SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs183809512 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136926822 | TCAGTTACGTGAACA[C/T]TGAGACATTCTTTAT | 4690 |
rs183900387 | snp | A/G | 0.00597247 | 0.0543191 | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136948924 | AAATAGCAATAATAA[A/G]TGGAAAATTAGAAAT | 4690 |
rs183955331 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NCK1 | GRCh38.p7 | 3:136904563 | AAGTGACTAGATGCT[C/T]TTCTTGCCATTTTTA | 4690 |
rs183958829 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136927645 | CCATGCCTCAGCCTC[C/T]TGAGTAGCTGGGACT | 4690 |
rs183987172 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136947254 | TTCTGTTAGTTGCCT[C/G]ATCTGGCTCACTGTT | 4690 |
rs184084692 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136878324 | TGAAGCAGGAGAGTC[A/G]TTTGAACTGGGGAGG | 4690 |
rs184102342 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136932133 | CAAAAAAAAAAAAAA[A/G]AAAAGAATCCATTGT | 4690 |
rs184119802 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136910457 | TTTTGTTGTGTAGTA[A/C]AGTTATGTTTAAAAA | 4690 |
rs184237992 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136922662 | CCTATTAGATTGGCA[A/G]AAATCCAAAAGATTG | 4690 |
rs184246472 | snp | A/T | 0.0085432 | 0.0647967 | intron-variant | NCK1 | GRCh38.p7 | 3:136901374 | CTTTCTTTTTTTTTT[A/T]AAATATTTTTTATTG | 4690 |
rs184249111 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136932723 | TCCCTTCTAACTCTA[A/T]AAGTCTTACATCCTG | 4690 |
rs184277110 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | NCK1 | GRCh38.p7 | 3:136890179 | GGCAAGAAATCGAGC[A/G]CAGCGCTGGTGGGCT | 4690 |
rs184348845 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136948170 | TAGGACTTAGTAAGT[G/T]CTTAGATTTTAGCTT | 4690 |
rs184360420 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | NCK1 | GRCh38.p7 | 3:136927133 | TGCGCCACCATACCT[A/T]GCTAATTTTTGTATT | 4690 |
rs184366069 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | NCK1 | GRCh38.p7 | 3:136904934 | TTAATCTAGTCTGTT[A/G]TTGACACTTTCCAAC | 4690 |
rs184402627 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136860922 | ATTTTGAAGTTAAAT[A/G]CAGAAAACTGCAAAC | 4690 |
rs184407016 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136884611 | ATGCCCGGCTAATTT[C/T]TGTATTTTTAGTAGA | 4690 |
rs184442405 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136933342 | GCATCCAGTATATCA[A/G]GGATTTGCAAACCAG | 4690 |
rs184537275 | snp | A/G | 0.00398564 | 0.0444627 | upstream-variant-2KB, intron-variant | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136861101 | ACATACAGGCAAACC[A/G]TTTCAATAGCTCGGA | 4690 |
rs184541353 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136905566 | CCTCAGAATTCTCTT[G/T]TATCTTACTGGGCTT | 4690 |
rs184547331 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136936004 | TCCATGTTGTAGCAT[A/C]TATCAGTAATTCATC | 4690 |
rs184623032 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136894642 | AACCATTGAGGTACT[A/G]TAAATGTCCAGAGAC | 4690 |
rs184636709 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | NCK1 | GRCh38.p7 | 3:136915604 | GCTATAAATAACTAC[A/T]TGAGACTGGGTAATT | 4690 |
rs184641337 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136915296 | ATTTGGTCTGTGGGG[A/G]GTTGACGTAGTAGCA | 4690 |
rs184648268 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | NCK1 | GRCh38.p7 | 3:136889301 | GCCGCGGACCCTCGC[C/G]GTGAGTGTTACAGCT | 4690 |
rs184681558 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136884919 | AGAGATGGTTTTTCA[C/T]CACGTTGGTCAGGCT | 4690 |
rs184766917 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136936198 | GGCACATGCCACCAC[A/G]CCTGGCTAATTTGTG | 4690 |
rs184824856 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136908241 | CTTCGTCATATTAAC[A/G]TTCCTTCACCAGTAG | 4690 |
rs184826709 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136866381 | GGTGCGATCTCGGCT[C/T]CCCGTAACCTCTGCC | 4690 |
rs184943181 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NCK1 | GRCh38.p7 | 3:136944457 | GGTATAGTTTATTCT[A/G]TAGGAAAATTGGACC | 4690 |
rs185006503 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | NCK1 | GRCh38.p7 | 3:136872449 | CTGTTAAAGGCATTC[A/C]GTTTTACAAGGGAGG | 4690 |
rs185020782 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136916828 | TATCCAGTTCAATTC[C/G]CTTATTTTGTAGATA | 4690 |
rs185121583 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136937660 | ATGAGTCTGATACTT[G/T]GTTAAAATTATTCCT | 4690 |
rs185124670 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136870121 | CCGAGGCAGGTGGAT[C/T]GCTTGAGGTCAGGAG | 4690 |
rs185125657 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NCK1 | GRCh38.p7 | 3:136895055 | TAATTTTGTATTTTT[A/G]GTAAAGACAGGGTTT | 4690 |
rs185133640 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136891925 | ACAAAGTCTCACTGT[A/G]TCACTCAGGCTGGAA | 4690 |
rs185144230 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NCK1 | GRCh38.p7 | 3:136945011 | CTGGGGTAAGGGGAG[A/G]AAAACAAATAATATT | 4690 |
rs185148271 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NCK1 | GRCh38.p7 | 3:136924160 | CTACCATTCAGTCTT[A/G]ACATCACAGAAAATG | 4690 |
rs185157512 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136901973 | AATCTTACTACTTTT[C/T]TGATGTAGGCATTTG | 4690 |
rs185201621 | snp | C/T | 0.00517822 | 0.0506191 | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136951069 | CTAAACAAAATAGGC[C/T]TCATGCAATCTATTG | 4690 |
rs185322039 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136900836 | GGTTTCTCTAGATAT[A/G]AAATCATATCATCAG | 4690 |
rs185352960 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NCK1 | GRCh38.p7 | 3:136942932 | CTTCAGGGAGCTGCC[A/G]GACAAGTTGAAACCC | 4690 |
rs185429077 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136918610 | GCGGGCTGCATGCAG[A/C]CCAGGATGGCTTTGA | 4690 |
rs185473549 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NCK1 | GRCh38.p7 | 3:136877037 | AAAAAATGGACAAAA[C/T]TAAAAGGAGAATTAG | 4690 |
rs185476635 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136873047 | TTCCTACTCGGGTAC[C/T]GCCTAGTGGAGCTGT | 4690 |
rs185480052 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136922059 | AAGTGCTGGGATTAC[A/G]GGCGTGAGCCACCGC | 4690 |
rs185483019 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | NCK1 | GRCh38.p7 | 3:136896471 | AATGACATGATTTCA[C/T]TATTTTTTAATGGCC | 4690 |
rs185485335 | snp | C/G | 0.000399281 | 0.0141238 | missense, downstream-variant-500B | NCK1, LOC107986136 | GRCh38.p7 | 3:136945634 | ATTCTGCATCTCCTG[C/G]TGATGATAGTTTTGT | 4690 |
rs185548991 | snp | A/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136926046 | GTAGTGACATCTCAG[A/T]GTGGTTTTAATTTGC | 4690 |
rs185557076 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136903310 | CATGGAATATCTTTT[G/T]CCATCCCTTAATTTC | 4690 |
rs185677683 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136886997 | TACAGGCAGGTGCCA[C/T]CATGCCCGGCTAATT | 4690 |
rs185700694 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | NCK1 | GRCh38.p7 | 3:136906569 | ATCTTTGAGCCTCCA[C/G]GTGTCTTGCTTGGGT | 4690 |
rs185716428 | snp | A/G | | | intron-variant, upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136863194 | CCTAGAAATTAGGAA[A/G]GAATTAGGTTAAAGA | 4690 |
rs185799181 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136879467 | AATTACTGTAACAGA[A/G]TCTAAAATAAAGAGT | 4690 |
rs185835242 | snp | C/T | 0.00358779 | 0.0422022 | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136950468 | TGTGTGCTAGTAATA[C/T]CTATTGTGTGCTCTT | 4690 |
rs185840945 | snp | A/G | 0.00279162 | 0.0372561 | upstream-variant-2KB, intron-variant | NCK1 | GRCh38.p7 | 3:136928943 | AATTTCATTTTTGGT[A/G]TTCAGGCAAACATGC | 4690 |
rs185927003 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136912882 | GTCTTGGTCTTGATA[C/T]CCTGGACTCAAGTGA | 4690 |
rs186013634 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136868520 | TTTAGCAGAGACAGG[A/G]TTTCACCATGTTGGC | 4690 |
rs186022180 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136890676 | CCCTTATGCCTATTA[C/G/T]GAGTAATATGGCTAC | 4690 |
rs186042541 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136911821 | CATAATTTTTCCCTC[A/C]CTTTTGAAGGAGAGT | 4690 |
rs186044174 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136934048 | ACACCATAAGCACTA[A/G]AAGGTAGGAAAATAG | 4690 |
rs186056454 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136907069 | TGTTACCGGGAAGGG[C/T]GGGGTTGCTGTCAGT | 4690 |
rs186066540 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136939600 | GGCTATAAATTTCCC[C/T]CTGAGCATTGCCTTT | 4690 |
rs186083874 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | NCK1 | GRCh38.p7 | 3:136864080 | CACTCCAGCCTGGGC[A/G]ACAGAGCGAGACTCC | 4690 |
rs186180475 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136862990 | ATGTTTGGTAAAACA[A/C]AAAACCATTTCGATA | 4690 |
rs186223734 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136887308 | GAGTAGCGGGGACTA[C/T]AGGAGTGCACCGCCA | 4690 |
rs186230008 | snp | A/G | 0.00398564 | 0.0444627 | upstream-variant-2KB, intron-variant | NCK1 | GRCh38.p7 | 3:136929911 | TCCAGGATGCATTCC[A/G]TACTACAGTATTCTG | 4690 |
rs186463892 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136890961 | ACAACTCCTGGAACC[A/G]TGTGTAAGTGAAATA | 4690 |
rs186464821 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136933647 | AGTGCTTAGATCTGA[A/G]CAGTTTCCTTCCAAC | 4690 |
rs186499563 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136940481 | TTTGTAACTGTTACA[C/T]TTCTTGATGGACTGA | 4690 |
rs186507255 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136918859 | CTTGATAAAGTGATA[C/T]ATATTCAGTGTTTTC | 4690 |
rs186513637 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136896966 | GTAGTTCTGTTTTCA[A/G]TTTTTTGAGAAATTT | 4690 |
rs186591627 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136936086 | CGCCCTGTCACACAG[G/T]CTGGAGTGCAGTGAC | 4690 |
rs186609392 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136912364 | GATGGGGTTTCGCCA[C/T]GTTTGGCCAGGCTGG | 4690 |
rs186621271 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136894417 | CATCCCAAATGACCA[C/G]CAGAATGACTTCTTA | 4690 |
rs186635380 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136915314 | TGACGTAGTAGCATT[A/T]ATTAATCCAGACAGC | 4690 |
rs186644222 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136947051 | TAATCTTGGCTTTGC[A/G]TGAGTATATTTGTAC | 4690 |
rs186647834 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | NCK1 | GRCh38.p7 | 3:136926369 | AAGCCCCGCCTCCCG[G/T]GTTCAAGCCATTCTC | 4690 |
rs186649447 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136869469 | AGAATCACTTAAACC[C/T]GGGAGGCAGGGGTTG | 4690 |
rs186744592 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136875572 | GGCCATTATGTAATG[A/G]TAAAGGGATCAATTC | 4690 |
rs186767567 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136920068 | TGCAAAAAGACAAGG[C/T]AATTCATAAGATGAT | 4690 |
rs186773767 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136898512 | AATTCTATTTGTTAT[A/T]GAATAACCATCTAAA | 4690 |
rs186888698 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136941044 | AGGAAGGATTTCTGC[C/T]ATTTTGCTGTTTTCA | 4690 |
rs186892547 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136903062 | CTGGTGTCCCTAACT[A/G]TTATCGTAGTGGAAT | 4690 |
rs186923231 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | NCK1 | GRCh38.p7 | 3:136945313 | GGACAACTTTATAAT[G/T]ATGTTATATAGTTAT | 4690 |
rs187066550 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136880589 | TTGATGTTGCCACTT[A/G]ATATCTCATGGATCT | 4690 |
rs187077734 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136924853 | AGGTCTGATTTTTCA[C/T]ACAAGAAATTGCAAC | 4690 |
rs187098947 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | NCK1 | GRCh38.p7 | 3:136880237 | TTGCAGTGAGCCGAG[A/G]TCATGCCACTGCACT | 4690 |
rs187296482 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136886138 | GAGGGAATACTTAAG[A/T]TGGAAGCATGGGTTA | 4690 |
rs187466546 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136906116 | GATGTATTTGTGGTG[G/T]TGGTTGAATATGGCA | 4690 |
rs187505639 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136931030 | TTTTAGCGGAACAGT[G/T]TAAAGATAATCTTTA | 4690 |
rs187510715 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | NCK1 | GRCh38.p7 | 3:136907934 | TAATAAGCTAGGAAC[C/T]GGTAATATCATGGTC | 4690 |
rs187515190 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136888346 | ACAGTTCACTCATTA[A/G]AAGTATACAATTCAG | 4690 |
rs187569946 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136874166 | TCAACATTCATTTAC[A/T]GTTTTTTACATTTTT | 4690 |
rs187574296 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136949796 | AATAGATATCTAATA[C/T]GCCAGAATTACTGAT | 4690 |
rs187582678 | snp | C/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136882446 | CACAGCAGCACACAA[C/G]AGCCAGAGAAATGTT | 4690 |
rs187601527 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | NCK1 | GRCh38.p7 | 3:136892441 | GGCTCTGGTAATCAC[A/G]AGAGTCCTTATCAGA | 4690 |
rs187626469 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136935204 | CGTGCTGGGCCATTC[C/T]TTTTTTGACAATGTG | 4690 |
rs187635702 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | NCK1 | GRCh38.p7 | 3:136913298 | GTTTTTCTTTTTGTT[C/T]TTAGAGTCTTGCTTT | 4690 |
rs187794038 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | NCK1 | GRCh38.p7 | 3:136941555 | TTTGAATTAATACCA[A/C]CTTAGTTTCAGTACT | 4690 |
rs187803081 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NCK1 | GRCh38.p7 | 3:136920962 | TTTGTCCCTTCAAAA[A/G]TTCACACATTGAAGT | 4690 |
rs187823090 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | NCK1 | GRCh38.p7 | 3:136904157 | CATTGAGCACTTTTT[A/T]AAAAAATTATTTTTT | 4690 |
rs187962168 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136888049 | TCCTAGGTTCAAGCT[A/G]TTCTCCTGCCTCAGC | 4690 |
rs187980799 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136935845 | CCCAAAAATAGTCAC[C/T]CTCAATCAGTCCCTG | 4690 |
rs188010475 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | NCK1 | GRCh38.p7 | 3:136893686 | ATGAGACTTTTGATA[C/G]AATCTACATCTTGCT | 4690 |
rs188107807 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136871729 | CTCCCACAATTCCCA[C/T]GTGTGGTTGGCAGAA | 4690 |
rs188199784 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136874375 | GAGATGGGGTTTCAC[C/T]ATGTTGGCTGGGCAG | 4690 |
rs188275849 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136914720 | ACTTCTGGCTTCCAG[C/T]CAGAAGATATTGGGA | 4690 |
rs188330959 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | NCK1 | GRCh38.p7 | 3:136871451 | TTTAAATGTTTATTG[A/G]AAACTGCACAAATTT | 4690 |
rs188336078 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136919357 | TATGTAAAATAAACA[A/G]CAAAAAAATATATGG | 4690 |
rs188501812 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136904628 | GATAATGTGCTGTGA[A/G]GAAGACCTTTTTGAT | 4690 |
rs188558157 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136944841 | CTGAAGTTGATGTAG[C/T]GTACATTTGTATTGA | 4690 |
rs188566458 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136923120 | ATGTGTGTGTGTGTG[C/T]GCGCGCCTGTGTGCA | 4690 |
rs188570644 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136878821 | TTTCTGACACTGAGG[A/G]TGGGCCCTAGACACA | 4690 |
rs188576686 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | NCK1 | GRCh38.p7 | 3:136901857 | CTTTTTAAAAAAGTC[A/G]TTTCATTTAGTTCTG | 4690 |
rs188627182 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136897799 | TTATACATTTTTAAT[A/G]GTTAATATGATTTGA | 4690 |
rs188638624 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136947512 | CACAGTGTTTTTTAA[A/T]CATTTAAATTCATTG | 4690 |
rs188658041 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136940636 | TGCAACCTCCGCCTC[C/G]CAGGTTCAAGCGATT | 4690 |
rs188700949 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136948194 | TTAGCTTTTAGTTTA[A/C]TATAAAAATACTGAT | 4690 |
rs188712786 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136860923 | TTTTGAAGTTAAATG[A/C]AGAAAACTGCAAACT | 4690 |
rs188712787 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136927214 | TGACCTCAGGTGATC[C/G]ACCAGCCTCGGCCTC | 4690 |
rs188722982 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136905076 | AGAGTGCTATGGCAC[A/G]ATCTCAGCTAACTGC | 4690 |
rs188723079 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NCK1 | GRCh38.p7 | 3:136884689 | TGCCTTGGCCTCCCA[A/G]AGTGCAGGCTTGAGC | 4690 |
rs188775902 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NCK1 | GRCh38.p7 | 3:136883606 | CTGCTAGAAAGAGGT[A/G]TCTGTCGTGCTCACT | 4690 |
rs188781181 | snp | A/T | 0.0115144 | 0.0749975 | intron-variant | NCK1 | GRCh38.p7 | 3:136899878 | CCATCCTTTTTTTTT[A/T]AGGGGTTTTCTCTTC | 4690 |
rs188788131 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | NCK1 | GRCh38.p7 | 3:136930812 | TTAGCATGAATGTTT[A/G]ACAAGTAGAGAAAGG | 4690 |
rs188845429 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136911939 | TGTGTTTTGGCCTAC[A/G]GAGCTGCTGATGAGA | 4690 |
rs188877138 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136890804 | ATATTCACATTGTTA[A/T]GCAGCCATCACCACC | 4690 |
rs188885400 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | NCK1 | GRCh38.p7 | 3:136933501 | TGGTTAAGAAACAGT[G/T]CTATAGGAAAAGAGA | 4690 |
rs188923231 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136926891 | GTTTTCTATTTGGAA[A/G]CAATATTCTGTATAT | 4690 |
rs188947670 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136864778 | TTTTTTTTTTTTTTT[C/T]TGAGACAGAGTCTCT | 4690 |
rs189058073 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136951675 | ATATACACAGACAGT[A/G]GTTTTTGGTATGTCT | 4690 |
rs189078213 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136907845 | CATAGAATCTTACCT[A/G]TTGTCCTCAGTGCTA | 4690 |
rs189081863 | snp | A/G | 0.00144283 | 0.0268204 | intron-variant | NCK1 | GRCh38.p7 | 3:136927963 | CAACCTTACATAAAA[A/G]TATTTTCCATGTGTT | 4690 |
rs189088738 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136876934 | TGCCAAACTGCTATT[G/T]AGAAAAGACATTCCA | 4690 |
rs189098914 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NCK1 | GRCh38.p7 | 3:136885046 | GTTTTAGAGATATTT[A/G]CTTAAATATTTATGG | 4690 |
rs189180935 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | NCK1 | GRCh38.p7 | 3:136916162 | CACCTGGAGATTACA[A/T]TTCGACATGAGATTT | 4690 |
rs189185110 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136886395 | GGGTACTATTTACAT[A/G]TAACCTATGCACATT | 4690 |
rs189216384 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | NCK1 | GRCh38.p7 | 3:136906330 | GCCCAGGCTGGTCTC[C/G]AACTCCTGAGCTCAA | 4690 |
rs189220310 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | NCK1 | GRCh38.p7 | 3:136894816 | TTTTGCTAGATTTTT[A/T]AAATCTTATTAGTAC | 4690 |
rs189222382 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136936659 | ATTTTCTTTCTTTCT[C/T]TGCTTATATCCATTG | 4690 |
rs189224550 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant, upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136863048 | CATACAAGTTAAATT[C/T]GCCGTTAGAAGCTCA | 4690 |
rs189292395 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136866543 | AACTCCTCACTTCAG[A/G]TGATCTACACATCTC | 4690 |
rs189331641 | snp | A/C/G | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136890397 | CCTCTACACCTCCCC[A/C/G]CAAGCTGAGGGAGCA | 4690 |
rs189355366 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136910826 | TTTTGAAATATATAA[C/T]ACATTAATACTGACT | 4690 |
rs189370253 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136868213 | GAGCCACCATGCCCA[A/G]CCTTACATTGTAAAT | 4690 |
rs189371306 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NCK1 | GRCh38.p7 | 3:136905641 | TTCTTTTTTTCCCCC[C/T]TGAGACAGGGTCTCA | 4690 |
rs189402625 | snp | A/G | 0.00318978 | 0.0398085 | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136949048 | CATACAGCAAGACAC[A/G]TGAGACATAGATTAG | 4690 |
rs189424795 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136862065 | CTCCCTCCACATCAG[G/T]CACGGCGCTTGATTG | 4690 |
rs189434329 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136908886 | ACCCCAAAGTTAATG[G/T]GTTGGAAAGTTGATG | 4690 |
rs189591681 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NCK1 | GRCh38.p7 | 3:136895303 | TATAAGGCTTTGGTA[C/T]GTTTTTGGTTTATTT | 4690 |
rs189616144 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136945232 | GTGTGGTGGAGCCTT[C/T]GTGTACTTAGATTGT | 4690 |
rs189701092 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136932241 | ATAGTTAATGCATTT[A/G]CAGACTGGGAGTCAG | 4690 |
rs189723245 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NCK1 | GRCh38.p7 | 3:136889439 | GACCTTCGCGGCGAG[C/T]GTTACAGCTCATAAA | 4690 |
rs189757502 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136939288 | ATAGTATTTGTTTAT[A/T]ATCCTTTTTAAAATA | 4690 |
rs189780277 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | NCK1 | GRCh38.p7 | 3:136939925 | GCATGATCATGGCTC[A/G]CTGTAGCCTTTGAAC | 4690 |
rs189788544 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136918666 | CGTTCTTAAAACATG[A/G]TGAGATTTTTTGGTG | 4690 |
rs189788795 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136874061 | GTTCCTTTTCAGTGA[C/T]AGTAGTATTCCATTG | 4690 |
rs189797286 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136896510 | TCCCATTGTGTATAT[A/G]TGCCACATATGTCCA | 4690 |
rs189855790 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136872570 | ATTTGCATAGGTAAT[A/G]AGGAGCTGAATATGA | 4690 |
rs189909278 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136922358 | TCACAAAGGGACAGA[C/G]AAAGGATTTATAATT | 4690 |
rs189918134 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | NCK1 | GRCh38.p7 | 3:136903842 | GCTGTTCAGTATATC[A/G]TCTATTCCCTCTGTC | 4690 |
rs189941771 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136881127 | TCTTTTCTACCTCCA[A/G]ATACATCTTGAAGTC | 4690 |
rs189948718 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136877144 | AAAGATTTAAACACT[A/G]TAATTATCAAATGAA | 4690 |
rs189958098 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | NCK1 | GRCh38.p7 | 3:136926240 | TTAATTTATTTTTAG[C/G]TCTTTTTAAAATTTT | 4690 |
rs190014379 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | NCK1 | GRCh38.p7 | 3:136917977 | CTTCTCTGGATCTGT[C/G]CTGTTTTATACCTGA | 4690 |
rs190153935 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136942955 | TGAAACCCACAATCA[C/T]AATTGTTTAAGAATG | 4690 |
rs190172400 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136868534 | GGTTTCACCATGTTG[A/G]CCAGGCTGATCTCCA | 4690 |
rs190201760 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136950336 | GTAAACTGCACTGAG[C/T]TGATATTAATAGAGC | 4690 |
rs190218535 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136901178 | AACATATGGTTTTGT[C/G]CTTTATTCTGTTGAG | 4690 |
rs190254166 | snp | A/C | | | intron-variant | NCK1 | GRCh38.p7 | 3:136874649 | TTCTGATAAAACTAG[A/C]GACTCCCTTTGTCTT | 4690 |
rs190258348 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136906771 | TTGCAGGTGGCACGT[A/G]TGGTTAGTTGCCAGC | 4690 |
rs190267219 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NCK1 | GRCh38.p7 | 3:136872266 | GGAGATGGGGAACTT[A/G]TTGGGAACTGGAGCA | 4690 |
rs190281148 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136863349 | CGATTTCTTCAGCAC[C/T]TGGAAACCAGTGTGC | 4690 |
rs190287965 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136887250 | ATAATGCTGTGTGGC[C/T]TCCAACTCTTGGCCT | 4690 |
rs190295853 | snp | A/G | 0.0023933 | 0.0345097 | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136950705 | CCTGGTGTCTGTATC[A/G]TGACACACTACTCTG | 4690 |
rs190401360 | snp | C/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136880454 | GAAGATGACTATCTA[C/G]AAGCCAACTAGGAGG | 4690 |
rs190511053 | snp | A/C | 0.0517044 | 0.152246 | upstream-variant-2KB, intron-variant | NCK1 | GRCh38.p7 | 3:136928795 | AGACAGTGGAGCCCA[A/C]TTCACACTGGACTTG | 4690 |
rs190558132 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | NCK1 | GRCh38.p7 | 3:136932780 | GTCATAGGAATTGAG[C/T]GAAAGCAATGAGTGA | 4690 |
rs190689676 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136935225 | TGACAATGTGTAATT[A/G]GTCTTAGACATAATG | 4690 |
rs190698294 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136887431 | TTGGAATAAAGGATA[A/G]GTTAAAAGGGCAGGA | 4690 |
rs190700704 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NCK1 | GRCh38.p7 | 3:136913435 | CACTATGCCTGCCTA[A/G]TGTTTTATTTTTTGT | 4690 |
rs190796203 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136924210 | GCCTCCTAATAAATG[A/G]CAATAACAAGTACAC | 4690 |
rs190841232 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | NCK1 | GRCh38.p7 | 3:136940488 | CTGTTACACTTCTTG[A/G]TGGACTGATTCTTTT | 4690 |
rs190844518 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | NCK1 | GRCh38.p7 | 3:136930190 | TGGATTTGTTTCGCA[A/G]TGGTTGTGCTGGTGG | 4690 |
rs190936876 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136864163 | GTCCAGGTTTCTGCA[A/G]TGCTTTCAGGTCCAT | 4690 |
rs190960054 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136907291 | AGGTGGAGAATGTCA[A/G]TGGGGTCTCCAGGGA | 4690 |
rs191005468 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | NCK1 | GRCh38.p7 | 3:136912763 | TGGGCTCAAGCAGTC[C/G]CCCTGCTTCAGCTTC | 4690 |
rs191038273 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136869506 | TGTGAGATCCCGCCA[C/T]TGCACTTTAGCCTGG | 4690 |
rs191091210 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136951611 | GTCAAAATATAGAGA[C/T]GAATCTCTGAAACGT | 4690 |
rs191215610 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136934210 | TTTTTTTTTTTAACT[G/T]TTAGGGTTGGGGGTA | 4690 |
rs191218019 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NCK1 | GRCh38.p7 | 3:136870239 | CCCAGCTACTTGGGA[A/G]GCTGCTGCAGGAGAA | 4690 |
rs191223814 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136913094 | TTGTCTATTAGGCCC[A/G]TCTTCTGATCTTTCT | 4690 |
rs191225453 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | NCK1 | GRCh38.p7 | 3:136892170 | TGGGATTATAGGTGT[G/T]AGTCACCACACCCAG | 4690 |
rs191239819 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NCK1 | GRCh38.p7 | 3:136933848 | CAGCTGGGACTACAG[A/G]TGCATGCCACCACAC | 4690 |
rs191292617 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136890985 | TGAAATAAATCATAC[A/G]ATATTTGTCCTTTAT | 4690 |
rs191307435 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136940878 | TATAGCCACCCCACT[C/G]TCTCAGTTATCCTTT | 4690 |
rs191332728 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136920222 | TAGTCAGAAATAAAG[C/G]CTACTTAAAAATTAA | 4690 |
rs191340989 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136899586 | CCTTCCAGAAAAATT[C/T]TCCTCTGTTGTACCG | 4690 |
rs191361754 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136876481 | ATATCACCACCGATC[C/T]CACAGAAATACAAAC | 4690 |
rs191371952 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136941048 | AGGATTTCTGCTATT[G/T]TGCTGTTTTCATTTA | 4690 |
rs191373562 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136898017 | ACTATTTGAAGAAAC[A/G]GCTTTCCCTTGTTTA | 4690 |
rs191510289 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136924940 | TTTTGAGGGGTATGG[A/G]TTTTTAATCTGTTAG | 4690 |
rs191605271 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136919550 | TAGACCCCTTAAGAG[A/T]TCCACTTTAGTAACC | 4690 |
rs191632549 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136884763 | TCTCACTCTGTTGCC[C/T]AGGTTGGAGTGCAGT | 4690 |
rs191664879 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136892680 | AAGACCTGTTTTAGA[C/T]TTAATGACCTCTAGA | 4690 |
rs191747517 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136927439 | GAACATTTTTCATTG[A/G]GTAGTGAACTTTATT | 4690 |
rs191755939 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NCK1 | GRCh38.p7 | 3:136905224 | ACAGGGTTTCACTGT[A/G]TTAGCCAGTCTTGTC | 4690 |
rs191776762 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | NCK1 | GRCh38.p7 | 3:136903084 | TAGTGGAATCTATCT[C/T]TCCTTACAGATCTAA | 4690 |
rs191798811 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136919022 | TACAATGGACTACTC[A/T]GCACTAAAAAGGAGT | 4690 |
rs191855040 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136874239 | GGAGTGCAGTGGTGC[A/G]ATCTCAGCTCACTGC | 4690 |
rs191866568 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136931276 | AGTGGCCTCCTTATG[A/G]TCTTATAGTGAACTT | 4690 |
rs191874897 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136908213 | TAGGGTACATAGGTC[C/T]GCAACCGTATCACTT | 4690 |
rs191952779 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136945431 | ATCTTATTTCCAAAA[A/T]GATGATTTTTAACTA | 4690 |
rs192104485 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136902309 | TTCAAGCAGTTCTTG[C/T]GCCTCAGCCTCCTGA | 4690 |
rs192107069 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136897249 | ATGTGCCACCATGCT[C/T]GGCTAATTTTTTGTA | 4690 |
rs192243288 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136860858 | GGGAACAAACATCTA[A/G]ATTACAGCACAGGCC | 4690 |
rs192254525 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | NCK1 | GRCh38.p7 | 3:136884601 | GTGTGGCACTATGCC[C/T]GGCTAATTTCTGTAT | 4690 |
rs192258915 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136904653 | TTTGATTTGTATTTA[A/C]TGAGAGATCCCTGAA | 4690 |
rs192315571 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136879821 | CACAGGGAGGGGAAC[A/T]TCACACATTGGGGCC | 4690 |
rs192375375 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136889910 | ATTCTCCAAGGCCCC[A/G]CCAGACTCAGGAGCC | 4690 |
rs192381032 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136864903 | GCTGGGACTACAGGT[A/G]TGTGCCACCATGCCT | 4690 |
rs192385217 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136930874 | ATTCAGTAATTTTCA[A/G]CTTAGCACAGACATT | 4690 |
rs192391139 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NCK1 | GRCh38.p7 | 3:136888230 | TTACAGGTGTGAGCC[A/G]CCGTGCCTGGCCCTC | 4690 |
rs192391378 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | NCK1 | GRCh38.p7 | 3:136907859 | TATTGTCCTCAGTGC[G/T]ACAGGTATTATATCC | 4690 |
rs192395053 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136932721 | AGTCCCTTCTAACTC[G/T]AAAAGTCTTACATCC | 4690 |
rs192557046 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136915167 | ACAGACAGACTAATA[C/T]GTACCTTAAGGAGGC | 4690 |
rs192570237 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136871563 | AAGGCTCTCTTGCGC[C/G]CCCTCCAATCAGTGT | 4690 |
rs192608525 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136915360 | ACTTTTTCTTGAATT[A/G]TAGGTCACAGAAGCA | 4690 |
rs192631543 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136871759 | ACCTGGTGGGAGGTA[A/G]TTGAACCATGGGGGT | 4690 |
rs192639152 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NCK1 | GRCh38.p7 | 3:136894513 | GTATGTGGTGTAGGA[C/T]CAGTGGATGCCATGG | 4690 |
rs192647905 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136936131 | CTGCAACCTCTGCCT[C/G]TTGGGTTCAAGTGAT | 4690 |
rs192758332 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NCK1 | GRCh38.p7 | 3:136910440 | AGCTTTTAGAGTAAT[A/G]TTTTTGTTGTGTAGT | 4690 |
rs192762265 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136867097 | TTCTTTCTTTCTTTC[C/T]TTCTTTCTTTCTTTC | 4690 |
rs192770673 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | NCK1 | GRCh38.p7 | 3:136943290 | CACCCCAAATGTAGG[G/T]ATTTCTCTGAAGGCT | 4690 |
rs192788191 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136866349 | GTCTCGCTCTGTTGC[C/T]CAGGCTGGAGTGCAA | 4690 |
rs192818365 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136893838 | TTGAGGCAGGAATTA[C/T]TATTCATCATTACCT | 4690 |
rs192828628 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | NCK1 | GRCh38.p7 | 3:136935884 | TAATCTGCTTTCTGT[C/G]TCTATGGATTTACCT | 4690 |
rs192947044 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | NCK1 | GRCh38.p7 | 3:136927034 | TGGAGTGCAGTGGCA[C/T]GATCTTGGCTAACTG | 4690 |
rs192999010 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136888717 | TTAGTTGTCACCCCT[A/G]ACCTCCCCTCTCCGT | 4690 |
rs193007281 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136876935 | GCCAAACTGCTATTT[A/G]GAAAAGACATTCCAA | 4690 |
rs193014801 | snp | A/G | | | downstream-variant-500B, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136951934 | AAACTGAGTTCTTGG[A/G]GCAGCTGCTATGTCC | 4690 |
rs193068145 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136870902 | GTATCAGACAGATGC[C/T]AAATATTAATTTCTC | 4690 |
rs193089060 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136921311 | AATATATTTTTAACT[C/T]AGGAAACAACTAGAG | 4690 |
rs193126828 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136947204 | CCCTCAGAAAAGCAG[G/T]TGGTTGGCAGTAGGG | 4690 |
rs193146784 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136904432 | TGCTAGGATTACAGG[C/T]GTGAGCCACCGTACC | 4690 |
rs193175719 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136947851 | GCTACTGTTAGCTAC[A/T]CATTGAAAAGGGGTT | 4690 |
rs193211868 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NCK1 | GRCh38.p7 | 3:136900310 | TCTATGTGTCTGTCT[C/T]ATACCAGTACCATGC | 4690 |
rs193244734 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136942741 | CCCATGTATATTCTT[A/T]CCCATCCCCTTTCTG | 4690 |
rs193252046 | snp | A/C | | | intron-variant | NCK1 | GRCh38.p7 | 3:136897179 | CTGCAACCTCTGCCT[A/C]CCAGGTTCAAGTGAT | 4690 |
rs193283591 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136926477 | AGACAGGGTTTTACC[A/G]TGTTAGCCAGGATGG | 4690 |
rs193293856 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136882493 | TAATGATACAACAAT[A/G]CCTCTTACTTGGCAG | 4690 |
rs199575387 | in-del | -/TTCTTTCTTTCTTTCTTTCTTTC | | | intron-variant | NCK1 | GRCh38.p7 | 3:136867050 | CTATGTTGCTTGCTT[-/TTCTTTCTTTCTTTCTTTCTTTC]TTTCTTTCTTTCTTT | 4690 |
rs199581766 | in-del | -/TT | | | intron-variant | NCK1 | GRCh38.p7 | 3:136888138 | TTAGTAGAGACAGGG[-/TT]TCGCCATGTTGGCCA | 4690 |
rs199606172 | snp | A/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136870363 | AAAAAAATTCATCCT[A/T]TTCTTCCAAAAATTT | 4690 |
rs199614850 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136912171 | TTTTTTCTTTTTTTT[C/T]TTTTTTTTTGAGACC | 4690 |
rs199633225 | in-del | -/A | | | intron-variant | NCK1 | GRCh38.p7 | 3:136926836 | ATTGAGACATTCTTT[-/A]TGGCCTGGCATTTGA | 4690 |
rs199716792 | snp | C/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136894344 | CTTGGTTTCTAAACC[C/G]GTGCATCTCAGGTAG | 4690 |
rs199723710 | in-del | -/ATTGGATGCA | | | intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136946665 | ATTTAAAAAATTGCT[-/ATTGGATGCA]ATGTGTAAGAAGGTA | 4690 |
rs199740258 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136934982 | TCTTGGCTCACTGCA[A/G]CCTCCGCCTCCTGGG | 4690 |
rs199750462 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136913466 | AGAGACAGGGTCTCA[C/T]TATGTTGCCCAAGCT | 4690 |
rs199761240 | in-del | -/G/TG | | | intron-variant | NCK1 | GRCh38.p7 | 3:136902194 | CTTTGTTTTTTTTTT[-/G/TG]TTTTTTTTGTTTTTG | 4690 |
rs199777441 | in-del | -/TTA | 0.0111196 | 0.0737302 | intron-variant | NCK1 | GRCh38.p7 | 3:136926265 | ATTTTATTTTAAATT[-/TTA]TTATTATTATTATTA | 4690 |
rs199841142 | snp | A/C/G/T | 0.00159649 | 0.0282165 | intron-variant | NCK1 | GRCh38.p7 | 3:136910463 | TGTGTAGTAAAGTTA[A/C/G/T]GTTTAAAAAATTACA | 4690 |
rs199841323 | in-del | -/TTTC | | | intron-variant | NCK1 | GRCh38.p7 | 3:136941107 | TGTCTTCTTTTGTGA[-/TTTC]TTTTTCTTTTTTTTT | 4690 |
rs199846693 | in-del | -/TTTA | | | intron-variant | NCK1 | GRCh38.p7 | 3:136913129 | GAAGGTTTCTGTTGG[-/TTTA]TTTTTTTTTCTTTCA | 4690 |
rs199863016 | snp | A/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136899433 | TCTTTTTTTTTTTTT[A/T]AAATTTCTTTAACTT | 4690 |
rs199869346 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136867427 | TTTTTTTTTTTTTTT[G/T]TAGAGATAGGGTCTC | 4690 |
rs199989902 | in-del | -/CTGGTC | | | intron-variant | NCK1 | GRCh38.p7 | 3:136912864 | TTGCTGTTTCCCAAA[-/CTGGTC]TTGGTCTTGATATCC | 4690 |
rs200016365 | snp | A/C/G | 3.29474e-05 | 0.00405867 | synonymous-codon, downstream-variant-500B | NCK1, LOC107986136 | GRCh38.p7 | 3:136945914 | AGTCGTCAATAACCT[A/C/G]AATACTGGGCAAGTG | 4690 |
rs200056826 | in-del | -/C | | | intron-variant | NCK1 | GRCh38.p7 | 3:136905988 | GGCGGTGTCATATTT[-/C]CTTGCTTTTTCATGT | 4690 |
rs200060986 | in-del | -/TTTA | 0.00557542 | 0.0525036 | intron-variant | NCK1 | GRCh38.p7 | 3:136939336 | AATGTTATTTCTGAT[-/TTTA]TTTATTTGAGTGTCT | 4690 |
rs200105301 | snp | A/T | | | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136949420 | CTCTTTTCAGCTTTA[A/T]GTTTTGTTGATTGGG | 4690 |
rs200116556 | snp | C/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136867120 | TTTCTTTCTTTCTTT[C/G]TTTCTTTCTTTCCTT | 4690 |
rs200116832 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136874077 | AGTAGTATTCCATTG[A/G]ATGAATATAATGTAA | 4690 |
rs200122433 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136931931 | TTGAGACCAGCCTGG[C/T]CAACATGGTGAAACA | 4690 |
rs200123303 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136867221 | TCCTTCCTTCCTTCC[G/T]TCCGTCCATCCATCC | 4690 |
rs200163744 | in-del | -/C | 0.00636936 | 0.0560724 | intron-variant | NCK1 | GRCh38.p7 | 3:136879133 | CAATCAGAACAACAA[-/C]AAAAAAAGGCTCAGT | 4690 |
rs200220540 | in-del | -/A | | | intron-variant | NCK1 | GRCh38.p7 | 3:136905982 | TCTTTTGGCGGTGTC[-/A]TATTTCCTTGCTTTT | 4690 |
rs200393406 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136878705 | GTTGTATCTCAATAA[A/G]GCTATTTTTTTTTAA | 4690 |
rs200430179 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136867073 | TTCTTTCTTTCTTTC[G/T]TTCTTTCTTTCTTTC | 4690 |
rs200457235 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136888142 | TAGAGACAGGGTTTC[A/G]CCATGTTGGCCAGGC | 4690 |
rs200460421 | in-del | -/GAT | | | intron-variant | NCK1 | GRCh38.p7 | 3:136878704 | GTTGTATCTCAATAA[-/GAT]AGCTATTTTTTTTTA | 4690 |
rs200466856 | snp | A/C | | | intron-variant | NCK1 | GRCh38.p7 | 3:136898407 | AAAAAAAAAAAAAGG[A/C]GGATGCAGTGGTATC | 4690 |
rs200498095 | in-del | -/CA | | | intron-variant | NCK1 | GRCh38.p7 | 3:136864484 | AGAGCAAGATTCCGT[-/CA]CACACACACACAAAA | 4690 |
rs200503410 | in-del | -/T | 0.00636936 | 0.0560724 | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136949520 | TAATTTTTTAATTTG[-/T]TTTTTTAACCAAGTA | 4690 |
rs200507573 | snp | A/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136867922 | TATTTACATTGTAAA[A/T]TTTTTTTTTTTTGAG | 4690 |
rs200551365 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136870365 | AAAAATTCATCCTTT[C/T]CTTCCAAAAATTTTA | 4690 |
rs200589808 | in-del | -/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136867934 | AATTTTTTTTTTTTT[-/T]GAGACAGAGTTTCGC | 4690 |
rs200610800 | in-del | -/ATAAGCC | 0.00953873 | 0.0683987 | intron-variant | NCK1 | GRCh38.p7 | 3:136915102 | AGAATTTTGAGCCAA[-/ATAAGCC]TTTTTTCTTTATAGA | 4690 |
rs200656170 | snp | C/T | 0.000150851 | 0.00868348 | intron-variant | NCK1 | GRCh38.p7 | 3:136927970 | ACATAAAAATATTTT[C/T]CATGTGTTTACAGTG | 4690 |
rs200674609 | snp | A/T | 0.000785731 | 0.0198053 | intron-variant | NCK1 | GRCh38.p7 | 3:136928263 | AAAGCAACTTTGTTT[A/T]AAATGAAACCTGCAA | 4690 |
rs200688923 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136867179 | CCTTCCTTCCTTCCT[C/T]CTTTCTTTCTTTTCT | 4690 |
rs200695817 | snp | A/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136903774 | GATCAGTTTACATTC[A/T]GAGTTATTGATGTGT | 4690 |
rs200798909 | in-del | -/TGA | 0.0162398 | 0.0886349 | intron-variant | NCK1 | GRCh38.p7 | 3:136892506 | TGAAAGCAGAAATCT[-/TGA]TGATGTGGCCAAGTG | 4690 |
rs200810131 | in-del | -/T | 0.0103295 | 0.0711199 | intron-variant | NCK1 | GRCh38.p7 | 3:136934153 | CATTTTATGAATTTA[-/T]TTTTTTACACACCAC | 4690 |
rs200851751 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136873361 | CCTTTGTTCTGGGCA[A/G]TTTCTCCCATTTGGA | 4690 |
rs200911098 | snp | C/G | | | intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136946679 | TATTGGATGCAATGT[C/G]TAAGAAGGTAGTCAC | 4690 |
rs200914165 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136871540 | GTGGAACATTTTTAG[C/T]GTTCGAAAAGGCTCT | 4690 |
rs200926211 | snp | C/T | | | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136949623 | GTCATAATTTGTCCC[C/T]CTATTATTCTGGAGA | 4690 |
rs200956853 | in-del | -/AA/TA | | | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136949418 | CCTCTTTTCAGCTTT[-/AA/TA]AAGTTTTGTTGATTG | 4690 |
rs201032539 | in-del | -/GA | 0.0414363 | 0.137845 | upstream-variant-2KB, intron-variant | NCK1 | GRCh38.p7 | 3:136928790 | CCTGAGACAGTGGAG[-/GA]CCCACTTCACACTGG | 4690 |
rs201089377 | in-del | -/TA | | | intron-variant | NCK1 | GRCh38.p7 | 3:136864933 | TAGCTAATTTTTTTG[-/TA]TATATATATATTTTT | 4690 |
rs201147055 | in-del | -/T | 0.0103295 | 0.0711199 | intron-variant | NCK1 | GRCh38.p7 | 3:136911561 | ATGTTTGTTCAAGTC[-/T]TTTGCCTATTCTAAA | 4690 |
rs201164685 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136902209 | TTTTTTTTTGTTTTT[G/T]TTTTTTGAGACAGAG | 4690 |
rs201167517 | in-del | -/TGGTCT | | | intron-variant | NCK1 | GRCh38.p7 | 3:136912871 | TTCCCAAACTGGTCT[-/TGGTCT]TGATATCCTGGACTC | 4690 |
rs201236804 | snp | A/G | 0.000176875 | 0.00940247 | intron-variant, nc-transcript-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136946310 | GGTAAGTTGATTTTC[A/G]GAGGTAAATACAAAT | 4690 |
rs201267667 | in-del | -/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136901377 | CTTTTTTTTTTTAAA[-/T]TATTTTTTATTGCAT | 4690 |
rs201270096 | in-del | -/A | 0.0154538 | 0.0865337 | intron-variant | NCK1 | GRCh38.p7 | 3:136942500 | AAAAAACAAACAAAC[-/A]AAAGAAAACCTCTCC | 4690 |
rs201317234 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136899440 | TTTTTTTTTAAATTT[G/T]TTTAACTTTACTTTT | 4690 |
rs201323970 | in-del | -/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136866474 | ACCATGCCTGGCTAA[-/T]TTTTGTATTTTTAGT | 4690 |
rs201351324 | snp | C/T | 0.000177409 | 0.00941663 | synonymous-codon, downstream-variant-500B | NCK1, LOC107986136 | GRCh38.p7 | 3:136945584 | TTTAATTTCAACAGG[C/T]ATTGGAAAAGTGAAA | 4690 |
rs201395064 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136867074 | TCTTTCTTTCTTTCT[C/T]TCTTTCTTTCTTTCT | 4690 |
rs201395230 | in-del | -/CCCT/GA | 0.0414363 | 0.137845 | upstream-variant-2KB, intron-variant | NCK1 | GRCh38.p7 | 3:136928788 | GGCCTGAGACAGTGG[-/CCCT/GA]AGCCCACTTCACACT | 4690 |
rs201412942 | snp | G/T | | | intron-variant, upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136863078 | AGGAAGCTGGGTTTT[G/T]TTCAGGGGTGAGGAC | 4690 |
rs201444058 | snp | A/C | 5.23729e-05 | 0.005117 | synonymous-codon | NCK1 | GRCh38.p7 | 3:136928223 | AAACCTAAAGGATAC[A/C]TTAGGTAAGATATTT | 4690 |
rs201450241 | snp | C/G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136867051 | TATGTTGCTTGCTTT[C/G/T]CTTTCTTTCTTTCTT | 4690 |
rs201476628 | in-del | -/A | 0.0107246 | 0.0724382 | intron-variant | NCK1 | GRCh38.p7 | 3:136881202 | ATCATCTCTTCACTT[-/A]ACACTATTGGCCTCT | 4690 |
rs201516376 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136867052 | ATGTTGCTTGCTTTT[C/T]TTTCTTTCTTTCTTT | 4690 |
rs201526093 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136936768 | TGCCTGTTGGCCATT[C/T]GTATACCGTAGTTGG | 4690 |
rs201617601 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136886423 | ATTCTCCTGTATACT[C/T]GAACTCATCTCTAGA | 4690 |
rs201695571 | in-del | -/GA | 0.0123036 | 0.0774623 | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136948884 | TGCTAAAATTTCTTG[-/GA]GAGTGTTAATCTTTT | 4690 |
rs201725436 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | NCK1 | GRCh38.p7 | 3:136867181 | TTCCTTCCTTCCTTC[C/T]TTCTTTCTTTTCTTT | 4690 |
rs201762990 | snp | A/G/T | | | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136949419 | CCTCTTTTCAGCTTT[A/G/T]AGTTTTGTTGATTGG | 4690 |
rs201784873 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136905025 | TTTTTTTTTTTTTTT[C/T]TTTTTGAGATGGAGT | 4690 |
rs201937748 | snp | C/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136903775 | ATCAGTTTACATTCA[C/G]AGTTATTGATGTGTG | 4690 |
rs201946585 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136867053 | TGTTGCTTGCTTTTC[C/T]TTCTTTCTTTCTTTC | 4690 |
rs201965958 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136905987 | TGGCGGTGTCATATT[C/T]CCTTGCTTTTTCATG | 4690 |
rs202048931 | in-del | -/GCGCCAC | | | intron-variant | NCK1 | GRCh38.p7 | 3:136866455 | TGGGACTACAGGCAT[-/GCGCCAC]CATGCCTGGCTAATT | 4690 |
rs202053308 | snp | A/G | | | intron-variant, upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136863021 | GGTTTTGTAACCTTT[A/G]TTCTGTATTAACATA | 4690 |
rs202070427 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136912469 | TGATAGTGTCTGTTT[G/T]CCTCTTTTGACTTTT | 4690 |
rs202079193 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136864765 | TTTTTTCTTTTCTTT[C/T]TTTTTTTTTTTTTTG | 4690 |
rs202089479 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136879141 | AACAACAAAAAAAAA[C/T]GCTCAGTAGAACAGT | 4690 |
rs202111998 | in-del | -/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136932133 | AAAAAAAAAAAAAAA[-/G]AAAAGAATCCATTGT | 4690 |
rs202218936 | in-del | -/TGATAGTAGTATTCCATT | | | intron-variant | NCK1 | GRCh38.p7 | 3:136874058 | GTAGTTCCTTTTCAG[-/TGATAGTAGTATTCCATT]GGATGAATATAATGT | 4690 |
rs202237179 | snp | G/T | 8.23716e-05 | 0.00641709 | missense, nc-transcript-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136946154 | ATCACCTCCACAGTG[G/T]GATTACATTAGGCCT | 4690 |
rs367598600 | snp | C/G | 0.0182019 | 0.0936463 | intron-variant, upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136862682 | CGAGTGTGCGGCGCG[C/G]TGGTTGACTTGTCTG | 4690 |
rs367652649 | in-del | -/A | | | intron-variant | NCK1 | GRCh38.p7 | 3:136870707 | AAAAAAAAAAAAAAA[-/A]GGCCTGTGAGGTCTT | 4690 |
rs367665146 | snp | A/C | 3.29511e-05 | 0.00405887 | missense, downstream-variant-500B | NCK1, LOC107986136 | GRCh38.p7 | 3:136945977 | CTCATCTAATGATGA[A/C]GAACTTAATTTCGAG | 4690 |
rs367674446 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136871226 | TATAGCAAGAGCCGG[C/T]CTTTACAAAAGTAAA | 4690 |
rs367731700 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136884807 | CTCACTGCAACCTCT[A/G]CCTCTTGAGTTCAAG | 4690 |
rs367746177 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136919485 | CCTCTGGAATCTCTA[G/T]TGAAAAGGGAAATTA | 4690 |
rs367927408 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136874481 | CACCACGCCCGGCCC[A/G]TTTACAGGTCTTTAA | 4690 |
rs367933872 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136876318 | CAGAGCAGAACTGAA[A/G]GAAATAGAGACACAA | 4690 |
rs368075741 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NCK1 | GRCh38.p7 | 3:136936102 | CTGGAGTGCAGTGAC[A/G]TGATCTCAGCTCACT | 4690 |
rs368078170 | snp | A/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136871233 | AGAGCCGGCCTTTAC[A/T]AAAGTAAAAAAAAAA | 4690 |
rs368146930 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136880100 | CCATCCTGGCTAACA[C/T]GGTGAAACCCCGACT | 4690 |
rs368149985 | snp | C/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136890145 | CGAGCCCTGCCCCAC[C/G]GGGAGGCAGCTGAGG | 4690 |
rs368212881 | snp | A/G | | | intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136947631 | TCCTGCAAGGCAACA[A/G]TCACAGCTGAGAAGT | 4690 |
rs368303784 | in-del | -/TTTTTTA | | | intron-variant | NCK1 | GRCh38.p7 | 3:136870045 | TTTTTTTTTTTTTTT[-/TTTTTTA]AAAGAATCATCCTGG | 4690 |
rs368340310 | snp | A/T | 9.885e-05 | 0.0070296 | missense, downstream-variant-500B | NCK1, LOC107986136 | GRCh38.p7 | 3:136945691 | TCAACATGCCCGCTT[A/T]TGTGAAATTTAACTA | 4690 |
rs368357832 | snp | A/C | | | intron-variant | NCK1 | GRCh38.p7 | 3:136870341 | GGAGAGACTTAATCT[A/C]AAAAAAAAAAAAATT | 4690 |
rs368377440 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136910922 | GACCAACACCTTCCC[A/G]TCCTGGCTTCTCCCC | 4690 |
rs368425994 | in-del | -/TTC | | | intron-variant | NCK1 | GRCh38.p7 | 3:136867186 | TCCTTCCTTCTTTCT[-/TTC]TTTTCTTTCTTTTCC | 4690 |
rs368447756 | snp | C/T | 3.55126e-05 | 0.00421367 | intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136948256 | CTTTTTTTTCTCTTT[C/T]AGCCAAATGATTTCT | 4690 |
rs368528029 | snp | C/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136934265 | AAATACATGTCATGG[C/G]GGTTTGCTGTTCATA | 4690 |
rs368557698 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136925432 | TTTCCTCCAGTGGCA[A/G]TACATCTGGCAGAAG | 4690 |
rs368595656 | snp | A/C | | | upstream-variant-2KB, intron-variant | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136861095 | AGGTAGACATACAGG[A/C]AAACCATTTCAATAG | 4690 |
rs368601944 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136889776 | TAGCTACGGAGTGTC[A/G]ATTGGTGCATTCACA | 4690 |
rs368795229 | in-del | -/CCTT | | | intron-variant | NCK1 | GRCh38.p7 | 3:136867203 | CTTTTCTTTCTTTTC[-/CCTT]CCTTCCTTCCTTCCT | 4690 |
rs368798199 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136906013 | TCATGTTTCCTGTGT[C/T]CTTACACTGGTATCT | 4690 |
rs368818457 | snp | C/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136864578 | GGGTAGTTCAAGCCT[C/G]TAATCCCAGCACTTG | 4690 |
rs368819291 | snp | A/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136865651 | CTAGAAAATTAAATG[A/T]TTATTTCATTAATAA | 4690 |
rs368823207 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NCK1 | GRCh38.p7 | 3:136892604 | CTGAAGGAATGCAGG[C/T]TTTGATTGTAGCTTT | 4690 |
rs368825244 | snp | A/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136879989 | GAACTTAAAGAATAT[A/T]AAAAAAAAAAAAAGG | 4690 |
rs368838634 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136887299 | TATCCTCTTGAGTAG[C/T]GGGGACTACAGGAGT | 4690 |
rs368962068 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136878445 | CTAAGTATACTAAAG[A/G]CCACATTGTATGATT | 4690 |
rs368977316 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136922523 | TCATTATTCTAGGAT[A/T]TGGGGAAAAGATATG | 4690 |
rs369029230 | in-del | -/CTC | | | upstream-variant-2KB, intron-variant | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136860290 | AACCCTTAGAATAAA[-/CTC]AAAATTCACCGCCAT | 4690 |
rs369078819 | in-del | -/TC | 0.499801 | 0.00998203 | intron-variant | NCK1 | GRCh38.p7 | 3:136867253 | CTGTCCGTCCGTCTG[-/TC]TCTCTCTCTCTCTTT | 4690 |
rs369086520 | snp | A/C | | | intron-variant | NCK1 | GRCh38.p7 | 3:136943743 | AGGAAGTTCACTCAT[A/C]TTGAGGAAGACAGAC | 4690 |
rs369131363 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136896543 | AATCTGTTTTTGTTT[C/T]GTTTTGTTTTTAAAG | 4690 |
rs369145816 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NCK1 | GRCh38.p7 | 3:136944205 | CTCACTGCAACCTCC[A/G]CCTGCCAGGTTCAAA | 4690 |
rs369181543 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136886595 | TCATAGATGCGGAAC[C/G]CATAGATACAGAGGG | 4690 |
rs369228707 | snp | A/C | | | intron-variant | NCK1 | GRCh38.p7 | 3:136872585 | GAGGAGCTGAATATG[A/C]ATCCCCAAGACAATG | 4690 |
rs369274656 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136937544 | AATTGCATTGAATCT[A/G]TGGATTGTTTTGGAT | 4690 |
rs369319231 | in-del | -/CC | | | upstream-variant-2KB, intron-variant | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136860300 | TAAACTCAAAATTCA[-/CC]CCGCCATTATTCACT | 4690 |
rs369369491 | snp | A/T | | | intron-variant, upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136862800 | CTCCAGCCCGAGAGG[A/T]GGGGAGGCGTCAGCC | 4690 |
rs369377924 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136873223 | GAGGTGCCCAAGACC[A/G]TGGAAATCCACTTCT | 4690 |
rs369379390 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136902836 | CACCAAAAAACTTAG[C/T]TCTGCTAAATAAATT | 4690 |
rs369385115 | snp | A/G | | | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136949717 | GTAGGATGTCGTATG[A/G]TACTTTCAACAAATT | 4690 |
rs369497053 | snp | C/T | | | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136949103 | TACAACTGTTGGAAA[C/T]AAAAATCACTTAATT | 4690 |
rs369555705 | snp | C/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136926511 | CGATCTCCTGAACTT[C/G]TGATTCACCCGCCTC | 4690 |
rs369562132 | snp | A/C | | | intron-variant | NCK1 | GRCh38.p7 | 3:136913899 | GGTCTCGATCTCCTG[A/C]CCTTGTGATCCTGGC | 4690 |
rs369641668 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136879983 | ACCCTAGAACTTAAA[A/G]AATATTAAAAAAAAA | 4690 |
rs369757191 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | NCK1 | GRCh38.p7 | 3:136937122 | GACATTTGGTCATTT[C/T]GAGTTAATTTTTATA | 4690 |
rs369787531 | snp | A/C | | | intron-variant | NCK1 | GRCh38.p7 | 3:136865000 | GTCTCACTCTGTTGC[A/C]CAGGCTGGAGTGCAG | 4690 |
rs369792707 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant, nc-transcript-variant | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136861713 | CAGACTCAGCTTCTT[C/T]TGGTCTGTGCCTCAA | 4690 |
rs369810148 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136934194 | ACAAGGATACTGGAG[G/T]TTTTTTTTTTTAACT | 4690 |
rs369833744 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NCK1 | GRCh38.p7 | 3:136882491 | ATTAATGATACAACA[A/G]TACCTCTTACTTGGC | 4690 |
rs369917231 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136870028 | GGATGTTTCTCAAAA[G/T]TTTTTTTTTTTTTTT | 4690 |
rs369995692 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136871397 | AGCGAGACGCTGTCT[A/G]AAAAAAACAAAATTA | 4690 |
rs370007678 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136913046 | TCTTCTTTTAGTTCT[G/T]TGAACACCTTTAAGG | 4690 |
rs370046464 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136907563 | GGTCTCTCAGCTCTC[C/T]GCTGATCCTGGTTGA | 4690 |
rs370136112 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136889640 | AGTGGTCTGTTTTGA[C/T]AGGGCACTGATTGGT | 4690 |
rs370148911 | in-del | -/T | 0.498945 | 0.0449638 | intron-variant | NCK1 | GRCh38.p7 | 3:136899419 | CCTTCATTTCTTTTC[-/T]TTTTTTTTTTTTTTA | 4690 |
rs370170350 | in-del | -/G | 0.00557542 | 0.0525036 | intron-variant | NCK1 | GRCh38.p7 | 3:136918421 | CATTTTATTATATTA[-/G]GTATTACAAGTAATC | 4690 |
rs370234907 | snp | A/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136871193 | TTGAGGGTAGGAGTT[A/T]GAGATCAGCCTGGGC | 4690 |
rs370253889 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136939124 | GCACATTTTTGATGC[A/G]AGATGTTTTGTTACT | 4690 |
rs370366721 | snp | C/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136933493 | CATTGTTCTGGTTAA[C/G]AAACAGTGCTATAGG | 4690 |
rs370492989 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136879906 | AAATGACAAGTTGAT[A/G]GGTGCAGCAAACCAA | 4690 |
rs370502348 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NCK1 | GRCh38.p7 | 3:136924082 | GTGGCAGGTAAAACC[A/G]TTGGGTAGAGGTTTG | 4690 |
rs370506982 | snp | A/G | | | intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136947031 | TCCATTTATTAAATC[A/G]TGGTTAATCTTGGCT | 4690 |
rs370540596 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136891942 | CACTCAGGCTGGAAT[A/G]GAGTGACATAATCAT | 4690 |
rs370575463 | snp | A/C | | | intron-variant | NCK1 | GRCh38.p7 | 3:136908433 | TAGTGGACTAGATGT[A/C]CAGCTTGCAAAGTGA | 4690 |
rs370583971 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136920266 | TTTTTTAAAAAATAG[C/T]GTAGGTCAAATAAAA | 4690 |
rs370612598 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136864039 | CCGGGAGGCGGAGCT[G/T]GCAGTGAGCCGAGAT | 4690 |
rs370617853 | snp | G/T | 1.65979e-05 | 0.00288074 | missense | NCK1 | GRCh38.p7 | 3:136928203 | CGGAAAGCATCTATT[G/T]TGAAAAACCTAAAGG | 4690 |
rs370629482 | snp | A/G | | | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136950164 | GTTGTAGGATGACTA[A/G]TAGTAAACATCATCT | 4690 |
rs370705394 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136882911 | TTATAATTTCCTTGC[C/T]TAAAACCCTTATTAC | 4690 |
rs370727973 | snp | C/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136915816 | CTGCAACCTCCACCT[C/G]CCAGGTTCAAGCAAT | 4690 |
rs370857782 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136867049 | CCTATGTTGCTTGCT[C/T]TTCTTTCTTTCTTTC | 4690 |
rs370876910 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136884448 | TTGAGTTCTTGTCTT[G/T]TCTTTTTTTTTGAAA | 4690 |
rs370918683 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | NCK1 | GRCh38.p7 | 3:136929722 | CAGTTAGACTTTTTT[C/G]TTCCATTTTAAGAGG | 4690 |
rs370941205 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136871211 | GATCAGCCTGGGCAA[C/T]ATAGCAAGAGCCGGC | 4690 |
rs370957495 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136875154 | TGAGGACTGTCATAA[C/T]AATACCACAGTCTGC | 4690 |
rs370974253 | snp | A/G | | | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136950825 | AATTTAAATACATGT[A/G]TCAGATGGAACCCTG | 4690 |
rs371078108 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136934512 | GCTGGTCTCGAACTC[C/T]CAACCTCATGTGATC | 4690 |
rs371079226 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136940759 | CATGTTGGCCAGGCT[A/G]GTCTTGAACTCCTGA | 4690 |
rs371087720 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136931573 | AGATCTTTGCATTTT[C/T]CATTTTTTGGGTAAG | 4690 |
rs371098026 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136909068 | ATGTAGTAGGAAGGC[C/T]TTCACCAGATGCTAG | 4690 |
rs371135567 | snp | C/T | | | intron-variant, upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136863983 | GCGGGCGCCTATAGT[C/T]CCAGCTACTCGGGAG | 4690 |
rs371141807 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136873753 | TTGTGATAGTGAATA[A/G]GTCTTTTGAGAACTG | 4690 |
rs371147224 | snp | A/G | 1.64746e-05 | 0.00287002 | synonymous-codon, nc-transcript-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136946139 | TTCAGGTTTGGAACC[A/G]TCACCTCCACAGTGT | 4690 |
rs371182102 | snp | A/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136904834 | ACACAGGCTTTTCTC[A/T]TTTTTTTTTTTTTAA | 4690 |
rs371207267 | snp | C/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136871221 | GGCAATATAGCAAGA[C/G]CCGGCCTTTACAAAA | 4690 |
rs371332692 | in-del | -/C | 0.00438332 | 0.0466095 | intron-variant | NCK1 | GRCh38.p7 | 3:136891985 | TCTCATCCTCCTGGG[-/C]TCAAGGGATCCTCCT | 4690 |
rs371366582 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136873844 | ATGCCTTTCACTATG[C/T]GCCATGATTGTGAGG | 4690 |
rs371372727 | snp | C/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136878759 | TGTTAGTTTGTATCA[C/G]TAAGTTACTGCCTTC | 4690 |
rs371375449 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136915646 | GAGGTTTAAAAGGTT[C/T]ACAGTTTCCTCAGGC | 4690 |
rs371535709 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136941883 | TTGCTCTGTCTCCCA[G/T]GCTGGAGTACAGTGG | 4690 |
rs371537381 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136871229 | AGCAAGAGCCGGCCT[C/T]TACAAAAGTAAAAAA | 4690 |
rs371541531 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136923195 | TTTTCAATTTTCTTA[C/T]ATATTTTTCTTGAAT | 4690 |
rs371565447 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136912560 | GCCTGCTCAAGTCTT[C/T]ATTCAAATCCCTGTA | 4690 |
rs371629761 | in-del | -/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136910989 | GAGTTCAACTTTTTT[-/T]AGATTCCACATGTAT | 4690 |
rs371731741 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136901210 | TTATGAATCATATTT[A/G]TTGATTTGTGTAACC | 4690 |
rs371818636 | snp | C/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136941921 | TTGGCTCACTACAAC[C/G]TCCACCTCCCGGGTT | 4690 |
rs371879871 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136869012 | GGAGGCTGAGGCATG[C/T]GGAGCCCCTGAGTCC | 4690 |
rs371880420 | snp | A/G | 1.64746e-05 | 0.00287002 | missense, nc-transcript-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136946068 | AGGAAGATCAATGGT[A/G]TGGTTGGTCTAGTAC | 4690 |
rs371919481 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136886341 | AGACTCCTTGCAGAT[A/G]CCAAAATTTGAGGAT | 4690 |
rs371928430 | in-del | -/TCTT | | | intron-variant, upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136863020 | AGGTTTTGTAACCTT[-/TCTT]CTGTATTAACATACA | 4690 |
rs371971935 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136910950 | CCCAGTCTCTGGTAA[A/G]CATCATTCTACTCTC | 4690 |
rs371998280 | in-del | -/TTATC | 0.00279162 | 0.0372561 | intron-variant | NCK1 | GRCh38.p7 | 3:136900594 | TGTGCCCTCTTTATT[-/TTATC]TAGTGTTTTGTAGTT | 4690 |
rs372161572 | snp | A/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136879986 | CTAGAACTTAAAGAA[A/T]ATTAAAAAAAAAAAA | 4690 |
rs372231637 | snp | A/G | 0.00199481 | 0.0315187 | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136948885 | GCTAAAATTTCTTGG[A/G]GAGTGTTAATCTTTT | 4690 |
rs372235501 | in-del | -/TTTTTA | | | intron-variant | NCK1 | GRCh38.p7 | 3:136870046 | TTTTTTTTTTTTTTT[-/TTTTTA]AAAGAATCATCCTGG | 4690 |
rs372279967 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136861176 | GCTTCCCTGAGGAGC[A/G]ATCCTAAACTGTGCC | 4690 |
rs372355611 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136871268 | AGCCAGGTTTGGCTG[G/T]GAGCGTCTGTAGTCC | 4690 |
rs372388356 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136870743 | ATTTGGCTTTTGTCT[A/G]CGTCTCACTTCATCT | 4690 |
rs372424696 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136871184 | GAGGATGCCTTGAGG[G/T]TAGGAGTTAGAGATC | 4690 |
rs372510063 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136927617 | ACCTTCGCCTCCCAG[A/G]TTCAAGCTATTCCCA | 4690 |
rs372616277 | snp | C/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136881915 | CCACATTTTGTTTAT[C/G]CATTCATTTGTTGAT | 4690 |
rs372652313 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136876950 | AGAAAAGACATTCCA[A/G]TTTACACCTTTACCA | 4690 |
rs372666726 | in-del | -/GTCCTGACCTCAG | 0.00914312 | 0.0669923 | intron-variant | NCK1 | GRCh38.p7 | 3:136874403 | CAGGCTGGTCTCGAA[-/GTCCTGACCTCAG]GTGACCCGCCCACCT | 4690 |
rs372721676 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136896873 | CTACAGTAAACATGC[A/G]AGTGCAGGTATCCCT | 4690 |
rs372877760 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136893492 | CTGTTTTTTGATGGG[A/G]TTGTTTTTTTCTTGC | 4690 |
rs372897097 | in-del | -/TT | | | intron-variant | NCK1 | GRCh38.p7 | 3:136936039 | TTATGTCTAAATAAC[-/TT]TTTTTTTTTTTTTTT | 4690 |
rs373028873 | snp | A/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136902851 | TTCTGCTAAATAAAT[A/T]CAGTAAAGTTGCAGG | 4690 |
rs373067110 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136877703 | CTGGAAACTGGAAAG[C/T]GAGTGAACTGATGGG | 4690 |
rs373122615 | in-del | -/TTTTTTTT | 0.135143 | 0.222054 | intron-variant | NCK1 | GRCh38.p7 | 3:136905008 | CTGTTTGGTTTTTCC[-/TTTTTTTT]TTTTTTTTTCTTTTT | 4690 |
rs373176308 | in-del | -/AGATAC | | | intron-variant | NCK1 | GRCh38.p7 | 3:136878703 | AGTTGTATCTCAATA[-/AGATAC]AAGCTATTTTTTTTT | 4690 |
rs373197808 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136878595 | TGGGGTGACAAAAAT[C/T]TTCTAAAATTCATTG | 4690 |
rs373273019 | in-del | -/GA | | | intron-variant | NCK1 | GRCh38.p7 | 3:136889043 | CCAGGCTAATTTTTT[-/GA]TTTTTTTTTTTTTTT | 4690 |
rs373324900 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136871199 | GTAGGAGTTAGAGAT[C/T]AGCCTGGGCAATATA | 4690 |
rs373343699 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136865339 | ATCTGCCCACCTCCG[C/T]CTCCCAAAGTGCTGA | 4690 |
rs373387220 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136933620 | AACTGCCTCAGAATG[G/T]TACACTTCCTCAGTG | 4690 |
rs373406327 | snp | C/T | 1.74424e-05 | 0.00295312 | missense, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136948259 | TTTTTTCTCTTTTAG[C/T]CAAATGATTTCTCAG | 4690 |
rs373411055 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136865787 | AAGGAAACTTTATGT[C/T]TGGCTGATCCTCACC | 4690 |
rs373433803 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | NCK1 | GRCh38.p7 | 3:136913685 | TTTTGTTTTGTTTTT[A/T]TGAGACGGAATCTCA | 4690 |
rs373448360 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136907055 | TTGTGCTGTGGCCTT[A/G]TTACCGGGAAGGGTG | 4690 |
rs373487588 | snp | A/C | | | intron-variant | NCK1 | GRCh38.p7 | 3:136918788 | ATTGGACACTCCTGC[A/C]TTAGATACTGAGGGC | 4690 |
rs373522891 | snp | C/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136907767 | AAGTTCCTCCCTTTC[C/G]TGTTTTTTTGATGAA | 4690 |
rs373610001 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136884747 | TTTTTTTGAGAGGGA[A/G]TCTCACTCTGTTGCC | 4690 |
rs373692055 | in-del | -/CT | | | intron-variant | NCK1 | GRCh38.p7 | 3:136944112 | AAAAGGAAAAACAAC[-/CT]TTTTTTTTTTTTTTT | 4690 |
rs373714308 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136927272 | CCACCAGGCCTGGCC[A/G]TTTTTATTTCTTTGT | 4690 |
rs373775669 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | NCK1 | GRCh38.p7 | 3:136901720 | ATTTCTGTGGAATTA[G/T]TTGTAATGTCTCTTT | 4690 |
rs373789090 | snp | A/G | | | intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136947997 | TGTTAAGAGACTTTT[A/G]ATTATGCAGGTTTGA | 4690 |
rs373811945 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136880141 | TACAAAAAAATTAGC[C/T]GGGTGTGGTGGTGGG | 4690 |
rs373816137 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136934261 | AGGTAAATACATGTC[A/T]TGGGGGTTTGCTGTT | 4690 |
rs373844047 | snp | C/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136887002 | GCAGGTGCCACCATG[C/G]CCGGCTAATTTTTGT | 4690 |
rs373869136 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NCK1 | GRCh38.p7 | 3:136867979 | CTGGAGTGCAGCAGC[A/G]TGATCTCGGCTCACT | 4690 |
rs373917552 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136891033 | GAGTATAGTGTCTTC[A/G]AGGTTTATTCACATT | 4690 |
rs373923128 | snp | A/C | | | intron-variant | NCK1 | GRCh38.p7 | 3:136936727 | ACATTTCTCTAATGA[A/C]TAATGATATTGAGGA | 4690 |
rs374022073 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136879929 | CAAACCAACGTGGCA[C/T]GTGTATACCTCTAAC | 4690 |
rs374041659 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136895935 | TTTTAATTATGATAT[A/G]TCTGGATTTTTGTCA | 4690 |
rs374137768 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136934611 | ATTATTTCATCACCC[A/G]GGTATTAAGCCCAGT | 4690 |
rs374144854 | in-del | -/C | | | intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136947898 | CTTTCTCATGTGTTT[-/C]TCTGACTGGAGAGAA | 4690 |
rs374161071 | snp | G/T | 1.65105e-05 | 0.00287315 | missense | NCK1 | GRCh38.p7 | 3:136928015 | AGATGGCAGAAGAAG[G/T]GGTGGTAGTAGCCAA | 4690 |
rs374194026 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136889969 | CAGGGGTTGCAGGTG[A/G]AGCTGCCTGCCAGTC | 4690 |
rs374233769 | snp | A/C | | | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136950916 | TAAGCTTTGTGACAA[A/C]AACAAATGCCATTGT | 4690 |
rs374243069 | in-del | -/TC | | | intron-variant | NCK1 | GRCh38.p7 | 3:136867179 | CCTTCCTTCCTTCCT[-/TC]TTTCTTTCTTTTCTT | 4690 |
rs374336115 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136871214 | CAGCCTGGGCAATAT[A/G]GCAAGAGCCGGCCTT | 4690 |
rs374353664 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NCK1 | GRCh38.p7 | 3:136903527 | CCTCCTGGGTTCAAG[C/T]GATTCTCCTGCCTCA | 4690 |
rs374361793 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136911482 | AATTGCATTTCCCTA[A/G]TGATTAGTGATGCTG | 4690 |
rs374362879 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136883140 | GGCTAAGGCTGGTCT[C/T]GTACTACTGGCGTCA | 4690 |
rs374379642 | in-del | -/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136905007 | CTGTTTGGTTTTTCC[-/T]TTTTTTTTTTTTTTT | 4690 |
rs374467312 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136925151 | TATTATACCAGTAAT[A/G]TAGTAGAATGCTATT | 4690 |
rs374467510 | snp | A/C | | | intron-variant | NCK1 | GRCh38.p7 | 3:136931574 | GATCTTTGCATTTTT[A/C]ATTTTTTGGGTAAGT | 4690 |
rs374473320 | snp | G/T | | | intron-variant, upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136863281 | CGGGTGTTGCCAAAA[G/T]GTACTCATTTTTAAA | 4690 |
rs374482338 | in-del | -/A | 0.00755907 | 0.0610114 | intron-variant | NCK1 | GRCh38.p7 | 3:136868818 | TAACTAAATGCAGTG[-/A]TCTAGCTGTAATGTT | 4690 |
rs374486224 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136903154 | TGCCTTATATGTTTG[C/G]AATTGTTAAATCCTC | 4690 |
rs374488270 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136882509 | CCTCTTACTTGGCAG[C/T]ATAATACAATGAAAG | 4690 |
rs374545343 | in-del | -/TATATA | | | intron-variant | NCK1 | GRCh38.p7 | 3:136893179 | GTGTGTGTGTGTGTG[-/TATATA]TATATATACACACAT | 4690 |
rs374586118 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136871232 | AAGAGCCGGCCTTTA[C/T]AAAAGTAAAAAAAAA | 4690 |
rs374620089 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | NCK1 | GRCh38.p7 | 3:136874024 | TTTGTGAGATTCATT[G/T]ATGATGTAGAGTGCA | 4690 |
rs374679476 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136941311 | TTTGGTATTTTTTTG[A/G]TAGAGACGAGGTCTC | 4690 |
rs374686288 | in-del | -/ATG | | | intron-variant | NCK1 | GRCh38.p7 | 3:136892511 | GCAGAAATCTTGATG[-/ATG]TGGCCAAGTGCAAAG | 4690 |
rs374706393 | snp | C/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136900080 | AGGCTGCACCATGGT[C/G]CCTTTCAGGGCTTGA | 4690 |
rs374736118 | snp | A/G | 2.2849e-05 | 0.00337994 | intron-variant, downstream-variant-500B | NCK1, LOC107986136 | GRCh38.p7 | 3:136945532 | TAAGTTCATTCTTTT[A/G]GTAATCATTTTTTTA | 4690 |
rs374819381 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136868708 | TTTAGTTTGTCTTTT[C/T]GAATCTCTTGATAAT | 4690 |
rs374852224 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136869839 | TTTTCTATTTGTTTA[A/G]ATTATCAGTTAAAAA | 4690 |
rs374873606 | in-del | -/CTTT | | | intron-variant | NCK1 | GRCh38.p7 | 3:136941110 | CTTCTTTTGTGATTT[-/CTTT]TTCTTTTTTTTTTTT | 4690 |
rs374903315 | snp | A/C | | | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136949707 | ACATAACTGAGTAGG[A/C]TGTCGTATGATACTT | 4690 |
rs374951738 | snp | A/G | 1.64732e-05 | 0.0028699 | synonymous-codon, downstream-variant-500B | NCK1, LOC107986136 | GRCh38.p7 | 3:136945884 | TGTGGGTTCTCTGTC[A/G]GAGAAATTAGCAGCA | 4690 |
rs375015872 | snp | A/G | | | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136949979 | CAAATTTTCATCTCT[A/G]TTACATCTGCTTTTA | 4690 |
rs375036620 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136864761 | GGGTTTTTTTCTTTT[C/T]TTTTTTTTTTTTTTT | 4690 |
rs375084826 | in-del | -/C | | | intron-variant | NCK1 | GRCh38.p7 | 3:136941116 | TTGTGATTTCTTTTT[-/C]TTTTTTTTTTTTTTT | 4690 |
rs375196356 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136878117 | ATAAACCTTTAAAAC[A/G]TGCTAAGTAGGCCGG | 4690 |
rs375208462 | in-del | -/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136900713 | ATGTTGATTTTTTTT[-/T]AACACTCCCTACTTC | 4690 |
rs375222376 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136871331 | TGAGTCCAAGAGGTC[A/G]AGGCTGCAGTGAGCT | 4690 |
rs375234927 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136924472 | TAGCTTAAGTGCAAT[A/G]TATCGACTTAGTTTG | 4690 |
rs375256364 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NCK1 | GRCh38.p7 | 3:136926504 | ATGGTCTCGATCTCC[C/T]GAACTTGTGATTCAC | 4690 |
rs375273239 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136898958 | TTATAGGACATGGTA[A/G]TGGATTCCTTTGTAT | 4690 |
rs375280377 | snp | A/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136905985 | TTTGGCGGTGTCATA[A/T]TTCCTTGCTTTTTCA | 4690 |
rs375431908 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136891383 | CAGGTGATCTACCCG[C/T]CTCAGCCTCCCAAAG | 4690 |
rs375522394 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136899265 | TGTAATGGTTTCCTA[G/T]TGGCATCTGAAGAAA | 4690 |
rs375529118 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136878813 | GACTATTGTTTCTGA[C/T]ACTGAGGGTGGGCCC | 4690 |
rs375536148 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136923277 | AATAGCTGTCCAGGC[C/T]GGGCGCGGTGGCTCA | 4690 |
rs375554492 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136946632 | AGTAGAATAATACTA[C/T]AGATTAAACTGGGAA | 4690 |
rs375564485 | snp | A/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136879988 | AGAACTTAAAGAATA[A/T]TAAAAAAAAAAAAAG | 4690 |
rs375593387 | snp | C/T | 0.426047 | 0.177503 | intron-variant | NCK1 | GRCh38.p7 | 3:136878710 | ATCTCAATAAAGCTA[C/T]TTTTTTTTAAGAAAG | 4690 |
rs375659091 | snp | C/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136871187 | GATGCCTTGAGGGTA[C/G]GAGTTAGAGATCAGC | 4690 |
rs375687300 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136886447 | CTCTAGATTACCTAA[C/T]ACATTGTAAATGGTA | 4690 |
rs375750084 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136915267 | AGTCCTATTGAGAAG[A/G]TAAAAGGGACATGAT | 4690 |
rs375778768 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136876541 | TATGAACATCCTTCC[A/G]TGTCAGTGTATATAT | 4690 |
rs375786026 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136916257 | ATTAAAAATGACATA[A/G]GCTCATGGAAGGCAT | 4690 |
rs375829999 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136877064 | TTAGACAAATCCATA[A/G]GCATAATATGAGATA | 4690 |
rs375896381 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136891851 | ATCTTCTTTGGAGAA[A/G]TGTCTATTCAATTCC | 4690 |
rs375909988 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136914162 | ACAATAGCTGCCTGC[G/T]TCTGTGTCTGTATCT | 4690 |
rs375915283 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136888781 | TATACATTTGCTCAT[C/T]CTGAACCTTTCATAT | 4690 |
rs376071168 | snp | C/T | | | upstream-variant-2KB, intron-variant | NCK1 | GRCh38.p7 | 3:136930191 | GGATTTGTTTCGCAA[C/T]GGTTGTGCTGGTGGA | 4690 |
rs376088893 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136909766 | TGATGGGCTGTCATT[A/G]CATGTTAAATGTTTA | 4690 |
rs376094468 | snp | A/C | | | intron-variant, upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136862789 | GGCGCTCTCACCTCC[A/C]GCCCGAGAGGAGGGG | 4690 |
rs376206146 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136924554 | AAATTGAATATTAGC[A/G]TTAGATGAAATAAGT | 4690 |
rs376214936 | snp | A/G | 0.000115732 | 0.00760609 | synonymous-codon, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136948399 | TTACAAAAAGGCACC[A/G]ATTTTTACAAGTGAA | 4690 |
rs376231702 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136939767 | TTTCCTTTCTGTTAT[G/T]GATTTCTAGGTTCAT | 4690 |
rs376233638 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136871224 | AATATAGCAAGAGCC[G/T]GCCTTTACAAAAGTA | 4690 |
rs376435532 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | NCK1 | GRCh38.p7 | 3:136883320 | CATCTCTAGCCATAC[G/T]GTCATTTTCTGTAAC | 4690 |
rs376538231 | snp | C/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136871207 | TAGAGATCAGCCTGG[C/G]CAATATAGCAAGAGC | 4690 |
rs376574104 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136886480 | TAGGTAGTTAATGCT[A/G]TATTGTTTAGGGAAT | 4690 |
rs376611325 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136912783 | GCTTCAGCTTCCTGA[A/G]TAGCTGGAACTACTT | 4690 |
rs376643488 | snp | C/T | 1.64741e-05 | 0.00286998 | missense, nc-transcript-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136946126 | ATAATCCATTAACTT[C/T]AGGTTTGGAACCATC | 4690 |
rs376669315 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136890395 | TCCCTCTACACCTCC[C/T]CCCAAGCTGAGGGAG | 4690 |
rs376716261 | in-del | -/TT | | | intron-variant, upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136863076 | CAGGAAGCTGKKTTT[-/TT]TGTTCAGGGGTGAGG | 4690 |
rs376716847 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136895126 | GTTATCCACCCGCCT[C/T]GGCCTCCCAAAGTGC | 4690 |
rs376779233 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136867133 | TTGTTTCTTTCTTTC[C/T]TTCCTTCCTTCCTTC | 4690 |
rs376886040 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136921930 | CTGGGACTACAGGCA[C/T]GCACCACCACGCCCA | 4690 |
rs376918868 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136922890 | GTTCATTGCAGCACT[A/G]TTTAATCCCAGAAAA | 4690 |
rs377070617 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136940275 | TGGGATATTCTCTAT[A/G]TGTCTATTAGGTCTA | 4690 |
rs377128809 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136893182 | TGTGTGTGTGTGTAT[A/G]TATATATATACACAC | 4690 |
rs377151132 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136903528 | CTCCTGGGTTCAAGC[A/G]ATTCTCCTGCCTCAG | 4690 |
rs377154149 | snp | C/T | | | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136951284 | GGCCCAGCCCTTCTC[C/T]AGAAGTTTGAATTTC | 4690 |
rs377203417 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136907411 | AGGTTTGTGGGACTT[A/G]GCGTGAGCTCTCTCT | 4690 |
rs377234848 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136887476 | GTGTTTAAAAATGAA[C/G]GCGAGAAGGAGAAAA | 4690 |
rs377340434 | in-del | -/TTC | | | intron-variant | NCK1 | GRCh38.p7 | 3:136917300 | CTGAGACAATTCTTC[-/TTC]CAGTATGATCCAGGG | 4690 |
rs377351824 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136867267 | TGTCTCTCTCTCTCT[C/T]TCTTTCTTTCTTCTT | 4690 |
rs377364825 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136888368 | ACAATTCAGCTTTTA[A/G]TATATTCAGAGTTGT | 4690 |
rs377372952 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136884731 | AGCTTTTTTTTTTTT[C/T]TTTTTTTGAGAGGGA | 4690 |
rs377423703 | in-del | -/AA | | | intron-variant | NCK1 | GRCh38.p7 | 3:136898385 | GCAAGACTCCCTCTC[-/AA]AAAAAAAAAAAAAAA | 4690 |
rs377565948 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136915752 | TTTTTTTGAGATGGA[A/G]TCTCACTCCGTCATC | 4690 |
rs377613376 | snp | C/G | | | intron-variant, upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136863808 | TGTAATGTTTTGTTC[C/G]ATACTGAGGGAGTCC | 4690 |
rs377649996 | snp | G/T | | | intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136946703 | TAGTCACTGTAGTCC[G/T]TATGACATAGGAAAT | 4690 |
rs377698151 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136871219 | TGGGCAATATAGCAA[A/G]AGCCGGCCTTTACAA | 4690 |
rs377708301 | snp | C/G | | | upstream-variant-2KB, intron-variant | NCK1 | GRCh38.p7 | 3:136930187 | TAATGGATTTGTTTC[C/G]CAATGGTTGTGCTGG | 4690 |
rs377710487 | snp | A/G | | | intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136947170 | TGTGAAGTTCAGGAA[A/G]ATGGGGCCTGTGCCT | 4690 |
rs377736740 | snp | A/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136937611 | TTTAAGTCTTCTTTA[A/T]TTTCTTTCAGCGGTG | 4690 |
rs377759052 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136927041 | CAGTGGCACGATCTT[A/G]GCTAACTGCAACCTC | 4690 |
rs377760409 | snp | A/G | | | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136950635 | ACCCTGGAAAACTCT[A/G]CATAGCTAGATAGTA | 4690 |
rs386398008 | in-del | -/TT | | | intron-variant, upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136863074 | CTCAGGAAGCTGGGT[-/TT]TTTGTTCAGGGGTGA | 4690 |
rs386666199 | multinucleotide-polymorphism | CGTGG/TGTGC | | | intron-variant | NCK1 | GRCh38.p7 | 3:136865374 | ACAGGTGTGCGCCAC[CGTGG/TGTGC]CTGGCCTATATTCAT | 4690 |
rs386666200 | multinucleotide-polymorphism | CGTGACAGTAATTAACAAAATATAGTGAAAAAACTAA/TGTGACAGTAATTAACAAAATATAGTGAAAAAACTAT | | | upstream-variant-2KB, intron-variant | NCK1 | GRCh38.p7 | 3:136929765 | TGGGATTAGAGTGAA[lengthTooLong]TATCATAGAGCAAAG | 4690 |
rs397690760 | in-del | -/A | 0.5 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136870354 | TCAAAAAAAAAAAAA[-/A]TTCATCCTTTTCTTC | 4690 |
rs397728080 | in-del | -/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136904847 | CATTTTTTTTTTTTT[-/T]AATTATTACTTTTTG | 4690 |
rs397730164 | in-del | -/CT/TT | | | intron-variant | NCK1 | GRCh38.p7 | 3:136867266 | TGTCTCTCTCTCTCT[-/CT/TT]TTCTTTCTTTCTTCT | 4690 |
rs397756003 | in-del | -/T | 0.375 | 0.216506 | intron-variant | NCK1 | GRCh38.p7 | 3:136931573 | AGATCTTTGCATTTT[-/T]CATTTTTTGGGTAAG | 4690 |
rs397760541 | in-del | -/A | 0.5 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136879140 | AACAACAAAAAAAAA[-/A]GGCTCAGTAGAACAG | 4690 |
rs397772960 | in-del | -/T | 0.5 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136933721 | TAATCTTTTTTTTTT[-/T]CTTGAGACAGTCTTG | 4690 |
rs397776778 | in-del | -/TT | | | intron-variant, upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136863077 | AGGAAGCTGGGTTTT[-/TT]GTTCAGGGGTGAGGA | 4690 |
rs397794763 | in-del | -/AA | 0.375 | 0.216506 | intron-variant | NCK1 | GRCh38.p7 | 3:136874815 | TCAAGCATGAACATG[-/AA]AAAAAGTTTTCATTA | 4690 |
rs397797060 | in-del | -/AG | | | intron-variant | NCK1 | GRCh38.p7 | 3:136903776 | TCAGTTTACATTCAG[-/AG]TTATTGATGTGTGAA | 4690 |
rs397805858 | in-del | -/A | 0.5 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136941722 | ATTTACAAAAAAAAA[-/A]CTGCAATACTACTGA | 4690 |
rs397874766 | in-del | -/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136866942 | TTAAAATTTTTTTTT[-/T]CTCCTAAATTACCAA | 4690 |
rs397874795 | in-del | -/A | | | intron-variant | NCK1 | GRCh38.p7 | 3:136923317 | CCCAGCACTTTGGGA[-/A]GGCCGAGGCAGGCGG | 4690 |
rs397875767 | in-del | -/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136867934 | AAATTTTTTTTTTTT[-/T]GAGACAGAGTTTCGC | 4690 |
rs397876995 | in-del | -/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136930992 | TAACTTTTTTTTTTT[-/T]AACTACTTTTTGCTT | 4690 |
rs397877751 | in-del | -/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136937954 | TAAAAGTGGTGGAAG[-/G]AGAGCATCCTTGTTC | 4690 |
rs397991173 | in-del | -/G | 0 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136944112 | AAAAAAAAAAAAAAA[-/G]GTTGTTTTTCCTTTT | 4690 |
rs398052301 | in-del | -/A | 0.5 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136918351 | TTCTGGAAAAAAAAA[-/A]TACACTAATTAAAAT | 4690 |
rs398091839 | in-del | -/A | | | intron-variant | NCK1 | GRCh38.p7 | 3:136893356 | ATTCTTGCAGGAGTA[-/A]GGTGGTACTGCATTG | 4690 |
rs398106491 | in-del | -/T | | | intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136946984 | TTAAAAATGGCCTTT[-/T]CTTTTTCCTTGATGA | 4690 |
rs527277535 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136873438 | TAACTACCTTGCTTT[C/T]GATTTTACAGGCTCA | 4690 |
rs527288589 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136881200 | GCCATCATCTCTTCA[C/T]TTACACTATTGGCCT | 4690 |
rs527309408 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136924083 | TGGCAGGTAAAACCA[C/T]TGGGTAGAGGTTTGA | 4690 |
rs527309802 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136932869 | AGAAGAAACAGAAAA[A/G]CTTTCTTTGGCCCCA | 4690 |
rs527332660 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136939070 | TAATTCCTCTTTAAA[C/T]GTTTAGTAAAATCCA | 4690 |
rs527433350 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136892608 | AGGAATGCAGGCTTT[G/T]ATTGTAGCTTTGTAA | 4690 |
rs527434470 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136900697 | TAGAAACAGGTTTTG[C/T]ATGTTGATTTTTTTT | 4690 |
rs527456355 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136946524 | AATTATTTCGTCTTG[C/T]CTAGTTCTGTTGATT | 4690 |
rs527457762 | snp | A/C | | | intron-variant | NCK1 | GRCh38.p7 | 3:136885982 | ACAAAAGCAGCAGTA[A/C]AGTGGTATTTCATCT | 4690 |
rs527469494 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136915452 | AAAGTTCTTTTATAC[C/T]CAGGATTTTTAAGTA | 4690 |
rs527495640 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136938278 | CTTTTAATATGCTTG[C/G]TGGATTTGGTTTTCC | 4690 |
rs527506079 | snp | A/T | | | intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136947699 | TCTGCCCATCTACCT[A/T]TCCACTCTGACACTT | 4690 |
rs527564874 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136907210 | ATGCACGGGTCCCCC[A/T]CTGCTGCAGTGTAGG | 4690 |
rs527628937 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136943785 | TACAATGCAGTGTTA[C/T]AATAACAAGGTTAGA | 4690 |
rs527709750 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136941431 | CTCTGTGACTGGACT[A/G]TTTTCTCTAATATAT | 4690 |
rs527760551 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NCK1 | GRCh38.p7 | 3:136910388 | TCTTATGTAGAAAAT[A/G]AAATGTGTAGTAACA | 4690 |
rs527811914 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136887948 | TTCTTTCTTTCTTTT[G/T]TTTTTTTTCTTTTGA | 4690 |
rs527825012 | snp | C/T | 3.32105e-05 | 0.00407482 | missense, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136948430 | CAAGGAGAAAAATTA[C/T]ATCTTGTCAAGCATT | 4690 |
rs527831425 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136861999 | GACAGTTCTGGTCCG[A/G]CCCAGCGCTTCTCAC | 4690 |
rs527903154 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136867555 | CTGGTCTGTTGCTTT[C/T]CTTTAAACCCATACC | 4690 |
rs527923301 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136909448 | AGGGATACAAAATGA[A/G]ACAAGGCTGTTTCCT | 4690 |
rs527940853 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136874082 | TATTCCATTGGATGA[A/G]TATAATGTAATTTTA | 4690 |
rs527950139 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136927058 | CTAACTGCAACCTCC[A/G]CCTCCCAGGTTCAAG | 4690 |
rs527981612 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136916549 | TTATGAATATGCTTA[C/T]TAGAAGAGATGACAC | 4690 |
rs528014465 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136910430 | CAATTATTCTAGCTT[C/T]TAGAGTAATGTTTTT | 4690 |
rs528082955 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136924535 | AAAAAAATACACTTA[A/G]CAAAAATTGAATATT | 4690 |
rs528130361 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136912267 | TTCCAGGTTCAAGCA[A/G]TTCTCCTGCCTCAGC | 4690 |
rs528137121 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136869209 | CATGCCATTCCACTC[C/T]GGCCTGGGTAACAGA | 4690 |
rs528140888 | in-del | -/A | 0.00676609 | 0.0577691 | intron-variant | NCK1 | GRCh38.p7 | 3:136877331 | AAGAAATGGATTACC[-/A]AAAAAAACTAGAAAA | 4690 |
rs528166937 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136924814 | TTGTGAGAGTTATTT[A/G]TATCATGCTCAAGGT | 4690 |
rs528178075 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136911288 | GTGGGATTGCTGGAT[A/C]ATATGGTAGCTCTAA | 4690 |
rs528192059 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136919136 | CTGGAAAAGGCAAAA[C/G]TACATAGGGACAGAA | 4690 |
rs528234652 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136920783 | AAAACGTGTAACATA[A/G]TGAATTTATTGTCAT | 4690 |
rs528269024 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136926008 | TTTGGTATTACCACT[C/G]TTAGCCATTCTGACA | 4690 |
rs528269156 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136934515 | GGTCTCGAACTCCCA[A/G]CCTCATGTGATCCAT | 4690 |
rs528292951 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136876123 | GAACAAAGACACAAC[A/G]TACCAGAATCTCTGG | 4690 |
rs528332313 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136934004 | TGAGCCACCTTGCCC[G/T]GCCAAGTTTAAGTAA | 4690 |
rs528349606 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136942340 | CTTATTGTGAGTGGT[G/T]GTTGTTTGCTTGTTT | 4690 |
rs528366720 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136889299 | AAGCCGCGGACCCTC[A/G]CGGTGAGTGTTACAG | 4690 |
rs528424995 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136879791 | TGCATGAGTTGAACA[A/G]TGAGAACACATGGAC | 4690 |
rs528432768 | snp | C/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136865148 | TTTTTAGTAGAGGCA[C/G]GGTTTCACCATCTTG | 4690 |
rs528463742 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136878141 | AGGCCGGACATGGTG[A/G]CTCACACCTGTAATC | 4690 |
rs528491635 | snp | C/T | 1.67038e-05 | 0.00288992 | intron-variant | NCK1 | GRCh38.p7 | 3:136927973 | TAAAAATATTTTCCA[C/T]GTGTTTACAGTGCTG | 4690 |
rs528511620 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136920333 | TTGAAATCATCCCCA[A/G]TATGAGAAGGCACAA | 4690 |
rs528557163 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136884467 | TTTTTTTTGAAACAC[A/G]GTCCTGCTCTGTGGC | 4690 |
rs528579174 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136890598 | TTGCTGAATAATATG[G/T]AATTTTACAGTTAAT | 4690 |
rs528584945 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136883554 | ACAGCATTTTTTGCA[A/G]CCTATAATTATTTTA | 4690 |
rs528634531 | in-del | -/TCTCT | | | intron-variant | NCK1 | GRCh38.p7 | 3:136871860 | TTTCCCTGCACAAAC[-/TCTCT]TCTCTTATCTGCCGC | 4690 |
rs528693362 | in-del | -/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136933568 | AAATTATCTTTACAC[-/T]TTTTTTTTTTTAATT | 4690 |
rs528707788 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136944281 | ACACCACTGCACCCA[A/G]CTAATTTTTGTATTT | 4690 |
rs528812601 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136896607 | CAGTGGTGCAATCAT[C/G]GCTCACTGCAGTGAG | 4690 |
rs528823042 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136951737 | AAAGAGAAATGTTAC[A/G]TATGTTTTGAAAGAA | 4690 |
rs528972382 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136899120 | GTGCTGATCTGGACA[A/G]GCCACAGCAGAGACT | 4690 |
rs528998886 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136891384 | AGGTGATCTACCCGC[C/T]TCAGCCTCCCAAAGT | 4690 |
rs529025515 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136945129 | TTTATATTGCATATC[A/G]TATTCTGATTTAAGA | 4690 |
rs529105558 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NCK1 | GRCh38.p7 | 3:136864353 | AAAATTATCCGGGCG[C/T]GGTGGCACGCACCTG | 4690 |
rs529110316 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136871282 | GTGAGCGTCTGTAGT[C/T]CTAGCTACTTGCAAG | 4690 |
rs529147055 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136912992 | TCTTTACTCATTTTC[C/T]TACTTTCTTTCTACA | 4690 |
rs529196327 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136913638 | TTTCCTGGACATGCA[C/T]AGTGATTTTCTTTTG | 4690 |
rs529297842 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136910329 | AGAGTAACTTCCTGT[A/G]CAGCTCCATCCCTAC | 4690 |
rs529317150 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136907999 | ATCACTTACTCTCTT[C/T]GGGAATATTTTTTCA | 4690 |
rs529352646 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136900113 | TTTACACTTCCCAAG[C/T]TCTTGTTGGCTGTAG | 4690 |
rs529377349 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136915656 | AGGTTCACAGTTTCC[C/T]CAGGCTGTATAGGAA | 4690 |
rs529426994 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136860769 | TATTCCTGAAGGAAC[C/T]ACCTCCATGACCCAA | 4690 |
rs529445792 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136931017 | TTGCTTACTTTTTTT[A/T]TAGCGGAACAGTGTA | 4690 |
rs529530061 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136887033 | GTTATTAGTAGAGAC[A/G]GGGTTTCATTATGTT | 4690 |
rs529543545 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136879502 | TAGCCAGATATTATG[C/G]GTTGAGTTATATCTT | 4690 |
rs529596956 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136886164 | GGTTAATAAAATTGT[A/G]TTAACACTAATTTCT | 4690 |
rs529632494 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136867635 | TCATAGAATTATAGA[A/G]CATTATTGCTGGAAT | 4690 |
rs529636617 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136874771 | GTATATCATACAATA[G/T]ATTCCTGTGGAAGAC | 4690 |
rs529641187 | snp | C/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136900864 | CAGCAAAGAGGGACA[C/G]TTTGACTTCCTCTTT | 4690 |
rs529669594 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NCK1 | GRCh38.p7 | 3:136874147 | ATTGTGAATAAAGCT[A/G]TTGTCAACATTCATT | 4690 |
rs529713801 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136932934 | AAAACAACATGCTTA[A/G]ACTAAAGAATACTGA | 4690 |
rs529747281 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136916635 | GTGTTAGTTTGTGTA[C/T]GTTGTTTTGGAAATA | 4690 |
rs529752135 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NCK1 | GRCh38.p7 | 3:136925693 | TCGTTTTGTGCATCA[A/G]TTGTTCTTTTTGGTA | 4690 |
rs529753629 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136881804 | TTCCGTGGCTGGCTT[A/G]TTTCACTTAATGTCT | 4690 |
rs529758549 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | NCK1 | GRCh38.p7 | 3:136888517 | AAGTGATTCTCCTGC[C/G]TCAGCCTCCGCAGTA | 4690 |
rs529843722 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136938193 | TTTGTTTTACTAATA[C/T]GAGGTGTCTTATATT | 4690 |
rs529852464 | snp | A/C | | | intron-variant | NCK1 | GRCh38.p7 | 3:136919807 | AAGTCAGTAGTTATA[A/C]CCTAAGGAAAATGTA | 4690 |
rs529871695 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136894045 | CCTGCATTCCAGACA[C/G]ATTGCTCCCTAATCT | 4690 |
rs529933220 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136932427 | TGTGCTTTTTGTGTG[A/G]CAGCCAGAGTATCTT | 4690 |
rs529942692 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NCK1 | GRCh38.p7 | 3:136887992 | TCTTGTCGCCCAGGC[C/T]GGAGTGCAATGGCAT | 4690 |
rs529981762 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136947340 | AACAACAACAACAAA[A/G]CTAATTAAAAAGAAG | 4690 |
rs530023944 | snp | A/G | 0.00398564 | 0.0444627 | upstream-variant-2KB, intron-variant | NCK1 | GRCh38.p7 | 3:136930189 | ATGGATTTGTTTCGC[A/G]ATGGTTGTGCTGGTG | 4690 |
rs530025860 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136942526 | TCTCCCCATCTTTAC[A/C]GATGGCTTTATGTTG | 4690 |
rs530059676 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136934575 | ACAGGTGTGCACCAC[C/T]GCGCCTGTCCTGTTG | 4690 |
rs530155721 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136889327 | CAGCTGTTAAGGTGG[C/T]GCGTCTGGAGTTTGC | 4690 |
rs530157486 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136911567 | GTTCAAGTCTTTTGC[C/T]TATTCTAAAACCAGG | 4690 |
rs530178986 | in-del | -/TA | | | intron-variant | NCK1 | GRCh38.p7 | 3:136924886 | CCGGCATATATGGGT[-/TA]AAAAAGGGAAAAGGT | 4690 |
rs530257544 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136941652 | CCCATTAACCTAGAA[C/T]TGAAATTTTTGTTTT | 4690 |
rs530275093 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136902549 | AGGAGATACTTGATA[C/T]GATTTCAATTTTTAA | 4690 |
rs530289493 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136868131 | ATGTTGGCCAGGCTG[G/T]TCTCAAACTCCTGAC | 4690 |
rs530371890 | snp | A/G | 0.198014 | 0.244535 | upstream-variant-2KB, intron-variant | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136861505 | AAAAAAAAAAAAAAA[A/G]AGGCAGGTTACGGCG | 4690 |
rs530388825 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136868362 | AGACGGAGTCCTGCT[C/G]TGTCACTCAGGATGG | 4690 |
rs530392140 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136917540 | TGCCCTCCACCTTAT[A/G]GCCCATGTAACCAAA | 4690 |
rs530407693 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136951965 | TTCATGTACTTTTTC[C/T]CCTTAATGCATTGAA | 4690 |
rs530426453 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136895254 | GATTCCATTTGTATG[C/G]AATTCAAGAAAAGGC | 4690 |
rs530532682 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136904306 | TACAGGAATGTATCA[C/T]CGTGCCCAGCTAATT | 4690 |
rs530562039 | snp | A/C | | | intron-variant | NCK1 | GRCh38.p7 | 3:136926521 | AACTTGTGATTCACC[A/C]GCCTCAGCCTCCTGA | 4690 |
rs530574878 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136863001 | AACAAAAAACCATTT[C/T]GATAGGTTTTGTAAC | 4690 |
rs530614779 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136918703 | TTAAGCTCATCAGCT[A/G]TCGTTAGTTTAGTGT | 4690 |
rs530650532 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136919314 | GTTTGTCAAATTTTA[C/T]TCACAACAAACAGTG | 4690 |
rs530676315 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136926678 | AGTTTTTAAAATTAT[G/T]TACTTCTAAGTATTT | 4690 |
rs530709903 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136890155 | CCCACGGGGAGGCAG[C/T]TGAGGCCCGGCAAGA | 4690 |
rs530715894 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136869757 | GGTAAAATCTCTCTG[G/T]GGAGGGAAAGGAATG | 4690 |
rs530718951 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NCK1 | GRCh38.p7 | 3:136882808 | TCTAATTGCAGGGGT[A/G]GCTGGGAAGTGTAGT | 4690 |
rs530785639 | in-del | -/T | 0.00835141 | 0.0640778 | intron-variant | NCK1 | GRCh38.p7 | 3:136874058 | GTAGTTCCTTTTCAG[-/T]GATAGTAGTATTCCA | 4690 |
rs530843138 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NCK1 | GRCh38.p7 | 3:136871354 | AGTGAGCTATGATCG[C/T]GCCACTGTACTCTAG | 4690 |
rs530902310 | snp | A/C | | | intron-variant | NCK1 | GRCh38.p7 | 3:136933833 | CCTCAGCCTCCCAAG[A/C]AGCTGGGACTACAGG | 4690 |
rs530924096 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NCK1 | GRCh38.p7 | 3:136921468 | ATCTTTGCTTTATGC[A/G]GGGATGTGTGGGGCT | 4690 |
rs530942309 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136931376 | CTTATGCACAACAAG[C/T]CTAAGGAAACAAAGA | 4690 |
rs530957553 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136905514 | TGCCTCAGCCTTCCA[A/G]AGTGCTGGGATTACA | 4690 |
rs530960821 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136922214 | AAATTAGGCCCACCA[A/G]TGTTTGGCCCTTACC | 4690 |
rs530962834 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136913691 | TTTGTTTTTTTGAGA[C/T]GGAATCTCACTCTTT | 4690 |
rs530990737 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NCK1 | GRCh38.p7 | 3:136944842 | TGAAGTTGATGTAGC[A/G]TACATTTGTATTGAT | 4690 |
rs531037913 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136885085 | ATTTTTTCAGGTATA[C/T]ACTGAAATATTTACA | 4690 |
rs531051314 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136884517 | TGCAGGCTTGCTCAC[C/G]GCAACCTCCGCTTCC | 4690 |
rs531087128 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136891217 | CGGCTCATTTGCAAC[C/T]TCCGCCTCCTGGGTT | 4690 |
rs531097184 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136878523 | GGTTGCATAGGACTG[A/G]GAGTAGGGGAGGTTA | 4690 |
rs531153938 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136936714 | GTGGTTTTGATTTAC[A/T]TTTCTCTAATGACTA | 4690 |
rs531216627 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136897417 | TTTAAATAACAGCCA[A/T]TTTAACTTGGCTGAA | 4690 |
rs531245421 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136887261 | TGGCCTCCAACTCTT[A/G]GCCTCAAACGATCTT | 4690 |
rs531252119 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NCK1 | GRCh38.p7 | 3:136898432 | GGTATCAAGAAAAAA[A/G]CATTTCAAAACATTT | 4690 |
rs531291226 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136899788 | TCTGCACATTAGTGG[C/T]GACTGTTGAAAGTTC | 4690 |
rs531292371 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136892117 | GGTCTTGAACTTTTA[C/G]CCTCAAGGGATCCTC | 4690 |
rs531326879 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136938116 | TTGTTATCATGAAAC[A/G]GTTTTGGATTTTGTC | 4690 |
rs531328138 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136892461 | TCCTTATCAGAGGGA[A/G]TCAATTAGTCCAGGA | 4690 |
rs531365096 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136938862 | ATTTATGGTAACTTT[A/G]TAGAACATAACTACT | 4690 |
rs531366269 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136931206 | TGTTATTGAGTTTGG[A/G]TCATGAAGTAAAACT | 4690 |
rs531416611 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136941545 | AACAATCATGTTTGA[A/G]TTAATACCAACTTAG | 4690 |
rs531554309 | snp | A/C/T | 3.29491e-05 | 0.00405877 | stop-gained, missense, downstream-variant-500B | NCK1, LOC107986136 | GRCh38.p7 | 3:136945733 | GAGAGGATGAATTAT[A/C/T]ATTGATAAAGGGGAC | 4690 |
rs531575492 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136887674 | AATTTATGTTTCCAT[A/G]AAATTGGTGGTAGAA | 4690 |
rs531584493 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136899162 | ACTTCATGGACACTC[A/C]TGCCAGTGCGCTGCT | 4690 |
rs531617823 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136948135 | GGAGATAATCTATGT[A/C]AATAATTTACCATGG | 4690 |
rs531665561 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136916462 | CACCTCCCATTAGGC[A/C]CCATTTCCAACATGG | 4690 |
rs531670901 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136908230 | CAACCGTATCACTTC[G/T]TCATATTAACATTCC | 4690 |
rs531702609 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136909308 | TTGGGTCTTAAAAAT[A/G]CGTAGAAGTTTGCTG | 4690 |
rs531737269 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136885547 | TGGGCTCAAGTGATT[C/T]GTCTACCTTGGCCTC | 4690 |
rs531788133 | in-del | -/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136899868 | CATCTAAAGCCATCC[-/T]TTTTTTTTTTAGGGG | 4690 |
rs531795037 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136867458 | ACTGTGTTGTTCAGA[C/T]TGGTTTTGAATTCCT | 4690 |
rs531795072 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136860700 | TTCTTTTTAACCAGC[C/T]CTGGTGGAAATAAAG | 4690 |
rs531808768 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | NCK1 | GRCh38.p7 | 3:136902113 | GTCTTCCTTGACCCA[G/T]TGGTCATTCAGAAGC | 4690 |
rs531827182 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | NCK1 | GRCh38.p7 | 3:136915747 | TTTTTTTTTTTTGAG[A/G]TGGAGTCTCACTCCG | 4690 |
rs531846343 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136901215 | AATCATATTTGTTGA[C/T]TTGTGTAACCATCCT | 4690 |
rs531875460 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | NCK1 | GRCh38.p7 | 3:136880259 | CACTGCACTCCAGCC[G/T]GGGTGACAGAGCGAG | 4690 |
rs531877604 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136932248 | ATGCATTTGCAGACT[C/G]GGAGTCAGGATTTGA | 4690 |
rs531898273 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136940791 | CTCAAGTGATCCACC[C/T]GCCTCGGCTTCCTAA | 4690 |
rs531915642 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136923925 | ACAGAAGTATATATT[C/G]TACCTTTTCTGTAAG | 4690 |
rs531988693 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136884973 | TGATCTGCCCACCTC[A/G]GCCTCCCAAAGTGTT | 4690 |
rs531995394 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | NCK1 | GRCh38.p7 | 3:136872820 | AGGGTGCAAGCCCCA[A/T]GCCTTGGTGTTGATG | 4690 |
rs532035192 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136879604 | AGCAAAGACTTGGAA[A/C]CAACCCAAATGTCCA | 4690 |
rs532038314 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136868273 | CAGTTTCTTTCCCCT[A/G]TACTTGTTAGGTGTA | 4690 |
rs532058836 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136932697 | GGGCAAGACTAAATG[A/G]TCCTGGAAAGTCCCT | 4690 |
rs532121997 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136869029 | GAGCCCCTGAGTCCA[A/G]GAGTTTGAGACCAGC | 4690 |
rs532155239 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136916665 | ATGTATAACTTGGAG[G/T]GACACTGAAATATAA | 4690 |
rs532160985 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | NCK1 | GRCh38.p7 | 3:136875798 | CAGCTCTGCACCAAG[G/T]GGACCTAATAGACAT | 4690 |
rs532234719 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136933872 | ACCACACCTGGCTAA[A/T]TTTTTTTGTATTTTT | 4690 |
rs532237621 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136926490 | CCGTGTTAGCCAGGA[C/T]GGTCTCGATCTCCTG | 4690 |
rs532250296 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136917677 | TTTTGAGGGTCAAGT[C/T]ACCTAGGTCAGTTCT | 4690 |
rs532282864 | snp | A/G | | | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136948926 | ATAGCAATAATAAGT[A/G]GAAAATTAGAAATTA | 4690 |
rs532292837 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136894120 | CTAGTATATTTATTC[A/C]TTTCTTTGCCTGCTC | 4690 |
rs532307232 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136889289 | TTCAAGAATGAAGCC[A/G]CGGACCCTCGCGGTG | 4690 |
rs532317878 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136889399 | GTGGAATCGTGATCT[C/T]GCTGGTTTCAGGAGT | 4690 |
rs532326500 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136933111 | CTGGCAGCAGCTTAC[A/G]TGAGTAAAAAACTTA | 4690 |
rs532424008 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | NCK1 | GRCh38.p7 | 3:136888656 | AGCCACCGCACCCAG[A/C]CATATTGGAACACTT | 4690 |
rs532426815 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136927324 | TAAAAATTGTCCTCT[C/G]TGGTAATGGGTTTGT | 4690 |
rs532457986 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136889817 | TAGACGCAGGGTGCT[C/G]ATTGGTGTGTTTACA | 4690 |
rs532490362 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136890077 | TTGGGGAGGCTCGGG[C/T]GGCACAGCAGCCCAT | 4690 |
rs532493879 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136890164 | AGGCAGCTGAGGCCC[A/G]GCAAGAAATCGAGCG | 4690 |
rs532515842 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136922630 | TACAAATTACAACTC[C/T]GAAATACTATTTCTC | 4690 |
rs532539022 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136896020 | TGTTTTTTATTGATA[C/T]ATAATATTTTACATA | 4690 |
rs532539807 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136935583 | AAGGAAACTAGTTTA[A/G]TGGGGTCACGAAACC | 4690 |
rs532548187 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136895807 | TGACCTCAGGTGATC[C/T]TCCCACCTTGGCCTC | 4690 |
rs532618014 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136862395 | CACACACACACCCCC[C/T]TTCAGTCCGCTGTCC | 4690 |
rs532627864 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136896563 | TGTTTTTAAAGGCAG[C/G]GTCTCACTCTGTCAC | 4690 |
rs532658734 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | NCK1 | GRCh38.p7 | 3:136940691 | CTGGGATTACAGGCA[C/T]CTGACATCATGCCTA | 4690 |
rs532690566 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136903846 | TTCAGTATATCATCT[A/G]TTCCCTCTGTCTCTT | 4690 |
rs532709677 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136903373 | ATTGTAGGTAGTATA[G/T]AGGTGGGTCATGCTT | 4690 |
rs532726337 | in-del | -/T | 0.00676609 | 0.0577691 | intron-variant | NCK1 | GRCh38.p7 | 3:136878289 | GGCAGGCACCTATAA[-/T]TCCCAGTTACATGGG | 4690 |
rs532764283 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136951662 | TGTAATTCAGGGCAT[A/G]TACACAGACAGTAGT | 4690 |
rs532767235 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136942797 | CTTGTCCCAGTTGTT[A/G]TCCCTTGCCCCAGGC | 4690 |
rs532840466 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | NCK1 | GRCh38.p7 | 3:136905036 | TTTTCTTTTTGAGAT[A/G]GAGTCTCGCTCTGTT | 4690 |
rs532840551 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136913549 | TTGGAATTACAAGTT[G/T]GAGACACTGCACCCA | 4690 |
rs532877212 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136905426 | TCAGAATTCTCTTGT[A/G]TCTTTTTTTTTTTGA | 4690 |
rs532892836 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136898463 | CCACTTTTATTAAAG[A/G]TTTTGACAATGAAGA | 4690 |
rs532907141 | snp | A/C | | | intron-variant | NCK1 | GRCh38.p7 | 3:136873947 | GCATGAAAGTGGACT[A/C]ATACAGTAACCATAT | 4690 |
rs533010616 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136864268 | GAGGCCGAGGCAGGC[A/G]GATCACGAGGTCAGG | 4690 |
rs533046623 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136919431 | TTGACAGTTTTGTAG[A/G]TCTTACAAATACTGA | 4690 |
rs533057838 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | NCK1 | GRCh38.p7 | 3:136884295 | AGTTGGCTGCATCCA[G/T]TAGAGCTATCCCTTG | 4690 |
rs533152090 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136864029 | TGGCGTGAACCCGGG[A/G]GGCGGAGCTTGCAGT | 4690 |
rs533178608 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136870596 | AGAAACATTTAGAAT[A/G]TTTAGTGTACAACCC | 4690 |
rs533218084 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136877542 | CTAAAAATAATTGAA[A/G]GGACTTCTAAATAAA | 4690 |
rs533267651 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | NCK1 | GRCh38.p7 | 3:136923122 | GTGTGTGTGTGTGTG[C/T]GCGCCTGTGTGCATG | 4690 |
rs533315065 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136904850 | TTTTTTTTTTTTTAA[C/T]TATTACTTTTTGTCT | 4690 |
rs533374495 | in-del | -/TT | 0.00159617 | 0.0282053 | intron-variant | NCK1 | GRCh38.p7 | 3:136937028 | TTTAGTGTCAGTATC[-/TT]TAAGAATCCATTGCT | 4690 |
rs533384905 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136865216 | CTGCCTCGGCCTCCC[A/G]AAGTGCTGGGATTAC | 4690 |
rs533399384 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136936769 | GCCTGTTGGCCATTC[A/G]TATACCGTAGTTGGA | 4690 |
rs533409097 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136906674 | ATGGCAGTAGCAGTG[C/G]TGGGATAACCTTTAG | 4690 |
rs533411887 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | NCK1, LOC107986136 | GRCh38.p7 | 3:136945507 | TTGAAGATCTCTTTT[C/T]AATAATGAATAAGTT | 4690 |
rs533429306 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136922306 | AGGTAGTTCTCAGGT[C/T]CTTGGGAAGATAGTT | 4690 |
rs533470779 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136914453 | GTTGTCTAGGTGGAG[A/G]GAAGATTCTTGTTGC | 4690 |
rs533483360 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136891879 | TCCTACTCCATTTTT[A/G]TGTTGGATTTTTATT | 4690 |
rs533535584 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136941864 | CTTCTTTTTTGAGAC[A/G]GTCTTGCTCTGTCTC | 4690 |
rs533543924 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136923331 | GAGGCCGAGGCAGGC[A/G]GATCACGAGGTCAGG | 4690 |
rs533581518 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136915303 | CTGTGGGGGGTTGAC[A/G]TAGTAGCATTAATTA | 4690 |
rs533588566 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136872867 | ATGCTGCAAGTGCAC[A/G]GAAGTCAAGAATTGG | 4690 |
rs533603848 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136886128 | AAAGTCAAATGAGGG[A/T]ATACTTAAGATGGAA | 4690 |
rs533604014 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136878277 | AGCCGGATGTGGTGG[C/T]AGGCACCTATAATCC | 4690 |
rs533641787 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136885246 | ATTTTAGCTACATGA[A/T]GGGTTTAAGGGGTTT | 4690 |
rs533650413 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136879081 | GAAAGCTTCTCATAT[A/G]AGAAACCTCTTAAAA | 4690 |
rs533664271 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136882160 | TGCATAAGAGTTCCA[A/G]TATCATTACATTTTC | 4690 |
rs533702442 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136908271 | GCTGCAGGGACCCAT[A/G]TAGTCTTAATAATTA | 4690 |
rs533749107 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136882948 | TTTTTAAAGACAGTC[G/T]CATTCTGTTGCCCAG | 4690 |
rs533783383 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136886441 | ACTCATCTCTAGATT[A/G]CCTAATACATTGTAA | 4690 |
rs533815764 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | NCK1 | GRCh38.p7 | 3:136865391 | TGGCTGGCCTATATT[A/C]ATTTTTCAAAAATTT | 4690 |
rs533823487 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136931553 | TGGGGAGTTACTAAA[A/C]TTTCAGATCTTTGCA | 4690 |
rs533824313 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136899293 | AAAGATAAATCTCTT[C/T]TGGCGAGGACTGAGA | 4690 |
rs533845312 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136922656 | TTCTCCCCTATTAGA[C/T]TGGCAAAAATCCAAA | 4690 |
rs533882688 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136910932 | TTCCCATCCTGGCTT[C/T]TCCCCAGTCTCTGGT | 4690 |
rs533882754 | in-del | -/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136881089 | TTCTAACTCACATAC[-/T]TCCAGTCCATCAGCA | 4690 |
rs534016741 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136893639 | GAAGCTTTTTAGTTT[A/G]AGTCCCATCTCTTTA | 4690 |
rs534073274 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136891701 | TCACCAACACTTGTT[A/G]TTTTCTGTCATCATC | 4690 |
rs534115342 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136916896 | CTGAGTGATCACTAA[C/T]GGCAGAGCAGTGGCT | 4690 |
rs534161541 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136887531 | TTTTCCTGTGCCTTA[A/G]TATCGACTTGCAGTG | 4690 |
rs534166908 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | NCK1 | GRCh38.p7 | 3:136901272 | ATTGTGGTGTATTTT[A/T]TTTTTTTTAATGTTG | 4690 |
rs534184217 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136940724 | TAATTTTTGTATTTT[C/T]GGTAGAGACGGAGTT | 4690 |
rs534189280 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136907664 | GTTCTCTCTTAGGTG[A/G]TCTATTTGAAGTGTG | 4690 |
rs534221511 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136924392 | TACAGGACAAGTGAA[C/G]CCAGCTTCTTAAATA | 4690 |
rs534224175 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136870824 | TGCTTTGGTGTCTGT[C/G]ATCATGCTCTTCCTC | 4690 |
rs534224962 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136908365 | AAGGAATGATAGAGG[A/G]TTTTAAAAGATAAAG | 4690 |
rs534226906 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136900375 | AAGTCAGGTAGTTTT[A/T]TTCTTTTTGCTTAAG | 4690 |
rs534230316 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136880638 | CAAACTTTGTTTGTT[C/T]GTTTTTTTGAGGCAG | 4690 |
rs534288766 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136949809 | TACGCCAGAATTACT[A/G]ATGGTAAAATTGAAG | 4690 |
rs534330384 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136941931 | ACAACCTCCACCTCC[C/T]GGGTTCAAGCAATTC | 4690 |
rs534376471 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136946799 | TTTTATTATAACCTC[A/T]AAAAACCTATTTTAG | 4690 |
rs534425833 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136914200 | CAGAAAGCGCAATTA[A/G]CTGTCAGAGCATAGA | 4690 |
rs534448246 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136892960 | TCTTTTATCCCTCAC[A/G]CCACCACCCTTATCA | 4690 |
rs534545236 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136944212 | CAACCTCCGCCTGCC[A/G]GGTTCAAACGATTCT | 4690 |
rs534562815 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136913633 | TGCCTTTTCCTGGAC[A/G]TGCACAGTGATTTTC | 4690 |
rs534566019 | in-del | -/A | | | intron-variant | NCK1 | GRCh38.p7 | 3:136938779 | TAGTGATTGGTTAAC[-/A]AAAACATGATTGGAG | 4690 |
rs534573846 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NCK1 | GRCh38.p7 | 3:136925017 | GGGATAGCTGAACCA[C/T]AAGGCATAATATTGA | 4690 |
rs534605016 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136914978 | CTTGCTTCATCTCTC[A/G]TCATGTGATCTGTGT | 4690 |
rs534612922 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136890253 | CGGGTGCTAAGCCCC[A/C]CACTGTCCGGCCGGC | 4690 |
rs534677966 | snp | C/G | 0.00159617 | 0.0282053 | upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136862188 | GAGTGGGTTTCCTGC[C/G]CGCGCGGATCCGCCT | 4690 |
rs534743366 | in-del | -/TAGTAGTATTCCATTGG | 0.00795532 | 0.062565 | intron-variant | NCK1 | GRCh38.p7 | 3:136874061 | GTTCCTTTTCAGTGA[-/TAGTAGTATTCCATTGG]ATGAATATAATGTAA | 4690 |
rs534757556 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NCK1 | GRCh38.p7 | 3:136889290 | TCAAGAATGAAGCCG[C/T]GGACCCTCGCGGTGA | 4690 |
rs534770317 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136918884 | GTTTTCACTAATGAC[C/T]GTGTAACCATGTGAG | 4690 |
rs534780163 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136869475 | ACTTAAACCCGGGAG[A/G]CAGGGGTTGCGGGGT | 4690 |
rs534781475 | in-del | -/AG | 0.00159617 | 0.0282053 | intron-variant | NCK1 | GRCh38.p7 | 3:136921676 | CTATTGCAGTAGGGA[-/AG]AGTGTCCAGTGTGAA | 4690 |
rs534800295 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NCK1 | GRCh38.p7 | 3:136876540 | TTATGAACATCCTTC[C/T]GTGTCAGTGTATATA | 4690 |
rs534802635 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136872103 | CTTTGGAACTGGGTA[A/G]CAGGCAGAGGTTGGA | 4690 |
rs534847723 | snp | A/G | 0 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136909818 | TTAAACTTTTTATTA[A/G]TGTATAGTATCCTTC | 4690 |
rs534853456 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136917752 | TTCCCACAGCACTTA[A/C]GAGTTAGAGGTGGTT | 4690 |
rs534900222 | in-del | -/AG | | | intron-variant | NCK1 | GRCh38.p7 | 3:136869657 | TAAAGTTTCTGTAAC[-/AG]AAACCATGTATGGTT | 4690 |
rs534966070 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136882438 | ATTCTTCACACAGCA[A/G]CACACAACAGCCAGA | 4690 |
rs534989191 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136889466 | TAAAGGCAGTGTGGA[C/T]CCAAAGAGTAAGCAG | 4690 |
rs535014233 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136863109 | GTAACCGTAGGAACG[C/G]TCTCGGTGTCAAACT | 4690 |
rs535024058 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136866780 | CACCACGCCTGGCTA[A/G]TTTTGTATTTTTAGT | 4690 |
rs535050175 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136912577 | TTCAAATCCCTGTAG[A/T]GAATTTTCCATTTTA | 4690 |
rs535076913 | in-del | -/AT | 0.0103295 | 0.0711199 | upstream-variant-2KB, intron-variant, nc-transcript-variant | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136861738 | CCTCAAATTAAGCAC[-/AT]GTCTTACATTTCTCC | 4690 |
rs535084157 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136927434 | GAGTAGAACATTTTT[C/T]ATTGGGTAGTGAACT | 4690 |
rs535089270 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136936855 | GTTCTAAGAGTTGTT[G/T]ATATGTTCTGGATAC | 4690 |
rs535100903 | snp | A/G | 0.0023933 | 0.0345097 | upstream-variant-2KB, intron-variant | NCK1 | GRCh38.p7 | 3:136929063 | CAAATATGAAATACT[A/G]TTGACTCACTACTTT | 4690 |
rs535148211 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136885352 | TAATCTAGGGCACAT[C/T]ACTTAACTTTTTTGA | 4690 |
rs535265378 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136883000 | CTCAGCTCACTGCAA[C/T]CTCCGCCTCCTGGGT | 4690 |
rs535265661 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136944045 | TAGAATGTTGGAGAC[A/G]AAGGATCAGATAATA | 4690 |
rs535303800 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136901666 | TTTTCCAGTATGTTA[A/G]TGTATCGTTGTTTGT | 4690 |
rs535310030 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136897738 | AATTAATTATTTTCA[C/T]GTTAACATAGATGTT | 4690 |
rs535315565 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136896019 | TTGTTTTTTATTGAT[A/G]TATAATATTTTACAT | 4690 |
rs535334710 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136904447 | CGTGAGCCACCGTAC[C/G]TGGCCTTCTTTCAGC | 4690 |
rs535344655 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | NCK1 | GRCh38.p7 | 3:136889924 | CACCAGACTCAGGAG[C/G]CCAGCTGGCTTCACC | 4690 |
rs535344800 | in-del | -/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136932322 | CCAAATTTTTATTTA[-/T]TTTTGCCAGGCAGTT | 4690 |
rs535375625 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136942929 | GTCCTTCAGGGAGCT[G/T]CCAGACAAGTTGAAA | 4690 |
rs535486931 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136877987 | TACTATTTGGCAGTA[A/T]AAAGGAATATAGAAC | 4690 |
rs535489492 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136946694 | GTAAGAAGGTAGTCA[C/G]TGTAGTCCTTATGAC | 4690 |
rs535513807 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136884649 | TTTCATCATGTTGGC[C/G]AGGCTGGTCTTGAGG | 4690 |
rs535548378 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136906749 | TGGACAGGCCAATCC[C/T]CCAGGCTTGCAGGTG | 4690 |
rs535647419 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136944494 | AGAAAAAATAAATAA[A/G]TTACCAAAATGTTAC | 4690 |
rs535656044 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136934122 | TACACATAGACTTCT[A/G]AAAATTTTTTACAAG | 4690 |
rs535668775 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136865260 | CACGCCCGGCCTGTA[G/T]TTTTAGTAGAGACGG | 4690 |
rs535702562 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136914525 | AAAGGTTTCATTAGA[A/G]TTAGAAGAGTTCTTT | 4690 |
rs535708275 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NCK1 | GRCh38.p7 | 3:136921757 | TGAGTATGCTAAGGG[A/G]AAGACACTGCTAAGG | 4690 |
rs535849828 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136937691 | ATGTATCTTATTCTT[A/C]TTAATGCTGTTATAA | 4690 |
rs535870229 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136916083 | CATGGAACAACAGCT[A/G]TCACAGAACAACAAG | 4690 |
rs535873071 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136866814 | GATGGGGTTTCACCA[C/T]GTTGGCCAGGCTGGT | 4690 |
rs535898746 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136892309 | GGTTACCTTTTCACT[A/G]TATTAATTTAGTGTC | 4690 |
rs535906126 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136908574 | ACCAAATCTGTGGAT[A/T]CTGAGTAAAACAAGA | 4690 |
rs535910536 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136866266 | GATTCTTATTTACTC[G/T]TTGTATTTTTGTACC | 4690 |
rs535923091 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136898888 | CTTACAAAGCTCTCA[C/T]TGAGATCTTGAAGAG | 4690 |
rs535948910 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136873011 | AGAAGGGAAATGTGG[G/T]GTCAGAGCCCCCACA | 4690 |
rs535962121 | snp | C/T | 0.0269139 | 0.112839 | intron-variant | NCK1 | GRCh38.p7 | 3:136899419 | ACCTTCATTTCTTTT[C/T]TTTTTTTTTTTTTTA | 4690 |
rs535994832 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136876585 | TTTTGTTTTTTTTTT[A/G]AACCAAAAAACTTTG | 4690 |
rs536045216 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136940099 | GACTCCTGGGCTCAA[A/G]TGATCCCCCGACCTT | 4690 |
rs536047194 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136913825 | AGGCGCCCGCCACCG[C/T]GCCCAACTAATTTTG | 4690 |
rs536074775 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136864723 | ATAAAGAAAAGAGAT[A/G]CTTAGTGATACTTCA | 4690 |
rs536082866 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136906159 | TTCTAGGTATGTGTC[A/T]TAGTGTAGTCTCTGT | 4690 |
rs536135225 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136887391 | TTTTCTCCTGATAAA[C/T]AGCAGCCTAAGTAAG | 4690 |
rs536160125 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | NCK1 | GRCh38.p7 | 3:136871102 | TACTAATTTTTTTTT[A/T]AAAAATTGTTTAGTC | 4690 |
rs536160210 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136878344 | AACTGGGGAGGTGGA[C/G]GTTACAGTGAGCCAA | 4690 |
rs536192575 | in-del | -/C | | | intron-variant | NCK1 | GRCh38.p7 | 3:136886342 | GACTCCTTGCAGATA[-/C]CAAAATTTGAGGATG | 4690 |
rs536220452 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136883923 | ATTATAATTAATAGA[C/T]TGGTAAAGAGGATAG | 4690 |
rs536244648 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136907702 | CCTCACTATTTTGTT[C/T]CCTTTTCATGGAAGA | 4690 |
rs536257256 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136911326 | TTTTGAGGACCCTCC[A/G]TACTCTTTTTCATAA | 4690 |
rs536268834 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NCK1 | GRCh38.p7 | 3:136916998 | ACAGGGCTGAAAACT[A/G]GGGTAAGATAAACAA | 4690 |
rs536306232 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136915418 | AGATGTGCCTATGCA[A/G]TAATATTGTAGAAGT | 4690 |
rs536309176 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136942210 | TATCTGGGAATGTCT[C/T]ATGTTCTCCTTCATT | 4690 |
rs536327347 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136881469 | ATGATCTGCCCGCCT[C/T]GGCCTCCCAAGTGCT | 4690 |
rs536363341 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136888910 | AAGGTTTGCTCTGTT[G/T]CTTGGACTGTAGTGC | 4690 |
rs536418785 | snp | C/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136874368 | TTTAGTAGAGATGGG[C/G]TTTCACTATGTTGGC | 4690 |
rs536426273 | in-del | -/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136890652 | TTACAGGCATTTGAG[-/T]TTTTTTCTCCCTTAT | 4690 |
rs536435829 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | NCK1 | GRCh38.p7 | 3:136931714 | AACTCTAGCAAATCT[G/T]ACATTCTGGTGGAGA | 4690 |
rs536461035 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136921542 | ATGCTTCTTTGGATA[C/T]TCTATGCATGTCCAA | 4690 |
rs536464471 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136940834 | ACAGGCATGAGACAC[C/T]GCGCCGGGCCTATGC | 4690 |
rs536472179 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136923412 | TACAAAAAAATTAGC[C/T]GGGCATGGTGGCGGG | 4690 |
rs536520797 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136901325 | TTGAGAATTTTTATC[C/T]CTGTGTTCATTAGGG | 4690 |
rs536558806 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136902141 | AGCATGTTGTTTAAC[C/T]TCTGTGTATTTATAT | 4690 |
rs536595577 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant | NCK1 | GRCh38.p7 | 3:136930508 | AGGAAGCTCACTGAG[A/T]ATTATCCTGAGCTGT | 4690 |
rs536626417 | snp | C/T | | | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136949248 | ACTTGTATTATTTTA[C/T]CTCTAGAGCATCTTG | 4690 |
rs536686583 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136874407 | CTGGTCTCGAAGTCC[C/T]GACCTCAGGTGACCC | 4690 |
rs536747427 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136890779 | CATTTTTAAGTGTAC[A/G]GTGATAAGTATATTC | 4690 |
rs536856542 | snp | C/T | 0.0023933 | 0.0345097 | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136949917 | CCACTGGGTGGCAGC[C/T]ATGGCTTCTCCCACT | 4690 |
rs536870170 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NCK1 | GRCh38.p7 | 3:136889419 | GTTTCAGGAGTGAAG[C/T]TGTAGACCTTCGCGG | 4690 |
rs536875345 | snp | C/T | 0.0023933 | 0.0345097 | utr-variant-5-prime, upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136862230 | GTGCCCCGCCTCTCT[C/T]CCAAGAGCTACGCGG | 4690 |
rs536883714 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136903046 | TGCTCACAGTGGGGT[C/G]CTGGTGTCCCTAACT | 4690 |
rs536939150 | in-del | -/A | 0.00517822 | 0.0506191 | intron-variant | NCK1 | GRCh38.p7 | 3:136919358 | TGTAAAATAAACAGC[-/A]AAAAAAATATATGGC | 4690 |
rs536989566 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136947531 | TTAAATTCATTGCCG[A/G]TATTTAAATATTAGG | 4690 |
rs537029696 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136870122 | CGAGGCAGGTGGATC[A/G]CTTGAGGTCAGGAGT | 4690 |
rs537066795 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136896912 | CTGATTTCTTTTCCT[A/G]TGGATAACTACCCAG | 4690 |
rs537092054 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136889988 | TGCCTGCCAGTCCTG[C/T]GCTGTGTGCCCGCAC | 4690 |
rs537121282 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136903421 | ATCTATTCAATCAGT[A/G]TCTATCTTATTTATT | 4690 |
rs537140314 | in-del | -/TTGA | | | intron-variant | NCK1 | GRCh38.p7 | 3:136927526 | CTCTTTATTGATTGG[-/TTGA]TTGATTGATTGATTG | 4690 |
rs537149473 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136870146 | CAGGAGTTCGAGACC[A/G]GCCTGGCCAACATGG | 4690 |
rs537151822 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136904551 | GCGTTCCTTTATAAG[C/T]GACTAGATGCTTTTC | 4690 |
rs537153079 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136896045 | TACATATTTACGAGG[C/T]ACATGTGACATTTTG | 4690 |
rs537233954 | in-del | -/ATTC | | | intron-variant | NCK1 | GRCh38.p7 | 3:136925666 | TATAATTCCCTGGAG[-/ATTC]ATTCATCCAGGTCGT | 4690 |
rs537236051 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136862476 | TAGCCCCGGGGGCGC[A/C]GTCTGCAGGCTCGGA | 4690 |
rs537275699 | snp | A/C/G | 4.95441e-05 | 0.00497694 | missense | NCK1 | GRCh38.p7 | 3:136928189 | GGAAAAACAGTGCTC[A/C/G]GAAAGCATCTATTGT | 4690 |
rs537287236 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136911399 | AATGTTTGCTTTTCT[C/T]TGCATCCTCATCAAC | 4690 |
rs537322946 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136876673 | TTATTCCTACAAAGA[A/T]TATACGTATTTTTTT | 4690 |
rs537346713 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136875275 | GCTTAAGGAGATTTT[A/G]GGCTGAGACAATGGG | 4690 |
rs537348669 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136867901 | TTCAGGGCAGGGGAA[C/G]CTTCATATTTACATT | 4690 |
rs537436579 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NCK1 | GRCh38.p7 | 3:136930164 | GTAACTTAAATATCC[A/G]GTGTAATTAATGGAT | 4690 |
rs537477090 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136922533 | AGGATATGGGGAAAA[G/T]ATATGAACAAGCACT | 4690 |
rs537488241 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | NCK1 | GRCh38.p7 | 3:136905182 | CACACCTGGTGTGGC[A/G]GCAATTTTTTTGTAT | 4690 |
rs537495132 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136927740 | TGGCCAAGCTGGTCT[C/T]GAACTCAACCTCAAG | 4690 |
rs537497763 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136937513 | GGAAAAAACAAAATG[A/G]TTGAACTTTAGTAAG | 4690 |
rs537507726 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136912750 | AGCCTCAAACTCCTG[A/G]GCTCAAGCAGTCCCC | 4690 |
rs537545653 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | NCK1 | GRCh38.p7 | 3:136913108 | CGTCTTCTGATCTTT[A/C]TCTGGGAAGGTTTCT | 4690 |
rs537562640 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136885510 | GGATTTTGCCATGTT[A/G]CCCAGGCTGGCCTCC | 4690 |
rs537661019 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136877373 | TTGAAGATAAGCAAT[A/G]TATTTCTGAGAAATT | 4690 |
rs537670196 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136919819 | ATACCCTAAGGAAAA[C/T]GTAAGGAACCAGCTA | 4690 |
rs537695830 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136891508 | AACATGGGTGTACAA[A/G]TATCTATTTGAGTTC | 4690 |
rs537705008 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136935831 | AATGTTTCCATCACC[C/T]CAAAAATAGTCACTC | 4690 |
rs537725857 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136890274 | TCCGGCCGGCAGGGC[C/T]GGCCGGCTGCTCTGA | 4690 |
rs537727098 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136883627 | CGTGCTCACTGTTGT[A/G]TCCCTGCATTAATTG | 4690 |
rs537761259 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136898627 | ACAAAACATCTTTGC[A/G]ATAAAACTGATAATA | 4690 |
rs537792591 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136872100 | CAACTTTGGAACTGG[G/T]TAACAGGCAGAGGTT | 4690 |
rs537825925 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136938468 | GCAATGTTCTTCCTT[A/C]TTATTTCAGCTTTCA | 4690 |
rs537827744 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136947438 | AATATATACCATTAT[C/T]TTTAGCAGTATACTT | 4690 |
rs537921552 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136878486 | GAAGTATCCAGAAAT[A/T]GTGTATTTGTAGAGA | 4690 |
rs538018438 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136945208 | TAAACTAAGACAAGA[A/G]GAGTATGGGTGTGGT | 4690 |
rs538023892 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136880814 | GGTTCTCACTTCTTT[A/G]CCCTGGCTGGTCTTG | 4690 |
rs538039773 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136887223 | GTACAGTGGCTGTTC[A/C/T]CAGGCACCATCATAA | 4690 |
rs538060869 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136936900 | AATTATGATTTGCAA[A/C]TATTCTCTTCTAATT | 4690 |
rs538113655 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136914699 | AATGTGACAACTAAT[A/G]TGACAACTTCTGGCT | 4690 |
rs538152224 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136915226 | GGGGTAGTAGTAGTG[A/T]GAATGGAGATACATG | 4690 |
rs538157400 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136872023 | CATGAAAACAGATTA[A/T]TACAGTAAATTGGTA | 4690 |
rs538177116 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136868839 | CTGTAATGTTCTTTT[C/T]CTCTTTTGAGTGTTA | 4690 |
rs538183233 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136944524 | CGGTTTAAAAGTTGT[A/G]GCAGAGTTAAAGTAA | 4690 |
rs538193312 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136893507 | ATTGTTTTTTTCTTG[C/T]TGATCTGAGTTCCTT | 4690 |
rs538203942 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | NCK1 | GRCh38.p7 | 3:136925172 | GAATGCTATTTTTGT[A/C]CATTCTGGGGAGGAC | 4690 |
rs538227612 | in-del | -/TTGT | | | intron-variant | NCK1 | GRCh38.p7 | 3:136888864 | TCAATGTTTTTTTTG[-/TTGT]TTGTTTTGTTTTTTT | 4690 |
rs538252061 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136931858 | GGCGTGGCAGCTCAA[A/G]CCTGTAATCTCAGCA | 4690 |
rs538275724 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant, nc-transcript-variant | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136861658 | TACTGCCGCCAAGAA[G/T]GTAAGCTGCCCAAGC | 4690 |
rs538291496 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136887451 | AAAGGGCAGGAAGGT[G/T]AGGAAAGAAGTGTTT | 4690 |
rs538296383 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | NCK1 | GRCh38.p7 | 3:136902199 | GTTTTTTTTTTTTTT[G/T]TTTGTTTTTGTTTTT | 4690 |
rs538310540 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136867771 | CCCTTGATCTTCTGA[A/C]GCAAGTTCTGTGTGT | 4690 |
rs538349278 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | NCK1 | GRCh38.p7 | 3:136866989 | AATTTGTTGAATTTT[C/G]GCTTTTGGTCCTTTG | 4690 |
rs538377090 | snp | A/G | | | upstream-variant-2KB, intron-variant | NCK1 | GRCh38.p7 | 3:136930085 | AACCTGTAAAGAGAT[A/G]TAAGTCCAGCTTTTA | 4690 |
rs538442143 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136914826 | GGAAGTGGGGCCTAA[C/T]GGGAGGTGTTTGGGT | 4690 |
rs538448438 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136924318 | GTTTATAGGAGATAG[A/G]GGGGATAGAGGAACA | 4690 |
rs538461313 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136935593 | GTTTAGTGGGGTCAC[A/G]AAACCTCTGGTACAA | 4690 |
rs538496758 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136873783 | GATGATTTTTAAAAA[C/T]GGGAGTTTCCCTGCA | 4690 |
rs538503645 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136865368 | GAGATTACAGGTGTG[C/T]GCCACCGTGGCTGGC | 4690 |
rs538511794 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136932513 | ATGTAGATGAAGTGA[A/G]CAGATGGACATATAA | 4690 |
rs538533593 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136906813 | AGGCAGGTTGAATAG[A/G]TCCAATCTCAGACCC | 4690 |
rs538621114 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136869133 | TAGTCCCAGCTACCC[A/G]GGAGGCAGAGGCAGG | 4690 |
rs538633901 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136922147 | GGGTTTGTTATTGGC[A/G]TTTATCTGGAAGAGA | 4690 |
rs538637560 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | NCK1 | GRCh38.p7 | 3:136886787 | TTACTTAGGCAGAGT[G/T]TGGAACTGTCCTGTA | 4690 |
rs538701706 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136908753 | AAGAAGAGAAAAGAT[A/G]TTAAAAGTAGACAGC | 4690 |
rs538705293 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136916763 | AGTTTGTTTAGTTCA[A/C]AAAATTGAAATTGTA | 4690 |
rs538708065 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136926338 | GGAGTGCAGTGGCGC[A/G]ATCTCGGCTCACTGC | 4690 |
rs538729006 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136874208 | TGAGATAGAGTCTTG[C/T]TCTGTCACCCAGGCT | 4690 |
rs538732552 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136875488 | GGAAAACAAAAAAAG[G/T]CAGGGATTGCAATCC | 4690 |
rs538738258 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136909647 | TCCTCTTTTGTCTGA[C/T]TATTCTACCCATTAT | 4690 |
rs538786176 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136913813 | AGCTGGGACTACAGG[C/T]GCCCGCCACCGCGCC | 4690 |
rs538799280 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NCK1 | GRCh38.p7 | 3:136889366 | ATGTTCAGATGTGTT[C/T]GGAGTTTCTTCCTTC | 4690 |
rs538828198 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136866022 | TGATTTTTCTCTCTA[C/T]TTAGTATGTCTTCCT | 4690 |
rs538854610 | snp | A/C | | | intron-variant | NCK1 | GRCh38.p7 | 3:136893324 | AACATCTATTTTTTG[A/C]TTTTTTGATTGTGGC | 4690 |
rs538857866 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136924902 | AAAAAAGGGAAAAGG[A/T]CAGGAGCCCTTGATT | 4690 |
rs538861678 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | NCK1 | GRCh38.p7 | 3:136916179 | TCGACATGAGATTTG[G/T]GTGGATACACAAATC | 4690 |
rs538875261 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136894215 | CTACTGTGGAAGCAT[C/T]ACCCTCAGGATCTCT | 4690 |
rs538931914 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136888994 | CCTGCCTCAGTCTCC[G/T]GAGTAGCTGGGACTG | 4690 |
rs538940880 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136894476 | TATGATTTTGTTAGC[C/T]GGACAGTTTCTAGGT | 4690 |
rs538992794 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136891415 | GCTGGGATTACAGGC[A/C]TGAGCCACCACGCCT | 4690 |
rs538995202 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136925271 | TCTTTAATTATAAAG[A/G]TATTCAGGATCTTTT | 4690 |
rs538996407 | in-del | -/C | 0.00517822 | 0.0506191 | intron-variant | NCK1 | GRCh38.p7 | 3:136913911 | TGACCTTGTGATCCT[-/C]GGCCTCCCAAAGTGC | 4690 |
rs539012022 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136926917 | TATATGTCTATTAAA[G/T]CAGACTTGCTGGTTG | 4690 |
rs539048890 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136918774 | AGGAAAGCCAAAAGA[C/T]TGGACACTCCTGCCT | 4690 |
rs539058627 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136936380 | TATCACATTTTGTTT[A/G]TCCACTCATCTGTTC | 4690 |
rs539059195 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NCK1 | GRCh38.p7 | 3:136876476 | AGGGGATATCACCAC[C/T]GATCCCACAGAAATA | 4690 |
rs539185687 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136943912 | AGTGGGCTGTGATCT[C/T]GGTTGCTGCATATAG | 4690 |
rs539317372 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136911557 | AGAAATGTTTGTTCA[A/G]GTCTTTTGCCTATTC | 4690 |
rs539332659 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136895169 | CATGAGCCACTGCGC[A/C]CAGCAAGCTGATTTT | 4690 |
rs539348364 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136912437 | TGGCATTCCCACAAT[A/G]TGTGTGTTCGTTCTC | 4690 |
rs539367541 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136949738 | TCAACAAATTCCCTA[A/G]TGCTGCCTAAGCATA | 4690 |
rs539401998 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136948532 | ATGTTGGGTCCAGTC[A/G]TGCTTGATTGGAAAT | 4690 |
rs539406761 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136892126 | CTTTTAGCCTCAAGG[G/T]ATCCTCCTGTCTCAG | 4690 |
rs539487502 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136883741 | GTTGAATTTTAACCA[A/G]GGGCTCTTATGATAA | 4690 |
rs539496608 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136896737 | AATTCCTGGGCTCAA[A/G]CAGTCCTCCTGCCTC | 4690 |
rs539530103 | snp | C/T | | | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136950704 | GCCTGGTGTCTGTAT[C/T]GTGACACACTACTCT | 4690 |
rs539536020 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136890335 | ACCCGGAACTCCAGC[G/T]GGCCCGCCAGCGTTG | 4690 |
rs539600104 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136907459 | TGGTTTCTAGGCACC[C/T]CTTTATGTTAGACTC | 4690 |
rs539606885 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136931977 | ATGCAAACATTAGCT[A/G]GGCGTGGTGGCGGGT | 4690 |
rs539671567 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136921655 | AGGACAGATTTTATT[C/T]AGTAACTATTGCAGT | 4690 |
rs539672253 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136863083 | GCTGGGTTTTGTTCA[A/G]GGGTGAGGACGTAAC | 4690 |
rs539681343 | in-del | -/TTTG | | | intron-variant | NCK1 | GRCh38.p7 | 3:136864958 | TATTTTTCTTTTTCT[-/TTTG]TTTGTTTTTTTTTTT | 4690 |
rs539705137 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136862634 | TGTGTCGGGCTGAGA[G/T]CCCGGGCGGCCGCCC | 4690 |
rs539754544 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136877364 | GTCAGCTGTTTGAAG[A/G]TAAGCAATATATTTC | 4690 |
rs539827534 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136877812 | TTGGCAGCATCAGGT[A/G]TTTTTGGCAGGGAGG | 4690 |
rs539848532 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136903262 | TGTTTGATACAAGTA[C/T]AGCTACTTCTAGTCA | 4690 |
rs539874760 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136906879 | ATGCTAGGTGATCGC[C/T]AGGCCCACGGATTGC | 4690 |
rs539907655 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136905208 | TGTATTCTTTGCAGA[A/G]ACAGGGTTTCACTGT | 4690 |
rs539909068 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NCK1 | GRCh38.p7 | 3:136913740 | GTGGCGCGATCTCGG[C/T]CCACTGCAAGCTCCG | 4690 |
rs539945079 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136906038 | GTATCTGTGCCTCTG[A/G]TGTAACAGTTGCTCC | 4690 |
rs539964462 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136896040 | TATTTTACATATTTA[A/C/T]GAGGCACATGTGACA | 4690 |
rs539983227 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136900780 | TGTCCTGCAACTTTA[C/T]TGAATTTATTTAGCA | 4690 |
rs540013499 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136920730 | AGAGCAATAATCTTG[C/T]TAAATTATGAGCAAT | 4690 |
rs540021850 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136864103 | GAGACTCCGTCTCAA[A/G]AAAATAAATAAAATG | 4690 |
rs540059270 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136913561 | GTTTGAGACACTGCA[C/T]CCAGCCCTTTTTATT | 4690 |
rs540077430 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136922062 | TGCTGGGATTACAGG[C/T]GTGAGCCACCGCGCC | 4690 |
rs540148290 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NCK1 | GRCh38.p7 | 3:136884576 | CTCCAGAGTAGCTGG[A/G]ATTAGAGGCGTGTGG | 4690 |
rs540156194 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136884963 | TGACCTCAAGTGATC[G/T]GCCCACCTCGGCCTC | 4690 |
rs540167647 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136936866 | TGTTTATATGTTCTG[A/G]ATACTAGACCCTTAT | 4690 |
rs540175677 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136883861 | CCAACACAAATTGAT[A/G]TGTGACTTAAGGGGA | 4690 |
rs540249772 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136923604 | AATAAATGGCTGTCC[A/G]GTGGGGTGGATGGGA | 4690 |
rs540255884 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136899054 | TCAGCCAAACATTTC[G/T]CTGGTACCACAGTCA | 4690 |
rs540288436 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136915584 | TATTAGTCTGCTCTC[A/T]CGTTGCTATAAATAA | 4690 |
rs540330389 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136864306 | GACCAGCCTGGCCAA[C/T]ACGGTGAAACCGCGT | 4690 |
rs540376461 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NCK1 | GRCh38.p7 | 3:136931973 | AAAAATGCAAACATT[A/G]GCTGGGCGTGGTGGC | 4690 |
rs540400744 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136937943 | ACAATGTTAAATAAA[A/C]GTGGTGGAAGGAGAG | 4690 |
rs540402382 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136922029 | ACCTCGTGATCTGCC[C/T]GCCTCGGCCTCCCAA | 4690 |
rs540407538 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136921216 | AACAGTAACTCCCCT[A/G]TATATAGATAGCCAA | 4690 |
rs540414443 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NCK1 | GRCh38.p7 | 3:136929267 | ACATTATTGTTATTC[C/T]AGAATGTTCTTCTAA | 4690 |
rs540437842 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136930997 | TTTTTTTTTTTAACT[A/G]CTTTTTGCTTACTTT | 4690 |
rs540495362 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136899647 | GAATACCACCATTGT[C/T]TTTCTTAGTAATCTT | 4690 |
rs540523090 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136912210 | CTCTGTCACCCAGGC[G/T]GGAGTGCAGTGGTGT | 4690 |
rs540569643 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | NCK1 | GRCh38.p7 | 3:136928566 | CACCAAGGCAACTTA[C/T]GTACATGGCACATAA | 4690 |
rs540577510 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136892425 | CTGGATTATCTGAGT[C/G]GGCTCTGGTAATCAC | 4690 |
rs540587592 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136898351 | CCAGTGAGCTGAGAT[C/T]GTGCCAGCCTGGGTG | 4690 |
rs540611424 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136908553 | GAGTCACACATGAAA[C/T]TGGAGACCAAATCTG | 4690 |
rs540654021 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NCK1 | GRCh38.p7 | 3:136880430 | GACACAGAGACAGAA[C/T]ACCAGGGAGAAGATG | 4690 |
rs540677659 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | NCK1 | GRCh38.p7 | 3:136873148 | AAAGCTGCAGACACT[C/G]AATGCAAGCCTGTGA | 4690 |
rs540705315 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136872624 | GTCTGCAGGGCGTGT[C/T]GGAGGTCTTCATGGC | 4690 |
rs540714397 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136880202 | AGGCAGGAGAATGGC[A/G]TGAACCCGGGAGGTG | 4690 |
rs540740946 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136887535 | CCTGTGCCTTAGTAT[C/T]GACTTGCAGTGAATT | 4690 |
rs540750736 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136879418 | AGATATACGCTTTCA[A/G]TTAAAGCCTAGTCAG | 4690 |
rs540771635 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136923131 | TGTGTGCGCGCCTGT[G/T]TGCATGTGTGTGTGT | 4690 |
rs540816908 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136874775 | ATCATACAATAGATT[C/T]CTGTGGAAGACTGAA | 4690 |
rs540860389 | in-del | -/A | | | intron-variant | NCK1 | GRCh38.p7 | 3:136919055 | ACTACTGATTTACAC[-/A]ACACAAATGAAACAA | 4690 |
rs540899051 | snp | C/T | | | downstream-variant-500B, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136951706 | AAAGAACAGAGAAGA[C/T]GGGGAGTTTTATTAT | 4690 |
rs540941790 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136860254 | GTCCATACCAGTCAT[G/T]ATAAAATATGCAGTT | 4690 |
rs540976521 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136866448 | TAGTAGCTGGGACTA[C/T]AGGCATGCGCCACCA | 4690 |
rs540978075 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136889130 | CTCCTGCGCTCAAGT[G/T]ATCTTCCCATCTCTG | 4690 |
rs541022237 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136903169 | GAATTGTTAAATCCT[C/T]CTCCTGAATTTTTCC | 4690 |
rs541036844 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136933525 | AAAGAGAAGTAAAGA[C/G]CAGTGGGTGGTAGTG | 4690 |
rs541042668 | snp | C/T | | | intron-variant, upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136862410 | CTTCAGTCCGCTGTC[C/T]GTCCATACAGCCTGT | 4690 |
rs541060868 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136895705 | GGGTAGCTGGGATTA[C/T]AGGTGCGTACCACCA | 4690 |
rs541079373 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136889806 | AAACCCTGAGCTAGA[C/T]GCAGGGTGCTGATTG | 4690 |
rs541129360 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136894646 | ATTGAGGTACTGTAA[A/G]TGTCCAGAGACACTC | 4690 |
rs541149972 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136949057 | AGACACATGAGACAT[A/G]GATTAGAAAACATGT | 4690 |
rs541169008 | snp | C/T | 0.00199481 | 0.0315187 | upstream-variant-2KB, nc-transcript-variant | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136862015 | CCCAGCGCTTCTCAC[C/T]CTCTAGCTCTCTACT | 4690 |
rs541221260 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136908972 | CACTCATGAATGAAT[G/T]AATGCTGTTATTTTA | 4690 |
rs541247900 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136917477 | ACAATCCTTTGGGGG[A/T]TTTTCTCCAGCTTTT | 4690 |
rs541259613 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136901650 | ATCCATTTCCTCTCA[A/G]TTTTCCAGTATGTTA | 4690 |
rs541269584 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136875508 | GATTGCAATCCTAGT[C/G]TCTGATAAAACAGAC | 4690 |
rs541290877 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136867172 | CTTCCTTCCTTCCTT[C/T]CTTCCTTCTTTCTTT | 4690 |
rs541296182 | in-del | -/TTTG | 0.0115144 | 0.0749975 | intron-variant | NCK1 | GRCh38.p7 | 3:136880628 | AGACAATCAACAAAC[-/TTTG]TTTGTTTGTTTTTTT | 4690 |
rs541407466 | in-del | -/ACTT | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136863472 | TTTTCTTTTTAAAAC[-/ACTT]AATTTTCTTGTGGGG | 4690 |
rs541448561 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136894921 | CTTGTTGCCCAGGCT[A/G]GAGTGCAGTGGCACT | 4690 |
rs541470137 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136923278 | ATAGCTGTCCAGGCC[A/G]GGCGCGGTGGCTCAC | 4690 |
rs541486793 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136862330 | CTCAGGTGAGCTGGA[C/G]CTGCCCGGCTCGGCA | 4690 |
rs541491452 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136926488 | TACCGTGTTAGCCAG[A/G]ATGGTCTCGATCTCC | 4690 |
rs541523500 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136868924 | GAACCATCACTTCTT[A/G]TTGAGCAAGACAAGA | 4690 |
rs541568642 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136927870 | ATGTATTTTTTTCCA[C/T]ATTTTTTACTTTTCA | 4690 |
rs541577373 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136884044 | ATGTTGAGGAACAGT[A/G]GCTTGGATTAGAGAA | 4690 |
rs541594417 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136935212 | GCCATTCTTTTTTTG[A/G]CAATGTGTAATTAGT | 4690 |
rs541605925 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136919145 | GCAAAACTACATAGG[A/G]ACAGAAAATAGATCA | 4690 |
rs541611959 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136897722 | TTTAATCACAGTTCT[A/G]AATTAATTATTTTCA | 4690 |
rs541635904 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136918231 | CTAAATAATATATAC[A/G]TATTATCTCTTAGTT | 4690 |
rs541661236 | snp | A/G | | | synonymous-codon, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136948447 | TCTTGTCAAGCATTT[A/G]TCATGATACTGCTGA | 4690 |
rs541667360 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136935890 | GCTTTCTGTCTCTAT[A/G]GATTTACCTATTCTG | 4690 |
rs541693504 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136896462 | GTTGCTGCAAATGAC[A/G]TGATTTCATTATTTT | 4690 |
rs541737520 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136927358 | GATCTCCTTGTGGTT[C/T]TGTCAACATATTTTG | 4690 |
rs541790888 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136925535 | CTGTTCCTGCTGCCC[C/T]GTTAACCCTGGCAAC | 4690 |
rs541811730 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136885890 | AAAGTTGGAATGGCT[A/G]ACTTAAAAGCTTCCA | 4690 |
rs541833365 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136912800 | AGCTGGAACTACTTG[C/T]GCTGCTGTGCTTGGC | 4690 |
rs541927740 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136869690 | CTTTCGTATTTTTCT[A/T]ATGTGTACGTAACAA | 4690 |
rs541962104 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136883239 | TTCTTATTACATGTA[G/T]AATAAAATTGGCCTG | 4690 |
rs541962509 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136876850 | TCCCTTCCTGCCTAA[C/G]ATCAATTTCTAAATG | 4690 |
rs541989658 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136945370 | TGGTGAACTGTCATA[C/T]AATAACAAATTAAAT | 4690 |
rs542023193 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136893840 | GAGGCAGGAATTACT[A/G]TTCATCATTACCTTC | 4690 |
rs542056933 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136905237 | GTGTTAGCCAGTCTT[C/G]TCTTGAACTCCTGAC | 4690 |
rs542058065 | snp | C/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136898364 | ATCGTGCCAGCCTGG[C/G]TGATAGGCAAGACTC | 4690 |
rs542060416 | in-del | -/CTT | | | intron-variant | NCK1 | GRCh38.p7 | 3:136867188 | CTTCCTTCTTTCTTT[-/CTT]TTCTTTCTTTTCCCT | 4690 |
rs542100726 | snp | A/T | 0.00318978 | 0.0398085 | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136951497 | GAGTTGAATTCCCAC[A/T]AGTCAACAATGAGCT | 4690 |
rs542115417 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136890078 | TGGGGAGGCTCGGGC[A/G]GCACAGCAGCCCATG | 4690 |
rs542124425 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | NCK1 | GRCh38.p7 | 3:136864153 | ATTATCCTTTGTCCA[C/G]GTTTCTGCAGTGCTT | 4690 |
rs542216181 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136899754 | TTGCCATGTTTTTCA[A/G]CTCTTTTATCTTGAG | 4690 |
rs542252192 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NCK1 | GRCh38.p7 | 3:136929484 | AATACTTTTGGGTTT[C/T]GTGATTAAGACCATT | 4690 |
rs542252462 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136892446 | TGGTAATCACAAGAG[A/T]CCTTATCAGAGGGAA | 4690 |
rs542276162 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NCK1 | GRCh38.p7 | 3:136881380 | GCACGCCACTACGCC[C/T]GGCTAATTTTTGTAT | 4690 |
rs542300125 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136885025 | TGCGCCTGCTGAAGT[C/T]CTTATGTTTTAGAGA | 4690 |
rs542318372 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136865449 | GTACTTTTACTTTGT[C/T]TTATTTTACTTTTTC | 4690 |
rs542351442 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136936666 | TTCTTTCTTTGCTTA[C/T]ATCCATTGTAGTTGG | 4690 |
rs542457040 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136872385 | TGATTTAGGGTGTCT[A/G]GTAGAAAAAATTTCT | 4690 |
rs542480387 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136914811 | TTTGATCCCCATGTT[G/T]GAAGTGGGGCCTAAT | 4690 |
rs542493976 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136871735 | CAATTCCCACGTGTG[A/G]TTGGCAGAACCTGGT | 4690 |
rs542503631 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136904766 | TTTGTTTTCTCTTCT[A/C]CTGAGACACTGAAAA | 4690 |
rs542514692 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136863591 | CATCTTGACCACAAA[C/T]TCTGAGACTTCTTTG | 4690 |
rs542583152 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136927678 | GGGTGTGCACCATCA[C/T]GCCCAGCTAATTTTT | 4690 |
rs542602652 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136916379 | TTAACACAGGTTTTA[C/T]GTATGTGAACTCACT | 4690 |
rs542612286 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136946412 | GGTAACAAGCTGGGA[C/T]GTAACATAAGCATAA | 4690 |
rs542639616 | in-del | -/AGAG | | | intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136946350 | GGTATTTTAAAAAAA[-/AGAG]AGAGAGAAATGGAGA | 4690 |
rs542644712 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136914672 | TTGTGTTTCAGATCT[C/T]TTTTGCGCCCTAATG | 4690 |
rs542676401 | snp | A/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136943057 | TGGGGGATGGTGGGC[A/T]GGCAACTTAGGATGC | 4690 |
rs542683345 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136909273 | ATATCTAGGCAAATG[G/T]TGCAAAGAAAATATG | 4690 |
rs542791443 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136914249 | CAGGTCTTATTGCCC[A/G]AAAGCTGTGGAACAC | 4690 |
rs542823789 | in-del | -/GG | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136880403 | GGGCCTTTTAAAAAA[-/GG]GAGAGATTTTGACAC | 4690 |
rs542829641 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136923873 | AAAAATGAAAACAAG[C/T]GAGCCTAACTCTACG | 4690 |
rs542830350 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136906499 | TGAAATTGCCTGTCC[C/T]TGGGCTTCAGGGCAG | 4690 |
rs542850520 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NCK1 | GRCh38.p7 | 3:136864981 | TTTTTTTTTTTGAGA[C/T]GGAGTCTCACTCTGT | 4690 |
rs542865309 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136915476 | TTAAGTAAGAATGTA[C/T]GGAGTGTACTGGTTC | 4690 |
rs542886796 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136893062 | ATTCCTGAGTTACTT[C/G]AGTTAGAATAATGGT | 4690 |
rs542908122 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136887478 | GTTTAAAAATGAAGG[C/T]GAGAAGGAGAAAAAG | 4690 |
rs542925950 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136869680 | TGTATGGTTGCTTTC[A/G]TATTTTTCTTATGTG | 4690 |
rs542941050 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136887633 | CATAACTTCTTTAGC[A/T]TACAATTCAGATACA | 4690 |
rs542957309 | in-del | -/AAATAAAT | 0.0103295 | 0.0711199 | intron-variant | NCK1 | GRCh38.p7 | 3:136923560 | GCGAGACTCCGTCTC[-/AAATAAAT]AAATAAATAAATAAA | 4690 |
rs542990455 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NCK1 | GRCh38.p7 | 3:136922190 | ATTTATGACAGGAGG[C/T]GGTGGTACAAATTAG | 4690 |
rs542994259 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136938702 | GATGTTGTGAATTCT[A/G]TGTTAATCACAATTT | 4690 |
rs542999632 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136885206 | ATGGATATTGTGGCC[A/G]TGGACAAGTGGCCAT | 4690 |
rs543082408 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | NCK1 | GRCh38.p7 | 3:136867305 | TGACAGGATCTCGCT[C/G]TGTTGCTCAGGCTGG | 4690 |
rs543120681 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136874021 | GTGTTTGTGAGATTC[A/G]TTTATGATGTAGAGT | 4690 |
rs543120763 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136866496 | ATTTTTAGTAGAGAC[A/G]GGGTTTCTCCGTGTT | 4690 |
rs543122290 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136880858 | AAGCAGTCCTTCCAC[C/G]TCAGCCTCCCAAAGT | 4690 |
rs543140453 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136881897 | TTCCATTGCTTATAT[A/T]TACCACATTTTGTTT | 4690 |
rs543157012 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136873249 | CTTCTTGGATCAGCA[C/T]GACCTGGATGTGAGA | 4690 |
rs543159793 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136899079 | CAGTCAGCCTCTAGT[A/C]GCATTTGGATGCAAA | 4690 |
rs543194581 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136933807 | TCTCTCAAGTTCAAA[C/T]GATTCTCGTCCCTCA | 4690 |
rs543205316 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136920707 | GCCATTATGTGACTA[C/T]AAACGTAAGAGCAAT | 4690 |
rs543224503 | snp | C/G | | | upstream-variant-2KB, intron-variant | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136861384 | GTAATCCCAGCTACT[C/G]GGGAGGCTGAGGCAG | 4690 |
rs543239680 | in-del | -/CGGAGCCGAGCCGGAGGGGGCG | 0.0123036 | 0.0774623 | intron-variant, upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136862488 | CGCCGTCTGCAGGCT[-/CGGAGCCGAGCCGGAGGGGGCG]CGGAGGCTGCTCGGA | 4690 |
rs543255789 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | NCK1 | GRCh38.p7 | 3:136941120 | GATTTCTTTTTCTTT[C/T]TTTTTTTTTTTTTTG | 4690 |
rs543315298 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136901730 | AATTAGTTGTAATGT[C/T]TCTTTTCATTTTCTG | 4690 |
rs543346455 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136948078 | AGCTTCTTTGAGACT[C/T]AGTTTTCACATGTGT | 4690 |
rs543357473 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136882581 | TGTGTGTGTGTGTGT[A/G]TGTGTGTGTTGAGGG | 4690 |
rs543358062 | snp | A/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136861084 | GTTTACAATCTAGGT[A/T]GACATACAGGCAAAC | 4690 |
rs543440687 | snp | C/T | | | downstream-variant-500B, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136951948 | GAGCAGCTGCTATGT[C/T]CTTCATGTACTTTTT | 4690 |
rs543450443 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136890156 | CCACGGGGAGGCAGC[G/T]GAGGCCCGGCAAGAA | 4690 |
rs543451589 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NCK1 | GRCh38.p7 | 3:136917352 | CTCTGTCCATGTTAA[A/G]CCTCATAGATCTTTC | 4690 |
rs543455928 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136935271 | TTCCAGAGAGAATCA[G/T]TCTAGGTTTTACTGA | 4690 |
rs543461020 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136926457 | TTTTTTTGTATTTTT[A/G]GTAGAGACAGGGTTT | 4690 |
rs543511690 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136896499 | GCCAAATAGTATCCC[A/G]TTGTGTATATATGCC | 4690 |
rs543511927 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136862801 | TCCAGCCCGAGAGGA[A/G]GGGAGGCGTCAGCCT | 4690 |
rs543568416 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136889247 | TGGTACTGTGTCTGG[A/C]ATTGGTGGGTTCTTG | 4690 |
rs543578817 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136908083 | AGTGTTTACCATTCA[A/G]AAGTACTTCAGTATT | 4690 |
rs543590536 | in-del | -/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136901267 | CTTCATTGTGGTGTA[-/T]TTTTTTTTTTTTTAA | 4690 |
rs543602102 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136902414 | TGCCCAGGCTGGTCT[C/T]GAGCTCCTGAGCTCA | 4690 |
rs543643147 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136910973 | CTACTCTCTACTTCT[A/G]TGAGTTCAACTTTTT | 4690 |
rs543648266 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136862391 | CAGACACACACACAC[A/C]CCCCTTCAGTCCGCT | 4690 |
rs543661247 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NCK1 | GRCh38.p7 | 3:136910178 | TTTGTGCTGAATTTA[A/G]TAGAATAATTCCATT | 4690 |
rs543670135 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136923327 | TTGGGAGGCCGAGGC[A/G]GGCGGATCACGAGGT | 4690 |
rs543678414 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136894801 | TGCTGTGATCCTAAA[A/T]TTTGCTAGATTTTTT | 4690 |
rs543685295 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136868964 | TTGTTGAGGCCGGGC[A/G]CGGTGGCTCACGTCT | 4690 |
rs543852739 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136894191 | TGTGGCTTTAGGCTC[C/T]GTGAACCCCTACTGT | 4690 |
rs543860222 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136912843 | TTTTTTTGTAGAAGC[A/G]GGGTCTTGCTGTTTC | 4690 |
rs543860351 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136921056 | AGGTAAAATGAGGTC[A/G]TTAAGATGGACCTTA | 4690 |
rs543863083 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | NCK1 | GRCh38.p7 | 3:136903835 | ATTTATGGCTGTTCA[C/G]TATATCATCTATTCC | 4690 |
rs543864439 | in-del | -/GTGATAC | | | upstream-variant-2KB, intron-variant | NCK1 | GRCh38.p7 | 3:136929676 | AAAGTATGCCTCATA[-/GTGATAC]GTGCACAGGGTACTA | 4690 |
rs543969152 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136951606 | TTCAAGTCAAAATAT[A/G]GAGACGAATCTCTGA | 4690 |
rs543986443 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136878066 | GAAGCCAGTCACAAA[C/T]GACCACAGTATTGTA | 4690 |
rs544068175 | snp | C/T | | | downstream-variant-500B, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136952029 | ATTTGTATAATTAAC[C/T]TTCACACTCCCAACC | 4690 |
rs544076167 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136890471 | GTGGTGGGCTGAAGG[G/T]CTCCTCAAGTGCTGC | 4690 |
rs544085053 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136918430 | ATATTAGGTATTACA[A/G]GTAATCTAGAGATGA | 4690 |
rs544093293 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136928438 | AGGCCCATGCTCCAA[A/G]TCAAGGCAGAGTGAT | 4690 |
rs544108186 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NCK1 | GRCh38.p7 | 3:136875635 | GCACCCAATACAGGA[A/G]CACCCAGATTCATAA | 4690 |
rs544202293 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136883302 | GCCCTTGTTCTCTGG[C/T]CACATCTCTAGCCAT | 4690 |
rs544264173 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136864220 | AATGTTGGCCGGGCT[C/T]GGTGGCTCACGCCTG | 4690 |
rs544293782 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136922968 | CTACTTACATAATGA[C/T]GACGCACTCTGCAAT | 4690 |
rs544296723 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136863889 | GGCGGATCACGAGGT[C/G]AGGAGATTGAAACCA | 4690 |
rs544300923 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136871158 | TCCTGCACTTTGGGA[A/G]GCTGAGGTGGGAGGA | 4690 |
rs544330717 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136879348 | CCCAGAATCAAGGAA[C/T]GTGATTTTGCAGAAT | 4690 |
rs544335406 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136870553 | TTTGCAAGTACTACA[C/T]GCTCTTGAATAATAT | 4690 |
rs544340151 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136937829 | ACTCTGTGTGAGTGT[G/T]TGGGTGTGTGTGTAT | 4690 |
rs544364534 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136945449 | TGATTTTTAACTACA[C/T]AGAAATTTGTTATAT | 4690 |
rs544370520 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136927906 | ATGTCTTTAGATTTT[C/T]AGGTGTGTCTCTTTT | 4690 |
rs544403184 | snp | A/G | 0.00095511 | 0.0218321 | missense, nc-transcript-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136946071 | AAGATCAATGGTATG[A/G]TTGGTCTAGTACCAA | 4690 |
rs544443790 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136877491 | CTTAGAGGAAGAGTT[A/G]TAGCCTTCAAATCTA | 4690 |
rs544528935 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136944969 | TAAACAAACAAAACT[C/T]CCTGTCCTTTTGGAG | 4690 |
rs544540098 | snp | C/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136873629 | TGGTTTGGCTGTGTC[C/G]CCACCCATATTTCAT | 4690 |
rs544563551 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136887773 | CTATTTTGTTAAATC[C/T]TCACAGCAACCCTGT | 4690 |
rs544575747 | in-del | -/AC | 0.00199481 | 0.0315187 | intron-variant | NCK1 | GRCh38.p7 | 3:136916746 | AACTTAGAAAATAAA[-/AC]AGTTTGTTTAGTTCA | 4690 |
rs544582184 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136898949 | AGAGATCATTTATAG[A/G]ACATGGTAATGGATT | 4690 |
rs544644115 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136871765 | TGGGAGGTAATTGAA[C/T]CATGGGGGTGGGCCT | 4690 |
rs544704180 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136886947 | CTCCCAGGTTCAAGC[A/G]ATTCTTATGCCTCAG | 4690 |
rs544745251 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136900658 | TCTTGATTTCTTTCT[C/T]AGCTAGTTTGTTTTA | 4690 |
rs544781945 | snp | A/G | 0.0322114 | 0.122752 | intron-variant | NCK1 | GRCh38.p7 | 3:136893178 | TGTGTGTGTGTGTGT[A/G]TATATATATATATAC | 4690 |
rs544786997 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136935377 | TATTTTCAGGTTTAA[-/C]TTTTTTTTTTTGTAT | 4690 |
rs544822635 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136884664 | CAGGCTGGTCTTGAG[A/G]TGATCCTTCTGCCTT | 4690 |
rs544839219 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136866306 | TTCCTTTTTCTTTCT[G/T]TCTTTCTTTTTTTTT | 4690 |
rs544859005 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136891826 | TCATGTGCTTATTCA[C/T]TGTTTGCATATCTTC | 4690 |
rs544877044 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136905043 | TTTGAGATGGAGTCT[C/T]GCTCTGTTTCCCAGG | 4690 |
rs544923409 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136891225 | TTGCAACCTCCGCCT[C/T]CTGGGTTCAAGTAAT | 4690 |
rs544985110 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136872489 | AGTTTGGAAAATTTG[C/T]AGCTTGACAGCGTGA | 4690 |
rs544987143 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136877418 | GAAATAACATTAAAC[G/T]ATTTAGAACAGAACC | 4690 |
rs544991506 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136932251 | CATTTGCAGACTGGG[A/C]GTCAGGATTTGAAAT | 4690 |
rs544994819 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136939003 | TCATAGAATGAGTTA[A/G]TAAGTATTCTCTCCT | 4690 |
rs545025122 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136887902 | TTCTTGTTATCTTTT[A/G]TTCATCGCCTTTATT | 4690 |
rs545026173 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136918658 | TTCACAAACGTTCTT[A/G]AAACATGATGAGATT | 4690 |
rs545030548 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136910700 | GGGTACAATGGGATG[C/T]TCTGACACATGTATA | 4690 |
rs545052750 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136917165 | CATCCTATGGGCTGC[A/T]TGCAGCCCAGGACAG | 4690 |
rs545057000 | snp | C/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136915133 | TATAGATTAGCCTCA[C/G]GCATTCCTTTGTAGC | 4690 |
rs545090158 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136901467 | GATGTTAGTTCTTCT[A/G]TGAGTGTTTGGTAGA | 4690 |
rs545100535 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136902467 | CCCAGAGTGCTAAGA[G/T]TACAGGCGCGAGCTA | 4690 |
rs545184235 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136867495 | AAACGATCCTCCCAC[C/G]TTGGCTTCTCAACGT | 4690 |
rs545193316 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136909661 | ATTATTCTACCCATT[A/C]TTGAGAGTCAGGTAT | 4690 |
rs545194154 | in-del | -/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136887943 | TTCTTTCTTTCTTTC[-/T]TTTTTTTTTTTTTCT | 4690 |
rs545213857 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NCK1 | GRCh38.p7 | 3:136916464 | CCTCCCATTAGGCCC[C/T]ATTTCCAACATGGGG | 4690 |
rs545218350 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136915473 | TTTTTAAGTAAGAAT[A/G]TACGGAGTGTACTGG | 4690 |
rs545235527 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NCK1 | GRCh38.p7 | 3:136923555 | GCAGTGCGAGACTCC[A/G]TCTCAAATAAATAAA | 4690 |
rs545238207 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136923516 | GCCAGGGTCGCTCCA[C/T]TGCACTCCAGCCTGG | 4690 |
rs545244482 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136881540 | TTATTGTGGTAAACT[A/G]CATAAGCATAAAGTT | 4690 |
rs545260647 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136873076 | GTGAGAAGAGGGCCA[C/T]CATCCTCCAGCCTCC | 4690 |
rs545281658 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136881011 | TCATTTCATTAAATG[A/G]TATTGCCATCCACTC | 4690 |
rs545326948 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136914165 | ATAGCTGCCTGCTTC[C/T]GTGTCTGTATCTCAG | 4690 |
rs545416668 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136862268 | GGAGCGCAGGCCTCG[C/T]GCCGTTACGGCCATC | 4690 |
rs545422464 | snp | A/G | | | upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136862072 | CACATCAGGCACGGC[A/G]CTTGATTGACATGAG | 4690 |
rs545451911 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136861990 | AAAAGCTAAGACAGT[C/T]CTGGTCCGGCCCAGC | 4690 |
rs545459084 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136868010 | GCAACCTCCGCCTCT[C/G]GGGTTCAAGCAATTC | 4690 |
rs545495727 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136874460 | GCTGGGATTACAGGC[A/G]TGAGCCACCACGCCC | 4690 |
rs545541756 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136935166 | TCGGCCTCCCAAAAT[C/G/T]CTGGGATTACAGTGT | 4690 |
rs545563637 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136875969 | TCTCAGGCCACAGTG[C/T]AATCAAACTAGAACT | 4690 |
rs545567927 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136942237 | CATTTTTGAAGGACA[C/G]TTTTGCTAAATATAG | 4690 |
rs545604994 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136934506 | GGCCAGGCTGGTCTC[A/G]AACTCCCAACCTCAT | 4690 |
rs545610160 | snp | A/G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136904586 | CATTTTTAGAATTCT[A/G/T]TGTATTTGATTTTTT | 4690 |
rs545725384 | in-del | -/TTTTCTTTGT | 0.00119737 | 0.0244387 | upstream-variant-2KB, nc-transcript-variant | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136861778 | AATTTTCAGGTCTGC[-/TTTTCTTTGT]TTTTCTTTGTCGCTC | 4690 |
rs545749902 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136884428 | GAGAATGATAGAGTA[C/T]AGCTTTGAGTTCTTG | 4690 |
rs545768025 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136949455 | TAAAACTGATGTATA[A/C]CTGAGGAAAAAATAG | 4690 |
rs545806148 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136919110 | CAGACTCAGCGTCTG[C/T]ATAAAACATTCTGGA | 4690 |
rs545809667 | snp | A/G | | | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136951173 | TATGGCACTTAAATT[A/G]TCTCCAGCTGTAATG | 4690 |
rs545811604 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136924203 | ATAATGTGCCTCCTA[A/G]TAAATGGCAATAACA | 4690 |
rs545821475 | snp | A/G | | | intron-variant, downstream-variant-500B | NCK1, LOC107986136 | GRCh38.p7 | 3:136945498 | TATATAGAGTTGAAG[A/G]TCTCTTTTTAATAAT | 4690 |
rs545830165 | in-del | -/GA | 0.00159617 | 0.0282053 | intron-variant | NCK1 | GRCh38.p7 | 3:136944348 | TGGTCTCGATCTCTT[-/GA]GCTTGTGATCTGCCC | 4690 |
rs545851602 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136944646 | AGAGTCAGGAAAGAT[A/C]GTATTAAGATCCTAG | 4690 |
rs545893137 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136890037 | TCAATGGGATTGGGC[A/G]CCCTGGAGCAGAGGG | 4690 |
rs545899078 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136883214 | GCATGAGCCCCCATG[C/T]CCAGCCTACTTCTTA | 4690 |
rs545919325 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136891075 | CTAAAGTTCCTCCCC[A/G]ACCAAAGGCTGGTAC | 4690 |
rs545934206 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136882627 | GCAGTCACTTGGAGC[A/G]CAGGCACCTGTATCT | 4690 |
rs546007683 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136897921 | ATCTGAGCTTCCTAA[A/G]AAGCTGTATTATCTA | 4690 |
rs546062556 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NCK1 | GRCh38.p7 | 3:136889558 | GCGGGTTGCCACTGC[C/T]GGCTCGGGCAGCCTG | 4690 |
rs546076659 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136926323 | TCTGCGGCCCAGGCT[A/G]GAGTGCAGTGGCGCG | 4690 |
rs546081695 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136895617 | TTGCCCAGGCTGGAG[C/T]GCAGTGGCACAATCT | 4690 |
rs546104291 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136950075 | GTAGTTAAGTTTTTA[A/G]TGGAAATAAAAATCA | 4690 |
rs546154535 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136870385 | CAAAAATTTTAGCAC[A/G]TATTTTCATATGTTA | 4690 |
rs546192375 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136936141 | TGCCTCTTGGGTTCA[A/G]GTGATTCTCCTGCCT | 4690 |
rs546229293 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136936605 | TCCAACCAGTATTGT[A/G]AGGGGGATTCCAGTT | 4690 |
rs546236199 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | NCK1 | GRCh38.p7 | 3:136945054 | TATGAGGTAAATAGA[G/T]CTACCTGGGTCTGGG | 4690 |
rs546246623 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | NCK1 | GRCh38.p7 | 3:136897097 | GTTTTACTTTTATTT[A/T]TTATTTTGAGACAGA | 4690 |
rs546247402 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136905542 | ACAGACAAGGGTCAC[A/T]GTGTCTGGCCTCAGA | 4690 |
rs546283570 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136890566 | GCTGTCACCTCTCAG[C/T]ACTTCATTCCTTTTT | 4690 |
rs546311594 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NCK1 | GRCh38.p7 | 3:136891332 | AGAGATGGGGGTTTC[A/G]CCATGTTGGTCAGGC | 4690 |
rs546354252 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136944267 | GGGACTACAGGTGCA[C/T]ACCACTGCACCCAGC | 4690 |
rs546371992 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136912899 | CTGGACTCAAGTGAT[C/T]CTTCTGCCTCAGCCT | 4690 |
rs546396318 | snp | A/G | | | upstream-variant-2KB, intron-variant | NCK1 | GRCh38.p7 | 3:136928507 | CTTTTTGAACCATGA[A/G]TCACTGTTGGAGTTT | 4690 |
rs546435149 | in-del | -/A | 0.00398564 | 0.0444627 | intron-variant | NCK1 | GRCh38.p7 | 3:136932896 | CCATTCTCAACACTT[-/A]ACTCAGTGATACAGG | 4690 |
rs546472785 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136912208 | CGCTCTGTCACCCAG[C/G]CTGGAGTGCAGTGGT | 4690 |
rs546483742 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136869606 | TTAGAGTGCTTTTAT[A/G]TGTTTGTTCTTCATG | 4690 |
rs546508951 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136877553 | TGAAAGGACTTCTAA[A/G]TAAAGATGGCTGAGT | 4690 |
rs546533455 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136912446 | CACAATGTGTGTGTT[C/T]GTTCTCTTGATAGTG | 4690 |
rs546571530 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136890931 | ACCATTCTACTTTCT[A/G]TCTCTATGAATTTGA | 4690 |
rs546626552 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136920280 | GTGTAGGTCAAATAA[A/G]ATTCCATCTAATTCT | 4690 |
rs546633089 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136897573 | CTTTTAAATGGGATT[A/G]TTGGTGGGGTTTTTG | 4690 |
rs546634519 | in-del | -/TTC | 0.00199481 | 0.0315187 | intron-variant | NCK1 | GRCh38.p7 | 3:136866614 | GCCTGGCCTCTTTCT[-/TTC]TTCTTTTTTTTTTTC | 4690 |
rs546634624 | snp | A/T | | | intron-variant, upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136863238 | CCTCTTTGGGTAGGG[A/T]GCAAAGCAGCTCAAT | 4690 |
rs546730427 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136879845 | TGGGGCCTGTTGGCG[A/G]GTGAGGGGCTGGGGG | 4690 |
rs546757142 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136865240 | GGATTACAGGCATGA[A/G]CCACCACGCCCGGCC | 4690 |
rs546796056 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136871868 | CACAAACTCTCTTCT[C/T]TTATCTGCCGCCATG | 4690 |
rs546856905 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136863099 | GGGTGAGGACGTAAC[C/G]GTAGGAACGCTCTCG | 4690 |
rs546921194 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NCK1 | GRCh38.p7 | 3:136929016 | CAATTTCTCCTTGTG[C/T]AGACAGTTTGGGAGC | 4690 |
rs546945542 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136873480 | GGCTTGCCTTGTTTT[A/G]GATGAGACTTTGGAC | 4690 |
rs546954847 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136915004 | TGTGTACATGCTGGC[G/T]TCTCTTTGCCATCTT | 4690 |
rs546966947 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136916318 | AATATGAAAAATTCT[C/T]AAATGTTATGATTAG | 4690 |
rs547003855 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136906697 | ACCTTTAGGACCCAA[A/G]CTGTCTGTGCTGGTG | 4690 |
rs547006244 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136880111 | AACACGGTGAAACCC[C/T]GACTCTACTAAAAAT | 4690 |
rs547042740 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NCK1 | GRCh38.p7 | 3:136875566 | AAAGAAGGCCATTAT[A/G]TAATGGTAAAGGGAT | 4690 |
rs547049386 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136924091 | AAAACCATTGGGTAG[A/C]GGTTTGATGGGGGAA | 4690 |
rs547079174 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136903487 | TGGAGTACAATGGTG[C/T]GGTCTTGGCTTACTG | 4690 |
rs547088303 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136916021 | GTGAGCCACTGGGCC[C/T]GGCCTAGCCAAACAC | 4690 |
rs547120268 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136879838 | CACACATTGGGGCCT[G/T]TTGGCGGGTGAGGGG | 4690 |
rs547170968 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136878783 | TGCCTTCTTGAGTAC[C/T]CCAGCAAGAAGACTG | 4690 |
rs547177916 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136887976 | TGAGATGGAGTCTTG[C/G]TCTTGTCGCCCAGGC | 4690 |
rs547191282 | in-del | -/A | 0.0126979 | 0.078662 | intron-variant | NCK1 | GRCh38.p7 | 3:136923572 | CTCAAATAAATAAAT[-/A]AATAAATAAATAAAT | 4690 |
rs547216368 | snp | A/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136886252 | ATAGTTATCCTTTTT[A/T]TTTTCTTTTGCAGTA | 4690 |
rs547242099 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136887333 | CCGCCATGCTCAGCA[A/T]TTTTTTTCTATCTTA | 4690 |
rs547267095 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136882181 | TTACATTTTCACTAA[C/T]ACTTGTTTCCTGCAT | 4690 |
rs547380109 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136944059 | CAAAGGATCAGATAA[C/T]AAAGAGTTGGGAGTG | 4690 |
rs547385221 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136894959 | CGGCTCACTGCAACC[A/T]CCACCTCCTGGGTTC | 4690 |
rs547393129 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136934027 | TTAAGTAATTTTGAA[A/G]ATTAAACACCATAAG | 4690 |
rs547422978 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NCK1 | GRCh38.p7 | 3:136924792 | TTCCATTATTGGAAC[A/G]CTAAGCTTGTGAGAG | 4690 |
rs547499477 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136887908 | TTATCTTTTATTCAT[C/T]GCCTTTATTGTTTCT | 4690 |
rs547534666 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NCK1 | GRCh38.p7 | 3:136894371 | GTAGTAGGGATATAA[C/T]ACCCTAGCCATTGGT | 4690 |
rs547549219 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136932312 | CTGCAGCAACCCCAA[A/C]TTTTTATTTATTTTG | 4690 |
rs547570469 | snp | A/G | 0.00358779 | 0.0422022 | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136948529 | AAAATGTTGGGTCCA[A/G]TCGTGCTTGATTGGA | 4690 |
rs547571453 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136938325 | TATTTTTCACAGATT[C/G]TGTATTTGTGAATTC | 4690 |
rs547603305 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136893349 | TGTGGCCATTCTTGC[A/G]GGAGTAAGGTGGTAC | 4690 |
rs547604613 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136940808 | CCTCGGCTTCCTAAA[A/G]TGCAGGGATTACAGG | 4690 |
rs547607746 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136902040 | TATCTCATAGATTTT[C/T]GGTATGTTGTATTAG | 4690 |
rs547667882 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NCK1 | GRCh38.p7 | 3:136901621 | AGATTGTATATGTCT[A/G]TGTCTAGGAATGCAT | 4690 |
rs547671041 | in-del | -/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136905428 | GAATTCTCTTGTATC[-/T]TTTTTTTTTTTGAGA | 4690 |
rs547673432 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136899978 | TGTTCTGGATTGCTT[G/T]TTTAAAGGTACAGTT | 4690 |
rs547675810 | snp | A/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136911039 | TGCCGGCTTATTTAA[A/T]TTAGCATAAAGTCCT | 4690 |
rs547700161 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136874106 | AATTTTAAAAAATTG[A/G]ACATTTGATTTTCAG | 4690 |
rs547731961 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136908444 | ATGTACAGCTTGCAA[A/C]GTGAGGGTGAGGCCA | 4690 |
rs547742450 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136950982 | TGAATATATATTCAC[A/C]CATGTATATTACACA | 4690 |
rs547749573 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136860805 | CCCATTAGTCCCCAC[C/T]TCCAACATTGGGGAT | 4690 |
rs547768383 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136910534 | ATACTAGCTTTTATA[C/T]TTGCCCATGCATTTA | 4690 |
rs547792915 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NCK1 | GRCh38.p7 | 3:136866739 | CTGTGTCAGTCTTCC[A/G]AGTAGCTAGGATTAC | 4690 |
rs547805639 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NCK1 | GRCh38.p7 | 3:136889300 | AGCCGCGGACCCTCG[C/T]GGTGAGTGTTACAGC | 4690 |
rs547844243 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | NCK1 | GRCh38.p7 | 3:136889122 | GTTTTGAACTCCTGC[A/G]CTCAAGTGATCTTCC | 4690 |
rs547861706 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136912282 | ATTCTCCTGCCTCAG[C/T]CTCCCACGTAGCTGG | 4690 |
rs547901011 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136949485 | GAATGTGCTCATGGT[A/T]AGGGAAAATTATATT | 4690 |
rs547974536 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136895344 | ATATATCATGTTTCC[A/G]TACCTTTTAATGTTG | 4690 |
rs547981869 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136920891 | TTATAGTTGATTGTA[A/G]TCATATTTTTAAATT | 4690 |
rs548009140 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136861356 | CATTAGCTGGGCGTG[A/G]TGGTACATGCCTGTA | 4690 |
rs548030977 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136868396 | GCAGTGGGGCAATCT[C/T]GGATCACTGTACCCT | 4690 |
rs548049419 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136867563 | TTGCTTTCCTTTAAA[C/T]CCATACCCCTTATTA | 4690 |
rs548059694 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136917781 | TTTAGGTTGAGTAAA[A/G]TCTCTGCTTCCATGT | 4690 |
rs548075238 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136944230 | TTCAAACGATTCTCC[C/T]GCCTCAGCCTCCTGA | 4690 |
rs548079779 | in-del | -/C | 0.00199481 | 0.0315187 | intron-variant | NCK1 | GRCh38.p7 | 3:136899422 | TCATTTCTTTTCTTT[-/C]TTTTTTTTTTTAAAT | 4690 |
rs548111643 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136934569 | GGGATTACAGGTGTG[A/C]ACCACCGCGCCTGTC | 4690 |
rs548127629 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136885120 | TTTTTAGAGGTATAC[A/G]CCGAAATATTTACAG | 4690 |
rs548128362 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136870868 | CCTTTAGGTTAATCA[A/G]CATTAAGTTTGGCTA | 4690 |
rs548193156 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136903416 | AAAAAATCTATTCAA[C/T]CAGTATCTATCTTAT | 4690 |
rs548200011 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136893055 | GTTTTCCATTCCTGA[A/G]TTACTTCAGTTAGAA | 4690 |
rs548232706 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136924709 | GTGAGTAGAGGTTCT[A/G]TGTTTCACCACACTG | 4690 |
rs548248687 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136862453 | CGCTTCCTCTTCTCG[C/G]GCTGAGTTAGCCCCG | 4690 |
rs548267560 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136877578 | CTGAGTGAAAGACAC[A/G]TTTACTTTTACTCCC | 4690 |
rs548358775 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | NCK1 | GRCh38.p7 | 3:136876177 | AGGGAAATTTATAGC[A/C]CTAAATGCCCAAAAG | 4690 |
rs548368126 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136874472 | GGCGTGAGCCACCAC[A/G]CCCGGCCCGTTTACA | 4690 |
rs548420798 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136884482 | GGTCCTGCTCTGTGG[A/C]CCAAGCTGGAGTGCA | 4690 |
rs548462278 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136944307 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCATGT | 4690 |
rs548468079 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136951758 | TTTGAAAGAAAACTC[A/G]TTGGTTCTAGATAAG | 4690 |
rs548491151 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136882149 | ACCACCAACCGTGCA[G/T]AAGAGTTCCAATATC | 4690 |
rs548502868 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136936223 | TTTGTGTATTTTTAG[C/T]AGAGATGGGGTTTCA | 4690 |
rs548551842 | in-del | -/CTTT | | | intron-variant | NCK1 | GRCh38.p7 | 3:136887943 | TTTCTTTCTTTCTTT[-/CTTT]TTTTTTTTTTCTTTT | 4690 |
rs548619565 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136921370 | GCAAGAAAAAGTAAG[A/G]CATAGGATCTAGGAA | 4690 |
rs548630319 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | NCK1 | GRCh38.p7 | 3:136899132 | ACAAGCCACAGCAGA[C/G]ACTCTGATTTGGAGA | 4690 |
rs548630448 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136891406 | TCCCAAAGTGCTGGG[A/G]TTACAGGCATGAGCC | 4690 |
rs548668456 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136937461 | GGTCCACCTTGCAGT[A/T]CTGTGTGAATATTAG | 4690 |
rs548727457 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136883578 | TATTTTATTTGAAAA[A/G]ATTTAATTTCCTCTG | 4690 |
rs548729586 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136935769 | TATGTAATTCAGTAG[C/T]ATTGAGTACATTAAC | 4690 |
rs548741298 | snp | G/T | 1.65061e-05 | 0.00287277 | missense | NCK1 | GRCh38.p7 | 3:136928020 | GCAGAAGAAGTGGTG[G/T]TAGTAGCCAAATTTG | 4690 |
rs548762311 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136890194 | GCAGCGCTGGTGGGC[A/T]GGCATTGCTGGGGGA | 4690 |
rs548792326 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136898612 | AAATTTGGCTAAAAT[A/G]CAAAACATCTTTGCA | 4690 |
rs548800547 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136937643 | TTTGCAGTGTTTAGT[A/G]TATGAGTCTGATACT | 4690 |
rs548830414 | in-del | -/TTG | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136900213 | GTGCAGAAGCCTTTT[-/TTG]TTGTTGTTGTTGTTG | 4690 |
rs548833073 | snp | C/T | 0.000461232 | 0.015179 | synonymous-codon, downstream-variant-500B | NCK1, LOC107986136 | GRCh38.p7 | 3:136945686 | TGACCTCAACATGCC[C/T]GCTTATGTGAAATTT | 4690 |
rs548851491 | in-del | -/TC | | | upstream-variant-2KB, intron-variant | NCK1 | GRCh38.p7 | 3:136928713 | CTTTTCTATTTTGTT[-/TC]TCTTTTTCCCTTTAT | 4690 |
rs548862407 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136896627 | ACTGCAGTGAGTAGC[C/T]GGGACCACAAGCATA | 4690 |
rs548865071 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136931262 | CTGCTGATTCTGCTA[A/G]TGGCCTCCTTATGAT | 4690 |
rs548878489 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NCK1 | GRCh38.p7 | 3:136871304 | ACTTGCAAGGCTGGC[A/G]GGAGGATTGCTTGAG | 4690 |
rs548893518 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136943714 | AAACGAATAAGATCT[C/G]GTTTTCTGCCCTCAG | 4690 |
rs548894366 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136905690 | AGTGCAATGGTGTGA[G/T]CATGGCTCAGTGCAG | 4690 |
rs548917711 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136946710 | TGTAGTCCTTATGAC[A/G]TAGGAAATCCCTGAA | 4690 |
rs548959561 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136913675 | TTTTTGTTTGTTTTG[A/T]TTTGTTTTTTTGAGA | 4690 |
rs549021080 | in-del | -/T | 0.00438332 | 0.0466095 | intron-variant | NCK1 | GRCh38.p7 | 3:136924638 | ATACTGATAATTTAA[-/T]TTTAGTATAATTGAC | 4690 |
rs549053554 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136945162 | GAAATAATTTTATTT[C/T]TATACAGCTCATTGT | 4690 |
rs549068816 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136941250 | TATATGTCAGCCTCT[C/T]GAGTAGCTGGGACTA | 4690 |
rs549090583 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136936858 | CTAAGAGTTGTTTAT[A/G]TGTTCTGGATACTAG | 4690 |
rs549138931 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136882310 | TTGTTGGCTATTTGT[A/G]TATATTTCGAGAAAT | 4690 |
rs549146581 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136923203 | TTTCTTATATATTTT[C/T]CTTGAATACTTTCCT | 4690 |
rs549157834 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136906241 | GGCTTAGATTGTGGT[G/T]GTTAGTGGAGGCTGT | 4690 |
rs549158581 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136868545 | GTTGGCCAGGCTGAT[C/T]TCCAACTCCTAACTT | 4690 |
rs549197876 | snp | C/G | 0.00557542 | 0.0525036 | upstream-variant-2KB, intron-variant | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136860807 | CATTAGTCCCCACCT[C/G]CAACATTGGGGATCA | 4690 |
rs549201735 | snp | G/T | | | intron-variant, upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136863100 | GGTGAGGACGTAACC[G/T]TAGGAACGCTCTCGG | 4690 |
rs549212881 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136905086 | GGCACGATCTCAGCT[A/G]ACTGCAACCTTCACC | 4690 |
rs549272540 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136864059 | TGAGCCGAGATCGCG[C/T]CACTGCACTCCAGCC | 4690 |
rs549308292 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136922399 | TAAGGTAACTGCTCT[A/G]AATGGGGGTTCAGGT | 4690 |
rs549349837 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136908214 | AGGGTACATAGGTCC[G/T]CAACCGTATCACTTC | 4690 |
rs549384667 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136900993 | TCGTCTTGTTCCAGT[A/T]CTTAGAAGAAAGGGT | 4690 |
rs549385921 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136900209 | TTGCTGTGCAGAAGC[C/T]TTTTTTGTTGTTGTT | 4690 |
rs549415571 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136880315 | ATGTGACCTTATTTC[A/G]AAGTGGGGTCTTTAC | 4690 |
rs549424627 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136892809 | AGATTATACATGAGA[C/T]TTTTAAAATACTTTA | 4690 |
rs549487593 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136873701 | AACCTGGTGGGAGGT[A/G]ATTGAATCGTGGGAG | 4690 |
rs549523975 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NCK1 | GRCh38.p7 | 3:136881833 | CTTGAAGGTTCATCC[A/G]TTTTGTAGCACATGT | 4690 |
rs549531678 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136914534 | ATTAGAGTTAGAAGA[C/G]TTCTTTTTCTCCTTA | 4690 |
rs549551828 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136872761 | TCCAGCTGCTCCAGC[C/T]GTGGCTGAAAGGGGC | 4690 |
rs549654924 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136947406 | GGGTAATTGAGTGTA[A/G]ATATTAGACAAAATG | 4690 |
rs549670120 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136880475 | AACTAGGAGGGAGCC[C/T]AGAGCAGATTCTTCC | 4690 |
rs549673788 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136932462 | AACAAAAATTGTACA[A/G]TGTTTTAAATAAAAC | 4690 |
rs549688799 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136872012 | TTTATCAGCAGCATG[A/G]AAACAGATTAATACA | 4690 |
rs549779555 | in-del | -/T | 0.00517822 | 0.0506191 | intron-variant | NCK1 | GRCh38.p7 | 3:136894810 | CTAAATTTTGCTAGA[-/T]TTTTTTAAATCTTAT | 4690 |
rs549827403 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136889328 | AGCTGTTAAGGTGGC[A/G]CGTCTGGAGTTTGCT | 4690 |
rs549834237 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136874162 | ATTGTCAACATTCAT[G/T]TACAGTTTTTTACAT | 4690 |
rs549864161 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136889768 | AGAGTAGCTAGCTAC[A/G]GAGTGTCGATTGGTG | 4690 |
rs549875986 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136944326 | GTTTCACCATGTTTG[C/G]CCAGGATGGTCTCGA | 4690 |
rs549913902 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136940508 | CTGATTCTTTTATCA[A/G]TATATGCTGTCCTTT | 4690 |
rs549950708 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136933036 | AATAGGAACAGACAG[C/T]ATTGTAAAACTCTAC | 4690 |
rs549990641 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136895154 | TGCTAGGATTATAGG[C/T]ATGAGCCACTGCGCC | 4690 |
rs550007469 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NCK1 | GRCh38.p7 | 3:136913360 | ATGGCTCACTGTAGC[C/T]TTGACCTCCTGGGCT | 4690 |
rs550041159 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136862038 | TCTCTACTCTCCGCC[G/T]CGCAGCCTCCGCTCC | 4690 |
rs550102002 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136893266 | AGGAGTGGGATTGCT[C/T]GATCTACTTTCAGTT | 4690 |
rs550111175 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136882858 | GAGAACACAGTCATT[A/G]GTGAATACTAGCAGT | 4690 |
rs550185058 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | NCK1 | GRCh38.p7 | 3:136935740 | TGTATAACATAAAAT[A/T]AACCATTTTAAAGTA | 4690 |
rs550222821 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136861576 | GAACCAACTTACTGA[C/T]GCCTCAGCCAGTGGC | 4690 |
rs550237390 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136880664 | GGCAGGTTCTTGCTC[C/T]GTGACCCATGCTAGA | 4690 |
rs550287140 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136941657 | TAACCTAGAATTGAA[A/T]TTTTTGTTTTATGCA | 4690 |
rs550297253 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136950552 | ACCAATTTTTAAAAA[A/G]TCTTAATCCAATGCT | 4690 |
rs550324003 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136942692 | CCTGGCCATGTGCAC[A/G]TCCTTCTTGATTGGT | 4690 |
rs550332605 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136897501 | GCATTTTTTCATATA[A/C]TTGTTTGCCATTTGT | 4690 |
rs550337365 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136902550 | GGAGATACTTGATAC[A/G]ATTTCAATTTTTAAA | 4690 |
rs550341689 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136911470 | CTTAGTGTTTTAAAT[C/T]GCATTTCCCTAATGA | 4690 |
rs550358866 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136949626 | ATAATTTGTCCCCCT[A/G]TTATTCTGGAGATTT | 4690 |
rs550378893 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136912417 | TCTCTTTGCCCCTCT[A/G]CTTTTGGCATTCCCA | 4690 |
rs550499973 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136918741 | GTGTGGCCCAAGACA[A/G]TTCTTCCATTGTGGC | 4690 |
rs550542346 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136896668 | CCTGGCTAATTAAAA[A/G]AGAATTTTTTTTGTA | 4690 |
rs550605637 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136904388 | GAACTCCTGGCCTCA[A/G]GTGATCCACCTGCCT | 4690 |
rs550610138 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | NCK1 | GRCh38.p7 | 3:136864573 | AGGCGGGGTAGTTCA[A/T]GCCTGTAATCCCAGC | 4690 |
rs550624016 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136890275 | CCGGCCGGCAGGGCC[A/G]GCCGGCTGCTCTGAG | 4690 |
rs550639184 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136927278 | GGCCTGGCCGTTTTT[A/C]TTTCTTTGTTTTGTT | 4690 |
rs550705135 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136863013 | TTTCGATAGGTTTTG[C/T]AACCTTTCTTCTGTA | 4690 |
rs550783588 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136871395 | AGAGCGAGACGCTGT[C/T]TAAAAAAAACAAAAT | 4690 |
rs550841852 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136862532 | TGCTCGGAGGGTCCA[G/T]ACTTCTGCACCGGGA | 4690 |
rs550843414 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136869886 | GATTCTCTTGTTTCT[A/G]TTCCTGAAATTGTAA | 4690 |
rs550851110 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136944387 | CCTCCCAGAATGCTG[G/T]GATTACTGGCATGAG | 4690 |
rs550858992 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136936738 | ATGACTAATGATATT[A/G]AGGATCTTTTCATGT | 4690 |
rs550876806 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136876406 | ATTGATAGACCGCTA[A/G]CAAGACTAATAAAGA | 4690 |
rs550914080 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136879575 | AATGTGACCTTATGT[A/G]CACTATTCACAATAG | 4690 |
rs550946039 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136871390 | GGGACAGAGCGAGAC[A/G]CTGTCTAAAAAAAAC | 4690 |
rs550994715 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136903068 | TCCCTAACTATTATC[A/G]TAGTGGAATCTATCT | 4690 |
rs551013083 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136914304 | GAATGGGTAGTCACT[A/G]CTGAACTAAGAGCTG | 4690 |
rs551047221 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136879720 | TTGCAGGGACATGGA[G/T]GAAGCTGGAAGCCAC | 4690 |
rs551063264 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136931371 | AGTCTCTTATGCACA[A/G]CAAGCCTAAGGAAAC | 4690 |
rs551134029 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136921515 | TGTACTTCATTTCTT[A/T]GTGCCTTTGTGATGC | 4690 |
rs551156258 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136885123 | TTAGAGGTATACACC[A/G]AAATATTTACAGACA | 4690 |
rs551191163 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136892123 | GAACTTTTAGCCTCA[A/G]GGGATCCTCCTGTCT | 4690 |
rs551233798 | snp | A/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136941739 | TGCAATACTACTGAC[A/T]TTTATATTTACTTAT | 4690 |
rs551272925 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136865118 | GCCTGCCACCACGCC[C/T]GACTAATTTTTGTAT | 4690 |
rs551277935 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136899190 | GCTGCTATTGCTGCT[A/T]CTTCCAGATGCTGGT | 4690 |
rs551293761 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136884518 | GCAGGCTTGCTCACC[A/G]CAACCTCCGCTTCCT | 4690 |
rs551322124 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136939729 | GAGAGTGTTAGTTGC[C/T]ACACACTTGTTAATT | 4690 |
rs551343189 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136906606 | AGTGGCACAGGTGAG[C/T]CAGGCAGGTTGACAG | 4690 |
rs551415747 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136909361 | TGAGGACTGAAACAC[C/T]GTGTGAAAGGAGCTG | 4690 |
rs551454041 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136878899 | CTCAATATTGAGACC[A/G]TTACTGAGGCCTCTT | 4690 |
rs551481925 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136947460 | AGTATACTTTTTAAG[A/G]TTAGAGGTCTCAAGT | 4690 |
rs551488977 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | NCK1 | GRCh38.p7 | 3:136930186 | TTAATGGATTTGTTT[C/T]GCAATGGTTGTGCTG | 4690 |
rs551499988 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136937536 | TTAGTAAGAATTGCA[A/T]TGAATCTGTGGATTG | 4690 |
rs551500008 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136946457 | AAGTCCGCATTCTTT[C/G]TAGCTATCTATTTTG | 4690 |
rs551514395 | in-del | -/C | 0.00597247 | 0.0543191 | intron-variant | NCK1 | GRCh38.p7 | 3:136924049 | ATTGAAATAGTTGAT[-/C]CTAGGCAGTGATCAT | 4690 |
rs551537276 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136915883 | GGTGTGCATCACCAC[A/G]CCTGGCTAACTTTTG | 4690 |
rs551543668 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136907564 | GTCTCTCAGCTCTCC[A/G]CTGATCCTGGTTGAG | 4690 |
rs551587397 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136911740 | TTTAGTTTGCTCTTT[C/T]AGCATTTCTTGCACA | 4690 |
rs551608414 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136898672 | TATAAGATTTCAGAA[A/G]TGTCTTATGAAAGAA | 4690 |
rs551679778 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136880263 | GCACTCCAGCCGGGG[A/T]GACAGAGCGAGACTC | 4690 |
rs551706701 | snp | C/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136869270 | TTATTTGTTCCGCTA[C/G]GCCTGATGGCTCACT | 4690 |
rs551769519 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136888071 | TGCCTCAGCCTCCCA[A/G]GTTGCTGGGATTACA | 4690 |
rs551777279 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136886075 | TTGAAAGACATTGTC[C/T]TTTAAAGTAGTTTGA | 4690 |
rs551782821 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136894139 | CTTTGCCTGCTCGTT[C/T]ATCAGTATGAGAAGC | 4690 |
rs551804762 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136862088 | CTTGATTGACATGAG[A/G]GCCCGCCCAATCCCA | 4690 |
rs551807654 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136872836 | GCCTTGGTGTTGATG[C/T]TGCAATGTGGTGTTG | 4690 |
rs551871808 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136918524 | GACTTGAGCATCTCT[A/G]GATTTTGGTATTGGG | 4690 |
rs551904408 | snp | A/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136942878 | ATGCCTGGGAATGAT[A/T]CAAGTCAGGCAAAGC | 4690 |
rs551911190 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136860705 | TTTAACCAGCTCTGG[C/T]GGAAATAAAGAGAAC | 4690 |
rs551928828 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136933874 | CACACCTGGCTAATT[C/T]TTTTTGTATTTTTAG | 4690 |
rs551995259 | snp | A/G | | | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136949181 | GTCTCTGAGATATTT[A/G]GCTTTTCAAACTGTA | 4690 |
rs552036957 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136873369 | CTGGGCAATTTCTCC[C/G]ATTTGGAATGGCTGT | 4690 |
rs552044716 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136874229 | CACCCAGGCTGGAGT[G/T]CAGTGGTGCGATCTC | 4690 |
rs552051595 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136940648 | CTCCCAGGTTCAAGC[A/G]ATTCTTCTGTCTCAG | 4690 |
rs552053969 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136866552 | CTTCAGGTGATCTAC[A/C]CATCTCAGCCTGCCA | 4690 |
rs552185212 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136910477 | ATGTTTAAAAAATTA[C/T]AAACTGAATAAACCT | 4690 |
rs552223877 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136911206 | GTGAATAATGCTGCA[A/G]TGAACATGGGAATAT | 4690 |
rs552247371 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136883424 | TATTTACATGACTGC[C/G]TCCTCTTCATCCTTA | 4690 |
rs552268334 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136875008 | ATTCTGAAATTTCAT[A/G]AGGTTGTAGCTTGGT | 4690 |
rs552297444 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136917739 | TTATAACAGTTCTTT[C/T]CCACAGCACTTACGA | 4690 |
rs552301873 | snp | C/T | 3.35525e-05 | 0.00409575 | intron-variant | NCK1 | GRCh38.p7 | 3:136927966 | CCTTACATAAAAATA[C/T]TTTCCATGTGTTTAC | 4690 |
rs552349746 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136899707 | TGCAATTAGAGATAC[A/G]AGGAGACTTACTCAC | 4690 |
rs552358885 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136925964 | CAGCAGTATACGTGT[A/G]ATCCAATTTCAACTT | 4690 |
rs552360208 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136882112 | CATACCATTTTCCAT[A/G]GCAGCTGCACCATTT | 4690 |
rs552382125 | snp | A/C | | | intron-variant | NCK1 | GRCh38.p7 | 3:136896305 | CACCCATGTACCCTT[A/C]TCAGATTTTGGTGTC | 4690 |
rs552411559 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136916778 | AAAAATTGAAATTGT[A/G]ATTTTGATACTCAAT | 4690 |
rs552458468 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136862406 | CCCCCTTCAGTCCGC[C/T]GTCCGTCCATACAGC | 4690 |
rs552494164 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136881327 | TGGGTTCAAGCAGTT[C/G]TTCTTCCTCAGCCTC | 4690 |
rs552509332 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136936389 | TTGTTTATCCACTCA[C/T]CTGTTCATAGATGGA | 4690 |
rs552511374 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136927744 | CAAGCTGGTCTCGAA[C/T]TCAACCTCAAGTGAT | 4690 |
rs552553472 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136919469 | ATTGAATTTCATGTA[A/G]CCTCTGGAATCTCTA | 4690 |
rs552599144 | in-del | -/TC | | | intron-variant | NCK1 | GRCh38.p7 | 3:136925312 | TGACTATTTGTGTTT[-/TC]TCTTTCAGTTTTTAT | 4690 |
rs552632744 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136935189 | TACAGTGTGAGCCCC[C/T]GTGCTGGGCCATTCT | 4690 |
rs552669451 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NCK1 | GRCh38.p7 | 3:136935871 | CCCTGGCAATTACTA[A/G]TCTGCTTTCTGTCTC | 4690 |
rs552699318 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136934742 | AAATAACTTGACCAA[A/G]ATCACACAACCAGTA | 4690 |
rs552732437 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136895919 | AATTCATTCACATCT[A/G]TTTTAATTATGATAT | 4690 |
rs552732625 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136904442 | ACAGGCGTGAGCCAC[C/T]GTACCTGGCCTTCTT | 4690 |
rs552751902 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NCK1 | GRCh38.p7 | 3:136890340 | GAACTCCAGCTGGCC[C/T]GCCAGCGTTGCACGC | 4690 |
rs552762606 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136942845 | GATTTTTGCAAAAAC[A/C]ACCCAGGAAGACTCC | 4690 |
rs552774321 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136943961 | ACTTTAAAAGTTACT[C/G]ATTTGACAGTAAGGA | 4690 |
rs552793462 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136943099 | CTTTACCACAAAGCA[C/G]CAACTTCTTTCTTTA | 4690 |
rs552862484 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136903375 | TGTAGGTAGTATATA[A/G]GTGGGTCATGCTTTA | 4690 |
rs552874799 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136938789 | TTAACAAAAACATGA[C/T]TGGAGCCTAACCCTG | 4690 |
rs552898302 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136903658 | TTGAACCCCTGACCT[C/T]AGGTGATCCACCTGC | 4690 |
rs552970919 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136877375 | GAAGATAAGCAATAT[A/T]TTTCTGAGAAATTCG | 4690 |
rs553012372 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136868925 | AACCATCACTTCTTG[G/T]TGAGCAAGACAAGAC | 4690 |
rs553024233 | in-del | -/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136943140 | CCTAGATTTTATAAG[-/T]TTTTTTTTTTTTACT | 4690 |
rs553048107 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136945321 | TTATAATTATGTTAT[A/G]TAGTTATTTCAGGGC | 4690 |
rs553113759 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136891728 | CATCATTTTTTTAAT[A/G]ATAACCATGGTGATG | 4690 |
rs553238990 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136951409 | AAATTAATTGCCAAC[A/T]TTTAAAAATCAGGGA | 4690 |
rs553246244 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136864113 | CTCAAAAAAATAAAT[A/G]AAATGTGTATTTATT | 4690 |
rs553247002 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136897978 | TTGACAACTACTTTC[C/T]GAAGACTGGCTTAAC | 4690 |
rs553337003 | in-del | -/CTA | | | intron-variant | NCK1 | GRCh38.p7 | 3:136884126 | TAATGAACGAGCTAT[-/CTA]GAGAGAGGGTATATG | 4690 |
rs553360559 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136907686 | TGAAGTGTGATTATC[C/T]CCTCACTATTTTGTT | 4690 |
rs553383813 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136871093 | TAAAAAGCTTACTAA[C/T]TTTTTTTTAAAAAAT | 4690 |
rs553444034 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136872916 | TGCATTTCAGAAGAT[A/G]TATGGAAATGCTTGG | 4690 |
rs553467279 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136872619 | AAAATGTCTGCAGGG[C/T]GTGTCGGAGGTCTTC | 4690 |
rs553504098 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136901306 | GATTCAGTTTGCCAG[C/T]ATTTTGAGAATTTTT | 4690 |
rs553505802 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136870945 | AATCCAGGGTTGGCA[C/T]GGCATTCATTTATTA | 4690 |
rs553517713 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136879118 | GAAAACAAACTGGGA[A/G]CAATCAGAACAACAA | 4690 |
rs553543571 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136913769 | CGCCTCCCGGGTTCA[C/T]GCCATTCTCCTGCCT | 4690 |
rs553551171 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136898042 | TGTTTATATTTACAA[C/G]AAAAAGGCTAACATT | 4690 |
rs553552598 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136878681 | TGAGTGAGTTTTATG[A/T]TAATCTGAGTTGTAT | 4690 |
rs553579911 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136865418 | ATTTTCTAGAGTTTT[A/G]CATTTTCATTGCTTT | 4690 |
rs553616397 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136905220 | AGAGACAGGGTTTCA[A/C]TGTGTTAGCCAGTCT | 4690 |
rs553620787 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136914753 | TGAAATTGGGAGATC[A/G]CTTGCTATGGTTTGA | 4690 |
rs553659852 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136870397 | CACGTATTTTCATAT[A/G]TTAGTGTGTAGATCA | 4690 |
rs553668719 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136903009 | GGCTTTCTTAATTTT[G/T]GTATCTACATGATCC | 4690 |
rs553684180 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136866135 | AGAATTCATAGCCTA[A/G]TAACAGTCTGCTCAA | 4690 |
rs553716629 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136924434 | GTGGGGAAAGAGAAC[A/G]GTGTCAGAGACTTAA | 4690 |
rs553718486 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136933201 | GATTCGAGTCTGAGA[A/C/G]GTGCTTAGGTGGAGG | 4690 |
rs553755188 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136925122 | AACTTAAAAGCATTA[C/T]ATAAATTTTTAGTTA | 4690 |
rs553811006 | snp | C/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136904584 | GCCATTTTTAGAATT[C/G]TGTGTATTTGATTTT | 4690 |
rs553845924 | snp | C/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136935276 | GAGAGAATCATTCTA[C/G]GTTTTACTGATCTTT | 4690 |
rs553866270 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136923337 | GAGGCAGGCGGATCA[C/T]GAGGTCAGGAGATCG | 4690 |
rs553877734 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136932683 | TAAAAGAGAGAGTTG[G/T]GCAAGACTAAATGAT | 4690 |
rs553881604 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136916333 | CAAATGTTATGATTA[A/G]TCATAAGTTAAATAC | 4690 |
rs553933218 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136901284 | TTTTTTTTTTTTAAT[G/T]TTGTTGGATTCAGTT | 4690 |
rs553967081 | snp | A/G | 0.00517822 | 0.0506191 | upstream-variant-2KB, intron-variant | NCK1 | GRCh38.p7 | 3:136930231 | TGAAAGTTGAGAAGG[A/G]AAAGGGGAAAACAAA | 4690 |
rs553994368 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136892236 | CTTGTAAGAGTTCTT[C/T]ATATATTCTGAATAT | 4690 |
rs554014914 | in-del | -/C | 0.00517822 | 0.0506191 | intron-variant, upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136862895 | TTTTCTAGTCTGGGG[-/C]TGTGACTTTAATGGT | 4690 |
rs554048294 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136887602 | GACTTTTAAGTTATT[A/T]GTCACCTGGAACAGA | 4690 |
rs554093925 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136900391 | TTCTTTTTGCTTAAG[A/T]TTGTTTTGGTTGTTT | 4690 |
rs554100389 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | NCK1 | GRCh38.p7 | 3:136915239 | TGAGAATGGAGATAC[A/G]TGGATTCATTTGAGT | 4690 |
rs554137901 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NCK1 | GRCh38.p7 | 3:136929424 | GTGTTCTAAAGGTAA[C/T]TAAGTAGATATAATG | 4690 |
rs554138250 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136937629 | TCTTTCAGCGGTGTT[C/T]TGCAGTGTTTAGTAT | 4690 |
rs554146918 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | NCK1 | GRCh38.p7 | 3:136914245 | AGGACAGGTCTTATT[G/T]CCCGAAAGCTGTGGA | 4690 |
rs554163566 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136898575 | TTAGTGTGTAAAATA[C/G]TTCTGAACTCTTACT | 4690 |
rs554170970 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136873960 | CTAATACAGTAACCA[C/T]ATAGCTTGTATACCT | 4690 |
rs554174737 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136881408 | TATTTTTAGTGGAGA[C/T]GGGATTTCACCATAT | 4690 |
rs554182529 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136936780 | ATTCGTATACCGTAG[C/T]TGGAACAATCTTTAT | 4690 |
rs554185572 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136946800 | TTTATTATAACCTCA[A/C/G]AAAACCTATTTTAGC | 4690 |
rs554280598 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136888176 | TCTCAAACTCCTGAC[C/G]TCGTGATCTGCCTGC | 4690 |
rs554300825 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136947529 | ATTTAAATTCATTGC[C/T]GATATTTAAATATTA | 4690 |
rs554301820 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NCK1 | GRCh38.p7 | 3:136873665 | ATTGTAGCTCCCACA[A/G]TTCCTGTGTGTGGTG | 4690 |
rs554314321 | snp | A/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136880975 | TGCGCTCTACCCTAC[A/T]TTTGTTCATTCCTGT | 4690 |
rs554353207 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136949073 | GATTAGAAAACATGT[C/T]GTACAATTTTAATTT | 4690 |
rs554379853 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136862201 | GCCCGCGCGGATCCG[C/T]CTGCCCACCGCGCGT | 4690 |
rs554384648 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136917307 | AATTCTTCTTCCAGT[A/G]TGATCCAGGGAAACC | 4690 |
rs554423784 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136949479 | AAAATAGAATGTGCT[C/T]ATGGTTAGGGAAAAT | 4690 |
rs554477902 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136910510 | GAGTTACAAACTAAA[A/G]TTACAGTAATACTAG | 4690 |
rs554519089 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136903815 | TTCTGTCATTTTATT[A/G]ACTGATTTATGGCTG | 4690 |
rs554534211 | in-del | -/T | 0.0126979 | 0.078662 | intron-variant | NCK1 | GRCh38.p7 | 3:136933872 | ACCACACCTGGCTAA[-/T]TTTTTTTGTATTTTT | 4690 |
rs554574816 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136889481 | CCCAAAGAGTAAGCA[C/G]TAGCAAGATTTATTG | 4690 |
rs554631706 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136870116 | GGAGGCCGAGGCAGG[C/T]GGATCGCTTGAGGTC | 4690 |
rs554637081 | snp | A/G | | | intron-variant, upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136863970 | GCCGGGCGTGGTGGC[A/G]GGCGCCTATAGTCCC | 4690 |
rs554643116 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136912611 | ATTGCCCTCAGGAGC[G/T]CCACAGTTTGTTTTT | 4690 |
rs554655724 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136894679 | GGCAGGAAAGGCAAA[C/G]TCATTTCTACAGTAA | 4690 |
rs554671158 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136949822 | CTGATGGTAAAATTG[A/G]AGTTGTGTAACTTGT | 4690 |
rs554705468 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136876609 | AACTTTGCCTATTTT[A/G]TCTCTGTTATAAAGT | 4690 |
rs554705671 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant, nc-transcript-variant | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136861687 | GCACGAGGACACTTT[C/T]AGAGGGCCCTCAGAC | 4690 |
rs554708956 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136889293 | AGAATGAAGCCGCGG[A/T]CCCTCGCGGTGAGTG | 4690 |
rs554728054 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136909888 | CTGATGTTAATACAG[A/C]CCACCTCACTTCTCT | 4690 |
rs554775662 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136923282 | CTGTCCAGGCCGGGC[A/G]CGGTGGCTCACGCCT | 4690 |
rs554809423 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136869699 | TTTTCTTATGTGTAC[A/G]TAACAATAGTTGAAT | 4690 |
rs554836597 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136867826 | CTCTTGTAATTTTGC[A/C]TTATTTGCCTCACAT | 4690 |
rs554865832 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136883068 | GGATTACAGGCATGC[A/G]CCACCACACCCAGCT | 4690 |
rs554889809 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136916843 | CCTTATTTTGTAGAT[A/G]AGGAAATGGAGTTTC | 4690 |
rs554905300 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136920968 | CCTTCAAAAATTCAC[A/C]CATTGAAGTCCTAAC | 4690 |
rs554926847 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136889951 | CACCCAGTGGATCCC[A/G]CACAGGGGTTGCAGG | 4690 |
rs554948493 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136921849 | AGTGCAGTGGCGTGA[A/T]CTCAGCTCACTGCAG | 4690 |
rs555019165 | snp | A/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136925513 | TATAGTCATACTTAC[A/T]TCCCTCCTGTTCCTG | 4690 |
rs555069449 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | NCK1 | GRCh38.p7 | 3:136928362 | GTTTGAGTCATAGCA[G/T]GTGGTCAACCCAGAA | 4690 |
rs555084850 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136911866 | ATTCTTAGCTGACAG[A/T]TTTTTTTTTATTCTC | 4690 |
rs555169305 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136927035 | GGAGTGCAGTGGCAC[G/T]ATCTTGGCTAACTGC | 4690 |
rs555170034 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136878009 | ATATAGAACTGATAC[A/G]TGTTATAACATGATG | 4690 |
rs555214957 | snp | A/C | | | intron-variant | NCK1 | GRCh38.p7 | 3:136934287 | CTGTTCATATTATTT[A/C]TTTCTTTCTTTTTTC | 4690 |
rs555223527 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136944504 | AATAAATTACCAAAA[C/T]GTTACGGTTTAAAAG | 4690 |
rs555226125 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136873881 | CAGCCACATGGAACT[A/G]TAAGTCCATTAAACC | 4690 |
rs555293898 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136934354 | GCAGTGGTGTGATCT[C/T]GGCTCACTGCAACCT | 4690 |
rs555306656 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136903717 | GGTGAGAGCCACACC[A/G]CGCCTGGCCAAATTA | 4690 |
rs555332608 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136926401 | TGCCTCAGCGTCCCA[A/G]GTAGCTGGGACTACA | 4690 |
rs555361611 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136871103 | ACTAATTTTTTTTTA[A/G]AAAATTGTTTAGTCT | 4690 |
rs555425338 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NCK1 | GRCh38.p7 | 3:136937700 | ATTCTTCTTAATGCT[A/G]TTATAAATGGATTAT | 4690 |
rs555454382 | snp | A/T | 1.64765e-05 | 0.00287019 | missense, nc-transcript-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136946010 | AGGAGATGTAATGGA[A/T]GTTATTGAAAAACCT | 4690 |
rs555511738 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136884099 | GCCAGAGGTGATACG[A/T]TGAAGTCATAATAAT | 4690 |
rs555658096 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136906161 | CTAGGTATGTGTCAT[A/G]GTGTAGTCTCTGTGT | 4690 |
rs555823530 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136913959 | GCCACCACGCCCAGC[C/T]GCACAGTGATTTTCT | 4690 |
rs555850745 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136899424 | CATTTCTTTTCTTTT[C/T]TTTTTTTTTAAATTT | 4690 |
rs555864481 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136866285 | TATTTTTGTACCTTC[A/G]TATCATTCCTTTTTC | 4690 |
rs555865501 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136900421 | TGGGCTCCTTTTTGG[C/T]TTCATATGAATTTTA | 4690 |
rs555939976 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136906763 | CCCCAGGCTTGCAGG[G/T]GGCACGTGTGGTTAG | 4690 |
rs555955702 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136911485 | TGCATTTCCCTAATG[A/G]TTAGTGATGCTGAGC | 4690 |
rs556010599 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136898917 | AGCTTTACAGAGAAC[A/G]TAATCATAAAATGGC | 4690 |
rs556029082 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136907729 | AAGAGGCAAGTACCA[A/C]ATGCATGTAGTCAGC | 4690 |
rs556045327 | in-del | -/C | | | intron-variant | NCK1 | GRCh38.p7 | 3:136940161 | AGCCACTGTGCCTGG[-/C]CTATTGAGCCTTGTT | 4690 |
rs556046393 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136864161 | TTGTCCAGGTTTCTG[C/G]AGTGCTTTCAGGTCC | 4690 |
rs556062059 | snp | C/T | | | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136949779 | AATTCTTTGCTGTTA[C/T]AAATAGATATCTAAT | 4690 |
rs556086056 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | NCK1 | GRCh38.p7 | 3:136864752 | CATGGTTCTGGGTTT[A/T]TTTCTTTTCTTTTTT | 4690 |
rs556103469 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136917006 | GAAAACTAGGGTAAG[A/G]TAAACAAGTTGCCTA | 4690 |
rs556109004 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | NCK1 | GRCh38.p7 | 3:136876421 | GCAAGACTAATAAAG[A/G]AAAAGAGAAGAATCA | 4690 |
rs556122812 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136871545 | ACATTTTTAGTGTTC[A/G]AAAAGGCTCTCTTGC | 4690 |
rs556140318 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136917945 | TTACAACCAGTGGGT[G/T]TAAATTTCTTGTGTT | 4690 |
rs556171103 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136860813 | TCCCCACCTCCAACA[C/T]TGGGGATCAAATTTC | 4690 |
rs556174578 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon, intron-variant | NCK1 | GRCh38.p7 | 3:136930575 | AATGGATTGGTTAAA[C/T]GTCTTTAAAGATTTT | 4690 |
rs556219474 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136879214 | AGTAGAGGAAAAGAT[A/G]GAAAATAAATGAGAA | 4690 |
rs556221681 | snp | C/T | | | intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136946741 | TTTAAAAAATTGATA[C/T]TAAGTTTCTTCATAA | 4690 |
rs556244024 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136875358 | TCTTTTCCTAATTGA[A/C]TACCCTTTATTTCCT | 4690 |
rs556247731 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136887391 | TTTTCTCCTGATAAA[-/T]AGCAGCCTAAGTAAG | 4690 |
rs556266655 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | NCK1 | GRCh38.p7 | 3:136925335 | AGTTTTTATTTTAAT[A/T]AAACTTTTTATTTTG | 4690 |
rs556284165 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NCK1 | GRCh38.p7 | 3:136892586 | ATTCTTCTCTAGAGC[C/T]TTCTGAAGGAATGCA | 4690 |
rs556286735 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136910266 | ATTTAACATTCTGAA[A/G]ATAAAACACTCCAAT | 4690 |
rs556304325 | in-del | -/AAAC | | | intron-variant | NCK1 | GRCh38.p7 | 3:136942487 | TGGAGCCAAAAGAAA[-/AAAC]AAACAAACAAACAAA | 4690 |
rs556311728 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136888963 | CAACCTCTGCCATCC[A/G]GGCACAAGTGATCCT | 4690 |
rs556336985 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136916131 | ATGATCCAGTCACCT[C/T]GCAGTCACCTCCAGT | 4690 |
rs556357468 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136923424 | AGCCGGGCATGGTGG[C/T]GGGCACCTGTAGTCC | 4690 |
rs556393969 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136893792 | AAGGGTTAGTGATAT[A/G]AGCCAGTGGTACCTG | 4690 |
rs556413109 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | NCK1 | GRCh38.p7 | 3:136938350 | GAATTCACTTATTGG[C/T]TAAAATTTATTTATA | 4690 |
rs556414616 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136921790 | AAGAAAGATGGTTTT[G/T]TTGTTTTGTTTTGAG | 4690 |
rs556423051 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136879962 | ACCTGCACGTTGTGC[A/G]CATGTACCCTAGAAC | 4690 |
rs556446252 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136918058 | GAGTTCAAGGCAGGC[C/T]GTTTGTTTTTATATT | 4690 |
rs556524561 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136922835 | GATTCTAACCCAAAG[A/G]TACACTAACAGAAAA | 4690 |
rs556553804 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136889433 | GCTGTAGACCTTCGC[A/G]GCGAGTGTTACAGCT | 4690 |
rs556559229 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136867975 | CTGGCTGGAGTGCAG[C/T]AGCATGATCTCGGCT | 4690 |
rs556589518 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136926739 | ATTAGTTTTTAGAAG[-/T]TTTCCAAACGTGGTA | 4690 |
rs556602832 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | NCK1 | GRCh38.p7 | 3:136940270 | TTTGATGGGATATTC[G/T]CTATATGTCTATTAG | 4690 |
rs556654109 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136881471 | GATCTGCCCGCCTCG[A/G]CCTCCCAAGTGCTGG | 4690 |
rs556661815 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136943005 | TGGCATTAGGAGTGC[A/G]GGTTACTGTCCACAC | 4690 |
rs556668535 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136940869 | TGATATTTATATAGC[C/T]ACCCCACTCTCTCAG | 4690 |
rs556711699 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136864221 | ATGTTGGCCGGGCTC[A/G]GTGGCTCACGCCTGT | 4690 |
rs556734993 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136896131 | GTATTTATCATTTCT[A/G]TGTGTTGGGAACATT | 4690 |
rs556748370 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NCK1 | GRCh38.p7 | 3:136890903 | TCTGCCATCCCCCCA[A/G]CCTCTGGCAATCACC | 4690 |
rs556759272 | snp | A/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136920258 | TCTTCTTTTTTTTTA[A/T]AAAATAGTGTAGGTC | 4690 |
rs556776427 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136949970 | TAATTAAGACAAATT[C/T]TCATCTCTATTACAT | 4690 |
rs556877280 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136935090 | TATTTTTAGTACTGA[C/T]AGGGTTTCGCATGTT | 4690 |
rs556887187 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136883157 | TACTACTGGCGTCAT[A/G]TGATCTGTCCACCTT | 4690 |
rs556920648 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136948618 | CCCATACATATATAC[G/T]ATGTATGCAGTGCAT | 4690 |
rs556930294 | snp | C/G | | | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136949385 | TAATTGTCAGGAATG[C/G]TATTACCTATTTTCA | 4690 |
rs557021784 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NCK1 | GRCh38.p7 | 3:136864089 | CTGGGCGACAGAGCG[A/G]GACTCCGTCTCAAAA | 4690 |
rs557053298 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136863202 | TTAGGAAAGAATTAG[C/G]TTAAAGAGAATTTCC | 4690 |
rs557076022 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136872211 | CCAAAATGCTGATTG[C/T]GATATGGACCATAAA | 4690 |
rs557184334 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136894261 | TTAAATTGTGGGGAT[A/G]GGAAATCCACATGCC | 4690 |
rs557195291 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136920450 | CTAGGAGACAGAGCA[A/G]AGGAATGAGAATAAA | 4690 |
rs557226026 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136869547 | GAGATTGTCTCAAAA[G/T]AAAAAAAAGAAAGAA | 4690 |
rs557275620 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136862264 | CGGCGGAGCGCAGGC[C/T]TCGTGCCGTTACGGC | 4690 |
rs557301482 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136914144 | TATTGGGAGGGAGGT[A/G]AAACAATAGCTGCCT | 4690 |
rs557306559 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136897058 | CTTTTTTTCTACATC[C/G]TTACCAGTGTCTTTT | 4690 |
rs557316472 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136868510 | TTTTTGTATTTTTAG[C/G]AGAGACAGGGTTTCA | 4690 |
rs557363772 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136870274 | TTGAACCCAGGAGCC[A/G]GAGGTTGCAGTGAGC | 4690 |
rs557377377 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136934926 | GTGAGGTCAGGAAGT[A/G]CTATGACCTGAGTGT | 4690 |
rs557410547 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136933229 | AGGTATGCTCCCTTA[C/T]GTGTGTGTTGGCCAA | 4690 |
rs557500251 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136885534 | GGCCTCCAACTCCTG[C/G]GCTCAAGTGATTCGT | 4690 |
rs557522894 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136891589 | TATGGTAATTTTGTT[G/T]CTAATTTTTTGAAGA | 4690 |
rs557530684 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136913262 | CTTTCCTCAGGATTT[C/G]CTGGGTTTTTGTGTG | 4690 |
rs557560888 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136919899 | TGTTGTACTTTAACA[C/T]ATAACTTGACAATTT | 4690 |
rs557567863 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NCK1 | GRCh38.p7 | 3:136929211 | TAGCTGGGACTACAG[A/T]TGCTTACTACCATAC | 4690 |
rs557598795 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136878487 | AAGTATCCAGAAATT[G/T]TGTATTTGTAGAGAT | 4690 |
rs557604669 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136922018 | TTAGTTTCCTGACCT[C/T]GTGATCTGCCTGCCT | 4690 |
rs557631568 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136927120 | GGGATTCCAAGTGTG[C/T]GCCACCATACCTAGC | 4690 |
rs557668697 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136876679 | CTACAAAGAATATAC[G/T]TATTTTTTTTAGGTG | 4690 |
rs557693081 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136872081 | ATACCCGAAAATGTG[C/G]AAGCAACTTTGGAAC | 4690 |
rs557709354 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136922604 | AAAAGAAATCACTGT[A/C]ATAAGAGAAATACAA | 4690 |
rs557744656 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136864861 | CTCCCGGGTTCAATC[A/G]ATTCTTGTGCCTCGG | 4690 |
rs557784089 | in-del | -/TT | 0.00159617 | 0.0282053 | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136951448 | TAAAATTCAGACTTC[-/TT]GTTTCCCTTTAAAAA | 4690 |
rs557824140 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | NCK1 | GRCh38.p7 | 3:136931929 | GTTTGAGACCAGCCT[C/G]GTCAACATGGTGAAA | 4690 |
rs557847316 | in-del | -/TA | 0.00874735 | 0.0655527 | intron-variant | NCK1 | GRCh38.p7 | 3:136895321 | TTTGGTTTATTTTAT[-/TA]TATATATATATATCA | 4690 |
rs557895104 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136928444 | ATGCTCCAAGTCAAG[A/G]CAGAGTGATACCAAT | 4690 |
rs557944992 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | NCK1 | GRCh38.p7 | 3:136937088 | TGTTTTCTTCTAAGA[A/G]TTTTATAGTTTTAGC | 4690 |
rs557946486 | in-del | -/C | 0.00597247 | 0.0543191 | intron-variant | NCK1 | GRCh38.p7 | 3:136866737 | TCCTGTGTCAGTCTT[-/C]CGAGTAGCTAGGATT | 4690 |
rs558068387 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136944603 | GGGACTAAATAGGAA[C/G]GAAAACAAGGATGTC | 4690 |
rs558076826 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136906831 | CAATCTCAGACCCTG[A/G]GAGGAGTGCTTAGGT | 4690 |
rs558087827 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136892382 | AAGTCCAGTTTGACT[A/C]TTTTCGGTTGCCTGT | 4690 |
rs558107063 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136936533 | TGCTGGATCGTATGG[A/T]AATTCTTTGCTTTTT | 4690 |
rs558146936 | in-del | -/A | | | intron-variant | NCK1 | GRCh38.p7 | 3:136942875 | CTATGCCTGGGAATG[-/A]ATTCAAGTCAGGCAA | 4690 |
rs558151884 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136880007 | AAAAAAAAAAAGGCT[A/G]GGCACAGTGGCTCAC | 4690 |
rs558188445 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NCK1 | GRCh38.p7 | 3:136892927 | CCAACAGCAATGTAC[A/G]CTGTACCCAATGTGT | 4690 |
rs558215904 | snp | A/T | 0.00358779 | 0.0422022 | upstream-variant-2KB, intron-variant, nc-transcript-variant | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136861665 | GCCAAGAATGTAAGC[A/T]GCCCAAGCACGAGGA | 4690 |
rs558372557 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136945339 | GTTATTTCAGGGCCT[C/T]TGACAAGAGAAAAGA | 4690 |
rs558375066 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136947784 | AAGTTTAGATTAATT[C/G]TCATTTGTGTATTCT | 4690 |
rs558389602 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136867772 | CCTTGATCTTCTGAC[A/G]CAAGTTCTGTGTGTT | 4690 |
rs558414941 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136901508 | GAAGCCATCCAGTCC[C/T]GGACTTCTGTTTGTT | 4690 |
rs558429057 | in-del | -/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136911865 | ATTCTTAGCTGACAG[-/T]TTTTTTTTTTATTCT | 4690 |
rs558503630 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136910735 | GTGAAATGATTAAAT[C/T]AAGCTAATTAACATA | 4690 |
rs558509360 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136902257 | GGCTGGAGTGCAGTG[A/G]CACTATCTCAGCTTA | 4690 |
rs558553415 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136894725 | CCCCTGGAATGCAAA[A/G]GTTCCAATTCCATCC | 4690 |
rs558570423 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136922205 | TGGTGGTACAAATTA[A/G]GCCCACCAATGTTTG | 4690 |
rs558570841 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136866338 | TTTGAGACAGAGTCT[C/T]GCTCTGTTGCCCAGG | 4690 |
rs558611471 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136873125 | ACAGCTTGCACCATG[A/C]GCCTGGAAAAGCTGC | 4690 |
rs558618632 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136876477 | GGGGATATCACCACC[A/G]ATCCCACAGAAATAC | 4690 |
rs558678254 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136866996 | TGAATTTTCGCTTTT[G/T]GTCCTTTGGTGCAGT | 4690 |
rs558694950 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136882345 | ATTTTGTTCGTTTGC[C/T]CATTTTTCATTTGGG | 4690 |
rs558731975 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136881597 | AGTTCAGTATTAAGT[A/G]TATTCACATTGTTGT | 4690 |
rs558734820 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | NCK1 | GRCh38.p7 | 3:136914851 | TTGGGTCGTGGGAGT[A/G]GATCCCTCATAATAT | 4690 |
rs558754888 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136916233 | GTAGAGTCCTAAAAC[C/T]ATTTTGTGATTAAAA | 4690 |
rs558789409 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136893340 | TTTTTTGATTGTGGC[C/T]ATTCTTGCAGGAGTA | 4690 |
rs558801379 | snp | G/T | | | downstream-variant-500B, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136951658 | GAATTGTAATTCAGG[G/T]CATATACACAGACAG | 4690 |
rs558809850 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136873821 | TCTTGTCTGCCGCCA[C/T]GTGAGACATGCCTTT | 4690 |
rs558825060 | snp | A/C | | | intron-variant | NCK1 | GRCh38.p7 | 3:136891444 | CTGGCCTGATCATGG[A/C]CACTTTGGTTGCTTC | 4690 |
rs558841377 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136925388 | AATTCTGAGAAACTT[C/T]AGAACTTATTGCGAG | 4690 |
rs558849572 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136924369 | CAAATTCACGATGTG[A/G]GAAATGCTACAGGAC | 4690 |
rs558864456 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136889090 | GTAGAGACAGTCTCA[C/G]TGTGTTGCCCAGGCT | 4690 |
rs558922625 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136915491 | CGGAGTGTACTGGTT[C/T]CCTGTAACTCCAGTA | 4690 |
rs558925452 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136880620 | TGAACTTAAGACAAT[A/C]AACAAACTTTGTTTG | 4690 |
rs558965382 | snp | A/C | | | intron-variant | NCK1 | GRCh38.p7 | 3:136886510 | TAATGACAAGGAAAA[A/C]ACGTCTGTATATGTT | 4690 |
rs559039711 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136875497 | AAAAAGGCAGGGATT[A/G]CAATCCTAGTCTCTG | 4690 |
rs559047001 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136919133 | ATTCTGGAAAAGGCA[A/G]AACTACATAGGGACA | 4690 |
rs559073749 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136881302 | TTGGCTCACTGCAAC[C/T]TCTGCCTCCTGGGTT | 4690 |
rs559133253 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136866491 | TTTGTATTTTTAGTA[A/G]AGACGGGGTTTCTCC | 4690 |
rs559153867 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136934256 | TACATAGGTAAATAC[A/G]TGTCATGGGGGTTTG | 4690 |
rs559201693 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136941422 | GGTGTGAGCCTCTGT[A/G]ACTGGACTATTTTCT | 4690 |
rs559204198 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136927158 | TGTATTTTTAGTAGA[A/G]ATGGGGTTTCACCAT | 4690 |
rs559240987 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136942327 | CTTATTACTGCTGCT[C/T]ATTGTGAGTGGTTGT | 4690 |
rs559254015 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NCK1 | GRCh38.p7 | 3:136924306 | AAATAATTACCAGTT[C/T]ATAGGAGATAGGGGG | 4690 |
rs559264432 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136862431 | TACAGCCTGTTACTC[C/G]CTGCGTCGCTTCCTC | 4690 |
rs559267121 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | NCK1 | GRCh38.p7 | 3:136889563 | TTGCCACTGCTGGCT[C/G]GGGCAGCCTGCTTTT | 4690 |
rs559299634 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136884972 | GTGATCTGCCCACCT[C/T]GGCCTCCCAAAGTGT | 4690 |
rs559301433 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136869103 | AAATGAGCCCACTGT[A/G]GTGGTGCATGCCTGT | 4690 |
rs559312692 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | NCK1 | GRCh38.p7 | 3:136941829 | TTTTTTCATTTTAGC[A/C]TGGAGGATTCTCTTT | 4690 |
rs559356835 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136911269 | TTTGGATATATACCC[A/G]GAAGTGGGATTGCTG | 4690 |
rs559391459 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136926544 | CCTCCTGAAGTGCTG[A/G]GATTACAGGCATGAG | 4690 |
rs559395189 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136876777 | GCTACAGTGAGAATT[C/T]ACGAATCAGTGTAAC | 4690 |
rs559400894 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136926330 | CCCAGGCTGGAGTGC[A/G]GTGGCGCGATCTCGG | 4690 |
rs559426649 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136918597 | CAACCTGTGGCCTGC[A/G]GGCTGCATGCAGCCC | 4690 |
rs559435804 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136895629 | GAGTGCAGTGGCACA[A/G]TCTCGGCTCACTGCA | 4690 |
rs559530030 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NCK1 | GRCh38.p7 | 3:136876087 | GAAGGCAGAAGTAAA[A/G]ATGTTCTTTGAAACC | 4690 |
rs559531958 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136883216 | ATGAGCCCCCATGCC[C/T]AGCCTACTTCTTATT | 4690 |
rs559565580 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136882659 | ATGTCACCACCATAA[G/T]CAGCTTTGGCTTCTC | 4690 |
rs559571648 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136944277 | GTGCACACCACTGCA[C/T]CCAGCTAATTTTTGT | 4690 |
rs559604023 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136882124 | CATAGCAGCTGCACC[A/T]TTTTACATTACCACC | 4690 |
rs559639507 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136890596 | TATTGCTGAATAATA[C/T]GTAATTTTACAGTTA | 4690 |
rs559643353 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136933364 | GCAAACCAGGTCACA[C/T]AAGGAATAGTTATGG | 4690 |
rs559666297 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136894632 | AACATTTTGAAACCA[C/T]TGAGGTACTGTAAAT | 4690 |
rs559685786 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136891086 | CCCCGACCAAAGGCT[A/G]GTACTGTTCCGTTGA | 4690 |
rs559701517 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136892454 | ACAAGAGTCCTTATC[A/G]GAGGGAATCAATTAG | 4690 |
rs559728022 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136899652 | CCACCATTGTCTTTC[G/T]TAGTAATCTTATCCA | 4690 |
rs559740500 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136936653 | ACACCTATTTTCTTT[C/T]TTTCTTTGCTTATAT | 4690 |
rs559794297 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136874065 | CTTTTCAGTGATAGT[A/G]GTATTCCATTGGATG | 4690 |
rs559815597 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136944694 | GACTTGAGTGAAGAA[C/T]GAGAGTGAGGATAAT | 4690 |
rs559826403 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136862865 | GCCCTCTCCCCTCCC[C/T]CCACCCACCGGCCGT | 4690 |
rs559871363 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NCK1 | GRCh38.p7 | 3:136896602 | GAGTGCAGTGGTGCA[A/G]TCATGGCTCACTGCA | 4690 |
rs559880016 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136871722 | ATTGTTACTCCCACA[A/G]TTCCCACGTGTGGTT | 4690 |
rs559901741 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136936155 | AAGTGATTCTCCTGC[C/T]TCAGCCTCCCAAGTA | 4690 |
rs559905443 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NCK1 | GRCh38.p7 | 3:136891989 | ATCCTCCTGGGCTCA[A/G]GGGATCCTCCTGTCT | 4690 |
rs559918962 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136905551 | GGTCACAGTGTCTGG[C/T]CTCAGAATTCTCTTG | 4690 |
rs559937039 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136943664 | TTTCCTTTGTTCCTA[C/T]TACTGATGTATGTAC | 4690 |
rs559955344 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136909018 | ACTCTTCCCCCACTC[A/G]CCCCCAGATATTTGA | 4690 |
rs559958930 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136904738 | TATTTTATTGAACAG[C/G]TTTTCTAACATTTTT | 4690 |
rs559988767 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136863365 | TGGAAACCAGTGTGC[C/T]TAGACTCTCAGCCTT | 4690 |
rs560090103 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136871267 | TAGCCAGGTTTGGCT[G/T]TGAGCGTCTGTAGTC | 4690 |
rs560124156 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136912786 | TCAGCTTCCTGAGTA[G/T]CTGGAACTACTTGCG | 4690 |
rs560207049 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136931988 | AGCTGGGCGTGGTGG[C/T]GGGTGCCTGTAATCC | 4690 |
rs560218585 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136864942 | TTTTTGTATATATAT[A/T]TATTTTTCTTTTTCT | 4690 |
rs560222369 | snp | C/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136890008 | TGTGCCCGCACTCCT[C/G]AGCCCTTGGGTGGTC | 4690 |
rs560242994 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136923640 | GAGAGAAAAGAGAAG[G/T]TATGGAAGAAGACCT | 4690 |
rs560259453 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136922098 | ACTGAGTGGTTTTTA[A/G]GGGCAATAGGTGGTC | 4690 |
rs560288934 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136865920 | CAAACTTTGGTTTTA[C/T]CTCTATGCGTGTAAC | 4690 |
rs560298013 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136914168 | GCTGCCTGCTTCTGT[A/G]TCTGTATCTCAGTGA | 4690 |
rs560331703 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136909330 | AGTTTGCTGAGAGGG[A/G]AAGGGCATGCTAGAC | 4690 |
rs560342029 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136939636 | CTCCCATAGGTTTTT[-/G]TATGTTGTGTTTTCA | 4690 |
rs560386342 | in-del | -/CAAT | 0.00874735 | 0.0655527 | downstream-variant-500B, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136951762 | AAGAAAACTCATTGG[-/CAAT]TTCTAGATAAGTTTT | 4690 |
rs560387832 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136920314 | CACTTTTGGAAATAT[A/C]ACTTTGAAATCATCC | 4690 |
rs560390297 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136937403 | AGAAAGGGAGAGTCC[G/T]CCCACTTGATTTTCC | 4690 |
rs560491128 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136873150 | AGCTGCAGACACTCA[A/C/G]TGCAAGCCTGTGAAA | 4690 |
rs560503472 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136866455 | TGGGACTACAGGCAT[C/G]CGCCACCATGCCTGG | 4690 |
rs560636254 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NCK1 | GRCh38.p7 | 3:136881243 | AATTTTTTTTGAGAT[A/G]GAGTCTCACTCTGTC | 4690 |
rs560672491 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136886154 | TGGAAGCATGGGTTA[A/G]TAAAATTGTATTAAC | 4690 |
rs560697663 | snp | G/T | | | upstream-variant-2KB, intron-variant | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136860308 | AAAATTCACCGCCAT[G/T]ATTCACTTTGGATGC | 4690 |
rs560776291 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136882189 | TCACTAACACTTGTT[C/T]CCTGCATGTTTTTTT | 4690 |
rs560816810 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136924798 | TATTGGAACGCTAAG[C/G]TTGTGAGAGTTATTT | 4690 |
rs560818156 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136946349 | GGGTATTTTAAAAAA[A/G]AGAGAGAGAGAAATG | 4690 |
rs560891742 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136892440 | GGGCTCTGGTAATCA[C/T]AAGAGTCCTTATCAG | 4690 |
rs560923236 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136895727 | GTACCACCACACCCC[A/G]CTAATTTTTGCATTT | 4690 |
rs560951324 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136881219 | CACTATTGGCCTCTT[A/G]TTTTATTTAATTTTT | 4690 |
rs560961977 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136896465 | GCTGCAAATGACATG[A/G]TTTCATTATTTTTTA | 4690 |
rs560970464 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136888178 | TCAAACTCCTGACCT[C/G]GTGATCTGCCTGCCT | 4690 |
rs560980318 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136864603 | CACTTGGGAGGCCAA[G/T]GCGGGAGGATAGCTG | 4690 |
rs561011068 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136915730 | AACACTTTTGCTTTT[A/G]TTTTTTTTTTTTTGA | 4690 |
rs561014751 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136940491 | TTACACTTCTTGATG[A/G]ACTGATTCTTTTATC | 4690 |
rs561017370 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136860946 | TGCAAACTTTTGAGG[C/T]TGATATCCAGGGCCA | 4690 |
rs561027223 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136947268 | TGATCTGGCTCACTG[C/T]TTGAAACTTTGGGAG | 4690 |
rs561039640 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136901680 | AGTGTATCGTTGTTT[C/G]TAATAGTTTTTAATG | 4690 |
rs561041651 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | NCK1 | GRCh38.p7 | 3:136893360 | TTGCAGGAGTAAGGT[A/G]GTACTGCATTGTGGT | 4690 |
rs561078871 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136894019 | TACCCTATTAGCAAG[C/T]ATGGAAATACCCTGC | 4690 |
rs561084137 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136903228 | TCTCTTTTTACTGTT[C/T]TTGACTTAAAGTTTG | 4690 |
rs561110651 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136868959 | ATATCTTGTTGAGGC[C/T]GGGCGCGGTGGCTCA | 4690 |
rs561151662 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136865937 | TCTATGCGTGTAACA[A/C]TATTGGCTGATTTTT | 4690 |
rs561152336 | snp | G/T | | | downstream-variant-500B, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136951710 | AACAGAGAAGATGGG[G/T]AGTTTTATTATAAAG | 4690 |
rs561184715 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136947894 | TAGACTTTCTCATGT[A/G]TTTCTCTGACTGGAG | 4690 |
rs561229092 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136879002 | AATCTGTGTTATTTA[C/T]AATAGCTTTTATGGC | 4690 |
rs561243976 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NCK1 | GRCh38.p7 | 3:136868056 | CTGAGGAGCTGGGAT[C/T]ACAGGCACCTGCCAC | 4690 |
rs561253170 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136862347 | TGCCCGGCTCGGCAG[C/T]GGGAAGGTGAGACGG | 4690 |
rs561282651 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136874707 | TTTCCATGAATCATA[C/T]AGTGTTTTTGTTTGT | 4690 |
rs561293892 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136918349 | ATATTCTGGAAAAAA[A/G]AATACACTAATTAAA | 4690 |
rs561313774 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136951555 | CTTTACCAGTGCACA[C/T]GGTGAAAAAATTCAA | 4690 |
rs561323818 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136910894 | TCCTCCTCTCTGAAA[C/T]TTGATATCCTTTGAC | 4690 |
rs561348920 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136889729 | ATACAGAATGTTGAC[A/G]CAAAGGTTCTCCAAG | 4690 |
rs561371440 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | NCK1 | GRCh38.p7 | 3:136942505 | ACAAACAAACAAAAG[A/G]AAACCTCTCCCCATC | 4690 |
rs561435999 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NCK1 | GRCh38.p7 | 3:136927894 | CTTTTCATCTTTATG[C/T]CTTTAGATTTTTAGG | 4690 |
rs561472051 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136920111 | AGCTTTTTAAACCCT[A/G]GTATCTCATCAAGTA | 4690 |
rs561487031 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136863694 | GCTGTTGGCTCATGT[A/G]TTAAATTTTAAAATG | 4690 |
rs561498580 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136927224 | TGATCCACCAGCCTC[A/G]GCCTCCCGAAGTGCT | 4690 |
rs561554074 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136925558 | CTGGCAACTACTAAT[C/T]TGTTTCTAATTTCCA | 4690 |
rs561615819 | snp | A/C | | | upstream-variant-2KB, intron-variant | NCK1 | GRCh38.p7 | 3:136930028 | TGCTACCTTTATTCC[A/C]GGGTGCTTGGAAACA | 4690 |
rs561651736 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | NCK1 | GRCh38.p7 | 3:136917520 | AATCTAGACCATCTT[C/T]CTAGTGCCCTCCACC | 4690 |
rs561720888 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NCK1 | GRCh38.p7 | 3:136871353 | CAGTGAGCTATGATC[A/G]CGCCACTGTACTCTA | 4690 |
rs561737104 | in-del | -/G | 0.00159617 | 0.0282053 | intron-variant | NCK1 | GRCh38.p7 | 3:136895465 | CCTTTTTAAAAAAAA[-/G]GTTTGTCAGAATTTA | 4690 |
rs561744168 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136883266 | CCTGTGTCTCTCCCA[A/G]CCTCACATTGTACCA | 4690 |
rs561764151 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136870501 | TATTTTATAAATTTA[A/G]TAGGGCTGGGCAGTT | 4690 |
rs561765305 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136903868 | CTGTCTCTTATTAAT[C/T]ATTATTTTGGCTTGG | 4690 |
rs561808307 | in-del | -/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136926503 | ATGGTCTCGATCTCC[-/T]TGAACTTGTGATTCA | 4690 |
rs561848388 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136935224 | TTGACAATGTGTAAT[C/T]AGTCTTAGACATAAT | 4690 |
rs561851075 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136912360 | TAGAGATGGGGTTTC[A/G]CCACGTTTGGCCAGG | 4690 |
rs561948718 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136878196 | GGCAGATCACTTGAG[C/G]TCAGGAGTTTGAGAC | 4690 |
rs561992913 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136934570 | GGATTACAGGTGTGC[A/G]CCACCGCGCCTGTCC | 4690 |
rs562015167 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136921445 | TAAACTTTTGCTGTG[G/T]TATTTGCATCTTTGC | 4690 |
rs562028342 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136936688 | TGTAGTTGGTGTGAG[G/T]TAGGGTCATTGTGGT | 4690 |
rs562066789 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NCK1 | GRCh38.p7 | 3:136929674 | AGAAAGTATGCCTCA[C/T]AGTGATACGTGCACA | 4690 |
rs562123519 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NCK1 | GRCh38.p7 | 3:136885963 | TTTTCTGATCTGAAC[A/G]TGTACAAAAGCAGCA | 4690 |
rs562177326 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NCK1 | GRCh38.p7 | 3:136928781 | TCCATTAGGGCCTGA[A/G]ACAGTGGAGCCCACT | 4690 |
rs562194033 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136944802 | ATCACACGCTAAGAA[A/G]TGGGCAGCAGTGAAA | 4690 |
rs562225196 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136937253 | GATCTTGGCACCATT[A/G]ATGAAAATCAATTGA | 4690 |
rs562246017 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136890778 | CCATTTTTAAGTGTA[C/T]AGTGATAAGTATATT | 4690 |
rs562246109 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136898247 | CTAAAAATACAAAAA[C/T]TAGCTGGGTATGGTG | 4690 |
rs562283970 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136891213 | ATCTCGGCTCATTTG[C/T]AACCTCCGCCTCCTG | 4690 |
rs562326179 | in-del | -/TT | 0.00159617 | 0.0282053 | intron-variant | NCK1 | GRCh38.p7 | 3:136891298 | GGCCACCATGCCTGG[-/TT]AATTTTGTATTTTTA | 4690 |
rs562351637 | in-del | -/GTCC | | | intron-variant | NCK1 | GRCh38.p7 | 3:136935854 | AGTCACTCTCAATCA[-/GTCC]CTGGCAATTACTAAT | 4690 |
rs562387668 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136933815 | GTTCAAACGATTCTC[A/G]TCCCTCAGCCTCCCA | 4690 |
rs562398529 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136938086 | AATTCCCTTCTAATC[C/T]TAGTTTGCTGAGCAT | 4690 |
rs562410532 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136897407 | TTTTTTGTTATTTAA[A/G]TAACAGCCATTTTAA | 4690 |
rs562446608 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136905245 | CAGTCTTGTCTTGAA[C/T]TCCTGACCTCCAGTG | 4690 |
rs562455122 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136878463 | ACATTGTATGATTCC[A/G]TTTGTATGAAGTATC | 4690 |
rs562581478 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136946422 | TGGGACGTAACATAA[A/G]CATAAATGTTCCAAA | 4690 |
rs562620708 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136933172 | AAACTCTCAACACAG[C/T]CCATGGTGACATTGA | 4690 |
rs562668886 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NCK1 | GRCh38.p7 | 3:136914267 | AGCTGTGGAACACAT[A/G]CGTGTCTGCCTGGAG | 4690 |
rs562702747 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136923888 | TGAGCCTAACTCTAC[A/G]TCCAGTTGGTGTCAT | 4690 |
rs562789747 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136885386 | AGGGTCTTGCTCTGT[C/T]ACCTAGGCTGGAGTA | 4690 |
rs562840904 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136860579 | AGCATCTGCATCTGA[G/T]GGTAGCCTAAGACTG | 4690 |
rs562875414 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136908219 | ACATAGGTCCGCAAC[C/T]GTATCACTTCGTCAT | 4690 |
rs562941841 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136884113 | GATGAAGTCATAATA[A/G]TGAACGAGCTATCTA | 4690 |
rs563002402 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136866509 | ACGGGGTTTCTCCGT[G/T]TTGGTCAGGCCAGTC | 4690 |
rs563084712 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136879586 | ATGTGCACTATTCAC[A/G]ATAGCAAAGACTTGG | 4690 |
rs563105904 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136880238 | TGCAGTGAGCCGAGA[C/T]CATGCCACTGCACTC | 4690 |
rs563108914 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136875745 | ATTAGACAGATCAAC[A/G]AGACAGAAAGTCAAC | 4690 |
rs563145294 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136882616 | CTTTGCTTTATGCAG[C/T]CACTTGGAGCACAGG | 4690 |
rs563191067 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136941279 | TACAGGTGCATGCCA[C/T]GATGCCTGGCTAATT | 4690 |
rs563207006 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136948117 | TTTGTTTTGAAGAGT[A/G]AAGGAGATAATCTAT | 4690 |
rs563236083 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136917665 | CTCCCATTTTACTTT[C/T]GAGGGTCAAGTTACC | 4690 |
rs563251834 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136940605 | GCTGGAGTGCAGTGG[A/C]GTGACCTCGGCTCAC | 4690 |
rs563261798 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136934493 | GTTTCACCATGTTGG[C/T]CAGGCTGGTCTCGAA | 4690 |
rs563304392 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136874913 | TGTTTTCTAGCTTGT[A/C]ATCCTTTTGAGAAGT | 4690 |
rs563360566 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136890491 | TCAAGTGCTGCCAAA[G/T]TGGGAGCCCAGGCAG | 4690 |
rs563422718 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136925863 | CCAGGGGTGCAGTTG[C/T]TAGCTTGTATGGTAG | 4690 |
rs563437449 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136900322 | TCTTATACCAGTACC[A/G]TGCTGTTTTGGTTAC | 4690 |
rs563454767 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136889262 | AATTGGTGGGTTCTT[A/G]GTCTCTCTGACTTCA | 4690 |
rs563475395 | in-del | -/TTTG | | | intron-variant | NCK1 | GRCh38.p7 | 3:136898504 | TGTCTTCAAATTCTA[-/TTTG]TTATAGAATAACCAT | 4690 |
rs563476551 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136902427 | CTCGAGCTCCTGAGC[C/T]CAGGCAATCTGCCCA | 4690 |
rs563492065 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136888647 | GACCTCGCGAGCCAC[C/T]GCACCCAGCCATATT | 4690 |
rs563498819 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136862829 | CCTGCGCGGTGCTGC[C/G]GGTGGACATCTTCGG | 4690 |
rs563528266 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136923001 | TTAGAAGTAGTAGAT[A/G]TATTAGTAAAGGAAG | 4690 |
rs563558714 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136923660 | GAAGAAGACCTCTCT[A/G]AATGTTTTAAATATG | 4690 |
rs563578882 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136910421 | CTAAAGTTACAATTA[G/T]TCTAGCTTTTAGAGT | 4690 |
rs563591387 | snp | A/G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136920385 | GCTGTGCATAGCACA[A/G/T]TTCATTCACTTATTC | 4690 |
rs563602961 | snp | C/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136867483 | ATTCCTGGCCTCAAA[C/G]GATCCTCCCACCTTG | 4690 |
rs563634535 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136862393 | GACACACACACACCC[C/G]CCTTCAGTCCGCTGT | 4690 |
rs563719503 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136944217 | TCCGCCTGCCAGGTT[C/G]AAACGATTCTCCTGC | 4690 |
rs563748749 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136935534 | GACTGGTTGATATGG[A/G]TGATGGGTCGACTGA | 4690 |
rs563815575 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136899268 | AATGGTTTCCTAGTG[A/G]CATCTGAAGAAAGAT | 4690 |
rs563833590 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | NCK1 | GRCh38.p7 | 3:136912875 | CAAACTGGTCTTGGT[C/T]TTGATATCCTGGACT | 4690 |
rs563842929 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136912143 | ATCAAATTTGGGAAG[C/T]TTTTAGCTATTATTT | 4690 |
rs563870660 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136913514 | CTCAAGCAGTCCTCC[C/T]GCTTTGGCCTCTCAA | 4690 |
rs563895697 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136905345 | TTTCCTTTGTGATAT[C/G]TAGTTCCTTTAGTAA | 4690 |
rs563901159 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136920256 | TTTCTTCTTTTTTTT[A/T]AAAAAATAGTGTAGG | 4690 |
rs563902584 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136950582 | TTATACCAGTGACTG[C/T]TTTTATAATACTTGA | 4690 |
rs563914328 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136895782 | GTTGACCAGGCTGAT[C/G]TCTAACTCCTGACCT | 4690 |
rs563970150 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136918447 | TAATCTAGAGATGAC[C/T]TAACGTATACAGGAG | 4690 |
rs564084095 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136884211 | CCAGAAGCAGGTGGC[A/G]TGGAGGGAGGGAAAC | 4690 |
rs564097913 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136870555 | TGCAAGTACTACATG[A/C]TCTTGAATAATATAT | 4690 |
rs564106593 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136865180 | CCAGGCTGGTCTTGA[A/T]CTCCTGACCTCGTGA | 4690 |
rs564109184 | snp | C/T | | | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136951533 | CTAATATGGATGGTC[C/T]TCTTATCTTTACCAG | 4690 |
rs564133235 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136946398 | CTAAAGTTAACCAGG[-/T]TAACAAGCTGGGACG | 4690 |
rs564166878 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136864259 | GCACTTTGGGAGGCC[A/G]AGGCAGGCGGATCAC | 4690 |
rs564204552 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136863917 | CCACCCTAGCAGACA[C/T]GGTGAAACCCCGTCT | 4690 |
rs564207337 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136921083 | CTTAATCCCTTATGA[C/G]TCCTCTTCCTGGTTC | 4690 |
rs564247191 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136927950 | ACTAATACTACCTCA[A/G]CCTTACATAAAAATA | 4690 |
rs564266231 | in-del | -/A | 0.12911 | 0.218828 | intron-variant | NCK1 | GRCh38.p7 | 3:136901374 | TTTCTTTTTTTTTTT[-/A]AAATATTTTTTATTG | 4690 |
rs564326828 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136871772 | TAATTGAACCATGGG[A/G]GTGGGCCTTTCTCGT | 4690 |
rs564384878 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136937340 | TCTGTCCTTATTCCA[A/G]TACCACACTGTTTTG | 4690 |
rs564408747 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136944990 | CCTTTTGGAGGTTAC[A/G]TATGACTGGGGTAAG | 4690 |
rs564434845 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136914418 | AATACTTAAATAAGA[C/T]AGATTATACTAGTAC | 4690 |
rs564446192 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136936751 | TTGAGGATCTTTTCA[C/T]GTGCCTGTTGGCCAT | 4690 |
rs564448025 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136945482 | AAAAGCTTTAAAGAT[C/T]TATATAGAGTTGAAG | 4690 |
rs564476750 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136879372 | GCAGAATGAGAGGCT[C/T]TATGGGTATCCTGGA | 4690 |
rs564518480 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136880289 | GACTCCGTCTCAAAA[A/C]AAAAAAAAGAATGTG | 4690 |
rs564555257 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | NCK1 | GRCh38.p7 | 3:136887885 | AAACTGTAATGTTTC[C/G]GTTCTTGTTATCTTT | 4690 |
rs564650711 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136886051 | AGCATTTATAAGGCA[C/G]GTGCCCCTTTGAAAG | 4690 |
rs564652827 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136891857 | TTTGGAGAAGTGTCT[A/T]TTCAATTCCTACTCC | 4690 |
rs564746412 | in-del | -/A | | | intron-variant | NCK1 | GRCh38.p7 | 3:136908111 | TTTTAGTAAAAACAT[-/A]ACATTATAGTAAACA | 4690 |
rs564775781 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136879761 | AAAATATCACAAGGA[C/T]GGAAAACCAAACACT | 4690 |
rs564816027 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136891238 | CTCCTGGGTTCAAGT[A/G]ATTCTCCTGCCTCAG | 4690 |
rs564818721 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136940613 | GCAGTGGCGTGACCT[C/T]GGCTCACTGCAACCT | 4690 |
rs564904375 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136899894 | AGGGGTTTTCTCTTC[C/T]AGTGGGATTTCTTCT | 4690 |
rs564919566 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136932309 | TCCCTGCAGCAACCC[C/G]AAATTTTTATTTATT | 4690 |
rs564975055 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136889662 | CTGATTGGTGCGTTT[A/G]CAATCCCTGAGCTAG | 4690 |
rs565036451 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136909427 | ATGATATTCTGTTGA[A/G]GTGCCAGGGATACAA | 4690 |
rs565038201 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | NCK1 | GRCh38.p7 | 3:136893186 | TGTGTGTGTATATAT[A/G]TATATACACACATGT | 4690 |
rs565075462 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136901905 | TCTTTCCTTCTACTA[A/G]TTTGGGGTTTGGTTC | 4690 |
rs565097785 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136900677 | TAGTTTGTTTTATTG[C/G]TATATAGAAACAGGT | 4690 |
rs565119436 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136946518 | ACACTGAATTATTTC[A/G]TCTTGTCTAGTTCTG | 4690 |
rs565210348 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136884337 | TGAAAGTTCTGAAAT[G/T]TTACCTTTTATTAAG | 4690 |
rs565214093 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136907194 | TCCTCAGTGCATGAA[A/G]ATGCACGGGTCCCCC | 4690 |
rs565224341 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136877442 | CAGAACCATGAAAAT[A/G]TAGTATAACTTAAAG | 4690 |
rs565229019 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NCK1 | GRCh38.p7 | 3:136917262 | TGCTTAATCAGCTAT[C/T]GTTAGTGTATTTTAT | 4690 |
rs565325720 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136949457 | AAACTGATGTATACC[C/T]GAGGAAAAAATAGAA | 4690 |
rs565341896 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136862130 | ACCGTTGTCGCGTCA[A/G]GGACCGGGGAAGGGG | 4690 |
rs565367397 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136861992 | AAGCTAAGACAGTTC[C/T]GGTCCGGCCCAGCGC | 4690 |
rs565444170 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136867534 | TATAGGGGTGAGCCA[C/T]TGTGCCTGGTCTGTT | 4690 |
rs565482887 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | NCK1 | GRCh38.p7 | 3:136927057 | GCTAACTGCAACCTC[C/T]GCCTCCCAGGTTCAA | 4690 |
rs565545536 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136943663 | TTTTCCTTTGTTCCT[A/G]CTACTGATGTATGTA | 4690 |
rs565560350 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136932827 | AAGTAGAAACATGGG[A/G]ACAGAATTGTAGTTG | 4690 |
rs565560662 | snp | A/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136908235 | GTATCACTTCGTCAT[A/T]TTAACATTCCTTCAC | 4690 |
rs565573587 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136862271 | GCGCAGGCCTCGTGC[C/T]GTTACGGCCATCACG | 4690 |
rs565608956 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136914859 | TGGGAGTGGATCCCT[C/T]ATAATATATTACTGC | 4690 |
rs565681477 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136903380 | GTAGTATATAGGTGG[C/G]TCATGCTTTAAAAAC | 4690 |
rs565690390 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136925999 | TTGTCAGCATTTGGT[A/G]TTACCACTCTTAGCC | 4690 |
rs565749521 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136877097 | TCAGCTTGCCTCTCT[G/T]AGTAATTAGAATAAT | 4690 |
rs565770881 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136909745 | TAGTTTTTGCTTTAT[A/G]TATTTTGATGGGCTG | 4690 |
rs565771147 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136889288 | CTTCAAGAATGAAGC[C/T]GCGGACCCTCGCGGT | 4690 |
rs565786719 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136883509 | CTCATATTCTCTGTC[C/T]TTTATGGTAGCACTG | 4690 |
rs565807793 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136916809 | AAAAGAGACTTTTTT[A/G]TATTATCCAGTTCAA | 4690 |
rs565822969 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136916819 | TTTTTATATTATCCA[A/G]TTCAATTCCCTTATT | 4690 |
rs565854402 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136875028 | TGTAGCTTGGTGTTA[C/T]GTCTATTTTTAACAA | 4690 |
rs565913227 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136870075 | ATCCTGGCCCAGCGC[A/G]GTGGCTCATGCCTGT | 4690 |
rs565915582 | in-del | -/A/AAAAAAAAA | | | upstream-variant-2KB, intron-variant | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136861488 | AGCGAAACTCGTTTC[-/A/AAAAAAAAA]AAAAAAAAAAAAAAA | 4690 |
rs565923686 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136882937 | ATTACATGACTTTTT[A/T]AAAGACAGTCTCATT | 4690 |
rs565979810 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136911095 | TGAAAGAATTTACTT[A/C/G]TTTTTTAAGGCTGAA | 4690 |
rs565980745 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NCK1 | GRCh38.p7 | 3:136924975 | TAATGAAATCATGGG[A/G]TTCCAGTTCCCCCAC | 4690 |
rs566000018 | in-del | -/TT | | | intron-variant | NCK1 | GRCh38.p7 | 3:136912494 | ACTTTTCTTCAGTCT[-/TT]TTTTTTTTTTTATGT | 4690 |
rs566025393 | snp | A/C | | | intron-variant | NCK1 | GRCh38.p7 | 3:136925320 | TGTGTTTTCTCTTTC[A/C]GTTTTTATTTTAATT | 4690 |
rs566080448 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136869470 | GAATCACTTAAACCC[A/G]GGAGGCAGGGGTTGC | 4690 |
rs566158602 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136935669 | TTGGCAATAAGGAGA[C/T]AGGATTGTGAGGATT | 4690 |
rs566183027 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | NCK1 | GRCh38.p7 | 3:136918882 | GTGTTTTCACTAATG[A/T]CCGTGTAACCATGTG | 4690 |
rs566195654 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136927396 | CTTGTTACTAGGTAC[A/G]TAGAAGTTTAGATAT | 4690 |
rs566214878 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136950860 | ACTCACTTCTACAAA[A/T]AACTTCCCCAAAATC | 4690 |
rs566232724 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136936441 | TTGGTTATTGTGAAC[A/G]GCGTTGTGATAAACA | 4690 |
rs566247083 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136871788 | GTGGGCCTTTCTCGT[A/G]CTGTTCTTGTGATAG | 4690 |
rs566282129 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136896017 | TTTTGTTTTTTATTG[A/G]TATATAATATTTTAC | 4690 |
rs566297974 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136901673 | GTATGTTAGTGTATC[A/G]TTGTTTGTAATAGTT | 4690 |
rs566331355 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136897726 | ATCACAGTTCTAAAT[G/T]AATTATTTTCACGTT | 4690 |
rs566409296 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136944467 | ATTCTATAGGAAAAT[C/T]GGACCAGTTAGAGAA | 4690 |
rs566438992 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136891382 | TCAGGTGATCTACCC[A/G]CCTCAGCCTCCCAAA | 4690 |
rs566450907 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NCK1 | GRCh38.p7 | 3:136885335 | ATTGTCTTTTCCAGC[C/T]GTAATCTAGGGCACA | 4690 |
rs566455640 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136904443 | CAGGCGTGAGCCACC[A/G]TACCTGGCCTTCTTT | 4690 |
rs566462920 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136877955 | GGTTACATGTAATGT[A/G]TATCCACACAATTAA | 4690 |
rs566478834 | in-del | -/CTGATG | 0.00279162 | 0.0372561 | intron-variant | NCK1 | GRCh38.p7 | 3:136938429 | AAAAATGTGAGTCAT[-/CTGATG]TGCACATTCCCAGTT | 4690 |
rs566484850 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136890932 | CCATTCTACTTTCTA[C/T]CTCTATGAATTTGAC | 4690 |
rs566509835 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136934104 | TATGTACTGTAAGTG[C/T]TTTACACATAGACTT | 4690 |
rs566544491 | in-del | -/AG | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136942455 | AGCTAGGGTTTTAAC[-/AG]AGTTTCGTTAAACAC | 4690 |
rs566564073 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NCK1 | GRCh38.p7 | 3:136945055 | ATGAGGTAAATAGAG[C/T]TACCTGGGTCTGGGA | 4690 |
rs566643124 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136912566 | TCAAGTCTTTATTCA[A/G]ATCCCTGTAGTGAAT | 4690 |
rs566661963 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136864034 | TGAACCCGGGAGGCG[A/G]AGCTTGCAGTGAGCC | 4690 |
rs566836410 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136907282 | AGCAGCTATAGGTGG[A/G]GAATGTCAATGGGGT | 4690 |
rs566836485 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136899415 | TTTTACCTTCATTTC[A/T]TTTCTTTTTTTTTTT | 4690 |
rs566837814 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NCK1 | GRCh38.p7 | 3:136929814 | TATTATCATAGAGCA[A/T]AGGGGGGAAGTAGTC | 4690 |
rs566872654 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136903622 | TGGAGATGGGGTTTC[A/G]CCGTGTAGGCCAGCC | 4690 |
rs566907447 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136913793 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGACTA | 4690 |
rs566933352 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136873621 | GAATAATATGGTTTG[A/G]CTGTGTCCCCACCCA | 4690 |
rs566944632 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136914491 | TCTGCTTTCTCCCCA[A/G]AATCCTCTAATGTTT | 4690 |
rs566994844 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136865247 | AGGCATGAGCCACCA[C/T]GCCCGGCCTGTATTT | 4690 |
rs566997347 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136906747 | ACTGGACAGGCCAAT[C/T]CCCCAGGCTTGCAGG | 4690 |
rs567010949 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136922377 | GGATTTATAATTTCA[A/G]GCTTTCTAAGGTAAC | 4690 |
rs567065191 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136921747 | TTTTAAAGGTTGAGT[A/T]TGCTAAGGGAAAGAC | 4690 |
rs567071939 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136880388 | ATCCACCATGACTTC[A/G]GGCCTTTTAAAAAAG | 4690 |
rs567071952 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NCK1 | GRCh38.p7 | 3:136872999 | CTAGGGCAGTGCAGA[A/G]GGGAAATGTGGGGTC | 4690 |
rs567081174 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136871457 | TGTTTATTGAAAACT[A/G]CACAAATTTAAATGT | 4690 |
rs567081329 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136878796 | ACCCCAGCAAGAAGA[C/G]TGACTATTGTTTCTG | 4690 |
rs567164042 | snp | C/G | | | upstream-variant-2KB, intron-variant | NCK1 | GRCh38.p7 | 3:136929536 | GACAAATCAGAAAGA[C/G]ATTTTCCTTCAGTAG | 4690 |
rs567205984 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136886337 | TCCAAGACTCCTTGC[A/G]GATACCAAAATTTGA | 4690 |
rs567208886 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136916050 | ACTTTTAAACAACCA[C/G]GTCTCATGAGAATTC | 4690 |
rs567214912 | snp | A/C | | | intron-variant | NCK1 | GRCh38.p7 | 3:136944064 | GATCAGATAATAAAG[A/C]GTTGGGAGTGTGAGT | 4690 |
rs567227170 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136866796 | TTTTGTATTTTTAGT[A/G]GAGATGGGGTTTCAC | 4690 |
rs567237523 | in-del | -/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136936040 | TATGTCTAAATAACT[-/T]TTTTTTTTTTTTTTT | 4690 |
rs567242681 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136883753 | CCAAGGGCTCTTATG[A/G]TAATTTAGGTGAGTT | 4690 |
rs567344793 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136932401 | TATAAAGTAGAAGAA[A/G]CAGAGTATTATGTGC | 4690 |
rs567352372 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136918209 | GATATTCTTTATAGA[C/T]ACATATCTAAATAAT | 4690 |
rs567386892 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136939143 | TGTTTTGTTACTGAT[C/T]GAATCTTTTACTTGT | 4690 |
rs567407428 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NCK1 | GRCh38.p7 | 3:136886567 | AATGTTTTAAATCCA[C/T]GGCTGGTTGAATTCA | 4690 |
rs567433130 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136933262 | AAAACATGATGTAAT[C/T]AATCCACTTTTGATA | 4690 |
rs567460081 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136894985 | GGTTCAAGCAGTTCT[C/T]CTGCCTCAGCCTCCC | 4690 |
rs567470451 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136868585 | AGCCTGCTTTGGCCT[C/T]CCAAAGTGCTGGGAT | 4690 |
rs567476639 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136887351 | TTTTTCTATCTTAAC[A/C]TAAAATGGAAAAGTT | 4690 |
rs567507994 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136931647 | ATCAACACATTCTTA[C/T]TGAGAGCCTACTCCA | 4690 |
rs567515818 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136946673 | AATTGCTATTGGATG[C/T]AATGTGTAAGAAGGT | 4690 |
rs567537879 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136882203 | TTCCTGCATGTTTTT[A/T]TAAAAATAGTAGCTA | 4690 |
rs567552596 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136938327 | TTTTTCACAGATTCT[A/G]TATTTGTGAATTCAC | 4690 |
rs567647285 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136901305 | GGATTCAGTTTGCCA[A/G]TATTTTGAGAATTTT | 4690 |
rs567654721 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136941649 | ATGCCCATTAACCTA[G/T]AATTGAAATTTTTGT | 4690 |
rs567673984 | snp | A/G/T | 0.00199481 | 0.0315187 | intron-variant | NCK1 | GRCh38.p7 | 3:136910945 | TTCTCCCCAGTCTCT[A/G/T]GTAAGCATCATTCTA | 4690 |
rs567707368 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136951000 | TGTATATTACACATA[A/T]ATCACTATACAGTTA | 4690 |
rs567710878 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136888908 | GCAAGGTTTGCTCTG[C/T]TGCTTGGACTGTAGT | 4690 |
rs567736206 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | NCK1 | GRCh38.p7 | 3:136890184 | GAAATCGAGCGCAGC[A/G]CTGGTGGGCTGGCAT | 4690 |
rs567779084 | in-del | -/CTGCCCA | 0.00517822 | 0.0506191 | intron-variant | NCK1 | GRCh38.p7 | 3:136913908 | TCCTGACCTTGTGAT[-/CTGCCCA]CCTGGCCTCCCAAAG | 4690 |
rs567859501 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136861385 | TAATCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 4690 |
rs567894981 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136909472 | GTTTCCTCTAAGAGC[A/T]TGCTCTGAGAGACAA | 4690 |
rs567942128 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136908494 | TGGAAACAGGGTTGA[C/G]GTGGTTCTGAATTCA | 4690 |
rs567981263 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136860806 | CCATTAGTCCCCACC[A/T]CCAACATTGGGGATC | 4690 |
rs567990841 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136926081 | CTTTAATAGCTAATG[A/T]TGAATACCTTTTCAT | 4690 |
rs568017651 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136904249 | CCTCTGCCTCCTGGG[C/T]TCAAGTGATTCTTCT | 4690 |
rs568041345 | snp | C/T | | | intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136948205 | TTTAATATAAAAATA[C/T]TGATAGAGGGCTTTC | 4690 |
rs568054685 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136911347 | TTTTTCATAATGGCT[A/G]TACTAATTTAATTTA | 4690 |
rs568066497 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136896648 | CACAAGCATACCCCA[C/T]CACACCTGGCTAATT | 4690 |
rs568083650 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136864072 | CGCCACTGCACTCCA[A/G]CCTGGGCGACAGAGC | 4690 |
rs568099537 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136862468 | CGCTGAGTTAGCCCC[A/G]GGGGCGCCGTCTGCA | 4690 |
rs568122483 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136870887 | TAAGTTTGGCTACTA[G/T]TATCAGACAGATGCC | 4690 |
rs568171909 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136890604 | AATAATATGTAATTT[G/T]ACAGTTAATACCACA | 4690 |
rs568216049 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136862218 | TGCCCACCGCGCGTG[C/T]CCCGCCTCTCTCCCA | 4690 |
rs568271829 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | NCK1 | GRCh38.p7 | 3:136876381 | CTGGTTTTTTGAAAG[A/G]ATCAACAAAATTGAT | 4690 |
rs568273854 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136868412 | GGATCACTGTACCCT[C/T]TGCATCCCAGGTTCA | 4690 |
rs568346504 | in-del | -/CTGATGTC | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136892402 | CGGTTGCCTGTGCTA[-/CTGATGTC]CTGGATTATCTGAGT | 4690 |
rs568403981 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136896697 | TAGAAATGGGGGTCT[C/T]ACTATGTTGCCCAAA | 4690 |
rs568413282 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136875177 | CAGTCTGCTCTCTGT[G/T]TGTCTGTTATTGGTG | 4690 |
rs568421648 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136931336 | GTTTCTAGAAAAATG[A/G]ACAGAGGAATTATTA | 4690 |
rs568544740 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136877162 | ATTATCAAATGAATC[C/T]AATTGACATGCATTG | 4690 |
rs568552336 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136919782 | CATGATAAATATGAC[C/T]TTTTTTGGCAAGTCA | 4690 |
rs568622966 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136884514 | TGGTGCAGGCTTGCT[C/T]ACCGCAACCTCCGCT | 4690 |
rs568633754 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136943725 | ATCTCGTTTTCTGCC[C/T]TCAGGAAGTTCACTC | 4690 |
rs568646107 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136871990 | ATTGCCCAGTCTCAG[A/G]TATGTCTTTATCAGC | 4690 |
rs568653207 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136892110 | CCAAGCAGGTCTTGA[A/G]CTTTTAGCCTCAAGG | 4690 |
rs568672419 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136935771 | TGTAATTCAGTAGTA[C/T]TGAGTACATTAACAG | 4690 |
rs568677710 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136898620 | CTAAAATACAAAACA[C/T]CTTTGCAATAAAACT | 4690 |
rs568684483 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136900216 | GCAGAAGCCTTTTTT[G/T]TTGTTGTTGTTGTTT | 4690 |
rs568687632 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136874580 | GCAGTTTTTGAATCT[G/T]CTTGATCTGGCCCTC | 4690 |
rs568689170 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136891229 | AACCTCCGCCTCCTG[A/G]GTTCAAGTAATTCTC | 4690 |
rs568717798 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136927490 | TTTAAGTTTTGTTTG[A/T]TACTAATAGAGCAAC | 4690 |
rs568779811 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136878450 | TATACTAAAGACCAC[A/G]TTGTATGATTCCATT | 4690 |
rs568789952 | snp | A/G | | | upstream-variant-2KB, intron-variant | NCK1 | GRCh38.p7 | 3:136929003 | TAGAAGAAAAGTACA[A/G]TTTCTCCTTGTGCAG | 4690 |
rs568816384 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136885479 | CTGGTTAATTTTTGA[A/T]TTTTTTGTAGAGACA | 4690 |
rs568832928 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NCK1 | GRCh38.p7 | 3:136936899 | GAATTATGATTTGCA[A/G]ATATTCTCTTCTAAT | 4690 |
rs568844256 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136897845 | ATTGATCAGAAGCTA[A/G]TTGAAATTCTCACCA | 4690 |
rs568850171 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136864416 | GAATTGCATGAACCC[A/G]GGAGTCGGAGGTTGC | 4690 |
rs568871677 | snp | C/T | 0.0023933 | 0.0345097 | upstream-variant-2KB, intron-variant | NCK1 | GRCh38.p7 | 3:136929140 | GTCTTGCTCTGTTGT[C/T]CAGGCCAAACTTGAA | 4690 |
rs568907063 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136946711 | GTAGTCCTTATGACA[C/T]AGGAAATCCCTGAAT | 4690 |
rs568943541 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NCK1 | GRCh38.p7 | 3:136937483 | GAATATTAGAATCAG[C/T]CTTTTCATTTCTGTG | 4690 |
rs568945187 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136947430 | CAAAATGCAATATAT[A/G]CCATTATTTTTAGCA | 4690 |
rs568946678 | snp | C/T | 0.000230608 | 0.0107355 | synonymous-codon, downstream-variant-500B | NCK1, LOC107986136 | GRCh38.p7 | 3:136945701 | CGCTTATGTGAAATT[C/T]AACTACATGGCTGAG | 4690 |
rs569052527 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136905093 | TCTCAGCTAACTGCA[A/G]CCTTCACCTCCCAGG | 4690 |
rs569067484 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136915213 | ACATTACTACTAAGG[A/G]GTAGTAGTAGTGAGA | 4690 |
rs569107038 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136945165 | ATAATTTTATTTTTA[C/T]ACAGCTCATTGTAGA | 4690 |
rs569162374 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136905821 | TTAGAGATGGGGTCT[C/T]ACTATGTTGCCCTGG | 4690 |
rs569230332 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136914596 | TATAACTCAAAGAAA[A/T]TCCATTGGAGACCTT | 4690 |
rs569232484 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136923229 | TTCCTTAAATTATTT[A/T]AAAAAAAATAGAAAC | 4690 |
rs569246104 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136892904 | TCTGAGATTGGTACA[A/G]CCATCACCCAACAGC | 4690 |
rs569280590 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136893462 | GTTTGAGAATTGTCT[A/G]TTCACGTCCTTAGGC | 4690 |
rs569319811 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136867705 | AAATACAAATAGACT[A/G]GATGCACCAAAATTC | 4690 |
rs569384874 | in-del | -/C | | | intron-variant | NCK1 | GRCh38.p7 | 3:136867085 | TCTTTCTTTCTTTCT[-/C]TTCTTTCTTTCTTTC | 4690 |
rs569452918 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136866892 | TGTTGGGATTACAGG[C/T]GTGAGCCACTGTGCC | 4690 |
rs569479772 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136872780 | GCTGAAAGGGGCCAG[C/T]GTAGAGCTTGGGCTG | 4690 |
rs569481852 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136865365 | GCTGAGATTACAGGT[G/T]TGCGCCACCGTGGCT | 4690 |
rs569498577 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136864564 | AGGGAGACCAGGCGG[A/G]GTAGTTCAAGCCTGT | 4690 |
rs569592518 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136909560 | CCCATGTGCACTTGA[A/G]AAGAATATGATTTGT | 4690 |
rs569637992 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NCK1 | GRCh38.p7 | 3:136924894 | TATGGGTTAAAAAAG[A/G]GAAAAGGTCAGGAGC | 4690 |
rs569733794 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136881275 | CCCAGGCTGGAGTGC[A/G]GTGGTGCAATCTTGG | 4690 |
rs569741467 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NCK1 | GRCh38.p7 | 3:136892975 | GCCACCACCCTTATC[A/G]TTCATATGCTTTTGC | 4690 |
rs569759802 | in-del | -/T | | | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136948675 | CCTTCTGTTTTATTG[-/T]TTTTTTTCTTTGCTG | 4690 |
rs569799198 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136862853 | TCTTCGGGACGCGCC[C/G]TCTCCCCTCCCCCCA | 4690 |
rs569812420 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136873725 | GTGGGAGTGGGCCTT[C/T]CCTGTGCTTTTCTTG | 4690 |
rs569895313 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136912343 | GATTTTTGTGTTTTT[A/G]GTAGAGATGGGGTTT | 4690 |
rs569903088 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136939571 | TCTTTCTTCTTTTTT[A/G]TGCAAGCTTTTAGGG | 4690 |
rs569911779 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | NCK1 | GRCh38.p7 | 3:136870350 | AATCTCAAAAAAAAA[-/T]AAAATTCATCCTTTT | 4690 |
rs569921484 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136888030 | GCTCACTGTAACCTC[C/T]GACTCCTAGGTTCAA | 4690 |
rs569924213 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136889362 | TCTGATGTTCAGATG[C/T]GTTCGGAGTTTCTTC | 4690 |
rs569940378 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136932477 | ATGTTTTAAATAAAA[C/T]AATAAAAAATAATTT | 4690 |
rs569948456 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136888731 | TAACCTCCCCTCTCC[A/G]TGTCCTAGGAAACCA | 4690 |
rs569980357 | in-del | -/TTT | 0.00597247 | 0.0543191 | intron-variant | NCK1 | GRCh38.p7 | 3:136913105 | GCCCGTCTTCTGATC[-/TTT]CTCTGGGAAGGTTTC | 4690 |
rs569995404 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136926858 | GGCATTTGATTGCTT[G/T]TTGTATGTGTTTCAT | 4690 |
rs569999095 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136864408 | AGGCAGGAGAATTGC[A/G]TGAACCCGGGAGTCG | 4690 |
rs570006367 | snp | A/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136925016 | GGGGATAGCTGAACC[A/T]CAAGGCATAATATTG | 4690 |
rs570020112 | snp | A/C | | | intron-variant | NCK1 | GRCh38.p7 | 3:136940599 | GCCCAGGCTGGAGTG[A/C]AGTGGCGTGACCTCG | 4690 |
rs570044842 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136921974 | TATTTTAGTAGAGAC[A/G]GGGTTTCACCATGTT | 4690 |
rs570047611 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136875452 | GGCATCCCTGTCTTG[G/T]GCCAGTTTTCAAAGG | 4690 |
rs570048845 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136894436 | AATGACTTCTTAATC[A/G]AGCTTTTAATTTAAT | 4690 |
rs570086788 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136882318 | TATTTGTATATATTT[A/C/T]GAGAAATGTCTATTT | 4690 |
rs570121311 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136895167 | GGCATGAGCCACTGC[A/G]CCCAGCAAGCTGATT | 4690 |
rs570142307 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136926324 | CTGCGGCCCAGGCTG[A/G]AGTGCAGTGGCGCGA | 4690 |
rs570162547 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136914269 | CTGTGGAACACATGC[A/G]TGTCTGCCTGGAGAT | 4690 |
rs570165137 | in-del | -/ATT | | | intron-variant | NCK1 | GRCh38.p7 | 3:136925118 | ATAAAACTTAAAAGC[-/ATT]ATATAAATTTTTAGT | 4690 |
rs570218680 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136943812 | TAGAGGAGCCTAGAC[A/G]GAGGTAAACAAGAAT | 4690 |
rs570226929 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136895757 | TTTAGTAGAGACAGG[G/T]TTTTGCTATGTTGAC | 4690 |
rs570285345 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136902582 | ATTTGTTGACACTTG[C/T]TTTGTGTCCTAACTT | 4690 |
rs570324938 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136902178 | CAGAGTTCTTCTTAA[C/G]TCTTTGTTTTTTTTT | 4690 |
rs570395820 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136918750 | AAGACAATTCTTCCA[C/T]TGTGGCCCAGGAAAG | 4690 |
rs570397699 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136897502 | CATTTTTTCATATAC[C/T]TGTTTGCCATTTGTA | 4690 |
rs570405482 | snp | C/T | | | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136948727 | TACAGTTTTGTATTT[C/T]GTAAACAAAAATCAA | 4690 |
rs570430976 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136869050 | TGAGACCAGCCTGGC[C/T]GGCATGGTGAAACCC | 4690 |
rs570433090 | snp | A/G | 0 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136919391 | TATTTTTATCCATCT[A/G]TTATGTATCATTCCT | 4690 |
rs570434347 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136890298 | GCTCTGAGTGCGTGC[A/G]GGGCCTGCCAAGCCC | 4690 |
rs570437309 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136911529 | TCTGTTGCCATTTTC[A/G]TGTCTTTTTTTGAGA | 4690 |
rs570452686 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136883685 | CAGTAGATATGTTGT[A/T]GGAGGGAATCTATTA | 4690 |
rs570471099 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136890892 | CAACTCCCAAGTCTG[C/T]CATCCCCCCAACCTC | 4690 |
rs570488272 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NCK1 | GRCh38.p7 | 3:136896701 | AATGGGGGTCTCACT[A/G]TGTTGCCCAAACTGG | 4690 |
rs570516739 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136864625 | GGATAGCTGGAGGCC[A/G]GGAGTTTGAGATCAG | 4690 |
rs570630444 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NCK1 | GRCh38.p7 | 3:136870014 | ATATTTAAAAGAATG[A/G]ATGTTTCTCAAAAGT | 4690 |
rs570653795 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136864095 | GACAGAGCGAGACTC[C/T]GTCTCAAAAAAATAA | 4690 |
rs570780634 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NCK1 | GRCh38.p7 | 3:136936304 | CCTCGGCCTCCCAAA[A/G]TGCTGGGATTACAGA | 4690 |
rs570907636 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136921619 | ATGTCGAAGATAAAC[C/T]GGACACTAGTTAAAA | 4690 |
rs570937532 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136870995 | TGTATGTGTTTTGCT[A/G]TTGTAAATTCTGCAA | 4690 |
rs570938002 | in-del | -/TTG | 0.0119091 | 0.0762411 | intron-variant | NCK1 | GRCh38.p7 | 3:136892192 | ACACCCAGCTGGATT[-/TTG]TTGTTGTTGTTGTTG | 4690 |
rs570950953 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136933863 | GTGCATGCCACCACA[C/T]CTGGCTAATTTTTTT | 4690 |
rs570961811 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136878938 | CTTCCAGAATTCTGG[C/T]AATCAAGTAGGAATT | 4690 |
rs570968692 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136871409 | TCTAAAAAAAACAAA[A/G]TTAAAAATTTGTTTA | 4690 |
rs570981471 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136913738 | CAGTGGCGCGATCTC[A/G]GCCCACTGCAAGCTC | 4690 |
rs570983656 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136931642 | TGTTTATCAACACAT[C/T]CTTATTGAGAGCCTA | 4690 |
rs571003492 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136878266 | ACACACAAATTAGCC[A/G]GATGTGGTGGCAGGC | 4690 |
rs571023108 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136924897 | GGGTTAAAAAAGGGA[A/G]AAGGTCAGGAGCCCT | 4690 |
rs571072873 | snp | A/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136875082 | TTCTGAATCTGTAAA[A/T]TTCATTAGTTCTGGG | 4690 |
rs571177287 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | NCK1 | GRCh38.p7 | 3:136923330 | GGAGGCCGAGGCAGG[C/T]GGATCACGAGGTCAG | 4690 |
rs571199273 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136872864 | TTGATGCTGCAAGTG[A/C]ACAGAAGTCAAGAAT | 4690 |
rs571200472 | snp | A/C | | | intron-variant | NCK1 | GRCh38.p7 | 3:136910915 | ATCCTTTGACCAACA[A/C]CTTCCCATCCTGGCT | 4690 |
rs571336763 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136931394 | AAGGAAACAAAGAGT[A/G]ACCTGACAAGAGATT | 4690 |
rs571345795 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136938157 | TCTGCATCAATTGAG[A/G]TAGTCATTTGTTTTT | 4690 |
rs571349802 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136932630 | AAGCCATGTGGCCTG[A/C]AAAATATAACTGAAC | 4690 |
rs571410534 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136939813 | AAAGATACTTTGTAT[A/G]ACTTCAATCTCAAAT | 4690 |
rs571450393 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136898729 | AAACTGAACGGTTAA[A/C]GTTAAGGTGCTATAA | 4690 |
rs571486901 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136891637 | CACAGTGGCTGTACC[A/G]TCTTATCTTCCCACC | 4690 |
rs571510532 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136937567 | TTTTGGATACTGTTG[A/C]CATCTTACACAGAAT | 4690 |
rs571534376 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136945285 | TACATTTAAGAGGGA[A/G]TTCATTAATTTAGGA | 4690 |
rs571543881 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136941787 | TGTTCTTTATTTCTT[C/T]ATATGACTTCAAATT | 4690 |
rs571556766 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NCK1 | GRCh38.p7 | 3:136869501 | GGGGTTGTGAGATCC[C/T]GCCACTGCACTTTAG | 4690 |
rs571565419 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NCK1 | GRCh38.p7 | 3:136906652 | TGCAGTGGGCATGGT[A/G]TGGATGATGGCAGTA | 4690 |
rs571628107 | snp | C/T | | | intron-variant, upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136863927 | AGACACGGTGAAACC[C/T]CGTCTCTACTAAAAA | 4690 |
rs571630515 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136915938 | ACCACGTTGGCCATG[C/T]TGGTCTCGAACTCCT | 4690 |
rs571630629 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136907624 | GCTTTCAGTGCTTCT[C/G]GTCACCACCCTGCTG | 4690 |
rs571655772 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136880630 | ACAATCAACAAACTT[C/T]GTTTGTTTGTTTTTT | 4690 |
rs571657648 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136888730 | CTAACCTCCCCTCTC[C/T]GTGTCCTAGGAAACC | 4690 |
rs571694367 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136888141 | GTAGAGACAGGGTTT[C/T]GCCATGTTGGCCAGG | 4690 |
rs571706062 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136880159 | GTGTGGTGGTGGGCG[C/T]CTGTAGTCCCAGCTA | 4690 |
rs571713799 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136901247 | GCCTCTCTGGGATAA[A/G]TCTCACTTCATTGTG | 4690 |
rs571748342 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136893563 | TCAGATGTATAGATG[A/G]TGAAGATTTTCTCCC | 4690 |
rs571846015 | snp | A/C | | | intron-variant, downstream-variant-500B | NCK1, LOC107986136 | GRCh38.p7 | 3:136945518 | TTTTTAATAATGAAT[A/C]AGTTCATTCTTTTGG | 4690 |
rs571926798 | snp | G/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136860222 | TCAGTATGAATTTTT[G/T]GGGGGGATGCAATTC | 4690 |
rs571945933 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136866062 | AATTATGCTTCAAAC[A/C]CATCCTTCACTTTTC | 4690 |
rs571954084 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136887142 | AGCCACTGCACCCAG[C/T]CCCTATCTTTTATAT | 4690 |
rs572034541 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136898589 | ACTTCTGAACTCTTA[C/T]TATGAAAAAATTTGG | 4690 |
rs572042204 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136888341 | ACTATACAGTTCACT[C/T]ATTAAAAGTATACAA | 4690 |
rs572045402 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136895217 | TGATAAACAGTTTTC[A/G]CTTTAACGTAGTCAA | 4690 |
rs572059702 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136911618 | TGTCTGGAGTTCCTT[A/G]TATATTTTGGATATT | 4690 |
rs572068429 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136947806 | GTGTATTCTTCATTT[G/T]TGGGAATTCAGCATG | 4690 |
rs572162343 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136867063 | TTTTCTTTCTTTCTT[C/T]CTTTCTTTCTTTCTT | 4690 |
rs572180450 | snp | C/T | | | downstream-variant-500B, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136951659 | AATTGTAATTCAGGG[C/T]ATATACACAGACAGT | 4690 |
rs572196378 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136902294 | CCTCCGCCTCCTGGG[C/T]TCAAGCAGTTCTTGT | 4690 |
rs572220956 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NCK1 | GRCh38.p7 | 3:136908916 | GCAGTGGTGTTGGGA[A/G]GTGGGGCATAATGGG | 4690 |
rs572226149 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136924378 | GATGTGGGAAATGCT[A/G]CAGGACAAGTGAAGC | 4690 |
rs572226263 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136910753 | GCTAATTAACATATC[C/T]ATAACCTTGTTTACA | 4690 |
rs572257262 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136866434 | TACCTCAGCCTCCCT[A/G]GTAGCTGGGACTACA | 4690 |
rs572264652 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136916245 | AACCATTTTGTGATT[A/G]AAAATGACATAAGCT | 4690 |
rs572279751 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136915551 | TAATGGGAGGCATGA[G/T]AAACTTTAATAGGGC | 4690 |
rs572327745 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136874606 | CCCTCTATGGCTGAT[A/G]CATAGTAGTTTCCTG | 4690 |
rs572329868 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NCK1 | GRCh38.p7 | 3:136882394 | TGAACAGGTCTTTTT[A/G]TTTTTACTTTTGTCT | 4690 |
rs572365610 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136881710 | AGCCCCTGGCAACCA[C/G]TATTCTTCATGTTTC | 4690 |
rs572382024 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136862743 | GTGGCGTAATCCGAG[G/T]CCGGGAAGGTAGGGA | 4690 |
rs572388780 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136866495 | TATTTTTAGTAGAGA[C/T]GGGGTTTCTCCGTGT | 4690 |
rs572446569 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136922275 | AGTTATCTTTTTGAT[G/T]GTTTGCATTCCAAAG | 4690 |
rs572585742 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136868013 | ACCTCCGCCTCTCGG[C/G]TTCAAGCAATTCTCT | 4690 |
rs572591268 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136926367 | GCAAGCCCCGCCTCC[C/T]GGGTTCAAGCCATTC | 4690 |
rs572737090 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136870413 | TTAGTGTGTAGATCA[A/G]TTCAAATAATAGATA | 4690 |
rs572766209 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136926360 | GCTCACTGCAAGCCC[C/G/T]GCCTCCCGGGTTCAA | 4690 |
rs572789900 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136920024 | GGGAGAAAGTCCCCA[A/G]TTAACTAACTTGGAT | 4690 |
rs572897562 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136877410 | TTAGAGAAGAAATAA[A/C]ATTAAACTATTTAGA | 4690 |
rs572916742 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136890074 | TTGTTGGGGAGGCTC[A/G]GGCGGCACAGCAGCC | 4690 |
rs572940217 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136943102 | TACCACAAAGCAGCA[A/G]CTTCTTTCTTTACCA | 4690 |
rs572995748 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136890347 | AGCTGGCCCGCCAGC[A/G]TTGCACGCAGCCCCA | 4690 |
rs573020085 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136943970 | GTTACTGATTTGACA[C/G]TAAGGAGAGATGACA | 4690 |
rs573031360 | in-del | -/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136871038 | GTATAAGGCTTTACA[-/T]TTTTTTTTCCTTTTG | 4690 |
rs573072078 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136883226 | ATGCCCAGCCTACTT[C/T]TTATTACATGTAGAA | 4690 |
rs573081799 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | NCK1 | GRCh38.p7 | 3:136896429 | TCACTTAACATAGTG[A/T]CCTCCAGGTCCATCC | 4690 |
rs573083554 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136895689 | TGTGCCACAGCCTCC[C/T]GGGTAGCTGGGATTA | 4690 |
rs573091986 | snp | C/G | | | upstream-variant-2KB, intron-variant | NCK1 | GRCh38.p7 | 3:136928666 | GATAAGAGAACTGTG[C/G]ATCATTACTGTACAT | 4690 |
rs573158290 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136891767 | GTGGTATTATTGTGG[G/T]TTTGATTTGGATTTT | 4690 |
rs573169288 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136898163 | CACTTTGGGAGGCCA[A/G]GGCAGGCAGATCACT | 4690 |
rs573187133 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136885866 | GATATGTTCTTTTTA[C/G]AATGTTATAAAGTTG | 4690 |
rs573189414 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136945357 | ACAAGAGAAAAGATG[G/T]TGAACTGTCATATAA | 4690 |
rs573190473 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136884978 | TGCCCACCTCGGCCT[C/T]CCAAAGTGTTGAGAT | 4690 |
rs573217518 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136944704 | AAGAACGAGAGTGAG[A/G]ATAATGAGAGTTTTG | 4690 |
rs573225980 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136937184 | TTTTGTTTATAGATA[A/C/T]CCATTTGTTCCAGTA | 4690 |
rs573299787 | in-del | -/AGTAG | 0.00159617 | 0.0282053 | intron-variant | NCK1 | GRCh38.p7 | 3:136872041 | CAGTAAATTGGTACC[-/AGTAG]AGTAGAGTGCTCCTG | 4690 |
rs573381972 | in-del | -/TTCC | | | intron-variant | NCK1 | GRCh38.p7 | 3:136867221 | TCCTTCCTTCCTTCC[-/TTCC]GTCCATCCATCCGTC | 4690 |
rs573393218 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136872620 | AAATGTCTGCAGGGC[A/G]TGTCGGAGGTCTTCA | 4690 |
rs573400965 | snp | C/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136877917 | AAAGTAGAAGCAACT[C/G]AGATGTCCATCAGCT | 4690 |
rs573403516 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136898886 | TTCTTACAAAGCTCT[A/C]ATTGAGATCTTGAAG | 4690 |
rs573437174 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136912796 | GAGTAGCTGGAACTA[C/T]TTGCGCTGCTGTGCT | 4690 |
rs573459128 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136920908 | CATATTTTTAAATTT[C/T]TAAAAAATTGTGGTA | 4690 |
rs573487999 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | NCK1 | GRCh38.p7 | 3:136872306 | CTTGTTATGTTTTAG[A/C]AAAGAAACTGGCAAC | 4690 |
rs573511538 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136907687 | GAAGTGTGATTATCT[C/T]CTCACTATTTTGTTC | 4690 |
rs573567820 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136866192 | TTCTTTCTTTTTTTT[A/T]AATCAGTGCCAGCAC | 4690 |
rs573578189 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136946358 | AAAAAAAAGAGAGAG[A/C]GAAATGGAGAGGTTA | 4690 |
rs573594548 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136904752 | GGTTTTCTAACATTT[G/T]TGTTTTCTCTTCTCC | 4690 |
rs573595926 | in-del | -/A | | | intron-variant | NCK1 | GRCh38.p7 | 3:136880285 | GCGAGACTCCGTCTC[-/A]AAAAAAAAAAAAGAA | 4690 |
rs573627508 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136871101 | TTACTAATTTTTTTT[A/T]AAAAAATTGTTTAGT | 4690 |
rs573659725 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136914803 | TGTTGAAATTTGATC[A/C]CCATGTTGGAAGTGG | 4690 |
rs573680165 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136907021 | TGCCATCAGAATGCT[C/T]TGGTGGCAACAGCAG | 4690 |
rs573691429 | in-del | -/CAGGC | | | intron-variant | NCK1 | GRCh38.p7 | 3:136904822 | GTTCCATATGTCACA[-/CAGGC]TTTTCTCATTTTTTT | 4690 |
rs573706464 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136943015 | AGTGCAGGTTACTGT[C/T]CACACAGCCATCACT | 4690 |
rs573712719 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136940079 | TCTTGCCCAGGCTGC[C/T]GTCAGACTCCTGGGC | 4690 |
rs573729422 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136865446 | TTTGTACTTTTACTT[C/T]GTCTTATTTTACTTT | 4690 |
rs573769299 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136923797 | CTTTTAGAACCATCC[A/G]AATGTTTTACATAAT | 4690 |
rs573807808 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136924470 | GTTAGCTTAAGTGCA[A/C]TATATCGACTTAGTT | 4690 |
rs573863122 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136893675 | GTTTTTGAGGCATGA[A/G]ACTTTTGATAGAATC | 4690 |
rs573922083 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136922728 | ATCACTGATATATTG[C/T]TAGGAGTTTTTAAAA | 4690 |
rs573924409 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136912711 | GGAGTTTGGCTGTGT[G/T]ATCACGGTTCATGGG | 4690 |
rs573933326 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136932039 | GCAGGAGAATCACTT[G/T]AAACCAGAGGTAGAG | 4690 |
rs573956158 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NCK1 | GRCh38.p7 | 3:136929435 | GTAATTAAGTAGATA[C/T]AATGTGATGTTTAAC | 4690 |
rs573985867 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NCK1 | GRCh38.p7 | 3:136930343 | GTCATATTTTTGGCC[A/C]TGATTATTTACTTGT | 4690 |
rs573987471 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136900392 | TCTTTTTGCTTAAGA[C/T]TGTTTTGGTTGTTTG | 4690 |
rs574008987 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136880844 | GAACTCCTGGTCTCA[A/G]GCAGTCCTTCCACCT | 4690 |
rs574024315 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136893039 | GAATATACGATGTTT[C/G]GTTTTCCATTCCTGA | 4690 |
rs574025462 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136916365 | TCTGATATTTCAGGT[G/T]AACACAGGTTTTATG | 4690 |
rs574065110 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136874400 | GGGCAGGCTGGTCTC[A/G]AAGTCCTGACCTCAG | 4690 |
rs574065183 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136867185 | TTCCTTCCTTCTTTC[C/T]TTCTTTTCTTTCTTT | 4690 |
rs574081978 | snp | C/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136916978 | TTGCTTATAGGGGCA[C/G]CCAAACAGGGCTGAA | 4690 |
rs574113924 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136889341 | GCGCGTCTGGAGTTT[G/T]CTCCTTCTGATGTTC | 4690 |
rs574139941 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136873167 | GCAAGCCTGTGAAAG[C/T]AGCCAGGAGAGAGGC | 4690 |
rs574145757 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136898591 | TTCTGAACTCTTACT[A/G]TGAAAAAATTTGGCT | 4690 |
rs574171831 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NCK1 | GRCh38.p7 | 3:136880214 | GGCGTGAACCCGGGA[A/G]GTGGAGCTTGCAGTG | 4690 |
rs574175680 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136938683 | TTTAGGCATGAGTTA[C/T]AGTGATGTTGTGAAT | 4690 |
rs574189618 | snp | C/T | 0 | 0 | intron-variant | NCK1 | GRCh38.p7 | 3:136940108 | GCTCAAGTGATCCCC[C/T]GACCTTGGACTCCCA | 4690 |
rs574207161 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136873745 | TGCTTTTCTTGTGAT[A/G]GTGAATAAGTCTTTT | 4690 |
rs574209899 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136887604 | CTTTTAAGTTATTTG[G/T]CACCTGGAACAGACA | 4690 |
rs574308772 | in-del | -/AG | | | intron-variant | NCK1 | GRCh38.p7 | 3:136914341 | ACTAAAAGTAACAGC[-/AG]TTTATTTTCAGGCCC | 4690 |
rs574320382 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136889505 | TTTATTGCAAAGAGC[A/G]AAAGAACAAAGCTTC | 4690 |
rs574348479 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NCK1 | GRCh38.p7 | 3:136941984 | GCTGGGACTACAAGC[A/G]TGTGCCACCACGCCC | 4690 |
rs574373068 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136933691 | AGCTATATAATGCAA[C/G]AATAAAGATTTAAGT | 4690 |
rs574384073 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136934410 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGATTA | 4690 |
rs574442368 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136889190 | AGCCACTGCACCCAG[A/C]AGCTTGATGTTTCTA | 4690 |
rs574576895 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136902896 | CATAAATCAATATGC[A/G]TCCACCTGTGAAGTA | 4690 |
rs574579180 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136894732 | AATGCAAAGGTTCCA[A/G]TTCCATCCTGCCACC | 4690 |
rs574582417 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136864661 | GCAATGTAGTGATAC[C/T]CTGTCTCTAAATTAA | 4690 |
rs574615627 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136895297 | GATGTGTATAAGGCT[G/T]TGGTATGTTTTTGGT | 4690 |
rs574629253 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136916912 | GGCAGAGCAGTGGCT[A/G]CAACCCAAGTGTGTG | 4690 |
rs574642669 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136902372 | CTGGCTGATTTGTAT[G/T]TTAGTAAAAACGGGG | 4690 |
rs574659647 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136909035 | CCCCAGATATTTGAT[A/G]CCTTCCTCCTTGTTG | 4690 |
rs574665356 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136910005 | GATAGCATATATTTA[G/T]AATTTTTTTTCTATT | 4690 |
rs574684469 | snp | C/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136897720 | ACTTTAATCACAGTT[C/G]TAAATTAATTATTTT | 4690 |
rs574711374 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136876619 | ATTTTGTCTCTGTTA[C/T]AAAGTTCCTGATTTT | 4690 |
rs574713635 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136868960 | TATCTTGTTGAGGCC[A/G]GGCGCGGTGGCTCAC | 4690 |
rs574713800 | snp | C/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136930944 | GATAAAAAGGATTAG[C/G]TGAACAAATTTCTTC | 4690 |
rs574724864 | snp | A/G | 0 | 0 | upstream-variant-2KB, intron-variant | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136860994 | ATTAATGCCTTAAAC[A/G]GTATTTACTGACCAT | 4690 |
rs574734938 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136904544 | TTGATGGGCGTTCCT[C/T]TATAAGTGACTAGAT | 4690 |
rs574857640 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136903822 | ATTTTATTAACTGAT[G/T]TATGGCTGTTCAGTA | 4690 |
rs574865263 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136951587 | CAGTATAATAAAGTC[G/T]TCTTTCAAGTCAAAA | 4690 |
rs574870004 | snp | A/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136925514 | ATAGTCATACTTACT[A/T]CCCTCCTGTTCCTGC | 4690 |
rs574881898 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136862780 | AGGAGGAAGGGCGCT[C/T]TCACCTCCAGCCCGA | 4690 |
rs574913105 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136873604 | GGGAGGGGCCGGGGG[C/T]GGAATAATATGGTTT | 4690 |
rs574944325 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136921973 | GTATTTTAGTAGAGA[C/T]GGGGTTTCACCATGT | 4690 |
rs574984796 | in-del | -/CTA | 0.0023933 | 0.0345097 | intron-variant | NCK1 | GRCh38.p7 | 3:136943256 | TTGGAGTTCCTTACT[-/CTA]CTATTTTTGGTGGTA | 4690 |
rs575035184 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136883092 | CCCAGCTAATTTTTT[A/G]TGTTTTTTAGTAGAC | 4690 |
rs575049614 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136934912 | GATTGTGGTGAACTG[G/T]GAGGTCAGGAAGTGC | 4690 |
rs575135409 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136918887 | TTCACTAATGACCGT[G/T]TAACCATGTGAGTAT | 4690 |
rs575140762 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136899093 | TAGCATTTGGATGCA[A/G]AGGTTTAACTGGTGC | 4690 |
rs575159997 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136926423 | GGGACTACAGGCACC[C/T]GCCACCACGCCTGTC | 4690 |
rs575179408 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136896988 | GAGAAATTTTTGTAG[C/G]TTTCCAAAAAGTATG | 4690 |
rs575254544 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136878035 | TGATGAACCTTGAAA[A/G]CATTATGCTGTGAAA | 4690 |
rs575292716 | snp | A/G | 1.64754e-05 | 0.00287009 | synonymous-codon, nc-transcript-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136946058 | GTGGAAATGCAGGAA[A/G]ATCAATGGTATGGTT | 4690 |
rs575333588 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136871128 | TAGTCTGGGCATGGT[A/G]GCTTATGCTTGTAAT | 4690 |
rs575338868 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136877485 | GCCATGCTTAGAGGA[A/G]GAGTTATAGCCTTCA | 4690 |
rs575341142 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136936062 | TTTTTTTTTTCTGAG[A/G]CAGAGTCTCGCCCTG | 4690 |
rs575349153 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136877349 | AAAAACTAGAAAATT[G/T]TCAGCTGTTTGAAGA | 4690 |
rs575391411 | in-del | -/AAAT | 0.00279162 | 0.0372561 | intron-variant | NCK1 | GRCh38.p7 | 3:136876436 | AAAAAGAGAAGAATC[-/AAAT]AGACACAATAAAAAA | 4690 |
rs575428605 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136936508 | TTAAGTGTATACCTA[A/T]AAGTGGAATTGCTGG | 4690 |
rs575476807 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136901997 | GCATTTGTTGATATA[A/G]ATTTCCCTCTTTGCA | 4690 |
rs575514521 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136913993 | TTCCCCATTTATATG[A/G]TTGCTTCTGAATGTC | 4690 |
rs575587499 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136879248 | AAAATTAAAAGGTCC[A/G]TCAGAGGTCAACTTC | 4690 |
rs575592749 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136893160 | ATAGTGTGTGTGTGT[G/T]TGTGTGTGTGTGTGT | 4690 |
rs575606607 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136937254 | ATCTTGGCACCATTG[A/G]TGAAAATCAATTGAC | 4690 |
rs575738638 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136886890 | CTCTTATTGCCCAGG[C/G]TGGAATGCAATGGCA | 4690 |
rs575752923 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136898940 | AAAATGGCTAGAGAT[A/C]ATTTATAGGACATGG | 4690 |
rs575774921 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136885991 | GCAGTACAGTGGTAT[C/T]TCATCTGTTCTAAAC | 4690 |
rs575803643 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136891813 | TATGATCATCTTTTC[A/G]TGTGCTTATTCACTG | 4690 |
rs575830613 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136905249 | CTTGTCTTGAACTCC[C/T]GACCTCCAGTGATTT | 4690 |
rs575842125 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136892324 | GTATTAATTTAGTGT[C/G]CTTTCATATACAAAG | 4690 |
rs575915830 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136940354 | ATTTAGTTCTGTCCC[G/T]TACAGAAAGTGGGGT | 4690 |
rs575990189 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136918242 | ATACATATTATCTCT[C/T]AGTTCATTTCTATTA | 4690 |
rs576054277 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136864817 | GGCTGGAGTGCAGTG[A/G]CACGATCTTGGCTCA | 4690 |
rs576076221 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NCK1 | GRCh38.p7 | 3:136884602 | TGTGGCACTATGCCC[A/G]GCTAATTTCTGTATT | 4690 |
rs576081694 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136908637 | GGTGAACTGCGACTG[A/G]TTACTGCCAATGTGG | 4690 |
rs576081939 | snp | A/C | | | intron-variant | NCK1 | GRCh38.p7 | 3:136881603 | GTATTAAGTATATTC[A/C]CATTGTTGTACAACC | 4690 |
rs576101157 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136947107 | ATTTTGAAAGAAAAT[G/T]TGTGGAAGTGGGGTG | 4690 |
rs576125821 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136947692 | CATTTCCTCTGCCCA[G/T]CTACCTTTCCACTCT | 4690 |
rs576137061 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136917069 | ATGTATTCATATGTA[A/G]TATGTAAACATAGTA | 4690 |
rs576214146 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136879967 | CACGTTGTGCACATG[C/T]ACCCTAGAACTTAAA | 4690 |
rs576226224 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136931846 | CCATTGTGGCTAGGC[A/G]TGGCAGCTCAAGCCT | 4690 |
rs576231162 | snp | C/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136911736 | GCTTTTTAGTTTGCT[C/G]TTTTAGCATTTCTTG | 4690 |
rs576240740 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136872461 | TTCAGTTTTACAAGG[G/T]AGGCAGAGCATAAGT | 4690 |
rs576242828 | snp | C/G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136877301 | TTGAGTGTTTTCTGA[C/G/T]GTGTTGGAATTAAGC | 4690 |
rs576258213 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | NCK1 | GRCh38.p7 | 3:136888979 | GGCACAAGTGATCCT[C/G]CTGCCTCAGTCTCCT | 4690 |
rs576325091 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136893816 | GTACCTGCTACTGCA[A/T]CTGGTATTGAGGCAG | 4690 |
rs576375199 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136922953 | TAGTTGAAGAAAGTG[C/T]TACTTACATAATGAT | 4690 |
rs576411726 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136923425 | GCCGGGCATGGTGGC[A/G]GGCACCTGTAGTCCC | 4690 |
rs576415071 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136874459 | TGCTGGGATTACAGG[C/T]GTGAGCCACCACGCC | 4690 |
rs576481912 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136861961 | AAGTAACCAACCAGA[A/G]CAGCCGCAGAGGGAA | 4690 |
rs576484209 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136868511 | TTTTGTATTTTTAGC[A/G]GAGACAGGGTTTCAC | 4690 |
rs576551979 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136881508 | AGGCATGAGCCACCA[C/T]GCCCAGCTTCTATTT | 4690 |
rs576574994 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NCK1 | GRCh38.p7 | 3:136932768 | AGTCTTAGGTGTGTC[A/G]TAGGAATTGAGCGAA | 4690 |
rs576609891 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136924698 | TCAGAAACATTGTGA[A/G]TAGAGGTTCTATGTT | 4690 |
rs576656993 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136942217 | GAATGTCTTATGTTC[G/T]CCTTCATTTTTGAAG | 4690 |
rs576752824 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136876757 | AGTCAAAGGATAGCT[A/G]TAAGGCTACAGTGAG | 4690 |
rs576819070 | snp | A/C | 0.00517822 | 0.0506191 | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136950036 | TTTTCTAACTCAGTA[A/C]TCCTTTGTTGAGGGT | 4690 |
rs576840409 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136934505 | TGGCCAGGCTGGTCT[C/T]GAACTCCCAACCTCA | 4690 |
rs576869614 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136935122 | GCCAGGCTGGTCTTG[A/G]ACTCCTGGCCTCAGG | 4690 |
rs576870354 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136896194 | ACAGTTTTGCTAGCT[A/G]TAGTCACCTTAGTCT | 4690 |
rs576902477 | in-del | -/GTGTGTGTGTGTGTGTGTGTATATATATATATACAC | 0.0150606 | 0.0854603 | intron-variant | NCK1 | GRCh38.p7 | 3:136893167 | TGTGTGTGTGTGTGT[lengthTooLong]GTGTGTGTGTGTATA | 4690 |
rs576904631 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136921551 | TGGATATTCTATGCA[C/T]GTCCAATTTGGGAGA | 4690 |
rs576976879 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136882622 | TTTATGCAGTCACTT[A/G]GAGCACAGGCACCTG | 4690 |
rs577004674 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136863314 | TTTACTTTGATAGAC[A/G]TATGACAAACCAACT | 4690 |
rs577011367 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | NCK1 | GRCh38.p7 | 3:136889545 | GAAGGGGACCCGAGC[C/G]GGTTGCCACTGCTGG | 4690 |
rs577046959 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NCK1 | GRCh38.p7 | 3:136890036 | GTCAATGGGATTGGG[C/T]GCCCTGGAGCAGAGG | 4690 |
rs577051524 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136902436 | CTGAGCTCAGGCAAT[C/G]TGCCCACCTCGGCCT | 4690 |
rs577075504 | snp | C/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136928343 | AAAGGCAAGGGCTAG[C/G]TAAGTTTGAGTCATA | 4690 |
rs577221624 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136902476 | CTAAGATTACAGGCG[C/T]GAGCTATCCCACCTG | 4690 |
rs577253421 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136904631 | AATGTGCTGTGAAGA[A/C]GACCTTTTTGATTTG | 4690 |
rs577290543 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | NCK1 | GRCh38.p7 | 3:136897093 | TTTTGTTTTACTTTT[A/T]TTTATTATTTTGAGA | 4690 |
rs577339072 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136944634 | GAGAGTCCCAAGAGA[A/G]TCAGGAAAGATAGTA | 4690 |
rs577386924 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136870291 | AGGTTGCAGTGAGCC[A/G]AGATCATGCCACTGC | 4690 |
rs577405122 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136878502 | GTGTATTTGTAGAGA[G/T]AGAGTGGTTGCATAG | 4690 |
rs577416446 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136869594 | CCATTTGGTGAGTTA[C/G]AGTGCTTTTATATGT | 4690 |
rs577421674 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136877334 | GAAATGGATTACCAA[A/G]AAAACTAGAAAATTG | 4690 |
rs577438016 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136927662 | GAGTAGCTGGGACTA[C/T]GGGTGTGCACCATCA | 4690 |
rs577443039 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136885622 | CTTAAACCTTTGAAG[C/T]CTTAGTTTCTTCAGT | 4690 |
rs577444251 | snp | C/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136897910 | AGTAAATTGAGATCT[C/G]AGCTTCCTAAAAAGC | 4690 |
rs577474571 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136919934 | CTTCTGATAAGAATC[A/G]GCTAAGTAACAATAC | 4690 |
rs577544432 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136877606 | CCCTTTGATAGCCCA[A/G]CAAGGTGACAGTAAA | 4690 |
rs577561170 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NCK1 | GRCh38.p7 | 3:136912765 | GGCTCAAGCAGTCCC[C/T]CTGCTTCAGCTTCCT | 4690 |
rs577569843 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136934952 | AGTGTTTGTGTCCCC[C/T]AAAACTCCGCATGAT | 4690 |
rs577580289 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136864866 | GGGTTCAATCGATTC[C/T]TGTGCCTCGGCCTCC | 4690 |
rs577591238 | in-del | -/GCAC | 0.00279162 | 0.0372561 | intron-variant | NCK1 | GRCh38.p7 | 3:136938436 | TGAGTCATCTGATGT[-/GCAC]ATTCCCAGTTGAGGC | 4690 |
rs577617184 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136871640 | AAACTATTTTTGCCT[A/G]TTTTTGAACTTTATA | 4690 |
rs577721107 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136931932 | TGAGACCAGCCTGGT[C/T]AACATGGTGAAACAC | 4690 |
rs577752387 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136871223 | CAATATAGCAAGAGC[C/T]GGCCTTTACAAAAGT | 4690 |
rs577803141 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | NCK1 | GRCh38.p7 | 3:136921165 | CTATTTCCAGAATAA[A/T]CTTCATCTTGCAAAA | 4690 |
rs577809928 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | NCK1 | GRCh38.p7 | 3:136929254 | TTATTCTTATTCAAC[A/G]TTATTGTTATTCTAG | 4690 |
rs577844155 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NCK1 | GRCh38.p7 | 3:136937894 | CTGTGGATACTTTTT[C/T]CCCTCCCTAATTGCT | 4690 |
rs577864521 | snp | G/T | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | NCK1 | GRCh38.p7 | 3:136928527 | TGTTGGAGTTTAGAC[G/T]TATAGGCAGAATTGC | 4690 |
rs577918688 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136909399 | TAATTTGTAAATGCT[A/G]AAAACCACGTGTATG | 4690 |
rs577932121 | in-del | -/TT | | | intron-variant | NCK1 | GRCh38.p7 | 3:136867054 | GTTGCTTGCTTTTCT[-/TT]CTTTCTTTCTTTCTT | 4690 |
rs577961213 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136873126 | CAGCTTGCACCATGC[A/G]CCTGGAAAAGCTGCA | 4690 |
rs577963034 | in-del | -/CTTTT | | | intron-variant | NCK1 | GRCh38.p7 | 3:136944112 | AAAAGGAAAAACAAC[-/CTTTT]TTTTTTTTTTTTTTT | 4690 |
rs577974056 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NCK1 | GRCh38.p7 | 3:136936570 | CCATCTGTTTTTCAC[A/G]TGGTGGCACCATTTT | 4690 |
rs578002983 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136937092 | TTCTTCTAAGAGTTT[C/T]ATAGTTTTAGCTCTG | 4690 |
rs578010248 | in-del | -/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136886537 | GTTTAGTACAGGTGC[-/T]TTTTTTTTTTCCTGA | 4690 |
rs578115658 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136879410 | AAGAAAATAGATATA[C/T]GCTTTCAATTAAAGC | 4690 |
rs578187135 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136914183 | GTCTGTATCTCAGTG[A/G]TCAGAAAGCGCAATT | 4690 |
rs578216528 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136899604 | CTCTGTTGTACCGCA[C/G]CTTTAGATGCTGCTT | 4690 |
rs578217635 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136886970 | TGCCTCAGCCTCCCA[A/G]GTAGCTGGGACTACA | 4690 |
rs578249163 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NCK1 | GRCh38.p7 | 3:136911904 | GTAGTTAATTAGACT[A/G]TTAGACTATATTAGC | 4690 |
rs745336610 | snp | A/C | | | intron-variant | NCK1 | GRCh38.p7 | 3:136878942 | CAGAATTCTGGCAAT[A/C]AAGTAGGAATTTGGA | 4690 |
rs745339160 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136924943 | TGAGGGGTATGGGTT[C/T]TTAATCTGTTAGTGC | 4690 |
rs745361386 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136879688 | TGCAGCCATAAAAAA[G/T]AATGAGTTCATGTCC | 4690 |
rs745389383 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136892883 | GTAAGTTCTTTAGTG[A/G]TGATTTCTGAGATTG | 4690 |
rs745389538 | snp | A/C | | | intron-variant | NCK1 | GRCh38.p7 | 3:136877878 | GAAAATCTGTTTAAG[A/C]AGCAGCTCAGTCATA | 4690 |
rs745407229 | snp | C/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136926560 | GATTACAGGCATGAG[C/G]CACCGCGCCCGGCCA | 4690 |
rs745484690 | snp | C/T | 1.64768e-05 | 0.00287021 | synonymous-codon, nc-transcript-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136946001 | TTTCGAGAAAGGAGA[C/T]GTAATGGATGTTATT | 4690 |
rs745536121 | snp | C/T | 1.64735e-05 | 0.00286993 | synonymous-codon, downstream-variant-500B | NCK1, LOC107986136 | GRCh38.p7 | 3:136945878 | TGACCATGTGGGTTC[C/T]CTGTCAGAGAAATTA | 4690 |
rs745569303 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136938946 | TAAGTGATATTAGCC[A/G]GTTGTCTTGTGATAG | 4690 |
rs745579367 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136891617 | AGAACTGCCATATGG[G/T]TTTCCACAGTGGCTG | 4690 |
rs745594768 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136924060 | TTGATCTAGGCAGTG[A/G]TCATCAGTGGCAGGT | 4690 |
rs745626257 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136933282 | CACTTTTGATAGATA[C/T]TCTTTAACAATGGTA | 4690 |
rs745647414 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136926976 | ATGTTTGTATTTATT[C/T]ATTTATTTTTTTGAG | 4690 |
rs745677094 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136934359 | GGTGTGATCTCGGCT[C/T]ACTGCAACCTCTGCC | 4690 |
rs745679283 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136919651 | CCAAACTACTTTTAT[A/G]AATTCTATAGGTATA | 4690 |
rs745688475 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136885987 | AGCAGCAGTACAGTG[A/G]TATTTCATCTGTTCT | 4690 |
rs745844923 | in-del | -/AAAC | | | intron-variant | NCK1 | GRCh38.p7 | 3:136942491 | GCCAAAAGAAAAAAC[-/AAAC]AAACAAACAAAAGAA | 4690 |
rs745864996 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136899359 | GTCACTAAAGCATTA[C/T]ATTTGGATTTAGGTT | 4690 |
rs745866583 | snp | G/T | | | intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136947375 | CTTGAATGCAGAATT[G/T]TATGTATTTTCTTGT | 4690 |
rs745879846 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136912193 | TTTGAGACCGAGTCT[C/T]GCTCTGTCACCCAGG | 4690 |
rs745898366 | snp | C/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136897701 | TTTTTTTAGACAAAT[C/G]CTCACTTTAATCACA | 4690 |
rs745905713 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136944018 | AGAATGGTTTTAATT[G/T]AGTAGTTTTGTTAGA | 4690 |
rs745923740 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136882810 | TAATTGCAGGGGTGG[C/T]TGGGAAGTGTAGTAT | 4690 |
rs745960463 | in-del | -/AAGG | | | intron-variant | NCK1 | GRCh38.p7 | 3:136941028 | AAAGTTATATCTGAT[-/AAGG]AAGGATTTCTGCTAT | 4690 |
rs745976194 | snp | C/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136896210 | TAGTCACCTTAGTCT[C/G]CTATAGAATATTAGA | 4690 |
rs745994136 | snp | A/G | 1.65252e-05 | 0.00287443 | missense, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136948340 | GAGACTGTCTACTGC[A/G]TTGGGCAGCGTAAAT | 4690 |
rs746052654 | snp | A/C | | | intron-variant | NCK1 | GRCh38.p7 | 3:136869283 | TAGGCCTGATGGCTC[A/C]CTCCTGTAATCCCAG | 4690 |
rs746076163 | snp | C/T | 0.000307464 | 0.0123951 | intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136948217 | ATACTGATAGAGGGC[C/T]TTCAAAATGTTTACT | 4690 |
rs746102200 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136897785 | AACTGAGCTAAGTAT[C/T]ATACATTTTTAATGG | 4690 |
rs746133165 | snp | A/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136874107 | ATTTTAAAAAATTGG[A/T]CATTTGATTTTCAGT | 4690 |
rs746145509 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136943299 | TGTAGGGATTTCTCT[A/G]AAGGCTATCATTAAC | 4690 |
rs746200486 | in-del | -/TT/TTT | | | intron-variant | NCK1 | GRCh38.p7 | 3:136867405 | TCAATGTCTGGCTAA[-/TT/TTT]TTTTTTTTTTTTTTT | 4690 |
rs746238278 | snp | C/T | | | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136949014 | CATAATTTTTAAAAA[C/T]ACATTCATTGTCTTC | 4690 |
rs746239594 | snp | C/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136903636 | CACCGTGTAGGCCAG[C/G]CTGGTCTTGAACCCC | 4690 |
rs746285510 | in-del | -/TTTT | | | intron-variant | NCK1 | GRCh38.p7 | 3:136886818 | GTTACATGATCAGTC[-/TTTT]TTTTTTTTTTTTTTC | 4690 |
rs746338229 | snp | A/G | 1.73e-05 | 0.00294104 | missense, downstream-variant-500B | NCK1, LOC107986136 | GRCh38.p7 | 3:136945594 | ACAGGCATTGGAAAA[A/G]TGAAAAGAAAACCTA | 4690 |
rs746376811 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136869629 | TCTTCATGTTTATTT[C/T]TCCTCTTAACTCTAA | 4690 |
rs746377943 | in-del | -/AAACCTAG | | | frameshift-variant, downstream-variant-500B | NCK1, LOC107986136 | GRCh38.p7 | 3:136945603 | GGAAAAGTGAAAAGA[-/AAACCTAG]TGTGCCAGATTCTGC | 4690 |
rs746401849 | snp | A/T | 2.17554e-05 | 0.00329807 | intron-variant | NCK1 | GRCh38.p7 | 3:136928258 | AAAGAAAAGCAACTT[A/T]GTTTTAAATGAAACC | 4690 |
rs746411259 | snp | C/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136884691 | CCTTGGCCTCCCAAA[C/G]TGCAGGCTTGAGCCA | 4690 |
rs746429448 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136916022 | TGAGCCACTGGGCCC[A/G]GCCTAGCCAAACACT | 4690 |
rs746446300 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136931208 | TTATTGAGTTTGGGT[C/T]ATGAAGTAAAACTAA | 4690 |
rs746479275 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136937595 | AATATCTTTCCGTTT[A/G]TTTAAGTCTTCTTTA | 4690 |
rs746531383 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136890527 | GTGCCAAGAGCGAGC[A/G]AGGGCTTTGAGGACT | 4690 |
rs746534233 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136923509 | GCAGTGAGCCAGGGT[C/T]GCTCCACTGCACTCC | 4690 |
rs746572239 | in-del | -/GT | | | intron-variant | NCK1 | GRCh38.p7 | 3:136881971 | TAGCTGTTAAGAATA[-/GT]GTGTTTCCATGAACA | 4690 |
rs746654195 | snp | A/G | 1.64751e-05 | 0.00287007 | synonymous-codon, nc-transcript-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136946151 | ACCATCACCTCCACA[A/G]TGTGATTACATTAGG | 4690 |
rs746702029 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136869500 | CGGGGTTGTGAGATC[C/T]CGCCACTGCACTTTA | 4690 |
rs746715971 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136936496 | ATCTATTTTCAGTTA[A/G]GTGTATACCTAAAAG | 4690 |
rs746719936 | snp | G/T | | | intron-variant, upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136863765 | GACAGTGCTTTCAGG[G/T]CCATCTAAATAAAAT | 4690 |
rs746727642 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136903488 | GGAGTACAATGGTGC[A/G]GTCTTGGCTTACTGC | 4690 |
rs746748137 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136899010 | AAACACAAATCAAAT[A/G]TAAACACCCTTGTAA | 4690 |
rs746766223 | snp | G/T | | | missense, downstream-variant-500B | NCK1, LOC107986136 | GRCh38.p7 | 3:136945873 | TTGGGTGACCATGTG[G/T]GTTCTCTGTCAGAGA | 4690 |
rs746772925 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136902434 | TCCTGAGCTCAGGCA[A/G]TCTGCCCACCTCGGC | 4690 |
rs746781596 | snp | C/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136911382 | CCCACCAGCAATGTA[C/G]AAATGTTTGCTTTTC | 4690 |
rs746819163 | snp | G/T | | | intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136947283 | TTTGAAACTTTGGGA[G/T]TAACTGTAGAAAAAG | 4690 |
rs746863854 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136898576 | TAGTGTGTAAAATAC[G/T]TCTGAACTCTTACTA | 4690 |
rs746880173 | snp | A/G | 1.64754e-05 | 0.00287009 | stop-gained, nc-transcript-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136946043 | AAATGACCCAGAGTG[A/G]TGGAAATGCAGGAAG | 4690 |
rs746958588 | snp | A/G | | | upstream-variant-2KB, nc-transcript-variant | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136862004 | TTCTGGTCCGGCCCA[A/G]CGCTTCTCACCCTCT | 4690 |
rs747028301 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136908681 | CAAAGGAGACTGACA[A/G]TATATATTTTTTACT | 4690 |
rs747092057 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136943190 | AAGTTGAGTCTGACA[G/T]TATTTACCAGCTCAT | 4690 |
rs747101307 | in-del | -/GG | | | intron-variant | NCK1 | GRCh38.p7 | 3:136865942 | GCGTGTAACAATATT[-/GG]CTGATTTTTGCCAGC | 4690 |
rs747116030 | snp | C/T | 0.00515615 | 0.0505123 | synonymous-codon | NCK1 | GRCh38.p7 | 3:136928095 | GAGAGATTATGGCTT[C/T]TGGATGATTCTAAGT | 4690 |
rs747226627 | in-del | -/A | 0.000152659 | 0.00873533 | intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136946342 | AGCTCTGGGTATTTT[-/A]AAAAAAAAGAGAGAG | 4690 |
rs747234609 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136944366 | CTTGTGATCTGCCCG[C/T]CTCAGCCTCCCAGAA | 4690 |
rs747241149 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136872318 | TAGCAAAGAAACTGG[C/T]AACATTTTGCCCCTG | 4690 |
rs747247914 | snp | A/G | 1.65214e-05 | 0.0028741 | missense, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136948350 | ACTGCATTGGGCAGC[A/G]TAAATTCAGCACCAT | 4690 |
rs747252816 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136873231 | CAAGACCATGGAAAT[C/T]CACTTCTTGGATCAG | 4690 |
rs747308475 | snp | A/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136914668 | GAATTTGTGTTTCAG[A/T]TCTTTTTTGCGCCCT | 4690 |
rs747325125 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136868032 | AAGCAATTCTCTTGC[C/T]TCAGCCTCCTGAGGA | 4690 |
rs747371796 | in-del | -/A | | | intron-variant | NCK1 | GRCh38.p7 | 3:136924316 | CAGTTTATAGGAGAT[-/A]GGGGGGATAGAGGAA | 4690 |
rs747373158 | snp | A/G | | | upstream-variant-2KB, intron-variant | NCK1 | GRCh38.p7 | 3:136929563 | GTAGCAGAAGAGACC[A/G]GGGTTAGAATCAGCA | 4690 |
rs747404063 | snp | C/T | | | downstream-variant-500B, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136951745 | ATGTTACGTATGTTT[C/T]GAAAGAAAACTCATT | 4690 |
rs747435296 | snp | G/T | | | upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136862203 | CCGCGCGGATCCGCC[G/T]GCCCACCGCGCGTGC | 4690 |
rs747529728 | snp | C/T | 1.64749e-05 | 0.00287005 | synonymous-codon, downstream-variant-500B | NCK1, LOC107986136 | GRCh38.p7 | 3:136945707 | TGTGAAATTTAACTA[C/T]ATGGCTGAGAGAGAG | 4690 |
rs747546995 | in-del | -/TTGT | | | intron-variant | NCK1 | GRCh38.p7 | 3:136887916 | TATTCATCGCCTTTA[-/TTGT]TTCTTTTCTTTCTTT | 4690 |
rs747572687 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136881924 | GTTTATCCATTCATT[C/T]GTTGATGAACAGCTT | 4690 |
rs747573950 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136888526 | TCCTGCCTCAGCCTC[C/T]GCAGTAGCTGGGACT | 4690 |
rs747576826 | snp | C/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136943824 | GACAGAGGTAAACAA[C/G]AATATGTAAACAGGT | 4690 |
rs747588071 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136898923 | ACAGAGAACATAATC[A/G]TAAAATGGCTAGAGA | 4690 |
rs747617745 | snp | C/T | | | downstream-variant-500B, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136951624 | GACGAATCTCTGAAA[C/T]GTTTTATTTGGGAAG | 4690 |
rs747670701 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136936354 | CTGGCTGAATAACTA[C/T]TATATGTATATATCA | 4690 |
rs747727219 | snp | C/G | 1.66941e-05 | 0.00288908 | missense, downstream-variant-500B | NCK1, LOC107986136 | GRCh38.p7 | 3:136945618 | AAACCTAGTGTGCCA[C/G]ATTCTGCATCTCCTG | 4690 |
rs747737963 | in-del | -/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136896572 | GGCAGGGTCTCACTC[-/T]TGTCACCCAGGCTGG | 4690 |
rs747749571 | snp | A/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136867809 | ACCATACTACTTCTC[A/T]TCTCTTGTAATTTTG | 4690 |
rs747788921 | in-del | -/TTTTA | | | intron-variant | NCK1 | GRCh38.p7 | 3:136939859 | TTTTTTTTTTTTTTT[-/TTTTA]AAATAGAGACAGGGT | 4690 |
rs747804500 | snp | A/C | | | intron-variant | NCK1 | GRCh38.p7 | 3:136882486 | TCTGCATTAATGATA[A/C]AACAATACCTCTTAC | 4690 |
rs747847948 | snp | G/T | | | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136949545 | CAAGTAGGAATTTGG[G/T]TGTATGGATAAGAGG | 4690 |
rs747869819 | snp | A/C | | | intron-variant | NCK1 | GRCh38.p7 | 3:136923265 | CCAAAACAAATAAAT[A/C]GCTGTCCAGGCCGGG | 4690 |
rs747882150 | snp | A/C | | | intron-variant | NCK1 | GRCh38.p7 | 3:136873950 | TGAAAGTGGACTAAT[A/C]CAGTAACCATATAGC | 4690 |
rs747883374 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136865789 | GGAAACTTTATGTCT[A/G]GCTGATCCTCACCTT | 4690 |
rs747923239 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136910334 | AACTTCCTGTACAGC[C/T]CCATCCCTACCCCCT | 4690 |
rs747974189 | in-del | -/TTT | | | intron-variant | NCK1 | GRCh38.p7 | 3:136864762 | GGTTTTTTTCTTTTC[-/TTT]TTTTTTTTTTTTTTT | 4690 |
rs748000220 | snp | A/C | | | intron-variant | NCK1 | GRCh38.p7 | 3:136909201 | TGGACTAAGACAGTA[A/C]GAGAGAGGCAGAAGT | 4690 |
rs748014796 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136871910 | GCCTTTAACCTTGTG[C/T]CATGATTGTGAGGCC | 4690 |
rs748086365 | snp | C/T | 1.64751e-05 | 0.00287007 | missense, nc-transcript-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136946158 | CCTCCACAGTGTGAT[C/T]ACATTAGGCCTTCAC | 4690 |
rs748146955 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136873515 | AACTTCTAAGTTAAT[G/T]CTGAAATGAGTTAAG | 4690 |
rs748163042 | in-del | -/C | | | intron-variant | NCK1 | GRCh38.p7 | 3:136864999 | AGTCTCACTCTGTTG[-/C]CCAGGCTGGAGTGCA | 4690 |
rs748172127 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136890368 | CGCAGCCCCAGTTCC[C/T]GCTGGCGCCTCTCCC | 4690 |
rs748174332 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136872201 | ATGACTTTGCCCAAA[A/G]TGCTGATTGCGATAT | 4690 |
rs748212318 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136906402 | GGTATGAGCCACCAT[A/G]CCTGGCCTGTGATAA | 4690 |
rs748233366 | snp | A/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136919488 | CTGGAATCTCTAGTG[A/T]AAAGGGAAATTAACA | 4690 |
rs748296383 | in-del | -/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136915730 | ACACTTTTGCTTTTG[-/T]TTTTTTTTTTTTTGA | 4690 |
rs748325789 | snp | A/G | 5.04978e-05 | 0.00502458 | synonymous-codon | NCK1 | GRCh38.p7 | 3:136928214 | TATTGTGAAAAACCT[A/G]AAGGATACCTTAGGT | 4690 |
rs748344901 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136917134 | ACAATGTGGCATGTT[C/T]TGTGTCAAGCTTGTC | 4690 |
rs748380862 | snp | C/G | 1.64803e-05 | 0.00287052 | missense | NCK1 | GRCh38.p7 | 3:136928111 | TGGATGATTCTAAGT[C/G]CTGGTGGCGAGTTCG | 4690 |
rs748423804 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136885853 | ACCTTTCATAAGAGA[G/T]ATGTTCTTTTTAGAA | 4690 |
rs748466468 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136932890 | TTTGGCCCCATTCTC[A/G]ACACTTACTCAGTGA | 4690 |
rs748479594 | snp | A/G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136937072 | CAGATATTTGCTCCT[A/G/T]TGTTTTCTTCTAAGA | 4690 |
rs748503376 | snp | A/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136881638 | CCCAGAACTTTTTCA[A/T]CTTGTAAAACTGAAA | 4690 |
rs748522898 | snp | A/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136907223 | CCTCTGCTGCAGTGT[A/T]GGGAGACAGTTGCTG | 4690 |
rs748532304 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136927700 | CTAATTTTTGTATTT[C/T]AGTACAGATGGGGTT | 4690 |
rs748661422 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136941273 | TGGGACTACAGGTGC[A/G]TGCCACGATGCCTGG | 4690 |
rs748702315 | snp | G/T | | | intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136947743 | TTTTGGCTCTTGTAG[G/T]CATTTGAGTTTGTAG | 4690 |
rs748723097 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136913163 | TATAGGCCATACTTT[C/T]CCATTTCTTTGTATC | 4690 |
rs748729294 | snp | A/C | | | intron-variant | NCK1 | GRCh38.p7 | 3:136893688 | GAGACTTTTGATAGA[A/C]TCTACATCTTGCTTT | 4690 |
rs748738721 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136865606 | TTTACCTTTATAATA[C/T]AGAAAAATACCAAAT | 4690 |
rs748740667 | in-del | -/A | | | upstream-variant-2KB, intron-variant | NCK1 | GRCh38.p7 | 3:136930244 | GGAAAAGGGGAAAAC[-/A]AAAGGATTAATTCAT | 4690 |
rs748771673 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136933371 | AGGTCACATAAGGAA[C/T]AGTTATGGGTACAAA | 4690 |
rs748778418 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136901160 | TCTGTGTCTGTTGAG[A/G]TGAACATATGGTTTT | 4690 |
rs748838309 | snp | C/T | | | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136949234 | ATTTTTTTAATCCCA[C/T]TTGTATTATTTTACC | 4690 |
rs748850817 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136871883 | CTTATCTGCCGCCAT[A/G]TGAGAAGACATGCCT | 4690 |
rs748857974 | snp | A/T | 1.64743e-05 | 0.00287 | missense, downstream-variant-500B | NCK1, LOC107986136 | GRCh38.p7 | 3:136945732 | AGAGAGGATGAATTA[A/T]CATTGATAAAGGGGA | 4690 |
rs748858960 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136914127 | GAGCAGTGGCCTCTA[A/G]CTATTGGGAGGGAGG | 4690 |
rs748948432 | in-del | -/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136897278 | ATTTTTAGTAGAGAT[-/G]GGGGTTTTGCAAAGT | 4690 |
rs749002889 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136936197 | AGGCACATGCCACCA[C/T]GCCTGGCTAATTTGT | 4690 |
rs749020115 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136879233 | AATAAATGAGAAAAG[A/G]AAATTAAAAGGTCCG | 4690 |
rs749053242 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136921639 | ACTAGTTAAAATGGT[A/G]AGGACAGATTTTATT | 4690 |
rs749059823 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136907668 | TCTCTTAGGTGATCT[A/G]TTTGAAGTGTGATTA | 4690 |
rs749100401 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136888323 | TTGAGATATGATTCA[C/T]ATACTATACAGTTCA | 4690 |
rs749103421 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136922181 | AAACTTATTATTTAT[A/G]ACAGGAGGTGGTGGT | 4690 |
rs749180139 | in-del | -/AGAGC | 1.81694e-05 | 0.00301403 | intron-variant, nc-transcript-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136946326 | GAGGTAAATACAAAT[-/AGAGC]TCTGGGTATTTTAAA | 4690 |
rs749247395 | snp | A/T | 5.72525e-05 | 0.00535004 | intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136946342 | GAGCTCTGGGTATTT[A/T]AAAAAAAAGAGAGAG | 4690 |
rs749254667 | in-del | -/TT | | | intron-variant | NCK1 | GRCh38.p7 | 3:136865780 | AAGATTTAAGGAAAC[-/TT]TATGTCTGGCTGATC | 4690 |
rs749307022 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136902429 | CGAGCTCCTGAGCTC[A/G]GGCAATCTGCCCACC | 4690 |
rs749307037 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136934721 | GTGTTAGAAATAAAA[A/G]AGATTAAATAACTTG | 4690 |
rs749341381 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136869843 | CTATTTGTTTAAATT[A/G]TCAGTTAAAAAAACC | 4690 |
rs749371503 | in-del | -/TTAC | | | intron-variant | NCK1 | GRCh38.p7 | 3:136865440 | CATTGCTTTGTACTT[-/TTAC]TTTGTCTTATTTTAC | 4690 |
rs749400802 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136917464 | TGTTTTAACCTTCAC[A/G]ATCCTTTGGGGGTTT | 4690 |
rs749443818 | snp | A/G | 1.65143e-05 | 0.00287348 | missense, nc-transcript-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136946221 | TATGGCAAAGTCACC[A/G]GGCATCAAGCAGAAA | 4690 |
rs749529285 | snp | C/T | | | upstream-variant-2KB, intron-variant | NCK1 | GRCh38.p7 | 3:136929856 | ATTACTGTATGTAAA[C/T]CTAAAATCCCATTTA | 4690 |
rs749532686 | snp | A/G | 3.61272e-05 | 0.00424997 | intron-variant, downstream-variant-500B | NCK1, LOC107986136 | GRCh38.p7 | 3:136945579 | CCCTTTTTAATTTCA[A/G]CAGGCATTGGAAAAG | 4690 |
rs749577849 | snp | G/T | | | synonymous-codon, downstream-variant-500B | NCK1, LOC107986136 | GRCh38.p7 | 3:136945824 | AGTTGGATGGTTCCC[G/T]TCAAACTATGTAACT | 4690 |
rs749611471 | snp | A/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136939429 | TTGGTTTTGTTGATT[A/T]CCTCTGTTTTTCTGT | 4690 |
rs749662094 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136911614 | GAATTGTCTGGAGTT[C/T]CTTATATATTTTGGA | 4690 |
rs749663216 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136941226 | TGCCTCCCAGGTTCA[A/G]GCGACACTTATATGT | 4690 |
rs749678194 | snp | A/G | 1.88035e-05 | 0.00306617 | intron-variant | NCK1 | GRCh38.p7 | 3:136928235 | TACCTTAGGTAAGAT[A/G]TTTTTTAAAAGAAAA | 4690 |
rs749686192 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136906357 | TCAAGTGATCCTCCC[A/G]CCTCAGCCTCCCAAA | 4690 |
rs749743279 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136919293 | GTGATTACATAACTC[C/T]TAAATGTTTGTCAAA | 4690 |
rs749807329 | in-del | -/TTT | | | intron-variant | NCK1 | GRCh38.p7 | 3:136870035 | CTCAAAAGTTTTTTT[-/TTT]TTTTTTTTTTTTTTT | 4690 |
rs749932433 | snp | A/G | 1.69971e-05 | 0.00291518 | missense, nc-transcript-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136946279 | GGGATTTCCTCATTC[A/G]TGATAGTGAATCTTC | 4690 |
rs749956215 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136906983 | TACTGGCTGTGGTAG[A/G]CAGGGGAGAGTGATC | 4690 |
rs749971575 | in-del | -/TG | | | intron-variant | NCK1 | GRCh38.p7 | 3:136923106 | CTATGCCTATGTGTA[-/TG]TGTGTGTGTGTGTGC | 4690 |
rs749980527 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136939329 | CTGTAGAAATGTTAT[G/T]TCTGATTTTATTTAT | 4690 |
rs749985486 | snp | G/T | 1.64741e-05 | 0.00286998 | missense, nc-transcript-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136946129 | ATCCATTAACTTCAG[G/T]TTTGGAACCATCACC | 4690 |
rs750076113 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136896163 | AAAGTCCTCTCTTCT[A/G]TCTACTTTGAAATAC | 4690 |
rs750101994 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136906293 | AAATTTTAACTTTCA[A/G]TAAAAGAGGTCTCAC | 4690 |
rs750120282 | in-del | -/ATTT | | | intron-variant | NCK1 | GRCh38.p7 | 3:136910620 | TTGACTCCTCTTAGC[-/ATTT]ATTTATTCCAGTTTT | 4690 |
rs750122654 | in-del | -/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136876970 | ACCTTTACCACAGTG[-/T]TTTTTTAACTCTGTG | 4690 |
rs750153677 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136866909 | TGAGCCACTGTGCCC[A/G]TCCAGTTTGCCTAGT | 4690 |
rs750203454 | snp | C/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136902276 | TATCTCAGCTTACTG[C/G]AACCTCCGCCTCCTG | 4690 |
rs750217969 | snp | A/C | | | upstream-variant-2KB, intron-variant | NCK1 | GRCh38.p7 | 3:136928763 | TTTTATTTTTACTGG[A/C]CCTCCATTAGGGCCT | 4690 |
rs750248734 | snp | A/T | | | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136951116 | AAATAGGCCTAGCAG[A/T]TGGGCAACTTGGGTT | 4690 |
rs750281139 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136915122 | CCTTTTTTCTTTATA[A/G]ATTAGCCTCAGGCAT | 4690 |
rs750326518 | snp | A/G | 6.59359e-05 | 0.00574139 | missense | NCK1 | GRCh38.p7 | 3:136928065 | CAAGAACAAGAGTTG[A/G]ACATCAAGAAGAATG | 4690 |
rs750371785 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136895726 | CGTACCACCACACCC[C/T]GCTAATTTTTGCATT | 4690 |
rs750381343 | snp | A/T | 1.72994e-05 | 0.00294099 | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136948491 | CTGTGTAGCTGTAAT[A/T]TGTCATGTAATTGAA | 4690 |
rs750401808 | in-del | -/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136932138 | AAAAAAAAAAAAAAA[-/G]AATCCATTGTATCAT | 4690 |
rs750404455 | snp | C/T | | | upstream-variant-2KB, intron-variant | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136861070 | ACTGATTCAACGGAG[C/T]TTACAATCTAGGTAG | 4690 |
rs750405087 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136881214 | ACTTACACTATTGGC[C/T]TCTTATTTTATTTAA | 4690 |
rs750451595 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136904243 | CTGCAGCCTCTGCCT[C/T]CTGGGTTCAAGTGAT | 4690 |
rs750455635 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136924526 | AGAATGTTTAAAAAA[A/G]TACACTTAGCAAAAA | 4690 |
rs750488135 | snp | A/C | | | intron-variant | NCK1 | GRCh38.p7 | 3:136910016 | TTTAGAATTTTTTTT[A/C]TATTCATCTTGCCAA | 4690 |
rs750540753 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136938192 | CTTTGTTTTACTAAT[A/G]TGAGGTGTCTTATAT | 4690 |
rs750575913 | in-del | -/C | | | intron-variant | NCK1 | GRCh38.p7 | 3:136932111 | CAACAGAGCGAGACT[-/C]CCATCTCAAAAAAAA | 4690 |
rs750591273 | snp | C/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136922975 | CATAATGATGACGCA[C/G]TCTGCAATTGTTAGA | 4690 |
rs750622340 | snp | A/G | 1.64751e-05 | 0.00287007 | synonymous-codon, downstream-variant-500B | NCK1, LOC107986136 | GRCh38.p7 | 3:136945929 | AAATACTGGGCAAGT[A/G]TTGCATGTGGTACAG | 4690 |
rs750636814 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136901114 | AAGAGTTTTTATCAC[A/G]AAGGGACACTGAATT | 4690 |
rs750677530 | snp | C/T | 1.64765e-05 | 0.00287019 | synonymous-codon, downstream-variant-500B | NCK1, LOC107986136 | GRCh38.p7 | 3:136945821 | ACAAGTTGGATGGTT[C/T]CCTTCAAACTATGTA | 4690 |
rs750699277 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136886451 | AGATTACCTAATACA[C/T]TGTAAATGGTATTTA | 4690 |
rs750776032 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136919750 | GAGGAAGGGTACTGT[C/T]GGCTGTGTATATAGG | 4690 |
rs750785031 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136918878 | TTCAGTGTTTTCACT[A/G]ATGACCGTGTAACCA | 4690 |
rs750793845 | snp | A/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136932318 | CAACCCCAAATTTTT[A/T]TTTATTTTGCCAGGC | 4690 |
rs750848915 | snp | A/C | | | intron-variant | NCK1 | GRCh38.p7 | 3:136933939 | TCTCGAACTCCTGGC[A/C]TCAAGTTATCTGCCT | 4690 |
rs750918907 | in-del | -/A | 1.85503e-05 | 0.00304546 | intron-variant | NCK1 | GRCh38.p7 | 3:136928235 | TACCTTAGGTAAGAT[-/A]TTTTTTAAAAGAAAA | 4690 |
rs750927429 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136900165 | AAAACCAGACATTGG[C/T]GCTCTCCCTTCACTC | 4690 |
rs750940005 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136885444 | TACGTAGCTGGAACT[A/G]TAGGTGCATGCCACC | 4690 |
rs750948665 | in-del | -/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136864215 | CGTGTAATGTTGGCC[-/G]GGCTCGGTGGCTCAC | 4690 |
rs751024787 | in-del | -/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136885070 | TTATGGATGAAAATA[-/T]TTTTTTCAGGTATAC | 4690 |
rs751028130 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136906147 | CTTTGGCTTTGATTC[C/T]AGGTATGTGTCATAG | 4690 |
rs751028905 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136924816 | GTGAGAGTTATTTAT[A/G]TCATGCTCAAGGTCG | 4690 |
rs751035568 | snp | A/T | | | intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136946880 | GTAAACAATAAAACT[A/T]TAAAACCATAAAAGT | 4690 |
rs751039709 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136873031 | GAGCCCCCACACAGA[G/T]TTCCTACTCGGGTAC | 4690 |
rs751067471 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136918084 | ATATTACATTTAAAA[A/G]TAAATTGTTTATGTG | 4690 |
rs751078214 | snp | A/C | 1.67722e-05 | 0.00289583 | stop-gained, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136948278 | ATGATTTCTCAGTAT[A/C]ACTAAAAGCACAAGG | 4690 |
rs751094369 | in-del | -/TTGTTTCTTTCTTTCC | | | intron-variant | NCK1 | GRCh38.p7 | 3:136867118 | TCTTTCTTTCTTTCT[-/TTGTTTCTTTCTTTCC]TTCCTTCCTTCCTTC | 4690 |
rs751095814 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136938806 | GGAGCCTAACCCTGT[C/T]TTTCCCTTAGGAGCT | 4690 |
rs751096958 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136885496 | TTTTTGTAGAGACAG[A/G]ATTTTGCCATGTTGC | 4690 |
rs751159113 | snp | C/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136932218 | TTTTGCTGAGTCTTA[C/G]GAAGTTGATAGTTAA | 4690 |
rs751181898 | snp | C/T | 1.73564e-05 | 0.00294583 | splice-donor-variant, nc-transcript-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136946297 | ATAGTGAATCTTCGG[C/T]AAGTTGATTTTCGGA | 4690 |
rs751186158 | in-del | -/TGGAT/TGGATTAT | 5.1548e-05 | 0.00507659 | frameshift-variant, nc-transcript-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136946289 | ATTCGTGATAGTGAA[-/TGGAT/TGGATTAT]TCTTCGGTAAGTTGA | 4690 |
rs751277309 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136870594 | TTAGAAACATTTAGA[A/G]TATTTAGTGTACAAC | 4690 |
rs751312715 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136881159 | TCTGTTCTTTATCTG[C/T]ATCACCATACTACTC | 4690 |
rs751335085 | in-del | -/CCGTGCGAGCCTGGGAGGTCGA | | | intron-variant, upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136862648 | AGCCCGGGCGGCCGC[-/CCGTGCGAGCCTGGGAGGTCGA]GTGTGCGGCGCGCTG | 4690 |
rs751434194 | snp | A/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136912975 | CTTTGAGGTTTTCTA[A/T]CTCTTTACTCATTTT | 4690 |
rs751444012 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136878803 | CAAGAAGACTGACTA[C/T]TGTTTCTGACACTGA | 4690 |
rs751517125 | snp | A/G | 3.31049e-05 | 0.00406834 | synonymous-codon | NCK1 | GRCh38.p7 | 3:136928196 | CAGTGCTCGGAAAGC[A/G]TCTATTGTGAAAAAC | 4690 |
rs751519386 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136940733 | TATTTTTGGTAGAGA[C/T]GGAGTTTCACCATGT | 4690 |
rs751523481 | snp | A/T | | | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136951080 | AGGCTTCATGCAATC[A/T]ATTGCCATTGCTAGA | 4690 |
rs751540021 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136873973 | CATATAGCTTGTATA[C/T]CTTTTTGTGGATGGC | 4690 |
rs751562818 | in-del | -/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136883880 | ACTTAAGGGGAGCCT[-/G]GGGTGAATTGGAAGA | 4690 |
rs751566615 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136877778 | AGCAAAAGTAGAAAA[C/T]ACTTCTTAGGCTCAG | 4690 |
rs751619081 | snp | C/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136922080 | GAGCCACCGCGCCCG[C/G]CCACTGAGTGGTTTT | 4690 |
rs751670516 | snp | A/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136922936 | TGACCATCAGTAAGG[A/T]CTAGTTGAAGAAAGT | 4690 |
rs751689598 | snp | A/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136905967 | CGTGAATTATTGTGG[A/T]CTTTTGGCGGTGTCA | 4690 |
rs751726662 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136889701 | TTCTCCACCTCCCCA[C/T]CAGATTAGCTAGATA | 4690 |
rs751794824 | snp | C/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136878706 | TTGTATCTCAATAAA[C/G]CTATTTTTTTTTAAG | 4690 |
rs751801783 | in-del | -/CCTT | | | intron-variant | NCK1 | GRCh38.p7 | 3:136867207 | TCTTTCTTTTCCCTT[-/CCTT]CCTTCCTTCCTTCCG | 4690 |
rs751815969 | snp | C/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136904492 | ATTTCATTCTCTACT[C/G]GCCTATAAGGTTTCT | 4690 |
rs751822521 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136898799 | AGAACGGCATGTGAT[A/G]TGGACTTCCTCCATG | 4690 |
rs751866793 | in-del | -/TG | | | intron-variant | NCK1 | GRCh38.p7 | 3:136895355 | TTCCGTACCTTTTAA[-/TG]TTGCAATAAAATTGT | 4690 |
rs751881674 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136902800 | GATGATATGATCTTA[C/T]ATTTAGAAAAACCTA | 4690 |
rs751892472 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136930766 | AAAAATTGTAGTTTC[A/G]ACTTGGTAAGTAAAA | 4690 |
rs751905277 | snp | A/C | | | intron-variant | NCK1 | GRCh38.p7 | 3:136894405 | GTGCATATGCTGCAT[A/C]CCAAATGACCAGCAG | 4690 |
rs751945293 | snp | C/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136945228 | ATGGGTGTGGTGGAG[C/G]CTTTGTGTACTTAGA | 4690 |
rs751989856 | in-del | -/TGG | | | intron-variant | NCK1 | GRCh38.p7 | 3:136923615 | GTCCAGTGGGGTGGA[-/TGG]GAGAGGGGAGAGAAA | 4690 |
rs751996567 | snp | A/G | | | intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136946362 | AAAAGAGAGAGAGAA[A/G]TGGAGAGGTTAAGTG | 4690 |
rs752025317 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136920224 | GTCAGAAATAAAGGC[C/T]ACTTAAAAATTAAGT | 4690 |
rs752040839 | snp | A/G | | | upstream-variant-2KB, intron-variant | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136860577 | TGAGCATCTGCATCT[A/G]ATGGTAGCCTAAGAC | 4690 |
rs752046581 | snp | C/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136909673 | ATTATTGAGAGTCAG[C/G]TATTGAAGTTTCCAA | 4690 |
rs752071867 | snp | C/T | 1.64738e-05 | 0.00286995 | synonymous-codon, downstream-variant-500B | NCK1, LOC107986136 | GRCh38.p7 | 3:136945851 | AACTGAAGAAGGTGA[C/T]AGTCCTTTGGGTGAC | 4690 |
rs752134960 | in-del | -/AACTC | | | intron-variant | NCK1 | GRCh38.p7 | 3:136869637 | TTTATTTTTCCTCTT[-/AACTC]TAAAGTTTCTGTAAC | 4690 |
rs752140185 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136876969 | ACACCTTTACCACAG[G/T]GTTTTTTAACTCTGT | 4690 |
rs752183903 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136930658 | TAGATTTTCTGCTTT[C/T]GTAAATTTAAAGGAA | 4690 |
rs752191407 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136869313 | GCGCTTTGGGAGGCT[A/G]AGGTGGGCGGATAAC | 4690 |
rs752194828 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136885197 | GGTGAGAATATGGAT[A/G]TTGTGGCCGTGGACA | 4690 |
rs752232185 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136890862 | GCCACCTGAAACTCT[A/G]TACCCATTAAACAAC | 4690 |
rs752239151 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136916522 | GAACCTTCAAGTAAG[C/T]ATATTCAGGTTTTAT | 4690 |
rs752250255 | snp | C/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136888054 | GGTTCAAGCTATTCT[C/G]CTGCCTCAGCCTCCC | 4690 |
rs752298831 | in-del | -/ACAT | 1.73936e-05 | 0.00294898 | intron-variant, nc-transcript-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136946298 | AGTGAATCTTCGGTA[-/ACAT]AGTTGATTTTCGGAG | 4690 |
rs752305358 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136915978 | TGATCTGCCCACCTC[A/G]GCCTCCTAAAGTGCT | 4690 |
rs752345876 | snp | A/G | 1.6609e-05 | 0.0028817 | missense, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136948431 | AAGGAGAAAAATTAT[A/G]TCTTGTCAAGCATTT | 4690 |
rs752368044 | in-del | -/TCTTTC | | | intron-variant | NCK1 | GRCh38.p7 | 3:136867179 | CCTTCCTTCCTTCCT[-/TCTTTC]TTTCTTTTCTTTCTT | 4690 |
rs752392931 | snp | C/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136884330 | ATGCATTTGAAAGTT[C/G]TGAAATGTTACCTTT | 4690 |
rs752399185 | snp | A/G | 1.66172e-05 | 0.00288242 | missense, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136948293 | CACTAAAAGCACAAG[A/G]GAAAAACAAGCATTT | 4690 |
rs752445841 | snp | A/C | | | intron-variant | NCK1 | GRCh38.p7 | 3:136897122 | GACAGAATCTCACTC[A/C]CTGTCACCTAGGCTG | 4690 |
rs752463456 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136944831 | AAATGCCTGACTGAA[G/T]TTGATGTAGCGTACA | 4690 |
rs752466994 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136936109 | GCAGTGACGTGATCT[C/T]AGCTCACTGCAACCT | 4690 |
rs752476069 | snp | C/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136905999 | ATTTCCTTGCTTTTT[C/G]ATGTTTCCTGTGTCC | 4690 |
rs752483937 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136892248 | CTTTATATATTCTGA[A/G]TATCAGTGTCCTATC | 4690 |
rs752490929 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136877558 | GGACTTCTAAATAAA[G/T]ATGGCTGAGTGAAAG | 4690 |
rs752517381 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136938441 | CATCTGATGTGCACA[C/T]TCCCAGTTGAGGCAA | 4690 |
rs752527271 | snp | C/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136904692 | ATCTGATGTGTAAAT[C/G]TGTTGCTAGACTTGG | 4690 |
rs752564457 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136940631 | CTCACTGCAACCTCC[A/G]CCTCCCAGGTTCAAG | 4690 |
rs752669440 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136887909 | TATCTTTTATTCATC[A/G]CCTTTATTGTTTCTT | 4690 |
rs752691664 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136934227 | TAGGGTTGGGGGTAC[A/G]TGTGAAGGTTTGTTA | 4690 |
rs752712322 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136923808 | ATCCAAATGTTTTAC[A/G]TAATTATGAAACAAT | 4690 |
rs752742130 | snp | C/T | | | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136950691 | TTCCTTATTCCCAGC[C/T]TGGTGTCTGTATCGT | 4690 |
rs752752493 | snp | G/T | | | intron-variant, upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136862887 | ACCGGCCGTTTTCTA[G/T]TCTGGGGCTGTGACT | 4690 |
rs752774458 | snp | G/T | 1.64871e-05 | 0.00287111 | stop-gained, downstream-variant-500B | NCK1, LOC107986136 | GRCh38.p7 | 3:136945660 | TTTGTTGACCCAGGG[G/T]AACGTCTCTATGACC | 4690 |
rs752819563 | snp | A/G | 7.95814e-05 | 0.00630749 | intron-variant, downstream-variant-500B | NCK1, LOC107986136 | GRCh38.p7 | 3:136945560 | TTATATTCTCCTCTC[A/G]TGGCCCTTTTTAATT | 4690 |
rs752858040 | in-del | -/AA | | | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136950066 | TAATTATTAGTAGTT[-/AA]GTTTTTAATGGAAAT | 4690 |
rs752921760 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136908732 | TCAAAATTGGTAGCT[C/T]TTAGGAAGAAGAGAA | 4690 |
rs752966417 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136878093 | TGTATGATACATGCT[A/G]TAACACAGATAAACC | 4690 |
rs752992119 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136922768 | GAATACAGAATTTAG[C/T]AGTATCTCACAAAAT | 4690 |
rs752998880 | snp | A/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136865312 | CTGGTCTCGAACTCC[A/T]GACCTCAAGCAATCT | 4690 |
rs753009568 | in-del | -/TTTC | | | intron-variant | NCK1 | GRCh38.p7 | 3:136887927 | TTATTGTTTCTTTTC[-/TTTC]TTTCTTTCTTTCTTT | 4690 |
rs753045375 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136909596 | TGGATAGTGTTCTCT[A/G]ATACAGCTAATTGGT | 4690 |
rs753105157 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136940519 | ATCAATATATGCTGT[C/T]CTTTGTCTTTAAGTC | 4690 |
rs753184682 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136922044 | TGCCTCGGCCTCCCA[A/G]AGTGCTGGGATTACA | 4690 |
rs753187246 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136873870 | TGAGGCCTCTCCAGC[C/T]ACATGGAACTGTAAG | 4690 |
rs753207597 | in-del | -/CAAT | | | intron-variant | NCK1 | GRCh38.p7 | 3:136896523 | TATGCCACATATGTC[-/CAAT]CATTAATCTGTTTTT | 4690 |
rs753228949 | in-del | -/TTGCCAGTATTTTG | | | intron-variant | NCK1 | GRCh38.p7 | 3:136901299 | GTTGTTGGATTCAGT[-/TTGCCAGTATTTTG]AGAATTTTTATCTCT | 4690 |
rs753238692 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136873048 | TCCTACTCGGGTACC[A/G]CCTAGTGGAGCTGTG | 4690 |
rs753322905 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136943527 | ATAGAAAATGAAAGT[G/T]TATGATTTCCTTGGA | 4690 |
rs753373777 | snp | C/G | | | upstream-variant-2KB, intron-variant | NCK1 | GRCh38.p7 | 3:136928975 | ATTTGCGTAATTGTT[C/G]TTTGTCTAGGTGTAG | 4690 |
rs753389526 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136895854 | ACAGGTATGAGCCAC[C/T]ATGCCCAGTCTGTAT | 4690 |
rs753441735 | in-del | -/TT | | | intron-variant | NCK1 | GRCh38.p7 | 3:136891448 | CCTGATCATGGACAC[-/TT]TGGTTGCTTCCACTT | 4690 |
rs753551735 | snp | A/C | | | intron-variant | NCK1 | GRCh38.p7 | 3:136942509 | ACAAACAAAAGAAAA[A/C]CTCTCCCCATCTTTA | 4690 |
rs753570558 | in-del | -/GTCT | | | intron-variant | NCK1 | GRCh38.p7 | 3:136867249 | TCCGTCTGTCCGTCC[-/GTCT]GTCTCTCTCTCTCTT | 4690 |
rs753579948 | in-del | -/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136915653 | AAAAGGTTCACAGTT[-/T]CCTCAGGCTGTATAG | 4690 |
rs753623410 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136904286 | GCCTCCTGAATAGCT[A/G]GGATTACAGGAATGT | 4690 |
rs753658983 | snp | A/C | | | intron-variant | NCK1 | GRCh38.p7 | 3:136916348 | GTCATAAGTTAAATA[A/C]GTCTGATATTTCAGG | 4690 |
rs753672797 | in-del | -/CTTT | | | intron-variant, upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136863016 | GATAGGTTTTGTAAC[-/CTTT]CTTTCTTCTGTATTA | 4690 |
rs753680418 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136909521 | TCAATGGCAGAATGT[C/T]GAGTGCTGTAATAAT | 4690 |
rs753683359 | snp | A/G | 4.94703e-05 | 0.0049732 | synonymous-codon | NCK1 | GRCh38.p7 | 3:136928043 | CAAATTTGATTATGT[A/G]GCCCAACAAGAACAA | 4690 |
rs753706218 | in-del | -/AGCC | | | intron-variant | NCK1 | GRCh38.p7 | 3:136871253 | TAAAAAAAAAAAATT[-/AGCC]AGGTTTGGCTGTGAG | 4690 |
rs753738439 | snp | C/T | 1.68709e-05 | 0.00290434 | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136948456 | GCATTTATCATGATA[C/T]TGCTGACCAGAAGTG | 4690 |
rs753758214 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136884124 | AATAATGAACGAGCT[A/G]TCTAGAGAGAGGGTA | 4690 |
rs753774461 | snp | C/T | | | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136951549 | TCTTATCTTTACCAG[C/T]GCACATGGTGAAAAA | 4690 |
rs753789797 | snp | C/G | 1.65343e-05 | 0.00287521 | missense, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136948327 | AGTCCAACTAAAAGA[C/G]ACTGTCTACTGCATT | 4690 |
rs753830178 | snp | A/G | | | intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136947200 | TAATCCCTCAGAAAA[A/G]CAGTTGGTTGGCAGT | 4690 |
rs753853018 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136912761 | CCTGGGCTCAAGCAG[C/T]CCCCCTGCTTCAGCT | 4690 |
rs753870409 | snp | C/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136900280 | ATTTCTGAATTATCT[C/G]TTTTATTCCATTAGT | 4690 |
rs753973486 | snp | A/G | | | intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136948239 | ATGTTTACTATATGT[A/G]TCTTTTTTTTCTCTT | 4690 |
rs754035940 | in-del | -/ACTT | | | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136950849 | AACCCTGCCTAACTC[-/ACTT]CTACAAATAACTTCC | 4690 |
rs754093070 | snp | C/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136872900 | TTTGGGAACCTCCAC[C/G]TGCATTTCAGAAGAT | 4690 |
rs754097336 | snp | A/G | | | intron-variant, upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136863344 | TATAACGATTTCTTC[A/G]GCACCTGGAAACCAG | 4690 |
rs754152871 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136878508 | TTGTAGAGATAGAGT[A/G]GTTGCATAGGACTGG | 4690 |
rs754236805 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136920938 | AAAAACAAATGTTAT[A/G]AACTGAATTTTGTCC | 4690 |
rs754276304 | in-del | -/CCTTTT | | | intron-variant | NCK1 | GRCh38.p7 | 3:136944111 | GAAAAGGAAAAACAA[-/CCTTTT]TTTTTTTTTTTTTTT | 4690 |
rs754360423 | in-del | -/TA | | | intron-variant | NCK1 | GRCh38.p7 | 3:136895323 | TGGTTTATTTTATTA[-/TA]TATATATATATCATG | 4690 |
rs754364138 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136872056 | AGTAGAGTAGAGTGC[C/T]CCTGAAAAGATACCC | 4690 |
rs754388469 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136886914 | AATGGCACAATCTCA[C/T]CTCACTGCAACCTCC | 4690 |
rs754395252 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136914193 | CAGTGATCAGAAAGC[A/G]CAATTAGCTGTCAGA | 4690 |
rs754461919 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136867692 | GATAAGGAAACTGAA[A/G]TACAAATAGACTAGA | 4690 |
rs754475387 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136882459 | AACAGCCAGAGAAAT[A/G]TTTTTAAGATTTCTG | 4690 |
rs754510347 | in-del | -/TTTTTA | | | intron-variant | NCK1 | GRCh38.p7 | 3:136939858 | TTTTTTTTTTTTTTT[-/TTTTTA]AAATAGAGACAGGGT | 4690 |
rs754517071 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136915513 | ACTCCAGTAGGTCTT[A/G]TGGCTTGCATAGGCC | 4690 |
rs754616883 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136895970 | GCTTTGTTTGCCATC[C/T]TTTTTCTTTGCTTCT | 4690 |
rs754626434 | snp | A/G | 3.48384e-05 | 0.00417348 | intron-variant, nc-transcript-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136946299 | AGTGAATCTTCGGTA[A/G]GTTGATTTTCGGAGG | 4690 |
rs754642801 | in-del | -/CC | | | intron-variant | NCK1 | GRCh38.p7 | 3:136864498 | TCACACACACACAAA[-/CC]AAAAAAACAGAAACA | 4690 |
rs754662512 | snp | C/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136927676 | ACGGGTGTGCACCAT[C/G]ACGCCCAGCTAATTT | 4690 |
rs754677672 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136904493 | TTTCATTCTCTACTG[G/T]CCTATAAGGTTTCTG | 4690 |
rs754752026 | snp | A/G | 3.295e-05 | 0.00405881 | missense, nc-transcript-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136946153 | CATCACCTCCACAGT[A/G]TGATTACATTAGGCC | 4690 |
rs754891005 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136903263 | GTTTGATACAAGTAT[A/G]GCTACTTCTAGTCAC | 4690 |
rs754971734 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136936292 | GTCATCTGCCCGCCT[C/T]GGCCTCCCAAAGTGC | 4690 |
rs755008602 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136869112 | CACTGTGGTGGTGCA[C/T]GCCTGTAGTCCCAGC | 4690 |
rs755023227 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136932824 | AAGAAGTAGAAACAT[A/G]GGAACAGAATTGTAG | 4690 |
rs755089718 | in-del | -/TTTTAA | | | intron-variant | NCK1 | GRCh38.p7 | 3:136939859 | TTTTTTTTTTTTTTT[-/TTTTAA]AATAGAGACAGGGTC | 4690 |
rs755093574 | snp | A/G | | | intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136947977 | TCTGCTGTTGGAGCC[A/G]TGGGTGTTAAGAGAC | 4690 |
rs755120153 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136873525 | TTAATGCTGAAATGA[A/G]TTAAGACTTCGGGGG | 4690 |
rs755154985 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136911338 | TCCATACTCTTTTTC[A/G]TAATGGCTGTACTAA | 4690 |
rs755249438 | snp | C/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136926075 | GCATTTCTTTAATAG[C/G]TAATGATGAATACCT | 4690 |
rs755259911 | snp | C/T | | | intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136947231 | AGGGAAGAGTGATGA[C/T]ATCCATTTTCTGTTA | 4690 |
rs755280574 | snp | C/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136912805 | GAACTACTTGCGCTG[C/G]TGTGCTTGGCTAATT | 4690 |
rs755316604 | snp | C/T | | | intron-variant, upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136863521 | ATTCTTAAATAGGCA[C/T]CCCATTCACAACTTG | 4690 |
rs755356875 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136872969 | CAGGGGTAGAGCATT[C/T]GTGGAGAACCTCTGC | 4690 |
rs755359806 | in-del | -/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136936852 | GGGTTCTAAGAGTTG[-/T]TTTATATGTTCTGGA | 4690 |
rs755360228 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136894669 | AGACACTCAGGGCAG[A/G]AAAGGCAAACTCATT | 4690 |
rs755386281 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136908341 | TCATGTATGCCTGGT[G/T]TAAATACAAAGGAAT | 4690 |
rs755399795 | snp | C/G | | | intron-variant, upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136863842 | CGGGGTAGCTCAAAC[C/G]TGTAATCCCAGCACT | 4690 |
rs755407658 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136887775 | ATTTTGTTAAATCCT[C/T]ACAGCAACCCTGTAG | 4690 |
rs755411716 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136872102 | ACTTTGGAACTGGGT[A/G]ACAGGCAGAGGTTGG | 4690 |
rs755414302 | in-del | -/GGGAGAGAA | | | intron-variant | NCK1 | GRCh38.p7 | 3:136923623 | GGGTGGATGGGAGAG[-/GGGAGAGAA]AAGAGAAGGTATGGA | 4690 |
rs755422684 | snp | C/T | 3.29506e-05 | 0.00405884 | synonymous-codon, downstream-variant-500B | NCK1, LOC107986136 | GRCh38.p7 | 3:136945971 | ATTCAGCTCATCTAA[C/T]GATGAAGAACTTAAT | 4690 |
rs755523154 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136926566 | AGGCATGAGCCACCG[C/T]GCCCGGCCACTCTTT | 4690 |
rs755534657 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136919320 | CAAATTTTATTCACA[A/G]CAAACAGTGAAAATC | 4690 |
rs755560496 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136942297 | ATCAGATCAGATTCT[A/G]TCCCCTCCCCAGGGC | 4690 |
rs755613442 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136894477 | ATGATTTTGTTAGCC[A/G]GACAGTTTCTAGGTG | 4690 |
rs755666267 | in-del | -/TTGA | 1.74821e-05 | 0.00295647 | intron-variant, nc-transcript-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136946301 | TGAATCTTCGGTAAG[-/TTGA]TTTTCGGAGGTAAAT | 4690 |
rs755734721 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136892973 | ACGCCACCACCCTTA[C/T]CATTCATATGCTTTT | 4690 |
rs755746200 | snp | C/T | | | upstream-variant-2KB, intron-variant | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136861089 | CAATCTAGGTAGACA[C/T]ACAGGCAAACCATTT | 4690 |
rs755763292 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136888055 | GTTCAAGCTATTCTC[C/T]TGCCTCAGCCTCCCA | 4690 |
rs755770014 | in-del | -/A | | | upstream-variant-2KB, intron-variant | NCK1 | GRCh38.p7 | 3:136928862 | AATGGCCTCTTCTTT[-/A]AAAAAAAAAAAAAAA | 4690 |
rs755802739 | snp | C/T | | | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136951182 | TAAATTATCTCCAGC[C/T]GTAATGTCCTACCAT | 4690 |
rs755879963 | in-del | -/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136931971 | CTAAAAATGCAAACA[-/T]TAGCTGGGCGTGGTG | 4690 |
rs755912060 | snp | A/G | 1.6609e-05 | 0.0028817 | synonymous-codon, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136948294 | ACTAAAAGCACAAGG[A/G]AAAAACAAGCATTTT | 4690 |
rs756001377 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136913136 | TCTGTTGGTTTATTT[C/T]TTTTTCTTTCATATA | 4690 |
rs756072556 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136927582 | GCTGGAGTGCAGTGG[C/T]GCGATATCGGCTCAC | 4690 |
rs756103637 | snp | C/T | | | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136948895 | CTTGGAGAGTGTTAA[C/T]CTTTTCTGTGACTAA | 4690 |
rs756111647 | snp | A/C | 1.80807e-05 | 0.00300667 | intron-variant, nc-transcript-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136946323 | TCGGAGGTAAATACA[A/C]ATAGAGCTCTGGGTA | 4690 |
rs756112764 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136882264 | TTGCATTTCCATAAT[A/G]GCTAGTGATGATGAG | 4690 |
rs756116416 | snp | A/G | | | intron-variant, upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136863330 | TATGACAAACCAACT[A/G]TAACGATTTCTTCAG | 4690 |
rs756123065 | snp | A/G | 1.6483e-05 | 0.00287076 | missense, downstream-variant-500B | NCK1, LOC107986136 | GRCh38.p7 | 3:136945664 | TTGACCCAGGGGAAC[A/G]TCTCTATGACCTCAA | 4690 |
rs756143637 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136911028 | ATGTCTTTCTGTGCC[A/G]GCTTATTTAATTTAG | 4690 |
rs756148728 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136945369 | ATGGTGAACTGTCAT[A/G]TAATAACAAATTAAA | 4690 |
rs756169292 | in-del | -/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136894879 | TTTTGTTTTGTTTTG[-/T]TTTTTTTTTTGAGAT | 4690 |
rs756227489 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136897739 | ATTAATTATTTTCAC[A/G]TTAACATAGATGTTC | 4690 |
rs756228735 | in-del | -/TTTAA | | | intron-variant | NCK1 | GRCh38.p7 | 3:136939860 | TTTTTTTTTTTTTTT[-/TTTAA]AATAGAGACAGGGTC | 4690 |
rs756238885 | snp | A/C | | | upstream-variant-2KB, intron-variant | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136861316 | CCATCCTGGTGAAAC[A/C]CCGTCACTGCTAAAA | 4690 |
rs756285931 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136923046 | GTGGAATGATCTTAA[A/G]GATAGATTGTTAAAC | 4690 |
rs756336227 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136877474 | ATGTGTATAGAGCCA[C/T]GCTTAGAGGAAGAGT | 4690 |
rs756374791 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136910031 | CTATTCATCTTGCCA[A/G]TCTCTGTCTTTTGAT | 4690 |
rs756404140 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136924645 | TAATTTAATTTTAGT[A/G]TAATTGACTTGTTTG | 4690 |
rs756447971 | in-del | -/TTG | | | intron-variant | NCK1 | GRCh38.p7 | 3:136892195 | CCCAGCTGGATTTTG[-/TTG]TTGTTGTTGTTGTTG | 4690 |
rs756457784 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136871016 | AATTCTGCAATAAAG[A/G]TCTTTGTGTATAAGG | 4690 |
rs756471691 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136871940 | CTCTCCTGCCATGTG[G/T]AACTGTAAGCCCATT | 4690 |
rs756496706 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136940789 | AGCTCAAGTGATCCA[C/T]CCGCCTCGGCTTCCT | 4690 |
rs756526755 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136886500 | GTTTAGGGAATAATG[A/G]CAAGGAAAAAACGTC | 4690 |
rs756561956 | snp | C/T | | | intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136946895 | ATAAAACCATAAAAG[C/T]TGAAAAATAATATGG | 4690 |
rs756570972 | in-del | -/TT | | | intron-variant | NCK1 | GRCh38.p7 | 3:136867267 | GTCTCTCTCTCTCTT[-/TT]TCTTTCTTTCTTCTT | 4690 |
rs756573751 | in-del | -/GC | | | intron-variant | NCK1 | GRCh38.p7 | 3:136900792 | TACTGAATTTATTTA[-/GC]GCAGAACTAAGTTTT | 4690 |
rs756655669 | snp | C/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136938883 | CATAACTACTGCAAA[C/G]AATGAAAATCAACTG | 4690 |
rs756673635 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136931309 | TTTGATCTCCTTGAA[C/T]ATTTGCTTGGTGTTT | 4690 |
rs756738301 | snp | C/T | 1.64754e-05 | 0.00287009 | synonymous-codon, nc-transcript-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136945989 | TGAAGAACTTAATTT[C/T]GAGAAAGGAGATGTA | 4690 |
rs756768183 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136864853 | ACCTCTGCCTCCCGG[A/G]TTCAATCGATTCTTG | 4690 |
rs756782511 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136936745 | ATGATATTGAGGATC[C/T]TTTCATGTGCCTGTT | 4690 |
rs756799050 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136891457 | GGACACTTTGGTTGC[C/T]TCCACTTTTTGGCTG | 4690 |
rs756799423 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136906188 | GTGTGTTTTCTTTCA[A/G]TGTGAATGCTGTCAG | 4690 |
rs756804203 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136939034 | TTTTTCTTTTTAGAG[A/G]TGTTTTAGAAGCATT | 4690 |
rs756910902 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136918651 | ACACAAATTCACAAA[C/T]GTTCTTAAAACATGA | 4690 |
rs756996793 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136900398 | TGCTTAAGATTGTTT[G/T]GGTTGTTTGGGCTCC | 4690 |
rs757027820 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136881204 | TCATCTCTTCACTTA[C/T]ACTATTGGCCTCTTA | 4690 |
rs757037296 | in-del | -/TTT/TTTT | | | intron-variant | NCK1 | GRCh38.p7 | 3:136902184 | CTTCTTAACTCTTTG[-/TTT/TTTT]TTTTTTTTTTTTTTT | 4690 |
rs757047082 | in-del | -/TTTTTTAA | | | intron-variant | NCK1 | GRCh38.p7 | 3:136870045 | TTTTTTTTTTTTTTT[-/TTTTTTAA]AAGAATCATCCTGGC | 4690 |
rs757047629 | snp | A/G | 1.6486e-05 | 0.00287102 | synonymous-codon | NCK1 | GRCh38.p7 | 3:136928055 | TGTGGCCCAACAAGA[A/G]CAAGAGTTGGACATC | 4690 |
rs757071540 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136912998 | CTCATTTTCCTACTT[C/T]CTTTCTACATTGTTT | 4690 |
rs757077753 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136924414 | TCTTAAATAAATGAC[A/G]TAGAGTGGGGAAAGA | 4690 |
rs757100926 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136864133 | GTGTATTTATTTTTC[G/T]AGGCATTATCCTTTG | 4690 |
rs757122012 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136894299 | AGTTACTGGGAGTGA[C/T]GGTGAAGAGTCAATC | 4690 |
rs757122834 | snp | A/C | | | intron-variant | NCK1 | GRCh38.p7 | 3:136913823 | ACAGGCGCCCGCCAC[A/C]GCGCCCAACTAATTT | 4690 |
rs757156731 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136878923 | GCCTCTTCTCTTTGG[C/T]TTCCAGAATTCTGGC | 4690 |
rs757190677 | in-del | -/CTT | | | intron-variant | NCK1 | GRCh38.p7 | 3:136909848 | CCTTGTCTCTTACAC[-/CTT]CTTGTTTTATAGTCT | 4690 |
rs757251380 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136924915 | GGTCAGGAGCCCTTG[A/G]TTTGTTCATTTTTGA | 4690 |
rs757276739 | in-del | -/TTTTTAA | | | intron-variant | NCK1 | GRCh38.p7 | 3:136939858 | TTTTTTTTTTTTTTT[-/TTTTTAA]AATAGAGACAGGGTC | 4690 |
rs757277499 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136922950 | GTCTAGTTGAAGAAA[A/G]TGCTACTTACATAAT | 4690 |
rs757300764 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136926539 | CTCAGCCTCCTGAAG[C/T]GCTGGGATTACAGGC | 4690 |
rs757304667 | snp | A/T | 4.96011e-05 | 0.00497977 | missense, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136948328 | GTCCAACTAAAAGAG[A/T]CTGTCTACTGCATTG | 4690 |
rs757334043 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136909688 | GTATTGAAGTTTCCA[A/G]TGATTACTGTAGAAC | 4690 |
rs757355145 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136900614 | TAGTGTTTTGTAGTT[C/T]TTATAGCTATTGTAA | 4690 |
rs757359581 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136873248 | ACTTCTTGGATCAGC[A/G]TGACCTGGATGTGAG | 4690 |
rs757407166 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136908837 | TTCAGATTCAGTGGG[A/G]TATATACAGTATAGT | 4690 |
rs757458865 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136935906 | GATTTACCTATTCTG[G/T]ATAATTTATATAAAT | 4690 |
rs757481715 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136897250 | TGTGCCACCATGCTC[G/T]GCTAATTTTTTGTAT | 4690 |
rs757488040 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136889989 | GCCTGCCAGTCCTGC[A/G]CTGTGTGCCCGCACT | 4690 |
rs757531453 | snp | C/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136926949 | GATATGAGTTCTTCT[C/G]TAGCCTTAATAATGT | 4690 |
rs757532603 | snp | C/T | 1.6476e-05 | 0.00287014 | missense, downstream-variant-500B | NCK1, LOC107986136 | GRCh38.p7 | 3:136945684 | TATGACCTCAACATG[C/T]CCGCTTATGTGAAAT | 4690 |
rs757555135 | in-del | -/TCTT | | | intron-variant | NCK1 | GRCh38.p7 | 3:136886816 | TAGTTACATGATCAG[-/TCTT]TTTTTTTTTTTTTTT | 4690 |
rs757566786 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136914073 | GAAATAAAAATAAAA[A/G]GCCCTGGTCTTTTAA | 4690 |
rs757583152 | in-del | -/A | | | intron-variant | NCK1 | GRCh38.p7 | 3:136944784 | GGTAAAGTAGAGCAT[-/A]AAATCACACGCTAAG | 4690 |
rs757583855 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136930954 | ATTAGGTGAACAAAT[G/T]TCTTCATCCTCAACT | 4690 |
rs757593808 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136916047 | AACACTTTTAAACAA[C/T]CAGGTCTCATGAGAA | 4690 |
rs757620427 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136885395 | CTCTGTCACCTAGGC[G/T]GGAGTACAGTGGCCT | 4690 |
rs757648400 | snp | A/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136897469 | ATTTGCATTTCCTTA[A/T]TGATTAGTGATGTTG | 4690 |
rs757704723 | in-del | -/TT | | | intron-variant | NCK1 | GRCh38.p7 | 3:136943394 | GACATGAGTGTTGGG[-/TT]TTTGAGGTACTGATG | 4690 |
rs757729636 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136884651 | TCATCATGTTGGCCA[A/G]GCTGGTCTTGAGGTG | 4690 |
rs757764919 | snp | C/G | | | upstream-variant-2KB, intron-variant | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136860594 | TGGTAGCCTAAGACT[C/G]CTTCTACTCATGCCA | 4690 |
rs757791563 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136881515 | AGCCACCACGCCCAG[C/T]TTCTATTTTTTATTG | 4690 |
rs757817586 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136943884 | TCAAAGAAGAAGAAA[A/G]CATAATGGAGAGAGT | 4690 |
rs757837731 | snp | A/C | 1.7257e-05 | 0.00293738 | missense, nc-transcript-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136946291 | TTCGTGATAGTGAAT[A/C]TTCGGTAAGTTGATT | 4690 |
rs757874778 | snp | A/C | | | intron-variant | NCK1 | GRCh38.p7 | 3:136945267 | ATGAAAGAAATCTAT[A/C]TTTACATTTAAGAGG | 4690 |
rs758030647 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136930730 | GTATGTAATATAAAC[C/T]AAATGATTGGTGATA | 4690 |
rs758035664 | snp | A/G | 1.64735e-05 | 0.00286993 | synonymous-codon, nc-transcript-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136946136 | AACTTCAGGTTTGGA[A/G]CCATCACCTCCACAG | 4690 |
rs758056781 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136884409 | TAAGAAAGTATAGCT[G/T]AATGAGAATGATAGA | 4690 |
rs758059769 | snp | A/G | | | upstream-variant-2KB, intron-variant | NCK1 | GRCh38.p7 | 3:136929316 | TATTTAATGTTTTTA[A/G]CCATTGTAAAACTGC | 4690 |
rs758078557 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136867811 | CATACTACTTCTCAT[C/T]TCTTGTAATTTTGCC | 4690 |
rs758088827 | snp | A/T | 1.64762e-05 | 0.00287016 | synonymous-codon, nc-transcript-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136946004 | CGAGAAAGGAGATGT[A/T]ATGGATGTTATTGAA | 4690 |
rs758090996 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136915564 | GATAAACTTTAATAG[G/T]GCTGTATTAGTCTGC | 4690 |
rs758243920 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136877613 | ATAGCCCAGCAAGGT[A/G]ACAGTAAAGGATACT | 4690 |
rs758244696 | snp | A/G | | | upstream-variant-2KB, nc-transcript-variant | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136861747 | AAGCACATGTCTTAC[A/G]TTTCTCCCAGGTCCC | 4690 |
rs758266779 | in-del | -/TATTTTT | | | intron-variant | NCK1 | GRCh38.p7 | 3:136878708 | GTATCTCAATAAAGC[-/TATTTTT]TTTTAAGAAAGGTTG | 4690 |
rs758294882 | snp | C/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136891197 | GGAGTGCAGTGGCAC[C/G]ATCTCGGCTCATTTG | 4690 |
rs758298707 | snp | C/T | 1.64841e-05 | 0.00287085 | synonymous-codon | NCK1 | GRCh38.p7 | 3:136928067 | AGAACAAGAGTTGGA[C/T]ATCAAGAAGAATGAG | 4690 |
rs758353596 | snp | C/G | 1.74099e-05 | 0.00295037 | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136948495 | GTAGCTGTAATTTGT[C/G]ATGTAATTGAAGACT | 4690 |
rs758372506 | in-del | -/GACT | | | intron-variant | NCK1 | GRCh38.p7 | 3:136878794 | GTACCCCAGCAAGAA[-/GACT]GACTATTGTTTCTGA | 4690 |
rs758448764 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136921134 | ATTAAGTACATTCAC[A/G]TTGTTGTACAACCAT | 4690 |
rs758471441 | snp | G/T | | | intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136947317 | CTTTGGGGGTTGATA[G/T]AGACTGTAACAACAA | 4690 |
rs758491058 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136887035 | TATTAGTAGAGACGG[A/G]GTTTCATTATGTTGG | 4690 |
rs758519894 | in-del | -/TG | | | intron-variant | NCK1 | GRCh38.p7 | 3:136901327 | GAGAATTTTTATCTC[-/TG]TGTTCATTAGGGATA | 4690 |
rs758567141 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136904307 | ACAGGAATGTATCAC[C/T]GTGCCCAGCTAATTT | 4690 |
rs758588289 | snp | A/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136902050 | ATTTTCGGTATGTTG[A/T]ATTAGATTTTCATTT | 4690 |
rs758599446 | snp | C/T | | | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136948574 | AATCTATATGAGAAT[C/T]GACAATAAGTATTTT | 4690 |
rs758650793 | snp | A/G | | | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136950712 | TCTGTATCGTGACAC[A/G]CTACTCTGTGTATGC | 4690 |
rs758654513 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136934251 | TTTGTTACATAGGTA[A/G]ATACATGTCATGGGG | 4690 |
rs758708050 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136891935 | ACTGTATCACTCAGG[C/T]TGGAATAGAGTGACA | 4690 |
rs758751585 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136909615 | CAGCTAATTGGTTTA[C/T]AGTATTAAGTCCTCT | 4690 |
rs758758837 | in-del | -/TTTTTTA | | | intron-variant | NCK1 | GRCh38.p7 | 3:136870044 | TTTTTTTTTTTTTTT[-/TTTTTTA]TTTTTTAAAAGAATC | 4690 |
rs758777810 | snp | A/C | 1.64749e-05 | 0.00287005 | synonymous-codon, downstream-variant-500B | NCK1, LOC107986136 | GRCh38.p7 | 3:136945836 | CCCTTCAAACTATGT[A/C]ACTGAAGAAGGTGAC | 4690 |
rs758778972 | snp | A/T | | | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136949830 | AAAATTGAAGTTGTG[A/T]AACTTGTGAATTTTT | 4690 |
rs758818693 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136882512 | CTTACTTGGCAGCAT[A/G]ATACAATGAAAGTTT | 4690 |
rs758820766 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136897198 | GGTTCAAGTGATTCT[C/T]CTGTCTCAGCCTCCC | 4690 |
rs758828933 | snp | A/C | | | intron-variant | NCK1 | GRCh38.p7 | 3:136922057 | CAAAGTGCTGGGATT[A/C]CAGGCGTGAGCCACC | 4690 |
rs758830972 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136919758 | GTACTGTTGGCTGTG[C/T]ATATAGGTCATGATA | 4690 |
rs758881659 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136916370 | TATTTCAGGTTAACA[C/T]AGGTTTTATGTATGT | 4690 |
rs758900228 | snp | A/G | 1.66062e-05 | 0.00288146 | synonymous-codon, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136948429 | ACAAGGAGAAAAATT[A/G]TATCTTGTCAAGCAT | 4690 |
rs758945424 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136907337 | TCTGTTGGGTTCCCG[A/G]GCATGACAAAGTCTG | 4690 |
rs758973674 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136873898 | AAGTCCATTAAACCT[C/T]TTTCTTTTGTAAATT | 4690 |
rs759012420 | in-del | -/GTT | | | intron-variant | NCK1 | GRCh38.p7 | 3:136939266 | ATTTATTGGCATACA[-/GTT]GTTCATAGTATTTGT | 4690 |
rs759027281 | snp | A/C | | | intron-variant | NCK1 | GRCh38.p7 | 3:136918104 | TTGTTTATGTGGAGC[A/C]TTCTGGGAGCTTAGA | 4690 |
rs759049110 | snp | G/T | | | utr-variant-5-prime, intron-variant | NCK1 | GRCh38.p7 | 3:136930517 | ACTGAGAATTATCCT[G/T]AGCTGTGTTAACAAA | 4690 |
rs759063912 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136884257 | GTAAGGAAACCAGCA[G/T]TTTCAAGAAAGAGGG | 4690 |
rs759086494 | snp | A/G | | | upstream-variant-2KB, intron-variant | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136860294 | CTTAGAATAAACTCA[A/G]AATTCACCGCCATTA | 4690 |
rs759090640 | snp | A/G | | | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136949564 | ATGGATAAGAGGCCA[A/G]TCTGCTTCTGTAGGC | 4690 |
rs759093663 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136898323 | AATCACTTGAACCCG[G/T]GAGGCGGAGGTTCCA | 4690 |
rs759136205 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136872475 | GGAGGCAGAGCATAA[G/T]TTTGGAAAATTTGCA | 4690 |
rs759146544 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136896967 | TAGTTCTGTTTTCAA[C/T]TTTTTGAGAAATTTT | 4690 |
rs759209647 | snp | C/G | 1.66615e-05 | 0.00288626 | missense, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136948287 | CAGTATCACTAAAAG[C/G]ACAAGGGAAAAACAA | 4690 |
rs759241295 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136874697 | TTTTTTTCCCTTTCC[A/G]TGAATCATATAGTGT | 4690 |
rs759259254 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136870189 | TCTACTAATAATACA[A/G]AATTTAGCTGGGCGT | 4690 |
rs759290581 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136917753 | TCCCACAGCACTTAC[A/G]AGTTAGAGGTGGTTT | 4690 |
rs759323484 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136909451 | GATACAAAATGAAAC[A/G]AGGCTGTTTCCTCTA | 4690 |
rs759332467 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136871525 | CACTCAAATCCAGAT[G/T]TGGAACATTTTTAGT | 4690 |
rs759358790 | snp | A/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136905708 | TGGCTCAGTGCAGCC[A/T]CGACCTCCCTGGGCT | 4690 |
rs759399063 | in-del | -/TTT | | | intron-variant | NCK1 | GRCh38.p7 | 3:136899037 | GTAAAGCTGTGCTTC[-/TTT]CAGCCAAACATTTCT | 4690 |
rs759403238 | in-del | -/CA | | | intron-variant | NCK1 | GRCh38.p7 | 3:136864486 | AGCAAGATTCCGTCA[-/CA]CACACACACAAAAAA | 4690 |
rs759422849 | snp | A/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136921945 | CGCACCACCACGCCC[A/T]GCTAATTTTATTGTA | 4690 |
rs759443661 | snp | C/G | 3.30169e-05 | 0.00406293 | missense, downstream-variant-500B | NCK1, LOC107986136 | GRCh38.p7 | 3:136945648 | GCTGATGATAGTTTT[C/G]TTGACCCAGGGGAAC | 4690 |
rs759457674 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136885122 | TTTAGAGGTATACAC[C/T]GAAATATTTACAGAC | 4690 |
rs759465760 | snp | A/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136880588 | CTTGATGTTGCCACT[A/T]GATATCTCATGGATC | 4690 |
rs759521512 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136931702 | AAAACTAATACTAAC[C/T]CTAGCAAATCTTACA | 4690 |
rs759545424 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136882128 | GCAGCTGCACCATTT[C/T]ACATTACCACCAACC | 4690 |
rs759576877 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136890331 | GCCCACCCGGAACTC[C/T]AGCTGGCCCGCCAGC | 4690 |
rs759650413 | snp | A/C | | | intron-variant | NCK1 | GRCh38.p7 | 3:136928455 | CAAGGCAGAGTGATA[A/C]CAATGAGTAGAACTA | 4690 |
rs759652592 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136866435 | ACCTCAGCCTCCCTA[A/G]TAGCTGGGACTACAG | 4690 |
rs759668460 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136908510 | GTGGTTCTGAATTCA[G/T]GTCCTTATAAGATCA | 4690 |
rs759689178 | in-del | -/TTT | | | intron-variant | NCK1 | GRCh38.p7 | 3:136886819 | TTACATGATCAGTCT[-/TTT]TTTTTTTTTTTTTTC | 4690 |
rs759702549 | snp | C/T | 1.65751e-05 | 0.00287876 | missense, nc-transcript-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136946240 | ATCAAGCAGAAATGG[C/T]ATTAAATGAAAGAGG | 4690 |
rs759721832 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136905972 | ATTATTGTGGTCTTT[G/T]GGCGGTGTCATATTT | 4690 |
rs759828280 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136922636 | TTACAACTCTGAAAT[A/G]CTATTTCTCCCCTAT | 4690 |
rs759858645 | snp | C/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136873768 | AGTCTTTTGAGAACT[C/G]ATGATTTTTAAAAAC | 4690 |
rs759860758 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136890727 | TTAAAAAGTTATTGT[G/T]GTAAGATATGTGTAA | 4690 |
rs759875342 | snp | C/T | 1.64738e-05 | 0.00286995 | missense, nc-transcript-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136946105 | ACTATGTTACCGTTA[C/T]GCAGAATAATCCATT | 4690 |
rs759907208 | in-del | -/CT | | | intron-variant | NCK1 | GRCh38.p7 | 3:136869020 | AGGCATGCGGAGCCC[-/CT]GAGTCCAGGAGTTTG | 4690 |
rs759915743 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136889330 | CTGTTAAGGTGGCGC[A/G]TCTGGAGTTTGCTCC | 4690 |
rs760010228 | in-del | -/AGAT | | | intron-variant | NCK1 | GRCh38.p7 | 3:136926207 | TTTTCTAACTGCTTA[-/AGAT]AGATACTCAGTTCAT | 4690 |
rs760024244 | snp | A/G | | | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136950060 | TGAGGGTAATTATTA[A/G]TAGTTAAGTTTTTAA | 4690 |
rs760131178 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136935532 | CAGACTGGTTGATAT[A/G]GATGATGGGTCGACT | 4690 |
rs760172881 | snp | C/T | 1.64808e-05 | 0.00287057 | synonymous-codon | NCK1 | GRCh38.p7 | 3:136928160 | AGGTTTTGTGCCTTC[C/T]AACTATGTGGAAAGG | 4690 |
rs760229393 | snp | A/G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136922496 | CAGGTAAGGAACTTG[A/G/T]TGGAGTTGGAGTCAT | 4690 |
rs760245467 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136873654 | TTTCATCTTGAATTG[C/T]AGCTCCCACAATTCC | 4690 |
rs760279843 | in-del | -/TTTTT | | | intron-variant | NCK1 | GRCh38.p7 | 3:136939840 | AAATTTATTGAGGCC[-/TTTTT]TTTTTTTTTTTTTTT | 4690 |
rs760332786 | in-del | -/TTTTTTT | | | intron-variant | NCK1 | GRCh38.p7 | 3:136870029 | GATGTTTCTCAAAAG[-/TTTTTTT]TTTTTTTTTTTTTTT | 4690 |
rs760370025 | in-del | -/TTATTA | | | intron-variant | NCK1 | GRCh38.p7 | 3:136926266 | ATTTTATTTTAAATT[-/TTATTA]TTATTATTATTATTA | 4690 |
rs760404440 | in-del | -/AT | | | intron-variant | NCK1 | GRCh38.p7 | 3:136908836 | TTCAGATTCAGTGGG[-/AT]ATATATACAGTATAG | 4690 |
rs760422921 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136868971 | GGCCGGGCGCGGTGG[C/T]TCACGTCTGTAATCC | 4690 |
rs760428778 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136884982 | CACCTCGGCCTCCCA[A/G]AGTGTTGAGATTATA | 4690 |
rs760460314 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136921940 | AGGCACGCACCACCA[C/T]GCCCAGCTAATTTTA | 4690 |
rs760478113 | snp | A/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136883909 | GATAATGATTTACAA[A/T]TATAATTAATAGATT | 4690 |
rs760556996 | snp | A/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136895289 | TGATGATAGATGTGT[A/T]TAAGGCTTTGGTATG | 4690 |
rs760596684 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136943470 | AATTCCAGAAAGGTC[G/T]TAGAGCTGCAAAGAG | 4690 |
rs760599913 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136896752 | GCAGTCCTCCTGCCT[C/T]GGCCTCCCAGAGTGC | 4690 |
rs760631298 | snp | A/T | 1.6476e-05 | 0.00287014 | missense, downstream-variant-500B | NCK1, LOC107986136 | GRCh38.p7 | 3:136945756 | AAGGGGACAAAGGTG[A/T]TCGTCATGGAGAAAT | 4690 |
rs760653866 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136944432 | CGGGAAAGACAACTT[C/T]TAAAAGAGTGGTATA | 4690 |
rs760690240 | snp | A/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136893882 | ATTCTAGATTTCCTT[A/T]ATGCTGGGCCAGCAT | 4690 |
rs760794568 | in-del | -/TAGCTGGGAT | | | intron-variant | NCK1 | GRCh38.p7 | 3:136884569 | CCTCAGCCTCCAGAG[-/TAGCTGGGAT]TAGAGGCGTGTGGCA | 4690 |
rs760947343 | snp | A/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136938310 | AGTACAAATGATCCT[A/T]ATTTTTCACAGATTC | 4690 |
rs760954181 | in-del | -/TTTT | | | intron-variant | NCK1 | GRCh38.p7 | 3:136939841 | AATTTATTGAGGCCT[-/TTTT]TTTTTTTTTTTTTTT | 4690 |
rs761001241 | snp | A/C | | | intron-variant | NCK1 | GRCh38.p7 | 3:136902575 | TTTAAAAATTTGTTG[A/C]CACTTGTTTTGTGTC | 4690 |
rs761054574 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136901613 | ATCTTGGTAGATTGT[A/G]TATGTCTATGTCTAG | 4690 |
rs761072186 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136934003 | CTGAGCCACCTTGCC[C/T]GGCCAAGTTTAAGTA | 4690 |
rs761107570 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136900166 | AAACCAGACATTGGC[A/G]CTCTCCCTTCACTCT | 4690 |
rs761121478 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136935152 | GTGATCTGCCTGCCT[C/T]GGCCTCCCAAAATGC | 4690 |
rs761123243 | snp | C/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136865985 | TTGAACTACTCACTA[C/G]CCTTTAATTGGGTTT | 4690 |
rs761148513 | snp | A/G | 1.67013e-05 | 0.0028897 | missense, nc-transcript-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136946258 | TAAATGAAAGAGGAC[A/G]TGAAGGGGATTTCCT | 4690 |
rs761241226 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136921808 | GTTTTGTTTTGAGAC[A/G]GAGTCTGTCTCTGTC | 4690 |
rs761318409 | snp | A/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136867586 | CCTTATTATTTTAGT[A/T]TTCCCTTGGTTTTTA | 4690 |
rs761323341 | in-del | -/CTGA | | | intron-variant | NCK1 | GRCh38.p7 | 3:136876911 | TTATTTAAAATGTTG[-/CTGA]CTGTTGCCAAACTGC | 4690 |
rs761345262 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136920379 | AAAAGTGCTGTGCAT[A/G]GCACAATTCATTCAC | 4690 |
rs761366485 | snp | A/C | | | intron-variant | NCK1 | GRCh38.p7 | 3:136935037 | CACCCAAGTAGCTGG[A/C]ATTACAGGTGTGCGC | 4690 |
rs761367212 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136895856 | AGGTATGAGCCACCA[G/T]GCCCAGTCTGTATGT | 4690 |
rs761368381 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136872565 | CAGAAATTTGCATAG[A/G]TAATGAGGAGCTGAA | 4690 |
rs761369991 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136932237 | GTTGATAGTTAATGC[A/G]TTTGCAGACTGGGAG | 4690 |
rs761373708 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136906850 | GAGTGCTTAGGTGCC[A/G]ACAGTGGTGGTCTAT | 4690 |
rs761379673 | snp | C/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136875896 | aaaattgaccacata[C/G]ttggaagtaaagctc | 4690 |
rs761404166 | snp | C/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136887374 | GAAAAGTTACTGTTG[C/G]CTTTTCTCCTGATAA | 4690 |
rs761419722 | in-del | -/A | | | intron-variant | NCK1 | GRCh38.p7 | 3:136925908 | TTATGAGAAACTGTC[-/A]GACAATTTTGCGGAG | 4690 |
rs761422341 | snp | C/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136871840 | GATGGTTTTAAAAAC[C/G]GGAGTTTCCCTGCAC | 4690 |
rs761527835 | snp | A/G | 4.59834e-05 | 0.00479474 | intron-variant | NCK1 | GRCh38.p7 | 3:136928266 | GCAACTTTGTTTTAA[A/G]TGAAACCTGCAACTT | 4690 |
rs761550449 | snp | A/G | | | intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136947793 | TTAATTCTCATTTGT[A/G]TATTCTTCATTTTTG | 4690 |
rs761569316 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136882158 | CGTGCATAAGAGTTC[C/T]AATATCATTACATTT | 4690 |
rs761581267 | snp | A/G | 1.64963e-05 | 0.00287192 | missense | NCK1 | GRCh38.p7 | 3:136928182 | GTGGAAAGGAAAAAC[A/G]GTGCTCGGAAAGCAT | 4690 |
rs761596292 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136901422 | GGTGTTAAGGTAATG[G/T]TGGCCTTGTAGAATG | 4690 |
rs761623102 | snp | C/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136943404 | GTTGGGTTTGAGGTA[C/G]TGATGGCACAATCTG | 4690 |
rs761706096 | snp | A/C | | | upstream-variant-2KB, intron-variant | NCK1 | GRCh38.p7 | 3:136928616 | ACCTTATGTTTTGAA[A/C]TTCACTTAAAACCCT | 4690 |
rs761726043 | in-del | -/A | | | intron-variant | NCK1 | GRCh38.p7 | 3:136870689 | TAGCTATAGTCTTTA[-/A]AAAAAAAAAAAAAAA | 4690 |
rs761799627 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136942420 | GGGCCGCTGAAGTCT[A/G]TTCCATTTGCTTAGT | 4690 |
rs761884120 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136924422 | AAATGACATAGAGTG[A/G]GGAAAGAGAACAGTG | 4690 |
rs761937235 | in-del | -/T | 0.165289 | 0.235211 | intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136948241 | TTTACTATATGTATC[-/T]TTTTTTTTCTCTTTT | 4690 |
rs761955307 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136892049 | GCATGCCACTGCTTG[G/T]CTCATTTATTTATTT | 4690 |
rs762003763 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136917685 | GTCAAGTTACCTAGG[C/T]CAGTTCTCTCTCCTT | 4690 |
rs762053185 | snp | A/G | | | upstream-variant-2KB, intron-variant | NCK1 | GRCh38.p7 | 3:136928843 | GAAATATGCATGGGC[A/G]AGGAATGGCCTCTTC | 4690 |
rs762063298 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136904174 | AAAAATTATTTTTTT[A/G]GACAGTCTCGCTCTG | 4690 |
rs762142393 | snp | A/G | | | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136949751 | TAATGCTGCCTAAGC[A/G]TATGGATGTTTTAAT | 4690 |
rs762214579 | snp | A/G | | | intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136946398 | CCTAAAGTTAACCAG[A/G]TAACAAGCTGGGACG | 4690 |
rs762265694 | in-del | -/C | | | intron-variant | NCK1 | GRCh38.p7 | 3:136864132 | TGTGTATTTATTTTT[-/C]TAGGCATTATCCTTT | 4690 |
rs762285377 | snp | A/T | 1.65255e-05 | 0.00287445 | missense, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136948392 | TAGAACATTACAAAA[A/T]GGCACCAATTTTTAC | 4690 |
rs762442083 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136878180 | TTGGGAGGCCAAGAC[A/G]GGCAGATCACTTGAG | 4690 |
rs762456880 | snp | C/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136917890 | CTTTTTGGCATCACC[C/G]TTTGTGAGGAGAATA | 4690 |
rs762500385 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136944896 | TTTCTTTCAACACAT[A/G]TGTGTTAAGCATTTA | 4690 |
rs762533477 | snp | C/T | 4.94336e-05 | 0.00497135 | missense, downstream-variant-500B | NCK1, LOC107986136 | GRCh38.p7 | 3:136945789 | AGTGATGGGTGGTGG[C/T]GTGGTAGCTACAATG | 4690 |
rs762575890 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136899589 | TCCAGAAAAATTTTC[C/T]TCTGTTGTACCGCAG | 4690 |
rs762585989 | snp | G/T | 0.000185271 | 0.00962295 | utr-variant-5-prime, intron-variant | NCK1 | GRCh38.p7 | 3:136930546 | AACTGACAGAACACA[G/T]AATTTTTACTCAAAA | 4690 |
rs762627225 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136898722 | CGAGATAAAACTGAA[C/T]GGTTAACGTTAAGGT | 4690 |
rs762646033 | snp | A/G | | | intron-variant, upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136862725 | AAAGTCCTTTTGCCA[A/G]CTGTGGCGTAATCCG | 4690 |
rs762687588 | snp | C/G | 4.97269e-05 | 0.00498608 | missense, downstream-variant-500B | NCK1, LOC107986136 | GRCh38.p7 | 3:136945633 | GATTCTGCATCTCCT[C/G]CTGATGATAGTTTTG | 4690 |
rs762707873 | snp | A/C | | | missense, nc-transcript-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136946150 | AACCATCACCTCCAC[A/C]GTGTGATTACATTAG | 4690 |
rs762732613 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136912073 | TGTGCATCTCCTTGT[A/G]TTCATGCTACTTGGA | 4690 |
rs762766780 | snp | C/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136906607 | GTGGCACAGGTGAGC[C/G]AGGCAGGTTGACAGG | 4690 |
rs762785420 | snp | A/C/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136894160 | TATGAGAAGCCCATA[A/C/G]TGACCAAGTGGTGGT | 4690 |
rs762817643 | snp | C/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136906035 | CTGGTATCTGTGCCT[C/G]TGGTGTAACAGTTGC | 4690 |
rs762878805 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136905964 | GCCCGTGAATTATTG[C/T]GGTCTTTTGGCGGTG | 4690 |
rs762897283 | snp | A/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136917717 | GGTAAAGGTCACGTT[A/T]CTTTATTTATAACAG | 4690 |
rs762950267 | in-del | -/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136934909 | AAGATTGTGGTGAAC[-/T]TGTGAGGTCAGGAAG | 4690 |
rs763191799 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136877924 | AAGCAACTCAGATGT[C/T]CATCAGCTGATAAAT | 4690 |
rs763240523 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136910756 | AATTAACATATCCAT[A/G]ACCTTGTTTACATAT | 4690 |
rs763241416 | snp | A/T | 1.64746e-05 | 0.00287002 | missense, nc-transcript-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136946081 | GTATGGTTGGTCTAG[A/T]ACCAAAAAACTATGT | 4690 |
rs763254344 | in-del | -/GCCCGTGCGAGCCTGGGAGGTC | | | intron-variant, upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136862646 | AGAGCCCGGGCGGCC[-/GCCCGTGCGAGCCTGGGAGGTC]GAGTGTGCGGCGCGC | 4690 |
rs763267267 | snp | C/T | | | upstream-variant-2KB, intron-variant | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136860414 | TACAGCATAAATAGG[C/T]AAATTTGTGCTTGAC | 4690 |
rs763295518 | in-del | -/ATGTAAGGTTGAGG | 1.92578e-05 | 0.00310299 | intron-variant | NCK1 | GRCh38.p7 | 3:136928240 | AGGTAAGATATTTTT[-/ATGTAAGGTTGAGG]TAAAAGAAAAGCAAC | 4690 |
rs763324425 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136876855 | TCCTGCCTAAGATCA[A/G]TTTCTAAATGTAAAA | 4690 |
rs763324953 | in-del | -/AC | | | upstream-variant-2KB, intron-variant | NCK1 | GRCh38.p7 | 3:136929019 | TTTCTCCTTGTGCAG[-/AC]AGTTTGGGAGCAATA | 4690 |
rs763325637 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136915107 | TTTGAGCCAAATAAG[C/T]CTTTTTTCTTTATAG | 4690 |
rs763450332 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136936942 | CTTTTCACTTCTTGA[C/T]AGTGTGTTATACACA | 4690 |
rs763455231 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136880369 | GTTATTAGGGTGGAC[C/T]CTAATCCACCATGAC | 4690 |
rs763459609 | in-del | -/CTGCTG | 3.41192e-05 | 0.00413019 | cds-indel, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136948473 | GCTGACCAGAAGTGA[-/CTGCTG]TGTAGCTGTAATTTG | 4690 |
rs763481977 | snp | G/T | 1.64787e-05 | 0.00287038 | synonymous-codon | NCK1 | GRCh38.p7 | 3:136928148 | CATGAATAAAACAGG[G/T]TTTGTGCCTTCTAAC | 4690 |
rs763503439 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136937892 | ATCTGTGGATACTTT[C/T]TCCCCTCCCTAATTG | 4690 |
rs763545226 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136907493 | GCCTGCAGCACTTGA[A/G]GGCTTCTCCCATGGC | 4690 |
rs763561470 | in-del | -/TTTCTTTCTTTCTTTG | | | intron-variant | NCK1 | GRCh38.p7 | 3:136867105 | TTCTTTCTTTCTTTC[-/TTTCTTTCTTTCTTTG]TTTCTTTCTTTCCTT | 4690 |
rs763641161 | in-del | -/AAAC | | | intron-variant | NCK1 | GRCh38.p7 | 3:136942488 | TGGAGCCAAAAGAAA[-/AAAC]AAACAAACAAAAGAA | 4690 |
rs763662544 | snp | A/C | | | intron-variant | NCK1 | GRCh38.p7 | 3:136917925 | CAGAATCCATAGTCT[A/C]TATCTTACAACCAGT | 4690 |
rs763667689 | snp | A/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136932217 | TTTTTGCTGAGTCTT[A/T]GGAAGTTGATAGTTA | 4690 |
rs763704002 | snp | C/T | 4.94409e-05 | 0.00497172 | synonymous-codon | NCK1 | GRCh38.p7 | 3:136928163 | TTTTGTGCCTTCTAA[C/T]TATGTGGAAAGGAAA | 4690 |
rs763734085 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136923020 | TAGTAAAGGAAGTCT[C/T]ATGTGCTGCTGTGGA | 4690 |
rs763748888 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136870635 | CAGTAATTCTGCTGC[C/T]CAAGGAAATCAGTTA | 4690 |
rs763778861 | in-del | -/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136876567 | ATATAAATCTAAAGG[-/T]TTTTTTGTTTTTTTT | 4690 |
rs763787178 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136919721 | TCAGTCATATTGTGT[A/G]TAATTTGTAAACTGA | 4690 |
rs763798996 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136891096 | AGGCTGGTACTGTTC[C/T]GTTGAATCTATATTT | 4690 |
rs763801972 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136885230 | TGGCCATGAGTTGAT[G/T]ATTTTAGCTACATGA | 4690 |
rs763803894 | snp | C/G | | | intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136946357 | TAAAAAAAAGAGAGA[C/G]AGAAATGGAGAGGTT | 4690 |
rs763822355 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136898788 | GTAACTAGAAAAGAA[C/T]GGCATGTGATGTGGA | 4690 |
rs763900564 | snp | C/T | 1.64991e-05 | 0.00287215 | synonymous-codon | NCK1 | GRCh38.p7 | 3:136928028 | AGTGGTGGTAGTAGC[C/T]AAATTTGATTATGTG | 4690 |
rs763952081 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136936353 | GCTGGCTGAATAACT[A/G]TTATATGTATATATC | 4690 |
rs763953586 | snp | C/T | 1.66696e-05 | 0.00288696 | synonymous-codon, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136948438 | AAAATTATATCTTGT[C/T]AAGCATTTATCATGA | 4690 |
rs763987531 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136906656 | GTGGGCATGGTGTGG[A/G]TGATGGCAGTAGCAG | 4690 |
rs764040380 | snp | C/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136906083 | ATTGTCTTTCATAGG[C/G]GAGGACATTTTCCTG | 4690 |
rs764042177 | snp | C/T | 6.59174e-05 | 0.00574059 | synonymous-codon, downstream-variant-500B | NCK1, LOC107986136 | GRCh38.p7 | 3:136945758 | GGGGACAAAGGTGAT[C/T]GTCATGGAGAAATGC | 4690 |
rs764043462 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136926099 | AATACCTTTTCATCT[G/T]CTTATTTGCCATCTG | 4690 |
rs764087868 | in-del | -/TGGCCCTAA | | | upstream-variant-2KB, intron-variant | NCK1 | GRCh38.p7 | 3:136928785 | TAGGGCCTGAGACAG[-/TGGCCCTAA]TGGAGCCCACTTCAC | 4690 |
rs764183035 | in-del | -/CTTAT | | | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136950097 | TAAAAATCATGTATG[-/CTTAT]CTTTGCTGTAAAATC | 4690 |
rs764224331 | in-del | -/CCTTT | | | intron-variant | NCK1 | GRCh38.p7 | 3:136944111 | GAAAAGGAAAAACAA[-/CCTTT]TTTTTTTTTTTTTTT | 4690 |
rs764250587 | snp | C/G/T | 4.9442e-05 | 0.00497182 | synonymous-codon, downstream-variant-500B | NCK1, LOC107986136 | GRCh38.p7 | 3:136945668 | CCCAGGGGAACGTCT[C/G/T]TATGACCTCAACATG | 4690 |
rs764293613 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136889655 | CAGGGCACTGATTGG[C/T]GCGTTTACAATCCCT | 4690 |
rs764299423 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136926686 | AAATTATTTACTTCT[A/G]AGTATTTTCAAAATT | 4690 |
rs764304916 | snp | A/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136935785 | ATTGAGTACATTAAC[A/T]GTGTTGTGCAGCCAT | 4690 |
rs764322111 | snp | C/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136868553 | GGCTGATCTCCAACT[C/G]CTAACTTCAGTTAAT | 4690 |
rs764327999 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136903934 | TGTTTGGTCTATCAG[G/T]GGTTTTTATATTTTT | 4690 |
rs764380830 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136902788 | TCCCCCTTTGCTGAT[G/T]ATATGATCTTATATT | 4690 |
rs764382133 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136870876 | TTAATCAGCATTAAG[C/T]TTGGCTACTAGTATC | 4690 |
rs764432975 | snp | C/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136897246 | GGTATGTGCCACCAT[C/G]CTCGGCTAATTTTTT | 4690 |
rs764454369 | in-del | -/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136916750 | TAGAAAATAAAACAG[-/T]TTGTTTAGTTCAAAA | 4690 |
rs764463773 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136876947 | TTTAGAAAAGACATT[C/T]CAATTTACACCTTTA | 4690 |
rs764486498 | snp | A/G | | | upstream-variant-2KB, intron-variant | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136860495 | AAAGGAATACCCAAA[A/G]CTGGATAATTTAGAA | 4690 |
rs764531380 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136909634 | ATTAAGTCCTCTTTC[C/T]TCTTTTGTCTGATTA | 4690 |
rs764609239 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136924404 | GAAGCCAGCTTCTTA[A/G]ATAAATGACATAGAG | 4690 |
rs764643858 | snp | C/T | 0.000135646 | 0.00823436 | synonymous-codon, nc-transcript-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136946277 | AGGGGATTTCCTCAT[C/T]CGTGATAGTGAATCT | 4690 |
rs764669731 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136873953 | AAGTGGACTAATACA[A/G]TAACCATATAGCTTG | 4690 |
rs764712358 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136884262 | GAAACCAGCAGTTTC[A/G]AGAAAGAGGGATGAT | 4690 |
rs764743140 | snp | C/T | | | upstream-variant-2KB, intron-variant | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136860343 | AACAGAATGTAGACA[C/T]AGAGTAGCTGTTGCC | 4690 |
rs764746767 | in-del | -/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136914670 | TTTGTGTTTCAGATC[-/T]TTTTTTGCGCCCTAA | 4690 |
rs764746996 | snp | A/C | | | upstream-variant-2KB, intron-variant | NCK1 | GRCh38.p7 | 3:136928688 | ACTGTACATTAGCAC[A/C]TACAGAGCTCTTTTC | 4690 |
rs764844786 | in-del | -/TT | | | intron-variant | NCK1 | GRCh38.p7 | 3:136915444 | GAAGTTGCAAAGTTC[-/TT]TTATACCCAGGATTT | 4690 |
rs764862777 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136896021 | GTTTTTTATTGATAT[A/G]TAATATTTTACATAT | 4690 |
rs764877596 | snp | C/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136939168 | ACTTGTTATATGTCT[C/G]TTCAGATTTTCTATT | 4690 |
rs764913666 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136894324 | TCAATCTAACTTCTC[C/T]ACCCCTTGGTTTCTA | 4690 |
rs764936111 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136864876 | GATTCTTGTGCCTCG[G/T]CCTCCTAAGTAGCTG | 4690 |
rs764959958 | snp | A/C | | | intron-variant | NCK1 | GRCh38.p7 | 3:136915108 | TTGAGCCAAATAAGC[A/C]TTTTTTCTTTATAGA | 4690 |
rs765005456 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136905878 | AGTCTGCCTGCCTCA[A/G]TCTCCCAAAGTGCTA | 4690 |
rs765039223 | snp | A/T | 4.79777e-05 | 0.00489761 | intron-variant | NCK1 | GRCh38.p7 | 3:136928271 | TTTGTTTTAAATGAA[A/T]CCTGCAACTTAGTTC | 4690 |
rs765089285 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136869262 | AAAAAATTTTATTTG[C/T]TCCGCTAGGCCTGAT | 4690 |
rs765097699 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136884828 | TGAGTTCAAGGGATT[C/T]TCCTGCCTCAGCCTC | 4690 |
rs765131680 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136916454 | AACCCAAACACCTCC[C/T]ATTAGGCCCCATTTC | 4690 |
rs765169232 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136870208 | TTAGCTGGGCGTGGT[G/T]GTGCATGCCTGTAAT | 4690 |
rs765184614 | snp | A/C | | | intron-variant | NCK1 | GRCh38.p7 | 3:136917806 | CCATGTCTCAGGAAG[A/C]TAATTCCCAGAACCT | 4690 |
rs765194182 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136904414 | TGCCTCAGCCTCCCA[A/G]AGTGCTAGGATTACA | 4690 |
rs765224549 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136885131 | ATACACCGAAATATT[G/T]ACAGACAAAAGTTTT | 4690 |
rs765244758 | snp | C/G | 3.29484e-05 | 0.00405871 | missense, downstream-variant-500B | NCK1, LOC107986136 | GRCh38.p7 | 3:136945921 | AATAACCTAAATACT[C/G]GGCAAGTGTTGCATG | 4690 |
rs765271528 | in-del | -/GTT | | | intron-variant | NCK1 | GRCh38.p7 | 3:136942791 | CTGTTCCTTGTCCCA[-/GTT]GTTGTCCCTTGCCCC | 4690 |
rs765298879 | in-del | -/TA | | | intron-variant | NCK1 | GRCh38.p7 | 3:136864934 | GCTAATTTTTTTGTA[-/TA]TATATATATATTTTT | 4690 |
rs765402504 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136866577 | CTGCCAAAGTGCTGG[A/G]ATTACAGGTGTGAGC | 4690 |
rs765415149 | in-del | -/A | | | intron-variant | NCK1 | GRCh38.p7 | 3:136887353 | TTTCTATCTTAACAT[-/A]AAATGGAAAAGTTAC | 4690 |
rs765448509 | snp | A/C/G | 3.42837e-05 | 0.00414016 | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136948478 | CCAGAAGTGACTGCT[A/C/G]TGTAGCTGTAATTTG | 4690 |
rs765453047 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136882135 | CACCATTTTACATTA[C/T]CACCAACCGTGCATA | 4690 |
rs765520867 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136913637 | TTTTCCTGGACATGC[A/G]CAGTGATTTTCTTTT | 4690 |
rs765526015 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136927121 | GGATTCCAAGTGTGC[A/G]CCACCATACCTAGCT | 4690 |
rs765545748 | in-del | -/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136895304 | ATAAGGCTTTGGTAT[-/G]TTTTTGGTTTATTTT | 4690 |
rs765553907 | snp | C/G | 1.64754e-05 | 0.00287009 | missense, downstream-variant-500B | NCK1, LOC107986136 | GRCh38.p7 | 3:136945818 | TGGACAAGTTGGATG[C/G]TTCCCTTCAAACTAT | 4690 |
rs765583979 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136874770 | AGTATATCATACAAT[A/G]GATTCCTGTGGAAGA | 4690 |
rs765624417 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136935553 | TGGGTCGACTGAGGG[A/G]GAAACTGAATTAATA | 4690 |
rs765627315 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136908600 | CAAGAAACAGGGATA[A/G]GTTGTCCCACCTGTT | 4690 |
rs765636860 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136873816 | AGCTCTCTTGTCTGC[C/T]GCCACGTGAGACATG | 4690 |
rs765675333 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136902642 | GATGAAAAGAATGTG[C/T]TCACAGTGGGGTGCT | 4690 |
rs765681184 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136922019 | TAGTTTCCTGACCTC[A/G]TGATCTGCCTGCCTC | 4690 |
rs765703135 | snp | A/C | | | intron-variant | NCK1 | GRCh38.p7 | 3:136876914 | TTTAAAATGTTGCTG[A/C]CTGTTGCCAAACTGC | 4690 |
rs765703527 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136922694 | CAACATAGTTTGTTG[A/G]CAAGGCTGTGGGGAA | 4690 |
rs765780044 | in-del | -/GTG | 1.65124e-05 | 0.00287331 | cds-indel | NCK1 | GRCh38.p7 | 3:136928014 | AAGATGGCAGAAGAA[-/GTG]GTGGTAGTAGCCAAA | 4690 |
rs765827503 | snp | A/C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136873014 | AGGGAAATGTGGGGT[A/C/T]AGAGCCCCCACACAG | 4690 |
rs765827604 | in-del | -/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136922649 | ATACTATTTCTCCCC[-/T]ATTAGATTGGCAAAA | 4690 |
rs765865474 | snp | A/C | | | intron-variant | NCK1 | GRCh38.p7 | 3:136895795 | ATCTCTAACTCCTGA[A/C]CTCAGGTGATCCTCC | 4690 |
rs765895012 | snp | G/T | 1.73384e-05 | 0.0029443 | synonymous-codon, nc-transcript-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136946295 | TGATAGTGAATCTTC[G/T]GTAAGTTGATTTTCG | 4690 |
rs765898079 | snp | A/C | | | intron-variant | NCK1 | GRCh38.p7 | 3:136873702 | ACCTGGTGGGAGGTA[A/C]TTGAATCGTGGGAGT | 4690 |
rs765925170 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136909362 | GAGGACTGAAACACC[A/G]TGTGAAAGGAGCTGA | 4690 |
rs765927761 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136943508 | AACCTTCTGCACAGA[A/G]ATTATAGAAAATGAA | 4690 |
rs765949151 | in-del | -/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136930809 | GTTTTAGCATGAATG[-/T]TTAACAAGTAGAGAA | 4690 |
rs765999993 | in-del | -/GC/GTGG | | | intron-variant | NCK1 | GRCh38.p7 | 3:136923120 | TGTGTGTGTGTGTGT[-/GC/GTGG]GCGCGCCTGTGTGCA | 4690 |
rs766021536 | snp | A/C | | | intron-variant | NCK1 | GRCh38.p7 | 3:136942411 | GGTCATGTGGGGCCG[A/C]TGAAGTCTATTCCAT | 4690 |
rs766058002 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136872861 | GTGTTGATGCTGCAA[A/G]TGCACAGAAGTCAAG | 4690 |
rs766093032 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136899468 | TTTTCTCATAGAGGA[A/G]TCTTTGTCATTATCC | 4690 |
rs766102125 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136908229 | GCAACCGTATCACTT[C/T]GTCATATTAACATTC | 4690 |
rs766103903 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136921946 | GCACCACCACGCCCA[G/T]CTAATTTTATTGTAT | 4690 |
rs766207987 | snp | A/T | 0.00246739 | 0.0350372 | intron-variant | NCK1 | GRCh38.p7 | 3:136930617 | AATCTGTTTATTAAA[A/T]CCACTGTTTTCTTGA | 4690 |
rs766233384 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136882330 | TTTCGAGAAATGTCT[A/G]TTTTGTTCGTTTGCC | 4690 |
rs766245769 | snp | A/G | | | upstream-variant-2KB, intron-variant | NCK1 | GRCh38.p7 | 3:136930327 | AAGTCTGAATAATAA[A/G]GTCATATTTTTGGCC | 4690 |
rs766297864 | snp | A/C | | | intron-variant | NCK1 | GRCh38.p7 | 3:136884097 | AGGCCAGAGGTGATA[A/C]GATGAAGTCATAATA | 4690 |
rs766307360 | in-del | -/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136866312 | TTCTTTCTTTCTTTC[-/T]TTTTTTTTTTTTTGA | 4690 |
rs766346337 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136903018 | AATTTTTGTATCTAC[A/G]TGATCCATTTAATGC | 4690 |
rs766350722 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136896768 | GGCCTCCCAGAGTGC[C/T]AGGATTACAGACCTA | 4690 |
rs766411952 | snp | A/C | | | intron-variant | NCK1 | GRCh38.p7 | 3:136912737 | ATGGGCTCACTGCAG[A/C]CTCAAACTCCTGGGC | 4690 |
rs766469500 | in-del | -/CTT | | | intron-variant | NCK1 | GRCh38.p7 | 3:136886817 | AGTTACATGATCAGT[-/CTT]TTTTTTTTTTTTTTT | 4690 |
rs766476990 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136924672 | TTTGCAATCTTATAT[A/G]TTTTTATGCATCAGA | 4690 |
rs766500118 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136905965 | CCCGTGAATTATTGT[G/T]GTCTTTTGGCGGTGT | 4690 |
rs766528018 | snp | A/C | | | intron-variant | NCK1 | GRCh38.p7 | 3:136932374 | TTCATCTACTTCCTA[A/C]CTGAATGGGCTTATA | 4690 |
rs766559723 | snp | A/G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136864969 | TTCTTTTGTTTGTTT[A/G/T]TTTTTTTGAGACGGA | 4690 |
rs766578759 | in-del | -/A | | | intron-variant | NCK1 | GRCh38.p7 | 3:136899716 | GATACGAGGAGACTT[-/A]ACTCACTGTTTCTGT | 4690 |
rs766611009 | snp | A/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136880446 | ACCAGGGAGAAGATG[A/T]CTATCTACAAGCCAA | 4690 |
rs766643212 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136925978 | TGATCCAATTTCAAC[G/T]TACCCTTGTCAGCAT | 4690 |
rs766700438 | in-del | -/TGA | 1.657e-05 | 0.00287832 | cds-indel, downstream-variant-500B | NCK1, LOC107986136 | GRCh38.p7 | 3:136945635 | TTCTGCATCTCCTGC[-/TGA]TGATAGTTTTGTTGA | 4690 |
rs766756489 | snp | A/C | | | intron-variant | NCK1 | GRCh38.p7 | 3:136923551 | CAGTGCAGTGCGAGA[A/C]TCCGTCTCAAATAAA | 4690 |
rs766777490 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136913588 | TATTTTTTGATTGTT[A/G]TAGGCTATCTCAGAT | 4690 |
rs766816380 | snp | A/G | 1.64757e-05 | 0.00287012 | missense, downstream-variant-500B | NCK1, LOC107986136 | GRCh38.p7 | 3:136945960 | GCTCTTTACCCATTC[A/G]GCTCATCTAATGATG | 4690 |
rs766838274 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136886507 | GAATAATGACAAGGA[A/G]AAAACGTCTGTATAT | 4690 |
rs766889260 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136900181 | GCTCTCCCTTCACTC[C/T]TCATTGTTTCCTTTG | 4690 |
rs766914546 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136920875 | TTAAACATAAATGGC[C/T]TTATAGTTGATTGTA | 4690 |
rs766958324 | snp | A/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136918166 | TGATCCAGCAAGAGT[A/T]GGCTAAATGTATAGC | 4690 |
rs766964624 | in-del | -/G | | | upstream-variant-2KB, intron-variant | NCK1 | GRCh38.p7 | 3:136928790 | GCCTGAGACAGTGGA[-/G]CCCACTTCACACTGG | 4690 |
rs767003507 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136906888 | GATCGCCAGGCCCAC[G/T]GATTGCATGCTTGGT | 4690 |
rs767008989 | snp | A/T | 1.65135e-05 | 0.00287341 | missense | NCK1 | GRCh38.p7 | 3:136928012 | GAAAGATGGCAGAAG[A/T]AGTGGTGGTAGTAGC | 4690 |
rs767031974 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136887408 | GCAGCCTAAGTAAGA[C/T]TGGTAGTTTGGAATA | 4690 |
rs767138188 | snp | A/G | 4.98699e-05 | 0.00499324 | missense, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136948292 | TCACTAAAAGCACAA[A/G]GGAAAAACAAGCATT | 4690 |
rs767207332 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136886397 | GTACTATTTACATAT[A/G]ACCTATGCACATTCT | 4690 |
rs767231044 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136871881 | CTCTTATCTGCCGCC[A/G]TGTGAGAAGACATGC | 4690 |
rs767342936 | in-del | -/CATT | | | intron-variant | NCK1 | GRCh38.p7 | 3:136894379 | ATATAATACCCTAGC[-/CATT]CATTGGTTCAGTGCA | 4690 |
rs767366990 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136943415 | GGTACTGATGGCACA[A/G]TCTGTGGGTGTCTAG | 4690 |
rs767404296 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136895711 | CTGGGATTACAGGTG[C/T]GTACCACCACACCCC | 4690 |
rs767427500 | in-del | -/CA | | | intron-variant | NCK1 | GRCh38.p7 | 3:136864492 | ATTCCGTCACACACA[-/CA]CACAAAAAAAAAACA | 4690 |
rs767452337 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136941993 | ACAAGCGTGTGCCAC[C/T]ACGCCCGGCTAATTT | 4690 |
rs767491992 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136878227 | CAGCCTGGCCAACAT[A/G]GTGAAACCCCATCTC | 4690 |
rs767504687 | snp | G/T | 1.64906e-05 | 0.00287142 | missense, downstream-variant-500B | NCK1, LOC107986136 | GRCh38.p7 | 3:136945658 | GTTTTGTTGACCCAG[G/T]GGAACGTCTCTATGA | 4690 |
rs767505560 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136927379 | ACATATTTTGAAACT[A/G]TCTTGTTACTAGGTA | 4690 |
rs767505694 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136907951 | GTAATATCATGGTCA[A/G]CAAGAGAGAGAACAT | 4690 |
rs767549636 | snp | G/T | 4.51029e-05 | 0.00474863 | intron-variant, downstream-variant-500B | NCK1, LOC107986136 | GRCh38.p7 | 3:136945540 | TTCTTTTGGTAATCA[G/T]TTTTTTATATTCTCC | 4690 |
rs767592059 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136937139 | AGTTAATTTTTATAT[A/G]TGATGTGAAGTTGGA | 4690 |
rs767628712 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136877907 | TAATAGCCCCAAAGT[A/G]GAAGCAACTCAGATG | 4690 |
rs767630511 | snp | A/T | | | upstream-variant-2KB, intron-variant | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136860832 | GGATCAAATTTCAAC[A/T]GGAGGTTTAGGGGAA | 4690 |
rs767649955 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136924505 | TCCCAGTTCACACCA[A/G]CTGTAAGAATGTTTA | 4690 |
rs767721465 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136908636 | AGGTGAACTGCGACT[A/G]ATTACTGCCAATGTG | 4690 |
rs767749905 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136937998 | GTTCTTACGGTGGAA[A/G]ACTTTGTCTTTCACC | 4690 |
rs767763329 | in-del | -/C | | | intron-variant | NCK1 | GRCh38.p7 | 3:136914486 | CCTACTCTGCTTTCT[-/C]CCCAGAATCCTCTAA | 4690 |
rs767773801 | in-del | -/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136905642 | TCTTTTTTTCCCCCC[-/T]GAGACAGGGTCTCAC | 4690 |
rs767790090 | snp | A/C | 1.64738e-05 | 0.00286995 | missense, nc-transcript-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136946116 | GTTATGCAGAATAAT[A/C]CATTAACTTCAGGTT | 4690 |
rs767809990 | snp | A/C | | | intron-variant | NCK1 | GRCh38.p7 | 3:136891019 | TGGCTTATTTCACTG[A/C]GTATAGTGTCTTCAA | 4690 |
rs767843758 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136926556 | CTGGGATTACAGGCA[C/T]GAGCCACCGCGCCCG | 4690 |
rs767880979 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136898872 | GCATGAGAAGATAAT[C/T]CTTACAAAGCTCTCA | 4690 |
rs767888187 | snp | A/T | 1.65822e-05 | 0.00287938 | synonymous-codon, nc-transcript-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136946241 | TCAAGCAGAAATGGC[A/T]TTAAATGAAAGAGGA | 4690 |
rs767985669 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136925815 | ATTCATGTAAAATGT[A/G]AACATAAATTTTCAT | 4690 |
rs767986458 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136900155 | GTTCCCACCCAAAAC[C/T]AGACATTGGCGCTCT | 4690 |
rs767987691 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136910935 | CCATCCTGGCTTCTC[C/T]CCAGTCTCTGGTAAG | 4690 |
rs768040704 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136912398 | CCATTAGTTTTTCAA[A/G]TAATCTCTTTGCCCC | 4690 |
rs768049545 | snp | A/G | | | intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136947864 | ACACATTGAAAAGGG[A/G]TTGGGTGGGTATCTT | 4690 |
rs768050372 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136902474 | TGCTAAGATTACAGG[C/T]GCGAGCTATCCCACC | 4690 |
rs768125318 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136923717 | TAAACATTCATATAA[A/G]CAATATTAAACATAA | 4690 |
rs768174664 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136895681 | GTGGTTCTTGTGCCA[C/T]AGCCTCCCGGGTAGC | 4690 |
rs768179282 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136912325 | ATGCCACCACGCCTG[A/G]CTGATTTTTGTGTTT | 4690 |
rs768235189 | snp | G/T | 4.36815e-05 | 0.0046732 | intron-variant | NCK1 | GRCh38.p7 | 3:136928259 | AAGAAAAGCAACTTT[G/T]TTTTAAATGAAACCT | 4690 |
rs768262553 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136901169 | GTTGAGATGAACATA[C/T]GGTTTTGTCCTTTAT | 4690 |
rs768284048 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136926748 | TTAGAAGTTTCCAAA[C/T]GTGGTATTTCAAAAG | 4690 |
rs768338646 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136869798 | TGGTCTGTTTTTCAT[G/T]TATTTTTTGGTTGTT | 4690 |
rs768376509 | in-del | -/TT | | | intron-variant | NCK1 | GRCh38.p7 | 3:136912171 | TTTTTCTTTTTTTTT[-/TT]TTTTTTTTTGAGACC | 4690 |
rs768395599 | in-del | -/A | | | intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136946972 | ACACTCATTTTCCTT[-/A]AAAATGGCCTTTCTT | 4690 |
rs768397134 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136882119 | TTTTCCATAGCAGCT[A/G]CACCATTTTACATTA | 4690 |
rs768448288 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136871785 | GGGGTGGGCCTTTCT[C/T]GTGCTGTTCTTGTGA | 4690 |
rs768475356 | snp | A/G | 4.94262e-05 | 0.00497098 | stop-gained, nc-transcript-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136946046 | TGACCCAGAGTGGTG[A/G]AAATGCAGGAAGATC | 4690 |
rs768507142 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136921652 | GTAAGGACAGATTTT[A/G]TTCAGTAACTATTGC | 4690 |
rs768651316 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136869862 | GTTAAAAAAACCTGT[G/T]AAAACACTGATTCTC | 4690 |
rs768660089 | snp | A/C | | | intron-variant | NCK1 | GRCh38.p7 | 3:136888339 | ATACTATACAGTTCA[A/C]TCATTAAAAGTATAC | 4690 |
rs768660181 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136872500 | TTTGCAGCTTGACAG[C/T]GTGATAGAAAAGAAA | 4690 |
rs768676919 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136889291 | CAAGAATGAAGCCGC[A/G]GACCCTCGCGGTGAG | 4690 |
rs768730269 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136887004 | AGGTGCCACCATGCC[C/T]GGCTAATTTTTGTGT | 4690 |
rs768735016 | snp | A/G | 9.8837e-05 | 0.00702914 | missense, downstream-variant-500B | NCK1, LOC107986136 | GRCh38.p7 | 3:136945852 | ACTGAAGAAGGTGAC[A/G]GTCCTTTGGGTGACC | 4690 |
rs768767143 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136871385 | CTTGGGGGACAGAGC[A/G]AGACGCTGTCTAAAA | 4690 |
rs768792160 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136931475 | ATGTTGTAATTGTAA[C/T]GTGAAGACTCATTTG | 4690 |
rs768811695 | snp | C/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136884962 | CTGACCTCAAGTGAT[C/G]TGCCCACCTCGGCCT | 4690 |
rs768858423 | in-del | -/TTT | | | intron-variant | NCK1 | GRCh38.p7 | 3:136870028 | GATGTTTCTCAAAAG[-/TTT]TTTTTTTTTTTTTTT | 4690 |
rs768900211 | snp | C/T | | | upstream-variant-2KB, intron-variant | NCK1 | GRCh38.p7 | 3:136930086 | ACCTGTAAAGAGATA[C/T]AAGTCCAGCTTTTAC | 4690 |
rs768905808 | in-del | -/AAAG | 1.90721e-05 | 0.00308799 | intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136946348 | TGGGTATTTTAAAAA[-/AAAG]AGAGAGAGAAATGGA | 4690 |
rs768916731 | snp | G/T | 0.000577839 | 0.0169878 | synonymous-codon | NCK1 | GRCh38.p7 | 3:136928097 | GAGATTATGGCTTCT[G/T]GATGATTCTAAGTCC | 4690 |
rs768938625 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136941230 | TCCCAGGTTCAAGCG[A/G]CACTTATATGTCAGC | 4690 |
rs768940605 | snp | C/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136925438 | CCAGTGGCAATACAT[C/G]TGGCAGAAGTATAGT | 4690 |
rs768951389 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136944673 | CTAGAAGGATCAGGA[G/T]TTGGAGACTTGAGTG | 4690 |
rs768967319 | snp | A/G | 1.65157e-05 | 0.0028736 | missense, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136948364 | CGTAAATTCAGCACC[A/G]TGGAAGAACTTGTAG | 4690 |
rs768982230 | in-del | -/C | | | intron-variant | NCK1 | GRCh38.p7 | 3:136867077 | TCTTTCTTTCTTTCT[-/C]TTCTTTCTTTCTTTC | 4690 |
rs769014288 | snp | A/G | 6.87474e-05 | 0.00586251 | missense, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136948262 | TTTCTCTTTTAGCCA[A/G]ATGATTTCTCAGTAT | 4690 |
rs769029767 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136916132 | TGATCCAGTCACCTC[A/G]CAGTCACCTCCAGTC | 4690 |
rs769104759 | snp | C/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136878045 | TGAAAGCATTATGCT[C/G]TGAAAGAAGCCAGTC | 4690 |
rs769135774 | snp | A/G | 1.64743e-05 | 0.00287 | missense, downstream-variant-500B | NCK1, LOC107986136 | GRCh38.p7 | 3:136945708 | GTGAAATTTAACTAC[A/G]TGGCTGAGAGAGAGG | 4690 |
rs769139513 | snp | C/G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136922798 | TTATACAAACTTTAG[C/G/T]TGTAACTCAGCATTC | 4690 |
rs769161763 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136891824 | TTTCATGTGCTTATT[C/T]ACTGTTTGCATATCT | 4690 |
rs769175153 | in-del | -/TT | | | intron-variant | NCK1 | GRCh38.p7 | 3:136921703 | GTGAACTCAACTCAC[-/TT]TTGCCAAAACAAAAG | 4690 |
rs769207179 | in-del | -/AA | | | intron-variant | NCK1 | GRCh38.p7 | 3:136897034 | TTACCAACACTGTAT[-/AA]GAGTTCCCTTTTTTT | 4690 |
rs769240384 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136906388 | GTGCTAGGATTACAG[A/G]TATGAGCCACCATGC | 4690 |
rs769253366 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136870290 | GAGGTTGCAGTGAGC[C/T]GAGATCATGCCACTG | 4690 |
rs769283432 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136931850 | TGTGGCTAGGCGTGG[C/T]AGCTCAAGCCTGTAA | 4690 |
rs769329022 | snp | C/T | | | upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136862071 | CCACATCAGGCACGG[C/T]GCTTGATTGACATGA | 4690 |
rs769371596 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136911956 | AGCTGCTGATGAGAA[A/G]TCTGCTTATAATATC | 4690 |
rs769382078 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136877897 | AGCTCAGTCATAATA[G/T]CCCCAAAGTAGAAGC | 4690 |
rs769432770 | snp | C/T | 4.98318e-05 | 0.00499133 | missense, downstream-variant-500B | NCK1, LOC107986136 | GRCh38.p7 | 3:136945628 | TGCCAGATTCTGCAT[C/T]TCCTGCTGATGATAG | 4690 |
rs769519595 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136925066 | ATAGGATTCATTATA[C/T]TATTCTCTTCTGTAA | 4690 |
rs769560178 | in-del | -/TTTT | | | intron-variant | NCK1 | GRCh38.p7 | 3:136887944 | TTCTTTCTTTCTTTC[-/TTTT]TTTTTTTTTCTTTTG | 4690 |
rs769567695 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136886025 | ATCCTTTTACTGAAT[A/G]TTATTCCGGAAGCAT | 4690 |
rs769621653 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136872396 | GTCTGGTAGAAAAAA[C/T]TTCTAAGCAGCAAAG | 4690 |
rs769693593 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136871929 | GATTGTGAGGCCTCT[C/T]CTGCCATGTGGAACT | 4690 |
rs769745049 | in-del | -/A | | | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136949176 | AACAGTCTCTGAGAT[-/A]ATTTAGCTTTTCAAA | 4690 |
rs769765192 | snp | C/T | | | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136948605 | TATTATAACTCAGCC[C/T]ATACATATATACTAT | 4690 |
rs769806256 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136901012 | AGAAGAAAGGGTTTC[A/G]ACTTTTCCCCATTCA | 4690 |
rs769809039 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136882856 | AAGAGAACACAGTCA[C/T]TAGTGAATACTAGCA | 4690 |
rs769862757 | in-del | -/T | 0.165289 | 0.235211 | intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136948242 | TTTACTATATGTATC[-/T]TTTTTTTCTCTTTTA | 4690 |
rs769894299 | in-del | -/TGGATGCAATGTGTAA | | | intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136946666 | TTAAAAAATTGCTAT[-/TGGATGCAATGTGTAA]TGGATGCAATGTGTA | 4690 |
rs769898121 | snp | C/T | 1.64784e-05 | 0.00287035 | synonymous-codon, nc-transcript-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136946175 | CATTAGGCCTTCACT[C/T]ACTGGAAAGTTTGCT | 4690 |
rs769930759 | snp | A/G | | | upstream-variant-2KB, intron-variant | NCK1 | GRCh38.p7 | 3:136929819 | TCATAGAGCAAAGGG[A/G]GGAAGTAGTCCAGTA | 4690 |
rs769954528 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136896337 | GTCATTCTACTGTCT[A/G]CCTCCATGAGATCAT | 4690 |
rs770009587 | snp | A/C | | | intron-variant | NCK1 | GRCh38.p7 | 3:136895447 | TAAAAAATTGCCATA[A/C]CACCTTTTTAAAAAA | 4690 |
rs770029732 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136943347 | GGAAGGAAGAAGTTG[A/G]TTTAGGGGTATAGAC | 4690 |
rs770040215 | snp | C/G | 1.71334e-05 | 0.00292684 | missense | NCK1 | GRCh38.p7 | 3:136928218 | GTGAAAAACCTAAAG[C/G]ATACCTTAGGTAAGA | 4690 |
rs770041759 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136889750 | GTTCTCCAAGTCCCC[A/G]CCAGAGTAGCTAGCT | 4690 |
rs770051515 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136891755 | GATGGTTGTGAGGTG[G/T]TATTATTGTGGTTTT | 4690 |
rs770077228 | in-del | -/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136867277 | CTCTTTCTTTCTTTC[-/T]TTCTTTCTTTTTTGA | 4690 |
rs770090971 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136917177 | TGCATGCAGCCCAGG[A/G]CAGCTTTAAATGTGG | 4690 |
rs770125861 | snp | A/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136920682 | TATTACATTTTATCT[A/T]AAGAAAGAAGCCATT | 4690 |
rs770146973 | snp | A/G | 0.000100155 | 0.00707585 | intron-variant | NCK1 | GRCh38.p7 | 3:136927974 | AAAAATATTTTCCAT[A/G]TGTTTACAGTGCTGA | 4690 |
rs770201827 | in-del | -/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136871830 | TGTGGGATCTGATGG[-/T]TTTAAAAACGGGAGT | 4690 |
rs770231243 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136934209 | GTTTTTTTTTTTAAC[G/T]TTTAGGGTTGGGGGT | 4690 |
rs770241980 | snp | A/C | | | intron-variant | NCK1 | GRCh38.p7 | 3:136890806 | ATTCACATTGTTATG[A/C]AGCCATCACCACCAC | 4690 |
rs770247331 | snp | A/G | | | downstream-variant-500B, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136951997 | CTGATTTGGTTGGGT[A/G]TGACAATAATTACCC | 4690 |
rs770270613 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136869668 | TAACAGAAACCATGT[A/G]TGGTTGCTTTCGTAT | 4690 |
rs770295231 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136903679 | ATCCACCTGCCTCAG[C/T]CTCCCAAAGTGCTGG | 4690 |
rs770414450 | snp | A/C | | | intron-variant | NCK1 | GRCh38.p7 | 3:136905588 | ACTGGGCTTCTTTAA[A/C]ATCAGTATTTGAGTT | 4690 |
rs770463304 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136917345 | TGGACACCTCTGTCC[A/G]TGTTAAGCCTCATAG | 4690 |
rs770466237 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136936497 | TCTATTTTCAGTTAA[G/T]TGTATACCTAAAAGT | 4690 |
rs770479572 | in-del | -/TA | | | intron-variant | NCK1 | GRCh38.p7 | 3:136895322 | TTTGGTTTATTTTAT[-/TA]TATATATATATCATG | 4690 |
rs770511764 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136874522 | CACTCATTTCTCCTG[A/G]CTGTATATACACATT | 4690 |
rs770521089 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136890652 | TTTACAGGCATTTGA[A/G]TTTTTTCTCCCTTAT | 4690 |
rs770529690 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136931196 | AATTCTTGACTGTTA[C/T]TGAGTTTGGGTCATG | 4690 |
rs770640721 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136937622 | TTTAATTTCTTTCAG[C/T]GGTGTTTTGCAGTGT | 4690 |
rs770642106 | in-del | -/TAC | 1.85544e-05 | 0.0030458 | intron-variant, splice-acceptor-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136946331 | AATACAAATAGAGCT[-/TAC]CTGGGTATTTTAAAA | 4690 |
rs770643567 | snp | A/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136931627 | ATTTGCTCATTCATT[A/T]GTTTATCAACACATT | 4690 |
rs770779379 | in-del | -/TTA | | | intron-variant | NCK1 | GRCh38.p7 | 3:136926268 | TTATTTTAAATTTTA[-/TTA]TTATTATTATTATTA | 4690 |
rs770851116 | in-del | -/TT | | | intron-variant | NCK1 | GRCh38.p7 | 3:136941118 | GTGATTTCTTTTTCT[-/TT]TTTTTTTTTTTTTTT | 4690 |
rs770862134 | snp | A/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136921122 | AGAAATATTGGCATT[A/T]AGTACATTCACATTG | 4690 |
rs770876265 | in-del | -/TTG | | | intron-variant | NCK1 | GRCh38.p7 | 3:136892193 | ACACCCAGCTGGATT[-/TTG]TTGTTGTTGTTGTTG | 4690 |
rs770985698 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136865879 | TTTGTTTTGGTGACA[G/T]TACCATGCTTTCAAT | 4690 |
rs771018167 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136907593 | AGCAGGCTGTCTTGC[C/T]TCCTCCTCCTTTCTT | 4690 |
rs771035547 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136911530 | CTGTTGCCATTTTCA[C/T]GTCTTTTTTTGAGAA | 4690 |
rs771037228 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136896179 | TCTACTTTGAAATAC[A/G]CAGTTTTGCTAGCTA | 4690 |
rs771053386 | in-del | -/TTTA | | | intron-variant | NCK1 | GRCh38.p7 | 3:136939859 | TTTTTTTTTTTTTTT[-/TTTA]TTTAAAATAGAGACA | 4690 |
rs771088876 | snp | A/T | 1.91657e-05 | 0.00309556 | intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136946343 | AGCTCTGGGTATTTT[A/T]AAAAAAAGAGAGAGA | 4690 |
rs771127463 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136881970 | TTTAGCTGTTAAGAA[C/T]AGTGTTTCCATGAAC | 4690 |
rs771130343 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136921387 | ATAGGATCTAGGAAG[C/T]GGAGGAACTGTGGGC | 4690 |
rs771135953 | snp | C/T | 1.65712e-05 | 0.00287843 | missense, nc-transcript-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136946237 | GGCATCAAGCAGAAA[C/T]GGCATTAAATGAAAG | 4690 |
rs771159703 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136864449 | TGAGCCAAGATCGCC[A/G]CTGCACTCCAGCCTG | 4690 |
rs771194847 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136906562 | TAAGCCAATCTTTGA[A/G]CCTCCAGGTGTCTTG | 4690 |
rs771258290 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136894988 | TCAAGCAGTTCTCCT[A/G]CCTCAGCCTCCCAAG | 4690 |
rs771265708 | snp | A/G | | | downstream-variant-500B, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136951803 | CAAGCTCTGATTGGT[A/G]TGTGACAGTGATAGG | 4690 |
rs771293429 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136941414 | GGATTACAGGTGTGA[A/G]CCTCTGTGACTGGAC | 4690 |
rs771304838 | in-del | -/AAAT/AAATAAAT | | | intron-variant | NCK1 | GRCh38.p7 | 3:136923559 | GCGAGACTCCGTCTC[-/AAAT/AAATAAAT]AAATAAATAAATAAA | 4690 |
rs771345810 | in-del | -/C | | | intron-variant | NCK1 | GRCh38.p7 | 3:136873488 | TTGTTTTGGATGAGA[-/C]TTTGGACTGTGAACT | 4690 |
rs771394511 | snp | A/G | 1.64787e-05 | 0.00287038 | missense | NCK1 | GRCh38.p7 | 3:136928152 | AATAAAACAGGTTTT[A/G]TGCCTTCTAACTATG | 4690 |
rs771451936 | snp | A/G | 3.31576e-05 | 0.00407157 | missense | NCK1 | GRCh38.p7 | 3:136928200 | GCTCGGAAAGCATCT[A/G]TTGTGAAAAACCTAA | 4690 |
rs771454065 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136911810 | TTTTGGAAAGTCATA[A/G]TTTTTCCCTCACTTT | 4690 |
rs771468274 | snp | C/T | 1.92578e-05 | 0.00310299 | intron-variant | NCK1 | GRCh38.p7 | 3:136928240 | TAGGTAAGATATTTT[C/T]TAAAAGAAAAGCAAC | 4690 |
rs771476014 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136890408 | CCCCCCAAGCTGAGG[G/T]AGCAGGCTCTGCCCT | 4690 |
rs771503546 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136866243 | CCACTCTAACCAAAC[C/T]AATCTCTGATTCTTA | 4690 |
rs771503925 | snp | C/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136882786 | AGAACTGAGTCATGT[C/G]ATCTTATCTAATTGC | 4690 |
rs771505410 | in-del | -/AT | | | intron-variant | NCK1 | GRCh38.p7 | 3:136941106 | CTGTCTTCTTTTGTG[-/AT]TTCTTTTTCTTTTTT | 4690 |
rs771542250 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136921869 | GCTCACTGCAGTCTC[C/T]GCCTCCCAGACTCAA | 4690 |
rs771631607 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136901473 | AGTTCTTCTATGAGT[A/G]TTTGGTAGAATTTGG | 4690 |
rs771640823 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136936444 | GTTATTGTGAACAGC[A/G]TTGTGATAAACATTC | 4690 |
rs771658678 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136888748 | GTCCTAGGAAACCAT[C/T]AATCTGCCTTCTGTC | 4690 |
rs771667760 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136902541 | CTTATCTGAGGAGAT[A/G]CTTGATACGATTTCA | 4690 |
rs771683116 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136879802 | AACAATGAGAACACA[C/T]GGACACAGGGAGGGG | 4690 |
rs771702229 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136873554 | GGACTGTTGGGAAGG[C/T]ATGATTGGTTTTGAA | 4690 |
rs771768700 | snp | A/C | | | intron-variant | NCK1 | GRCh38.p7 | 3:136895161 | ATTATAGGCATGAGC[A/C]ACTGCGCCCAGCAAG | 4690 |
rs771851523 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136883700 | TGGAGGGAATCTATT[A/G]TATAGAACCGACTGA | 4690 |
rs771853836 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136897950 | TAATATCATAATAGG[A/G]ATGACTAAATACTTG | 4690 |
rs771863858 | snp | A/G | 1.64746e-05 | 0.00287002 | missense, downstream-variant-500B | NCK1, LOC107986136 | GRCh38.p7 | 3:136945744 | TTATCATTGATAAAG[A/G]GGACAAAGGTGATCG | 4690 |
rs771866777 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136909257 | CACTGACTACTCAGA[A/G]ATATCTAGGCAAATG | 4690 |
rs771871797 | snp | C/T | | | downstream-variant-500B, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136951677 | ATACACAGACAGTAG[C/T]TTTTGGTATGTCTAA | 4690 |
rs771949191 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136866908 | GTGAGCCACTGTGCC[C/T]GTCCAGTTTGCCTAG | 4690 |
rs771965220 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136944408 | CTGGCATGAGCCACC[A/G]TGCCCAGCCGGGAAA | 4690 |
rs772007596 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136883749 | TTAACCAAGGGCTCT[C/T]ATGATAATTTAGGTG | 4690 |
rs772123306 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136893217 | GCAAGTATCTTTTTC[A/G]TATAATAACTTCTTC | 4690 |
rs772232599 | snp | C/T | 2.13696e-05 | 0.00326869 | intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136948242 | TTTACTATATGTATC[C/T]TTTTTTTCTCTTTTA | 4690 |
rs772271183 | snp | C/T | | | upstream-variant-2KB, nc-transcript-variant | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136862032 | TCTAGCTCTCTACTC[C/T]CCGCCGCGCAGCCTC | 4690 |
rs772309873 | snp | A/C | | | intron-variant | NCK1 | GRCh38.p7 | 3:136865898 | CATGCTTTCAATTAC[A/C]CAGACACAAACTTTG | 4690 |
rs772320995 | snp | C/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136917695 | CTAGGTCAGTTCTCT[C/G]TCCTTAGGTAAAGGT | 4690 |
rs772334995 | snp | C/T | 1.65231e-05 | 0.00287424 | synonymous-codon, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136948342 | GACTGTCTACTGCAT[C/T]GGGCAGCGTAAATTC | 4690 |
rs772392097 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136869290 | GATGGCTCACTCCTG[G/T]AATCCCAGCGCTTTG | 4690 |
rs772406798 | in-del | -/TT | | | intron-variant | NCK1 | GRCh38.p7 | 3:136864762 | GGTTTTTTTCTTTTC[-/TT]TTTTTTTTTTTTTTT | 4690 |
rs772508754 | in-del | -/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136874726 | TTTTTGTTTGTTTTG[-/T]TTTTTTGTTTAACCT | 4690 |
rs772550419 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136908080 | GAAAGTGTTTACCAT[G/T]CAAAAGTACTTCAGT | 4690 |
rs772596677 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136926871 | TTTTTGTATGTGTTT[C/T]ATTTGTTTTCTATTT | 4690 |
rs772631737 | in-del | -/ATTT | | | intron-variant | NCK1 | GRCh38.p7 | 3:136881921 | TTTGTTTATCCATTC[-/ATTT]GTTGATGAACAGCTT | 4690 |
rs772639807 | snp | C/T | 4.94434e-05 | 0.00497184 | synonymous-codon | NCK1 | GRCh38.p7 | 3:136928166 | TGTGCCTTCTAACTA[C/T]GTGGAAAGGAAAAAC | 4690 |
rs772680921 | snp | C/G | 1.65968e-05 | 0.00288065 | missense, downstream-variant-500B | NCK1, LOC107986136 | GRCh38.p7 | 3:136945630 | CCAGATTCTGCATCT[C/G]CTGCTGATGATAGTT | 4690 |
rs772723804 | snp | C/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136888936 | AGTGCAGTGCTTGAT[C/G]ACAGCTCACTGCAAC | 4690 |
rs772799181 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136899318 | CTGAGATTCTGATTT[A/G]ATGGCAGCCAGAGCA | 4690 |
rs772819979 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136897953 | TATCATAATAGGGAT[G/T]ACTAAATACTTGACA | 4690 |
rs772841142 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136921872 | CACTGCAGTCTCCGC[C/T]TCCCAGACTCAAGCA | 4690 |
rs772896055 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136922235 | GGCCCTTACCCTCTC[G/T]CCAGGGACTGGGAAC | 4690 |
rs772926683 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136883846 | ATTTCAAGAGAAAAA[C/T]CAACACAAATTGATG | 4690 |
rs772937707 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136935134 | TTGAACTCCTGGCCT[C/T]AGGTGATCTGCCTGC | 4690 |
rs772938270 | in-del | -/TG | | | intron-variant | NCK1 | GRCh38.p7 | 3:136923107 | ATGCCTATGTGTATG[-/TG]TGTGTGTGTGTGTGC | 4690 |
rs772974121 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136944417 | GCCACCGTGCCCAGC[C/T]GGGAAAGACAACTTT | 4690 |
rs773034677 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136887428 | AGTTTGGAATAAAGG[A/G]TAAGTTAAAAGGGCA | 4690 |
rs773055166 | snp | A/T | 7.69004e-05 | 0.00620035 | intron-variant | NCK1 | GRCh38.p7 | 3:136928278 | TAAATGAAACCTGCA[A/T]CTTAGTTCTTTGTAC | 4690 |
rs773120335 | in-del | -/GTGG/GTGTGG | | | intron-variant | NCK1 | GRCh38.p7 | 3:136882590 | TGTGTGTGTGTGTGT[-/GTGG/GTGTGG]TGAGGGGCACCTTTG | 4690 |
rs773132768 | snp | C/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136943445 | GTGACAGTTGGAATT[C/G]TAATGCCTGAATTCC | 4690 |
rs773173936 | in-del | -/TG | | | intron-variant | NCK1 | GRCh38.p7 | 3:136882549 | TTTCCCACATCACTG[-/TG]TGTGTGTGTGTGTGT | 4690 |
rs773188428 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136872036 | TAATACAGTAAATTG[A/G]TACCAGTAGAGTAGA | 4690 |
rs773203822 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136941368 | CTTCTGACCTCAAGT[A/G]ATCCGCCCACCTTGG | 4690 |
rs773222966 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136874464 | GGATTACAGGCGTGA[A/G]CCACCACGCCCGGCC | 4690 |
rs773245202 | snp | C/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136909313 | TCTTAAAAATACGTA[C/G]AAGTTTGCTGAGAGG | 4690 |
rs773256240 | snp | A/G | | | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136948977 | CACAGGCCATTGTAA[A/G]TACCAAGTATATTGT | 4690 |
rs773327519 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136940198 | CCTAATATATGGTCT[A/G]TCTTGCAGAATATTC | 4690 |
rs773342253 | in-del | -/TTCTC | | | intron-variant | NCK1 | GRCh38.p7 | 3:136904757 | TCTAACATTTTTGTT[-/TTCTC]TTCTCCTGAGACACT | 4690 |
rs773344757 | snp | C/T | | | missense, downstream-variant-500B | NCK1, LOC107986136 | GRCh38.p7 | 3:136945663 | GTTGACCCAGGGGAA[C/T]GTCTCTATGACCTCA | 4690 |
rs773363408 | snp | C/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136893855 | ATTCATCATTACCTT[C/G]TTTTACTACCTATTC | 4690 |
rs773369716 | snp | C/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136890013 | CCGCACTCCTGAGCC[C/G]TTGGGTGGTCAATGG | 4690 |
rs773378416 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136925878 | CTAGCTTGTATGGTA[G/T]TTGCATGTTTAGTTT | 4690 |
rs773408330 | snp | A/G | 4.94621e-05 | 0.00497279 | missense, nc-transcript-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136946195 | GAAAGTTTGCTGGCA[A/G]TCCTTGGTATTATGG | 4690 |
rs773423077 | snp | C/G | | | intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136947953 | TAACTAAAGGATTTG[C/G]TGTGGGTGTCTGCTG | 4690 |
rs773439768 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136919591 | GAACTGCTAATGTAA[A/G]TACATGAATAATGCT | 4690 |
rs773442253 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136871486 | GTATAGAATGTTTAT[A/G]TTTGTAGATATCTGT | 4690 |
rs773465348 | snp | A/G | 6.58989e-05 | 0.00573978 | synonymous-codon, nc-transcript-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136946079 | TGGTATGGTTGGTCT[A/G]GTACCAAAAAACTAT | 4690 |
rs773539436 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136907472 | CCTCTTTATGTTAGA[C/T]TCAGGGCCTGCAGCA | 4690 |
rs773539681 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136926894 | TTCTATTTGGAAGCA[A/G]TATTCTGTATATGTC | 4690 |
rs773593965 | snp | A/G | 1.64798e-05 | 0.00287047 | missense | NCK1 | GRCh38.p7 | 3:136928120 | CTAAGTCCTGGTGGC[A/G]AGTTCGAAATTCCAT | 4690 |
rs773598793 | in-del | -/TT | 2.18079e-05 | 0.00330204 | intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136948242 | TTTACTATATGTATC[-/TT]TTTTTTCTCTTTTAG | 4690 |
rs773620261 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136914323 | AACTAAGAGCTGAAA[C/T]TGACTAAAAGTAACA | 4690 |
rs773648764 | snp | C/G/T | 3.32387e-05 | 0.00407658 | intron-variant | NCK1 | GRCh38.p7 | 3:136927981 | TTTTCCATGTGTTTA[C/G/T]AGTGCTGAAGCTGCT | 4690 |
rs773678617 | snp | A/G | | | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136949480 | AAATAGAATGTGCTC[A/G]TGGTTAGGGAAAATT | 4690 |
rs773708436 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136913482 | TATGTTGCCCAAGCT[C/T]GTCTAGAACTCCTAG | 4690 |
rs773770914 | snp | C/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136905963 | TGCCCGTGAATTATT[C/G]TGGTCTTTTGGCGGT | 4690 |
rs773804607 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136877269 | TGGACAATAAAAAAG[A/G]TCAAAATAATCAATT | 4690 |
rs773833312 | snp | A/C | | | intron-variant | NCK1 | GRCh38.p7 | 3:136881849 | TTTTGTAGCACATGT[A/C]AAAATTTTCTTCCTT | 4690 |
rs773864662 | snp | A/C | | | intron-variant | NCK1 | GRCh38.p7 | 3:136901233 | GTGTAACCATCCTTG[A/C]CTCTCTGGGATAAAT | 4690 |
rs773904004 | snp | A/C | 1.65778e-05 | 0.002879 | missense, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136948424 | AGTGAACAAGGAGAA[A/C]AATTATATCTTGTCA | 4690 |
rs773950900 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136934961 | GTCCCCCAAAACTCC[A/G]CATGATCTTGGCTCA | 4690 |
rs774048564 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136943386 | TTTTATTTGGACATG[A/G]GTGTTGGGTTTGAGG | 4690 |
rs774075820 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136909108 | CTTGAACTTCCCACC[C/T]TTCAGAACTATGAGG | 4690 |
rs774075870 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136895555 | ATTTGTATGTTGTTT[C/T]TATTTTATTTTATAT | 4690 |
rs774095014 | snp | C/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136900060 | ATTGGTTTCTTACAT[C/G]TCACAGGCTGCACCA | 4690 |
rs774176911 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136941902 | GGAGTACAGTGGTGC[A/G]GTCTTGGCTCACTAC | 4690 |
rs774239593 | snp | G/T | 4.95503e-05 | 0.00497722 | missense, downstream-variant-500B | NCK1, LOC107986136 | GRCh38.p7 | 3:136945643 | CTCCTGCTGATGATA[G/T]TTTTGTTGACCCAGG | 4690 |
rs774256274 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136892929 | AACAGCAATGTACAC[C/T]GTACCCAATGTGTAG | 4690 |
rs774267956 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136907887 | TCCTTATATATGTGG[C/T]GTCAGCCTCAGTCCC | 4690 |
rs774295017 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136921807 | TGTTTTGTTTTGAGA[C/T]GGAGTCTGTCTCTGT | 4690 |
rs774295095 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136921937 | TACAGGCACGCACCA[C/T]CACGCCCAGCTAATT | 4690 |
rs774346224 | in-del | -/AGA | | | intron-variant | NCK1 | GRCh38.p7 | 3:136897765 | TGTTCCCATAAACTG[-/AGA]AGAACTGAGCTAAGT | 4690 |
rs774401651 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136873478 | GGGGCTTGCCTTGTT[C/T]TGGATGAGACTTTGG | 4690 |
rs774443465 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136938107 | TGCTGAGCATTGTTA[C/T]CATGAAACGGTTTTG | 4690 |
rs774452907 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136872501 | TTGCAGCTTGACAGC[A/G]TGATAGAAAAGAAAA | 4690 |
rs774466407 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136908481 | CAGCATTTGGATATG[A/G]AAACAGGGTTGACGT | 4690 |
rs774533023 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136869873 | CTGTTAAAACACTGA[G/T]TCTCTTGTTTCTATT | 4690 |
rs774572688 | snp | A/G | 1.64741e-05 | 0.00286998 | missense, nc-transcript-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136946101 | AAAAACTATGTTACC[A/G]TTATGCAGAATAATC | 4690 |
rs774578403 | snp | G/T | 1.65721e-05 | 0.0028785 | missense, nc-transcript-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136946239 | CATCAAGCAGAAATG[G/T]CATTAAATGAAAGAG | 4690 |
rs774579734 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136868747 | ATCTTTGGAGGCCTT[A/G]AATGTGGATACAGAA | 4690 |
rs774580286 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136931494 | AAGACTCATTTGTTA[A/G]CTTTAGTGACTCCCT | 4690 |
rs774616779 | snp | C/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136935306 | TTGCATTTCTTTTAC[C/G]ATACAAAACTGTGCA | 4690 |
rs774635559 | snp | A/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136917678 | TTTGAGGGTCAAGTT[A/T]CCTAGGTCAGTTCTC | 4690 |
rs774656852 | snp | G/T | 2.06081e-05 | 0.00320993 | intron-variant | NCK1 | GRCh38.p7 | 3:136928251 | TTTTTTAAAAGAAAA[G/T]CAACTTTGTTTTAAA | 4690 |
rs774665218 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136916203 | ACAAATCCAAACTGT[A/G]TCAAGGGCTAAGTGG | 4690 |
rs774699527 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136878128 | AAACATGCTAAGTAG[A/G]CCGGACATGGTGGCT | 4690 |
rs774712313 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136904022 | AGCATTTCTTCTAGG[A/G]CCAGTCTAGTGGTGA | 4690 |
rs774778303 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136939956 | TCCTGGGTTCAAGCA[A/G]TCCTCCCAACTCAGC | 4690 |
rs774789877 | in-del | -/TTTTTTTTTTTTTT | | | intron-variant | NCK1 | GRCh38.p7 | 3:136889045 | AGGCTAATTTTTTGA[-/TTTTTTTTTTTTTT]TTTTTTTTTTTTTTT | 4690 |
rs774814996 | in-del | -/TTT | | | intron-variant | NCK1 | GRCh38.p7 | 3:136941117 | TGTGATTTCTTTTTC[-/TTT]TTTTTTTTTTTTTTT | 4690 |
rs774825920 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136912337 | CTGGCTGATTTTTGT[A/G]TTTTTAGTAGAGATG | 4690 |
rs774848163 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136879480 | GAATCTAAAATAAAG[A/G]GTTGTTTAGCCAGAT | 4690 |
rs774897968 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136932009 | CCTGTAATCCCAGCT[A/G]CTTGGGAAGCTGAGG | 4690 |
rs774913149 | in-del | -/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136942033 | TTAGTAGAGACGGGG[-/T]TTCACCATGTTGGCC | 4690 |
rs774926219 | in-del | -/TTTTTT | | | intron-variant | NCK1 | GRCh38.p7 | 3:136870030 | ATGTTTCTCAAAAGT[-/TTTTTT]TTTTTTTTTTTTTTT | 4690 |
rs774942558 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136880067 | AGATGGGTGGATCAC[A/G]AGGTCAGGAGAATGA | 4690 |
rs774989176 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136880564 | TCCAGAACAGTGAGA[A/G]TGTGTTTCCTTGATG | 4690 |
rs775010222 | snp | C/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136911982 | ATATCATTGAGGATC[C/G]CTTATATGTGACAGA | 4690 |
rs775056529 | snp | C/G | 1.64798e-05 | 0.00287047 | missense | NCK1 | GRCh38.p7 | 3:136928159 | CAGGTTTTGTGCCTT[C/G]TAACTATGTGGAAAG | 4690 |
rs775082088 | snp | C/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136899518 | AATCATCCTCAGAAT[C/G]TTCACCAGTTGCCAA | 4690 |
rs775144130 | in-del | -/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136939378 | GGTCTAGCTAAAGAG[-/T]TTTCAATTTTACTGA | 4690 |
rs775160961 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136910669 | AATTGACAAATCATA[A/G]TTTTATACTTTTCTG | 4690 |
rs775218595 | snp | A/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136872398 | CTGGTAGAAAAAATT[A/T]CTAAGCAGCAAAGCA | 4690 |
rs775274058 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136875220 | TGTGATTTTTGCCCA[C/T]TGATTTTGTATCCTG | 4690 |
rs775277053 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136898494 | TATCACTAAATGTCT[C/T]CAAATTCTATTTGTT | 4690 |
rs775314047 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136921453 | TGCTGTGGTATTTGC[A/G]TCTTTGCTTTATGCA | 4690 |
rs775327180 | in-del | -/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136936309 | GCCTCCCAAAGTGCT[-/G]GGATTACAGACGTGA | 4690 |
rs775351154 | snp | A/G | 1.64743e-05 | 0.00287 | missense, downstream-variant-500B | NCK1, LOC107986136 | GRCh38.p7 | 3:136945747 | TCATTGATAAAGGGG[A/G]CAAAGGTGATCGTCA | 4690 |
rs775444089 | in-del | -/GAA | | | intron-variant | NCK1 | GRCh38.p7 | 3:136865815 | ACCTTAAACTCTAAT[-/GAA]GATAGAATTTATAGT | 4690 |
rs775456124 | snp | C/T | 1.68485e-05 | 0.00290241 | intron-variant | NCK1 | GRCh38.p7 | 3:136927951 | CTAATACTACCTCAA[C/T]CTTACATAAAAATAT | 4690 |
rs775457001 | in-del | -/TCTC | | | intron-variant | NCK1 | GRCh38.p7 | 3:136867254 | CTGTCCGTCCGTCTG[-/TCTC]TCTCTCTCTTTCTTT | 4690 |
rs775518618 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136884062 | TTGGATTAGAGAACA[C/T]AATTCAAATTACAGA | 4690 |
rs775545841 | in-del | -/CGCCCGTGCGAGCCTGGGAGGT | | | intron-variant, upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136862644 | GAGAGCCCGGGCGGC[-/CGCCCGTGCGAGCCTGGGAGGT]CGCCCGTGCGAGCCT | 4690 |
rs775546952 | snp | C/G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136887318 | GACTACAGGAGTGCA[C/G/T]CGCCATGCTCAGCAT | 4690 |
rs775590553 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136902768 | GAAAAGAGGAAGTCA[A/G]ACTGTCCCCCTTTGC | 4690 |
rs775597855 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136886032 | TACTGAATGTTATTC[C/T]GGAAGCATTTATAAG | 4690 |
rs775598762 | in-del | -/CT | | | intron-variant, upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136863370 | ACCAGTGTGCCTAGA[-/CT]CTCAGCCTTCGGCGA | 4690 |
rs775609617 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136882150 | CCACCAACCGTGCAT[A/G]AGAGTTCCAATATCA | 4690 |
rs775693583 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136900016 | CAAAATCATCATCAC[C/T]GTCAGAGTCGCCAAA | 4690 |
rs775709249 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136868397 | CAGTGGGGCAATCTC[A/G]GATCACTGTACCCTC | 4690 |
rs775758517 | in-del | -/TCA | | | intron-variant | NCK1 | GRCh38.p7 | 3:136920117 | TTAAACCCTAGTATC[-/TCA]TCAAGTAATTTTAAT | 4690 |
rs775761011 | snp | A/G | 1.66682e-05 | 0.00288684 | synonymous-codon, nc-transcript-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136946253 | GGCATTAAATGAAAG[A/G]GGACATGAAGGGGAT | 4690 |
rs775761257 | snp | C/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136916121 | ATCTGTCCCCATGAT[C/G]CAGTCACCTCGCAGT | 4690 |
rs775783469 | in-del | -/AAAG | | | intron-variant | NCK1 | GRCh38.p7 | 3:136914589 | AGTTCATTATAACTC[-/AAAG]AAAATCCATTGGAGA | 4690 |
rs775800014 | snp | A/T | | | upstream-variant-2KB, intron-variant | NCK1 | GRCh38.p7 | 3:136928610 | CTAATGACCTTATGT[A/T]TTGAACTTCACTTAA | 4690 |
rs775823048 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136937879 | ATAAGATCATGTCAT[C/T]TGTGGATACTTTTTC | 4690 |
rs775848837 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136890824 | CCATCACCACCACCT[G/T]TTTGCATAAGTTTTT | 4690 |
rs775913291 | snp | C/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136936876 | TTCTGGATACTAGAC[C/G]CTTATCAGAATTATG | 4690 |
rs775962974 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136924304 | AGAAATAATTACCAG[C/T]TTATAGGAGATAGGG | 4690 |
rs775975898 | in-del | -/TAA | | | intron-variant | NCK1 | GRCh38.p7 | 3:136931221 | GTCATGAAGTAAAAC[-/TAA]TAATAATTTATAAGA | 4690 |
rs776093056 | snp | A/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136927357 | AGATCTCCTTGTGGT[A/T]CTGTCAACATATTTT | 4690 |
rs776239408 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136874650 | TCTGATAAAACTAGC[G/T]ACTCCCTTTGTCTTT | 4690 |
rs776280952 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136909416 | AAACCACGTGTATGA[C/T]ATTCTGTTGAGGTGC | 4690 |
rs776296385 | snp | C/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136890668 | TTTTTTCTCCCTTAT[C/G]CCTATTACGAGTAAT | 4690 |
rs776332362 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136910519 | ACTAAAGTTACAGTA[A/G]TACTAGCTTTTATAC | 4690 |
rs776341183 | snp | A/C | | | intron-variant | NCK1 | GRCh38.p7 | 3:136870135 | TCGCTTGAGGTCAGG[A/C]GTTCGAGACCAGCCT | 4690 |
rs776367906 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136922531 | CTAGGATATGGGGAA[A/G]AGATATGAACAAGCA | 4690 |
rs776373234 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136873761 | GTGAATAAGTCTTTT[G/T]AGAACTGATGATTTT | 4690 |
rs776468487 | in-del | -/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136913105 | GCCCGTCTTCTGATC[-/T]TTCTCTGGGAAGGTT | 4690 |
rs776490617 | snp | A/G | | | upstream-variant-2KB, intron-variant | NCK1 | GRCh38.p7 | 3:136930360 | GATTATTTACTTGTT[A/G]TACAGGCTGTGTTAT | 4690 |
rs776523624 | in-del | -/TG | | | intron-variant | NCK1 | GRCh38.p7 | 3:136913229 | CTAATGTGATAACTC[-/TG]GAAATCAGATTGTCT | 4690 |
rs776572041 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136869810 | CATTTATTTTTTGGT[C/T]GTTAATAGTTGCTTT | 4690 |
rs776623359 | in-del | -/TT | | | intron-variant | NCK1 | GRCh38.p7 | 3:136864763 | GTTTTTTTCTTTTCT[-/TT]TTTTTTTTTTTTTTT | 4690 |
rs776667877 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136898321 | AGAATCACTTGAACC[C/T]GGGAGGCGGAGGTTC | 4690 |
rs776700361 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136880930 | ACTCTTGATCCCTTC[A/G]TTCTTAAAGTACACT | 4690 |
rs776726116 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136889509 | TTGCAAAGAGCGAAA[G/T]AACAAAGCTTCCACA | 4690 |
rs776762628 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136927028 | CAGGCCTGGAGTGCA[A/G]TGGCACGATCTTGGC | 4690 |
rs776789808 | snp | A/C | | | intron-variant | NCK1 | GRCh38.p7 | 3:136915063 | ACCAGATGAAGATGC[A/C]CAATCTTGAACTTTC | 4690 |
rs776810119 | in-del | -/A | 2.55647e-05 | 0.00357515 | intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136948221 | TGATAGAGGGCTTTC[-/A]AAATGTTTACTATAT | 4690 |
rs776815486 | snp | C/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136913599 | TGTTGTAGGCTATCT[C/G]AGATCTTTTCTGAGC | 4690 |
rs776843788 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136935315 | TTTTACCATACAAAA[C/T]TGTGCAAATTCTGAA | 4690 |
rs776877968 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136907632 | TGCTTCTCGTCACCA[C/T]CCTGCTGAATTCCAG | 4690 |
rs776928160 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136941453 | CTAATATATTGTTTT[A/G]TTACCCTTCTTGTTT | 4690 |
rs777018926 | snp | A/G | 1.65187e-05 | 0.00287386 | missense, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136948383 | AAGAACTTGTAGAAC[A/G]TTACAAAAAGGCACC | 4690 |
rs777032717 | snp | C/G | | | downstream-variant-500B, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136951864 | TTTCAGCAGCTACTA[C/G]GTAAAACTGGTCTTA | 4690 |
rs777069160 | in-del | -/A | | | intron-variant | NCK1 | GRCh38.p7 | 3:136922512 | GGAGTTGGAGTCATT[-/A]ATTCTAGGATATGGG | 4690 |
rs777117080 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136902614 | ATCTATCCTGGAGAA[C/T]GTTCTATATGCTGAT | 4690 |
rs777123597 | snp | A/C | 1.64735e-05 | 0.00286993 | missense, downstream-variant-500B | NCK1, LOC107986136 | GRCh38.p7 | 3:136945855 | GAAGAAGGTGACAGT[A/C]CTTTGGGTGACCATG | 4690 |
rs777158338 | in-del | -/GTA | | | intron-variant | NCK1 | GRCh38.p7 | 3:136901604 | CCTGATTCAATCTTG[-/GTA]GATTGTATATGTCTA | 4690 |
rs777178492 | snp | A/C | | | utr-variant-5-prime, intron-variant, upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136862336 | TGAGCTGGAGCTGCC[A/C]GGCTCGGCAGCGGGA | 4690 |
rs777181101 | in-del | -/TC | | | intron-variant | NCK1 | GRCh38.p7 | 3:136867178 | CCTTCCTTCCTTCCT[-/TC]TCTTTCTTTCTTTTC | 4690 |
rs777195858 | in-del | -/TTA | | | intron-variant | NCK1 | GRCh38.p7 | 3:136926266 | ATTTTATTTTAAATT[-/TTA]TTATTATTATTATTA | 4690 |
rs777196674 | snp | C/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136904560 | TATAAGTGACTAGAT[C/G]CTTTTCTTGCCATTT | 4690 |
rs777240404 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136930757 | GATATATCCAAAAAT[C/T]GTAGTTTCGACTTGG | 4690 |
rs777250828 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136868221 | ATGCCCAGCCTTACA[C/T]TGTAAATTATTTAAA | 4690 |
rs777267688 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136890522 | AGGAGGTGCCAAGAG[C/T]GAGCGAGGGCTTTGA | 4690 |
rs777283783 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136931936 | ACCAGCCTGGTCAAC[A/G]TGGTGAAACACTGTC | 4690 |
rs777289285 | snp | A/G | | | upstream-variant-2KB, intron-variant | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136861340 | GCTAAAAATACAAAA[A/G]CATTAGCTGGGCGTG | 4690 |
rs777296022 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136866421 | CAAGCGATTCTCCTA[C/T]CTCAGCCTCCCTAGT | 4690 |
rs777366673 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136915592 | TGCTCTCACGTTGCT[A/G]TAAATAACTACTTGA | 4690 |
rs777371332 | snp | A/G | 0.000197668 | 0.00993955 | synonymous-codon, downstream-variant-500B | NCK1, LOC107986136 | GRCh38.p7 | 3:136945722 | CATGGCTGAGAGAGA[A/G]GATGAATTATCATTG | 4690 |
rs777388707 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136903461 | TGGAGTTTTGCTCTT[A/G]TTGCCCAGACTGGAG | 4690 |
rs777419925 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136916630 | TCTCTGTGTTAGTTT[A/G]TGTATGTTGTTTTGG | 4690 |
rs777536280 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136877673 | AGAATAAAGAAAAGA[C/T]GGCAACAATAAAATC | 4690 |
rs777547782 | in-del | -/CCTTCCTT | | | intron-variant | NCK1 | GRCh38.p7 | 3:136867203 | CTTTTCTTTCTTTTC[-/CCTTCCTT]CCTTCCTTCCTTCCG | 4690 |
rs777568480 | in-del | -/AAAC | | | intron-variant | NCK1 | GRCh38.p7 | 3:136878411 | GGGATTCTGTCTCAA[-/AAAC]AAACAAACAAATGTG | 4690 |
rs777580097 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136884419 | TAGCTTAATGAGAAT[A/G]ATAGAGTACAGCTTT | 4690 |
rs777593362 | snp | A/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136891391 | CTACCCGCCTCAGCC[A/T]CCCAAAGTGCTGGGA | 4690 |
rs777621447 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136906329 | TGCCCAGGCTGGTCT[C/T]GAACTCCTGAGCTCA | 4690 |
rs777663902 | snp | A/G | | | downstream-variant-500B, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136951946 | TGGAGCAGCTGCTAT[A/G]TCCTTCATGTACTTT | 4690 |
rs777685775 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136911368 | ATTTAATTTACATCC[C/T]CACCAGCAATGTACA | 4690 |
rs777735558 | snp | A/G | 1.6577e-05 | 0.00287893 | synonymous-codon, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136948303 | ACAAGGGAAAAACAA[A/G]CATTTTAAAGTCCAA | 4690 |
rs777766019 | snp | A/G | | | upstream-variant-2KB, nc-transcript-variant | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136861967 | CCAACCAGAGCAGCC[A/G]CAGAGGGAAAAGCTA | 4690 |
rs777784341 | snp | C/G | 0.000112137 | 0.00748705 | intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136946335 | ACAAATAGAGCTCTG[C/G]GTATTTTAAAAAAAA | 4690 |
rs777824563 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136888100 | CAGGCGTCTGCCAGC[A/G]CGCCTGGCTAATTTT | 4690 |
rs777865238 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136921161 | CCATCTATTTCCAGA[A/G]TAATCTTCATCTTGC | 4690 |
rs777921581 | in-del | -/AGAGAGCTGTGGCAGTGTTGC | 1.79522e-05 | 0.00299596 | intron-variant, nc-transcript-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136946318 | ATTTTCGGAGGTAAA[-/AGAGAGCTGTGGCAGTGTTGC]TACAAATAGAGCTCT | 4690 |
rs777928916 | snp | A/G | 1.85479e-05 | 0.00304526 | intron-variant, downstream-variant-500B | NCK1, LOC107986136 | GRCh38.p7 | 3:136945572 | CTCATGGCCCTTTTT[A/G]ATTTCAACAGGCATT | 4690 |
rs777996754 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136943814 | GAGGAGCCTAGACAG[A/G]GGTAAACAAGAATAT | 4690 |
rs778052253 | snp | C/T | | | upstream-variant-2KB, intron-variant | NCK1 | GRCh38.p7 | 3:136929528 | CAATGGAAGACAAAT[C/T]AGAAAGAGATTTTCC | 4690 |
rs778077248 | snp | A/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136887255 | GCTGTGTGGCCTCCA[A/T]CTCTTGGCCTCAAAC | 4690 |
rs778106556 | in-del | -/GGGTAACA | | | intron-variant | NCK1 | GRCh38.p7 | 3:136872098 | AGCAACTTTGGAACT[-/GGGTAACA]GGCAGAGGTTGGAAC | 4690 |
rs778189290 | in-del | -/TACTTT | | | intron-variant | NCK1 | GRCh38.p7 | 3:136865435 | ATTTTCATTGCTTTG[-/TACTTT]TACTTTGTCTTATTT | 4690 |
rs778198006 | snp | C/T | 1.64792e-05 | 0.00287042 | stop-gained | NCK1 | GRCh38.p7 | 3:136928119 | TCTAAGTCCTGGTGG[C/T]GAGTTCGAAATTCCA | 4690 |
rs778206394 | snp | A/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136920939 | AAAACAAATGTTATG[A/T]ACTGAATTTTGTCCC | 4690 |
rs778254847 | in-del | -/TCTC | | | intron-variant | NCK1 | GRCh38.p7 | 3:136940267 | TGTTTGATGGGATAT[-/TCTC]TCTCTATATGTCTAT | 4690 |
rs778345470 | snp | C/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136882704 | GGGGAAGTGTGTGTG[C/G]AGAAAGATTTTAGGG | 4690 |
rs778373683 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136908643 | CTGCGACTGATTACT[G/T]CCAATGTGGTGACAT | 4690 |
rs778374935 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136905146 | GCCTCCGAAGTAGCT[A/G]GGACTACAGGTGCCT | 4690 |
rs778392141 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136896922 | TTCCTATGGATAACT[A/G]CCCAGTAGTGGGATT | 4690 |
rs778397802 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136865782 | GATTTAAGGAAACTT[C/T]ATGTCTGGCTGATCC | 4690 |
rs778402560 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136896106 | GTATTTGGGATATCT[A/G]TCACCTTGAGTATTT | 4690 |
rs778419590 | snp | A/G | 3.29527e-05 | 0.00405898 | missense, nc-transcript-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136945990 | GAAGAACTTAATTTC[A/G]AGAAAGGAGATGTAA | 4690 |
rs778458420 | snp | C/G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136915555 | GGGAGGCATGATAAA[C/G/T]TTTAATAGGGCTGTA | 4690 |
rs778471370 | snp | C/T | | | intron-variant, upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136863343 | CTATAACGATTTCTT[C/T]AGCACCTGGAAACCA | 4690 |
rs778474804 | snp | A/T | 1.64732e-05 | 0.0028699 | missense, downstream-variant-500B | NCK1, LOC107986136 | GRCh38.p7 | 3:136945868 | GTCCTTTGGGTGACC[A/T]TGTGGGTTCTCTGTC | 4690 |
rs778519115 | in-del | -/CTA | | | intron-variant | NCK1 | GRCh38.p7 | 3:136910222 | GTGTCTATTCAGTAG[-/CTA]CTTTTTGTAGTTACC | 4690 |
rs778540986 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136924419 | AATAAATGACATAGA[A/G]TGGGGAAAGAGAACA | 4690 |
rs778546573 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136914243 | GGAGGACAGGTCTTA[C/T]TGCCCGAAAGCTGTG | 4690 |
rs778596327 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136882464 | CCAGAGAAATGTTTT[C/T]AAGATTTCTGCATTA | 4690 |
rs778603330 | snp | C/T | | | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136951593 | AATAAAGTCTTCTTT[C/T]AAGTCAAAATATAGA | 4690 |
rs778663268 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136936321 | GCTGGGATTACAGAC[A/G]TGAGCCACTGTGCCC | 4690 |
rs778693151 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136936801 | CAATCTTTATTCAAG[C/T]CCTTTGCCCATTTTT | 4690 |
rs778716957 | in-del | -/C | 1.65754e-05 | 0.00287879 | | | GRCh38.p7 | 3:136946337 | AATAGAGCTCTGGGT[-/C]ATTTTAAAAAAAAGA | 4690 |
rs778725829 | snp | A/T | | | | | GRCh38.p7 | 3:136896002 | TTCTCCTTTCCTGTT[A/T]TTTGTTTTTTATTGA | 4690 |
rs778741244 | snp | A/G | | | | | GRCh38.p7 | 3:136903303 | CTGTTTGCATGGAAT[A/G]TCTTTTTCCATCCCT | 4690 |
rs778823142 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136923124 | GTGTGTGTGTGTGCG[C/T]GCCTGTGTGCATGTG | 4690 |
rs778866578 | snp | A/G | 3.29712e-05 | 0.00406011 | synonymous-codon | NCK1 | GRCh38.p7 | 3:136928061 | CCAACAAGAACAAGA[A/G]TTGGACATCAAGAAG | 4690 |
rs778894535 | snp | A/C | 1.91382e-05 | 0.00309334 | intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136946344 | GCTCTGGGTATTTTA[A/C]AAAAAAGAGAGAGAG | 4690 |
rs778914567 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136919377 | AAAATATATGGCCCT[A/G]TTTTTATCCATCTAT | 4690 |
rs778958338 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136879405 | AATGAAAGAAAATAG[A/G]TATACGCTTTCAATT | 4690 |
rs778978028 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136900316 | TGTCTGTCTTATACC[A/G]GTACCATGCTGTTTT | 4690 |
rs778997826 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136937246 | ATTGAGTGATCTTGG[C/T]ACCATTGATGAAAAT | 4690 |
rs779031906 | snp | C/T | 3.30595e-05 | 0.00406554 | synonymous-codon, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136948336 | AAAAGAGACTGTCTA[C/T]TGCATTGGGCAGCGT | 4690 |
rs779105305 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136934171 | TTTTACACACCACCA[C/T]TGTACAAACAAGGAT | 4690 |
rs779160872 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136869069 | ATGGTGAAACCCCAT[C/T]TCTACTAAAGATATA | 4690 |
rs779193394 | snp | A/C | | | intron-variant | NCK1 | GRCh38.p7 | 3:136942850 | TTGCAAAAACCACCC[A/C]GGAAGACTCCCTATG | 4690 |
rs779210282 | snp | A/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136897255 | CACCATGCTCGGCTA[A/T]TTTTTTGTATTTTTA | 4690 |
rs779222892 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136899009 | TAAACACAAATCAAA[G/T]ATAAACACCCTTGTA | 4690 |
rs779277788 | snp | C/T | | | intron-variant, upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136863629 | TGTGATCTGTGGAAA[C/T]TGGCTGTAATATCCA | 4690 |
rs779280861 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136916154 | CCTCCAGTCACCTGG[A/G]GATTACAATTCGACA | 4690 |
rs779298865 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136926814 | GTAGGATATCAGTTA[C/T]GTGAACATTGAGACA | 4690 |
rs779317785 | in-del | -/TTT | | | intron-variant | NCK1 | GRCh38.p7 | 3:136939842 | ATTTATTGAGGCCTT[-/TTT]TTTTTTTTTTTTTTT | 4690 |
rs779327251 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136941237 | TTCAAGCGACACTTA[C/T]ATGTCAGCCTCTCGA | 4690 |
rs779338702 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136895011 | CTCCCAAGTAGCTGG[A/G]ATTACAGGCATGTGC | 4690 |
rs779358036 | snp | A/G | 1.75256e-05 | 0.00296015 | missense, downstream-variant-500B | NCK1, LOC107986136 | GRCh38.p7 | 3:136945588 | ATTTCAACAGGCATT[A/G]GAAAAGTGAAAAGAA | 4690 |
rs779368105 | snp | A/C | | | intron-variant | NCK1 | GRCh38.p7 | 3:136885957 | TAGGAGTTTTCTGAT[A/C]TGAACGTGTACAAAA | 4690 |
rs779405443 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136872173 | AAAGTTTGGAACTTT[C/T]TAGACTTGTTGAATG | 4690 |
rs779544541 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136907274 | CCCTGTGGAGCAGCT[A/G]TAGGTGGAGAATGTC | 4690 |
rs779555216 | in-del | -/TTG | | | intron-variant | NCK1 | GRCh38.p7 | 3:136900216 | CAGAAGCCTTTTTTG[-/TTG]TTGTTGTTGTTGTTT | 4690 |
rs779597675 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136906392 | TAGGATTACAGGTAT[A/G]AGCCACCATGCCTGG | 4690 |
rs779598851 | snp | C/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136881338 | AGTTCTTCTTCCTCA[C/G]CCTCCTTAGTAGCTG | 4690 |
rs779631566 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136941016 | CTATTTACATTTAAA[G/T]TTATATCTGATAAGG | 4690 |
rs779650513 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136879175 | TAGAAAAGTTGAAGT[C/T]AGAGTAAAGGAGTTC | 4690 |
rs779672104 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136913156 | TCTTTCATATAGGCC[A/G]TACTTTCCCATTTCT | 4690 |
rs779711224 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136934697 | GGAAGCATTTGGTTT[C/T]CTGTTCCTGTGTTAG | 4690 |
rs779727952 | in-del | -/TTT | | | intron-variant | NCK1 | GRCh38.p7 | 3:136912493 | GACTTTTCTTCAGTC[-/TTT]TTTTTTTTTTTATGT | 4690 |
rs779755769 | in-del | -/GTTA | | | intron-variant | NCK1 | GRCh38.p7 | 3:136916622 | GTCAGTGTTCTCTGT[-/GTTA]GTTTGTGTATGTTGT | 4690 |
rs779922033 | snp | A/G | 1.65184e-05 | 0.00287384 | missense | NCK1 | GRCh38.p7 | 3:136928191 | AAAAACAGTGCTCGG[A/G]AAGCATCTATTGTGA | 4690 |
rs779933909 | snp | A/G | | | upstream-variant-2KB, intron-variant | NCK1 | GRCh38.p7 | 3:136929666 | TTCTGTCAAGAAAGT[A/G]TGCCTCATAGTGATA | 4690 |
rs779973523 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136865503 | GGTATATTTGATGTG[A/G]TTATTATAAATCACT | 4690 |
rs780075424 | snp | C/G | 1.65206e-05 | 0.00287403 | missense, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136948348 | CTACTGCATTGGGCA[C/G]CGTAAATTCAGCACC | 4690 |
rs780136771 | snp | A/G | 1.74781e-05 | 0.00295614 | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136948501 | GTAATTTGTCATGTA[A/G]TTGAAGACTGAGAAA | 4690 |
rs780159643 | snp | C/T | 1.64817e-05 | 0.00287064 | missense | NCK1 | GRCh38.p7 | 3:136928089 | AAGAATGAGAGATTA[C/T]GGCTTCTGGATGATT | 4690 |
rs780196268 | in-del | -/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136932215 | TCTTTTTGCTGAGTC[-/T]TAGGAAGTTGATAGT | 4690 |
rs780215846 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136910137 | CCTTACAGCTTTCTT[G/T]TCACTCATTTGCTGC | 4690 |
rs780228354 | snp | A/G | | | intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136947057 | TGGCTTTGCGTGAGT[A/G]TATTTGTACAAAAGG | 4690 |
rs780235746 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136897817 | TAATATGATTTGAAA[A/G]TTTTTTATAAAAATT | 4690 |
rs780328303 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136931326 | TTTGCTTGGTGTTTC[C/T]AGAAAAATGAACAGA | 4690 |
rs780348158 | in-del | -/A | | | intron-variant | NCK1 | GRCh38.p7 | 3:136887505 | AAGAAGTTGAGAGAT[-/A]AAAGTTTATATTTTC | 4690 |
rs780439959 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136939409 | TATTTTCAAATAACC[A/G]CATTTTGGTTTTGTT | 4690 |
rs780476942 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136888475 | TGGCAAAATCTTGGC[G/T]GACTGCAACCTCTGC | 4690 |
rs780572361 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136871225 | ATATAGCAAGAGCCG[A/G]CCTTTACAAAAGTAA | 4690 |
rs780585889 | snp | A/C | 1.64738e-05 | 0.00286995 | missense, downstream-variant-500B | NCK1, LOC107986136 | GRCh38.p7 | 3:136945842 | AAACTATGTAACTGA[A/C]GAAGGTGACAGTCCT | 4690 |
rs780599468 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136916430 | TATTCATGAGGTATC[C/T]ACTCCCACAACCCAA | 4690 |
rs780640959 | snp | C/T | 1.64743e-05 | 0.00287 | missense, downstream-variant-500B | NCK1, LOC107986136 | GRCh38.p7 | 3:136945705 | TATGTGAAATTTAAC[C/T]ACATGGCTGAGAGAG | 4690 |
rs780665498 | snp | A/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136917384 | CAGGCCTGGCCTGGT[A/T]CCTATTCTCATTTTT | 4690 |
rs780671824 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136881908 | ATATATACCACATTT[C/T]GTTTATCCATTCATT | 4690 |
rs780739461 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136904664 | TTTACTGAGAGATCC[C/T]TGAACTTGGTGTATC | 4690 |
rs780754188 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136938924 | AGGATTTTTGCATCT[A/G]TATTTCTAAGTGATA | 4690 |
rs780764185 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136913762 | CAAGCTCCGCCTCCC[A/G]GGTTCACGCCATTCT | 4690 |
rs780799701 | snp | C/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136891462 | CTTTGGTTGCTTCCA[C/G]TTTTTGGCTGTTGTG | 4690 |
rs780805287 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136924920 | GGAGCCCTTGATTTG[C/T]TCATTTTTGAGGGGT | 4690 |
rs780860184 | in-del | -/GAAAG | | | upstream-variant-2KB, intron-variant | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136860669 | GAGGACGCAAAAGAA[-/GAAAG]GAAGTGCGACGTTCT | 4690 |
rs780875184 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136906204 | TGTGAATGCTGTCAG[C/T]GGTGTCTGTGATTTC | 4690 |
rs780884242 | in-del | -/GCA | 1.72907e-05 | 0.00294025 | cds-indel, nc-transcript-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136946292 | CGTGATAGTGAATCT[-/GCA]TCGGTAAGTTGATTT | 4690 |
rs780924907 | snp | A/C | | | intron-variant | NCK1 | GRCh38.p7 | 3:136885658 | ATGGTGATATTAATA[A/C]TGATTGTATCAGTTT | 4690 |
rs780953338 | snp | A/C | | | intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136947349 | AACAAAACTAATTAA[A/C]AAGAAGATAGCTTGA | 4690 |
rs780973859 | in-del | -/GC | | | intron-variant | NCK1 | GRCh38.p7 | 3:136923280 | AGCTGTCCAGGCCGG[-/GC]GCGGTGGCTCACGCC | 4690 |
rs781000544 | snp | A/C | | | intron-variant | NCK1 | GRCh38.p7 | 3:136870873 | AGGTTAATCAGCATT[A/C]AGTTTGGCTACTAGT | 4690 |
rs781006157 | snp | C/T | | | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136948593 | AATAAGTATTTTTAT[C/T]ATAACTCAGCCCATA | 4690 |
rs781018015 | snp | C/T | 1.76561e-05 | 0.00297115 | intron-variant, nc-transcript-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136946309 | CGGTAAGTTGATTTT[C/T]GGAGGTAAATACAAA | 4690 |
rs781045285 | snp | A/C | | | intron-variant | NCK1 | GRCh38.p7 | 3:136902486 | AGGCGCGAGCTATCC[A/C]ACCTGGCCTATTATT | 4690 |
rs781045600 | in-del | -/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136882160 | GCATAAGAGTTCCAA[-/T]TATCATTACATTTTC | 4690 |
rs781066347 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136900584 | TCCATTTGTTTGTGC[C/T]CTCTTTATTTTATCT | 4690 |
rs781068447 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136896196 | AGTTTTGCTAGCTAT[A/G]GTCACCTTAGTCTGC | 4690 |
rs781124660 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136878936 | GGCTTCCAGAATTCT[G/T]GCAATCAAGTAGGAA | 4690 |
rs781238193 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136911899 | CTTTGGTAGTTAATT[A/G]GACTATTAGACTATA | 4690 |
rs781293100 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136913019 | TACATTGTTTTCTTG[C/T]CTTTCTCTGTGTCTT | 4690 |
rs781314654 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136909988 | AAAGTGAGTCTCTTA[C/T]GGATAGCATATATTT | 4690 |
rs781322778 | snp | A/G | 6.60491e-05 | 0.00574632 | missense | NCK1 | GRCh38.p7 | 3:136928099 | GATTATGGCTTCTGG[A/G]TGATTCTAAGTCCTG | 4690 |
rs781353217 | snp | C/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136922133 | TGAGTAGGCCATCTG[C/G]GTTTGTTATTGGCAT | 4690 |
rs781379715 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136908852 | ATATATACAGTATAG[C/T]GCTGTGGTTTGAATG | 4690 |
rs781422117 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136916897 | TGAGTGATCACTAAC[A/G]GCAGAGCAGTGGCTA | 4690 |
rs781429964 | in-del | -/AA | | | intron-variant | NCK1 | GRCh38.p7 | 3:136870688 | TTAGCTATAGTCTTT[-/AA]AAAAAAAAAAAAAAA | 4690 |
rs781466652 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136943908 | AGAGAGTGGGCTGTG[A/G]TCTTGGTTGCTGCAT | 4690 |
rs781468177 | snp | A/C | | | intron-variant | NCK1 | GRCh38.p7 | 3:136885409 | CTGGAGTACAGTGGC[A/C]TGATAACTCTTCAGC | 4690 |
rs781468189 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136916889 | ACAGGCCCTGAGTGA[C/T]CACTAACGGCAGAGC | 4690 |
rs781479841 | in-del | -/TC | | | intron-variant | NCK1 | GRCh38.p7 | 3:136867255 | GTCCGTCCGTCTGTC[-/TC]TCTCTCTCTCTTTCT | 4690 |
rs781493871 | snp | A/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136873276 | GAGACATGGAGTCAA[A/T]GGAGATCATTTTGGA | 4690 |
rs781546583 | in-del | -/CTT | | | cds-indel, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136951444 | CACATAAAATTCAGA[-/CTT]CTTGTTTCCCTTTAA | 4690 |
rs781565072 | snp | C/T | 1.6918e-05 | 0.00290839 | synonymous-codon, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136948270 | TTAGCCAAATGATTT[C/T]TCAGTATCACTAAAA | 4690 |
rs781567590 | in-del | -/TTG | | | intron-variant | NCK1 | GRCh38.p7 | 3:136900214 | GTGCAGAAGCCTTTT[-/TTG]TTGTTGTTGTTGTTT | 4690 |
rs781610950 | snp | A/T | | | intron-variant, upstream-variant-2KB | NCK1, NCK1-AS1 | GRCh38.p7 | 3:136863896 | CACGAGGTCAGGAGA[A/T]TGAAACCACCCTAGC | 4690 |
rs781705700 | snp | A/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136899180 | CCAGTGCGCTGCTGC[A/T]ATTGCTGCTACTTCC | 4690 |
rs781725742 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136916009 | GGGATTACAGGTGTG[A/G]GCCACTGGGCCCGGC | 4690 |
rs781746937 | snp | A/C | | | intron-variant | NCK1 | GRCh38.p7 | 3:136945308 | ATTTAGGACAACTTT[A/C]TAATTATGTTATATA | 4690 |
rs781754743 | snp | A/C | 1.64757e-05 | 0.00287012 | missense, downstream-variant-500B | NCK1, LOC107986136 | GRCh38.p7 | 3:136945973 | TCAGCTCATCTAATG[A/C]TGAAGAACTTAATTT | 4690 |
rs796095560 | in-del | -/TC | | | intron-variant | NCK1 | GRCh38.p7 | 3:136912167 | TTATTTTTTCTTTTT[-/TC]TTTTTTTTTTTTTGA | 4690 |
rs796115768 | in-del | -/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136878709 | ATCTCAATAAAGCTA[-/T]TTTTTTTTTAAGAAA | 4690 |
rs796193940 | in-del | -/AA | | | intron-variant | NCK1 | GRCh38.p7 | 3:136864496 | CCGTCACACACACAC[-/AA]AAAAAAAACAGAAAC | 4690 |
rs796247962 | in-del | -/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136904133 | ATCCTTGACTGACAG[-/T]TTTTTTTTCATTGAG | 4690 |
rs796259770 | in-del | -/TGTGTGTGTA | | | intron-variant | NCK1 | GRCh38.p7 | 3:136893171 | GTGTGTGTGTGTGTG[-/TGTGTGTGTA]TATATATATATACAC | 4690 |
rs796360177 | snp | A/G | | | intron-variant, downstream-variant-500B | NCK1, LOC107986136 | GRCh38.p7 | 3:136945508 | TGAAGATCTCTTTTT[A/G]ATAATGAATAAGTTC | 4690 |
rs796398989 | in-del | -/TTA | | | intron-variant | NCK1 | GRCh38.p7 | 3:136939861 | TTTTTTTTTTTTTTT[-/TTA]AAATAGAGACAGGGT | 4690 |
rs796480317 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136878667 | TTGTATACTTTAAAT[A/G]AGTGAGTTTTATGAT | 4690 |
rs796492815 | in-del | -/TC | | | intron-variant | NCK1 | GRCh38.p7 | 3:136867254 | CTGTCCGTCCGTCTG[-/TC]TCTCTCTCTCTTTCT | 4690 |
rs796540309 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136927258 | ATTACAGGTGTGTGC[C/T]ACCAGGCCTGGCCGT | 4690 |
rs796575591 | in-del | -/TA | | | utr-variant-3-prime, intron-variant | NCK1, LOC107986136 | GRCh38.p7 | 3:136949418 | TCCTCTTTTCAGCTT[-/TA]AGTTTTGTTGATTGG | 4690 |
rs796610623 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136874946 | GAAGACATTCTGATT[C/T]TTGATTGTAAAAATG | 4690 |
rs796673405 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136941099 | TCTATTACTGTCTTC[C/T]TTTGTGATTTCTTTT | 4690 |
rs796673649 | in-del | -/GA | | | upstream-variant-2KB, intron-variant | NCK1 | GRCh38.p7 | 3:136928788 | GGGCCTGAGACAGTG[-/GA]GCCCACTTCACACTG | 4690 |
rs796724472 | in-del | -/TT | | | intron-variant | NCK1 | GRCh38.p7 | 3:136867266 | CTGTCTCTCTCTCTC[-/TT]TCTTTCTTTCTTCTT | 4690 |
rs796774979 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136912162 | TAGCTATTATTTTTT[C/T]TTTTTTTTTTTTTTT | 4690 |
rs796798023 | in-del | -/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136900705 | GGTTTTGTATGTTGA[-/T]TTTTTTTTAACACTC | 4690 |
rs796840698 | snp | C/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136925339 | TTTATTTTAATTAAA[C/G]TTTTTATTTTGAGAT | 4690 |
rs796859151 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136865145 | GTATTTTTAGTAGAG[A/G]CAGGGTTTCACCATC | 4690 |
rs796866284 | snp | G/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136864117 | AAAAAATAAATAAAA[G/T]GTGTATTTATTTTTC | 4690 |
rs796940444 | snp | A/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136864620 | CGGGAGGATAGCTGG[A/G]GGCCAGGAGTTTGAG | 4690 |
rs796951962 | snp | C/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136870149 | GAGTTCGAGACCAGC[C/T]TGGCCAACATGGTGA | 4690 |
rs796953904 | snp | A/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136893147 | TAAGTAATATTCCAT[A/T]GTGTGTGTGTGTGTG | 4690 |
rs796982460 | in-del | -/T | | | intron-variant | NCK1 | GRCh38.p7 | 3:136905987 | TGGCGGTGTCATATT[-/T]CCTTGCTTTTTCATG | 4690 |
rs797002813 | snp | C/G | | | intron-variant | NCK1 | GRCh38.p7 | 3:136920061 | TAAGTAATGCAAAAA[C/G]ACAAGGCAATTCATA | 4690 |