GTAAGGCAGATTTTA | 8440 |
rs560355895 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105856651 | AGGTAGTATTTTTGT[C/G]TATGGATTAGGTTCT | 8440 |
rs560376051 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105781386 | CATCCCTTCCCACAC[C/T]GCAAGACTTGACTAA | 8440 |
rs560378398 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105805257 | GTGCAAAGATGTTCC[C/T]AGTACGGGGAGGAAA | 8440 |
rs560378872 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105768676 | TGATGAGTTTTTTTT[G/T]AAATTTTCTTTTTCT | 8440 |
rs560407664 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105893731 | TTTGGGGCTGTGCTT[A/G]CAATAAAGAATTTCC | 8440 |
rs560419155 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105804555 | TTGGATTTCAGCCCA[C/G]ACACAGTATTTGAAT | 8440 |
rs560455517 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105862089 | GTTAGCCTGCATAAA[C/T]ACATGTAATGAGAGC | 8440 |
rs560473371 | in-del | -/T | 0.0660258 | 0.169273 | intron-variant | NCK2 | GRCh38.p7 | 2:105795303 | TGATATATTTTTAAT[-/T]TTTTTTTTTCCTCAA | 8440 |
rs560482753 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105756570 | AAGTGTGGGTCCCTC[A/G]CCAGGGCACACTGAC | 8440 |
rs560492718 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105763166 | TCATGCCACCGCACT[C/G]CAGCCTGGGCGACAG | 8440 |
rs560496560 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105787206 | ACACTGAAGGAAGCT[A/C]AGCTCAGCGCCGTGG | 8440 |
rs560507075 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105810604 | AAAGGCAATATGTAA[A/T]TAAATTGTCTAGTTA | 8440 |
rs560530304 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105800126 | TTGTGAGAAGAGAGG[A/G]TCAGTGCAGCCATGT | 8440 |
rs560567898 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105781449 | CCCCAGCCAGAACTA[C/G]TGACCCTCCTTGGCC | 8440 |
rs560572783 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105847526 | TGCAGGTGTGCAGCG[C/G/T]AACTGGCCTCCCTAG | 8440 |
rs560584160 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105855007 | AGGATGAAGTGTCCG[C/G]GTAGTTCTCTAATGA | 8440 |
rs560601445 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105817972 | CTGCTATAAAGACAC[A/G]TGCACACGTATGTTT | 8440 |
rs560630021 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105784008 | CAGGACCTGCTTCAG[C/T]TGGACGGCAGGTCCC | 8440 |
rs560632311 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105827783 | GATAGAGAGCAGGTT[A/G]GTGTTTACAAGGGGT | 8440 |
rs560636243 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105749191 | AAACGCTGGGCAGAC[C/T]GTTTGTGATCCTGGC | 8440 |
rs560709917 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105879044 | TTATAAAGTGTCTTT[A/G]TAACGTATTGTGATG | 8440 |
rs560756678 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105846363 | AATGAGTTGCTCAAT[A/G]ATGAACTCCTGAAAA | 8440 |
rs560816273 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105824627 | TAAGTACCACGTCTC[A/G]GCGGCGTGTGCTTAG | 8440 |
rs560817330 | snp | C/T | | | upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105743363 | ATATTGCTATACTTA[C/T]TTTGAGTAAATTAAT | 8440 |
rs560824221 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105825317 | ATTTGCGAGTTTTCA[G/T]GTATTCACACCTGAG | 8440 |
rs560828547 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105867524 | GTGGGAGGATACTTC[A/G]AGAGAAAATAGACAC | 8440 |
rs560830020 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105818801 | TTCTGGAAATTTTCT[C/T]CTTTAATATTAAAAG | 8440 |
rs560862473 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105786878 | GGCTGACTCCCTTAC[A/C]TCTGCTGCTCAGGCA | 8440 |
rs560866092 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105853954 | TTGAGAGTGGAGGAT[G/T]CCAGCTAGAGCACCT | 8440 |
rs560909684 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105824637 | GTCTCGGCGGCGTGT[A/G]CTTAGAACAGAGGTC | 8440 |
rs560994306 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105787300 | ACCTGCAAGTGCAAT[G/T]GACTGAAATTTTATG | 8440 |
rs561013416 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105793725 | CCCAGCCTTGGCCAG[C/G/T]GAAAGCTGCCTTAGG | 8440 |
rs561032490 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105766767 | ACCTTTCCTTTACTC[A/G]GCTATCCCTCCATCT | 8440 |
rs561041779 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105852941 | CTCCTTCCCAAAAGG[A/T]TTGTTATCTTTAAAT | 8440 |
rs561041803 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105820727 | GGCCATTACTAGGGA[C/T]GGAAGATGCAAAGGG | 8440 |
rs561056326 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105800175 | AGTCTGGCTCTCCCT[C/G]GTCTCCGGCACGGGG | 8440 |
rs561062679 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105761433 | CTCCTAGTGATGGGA[C/T]GATTCCAGGCTTGGG | 8440 |
rs561064719 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105893202 | GCCCCACACTCGCCT[C/T]CCGGGCCCCACGGTG | 8440 |
rs561099402 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105886889 | AGTTGATGATTGACT[C/T]TTCATTTATGTAAAT | 8440 |
rs561109027 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105839195 | AGAGTTTGGAAAAAC[C/T]GCCCAGGGTCAAGGT | 8440 |
rs561111334 | snp | A/G | | | upstream-variant-2KB, intron-variant | NCK2 | GRCh38.p7 | 2:105850636 | GAAGCCAAAAATTAG[A/G]TTTCCTTGAACTGCT | 8440 |
rs561175301 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105805487 | TAAGTTAAATTTTTA[C/T]AACTATTAGCCTTTT | 8440 |
rs561240389 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105750368 | ATTGCCTCCTGAAGC[A/G]TCCTGTCTCCAAATA | 8440 |
rs561245179 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105781503 | CGTAATATTTCTGCA[C/T]TCATTCCTGGAAGGC | 8440 |
rs561272067 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105767564 | GAACCCAGCTGGGCT[C/T]ATTCATTTCCACAGC | 8440 |
rs561274686 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105773979 | GTGCATCTGGAAGTC[C/T]TCAGGTGGAAGATGT | 8440 |
rs561279135 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105757268 | GTCTTCTGTGAAACT[A/G]GGGGTTGCCTGTAAT | 8440 |
rs561279237 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105749873 | CTGCCTTAAGAGAAT[A/T]ACACACAGAGGCCGG | 8440 |
rs561298549 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105881032 | CTCAAGCAATCTTCC[C/T]GCCTGGGCCTCTCAA | 8440 |
rs561328643 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105765339 | CCATGTCCTTTTAAA[A/G]CAGGCTGACTTTAAA | 8440 |
rs561335963 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NCK2 | GRCh38.p7 | 2:105782150 | CCGCGAGAGTGGGAG[C/T]CTATCACCGATCATC | 8440 |
rs561348664 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105813688 | AGTGCTCAGCACACT[C/T]GCCCAACACTGCAGC | 8440 |
rs561366633 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105756635 | GGGAATGTCAGGCCC[A/C]AGCAGTGTGGTATGT | 8440 |
rs561367067 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105783652 | TGAAATACCTTAGCA[C/T]GAAGAAACCCTGTAA | 8440 |
rs561427327 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105802213 | TGTGATGAAGTGGAA[C/T]GGGAAGATGTGCACA | 8440 |
rs561427364 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105825252 | GACCTGGGCATCTGT[C/G]CTGTTAACGCTGATC | 8440 |
rs561432081 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105861569 | ACCTAGGCTGGAGTG[A/C]AGTGGCACAATCTCG | 8440 |
rs561468718 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105763184 | GCCTGGGCGACAGAA[C/T]GAGACTCTTGTCTCC | 8440 |
rs561487184 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105883928 | CTTTACTGGGACTTG[C/G]ATCGGCTCTGCACAC | 8440 |
rs561514617 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105809011 | AAACATCACAATTCA[A/G]ATGCAAAATGGCATG | 8440 |
rs561518904 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105757282 | TAGGGGTTGCCTGTA[A/G]TGTACTTTCACAACC | 8440 |
rs561527741 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105806933 | TACTTCTCAGATGCC[C/T]GTGGTCATGGGGTGA | 8440 |
rs561538718 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105844097 | TTTTGCAGAAGGTCC[C/T]CCACTTAGGATTTGT | 8440 |
rs561553839 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105891580 | TTTTGAGATTTTTCG[C/T]TCTTGTTGCCCAGAC | 8440 |
rs561561726 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105812864 | AAGAGAAGCAGTAAC[A/G]TTGAAAACAAACTTG | 8440 |
rs561587780 | snp | G/T | 0 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105819460 | CAGATCTTCTGATTG[G/T]ATCATCAGAACTCAT | 8440 |
rs561605347 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105777795 | GTTTGCTCCTGTCAA[A/G]CAGGAAACAAACACG | 8440 |
rs561607650 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105758514 | CCCCGGGTTCAAGCA[C/G]TTCTTCTGCCTCAGC | 8440 |
rs561618948 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105862119 | CAGCAACAGCTTGCA[A/G]TTTATACAGCACTTT | 8440 |
rs561640651 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105753649 | GTGTCTTCTCACTCT[C/T]CCAAGTGGCCCCCGG | 8440 |
rs561678665 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105752830 | TCATCTGTAGTATTC[A/G]TATTTCTGATAACAT | 8440 |
rs561678812 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105760355 | ACTGCCTGACTTCCC[A/G]CGTGGGATAGGTTGG | 8440 |
rs561688070 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105873652 | TGAGGCTGGGGGAAG[A/G]GTGGTTTTATTTTTT | 8440 |
rs561694087 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | NCK2 | GRCh38.p7 | 2:105784796 | TGTTTCCCACACTTC[C/G]CATTTCAACATTCTT | 8440 |
rs561719427 | snp | G/T | 0.00795532 | 0.062565 | utr-variant-5-prime, intron-variant | NCK2 | GRCh38.p7 | 2:105851828 | TCTGATATGAGGTGG[G/T]GGTGAATTGGTGGGC | 8440 |
rs561720452 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105775420 | ATAATTATTTTTAAC[C/T]GAAATTTAGTTTTTA | 8440 |
rs561752721 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105771238 | AATATCACTATTTCT[A/G]TCCCCTTTTATATTT | 8440 |
rs561818377 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105843492 | GTTACAATCAAGGCA[A/G]ATATACTGATTCTGG | 8440 |
rs561820172 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NCK2 | GRCh38.p7 | 2:105834059 | CGTTTATGACCAAAC[A/G]TACTGTAAATCCTAG | 8440 |
rs561820599 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105766295 | CCTGATGTATTTCTT[C/T]CTCCTTCTCTCACCT | 8440 |
rs561826933 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105817358 | AGACAAAAACATGTC[A/G]CTGTGCAACAAAAAT | 8440 |
rs561828203 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | NCK2 | GRCh38.p7 | 2:105864681 | GCTGGCACTTCTGAG[C/G]CAGCTGATTAGGTAC | 8440 |
rs561840398 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105870687 | TTGAACCTGGGAGGC[A/G]GAGGTTGCAGCCAAG | 8440 |
rs561841700 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105888505 | AAACCCGGGGACTGA[A/G]TCTAGTTAGGTTTTA | 8440 |
rs561897989 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105855454 | GAGATGAAGATGGAG[-/A]AAGAGGATGTTTTTC | 8440 |
rs561904560 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105860278 | GCCACAGAGTGAGAC[A/C]CTGTCTCAAAAAATG | 8440 |
rs561967202 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105836005 | TGAATTTCTCCATGA[A/G]TTCTCATGAATTGTT | 8440 |
rs561970865 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105811124 | AGGTTGCAGTGAGCC[A/G]AGATTGCACCACTGC | 8440 |
rs561986349 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105822163 | AATCTCCTGCAACTA[A/T]GTGCAGTTTGGAGAG | 8440 |
rs561994086 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105829210 | GGCATAATAATAAGA[A/C]AAATGCCTGTGAACC | 8440 |
rs562021773 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105864185 | CTTAAGGGGGAGATG[A/G]GTGCTGGGGTGTCCG | 8440 |
rs562046351 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105866233 | TATTACTTTTAAAAT[C/T]TGGAAACTATAGAAA | 8440 |
rs562120930 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105791700 | TTTTTCTACTTGACA[A/G]TTCAGGCAAATCAGT | 8440 |
rs562122060 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105772669 | AAAAACACTGTGCTT[C/T]TGACTTCAGGGAGGC | 8440 |
rs562141983 | in-del | -/TTC | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105868719 | CTGTGGGTTTTCTTT[-/TTC]TTCTTCAAAGCCTGC | 8440 |
rs562143481 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105860529 | AGTGAAGTTCACAGC[A/G]GGGCATGGAGGATGA | 8440 |
rs562145449 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105817756 | ACCAGTTAGAATGGT[C/G]ATCATTAAAAAGTCA | 8440 |
rs562179975 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105754437 | TGTCTCCCATTTAAT[A/T]TCTTAAGAATTTTGG | 8440 |
rs562202794 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105866751 | TGTGGCCCCGGGGGG[C/T]TGGGGACCCCTGGTC | 8440 |
rs562217448 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105798190 | TTTGTTTTCTTCTGA[A/T]ATGATGATTTTGTTG | 8440 |
rs562239069 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105867514 | CAACAGATTAGTGGG[A/G]GGATACTTCGAGAGA | 8440 |
rs562277590 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105892584 | CTCATGCCTGTAATC[C/T]GAGCAATTTGGAAGG | 8440 |
rs562291085 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105786149 | ATCTGTTGTGTCTAG[A/G]GCAGCATGATTAGCG | 8440 |
rs562302310 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105878269 | GGTGCCTGTCATGGG[C/T]CAGATTGCATCTTCC | 8440 |
rs562319431 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105835272 | TCTACTGGTGATGAA[C/T]TCCTCCAATTTTTGC | 8440 |
rs562337098 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105891800 | GATCCACCTGCCTTG[A/G]CCTCCCAAAGTGCTG | 8440 |
rs562344991 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105766454 | TCAGTCACCTGAGTA[C/G]CTGAGACTACAGGCA | 8440 |
rs562408573 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NCK2 | GRCh38.p7 | 2:105877429 | CCCAGCAACTTGGTC[C/T]CATTGACGTCTTTCC | 8440 |
rs562422204 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105753725 | TTCTGTTTTTCCTTA[A/G]TGAGTTGCTGTTGTT | 8440 |
rs562426165 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105787499 | GCAGCCATCGGCAAG[C/T]CAGAAAGTGGCCCCC | 8440 |
rs562444376 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105884640 | TCAGGGAAGACAAAC[A/G]TTGCCACATGCTACA | 8440 |
rs562449848 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105865308 | AAATCATAATAGCCT[C/T]ATTTTGCATGTGAGA | 8440 |
rs562506396 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105747236 | TCGGTTATTTAGCTT[G/T]TCCAACAAACAGCAG | 8440 |
rs562506889 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105760492 | GGAGTCAGGCCCTCA[C/T]CTCCATCCTTGCCGT | 8440 |
rs562521954 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105788079 | AAAGTGAGGGTGCTA[A/G]CTTTGAAAAAGCTTC | 8440 |
rs562541523 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105804008 | GGAGTAAATTAACAC[A/G]TTGAGTGCATCTCTG | 8440 |
rs562542093 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105754281 | CTTAATTTCCCAGCA[A/G]TGGTGGGGGCAGCCA | 8440 |
rs562547219 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105815556 | GTTAGTCAAGGACTG[A/G]AAATACTTACCAAGT | 8440 |
rs562561027 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105837034 | GCTTACTTTTTCCTA[G/T]AACAGGGAGTCCCCC | 8440 |
rs562575860 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105810368 | CAAGCTGGCAGTAGA[A/G]GGAGGGAGAGAGAGA | 8440 |
rs562578614 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105812280 | GGTCATCTCCTTGGA[C/T]ACCTTTGAGTTTCGG | 8440 |
rs562582171 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105761207 | CTGGGAGGTTTGGGT[A/G]TGTATGGGAGCGGTG | 8440 |
rs562584207 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105789905 | TAACGAACAGGTTGG[A/G]TATGAGTGGTCGCCA | 8440 |
rs562600292 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105844150 | AGACAAATCCTAACG[G/T]GTGGGGGGACATTCT | 8440 |
rs562622691 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105852925 | TTATGCAGAGGCTTT[C/T]CTCCTTCCCAAAAGG | 8440 |
rs562636964 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NCK2 | GRCh38.p7 | 2:105884032 | GCCGTGACACGGGCC[A/G]TTTTCAGCTGTTAGT | 8440 |
rs562640359 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105813142 | TTTGGTTCCTGGGCT[A/G]AATGATAAGATGTAT | 8440 |
rs562666814 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105888291 | CATTCCTTATAAGGA[A/G]TACTCATAGAAGGAC | 8440 |
rs562675502 | in-del | -/GTT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105832403 | TCTTATATTTTTCCA[-/GTT]GTTAGAGGAAAAGTT | 8440 |
rs562695433 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105817872 | GGAAGACAGTGTGGC[A/G]ATTCCTCAGGGATCT | 8440 |
rs562744538 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105762189 | GCACAGTTTCTGTGC[A/G]TAAGAGTGGGCTTAA | 8440 |
rs562767056 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105805574 | CATAACCAAAATTTT[A/G]TACCCATCCACCAAA | 8440 |
rs562824226 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NCK2 | GRCh38.p7 | 2:105810014 | AGGAGAGTGGGTGCT[A/G]AGGTCTCATTCAGTG | 8440 |
rs562832239 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | NCK2 | GRCh38.p7 | 2:105778904 | ATTGAGATAATGGTT[A/T]TTTTTTTTTTCAAGA | 8440 |
rs562838869 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105853996 | TCTTGCAAAAATTGG[C/G]CAATGCAGAGATGGA | 8440 |
rs562864866 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NCK2 | GRCh38.p7 | 2:105762829 | TACGTAGATTACTAT[A/G]TCTCAAGTTTGTTTT | 8440 |
rs562868129 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105751252 | ATCCTTGAATTCTCC[C/T]TCAGCTCCCAACTAG | 8440 |
rs562888558 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105893263 | TCCTCCCGCGGGGAC[A/G]GCCCCGACGGCTTCT | 8440 |
rs562893234 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105787280 | AGGCTTGGGCTGAGT[C/G]TTCCACCTGCAAGTG | 8440 |
rs562899726 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105806181 | TGCTCAGCCTTGTAT[A/G]TGTATGTGTGTGTGT | 8440 |
rs562963606 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105767716 | ACAGAAATCAGGAGA[A/G]CTGCATTGGAGTCCC | 8440 |
rs562976552 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105849277 | TGCACACCTACAGCT[A/G]CTCAGGAGGCTGAGG | 8440 |
rs562980492 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105815016 | CCTTTGCTGATGTTC[A/G]GTGGTGTCAGCATGA | 8440 |
rs562995107 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105861384 | TGCACCAGGTTCTGA[C/T]CACCTCTCTATGGGG | 8440 |
rs563106695 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105841813 | TTTTATACGGTATCA[C/T]AGAAGGTCATTCATC | 8440 |
rs563110375 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105780778 | AGGGCCCCCTCACCC[C/T]TTCAGCATGTGAGGA | 8440 |
rs563138682 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105824151 | TTTTGGGTTTTGCTT[C/G]TGATTGTTACCTTAT | 8440 |
rs563138949 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105785188 | TTTCACTGTGTTAGC[C/G]AGGATGGTCTCCATC | 8440 |
rs563149140 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105786708 | CAGGGCTTCCTGTCT[C/T]CATCGCTGTCTCTTA | 8440 |
rs563162832 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105866367 | GATCCTGTTACACAG[A/T]TGGCTTCTTGCTGTT | 8440 |
rs563188889 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | NCK2 | GRCh38.p7 | 2:105820017 | AACTGCTGTAGTGGA[G/T]GTTCTTACAGCCAGT | 8440 |
rs563223743 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105871830 | TAAACTACTAGAGGT[A/G]AAAAGTTTCCTGGGT | 8440 |
rs563240341 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NCK2 | GRCh38.p7 | 2:105878865 | GTCTTGATGGAGAAG[C/T]ATAAGCTCTATGCAG | 8440 |
rs563260116 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105758464 | CACCCATGCTGGAGT[A/G]CAGTCGCTTGATCTC | 8440 |
rs563268969 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NCK2 | GRCh38.p7 | 2:105872947 | AGTGGACATTAGCAG[C/T]GCCTGTCCTCTGCCT | 8440 |
rs563270674 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105801684 | ATTGTTCTTTGGCAG[A/G]CTCATCTCAAGGGCT | 8440 |
rs563298096 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105764513 | TGAGACAGGTGAGCA[A/G]GAGGCAGAATGATAC | 8440 |
rs563313355 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105871109 | AGTGCGTGTGAAATC[A/G]GGGTGATGAGACAGC | 8440 |
rs563348634 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105847435 | TTTGCTGAATAATAT[A/G]TACTATAATTACTGT | 8440 |
rs563390871 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105760674 | TTGGTGGGCCCAGAG[C/T]TCCAGTGAAGGGAGA | 8440 |
rs563392023 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105857184 | CTCAGTTTTCTAGAA[A/G]CAGAAAAGACAAAGC | 8440 |
rs563406500 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105863622 | TAATCGGGAAAATAA[C/T]ACTGGCACAAGATGG | 8440 |
rs563409145 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105878586 | GGACTTCCAGCCTCC[A/G]GAATTGTGAGGAAAT | 8440 |
rs563423748 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105870765 | CAAAAAAGAAAGAAA[G/T]AAAGAATAAAGGTAA | 8440 |
rs563425748 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105836548 | AAAGTTGTTGGTGGA[G/T]GTAGTAGCAGGCCCC | 8440 |
rs563444228 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105869380 | CTCAGTTACTGGGCC[C/T]TCATAACAGCCCCAC | 8440 |
rs563466729 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105759772 | ACAGTTTCTTAGACT[C/T]GCCTTGTTTTTAATG | 8440 |
rs563484511 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105816741 | TCACATTAAATTTAA[C/G]CTTTCAATGAGGGAG | 8440 |
rs563491039 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105745421 | CGCCAGCCAAGGGCG[A/C]GGGCGAGGATCAGGG | 8440 |
rs563491939 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | NCK2 | GRCh38.p7 | 2:105776086 | GAGCATGTCCCTTAC[C/T]GCAGGCCACCTCTGG | 8440 |
rs563508447 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105816735 | GTTGAATCACATTAA[A/G]TTTAAGCTTTCAATG | 8440 |
rs563540976 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105799101 | ATTTAAGAAGCTCTC[A/G]CTGTGTCCTGTCTGT | 8440 |
rs563546084 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105843119 | ATTTTTTGAGGTTTT[A/G]GAATATCTACATATA | 8440 |
rs563556981 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105869028 | TTATGTCTCAGTAAC[A/G]TTTGTTTGTCCAAAG | 8440 |
rs563572773 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105757056 | GTGATCTGCCTGCCT[C/T]GGCCTCCCAGAGTGC | 8440 |
rs563578811 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | NCK2 | GRCh38.p7 | 2:105751756 | CTGTCATGGGAGGAG[A/G]AGAGACTAACTGCAG | 8440 |
rs563585809 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105785001 | TTGTTTGTTTTGAGA[C/T]GGAGTCTCGCTCTGT | 8440 |
rs563587914 | snp | A/G | 0.00199481 | 0.0315187 | upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105743493 | TTCTTTCACAAGGTC[A/G]AAACAAGGAAAAATG | 8440 |
rs563607091 | in-del | -/TTC | 0.00199481 | 0.0315187 | upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105744228 | CAACAGAGGTCGAGT[-/TTC]TTCTTCTTTTAGGAA | 8440 |
rs563623576 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105874357 | CTTTGGTCACTTTAT[A/G]CCATAATCAGATCTT | 8440 |
rs563641873 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | NCK2 | GRCh38.p7 | 2:105858253 | ATGTATACTGACCAC[A/G]GTTTGTTTTTGTTTT | 8440 |
rs563658459 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NCK2 | GRCh38.p7 | 2:105850035 | TTGCCCTCTAAAGCA[C/T]TTTGTATTCATGTCT | 8440 |
rs563704298 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105862752 | GGGTAATGGAACATC[A/G]TCTTGGCAGCTTAGT | 8440 |
rs563719355 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105822260 | GAACCTGAATCCCCC[A/G]AGGGCCTCTGCTGCT | 8440 |
rs563739427 | snp | G/T | | | utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105893475 | TCATGGAACCCCTCT[G/T]TAAAAAGACGCAGGG | 8440 |
rs563752382 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105842669 | TTATGTTTTGTTGCC[C/T]CTAAGTCAAGGGTAC | 8440 |
rs563754152 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | NCK2 | GRCh38.p7 | 2:105880161 | TTCTCAATCTGATTC[A/G]ATACTCGTATCTGTG | 8440 |
rs563787937 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105865774 | ATGAGTCATCTTCAG[C/T]ATCTTTGTCATCAGT | 8440 |
rs563813804 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105790572 | CTTTGAGAAGTGTGC[C/T]AGGTGTTGCTGCCTG | 8440 |
rs563852156 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105808914 | TTTGCTTGTGATTTG[C/T]TTTAGCCATCTTGTG | 8440 |
rs563888938 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105815262 | CAGTGCTAGAGAATA[C/T]ATAAAAAGGAATTAA | 8440 |
rs563892685 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105890913 | TGGGAGGTCGCAGAG[C/T]AGGGCTGAGCTGCTG | 8440 |
rs563905608 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105819009 | GTGTCTTAGTGTTCT[C/T]GTCGTGTTACGCTTT | 8440 |
rs563917348 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105803114 | CTAGCTTTGAAGGTC[A/G]GTCTTGGGAAAGCAA | 8440 |
rs563943783 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105795862 | TCCTCTCATCTTCCA[C/T]GCACCCTCCCCCCAG | 8440 |
rs563962420 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | NCK2 | GRCh38.p7 | 2:105850969 | CGTCCAAGGGATGCA[A/G]CTTCAACTCTCGGCC | 8440 |
rs564160548 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105765129 | GCCCTTACAAAGGGT[C/T]ATGCCAGTTTTCAGT | 8440 |
rs564166054 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105866165 | GTGATCCACCCACCT[C/T]GGCCTCCCAAAGTGC | 8440 |
rs564170806 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105858229 | GAAACAGCATCAAAA[A/G]TACACCACATGTATA | 8440 |
rs564185164 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105775975 | GGGATAATTGTTGAC[C/T]GTCAGTTGCTTAGGG | 8440 |
rs564196741 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105770827 | TCATTTTGGGTTAAA[C/T]AGTTTGGCATTTCAG | 8440 |
rs564197559 | in-del | -/TT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105845399 | ATTTATATTTTGAAT[-/TT]TTTTTTTTTTTTTGA | 8440 |
rs564209802 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105869824 | AATTAAAAATTATAA[C/T]GAAAAAAATTTTTAA | 8440 |
rs564233998 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105860698 | TGGGGATGAAGAAAC[A/G]TGGAAAGCTCAGAGA | 8440 |
rs564245841 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105864055 | GTGGGGAAGGCCATC[A/G]GCGAGCCAGCCGGAC | 8440 |
rs564294905 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105770024 | AAAATGGGTGATTGT[A/G]CAGAGTACAGTGAGT | 8440 |
rs564342387 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105836761 | GGATACGGTGAGATG[C/T]TGACAGGACCCCAGG | 8440 |
rs564367063 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105776694 | CCTCCCTCGTTTTAG[C/T]TCAGCCATCCCAGCA | 8440 |
rs564375709 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105869529 | AAGCTGGCACAAGTA[C/T]GGTTCGGCTGTGTCT | 8440 |
rs564376572 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105771112 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACTCTGT | 8440 |
rs564381455 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105820627 | CCAGAAGGCCACCAG[A/G]GTTGTCATTTTGGCA | 8440 |
rs564384945 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105779088 | GAGGCAGGTGGATCA[A/C]TTGAGGTCATGAGTT | 8440 |
rs564388069 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105745209 | GGAGTTGGGAGCGCG[G/T]CGGGGCTCGCGGGCC | 8440 |
rs564400902 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105822797 | AAGGAATTTTCGTGA[A/G]TTCTCTTTAATGCCA | 8440 |
rs564425154 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105871201 | CACGATGGTGACTTT[G/T]TTTGTCCTTCCCAAG | 8440 |
rs564453561 | in-del | -/TTTGT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105890607 | TTTTCGCCTCAAAGG[-/TTTGT]TCTTATTTGGTCTAT | 8440 |
rs564454492 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105783813 | CACAGAGAGGGTTTT[C/G]CAGCTGGAAACAAGG | 8440 |
rs564492325 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105862291 | TGCTGATTTTACTTA[C/G]ATCAAAAGACCCAGG | 8440 |
rs564512766 | in-del | -/GT | 0.00398564 | 0.0444627 | intron-variant | NCK2 | GRCh38.p7 | 2:105770576 | TCTGTCATTTTTAGA[-/GT]GTGTAGATATGCTCT | 8440 |
rs564513526 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105868867 | CCGGGGCAGCCAAGC[A/G]ACTTGGCCAGGGCTA | 8440 |
rs564542105 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105823390 | TGTGCTCCCCATTCC[C/T]GTGCTGCAGGTGCCT | 8440 |
rs564544849 | snp | A/G | | | upstream-variant-2KB, intron-variant | NCK2 | GRCh38.p7 | 2:105850347 | AGAGTAGGATTGCTC[A/G]TATTTTAGGCGTTAG | 8440 |
rs564595129 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | NCK2 | GRCh38.p7 | 2:105871591 | ACCTCCGACTCCCAG[C/G]TTCAAGCAATTCTCC | 8440 |
rs564624569 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105868312 | GGAATTCACAGATTT[C/T]GGGCACGCACTCAGG | 8440 |
rs564627153 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105796767 | ATTGGAAAAATAACT[A/G]AGCATTTCTCTTTGA | 8440 |
rs564653170 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105778121 | GAAATTTGTCCTAAG[A/G]ACAAGATGTGTTGTG | 8440 |
rs564656527 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105791294 | TTACAGCCACACTGA[C/T]AAGAAACTGGTCATT | 8440 |
rs564656950 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105747038 | GGCTGCTGCATAACC[C/G]CCTCTGTCCACTTGT | 8440 |
rs564742423 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105790627 | CTTACTGCATCCCCC[A/G]CACCTGTCCTCATCT | 8440 |
rs564773871 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105764956 | TTTGGACATCTAAAT[A/T]TTTGCTCCTGTAGAC | 8440 |
rs564775013 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105883084 | GACGGAGCATCGTGG[C/T]GGTGGAAACTGGACT | 8440 |
rs564778121 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105749315 | AGTATTGCAGTTGCT[G/T]CTTTTGAGACAATTT | 8440 |
rs564818057 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105879671 | TGCCTCCTGGCGCCG[C/T]GTGGGCACATGTCCC | 8440 |
rs564821343 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105813015 | GCGATTTGCAGAATG[C/T]GACTGTCAAGGTTCT | 8440 |
rs564890003 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105873026 | CTGGTGCCCTCACCC[A/G]GCTGCCAGGAAAGGT | 8440 |
rs564910797 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105774784 | TTTTGTGAAGCATTC[A/G]TTGGACACTGAGTAC | 8440 |
rs564937090 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105831888 | GAGGTCTTTTGTGGT[G/T]GCATACAAATTTTAG | 8440 |
rs564956618 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | NCK2 | GRCh38.p7 | 2:105760497 | CAGGCCCTCACCTCC[A/C]TCCTTGCCGTTCACA | 8440 |
rs564973503 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105825363 | TTCAAAAATCCCATT[C/T]CGTTACTAGTGTTTA | 8440 |
rs565001962 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105795304 | TGATATATTTTTAAT[A/T]TTTTTTTTCCTCAAA | 8440 |
rs565019563 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105876094 | CTAATACACAGCATG[C/G]CAGCCATTGGAAGGG | 8440 |
rs565038020 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105873523 | CACCACCCTCACTCC[C/T]ACACCCAAAACCCTT | 8440 |
rs565044840 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105801830 | GGGACTTTACAGGGC[A/G]CTTTTTAGAGTATCT | 8440 |
rs565049804 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105793539 | CACTGGCTAACAAGT[G/T]TATTTGGCAGTTTTC | 8440 |
rs565049913 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105787370 | GTGACTATATTTGGA[A/G]ATGAGCCCTCTGAGG | 8440 |
rs565054281 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105791641 | CTGACTCCATAATAG[A/G]TCTGATCATAGTGAC | 8440 |
rs565056811 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105832372 | CATTGAATAAGAGTC[A/G]TGAAGGAATAGGCAT | 8440 |
rs565080936 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105889310 | GGAAAAGTATCCACA[C/G]ACTGGAGCTCCCTCC | 8440 |
rs565092779 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105888690 | AAGATGTGGCAGAAG[C/T]GATGGAGGGCAGCTT | 8440 |
rs565095529 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105887828 | CAAGTATTTGAGGCA[A/G]TGGATCAAGCTGGCA | 8440 |
rs565164198 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105755595 | TCATTCATTTTAGAT[C/T]GTATTAGTTATTAGA | 8440 |
rs565176133 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105751019 | ACCTAGGCCATTTTG[C/T]CTTGTTCAGACATAA | 8440 |
rs565197973 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105799614 | TTATTTGAAAACTTC[A/C]TATTTTAAAGCAGAA | 8440 |
rs565210149 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105887057 | GGCAAGGAAGAGATA[A/C]TCTGATGTAAAAACA | 8440 |
rs565215005 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105758226 | GCCATTATGCCATCA[C/T]ATTTGATATAGAGAT | 8440 |
rs565227175 | in-del | -/AG | 0.00636936 | 0.0560724 | intron-variant | NCK2 | GRCh38.p7 | 2:105750681 | AAGTAGAGTGATTGA[-/AG]AGAGAGAAAAATCTT | 8440 |
rs565229688 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105763264 | ATTCTGCCAAGGGGA[G/T]AGCGGGACCTCGCCA | 8440 |
rs565246739 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105826730 | TTCTGGCCAAGTAAG[G/T]ATCCTTTCCTCTGAG | 8440 |
rs565248792 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105874998 | ATTATACTTTCTGTC[G/T]GCTCACTGAGTGACA | 8440 |
rs565250485 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105744426 | GGAATGCTTCCGGGA[A/G]GGGGGCGGCTGCCCA | 8440 |
rs565281593 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105834112 | AAGGGTGTATATTCT[A/G]TAGCTGTTAGATGAA | 8440 |
rs565304291 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105822475 | GCCATCTCTAAGGTC[C/T]CTGACGCTTCCCACA | 8440 |
rs565312222 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105743558 | CCTGCTCAGTGTACT[A/G]TGCTTCCTTCCACTT | 8440 |
rs565319761 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105801978 | TTGTAGATTGGTAGC[A/G]ATTGGACAGCCATGC | 8440 |
rs565347182 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105759183 | AGGAGAGAATTTCAC[C/G/T]TGTTAAGTCCTTATT | 8440 |
rs565360211 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105763312 | CGTCCTCTGATGACC[A/G]AGCTGCTGGGACCGA | 8440 |
rs565398941 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105763042 | TCTACTAAAGAATAC[A/T]AAAGAATTAGCCAGG | 8440 |
rs565429967 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105855857 | TTTTTTTTTTTGAGA[C/T]GGAGTCTCACACTCT | 8440 |
rs565442955 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105862247 | AGTGGGAAGGGGGTC[G/T]GTCTTGAGCCTGTGC | 8440 |
rs565450801 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105855782 | TGTGACATCAGAGGC[C/T]GCTCCATGGTGGGGG | 8440 |
rs565452509 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105807020 | CACCCTCATGCTGAA[A/G]AGTCCTATTGTGACT | 8440 |
rs565465106 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | NCK2 | GRCh38.p7 | 2:105775739 | GCCTGGCTGGCATCA[C/T]TGGGAGCACCACACC | 8440 |
rs565467284 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105871281 | CGCTCCCACAGCCTG[C/T]GGGAGACAGGCCTTT | 8440 |
rs565506448 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105861639 | CCTGCTTCAGCCTCC[C/T]TAGTAGCTGGGACTA | 8440 |
rs565591349 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105813603 | TGGGGATGCAGAATC[A/G]GCCACGACTGCTTGC | 8440 |
rs565607332 | in-del | -/GT | 0.0186602 | 0.094773 | intron-variant | NCK2 | GRCh38.p7 | 2:105884090 | CAAGAGCCCTGAGGT[-/GT]GTGTGTGTGGCTTCT | 8440 |
rs565660051 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105813031 | GACTGTCAAGGTTCT[A/G]GCCCTTTCGTGGTGA | 8440 |
rs565664159 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105840141 | GGTGGGGTTAGGGGC[A/G]AGGGAATGTAATCAC | 8440 |
rs565668945 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105888146 | GAGAGGTTGGTTTTC[A/C/T]GCCAACCTATTAATT | 8440 |
rs565675383 | in-del | -/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105765023 | CTTCAGTGGAACCAT[-/T]TTTTTTTTTTTAGTG | 8440 |
rs565681924 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105774953 | TAATCCCAGTGCAGG[A/G]GGATCAGTTGAGGCC | 8440 |
rs565687824 | in-del | -/TTTG | | | intron-variant | NCK2 | GRCh38.p7 | 2:105871198 | GGCCACGATGGTGAC[-/TTTG]TTTGTCCTTCCCAAG | 8440 |
rs565697619 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105847931 | GTGACCCAAGACTTA[C/T]TGGGATCTCTTCGTA | 8440 |
rs565698865 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105776707 | AGCTCAGCCATCCCA[A/G/T]CAGGGCTGGACTTAG | 8440 |
rs565712332 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105807079 | ATGAAGGTAGAGTCT[C/G]AGTAACACTTGGAAT | 8440 |
rs565805343 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105783922 | TATTTGGAATTTGCA[C/T]GAGAAAATGAAACAC | 8440 |
rs565807192 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105776246 | GTCCCAGCGACAGAA[A/G]CCGTACATCCTGGGT | 8440 |
rs565816898 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105768550 | ACTCACAGAACTCAG[A/G]AAGGCACTTTGCTTA | 8440 |
rs565843951 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105783271 | GCGTGCTGTTTGTAG[C/G]CTCGCTAGAGCTTGG | 8440 |
rs565849840 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105774286 | AGTGCTGGGATTACA[C/G]GTGTGAGCCACTGTG | 8440 |
rs565875353 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105875037 | TACCTGCAGTACACA[C/T]GTTATTTTATTATTA | 8440 |
rs565902566 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105863756 | TGTGGGCAGGAGGGA[A/G]GACTCTGGAGTCTTC | 8440 |
rs565908835 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NCK2 | GRCh38.p7 | 2:105804030 | GCATCTCTGCCATCC[C/T]TCTCCCTCTCAGTTA | 8440 |
rs565936307 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105816360 | GCAAATAAATAACCA[A/G]TTATTTTTAAAAGTG | 8440 |
rs565948567 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105881273 | TCCCGGTAGGCTAGG[G/T]AGTGTGGTGGTGCCC | 8440 |
rs565988305 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105781052 | TCGTGGTCTTCCTGT[A/C]TTCTTGCTTTCAGAT | 8440 |
rs565988323 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105787407 | GGTTGAGAGTAGGGC[C/T]CCCATAATGGGATTC | 8440 |
rs566003202 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105873075 | CACACCCCCAGTTCC[A/G]TGATCTTTGGCCAGC | 8440 |
rs566020373 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105869539 | AAGTACGGTTCGGCT[A/G]TGTCTTTGCCAACCA | 8440 |
rs566028881 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105757550 | TCACTCAGTTGTGTA[C/G]CTGCAGTTCATACCT | 8440 |
rs566046516 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105830020 | AGAGTGGTATTTTGA[A/T]ACCTGTATATAGTGT | 8440 |
rs566049812 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105769435 | CTTGCTTCTCAGGAA[A/G]CAAATGTAGGAAAAA | 8440 |
rs566067822 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105880610 | TCTTAGAGTTCTAAC[A/G]GGTCTTTGAATTCAT | 8440 |
rs566085246 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105832919 | AATAGTTTGAAAAGA[A/G]TTGGTGTTAGTTTGT | 8440 |
rs566094102 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105743719 | ACAGTCAAACACTCA[C/G]CTGTCTGACTTCAAA | 8440 |
rs566109397 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105814066 | ATCTTTCAGGCTGAT[A/G]CTGTTTTTTGCACAA | 8440 |
rs566137130 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NCK2 | GRCh38.p7 | 2:105788901 | ATCTCTTATCTGCTC[A/G]TTTGGGTTTCTAAAA | 8440 |
rs566151493 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105750531 | TGGGATCTCTGTTTA[G/T]TTGGGGACACCTACC | 8440 |
rs566152199 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105820127 | GTTTTAAAGAATGAG[A/G]AGACGTGTACAGAGG | 8440 |
rs566202015 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105786331 | TCTGAGCACGGACTT[C/G]TTCCATTAGCCCTGG | 8440 |
rs566220300 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105801182 | CCATAAATCTGTGGT[A/G]TTAATATGCCTCCTT | 8440 |
rs566250528 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105826196 | CCTTCTTCACAGGGT[A/G]GCAAGAAGAAGTTCT | 8440 |
rs566258987 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105848349 | TTTCACAAAAGTGGT[C/T]CTATCAGTGTCCACA | 8440 |
rs566269412 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NCK2 | GRCh38.p7 | 2:105888747 | TTGCTCTCTCTTGGG[C/T]CACTTGATCTAGGGT | 8440 |
rs566273189 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105836866 | GCAGCCTGGGACTCA[G/T]GGAGTAGGGGCTACC | 8440 |
rs566277590 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105743090 | AACAACCTCTCTAGA[A/G]GAGGCAGATGGGCAG | 8440 |
rs566327379 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105785182 | ACAGGATTTCACTGT[A/G]TTAGCCAGGATGGTC | 8440 |
rs566330620 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105788430 | TTTTTCCTCTGGTTT[A/G]TATATTTATAGTCAT | 8440 |
rs566359368 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105749995 | AGATCACACCACTGC[A/C]CTCCTGGGTGACAGC | 8440 |
rs566373215 | snp | A/G | | | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105771750 | CTTTCTAGAAAAAGC[A/G]TGTACCTGGGTTGAC | 8440 |
rs566390929 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105816623 | CCAAAGGTAAGTCTG[C/T]AGTTTTCTGCTTAAA | 8440 |
rs566393573 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105801073 | GAGGTGAAAGCTGGG[C/T]GTGCTGAGCCCGTCA | 8440 |
rs566415321 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105779618 | CACTTGGCCTTGTGG[C/G]CAGATGGAAAGGAGA | 8440 |
rs566425310 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105760505 | CACCTCCATCCTTGC[C/T]GTTCACACCTCTTCC | 8440 |
rs566443344 | snp | A/C/T | 0.00398564 | 0.0444627 | utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105893369 | TCGAGCCCACCCGGC[A/C/T]GGCCAGCTTTAGAGG | 8440 |
rs566463862 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105760061 | CTCTTTTCCCTTCTT[C/T]CCATACTGCTGCAGT | 8440 |
rs566542599 | in-del | -/TA/TATA | 0.0338446 | 0.126129 | intron-variant | NCK2 | GRCh38.p7 | 2:105835363 | ATTCTTGGCTGGTTT[-/TA/TATA]TATATATATATACAT | 8440 |
rs566552854 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NCK2 | GRCh38.p7 | 2:105865798 | CATCAGTTTCTTTGT[A/G]TGGCACAGTTTTCTG | 8440 |
rs566555989 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105746689 | TGGAGGTTTTTTGAC[G/T]TTTGGAACAGGGGTT | 8440 |
rs566558900 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105829541 | AGCTCTTCTTGGCTG[G/T]GACAGTTTCTCAGAC | 8440 |
rs566629774 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105747364 | TAAAATACCCTAAGA[C/T]TCCCGGAATGGCGCA | 8440 |
rs566659283 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | NCK2 | GRCh38.p7 | 2:105838135 | GCAATAGATAACCAC[A/T]ATTTATAAACCTTAG | 8440 |
rs566662018 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105806851 | TAAAAAAAAACCCAA[C/G/T]CAACCATCCTACAGA | 8440 |
rs566669556 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105797208 | CTGGCCAAATTCAGG[A/C]TCTTAGAAAGGACAC | 8440 |
rs566671967 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105876921 | TGCCCTCGGTCTGGA[C/T]GCACAGCTGCAGTGC | 8440 |
rs566688234 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105797759 | AAAACACCTGATGTT[A/G]TGGCCTCCTGTCAGC | 8440 |
rs566689710 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105843616 | CAGTGATGGTGATAC[A/G]TCACAGGGACACAGT | 8440 |
rs566747194 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105793157 | GGTGGGAAGCCACAG[A/G]TGTAGGACATCTTTA | 8440 |
rs566748042 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105827044 | TTGCTCTGTTGCCCA[A/G]GCTGGAGTGCAGTGG | 8440 |
rs566763117 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105839410 | GAGAGAAGGGGTGGA[C/T]CTGAGGCATATTTTG | 8440 |
rs566766293 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105811771 | TCTCTGTAAGCCCCT[A/C]ATAAAACCCTGGCTG | 8440 |
rs566766345 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105805009 | AATGGGGGAGAAGAG[A/T]CATTTTATCCAGAGC | 8440 |
rs566787920 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105862921 | TCCCCTGCTGTGCCT[A/G]GGCAGTGCCCTAAGT | 8440 |
rs566797728 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105848075 | TCCCCGTGAACCTTA[A/T]GTTCAAGCCATTGAG | 8440 |
rs566823909 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105879753 | ACAATCAGCCTTTTT[A/G]CCCTCTTCACCTCCT | 8440 |
rs566885277 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105887303 | ACTTCTGTGGACAGA[A/G]GAGTGCCTTCTGTAA | 8440 |
rs566907412 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105798483 | ACTTTAAACAGTGAA[C/T]CAGTTTGGGGTCTGG | 8440 |
rs566921752 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105874117 | TAATCTCATGTGGCC[A/G]CCCTTTCAAAAAATC | 8440 |
rs566939708 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105773582 | CCCCAGTCCTCTGTC[A/G]GCACCCAATACCATA | 8440 |
rs566971685 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105767868 | TTCCCAGCACTTAAT[A/G]TGCACTTAATAAATA | 8440 |
rs566976437 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105780934 | CCACCATTCTGTGGT[A/G]TTTTGTTACAGCCAG | 8440 |
rs566977992 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105773070 | CAAATTTTTTTTTTT[A/T]AATTTTTCTGTAGAG | 8440 |
rs566990560 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105846031 | TACAGTTAACATCAT[A/G]TAAGAAAATTGGCTT | 8440 |
rs566997235 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105886259 | CTTGAAGATGGAAAG[A/G]CCTGCAAGATCATGC | 8440 |
rs567007943 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105806765 | GATAACATGCAGTGC[A/G]GTATTTTCAGTTTCT | 8440 |
rs567043829 | snp | A/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105893276 | ACGGCCCCGACGGCT[A/T]CTCTGCGAGTCTCTC | 8440 |
rs567070143 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105872289 | ACCTTCCCCCCGCCA[C/T]CAGGCCTGCCCTGTG | 8440 |
rs567089081 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105761566 | TATAATAATGCATTT[C/T]GTTTATTAAAAAATG | 8440 |
rs567095592 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105804085 | TTTACGGGGCAAATT[A/G]TATACATAGAGGCAG | 8440 |
rs567108487 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105756689 | CAGGTCCTGGACTTC[A/G]TTCTGGCTTTGTATT | 8440 |
rs567146075 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105802843 | ATGACTGATCATCTG[G/T]AATTCCCCTTTTTTG | 8440 |
rs567146140 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105779808 | GAAATGTAGCTTTGT[A/G]GAGTCCTCACGTTCT | 8440 |
rs567164539 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105767161 | ACCCCCGTCTGTGTT[C/T]ATCTCATAGATACCA | 8440 |
rs567206826 | in-del | -/A | 0.340784 | 0.232934 | intron-variant | NCK2 | GRCh38.p7 | 2:105765990 | CAGCAGGTGACGCTT[-/A]ACACTGCACAGGTAT | 8440 |
rs567215182 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105811908 | TTCTGGAGTATTTGA[A/C]GGCAGAAATCATTAT | 8440 |
rs567220807 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105766750 | CCTGGCTCTGTCCCC[A/G]GACCTTTCCTTTACT | 8440 |
rs567232227 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | NCK2 | GRCh38.p7 | 2:105874448 | TGACTCTAGTGGGGG[-/A]AACCCCCACAGATCA | 8440 |
rs567235934 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105817412 | GACATTTAACTTAAA[A/C]TATGAATTGCTGTTT | 8440 |
rs567255018 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | NCK2 | GRCh38.p7 | 2:105844689 | GCAGTGAGCTGAGAT[A/C]GCGCCACTGCACTCC | 8440 |
rs567260813 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105877823 | GAGTACAGTCTGTGC[C/G]ACATCACTGGTGGGT | 8440 |
rs567287722 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105819133 | GGTTGGCACTCACAC[C/T]GCATACCTGACTTCA | 8440 |
rs567293659 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105825490 | CACTGGGCACTGCAG[C/T]GCTTTGGAACATAGC | 8440 |
rs567300991 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105784264 | ATGAGACACCACGCC[C/T]GGCTGTTATTTCTAA | 8440 |
rs567326798 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105825070 | GTGCTTGGGGACGGA[A/G]TGGAGGTAGACATGG | 8440 |
rs567370554 | in-del | -/A | 0.0158469 | 0.0875917 | intron-variant | NCK2 | GRCh38.p7 | 2:105752542 | CACCATAGGAAAGGT[-/A]AAAAAACAACATTGT | 8440 |
rs567439086 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105823883 | CTGCTCTGGCTGTTT[C/G]GTGATCAAACGCCTT | 8440 |
rs567447990 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105747513 | TGCACTGGGGGAGAC[A/G]GGGCTTGCGGAAATC | 8440 |
rs567452247 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105791465 | AGTGCACCCTCGCCC[C/T]GTTGCCGTGCTTACC | 8440 |
rs567516806 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105799749 | GGAGGGATGCTTCCC[C/T]CTACCTCAAGCCTAA | 8440 |
rs567528806 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105893902 | TCTCAAAGAAATATG[G/T]ATCTGTAGCCGTTTG | 8440 |
rs567572404 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105871622 | TGCCTCAGCCTCCCC[A/G]GTGGCTATCATAGGC | 8440 |
rs567574016 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105798309 | GCCCGGATAGCCTCA[C/T]TGTGGCCTCTTGTTT | 8440 |
rs567577781 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105880380 | CTAATGCACTCATCA[C/T]AATCTGTTGTGGGAA | 8440 |
rs567583047 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105873614 | TTTGGCTCGTTTAAG[G/T]GGATGGTTGGGGAGA | 8440 |
rs567590526 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105893346 | CCATCCAGGCCTCAC[A/G]CCCACACTCGAGCCC | 8440 |
rs567628248 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105781707 | GAAAAGTACAGAGCC[C/T]GTGGCTTGGCAAGTG | 8440 |
rs567664575 | in-del | -/TTC | 0.00676609 | 0.0577691 | intron-variant | NCK2 | GRCh38.p7 | 2:105866551 | TCAGCATTAGATAGA[-/TTC]TGCTCAAAAGGAGCT | 8440 |
rs567683424 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105873212 | TTGTCTGAAATCGAT[A/T]TGTACCCAAAAGTCT | 8440 |
rs567688627 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NCK2 | GRCh38.p7 | 2:105828002 | TTATGTAGAATGTAG[C/T]CATTAGGAGGAACAA | 8440 |
rs567714761 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105787493 | GAGAAGGCAGCCATC[A/G]GCAAGCCAGAAAGTG | 8440 |
rs567748998 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105792942 | CAGCTATTACCCCGA[C/T]GTGCAGTTTAGATGG | 8440 |
rs567772168 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105886451 | AGATTGCCCCAGCTT[A/G]CTGACTTCGAATCTC | 8440 |
rs567779319 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105879878 | TACCCATGGAAGTGC[C/T]TGGAGGAAGTCATTT | 8440 |
rs567798246 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105806384 | CTGGGACTACAGGCA[C/G]CCACCACCACGTCCG | 8440 |
rs567805903 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105779597 | CTGCCCATTCTTTGT[A/G]CTTTACACTTGGCCT | 8440 |
rs567823226 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105755719 | CCATGCCTATAAATT[C/T]GTGGTTCTCAGCTGG | 8440 |
rs567844387 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105887428 | AAGGAGATGTGTAGA[C/T]TATTGATGCTTGGAG | 8440 |
rs567860086 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105755218 | CTAGGTCTATTTTAC[A/G]TGGTTCGGTAGACAA | 8440 |
rs567890222 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105846692 | GGCGTTGACAAGGAT[G/T]TAGAGAACTTGGTAC | 8440 |
rs567908876 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105802445 | GTTTATTTGGTTCAC[A/G]GTTCTGCAGGAGGTA | 8440 |
rs567912824 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105846187 | GTACTTTTGTAGCTG[A/G]AGTGGTAAATTATGT | 8440 |
rs567947915 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105801829 | TGGGACTTTACAGGG[C/T]GCTTTTTAGAGTATC | 8440 |
rs567973997 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-5-prime | NCK2 | GRCh38.p7 | 2:105745654 | CGGGAGAACTTAACC[A/G]TGTTTATTACAACTA | 8440 |
rs567976847 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105767946 | AGTAGTTGCTGTCTT[G/T]CTACATGTGAAAAAT | 8440 |
rs568007556 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105870419 | GGGATTTTGAATGGC[A/G]CACAGTAGAATGTTT | 8440 |
rs568018590 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105876756 | ACTTTAATGAAAGAT[G/T]AGGCGATGAAGCGGA | 8440 |
rs568030820 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105790262 | TAAAATGACAGACTC[A/G]TTTCTTGGCTTCCTG | 8440 |
rs568043791 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105784676 | TTGCCATAAAAGATT[C/T]TCATTTAGTCTAGTG | 8440 |
rs568070947 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105796323 | ACACAGGAGAGTGCT[A/G]GAGGTTAGTGTCAGT | 8440 |
rs568075065 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105866610 | TCACAATAGTGTTTG[C/T]GCTCCTGTGAGAATC | 8440 |
rs568085027 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105875881 | ATTTTATGATGATAG[A/T]TTTAAAGTGCTTGAG | 8440 |
rs568095715 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105842734 | ACAGCAAAGACTGCA[G/T]GTGGGCTCTGGGAGG | 8440 |
rs568138143 | in-del | -/TT | 0.00517822 | 0.0506191 | intron-variant | NCK2 | GRCh38.p7 | 2:105830644 | AAATTAGTGTTCCTC[-/TT]TGTTTGCATCCTTGC | 8440 |
rs568146957 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105838334 | TTTTTGGCCAGGTAA[A/C]TAGTCTTAGACAATT | 8440 |
rs568160632 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105890353 | TATCTTACATCTACC[A/G]TGATTCACTCCCATA | 8440 |
rs568194907 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105882911 | ATTTTTAAATGCACG[C/T]TATAAGACTAGTAAG | 8440 |
rs568198672 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105751368 | CACTTTTTAACCATT[C/G]CTGCCAATCCATCCC | 8440 |
rs568223034 | snp | A/G | 0.00478085 | 0.0486577 | upstream-variant-2KB, intron-variant | NCK2 | GRCh38.p7 | 2:105851480 | GCCAGGATGGTTTCC[A/G]TCTCCTGACCTCGTG | 8440 |
rs568235921 | in-del | -/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105861513 | CGTTGAGGTTTTTCT[-/C]TTTTTTTTTTTTTTT | 8440 |
rs568242032 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105795636 | TATTCAGCAGGCAGT[A/G]TCTGCAGGCGTTGTT | 8440 |
rs568264905 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105842110 | TTTTTTTTTTGAGCC[A/G]GAGTTTCTCTCGTTT | 8440 |
rs568284677 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105858530 | CCATTTTTACTGCTT[G/T]GGGAGTCCACCTAAT | 8440 |
rs568362115 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105884261 | TCCACTGCCTCCCCC[C/T]GTCCCCATGTGTTTT | 8440 |
rs568369437 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105857278 | TCGGTTCAGCCAATG[A/C]GTGTACTCCCAGGCT | 8440 |
rs568372426 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105830487 | AATCTGTTAATGGAC[A/G]CTTAGGTTGATTACA | 8440 |
rs568380885 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105844318 | GGGAAAGCTAAGGAC[A/T]TCTGAATAAACCATG | 8440 |
rs568459467 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105855625 | GCCAGTGTCGTGACA[C/T]GAAGTTCTTTCTCTC | 8440 |
rs568499384 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105804119 | CGACTCTCAGGATTT[A/G]CTAATTTCAAGGGTG | 8440 |
rs568500988 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105766634 | GGCCTAGGTTTTCTT[C/T]TTCTCCACTGCTTTG | 8440 |
rs568518659 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105822549 | GTTCTTGCATAGTCA[A/G]TAACATAATTATTTT | 8440 |
rs568541241 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NCK2 | GRCh38.p7 | 2:105869706 | GTGCTCCAGAATGCC[A/G]TGTCTCATCCTTGCC | 8440 |
rs568545668 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105859311 | ATTACCCAAAAAGTT[A/T]CGGTTCCATTTACAA | 8440 |
rs568557468 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105750266 | TCTGGTGTTTCTTCC[A/T]CTTATAAGAACATCT | 8440 |
rs568558732 | in-del | -/GCTT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105836179 | TTTTATTGTTTCCTT[-/GCTT]TTTCGTGTTTCTTGT | 8440 |
rs568560073 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105810640 | CTGAGATGTATAGCA[A/C]GGTTTTTATGTTGAT | 8440 |
rs568603923 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105888907 | CAGCATCCTGACTGC[A/G]TGTTTCAAAAATGTG | 8440 |
rs568609760 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105816073 | AGGTGGGAAGAGGGA[A/G]TACATGTGTGTTGAT | 8440 |
rs568610816 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | NCK2 | GRCh38.p7 | 2:105884893 | TATTCTCCATATTTC[A/G]TTATCATACCTTCAC | 8440 |
rs568611566 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105790800 | TGCCAGCTGATGCAC[A/G]TAGGCAAGACTTGGG | 8440 |
rs568614815 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105796181 | ATAGTCTCTGTATTG[A/G]CCGCCCTCTGGGCAC | 8440 |
rs568699605 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | NCK2 | GRCh38.p7 | 2:105745909 | TTTAAGGCATGGAGG[C/G]TAACTGCCTTATGAG | 8440 |
rs568710802 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105790333 | TGCCCTGCTGACTCA[C/G]AGTGGGAACAGTTGC | 8440 |
rs568725844 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105778172 | CTGGGACTGGGTCCC[A/G]GGCTTAGAGGGGGAC | 8440 |
rs568737219 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105796548 | CATGAGTGTGTGGCA[A/C]AGAACGCAGGTGTTC | 8440 |
rs568810063 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105785565 | ACTGACAGGTTTCCC[A/G]CTGTGAACAGTAAAG | 8440 |
rs568813452 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105784993 | TTTTGTTTTTGTTTG[C/T]TTTGAGACGGAGTCT | 8440 |
rs568840714 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105828675 | AGGAAGAGGTCTCAG[C/T]TTGTCTTTGATCACC | 8440 |
rs568851525 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105828236 | GAAGATGGAAATAGG[A/G]GAGGGGCCAGGGAGA | 8440 |
rs568888301 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105836283 | AGGGAACAGAGTTTT[C/T]TGTAGATGTATGCTA | 8440 |
rs568893231 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105870948 | GATCTTGGTGGAAGG[A/G]AAGGAGGAAGAAATA | 8440 |
rs568894022 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105876818 | AAGGAAACTGGGATC[A/T]GGGTGCCGCCTCTTT | 8440 |
rs568926823 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105837993 | TATATGTGCTGTTTC[C/T]AACAGTTTCTTTACA | 8440 |
rs568954369 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105883505 | GTGGAGACATTGGTC[C/G]CAGTCATTATTCTTT | 8440 |
rs568963461 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | NCK2 | GRCh38.p7 | 2:105844947 | AATAAATATTAGCAT[G/T]TATTGTTCCAAACTC | 8440 |
rs569036955 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105752881 | ATGTATTTTTAAAGT[A/G]AACATTAGCTTCTCT | 8440 |
rs569038867 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | NCK2 | GRCh38.p7 | 2:105745743 | AAGGGAGCTTTTGTG[C/T]CCGGCTTCAGGCTCT | 8440 |
rs569049418 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105844423 | AAAGGAACCTATTTT[A/C]GTCTAAAAAATATTT | 8440 |
rs569063119 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105811231 | GATACATTTTTGGCA[A/C]CACATCATCAATTTT | 8440 |
rs569070318 | snp | A/G | 0 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105803258 | TTAGATAGCACACAT[A/G]TGTTTTAGAAGTTAC | 8440 |
rs569070972 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105802539 | GAAGGTGAAGGGGGC[C/T]GATGGGTAGAGATCC | 8440 |
rs569077948 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105752308 | TGGGAAAGGTGTAAC[C/T]TTTTTAAATATGAGG | 8440 |
rs569078439 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105786523 | ATGAGATGCTGAGTC[A/G]GTTCCTTTAGCTCAG | 8440 |
rs569087528 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105765234 | TTTTGGATTGATCTA[G/T]TCTAGAGGACCGTGT | 8440 |
rs569088621 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105843583 | ATGTGCTCAAAGAAA[C/G]AAACGAACGAACACT | 8440 |
rs569156041 | in-del | -/ATA | 0.00199481 | 0.0315187 | intron-variant | NCK2 | GRCh38.p7 | 2:105830354 | CTTATTTCATGTAAT[-/ATA]ATAACATTATCCAGG | 8440 |
rs569184095 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-5-prime | NCK2 | GRCh38.p7 | 2:105816563 | GCTGAAAACATCATC[A/G]TTTTGAAGAGTTCTG | 8440 |
rs569242912 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105753985 | GTGAGTTGTCTGTGC[C/G]AGCTTCTCGAACCTA | 8440 |
rs569250884 | snp | C/G | | | missense, intron-variant | NCK2 | GRCh38.p7 | 2:105881448 | ACCTCAACATCCCGG[C/G]CTTCGTCAAGTTCGC | 8440 |
rs569282718 | snp | C/T | | | upstream-variant-2KB, intron-variant | NCK2 | GRCh38.p7 | 2:105851326 | TGGAGTGCAGTGGCG[C/T]GATCTCGGCTCACTG | 8440 |
rs569299519 | in-del | -/T | 0.0023933 | 0.0345097 | intron-variant | NCK2 | GRCh38.p7 | 2:105755888 | GTCACATATGTTAGC[-/T]TTTGAATGTTTAATT | 8440 |
rs569327807 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105841044 | CTCCACACTGATAGT[A/G]TGGATTACAAGCTTA | 8440 |
rs569344370 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105853263 | TCTTCTACCTAAGAA[C/G]TAGAGAGTTGCTAAA | 8440 |
rs569346451 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105804863 | GTTAGGGATTCAGTG[A/T]GTCTTAGATTGCAAA | 8440 |
rs569369101 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105848318 | AAACCCTGGCTTTCT[A/G/T]CAGCTGAAGAGGATC | 8440 |
rs569369379 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105878709 | GTACACAGAGAGACA[C/T]TTATTAAGTAATTTG | 8440 |
rs569387356 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105798039 | CATTTTTATTAATTT[A/G]TGGTTTTGATCCATC | 8440 |
rs569388533 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105810756 | ATTTAAGAGGCTAGC[A/G]TTAAATATATCAAGA | 8440 |
rs569404758 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105767035 | TCACACCTACTCTTA[C/T]GGTCAGCTACTCGTA | 8440 |
rs569406187 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105859805 | AAGATTACAGTACTC[C/T]GGAGGGAGGGAGGCA | 8440 |
rs569420273 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105847975 | CTATGTCATCCCAAT[C/T]TTACTACCTTTGAGT | 8440 |
rs569486506 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105821969 | TGGTGACATGGTAAC[A/G]ACCCATTCTCCAAGT | 8440 |
rs569524126 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105772115 | AGGATGGCGGAGGGG[G/T]TAGCGTTTGCAGAGG | 8440 |
rs569567520 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105783516 | GCTTGTGGGAAGCTT[C/T]GTACACCACCAAGGC | 8440 |
rs569574286 | snp | C/G | 0.0126979 | 0.078662 | intron-variant | NCK2 | GRCh38.p7 | 2:105779486 | GTCTGAATATGGCTG[C/G]ATCTCTGCCACCTAC | 8440 |
rs569598909 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105819669 | TAGACAAGACGGTAC[A/G]TGGAGACCATGAGAG | 8440 |
rs569610220 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105771550 | AGCCTGGGCGACAAG[A/G]GTGGAACTCCCTCTC | 8440 |
rs569638372 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105763965 | CAATAATAATAGCTG[A/C]TATTTATTGAGCACT | 8440 |
rs569639417 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105888900 | CCTCAGCCAGCATCC[C/T]GACTGCATGTTTCAA | 8440 |
rs569639500 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105839810 | GGGGAGGCTCCTAGA[C/T]GGCCTGGCTACCCCT | 8440 |
rs569640640 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105820605 | GGAGCGGAGACCATA[A/G]GAAGAGCCAGAAGGC | 8440 |
rs569681912 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105864246 | CGACTGGAAGGGCCT[C/G]AGCCTGGCAGTGGGA | 8440 |
rs569721461 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | NCK2 | GRCh38.p7 | 2:105765742 | TTAGATTTTCACACC[C/T]GTAACAGGCAGATAG | 8440 |
rs569722576 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105756867 | TGGAGTGCAATGGCA[C/T]GATCTTGGCTCATCA | 8440 |
rs569725549 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105814824 | AGGGGGGAGGCCTGT[A/G]TTTGGACAGCCCAAA | 8440 |
rs569728055 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | NCK2 | GRCh38.p7 | 2:105771047 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGACTA | 8440 |
rs569759210 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105763417 | CCAGTCATGCAGTAA[A/C/T]GACAAAACATGCCCC | 8440 |
rs569767905 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105837748 | CCATTGATTTTCAAC[C/T]TTCCTAACACATTAT | 8440 |
rs569768989 | in-del | -/A | 0.00597247 | 0.0543191 | upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105744648 | CTGCGCCTCCAGAGC[-/A]GGAGCGTCCCGCAGC | 8440 |
rs569777133 | in-del | -/AG | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105882148 | TTGTGTGAGTACACT[-/AG]AAAGAGCGGGAGACG | 8440 |
rs569852831 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105776867 | TAATCTCTGCTCTCC[G/T]CTGGCCTTGGGGTTC | 8440 |
rs569864921 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105870129 | GACTACCTGCGCATA[A/G]AGATGTTGGAAGACA | 8440 |
rs569885649 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NCK2 | GRCh38.p7 | 2:105835154 | CTCATTTATGTTTTC[A/G]CACTACCAGTGAGTT | 8440 |
rs569897272 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105758111 | TTGAGAGCTTTATCT[A/C]TTAAAAATGAGTTAA | 8440 |
rs569908525 | snp | G/T | | | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105771753 | TCTAGAAAAAGCATG[G/T]ACCTGGGTTGACCGC | 8440 |
rs569923051 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105835903 | TCTTTCTTCTGCTTG[A/G]TCTAGTCTCTTTTTG | 8440 |
rs569934771 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105875169 | ATCTTGGGCAGCTCT[A/T]TGCTCAGGAGCTCTG | 8440 |
rs569954368 | snp | A/G | 0.00835141 | 0.0640778 | upstream-variant-2KB, utr-variant-5-prime | NCK2 | GRCh38.p7 | 2:105744689 | CCCGGCGCCCGTACC[A/G]GGACCCGGGCGCGGA | 8440 |
rs569983401 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | NCK2 | GRCh38.p7 | 2:105756123 | CTTACTTGATCAAGT[A/C]GGATCAGCCTAGAGA | 8440 |
rs569990231 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105751197 | TCCTGCAACCTGCCC[A/G]CCTTCTCAGTTATAT | 8440 |
rs570004389 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105774374 | TAGCTGAGCCCTTAC[A/G]GCAAGCCTTAACTTG | 8440 |
rs570008867 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105868452 | AGCTGTTGATGGGGA[A/G]TCTTGCTTGGTTTTG | 8440 |
rs570044779 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105841911 | GAGAGGGGAAGGGAG[C/G]TCGCTTAGAAAATGG | 8440 |
rs570083660 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | NCK2 | GRCh38.p7 | 2:105744726 | CGACGACGGGGGGCG[C/T]CCCAGGTGGGTCTCG | 8440 |
rs570090716 | in-del | -/C | 0.00835141 | 0.0640778 | intron-variant | NCK2 | GRCh38.p7 | 2:105867605 | AAGTGAAGGTGGGGT[-/C]CCGTACCCTTGGAAT | 8440 |
rs570104396 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105815468 | ACAGATCCCCATTGG[A/G]TTTGAAATGTAATTA | 8440 |
rs570120472 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105857322 | AGCCGCCCGTCCTGG[A/T]GCCGGCACTGGGCCC | 8440 |
rs570143136 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105821684 | GCAGGTGCCCGGCAC[A/G]GGGCTTGTCACTGCT | 8440 |
rs570158683 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105826949 | AGTAGAGAGTTACCA[A/G]GGACATAAAAGAGTG | 8440 |
rs570163395 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105842055 | GACCTGAGATGTGGT[A/G]AAGGGAAAGTAGTAA | 8440 |
rs570218169 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105789643 | TAAAACCTGCCTTCG[G/T]AACCAGCTGTAAAGC | 8440 |
rs570242283 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105860871 | ACTTGTGGGGCACAC[A/G]AGATGGGGAATTTTC | 8440 |
rs570262959 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105826724 | TCCAAGTTCTGGCCA[A/G]GTAAGTATCCTTTCC | 8440 |
rs570279488 | in-del | -/A | | | intron-variant | NCK2 | GRCh38.p7 | 2:105892184 | GCAAAACTGCGTCTC[-/A]AAAAAAAAAAAGAAT | 8440 |
rs570293170 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105783370 | CCTTCCTCGGAGTGA[A/G]GCATTAAATTGTGCC | 8440 |
rs570324907 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | NCK2 | GRCh38.p7 | 2:105804421 | GGCATGTAGGTTTTC[A/G]TGCTCTTGTCTGGTT | 8440 |
rs570374557 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105795476 | TATAAAAACTGCTGC[A/G]TAAATATTTGAGTCA | 8440 |
rs570380802 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105795556 | TTTAACAAACTTGGT[C/T]TATTTAGTTTACATG | 8440 |
rs570383330 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105875286 | ATCTGTGGAGCACAC[C/G/T]GTCAAGCACCCAGGG | 8440 |
rs570393759 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105813959 | AAAAGCACACACTCC[G/T]TCTGTATATTCCTGT | 8440 |
rs570469772 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105801725 | GGACAGAGTGGCCCT[C/T]GGCTCAGTCCCTTTA | 8440 |
rs570477216 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105863739 | CAGAGAGCATGTAGC[A/G]TTGTGGGCAGGAGGG | 8440 |
rs570479509 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NCK2 | GRCh38.p7 | 2:105882143 | TCACATTGTGTGAGT[A/G]CACTAGAAAGAGCGG | 8440 |
rs570480660 | snp | A/C | | | utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105894259 | TATTGTAATAAAAAA[A/C]AGTATTATGACAAGG | 8440 |
rs570492288 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105892058 | ATTAGAAAAATTAGC[C/T]AGGCATGGTGGCACA | 8440 |
rs570512670 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105863728 | ACCTGTGCTTTCAGA[A/G]AGCATGTAGCATTGT | 8440 |
rs570521197 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105750766 | TTTGGGGGTTGGTTT[A/G]TCTTTAATTGAGACC | 8440 |
rs570559865 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105757843 | AATATTTTCTTCAAG[A/G]TCCTCAGAAGCTCTT | 8440 |
rs570580819 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105857229 | ATGAACCACATCTTC[A/C]GCCCAGCATGCTTAG | 8440 |
rs570581860 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105801363 | ACTCGGCTTGCCTCC[C/G]CCCTTCCCCATGTCA | 8440 |
rs570615158 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105857880 | AGAGGAGGCACCCCC[A/G]ATCAGGTCTCACCAT | 8440 |
rs570674539 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105864449 | CCTGAAGGACCAACA[A/G]TGACCCAGAGAGTGG | 8440 |
rs570699932 | snp | C/T | | | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105771513 | AATGTTGCAGTAAGC[C/T]GAGATTGGGCCACTG | 8440 |
rs570701770 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105792749 | CAGAGCCAGTCTGGT[A/G]CGATTTTCTGGCAAG | 8440 |
rs570702889 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105776160 | CTAGGAATCTCAGTG[C/T]TCTGCCCTGCCATTC | 8440 |
rs570713940 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105856599 | TGTTGAAAAGTCTAA[A/G]CTCCCTCTGCAAAAT | 8440 |
rs570720274 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105769413 | CTGTGCTGGTAACTC[C/G]CCCGTTCTTGCTTCT | 8440 |
rs570782602 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NCK2 | GRCh38.p7 | 2:105851349 | GCTCACTGCAACATC[C/T]GCCTCCCGGGTTCAA | 8440 |
rs570790914 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105745510 | TGGCCTGCAGGCGGG[C/T]GGCCGGCACGGAGCT | 8440 |
rs570826592 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105790810 | TGCACATAGGCAAGA[A/C]TTGGGTGGAGGGAAC | 8440 |
rs570836021 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105835314 | AGACTTTTATTTCTT[C/T]TTCCTTTTTGAAGGA | 8440 |
rs570900625 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105894039 | ATATATATATATTAT[G/T]TACAGGGAAATTTTT | 8440 |
rs570901888 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105810044 | GGCAGGGCCAGGGCT[G/T]AGAGGGAGGGAGAAA | 8440 |
rs570927021 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105768491 | ACTGGCTGTAAATTG[G/T]GGTTCCCATGACCTC | 8440 |
rs570936693 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105809339 | GTACCACAGACTGAG[A/G]TGCTTACACAGCAAT | 8440 |
rs570958319 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105821810 | GCTGTGCATGCTCAA[C/T]TGTGTGACTCTGGAG | 8440 |
rs571033649 | snp | A/G | 0 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105870318 | CAGGGTGGCTGCTTG[A/G]GGTTTCCCTCAGGGA | 8440 |
rs571039781 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105822887 | TTTCCTTGCCTAGTA[C/T]GGCCCAGCGTTGGAT | 8440 |
rs571045676 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105827316 | CATAGCATTCTTAAG[C/T]ATGCATGCACCAAAC | 8440 |
rs571056476 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105773633 | TTCATTTCTTATATG[A/C]TAGAGCATCCTGGTT | 8440 |
rs571058256 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105860971 | GGAGGAACCCAAGGT[C/T]GTTGTGGATCCCGAA | 8440 |
rs571074211 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105867072 | AGGAACCACTTTTTC[C/T]TTTCAAATCAGTACA | 8440 |
rs571082662 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105835407 | TATATATATATATAC[A/G]TGTATATATATATAT | 8440 |
rs571100740 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105875862 | CTAGAACTTAAACAC[C/T]GTAATTTTATGATGA | 8440 |
rs571124336 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105806533 | GTGAGCCACCACTCC[C/T]GGCCACATATATTCT | 8440 |
rs571148377 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NCK2 | GRCh38.p7 | 2:105863306 | ATCTCTGAAATGAAA[C/T]GTGGGTAACAAATGC | 8440 |
rs571161029 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105869630 | CACTTTCCTGAGCAG[A/G]TGTGGTCCTGCAGAA | 8440 |
rs571170423 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105790205 | ACATAAAAGTAAACC[A/G]TTAGAAATAGTGTGC | 8440 |
rs571172260 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105784057 | GCCTCAACACCATGC[A/G]TGGCATTGGCAGTGA | 8440 |
rs571175349 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | NCK2 | GRCh38.p7 | 2:105806396 | GCACCCACCACCACG[C/T]CCGGCTAACTTTTTG | 8440 |
rs571187842 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105748704 | ATTACAGGCCAGAGC[C/T]ACCATACCCTGCCCT | 8440 |
rs571195450 | snp | C/T | 7.21293e-05 | 0.00600495 | synonymous-codon | NCK2 | GRCh38.p7 | 2:105855228 | TGTACCGTCCAACTA[C/T]GTGGAGCGGAAGAAC | 8440 |
rs571207169 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105774155 | CTGAGACTACAGGCA[C/T]GTGCCACCACACCCA | 8440 |
rs571219834 | in-del | -/AAG | 0.00358779 | 0.0422022 | intron-variant | NCK2 | GRCh38.p7 | 2:105798238 | GAGTAACGTGTAGGT[-/AAG]AAATAAGTTAGCCAA | 8440 |
rs571227900 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105803472 | CATTTTCATTGAATA[C/T]GTGTGACTGATTTCA | 8440 |
rs571241315 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105854507 | GAGATTGACAATTAT[C/T]TATTGTTATTATTAT | 8440 |
rs571265459 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105761692 | AGACCAGCCTGGGCA[A/G]CATGGCGAAACCCTG | 8440 |
rs571341708 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105812055 | CTCGTGTTTTCATTA[A/G]TCAGCTTCTAATTAA | 8440 |
rs571353726 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105760291 | GGTGCCCCAGCATGG[A/G]GTTTCCAGAATGTGG | 8440 |
rs571386471 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105777183 | CACCGATGGCAGCTG[A/G]AACCTTCTACTCTCG | 8440 |
rs571400121 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105767406 | TGAAAGGTGTTCTTT[A/G]TAAGTGTTACATTCT | 8440 |
rs571405443 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105781036 | TTTGTCTCTCACCTG[C/G]TCGTGGTCTTCCTGT | 8440 |
rs571420971 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105824317 | GCAGATCTGACAGTG[A/G]GAGCCCAGTCACTCC | 8440 |
rs571436738 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105818415 | ACATGTACCCTAGAA[A/C]TTAAAAGTGTAATAA | 8440 |
rs571462503 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105786518 | TAAGCATGAGATGCT[A/G]AGTCGGTTCCTTTAG | 8440 |
rs571476827 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105830155 | TACAGTGCTATCAAA[C/T]ACTAGAACTTATTCC | 8440 |
rs571496824 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105872393 | CCGTGGTGTAGCCTG[A/T]CTTCCTTGCCACGGG | 8440 |
rs571503996 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105787857 | TTGGGCTACATCCAT[A/G]TTATAAGATGATCTC | 8440 |
rs571507150 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105831029 | TCCCCTATTCCAGAG[C/T]GTCTCTTCATTTGAT | 8440 |
rs571515420 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105820048 | CCCTAATACTTGAGG[C/G]AGGGATCAACTGACC | 8440 |
rs571522476 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105888098 | ACACAGAATCTAAAG[C/G]CTAAACAAAAATAAT | 8440 |
rs571538118 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105783236 | TTTGAAGATGGAAAG[A/T]AATGGCAGTGGAATG | 8440 |
rs571540569 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105786936 | AGCACCGTCCAGACT[C/T]GAAGCAGGGGACCTG | 8440 |
rs571543179 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105793329 | TGTCATGGTCCTAGT[C/G]GGAGTGTCATTTAGT | 8440 |
rs571550580 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105826089 | GACTGGGTTATTTAT[A/T]CAGGAAAGAGATTTA | 8440 |
rs571559487 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105879167 | TCTCAAGTAGCTTTT[A/G]TAATTCACATGTTTG | 8440 |
rs571577209 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105792817 | GAGGCCCATGTGAGC[A/T]ACCTGGATGGCCGTG | 8440 |
rs571633143 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105869063 | ATACGATCCAGCCCC[A/G]CTGCCCACCCTTACC | 8440 |
rs571636744 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | NCK2 | GRCh38.p7 | 2:105894622 | AGCATTTATATTGAT[A/G]TGCCAGGCCCTGGGG | 8440 |
rs571667291 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105831891 | GTCTTTTGTGGTTGC[A/G]TACAAATTTTAGGAT | 8440 |
rs571731248 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105756047 | TCTGCAAAGCTGCCT[C/G]TTACCTGGCCTAGCA | 8440 |
rs571765301 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105742985 | CAAAAAACAATCAAC[C/T]CTCTCTTTAAAAAAA | 8440 |
rs571766966 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105879960 | AGCAGAGCTGTGGTG[G/T]GAGCACTCATCTCTC | 8440 |
rs571770221 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105755464 | GTGGGTGCAGCCGAT[C/T]CCGTCTTCCATAAGA | 8440 |
rs571842102 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105879490 | GGTTTGTGTTTTTAT[A/G]TAAGTTAACACAAAG | 8440 |
rs571842449 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105803928 | TGGTTCTGGCTGTTG[C/G]ATGAAAGCTGAGGAT | 8440 |
rs571846261 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105847865 | GGCTAGCTAGATACA[A/C]GCTGATAGCATTAGC | 8440 |
rs571858993 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105754940 | TTTTTCCAGCCATTT[C/G]CATTCTTTCTTTCCA | 8440 |
rs571875674 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105749582 | CATGAGGAACACCAA[C/T]GTGTTGCTGGGTAGA | 8440 |
rs571877325 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105854747 | TTACTTAATGAAATG[A/G]ACTCATTTAATTATA | 8440 |
rs571919539 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105846873 | GATATTTGCATACTC[A/G]TGTTCATAGCATTAT | 8440 |
rs571919820 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105759578 | TCTGATATAAACTGT[A/G]TCTACTTTCCCCTGT | 8440 |
rs571963083 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105839406 | ATGGGAGAGAAGGGG[C/T]GGATCTGAGGCATAT | 8440 |
rs571965727 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105864967 | ACCATCCAAATAACA[C/T]GAGTACCTTCAACTA | 8440 |
rs571988168 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105861080 | TGTTTACGGAAAACT[A/G]TCAACCATTTTCTAA | 8440 |
rs572034269 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105820929 | CAGTTGGTGATGTGC[A/C]TGTCCAGCGTGTAAA | 8440 |
rs572037671 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105793041 | CATGAAGCCAACCCA[C/T]GAAACTGAAGGTGAG | 8440 |
rs572051627 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NCK2 | GRCh38.p7 | 2:105860475 | GGGACCTGCTAAGCC[A/G]TAGGCGTCTCAGAAT | 8440 |
rs572064347 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105839098 | GACATTTGAATGGCG[C/G]CTTGAACAAAGTAAC | 8440 |
rs572092735 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105831659 | AGGCTCTCCTTTTCC[C/G]TAATCTATGTTCTTG | 8440 |
rs572104593 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105799838 | CGCCATCTTGCCACT[A/G]TGTTCTTGGCTATGG | 8440 |
rs572127226 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105799437 | CCAGAGTACCCCATG[A/G]CCATTTATTGAGAAG | 8440 |
rs572129801 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105845694 | CCACCACGCCCAGCC[A/G]AGGTTTTTTTGAAGT | 8440 |
rs572133828 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105768216 | GTCTGTAGAGTCCAG[C/T]GTGTGTTTGCCCTCA | 8440 |
rs572151640 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105846353 | TCAGAGAGTAAATGA[A/G]TTGCTCAATGATGAA | 8440 |
rs572197443 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105836128 | ATTTCCTTTTCTTTG[C/T]TCTGTTATTAGAGAA | 8440 |
rs572203319 | snp | A/C | | | upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105743717 | CAACAGTCAAACACT[A/C]ACCTGTCTGACTTCA | 8440 |
rs572217702 | in-del | -/GAGA | 0.00597247 | 0.0543191 | intron-variant | NCK2 | GRCh38.p7 | 2:105760792 | GGTTTTGTCACATGT[-/GAGA]GAGAGAGAGAGGCAG | 8440 |
rs572219296 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105838077 | TTCACTGTTAAGCCA[A/G]ACTTTCTGTTTAACT | 8440 |
rs572230841 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105806009 | AATTTTATTTTTTTT[A/C]TTGGGGGTGCTGGGT | 8440 |
rs572284347 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105782660 | ATGCAACGTCAAATG[A/G]TAGAACCTGATCGTT | 8440 |
rs572315046 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105805264 | GATGTTCCCAGTACG[A/G]GGAGGAAATAGCAGA | 8440 |
rs572327672 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105873860 | ATGAACCTCTGCAGC[A/G]TGGGCAGATGCTGCT | 8440 |
rs572352855 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105811565 | CTTGTCTTTAAGGAG[C/T]ATCTGAGTCCCTGCA | 8440 |
rs572369763 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105781938 | TTTTAACTGAAATAG[C/G]TACATACAGCTGTCA | 8440 |
rs572390156 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105888496 | GATGTTTCAAAACCC[A/G]GGGACTGAGTCTAGT | 8440 |
rs572412266 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105787902 | ACATGCGTATACCGC[C/T]CCCCACCGCCCCCGA | 8440 |
rs572435024 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105813404 | GTGGTATTATGTCCA[C/T]AAAGCTCACAGCCTT | 8440 |
rs572439879 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105856704 | TGAGACATGGAACTT[C/T]GTATGAATCATACCA | 8440 |
rs572462602 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105803768 | TCTAGAGTAGTGATT[C/T]TGAATGGGGCTGGGC | 8440 |
rs572487992 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105763661 | CATTGGGAACTTAGG[C/G]GTTTATAATAACTTC | 8440 |
rs572493127 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105862525 | TCTACCAAATTGACT[A/G]TCTGGATTTAGTGGT | 8440 |
rs572505606 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105868826 | CCTGGCTCAGCGCTT[C/T]TCTATGAAAATGAAG | 8440 |
rs572517470 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105819868 | CATCTATTGTGAACA[A/C]CCCACCTGTATTTTG | 8440 |
rs572608439 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105819399 | TGCAGTCATGTATCA[A/G]TCCACTTGTCAGATT | 8440 |
rs572666986 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105784527 | ACTATGTGGAGCCTC[A/G]CTTGTGGAGGGTACA | 8440 |
rs572703340 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105782995 | TGCAGCTGAGTTGGT[C/T]GACTATCATTTGCAA | 8440 |
rs572725210 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105833504 | TTCATATTAGTCTCT[A/T]ATGATCTTTTATATT | 8440 |
rs572732010 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | NCK2 | GRCh38.p7 | 2:105784760 | TCCATCCGTTCCTCA[C/G]CAGCCACTGTTCCAG | 8440 |
rs572737182 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105891466 | CTTGATATTTTTGTA[C/G]AAAGAACATTTATCG | 8440 |
rs572737722 | snp | C/T | 0.00438332 | 0.0466095 | upstream-variant-2KB, intron-variant | NCK2 | GRCh38.p7 | 2:105850417 | ATTTGTTTTTAAACC[C/T]ATTCCCATCCAAGAC | 8440 |
rs572752964 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105874139 | CAAAAAATCCTTAAG[G/T]TGAGTGAATTTGAGT | 8440 |
rs572809728 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105832247 | CTGCAATTTCACCGG[A/C]TCTGTTTACCAATTC | 8440 |
rs572820428 | snp | A/C/T | 0.00279162 | 0.0372561 | intron-variant | NCK2 | GRCh38.p7 | 2:105784257 | TACAGGCATGAGACA[A/C/T]CACGCCCGGCTGTTA | 8440 |
rs572820442 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NCK2 | GRCh38.p7 | 2:105790366 | AGCCCTGGGCTTCTC[A/G]ATGCCATAGGCTGGC | 8440 |
rs572830445 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105801862 | GCTCTAGAGTTAGTC[A/G]TCTTGCTGAGAGAAA | 8440 |
rs572835528 | snp | A/C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105886765 | GACTTTAGGAAATAC[A/C/G]TTTGGGGATAGGGAG | 8440 |
rs572859136 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105843870 | GCGTGGGCTGTTCCT[G/T]GAGACTTCCTTCCAA | 8440 |
rs572865538 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105771711 | CAAATAGAGGCTACT[C/G]AGATTTGCTTTGAGT | 8440 |
rs572878103 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105816207 | GCTAATGGGGAGACT[C/T]AGGCAGGAGGATCAC | 8440 |
rs572920937 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105815747 | GTGGCTTCTCAACAA[A/G]TGGCTGGTGCAACAG | 8440 |
rs572948025 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105765791 | TAGAATAGGGGGTGT[A/G]TGTGTGTGTGTGTGT | 8440 |
rs572954080 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105858764 | AGCTTGAGGAAAGAC[A/G]TGAGAACCTTTGACA | 8440 |
rs572964667 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | NCK2 | GRCh38.p7 | 2:105822026 | TCTGGGAGATTAAAT[A/G]ACTTGGCCGGGGCTC | 8440 |
rs572965787 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105764854 | GAATATTTTTTCCAC[G/T]TTACTAGTTTTTCAA | 8440 |
rs572970733 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105870611 | AAATATAAAAATTAG[C/T]CAGGGTGGTGGCACA | 8440 |
rs572992660 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105853102 | CCTAAAGTCATCCCT[A/G]TACAATAATGAGAAC | 8440 |
rs573022496 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105791486 | CGTGCTTACCGGCCA[G/T]AGTGCTGCTGCAGAT | 8440 |
rs573028976 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105864661 | TCCAGGGCCTACCTC[A/G]GAGAGCTGGCACTTC | 8440 |
rs573031333 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105856130 | TGAGCCACCGTGCCC[A/G]GCTCCCCATGTGCCT | 8440 |
rs573043204 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105805047 | GGGCCTCCCCATATG[G/T]GTATCAGGACATGAA | 8440 |
rs573087658 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | NCK2 | GRCh38.p7 | 2:105745831 | CACAATCGCTCGGCT[C/T]TCTCGGTTTTTTTCA | 8440 |
rs573125836 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105752455 | TGTGGTTTGAATTCT[A/G]GAAGTTACCAGTGTA | 8440 |
rs573133694 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105772562 | AGCCGCATGTTACTG[A/T]TGCTGGGTTAAACAT | 8440 |
rs573146180 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105866697 | CTGCTCATCTCCTGC[C/T]GTGCAGCCCATTCCT | 8440 |
rs573160533 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105817645 | ACACTGCTCAAAAGA[A/G]GACATTTATGCAGCC | 8440 |
rs573169116 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105825486 | GCAGCACTGGGCACT[A/G]CAGCGCTTTGGAACA | 8440 |
rs573173525 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105827673 | TTCTATCTTTTAATA[C/G]AATTTCTTCTTTTTG | 8440 |
rs573178197 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105866184 | CTCCCAAAGTGCCGG[A/G]ATTACAGGCGTGAGC | 8440 |
rs573201621 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NCK2 | GRCh38.p7 | 2:105823953 | AGTGTGAACAACCCA[C/T]GGTCCGGAGCAGTCC | 8440 |
rs573207440 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105823715 | GTAAGGTCCGTGGCC[A/G]TGGAGGCAGGCCTTG | 8440 |
rs573208170 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105745230 | CTCGCGGGCCGGGGT[A/G]CGCCCGGGAAGGGGC | 8440 |
rs573209871 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NCK2 | GRCh38.p7 | 2:105835794 | AATAGGATCCCACAT[A/G]TCAGGTAGGCTTTCT | 8440 |
rs573210336 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105827232 | TCTCGATCTCCTGAC[C/G]TCGTGATCTACCCGC | 8440 |
rs573244442 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105843525 | CTGGGGTAGAAAATA[C/T]GCAAGAAAAGCCCAG | 8440 |
rs573261935 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105798162 | TAGGAGCTAATGTTC[A/G]CTTGTTGTAATGTTT | 8440 |
rs573263742 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105805108 | CTATCTGGACAGTTT[C/T]GTAAATGACAGTTGA | 8440 |
rs573271196 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105780620 | GCCCCTGGTCACTGA[C/T]GTGGTCTGAATGTGT | 8440 |
rs573300316 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105841371 | AATGTCTACCTCAGT[C/T]ACTCATTTTGGGTGT | 8440 |
rs573307782 | in-del | -/AGAA | 0.00676609 | 0.0577691 | intron-variant | NCK2 | GRCh38.p7 | 2:105883862 | ATTCTCTCCTAACTT[-/AGAA]AGTCAAGGAACAACA | 8440 |
rs573321910 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105747778 | AATACTTCACGGCAC[A/G]TTTTCAAAGGGCCTA | 8440 |
rs573351935 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105804332 | GAAGACCTGGTGGAC[A/G]AGAAAATGGGTTTGA | 8440 |
rs573379165 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105791632 | CATTTCGAACTGACT[C/T]CATAATAGATCTGAT | 8440 |
rs573379909 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105747040 | CTGCTGCATAACCCC[C/G]TCTGTCCACTTGTGG | 8440 |
rs573380680 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105786139 | TTTATTGATCATCTG[G/T]TGTGTCTAGGGCAGC | 8440 |
rs573403062 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105878740 | ACTAAGAGCATGCAG[C/T]TCTCTGTCAGTCTGC | 8440 |
rs573407770 | snp | C/G | 0 | 0 | intron-variant | NCK2 | GRCh38.p7 | 2:105753997 | TGCCAGCTTCTCGAA[C/G]CTACCCTTTTGTGTT | 8440 |
rs573416114 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105798134 | TTTAGGATTTAATAT[C/T]CTATGAAAGGAGTAG | 8440 |
rs573418419 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105753605 | CACCCTTGTCTCCTC[A/C]ACACTGGGGGCTGAG | 8440 |
rs573445577 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105772365 | CCTGTGTTTGGTCAG[A/G]ATAAGAACCTAGAAA | 8440 |
rs573452163 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105870195 | GAGACCACAGTGCCA[C/T]GGGGCCAAGCAGGGG | 8440 |
rs573456982 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105892267 | AAAATTTCTAGCTAC[C/T]GCCTGCATGCAAACC | 8440 |
rs573469146 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105760520 | CGTTCACACCTCTTC[C/T]CTGCTGGTGGCACCT | 8440 |
rs573481797 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105779703 | TTTGATTTTTTTTTT[C/T]CCCACTAATCAGCTT | 8440 |
rs573481972 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105771841 | GTGAAAGCTGCCATT[A/C]CTTTGTGAGGCCTGC | 8440 |
rs573520561 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105871461 | GCTCAGGGAGATGGG[A/G]ATTTGCTAAGCTTTT | 8440 |
rs573539950 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105884646 | AAGACAAACATTGCC[A/G]CATGCTACACTATCC | 8440 |
rs573550427 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105883876 | TAGAAAGTCAAGGAA[C/G]AACATATATGATTCT | 8440 |
rs573564179 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105892863 | AAAAAAAAAAAAAAG[C/G]AGAGACCCAGTGTTT | 8440 |
rs573594970 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105761187 | GGTTGTGCCCTACCC[A/G]GGTGCTGGGAGGTTT | 8440 |
rs573595502 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105823214 | TTTTAGTAAACTGGA[C/G]CTTGAACAGGTAATT | 8440 |
rs573597575 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105799147 | TTGCAAATGTTTTCT[C/T]CTAGCTTTTTATTTG | 8440 |
rs573599773 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105892561 | AGAGACCCGGCTGGG[C/T]GTGGTGGCTCATGCC | 8440 |
rs573666013 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NCK2 | GRCh38.p7 | 2:105810915 | GTGCAGTGGCTCACA[C/T]CTGTAATCTCAGCAC | 8440 |
rs573712133 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105858990 | GCTGGCAGAATCCAG[C/T]TGATGTTTTTGAAGG | 8440 |
rs573738073 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105865988 | GGCAATATCTTGGCT[C/T]ACCGCAACCTCCGCC | 8440 |
rs573774578 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105865183 | TCACAAGCGTTTTCC[A/C]AGCAAATGGGCCGTG | 8440 |
rs573785531 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | NCK2 | GRCh38.p7 | 2:105817787 | GGAAACAACAGGTGC[C/T]GGAGAGGATGTGGAG | 8440 |
rs573838747 | in-del | -/C | 0.0023933 | 0.0345097 | intron-variant | NCK2 | GRCh38.p7 | 2:105809864 | AGAGATCTTACCTCA[-/C]CCACTGAGCACTGCT | 8440 |
rs573849092 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105760372 | GTGGGATAGGTTGGT[C/G]TGGAATTCTTCCTGT | 8440 |
rs573874255 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105877216 | ACTGAGACACCTTGC[C/T]CAGGCACCCTTCCCC | 8440 |
rs573943670 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105812219 | TCAGCTGTTTCTAAA[A/C]CCTGCCTGGGAACCA | 8440 |
rs574012585 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105828411 | TAATGTTGGTCAAAT[G/T]TAAAAAATGGCACTG | 8440 |
rs574037989 | in-del | -/GTG | | | intron-variant | NCK2 | GRCh38.p7 | 2:105870032 | GACACAAGGACCCAT[-/GTG]GTGGTCGGGAGGGTG | 8440 |
rs574053697 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105787054 | TTCTGCCCTTTGCTG[C/T]GACTCCTCTGCTGTC | 8440 |
rs574078536 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105831407 | ACCAAATAAGCATGA[C/T]ATCTTTTTTTTTTTT | 8440 |
rs574145699 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105816621 | TGCCAAAGGTAAGTC[-/T]GCAGTTTTCTGCTTA | 8440 |
rs574146040 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105781141 | TTTTACTTCTCTTCT[C/T]ATAAACTATTAGCTT | 8440 |
rs574146117 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | NCK2 | GRCh38.p7 | 2:105773331 | TCCTTTCCAGCCACC[C/T]GCTTGAGGCAGACCT | 8440 |
rs574146664 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105879323 | TCCTGGTTGAGCTTC[A/G]GGCACCACTGCCTTC | 8440 |
rs574167673 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105786689 | ACTCTCCTGGGTCCC[C/T]GGGCAGGGCTTCCTG | 8440 |
rs574182317 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105780661 | TTGAGATCCTACCCC[C/G]CAAGGTGATGGTATT | 8440 |
rs574187315 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105864501 | CCACGGTGCGTAGTG[G/T]AGTTTGAGGTTAGGG | 8440 |
rs574190713 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105820572 | GGACCCTGCGGCTCT[C/G]ACCCTGCCTTCTTTG | 8440 |
rs574199191 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105867607 | AGTGAAGGTGGGGTC[C/T]GTACCCTTGGAATAC | 8440 |
rs574217781 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105872512 | ATTGCGATTGTCACC[A/G]TTGGTCATCTGCAAC | 8440 |
rs574226302 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105826565 | TTAATGCAAAAATGT[A/G]ACTAATAAAGCAAGA | 8440 |
rs574238366 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105870707 | TTGCAGCCAAGATCG[C/T]GCCACCTCACTCCAG | 8440 |
rs574247338 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105885416 | CTGGGAAATAAAATA[A/G]AATAGCTCCTTTCTG | 8440 |
rs574259768 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105775220 | GTGTGTGGCATGTGG[A/G]TGCCTAATCAATGAG | 8440 |
rs574265011 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105791683 | CTTGATACAGGGTTT[A/C]GTTTTTCTACTTGAC | 8440 |
rs574277163 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | NCK2 | GRCh38.p7 | 2:105761699 | CCTGGGCAACATGGC[A/G]AAACCCTGTCTCTAC | 8440 |
rs574282826 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105872074 | TTCCTTAAACGTACG[C/T]AGTTCTTAATGGTGA | 8440 |
rs574286613 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105748355 | TCTTTGTGTCCCTGA[A/T]TTGTCATCTGTGACA | 8440 |
rs574291105 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105878803 | AGATCACATTCAAGC[A/T]AAACAGGTAAAATTT | 8440 |
rs574304878 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105809067 | CTTGGCCCAGGAAGC[C/T]AGCTGTAGTGCTTAA | 8440 |
rs574369434 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105869668 | CGTGCTGAACTTTTG[C/T]CAGTGGATTGACACT | 8440 |
rs574376886 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105747824 | TCGTGTATCTTGTTC[C/T]ATGCCTGAGTTAAGG | 8440 |
rs574381829 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105812899 | GTGTACATTCATGGG[C/T]TTGCTTCTTGATGTA | 8440 |
rs574393139 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105863575 | AAGGATAAGGCTTAG[C/T]CCCTGACTTTCTGAA | 8440 |
rs574412562 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105801380 | CCTTCCCCATGTCAT[C/T]GTGTGCACCAGCACG | 8440 |
rs574414071 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105840218 | AGAAAGACACAGTAG[C/T]TCCAGGGAATAATTA | 8440 |
rs574439158 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105828105 | AAAGTTTAAACTTTT[C/T]TAAAAAGAAAAAAAT | 8440 |
rs574473456 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NCK2 | GRCh38.p7 | 2:105744813 | GCCGGGGAGGAGCGC[C/G]GGAGGAGGAGGAAGA | 8440 |
rs574498856 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105876228 | GTGCAGTAGGATTTT[A/G]TGATTAACTTGAGAA | 8440 |
rs574514096 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105854035 | TGCAAAAGTTGAGGC[C/G]TTAAAGGGAAGAAGA | 8440 |
rs574526355 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105750848 | GAAGAGAGCAAAGCA[A/G]GAGGTGGGGCCAATG | 8440 |
rs574537223 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105789411 | CAGGCTGGTCTCCCA[A/G]CTCCTGGCCTCAAGT | 8440 |
rs574550515 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105784146 | TCTCCCTCTGTCACC[C/G]AGGCTGGCGTGCAGT | 8440 |
rs574552150 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105764953 | TCATTTGGACATCTA[A/C]ATTTTTGCTCCTGTA | 8440 |
rs574579999 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105795123 | CATCCCCGACAGGGT[A/G]CTGCATTTGTTTCTG | 8440 |
rs574580471 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105752575 | ACAGTGATGGGGTAC[A/G]GGTGTTATTTTGTTA | 8440 |
rs574584021 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105747773 | ATGGAAATACTTCAC[A/G]GCACGTTTTCAAAGG | 8440 |
rs574636986 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105750277 | TTCCTCTTATAAGAA[A/C]ATCTGTCCTGTTGGA | 8440 |
rs574681234 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105768728 | GTGTATTTTATGTAT[C/G]GCCCAAGATGATTCT | 8440 |
rs574683551 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105874762 | ATATAAAAGATTTTG[A/G]CTTTAAATTTACTGA | 8440 |
rs574685174 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105882177 | ACGCAGATGAATGCA[A/G]TTTAGTATAATGTTT | 8440 |
rs574696529 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105783855 | CAGAAAGTGGGAGTT[G/T]TTTCGCTTCTCCCTT | 8440 |
rs574698550 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105794350 | CGCCACCATGCCTGG[C/G]TGAATCCTTTGATTT | 8440 |
rs574707478 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105759147 | TCGAATACCTAGATT[A/C]CTGGTTCTTGGGCCT | 8440 |
rs574710301 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105750888 | GTGGAGAGGCCGTCT[C/T]CTCTGAGCCTGCCAT | 8440 |
rs574720537 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105840629 | AGATGCCAGTTGCAC[A/G]TCCCAGGTTGTTTTA | 8440 |
rs574740921 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105825182 | ATCTGGGATGCTTGG[A/G]GGTGACTTAGGATGC | 8440 |
rs574746355 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105757984 | CTCATGCCAGGGTGG[A/G]TGTTATTATTCCAGG | 8440 |
rs574758107 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105880862 | CTCACTGCAGTCTCA[A/C]CTCTGGCTCAAGCCA | 8440 |
rs574765770 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105791119 | GCCACTTGGAAGCCC[C/T]TGCGGCCCTGGGCTC | 8440 |
rs574768944 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105790435 | TGGGCAGCAGGAGAG[C/T]CTGTGCCTGTGAGGA | 8440 |
rs574774661 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105857974 | GTGAGAATGCTTTCC[A/G]TAGCCCCTCCTGCCT | 8440 |
rs574774824 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NCK2 | GRCh38.p7 | 2:105849963 | TTACCCTGGGCTATT[A/G]AAGAGGCAGCTGGGC | 8440 |
rs574808798 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105883259 | TTGTTCTCACATGAC[G/T]AGAGCTCTGTGCACC | 8440 |
rs574812112 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NCK2 | GRCh38.p7 | 2:105757097 | AGTGTGAGCCACCGC[A/G]CCTGGCCCCATTCTG | 8440 |
rs574835586 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105874672 | CAGCTTAAATCTCCC[A/G]AACTCCAGCTGGAAG | 8440 |
rs574837726 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105857379 | CAGCCCTGCTGGAGC[A/G]CAGCGTCGGTTCGAG | 8440 |
rs574855385 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105879299 | TGTTTTGATAAGGCC[A/G]TGAGGCCTTCCTGGT | 8440 |
rs574897983 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105785010 | TTGAGACGGAGTCTC[A/G]CTCTGTCGCCCAGGC | 8440 |
rs574918932 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105890784 | ATTGGTAGAAATGGA[C/G]TGATTCCTTGTTTTG | 8440 |
rs574920589 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105797376 | TCTAGGACCGGAAGA[C/G]ACTGCCAGCCATGCG | 8440 |
rs574939583 | in-del | -/TT | 0.00358779 | 0.0422022 | intron-variant | NCK2 | GRCh38.p7 | 2:105758414 | TTTTTGTTGTTTTTG[-/TT]TTTTTTTTTTTTTGA | 8440 |
rs574949609 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105849524 | CTCCTTCAGCTTCCC[A/T]TTAAACCAGGTGGCT | 8440 |
rs574986169 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105765069 | GGCATTGCAGAGTTA[C/T]ATGGTATGGACATCT | 8440 |
rs574988005 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105821948 | GCTGTCTCTGACACA[C/T]GATGGTGGTGACATG | 8440 |
rs574990981 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105765522 | ACATTCTCAGCCATG[A/G]TATGACTTTTCCCTT | 8440 |
rs575013366 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105747447 | GATAGACCAGGCTGC[A/G]AGGCTCTATGGGACA | 8440 |
rs575020338 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NCK2 | GRCh38.p7 | 2:105808730 | GGACATGACTTGGAT[C/T]CTGATTCAAGTAAAT | 8440 |
rs575027040 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105809451 | CGCTTGCAGACAGAT[A/G]CCTTCTTGCTGTGTC | 8440 |
rs575029344 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105846643 | ATACGTTACACCCAA[C/T]AGGATGACTGCTGTC | 8440 |
rs575031241 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105771085 | CCGCCACCATGCCCA[C/G]CTACTTTTTTGTATT | 8440 |
rs575052037 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105767896 | ATACTAATTCCTTCC[C/T]TCTCTATTACTCACA | 8440 |
rs575052149 | snp | A/T | | | upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105743051 | ATCTGCCTTGGGGAT[A/T]TCACTTTTACAGGGT | 8440 |
rs575092096 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | NCK2 | GRCh38.p7 | 2:105858048 | CTTTGTTTTTTGGGG[G/T]TTTTTTTTTGTTTTT | 8440 |
rs575095198 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105809802 | TGTCCATGGAGCCAT[C/T]CAGGAGGTCTTCCTG | 8440 |
rs575100773 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105825403 | TTTGATCCTTACAGC[A/G/T]AGCTGACCCTCAGTG | 8440 |
rs575133207 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105789926 | GTGGTCGCCAACTAA[A/G]TGTTCACGAATGGAT | 8440 |
rs575151431 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105818702 | TGTATAAAAAAACTT[C/T]AATTTGCTTCTATTA | 8440 |
rs575184222 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105795651 | GTCTGCAGGCGTTGT[A/T]GATTGTCACCAATTT | 8440 |
rs575184870 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105843602 | CGAACGAACACTCGC[A/T]GTGATGGTGATACGT | 8440 |
rs575287379 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105837443 | ATTGTGTGGGGAGTG[A/G]TGATTTCTTGGTTTT | 8440 |
rs575289579 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105771157 | TCGATCTCCTGACCT[C/T]GTGATCCGCCTGCCT | 8440 |
rs575298716 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105784737 | GAGGAGCAGTGTGTC[C/T]GTTGAGGTCCATCCG | 8440 |
rs575324782 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105876702 | CACATTGGACTTCAA[A/G]TTGTGCTTCTGTTAC | 8440 |
rs575327369 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105827555 | AGTAGCAGGATACAC[A/G]TTCTTTTTAGGCACC | 8440 |
rs575328039 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105746922 | CTGTCCCGGAGGCCT[A/C]GCCTGGATTCTGAGC | 8440 |
rs575335731 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105758000 | TGTTATTATTCCAGG[A/G]CCTGGATGAAGCTCA | 8440 |
rs575344959 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105784215 | CTCAAGTAATCCGCC[C/T]GCCTCAGCCTCCCAA | 8440 |
rs575349703 | in-del | -/CAC | 0.00398564 | 0.0444627 | intron-variant | NCK2 | GRCh38.p7 | 2:105777906 | GGATTCCAGCAGCAG[-/CAC]CACCTTGGTTTCGCC | 8440 |
rs575401303 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105834756 | CCCTGTAGCCTTGAA[A/C]TGTTGGGTTTAAGTG | 8440 |
rs575445746 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105870503 | CTCACACCTGTAATT[C/T]CCAGCACAGTGGGAG | 8440 |
rs575514133 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, intron-variant | NCK2 | GRCh38.p7 | 2:105745105 | CCGGGACCCGCGCCG[C/T]TGCCCTCCGGCTCCG | 8440 |
rs575525858 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105758947 | AGTGATTCGTCCTCT[A/G]TTTGACACTGAACCA | 8440 |
rs575563935 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105822737 | GAATACATAACATTC[C/T]ATTCATTTTTCAGTG | 8440 |
rs575593631 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105786062 | CTTATTTGCCTTATT[C/G]TCACGTCCCTTCCAC | 8440 |
rs575603685 | in-del | -/TG | | | intron-variant | NCK2 | GRCh38.p7 | 2:105805802 | ATTGAATAATATTCT[-/TG]TGTGTGTGTATATAT | 8440 |
rs575627844 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105873976 | GAGTCATGGGCCTTC[C/T]CCCATGGCCAGCAAA | 8440 |
rs575635750 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105750107 | GCTAAAGCTGCAGAC[A/G]TTTATTTTCTCACAG | 8440 |
rs575638986 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105750958 | CCTTAGCAGAATGTG[C/T]ATGACGGTGGTGAGG | 8440 |
rs575685393 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105840353 | ATGTTTTCTTCCGAT[G/T]GCCTGAATTTCTGTT | 8440 |
rs575722148 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105749708 | CTGGATGTGAGTTGA[C/T]TGAGGTTGAGCGGTG | 8440 |
rs575723842 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105753342 | CCATTGGCCTGGCTG[C/T]TCCTCTCCCCCAGCC | 8440 |
rs575803359 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105824993 | GCTGCAGGCAAGTGA[C/T]GCTGCCCACATTTGT | 8440 |
rs575804857 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105847369 | TTGTTAAATATATTT[C/T]ATCACAACTTTGTAG | 8440 |
rs575810732 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105760239 | GTGGCACAGACAGCC[C/T]CTTGGCACTGTTGCG | 8440 |
rs575840298 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105846227 | CATTTCCCAGATTCT[A/G]GTTGAAGCGACAGTG | 8440 |
rs575857465 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105872837 | GAGTCAGAAATGATT[C/T]GGAGAAATCTCTGAA | 8440 |
rs575861287 | in-del | -/TC | 0.00318978 | 0.0398085 | intron-variant | NCK2 | GRCh38.p7 | 2:105832261 | GATCTGTTTACCAAT[-/TC]TACAGTATTTTGCTG | 8440 |
rs575869887 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105810233 | CTCACCCCCGATTCT[A/C]CTCCCTAAAAGTGTT | 8440 |
rs575897032 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105846497 | AAAAAAAATAATAGG[A/C]GGGTGTAGCAGAAAA | 8440 |
rs575897403 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NCK2 | GRCh38.p7 | 2:105850675 | GAGAAAAACATGCGT[G/T]GTTCTTTGGATCAGA | 8440 |
rs575907882 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105743163 | TGAAAAGATGATGGT[A/G]TTTCAGGAAATAGCA | 8440 |
rs575913587 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105891304 | ACTTACTGCCCTGTG[C/T]AGCCATCTGTACACC | 8440 |
rs575942510 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105858666 | TAACTCTGTGTAGTT[C/T]TCTCCTGCTTTCTTG | 8440 |
rs575964489 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105832873 | TATTTTGTTTCGTTT[C/T]GTTTTTGTTTCGTTT | 8440 |
rs575965507 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105795383 | TGGTTTTCTAATTAT[A/G]TGGTATATTGTAACT | 8440 |
rs575976209 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105890939 | TGCTGGACCCTCAGA[A/G]CAGGAAGTTTCTGGG | 8440 |
rs576014783 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105787915 | GCCCCCCACCGCCCC[C/T]GACTTGTAGATCCCT | 8440 |
rs576020210 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105889868 | AGGGATTACAGGTGT[C/G]AGCTTCCATGGCTGG | 8440 |
rs576034368 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105889226 | TACAGCAGTGTCCCA[C/G]CTGTCCCTTCAGGGG | 8440 |
rs576104855 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105755466 | GGGTGCAGCCGATTC[C/T]GTCTTCCATAAGAAG | 8440 |
rs576117835 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105819114 | CTCCTGGTCGGCAGT[A/C/T]GGGGGTTGGCACTCA | 8440 |
rs576144055 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105794166 | TGATTCTCCTGCTTC[A/T]GCCTCCCAAGTAGCT | 8440 |
rs576209571 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105769160 | ACTAAGGGCACTCTT[A/G]TTGCTCAGTAAATAC | 8440 |
rs576212504 | snp | A/C/G | | | upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105744003 | TGTGTCTGTGAAAGG[A/C/G]AAACTTGTGTCTTTC | 8440 |
rs576216130 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105860013 | ATCAGGGCTGGGCAC[A/G]ATGGTTTATGCCTGT | 8440 |
rs576237753 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105812267 | AAGAGACAGCTGAGG[G/T]CATCTCCTTGGACAC | 8440 |
rs576242687 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105762816 | GTTAATAAGGAAATA[C/T]GTAGATTACTATGTC | 8440 |
rs576266048 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105799950 | CATTTTGCAAAGTTT[A/G]TAAGAATCCCTCCCA | 8440 |
rs576292577 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105775662 | AAGAATAATCAGCTA[A/G]TTACAACTGTTTGAA | 8440 |
rs576307603 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NCK2 | GRCh38.p7 | 2:105861804 | ATAGGCATGAGCCAC[C/T]GCACCCGGCCAGTTT | 8440 |
rs576327134 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105810534 | TGGTGTTGTCACTAC[A/C]TAGACAATGGCTGAA | 8440 |
rs576328892 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105768257 | TAGCTGGACTCACCA[C/T]CCCTTGAGTGCTCAG | 8440 |
rs576348817 | snp | A/C | 0.000399281 | 0.0141238 | downstream-variant-500B | NCK2 | GRCh38.p7 | 2:105894320 | AGACTCAATCATGGG[A/C]GAGTAATTACTGAAG | 8440 |
rs576365817 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105829383 | ATTTAGCATCTAGTT[A/G]CCCTTATGATGAACT | 8440 |
rs576396749 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105801402 | ACCAGCACGTGGTTG[A/C]GGGATGTGCTTTTTT | 8440 |
rs576415003 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105764154 | TCACGTGGGTGCATG[C/T]TGTTTGCACGCCTGT | 8440 |
rs576449211 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105744125 | ACTCCTTCTAGGGGC[A/C]CATTCGGGCAGCTCC | 8440 |
rs576507284 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105856734 | AGCTCACTGGCCATC[A/G]TAGATTCTCAGCCTG | 8440 |
rs576529196 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105833861 | CTGTGTTTCCATTTT[A/T]ATGTTGTTTCAGATT | 8440 |
rs576542378 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105856263 | ACAGTATTTACTGCC[C/T]CAGATTACCTGAGAA | 8440 |
rs576581048 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105813542 | ATAGTTGGAGGAAAC[C/T]AGCCCAGGTGCAGCA | 8440 |
rs576590444 | in-del | -/AT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105780319 | TAATATGGGAGAGAG[-/AT]ATATATACACACACA | 8440 |
rs576592867 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105773710 | CAACAACTATTTGAG[C/T]ACCTACTCTGAGCCA | 8440 |
rs576596211 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105848800 | TCAGTTGCATTTTAA[A/G]GCATGAGATATTACA | 8440 |
rs576599492 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105862559 | CCGCTTTGTACGTTT[G/T]GGGGGACTCTGTCCC | 8440 |
rs576674379 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105814235 | AGAGATGTTGACCAC[C/T]ATGTTTTATTCTACT | 8440 |
rs576695965 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | NCK2 | GRCh38.p7 | 2:105825783 | GCAGTAAATATACAC[C/T]CTGCTCTGTCAGTTA | 8440 |
rs576707830 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105807224 | GTTACTGTCCTGTGA[C/T]GCACCTGCGTGGGAA | 8440 |
rs576709695 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105856083 | TTGTGATCCGCCCAC[C/G]TTGGCCTCCCAAAGT | 8440 |
rs576715106 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105820306 | ACAGCTCGGTCAGCC[A/G]TACACTTCGGCATGT | 8440 |
rs576736829 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105820415 | GACACTCAAGGTTTG[C/T]GTGCCTGGGGCTGGG | 8440 |
rs576768587 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NCK2 | GRCh38.p7 | 2:105775944 | AGCACCACCACCAAC[A/G]AAAAAAACAGTGCGA | 8440 |
rs576775561 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105874694 | AGCTGGAAGATGACA[G/T]GCAGAGCATGTTTTA | 8440 |
rs576789332 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105868870 | GGGCAGCCAAGCGAC[C/T]TGGCCAGGGCTATGA | 8440 |
rs576829075 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105882435 | CCCAGAGAAAGCATT[A/C]TTTGCAAGACTGGTG | 8440 |
rs576845652 | in-del | -/TGTGTGTGTGTGTGTA | 0.240478 | 0.249819 | intron-variant | NCK2 | GRCh38.p7 | 2:105830693 | GTGTGTGTGTGTGTG[-/TGTGTGTGTGTGTGTA]TGTGTGTGTGTGTGT | 8440 |
rs576868572 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105825910 | TGATCCGTCAGGTTT[A/G]GAGTTCCTGGCTCCA | 8440 |
rs576884066 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105759074 | AGTGTTTTGAATGAA[C/G]TTAATTTGCAAATAA | 8440 |
rs576890843 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105889937 | GCTCATGCTGCTGGT[C/T]TTGAGAGCACACTTG | 8440 |
rs576896644 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105874012 | GGGAAGGCTCGGGGT[C/G]AGATGGGGCCCTTCA | 8440 |
rs576903637 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105783428 | CCGCGTGGAACATGG[C/T]TTTTATTTAGAGTAA | 8440 |
rs576945701 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105889172 | CTCCATCTCCATCAG[A/T]TGCAGGGACTGGTGG | 8440 |
rs576966318 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105779079 | TGGGAGGCTGAGGCA[A/G]GTGGATCACTTGAGG | 8440 |
rs576983776 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105757033 | TGGTCTTGAACTCCT[C/G]ACCTCGGGTGATCTG | 8440 |
rs576988546 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105857346 | TGGGCCCGCGCCCGT[C/T]CCCGACAGATGGCCA | 8440 |
rs577005666 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105800528 | TACAATTCAGGATTA[C/T]GTAAGAGTGGCATAT | 8440 |
rs577023843 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105888129 | GATGATAGAGGCCCC[A/G]AGAGAGGTTGGTTTT | 8440 |
rs577026610 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105807480 | AGCATACAGCTGATA[C/T]CTATGTAATTTGAGA | 8440 |
rs577069627 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105847523 | AAATGCAGGTGTGCA[A/G]CGGAACTGGCCTCCC | 8440 |
rs577091248 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105769689 | GCCAGGGGTCCACGC[A/G]GCTTCCGCCCTGAGG | 8440 |
rs577099889 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105880778 | GTCACTGGTATTCCC[A/G]CATTTTTTGGTTTTA | 8440 |
rs577100878 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | NCK2 | GRCh38.p7 | 2:105856823 | TTCATCTTTTCTTCC[C/T]CCACATAAGCATGCC | 8440 |
rs577153739 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105793559 | TGGCAGTTTTCAGAG[C/T]AAATAGTTCTGGTTC | 8440 |
rs577158866 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105875623 | CAGAGAGCACCCTTG[C/T]TGCTTCTGCCATGTG | 8440 |
rs577188352 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105751551 | CCTTCCCCATATACA[C/T]ACATGCTGAGCTACA | 8440 |
rs577221296 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105885629 | CAGGAGGTCTGGGGC[C/T]CAAGAATTTGCATTT | 8440 |
rs577223281 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105893394 | TAGAGGAGGGGAGGA[A/G]CAGGGCGAGTTCACA | 8440 |
rs577226829 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK2 | GRCh38.p7 | 2:105842283 | TAGAGACAGGGTTTC[A/G]CCATGTTGGTCAGGC | 8440 |
rs577247294 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105802006 | TGCCCTGTCACCTGC[C/T]GGTTCAGTGCTCCTC | 8440 |
rs577269764 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NCK2 | GRCh38.p7 | 2:105849916 | TGGCACATCCGGCCT[C/T]AGGACTTTGTTTACA | 8440 |
rs577283510 | snp | A/G | 1.68255e-05 | 0.00290043 | missense, synonymous-codon | NCK2 | GRCh38.p7 | 2:105892986 | TTCCTCCCCAGCCCA[A/G]CGACTTCTCCGTGTC | 8440 |
rs577308278 | in-del | -/GACTCCACTGTCAAGT | 0.0023933 | 0.0345097 | intron-variant | NCK2 | GRCh38.p7 | 2:105760012 | TAGTGTTTGTCAGGG[-/GACTCCACTGTCAAGT]GACTCCACTGTCAAG | 8440 |
rs577315730 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105758235 | CCATCACATTTGATA[C/T]AGAGATGTAAGTAAT | 8440 |
rs577325584 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105801438 | TTTTTTTTTCTCCTC[A/G]CAGTCTATTTACACA | 8440 |
rs577332876 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105834832 | GATGTGTGCTACCAT[A/G]TCTGGCTAAATTTTA | 8440 |
rs577355728 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105770489 | TAAGGTTGTGTGTGT[A/G]TATGCGAATGTGTGT | 8440 |
rs577400655 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | NCK2 | GRCh38.p7 | 2:105773186 | TTACAGGCATGAGCC[A/G]CCTACCATCTGGCCG | 8440 |
rs577488218 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105772422 | CGGGGAATGTGGGCA[A/T]AGTCCTGGGTTTCAC | 8440 |
rs577513115 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105840408 | AAAATATGCAGTTTC[G/T]CCTACTCTACTCTAC | 8440 |
rs577518145 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105814847 | AGCCCAAACAACTGC[A/G]TAAAACAATTCCTTG | 8440 |
rs577519714 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105799347 | TTTACTTTTTCATTG[C/T]AAATCTTGGATACCT | 8440 |
rs577554082 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105878875 | AGAAGTATAAGCTCT[A/G]TGCAGGCAGAAAGCA | 8440 |
rs577556472 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105866071 | AGGCATGCGCCGCCA[C/T]ACCCAGTTGATTTTG | 8440 |
rs577577812 | in-del | -/CTA | 0.00914312 | 0.0669923 | intron-variant | NCK2 | GRCh38.p7 | 2:105848934 | GACTCAATTTTTTTT[-/CTA]CTAACTGAACTCTAA | 8440 |
rs577586252 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105754903 | GCAGAATCTAGCAAG[A/G]TGGTTATAGAAACAG | 8440 |
rs577596848 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105814328 | GCATGCAACCTTCAC[A/G]TTTTACACTTGAATC | 8440 |
rs577608591 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105798714 | AACAGAATGAAAATA[A/T]ACTGTGGGTGTCTAT | 8440 |
rs577638890 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105865430 | CTTGTGATTGCTGTT[C/T]AGTCTCAGGAATTGG | 8440 |
rs577656888 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105800321 | ACGGGGTAATGAGGT[A/G]TTGTCTTGTTGTAAA | 8440 |
rs577681096 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105762499 | GTGTGAAGTTCTGAG[G/T]GATTTCCTAAAGACG | 8440 |
rs577717847 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105780104 | TGAGCATATTTTGGA[C/T]GTACTAGAAATGAAG | 8440 |
rs577728694 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105852939 | TCCTCCTTCCCAAAA[A/G]GTTTGTTATCTTTAA | 8440 |
rs577730045 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105860128 | CATCTCTACAAAAAA[A/T]TTTTTTAAAAAATAG | 8440 |
rs577737584 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105838532 | GAATAATATAAAATT[G/T]AAATTTTTTAATGGA | 8440 |
rs577774072 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105845554 | ATGTACCAGCATGCC[C/T]GGCTAATTTTTTGTA | 8440 |
rs577784829 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105756886 | CTTGGCTCATCACAA[C/T]CTCCCCCCTCCTGGG | 8440 |
rs577794233 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105777629 | CTATAAATGACTTCA[A/G]TTGCAGCTGTTCTCC | 8440 |
rs577821731 | snp | A/G | | | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105772327 | CCCATGGAATAAACA[A/G]CACTAAGCATCCTTC | 8440 |
rs577835641 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105859502 | GAAACTTGCATGATC[A/T]GCCCCAGAACTCCTG | 8440 |
rs577847752 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105880461 | GTGAAGATGATGGGT[G/T]TTGCCCAGTAGGGCT | 8440 |
rs577852436 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NCK2 | GRCh38.p7 | 2:105787098 | TGCAGGCGTGGTGGC[A/G]CTGGGCAGCTGCTGT | 8440 |
rs577856103 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105819612 | GTGGCATGCTCACCC[A/G]GCAGCTCAGTCTGCA | 8440 |
rs577880895 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105846795 | AAACTAGAATTACCA[C/T]ATGACCCAGCAATTT | 8440 |
rs577894835 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105869108 | CCTCTCATAGACCCA[C/T]AGTGCTCCCCCTAGC | 8440 |
rs577918839 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105810989 | GACCATCCTGGCCAA[C/T]ATGGTGAAACCCCGT | 8440 |
rs577934420 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105855450 | TTAAGAGATGAAGAT[A/G]GAGAAAGAGGATGTT | 8440 |
rs577938676 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105786710 | GGGCTTCCTGTCTCC[A/C]TCGCTGTCTCTTATT | 8440 |
rs577938992 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105792974 | AGTCTTTCCCTTTCT[C/T]ACCAACCGAGTCAGC | 8440 |
rs577946338 | snp | A/G | 0.00318978 | 0.0398085 | downstream-variant-500B | NCK2 | GRCh38.p7 | 2:105894454 | TGAGTTTTAATTAGT[A/G]AAACCCCAAGGGAAC | 8440 |
rs577993437 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105816775 | ATTAGATTATCTCTG[C/T]TCCTGCTTTAGTGTG | 8440 |
rs578014516 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105774526 | TGGTGTGTTGAGCCC[C/T]TGGAACAATGTATTT | 8440 |
rs578028903 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105819248 | AAGACAGACACCATC[A/G]GGGTGTTCCTGTTCC | 8440 |
rs578042582 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105781769 | AGCTGTCGCCTCTCC[A/G]CAGTACGAAAATTTG | 8440 |
rs578048595 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105873394 | ATGTGGCCTCCCAGC[A/C]TCACAGGTTTCTCAT | 8440 |
rs578054627 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105825147 | AGTCCATGCCTACCA[G/T]CTGTAATGTAATGGG | 8440 |
rs578058134 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105768654 | ATACTTAAACTTTCT[C/T]AAAACATGATGAGTT | 8440 |
rs578077653 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105873281 | CCACTGTGCCTAAGA[C/T]ACTGGCCCCAGTGAA | 8440 |
rs578098897 | in-del | -/AAAAC | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105778981 | CAATATTTAAATGTT[-/AAAAC]AAATAATTGAGAATA | 8440 |
rs578126291 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | NCK2 | GRCh38.p7 | 2:105861941 | TCCCTCCCTCCTGCC[C/G]GCTCCCCCCTTCCCT | 8440 |
rs578193608 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105843325 | TCAAGTTTTGGATTC[A/G]GAGCATTTTGGATTT | 8440 |
rs578209424 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK2 | GRCh38.p7 | 2:105755303 | AGGAGGGTGTCAGAC[A/G]TCGTGCTGTTGTGAT | 8440 |
rs578212792 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NCK2 | GRCh38.p7 | 2:105830428 | TTTTTTTCTGGCTGA[A/G]TAGTATTCCACTGTG | 8440 |
rs578219615 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NCK2 | GRCh38.p7 | 2:105879436 | GTTGAACCATCCTGC[A/C]TTTGAAATCCTATGA | 8440 |
rs578241507 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105778531 | CTTGGTTCTGGGCAG[C/G]CTCTCCATGGGGATT | 8440 |
rs578257956 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | NCK2 | GRCh38.p7 | 2:105748395 | GCAGTTGTTTTTTTT[C/T]TTTTTTTAAGGCAGG | 8440 |
rs745313669 | in-del | -/TTC | | | intron-variant | NCK2 | GRCh38.p7 | 2:105807700 | TTTTTTTTTTCTCTT[-/TTC]TTTTTTCCTTCCTTC | 8440 |
rs745334779 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105873589 | CACGTTTTCAGATGG[G/T]AATCAACAGTTTGGC | 8440 |
rs745361416 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105765576 | AGACTGTTCTGTGGG[G/T]ACTTGTTTGGGGCAT | 8440 |
rs745406503 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105864490 | AGGAGACTGAGCCAC[A/G]GTGCGTAGTGGAGTT | 8440 |
rs745424219 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105775406 | TTCCAGGTAGATAGA[C/T]AATTATTTTTAACCG | 8440 |
rs745426812 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105843142 | TACATATACATAAAT[C/G]AGATATCTTGGGAAT | 8440 |
rs745446434 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105857272 | CTGTGATCGGTTCAG[C/T]CAATGCGTGTACTCC | 8440 |
rs745496863 | snp | C/T | 1.72913e-05 | 0.0029403 | intron-variant | NCK2 | GRCh38.p7 | 2:105892963 | GCCCGGCTGTAACTG[C/T]GTTCTGTTTCCTCCC | 8440 |
rs745514962 | snp | C/T | 3.33667e-05 | 0.00408439 | missense | NCK2 | GRCh38.p7 | 2:105855194 | GGCGGGTGAGGAACG[C/T]GGCCAACAGGACGGG | 8440 |
rs745535594 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105869401 | ACAGCCCCACGGGTA[A/C]CAGGGGTTTCCTTGT | 8440 |
rs745535939 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105856091 | CGCCCACCTTGGCCT[C/T]CCAAAGTGCTGGGAT | 8440 |
rs745542773 | snp | C/T | 1.65957e-05 | 0.00288055 | intron-variant | NCK2 | GRCh38.p7 | 2:105855302 | TAGGTGAGTGTTTCA[C/T]CCTCGAGAGAGGAAG | 8440 |
rs745544346 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105774589 | TGGGCAGGTGTCCAC[C/T]GCAGGTCTGGTCATG | 8440 |
rs745544406 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105785412 | GGACACAGGAAAAAA[A/T]TGTTGTGTTGTCCTA | 8440 |
rs745608918 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105796556 | TGTGGCACAGAACGC[A/T]GGTGTTCAGATCGGC | 8440 |
rs745616415 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105746874 | ATGGAGAACTTTAGG[C/T]ATAGGAAGCTGTGGA | 8440 |
rs745646266 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105758008 | TTCCAGGGCCTGGAT[A/G]AAGCTCAGTTAGTTT | 8440 |
rs745660545 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105773857 | CTTTTGTTCTTATGC[A/G]GTGTTTTGGGTAGTC | 8440 |
rs745661855 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105775734 | TGGGAGCCTGGCTGG[C/T]ATCACTGGGAGCACC | 8440 |
rs745695284 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105868157 | TAACCGATGGACCTT[C/G]GCAAGTATGGGTGGA | 8440 |
rs745711187 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105880656 | ACCCATTCTAGGAAT[G/T]AAAAAGATATTTTCT | 8440 |
rs745744730 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105848278 | CCCAAAGTCACCCAG[A/C]TGGTTGATATGAAGC | 8440 |
rs745761417 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105806388 | GACTACAGGCACCCA[A/C]CACCACGTCCGGCTA | 8440 |
rs745828163 | snp | A/G | 1.6519e-05 | 0.00287388 | missense, intron-variant | NCK2 | GRCh38.p7 | 2:105881738 | TCAGTCACCGAGGAG[A/G]AGCTCAACTTCGAGA | 8440 |
rs745834850 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105847440 | TGAATAATATGTACT[A/T]TAATTACTGTTTAAG | 8440 |
rs745908571 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105832180 | TTTCAGCTAGTTTGT[C/T]ATTGGTATATAGAAG | 8440 |
rs745938085 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105749839 | ATTCCTGTTTAGTGC[A/G]TGTATTAGTCAGCTC | 8440 |
rs745944583 | in-del | -/TT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105861514 | GTTGAGGTTTTTCTC[-/TT]TTTTTTTTTTTTTTT | 8440 |
rs745955753 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105787935 | TGTAGATCCCTGGCC[C/T]ATTGGCAGAAGTGAG | 8440 |
rs745963941 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105781338 | CTGACACAGGGGCAG[C/G]CTTCTCCCATCTCCG | 8440 |
rs746038704 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105789702 | AGGACCTTGCTCCCC[A/G]GCTTGTGATTCTCAA | 8440 |
rs746094322 | snp | C/T | | | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105771990 | AAAATTGGATATTGT[C/T]GTCAAAGTGTCCAGG | 8440 |
rs746094550 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105883788 | TAAAGAACTAAAGCA[C/T]GAATTGTTTGTATTT | 8440 |
rs746163342 | snp | A/G | 5.7063e-05 | 0.00534118 | utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105893187 | AGTGACGGCGCCCCG[A/G]CCCCACACTCGCCTC | 8440 |
rs746174788 | snp | A/G | 0.000121506 | 0.00779346 | synonymous-codon, intron-variant | NCK2 | GRCh38.p7 | 2:105881386 | CCCCACGCCCAGCAC[A/G]GACGCCGAGTACCCC | 8440 |
rs746216795 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105782136 | TTGCTTTTGGGCTTC[C/T]GCGAGAGTGGGAGCC | 8440 |
rs746258734 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105749860 | TAGTCAGCTCCAGCT[A/G]CCTTAAGAGAATAAC | 8440 |
rs746284953 | snp | A/G | | | upstream-variant-2KB, intron-variant | NCK2 | GRCh38.p7 | 2:105850673 | GAGAGAAAAACATGC[A/G]TTGTTCTTTGGATCA | 8440 |
rs746367074 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105831870 | GTATTTCTTTGGCTA[G/T]TTGAGGTCTTTTGTG | 8440 |
rs746393916 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105766724 | GGTCTGCAGGTGAAC[A/G]TCGAACCAGCCCTGG | 8440 |
rs746404630 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105852723 | ATTCCTGTTACTGCT[A/G]TTGCTCTTCTTCTTG | 8440 |
rs746455916 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105886059 | CCGTGATCCATGGTG[C/T]TTCTTCATAAATGAG | 8440 |
rs746484624 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105774410 | GTGATGATGGTCTGA[C/T]TGGTCTGACAGATGC | 8440 |
rs746565352 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105773629 | ATGGTTCATTTCTTA[C/T]ATGCTAGAGCATCCT | 8440 |
rs746585225 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105824379 | GGAATATGCCACTTA[C/T]GATCTTACCCAGAGG | 8440 |
rs746592318 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105825626 | ACATAGCAATGTCCA[C/T]GTTATCACATAGCAG | 8440 |
rs746638698 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105823631 | AGAGTATATTAACAA[G/T]ATGCCAGTTTTGGAT | 8440 |
rs746651316 | snp | A/G | 5.66257e-05 | 0.00532068 | synonymous-codon, intron-variant | NCK2 | GRCh38.p7 | 2:105881974 | CTACGGGAACGTGAC[A/G]CGGCACCAGGCCGAG | 8440 |
rs746669898 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105854041 | AGTTGAGGCCTTAAA[A/G]GGAAGAAGATTCAAA | 8440 |
rs746682649 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105783742 | GGTGAAAAATGATGA[A/C]CTCCACTCTTTCCAA | 8440 |
rs746688013 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105866934 | AGAAGCTGATTCTTT[A/G]TGGTGCATTTGTCTT | 8440 |
rs746692898 | snp | A/G | 1.6686e-05 | 0.00288838 | intron-variant | NCK2 | GRCh38.p7 | 2:105855043 | TCCAAATGTTTTGCT[A/G]GCAGAAGGACTCCAT | 8440 |
rs746745967 | snp | C/T | 1.65644e-05 | 0.00287783 | missense | NCK2 | GRCh38.p7 | 2:105855181 | TCCAAGACGTGGTGG[C/T]GGGTGAGGAACGCGG | 8440 |
rs746754605 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105757222 | GCTAAAATTGCATAG[C/T]GAAGTTTTAAACTCT | 8440 |
rs746789660 | snp | A/G | | | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105771514 | ATGTTGCAGTAAGCC[A/G]AGATTGGGCCACTGT | 8440 |
rs746806094 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105791253 | AATGTTGATTCATCT[A/G]GAGAAACCTGAGGCA | 8440 |
rs746819868 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105842602 | GACATCTGACTCTTG[A/G]GTTATAGCCACTGAG | 8440 |
rs746842801 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105778264 | TCCCTATCCCAGCAC[A/G]TGTGGTAGTGACCTT | 8440 |
rs746850875 | in-del | -/TTGT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105884229 | GGACAAGTCCTTTGC[-/TTGT]TTTTTTCCCACCATC | 8440 |
rs746893563 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105815957 | CCTTGATTATGGGCT[A/G]GCTGTTCCCCCACAC | 8440 |
rs746900978 | in-del | -/TTG | | | intron-variant | NCK2 | GRCh38.p7 | 2:105891567 | TTTTTTTTTTTTTTT[-/TTG]AGATTTTTCGCTCTT | 8440 |
rs746955345 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105777566 | CCAAAATGGAAAAAC[A/G]AAACAAATGAAAAGT | 8440 |
rs746972416 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105859998 | CAGTTCAAAACAACA[A/G]TCAGGGCTGGGCACG | 8440 |
rs746987219 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105845104 | ATCCACTCTCCCACT[G/T]CAATAGGAAAATCTA | 8440 |
rs747004722 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105751545 | ATATCCCCTTCCCCA[C/T]ATACACACATGCTGA | 8440 |
rs747008561 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105891203 | TCTCACATCTGCGCA[C/T]GCTCACACACTTAGA | 8440 |
rs747014757 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105785661 | AACATCCGCTCAGGT[A/G]TTTGCAGGTATGCCC | 8440 |
rs747018579 | snp | A/G | 3.31741e-05 | 0.00407259 | missense, intron-variant | NCK2 | GRCh38.p7 | 2:105881670 | GCGCCTCGCTGAGCA[A/G]TGGCCAGGGCTCCCG | 8440 |
rs747020004 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105838495 | ATACTCCCTGTACTT[C/T]CACCCTTTTACCAAA | 8440 |
rs747022768 | snp | C/G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105797583 | ATGGCTGGAATGGAG[C/G/T]GTGGAGCCTGGTCTG | 8440 |
rs747053789 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105869574 | CCACCTGCGTGTTCC[A/C]CCGTGAATGTGCTGT | 8440 |
rs747067645 | in-del | -/A | | | intron-variant | NCK2 | GRCh38.p7 | 2:105801329 | CCAGCCCCAGCCCTT[-/A]ACGTCTGTTGACCAG | 8440 |
rs747070744 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105825900 | AGTGTCCTGGTGATC[C/T]GTCAGGTTTGGAGTT | 8440 |
rs747074489 | in-del | -/TT/TTT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105758413 | TTTTTGTTGTTTTTG[-/TT/TTT]TTTTTTTTTTTTTTT | 8440 |
rs747086963 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105761209 | GGGAGGTTTGGGTGT[C/G]TATGGGAGCGGTGGT | 8440 |
rs747100896 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105777171 | CACTGGGCACTCCAC[C/T]GATGGCAGCTGGAAC | 8440 |
rs747123934 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105837456 | TGGTGATTTCTTGGT[G/T]TTCACTTTCTTGGTA | 8440 |
rs747147634 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105796681 | ATTCCAGAAGCTCTC[A/G]GCATCATGTTTATTC | 8440 |
rs747163708 | snp | A/G | | | upstream-variant-2KB, intron-variant | NCK2 | GRCh38.p7 | 2:105850429 | ACCCATTCCCATCCA[A/G]GACTTGAAAAGGCAG | 8440 |
rs747165313 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105807415 | TACAAGTTGTTCTTT[A/G]TAGAAATAAAAAGTG | 8440 |
rs747173225 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105808567 | GTAACCACCAGTTTA[C/T]TACAAATGCCAGGGC | 8440 |
rs747216689 | in-del | -/TTAC | | | intron-variant | NCK2 | GRCh38.p7 | 2:105854732 | TATCAGGAGGCAGTG[-/TTAC]TTAATGAAATGGACT | 8440 |
rs747217047 | snp | A/C | 1.65228e-05 | 0.00287422 | synonymous-codon, intron-variant | NCK2 | GRCh38.p7 | 2:105881725 | GTACCCCTTCAGCTC[A/C]GTCACCGAGGAGGAG | 8440 |
rs747217650 | snp | C/T | 1.65864e-05 | 0.00287974 | synonymous-codon, intron-variant | NCK2 | GRCh38.p7 | 2:105881563 | GCGGGGCAGCTACAA[C/T]GGGCAGATCGGCTGG | 8440 |
rs747244269 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105781137 | ATTGTTTTACTTCTC[C/T]TCTTATAAACTATTA | 8440 |
rs747245954 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105769473 | ACATTTCTAAGGAAG[C/T]TTAGAGATACAAAAT | 8440 |
rs747257654 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105863743 | GAGCATGTAGCATTG[C/T]GGGCAGGAGGGAGGA | 8440 |
rs747259951 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105848903 | TCAAGGTAGGGATGA[C/T]AGTATTTTTCATATA | 8440 |
rs747265944 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105828267 | ATTGGGCACCGTTCA[A/G]GATTGCTGAAAATGT | 8440 |
rs747304524 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105817247 | AAGGTTTTACCTGTT[A/C]ATATGAAAAACCTAC | 8440 |
rs747364824 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105780432 | TCGTTTGGTATCTGG[A/G]TTAAAATTCTAATGT | 8440 |
rs747377712 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105874289 | AGCAACACAAAAACT[G/T]GTAGAAGCTGAGCTG | 8440 |
rs747378725 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105830263 | AGTAACCTCTATTCT[A/G]TTCTCTACTTTTATG | 8440 |
rs747446871 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105790369 | CCTGGGCTTCTCAAT[A/G]CCATAGGCTGGCAAG | 8440 |
rs747449570 | snp | A/G | 7.93966e-05 | 0.00630016 | missense, utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105893117 | GAACACTACAAAAAG[A/G]CGCCCATCTTCACCA | 8440 |
rs747482512 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105753857 | AATTCCAAGGTGGCT[G/T]TGAAATCTGCTTCTG | 8440 |
rs747497677 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105765360 | TGACTTTAAAATGGC[C/T]CTTGAATTTCAGGGA | 8440 |
rs747500810 | snp | C/T | 1.74967e-05 | 0.00295771 | missense, intron-variant | NCK2 | GRCh38.p7 | 2:105881376 | GGGATGCGTCCCCCA[C/T]GCCCAGCACGGACGC | 8440 |
rs747525415 | in-del | -/CCTG | 1.94801e-05 | 0.00312084 | intron-variant | NCK2 | GRCh38.p7 | 2:105881294 | GTGGTGCCCAAGTGC[-/CCTG]CCTGCGCCACTGAGC | 8440 |
rs747547016 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105841594 | GGCCATGGATAATCA[A/C]CTTGACCTCAGCCCC | 8440 |
rs747566679 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105749671 | GTGTCGCAGCTGTGT[C/G]TAGATATTGGTGGAG | 8440 |
rs747585294 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105800570 | TAGCCCATAGAAGGC[A/G]GAAACCCAGCTGACA | 8440 |
rs747604745 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105783643 | TGAGCATCATGAAAT[A/G]CCTTAGCACGAAGAA | 8440 |
rs747622762 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105758252 | GAGATGTAAGTAATT[G/T]AATCACATTACTTCT | 8440 |
rs747636275 | snp | A/C/T | 6.69718e-05 | 0.00578637 | synonymous-codon, intron-variant | NCK2 | GRCh38.p7 | 2:105881443 | CTACGACCTCAACAT[A/C/T]CCGGCCTTCGTCAAG | 8440 |
rs747637204 | snp | A/G | | | upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105744226 | GGCAACAGAGGTCGA[A/G]TTTCTTCTTCTTTTA | 8440 |
rs747643428 | in-del | -/TTT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105845398 | CATTTATATTTTGAA[-/TTT]TTTTTTTTTTTTTGA | 8440 |
rs747649369 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105755295 | AAAAAAGGAGGAGGG[A/T]GTCAGACATCGTGCT | 8440 |
rs747743332 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105878351 | TGGAGACAAAGCCTT[A/T]ACAGGGGTGATTAAG | 8440 |
rs747746274 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105782673 | TGATAGAACCTGATC[A/G]TTTCTGAGAGTGGGG | 8440 |
rs747788968 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105890211 | GCGAAAATTTTATTG[C/T]TGCAACTCATGCATG | 8440 |
rs747791836 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105865605 | ACCCTAGGGATTCAC[A/G]TCTTTGTAACTTTTC | 8440 |
rs747811244 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105888656 | ATGGGCTGCACTGAG[C/G]AACTCACTTCTAATG | 8440 |
rs747822398 | snp | A/G | 1.80546e-05 | 0.00300449 | missense, intron-variant | NCK2 | GRCh38.p7 | 2:105881886 | ACGGGCCTGCCCTGC[A/G]CCCTGCGCACGCCCC | 8440 |
rs747832804 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105804553 | AATTGGATTTCAGCC[C/T]AGACACAGTATTTGA | 8440 |
rs747840426 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105767453 | AGTAATTGATTTAGG[A/G]ATATCTGTTACTCTT | 8440 |
rs747848519 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105876564 | ATGTTCTGGTTGGCT[A/G]TGGTTTCATTATGGT | 8440 |
rs747868740 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105846085 | AAATGCTGGCACCAG[A/G]GAATCACTTGACAGT | 8440 |
rs747869239 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105793174 | GTAGGACATCTTTAA[G/T]GAAGGGATTGGGCAT | 8440 |
rs747869528 | snp | C/T | 3.73406e-05 | 0.00432075 | synonymous-codon, intron-variant | NCK2 | GRCh38.p7 | 2:105881962 | CAGAGAGTGGTACTA[C/T]GGGAACGTGACGCGG | 8440 |
rs747945951 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105845052 | AGGTAGGTACAGGTT[A/C]TTGTCCCTAGAGCGG | 8440 |
rs747972635 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105750309 | GAGGGCCCCACCCTT[A/G]TGGTGACCTTTTTTA | 8440 |
rs747986593 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105867870 | AAGTTTACGAATAAA[C/G]AAACGTGAACCAAAT | 8440 |
rs747999247 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105790995 | GTGTTAGAACCTGCA[A/G]GAGTTGGAAGGCACT | 8440 |
rs748000839 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105815147 | ATCTGCCTAGTATAC[A/G]TTTGAACTTCTTGCC | 8440 |
rs748028708 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105859754 | TTGTTACGTAAGATC[C/T]AAAAGCAGTGAAAAG | 8440 |
rs748051937 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105814635 | GATTAGAGATGTGCA[A/G]AGCCCACTCATCCGG | 8440 |
rs748090753 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105871904 | ACTACATGACACCTG[A/C]CAACAACAGGAACCT | 8440 |
rs748114244 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105786775 | CCTCCCTTCTGCCTC[C/T]CCCACGCATTGCTTC | 8440 |
rs748149589 | in-del | -/AA | | | intron-variant | NCK2 | GRCh38.p7 | 2:105795158 | TGAAACTGCACTGAC[-/AA]AAACCAATCACCCAA | 8440 |
rs748177897 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105749161 | GGTTAGTCTGTTCCT[A/G]TCAACCTGAATTCAA | 8440 |
rs748203090 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105794872 | GTTCGCATGGTTCCG[C/T]AGCCAAAGATGGTTA | 8440 |
rs748216799 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105879943 | ATTAAGGTAGAGGTC[A/G]AAGCAGAGCTGTGGT | 8440 |
rs748220802 | in-del | -/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105754679 | AGCTCCCCCAACAAC[-/T]TTTTTTTTTTTTTTT | 8440 |
rs748236441 | in-del | -/TGTGTGTGTGTGTGTG | | | intron-variant | NCK2 | GRCh38.p7 | 2:105823135 | AGTCCTCTCATGCTG[-/TGTGTGTGTGTGTGTG]TGTGTGTGTGTGTGT | 8440 |
rs748242094 | in-del | -/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105843394 | ACTGTGGTCCCATAA[-/G]GAAAAAAAAAAAAAA | 8440 |
rs748247708 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105769222 | AGGGACCAAGACCAG[A/C]GATCTTTTTTATTAT | 8440 |
rs748282022 | snp | A/G | 0.000489596 | 0.0156384 | synonymous-codon, intron-variant | NCK2 | GRCh38.p7 | 2:105882007 | CGCCCTCAACGAGCG[A/G]GGCGTGGAGGGCGAC | 8440 |
rs748291823 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105817108 | TTGAACCTGGGAGGC[A/G]GAGGTTGCAGTGAGC | 8440 |
rs748295860 | snp | A/T | 1.65883e-05 | 0.00287991 | missense, intron-variant | NCK2 | GRCh38.p7 | 2:105881571 | GCTACAACGGGCAGA[A/T]CGGCTGGTTCCCCTC | 8440 |
rs748299981 | in-del | -/CTCG | 0.000140657 | 0.00838502 | utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105893195 | CGCCCCGGCCCCACA[-/CTCG]CCTCCCGGGCCCCAC | 8440 |
rs748304411 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105806427 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCGTGT | 8440 |
rs748314858 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105848447 | ATAAAAACAGAAGAC[A/C]GATCATGAAAGGACT | 8440 |
rs748327037 | in-del | -/A | | | intron-variant | NCK2 | GRCh38.p7 | 2:105844575 | AAAGTAGAAAAAAAC[-/A]AAAAAAAAAAAAAAC | 8440 |
rs748391607 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105800370 | ATAAAGAGGGCCTAG[C/T]CTGGTCTGTGGTACC | 8440 |
rs748395451 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105790220 | GTTAGAAATAGTGTG[C/T]ATGTCATTAGGATCT | 8440 |
rs748414848 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105848160 | TTGTCCAGCACAGAC[C/T]GAGTGTTAGGTATTT | 8440 |
rs748434616 | in-del | -/TTTTG | | | intron-variant | NCK2 | GRCh38.p7 | 2:105767981 | ACAAAAAAATGGACA[-/TTTTG]TCAGTACTTGTGTTT | 8440 |
rs748435528 | snp | G/T | 1.66029e-05 | 0.00288117 | synonymous-codon, intron-variant | NCK2 | GRCh38.p7 | 2:105881662 | GCGCAAGGGCGCCTC[G/T]CTGAGCAATGGCCAG | 8440 |
rs748500339 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105764282 | ATCCGCACCCTGCAG[A/G]TTAAGGAGAGCCTGT | 8440 |
rs748503933 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105861344 | ATACAGACGTCACAT[A/G]TCTTGTGAAAGGAAG | 8440 |
rs748561841 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105872285 | CGCTACCTTCCCCCC[A/G]CCACCAGGCCTGCCC | 8440 |
rs748569630 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105799160 | CTCCTAGCTTTTTAT[G/T]TGTCTTTGGAATCTA | 8440 |
rs748573125 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105841434 | TAGAGGTGTAGGTAG[C/G]GTGAGGTACAGGGGA | 8440 |
rs748592885 | in-del | -/TCT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105832840 | AGTTAGGAAGAATTC[-/TCT]TCTCTTTTTTTTTTT | 8440 |
rs748601250 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105799750 | GAGGGATGCTTCCCT[C/T]TACCTCAAGCCTAAA | 8440 |
rs748625193 | snp | C/G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105774255 | CTCAAGTTATCCCCC[C/G/T]GCCTCAGTCCTCTAA | 8440 |
rs748625327 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105763276 | GGAGAGCGGGACCTC[A/G]CCAGGGACCAGGTGT | 8440 |
rs748639099 | snp | G/T | | | intron-variant, utr-variant-5-prime | NCK2 | GRCh38.p7 | 2:105745620 | CCCCGGCGCAGGGAC[G/T]GGGGAGGCCGCGATC | 8440 |
rs748639333 | snp | C/T | 2.28464e-05 | 0.00337975 | intron-variant | NCK2 | GRCh38.p7 | 2:105882078 | GCCCACAGCTCCGGC[C/T]GCAGGCAGTAAATGC | 8440 |
rs748646636 | in-del | -/TCTT | | | upstream-variant-2KB, intron-variant | NCK2 | GRCh38.p7 | 2:105850869 | GGGTCATCTGCAGTC[-/TCTT]TCTGTTCAAATCCAT | 8440 |
rs748654239 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105811564 | CCTTGTCTTTAAGGA[A/G]CATCTGAGTCCCTGC | 8440 |
rs748676364 | snp | C/T | | | intron-variant, utr-variant-5-prime | NCK2 | GRCh38.p7 | 2:105773443 | CCTCCTTGTTTCCCA[C/T]ATGCTCAGCTCAGGG | 8440 |
rs748679430 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105853833 | ACATCAGGGGTGGAG[C/T]GTGGGGATTCTGGCT | 8440 |
rs748681921 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105793002 | AGCTTTTCCCTAATG[A/G]TGGGATTCTTTCCTG | 8440 |
rs748686837 | snp | C/T | 3.36389e-05 | 0.00410101 | synonymous-codon, stop-gained | NCK2 | GRCh38.p7 | 2:105892987 | TCCTCCCCAGCCCAG[C/T]GACTTCTCCGTGTCC | 8440 |
rs748708999 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105767677 | TCCAGAAGAAGAACC[G/T]CAGCCCCTAGTGTGC | 8440 |
rs748724222 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105746582 | GGTGAATTAGTAACA[C/G]GATTCAAGCCTTGCG | 8440 |
rs748792551 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105839657 | GACGTGAGATTTGAA[A/G]TGCATGTTAGACATC | 8440 |
rs748806487 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105803572 | ATTTCTACAGCTAGG[A/G]AAGTGCGGAACTGGC | 8440 |
rs748832890 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105876102 | CAGCATGCCAGCCAT[C/T]GGAAGGGTTTTGTAA | 8440 |
rs748836635 | in-del | -/TTTT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105748387 | TCTTTCCTGCAGTTG[-/TTTT]TTTTCTTTTTTTAAG | 8440 |
rs748836666 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105864027 | GAGGATGTGAAGACG[C/G]AAACCCATAGGTGTG | 8440 |
rs748860185 | in-del | -/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105881093 | TGGCCCTGTGACATG[-/T]TTTTTATGGATAAAA | 8440 |
rs748866548 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105791887 | AGTGAACTGATTTTT[A/C]TTTTTGGGAGGAGCA | 8440 |
rs748876363 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105891051 | ATGTCCGAGGTACCA[G/T]CCCTGCCTCGGAGAG | 8440 |
rs748910074 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105821911 | TTGCTTACCAGCCCA[C/T]GTTCCTTCTGCTTCC | 8440 |
rs748913648 | in-del | -/AG | | | intron-variant | NCK2 | GRCh38.p7 | 2:105871228 | CAAGGAGATAAATAC[-/AG]AGAGATGAGGAGGAT | 8440 |
rs748918155 | in-del | -/TAAAA | | | intron-variant | NCK2 | GRCh38.p7 | 2:105770124 | TAAAGCACTAATAAG[-/TAAAA]AAAAAAAAAAAAAAG | 8440 |
rs748935902 | snp | C/G | 1.78554e-05 | 0.00298787 | missense, intron-variant | NCK2 | GRCh38.p7 | 2:105881361 | GGAAGACCAGCGCGC[C/G]GGATGCGTCCCCCAC | 8440 |
rs748976988 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105858384 | GCCTCCCGAGTATCT[C/G]GGACTACGGGCATGC | 8440 |
rs748983870 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105752721 | CAAGTCTCTGGTTCC[A/G]TCTGGATAATGGCCT | 8440 |
rs748987312 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105776638 | GGTTAGCTGGTGAGC[A/G]GATGATGCCAGCTAG | 8440 |
rs749083344 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105825671 | TCTTGTTTTATTAGA[C/G]ATTTTTTACGGAGCC | 8440 |
rs749128300 | snp | C/T | | | utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105893265 | CTCCCGCGGGGACGG[C/T]CCCGACGGCTTCTCT | 8440 |
rs749130766 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105760994 | GGGATTGGGATCTGG[A/G]TGGCCCTCATCCTGC | 8440 |
rs749139474 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105857386 | GCTGGAGCGCAGCGT[A/C]GGTTCGAGTAGGCCA | 8440 |
rs749163599 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105837256 | AGGCCATCTTAATGA[C/T]GTCAAGCTCCTTGAT | 8440 |
rs749184973 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105770037 | GTGCAGAGTACAGTG[A/T]GTCAAACCATTGAGA | 8440 |
rs749212106 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105867580 | GAGGACAAGGCAGGA[A/G]AGACCCTGGGAAGTG | 8440 |
rs749219349 | snp | A/G | | | upstream-variant-2KB, intron-variant | NCK2 | GRCh38.p7 | 2:105850207 | TTCACCTTGATCCCC[A/G]TGACCTCTTTGGAAA | 8440 |
rs749231203 | snp | G/T | 1.7958e-05 | 0.00299644 | synonymous-codon, intron-variant | NCK2 | GRCh38.p7 | 2:105881875 | GGTCCTCAGTGACGG[G/T]CCTGCCCTGCACCCT | 8440 |
rs749251935 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105760042 | TGACTCCACTGTCAA[A/G]TGACTCTTTTCCCTT | 8440 |
rs749325039 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105816879 | CACACTCAGATATTA[C/G]TGACTCTTGAATCCA | 8440 |
rs749337403 | snp | C/T | | | missense, utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105893064 | ACAATGTCTACTGCA[C/T]TGGGCAGCGGCGCTT | 8440 |
rs749381790 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105778439 | CGTGGGAAGTGGTGG[A/T]GTGTAAGAACACACC | 8440 |
rs749420938 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105793240 | GGAATGGGTGGAGAA[C/T]TTCTGGAAACCAGAG | 8440 |
rs749430904 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105751782 | TGCAGAAAATGGTGC[A/G]TATGTGTGTTTTAAT | 8440 |
rs749434603 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105861016 | GCAGGTGGCTTAGGA[A/G]AGTCAAACCTGGTGT | 8440 |
rs749436694 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105789452 | CCTCGGCCTCCCAAG[A/G]TGCTGGGCTTACAGG | 8440 |
rs749440596 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105813584 | GCCAGCACCACACAG[A/G]CATTGGGGATGCAGA | 8440 |
rs749441352 | snp | A/G | 8.57008e-05 | 0.00654546 | utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105893198 | CCCGGCCCCACACTC[A/G]CCTCCCGGGCCCCAC | 8440 |
rs749453821 | in-del | -/CA | | | intron-variant | NCK2 | GRCh38.p7 | 2:105891207 | ACATCTGCGCACGCT[-/CA]CACACTTAGAGCTGC | 8440 |
rs749455741 | in-del | -/TTTTTTTTTTTTT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105880942 | AGGTGGCTAATTTTT[-/TTTTTTTTTTTTT]TTTTTTTTTTTTTTG | 8440 |
rs749460243 | in-del | -/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105876344 | GGGAGGCATTGGAAC[-/T]TGTCTGGGTGTTCTG | 8440 |
rs749465792 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105860110 | GGGAACATAGCAAGA[C/T]TTCATCTCTACAAAA | 8440 |
rs749516650 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105872161 | TGCTTTGCTCGACAC[A/G]TTTCTGCCAGCCTCA | 8440 |
rs749531743 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105885398 | TATATGAAAAGTATT[A/T]GGCTGGGAAATAAAA | 8440 |
rs749533189 | in-del | -/ATCT | | | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105771867 | CTGCCCATCACTCAG[-/ATCT]ATCTATATTTTTCTC | 8440 |
rs749536605 | snp | A/G/T | 3.33229e-05 | 0.00408173 | missense, intron-variant | NCK2 | GRCh38.p7 | 2:105881462 | GCCTTCGTCAAGTTC[A/G/T]CCTATGTGGCCGAGC | 8440 |
rs749542425 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105799662 | ACTATATGAAAGCCT[A/G]TAAAAAGCTAATTAC | 8440 |
rs749548214 | in-del | -/AGACAAT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105874082 | GTTCTGAACAGATTA[-/AGACAAT]AGAACCATGACATTA | 8440 |
rs749582191 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105839992 | ACATGCAGGTAACAA[A/G]AGGACCTTTGGATCT | 8440 |
rs749591659 | snp | A/G | 1.65743e-05 | 0.00287869 | missense, intron-variant | NCK2 | GRCh38.p7 | 2:105881550 | GCGACGGTTGGTGGC[A/G]GGGCAGCTACAACGG | 8440 |
rs749621537 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105797765 | CCTGATGTTGTGGCC[G/T]CCTGTCAGCTTTTGT | 8440 |
rs749652019 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105888219 | TCAAATGAATGGGTT[C/G]TACTAATTGTTCATT | 8440 |
rs749657700 | in-del | -/TC | | | intron-variant | NCK2 | GRCh38.p7 | 2:105754094 | ACGGTGAGTCTGGCG[-/TC]TCTGTTGGGAGAAGC | 8440 |
rs749668298 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105853348 | CAAAATTGACTTTAC[A/T]GGATATATAATACAC | 8440 |
rs749703296 | snp | A/G | | | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105772070 | GCCTGTGGAACTGCC[A/G]ATCCTGGCTCAGCCG | 8440 |
rs749724375 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105832580 | TTGTTCTTCATTTTG[G/T]TGATGTGATGTATCA | 8440 |
rs749752785 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105847101 | TAAATGAGGTACCTG[A/G]AGTTGTCAAATTCGC | 8440 |
rs749765385 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105808737 | ACTTGGATCCTGATT[C/G]AAGTAAATCAGCTAC | 8440 |
rs749769741 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105783779 | TGGCCTGTTCCTGAG[C/T]GACTTCAGTGTGCTT | 8440 |
rs749778887 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105822119 | TGTACCAGGAATTTC[A/G]TGAGATTTATTTTTT | 8440 |
rs749800047 | in-del | -/TG | | | intron-variant | NCK2 | GRCh38.p7 | 2:105816078 | GGAAGAGGGAGTACA[-/TG]TGTGTTGATGGAGGT | 8440 |
rs749917160 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105859388 | TGGCTCACCCTGCCA[C/T]CCTACCTACCTGGGA | 8440 |
rs749973874 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105870325 | GCTGCTTGGGGTTTC[C/G]CTCAGGGATGGCAAC | 8440 |
rs750010957 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105870983 | CAGAGCAGGGTCAGC[A/G]TGTTGTGTGCTTGGG | 8440 |
rs750011086 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105858059 | GGGGTTTTTTTTTTG[G/T]TTTTTTTTTTGCTAA | 8440 |
rs750014790 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105825476 | GAAGTAGGAAGCAGC[A/C]CTGGGCACTGCAGCG | 8440 |
rs750023932 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105883213 | ATCAAGTCACCAGAG[G/T]TTATCATTCCTGGCA | 8440 |
rs750029278 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105748644 | GCTGGTCTCAAACTC[C/T]TGGGCTCAAGTGAGC | 8440 |
rs750051010 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105837769 | AACACATTATCAACC[A/T]TTTTCATTTTTACCC | 8440 |
rs750063366 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105797238 | CCCCTATTTCAGCTC[C/T]TATACTAGTGTTTTA | 8440 |
rs750069895 | in-del | -/TAAA | | | intron-variant | NCK2 | GRCh38.p7 | 2:105770124 | TAAAGCACTAATAAG[-/TAAA]AAAAAAAAAAAAAAA | 8440 |
rs750135733 | snp | C/T | 1.68724e-05 | 0.00290446 | missense, utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105893075 | TGCATTGGGCAGCGG[C/T]GCTTCCACACCATGG | 8440 |
rs750166680 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105760817 | GAGAGGCAGAGACAC[C/T]GAGACCCCACGTGGA | 8440 |
rs750177299 | snp | G/T | 1.87205e-05 | 0.00305939 | synonymous-codon, intron-variant | NCK2 | GRCh38.p7 | 2:105881341 | AGGCCTCGGCAAGAC[G/T]CGCAGGAAGACCAGC | 8440 |
rs750189009 | snp | C/T | 3.032e-05 | 0.00389347 | synonymous-codon, utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105893158 | GGAGAAGCTCTACCT[C/T]GTCAGGGCCCTGCAG | 8440 |
rs750192683 | snp | A/G | | | upstream-variant-2KB, intron-variant | NCK2 | GRCh38.p7 | 2:105851224 | TGCCTCCTTCATTGA[A/G]GATACCGGGCTGCTA | 8440 |
rs750221277 | in-del | -/CTG | | | intron-variant | NCK2 | GRCh38.p7 | 2:105818839 | TTCCTCTTACTTGGT[-/CTG]CTACTACTACAAACA | 8440 |
rs750260726 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105748842 | TGTGAATAATGAGTG[C/T]CCAGCCTGTTAATAT | 8440 |
rs750287761 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105807048 | ACTTTTCAAATGACC[C/T]GTGATGTAATGTGGA | 8440 |
rs750297390 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105820383 | ATGTCAGCCTTGGAT[A/G]CATTTCCCAGTTATT | 8440 |
rs750306092 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105755570 | ATTGCACGTTCATGC[A/G]TGTGGCTTCTCATTC | 8440 |
rs750314125 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105863443 | GAGAACAGTAACCAA[A/G]GGCTTTGAAACAGGG | 8440 |
rs750336837 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105780885 | GGACTTCCAGCTTCC[A/G]CAACTGTGGGAAATA | 8440 |
rs750352344 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105819185 | CTAGCTTTGGGTCCC[C/T]TCATGCATTCATAGG | 8440 |
rs750353533 | snp | A/G | | | upstream-variant-2KB, intron-variant | NCK2 | GRCh38.p7 | 2:105851518 | TGCCTGGGGCTCCCA[A/G]AGTGCTGGGATTACA | 8440 |
rs750384319 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105754523 | AGCCTGGCTACAGGA[A/G]AGGAGAGCAGTTGCT | 8440 |
rs750404069 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105873887 | TGCTGCAACCCTGGC[C/T]ATGTCCTCCTAGGGA | 8440 |
rs750411829 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105882375 | TGCCCATTCTGTGTA[C/T]GTAGAAGGCCCGAGT | 8440 |
rs750455423 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105783424 | AGGCCCGCGTGGAAC[A/G]TGGTTTTTATTTAGA | 8440 |
rs750464687 | snp | C/G | 1.79425e-05 | 0.00299515 | missense, intron-variant | NCK2 | GRCh38.p7 | 2:105881872 | GGTGGTCCTCAGTGA[C/G]GGGCCTGCCCTGCAC | 8440 |
rs750465829 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105799588 | TGCCACACCAAACAC[A/G]AGCTGATGAGTTATT | 8440 |
rs750471308 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105800667 | TTGAGATAAATGGAC[C/T]GAGAGAGTGGGTTTG | 8440 |
rs750476066 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105860422 | AGGATGGACAGAGCC[C/T]CTGCTCTGGTGTAGT | 8440 |
rs750482346 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105763067 | GCCAGGCGTGGTGGT[A/G]TGTGCCTGTAGTCCC | 8440 |
rs750505904 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105840913 | GGTAAAAGGCCGTGG[C/G]CATCTGAAAGGCTGC | 8440 |
rs750512578 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105885237 | TAAGATTTTAGTTCC[C/T]GAAGATATCATGTAT | 8440 |
rs750532600 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105855014 | AGTGTCCGGGTAGTT[C/T]TCTAATGAGCATCTC | 8440 |
rs750536539 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105839918 | GCTGTGTGATCTCCG[C/T]GCAGCTGGTGGACGG | 8440 |
rs750553259 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105867653 | GTGGAGTTCACAGTG[G/T]GGTGTGTGGGATTCA | 8440 |
rs750565855 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105889566 | GAGCCTGAGAATTTG[A/C]ATTTCTTTTTTTTTT | 8440 |
rs750621886 | snp | C/G | | | intron-variant, utr-variant-5-prime | NCK2 | GRCh38.p7 | 2:105773267 | CAACATCAGCAATTG[C/G]AGTTGTTTCTCGAAT | 8440 |
rs750622265 | in-del | -/TTT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105794046 | TATTGTATCTTTCGA[-/TTT]TTTTTTTTTTTTTTT | 8440 |
rs750648011 | snp | A/G | 1.8275e-05 | 0.00302278 | missense, intron-variant | NCK2 | GRCh38.p7 | 2:105881918 | CAGATAAGCTACACC[A/G]GGCCCTCGTCCAGCG | 8440 |
rs750656280 | snp | C/T | 1.97322e-05 | 0.00314098 | synonymous-codon, intron-variant | NCK2 | GRCh38.p7 | 2:105882019 | GCGGGGCGTGGAGGG[C/T]GACTTCCTCATTAGG | 8440 |
rs750715370 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105757635 | GCAAACCAGACAAAC[A/G]CCAGCCTTTGGGGAG | 8440 |
rs750764777 | in-del | -/CT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105770000 | TGGTGCCTCCATTTC[-/CT]TCACTGGAAAATGGG | 8440 |
rs750771445 | snp | A/G | 3.2963e-05 | 0.00405961 | missense | NCK2 | GRCh38.p7 | 2:105855130 | GACCAGGAGCTGGAC[A/G]TCAAGAAGAACGAGC | 8440 |
rs750792914 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105771134 | TCACTCTGTTAGCCA[A/G]GATGCTCTCGATCTC | 8440 |
rs750798227 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105821407 | AAATGGGCCCATCTC[A/G]GCCTCCTTCTGCCGC | 8440 |
rs750822216 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105832744 | GCATCTATGTTCATC[A/G]GGCACATTGGCCTGT | 8440 |
rs750865270 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105804387 | GTCTTTTCTGTCTTT[A/G]TGCCCAGTTAAAAGG | 8440 |
rs750871633 | in-del | -/TTTTTGGG | | | intron-variant | NCK2 | GRCh38.p7 | 2:105841526 | CATCTGAACCCTGTC[-/TTTTTGGG]TTTTTATGGAAGCTT | 8440 |
rs750924189 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105815587 | GCAGTGAACATAACG[C/G]AGCTGCCAGCTCTCC | 8440 |
rs750929190 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105892011 | ATGCGACCGGAATTT[C/T]CCACTGCTGTTCATA | 8440 |
rs750977650 | snp | A/G | 1.662e-05 | 0.00288266 | missense, intron-variant | NCK2 | GRCh38.p7 | 2:105881633 | GCTGCGGAGTCCCCA[A/G]GCTTCCTGAGCCTGC | 8440 |
rs750997508 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105803375 | GACTTTGAACTCTAA[A/T]TAGGCTGAGCTCCTT | 8440 |
rs751050312 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105827340 | ACCAAACAACAGAGC[A/T]GTGAAATAAGAAGTA | 8440 |
rs751056357 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105785327 | TGTGTGTCCAAGTGT[A/G]AAAAGAACCAGAGGA | 8440 |
rs751064755 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105797048 | TCATCACAGTCCCTT[G/T]TTTATTTTAACTTTA | 8440 |
rs751109991 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105796445 | TTGCTGTTTTAAGGG[A/T]CATGTATGTAAATAT | 8440 |
rs751127594 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105774882 | CGTGTAGATGTACAG[C/G]TGAAAAAACGCTTTC | 8440 |
rs751128620 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105807692 | CTCTCTCCTTTTTTT[C/T]TTCTCTTTTCTTTTT | 8440 |
rs751136694 | snp | C/G | | | upstream-variant-2KB, intron-variant | NCK2 | GRCh38.p7 | 2:105850976 | GGGATGCAACTTCAA[C/G]TCTCGGCCAACAAGA | 8440 |
rs751149846 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105835930 | TTTGAGGCTCTCAAT[G/T]TTTTTATTTAATTCA | 8440 |
rs751150918 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105836875 | GACTCAGGGAGTAGG[A/G]GCTACCCAGCATGAA | 8440 |
rs751162805 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105849533 | CTTCCCATTAAACCA[A/G]GTGGCTGAAGCCTAA | 8440 |
rs751211620 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105769739 | GCCAGGCGGCCACAG[A/G]AGCCACTGTGGCAGG | 8440 |
rs751218903 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105761310 | CTGACTGACTTCCAG[A/G]GAATCTTTTTTTGGG | 8440 |
rs751256548 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105880505 | GGGGTGAGGGTGGGG[C/G]CAGTGAGTGTCCCAG | 8440 |
rs751262557 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105780807 | GACACAGCAAGAAGC[C/T]GCCGTGTAGGAACCA | 8440 |
rs751376214 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105815037 | GTCAGCATGAGAAAC[A/G]AGAACTCTTGGTCAA | 8440 |
rs751430450 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105752965 | TTCCATGTAATAACT[C/G]ATTGAGTCCTCACCA | 8440 |
rs751433196 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105816744 | CATTAAATTTAAGCT[C/T]TCAATGAGGGAGAAA | 8440 |
rs751441679 | snp | A/G | 3.3095e-05 | 0.00406773 | missense, utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105893052 | TGCAGCTCGTGGACA[A/G]TGTCTACTGCATTGG | 8440 |
rs751445334 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105872912 | TTGAGCAGTGAGTAC[A/G]TTCTGATGCCCTTCC | 8440 |
rs751474429 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105875871 | AAACACCGTAATTTT[A/G]TGATGATAGATTTAA | 8440 |
rs751501433 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105794405 | TTTGTCCCTAGGATC[A/G]TTTACGTAATGACTT | 8440 |
rs751514128 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105828505 | AGTGCAGAATTTAAG[C/G]ATGTGATAGGTAATG | 8440 |
rs751522745 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105872075 | TCCTTAAACGTACGC[A/G]GTTCTTAATGGTGAG | 8440 |
rs751531697 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105809569 | TTCATTTTAACCACC[G/T]CTTTAAAGACCTTTT | 8440 |
rs751537554 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105800181 | GCTCTCCCTGGTCTC[C/T]GGCACGGGGGCCACA | 8440 |
rs751541163 | snp | A/C | 3.81105e-05 | 0.00436506 | missense, intron-variant | NCK2 | GRCh38.p7 | 2:105881330 | TGTGTCTCCACAGGC[A/C]TCGGCAAGACGCGCA | 8440 |
rs751565739 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105764138 | TCGCTTTGCAGAGCT[C/T]TCACGTGGGTGCATG | 8440 |
rs751568264 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105783018 | ATTTGCAACAGGTAA[G/T]CCTTAAGGCCAGAGC | 8440 |
rs751648952 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105821768 | GGGGACACAAAGCCT[C/T]AGGAGAGGTTAAGGA | 8440 |
rs751659598 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105853109 | TCATCCCTATACAAT[A/G]ATGAGAACTTCTCTG | 8440 |
rs751676420 | in-del | -/TGTCAGGGGACTCCAC | | | intron-variant | NCK2 | GRCh38.p7 | 2:105760004 | GGCCCAGGTAGTGTT[-/TGTCAGGGGACTCCAC]TGTCAAGTGACTCCA | 8440 |
rs751691726 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105793533 | GCATTGCACTGGCTA[A/G]CAAGTTTATTTGGCA | 8440 |
rs751708723 | snp | C/T | | | upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105743739 | CTGACTTCAAAGCTA[C/T]GCTGACTCTAGTTAC | 8440 |
rs751747464 | snp | A/G | | | upstream-variant-2KB, intron-variant | NCK2 | GRCh38.p7 | 2:105851624 | GTTTCAGAAGCGGAA[A/G]CGTTCAGGGATTGGT | 8440 |
rs751752022 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105832546 | GTTTTCTACATTTAT[C/T]GAGATGATCATATGG | 8440 |
rs751764931 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105781982 | GAAGTTGAGAATGTC[C/G]AAGTGAGTCCAAATT | 8440 |
rs751765891 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105865004 | GGTCACCAGAGCCCT[C/T]CCCAGCAGGAGGCCT | 8440 |
rs751776241 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105756417 | AGTAATTCTTTGCAC[A/C]GACTGGAAAGTTCTG | 8440 |
rs751779511 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105749212 | TGATCCTGGCCTGGT[A/G]AGTTAGTTATTTGTG | 8440 |
rs751819709 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105781093 | CCCACCCACCTATTC[C/T]GGGGTTGGCTTTCAA | 8440 |
rs751821862 | in-del | -/TG | | | intron-variant | NCK2 | GRCh38.p7 | 2:105848005 | GTTGGCACATCTTTC[-/TG]TGTTTAAGTTTTCTG | 8440 |
rs751850850 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105800355 | TGATTGAGATAGTGC[A/T]TAAAGAGGGCCTAGT | 8440 |
rs751867472 | snp | A/G | 0.000176682 | 0.00939732 | missense, intron-variant | NCK2 | GRCh38.p7 | 2:105881847 | TGGGCCTCGTCCCCA[A/G]AAACTACGTGGTGGT | 8440 |
rs751879373 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105767117 | GCTTATCTCTCTGGA[A/G]CCAGGGAGGCTCCGA | 8440 |
rs751920917 | snp | C/G | 1.82065e-05 | 0.0030171 | missense, intron-variant | NCK2 | GRCh38.p7 | 2:105881910 | ACGCCCCACAGATAA[C/G]CTACACCGGGCCCTC | 8440 |
rs751928560 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105845550 | AGGCATGTACCAGCA[C/T]GCCCGGCTAATTTTT | 8440 |
rs751947127 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105870041 | ACCCATGTGGTGGTC[A/G]GGAGGGTGGGTCCTT | 8440 |
rs751949148 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105838902 | TCAGAGAAAATAAAC[A/G]ATAAATAAATTAAAA | 8440 |
rs751970413 | in-del | -/AA | | | intron-variant | NCK2 | GRCh38.p7 | 2:105811163 | CTGGTGACAGAGTGC[-/AA]AAAAAAAAAAAAAAT | 8440 |
rs751972323 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105776326 | CTCCAAATATCTTAA[C/T]ATTTCAACATCTTCT | 8440 |
rs751987233 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105844257 | GTGACAACTAAATGT[A/G]GTGTGGGATCCTGGG | 8440 |
rs752020831 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105801766 | TCATTTTCGTGTCCA[C/G]TCGGGGGAACAAAGT | 8440 |
rs752035585 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105870277 | CTGAGGAGGCAGGGG[G/T]CCAGCAGCCCTAACC | 8440 |
rs752041841 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105826133 | TCAGCATAACTGGGA[A/G]GCCTCAGGAAACTTA | 8440 |
rs752075505 | snp | A/G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105786262 | GATTATTTTGAATCT[A/G/T]TGTAATAACCGTAGT | 8440 |
rs752109757 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105775215 | GCACTGTGTGTGGCA[A/T]GTGGGTGCCTAATCA | 8440 |
rs752134465 | snp | A/G | 4.78641e-05 | 0.0048918 | utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105893178 | GGGCCCTGCAGTGAC[A/G]GCGCCCCGGCCCCAC | 8440 |
rs752142101 | in-del | -/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105837572 | GCCCTGAGCACTGTG[-/C]CATGTCCCTGAGGCA | 8440 |
rs752147534 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105813862 | AAGAGATACGTACGG[A/T]ATCAGTGTTAATTGC | 8440 |
rs752158645 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105769687 | GGGCCAGGGGTCCAC[A/G]CAGCTTCCGCCCTGA | 8440 |
rs752235841 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105847114 | TGGAGTTGTCAAATT[C/T]GCAGGGACAGAAAGT | 8440 |
rs752238129 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105768280 | GTGCTCAGTGGCCGC[A/G]TGTGGCCGGTGGCTG | 8440 |
rs752248805 | snp | A/G | | | intron-variant, utr-variant-5-prime | NCK2 | GRCh38.p7 | 2:105773369 | CGCCGTCTGGTACAC[A/G]TGCCGGCCTCCATCA | 8440 |
rs752262504 | in-del | -/TGA | | | intron-variant | NCK2 | GRCh38.p7 | 2:105880209 | TACTGTAATTGTGTT[-/TGA]TGCACTGAAATTTTC | 8440 |
rs752283243 | snp | A/G | 1.65877e-05 | 0.00287986 | synonymous-codon, intron-variant | NCK2 | GRCh38.p7 | 2:105881488 | CGAGCGGGAGGATGA[A/G]TTGTCCCTGGTGAAG | 8440 |
rs752297150 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105778155 | GAGATGTTGGCAGGC[C/T]TCTGGGACTGGGTCC | 8440 |
rs752318410 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105848051 | ATCTATTGCACATAC[A/G]TTTTTGAGTCCCCGT | 8440 |
rs752344128 | in-del | -/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105774803 | ACACTGAGTACTGGG[-/T]TATCATCTATAAAGC | 8440 |
rs752379954 | snp | C/T | | | utr-variant-5-prime | NCK2 | GRCh38.p7 | 2:105816558 | AATTAGCTGAAAACA[C/T]CATCGTTTTGAAGAG | 8440 |
rs752414000 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105833324 | CTGATCTCGAACTCC[G/T]GGCCTCAGGTGATCC | 8440 |
rs752415784 | in-del | -/TGTGTGTGTGTGTGTC | | | intron-variant | NCK2 | GRCh38.p7 | 2:105823159 | GTGTGTGTGTGTGTG[-/TGTGTGTGTGTGTGTC]ACAATGGAGGGGGTG | 8440 |
rs752416456 | in-del | -/TTG | | | intron-variant | NCK2 | GRCh38.p7 | 2:105884228 | GGACAAGTCCTTTGC[-/TTG]TTGTTTTTTTCCCAC | 8440 |
rs752423174 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105765325 | ACATACTGTGACTAC[C/G]ATGTCCTTTTAAAAC | 8440 |
rs752433394 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105815829 | CTTCTCCGTCATTAG[A/C]CTCTCAGACTGGCCA | 8440 |
rs752440879 | snp | A/G | 6.65126e-05 | 0.00576644 | synonymous-codon, intron-variant | NCK2 | GRCh38.p7 | 2:105881623 | GGACGAGGCGGCTGC[A/G]GAGTCCCCAAGCTTC | 8440 |
rs752461932 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105764102 | GCTAAGCAATTTGTC[C/T]GAGTGCTAGTCCTGG | 8440 |
rs752525846 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105788779 | TCTTATATAGCTTAA[A/C]TCAGTTACAAACAAG | 8440 |
rs752570009 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105762989 | TGCCTGAGCTCAGGA[C/G]TTCGAAACCAGCCTG | 8440 |
rs752575936 | in-del | -/CTTTACC | | | intron-variant | NCK2 | GRCh38.p7 | 2:105769976 | GACTTGTGCTGGCTA[-/CTTTACC]CTTGGTGCCTCCATT | 8440 |
rs752583252 | in-del | -/GTA | | | intron-variant | NCK2 | GRCh38.p7 | 2:105799694 | ATGTTTACATAAATG[-/GTA]CAATAGCAGCCCAGA | 8440 |
rs752592960 | in-del | -/TT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105855835 | CCCCATGTGCCTCTT[-/TT]TTTTTTTTTTTTTTT | 8440 |
rs752615401 | snp | C/T | 2.06896e-05 | 0.00321627 | synonymous-codon, intron-variant | NCK2 | GRCh38.p7 | 2:105882046 | TAGGGACAGCGAGTC[C/T]TCGGTAAGTGCGCTG | 8440 |
rs752627258 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105871189 | CAGATCTGAGGCCAC[A/G]ATGGTGACTTTGTTT | 8440 |
rs752629376 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105884917 | CCTTCACCTGTGAGC[C/T]ATACCTGCTTAAATC | 8440 |
rs752646067 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105883449 | TCTTGGCTTAAAATT[A/T]TTTGAGTTTGAGGAG | 8440 |
rs752657608 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105839835 | ACCCCTCCATCTTTA[G/T]TTCAGAAGCACAAGT | 8440 |
rs752670187 | snp | A/G | 3.3006e-05 | 0.00406226 | missense | NCK2 | GRCh38.p7 | 2:105855163 | CTGTGGTTGCTGGAC[A/G]ACTCCAAGACGTGGT | 8440 |
rs752670557 | snp | C/T | 1.75838e-05 | 0.00296506 | intron-variant | NCK2 | GRCh38.p7 | 2:105892941 | TTAGACACAGCTCCC[C/T]GCTGTGGCCCGGCTG | 8440 |
rs752696692 | snp | C/T | | | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105773032 | TAGTAGCTGGGACTA[C/T]AGGTGTGTAGCACCC | 8440 |
rs752702780 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105810707 | CCTTAGAGAAACACC[A/T]GGGCAGACCTTTTAG | 8440 |
rs752720043 | snp | A/G | | | intron-variant, utr-variant-5-prime | NCK2 | GRCh38.p7 | 2:105745727 | GGTCCTCGCTTCGGC[A/G]AAGGGAGCTTTTGTG | 8440 |
rs752723534 | snp | A/G | 2.08792e-05 | 0.00323097 | synonymous-codon | NCK2 | GRCh38.p7 | 2:105855255 | GAACAGCCTGAAGAA[A/G]GGCTCCCTCGTGAAG | 8440 |
rs752752217 | in-del | -/AT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105819391 | TTTGCAAATGCAGTC[-/AT]GTATCAATCCACTTG | 8440 |
rs752758092 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105792652 | TTTGTTGGCAAAACC[C/T]GGTCTTTTGTCATTT | 8440 |
rs752761494 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105802831 | GGGCCATGGATGATG[A/T]CTGATCATCTGGAAT | 8440 |
rs752777726 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105838637 | ATTGTTTTAAATGAA[A/G]CACCTTAAATTTGAA | 8440 |
rs752784010 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105831240 | AGTGCAATCCCTATC[A/C]AAATACAATGATATT | 8440 |
rs752811237 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105791469 | CACCCTCGCCCCGTT[A/G]CCGTGCTTACCGGCC | 8440 |
rs752873337 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105875374 | CTCCTGCCCCGCCCA[G/T]TCCCCTGGGCTGTAC | 8440 |
rs752876777 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105820595 | CTTCTTTGGGGGAGC[A/G]GAGACCATAGGAAGA | 8440 |
rs752905710 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105766043 | CCAGACTTTGCTTCC[C/T]GCCAAGCAGGACTCC | 8440 |
rs752907062 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105882822 | TTCTACAATCGAGAG[A/G]CTTCCAAAACAAGCA | 8440 |
rs752908626 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105780361 | ACACACACACACACA[C/T]ACATTCATCTAAAGG | 8440 |
rs752930745 | in-del | -/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105873995 | ATGGCCAGCAAAGGC[-/G]GGGGAAGGCTCGGGG | 8440 |
rs752941450 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105830069 | TAATTAGCATATTCA[C/T]TCCCTCAAACATTTA | 8440 |
rs752945323 | snp | C/T | 1.65288e-05 | 0.00287474 | missense, intron-variant | NCK2 | GRCh38.p7 | 2:105881714 | GTCCAGACGCTGTAC[C/T]CCTTCAGCTCAGTCA | 8440 |
rs753008858 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105804491 | TGATGATTTCCACTT[G/T]GAGCTCAGCAGGAGG | 8440 |
rs753029975 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105857542 | GTCAGATCCTCTTCT[A/G]TAGAGTGTCAGCCCT | 8440 |
rs753031889 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105842801 | GACGGGACCCAGCCC[A/G]TGGCAGGAGAGGGCG | 8440 |
rs753033277 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105759664 | GTACATTATTGTTAA[C/G]TCCATAGTTTATTTG | 8440 |
rs753041762 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105813652 | CTGGCCCTGCGCCTG[A/G]GACAAGTAGTGTGGC | 8440 |
rs753059522 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105812907 | TCATGGGCTTGCTTC[C/T]TGATGTAGCCTGACA | 8440 |
rs753079921 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105869023 | AGCACTTATGTCTCA[A/G]TAACGTTTGTTTGTC | 8440 |
rs753089756 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105775088 | GAGTCACACCATGGT[G/T]TCTGAATACCTTGTC | 8440 |
rs753090615 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105760533 | TCCCTGCTGGTGGCA[C/T]CTAGCTCTAAGGCTC | 8440 |
rs753122043 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105856686 | ATGATTTGGAGAGAT[A/G]AGTGAGACATGGAAC | 8440 |
rs753148575 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105747502 | GGCTTGCCGTGTGCA[C/T]TGGGGGAGACAGGGC | 8440 |
rs753159981 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105796283 | GGCTTTGCTGCTCTT[G/T]CAAGGCTGTTTTGTC | 8440 |
rs753168125 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105880223 | TTGATGCACTGAAAT[G/T]TTCTACTTTATTCCC | 8440 |
rs753186132 | in-del | -/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105841432 | GTAGAGGTGTAGGTA[-/G]GGGTGAGGTACAGGG | 8440 |
rs753222918 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105824359 | TGTTTTATTTAGTGC[C/G]TTCCGGAATATGCCA | 8440 |
rs753224876 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105836650 | GTGCTGGACCACCTG[C/T]TCTACAGGGTGTAGG | 8440 |
rs753243958 | snp | C/T | 3.43342e-05 | 0.00414318 | missense, intron-variant | NCK2 | GRCh38.p7 | 2:105881820 | GGAAATGCAAAAATG[C/T]CCGGGGCCAGGTGGG | 8440 |
rs753270807 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105867890 | GTGAACCAAATATGC[C/G]AGGGAATTAGAGAAC | 8440 |
rs753272591 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105863407 | TCTGAGCCACTGCAT[C/T]CTCTGCTGTGAGTGA | 8440 |
rs753316459 | in-del | -/CT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105805637 | TTAACTACCGTTCTA[-/CT]CTCTATTTCCATGAA | 8440 |
rs753332048 | in-del | -/AT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105891358 | AGATTGTCACAGAGC[-/AT]ATGTCCTGCATGCAC | 8440 |
rs753363002 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105778041 | TCCTCACCTTCTTCA[G/T]CTGTGCTTGGAGGAG | 8440 |
rs753372876 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105790891 | GCAAGGGAGGAGAGT[C/T]CTCATCTGCAGGGCT | 8440 |
rs753391457 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105812307 | TCGGATTGATAAACA[C/T]ATCTAAGCTGCTCAG | 8440 |
rs753442099 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105787668 | TCTCTCCCTGCGGTG[C/G]AGACTCCACCCCATG | 8440 |
rs753448656 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105860670 | ATGTTCCTCTGCAGA[A/G]CTGGGGAGGAATTGG | 8440 |
rs753456462 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105871089 | ACAGGCCTGGAGGGT[C/T]GATGAGTGCGTGTGA | 8440 |
rs753461255 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105845802 | ATGGTGACTGTTATC[C/T]GTCTACTTTGGGAGC | 8440 |
rs753465168 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105871881 | GGACCTTAGAGAGCG[A/G]GGAGGAAACTACATG | 8440 |
rs753477649 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105859520 | CCCAGAACTCCTGCC[C/T]CTGATCCAACCCAGA | 8440 |
rs753485481 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105788725 | ATCCATAGAATGCAT[A/G]ATTTTTTTTGTTTGT | 8440 |
rs753525782 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105839500 | GGGATGAGTCTCAGA[C/T]TGGGGGCTGGGTCAG | 8440 |
rs753530666 | snp | C/T | 0.00013887 | 0.0083316 | synonymous-codon, utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105893168 | TACCTCGTCAGGGCC[C/T]TGCAGTGACGGCGCC | 8440 |
rs753546750 | in-del | -/TA | | | intron-variant | NCK2 | GRCh38.p7 | 2:105826806 | TTTTATATATGTGTA[-/TA]TATATATATATGTAT | 8440 |
rs753575284 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105780785 | CCTCACCCCTTCAGC[A/C]TGTGAGGACACAGCA | 8440 |
rs753586078 | snp | A/T | 0.000252162 | 0.0112258 | missense, intron-variant | NCK2 | GRCh38.p7 | 2:105881433 | CCGACCGCATCTACG[A/T]CCTCAACATCCCGGC | 8440 |
rs753614521 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105749890 | CACACAGAGGCCGGG[C/T]GCAGTGGCTCACGGC | 8440 |
rs753635815 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105762098 | AAAACAAGGACTTTC[A/G]CTTTGCTAGAAAATT | 8440 |
rs753636963 | snp | A/C | 1.66142e-05 | 0.00288216 | synonymous-codon, intron-variant | NCK2 | GRCh38.p7 | 2:105881477 | GCCTATGTGGCCGAG[A/C]GGGAGGATGAGTTGT | 8440 |
rs753644320 | in-del | -/ATGGTAAA | | | intron-variant | NCK2 | GRCh38.p7 | 2:105886635 | ATACTGTTGTGTAAT[-/ATGGTAAA]ATTCTGACTTAAATG | 8440 |
rs753683597 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105779055 | CTCACACCTGTAGTC[C/T]CAGCACTTTGGGAGG | 8440 |
rs753732231 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105809328 | GCCATGGGAAAGTAC[C/T]ACAGACTGAGGTGCT | 8440 |
rs753753402 | snp | C/G/T | | | upstream-variant-2KB, intron-variant | NCK2 | GRCh38.p7 | 2:105851551 | CGTGAGCCACCGCAC[C/G/T]CGGCCAGAGCTGAGC | 8440 |
rs753754809 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105854185 | TTCATGGCTTGATAG[C/T]TCATTTCTTTTTGGT | 8440 |
rs753775988 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105781879 | TGAATGAACTGGTAT[A/G]CGTGCATATGTATTC | 8440 |
rs753809385 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105882221 | TTACTTGCATCTGTT[A/T]TGGGGATAGTGGGTG | 8440 |
rs753855310 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105808468 | AAATCACGGATTAAT[C/T]GGGTGGTTCTCAGTG | 8440 |
rs753871179 | in-del | -/A | | | intron-variant | NCK2 | GRCh38.p7 | 2:105866360 | AATCAAGATCCTGTT[-/A]ACACAGATGGCTTCT | 8440 |
rs753883653 | in-del | -/GCAC | | | utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105893999 | TACACACACACACGT[-/GCAC]ACACACACACACACA | 8440 |
rs753894868 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105836227 | ATCTGCACTGTTAGC[A/G]AAATAGTTTCTTTTT | 8440 |
rs753913070 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105790142 | AGCTAAAAATACGGG[C/T]AGCCGTTTCTTCTTC | 8440 |
rs753913988 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105872973 | TGCCTGTCTTGGCAG[G/T]TGTGCTGTGACCCTG | 8440 |
rs753916614 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105829851 | AGATGGAGTGTCTAC[A/G]TAAGTTATTTAGAGT | 8440 |
rs753928335 | in-del | -/TTTTTTTTTTTTTTTTTT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105880937 | ACCACAGGTGGCTAA[-/TTTTTTTTTTTTTTTTTT]TTTTTTTTTTTTTTG | 8440 |
rs754019649 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105888679 | TTCTAATGACCAAGA[C/T]GTGGCAGAAGCGATG | 8440 |
rs754022221 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105838445 | TTGGAAGATTCACTC[G/T]TTATTACTGATCTGT | 8440 |
rs754039101 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105841101 | ACTCATTTCTTCCAC[C/T]TACCCAGAGATGACT | 8440 |
rs754043467 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105764245 | CTGTGGCACCACAGC[C/G]TTGACCCTTCAGCAC | 8440 |
rs754056117 | snp | C/G | 1.87064e-05 | 0.00305825 | synonymous-codon | NCK2 | GRCh38.p7 | 2:105855237 | CAACTACGTGGAGCG[C/G]AAGAACAGCCTGAAG | 8440 |
rs754062590 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105774923 | ACCAGTCCAGGCACC[A/G]GTGGCTTATGCCTGT | 8440 |
rs754086407 | snp | C/T | 1.6483e-05 | 0.00287076 | synonymous-codon | NCK2 | GRCh38.p7 | 2:105855141 | GGACATCAAGAAGAA[C/T]GAGCGGCTGTGGTTG | 8440 |
rs754119859 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105774089 | TCTTGGCTCACTGCA[A/G]CCTCTGTCTCCCAGG | 8440 |
rs754131355 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105747217 | GGCTTTGTCATTTAC[A/G]TTTTCGGTTATTTAG | 8440 |
rs754178751 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105746436 | GTTTTTCATGCCTCT[C/G]TTTTAGATGTAGTTA | 8440 |
rs754221666 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105823296 | CAGAACTGAAGGGAA[C/T]ACGTGGAACTGCAGA | 8440 |
rs754227086 | snp | C/T | | | intron-variant, utr-variant-5-prime | NCK2 | GRCh38.p7 | 2:105773166 | AGCCTCCCAAAGTGT[C/T]GGAATTACAGGCATG | 8440 |
rs754257460 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105867704 | TGGGTGAGAGCCAGT[C/T]GTGTCCTGGTGAAAG | 8440 |
rs754276004 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105879235 | CTTGACATCATTGTT[A/G]CCAATAAAAGTTGGC | 8440 |
rs754288623 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105847115 | GGAGTTGTCAAATTC[A/G]CAGGGACAGAAAGTA | 8440 |
rs754318345 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105835106 | GTGGTTTGCTGGTTT[C/T]CTTCAGTGGTAATAT | 8440 |
rs754321714 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105805675 | TTCTTTAGATTCCAC[A/G]TATAAATGAGATCAT | 8440 |
rs754330998 | snp | A/G | 3.32336e-05 | 0.00407624 | missense, intron-variant | NCK2 | GRCh38.p7 | 2:105881649 | GCTTCCTGAGCCTGC[A/G]CAAGGGCGCCTCGCT | 8440 |
rs754384046 | snp | A/C | 1.6549e-05 | 0.0028765 | missense, intron-variant | NCK2 | GRCh38.p7 | 2:105881694 | GCTCCCGCGTGCTGC[A/C]TGTGGTCCAGACGCT | 8440 |
rs754394865 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105793824 | GGGGTTTCAGGCTCC[G/T]TTAGACAGTGCCTAC | 8440 |
rs754407970 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105842147 | CTGGAGTGCAATGGC[A/G]CGACCTCGGCTCACT | 8440 |
rs754409792 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105793826 | GGTTTCAGGCTCCTT[G/T]AGACAGTGCCTACCC | 8440 |
rs754417101 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105756943 | CCCGAGTAGCTGGGA[C/T]TACAGGCATACACCA | 8440 |
rs754448748 | snp | A/G | | | upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105744069 | TATAGGCTAGCCACA[A/G]CTCGAGGCTGGGTGA | 8440 |
rs754455009 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105804466 | GCTTACACAGCTAAT[C/T]TGGCATTTATGATGA | 8440 |
rs754468383 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105805840 | AAGAATTCCTTAACC[C/T]GAATACCTGGAACCA | 8440 |
rs754500477 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105846940 | GAGTGATGGATGAAC[A/G]GACCAACAAAATGTG | 8440 |
rs754538273 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105767371 | TCCCTTGTTTCCACA[A/G]TAACCTAGTTAGTAT | 8440 |
rs754543630 | in-del | -/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105830716 | TGTGTGTGTGTGTGT[-/G]TTGGTCTGATAATAC | 8440 |
rs754562294 | snp | G/T | 3.87244e-05 | 0.00440008 | synonymous-codon, utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105893170 | CCTCGTCAGGGCCCT[G/T]CAGTGACGGCGCCCC | 8440 |
rs754567416 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105860740 | TGGTCCATAGAGAGC[C/T]GTGGATGCCGGCGGC | 8440 |
rs754598923 | in-del | -/AAC | | | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105771554 | GGGCGACAAGAGTGG[-/AAC]AACTCCCTCTCAAAA | 8440 |
rs754617716 | snp | C/G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105815820 | TTTGTAACCCTTCTC[C/G/T]GTCATTAGACTCTCA | 8440 |
rs754635258 | snp | C/T | 1.68086e-05 | 0.00289896 | synonymous-codon, intron-variant | NCK2 | GRCh38.p7 | 2:105881434 | CGACCGCATCTACGA[C/T]CTCAACATCCCGGCC | 8440 |
rs754643851 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105823465 | TCAGAATCAATTTTC[C/T]GGTTGACTTTTATTA | 8440 |
rs754659498 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105845888 | CCACCAAAGACATCT[A/G]TGTCCATTTTCATAC | 8440 |
rs754666402 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105751286 | TCAACCCCTATTGAT[C/T]CTACCTCCAAAAGAT | 8440 |
rs754686314 | in-del | -/AAAG | | | intron-variant | NCK2 | GRCh38.p7 | 2:105878441 | AGGAGATTGGAACAC[-/AAAG]AAAAGGAGATTGGAA | 8440 |
rs754718543 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105750247 | GAGTGCACTGAGAGA[A/G]AGGTCTGGTGTTTCT | 8440 |
rs754745928 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105871099 | AGGGTCGATGAGTGC[A/G]TGTGAAATCGGGGTG | 8440 |
rs754778445 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105829288 | TCCTCTTTTGCCATT[A/G]CCTTTTCCCCCAGAA | 8440 |
rs754799695 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105883362 | ACTTAGAGAAAGCGC[A/T]GGAAAACCAATTACA | 8440 |
rs754829118 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105798298 | CTATCCTGGGAGCCC[A/G]GATAGCCTCACTGTG | 8440 |
rs754829673 | in-del | -/TT/TTT | | | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105772896 | CCCACGTGTCCACAT[-/TT/TTT]TTTTTTTTTTTTTTT | 8440 |
rs754838854 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105870492 | AGGCACAGTGGCTCA[C/T]ACCTGTAATTCCCAG | 8440 |
rs754867883 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105812536 | CTCCGTACTCTGAAC[A/G]GGAGATCCACTTGCA | 8440 |
rs754935223 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105789337 | GGATTACAAGTGTGC[A/G]CCACCATGCCCAGCT | 8440 |
rs754935625 | snp | C/T | | | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105771647 | TTAGGTAGAAAGTAA[C/T]GTTCTTTTCTTATCA | 8440 |
rs754953691 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105810417 | CTGACTCCTCACTCT[A/T]CCCTCCCTCTTTCCT | 8440 |
rs754966125 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105882312 | GCTTCTCTCCCAAGA[C/T]TCCCCCTCTTGTATT | 8440 |
rs755041275 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105780228 | TTTCTATTAATAAAA[C/T]CATTGCTTCTCAGCA | 8440 |
rs755052861 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105753191 | AATCATTGATAGGGA[G/T]TGTAGCTTGCATACA | 8440 |
rs755070830 | snp | A/G | 1.64904e-05 | 0.00287139 | synonymous-codon | NCK2 | GRCh38.p7 | 2:105855150 | GAAGAACGAGCGGCT[A/G]TGGTTGCTGGACGAC | 8440 |
rs755101911 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105748865 | GTTAATATTGGGGCT[C/G]TAGCCTCCCACTGAG | 8440 |
rs755114773 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105829885 | TCTTCCAACAAGATT[C/T]GTCTCTTTCACTTAT | 8440 |
rs755135222 | snp | C/G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105765093 | GACATCTTTATGGCT[C/G/T]TTGATGCATCTTGCC | 8440 |
rs755185576 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105764259 | CCTTGACCCTTCAGC[A/G]CCTTTGCATCCGCAC | 8440 |
rs755205313 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105816899 | TCTTGAATCCATAAC[A/G]AATCCTGGTCCCTGT | 8440 |
rs755217315 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105842749 | GGTGGGCTCTGGGAG[G/T]CCTGACTGGGTTGGG | 8440 |
rs755220495 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105873040 | CGGCTGCCAGGAAAG[C/G]TCACTGTCCTTCCAT | 8440 |
rs755231174 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105879773 | CTTCACCTCCTGCCC[A/G]CTCAGCAAGGCCATA | 8440 |
rs755231912 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105799732 | CTGGGTTGTTTTGGC[A/G]TGGAGGGATGCTTCC | 8440 |
rs755289426 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105855476 | ATGTTTTTCATTTCC[C/T]GGAGATTCTGGAGTT | 8440 |
rs755306585 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105876486 | GCGAATGTGCTCTTC[C/G]AAAATGCAACATAGA | 8440 |
rs755308518 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105887879 | AAGAGTGTGCTCTCT[A/G]CTGTTCTTTTCTAAA | 8440 |
rs755324913 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105885589 | TAAAACAAATTGCTG[A/G]GTCCTACCTGAAATG | 8440 |
rs755334168 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105747315 | TAAATACACCGGAAA[C/T]CTTCCTTGCATGTGC | 8440 |
rs755335093 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105774156 | TGAGACTACAGGCAC[A/G]TGCCACCACACCCAG | 8440 |
rs755385208 | snp | A/G | 1.66103e-05 | 0.00288182 | missense, intron-variant | NCK2 | GRCh38.p7 | 2:105881657 | AGCCTGCGCAAGGGC[A/G]CCTCGCTGAGCAATG | 8440 |
rs755399506 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105756377 | CTATCTCATATGGAC[C/T]GAGAAAGACCTGTGA | 8440 |
rs755421453 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105746491 | TGAAATTAACCTGGG[C/T]CGCTTTAACTTACCA | 8440 |
rs755440418 | snp | C/T | 1.65392e-05 | 0.00287564 | missense, intron-variant | NCK2 | GRCh38.p7 | 2:105881706 | TGCATGTGGTCCAGA[C/T]GCTGTACCCCTTCAG | 8440 |
rs755442214 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105823043 | AGAGCTTGAAATGAG[C/T]GCATTGCTGCAGTTG | 8440 |
rs755448690 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105867737 | AAAACATTAGGCAGA[A/G]CATTTCCCAGGAACT | 8440 |
rs755452781 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105834025 | CCTGACTTTGATTTA[C/T]AAAAATTTCTTATGA | 8440 |
rs755452826 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105853370 | ATAATACACGCATCT[A/G]TTTATTGTTGTTTTG | 8440 |
rs755462056 | snp | G/T | | | intron-variant, utr-variant-5-prime | NCK2 | GRCh38.p7 | 2:105773391 | CCTCCATCAGTCCAT[G/T]CACCTTTGCTCATGC | 8440 |
rs755480803 | in-del | -/CATTATAGGATTGTGGGTCTGTCAT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105863218 | AAATTCTCATTTCGG[-/CATTATAGGATTGTGGGTCTGTCAT]CATTATAGGATTGTG | 8440 |
rs755522239 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105783585 | TACTAGGAAGGCAGC[C/T]GTTCGCGGAGAATAA | 8440 |
rs755544286 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105866703 | ATCTCCTGCCGTGCA[G/T]CCCATTCCTAACAGG | 8440 |
rs755561819 | in-del | -/GG | | | intron-variant | NCK2 | GRCh38.p7 | 2:105765782 | ATACAGCTTAGAATA[-/GG]GGGGGTGTGTGTGTG | 8440 |
rs755564569 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105766781 | CGGCTATCCCTCCAT[C/T]TTGTGGGCATGCAGG | 8440 |
rs755644764 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105835400 | ACACATATATATATA[C/T]ATATACGTGTATATA | 8440 |
rs755693604 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105826340 | CCATTAACACATGGG[C/G]ATTATAGGGATTACA | 8440 |
rs755695461 | in-del | -/GGAAG | | | intron-variant | NCK2 | GRCh38.p7 | 2:105770002 | TGCCTCCATTTCCTT[-/GGAAG]CACTGGAAAATGGGT | 8440 |
rs755727286 | snp | A/G | 1.824e-05 | 0.00301988 | missense, intron-variant | NCK2 | GRCh38.p7 | 2:105881354 | ACGCGCAGGAAGACC[A/G]GCGCGCGGGATGCGT | 8440 |
rs755729599 | snp | C/T | 3.42477e-05 | 0.00413796 | intron-variant | NCK2 | GRCh38.p7 | 2:105892974 | ACTGTGTTCTGTTTC[C/T]TCCCCAGCCCAGCGA | 8440 |
rs755778856 | snp | C/T | 1.70017e-05 | 0.00291558 | synonymous-codon, utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105893080 | TGGGCAGCGGCGCTT[C/T]CACACCATGGACGAG | 8440 |
rs755788163 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105814313 | CTCAAGGAAAACATC[G/T]CATGCAACCTTCACG | 8440 |
rs755803190 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105858238 | TCAAAAGTACACCAC[A/T]TGTATACTGACCACG | 8440 |
rs755816033 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105825491 | ACTGGGCACTGCAGC[A/G]CTTTGGAACATAGCA | 8440 |
rs755852921 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105762074 | TCTGTAGATGAATCA[C/G]TTGACCTGAAAACAA | 8440 |
rs755878993 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105882200 | TAATGTTTGCTACTC[C/T]GTGATTTACTTGCAT | 8440 |
rs755895475 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105797270 | GGGGAACCTTTAAAA[C/T]GGGATTCTGAAGCCT | 8440 |
rs755906200 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105760838 | CCCACGTGGACTGTG[C/T]TCAGGTTTGAGCAAA | 8440 |
rs755910303 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105869443 | AGACATGTAGATGCA[A/G]AGAGATGTTACAGAA | 8440 |
rs755921990 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105769842 | ATTTTAATCCCTCGG[A/G]GTAATCTTTGGCCTC | 8440 |
rs755977186 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105780891 | CCAGCTTCCACAACT[A/G]TGGGAAATAACTTCC | 8440 |
rs755984710 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105795957 | AAACACATCAACGAT[A/G]TATTCTTTATTACCA | 8440 |
rs755987478 | snp | A/C | | | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105849715 | TGTTCACTGGCTTGA[A/C]TCACAGAAGAGCAGC | 8440 |
rs755989418 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105828848 | CAGTGGCCACTGTCT[A/G]AAATGTCTTCTTTTA | 8440 |
rs755994999 | snp | C/T | 1.70043e-05 | 0.0029158 | missense, intron-variant | NCK2 | GRCh38.p7 | 2:105881418 | CCAATGGCAGCGGCG[C/T]CGACCGCATCTACGA | 8440 |
rs756048096 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105769116 | TTAGCATAAGCTCAG[G/T]TGTGGTGCACTGGGG | 8440 |
rs756086507 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105887599 | ACCTGGAGCAAGGCC[C/T]CTCCCTCCCGTTTCC | 8440 |
rs756090708 | in-del | -/ACACACACAC | | | intron-variant | NCK2 | GRCh38.p7 | 2:105864839 | CATGTACACACACAC[-/ACACACACAC]ACACACACACACACA | 8440 |
rs756145447 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105800202 | GGGGGCCACATGCCC[A/G]GGGTGAACACCAAGG | 8440 |
rs756157121 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105872111 | TTTCTGCCAGCAGGA[C/T]ACTTAGAAGAGAAAG | 8440 |
rs756166469 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105819204 | TGCATTCATAGGGCA[C/T]TCCCAGGTCTCTCTT | 8440 |
rs756202194 | snp | A/G | 1.83424e-05 | 0.00302834 | synonymous-codon, intron-variant | NCK2 | GRCh38.p7 | 2:105881926 | CTACACCGGGCCCTC[A/G]TCCAGCGGGCGCTTC | 8440 |
rs756217972 | snp | A/G | 1.79393e-05 | 0.00299488 | missense, intron-variant | NCK2 | GRCh38.p7 | 2:105881873 | GTGGTCCTCAGTGAC[A/G]GGCCTGCCCTGCACC | 8440 |
rs756244834 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105885257 | ATATCATGTATTTAT[C/T]ATGTCCTGCAATAGT | 8440 |
rs756263652 | snp | C/G | | | intron-variant, utr-variant-5-prime | NCK2 | GRCh38.p7 | 2:105773296 | ATCCTCTAACACTGG[C/G]TTAGTCCCCCTTGTC | 8440 |
rs756288467 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105815084 | CCAATACTTCCATCT[C/T]GAGAGGACCTGTCAT | 8440 |
rs756294224 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105853286 | TTGCTAAAATAGTTG[A/T]TTATTTATTTTATTT | 8440 |
rs756295094 | in-del | -/TT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105812129 | CTAGTGCAGAAAAAC[-/TT]GATACTTTTACTTTT | 8440 |
rs756297316 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105827459 | CACACAGAAAGTACA[C/T]AGAAAGTCAGCAGGG | 8440 |
rs756342728 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105855042 | CTCCAAATGTTTTGC[C/T]GGCAGAAGGACTCCA | 8440 |
rs756380327 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105866600 | CAGGCGTAGTTCACA[A/G]TAGTGTTTGCGCTCC | 8440 |
rs756388272 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105843942 | AATCCTGACAAACAC[C/T]GCCTCAGCCAGGTGA | 8440 |
rs756406605 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105754452 | ATCTTAAGAATTTTG[G/T]TTGCGTGTTTAAGGA | 8440 |
rs756417506 | in-del | -/AGC | | | intron-variant | NCK2 | GRCh38.p7 | 2:105883946 | CGGCTCTGCACACAT[-/AGC]AGCACCGTCTTTGTC | 8440 |
rs756429484 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105757809 | CCAGGCAGAATTCAT[C/T]TGAAGCATTCTGGAG | 8440 |
rs756551510 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105756835 | TTGAGACGGAGTTTC[A/G]CTCTTGTCACCCAGG | 8440 |
rs756552772 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105782189 | CTCTCTTTATAGGAG[C/T]AAGGGGACAACCCTC | 8440 |
rs756554724 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105793743 | AAGCTGCCTTAGGTG[A/G]CCTTCGTGTTCTCTT | 8440 |
rs756566928 | snp | A/G | 3.31296e-05 | 0.00406985 | missense, intron-variant | NCK2 | GRCh38.p7 | 2:105881519 | GGGTCGCGCGTCACC[A/G]TCATGGAGAAGTGCA | 8440 |
rs756579119 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105878052 | GTTTGCTTCCCAGGT[A/G]TCAAAGTCTGGCAGG | 8440 |
rs756612606 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105865259 | AGGTGCCCGAATATG[G/T]TTTTATTTCATCTTC | 8440 |
rs756617702 | in-del | -/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105880285 | AGCCCATTAAAGTGA[-/T]TTTTTTATGATCCAC | 8440 |
rs756619375 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105803409 | AAGGGCCACTTCTGT[C/G]CTGTGCCTTATGTAT | 8440 |
rs756622014 | snp | A/C | 1.66214e-05 | 0.00288278 | missense, intron-variant | NCK2 | GRCh38.p7 | 2:105881638 | GGAGTCCCCAAGCTT[A/C]CTGAGCCTGCGCAAG | 8440 |
rs756681639 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105800734 | AGTTGATCAACTGTC[A/T]TGAACGTCTGTGTTT | 8440 |
rs756707892 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105786272 | AATCTATGTAATAAC[C/T]GTAGTGATCATTAGC | 8440 |
rs756709601 | in-del | -/AAGT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105770121 | ACATAAAGCACTAAT[-/AAGT]AAAAAAAAAAAAAAA | 8440 |
rs756775639 | snp | A/G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105870306 | CCCCCACCCAGGCAG[A/G/T]GTGGCTGCTTGGGGT | 8440 |
rs756789151 | in-del | -/TCAGGATTTACTAAA | | | intron-variant | NCK2 | GRCh38.p7 | 2:105804109 | AGGCAGTGGCGACTC[-/TCAGGATTTACTAAA]TCAGGATTTACTAAT | 8440 |
rs756828418 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105747716 | CATCCAGAGGGTTTG[C/G]GAGTGGCACTTCCAA | 8440 |
rs756877870 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105760694 | GTGAAGGGAGAAACC[A/G]GTTACAGCTGAGAAC | 8440 |
rs756881015 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105796511 | GGTATTATTGGCACC[A/G]GTTGCAGAGAGGGCC | 8440 |
rs756881654 | snp | C/T | 2.16706e-05 | 0.00329163 | intron-variant | NCK2 | GRCh38.p7 | 2:105882062 | TCGGTAAGTGCGCTG[C/T]GCCCACAGCTCCGGC | 8440 |
rs756886237 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105759889 | TTAGTGTAGAGTTAC[C/T]GGTTTGGGGAGGAAG | 8440 |
rs756937437 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105866933 | GAGAAGCTGATTCTT[C/T]ATGGTGCATTTGTCT | 8440 |
rs756952374 | in-del | -/TGTT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105800649 | ATCCTGTTTTTGGTC[-/TGTT]TGAGATAAATGGACC | 8440 |
rs756977017 | in-del | -/ACACACACAC | | | intron-variant | NCK2 | GRCh38.p7 | 2:105864829 | CTCACATGTGCATGT[-/ACACACACAC]ACACACACACACACA | 8440 |
rs756993891 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105835939 | CTCAATTTTTTTATT[G/T]AATTCATTTAATTAT | 8440 |
rs757003768 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105848149 | ATGGCTAACACTTGT[C/G]CAGCACAGACTGAGT | 8440 |
rs757005433 | in-del | -/GTTT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105874642 | TTTCCAAAGTACCAA[-/GTTT]GTTTGACGCTTCAGC | 8440 |
rs757017667 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105806176 | AGGGATGCTCAGCCT[A/T]GTATATGTATGTGTG | 8440 |
rs757029352 | in-del | -/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105757267 | TGTCTTCTGTGAAAC[-/T]AGGGGTTGCCTGTAA | 8440 |
rs757031471 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105880540 | GGAGGAGGCAGCGGC[A/G]AGGCAGCTGGGGGCA | 8440 |
rs757032718 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105875889 | ATGATAGATTTAAAG[G/T]GCTTGAGATGCTTTT | 8440 |
rs757038734 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105806852 | AAAAAAAAACCCAAC[C/T]AACCATCCTACAGAA | 8440 |
rs757054911 | snp | A/G | 2.4956e-05 | 0.00353233 | missense | NCK2 | GRCh38.p7 | 2:105855278 | TCGTGAAGAACCTGA[A/G]GGACACACTAGGTGA | 8440 |
rs757066638 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105780031 | CTCTTTTCATAAACT[A/G]CTCTAATTTCCGTTT | 8440 |
rs757090690 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105819094 | GTTGTGATTTCCAGA[A/G]CTAGCTCCTGGTCGG | 8440 |
rs757106755 | in-del | -/CTA | | | intron-variant | NCK2 | GRCh38.p7 | 2:105786751 | CTTCAGGTCCAGCTT[-/CTA]CTCTCTCCTCCCTTC | 8440 |
rs757121571 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105790005 | AACACTAGCGTGTTC[A/G]TGTATTGAGTGCAAG | 8440 |
rs757135700 | in-del | -/AT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105780320 | TAATATGGGAGAGAG[-/AT]ATATACACACACACA | 8440 |
rs757152355 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105879486 | TAGAGGTTTGTGTTT[C/T]TATATAAGTTAACAC | 8440 |
rs757163165 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105862182 | ATTTTTTTATATCAG[C/T]GGTAAAGACTCTAGA | 8440 |
rs757182579 | snp | A/G | 3.79319e-05 | 0.00435483 | missense, intron-variant | NCK2 | GRCh38.p7 | 2:105881333 | GTCTCCACAGGCCTC[A/G]GCAAGACGCGCAGGA | 8440 |
rs757239739 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105794559 | TATCTCACAGGGGAA[A/G]TACAGTCCAATTATT | 8440 |
rs757250945 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105860922 | CCACTCAGTGAAGCC[A/G]TGGATGGAGCCCCAA | 8440 |
rs757257611 | in-del | -/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105827480 | GTCAGCAGGGCTATA[-/G]GAACACTCACCACCA | 8440 |
rs757263330 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105883631 | TCTGTGGAACATGCA[C/T]AGGTGGTCATTGCTG | 8440 |
rs757316144 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105828511 | GAATTTAAGCATGTG[A/G]TAGGTAATGACTTTG | 8440 |
rs757321580 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105798554 | CCATATCTGATTCAT[A/G]TAATCAGATATGAAT | 8440 |
rs757342995 | in-del | -/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105747392 | GCAGAATGCACTGGA[-/G]TCCTTTACTTGATCA | 8440 |
rs757409053 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105832085 | ATCTTTCACTTTCTT[C/G]GTTAAATTTGTTCTT | 8440 |
rs757409597 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105799248 | CCCTCTTTTATGGTT[G/T]CTGGAATTTGAGTCC | 8440 |
rs757431499 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105857315 | CTGAGCCAGCCGCCC[A/G]TCCTGGAGCCGGCAC | 8440 |
rs757457379 | snp | G/T | 1.65222e-05 | 0.00287417 | missense, intron-variant | NCK2 | GRCh38.p7 | 2:105881726 | TACCCCTTCAGCTCA[G/T]TCACCGAGGAGGAGC | 8440 |
rs757459190 | snp | A/G | | | upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105743749 | AGCTACGCTGACTCT[A/G]GTTACCTATCCTTGG | 8440 |
rs757466970 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105821800 | ACTGTCCACAGCTGT[A/G]CATGCTCAACTGTGT | 8440 |
rs757476795 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105866404 | ACTAGCTGTCACAGT[A/G]CAGTTCATCTGTAAC | 8440 |
rs757479933 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105754216 | TGGCCACTTCTACAC[A/G]TAGCAGGTTCCAGGA | 8440 |
rs757488766 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105865062 | CTCCCTCAGCCAGCA[G/T]CAGTGCTCCCTGACC | 8440 |
rs757509012 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105875805 | TATTTTGTTATAGGC[A/G]CCTGAACCAATTAAG | 8440 |
rs757510743 | snp | A/G | 1.78064e-05 | 0.00298377 | missense, intron-variant | NCK2 | GRCh38.p7 | 2:105881861 | AAAAACTACGTGGTG[A/G]TCCTCAGTGACGGGC | 8440 |
rs757531438 | snp | G/T | | | upstream-variant-2KB, intron-variant | NCK2 | GRCh38.p7 | 2:105851637 | AAGCGTTCAGGGATT[G/T]GTTAACCTTTAGCTA | 8440 |
rs757582430 | snp | C/T | | | upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105743061 | GGGATATCACTTTTA[C/T]AGGGTGGGAAGACAA | 8440 |
rs757598660 | in-del | -/TTTTTTTTTTTTTTTT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105891533 | GAGATAAAAGACCAA[-/TTTTTTTTTTTTTTTT]TTTTTTTTTTTTTTT | 8440 |
rs757609586 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105788711 | TTTCAATATGCTTTA[C/T]CCATAGAATGCATAA | 8440 |
rs757631811 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105755720 | CATGCCTATAAATTC[A/G]TGGTTCTCAGCTGGG | 8440 |
rs757652452 | snp | A/G | 5.10556e-05 | 0.00505225 | utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105893181 | CCCTGCAGTGACGGC[A/G]CCCCGGCCCCACACT | 8440 |
rs757653580 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105890410 | TTATCTCTAAATTGA[C/G]CCTGGCTTATAGTAA | 8440 |
rs757699924 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105768749 | AGATGATTCTTACAG[C/T]GTGTGTGGCCCAGGG | 8440 |
rs757701167 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105803292 | GAAAAGTTTAGCTGC[C/T]GTTTTTTATAGGCAC | 8440 |
rs757709667 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105842868 | GACGCTGTGAGAAAT[A/G]TGATAGGCAACCAGT | 8440 |
rs757717715 | in-del | -/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105773820 | GCTGCCTGGAGAATC[-/G]GGTAGTGGTGTGGAC | 8440 |
rs757785848 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105857925 | TGTGCACTTCTGTGC[A/G]AAGCTTATAGATGTG | 8440 |
rs757793720 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105784698 | AGTCTAGTGAAAACT[A/G]TAACACCATCAAACT | 8440 |
rs757794796 | in-del | -/GAGGCAT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105890635 | GGTCTATTTGAGACA[-/GAGGCAT]GCATAAATACAAACT | 8440 |
rs757797389 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105777064 | TGAAGGGCAAAATGA[C/G]GCCTTGAGAGTTCCC | 8440 |
rs757856192 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105796300 | AAGGCTGTTTTGTCA[C/T]TGATGGCACACAGGA | 8440 |
rs757869986 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105880383 | ATGCACTCATCACAA[C/T]CTGTTGTGGGAAATT | 8440 |
rs757877405 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105835633 | TCTTAGGTTGAATAT[A/G]TTTAAGGATCTTAGA | 8440 |
rs757879107 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105813869 | ACGTACGGTATCAGT[C/G]TTAATTGCCTTCCAG | 8440 |
rs757879417 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105879595 | GGTACAAAGAGAAAC[A/G]GCAGAGGCCATTAGC | 8440 |
rs757879534 | in-del | -/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105798469 | CACTGAATTGTACAC[-/T]TTTAAACAGTGAACC | 8440 |
rs757894428 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105774838 | TTTCTTTTTGAGTTA[C/T]GTGTTGAAAGAAATG | 8440 |
rs757894907 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105746648 | GTGGAGAAGAAATTG[A/T]CTTCACCTGGAGATT | 8440 |
rs757971955 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105758269 | ATCACATTACTTCTC[C/T]TGGATTAGTAATGAA | 8440 |
rs757980179 | snp | C/T | 1.65809e-05 | 0.00287926 | synonymous-codon, intron-variant | NCK2 | GRCh38.p7 | 2:105881495 | GAGGATGAGTTGTCC[C/T]TGGTGAAGGGGTCGC | 8440 |
rs758011747 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105823483 | TTGACTTTTATTATA[A/G]CTAACGTTGAAATGG | 8440 |
rs758036058 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105805994 | ACATAGCCTGCAGGT[A/C]ATTTTATTTTTTTTC | 8440 |
rs758040613 | in-del | -/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105849256 | AAACTAGCAGGGCGC[-/G]GGTGGTGCACACCTA | 8440 |
rs758062253 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105825364 | TCAAAAATCCCATTC[C/T]GTTACTAGTGTTTAG | 8440 |
rs758065144 | snp | A/C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105834250 | GTGTTGAAGCCCCCA[A/C/G]CTGTTGTTCTATTGG | 8440 |
rs758090937 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105804671 | ATTCTGTCCCTCTTC[A/G]TTGACTGCTTGCAAA | 8440 |
rs758153248 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105815896 | GGCTTTTAAAGGTGG[G/T]GCTCATTGGGAGGAG | 8440 |
rs758163709 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105751508 | ACGACTGGGCTGCCT[C/G]TCTGTTTCTCCCAGC | 8440 |
rs758191859 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105890213 | GAAAATTTTATTGCT[A/G]CAACTCATGCATGCA | 8440 |
rs758230007 | in-del | -/CC | | | intron-variant | NCK2 | GRCh38.p7 | 2:105869863 | ATTGGCATCTGTGTT[-/CC]CATTTGACTTTCATT | 8440 |
rs758231127 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105799820 | TTACCTGGCCTTCCC[C/G]TCCGCCATCTTGCCA | 8440 |
rs758235338 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105875757 | GAGAAATAAATGTCT[A/G]TAATTTTACTTTATA | 8440 |
rs758238053 | snp | A/G | 2.12344e-05 | 0.00325833 | intron-variant | NCK2 | GRCh38.p7 | 2:105882056 | GAGTCCTCGGTAAGT[A/G]CGCTGCGCCCACAGC | 8440 |
rs758239011 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105859927 | TTGCAAAGCTGACTG[C/G]TTATTTCTGTTGGTA | 8440 |
rs758291179 | snp | C/T | 1.65056e-05 | 0.00287272 | synonymous-codon | NCK2 | GRCh38.p7 | 2:105855165 | GTGGTTGCTGGACGA[C/T]TCCAAGACGTGGTGG | 8440 |
rs758299740 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105844690 | CAGTGAGCTGAGATC[A/G]CGCCACTGCACTCCA | 8440 |
rs758329030 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105884953 | AACTCAGAAATCCTA[A/C]TCACCCTGTGTGTGT | 8440 |
rs758332927 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105789010 | GAACGATTTAATGCA[C/T]GCTTCTCTGCCAATC | 8440 |
rs758342518 | snp | A/C | 2.12289e-05 | 0.00325792 | synonymous-codon | NCK2 | GRCh38.p7 | 2:105855258 | CAGCCTGAAGAAGGG[A/C]TCCCTCGTGAAGAAC | 8440 |
rs758387939 | in-del | -/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105828039 | GAGCACAAGGGACCA[-/C]TCTGCACACCCTTTG | 8440 |
rs758392083 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105871246 | GAGATGAGGAGGATG[A/G]TGAGCTGAGCACCAG | 8440 |
rs758410656 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105781915 | TCTTTATTTCTTGCC[A/G]TAAATGCTTTTAACT | 8440 |
rs758437340 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105791240 | TAATTCTTAAGAGAA[C/T]GTTGATTCATCTAGA | 8440 |
rs758458752 | snp | C/T | | | upstream-variant-2KB, intron-variant | NCK2 | GRCh38.p7 | 2:105850283 | AGGAGTGTGTTAACC[C/T]AGCAAGATACGGTTC | 8440 |
rs758468230 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105839844 | TCTTTAGTTCAGAAG[C/T]ACAAGTAGAGTGAGC | 8440 |
rs758470325 | in-del | -/GTGT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105830683 | TTGGTGTGTGTGTGT[-/GTGT]GTGTGTGTGTGTGTG | 8440 |
rs758482766 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105819463 | ATCTTCTGATTGGAT[A/C]ATCAGAACTCATTAA | 8440 |
rs758499201 | snp | C/T | 1.66034e-05 | 0.00288122 | synonymous-codon, intron-variant | NCK2 | GRCh38.p7 | 2:105881663 | CGCAAGGGCGCCTCG[C/T]TGAGCAATGGCCAGG | 8440 |
rs758526232 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105820594 | CCTTCTTTGGGGGAG[C/T]GGAGACCATAGGAAG | 8440 |
rs758536959 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105781011 | CTTTTCTCATTGCCC[A/G]AATCTAGATTTTGTC | 8440 |
rs758549544 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105799100 | TATTTAAGAAGCTCT[C/T]GCTGTGTCCTGTCTG | 8440 |
rs758579887 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105831248 | CCCTATCAAAATACA[A/G]TGATATTTTTCACAG | 8440 |
rs758587621 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105755666 | ACGAATACCTTTTTA[A/T]ATGTTAGTATTTTGA | 8440 |
rs758604992 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105830160 | TGCTATCAAACACTA[A/G]AACTTATTCCTCCTA | 8440 |
rs758622270 | in-del | -/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105887275 | TTCTCACTTTTGGGA[-/G]GGTAAATGAACCACT | 8440 |
rs758649473 | snp | G/T | 3.30469e-05 | 0.00406477 | missense, intron-variant | NCK2 | GRCh38.p7 | 2:105881723 | CTGTACCCCTTCAGC[G/T]CAGTCACCGAGGAGG | 8440 |
rs758663316 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105854302 | AATTTGAGCAATTAT[G/T]AATAAAGCTGCTACA | 8440 |
rs758665588 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105863652 | GACAGTCCTCATTCA[A/G]ACAATAGCACTGTCC | 8440 |
rs758698542 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105856320 | ATGACTCATCTGAGC[G/T]GACATTTAAAACGTT | 8440 |
rs758712642 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105754806 | TTCAGGGAGTTATTT[G/T]GAGACAGTTTTTGGG | 8440 |
rs758718100 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105790288 | TCCTGCAGCTCTCGT[C/T]ATTGCCCACCATCTA | 8440 |
rs758724129 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105842815 | CGTGGCAGGAGAGGG[C/T]GGCTGTGGTTTTGGA | 8440 |
rs758746326 | snp | A/G | 1.7257e-05 | 0.00293738 | missense, intron-variant | NCK2 | GRCh38.p7 | 2:105881823 | AATGCAAAAATGCCC[A/G]GGGCCAGGTGGGCCT | 8440 |
rs758751401 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105874243 | CTTAGCAGCATAACT[A/G]AAAAAGTAGATGCAA | 8440 |
rs758765455 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105765216 | GGTCCCTCCATAAAG[C/G]CATTTTGGATTGATC | 8440 |
rs758813201 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105888036 | TACTCTGAGCCCGGT[G/T]TGGGGATGTGGAGCT | 8440 |
rs758845993 | in-del | -/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105860569 | TAGTCAGAACCGCAT[-/G]GGGAGGCCTTACTGG | 8440 |
rs758850101 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105785230 | TGATCCGCCCATCTC[A/G]GCCTCCCAAAGTGTT | 8440 |
rs758854195 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105775176 | GGGGTGGTTTTTACG[G/T]GTTAGTCATGTTGTA | 8440 |
rs758891939 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105817036 | CAAAGGATAGCTGGG[C/T]ATGGTGGCGTGCACA | 8440 |
rs758898610 | snp | A/T | 1.64866e-05 | 0.00287106 | synonymous-codon | NCK2 | GRCh38.p7 | 2:105855081 | GACAGAAGAAGTTAT[A/T]GTGATAGCCAAGTGG | 8440 |
rs758930795 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105747565 | GGCTTAAAGACTGAA[G/T]AGCTCAGAATTGCTT | 8440 |
rs758972786 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105812911 | GGGCTTGCTTCTTGA[A/T]GTAGCCTGACATGGT | 8440 |
rs758985498 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105866244 | AAATTTGGAAACTAT[A/G]GAAAAGCATAAAAGA | 8440 |
rs759029157 | snp | C/T | | | downstream-variant-500B | NCK2 | GRCh38.p7 | 2:105894395 | AACATTTATTACTTG[C/T]GTGTTTTCATTTTCT | 8440 |
rs759047475 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105861734 | TGGCCAGGCTGGTCT[C/T]GAACTCCTGACCTCA | 8440 |
rs759053273 | in-del | -/A | | | intron-variant | NCK2 | GRCh38.p7 | 2:105833117 | TCTTTTTTTTGAGAC[-/A]AAGTCTCACTGTTGT | 8440 |
rs759059155 | snp | A/G | | | utr-variant-5-prime | NCK2 | GRCh38.p7 | 2:105816537 | GCTTTGTAACTTCAG[A/G]GGTGTAATTAGCTGA | 8440 |
rs759061227 | snp | C/T | | | utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105894190 | GATGGCACATTCCTA[C/T]GATTGAAGAAGGGGT | 8440 |
rs759066450 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105752720 | TCAAGTCTCTGGTTC[C/T]GTCTGGATAATGGCC | 8440 |
rs759068326 | snp | A/G | 0.000119296 | 0.0077223 | utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105893215 | CTCCCGGGCCCCACG[A/G]TGGAGCTGCCCGCCC | 8440 |
rs759070822 | in-del | -/CTTA | | | intron-variant | NCK2 | GRCh38.p7 | 2:105748262 | TCCCAAGGGTCGTCT[-/CTTA]CTTCTTTTCTTCCCC | 8440 |
rs759078250 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105753993 | TCTGTGCCAGCTTCT[A/C]GAACCTACCCTTTTG | 8440 |
rs759129555 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105764576 | TTTCAGCAGTACCAG[C/G]TAAAAAGATCTCAAA | 8440 |
rs759142593 | in-del | -/TTGT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105882475 | TGACACCTCCTTTTG[-/TTGT]TTGCTTGCTTTCTCT | 8440 |
rs759167397 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105835260 | TCATAGGGCCAGTCT[A/G]CTGGTGATGAATTCC | 8440 |
rs759173316 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105789893 | CTCACCATCAGATAA[C/T]GAACAGGTTGGATAT | 8440 |
rs759176703 | in-del | -/AC | | | intron-variant, utr-variant-5-prime | NCK2 | GRCh38.p7 | 2:105773173 | CAAAGTGTTGGAATT[-/AC]AGGCATGAGCCACCT | 8440 |
rs759178783 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105871938 | GGGACAGTTTTGGAG[A/G]TGGGCTGAGATTTCG | 8440 |
rs759182226 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105878182 | CAACAAGAAAGCCAC[A/C]GCTTAGTTAATAAGG | 8440 |
rs759183991 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105828261 | GGGAGAATTGGGCAC[C/T]GTTCAAGATTGCTGA | 8440 |
rs759206258 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105811880 | ACTGCTTGCTATTTC[C/T]TTCTTTTCTCAGTTC | 8440 |
rs759231349 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105788753 | TGTTCTCCTTCATTC[A/G]TTTTCTTCATTCTTA | 8440 |
rs759235416 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105800117 | GCCCTTACTTTGTGA[A/G]AAGAGAGGGTCAGTG | 8440 |
rs759253677 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105886839 | ACGCTCCGTTTGCCT[A/G]GATTAGGTAGATGGG | 8440 |
rs759291775 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105854657 | TTTGGTTATGTTGAC[G/T]TATTAAATATGTTTA | 8440 |
rs759298759 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105802984 | TAAATACTTGTTGGA[C/T]GAATTAACTTGAAGT | 8440 |
rs759301819 | in-del | -/TTT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105855834 | TCCCCATGTGCCTCT[-/TTT]TTTTTTTTTTTTTTT | 8440 |
rs759330804 | in-del | -/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105835424 | GTATATATATATATA[-/T]TTTTTTTTTGGTCAG | 8440 |
rs759374096 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105783935 | CACGAGAAAATGAAA[C/T]ACCCTTTCTCTGCAG | 8440 |
rs759383514 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105810513 | TTTTGTCAGCATGCT[C/T]TTTACTGGTGTTGTC | 8440 |
rs759388431 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105800283 | TGTCCTCCCTGTGCA[C/T]GCCACCTAATTCTCT | 8440 |
rs759466997 | snp | C/G | | | intron-variant, utr-variant-5-prime | NCK2 | GRCh38.p7 | 2:105745629 | AGGGACGGGGGAGGC[C/G]GCGATCGGCCGGGAG | 8440 |
rs759485892 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105865628 | AACTTTTCCTGGTTC[C/T]TTAATGTTGAGGTGA | 8440 |
rs759506131 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105852971 | TTTGGAAGTTAATTC[A/G]TGAAAGAAACGTGTA | 8440 |
rs759552292 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105866196 | CGGGATTACAGGCGT[C/G]AGCCACCGTGGCCAG | 8440 |
rs759566423 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105802698 | GATCCGCCCTCGCGA[A/T]GCAGACACCTCCCTT | 8440 |
rs759613131 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105801298 | GCCCCCTTGTTGGAC[A/G]TCATTGTAGGGATCC | 8440 |
rs759654039 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105858670 | TCTGTGTAGTTCTCT[C/T]CTGCTTTCTTGTACT | 8440 |
rs759660882 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105788187 | AGATAAGTTTTTTCA[C/T]CAGCTATGTGAATTG | 8440 |
rs759683385 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105776951 | TATAGGCAGAATCTA[A/G]TATGGGGAGTGGCTT | 8440 |
rs759749815 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105786293 | GATCATTAGCTGAGC[A/G]TGTGCTATGTGCCAG | 8440 |
rs759750149 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105818908 | AAAAGAAAAATCTCT[A/T]GGAACCTTTTCAATT | 8440 |
rs759770846 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105748257 | ACTCATCCCAAGGGT[C/T]GTCTCTTACTTCTTT | 8440 |
rs759773179 | snp | C/T | 1.92151e-05 | 0.00309954 | synonymous-codon | NCK2 | GRCh38.p7 | 2:105855243 | CGTGGAGCGGAAGAA[C/T]AGCCTGAAGAAGGGC | 8440 |
rs759810195 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105868509 | TTGTTGATTGTCTGA[C/T]TTGTGAAATTTACAA | 8440 |
rs759831058 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105786035 | CTGTCAATTTTCTCA[C/T]TTACCTTCTGCCTTA | 8440 |
rs759840609 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105824969 | AAAGAGCATCAGGGA[C/T]TCCCCCAAGCTGCAG | 8440 |
rs759846325 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105868754 | TACACAGTTACGTTT[A/C]AAAAGTGAAGTTAAT | 8440 |
rs759869027 | in-del | -/TG | | | intron-variant | NCK2 | GRCh38.p7 | 2:105759575 | AATTCTGATATAAAC[-/TG]TGTCTACTTTCCCCT | 8440 |
rs759874772 | in-del | -/AG | | | intron-variant | NCK2 | GRCh38.p7 | 2:105791613 | ACTTCTCTAGAGCAA[-/AG]AGCATTTCGAACTGA | 8440 |
rs759888558 | in-del | -/GG | | | intron-variant | NCK2 | GRCh38.p7 | 2:105774700 | GGTGTCAAGTTGTCT[-/GG]GGGGCCTGGATGACG | 8440 |
rs759888645 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105796117 | ACAGAATTTTATTAG[A/G]TGCATGCACATGGAA | 8440 |
rs759897836 | snp | C/T | | | synonymous-codon, intron-variant | NCK2 | GRCh38.p7 | 2:105881881 | CAGTGACGGGCCTGC[C/T]CTGCACCCTGCGCAC | 8440 |
rs759929583 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105880134 | TTTTTCCTCATGCAC[A/G]GGAAGAAATGTTTCT | 8440 |
rs759932083 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105759570 | CAGAGAATTCTGATA[A/T]AAACTGTGTCTACTT | 8440 |
rs759941632 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105806692 | AATATCTATGTGAAT[A/G]TCTGCTACTTAATGA | 8440 |
rs759964848 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105807481 | GCATACAGCTGATAT[C/G]TATGTAATTTGAGAA | 8440 |
rs759974750 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105862800 | AAATAATGTTTTTTG[C/T]GCCGTTTTTGTAATT | 8440 |
rs759982804 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105780549 | ATACCTGGGCACTAT[G/T]GAGAGTGGGAGGGGT | 8440 |
rs760000718 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105836543 | GGAGCAAAGTTGTTG[G/T]TGGAGGTAGTAGCAG | 8440 |
rs760016455 | in-del | -/TT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105795344 | GCATACTCTATACAC[-/TT]TTCCCAAGCAAGAGG | 8440 |
rs760108243 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105768861 | GGGAGTCCCCATGCC[C/T]CCTGGGGGAGACACC | 8440 |
rs760110683 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105827178 | CTAATTTTTGGTATT[A/T]TTAGTAGAGACGGGG | 8440 |
rs760117014 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105849297 | GGAGGCTGAGGCAGA[C/T]GGATCGCTTGAGCCC | 8440 |
rs760168625 | snp | A/G | 1.80941e-05 | 0.00300778 | synonymous-codon, intron-variant | NCK2 | GRCh38.p7 | 2:105881893 | TGCCCTGCACCCTGC[A/G]CACGCCCCACAGATA | 8440 |
rs760176997 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105814128 | CTGATTATAATTAAG[A/C]CCTGCTTTGAAATGC | 8440 |
rs760190378 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105871822 | TCTAAAGCTAAACTA[C/T]TAGAGGTAAAAAGTT | 8440 |
rs760230342 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105840470 | GGGTATCTCTCCCCA[A/G]CAGCAAGTAAGCAGT | 8440 |
rs760251010 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105839437 | TTTGAAGGCAAGTCT[A/G]TGGGGTTTGCTGCTG | 8440 |
rs760260840 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105852532 | TGCGTGAAAATAGAT[C/G]CTGCCCAGCCAGCTC | 8440 |
rs760270079 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105831163 | GATATCTCATATTCA[C/T]GGATTAGAAGAATTA | 8440 |
rs760294627 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105799292 | AAAAAGTTCTTCCTT[C/T]AGGGTTATAAAGGGT | 8440 |
rs760343464 | in-del | -/TGTGTGTGT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105823159 | GTGTGTGTGTGTGTG[-/TGTGTGTGT]GTGTGTCACAATGGA | 8440 |
rs760353547 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105884811 | TTCTTCCTCCTCCCT[C/T]GCTCTCCTCTCTCAT | 8440 |
rs760354750 | in-del | -/ACAA/ACACAA | | | intron-variant | NCK2 | GRCh38.p7 | 2:105750067 | CACACACACACACAC[-/ACAA/ACACAA]AAAACAACAACAACA | 8440 |
rs760396860 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105812030 | ATTAGAAATTAGTTC[C/T]GTTTTTTCCCTCGTG | 8440 |
rs760411606 | snp | A/G | 0.000160867 | 0.00896704 | synonymous-codon, utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105893164 | GCTCTACCTCGTCAG[A/G]GCCCTGCAGTGACGG | 8440 |
rs760475257 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105780704 | CTTTGGGAGGTGATT[A/G]GGTCGTAAGAGGGGA | 8440 |
rs760490485 | snp | A/C | | | upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105743517 | AAAAATGAGGCTGTT[A/C]TGATTCCCTGAGCTT | 8440 |
rs760503244 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105809270 | GCGTGTGTCATATGT[C/T]GTGACACATATGTAT | 8440 |
rs760511385 | in-del | -/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105881162 | TACAGGAGGCAGCTG[-/C]CCAGCAACCGTATTT | 8440 |
rs760519482 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105751277 | AACTAGTTATCAACC[C/T]CTATTGATTCTACCT | 8440 |
rs760552536 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105770735 | TATTTTAAACTTAAA[C/G]ATCTTTAACAGGTCA | 8440 |
rs760558780 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105821622 | ATTCCACAGTGCCCC[A/G]GTGGTGCAGTCAGTG | 8440 |
rs760570019 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105792497 | GTCAGTGTTCAAATT[C/T]TCCCACCTGTCTCAA | 8440 |
rs760604948 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105800024 | TGTCATTTGGAAACA[A/C]CATCTTTGTTCATGT | 8440 |
rs760607635 | snp | A/T | 1.76235e-05 | 0.0029684 | utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105893212 | CGCCTCCCGGGCCCC[A/T]CGGTGGAGCTGCCCG | 8440 |
rs760617670 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105756206 | TTTAAATTATTTCCT[A/G]TTCCATTATTCTTCC | 8440 |
rs760632851 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105891807 | CTGCCTTGGCCTCCC[A/G]AAGTGCTGAGATTAC | 8440 |
rs760642849 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105748216 | CTCAACTCCTTGGCT[C/T]AGTCTCCTCCGTGTC | 8440 |
rs760679946 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105824801 | ATTCTAAGGACAGTC[C/T]TGCACAGGCAGGACA | 8440 |
rs760685033 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105845252 | GTTTTTAAAAATCAC[C/T]GTGCTTCTTGTTTCA | 8440 |
rs760710223 | snp | C/T | 8.3013e-05 | 0.00644202 | synonymous-codon, intron-variant | NCK2 | GRCh38.p7 | 2:105881593 | GTTCCCCTCCAACTA[C/T]GTCTTGGAGGAGGTG | 8440 |
rs760757698 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105812582 | TCCTTGGTCAGGGAG[A/G]GAGGAGGGAAGGGTA | 8440 |
rs760763020 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105875350 | CTGGAGGTGCTGGCG[G/T]TACGGGGTCTCCTGC | 8440 |
rs760872323 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105868614 | TAAATCTGTAATGTT[C/T]AACCGGCTGTGCTAA | 8440 |
rs760886745 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105865197 | CCAGCAAATGGGCCG[G/T]GATAATTATTTCTCC | 8440 |
rs760899901 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105785126 | TGGGACTACAGGCGC[C/T]GGCCACCACACCTGG | 8440 |
rs760902739 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105747075 | ACTGACCCTGTTAAC[C/T]GTCGGGCTTGCTGAA | 8440 |
rs760903125 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105862312 | AAGACCCAGGTTAGT[C/T]GAGTAGTCAAGCAAG | 8440 |
rs760948748 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105805462 | GGAATAATAATAAAT[G/T]TGTTTTCTATAAGTT | 8440 |
rs760970305 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105782428 | ATGGCCATTTGAGGA[C/T]TTGAGAAGAAACAGT | 8440 |
rs760977875 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105879226 | ATGTTATTTCTTGAC[A/G]TCATTGTTGCCAATA | 8440 |
rs760992976 | snp | A/G | | | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105773004 | TCAAGCAATCCTCCT[A/G]CCTCTGCCTCCTTAG | 8440 |
rs761073622 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105816331 | TAAATAACAAAAAAA[A/C]CCATTAGTTTTAGGC | 8440 |
rs761074516 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105779077 | TTTGGGAGGCTGAGG[C/T]AGGTGGATCACTTGA | 8440 |
rs761074924 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105768105 | AACCACATGAAAAAG[G/T]CTACAAATTTTAAGT | 8440 |
rs761093928 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105872430 | CTGTCCTCACCTGAG[C/G]GCCTCCGTGTCCTGC | 8440 |
rs761126487 | in-del | -/GG | | | intron-variant | NCK2 | GRCh38.p7 | 2:105785001 | TGTTTGTTTTGAGAC[-/GG]GGAGTCTCGCTCTGT | 8440 |
rs761166110 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105847651 | CAGGGTACATCAGGG[A/G]AGGAGCAGATGGCAA | 8440 |
rs761188698 | snp | A/G | 1.80968e-05 | 0.003008 | missense | NCK2 | GRCh38.p7 | 2:105855229 | GTACCGTCCAACTAC[A/G]TGGAGCGGAAGAACA | 8440 |
rs761205336 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105777884 | CGGTACTGGGGTGAC[A/G]GCTCACAGGATTCCA | 8440 |
rs761245121 | in-del | -/TGT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105884230 | GACAAGTCCTTTGCT[-/TGT]TTTTTTCCCACCATC | 8440 |
rs761251268 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105846729 | GTACTGTTGGTGGAA[C/T]TGTAGATGCAGCCTC | 8440 |
rs761256323 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105824663 | AGGTCTCTGGAGGAA[A/T]CACTGGGGCGTGCTC | 8440 |
rs761280496 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105752475 | TTACCAGTGTAAAAT[A/C]ACATTTTTGTATATC | 8440 |
rs761283894 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105815641 | CTTTGTCAGGTGCCT[C/G]TCATCTTAACTTCCT | 8440 |
rs761316119 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105797138 | ACCATCTTTTCTTTC[A/G]GCATCTCCCCCACCC | 8440 |
rs761356249 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105883083 | GGACGGAGCATCGTG[A/G]TGGTGGAAACTGGAC | 8440 |
rs761363952 | in-del | -/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105841306 | GCTCTGTGGCTTATG[-/T]TTTTTCCCTCGAAAA | 8440 |
rs761375052 | snp | C/G | 1.65531e-05 | 0.00287686 | synonymous-codon, intron-variant | NCK2 | GRCh38.p7 | 2:105881692 | GGGCTCCCGCGTGCT[C/G]CATGTGGTCCAGACG | 8440 |
rs761380496 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105856184 | GTTATGGGCAGTGCC[A/C]TCCTGGAGTTACACA | 8440 |
rs761390287 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105809115 | GAATAGGTGTTGAAA[A/C]TGGAAGAATCAGTTC | 8440 |
rs761403971 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105761951 | CTCTGTGTTACAGTT[G/T]ATGTTTTCTCTTTTG | 8440 |
rs761405829 | snp | A/G | | | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105772234 | GTTTGAGAACCATAG[A/G]TTTATTTAGACTGTT | 8440 |
rs761407037 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105781664 | TCTTGTAAGGTAGTT[A/G]TTAGGTTTATAATAA | 8440 |
rs761417539 | snp | A/T | | | upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105743349 | TACAAACTGGGTCAA[A/T]ATTGCTATACTTATT | 8440 |
rs761423872 | snp | C/T | 1.65433e-05 | 0.002876 | missense, intron-variant | NCK2 | GRCh38.p7 | 2:105881766 | AGAAGGGGGAGACCA[C/T]GGAGGTGATTGAGAA | 8440 |
rs761448279 | snp | C/T | | | upstream-variant-2KB, intron-variant | NCK2 | GRCh38.p7 | 2:105851096 | CACTCTTCCTTCCCA[C/T]TTGTTTTGGGGTCTC | 8440 |
rs761460122 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105792115 | TTTGGAGACCCCTCC[A/T]GCTCAGCCTCACCAC | 8440 |
rs761464719 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105864498 | GAGCCACGGTGCGTA[A/G]TGGAGTTTGAGGTTA | 8440 |
rs761474504 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105875141 | AGGAGTTTGTTCACA[C/T]TCCTTGCTGTCCATC | 8440 |
rs761521907 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105882120 | TGGGTCTGTGTGCCG[C/T]GCCCTTTTCACATTG | 8440 |
rs761540303 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105821280 | GAAAGATTTTTTACA[C/T]GCAAAGCCCAGTGCT | 8440 |
rs761551231 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105863251 | TCTGTCATCGTGATT[A/G]TAAATATTCTCACAG | 8440 |
rs761578398 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105787860 | GGCTACATCCATGTT[A/G]TAAGATGATCTCATT | 8440 |
rs761595502 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105820206 | CATGGTTCCTGGAGA[C/T]TGCAGGTCATTCAGA | 8440 |
rs761617257 | snp | C/T | 2.80257e-05 | 0.00374327 | synonymous-codon, utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105893152 | GCACGGGGAGAAGCT[C/T]TACCTCGTCAGGGCC | 8440 |
rs761661296 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105802603 | GGGATGTGCCAGGCT[C/G]TTTTTAACCATCACT | 8440 |
rs761674486 | snp | C/G | 1.71182e-05 | 0.00292554 | missense, intron-variant | NCK2 | GRCh38.p7 | 2:105881408 | GAGTACCCCGCCAAT[C/G]GCAGCGGCGCCGACC | 8440 |
rs761680676 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105764931 | CACACTTGCATAAGT[A/G]GTGTGCTCATTTGGA | 8440 |
rs761701786 | in-del | -/GTGTGTGTGTGTGTGT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105830671 | CTTGCCAGGAATTTG[-/GTGTGTGTGTGTGTGT]GTGTGTGTGTGTGTG | 8440 |
rs761702189 | in-del | -/T | | | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105773058 | ACCCCACTCAGCAAA[-/T]TTTTTTTTTTTTAAT | 8440 |
rs761706857 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105765839 | TGTGTGTGTAAGTCT[C/G]TGGAGGTATGTGTGT | 8440 |
rs761713187 | in-del | -/GTATT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105879049 | AAGTGTCTTTATAAC[-/GTATT]GTGATGGCCACTATC | 8440 |
rs761741680 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105820222 | TGCAGGTCATTCAGA[C/G]AATACTGGCTTGGGG | 8440 |
rs761756237 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105867483 | GTATTTAGAACCAAA[A/C]ATGTAAAACAAATCA | 8440 |
rs761758661 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105810862 | CAGCAGACTGTAAAT[A/C]TTAAATTTATATTAA | 8440 |
rs761784547 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105873821 | TGAGCCTCTCCCTGC[G/T]CACCTCTGCCCTTCA | 8440 |
rs761786969 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105759239 | TTTTGTTTGTTTATA[A/G]ACACATGCAGTATAT | 8440 |
rs761807304 | in-del | -/AAATG | | | intron-variant | NCK2 | GRCh38.p7 | 2:105847087 | CAAGTGATTCCACTT[-/AAATG]AGGTACCTGGAGTTG | 8440 |
rs761809320 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105843662 | CTCCCATACACAAAG[C/T]TGGAACAATTCAAGA | 8440 |
rs761827221 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105857415 | CAATCCCATTTTTGG[C/T]GAAAACAGATTGTTA | 8440 |
rs761829750 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105775952 | CACCAACAAAAAAAA[C/T]AGTGCGAGGGATAAT | 8440 |
rs761874526 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105888577 | TGATGGCTTAAAAAG[A/G]TGTCCATAAATTCTT | 8440 |
rs761898451 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105834773 | GTTGGGTTTAAGTGA[C/T]TGCCCCCCTGCTTCA | 8440 |
rs762019822 | snp | C/T | 1.66388e-05 | 0.00288429 | synonymous-codon, intron-variant | NCK2 | GRCh38.p7 | 2:105881467 | CGTCAAGTTCGCCTA[C/T]GTGGCCGAGCGGGAG | 8440 |
rs762031430 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105889257 | AAATTCCCTATGAGA[A/G]ATGTCTGGAGCAGAG | 8440 |
rs762037145 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105846101 | GAATCACTTGACAGT[C/T]ACAGCCTTCCTCCCA | 8440 |
rs762086724 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105860071 | AGAAGGATCAGTTGA[A/G]GCCACGAATTTGAGA | 8440 |
rs762103396 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105777809 | AGCAGGAAACAAACA[C/T]GTGCATCTTGAAAAT | 8440 |
rs762103913 | in-del | -/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105866133 | GGCCAGGCTGGTCTC[-/G]GAACTCCTGACCTCA | 8440 |
rs762104451 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105805180 | CCTAGAAGAGAGCAC[A/G]TTTGAGTTCCTTCCT | 8440 |
rs762111772 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105891806 | CCTGCCTTGGCCTCC[C/G]AAAGTGCTGAGATTA | 8440 |
rs762113310 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105824502 | CCCTGCCTGGAGTCT[A/G]GGTCTGGTACAGGCC | 8440 |
rs762114901 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105846616 | AATACTGTTCAGTTA[A/G]GAAATTGATGTATAC | 8440 |
rs762133170 | snp | A/G | 1.82207e-05 | 0.00301828 | missense, intron-variant | NCK2 | GRCh38.p7 | 2:105881913 | CCCCACAGATAAGCT[A/G]CACCGGGCCCTCGTC | 8440 |
rs762158229 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105877695 | GTCCTAGTTTCATTT[A/C]CTATAGAAATCATAT | 8440 |
rs762177582 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105751043 | GACATAAGGCAGGGG[A/C]AATGCCTGCATGACT | 8440 |
rs762212270 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105859273 | CTTTTCGGTGGTTAA[C/T]ATAGGCTTAAGGGCT | 8440 |
rs762223890 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105777158 | GCCCTGCGGCTGTCA[C/T]TGGGCACTCCACCGA | 8440 |
rs762250373 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105791723 | AAATCAGTGGTATAC[A/G]TTCTTCGTAGAGCTT | 8440 |
rs762271489 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105839183 | AAGGTGAGAATCAGA[A/G]TTTGGAAAAACTGCC | 8440 |
rs762274426 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105860479 | CCTGCTAAGCCGTAG[C/G]CGTCTCAGAATGAGG | 8440 |
rs762278980 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105787357 | TCTAACCCCCAGTGT[A/G]ACTATATTTGGAGAT | 8440 |
rs762336248 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105813618 | GGCCACGACTGCTTG[C/T]AGGGGGGCATCTCAC | 8440 |
rs762382562 | snp | C/T | 1.648e-05 | 0.0028705 | synonymous-codon | NCK2 | GRCh38.p7 | 2:105855105 | CAAGTGGGACTACAC[C/T]GCCCAGCAGGACCAG | 8440 |
rs762392609 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105843599 | AAACGAACGAACACT[C/T]GCAGTGATGGTGATA | 8440 |
rs762403632 | snp | C/G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105807636 | GCCCTTGAGCCCCTG[C/G/T]GGAGGCTGATCTGAC | 8440 |
rs762442376 | in-del | -/TGT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105765788 | GCTTAGAATAGGGGG[-/TGT]GTGTGTGTGTGTGTG | 8440 |
rs762460802 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105769659 | TGGGGTAATTAGAGT[C/T]ATTGGCCAAGAAGGG | 8440 |
rs762479770 | snp | A/C | 1.6625e-05 | 0.00288309 | missense, intron-variant | NCK2 | GRCh38.p7 | 2:105881625 | ACGAGGCGGCTGCGG[A/C]GTCCCCAAGCTTCCT | 8440 |
rs762486458 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105781537 | ACAGCCTAGCAGTTA[A/G]GATCTGGTTTGCTGG | 8440 |
rs762504423 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105818999 | ATAGGATTAAGTGTC[G/T]TAGTGTTCTCGTCGT | 8440 |
rs762514864 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105754080 | GGGACTGAGATAGGA[C/T]GGTGAGTCTGGCGTC | 8440 |
rs762530190 | in-del | -/GTT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105748383 | ACATTCTTTCCTGCA[-/GTT]GTTTTTTTTCTTTTT | 8440 |
rs762554910 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105755384 | CCTATAGATTAGGTG[C/T]CTAGTGTTGAATTTG | 8440 |
rs762564740 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105849395 | TGCCATCAGAAAGAA[C/G]GAAAGAAGGAGGGAG | 8440 |
rs762578847 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105863150 | TCTTGCTGGGTCACC[C/G]CAGGCTGTTTTGAGC | 8440 |
rs762591065 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105827262 | CCTTGGCCTCCCAAA[A/G]TGCTGGGTTTACAGG | 8440 |
rs762595150 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105873762 | GATGATTGGGAAGTA[C/T]GATTGGATCCAGGGG | 8440 |
rs762600919 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105861811 | TGAGCCACCGCACCC[A/G]GCCAGTTTCTCTCAT | 8440 |
rs762602257 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105888439 | TGCGGACAGTGGGAG[G/T]TAGCACAAAGGTGGC | 8440 |
rs762606119 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105800878 | TTTTCAATCCAAGCT[C/G]GAGGTTCCATGGGAT | 8440 |
rs762624636 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105785652 | AGCCACCTCAACATC[C/T]GCTCAGGTGTTTGCA | 8440 |
rs762637461 | in-del | -/CCTG | | | intron-variant | NCK2 | GRCh38.p7 | 2:105778832 | GGTTCCAGTGATCCT[-/CCTG]CCTCAGCTTCCCAAG | 8440 |
rs762683461 | snp | A/G | 1.65641e-05 | 0.00287781 | missense, intron-variant | NCK2 | GRCh38.p7 | 2:105881687 | GGCCAGGGCTCCCGC[A/G]TGCTGCATGTGGTCC | 8440 |
rs762690993 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105872849 | ATTCGGAGAAATCTC[C/T]GAAAAAGTAACTGAG | 8440 |
rs762725085 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105779907 | TAGCCTACGAGACCG[C/T]CTTCACCCTCTCATT | 8440 |
rs762735951 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105764677 | TTCTTGGTGTGAATT[A/T]ACTTTTAAAGATAGA | 8440 |
rs762788442 | in-del | -/GC | | | utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105894000 | CACACACACACGTGC[-/GC]ACACACACACACACA | 8440 |
rs762825671 | in-del | -/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105835825 | CATTCTTTTTTATTC[-/T]TTTTTTTCTGAATTC | 8440 |
rs762827040 | in-del | -/A | | | intron-variant | NCK2 | GRCh38.p7 | 2:105760854 | CAGGTTTGAGCAAAT[-/A]AAAAAATCACCGAAA | 8440 |
rs762827810 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105768381 | AGCTTTTCAGGGTTC[A/G]TGCCGGCCTCACAAG | 8440 |
rs762873971 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105800173 | ATAGTCTGGCTCTCC[C/T]TGGTCTCCGGCACGG | 8440 |
rs762882581 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105793513 | AATTCACCTAGGTCA[A/T]GTAGGCATTGCACTG | 8440 |
rs762886310 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105837592 | TCCCTGAGGCACAGT[A/G]CAAGAGTTTCTGTAC | 8440 |
rs762887511 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105842146 | GCTGGAGTGCAATGG[C/T]GCGACCTCGGCTCAC | 8440 |
rs762912456 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105773802 | CTGAGCTTGTGTCTG[G/T]CAGGCTGCCTGGAGA | 8440 |
rs762921030 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105887422 | GGGTAGAAGGAGATG[A/T]GTAGATTATTGATGC | 8440 |
rs762953356 | in-del | -/AAAC | | | intron-variant | NCK2 | GRCh38.p7 | 2:105878804 | GATCACATTCAAGCA[-/AAAC]AGGTAAAATTTCCGC | 8440 |
rs762957590 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105868426 | TTCCTGGAAGCAGGC[C/G]GTGCTGAGGCAGCTG | 8440 |
rs762978637 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105840883 | CATTATGCATCAGCC[A/G]GGTCCCCACGGAAAG | 8440 |
rs762980348 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105784992 | TTTTTGTTTTTGTTT[A/G]TTTTGAGACGGAGTC | 8440 |
rs762997273 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105746966 | CATAAACATTCAGGG[A/G]GGTTGGTCATGAAAC | 8440 |
rs763011883 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105804104 | ACATAGAGGCAGTGG[C/T]GACTCTCAGGATTTA | 8440 |
rs763052587 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105891358 | AGATTGTCACAGAGC[A/G]TATGTCCTGCATGCA | 8440 |
rs763054555 | in-del | -/TGTGTGTGTGTGTGTGTA | | | intron-variant | NCK2 | GRCh38.p7 | 2:105830691 | GTGTGTGTGTGTGTG[-/TGTGTGTGTGTGTGTGTA]TGTGTGTGTGTGTGT | 8440 |
rs763069551 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105846457 | TGGCAGTAAAGATAA[A/G]TTAATGGTAGATACT | 8440 |
rs763082202 | snp | C/T | 1.93463e-05 | 0.00311011 | intron-variant | NCK2 | GRCh38.p7 | 2:105881310 | CCTGCGCCACTGAGC[C/T]TTGCTGTGTCTCCAC | 8440 |
rs763085878 | snp | A/T | 2.41036e-05 | 0.00347149 | missense, utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105893139 | TCTTCACCAGCGAGC[A/T]CGGGGAGAAGCTCTA | 8440 |
rs763103561 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105771018 | AGCTCTGCCTCCCGG[G/T]TTCACGCCATTCTCC | 8440 |
rs763108094 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105820646 | GTCATTTTGGCAAAC[A/G]CATAATCTGCACTTA | 8440 |
rs763125728 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105756265 | CTTCCTGTGCTGTTT[C/T]TAGGATAAACACGAA | 8440 |
rs763135850 | snp | A/C | 0.000474129 | 0.0153896 | missense, intron-variant | NCK2 | GRCh38.p7 | 2:105881397 | GCACGGACGCCGAGT[A/C]CCCCGCCAATGGCAG | 8440 |
rs763147739 | in-del | -/AT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105877943 | GAGGGTTTAGATAAC[-/AT]AGTAAAGTCAGGTCC | 8440 |
rs763157616 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105792653 | TTGTTGGCAAAACCC[A/G]GTCTTTTGTCATTTG | 8440 |
rs763174250 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105750688 | GTGATTGAAGAGAGA[C/G]AAAAATCTTGACTTG | 8440 |
rs763187728 | in-del | -/A | | | intron-variant | NCK2 | GRCh38.p7 | 2:105811164 | TGGTGACAGAGTGCA[-/A]AAAAAAAAAAAAAAT | 8440 |
rs763206461 | in-del | -/TCAC | | | intron-variant | NCK2 | GRCh38.p7 | 2:105886660 | TCTGACTTAAATGTA[-/TCAC]TCAGTCACATCAGGT | 8440 |
rs763265595 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105857559 | AGAGTGTCAGCCCTC[C/G]CATAGGCTTGGTCTC | 8440 |
rs763268706 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105777121 | ACTGCTGCTGCCGCC[A/G]AGCAGGAATTCTGAG | 8440 |
rs763285298 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105786145 | GATCATCTGTTGTGT[C/T]TAGGGCAGCATGATT | 8440 |
rs763293648 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105760903 | ATGTGTCATGCCTTG[C/T]GCTTTGGGACACCCC | 8440 |
rs763349749 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105870215 | CCAAGCAGGGGCCCT[A/G]CAGGTGCTCCTCCTA | 8440 |
rs763352916 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105748447 | TGGAGTACAGTAGCA[C/T]GATCACAGCTCACTG | 8440 |
rs763353259 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105762840 | CTATGTCTCAAGTTT[A/G]TTTTTAAGTAATATA | 8440 |
rs763360828 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105828645 | ACAAGCACTAACCCT[A/G]GGGTCAAGAGACCCA | 8440 |
rs763366761 | in-del | -/ACTA | | | utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105894019 | CACACACACACACAC[-/ACTA]TATATATATATATTA | 8440 |
rs763374583 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105814810 | GACACAGGGCACACA[G/T]GGGGGAGGCCTGTAT | 8440 |
rs763390583 | snp | C/G | | | upstream-variant-2KB, intron-variant | NCK2 | GRCh38.p7 | 2:105850954 | GGTTTTAAGAAACAG[C/G]GTCCAAGGGATGCAA | 8440 |
rs763419863 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105797034 | AGAAATGGATTTAGT[C/T]ATCACAGTCCCTTTT | 8440 |
rs763482146 | snp | A/G | 3.62325e-05 | 0.00425617 | missense, intron-variant | NCK2 | GRCh38.p7 | 2:105881897 | CTGCACCCTGCGCAC[A/G]CCCCACAGATAAGCT | 8440 |
rs763491670 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105867371 | AGATTGTTCATAATA[C/G]GAAGGGCCCACATAA | 8440 |
rs763498416 | in-del | -/GG | | | intron-variant | NCK2 | GRCh38.p7 | 2:105765784 | ACAGCTTAGAATAGG[-/GG]GGGTGTGTGTGTGTG | 8440 |
rs763509485 | in-del | -/GA | | | intron-variant | NCK2 | GRCh38.p7 | 2:105761511 | CCATTATACACAGAT[-/GA]GAGAGAGACTCTGTT | 8440 |
rs763534960 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105882891 | TTCTAGGAGGCTTCA[A/G]TTTCATTTTTAAATG | 8440 |
rs763541882 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105849418 | GGAGGGAGGGAAGAC[G/T]CTGGTCTTCTCTGTG | 8440 |
rs763545854 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105807665 | ACCCACAAGGTAGTT[A/G]TTTTTTTCAACCTCT | 8440 |
rs763551203 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105825067 | GAGGTGCTTGGGGAC[A/G]GAGTGGAGGTAGACA | 8440 |
rs763564259 | in-del | -/TTTATA | | | intron-variant | NCK2 | GRCh38.p7 | 2:105854366 | GTTTTGGGGAATAAT[-/TTTATA]TTTATAAAAAAGTTC | 8440 |
rs763565809 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105836742 | ACACTGCAGCTCTTT[C/G]GGTGGATACGGTGAG | 8440 |
rs763589848 | snp | C/T | 1.65633e-05 | 0.00287774 | missense, intron-variant | NCK2 | GRCh38.p7 | 2:105881688 | GCCAGGGCTCCCGCG[C/T]GCTGCATGTGGTCCA | 8440 |
rs763627518 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105796330 | AGAGTGCTGGAGGTT[A/G]GTGTCAGTTTATCTT | 8440 |
rs763646517 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105795410 | AACTTAATCATGATA[G/T]TGAGTTAAACTGAAT | 8440 |
rs763666468 | in-del | -/CA/CACC | | | utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105894009 | ACGTGCACACACACA[-/CA/CACC]CACACACACACTATA | 8440 |
rs763667597 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105877694 | AGTCCTAGTTTCATT[G/T]CCTATAGAAATCATA | 8440 |
rs763774390 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105807335 | GCAGGGGAAATAAAG[A/G]TTTTGAGGTTTCTGA | 8440 |
rs763784905 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105863220 | AATTCTCATTTCGGC[A/G]TTATAGGATTGTGGG | 8440 |
rs763788596 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105761159 | ACCCTACTGGGCCTC[C/T]TCTGGGCAGCAGGGT | 8440 |
rs763813415 | snp | A/G | 1.75299e-05 | 0.00296051 | intron-variant | NCK2 | GRCh38.p7 | 2:105892947 | ACAGCTCCCCGCTGT[A/G]GCCCGGCTGTAACTG | 8440 |
rs763827166 | in-del | -/TTTTTGT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105829919 | TAGTCATTCATTCTC[-/TTTTTGT]TTTTTGTTTTTTTGA | 8440 |
rs763829624 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105833543 | AACTTGTAAAATGTC[G/T]TCTGATATTATTTAT | 8440 |
rs763835058 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105780755 | TTTCCTTACGGAAGA[C/T]ACCCCAGAGGGCCCC | 8440 |
rs763855184 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105848084 | ACCTTATGTTCAAGC[A/C]ATTGAGCCTAGTGAT | 8440 |
rs763870719 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105862099 | ATAAATACATGTAAT[G/T]AGAGCAGCAACAGCT | 8440 |
rs763877585 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105819013 | CTTAGTGTTCTCGTC[A/G]TGTTACGCTTTATGT | 8440 |
rs763887380 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105752903 | AGCTTCTCTCCCACA[C/T]GGACACAGACACACA | 8440 |
rs763894774 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105887443 | TTATTGATGCTTGGA[A/G]ACTTCAGCGTGGCTG | 8440 |
rs763899181 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105828486 | CCACCGCAGATCAGT[G/T]TGGAGTGCAGAATTT | 8440 |
rs763929530 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105774713 | TCTGGGGCCTGGATG[A/T]CGAAATCTGTGTTCC | 8440 |
rs764022792 | snp | A/G | 1.65444e-05 | 0.00287609 | missense, utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105893051 | GTGCAGCTCGTGGAC[A/G]ATGTCTACTGCATTG | 8440 |
rs764040005 | in-del | -/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105788884 | ACTAGTCAGGGCAGC[-/G]GATCTCTTATCTGCT | 8440 |
rs764088859 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105842148 | TGGAGTGCAATGGCG[C/T]GACCTCGGCTCACTG | 8440 |
rs764094198 | in-del | -/TTTT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105855833 | GTCCCCATGTGCCTC[-/TTTT]TTTTTTTTTTTTTTT | 8440 |
rs764141400 | snp | C/T | 1.92628e-05 | 0.00310339 | intron-variant | NCK2 | GRCh38.p7 | 2:105881320 | TGAGCCTTGCTGTGT[C/T]TCCACAGGCCTCGGC | 8440 |
rs764150717 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105799587 | CTGCCACACCAAACA[C/T]GAGCTGATGAGTTAT | 8440 |
rs764180187 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105781929 | CGTAAATGCTTTTAA[C/T]TGAAATAGGTACATA | 8440 |
rs764189381 | snp | C/T | | | upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105743721 | AGTCAAACACTCACC[C/T]GTCTGACTTCAAAGC | 8440 |
rs764192536 | snp | C/G | 1.71658e-05 | 0.00292961 | missense, intron-variant | NCK2 | GRCh38.p7 | 2:105881402 | GACGCCGAGTACCCC[C/G]CCAATGGCAGCGGCG | 8440 |
rs764223468 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105757337 | GTTAAAATTGAGATG[G/T]GACAGGTCCTTGATT | 8440 |
rs764265231 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105777133 | GCCGAGCAGGAATTC[C/T]GAGCCCACGGCCCTG | 8440 |
rs764266457 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105866243 | AAAATTTGGAAACTA[C/T]AGAAAAGCATAAAAG | 8440 |
rs764271339 | in-del | -/AGG | | | intron-variant | NCK2 | GRCh38.p7 | 2:105887003 | AGAGTGAACATTGAT[-/AGG]AGAATAGGAAAAGCT | 8440 |
rs764276840 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105756413 | TAATAGTAATTCTTT[C/G]CACAGACTGGAAAGT | 8440 |
rs764282009 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105802900 | ATCTGCTGCTTTCTC[A/G]GGGGTGAGGTGGTGT | 8440 |
rs764292037 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105822696 | AATTCTGTACCCCTC[A/G]ACCTTCTTTTCCTTA | 8440 |
rs764310082 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105804120 | GACTCTCAGGATTTA[C/T]TAATTTCAAGGGTGT | 8440 |
rs764334314 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105891457 | TGATCAAAACTTGAT[A/G]TTTTTGTACAAAGAA | 8440 |
rs764357743 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105845540 | CTGAAATTACAGGCA[G/T]GTACCAGCATGCCCG | 8440 |
rs764376305 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105844154 | AAATCCTAACGGGTG[A/G]GGGGACATTCTTTAA | 8440 |
rs764386079 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105870902 | GCAACATCACTGACA[C/T]ACGGGTGTGTGAGTG | 8440 |
rs764424085 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105753909 | CAAGTCCAAATGTAG[A/G]TTCTTGGGAGACTGC | 8440 |
rs764487273 | in-del | -/GTA | | | intron-variant | NCK2 | GRCh38.p7 | 2:105817053 | TGGTGGCGTGCACAT[-/GTA]GTCTCAGCTATTCGG | 8440 |
rs764493809 | snp | A/G | 1.7271e-05 | 0.00293857 | synonymous-codon, intron-variant | NCK2 | GRCh38.p7 | 2:105881824 | ATGCAAAAATGCCCG[A/G]GGCCAGGTGGGCCTC | 8440 |
rs764581321 | snp | G/T | 1.81496e-05 | 0.00301239 | missense, intron-variant | NCK2 | GRCh38.p7 | 2:105881905 | TGCGCACGCCCCACA[G/T]ATAAGCTACACCGGG | 8440 |
rs764641239 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105761877 | AGTGAGACCAAAAAA[C/G]ACTGAATACAGACAT | 8440 |
rs764650739 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105813754 | GTGGCTTTAGTGGAA[A/C]AAAAGCAAATTTTAA | 8440 |
rs764650740 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105826114 | GATTTAATTTACTCA[C/T]AGTTCAGCATAACTG | 8440 |
rs764702270 | in-del | -/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105746600 | TTCAAGCCTTGCGAG[-/T]TTTACGTAAAGAGAA | 8440 |
rs764703602 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105870258 | GAGAGCAGCCAGCTG[A/G]AGGCTGAGGAGGCAG | 8440 |
rs764736765 | in-del | -/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105869855 | TTCTCTTCATTGGCA[-/T]CTGTGTTCCCATTTG | 8440 |
rs764821563 | snp | C/T | 1.79306e-05 | 0.00299416 | utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105893221 | GGCCCCACGGTGGAG[C/T]TGCCCGCCCGGCCTT | 8440 |
rs764909967 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105847351 | TGGTTAAAATGTTAA[A/G]CTTTGTTAAATATAT | 8440 |
rs764913999 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105872707 | ATTTGTAGGTATTCT[A/C]GTGTAAATTCATGGC | 8440 |
rs764934021 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105778133 | AAGGACAAGATGTGT[C/T]GTGAAGGAGATGTTG | 8440 |
rs764948111 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105828344 | GCCTAACCATATTTT[A/T]GTTGTTGTTGTTTTG | 8440 |
rs764971775 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105856999 | TTAGTGATGCCAAAC[A/G]TTGTTACGTTGTTGA | 8440 |
rs764985286 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105860741 | GGTCCATAGAGAGCC[A/G]TGGATGCCGGCGGCG | 8440 |
rs765004749 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105871940 | GACAGTTTTGGAGAT[A/G]GGCTGAGATTTCGTG | 8440 |
rs765006871 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105887088 | AAGAACATAGGGTCA[A/G]CTGACAGCTAGCAGC | 8440 |
rs765024335 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105840633 | GCCAGTTGCACGTCC[C/T]AGGTTGTTTTAACCA | 8440 |
rs765026598 | in-del | -/TTTTTTTTTTTTTTT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105891534 | AGATAAAAGACCAAT[-/TTTTTTTTTTTTTTT]TTTTTTTTTTTTTTT | 8440 |
rs765030060 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105810599 | GTTAAAAAGGCAATA[A/T]GTAATTAAATTGTCT | 8440 |
rs765048560 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105780333 | AGATATATACACACA[C/T]ACACACACACACACA | 8440 |
rs765059372 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105831952 | GATATATTGATAGGG[A/G]TCACATTGAAAATGT | 8440 |
rs765106638 | snp | C/T | 1.66299e-05 | 0.00288352 | missense, intron-variant | NCK2 | GRCh38.p7 | 2:105881622 | TGGACGAGGCGGCTG[C/T]GGAGTCCCCAAGCTT | 8440 |
rs765157659 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105799457 | TTATTGAGAAGGCTG[A/T]CTCTTCCCTGGGGAC | 8440 |
rs765223593 | snp | A/C | 2.02308e-05 | 0.00318041 | missense, intron-variant | NCK2 | GRCh38.p7 | 2:105882036 | ACTTCCTCATTAGGG[A/C]CAGCGAGTCCTCGGT | 8440 |
rs765241366 | snp | A/C | | | intron-variant, utr-variant-5-prime | NCK2 | GRCh38.p7 | 2:105745666 | ACCGTGTTTATTACA[A/C]CTATTTATGTTCGCG | 8440 |
rs765262710 | snp | C/T | 1.95074e-05 | 0.00312303 | synonymous-codon | NCK2 | GRCh38.p7 | 2:105855246 | GGAGCGGAAGAACAG[C/T]CTGAAGAAGGGCTCC | 8440 |
rs765278508 | snp | C/G | 1.75922e-05 | 0.00296577 | intron-variant | NCK2 | GRCh38.p7 | 2:105892940 | TTTAGACACAGCTCC[C/G]CGCTGTGGCCCGGCT | 8440 |
rs765331885 | snp | A/G | 1.65198e-05 | 0.00287395 | missense, utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105893025 | CGTCAGGGAAGAACA[A/G]ACACTTCAAGGTGCA | 8440 |
rs765370334 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105768552 | TCACAGAACTCAGAA[A/G]GGCACTTTGCTTATT | 8440 |
rs765372218 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105788366 | CTCCATTTCTATCAA[C/T]GCCATTTAGATGATG | 8440 |
rs765412850 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105874063 | CTAAGAGAAGGGACA[A/G]AGGGTTCTGAACAGA | 8440 |
rs765429457 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105842781 | ACAGTGAATGCAGAG[A/G]TGGGGACGGGACCCA | 8440 |
rs765438756 | snp | C/T | 1.65803e-05 | 0.00287922 | intron-variant | NCK2 | GRCh38.p7 | 2:105881297 | GGTGCCCAAGTGCCC[C/T]GCGCCACTGAGCCTT | 8440 |
rs765441804 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105813647 | ACTGCCTGGCCCTGC[A/G]CCTGGGACAAGTAGT | 8440 |
rs765463213 | snp | C/T | | | missense | NCK2 | GRCh38.p7 | 2:105855173 | TGGACGACTCCAAGA[C/T]GTGGTGGCGGGTGAG | 8440 |
rs765493654 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105857473 | TTTTTACATTTCTTT[A/G]ACTTTCTTCCTTCCT | 8440 |
rs765500142 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105819247 | CAAGACAGACACCAT[C/T]GGGGTGTTCCTGTTC | 8440 |
rs765515870 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105888736 | TGGCTGCCTCTTTGC[A/T]CTCTCTTGGGTCACT | 8440 |
rs765542463 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105776216 | AGTGTCCTGGGTGGG[G/T]ACACCCCAACTTCCG | 8440 |
rs765555796 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105819767 | AGTTCCACACAAAAC[C/G]TTGATTCACCTATTA | 8440 |
rs765573075 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105769598 | TCTAAGAAATGGGAC[A/G]TGTGGGTGACCTACT | 8440 |
rs765593290 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105775003 | GGGCTGTATAGCAAG[C/G]CCCTGTCTCTACAAT | 8440 |
rs765594937 | snp | C/G | 1.71375e-05 | 0.00292719 | missense, intron-variant | NCK2 | GRCh38.p7 | 2:105881819 | TGGAAATGCAAAAAT[C/G]CCCGGGGCCAGGTGG | 8440 |
rs765600115 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105868874 | AGCCAAGCGACTTGG[C/G]CAGGGCTATGAGTCT | 8440 |
rs765632081 | in-del | -/AC | | | intron-variant | NCK2 | GRCh38.p7 | 2:105752913 | CACACGGACACAGAC[-/AC]ACACACACACACATT | 8440 |
rs765651466 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105747488 | TAACTGCTCAAACTG[G/T]CTTGCCGTGTGCACT | 8440 |
rs765653352 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105760531 | CTTCCCTGCTGGTGG[C/T]ACCTAGCTCTAAGGC | 8440 |
rs765658364 | snp | A/G | 8.26863e-05 | 0.00642933 | synonymous-codon, intron-variant | NCK2 | GRCh38.p7 | 2:105881707 | GCATGTGGTCCAGAC[A/G]CTGTACCCCTTCAGC | 8440 |
rs765666439 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105825101 | CCTGGCTCCTGCCTC[C/G]TCCTCTCCCTCCAGG | 8440 |
rs765718190 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105795115 | ACTAGCAACATCCCC[G/T]ACAGGGTGCTGCATT | 8440 |
rs765732618 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105807004 | AAGACATCCTATCCC[A/G]CACCCTCATGCTGAA | 8440 |
rs765736322 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105880185 | ATCTGTGACTGAAGA[A/G]ACAGTACTTACTGTA | 8440 |
rs765757311 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105760641 | GGTCTTTGCTTTCTG[C/G]ATAACTTCATCCTTC | 8440 |
rs765832059 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105849354 | GATTGTGCCACTGCA[C/T]TCCAGCCTCAGATGC | 8440 |
rs765851514 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105828150 | TCATTTCCTCTTTTT[A/G]TAGTAGTTTGTAGTT | 8440 |
rs765896708 | in-del | -/ACACACACACACGTGCACACAC | | | utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105893985 | CTACCAACACTTTAT[-/ACACACACACACGTGCACACAC]ACACACACACACACT | 8440 |
rs765924655 | in-del | -/T | | | upstream-variant-2KB, intron-variant | NCK2 | GRCh38.p7 | 2:105850869 | GGTCATCTGCAGTCT[-/T]CTTTCTGTTCAAATC | 8440 |
rs765993944 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105787664 | TCAGTCTCTCCCTGC[G/T]GTGGAGACTCCACCC | 8440 |
rs766006920 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105859505 | ACTTGCATGATCAGC[C/G]CCAGAACTCCTGCCT | 8440 |
rs766029644 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105792313 | GTGTAGTCCTAAGGT[A/G]GAATCAGAATAAATT | 8440 |
rs766031821 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105839486 | AGACAAGAGCTTGAG[A/G]GATGAGTCTCAGATT | 8440 |
rs766046874 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105751234 | TCACCGACTCACTCG[A/G]TTATCCTTGAATTCT | 8440 |
rs766093008 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105871077 | GTCACTGCAGACACA[A/G]GCCTGGAGGGTCGAT | 8440 |
rs766100407 | snp | A/T | | | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105771621 | TTTCCCATTGTTTCT[A/T]ATCATGTCACTTAGG | 8440 |
rs766109362 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105798191 | TTGTTTTCTTCTGAT[A/C]TGATGATTTTGTTGA | 8440 |
rs766157739 | snp | C/T | | | upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105743523 | GAGGCTGTTCTGATT[C/T]CCTGAGCTTGTACCT | 8440 |
rs766185087 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105886166 | GTTATTTTTAATTGC[A/C]AGGCTTTTTGCCCAG | 8440 |
rs766192439 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105756212 | TTATTTCCTGTTCCA[C/T]TATTCTTCCTTTTGA | 8440 |
rs766204961 | snp | C/T | 3.45728e-05 | 0.00415755 | synonymous-codon, utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105893167 | CTACCTCGTCAGGGC[C/T]CTGCAGTGACGGCGC | 8440 |
rs766217195 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105782672 | ATGATAGAACCTGAT[C/G]GTTTCTGAGAGTGGG | 8440 |
rs766223855 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105866029 | GAGCAATTTTCCTGA[C/T]TCAGCTTCCCAAGTA | 8440 |
rs766243844 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105809315 | AAAGTCCCAGGCTGC[C/T]ATGGGAAAGTACCAC | 8440 |
rs766256305 | snp | A/G | 1.68224e-05 | 0.00290016 | missense, intron-variant | NCK2 | GRCh38.p7 | 2:105881432 | GCCGACCGCATCTAC[A/G]ACCTCAACATCCCGG | 8440 |
rs766264690 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105854058 | GAAGAAGATTCAAAG[C/G]AATTTGGCTGAAGTT | 8440 |
rs766270279 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105864953 | AACACTGGAATAACA[C/T]CATCCAAATAACACG | 8440 |
rs766282617 | in-del | -/A | | | intron-variant | NCK2 | GRCh38.p7 | 2:105882769 | GTGTGTGAAGGAAAT[-/A]ACTCGACCAGTTTTG | 8440 |
rs766346819 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105780740 | TGCAAATGGGATTAA[C/T]TTCCTTACGGAAGAC | 8440 |
rs766356041 | in-del | -/A | | | upstream-variant-2KB, intron-variant | NCK2 | GRCh38.p7 | 2:105850622 | CTAGCTGTAGTAATG[-/A]AGCCAAAAATTAGGT | 8440 |
rs766356399 | in-del | -/TTG | | | intron-variant | NCK2 | GRCh38.p7 | 2:105879204 | TCTATTAAAAGTTTA[-/TTG]TTCAATGTTATTTCT | 8440 |
rs766366565 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105808228 | TAAGAAAAGAACATT[A/G]CATCATTCAATGCTT | 8440 |
rs766392719 | snp | A/G | 4.03161e-05 | 0.00448959 | synonymous-codon, intron-variant | NCK2 | GRCh38.p7 | 2:105882034 | CGACTTCCTCATTAG[A/G]GACAGCGAGTCCTCG | 8440 |
rs766410683 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105813609 | TGCAGAATCGGCCAC[A/G]ACTGCTTGCAGGGGG | 8440 |
rs766423706 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105820425 | GTTTGCGTGCCTGGG[A/G]CTGGGCTGAGAGCAG | 8440 |
rs766446105 | snp | A/G | 3.29663e-05 | 0.00405981 | synonymous-codon | NCK2 | GRCh38.p7 | 2:105855138 | GCTGGACATCAAGAA[A/G]AACGAGCGGCTGTGG | 8440 |
rs766485850 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105891877 | TTAATTAAAATAATG[A/G]CATGTTTCTAAAATA | 8440 |
rs766493236 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105768455 | CAGTTGCATGTCCTA[A/G]GCCACCTGTACTTCT | 8440 |
rs766508291 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105856476 | CTAACAAGAGGATTT[G/T]TTTTCTTTTGGGGAA | 8440 |
rs766509319 | in-del | -/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105825916 | GTCAGGTTTGGAGTT[-/C]CTGGCTCCATTAGAT | 8440 |
rs766509881 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105824186 | CATGTGTGAGTGCCC[C/T]CTCCCTTTATTGACC | 8440 |
rs766511678 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105786239 | TACAAATGACTCTGA[C/T]AACAAATGATTATTT | 8440 |
rs766549348 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105748226 | TGGCTCAGTCTCCTC[C/T]GTGTCCTGAGTTCTT | 8440 |
rs766557465 | snp | A/G | 2.59017e-05 | 0.00359864 | intron-variant | NCK2 | GRCh38.p7 | 2:105882094 | GCAGGCAGTAAATGC[A/G]CCTTGCGCGGTGGGT | 8440 |
rs766597481 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105846896 | AGCATTATTGACAAC[A/T]GCCCAAAGGTGGAAG | 8440 |
rs766624888 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105767276 | AATGTAATACTGCTC[A/G]TGACGTGGCCTACTT | 8440 |
rs766631785 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105836213 | ATCTGTACGTTGATA[A/T]CTGCACTGTTAGCGA | 8440 |
rs766635732 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105868648 | ACTTCATTCAGTGGC[A/G]AGAAAGGTTGGTTGT | 8440 |
rs766636504 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105835024 | GCAAACTCTTGTAAC[C/T]ATGTTAAGTATTTTC | 8440 |
rs766679038 | snp | C/G | | | utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105893604 | CCTAGCAGCCCTCGC[C/G]CATGTCCTGTGCCCT | 8440 |
rs766680599 | in-del | -/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105799292 | AAAAAGTTCTTCCTT[-/C]AGGGTTATAAAGGGT | 8440 |
rs766685728 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105874750 | ATCTGAAAGGGGATA[C/T]AAAAGATTTTGACTT | 8440 |
rs766725763 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105880068 | GAATGTTCCGGAATT[C/T]CGTGCATTTTAACAC | 8440 |
rs766742007 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105879230 | TATTTCTTGACATCA[C/T]TGTTGCCAATAAAAG | 8440 |
rs766749091 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105890135 | TAAATTGGTTCTACA[A/T]CCTTAACTTTTAAAG | 8440 |
rs766749428 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105822959 | TCTGTCCTTGTCCTT[A/G]AGAGGCCCTGGGCCG | 8440 |
rs766753457 | snp | A/G | 7.4599e-05 | 0.00610688 | missense | NCK2 | GRCh38.p7 | 2:105855236 | CCAACTACGTGGAGC[A/G]GAAGAACAGCCTGAA | 8440 |
rs766769945 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105757834 | CTGGAGGATAATATT[A/T]TCTTCAAGATCCTCA | 8440 |
rs766849490 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105805540 | TTAAACATTTTAAAT[C/T]AAATTTCCCGAACTT | 8440 |
rs766856573 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105768197 | TCATTTGCTTTCTTT[A/G]CCTGTCTGTAGAGTC | 8440 |
rs766883850 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105847734 | TTTTTTCATTGACTG[A/G]TTCTCTAAAATGAAC | 8440 |
rs766889437 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105774631 | GGCACACACACAACG[A/G]ACTCTAGACCTGGCT | 8440 |
rs766897162 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105749720 | TGACTGAGGTTGAGC[A/G]GTGTGAGGGGAGGCC | 8440 |
rs766917555 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105826276 | TCAGTATCACCAAGA[C/T]AGCATGGGGGAAACC | 8440 |
rs766961295 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105804264 | TCAAAATGTGTGTAA[A/G]TGAACGGACCAGCGC | 8440 |
rs766966348 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105798024 | AGAAAATTATAACCA[C/T]ATTTTTATTAATTTA | 8440 |
rs766993432 | snp | C/T | 1.65518e-05 | 0.00287674 | missense, intron-variant | NCK2 | GRCh38.p7 | 2:105881693 | GGCTCCCGCGTGCTG[C/T]ATGTGGTCCAGACGC | 8440 |
rs766996959 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105856197 | CCCTCCTGGAGTTAC[A/G]CAAAGTTAACAGTAT | 8440 |
rs766999626 | in-del | -/TGTGTGTGTG | | | intron-variant | NCK2 | GRCh38.p7 | 2:105823139 | CTCTCATGCTGTGTG[-/TGTGTGTGTG]TGTGTGTGTGTGTGT | 8440 |
rs767019640 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105809190 | CACCTGGTGGTTTTG[A/G]CCTCGAGTTCTTTCA | 8440 |
rs767026903 | in-del | -/TT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105872494 | CCTGACCTCCTCCTC[-/TT]TATTGCGATTGTCAC | 8440 |
rs767075400 | in-del | -/TAAGT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105770120 | AACATAAAGCACTAA[-/TAAGT]AAAAAAAAAAAAAAA | 8440 |
rs767141358 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105761966 | TATGTTTTCTCTTTT[C/G]TCCTGCGGATTTTTG | 8440 |
rs767189307 | snp | A/G | 1.67894e-05 | 0.00289731 | synonymous-codon, utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105893071 | CTACTGCATTGGGCA[A/G]CGGCGCTTCCACACC | 8440 |
rs767210537 | snp | C/T | | | upstream-variant-2KB, intron-variant | NCK2 | GRCh38.p7 | 2:105851220 | GGGGTGCCTCCTTCA[C/T]TGAGGATACCGGGCT | 8440 |
rs767240597 | snp | C/T | 5.63703e-05 | 0.00530867 | missense, intron-variant | NCK2 | GRCh38.p7 | 2:105881340 | CAGGCCTCGGCAAGA[C/T]GCGCAGGAAGACCAG | 8440 |
rs767241991 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105781697 | AGCAATGCATGAAAA[G/T]TACAGAGCCTGTGGC | 8440 |
rs767242647 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105780868 | CCTGGTACTTTGATC[C/T]TGGACTTCCAGCTTC | 8440 |
rs767266233 | snp | A/G | | | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105771517 | TTGCAGTAAGCCGAG[A/G]TTGGGCCACTGTACT | 8440 |
rs767272808 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105864510 | GTAGTGGAGTTTGAG[C/G]TTAGGGTGGGACGTC | 8440 |
rs767283106 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105818773 | GGACTATGGAATCTT[C/T]TGGTGTGGTGGTTTC | 8440 |
rs767293809 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105791447 | CCTAACAACAATGTA[A/G]GGAGTGCACCCTCGC | 8440 |
rs767370787 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105792241 | TATCACATTTTATGA[C/T]GATCTTGACATTCTT | 8440 |
rs767394917 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105820347 | TGAAATAAATGCTGG[C/T]CTGGTAGAACAGTAA | 8440 |
rs767404982 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105879533 | CGTTTCACCTGTTCT[A/C]ATATTCTGGCTTACT | 8440 |
rs767425900 | snp | A/C | 5.13624e-05 | 0.0050674 | missense, intron-variant | NCK2 | GRCh38.p7 | 2:105881413 | CCCCGCCAATGGCAG[A/C]GGCGCCGACCGCATC | 8440 |
rs767498334 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105801167 | TCTTAGGTGAGTGTC[C/T]CATAAATCTGTGGTG | 8440 |
rs767509799 | in-del | -/ATCAGCTG | | | intron-variant | NCK2 | GRCh38.p7 | 2:105878240 | CCTGTGCTTTATAGC[-/ATCAGCTG]AACGCTGGTGCCTGT | 8440 |
rs767517666 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105831041 | GAGTGTCTCTTCATT[C/T]GATTATTTCCTTTGC | 8440 |
rs767519636 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105819141 | CTCACACTGCATACC[G/T]GACTTCACCCCAGCC | 8440 |
rs767535997 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105778252 | ACAGACTGGCCGTCC[C/G]TATCCCAGCACATGT | 8440 |
rs767555785 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105810887 | TATTAATATTTGCCC[A/G]GCTATGGGCCAGGTG | 8440 |
rs767555984 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105823952 | CAGTGTGAACAACCC[A/G]TGGTCCGGAGCAGTC | 8440 |
rs767571411 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105783124 | CCAGAGCCCTGGGAG[A/G]TGGTTTAACTTTCTC | 8440 |
rs767573276 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105800611 | CTCAAAGTTCTACTA[A/T]GGCCTAAGAACAAGA | 8440 |
rs767582966 | in-del | -/TTG | | | intron-variant | NCK2 | GRCh38.p7 | 2:105891264 | AACTCTTTTTTTTGT[-/TTG]TTTTCTTTTTTTTTT | 8440 |
rs767588515 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105887805 | AAAACTGCAAAGGTG[C/G]TTTTCAGCAAGTATT | 8440 |
rs767612614 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105757573 | TCATACCTACATAGG[A/T]CCAGCCATGGGCCAG | 8440 |
rs767613766 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105882341 | TTTCACAGGCTCAAA[C/T]ATCATTTTCTCTCCT | 8440 |
rs767616117 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105885007 | CATTTTGTCCACATT[A/G]ATTCTATGGATGTGG | 8440 |
rs767637978 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105747039 | GCTGCTGCATAACCC[C/G]CTCTGTCCACTTGTG | 8440 |
rs767641293 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105833971 | TTTCCAAAGTTGTTA[C/T]TGATTTTTAGTTTTA | 8440 |
rs767654668 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105867633 | AATACTAAGGAGAAT[C/G]AGGTGTGGAGTTCAC | 8440 |
rs767658854 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105784241 | CCCAAAATGCTGGGA[C/G]TACAGGCATGAGACA | 8440 |
rs767738357 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105749753 | CAGGAGCAATGTCAG[A/T]CTCTCTTGTCCCCAC | 8440 |
rs767755673 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105877718 | AATCATATTACAGAT[A/G]ATAATGCTTTCCATA | 8440 |
rs767764302 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105860247 | GCAGTGATTGCAACA[C/T]TGCACTCCAGCCTGG | 8440 |
rs767766061 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105891222 | CACACACTTAGAGCT[A/G]CGGTATCTCATGCTC | 8440 |
rs767818418 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105879176 | GCTTTTGTAATTCAC[A/G]TGTTTGCAAAGGTCT | 8440 |
rs767858559 | snp | A/G | | | utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105893754 | GAATTTCCTGGAAAG[A/G]CAGTCTGCAAAAGAG | 8440 |
rs767884529 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105756665 | TGGGATGGCCCAGCT[A/C]CAGAGCAGCAGGTCC | 8440 |
rs767885455 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105777828 | CATCTTGAAAATGCC[A/G]AGCTCCCTTTGCAGT | 8440 |
rs767899136 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105754416 | TTCGATTTTCCTTAA[C/T]GGTTATGTCTCCCAT | 8440 |
rs767904087 | in-del | -/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105818051 | CAACAATGATGGACT[-/G]GATTAAGAAAATGTG | 8440 |
rs767908154 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105805222 | TGGATTTGATTGCAC[A/G]ATGGCATTGGGAAGC | 8440 |
rs767953756 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105845618 | AGGCTGGTCTCGAAC[C/T]CCTGACCTCAGATGA | 8440 |
rs767967191 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105890711 | CTATGGCTGCTGGGT[A/G]AGCCCAGCTGCCTTG | 8440 |
rs767975664 | snp | A/G | 1.95957e-05 | 0.00313009 | missense, intron-variant | NCK2 | GRCh38.p7 | 2:105882011 | CTCAACGAGCGGGGC[A/G]TGGAGGGCGACTTCC | 8440 |
rs768017338 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105815574 | ATACTTACCAAGTGC[A/G]GTGAACATAACGCAG | 8440 |
rs768020923 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105860480 | CTGCTAAGCCGTAGG[C/T]GTCTCAGAATGAGGA | 8440 |
rs768027105 | snp | A/G | 1.648e-05 | 0.0028705 | missense | NCK2 | GRCh38.p7 | 2:105855106 | AAGTGGGACTACACC[A/G]CCCAGCAGGACCAGG | 8440 |
rs768065074 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105787376 | ATATTTGGAGATGAG[C/G]CCTCTGAGGAAATAG | 8440 |
rs768077646 | snp | C/T | 3.58963e-05 | 0.00423638 | utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105893228 | CGGTGGAGCTGCCCG[C/T]CCGGCCTTGTGGCAG | 8440 |
rs768093704 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105865510 | ACTGGCGACTCCCAC[C/G]CACACGACTGTTGAG | 8440 |
rs768122573 | in-del | -/AA | | | intron-variant | NCK2 | GRCh38.p7 | 2:105886691 | GGTATGACACTATGG[-/AA]AGACAAAGAATAACA | 8440 |
rs768160517 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105820207 | ATGGTTCCTGGAGAC[C/T]GCAGGTCATTCAGAC | 8440 |
rs768166080 | in-del | -/AT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105864768 | TTGTCCCTTTCACAC[-/AT]GAGTTTGGCCCTCCG | 8440 |
rs768185870 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105864158 | AAAGAACCCTCGGAG[A/G]TTTCCACAGGGCTTA | 8440 |
rs768212538 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105755938 | AAAATAAACTCCTCA[A/G]GGGAGAGAGACTAAA | 8440 |
rs768240667 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105802513 | CCTCAAGCTGCTTTC[C/T]ACTCATGGCAGAAGG | 8440 |
rs768244023 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105876164 | TGATTTATCCAAAGC[A/C]TGCTGCTGTGACACC | 8440 |
rs768245569 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105782506 | CTACACAAAATCTCA[C/T]TTGAGGAATGCTGGC | 8440 |
rs768267551 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105755460 | CCCAGTGGGTGCAGC[C/T]GATTCCGTCTTCCAT | 8440 |
rs768278565 | snp | C/T | 3.8211e-05 | 0.00437081 | intron-variant | NCK2 | GRCh38.p7 | 2:105855318 | CCTCGAGAGAGGAAG[C/T]CTTGTGCATTTCAAG | 8440 |
rs768282394 | in-del | -/CT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105790281 | CTTGGCTTCCTGCAG[-/CT]CTCGTCATTGCCCAC | 8440 |
rs768295726 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105808576 | AGTTTACTACAAATG[C/T]CAGGGCTGGGGAGCA | 8440 |
rs768370428 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105832156 | ACGAGATTGGTTTCT[G/T]TATTTCATTTTCAGC | 8440 |
rs768409289 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105799640 | CAGAAAAACAAAACG[G/T]AATACCACTATATGA | 8440 |
rs768470187 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105814600 | CATAAGGAGTCTCTC[C/G]TCTGTTCGCATGCAG | 8440 |
rs768473802 | snp | C/T | | | utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105893288 | GCTTCTCTGCGAGTC[C/T]CTCTTTATGTTCAGG | 8440 |
rs768493177 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105830921 | ACCAGATTATTTGGG[C/T]TTTTCTTTTTGTTTT | 8440 |
rs768505235 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105775504 | GCTTATTTTTTTCAG[G/T]TGTCATTGTAGCACA | 8440 |
rs768521472 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105813462 | CTCCCTTCTTAACCC[G/T]GAACTGCTCCTCTGG | 8440 |
rs768529029 | in-del | -/TTTTGC | | | intron-variant | NCK2 | GRCh38.p7 | 2:105770919 | TGTTTGTTTGTTTGT[-/TTTTGC]TTTTGCTTTTGTTTT | 8440 |
rs768567059 | in-del | -/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105862483 | AGACCCAGAGGGGAC[-/T]TCAGATCTAATCTGA | 8440 |
rs768598254 | snp | A/G | 2.46321e-05 | 0.00350933 | missense, utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105893141 | TTCACCAGCGAGCAC[A/G]GGGAGAAGCTCTACC | 8440 |
rs768626859 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105778633 | AACTGGAGTTTCTGC[A/G]CATTCCTCCTTAGGC | 8440 |
rs768641270 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105805159 | TATGGGCACGGAGGC[C/T]GGTCTCCTAGAAGAG | 8440 |
rs768644438 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105824692 | TCATGTGTGGGTGTT[G/T]TGCTTTCATGGCTGG | 8440 |
rs768670776 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105847493 | GTCCTGGCCTGTGTC[C/G]CGGTGGGCAGGTGGA | 8440 |
rs768695749 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105869555 | TGTCTTTGCCAACCA[C/T]GTGCCACCTGCGTGT | 8440 |
rs768705103 | in-del | -/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105760397 | CCTGTTGCACGAGTT[-/C]CCCCAGGTGATTCTG | 8440 |
rs768725117 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105861098 | AACCATTTTCTAAAT[A/T]GAGTTCTTGTGAAAG | 8440 |
rs768737651 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105748163 | GTCACAGTGATGTCA[C/T]ACGGTGTCACTGTCC | 8440 |
rs768773910 | snp | A/G | | | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105771625 | CCATTGTTTCTAATC[A/G]TGTCACTTAGGTAGA | 8440 |
rs768786696 | in-del | -/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105832719 | ATTTTTTTTTTTTTT[-/G]AGGATTTTTGCATCT | 8440 |
rs768814890 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105872200 | GCTCTATGCTCCTGC[C/T]CTGCCCAGATCCCTC | 8440 |
rs768834247 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105846566 | TTTATTGAGAATTGC[C/T]ATGTGCTAATAAATT | 8440 |
rs768863884 | in-del | -/T | 1.71088e-05 | 0.00292474 | frameshift-variant, intron-variant | NCK2 | GRCh38.p7 | 2:105881817 | GTGGAAATGCAAAAA[-/T]TGCCCGGGGCCAGGT | 8440 |
rs768910570 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105777693 | TCCTATCAAGGTCCT[A/G]TGTGTAGAGCCACTG | 8440 |
rs768934174 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105816094 | GTGTGTTGATGGAGG[G/T]CTTTAGGCACAGAGC | 8440 |
rs768944995 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105751978 | CCTATATTTTGCCCA[A/G]TATATATATAAACTC | 8440 |
rs768964917 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105830395 | TGTTGCCATGAGTGA[C/T]AAGTGACAGAATTTT | 8440 |
rs768970381 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105762735 | GTGTTGAAAGAGTGA[C/G]TGCTTTTATCATTGC | 8440 |
rs768979880 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105860139 | AAAAATTTTTTAAAA[A/C]ATAGAGCATGGTGTC | 8440 |
rs768981116 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105848028 | GTTTTCTGTTTTTCA[A/G]TGACATAATCTATTG | 8440 |
rs769002087 | in-del | -/AT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105844751 | GGCGGGGGGGGATAT[-/AT]ATATATATATATATA | 8440 |
rs769002441 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105857717 | GGGGATCAGTATCCC[C/T]GTCATGAGGGAGAAA | 8440 |
rs769007984 | snp | A/G | 3.31598e-05 | 0.00407171 | missense, intron-variant | NCK2 | GRCh38.p7 | 2:105881559 | GGTGGCGGGGCAGCT[A/G]CAACGGGCAGATCGG | 8440 |
rs769030336 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105799114 | TCGCTGTGTCCTGTC[C/T]GTCCTTCGTGTCCTA | 8440 |
rs769098848 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105822124 | CAGGAATTTCGTGAG[A/G]TTTATTTTTTTCTCC | 8440 |
rs769115741 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105826913 | AATTGTTATATTAAT[A/G]TCAGATAAAGAACTT | 8440 |
rs769126729 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105813595 | ACAGGCATTGGGGAT[C/G]CAGAATCGGCCACGA | 8440 |
rs769143397 | snp | C/G | | | upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105743119 | AGGTCAGAAAGGTAA[C/G]AGAATCAGAACTGGC | 8440 |
rs769159222 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105811560 | CAGTCCTTGTCTTTA[A/G]GGAGCATCTGAGTCC | 8440 |
rs769162706 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105884262 | CCACTGCCTCCCCCC[A/G]TCCCCATGTGTTTTC | 8440 |
rs769216329 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105851907 | AAGCAGGTTCGGTTT[G/T]GTTTTGTTTTGGTTT | 8440 |
rs769226018 | snp | C/T | 1.92177e-05 | 0.00309975 | synonymous-codon, intron-variant | NCK2 | GRCh38.p7 | 2:105881992 | GCACCAGGCCGAGTG[C/T]GCCCTCAACGAGCGG | 8440 |
rs769242134 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105754032 | GGGCCACTGGGGCCA[C/T]CAGAGTGTTGAGCAG | 8440 |
rs769262194 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105808833 | TGGTAATGATGTGGG[A/G]TGTGATACTGAAGTT | 8440 |
rs769264732 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105749980 | GGTTGCAGTGAGCCA[A/G]GATCACACCACTGCA | 8440 |
rs769264951 | snp | C/G | | | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105772083 | CCGATCCTGGCTCAG[C/G]CGAGGGCAGTGTCTG | 8440 |
rs769284797 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105829266 | ATTCTCAATACTGTT[C/T]TCTACCTCCTCTTTT | 8440 |
rs769306828 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105780581 | CTGTCTGTAATTATG[C/T]TGAAACATCAGTCAC | 8440 |
rs769312422 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105889170 | AACTCCATCTCCATC[A/T]GATGCAGGGACTGGT | 8440 |
rs769313630 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105764588 | CAGGTAAAAAGATCT[C/G]AAAGTGCAAACCAAA | 8440 |
rs769317329 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105830672 | TTGCCAGGAATTTGG[G/T]GTGTGTGTGTGTGTG | 8440 |
rs769321690 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105795349 | CTCTATACACTTTTC[C/G]CAAGCAAGAGGTCAA | 8440 |
rs769333109 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105787212 | AAGGAAGCTCAGCTC[A/G]GCGCCGTGGAAGGGG | 8440 |
rs769339535 | snp | G/T | 1.64866e-05 | 0.00287106 | missense | NCK2 | GRCh38.p7 | 2:105855082 | ACAGAAGAAGTTATT[G/T]TGATAGCCAAGTGGG | 8440 |
rs769363940 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105765630 | ATCGTATTTTTGGTC[A/G]CTGGCTAAAACAGAG | 8440 |
rs769383076 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105813259 | TCCCAGCCTGTCACC[A/G]TTTCTATCATTTGGA | 8440 |
rs769385681 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105837180 | GACATTTTACTTGCT[C/G]TGTGGTTATCTATTG | 8440 |
rs769399291 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105841972 | ACTTGAGGCCAGAGA[A/T]CAGAAATGTAAAATG | 8440 |
rs769418391 | snp | A/G/T | 4.54455e-05 | 0.00476666 | intron-variant | NCK2 | GRCh38.p7 | 2:105882075 | TGCGCCCACAGCTCC[A/G/T]GCTGCAGGCAGTAAA | 8440 |
rs769440978 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105791011 | GAGTTGGAAGGCACT[A/G]CTTAGAGGTTGTCCG | 8440 |
rs769450944 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105802161 | AGTGAGCCAGGATTT[A/G]GGACTCTTGAGAAGC | 8440 |
rs769480243 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105888240 | ATTGTTCATTCTCCA[A/G]AACCATTGATTCAAA | 8440 |
rs769563409 | snp | A/G | 1.65192e-05 | 0.00287391 | synonymous-codon, intron-variant | NCK2 | GRCh38.p7 | 2:105881740 | AGTCACCGAGGAGGA[A/G]CTCAACTTCGAGAAG | 8440 |
rs769566058 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105800715 | GGACCAGTTGCAGGA[A/G]CACAGTTGATCAACT | 8440 |
rs769620741 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105806080 | CATGAAGTTAGGTGT[C/T]GAATTTTTTACTTGC | 8440 |
rs769644402 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105784902 | CACTTAGGCAGCCTC[C/T]CAGTTTGAAATGCTT | 8440 |
rs769652105 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105856113 | TGCTGGGATTACAGG[C/T]GTGAGCCACCGTGCC | 8440 |
rs769654096 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105747842 | GCCTGAGTTAAGGCA[A/G]CTCAGAAGAAGGTCG | 8440 |
rs769662468 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105812160 | TCAGGACAGCTTTAT[C/G]TTGAGTGAAAAATCT | 8440 |
rs769704337 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105868822 | ATAGCCTGGCTCAGC[A/G]CTTTTCTATGAAAAT | 8440 |
rs769712082 | in-del | -/CTCCCTCCCTCCCTCCCTTCTATCTCTCC | | | intron-variant | NCK2 | GRCh38.p7 | 2:105807814 | CCCTCCCTTCTATCT[lengthTooLong]CTCCCTCCCTCCCTC | 8440 |
rs769769628 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105759970 | GGCTTATGATGGTTG[A/T]TGTTGATCTTGATCA | 8440 |
rs769777608 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105746914 | CCCACTTCCTGTCCC[G/T]GAGGCCTCGCCTGGA | 8440 |
rs769799123 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105815383 | CGATTTTTCTATGGG[A/G]TATTTAACATTTTGG | 8440 |
rs769799702 | in-del | -/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105842323 | CTCCTGACCTCAGGT[-/G]GATCTACCTGCCTCA | 8440 |
rs769807801 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105845398 | CATTTATATTTTGAA[A/T]TTTTTTTTTTTTTTT | 8440 |
rs769813255 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105763959 | ATGTGTCAATAATAA[C/T]AGCTGATATTTATTG | 8440 |
rs769815022 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105879900 | AAGTCATTTTGAGGA[A/G]TCTACAAATGACTAA | 8440 |
rs769824851 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105758864 | TGATTTCAGGGTTTA[C/T]ATTTAAGCTTTGTTT | 8440 |
rs769835570 | snp | A/G | 0.000158043 | 0.008888 | intron-variant | NCK2 | GRCh38.p7 | 2:105892942 | TAGACACAGCTCCCC[A/G]CTGTGGCCCGGCTGT | 8440 |
rs769895060 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105798975 | TCTTAGTATCATTTT[A/G]GTGAAGTTCAGATGT | 8440 |
rs769904198 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105867369 | CAAGATTGTTCATAA[C/T]AGGAAGGGCCCACAT | 8440 |
rs769926068 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105750625 | ACCCCATAACAGGGA[A/G]CAAGCCTTGGTGCTG | 8440 |
rs769943214 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105766981 | AAGAGACACGCTTGG[G/T]AGGAACTCTTCTCAC | 8440 |
rs769944376 | snp | C/T | 2.07717e-05 | 0.00322264 | synonymous-codon, utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105893122 | CTACAAAAAGGCGCC[C/T]ATCTTCACCAGCGAG | 8440 |
rs769962974 | in-del | -/TT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105794047 | ATTGTATCTTTCGAT[-/TT]TTTTTTTTTTTTTTT | 8440 |
rs769963176 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105883854 | TTTTTTGCATTCTCT[C/G]CTAACTTAGAAAGTC | 8440 |
rs769978716 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105749354 | GGGGTGCTTACGTTG[C/T]CAAATTGTTAGTGAA | 8440 |
rs769979850 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105891213 | GCGCACGCTCACACA[C/T]TTAGAGCTGCGGTAT | 8440 |
rs770041947 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105787019 | CTCAATGGGGTGAGC[A/T]TGTGCCCTGCTTTCC | 8440 |
rs770047813 | snp | A/G | 1.73468e-05 | 0.00294501 | missense, intron-variant | NCK2 | GRCh38.p7 | 2:105881387 | CCCACGCCCAGCACG[A/G]ACGCCGAGTACCCCG | 8440 |
rs770070509 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105813276 | TTCTATCATTTGGAC[A/G]GTGGGAGAGGAGGGA | 8440 |
rs770078323 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105796783 | AGCATTTCTCTTTGA[C/T]GCAGGTAAATGCAGT | 8440 |
rs770083415 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105826822 | TATATATATATGTAT[G/T]TGTGTGTATATATAT | 8440 |
rs770084359 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105881260 | AACTGCGTGGAAATC[C/G]CGGTAGGCTAGGGAG | 8440 |
rs770094271 | snp | C/T | | | upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105743144 | ACTGGCTGTGTTTGA[C/T]GAATGAAAAGATGAT | 8440 |
rs770096907 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105797690 | GTGTGGAGCCTCCCT[G/T]TTTAGGCTTAGTGAG | 8440 |
rs770107265 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105870715 | AAGATCGCGCCACCT[C/T]ACTCCAGCCTGGGTG | 8440 |
rs770138657 | snp | C/G | 6.31532e-05 | 0.00561895 | utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105893189 | TGACGGCGCCCCGGC[C/G]CCACACTCGCCTCCC | 8440 |
rs770154748 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105789740 | CTTAGGCTTGCTCCC[C/G]GTTAACGGGAGGGCT | 8440 |
rs770165493 | snp | A/G/T | 5.01847e-05 | 0.00500902 | synonymous-codon, intron-variant | NCK2 | GRCh38.p7 | 2:105881446 | CGACCTCAACATCCC[A/G/T]GCCTTCGTCAAGTTC | 8440 |
rs770167261 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105808648 | GGTGGATCACCCAGC[A/G]TCTTCAGTGCATTGT | 8440 |
rs770169824 | snp | C/G | | | upstream-variant-2KB, intron-variant | NCK2 | GRCh38.p7 | 2:105850707 | TTCTATGATGGTCTT[C/G]CCTAGACTAAATCAG | 8440 |
rs770182123 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105830253 | CCCCACCTCTAGTAA[C/T]CTCTATTCTATTCTC | 8440 |
rs770190296 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105781403 | CAAGACTTGACTAAA[C/T]GCAATCTCCCTTTTG | 8440 |
rs770209992 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105825948 | TTGATGGAGATTCTG[A/T]TTAACCAAAGTGATT | 8440 |
rs770218842 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105762792 | TGCTGCTACCCTCTC[A/G]TTTGGTGTGTTAATA | 8440 |
rs770222731 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105820741 | ACGGAAGATGCAAAG[G/T]GCCTTGTCTGCTATG | 8440 |
rs770222756 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105807482 | CATACAGCTGATATC[C/T]ATGTAATTTGAGAAG | 8440 |
rs770260084 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105863982 | GGCGAGGGGGGGTGG[A/G]GTCTCACTTGAGGGA | 8440 |
rs770261058 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105837532 | TCAGGGTTATTTTCT[C/G]TTCTTTAACTGTCAT | 8440 |
rs770264231 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105831941 | AAAAAGTCACTGATA[C/T]ATTGATAGGGATCAC | 8440 |
rs770343440 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105819898 | GGGCTATTTTTCTTG[C/T]AGTGACTGTTGTAGC | 8440 |
rs770356794 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105779776 | CTCACATACATATAC[A/G]TAGTAATTCCCTAGC | 8440 |
rs770384522 | snp | A/G | 1.89723e-05 | 0.0030799 | missense, intron-variant | NCK2 | GRCh38.p7 | 2:105881982 | ACGTGACGCGGCACC[A/G]GGCCGAGTGCGCCCT | 8440 |
rs770401379 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105828601 | GCAGCTACTGCAAAT[A/G]AAATACCTATTTTCA | 8440 |
rs770426291 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105841630 | CCTTCTTGGAGGGTG[A/G]AGGGTGGGGTTGAAA | 8440 |
rs770460763 | snp | A/G | 1.81017e-05 | 0.00300841 | missense, intron-variant | NCK2 | GRCh38.p7 | 2:105881895 | CCCTGCACCCTGCGC[A/G]CGCCCCACAGATAAG | 8440 |
rs770464319 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105773645 | ATGCTAGAGCATCCT[A/G]GTTTATGGATATTTT | 8440 |
rs770467338 | in-del | -/AAT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105748831 | CTTATTGAATATGTG[-/AAT]AATGAGTGCCCAGCC | 8440 |
rs770493722 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105890816 | AAGGGTTGCACACTT[A/C]TCATCAAACATTTAT | 8440 |
rs770507534 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105746782 | GTATATTCTGCCCTG[G/T]AGGTTGGTTAGATGT | 8440 |
rs770518975 | snp | A/G | 1.65828e-05 | 0.00287943 | utr-variant-5-prime, splice-acceptor-variant | NCK2 | GRCh38.p7 | 2:105855050 | GTTTTGCTGGCAGAA[A/G]GACTCCATGAAAGAT | 8440 |
rs770538445 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105774480 | TGGTCAGAATCTGGT[A/G]GCCCTCCCTGTGAAT | 8440 |
rs770547876 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105784791 | GCCCGTGTTTCCCAC[A/G]CTTCCCATTTCAACA | 8440 |
rs770577000 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105758470 | TGCTGGAGTGCAGTC[A/G]CTTGATCTCGGCTCA | 8440 |
rs770579775 | in-del | -/TTCTCAGA | | | intron-variant | NCK2 | GRCh38.p7 | 2:105823765 | ATATGCCTTCTCAGC[-/TTCTCAGA]GTCACACCTGACCAA | 8440 |
rs770587733 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105856038 | ATGGGGTTTCACTGT[C/G]TTAGCCAGGATGATC | 8440 |
rs770588061 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105859150 | ATGGGGAAGCTGCTC[C/T]CAGGGAGGTATTTTT | 8440 |
rs770592038 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105813038 | AAGGTTCTAGCCCTT[C/T]CGTGGTGATCTTTGT | 8440 |
rs770730516 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105822492 | TGACGCTTCCCACAG[C/T]GCCCCTGTTCAGGGC | 8440 |
rs770768035 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105868055 | ACTGAGAGAGCGCTC[A/G]TTTACTGGCTTGATG | 8440 |
rs770833657 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105847399 | GAAAAGAAATGATGT[G/T]GGATATTGTGTGCTT | 8440 |
rs770842142 | in-del | -/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105802304 | GTGCAGGGATGGTGC[-/T]TGTCTGCAGAGGCAT | 8440 |
rs770852493 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105857421 | CATTTTTGGCGAAAA[C/G]AGATTGTTAGAAAGC | 8440 |
rs770862782 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105749180 | ACCTGAATTCAAAAC[G/T]CTGGGCAGACCGTTT | 8440 |
rs770898319 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105804860 | GGTGTTAGGGATTCA[C/G]TGTGTCTTAGATTGC | 8440 |
rs770898868 | in-del | -/T | | | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105771518 | TGCAGTAAGCCGAGA[-/T]TGGGCCACTGTACTC | 8440 |
rs770903590 | snp | A/G | | | utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105893502 | AGGGCACCTGTGAGC[A/G]CAGGAGCGAGCCTAA | 8440 |
rs770921915 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105846368 | GTTGCTCAATGATGA[A/G]CTCCTGAAAACTGGA | 8440 |
rs770931972 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105870669 | CGGAGGCACAAGAAT[C/T]GCTTGAACCTGGGAG | 8440 |
rs771022062 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105869732 | TTGCCGCGTCTTGTA[C/T]ACTCTTTTGCATATT | 8440 |
rs771023780 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105882386 | TGTACGTAGAAGGCC[C/T]GAGTGATTTACTTTG | 8440 |
rs771033492 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105877006 | TTTGAGATGTCCCGG[C/T]TGCCACCTGGCGGGG | 8440 |
rs771048558 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105779520 | GTGGTGGGTGGCTGC[A/G]TCCAGCTGAACTTGG | 8440 |
rs771092665 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105776102 | GCAGGCCACCTCTGG[A/G]GGTGTGGGTGCGGAG | 8440 |
rs771175221 | in-del | -/CCT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105762341 | CCTGCTGTCAGACTG[-/CCT]CCTCACATCAGCAGG | 8440 |
rs771183263 | snp | A/C/G | 1.65825e-05 | 0.00287941 | missense, intron-variant | NCK2 | GRCh38.p7 | 2:105881676 | CGCTGAGCAATGGCC[A/C/G]GGGCTCCCGCGTGCT | 8440 |
rs771185679 | snp | A/G | 1.6628e-05 | 0.00288335 | synonymous-codon, missense | NCK2 | GRCh38.p7 | 2:105892999 | CAGCGACTTCTCCGT[A/G]TCCCTTAAAGCGTCA | 8440 |
rs771228700 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105806534 | TGAGCCACCACTCCC[A/G]GCCACATATATTCTC | 8440 |
rs771230148 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105877965 | AGTCAGGTCCCTCTC[C/T]ATCTCCAGACACCTG | 8440 |
rs771239243 | snp | G/T | 1.94812e-05 | 0.00312093 | intron-variant | NCK2 | GRCh38.p7 | 2:105881277 | GGTAGGCTAGGGAGT[G/T]TGGTGGTGCCCAAGT | 8440 |
rs771268459 | in-del | -/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105787867 | TCCATGTTATAAGAT[-/G]ATCTCATTCTGTTAG | 8440 |
rs771284885 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105808781 | TGAGACAGGAAAATC[A/G]GGACACTAATGAGAT | 8440 |
rs771318200 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105819564 | CTGAAGCTGTTGTTG[A/G]TGCTGGTTGAGAAGG | 8440 |
rs771365009 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105848909 | TAGGGATGACAGTAT[C/T]TTTCATATAGACTCA | 8440 |
rs771366302 | snp | C/T | 4.03047e-05 | 0.00448896 | missense, utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105893118 | AACACTACAAAAAGG[C/T]GCCCATCTTCACCAG | 8440 |
rs771417618 | snp | C/T | 1.74391e-05 | 0.00295283 | missense, intron-variant | NCK2 | GRCh38.p7 | 2:105881379 | ATGCGTCCCCCACGC[C/T]CAGCACGGACGCCGA | 8440 |
rs771456987 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105862725 | ATTTGTGGAAATACA[C/T]ATAAAGTATTCGGGT | 8440 |
rs771514676 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105853857 | TCTGGCTAAACTGAC[C/G]GAACAGGATTCTTCT | 8440 |
rs771535855 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105849121 | AGGTGTAATGGCTCA[C/T]ACCTGTAATCCAGCG | 8440 |
rs771554086 | in-del | -/CCT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105748672 | AGCCTCCTGCCTTGA[-/CCT]CCAAAAGTACTGGGA | 8440 |
rs771560522 | snp | C/G | | | intron-variant, utr-variant-5-prime | NCK2 | GRCh38.p7 | 2:105773465 | AGCTCAGGGCCATCA[C/G]CACTGCACCTGGAAC | 8440 |
rs771591716 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105753874 | GAAATCTGCTTCTGA[A/G]GTTGTGAGAGAGGCC | 8440 |
rs771604670 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105852433 | CTTGGATGCTCAGGC[A/C]TCTTTCATAAAGATA | 8440 |
rs771607077 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105782710 | GCCCGTTGAAATCAT[G/T]TGGCAAAATGGGCTG | 8440 |
rs771613648 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105783653 | GAAATACCTTAGCAC[A/G]AAGAAACCCTGTAAA | 8440 |
rs771637885 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105801649 | TGGCTTCTTACCTAC[C/T]CTGTGAGAGCAGCCT | 8440 |
rs771644404 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105866872 | CTGGGTGTTGAGTGC[G/T]TGGGATGCTCAGTGT | 8440 |
rs771651864 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105757060 | TCTGCCTGCCTCGGC[C/G]TCCCAGAGTGCTGGG | 8440 |
rs771658118 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105793186 | TAATGAAGGGATTGG[C/G]CATTAAAAGCCAGGA | 8440 |
rs771668617 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105755305 | GAGGGTGTCAGACAT[C/T]GTGCTGTTGTGATTT | 8440 |
rs771703040 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105767506 | AAAGTGGCCCATGGA[C/T]CAAATCCAGTTCACC | 8440 |
rs771710354 | snp | C/T | | | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105772321 | TTCTGCCCCATGGAA[C/T]AAACAGCACTAAGCA | 8440 |
rs771735345 | in-del | -/TCTTATTTGG | | | intron-variant | NCK2 | GRCh38.p7 | 2:105890612 | GCCTCAAAGGTTTGT[-/TCTTATTTGG]TCTATTTGAGACAGA | 8440 |
rs771735403 | snp | C/T | | | upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105743359 | GTCAATATTGCTATA[C/T]TTATTTTGAGTAAAT | 8440 |
rs771790225 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105840119 | ATCCCCTCTATAAAG[G/T]AGAGTTGGTGGGGTT | 8440 |
rs771791839 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105822355 | ATGGTGCTCAGAGTC[A/G]CCTTGTGTTGGGGAT | 8440 |
rs771805943 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105878567 | CCTGCCCACACCTTG[A/G]TTTGGACTTCCAGCC | 8440 |
rs771835741 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105753017 | GTTTGTATCTTCATC[A/G]CTAAGGAAAGGGAGG | 8440 |
rs771841202 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105764418 | CCTAGGACTGCATCC[C/G]TGCAGGAGCCTGCAG | 8440 |
rs771841995 | snp | C/T | 0.000318117 | 0.0126078 | utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105893208 | CACTCGCCTCCCGGG[C/T]CCCACGGTGGAGCTG | 8440 |
rs771849479 | snp | A/G | 1.87475e-05 | 0.0030616 | missense, intron-variant | NCK2 | GRCh38.p7 | 2:105881967 | AGTGGTACTACGGGA[A/G]CGTGACGCGGCACCA | 8440 |
rs771872369 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105803850 | GTCTCAGGTAGGGTC[C/T]GTTTGGAATGAATAG | 8440 |
rs771902940 | snp | C/T | 1.6951e-05 | 0.00291122 | intron-variant | NCK2 | GRCh38.p7 | 2:105855020 | CGGGTAGTTCTCTAA[C/T]GAGCATCTCCAAATG | 8440 |
rs771927961 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105770606 | CTAGAAACAGACCAC[C/T]GATCTGTAAAATGAT | 8440 |
rs771933718 | snp | A/G | | | utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105894198 | ATTCCTACGATTGAA[A/G]AAGGGGTCTTGAGAT | 8440 |
rs771968540 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105820358 | CTGGCCTGGTAGAAC[A/G]GTAAGCGGGATGTCA | 8440 |
rs771977205 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105815336 | GATAGCCCTATTTGA[A/G]TTATCTTCTTATCTT | 8440 |
rs772014764 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105891198 | CTCCCTCTCACATCT[A/G]CGCACGCTCACACAC | 8440 |
rs772018162 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105845144 | TACCATGCTTAGGAA[C/T]GTGGGCATAAACCAT | 8440 |
rs772032136 | snp | A/G | 1.66349e-05 | 0.00288395 | missense, intron-variant | NCK2 | GRCh38.p7 | 2:105881468 | GTCAAGTTCGCCTAT[A/G]TGGCCGAGCGGGAGG | 8440 |
rs772066787 | in-del | -/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105754633 | TGTGTCTGTGGGAGG[-/T]TGGGGGGAGCTGCTG | 8440 |
rs772070649 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105881194 | TCTCATGGTAATTAC[A/T]GTTTGTAAGCACTGT | 8440 |
rs772081026 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105774164 | CAGGCACGTGCCACC[A/G]CACCCAGCTAATTTT | 8440 |
rs772085846 | in-del | -/TTTTTTTTTTTTTTT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105891533 | GAGATAAAAGACCAA[-/TTTTTTTTTTTTTTT]TTTTTTTTTTTTTTT | 8440 |
rs772109696 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105769417 | GCTGGTAACTCCCCC[A/G]TTCTTGCTTCTCAGG | 8440 |
rs772110197 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105858502 | TAGTAACTCATGGCA[C/G]CACCCACATTTGCCA | 8440 |
rs772156881 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105848849 | AGCCACAGCGAAGTA[G/T]ATTGTGTTATTTGAA | 8440 |
rs772160435 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105880025 | GGGTGTGTCCCCAGC[C/T]CTGGGGCTGACATGC | 8440 |
rs772176002 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105889737 | CACAGGTATGCATCA[A/C]CACACCTGGCTAATT | 8440 |
rs772215138 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105848169 | ACAGACTGAGTGTTA[C/G]GTATTTCCTGTAGAC | 8440 |
rs772235220 | snp | C/T | 0.000132716 | 0.00814497 | synonymous-codon, intron-variant | NCK2 | GRCh38.p7 | 2:105881572 | CTACAACGGGCAGAT[C/T]GGCTGGTTCCCCTCC | 8440 |
rs772291952 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105816247 | GGAGGTGCAAGTTGC[C/T]GTGAAGTAAGATCGT | 8440 |
rs772292389 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105834795 | CCTGCTTCAGCCTCC[C/T]GGGTAGCTGGGCCTA | 8440 |
rs772292815 | in-del | -/ACACACACACACACACACAC | | | intron-variant | NCK2 | GRCh38.p7 | 2:105864831 | CACATGTGCATGTAC[-/ACACACACACACACACACAC]ACACACACACACACA | 8440 |
rs772296759 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105807324 | CTCCTCGAAGGGCAG[A/G]GGAAATAAAGGTTTT | 8440 |
rs772298728 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105795874 | CCACGCACCCTCCCC[A/C]CAGTCTTTTTCAGTA | 8440 |
rs772304873 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105846519 | AGCAGAAAACTGTAG[A/T]TGATCTTTATGATCA | 8440 |
rs772312517 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105806363 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGACTAC | 8440 |
rs772385711 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105752134 | TTGATTGGCCTTGGC[C/T]ACACGCGACTAGTGG | 8440 |
rs772388744 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105778900 | GCTAATTGAGATAAT[A/G]GTTATTTTTTTTTTC | 8440 |
rs772444058 | in-del | -/AGC | | | intron-variant | NCK2 | GRCh38.p7 | 2:105883948 | CTCTGCACACATAGC[-/AGC]AGCACCGTCTTTGTC | 8440 |
rs772447704 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105828774 | TGTTGACCTCTTAGT[A/G]AATTAGGCATGCTCT | 8440 |
rs772483265 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105862451 | TGAAGCCTGAGAACA[C/T]AGCAGTCACAGGTAC | 8440 |
rs772503351 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105885869 | GATTTATCTCTTGAA[C/G]TATATTTCTGTTGAG | 8440 |
rs772529607 | in-del | -/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105763335 | GGGACCGAGGCTGCT[-/G]GCCAGAGACAGTCTA | 8440 |
rs772570295 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105815534 | GCTCCAGGGTCCCCT[C/T]GAAAACGTTAGTCAA | 8440 |
rs772580744 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105799238 | TTGAATTCATCCCTC[C/T]TTTATGGTTTCTGGA | 8440 |
rs772595570 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105872341 | CCCTAACACCTCCTT[A/C]ACATCACTGAATGGC | 8440 |
rs772595934 | snp | A/G | 4.5939e-05 | 0.00479243 | intron-variant | NCK2 | GRCh38.p7 | 2:105882079 | CCCACAGCTCCGGCT[A/G]CAGGCAGTAAATGCG | 8440 |
rs772622223 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105764291 | CTGCAGGTTAAGGAG[A/G]GCCTGTGGGCAGACA | 8440 |
rs772626341 | in-del | -/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105875386 | CCAGTCCCCTGGGCT[-/G]TACACACATGGAATC | 8440 |
rs772650775 | snp | A/G | 3.35312e-05 | 0.00409444 | missense | NCK2 | GRCh38.p7 | 2:105892988 | CCTCCCCAGCCCAGC[A/G]ACTTCTCCGTGTCCC | 8440 |
rs772677900 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105874546 | TGTTACACATCTGAT[C/T]AGTAGCAAAAATTAA | 8440 |
rs772678873 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105783695 | ATAGCCCTACATAAA[G/T]GTATTCAGATTATGT | 8440 |
rs772711255 | snp | C/T | 5.41971e-05 | 0.00520535 | missense, intron-variant | NCK2 | GRCh38.p7 | 2:105881888 | GGGCCTGCCCTGCAC[C/T]CTGCGCACGCCCCAC | 8440 |
rs772725407 | in-del | -/A | | | intron-variant | NCK2 | GRCh38.p7 | 2:105857529 | TGTGCTGAGTAGGTC[-/A]AGATCCTCTTCTGTA | 8440 |
rs772755059 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105871665 | ACCCAGCTAATTTTT[G/T]TGTATTTTTAGTAGA | 8440 |
rs772807216 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105852504 | TTTTAAAGCTTCTAT[A/G]TGATGTTCGGTGTGC | 8440 |
rs772820371 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105858838 | AATAATTTAAAATTG[A/G]TAAAAGCAACCTGAG | 8440 |
rs772888372 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105838100 | GTTTAACTAGAACAG[C/T]CCTTTTTTTTTTTGT | 8440 |
rs772919085 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105856229 | CAGTCTTGCCTTTAC[A/G]TGCACACGGAACTGA | 8440 |
rs772936230 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105832276 | TCTACAGTATTTTGC[C/T]GGAATTTTCCGTTTT | 8440 |
rs772936723 | in-del | -/TA | | | intron-variant | NCK2 | GRCh38.p7 | 2:105761147 | CCTGCCCGCCCACCC[-/TA]TACTGGGCCTCTTCT | 8440 |
rs772957707 | snp | C/T | 1.68063e-05 | 0.00289877 | intron-variant | NCK2 | GRCh38.p7 | 2:105855034 | ATGAGCATCTCCAAA[C/T]GTTTTGCTGGCAGAA | 8440 |
rs772972128 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105766459 | CACCTGAGTAGCTGA[A/G]ACTACAGGCATACAC | 8440 |
rs772979556 | in-del | -/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105784185 | CTCTGTTCACTGCAG[-/C]CTCTACCTCTTGGGC | 8440 |
rs772981667 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105782743 | GCTGCCTGTAGAGGC[A/G]AAGTGGATGTCGGGG | 8440 |
rs772985133 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105845246 | GAATCTGTTTTTAAA[A/C]ATCACTGTGCTTCTT | 8440 |
rs773032479 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105865825 | TCTGCAAACAGATAT[C/T]CCTCAGAATCATAAT | 8440 |
rs773060471 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105764440 | AGCCTGCAGCCTGCT[C/G]TGCTTCGAGGCTCAG | 8440 |
rs773096302 | in-del | -/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105863731 | TGTGCTTTCAGAGAG[-/C]ATGTAGCATTGTGGG | 8440 |
rs773096771 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105803863 | TCCGTTTGGAATGAA[G/T]AGTCAGCCCAGAGTC | 8440 |
rs773118657 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105876939 | ACAGCTGCAGTGCTC[C/T]GTCTCCCAGACATGC | 8440 |
rs773126402 | snp | C/G | 1.65968e-05 | 0.00288065 | synonymous-codon, intron-variant | NCK2 | GRCh38.p7 | 2:105881587 | CGGCTGGTTCCCCTC[C/G]AACTACGTCTTGGAG | 8440 |
rs773140737 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105869556 | GTCTTTGCCAACCAC[G/T]TGCCACCTGCGTGTT | 8440 |
rs773143595 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105802685 | ACCATGCATGAGGGA[C/T]CCGCCCTCGCGATGC | 8440 |
rs773203210 | in-del | -/GT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105835407 | TATATATATATATAC[-/GT]GTATATATATATATA | 8440 |
rs773205035 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105824700 | GGGTGTTGTGCTTTC[A/G]TGGCTGGGTTTTAAC | 8440 |
rs773240714 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105759401 | AGCACAGTGTTTTAA[C/T]GTTTCCAAAGTGTAA | 8440 |
rs773242656 | in-del | -/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105845750 | GTACCTTACAGCTGT[-/G]GAAAAAAAAATAGGA | 8440 |
rs773257144 | in-del | -/TT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105833680 | CATTTTTTTGGCCTC[-/TT]TTGTTCAGTTCTCTG | 8440 |
rs773281489 | snp | C/G | 0.000322251 | 0.0126894 | utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105893209 | ACTCGCCTCCCGGGC[C/G]CCACGGTGGAGCTGC | 8440 |
rs773283981 | in-del | -/GGA | | | intron-variant | NCK2 | GRCh38.p7 | 2:105751749 | CAGCTCTCTGTCATG[-/GGA]GGAGAAGAGACTAAC | 8440 |
rs773307239 | in-del | -/TGGTCTGAC | | | intron-variant | NCK2 | GRCh38.p7 | 2:105774402 | TTGGCTGTGTGATGA[-/TGGTCTGAC]TGGTCTGACAGATGC | 8440 |
rs773314001 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105889856 | ATCCCAAAGGGCAGG[A/G]ATTACAGGTGTGAGC | 8440 |
rs773315347 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105856285 | ACCTGAGAAAATAAT[G/T]GCGAGGACTTTTTTG | 8440 |
rs773316556 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105806485 | CTCGTGATCCACCCC[A/G]CGTTGGCCTCCCAAA | 8440 |
rs773334365 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105823974 | GGAGCAGTCCCTGGC[C/T]GGCGTGAACTCCAAG | 8440 |
rs773336660 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105776905 | CCCCTTGGAGCCTCT[C/G]TCAGTAAATGGAAAC | 8440 |
rs773356406 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105769441 | TCTCAGGAAGCAAAT[A/G]TAGGAAAAATATAGT | 8440 |
rs773358457 | snp | C/T | | | utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105893449 | CGCTCGTGCATTCAA[C/T]TCGTTCCCGCTCATG | 8440 |
rs773362930 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105880061 | TCTCCTAGAATGTTC[C/T]GGAATTCCGTGCATT | 8440 |
rs773407248 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105868571 | GGTAAACATGCAGTT[C/T]GTTCTAATGCTGCTA | 8440 |
rs773455664 | snp | A/C | 1.67304e-05 | 0.00289222 | missense | NCK2 | GRCh38.p7 | 2:105892990 | TCCCCAGCCCAGCGA[A/C]TTCTCCGTGTCCCTT | 8440 |
rs773524832 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105795950 | TAAAATGAAACACAT[A/C]AACGATATATTCTTT | 8440 |
rs773618216 | snp | A/T | | | utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105893933 | TTGACACTAATACAG[A/T]TGATTAAGGAAAACA | 8440 |
rs773674978 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105816264 | TGAAGTAAGATCGTA[C/G]AACCACACTCCAGCC | 8440 |
rs773706609 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105805298 | GAGGGCAAAGAGTTA[C/T]GAAAGGGTCCAGCGT | 8440 |
rs773727726 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105808919 | TTGTGATTTGCTTTA[A/G]CCATCTTGTGAGGGC | 8440 |
rs773744009 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105820212 | TCCTGGAGACTGCAG[A/G]TCATTCAGACAATAC | 8440 |
rs773755187 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105793818 | GCTGTGGGGGTTTCA[A/G]GCTCCTTTAGACAGT | 8440 |
rs773788868 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105882151 | TGTGAGTACACTAGA[A/C]AGAGCGGGAGACGCA | 8440 |
rs773797530 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105827900 | TTGGCATGGTGGTTA[C/T]AGGAGTTTACACACA | 8440 |
rs773798742 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105872406 | TGTCTTCCTTGCCAC[C/G]GGTACTTCCTGTCCT | 8440 |
rs773802888 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105860565 | CATGTAGTCAGAACC[G/T]CATGGGGAGGCCTTA | 8440 |
rs773843788 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105752234 | AAGTTGAGATAGCTA[A/C]AGAGACAAAGTGGAA | 8440 |
rs773853198 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105865515 | CGACTCCCACCCACA[C/T]GACTGTTGAGGTTAT | 8440 |
rs773891810 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105884882 | TTGTTGTTGCTTATT[C/T]TCCATATTTCGTTAT | 8440 |
rs773896810 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105751218 | TCAGTTATATTCCCC[A/G]TCACCGACTCACTCG | 8440 |
rs773903072 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105763521 | GTTGTTGTTTTTATA[A/C]ATTTTATTTAATTAA | 8440 |
rs773990558 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105797941 | TTTAAGTGTTTAATC[A/G]TCCCAAGTCAGGTTT | 8440 |
rs773992501 | snp | C/T | 1.65542e-05 | 0.00287695 | missense, intron-variant | NCK2 | GRCh38.p7 | 2:105881691 | AGGGCTCCCGCGTGC[C/T]GCATGTGGTCCAGAC | 8440 |
rs774005469 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105791395 | GTGGTGGAAGGCTCG[A/G]TGGCTTTCACGATGG | 8440 |
rs774019276 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105856136 | ACCGTGCCCGGCTCC[C/T]CATGTGCCTCTTGTT | 8440 |
rs774052604 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105800899 | TCCATGGGATTACAT[G/T]CCTGTCCAGGTGGTT | 8440 |
rs774068733 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105873797 | ACTCTTGGTTGGGGC[A/C]TGTCTCTCTGAGCCT | 8440 |
rs774078454 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105820142 | GAGACGTGTACAGAG[A/G]TATAATGTGTTTCCT | 8440 |
rs774101471 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105775539 | TGTGTTCTTTCTTAT[C/T]TCCTTTTGGGTTTTA | 8440 |
rs774109858 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105839970 | TCAGCAGTGTCTGCT[C/G]TAGTGGACATGCAGG | 8440 |
rs774167621 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105814613 | TCCTCTGTTCGCATG[C/G]AGAAGAGATTAGAGA | 8440 |
rs774180665 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105802602 | AGGGATGTGCCAGGC[C/T]CTTTTTAACCATCAC | 8440 |
rs774225641 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105830973 | TTGAATATTTTGGAT[A/G]ATAAATAGTCCCTTA | 8440 |
rs774230225 | in-del | -/TA | | | intron-variant | NCK2 | GRCh38.p7 | 2:105749642 | CACAGTGTCCTTGGG[-/TA]TCTGCCTTTGCCGTG | 8440 |
rs774246902 | snp | C/T | 0.000507588 | 0.0159228 | utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105893204 | CCCACACTCGCCTCC[C/T]GGGCCCCACGGTGGA | 8440 |
rs774261278 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105879914 | AGTCTACAAATGACT[A/G]AACCTCCACACTGAT | 8440 |
rs774278796 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105845047 | CTGGCAGGTAGGTAC[A/G]GGTTCTTGTCCCTAG | 8440 |
rs774292518 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105813486 | CCTCTGGAGTTGCCT[G/T]AGTCAGGGACCTCAT | 8440 |
rs774351421 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105834608 | ATCCATCTGTCCAGT[C/T]TATATCTTTTAATTG | 8440 |
rs774367973 | snp | A/G | 3.42654e-05 | 0.00413902 | missense, intron-variant | NCK2 | GRCh38.p7 | 2:105881406 | CCGAGTACCCCGCCA[A/G]TGGCAGCGGCGCCGA | 8440 |
rs774394152 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105846598 | TATTGAGGATGCAGT[A/G]CAAATACTGTTCAGT | 8440 |
rs774421382 | snp | A/G | | | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105771976 | CCCAGACACCCTTCA[A/G]AATTGGATATTGTCG | 8440 |
rs774422971 | snp | C/G | 1.66521e-05 | 0.00288544 | synonymous-codon, intron-variant | NCK2 | GRCh38.p7 | 2:105881464 | CTTCGTCAAGTTCGC[C/G]TATGTGGCCGAGCGG | 8440 |
rs774455196 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105891649 | CTCCCAGGTTCAAGC[A/G]ATTCTCCTGCCTCAG | 8440 |
rs774476784 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105794411 | CCTAGGATCGTTTAC[A/G]TAATGACTTATTTGC | 8440 |
rs774486771 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105751993 | ATATATATATAAACT[C/G]TATGTGTAATCAACA | 8440 |
rs774505131 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105777778 | AAGCCCTGGTAGGAA[C/G]TGTTTGCTCCTGTCA | 8440 |
rs774521180 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105768546 | GACAACTCACAGAAC[C/T]CAGAAAGGCACTTTG | 8440 |
rs774556603 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105860456 | TATGTTCCACACAGG[C/T]TCAGGGACCTGCTAA | 8440 |
rs774578451 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105778682 | TTACTGCACTGGTTA[C/T]GTGTATCAATTGAGA | 8440 |
rs774588851 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105861311 | ATTAAGATCATGCAC[A/G]ATCTTTAAAGACAGT | 8440 |
rs774606080 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105757410 | ATCTATGTGTAAATT[A/G]ATGTTGCTGTTGCTT | 8440 |
rs774677974 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105788383 | CCATTTAGATGATGA[C/T]GTTTCAGTCTTTTTT | 8440 |
rs774685949 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105758599 | ATTTTTAGTAGAGAC[A/G]GGGTTTCACCATATT | 8440 |
rs774773148 | snp | A/G | 1.64825e-05 | 0.00287071 | missense | NCK2 | GRCh38.p7 | 2:105855092 | TTATTGTGATAGCCA[A/G]GTGGGACTACACCGC | 8440 |
rs774800601 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105787312 | AATGGACTGAAATTT[G/T]ATGTCCCCCAGAAAT | 8440 |
rs774829999 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105826954 | AGAGTTACCAGGGAC[A/G]TAAAAGAGTGTTCAT | 8440 |
rs774840387 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105849389 | CTGTGATGCCATCAG[A/C]AAGAAGGAAAGAAGG | 8440 |
rs774851851 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105797814 | TGCTTCTAGAAAACC[A/G]GTTTGTAAATTTGGC | 8440 |
rs774853396 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105815540 | GGGTCCCCTCGAAAA[C/T]GTTAGTCAAGGACTG | 8440 |
rs774874465 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105813613 | GAATCGGCCACGACT[C/G]CTTGCAGGGGGGCAT | 8440 |
rs774887451 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105755319 | TCGTGCTGTTGTGAT[A/T]TTCATTTTGAAGCTT | 8440 |
rs774928332 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105862849 | AGCAGACATATCAGC[A/G]GTGGTTTAGAGACTA | 8440 |
rs774934266 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105810183 | CCAAAGTAAAACATA[C/T]TATAAAAGTTCAGAT | 8440 |
rs774938993 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105870905 | ACATCACTGACATAC[G/T]GGTGTGTGAGTGCCC | 8440 |
rs774996531 | snp | A/G | 1.93718e-05 | 0.00311216 | missense, intron-variant | NCK2 | GRCh38.p7 | 2:105882002 | GAGTGCGCCCTCAAC[A/G]AGCGGGGCGTGGAGG | 8440 |
rs775028062 | snp | C/T | 1.69281e-05 | 0.00290925 | missense | NCK2 | GRCh38.p7 | 2:105855206 | ACGCGGCCAACAGGA[C/T]GGGCTATGTACCGTC | 8440 |
rs775029862 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105818996 | AGGATAGGATTAAGT[A/G]TCTTAGTGTTCTCGT | 8440 |
rs775045823 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105874653 | CCAAGTTTGTTTGAC[A/G]CTTCAGCTTAAATCT | 8440 |
rs775057638 | snp | A/G | | | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105772085 | GATCCTGGCTCAGCC[A/G]AGGGCAGTGTCTGAA | 8440 |
rs775104425 | snp | A/C | 1.6582e-05 | 0.00287936 | synonymous-codon, intron-variant | NCK2 | GRCh38.p7 | 2:105881680 | GAGCAATGGCCAGGG[A/C]TCCCGCGTGCTGCAT | 8440 |
rs775114112 | in-del | -/T | | | upstream-variant-2KB, intron-variant | NCK2 | GRCh38.p7 | 2:105851265 | GGCACAGAGCTGAGC[-/T]TTTTTTTTTTTTTTC | 8440 |
rs775119044 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105791850 | ATATTTAACACCCGA[A/G]TAACTTACCAAGATT | 8440 |
rs775159347 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105803574 | TTCTACAGCTAGGAA[A/C]GTGCGGAACTGGCAT | 8440 |
rs775213995 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105800780 | AAAGAAGAATCTTGA[A/C]AGTAGAGGCTTCAGA | 8440 |
rs775235923 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105774626 | GGGAAGGCACACACA[C/T]AACGAACTCTAGACC | 8440 |
rs775238929 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105868377 | CCCAGAGGGCAACTG[C/T]TCATAAGTTAAAGGC | 8440 |
rs775239239 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105864936 | ATAATACTAGAAAGA[A/G]TAACACTGGAATAAC | 8440 |
rs775258796 | in-del | -/TG | | | intron-variant | NCK2 | GRCh38.p7 | 2:105806674 | TCATTTATGGGACAC[-/TG]TAATATCTATGTGAA | 8440 |
rs775308036 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105824610 | GTCATTTTCCCAGTC[A/G]TTAAGTACCACGTCT | 8440 |
rs775316479 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105887217 | TGAGATAAAAACAGA[C/G]AAACTATTAATCAGT | 8440 |
rs775319926 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105843205 | CATATATACCTTATT[A/T]ATGTTTCATATATAT | 8440 |
rs775320774 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105862269 | AGCCTGTGCTTCATA[C/G]TAAGCATGCTGATTT | 8440 |
rs775322262 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105891154 | CTCACACGCTACGCA[C/T]ACTCTCACACACTCT | 8440 |
rs775334302 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105795370 | AAGAGGTCAAAGGTG[A/G]TTTTCTAATTATATG | 8440 |
rs775343365 | in-del | -/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105804047 | TCCCTCTCAGTTAGG[-/T]TTTTGGCTTTGCTTG | 8440 |
rs775343631 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105813316 | CCTCCTGAAGGCTGA[C/G]TTTAGTCTCTTGGTG | 8440 |
rs775361204 | in-del | -/CTACT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105840410 | AATATGCAGTTTCTC[-/CTACT]CTACTCTACTCTCAC | 8440 |
rs775361933 | snp | A/G | 1.65201e-05 | 0.00287398 | missense, intron-variant | NCK2 | GRCh38.p7 | 2:105881745 | CCGAGGAGGAGCTCA[A/G]CTTCGAGAAGGGGGA | 8440 |
rs775410043 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105842122 | GCCGGAGTTTCTCTC[A/G]TTTCCCAGGCTGGAG | 8440 |
rs775432832 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105823884 | TGCTCTGGCTGTTTC[C/G]TGATCAAACGCCTTG | 8440 |
rs775496029 | snp | A/C | 1.65266e-05 | 0.00287455 | missense, utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105893039 | AAACACTTCAAGGTG[A/C]AGCTCGTGGACAATG | 8440 |
rs775515605 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105777093 | CCAGAGCCTGAGAGC[A/T]GGTGCTCTCCTCACT | 8440 |
rs775518109 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105854935 | AAGACCCAGGAGAAA[A/G]CTGGTTGCAGAGTTG | 8440 |
rs775523889 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105843028 | GTGGGCTAGAGTCTG[C/T]ATAGGAGAAATCTTA | 8440 |
rs775534825 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105846429 | TCTATAATTTTGAGG[A/G]GTAACCTGATCCTGG | 8440 |
rs775551208 | snp | A/G | 2.36684e-05 | 0.00344 | missense, utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105893135 | CCCATCTTCACCAGC[A/G]AGCACGGGGAGAAGC | 8440 |
rs775551214 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105860022 | GGGCACGATGGTTTA[C/T]GCCTGTAATCCCAGT | 8440 |
rs775573095 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105819830 | TTTGGAAAATCGTGA[C/G]ATGTAGCCATTCATA | 8440 |
rs775580652 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105832436 | TTCAGCTTTTGCCTA[G/T]TCAGTATGATGTTAG | 8440 |
rs775601285 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105814800 | TTACTCATGAGACAC[A/C]GGGCACACAGGGGGG | 8440 |
rs775611088 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105777644 | GTTGCAGCTGTTCTC[C/T]GGGTAACAGTCTGTG | 8440 |
rs775618530 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105758940 | CATTATTAGTGATTC[A/G]TCCTCTATTTGACAC | 8440 |
rs775627582 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105804083 | TTTTTACGGGGCAAA[C/T]TATATACATAGAGGC | 8440 |
rs775627837 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105762702 | ACTATTTTCCTGTTA[C/G]ATAATAGTGATGCAC | 8440 |
rs775640517 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105787151 | GACCCTCAGCCCTGA[A/G]CACTCAGCTGGATTT | 8440 |
rs775641564 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105859098 | AGAAAATTGTGCAGG[C/T]GAGGTGTTGTAAAAG | 8440 |
rs775648643 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105779901 | ATGCCATAGCCTACG[A/C]GACCGCCTTCACCCT | 8440 |
rs775652539 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105839063 | AGGAATATGAGAGAG[G/T]CAGGGAGAGCAAGGG | 8440 |
rs775686602 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105891353 | ACACCAGATTGTCAC[A/C]GAGCATATGTCCTGC | 8440 |
rs775689506 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105870784 | GAATAAAGGTAAATA[C/T]CCTGGAGTTATTCCA | 8440 |
rs775695111 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105869086 | CCCTTACCTGGGAAA[C/T]GGGGCTCCTCTCATA | 8440 |
rs775740823 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105767010 | ACCTGAGGACACCTG[A/C]CCAGGTGTGTCACAC | 8440 |
rs775781097 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105882789 | GACCAGTTTTGCAAA[C/T]GTCTTTCCGAATACA | 8440 |
rs775791427 | in-del | -/CTTTC | | | intron-variant | NCK2 | GRCh38.p7 | 2:105810426 | CACTCTTCCCTCCCT[-/CTTTC]CTTCCTTCAGAAAAA | 8440 |
rs775810979 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105797723 | GATGCAAAGTCTTTC[A/G]TAACCATGATCAGTT | 8440 |
rs775843545 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105852826 | ATGGTATGCACTTGA[G/T]ATTTTCTGAAAGTGG | 8440 |
rs775878065 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105826850 | TATGTTGAAAATAAA[A/G]GGATGGAAAAAGATA | 8440 |
rs775899498 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105786129 | CAGCCAGCCTTTTAT[G/T]GATCATCTGTTGTGT | 8440 |
rs775905873 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105809722 | TATAAGCACTTATGA[C/T]TTATTCACAGAATAA | 8440 |
rs775912785 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105770995 | TGGTGCGATCTCAGC[C/T]CACTGCAAGCTCTGC | 8440 |
rs775946996 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105766679 | TCACCTTTCAGGGTA[A/G]TCTGTGAGGGAGAAT | 8440 |
rs775979429 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105789881 | GCCAGGGCACACCTC[A/T]CCATCAGATAACGAA | 8440 |
rs775990862 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105807557 | TAAAATGCCTCCTTC[C/G]TAGGGTGGTGTGAGG | 8440 |
rs776018493 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105841641 | GGTGGAGGGTGGGGT[G/T]GAAAGTCCCAACCCT | 8440 |
rs776019571 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105830301 | TTTTGTAGCTCCCAC[A/G]TGAGTGAGAACTCTG | 8440 |
rs776025898 | snp | A/C | | | upstream-variant-2KB, intron-variant | NCK2 | GRCh38.p7 | 2:105850787 | TTTTTTTCAGACTTT[A/C]TTCTGTTGAGGCTTT | 8440 |
rs776036780 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105784265 | TGAGACACCACGCCC[A/G]GCTGTTATTTCTAAT | 8440 |
rs776040750 | in-del | -/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105892921 | CACAAGAGATGTGGA[-/T]GGATTTAGACACAGC | 8440 |
rs776043132 | in-del | -/A | | | intron-variant | NCK2 | GRCh38.p7 | 2:105774872 | CTTAATGAGCCGTGT[-/A]GATGTACAGCTGAAA | 8440 |
rs776063432 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105872521 | GTCACCGTTGGTCAT[A/C]TGCAACTTGGGTTTG | 8440 |
rs776163110 | snp | C/G/T | 9.53142e-05 | 0.00690283 | synonymous-codon, intron-variant | NCK2 | GRCh38.p7 | 2:105881986 | GACGCGGCACCAGGC[C/G/T]GAGTGCGCCCTCAAC | 8440 |
rs776196468 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105774571 | GATTTGATCGTCTCA[A/G]TTTGGGCAGGTGTCC | 8440 |
rs776200243 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105875257 | AGCCTCTCCAAGCCT[C/T]TGTCACTCGTCTCAT | 8440 |
rs776265268 | in-del | -/TTT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105891548 | TTTTTTTTTTTTTTT[-/TTT]TTTTTTTTTTTTTTT | 8440 |
rs776268891 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105835153 | CCTCATTTATGTTTT[C/T]GCACTACCAGTGAGT | 8440 |
rs776275708 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105763658 | GTGCATTGGGAACTT[A/G]GGGGTTTATAATAAC | 8440 |
rs776288339 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105884852 | CATTTATCCTTAGCA[A/G]CTAAAGGTGATGCAT | 8440 |
rs776295166 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105861622 | CAGGTTCAAGCGATT[C/T]TCCTGCTTCAGCCTC | 8440 |
rs776308141 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105840608 | CTGCCCCTCCACCCC[C/T]ACTTCAGATGCCAGT | 8440 |
rs776315818 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105752702 | TTCCTACCCCATCAC[C/G]CTTCAAGTCTCTGGT | 8440 |
rs776378213 | in-del | -/ACCT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105816832 | AGCAGGATGGTAGAC[-/ACCT]ACAACCTGTAAGATG | 8440 |
rs776378837 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105783860 | AGTGGGAGTTGTTTC[A/G]CTTCTCCCTTTATAG | 8440 |
rs776386369 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105800029 | TTTGGAAACACCATC[C/T]TTGTTCATGTGGTAT | 8440 |
rs776387156 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105815779 | CCTCCAAGAGAGGAA[C/T]GAGTCTCTAAACAAT | 8440 |
rs776439132 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105804918 | GCCTAACATGGCACT[A/G]ACTGCTGCAGGGTAC | 8440 |
rs776439626 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105811866 | CCATCGATTGACCTA[C/T]TGCTTGCTATTTCCT | 8440 |
rs776465585 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105833317 | GGCCAGGCTGATCTC[A/G]AACTCCGGGCCTCAG | 8440 |
rs776481366 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105823776 | CAGCTTCTCAGAGTC[A/T]CACCTGACCAACAGT | 8440 |
rs776492005 | snp | A/G | | | intron-variant, utr-variant-5-prime | NCK2 | GRCh38.p7 | 2:105746307 | AGAAACAACCCTGAG[A/G]GGCCGGTGGGCGTGG | 8440 |
rs776510739 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105755561 | TTTCAACACATTGCA[C/T]GTTCATGCGTGTGGC | 8440 |
rs776566131 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105810505 | CAGTTTATTTTTGTC[A/C]GCATGCTTTTTACTG | 8440 |
rs776572130 | snp | A/G | 1.66131e-05 | 0.00288206 | missense, intron-variant | NCK2 | GRCh38.p7 | 2:105881604 | ACTACGTCTTGGAGG[A/G]GGTGGACGAGGCGGC | 8440 |
rs776620191 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105813611 | CAGAATCGGCCACGA[C/T]TGCTTGCAGGGGGGC | 8440 |
rs776645486 | in-del | -/TG | | | intron-variant | NCK2 | GRCh38.p7 | 2:105833847 | CAGTTTTTGGTATAC[-/TG]TGTTTCCATTTTTAT | 8440 |
rs776650832 | in-del | -/G | | | upstream-variant-2KB, intron-variant | NCK2 | GRCh38.p7 | 2:105851469 | TCACCGTGTTAGCCA[-/G]GATGGTTTCCATCTC | 8440 |
rs776652223 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105866181 | GGCCTCCCAAAGTGC[C/T]GGGATTACAGGCGTG | 8440 |
rs776654318 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105878821 | ACAGGTAAAATTTCC[A/G]CTGCATGCTTGCTAT | 8440 |
rs776673280 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105858628 | ACAGTGTTGTGTATT[C/G]CATCTCCAACTGTAG | 8440 |
rs776726523 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105796718 | TTTTTTTTCCCTTGT[A/G]CTTTCTCATACCTCT | 8440 |
rs776743782 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105877069 | GAAGGACAAGGGATC[A/G]CTGAGTCCCCTAAGC | 8440 |
rs776750326 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105865600 | CCTGGACCCTAGGGA[G/T]TCACGTCTTTGTAAC | 8440 |
rs776751269 | snp | A/G | | | missense, intron-variant | NCK2 | GRCh38.p7 | 2:105881732 | TTCAGCTCAGTCACC[A/G]AGGAGGAGCTCAACT | 8440 |
rs776754070 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105843741 | ACAGTGATATAAATG[A/G]TGGAATACGTTAATT | 8440 |
rs776758935 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105870679 | AGAATCGCTTGAACC[C/T]GGGAGGCGGAGGTTG | 8440 |
rs776762870 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105857448 | AAGCTCTTCCTTAAA[C/T]AGAATCAGATTTTTA | 8440 |
rs776770222 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105767754 | TCCCTTTATTGGCGC[A/G]AGGTTTGAGGTTTCC | 8440 |
rs776777209 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105869901 | TGTGAGAAAATTCTA[A/T]ACTTTTAGACCATTT | 8440 |
rs776780961 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105749234 | TTATTTGTGTCACCC[C/T]TTCTTTCTACTGTTG | 8440 |
rs776817344 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105776106 | GCCACCTCTGGGGGT[A/G]TGGGTGCGGAGCAGG | 8440 |
rs776830935 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105849258 | AACTAGCAGGGCGCG[A/G]TGGTGCACACCTACA | 8440 |
rs776848356 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105809030 | CAAAATGGCATGGCT[A/G]TGTTACAATGTGATG | 8440 |
rs776872198 | snp | C/T | 1.73854e-05 | 0.00294829 | missense, intron-variant | NCK2 | GRCh38.p7 | 2:105881385 | CCCCCACGCCCAGCA[C/T]GGACGCCGAGTACCC | 8440 |
rs776882768 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105817465 | CTCTTTCTGGCTGGG[A/C]AGTAAGAAGTGCTTT | 8440 |
rs776919956 | in-del | -/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105794048 | TTGTATCTTTCGATT[-/T]TTTTTTTTTTTTTTT | 8440 |
rs776942291 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105785869 | TGAAGAAAATAAATA[C/T]GATATCTAGTAGCAG | 8440 |
rs776954305 | in-del | -/AA | | | intron-variant | NCK2 | GRCh38.p7 | 2:105876486 | CGAATGTGCTCTTCC[-/AA]AAAATGCAACATAGA | 8440 |
rs776959381 | snp | G/T | 3.31565e-05 | 0.0040715 | synonymous-codon, stop-lost | NCK2 | GRCh38.p7 | 2:105893005 | CTTCTCCGTGTCCCT[G/T]AAAGCGTCAGGGAAG | 8440 |
rs777024116 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105837481 | TTGGTATGATAGTGA[A/G]TCATGTGACTATACC | 8440 |
rs777044980 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105796031 | TTGTAGTTTGCTCTG[A/G]TATAAATCATATGTG | 8440 |
rs777064008 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105768858 | GGTGGGAGTCCCCAT[A/G]CCCCCTGGGGGAGAC | 8440 |
rs777077157 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105836540 | GAGGGAGCAAAGTTG[G/T]TGGTGGAGGTAGTAG | 8440 |
rs777077575 | in-del | -/CGAGGTGGTTCTGCTTCTCTCCCAAGATTCCCC | 2.75912e-05 | 0.00371414 | cds-indel, utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105893149 | GAGCACGGGGAGAAG[lengthTooLong]CTCTACCTCGTCAGG | 8440 |
rs777096347 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105806540 | ACCACTCCCGGCCAC[A/G]TATATTCTCTTCATT | 8440 |
rs777123504 | snp | A/G | 1.65715e-05 | 0.00287845 | missense, intron-variant | NCK2 | GRCh38.p7 | 2:105881511 | TGGTGAAGGGGTCGC[A/G]CGTCACCGTCATGGA | 8440 |
rs777127535 | in-del | -/GGTGTGTGTGTGTGTG | | | intron-variant | NCK2 | GRCh38.p7 | 2:105830670 | CCTTGCCAGGAATTT[-/GGTGTGTGTGTGTGTG]TGTGTGTGTGTGTGT | 8440 |
rs777137088 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105780545 | ATCTATACCTGGGCA[C/T]TATTGAGAGTGGGAG | 8440 |
rs777147009 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105852409 | ATTACATGGCAAGAT[A/G]TAAAACTCCTTGGAT | 8440 |
rs777147658 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105818676 | CAAATGAGAATATTA[C/T]AGTGGACATTTGTAT | 8440 |
rs777242458 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105866881 | GAGTGCTTGGGATGC[C/T]CAGTGTGGCTTATAT | 8440 |
rs777259645 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105790790 | GGTCTCTCGCTGCCA[C/G]CTGATGCACATAGGC | 8440 |
rs777264543 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105785257 | TGTTGGGATTACAGG[C/T]GTGAGCGGCAGTTGG | 8440 |
rs777271976 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105801868 | GAGTTAGTCGTCTTG[C/G]TGAGAGAAAGTGATG | 8440 |
rs777273129 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105758323 | ACATTTTACAGGTTT[C/G]TTTTATCCTATTGAT | 8440 |
rs777315716 | in-del | -/CTCT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105794918 | TATTTTGTATGACTA[-/CTCT]CTCTATCTTCTTTTT | 8440 |
rs777348656 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105804865 | TAGGGATTCAGTGTG[G/T]CTTAGATTGCAAACT | 8440 |
rs777350948 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105795332 | AAATAAGCAATAGCA[C/T]ACTCTATACACTTTT | 8440 |
rs777388396 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105890502 | TAATCATCTATAGGC[C/T]GAGGCCTAATCTGAG | 8440 |
rs777424581 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105873577 | ACCCATATTTACCAC[G/T]TTTTCAGATGGGAAT | 8440 |
rs777433704 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105881272 | ATCCCGGTAGGCTAG[C/G]GAGTGTGGTGGTGCC | 8440 |
rs777472288 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105806122 | AGTGCTCAAAAATTA[C/T]CAGATTTTGGAGCAA | 8440 |
rs777513074 | snp | C/G/T | 0.000106619 | 0.0073007 | intron-variant | NCK2 | GRCh38.p7 | 2:105882057 | AGTCCTCGGTAAGTG[C/G/T]GCTGCGCCCACAGCT | 8440 |
rs777516671 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105892259 | GAAGTAGTAAAATTT[C/G]TAGCTACTGCCTGCA | 8440 |
rs777564175 | snp | G/T | 1.6546e-05 | 0.00287624 | synonymous-codon | NCK2 | GRCh38.p7 | 2:105855174 | GGACGACTCCAAGAC[G/T]TGGTGGCGGGTGAGG | 8440 |
rs777619212 | snp | C/T | 4.33398e-05 | 0.00465489 | synonymous-codon | NCK2 | GRCh38.p7 | 2:105855261 | CCTGAAGAAGGGCTC[C/T]CTCGTGAAGAACCTG | 8440 |
rs777638812 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105871466 | GGGAGATGGGGATTT[A/G]CTAAGCTTTTGAAAA | 8440 |
rs777644675 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105837299 | TTTTACCACATATGT[A/T]AGTCTAAACTACATT | 8440 |
rs777695593 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105808556 | AGCCCCCAGGAGTAA[C/T]CACCAGTTTACTACA | 8440 |
rs777726001 | snp | G/T | | | upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105743005 | CTTTAAAAAAAAAAG[G/T]TGCGTATCAGAATAA | 8440 |
rs777728428 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105880648 | GACTTCCCACCCATT[A/C]TAGGAATGAAAAAGA | 8440 |
rs777731987 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105763014 | AGCCTGGGCAACACA[A/G]TGAAACCCCGTCTCT | 8440 |
rs777768005 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105892513 | CTACCTCCAGGTCTT[C/T]CTGAACATCAGATGC | 8440 |
rs777779826 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105827355 | TGTGAAATAAGAAGT[A/G]AAAACTGCTAGAACT | 8440 |
rs777799501 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105882345 | ACAGGCTCAAACATC[A/G]TTTTCTCTCCTGGTT | 8440 |
rs777813254 | in-del | -/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105861515 | TTGAGGTTTTTCTCT[-/T]TTTTTTTTTTTTTTT | 8440 |
rs777864462 | in-del | -/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105794971 | CCATTTTTTAAAGAT[-/G]TTTTTTTCTTTCCCC | 8440 |
rs777913252 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105787916 | CCCCCCACCGCCCCC[A/G]ACTTGTAGATCCCTG | 8440 |
rs777919935 | snp | C/T | 6.6379e-05 | 0.00576065 | missense, intron-variant | NCK2 | GRCh38.p7 | 2:105881664 | GCAAGGGCGCCTCGC[C/T]GAGCAATGGCCAGGG | 8440 |
rs777924793 | snp | C/T | 1.65233e-05 | 0.00287426 | missense, intron-variant | NCK2 | GRCh38.p7 | 2:105881724 | TGTACCCCTTCAGCT[C/T]AGTCACCGAGGAGGA | 8440 |
rs778025040 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105780424 | TCTCATTTTCGTTTG[A/G]TATCTGGGTTAAAAT | 8440 |
rs778036531 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105762252 | TCAAGTTGAAAGAGG[C/G]CTTGCCGAGGAAACA | 8440 |
rs778085003 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105888051 | GTGGGGATGTGGAGC[C/T]AAATAGGGTTCTTGC | 8440 |
rs778097269 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105800468 | TTCTGAGGTGCACAG[A/T]TCCTGAGCTTTAAAC | 8440 |
rs778112176 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105791518 | ACTCTTCGCTCACTG[G/T]CTTTGGGATGTCCTT | 8440 |
rs778114653 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105755688 | GTATTTTGAGAGACT[G/T]CATTGAGACCCGAAC | 8440 |
rs778137876 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105775189 | CGTGTTAGTCATGTT[A/G]TAAGTAATTTGCACT | 8440 |
rs778151035 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105786810 | TGGGTTTGTTCCCCT[C/G]TGCCTCTCTTGGGCC | 8440 |
rs778171416 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105801706 | TCAAGGGCTGGGTGT[C/T]TGGGGACAGAGTGGC | 8440 |
rs778180056 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105828187 | CTAAGAAGTGTGCAA[A/G]CTTACATAGCAGTAG | 8440 |
rs778182861 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105838880 | GTCTTCAAGGAGTTA[A/G]GTGCAGTCAGAGAAA | 8440 |
rs778184225 | in-del | -/TTTG | | | intron-variant | NCK2 | GRCh38.p7 | 2:105885909 | GGGCTTTTTTGTGTT[-/TTTG]TTTGTTTGTTTTTTA | 8440 |
rs778185215 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105856763 | TGATGGAGAAATTTC[A/G]TTTTTGATTAGCAAT | 8440 |
rs778252444 | snp | C/T | 9.52426e-05 | 0.00690016 | utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105893177 | AGGGCCCTGCAGTGA[C/T]GGCGCCCCGGCCCCA | 8440 |
rs778286118 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105863459 | GGCTTTGAAACAGGG[A/T]TGCAGACACGATGCA | 8440 |
rs778292639 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105765246 | CTATTCTAGAGGACC[A/G]TGTCTCAGAGTGATG | 8440 |
rs778352094 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105758179 | AGCACACTAATACTT[C/T]CTTATTTTTTTTTAA | 8440 |
rs778367390 | in-del | -/T/TT/TTTT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105857030 | TTGTTGTGTGTCTTC[-/T/TT/TTTT]TTTTTTTTTTTTTTT | 8440 |
rs778389825 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105774329 | CTATCTTAGTAACAG[A/G]TGTTTTAGGTACCTG | 8440 |
rs778407234 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105757040 | GAACTCCTGACCTCG[G/T]GTGATCTGCCTGCCT | 8440 |
rs778417118 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105764297 | GTTAAGGAGAGCCTG[C/T]GGGCAGACATCCCAC | 8440 |
rs778426194 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105767399 | TATTTTGTGAAAGGT[G/T]TTCTTTATAAGTGTT | 8440 |
rs778431559 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105813002 | GGCATCAGCAGATGC[C/G]ATTTGCAGAATGCGA | 8440 |
rs778442896 | snp | C/T | | | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105771349 | AGGCAGGTGGATCAC[C/T]TGAGGTCAGGAGTTC | 8440 |
rs778477944 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105822302 | AGGATCAGCTTAACA[C/G]CTCCTGTGGCTTCCA | 8440 |
rs778489948 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105878313 | AAGTCCCAATCCCCA[A/G]GACCTCAGAATGGGA | 8440 |
rs778508759 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105846956 | GACCAACAAAATGTG[G/T]TATATGCATACATTG | 8440 |
rs778534616 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105763556 | TCACAGTGGGAAATA[C/T]TCAATTTGTTAGTTG | 8440 |
rs778538393 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105803668 | CACACCCAGGTTAGT[C/T]GTCTTTCACACTTGT | 8440 |
rs778560179 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105834070 | AAACATACTGTAAAT[C/T]CTAGAGAATGTCCCA | 8440 |
rs778577586 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105871112 | GCGTGTGAAATCGGG[A/G]TGATGAGACAGCGAG | 8440 |
rs778579946 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105892193 | GCGTCTCAAAAAAAA[A/G]AAGAATTAGAAAAAT | 8440 |
rs778588738 | snp | A/G | 1.67652e-05 | 0.00289522 | missense, intron-variant | NCK2 | GRCh38.p7 | 2:105881439 | GCATCTACGACCTCA[A/G]CATCCCGGCCTTCGT | 8440 |
rs778613251 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105832920 | ATAGTTTGAAAAGAA[C/T]TGGTGTTAGTTTGTC | 8440 |
rs778640285 | snp | C/T | 3.60231e-05 | 0.00424385 | synonymous-codon, intron-variant | NCK2 | GRCh38.p7 | 2:105881882 | AGTGACGGGCCTGCC[C/T]TGCACCCTGCGCACG | 8440 |
rs778695540 | snp | C/T | 1.86416e-05 | 0.00305294 | synonymous-codon, intron-variant | NCK2 | GRCh38.p7 | 2:105881959 | GGGCAGAGAGTGGTA[C/T]TACGGGAACGTGACG | 8440 |
rs778752100 | snp | C/T | | | | | GRCh38.p7 | 2:105846044 | ATGTAAGAAAATTGG[C/T]TTATTAAATTTATGT | 8440 |
rs778755115 | snp | C/T | | | | | GRCh38.p7 | 2:105761058 | CTCAGGAAGTGGTCC[C/T]GACCCAGTGTCTGAG | 8440 |
rs778775080 | in-del | -/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105871021 | TCATCGTGATCCTGG[-/C]CCTCCTACTTTCGCT | 8440 |
rs778796962 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105776790 | CACACGTGACTATTC[C/G]AGGGTACCATAGCCC | 8440 |
rs778808840 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105826674 | TGGATTTGGGTCATT[A/C]CTGAGTTATCCTCAC | 8440 |
rs778823483 | in-del | -/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105891272 | TTTTTGTTTGTTTTC[-/T]TTTTTTTTTTCATAG | 8440 |
rs778840688 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105825791 | TATACACTCTGCTCT[C/G]TCAGTTACAGTATAA | 8440 |
rs778849567 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105848421 | CGGCAGCAGATTTTG[A/G]CCATTACCCAATAAA | 8440 |
rs778852582 | in-del | -/GGTG | | | intron-variant | NCK2 | GRCh38.p7 | 2:105830670 | CCTTGCCAGGAATTT[-/GGTG]TGTGTGTGTGTGTGT | 8440 |
rs778858931 | snp | C/G | | | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105771656 | AAGTAATGTTCTTTT[C/G]TTATCAATAGAAGGC | 8440 |
rs778882378 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105790939 | GAGTCCAACCCCTCC[C/T]CTTTATATCACAGAT | 8440 |
rs778892270 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105836388 | GGACTGTAATCACTG[A/T]CAGTGGTGTCTGCAA | 8440 |
rs778892513 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105780257 | CATCTAGATTAAGTT[A/G]GGACCTGATAGTCAT | 8440 |
rs778896517 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105829978 | TCTGTTTACTTATTC[A/G]TTCTAATTGTTCCTA | 8440 |
rs778929842 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105838205 | GTGCCGAAAGGGCTA[C/T]ATGCATTTTGTTTTG | 8440 |
rs778932258 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105786771 | CTCTCCTCCCTTCTG[C/T]CTCCCCCACGCATTG | 8440 |
rs779053202 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105790217 | ACCGTTAGAAATAGT[A/G]TGCATGTCATTAGGA | 8440 |
rs779117347 | snp | A/T | 3.32077e-05 | 0.00407465 | missense, intron-variant | NCK2 | GRCh38.p7 | 2:105881660 | CTGCGCAAGGGCGCC[A/T]CGCTGAGCAATGGCC | 8440 |
rs779118232 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105819262 | CGGGGTGTTCCTGTT[C/G]CAAACCTAGGAGGTT | 8440 |
rs779160807 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105858194 | CCTGCAGAAATTATC[A/C]CTGCTGTGTATTAGG | 8440 |
rs779162818 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105840196 | CTTATGCTAAATGAG[A/G]TGATCCAGAAAGACA | 8440 |
rs779174961 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105801243 | CTGGCTAGAGGCCTG[C/T]CGGGCTGTCATCTCC | 8440 |
rs779206607 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105748928 | TAAATCTCAGAACTT[C/G]TGTCTACTGTGGAAG | 8440 |
rs779217228 | in-del | -/TTTTTTTTTTTTTT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105880941 | CAGGTGGCTAATTTT[-/TTTTTTTTTTTTTT]TTTTTTTTTTTTTTG | 8440 |
rs779251709 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105794871 | TGTTCGCATGGTTCC[G/T]CAGCCAAAGATGGTT | 8440 |
rs779257737 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105800352 | GATTGATTGAGATAG[C/T]GCATAAAGAGGGCCT | 8440 |
rs779276214 | in-del | -/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105800885 | TCCAAGCTCGAGGTT[-/C]CATGGGATTACATGC | 8440 |
rs779281957 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105804490 | ATGATGATTTCCACT[G/T]TGAGCTCAGCAGGAG | 8440 |
rs779312302 | in-del | -/T | | | upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105742990 | ACAATCAACTCTCTC[-/T]TTTAAAAAAAAAAGG | 8440 |
rs779335223 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105841334 | AAAGCCCTAAAGTTG[G/T]CTTAATAAACTTCTG | 8440 |
rs779354210 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105867797 | TCTCACCCTGCTTCA[A/G]CTTCCTAAAGATCAC | 8440 |
rs779361161 | in-del | -/AGC | | | intron-variant | NCK2 | GRCh38.p7 | 2:105783988 | GCAGGTCACTGAGTA[-/AGC]AGCAGGACCTGCTTC | 8440 |
rs779398143 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105888001 | AAATTTTTAAGTCTG[C/T]ACGTTTGTTGAACAC | 8440 |
rs779398281 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105872258 | GCCTGCTGCTGCTTG[C/T]ACGCTGTCACCCGCT | 8440 |
rs779428772 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105870655 | AGCTACTTGGGAGAC[A/G]GAGGCACAAGAATCG | 8440 |
rs779433416 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105853458 | GATTTTAACAAATGT[A/G]TAATGACAGGTGTCC | 8440 |
rs779485059 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105885633 | AGGTCTGGGGCCCAA[C/G]AATTTGCATTTCTAT | 8440 |
rs779528731 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105817248 | AGGTTTTACCTGTTC[A/G]TATGAAAAACCTACT | 8440 |
rs779533025 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105802203 | CGGAAACTGATGTGA[A/T]GAAGTGGAACGGGAA | 8440 |
rs779577834 | in-del | -/A | | | intron-variant | NCK2 | GRCh38.p7 | 2:105829163 | ATATTTGATAGGTAC[-/A]AAATACGTAGGTGTC | 8440 |
rs779591948 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105803531 | TCCAAGGAAACCTAG[C/T]TTCTGAGGTTAATTA | 8440 |
rs779608119 | in-del | -/ACAAATGTTATTACCTGCAGT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105875011 | TCTGCTCACTGAGTG[-/ACAAATGTTATTACCTGCAGT]ACACATGTTATTTTA | 8440 |
rs779645389 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105810333 | GTGTGAGAGAGAGAG[C/G]GAGCGAGCAAGCACA | 8440 |
rs779691258 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105826405 | AAGCCTAACCCCACC[A/G]CCCTTCGAGGACCAA | 8440 |
rs779699343 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105870429 | ATGGCGCACAGTAGA[A/G]TGTTTCATTATGGGG | 8440 |
rs779716893 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105814974 | CATACAGAGGTGGTG[C/T]TTGGGGCATGGTACC | 8440 |
rs779724766 | snp | A/T | 6.86672e-05 | 0.00585908 | missense, utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105893082 | GGCAGCGGCGCTTCC[A/T]CACCATGGACGAGCT | 8440 |
rs779744505 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105775439 | ATTTAGTTTTTAAAA[C/T]TTAACTTCAGATTGA | 8440 |
rs779746624 | in-del | -/TAAG | | | intron-variant | NCK2 | GRCh38.p7 | 2:105770078 | GCACACAGCATTATT[-/TAAG]TATTTTTGCACTTAA | 8440 |
rs779869297 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105837099 | TTTCCTCTGTGCTGC[C/T]ATCCTGAGCTTCTGT | 8440 |
rs779869388 | in-del | -/TTTCTGTTTAAGT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105848002 | GAGTGTTGGCACATC[-/TTTCTGTTTAAGT]TTTCTGTTTTTCAAT | 8440 |
rs779876358 | in-del | -/AA | | | intron-variant | NCK2 | GRCh38.p7 | 2:105770128 | GCACTAATAAGTAAA[-/AA]AAAAAAAAAAAAAGA | 8440 |
rs779901605 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105808286 | AATTTTCATATACCT[C/T]ATTCCAGTTGGAAAA | 8440 |
rs779903120 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105869516 | AGAGTGTTCTGAGAA[A/G]CTGGCACAAGTACGG | 8440 |
rs779907949 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105794836 | CTGCCTCAGCCTCCC[A/G]AATAGTTTATTATCT | 8440 |
rs779911259 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105760993 | TGGGATTGGGATCTG[G/T]GTGGCCCTCATCCTG | 8440 |
rs779917800 | snp | A/G | 1.79519e-05 | 0.00299593 | missense, intron-variant | NCK2 | GRCh38.p7 | 2:105881874 | TGGTCCTCAGTGACG[A/G]GCCTGCCCTGCACCC | 8440 |
rs779967001 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105789444 | TCCACCCGCCTCGGC[C/T]TCCCAAGGTGCTGGG | 8440 |
rs779989133 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105880852 | GCGATCATGGCTCAC[A/T]GCAGTCTCAACTCTG | 8440 |
rs779999689 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105872136 | AGAAAGGTCAGTTGA[C/T]GAATATTTTTGCTTT | 8440 |
rs780002604 | snp | G/T | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime | NCK2 | GRCh38.p7 | 2:105851701 | GATTGGCTGTCCCTC[G/T]GAAGCAGTCTCACTG | 8440 |
rs780007889 | in-del | -/A | | | intron-variant | NCK2 | GRCh38.p7 | 2:105892337 | GAAATGAAAAACAGC[-/A]AATTTCTTGAGCAGT | 8440 |
rs780012547 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105780941 | TCTGTGGTATTTTGT[C/T]ACAGCCAGCCAAATG | 8440 |
rs780024419 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105841052 | TGATAGTGTGGATTA[C/G]AAGCTTATCTTCCCA | 8440 |
rs780059338 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105753027 | TCATCGCTAAGGAAA[C/G]GGAGGCACTGAGGCT | 8440 |
rs780083790 | snp | A/C | | | upstream-variant-2KB, intron-variant | NCK2 | GRCh38.p7 | 2:105850053 | TGTATTCATGTCTCT[A/C]CTGAGCATCAGAAGT | 8440 |
rs780086558 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105885388 | TTTTTTAAAATATAT[A/G]AAAAGTATTTGGCTG | 8440 |
rs780093707 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105860972 | GAGGAACCCAAGGTC[A/G]TTGTGGATCCCGAAA | 8440 |
rs780136235 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105759991 | ATCTTGATCACCTGG[C/T]CCAGGTAGTGTTTGT | 8440 |
rs780144088 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105807156 | GAGGACCCAGCTGCC[C/T]AATCCTGAGTTCATT | 8440 |
rs780151498 | snp | A/G | 1.84735e-05 | 0.00303915 | missense, intron-variant | NCK2 | GRCh38.p7 | 2:105881937 | CCTCGTCCAGCGGGC[A/G]CTTCGCGGGCAGAGA | 8440 |
rs780244038 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105747367 | AATACCCTAAGACTC[C/G]CGGAATGGCGCAGAA | 8440 |
rs780271789 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105871564 | GCAGTGGCGCGATCT[C/T]GGCTCACTGCAACCT | 8440 |
rs780274232 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105788276 | GCCCTTGAAACTTCT[A/G]CACCCATAAAATGCA | 8440 |
rs780294037 | snp | C/G | | | utr-variant-5-prime, intron-variant | NCK2 | GRCh38.p7 | 2:105851886 | CGTCGATTGACTGGT[C/G]TTCAGAAGCAGGTTC | 8440 |
rs780305389 | snp | C/T | 0.000158366 | 0.00889706 | utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105893197 | CCCCGGCCCCACACT[C/T]GCCTCCCGGGCCCCA | 8440 |
rs780325930 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105827596 | TTGCCATGTTAGGGC[A/G]TGTCCTGGGCCAAAA | 8440 |
rs780370050 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105815263 | AGTGCTAGAGAATAC[A/G]TAAAAAGGAATTAAT | 8440 |
rs780372354 | snp | C/T | | | intron-variant, utr-variant-5-prime | NCK2 | GRCh38.p7 | 2:105773315 | GTCCCCCTTGTCCCT[C/T]TCCTTTCCAGCCACC | 8440 |
rs780388044 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105821953 | CTCTGACACATGATG[A/G]TGGTGACATGGTAAC | 8440 |
rs780409616 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105866601 | AGGCGTAGTTCACAA[C/T]AGTGTTTGCGCTCCT | 8440 |
rs780411756 | snp | C/T | 3.3134e-05 | 0.00407012 | synonymous-codon, intron-variant | NCK2 | GRCh38.p7 | 2:105881539 | GGAGAAGTGCAGCGA[C/T]GGTTGGTGGCGGGGC | 8440 |
rs780431403 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105883921 | GAAAGAGCTTTACTG[C/G]GACTTGCATCGGCTC | 8440 |
rs780443046 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105832836 | AGTGAGTTAGGAAGA[A/G]TTCTCTTCTCTTTTT | 8440 |
rs780459874 | in-del | -/ATTA | | | intron-variant | NCK2 | GRCh38.p7 | 2:105888155 | GTTTTCCGCCAACCT[-/ATTA]ATTGTCCTTAGATTC | 8440 |
rs780497600 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105865329 | GCATGTGAGAAAACT[C/G]ATACTCAGAAGTTAA | 8440 |
rs780578224 | snp | C/T | 0.000179909 | 0.00948272 | intron-variant | NCK2 | GRCh38.p7 | 2:105882073 | GCTGCGCCCACAGCT[C/T]CGGCTGCAGGCAGTA | 8440 |
rs780581009 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105767296 | GTGGCCTACTTGGAT[A/G]TCTGATATGAGCTTA | 8440 |
rs780590996 | in-del | -/A/AA/AAA | | | intron-variant | NCK2 | GRCh38.p7 | 2:105779306 | GCGAGACTCCGTCTC[-/A/AA/AAA]AAAAAAAAAAAAAAA | 8440 |
rs780600174 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105783348 | TAGAGGAGACTTCCC[C/T]GAGCTTCCTTCCTCG | 8440 |
rs780607036 | snp | C/G | | | upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105743195 | AAATGCCACATATTT[C/G]AGAAAACTCCACAGG | 8440 |
rs780611626 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105807602 | CACCAGCCTCTTGGA[A/G]TTGGAGTCACGCTGG | 8440 |
rs780613322 | in-del | -/GGCC | | | intron-variant | NCK2 | GRCh38.p7 | 2:105833674 | TTTTTGCATTTTTTT[-/GGCC]TCTTTTGTTCAGTTC | 8440 |
rs780615941 | in-del | -/A | | | intron-variant | NCK2 | GRCh38.p7 | 2:105767840 | GCATGAAATTGTGGG[-/A]CATACTGGGTGGTTC | 8440 |
rs780651062 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105782416 | AGAGTTGGGTTGATG[A/G]CCATTTGAGGACTTG | 8440 |
rs780652108 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105755841 | ACTAAGGTTCATAGG[A/G]TTCTAGGTTCAGCCT | 8440 |
rs780662125 | in-del | -/TTCT | | | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105849723 | GCTTGAATCACAGAA[-/TTCT]GAGCAGCCACTGGGC | 8440 |
rs780731933 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105814086 | TTTTTGCACAAAAGT[A/G]TATACTTTCCTGATG | 8440 |
rs780748328 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105842934 | TTGCTTAGCAGGAGG[A/G]ACAGTCTAGTGGAGA | 8440 |
rs780753687 | in-del | -/TG | | | intron-variant | NCK2 | GRCh38.p7 | 2:105867097 | AGTACAAAGCCAAAC[-/TG]TTCCCCTTAAAATGT | 8440 |
rs780761306 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105800880 | TTCAATCCAAGCTCG[A/G]GGTTCCATGGGATTA | 8440 |
rs780761768 | in-del | -/T | 1.94888e-05 | 0.00312154 | intron-variant | NCK2 | GRCh38.p7 | 2:105881284 | TAGGGAGTGTGGTGG[-/T]GCCCAAGTGCCCTGC | 8440 |
rs780764804 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105857230 | TGAACCACATCTTCC[A/G]CCCAGCATGCTTAGT | 8440 |
rs780766915 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105785355 | GGACGGTTCCCCCGT[C/G]CTGGCCAAGGAGGCT | 8440 |
rs780774064 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105792982 | CCTTTCTCACCAACC[A/G]AGTCAGCTTTTCCCT | 8440 |
rs780774299 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105796512 | GTATTATTGGCACCG[G/T]TTGCAGAGAGGGCCT | 8440 |
rs780845123 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105864281 | GGGGACGGGGCCTGA[G/T]AGTGACCCAGGGTGA | 8440 |
rs780860889 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105825378 | CCGTTACTAGTGTTT[A/T]GTTCTGATCTTTGAT | 8440 |
rs780879396 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105786967 | CGAAACTTCAGCTGG[C/T]GTGGTGCCGCACAGG | 8440 |
rs780949614 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105869261 | GCCACACCGGATCCT[A/G]CATGTGTCCCTAGCC | 8440 |
rs780951875 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105813068 | TCAGGAGAAGGAGCA[C/T]TCTGGCTTTAAAATC | 8440 |
rs780958750 | snp | G/T | 0.000104703 | 0.00723467 | intron-variant | NCK2 | GRCh38.p7 | 2:105892953 | CCCCGCTGTGGCCCG[G/T]CTGTAACTGTGTTCT | 8440 |
rs780985936 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105848250 | TGGGGGGCAGAGTGG[C/T]CAAGCACCTTCCCCC | 8440 |
rs781013802 | snp | A/G | 2.65312e-05 | 0.0036421 | synonymous-codon | NCK2 | GRCh38.p7 | 2:105855288 | CCTGAAGGACACACT[A/G]GGTGAGTGTTTCACC | 8440 |
rs781033433 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105759746 | AGTCTCCGTAGCGCC[C/T]CTGATCTGGGACAGT | 8440 |
rs781039313 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105836937 | TGCCAGGTACCTCCC[C/T]TTATGGGGCTCAAGG | 8440 |
rs781076725 | in-del | -/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105811507 | ACCTGAATGTGTGTT[-/C]CCAGCTAGGGAATCC | 8440 |
rs781084995 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105781249 | CCTTGTGAATTTTAT[A/G]AACATGATTACTCTA | 8440 |
rs781091603 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105834361 | TTGTTATGTCTTTTT[A/G]AATTCACTCCTTTAT | 8440 |
rs781103255 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105798766 | AGCAAAGCAGTAGCT[C/G]TGGTTCTTCATAGAT | 8440 |
rs781115104 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105868112 | TGGGCATCTGTAGGG[C/G]TCCTGCATGGCCCAC | 8440 |
rs781118251 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105780094 | TTATTTTAACTGAGC[A/G]TATTTTGGACGTACT | 8440 |
rs781129740 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105829793 | AAGTCTCTGGGTGCA[C/T]CCCATAGTTAAGGGA | 8440 |
rs781170309 | in-del | -/ACACTA | | | utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105894016 | CACACACACACACAC[-/ACACTA]ACACTATATATATAT | 8440 |
rs781199784 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105883782 | TTTTTCTAAAGAACT[A/G]AAGCACGAATTGTTT | 8440 |
rs781203600 | snp | A/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105879739 | CTCCACCATTGAGGA[A/C]AATCAGCCTTTTTAC | 8440 |
rs781276491 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105762299 | AGCATCAAACCAGGG[A/G]GGGTCTAGGTCCAGG | 8440 |
rs781343965 | in-del | -/CTTAA | | | intron-variant | NCK2 | GRCh38.p7 | 2:105775577 | TTTATGAATTTATGC[-/CTTAA]CTTAAATTGTCTACA | 8440 |
rs781362184 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105749780 | CCACATCCTGGTTAT[G/T]GGCCAGGGTTACCCT | 8440 |
rs781387075 | snp | C/G | 1.65236e-05 | 0.00287429 | synonymous-codon, intron-variant | NCK2 | GRCh38.p7 | 2:105881731 | CTTCAGCTCAGTCAC[C/G]GAGGAGGAGCTCAAC | 8440 |
rs781411928 | snp | C/G | | | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105771921 | TCAGACTGACTTCCT[C/G]CCTCCCAGGGCTGTT | 8440 |
rs781415303 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105863827 | CTTAATCATTGAGTG[A/G]CTTTGAACAAGCCGC | 8440 |
rs781425556 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105755761 | CTAATCAAAGACATC[C/T]GTTTTCTTAGCTCAG | 8440 |
rs781432567 | in-del | -/A | | | intron-variant | NCK2 | GRCh38.p7 | 2:105888027 | ACACCAGATACTCTG[-/A]AGCCCGGTGTGGGGA | 8440 |
rs781442001 | snp | C/T | 1.78401e-05 | 0.00298659 | synonymous-codon, intron-variant | NCK2 | GRCh38.p7 | 2:105881863 | AAACTACGTGGTGGT[C/T]CTCAGTGACGGGCCT | 8440 |
rs781444146 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105853220 | AGGACTGAATATTGA[A/G]TTTTTCTGCTTAAAG | 8440 |
rs781502696 | snp | G/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105880972 | TTTTTTTTTTTTGCA[G/T]ACACGGTCTCGCTAT | 8440 |
rs781505045 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105874422 | ATTTAGCTGACTTTA[A/G]TAATAGGTTCTGACT | 8440 |
rs781523130 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105820693 | CTTGAAAAGTGACTG[C/T]AATTGATTGTTGGAG | 8440 |
rs781528541 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105832142 | TTTAGCTATTATAAA[C/T]GAGATTGGTTTCTTT | 8440 |
rs781532125 | snp | A/G | | | upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105743851 | ATTATTGCCTTAATA[A/G]TAAGCAGAGACCAGG | 8440 |
rs781549575 | snp | C/T | 5.01375e-05 | 0.00500662 | utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105893185 | GCAGTGACGGCGCCC[C/T]GGCCCCACACTCGCC | 8440 |
rs781550103 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105766696 | CTGTGAGGGAGAATC[C/G]TGGCGGGGGCGGGGT | 8440 |
rs781578124 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105831786 | TACGATGCTGTTTTG[A/T]TTACTATAGCTTGTA | 8440 |
rs781610123 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105865127 | GCCAAACAGAAAGCT[C/T]ATGCAGTAGAAAAGC | 8440 |
rs781626101 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105875833 | AAGATACCATCAGAT[C/T]TCTAAGGTTTCTTCT | 8440 |
rs781725663 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105752073 | TTTGAAATTCAGCAT[A/G]TAGTATATACGTTTA | 8440 |
rs781743996 | in-del | -/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105878782 | AGTTGCGCCAAAGAC[-/T]TATTTAGATCACATT | 8440 |
rs781753779 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105797155 | CATCTCCCCCACCCA[C/T]AAGAAAAAAGTTGAC | 8440 |
rs781754645 | snp | C/T | 1.67385e-05 | 0.00289292 | missense, intron-variant | NCK2 | GRCh38.p7 | 2:105881444 | TACGACCTCAACATC[C/T]CGGCCTTCGTCAAGT | 8440 |
rs781758992 | in-del | -/A | | | intron-variant, upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105771829 | AAACCCTCTGGTGTG[-/A]AAGCTGCCATTCCTT | 8440 |
rs781780191 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105821254 | TGACTTTGCCCCCAA[C/G]AGGTTATTTAGAAAG | 8440 |
rs796079694 | in-del | -/A | | | intron-variant | NCK2 | GRCh38.p7 | 2:105892328 | ATAGTTTGGGAAATG[-/A]AAAACAGCAAATTTC | 8440 |
rs796108902 | in-del | -/A | | | intron-variant | NCK2 | GRCh38.p7 | 2:105806845 | CAAAATTAAAAAAAA[-/A]CCCAACCAACCATCC | 8440 |
rs796114630 | in-del | -/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105795312 | TTTTAATTTTTTTTT[-/T]CCTCAAATAAGCAAT | 8440 |
rs796125869 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105763058 | AAAGAATTAGCCAGG[C/T]GTGGTGGTATGTGCC | 8440 |
rs796132191 | snp | A/C | | | upstream-variant-2KB | NCK2 | GRCh38.p7 | 2:105744469 | TCGTGATAAGAACAA[A/C]GAACAAACAAAAAAG | 8440 |
rs796164361 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105791421 | GATGGGAGGATATAC[A/G]GTGTAAAGTGCCTAA | 8440 |
rs796169824 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105762293 | GGGCAGAGCATCAAA[C/T]CAGGGGGGGTCTAGG | 8440 |
rs796175932 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105792082 | TCCTGCCTTGGTGAC[C/G]GGAGAGATGGATGAG | 8440 |
rs796176824 | in-del | -/A | | | intron-variant | NCK2 | GRCh38.p7 | 2:105807524 | ATTATGTTTCTCAAT[-/A]AGGGTCACTTGGGGA | 8440 |
rs796200620 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105828512 | AATTTAAGCATGTGA[C/T]AGGTAATGACTTTGT | 8440 |
rs796207320 | in-del | -/CTAA | | | intron-variant | NCK2 | GRCh38.p7 | 2:105883762 | TTGTTAGAGAATGAG[-/CTAA]CTTTTTCTAAAGAAC | 8440 |
rs796257217 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105746451 | GTTTTAGATGTAGTT[A/G]TCAAGTCTCAAAAGT | 8440 |
rs796279224 | in-del | AGCTGCCTGCCTGCAA/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105868076 | GGCTTGATGTGTGAA[AGCTGCCTGCCTGCAA/C]CAGGTGGGCATCTGT | 8440 |
rs796296703 | in-del | -/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105792604 | GTCCAAACTCGTTTG[-/T]TTTTTTTTTTCCACC | 8440 |
rs796361323 | in-del | -/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105790555 | CCCTGGTTTCCTAGG[-/C]CCTTTGAGAAGTGTG | 8440 |
rs796363998 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105753381 | ATGTTCCGTAGGCTG[A/G]TGGTCCTCCACCTGC | 8440 |
rs796384396 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105847375 | AATATATTTTATCAC[A/G]ACTTTGTAGAAAAGA | 8440 |
rs796389038 | snp | A/G | | | utr-variant-3-prime | NCK2 | GRCh38.p7 | 2:105893186 | CAGTGACGGCGCCCC[A/G]GCCCCACACTCGCCT | 8440 |
rs796403018 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105760272 | GGAGGTGATAGGATA[A/G]GATGGTGCCCCAGCA | 8440 |
rs796412127 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105801556 | CGAGTGAGGAGAGGG[A/G]CCCATGGCACAAGGA | 8440 |
rs796418306 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105830677 | AGGAATTTGGTGTGT[A/G]TGTGTGTGTGTGTGT | 8440 |
rs796424750 | in-del | -/TTCC | | | intron-variant | NCK2 | GRCh38.p7 | 2:105807707 | TTTCTCTTTTCTTTT[-/TTCC]TTCCTTCCTTCCTTC | 8440 |
rs796454225 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105834621 | GTCTATATCTTTTAA[C/T]TGGGAAATTTAATTC | 8440 |
rs796457384 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105803330 | TGCAGCAGATATCAT[A/G]AATAGGCACTGCTAT | 8440 |
rs796508826 | in-del | -/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105801418 | GGATGTGCTTTTTTC[-/T]TTTTTTTTTTTTTCT | 8440 |
rs796517665 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105806971 | CTTTCTTAGCCCATC[C/G]CTTTGTCTAATTGCT | 8440 |
rs796608430 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105790384 | GCCATAGGCTGGCAA[A/G]TAGCCTGACTTCTAG | 8440 |
rs796614196 | in-del | -/A | | | intron-variant | NCK2 | GRCh38.p7 | 2:105811163 | CTGGTGACAGAGTGC[-/A]AAAAAAAAAAAAAAA | 8440 |
rs796616129 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105786932 | TAACAGCACCGTCCA[A/G]ACTCGAAGCAGGGGA | 8440 |
rs796620199 | in-del | -/A | | | intron-variant | NCK2 | GRCh38.p7 | 2:105819927 | GCAGTTAAAAAAAAA[-/A]TAGATAAAATATAGT | 8440 |
rs796679364 | multinucleotide-polymorphism | CT/TG | | | intron-variant | NCK2 | GRCh38.p7 | 2:105853903 | GATCAGCTGTCACCT[CT/TG]GGGATGGTAGAGGAT | 8440 |
rs796686402 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105800205 | GGCCACATGCCCAGG[A/G]TGAACACCAAGGAAG | 8440 |
rs796687474 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105747173 | AAATCTTCTTCATCC[C/T]TGCTCTGTTTGACCC | 8440 |
rs796723654 | snp | C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105840179 | AGGAGAATTTAGCAT[C/G]TCTTATGCTAAATGA | 8440 |
rs796729624 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105823753 | CTGGAAAGTAAAATA[C/T]GCCTTCTCAGCTTCT | 8440 |
rs796775607 | snp | A/C/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105752733 | TCCGTCTGGATAATG[A/C/G]CCTCCAGTTCCATCT | 8440 |
rs796780187 | in-del | -/AG | | | intron-variant | NCK2 | GRCh38.p7 | 2:105812790 | TCTGCTCATTACTGA[-/AG]CCAGGTGACACTATT | 8440 |
rs796801157 | in-del | -/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105793042 | ATGAAGCCAACCCAT[-/G]AAACTGAAGGTGAGC | 8440 |
rs796802215 | in-del | -/C | | | intron-variant | NCK2 | GRCh38.p7 | 2:105756347 | ACAATCAATCTTTCC[-/C]TTTCTTCAGTCATCC | 8440 |
rs796821213 | snp | A/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105889584 | TTCTTTTTTTTTTTT[A/T]TTTTTTTTAATTATT | 8440 |
rs796858083 | snp | C/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105857030 | CTTGTTGTGTGTCTT[C/T]TTTTTTTTTTTTTTT | 8440 |
rs796862962 | in-del | -/CCCTGGCC | | | intron-variant | NCK2 | GRCh38.p7 | 2:105787926 | CCCCGACTTGTAGAT[-/CCCTGGCC]CCCTGGCCCATTGGC | 8440 |
rs796870192 | in-del | A/TT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105889588 | TTTTTTTTTTTTTTT[A/TT]TTAATTATTTTGAGA | 8440 |
rs796873677 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105818376 | GGCACATGTATACAT[A/G]TATAACAAACCTGCA | 8440 |
rs796882000 | snp | A/G | | | intron-variant | NCK2 | GRCh38.p7 | 2:105789544 | TGTTACACATAAGAG[A/G]GTTCTTTCTAGTTGA | 8440 |
rs796894650 | in-del | -/A | | | intron-variant | NCK2 | GRCh38.p7 | 2:105846489 | ACTGAAAAAAAAAAA[-/A]TAATAGGAGGGTGTA | 8440 |
rs796916719 | in-del | -/AAAG | | | intron-variant | NCK2 | GRCh38.p7 | 2:105816389 | TGGTTACTTAAAATC[-/AAAG]AAGCAAGCAGACCTA | 8440 |
rs796948175 | in-del | -/TC | | | intron-variant | NCK2 | GRCh38.p7 | 2:105765836 | GTGTGTGTGTGTAAG[-/TC]TGTGGAGGTATGTGT | 8440 |
rs796976131 | in-del | -/T | | | intron-variant | NCK2 | GRCh38.p7 | 2:105832858 | TCTCTTTTTTTTTTT[-/T]ATTTTGTTTCGTTTC | 8440 |
rs796999315 | in-del | -/GGGT | | | intron-variant | NCK2 | GRCh38.p7 | 2:105765785 | ACAGCTTAGAATAGG[-/GGGT]GTGTGTGTGTGTGTG | 8440 |