SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs536876904 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NUB1 | GRCh38.p7 | 7:151350639 | TACAAACTAATAATG[A/G]TATTCATATATAATC | 51667 |
rs536903608 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151357127 | GCTTGAGCGATCCTC[C/T]CGCCTCCGCCTTCTG | 51667 |
rs537072572 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151349503 | TTTCTAGCGTGTGAA[C/T]GTTGAGAAATAATGG | 51667 |
rs537143153 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NUB1 | GRCh38.p7 | 7:151344880 | TGGCGCATGCCTGTA[A/G]TCCCAGTGAGTAGGG | 51667 |
rs537181845 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NUB1 | GRCh38.p7 | 7:151344739 | GAATTTACAAGCTCA[C/T]GCCTGTAATCCCAGC | 51667 |
rs537189776 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NUB1 | GRCh38.p7 | 7:151370084 | AAAGGCAGAGACTTT[C/G]AAAAGCTGAGTTCTT | 51667 |
rs537230768 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151373172 | TCTGTTTTCTCCCCC[A/G]TCCTCGCTGCTGCTG | 51667 |
rs537266567 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NUB1 | GRCh38.p7 | 7:151358489 | CTCCTGTCAGATCAG[C/T]GGCGGCATTAGAGTC | 51667 |
rs537394922 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151372691 | GCCCTGAGTAGCAGA[A/G]TAAGGAGCTGGTGCC | 51667 |
rs537463863 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime | NUB1, WDR86 | GRCh38.p7 | 7:151378715 | GGTGAGCTGAGGTGA[C/T]GCGGAGTCTCAGCCT | 51667 |
rs537505945 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | NUB1 | GRCh38.p7 | 7:151344683 | TTAACTACCAGGATG[A/G]TTGGCCTTTTGTTTT | 51667 |
rs537522633 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151357116 | TAACCTCCTGGGCTT[A/G]AGCGATCCTCCCGCC | 51667 |
rs537809591 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NUB1 | GRCh38.p7 | 7:151345218 | GAGCTCATTTAAACC[A/G]TAGTAATTTATATTT | 51667 |
rs537819378 | in-del | -/GCGGCG | 0.0185938 | 0.0946107 | upstream-variant-2KB, utr-variant-5-prime | NUB1 | GRCh38.p7 | 7:151341711 | CAACCCTCTTTCCAA[-/GCGGCG]GCGGCGGCGGCGGCG | 51667 |
rs537904893 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151359021 | AGTGAGCCGAGATCG[C/T]GCCACTGCACTCCAG | 51667 |
rs537999532 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151374878 | CAAACTCAGAGCACA[C/T]GTGGTGAGGGGTCCC | 51667 |
rs538050985 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151374429 | GGCCACGTGAGGCCC[A/C]ATGCTCAGTGCTTGG | 51667 |
rs538142210 | snp | C/T | | | upstream-variant-2KB | NUB1 | GRCh38.p7 | 7:151340286 | AGCAATCAACGGGCT[C/T]TTTCCTGATGTGCTA | 51667 |
rs538172592 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151346035 | ACAGTACTCATTTTT[A/G]CCAGAAATCTATCAT | 51667 |
rs538224048 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NUB1 | GRCh38.p7 | 7:151367300 | TTTTACAAATCTGGC[C/T]GTCTCTCTTACTTAG | 51667 |
rs538363705 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151376028 | AATCAGGCAGCAGGA[C/T]TGGGGGAGTCCGTGC | 51667 |
rs538399361 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151359698 | AGGAGAATCGCTTGA[A/G]CCCAGGAGGCAGAGG | 51667 |
rs538481853 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | NUB1 | GRCh38.p7 | 7:151372956 | CATGAGTCTACAGAT[A/G]TCTTCATCCCTGGAG | 51667 |
rs538590856 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | NUB1 | GRCh38.p7 | 7:151344921 | AGGGGAATTGCTTGA[A/C]CCCAGGGGGCGGAGC | 51667 |
rs538626889 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151358402 | AGATGGGTACCAGTC[C/T]GTGGCTTGTTAGGAA | 51667 |
rs538677937 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151365024 | AGAGACAGAGTCTCT[A/G]TGTTGTTCAGGCTGG | 51667 |
rs538691609 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151357870 | CCACCTCGGCCTCCC[A/G]AAGTGCTGGGATTAC | 51667 |
rs538719638 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151362189 | CATGTCCGGTAAGTG[A/G]TAGGTATAATAATGA | 51667 |
rs538840081 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151353101 | GAAGAAAGACACTCA[C/T]TACAGCTTAGATAAA | 51667 |
rs538899771 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151352426 | TAAAAGAGCTATCAT[G/T]ATTAAAGCCTTCTTT | 51667 |
rs539015076 | snp | A/G | 0.00767938 | 0.0614875 | intron-variant | NUB1 | GRCh38.p7 | 7:151374354 | CCTATGGGCTGCCCC[A/G]TCATCCGGATCTGAA | 51667 |
rs539042421 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | NUB1 | GRCh38.p7 | 7:151366553 | AGAAAGAACGTTGCT[C/G]TGGCCCAGGTGATGC | 51667 |
rs539058324 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | NUB1, WDR86 | GRCh38.p7 | 7:151377758 | TGCTGTGGGGCATAA[C/T]GATGAGGCGCTGGCC | 51667 |
rs539178322 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NUB1 | GRCh38.p7 | 7:151373601 | CCAGGCTGTGGGGGG[C/T]GGGTCACCAGCTTTG | 51667 |
rs539181604 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NUB1 | GRCh38.p7 | 7:151346781 | TAATGAACTATATTC[A/G]TAAGTATACCATTTT | 51667 |
rs539226134 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151368388 | GCATGCCATTGACTT[C/T]GACTTCACTACCTGG | 51667 |
rs539265498 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151369109 | GCCTCCCGGGTTCAA[A/G]CAATTCTCGTGCCTC | 51667 |
rs539274499 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151359657 | TGGCTCATGCCTGTA[A/G]TCCTAGCTGCTCGGC | 51667 |
rs539814003 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151348774 | GTTATGGGGTTTCAC[C/T]ATGTTGGCCAGGCTG | 51667 |
rs539876276 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NUB1 | GRCh38.p7 | 7:151354686 | ACTGAGTCCTAGAAG[A/G]TAGGTAGTTTATTCA | 51667 |
rs540048699 | snp | C/T | 3.57213e-05 | 0.00422604 | missense | NUB1 | GRCh38.p7 | 7:151376755 | TGCCTCCCGAGCTGC[C/T]GCTGTCGCCAGAAGA | 51667 |
rs540104141 | snp | C/T | 6.70657e-05 | 0.00579037 | intron-variant | NUB1 | GRCh38.p7 | 7:151349272 | AATTTGAGTAGGCAC[C/T]AATGTCCAGTTAGTG | 51667 |
rs540132216 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NUB1 | GRCh38.p7 | 7:151343515 | TTCCACTCTCTAGAA[C/T]TTGTCTTCATCATTC | 51667 |
rs540239148 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NUB1 | GRCh38.p7 | 7:151347172 | ATACAAAAATATAAA[C/G]AATGTATTTTTAAAA | 51667 |
rs540406081 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151359293 | AATACAAAAAAAAAA[A/G]TTAGCCAGGCGTGGT | 51667 |
rs540442909 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151359734 | GTGACCCGAGATCGC[A/G]CCACTGCCCTCCAGC | 51667 |
rs540521009 | in-del | -/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151373340 | AGCAGCAAAATCCCC[-/T]TTTTAAATGACATTT | 51667 |
rs540584760 | in-del | -/C | 0.00159617 | 0.0282053 | intron-variant | NUB1 | GRCh38.p7 | 7:151368261 | CCAGCCTCAGCGAGG[-/C]CGTCCTAGGTTGCTC | 51667 |
rs540641319 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NUB1 | GRCh38.p7 | 7:151354934 | ATTTTCTGTGGAGAC[A/G]GGGTCCACTGTGTTG | 51667 |
rs540807053 | snp | C/T | 1.73132e-05 | 0.00294216 | intron-variant | NUB1 | GRCh38.p7 | 7:151368688 | ACTTTGTATTAAGCT[C/T]TAAGTATTGCCGTGG | 51667 |
rs540840001 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151343230 | TGGAGGATTCTCCCA[C/T]GGGCCACCCAGGTTG | 51667 |
rs540879088 | snp | A/G | 3.94089e-05 | 0.00443879 | missense | NUB1 | GRCh38.p7 | 7:151355852 | AAGAGGACGCGAGGA[A/G]AAACTTCCAGTTAGA | 51667 |
rs541035315 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151361658 | TAATACTGTATACTC[A/C]CAGAAGATGAATGCA | 51667 |
rs541363895 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151347965 | ATGCAGATACAGATT[A/G]AGAGGAGTATCCCGT | 51667 |
rs541398116 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151367583 | ACCTGGTTTGGATTT[C/T]TGCATACTTCTCTGC | 51667 |
rs541437098 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151368442 | TGAGAAATGCCACGT[A/G]CACAGCTGAAATTCG | 51667 |
rs541437206 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151360497 | ACATGTGCTATGTTG[C/T]TAGTCGGAACTTTCC | 51667 |
rs541462596 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151372770 | ACTGGAATGACGGAG[A/C]CTGCTGCCCTGTGCA | 51667 |
rs541593174 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NUB1 | GRCh38.p7 | 7:151363458 | GAGAAAAGGCTAAAA[A/G]AAAAAAAAAATGAAC | 51667 |
rs541616721 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151356883 | CCACCACGGATGGCT[A/G]ATTTTGTATTTTTAG | 51667 |
rs541645146 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NUB1 | GRCh38.p7 | 7:151354805 | CTGGAGTGTGGTGTG[C/T]GATTGCAGCTCACTG | 51667 |
rs541661123 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151357376 | TGATCCGCCCGCCTC[A/G]GCCTCCCGAAGTTCT | 51667 |
rs541786679 | snp | A/G | | | missense | NUB1 | GRCh38.p7 | 7:151368780 | GATCCATCAAAAGTG[A/G]ACAATTTGTTGCAGT | 51667 |
rs541860975 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151376562 | GAGAGTCGGCTGTCC[A/G]CTCGTATGGCTGACG | 51667 |
rs542056043 | in-del | -/G | 0.00159617 | 0.0282053 | intron-variant | NUB1 | GRCh38.p7 | 7:151365760 | GAAATTAGAAATGTT[-/G]AGAGAGATGAAAATA | 51667 |
rs542198573 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151369649 | TCCAATATGTTCTGC[A/G]GTGAAAGAACTGAGG | 51667 |
rs542201322 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151349504 | TTCTAGCGTGTGAAC[A/G]TTGAGAAATAATGGG | 51667 |
rs542235287 | snp | C/G/T | 0.00239401 | 0.0345304 | intron-variant | NUB1 | GRCh38.p7 | 7:151343907 | AATAGTAGGGCCAGG[C/G/T]GCGGTGGCTCAGGCC | 51667 |
rs542245480 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151349726 | GTGGCAAGGCACCCA[A/G]AGCCTCTTGGGACTG | 51667 |
rs542349389 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NUB1 | GRCh38.p7 | 7:151348827 | TGATGCGCCTGCCTC[A/G]GCCTCCCAAAGTGCT | 51667 |
rs542381890 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NUB1 | GRCh38.p7 | 7:151370336 | TCAAGTGATCCTCCC[A/G]CCTTGGCCTCCCAAA | 51667 |
rs542417975 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NUB1 | GRCh38.p7 | 7:151361922 | GGTAAATTTTTCATT[C/T]CCTTCCATAGTTGTT | 51667 |
rs542425467 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | NUB1, WDR86 | GRCh38.p7 | 7:151377699 | GGGTTCCTGTGCCAC[C/G]CTTTCCCCGCCCCTC | 51667 |
rs542460022 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151371789 | TGCTCTCTTGTCCAG[A/G]CTGGAGGGCAGTGGC | 51667 |
rs542517462 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | NUB1, WDR86 | GRCh38.p7 | 7:151378153 | GGCTCCAGCAGTAAC[C/T]GTCCTCACTGCGCCA | 51667 |
rs542625131 | snp | A/C | | | intron-variant | NUB1 | GRCh38.p7 | 7:151344882 | GCGCATGCCTGTAAT[A/C]CCAGTGAGTAGGGAG | 51667 |
rs542625417 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151357967 | GAGTTATCAGTAGAT[G/T]GATGTTTGTCTTTTT | 51667 |
rs542631776 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151350076 | TAGACGAGGCGGAGA[A/G]AGAGGACAGCTTACG | 51667 |
rs542688541 | snp | A/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151343872 | TCAGCTGTAAAATGA[A/T]CCGATCAGTGTTAGA | 51667 |
rs542792425 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NUB1 | GRCh38.p7 | 7:151356808 | CTGCAACCTCCGCCT[C/T]CTGGGTTCAAGTGAT | 51667 |
rs542864397 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151358549 | GCATGTGAGGGATCT[A/G]GGCTGTGCACTCCTG | 51667 |
rs542928310 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NUB1 | GRCh38.p7 | 7:151359492 | CCCTTTTTAAAGATA[C/G]AAGCAGCCGGGCACC | 51667 |
rs542982376 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151357997 | TTTGTGTGTGTGTGA[A/G]GCGGAGTCTCGCTCT | 51667 |
rs543034081 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151348960 | TGGACTGCAGTGTAA[C/T]GGGGCGACCTCCACT | 51667 |
rs543194807 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151352040 | TCCAGGGCTAGCTAG[C/T]GGGTGTATTTCTTCA | 51667 |
rs543198795 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NUB1 | GRCh38.p7 | 7:151361739 | GTCCCAACTTTAACG[C/T]ACACAAAAAAGGAAT | 51667 |
rs543219864 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151343825 | TTGTGTCTTTGCCTG[A/C]GTCATGGTACAAACT | 51667 |
rs543267103 | snp | A/G | | | downstream-variant-500B, utr-variant-3-prime | NUB1, WDR86 | GRCh38.p7 | 7:151378586 | GATGATGGAAGGATG[A/G]TCTCAGAAGCAGAGG | 51667 |
rs543270916 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151349628 | CAGTCCGCTGAGTGC[C/T]CTCAAGCAGGGCCGA | 51667 |
rs543419661 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151363683 | AAAAACTACACTACA[A/G]CACACTATAATCCAA | 51667 |
rs543425159 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151356751 | AGACGGAGTTTTGCT[C/T]TTGTTGCTCAGGCTG | 51667 |
rs543546687 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NUB1 | GRCh38.p7 | 7:151370664 | CGTCATTTAGCATTA[A/G]GTATATCTCCTAAAG | 51667 |
rs543598645 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | NUB1 | GRCh38.p7 | 7:151344987 | CCTGGGCGACAGAGC[A/G]AGACTCCGTCTCAAA | 51667 |
rs543665584 | snp | C/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151367799 | GAATGACAGAGATGA[C/G]TATTATAGACCTGTA | 51667 |
rs543806324 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NUB1 | GRCh38.p7 | 7:151357413 | ACAGGTGTGAGCCAC[A/T]GCACCCAGCCCCTTG | 51667 |
rs543818603 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | NUB1, WDR86 | GRCh38.p7 | 7:151378415 | TTAAACGGATGATAC[C/T]GATGGAAATAAAAGG | 51667 |
rs543980026 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151357905 | ATGAGCCACTGCGCC[C/T]GGCCGGATTAAAGTT | 51667 |
rs544001575 | snp | C/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151343967 | CGGGCGGATCACAAG[C/G]TCAGGAGATTGAGAC | 51667 |
rs544085812 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151358797 | GGGCCGGGCGCGGTG[G/T]CTCACGCCTGTAATC | 51667 |
rs544144806 | snp | A/G | | | utr-variant-3-prime | NUB1, WDR86 | GRCh38.p7 | 7:151378135 | TGTAGTTCGCTGTGT[A/G]TCGGCTCCAGCAGTA | 51667 |
rs544178654 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NUB1 | GRCh38.p7 | 7:151345681 | ATTTTTCAGGCATAT[A/G]TTTTTAATACCATCA | 51667 |
rs544232773 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151344931 | CTTGAACCCAGGGGG[C/T]GGAGCTTGCAGTGAG | 51667 |
rs544263058 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151359707 | GCTTGAACCCAGGAG[G/T]CAGAGGTTGCAGTGA | 51667 |
rs544363393 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151344864 | AATTAGCCGGGCGTG[A/G]TGGCGCATGCCTGTA | 51667 |
rs544366519 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | NUB1 | GRCh38.p7 | 7:151341436 | CGACCCTTCCCCCAG[A/C]CTCTTTCAAGGATTC | 51667 |
rs544369914 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NUB1 | GRCh38.p7 | 7:151362353 | AAAGGAAATCAGCAG[C/T]AATGTAAGCCAAATA | 51667 |
rs544394386 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NUB1 | GRCh38.p7 | 7:151373612 | GGGGCGGGTCACCAG[C/T]TTTGGCATTGCCCAG | 51667 |
rs544398063 | in-del | -/TCTT | 0.00159617 | 0.0282053 | intron-variant | NUB1 | GRCh38.p7 | 7:151366176 | TGACTTCTGTTGCTG[-/TCTT]TCTTCCCTTTGCTGC | 51667 |
rs544545204 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151346200 | GGTGACAAACTGTAT[A/T]AGGGTCCTAGTTCTT | 51667 |
rs544630685 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151349842 | AGAGATCGTAGAAAT[A/G]AACACACAAGACAAA | 51667 |
rs544721138 | in-del | -/TTATTTG | 0.00199481 | 0.0315187 | intron-variant | NUB1 | GRCh38.p7 | 7:151354474 | TTTTAGTTCACAATA[-/TTATTTG]TTATTTTAAAATCTG | 51667 |
rs544740211 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NUB1 | GRCh38.p7 | 7:151359166 | AAGTGAGGCCGGGCA[C/T]GGTGGCTCATGCCTG | 51667 |
rs545188057 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime | NUB1, WDR86 | GRCh38.p7 | 7:151378951 | TTCTGGGCATGCGCT[A/G]TGTCCAGAATGGGCT | 51667 |
rs545205607 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151345541 | ATTCTGAATTGTCAG[A/G]CATGACCATATAAAC | 51667 |
rs545228643 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NUB1 | GRCh38.p7 | 7:151372888 | GCAAAGGGAGCTGGC[A/G]CTGTGGGCACTCCAG | 51667 |
rs545246795 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151362051 | AAGACATGGTTGATC[C/T]TCATACATCTGTGTG | 51667 |
rs545250801 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | NUB1 | GRCh38.p7 | 7:151352620 | GCTAATTTTTAAAAA[A/T]TTTTTGTAGAGATAG | 51667 |
rs545339051 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151344975 | ACTGCACTCCAGCCT[A/G]GGCGACAGAGCGAGA | 51667 |
rs545349942 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | NUB1, WDR86 | GRCh38.p7 | 7:151378368 | TGTGGGTGGTCCAGT[G/T]TGGACTGATGGGAAT | 51667 |
rs545353192 | in-del | -/A | 0.00398564 | 0.0444627 | intron-variant | NUB1 | GRCh38.p7 | 7:151342151 | AATAAATATGTCTAT[-/A]AAAAATTAGCCAAAT | 51667 |
rs545365558 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NUB1 | GRCh38.p7 | 7:151374609 | TAATTGTTTGGCATT[A/G]AAATTTTAAATGTAA | 51667 |
rs545367337 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151358727 | TGCGAACATTTAAAT[G/T]GAAAAATCTAATGAA | 51667 |
rs545487922 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151350434 | TAACGAGGGCCTTTC[C/T]GGGCACTGGAGTTAC | 51667 |
rs545527220 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NUB1 | GRCh38.p7 | 7:151373834 | CGGATGGTGGATGGC[A/G]GGGCTGGCGAGGCAC | 51667 |
rs545554832 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | NUB1 | GRCh38.p7 | 7:151339981 | CACCCCTTGAAGGTT[C/T]CTCATTCTCTGGAAT | 51667 |
rs545612723 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | NUB1 | GRCh38.p7 | 7:151340737 | CAGATTGGTCTGGTG[C/T]GGTTATACAGTTATT | 51667 |
rs545659645 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151360425 | ATTTCTAATTGACCT[C/T]TCCTCCCTGTAAAGA | 51667 |
rs546038413 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151353874 | CCAGCGTCATCTCTA[G/T]CAATTTCCCATTGTC | 51667 |
rs546186044 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | NUB1 | GRCh38.p7 | 7:151341589 | CGGCCACATCCTCGC[C/T]CAGCCCCGCCTCCGC | 51667 |
rs546188462 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151342356 | CTAAGAAAAAATGAA[C/T]GTGTCTTGACTAGAT | 51667 |
rs546227092 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151347786 | TATAAAGTTTTCCAA[C/T]TTCACTTTTATCATG | 51667 |
rs546241978 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NUB1 | GRCh38.p7 | 7:151373020 | CTACTGTGGGGCCTG[G/T]GGAGTCTGGTTCCAC | 51667 |
rs546328958 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151350509 | GAGGGCTCACACTTG[C/T]CTTCTGGTCACTTCT | 51667 |
rs546388765 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151369005 | GGGAAGGAAGGAGAA[A/G]CTTGTCCTTTTTTTT | 51667 |
rs546427707 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151369473 | CATGAGGTCATTATT[A/G]AAGTTGGGGATTGCA | 51667 |
rs546451772 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151346684 | ACACCCCCAACTCCA[C/T]GGGACAGAGGCTTCT | 51667 |
rs546457610 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151373332 | TGTTTTTAAGCAGCA[A/C]AATCCCCTTTTTAAA | 51667 |
rs546521070 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151370935 | CATAAAACATTGTCA[C/T]ACTCATGTCATTCAC | 51667 |
rs546552199 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NUB1 | GRCh38.p7 | 7:151376092 | TGCCCACCTCAGAGG[A/C]CACCCACGCAGTAAC | 51667 |
rs546623568 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151358391 | CCACAGGCTGCAGAT[A/G/T]GGTACCAGTCCGTGG | 51667 |
rs546706577 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NUB1 | GRCh38.p7 | 7:151372537 | AGAGGATGGGGCCAG[C/T]AAAGGCATTTTACAT | 51667 |
rs546758620 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NUB1 | GRCh38.p7 | 7:151345023 | AAAAAAGAAGTTCAC[A/G]ACTCGAGGGATTTAT | 51667 |
rs546794418 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151360028 | CTTTTAGATTGAGTT[A/C]TGATCTTGTTTTCAT | 51667 |
rs546794864 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151352337 | CAGTTTCAAATAGCC[A/G]TCTAGTAAGATGGCT | 51667 |
rs546826689 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NUB1 | GRCh38.p7 | 7:151345720 | CATAACATTATTTAT[A/C]TGGAACTCATTTTGA | 51667 |
rs546831579 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151352723 | GTTGGGATTACAGGC[A/G]TGAGCCACCGGGCCT | 51667 |
rs546936836 | snp | C/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151350157 | TCACTTTCTGCTGCT[C/G]CTATCTAGAAGGCGG | 51667 |
rs547083374 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151353559 | TAGCGCAGCTGTTGG[C/G]AAACGAGAAACTAGA | 51667 |
rs547264229 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151374257 | AGGTAGCAGCTCCCT[C/T]GGGGCCTCTGGCCTT | 51667 |
rs547329627 | in-del | -/CA | 0.0023933 | 0.0345097 | intron-variant | NUB1 | GRCh38.p7 | 7:151362735 | CCAGAGAGAGGGTGT[-/CA]CAGAGAGCTTCAGAG | 51667 |
rs547420736 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151365973 | GTTTTATACAAGAGC[A/G]TTCTTATTTTTAGTA | 51667 |
rs547421237 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | NUB1 | GRCh38.p7 | 7:151341714 | ACCCTCTTTCCAAGC[C/G]GCGGCGGCGGCGGCG | 51667 |
rs547441967 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151361159 | GTGGAGGTACAATTT[A/G]TATAGGAAAGTTAGA | 51667 |
rs547604539 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151369094 | CTCACTGCAAGCTCC[A/G]CCTCCCGGGTTCAAG | 51667 |
rs547736739 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NUB1 | GRCh38.p7 | 7:151369726 | TTCTTGCCAAAACAA[A/G]AAGTTGGTACTAGAT | 51667 |
rs547773069 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NUB1 | GRCh38.p7 | 7:151362163 | TACATCTTCAGTTCA[C/T]GATACATTAACATGT | 51667 |
rs547989893 | snp | A/G | 1.65773e-05 | 0.00287895 | missense, utr-variant-5-prime | NUB1 | GRCh38.p7 | 7:151349214 | ATTGCTACAATCGAG[A/G]TGTTTTTACCACCAA | 51667 |
rs548143886 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151352941 | TAGAAATAATGACTT[C/G]CCTTTTTTTCTCAAT | 51667 |
rs548153028 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151356358 | CTCGTAAACAGAAAA[C/T]GTCACCACGTGGTGA | 51667 |
rs548383013 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | NUB1 | GRCh38.p7 | 7:151341678 | CCGCCCACAGCTGGC[C/T]TCGCCTTGGCCCCGC | 51667 |
rs548528611 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151376101 | CAGAGGCCACCCACG[A/C]AGTAACAGAGGGCAG | 51667 |
rs548600372 | in-del | -/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | NUB1 | GRCh38.p7 | 7:151341365 | GTGAAAAGCCGCTGG[-/T]TTTAGGGAAGGGGTC | 51667 |
rs548603646 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151369084 | ACGATCTTGGCTCAC[G/T]GCAAGCTCCGCCTCC | 51667 |
rs548826633 | in-del | -/G | 0.00159617 | 0.0282053 | intron-variant | NUB1 | GRCh38.p7 | 7:151344820 | CCTGGCCAACATGGC[-/G]GAAACCCCGTCTCTA | 51667 |
rs548902039 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151354440 | GCTAGTTTTCCAGAA[A/T]TGTGTTCACATTTGT | 51667 |
rs549033078 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151369898 | GAGCAGGAAAGCCCC[A/G]TGGTTGTTTGCCTAC | 51667 |
rs549084000 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151349944 | AATGCCTGGCTGTGC[C/T]GTTATTTATTGGATA | 51667 |
rs549105880 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | NUB1 | GRCh38.p7 | 7:151363966 | TCCCGACTAGTTTTT[G/T]TATTTTTAGTAGAGA | 51667 |
rs549107964 | snp | G/T | | | upstream-variant-2KB | NUB1 | GRCh38.p7 | 7:151341637 | CGGCTCCGCCCCGCG[G/T]TAACCACGCCCACAC | 51667 |
rs549171318 | snp | A/G | | | upstream-variant-2KB | NUB1 | GRCh38.p7 | 7:151340094 | TTGTTGTTAGTGGGA[A/G]CCTTGGTCTACTGCA | 51667 |
rs549261670 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | NUB1, WDR86 | GRCh38.p7 | 7:151378107 | CATGTGACAGAGGCT[C/T]TTTCTAAAAGTATGT | 51667 |
rs549306742 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant | NUB1 | GRCh38.p7 | 7:151363666 | TACAAGAAATATCAG[-/A]AAAAAACTACACTAC | 51667 |
rs549381197 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant, utr-variant-5-prime | NUB1 | GRCh38.p7 | 7:151341918 | CCCCGGTTCCCGGTC[C/G]GACTGGGCACCTCTC | 51667 |
rs549383095 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151348100 | AGTGTGCATTTCCTT[A/T]GAGCATCTCCAGATG | 51667 |
rs549526402 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151369221 | CCATGTTGGCCAGGC[C/T]GTTCTCAAACTCCTG | 51667 |
rs549587223 | in-del | -/C | 0.466824 | 0.124448 | intron-variant | NUB1 | GRCh38.p7 | 7:151371363 | TGTCTTTTACCCCCA[-/C]CCCCCCACCCCATGT | 51667 |
rs549662717 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151371636 | AAAAACAATGTCCCA[C/T]AGAAAGTGAGCTCCT | 51667 |
rs549699475 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NUB1 | GRCh38.p7 | 7:151344580 | ACTCAGCCTCCCAAA[A/G]TGCTGGGGTTACAGG | 51667 |
rs549861874 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NUB1 | GRCh38.p7 | 7:151369795 | AGAAGTCTCTAGAAT[C/T]TTCACATGTATGTTA | 51667 |
rs549893786 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NUB1 | GRCh38.p7 | 7:151355162 | ACTTTCTCATTTTCC[A/G]TTTATATTGTCTAGC | 51667 |
rs550159930 | snp | A/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151355261 | GAAGATTAGAAAAGA[A/T]GAATTTAGTTGATTC | 51667 |
rs550209763 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151349423 | TGGAACATTCCCAAG[A/G]TAGGCTTTTAGAGAC | 51667 |
rs550239140 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151363817 | GAGTCTCACTCTGTC[A/G]CCCAGGCTGTAGTGC | 51667 |
rs550375261 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | NUB1 | GRCh38.p7 | 7:151344490 | TAATTGTTCATATAT[A/T]TTTTTTTTTTTAGTA | 51667 |
rs550388015 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime | NUB1 | GRCh38.p7 | 7:151377401 | TTCATGCGTGGTCTC[A/G]GGGAAGAAGCTTCCT | 51667 |
rs550482755 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | NUB1 | GRCh38.p7 | 7:151340401 | GCTCTGTCTCCTTGA[A/G]CTTGGGGCTGGGTTG | 51667 |
rs550555849 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151371905 | AGAAATGGGGTCTCA[C/T]CATGTTGCCCAGGCC | 51667 |
rs550577239 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151344989 | TGGGCGACAGAGCGA[A/G]ACTCCGTCTCAAAAA | 51667 |
rs550639086 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | NUB1 | GRCh38.p7 | 7:151357747 | CCCAAGTAGCTGGGA[C/G]TACAGGTGTGCCCCA | 51667 |
rs550723194 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NUB1 | GRCh38.p7 | 7:151358329 | TCTTACATTGAATGA[C/T]GACATCCAGATCTTT | 51667 |
rs550762049 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151351621 | AAATTGAGGCTTTGA[A/G]GTTGAAGGACTTATT | 51667 |
rs550768903 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NUB1 | GRCh38.p7 | 7:151358215 | TTGACCTCGTGATCC[A/G]CCTGCCTCGGCCTCC | 51667 |
rs550886920 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151376315 | ATTTGTGCCCCTACA[C/T]GCGTTAGCACGCCTG | 51667 |
rs550892492 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151364086 | GGTGTGAGCCACCGC[A/G]CCTGGCCTAAAATTT | 51667 |
rs550892586 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151372466 | TCTCTGTGCTTGGAT[A/G]TTAGGTGCGCTTCTT | 51667 |
rs550931460 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151364747 | TCTTGACCCTCTGAC[C/T]TCAGGTGATCTGCCC | 51667 |
rs551286272 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151365707 | TGTCTGCGTGCACAC[A/G]TGTGTAAAACATGGT | 51667 |
rs551309210 | in-del | -/A | 0.00279162 | 0.0372561 | intron-variant | NUB1 | GRCh38.p7 | 7:151344999 | GCGAGACTCCGTCTC[-/A]AAAAAAGAAAAAAAG | 51667 |
rs551356969 | snp | A/C | 0.000798403 | 0.0199641 | utr-variant-3-prime | NUB1 | GRCh38.p7 | 7:151377392 | CCCAGGGCCTTCATG[A/C]GTGGTCTCGGGGAAG | 51667 |
rs551420909 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151363135 | GAAACAAGCAAATGT[A/T]ACCTATAACAAGCAA | 51667 |
rs551499423 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151343933 | AGGCCTGTAATCCCA[C/G]CACTTTGGGAGGCCG | 51667 |
rs551502810 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151344632 | GAAAATATTTATTAT[C/G]GATAGTTTACAGTTC | 51667 |
rs551516736 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151372615 | CTGCTGGCATGTGTG[A/G]TTGGGGTGGTGTGGC | 51667 |
rs551557280 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151358986 | GGAAGAATGGCGTGA[A/G]CTCGGGAGGCAGAGG | 51667 |
rs551560138 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | NUB1 | GRCh38.p7 | 7:151357612 | TAAAGATTAAAGTTT[G/T]TTTTTTTTTTTTCTT | 51667 |
rs551625479 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NUB1 | GRCh38.p7 | 7:151358075 | CCGCCTCCCGGGTTC[A/C]AGCGATTCTCCTGCC | 51667 |
rs551752666 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NUB1 | GRCh38.p7 | 7:151356764 | CTCTTGTTGCTCAGG[C/T]TGGAGTGCAATGGCT | 51667 |
rs551767316 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151364354 | GGAACCCGGGAGGCG[A/G]AGCTTGCAGTGAGCC | 51667 |
rs552080994 | snp | C/T | 0.00716266 | 0.059414 | upstream-variant-2KB | NUB1 | GRCh38.p7 | 7:151340257 | GTCCTTCTACCTTGC[C/T]GCAATTGCTACTGAG | 51667 |
rs552081330 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151370235 | GGAATTACAGGTGCC[C/T]ACCACCACGCCCAGC | 51667 |
rs552122983 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151358979 | CTGAGGTGGAAGAAT[A/G]GCGTGAACTCGGGAG | 51667 |
rs552151173 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NUB1 | GRCh38.p7 | 7:151344425 | AAGCGATTCTCCTGC[C/T]TCAGTCTCCCGAGTA | 51667 |
rs552287589 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151351310 | GGCAGCATTTTAGTT[C/T]TTAACAGTGAACTCA | 51667 |
rs552328343 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | NUB1 | GRCh38.p7 | 7:151340270 | GCTGCAATTGCTACT[A/G]AGCAATCAACGGGCT | 51667 |
rs552349042 | snp | A/G | 1.6566e-05 | 0.00287797 | intron-variant | NUB1 | GRCh38.p7 | 7:151375822 | AGTTCTTAGTGATGG[A/G]TAAAGGGTGTTCCTG | 51667 |
rs552418288 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151345886 | TTTGATGCTCTCACT[A/G]TCAGTGTTCATTTTT | 51667 |
rs552466123 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151360629 | TTCCTTCTGTACTTA[C/T]TTTTTTTGAGACAGA | 51667 |
rs552504788 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151354428 | GAAAAAAATCCAGCT[A/G]GTTTTCCAGAAATGT | 51667 |
rs552550693 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NUB1 | GRCh38.p7 | 7:151352736 | GCGTGAGCCACCGGG[C/T]CTGGCTAATGTCTTT | 51667 |
rs552661728 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151350106 | GTCATTATTTCTTCT[A/G]TGCTCTTCTCAGAAA | 51667 |
rs552859178 | in-del | -/AG | 0.00159617 | 0.0282053 | intron-variant | NUB1 | GRCh38.p7 | 7:151365754 | TTCACGAAATTAGAA[-/AG]ATGTTGAGAGAGATG | 51667 |
rs552879973 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | NUB1 | GRCh38.p7 | 7:151344870 | CCGGGCGTGGTGGCG[C/G/T]ATGCCTGTAATCCCA | 51667 |
rs552899266 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NUB1 | GRCh38.p7 | 7:151375582 | AACCTGTTTTCTTGG[A/G]TGCTGCTTCCACCTG | 51667 |
rs552936424 | snp | C/T | 0.000139762 | 0.00835833 | intron-variant | NUB1 | GRCh38.p7 | 7:151367831 | TTAGAAATAAGGCAA[C/T]TTTATCCTTTTTTTC | 51667 |
rs552970844 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151357841 | TCTTGAACTCCTGAC[C/G]TCAGGTGATCCACCC | 51667 |
rs553119016 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NUB1 | GRCh38.p7 | 7:151352593 | GGCCACAGGCATGGG[C/T]TACCAGGCCTGGCTA | 51667 |
rs553192053 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NUB1 | GRCh38.p7 | 7:151344790 | GGATCACTTGAGGTC[A/G]GGAATTCGAGACCAG | 51667 |
rs553251159 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | NUB1, WDR86 | GRCh38.p7 | 7:151378279 | TCCAAGACTTTCCCT[C/G]CCTTCCAGAAGGCAC | 51667 |
rs553282597 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151359059 | GACAGAGCGAGACTC[C/T]GTCTCAAAAAAAAAA | 51667 |
rs553286313 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151365194 | TCAGGTTTAAATATA[A/G]TTTTATATATAATAA | 51667 |
rs553325568 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NUB1 | GRCh38.p7 | 7:151376325 | CTACACGCGTTAGCA[A/C]GCCTGTATGCTGTGG | 51667 |
rs553447892 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NUB1 | GRCh38.p7 | 7:151372827 | CCACTGAGAGGTAGA[A/G]CACGTAATGGGGGCA | 51667 |
rs553527182 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon, utr-variant-5-prime | NUB1 | GRCh38.p7 | 7:151345385 | TCAAGCAAAATTGAC[C/T]CAGTTTTTAAGGGAA | 51667 |
rs553545340 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151346129 | TTTATCAGGGACTAA[A/G]GATTGTCATGAGGCA | 51667 |
rs553632640 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | NUB1 | GRCh38.p7 | 7:151353494 | GCTGCTGAATGTGCA[A/G]TGCCCAGAACAGGCC | 51667 |
rs553936047 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151362270 | GGCATCTATTTATCC[C/T]GGGCATCTATTTATC | 51667 |
rs553968646 | snp | C/T | 0.00167785 | 0.0289156 | intron-variant | NUB1 | GRCh38.p7 | 7:151360309 | CCAGACTATACAGAA[C/T]ACCCTGCCATGCCCT | 51667 |
rs553980563 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151357861 | GTGATCCACCCACCT[C/T]GGCCTCCCAAAGTGC | 51667 |
rs554129255 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151343625 | GCCTTACATCTCAGC[C/T]GCCTCACTCACCTTT | 51667 |
rs554235724 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151368319 | GGGGGCAAGAGAGAG[A/T]CCAGAGCAGGCCACT | 51667 |
rs554270621 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | NUB1 | GRCh38.p7 | 7:151360973 | AATTATACAGATGGG[G/T]TCTCCCTGTGTTGCT | 51667 |
rs554338564 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151353837 | TAAGACAGCCCTTCA[C/T]AGCTCACCCTAGCCT | 51667 |
rs554362619 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151342965 | AGGTGTGAGCCACCG[A/C]GCCCGGCCTTGGATG | 51667 |
rs554418629 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NUB1 | GRCh38.p7 | 7:151374530 | GTTTCTGTGTGCAGC[A/G]GAGTTTAGTGAAACA | 51667 |
rs554666060 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NUB1 | GRCh38.p7 | 7:151344932 | TTGAACCCAGGGGGC[A/G]GAGCTTGCAGTGAGC | 51667 |
rs554669255 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | NUB1 | GRCh38.p7 | 7:151353750 | CAGCCATCCATACAA[A/G]CACTGTAGCCCACTG | 51667 |
rs554729884 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151342007 | CGGGGCCGGGGCCGG[A/G]GCCGGGAGCGGTGGG | 51667 |
rs554746540 | snp | C/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151364795 | TGCTGGGATTACAAG[C/G]GTGAGCCACTGTGCC | 51667 |
rs554851535 | in-del | -/TTG | 0.00835141 | 0.0640778 | intron-variant | NUB1 | GRCh38.p7 | 7:151364526 | AATGGGATTTAATTT[-/TTG]TTGTTGTTGTTTTTG | 51667 |
rs554889784 | snp | C/T | 0.00517822 | 0.0506191 | downstream-variant-500B, utr-variant-3-prime | NUB1, WDR86 | GRCh38.p7 | 7:151378801 | CAAATCGCTGTCCTG[C/T]GCTTGGTTCAGGCGT | 51667 |
rs554994944 | in-del | -/TTTTTT | | | intron-variant | NUB1 | GRCh38.p7 | 7:151348588 | TTTTTTTTTTTTTTT[-/TTTTTT]GAGGCGGAGTCTTGC | 51667 |
rs555008671 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151371481 | CTTGAACCTGTCACT[A/G]AGGCTGGAGGAACGC | 51667 |
rs555018341 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151368490 | AACAAAGTGGTTACC[A/T]GTCACTTCTGCAACA | 51667 |
rs555108702 | snp | C/T | 0.000216488 | 0.0104018 | synonymous-codon | NUB1 | GRCh38.p7 | 7:151355844 | ACAATCTGAAGAGGA[C/T]GCGAGGAAAAACTTC | 51667 |
rs555126363 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151367320 | CTCTTACTTAGCGTG[G/T]GAGCATTTAGCCCAA | 51667 |
rs555268590 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151348872 | GAGCCACCGCGCCCA[C/G]TCTCAAATAAGTGTT | 51667 |
rs555293575 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151376317 | TTGTGCCCCTACACG[C/T]GTTAGCACGCCTGTA | 51667 |
rs555462056 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151344053 | GGGCGTGGTGGCGGG[C/T]GCCTGTAGTCCCAGC | 51667 |
rs555628246 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NUB1 | GRCh38.p7 | 7:151369294 | ATTACAGGTGTGAGC[C/T]ACCGCGCCTGGCCGA | 51667 |
rs555654299 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NUB1 | GRCh38.p7 | 7:151342970 | TGAGCCACCGCGCCC[A/G]GCCTTGGATGGCATC | 51667 |
rs555753529 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NUB1 | GRCh38.p7 | 7:151343589 | GGGAAACCTTAAAGC[A/G]CTGTGCTACACCTGC | 51667 |
rs555761995 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NUB1 | GRCh38.p7 | 7:151376886 | TGTGGCCCTAAGCCA[C/T]GGCAGATGTGGAGAC | 51667 |
rs555815579 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151373768 | CATGCACCTCACACC[A/C/T]GCGACCTCTGCAGTG | 51667 |
rs555870235 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151349507 | TAGCGTGTGAACGTT[A/G]AGAAATAATGGGGAA | 51667 |
rs555882850 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NUB1 | GRCh38.p7 | 7:151371494 | CTGAGGCTGGAGGAA[C/T]GCCAAGACTGGCTCA | 51667 |
rs555883274 | snp | A/T | 0.000610294 | 0.0174578 | intron-variant | NUB1 | GRCh38.p7 | 7:151349032 | ATATTTTGCCTTTTT[A/T]TTTTTAAGTCAGTAT | 51667 |
rs555947681 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151359604 | CCAACATGGTGAAAC[C/T]CCATCTCTACTAAAA | 51667 |
rs556047635 | snp | A/G | 0.368119 | 0.220336 | intron-variant | NUB1 | GRCh38.p7 | 7:151360995 | TGTGTTGCTCAGGCT[A/G]ATCTTGAACTCCTGG | 51667 |
rs556247525 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NUB1 | GRCh38.p7 | 7:151357226 | AGTCTCGCTCTGTTG[A/C]CATTCTCCTGCTTCA | 51667 |
rs556401194 | in-del | -/T | 0.00318978 | 0.0398085 | intron-variant | NUB1 | GRCh38.p7 | 7:151348136 | TTTGGCGATTTCAGA[-/T]TTTTTAGATTAGAGA | 51667 |
rs556551876 | in-del | -/C | 0.00199481 | 0.0315187 | intron-variant | NUB1 | GRCh38.p7 | 7:151342023 | GCCGGGAGCGGTGGG[-/C]CGGGCTTCGGGACGC | 51667 |
rs556587795 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151343041 | TAACCAGCCTGTGAA[A/G]TTACTGTCCCCCAGT | 51667 |
rs556594689 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151376530 | CCATGGTGCACACGC[C/T]GGGAGCTCTTAAACA | 51667 |
rs556616499 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151361539 | CTAAGAGACTATGAT[A/G]CAGACATATTCAACA | 51667 |
rs556662146 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151350606 | AGATTATTGTAATAT[C/T]GAAATAAAGAGTAAT | 51667 |
rs556670832 | snp | A/G | 0.000188249 | 0.00969996 | synonymous-codon | NUB1 | GRCh38.p7 | 7:151376762 | CGAGCTGCCGCTGTC[A/G]CCAGAAGACTCTTTG | 51667 |
rs556848882 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151343518 | CACTCTCTAGAACTT[A/G]TCTTCATCATTCAGG | 51667 |
rs557029060 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime | NUB1, WDR86 | GRCh38.p7 | 7:151378716 | GTGAGCTGAGGTGAC[A/G]CGGAGTCTCAGCCTC | 51667 |
rs557134139 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151359022 | GTGAGCCGAGATCGC[A/G]CCACTGCACTCCAGC | 51667 |
rs557219886 | snp | A/C | 0.0119091 | 0.0762411 | intron-variant | NUB1 | GRCh38.p7 | 7:151364454 | AAACAAAAAAAAAAA[A/C]AAAAAAACTGTAAGA | 51667 |
rs557385623 | snp | C/G | | | utr-variant-3-prime, downstream-variant-500B | NUB1, WDR86 | GRCh38.p7 | 7:151377780 | GCGCTGGCCTTGGGG[C/G]CCACACCAGGTCGCA | 51667 |
rs557493128 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151358493 | TGTCAGATCAGCGGC[A/G]GCATTAGAGTCTTAG | 51667 |
rs557500388 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NUB1 | GRCh38.p7 | 7:151357087 | AGTGGCACCATCATA[A/G]CTCACTGCAGCCTTA | 51667 |
rs557532146 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151351941 | CACACACACACGTTT[A/G]CCACATACTAGTGAA | 51667 |
rs557661671 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151343705 | ACTTCTCTGGGAGAG[A/G]GAAGTTACATACCTG | 51667 |
rs557774016 | snp | A/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, downstream-variant-500B | NUB1, WDR86 | GRCh38.p7 | 7:151377575 | GGGAAGGGTGTCCCG[A/T]CCGCTTCCTCTCCAG | 51667 |
rs557873432 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NUB1 | GRCh38.p7 | 7:151376362 | ACCTCGCGGTGCTCG[C/T]GGTGAGGCTGGTGTG | 51667 |
rs558017380 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151371597 | CCACACCTCAGGGAG[C/G]GGTAGAATGGGTGCT | 51667 |
rs558050066 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151372104 | AACAGCTGTAGAAAC[A/G]GAGCTCACAGATCAT | 51667 |
rs558288601 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | NUB1 | GRCh38.p7 | 7:151364451 | AAAAAACAAAAAAAA[A/C]AACAAAAAAACTGTA | 51667 |
rs558616760 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151357875 | TCGGCCTCCCAAAGT[G/T]CTGGGATTACAGGCA | 51667 |
rs558707060 | in-del | -/A/AA | 0.252983 | 0.249982 | intron-variant | NUB1 | GRCh38.p7 | 7:151359282 | CTCTACTAAAAATAC[-/A/AA]AAAAAAAAAAATTAG | 51667 |
rs558717533 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151346861 | CTTGTGTGAACCCTC[A/G]ACTTTGTAGCTAAGT | 51667 |
rs558720028 | snp | C/G | 0.0146672 | 0.084371 | intron-variant | NUB1 | GRCh38.p7 | 7:151350898 | GTGGTCTATTCATAC[C/G]ATGGAAAACTGTTCA | 51667 |
rs558754386 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151346195 | TGGGAGGTGACAAAC[G/T]GTATTAGGGTCCTAG | 51667 |
rs558846398 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151345195 | ATATATATTTTTAGA[G/T]AAGTCTGGAGCTCAT | 51667 |
rs558871943 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151359145 | AACTAGATGATTAAG[A/T]ATAGAAAGTGAGGCC | 51667 |
rs559021658 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151353142 | ATGGAATGTAAGGTG[A/T]GCTGAGTGTAAGATG | 51667 |
rs559079657 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NUB1 | GRCh38.p7 | 7:151373602 | CAGGCTGTGGGGGGC[A/G]GGTCACCAGCTTTGG | 51667 |
rs559081697 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NUB1 | GRCh38.p7 | 7:151344359 | TCTGTTGCCCAGGCT[A/G]GAGTGCAGTGGTGCC | 51667 |
rs559096449 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | NUB1 | GRCh38.p7 | 7:151340752 | CGGTTATACAGTTAT[C/T]AATATCCCTTTGTCA | 51667 |
rs559118386 | snp | A/G | 0.000728067 | 0.0190658 | intron-variant | NUB1 | GRCh38.p7 | 7:151374385 | GGGCAGGTTTCTCCT[A/G]GGCTCCAGCCCAGAC | 51667 |
rs559369226 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151369020 | ACTTGTCCTTTTTTT[C/T]TTCTTGAGACAGAGT | 51667 |
rs559428619 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151349744 | CCTCTTGGGACTGAT[C/T]GATGCCAGCACTCTC | 51667 |
rs559483332 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151356828 | GTTCAAGTGATTCTC[C/T]TGCCTCAGCCTCCTG | 51667 |
rs559611060 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NUB1 | GRCh38.p7 | 7:151358599 | TGACCTGAGGTAGAA[C/T]GTTTTCACCCTGAAA | 51667 |
rs559612845 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151351156 | TGGTGGAAATGTTCT[C/G]AAATGTTAAAGACGT | 51667 |
rs559613256 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151364555 | TTTGAGACGGAGTCT[C/T]GCTCTGTCGCCCACG | 51667 |
rs559660462 | snp | C/T | 7.55601e-05 | 0.00614608 | utr-variant-3-prime | NUB1 | GRCh38.p7 | 7:151377243 | AATGAACAGAAATAG[C/T]GCTAATTTTCTGCTT | 51667 |
rs559696715 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, downstream-variant-500B | NUB1, WDR86 | GRCh38.p7 | 7:151377708 | TGCCACCCTTTCCCC[A/G]CCCCTCAAATCGTCC | 51667 |
rs559729185 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151344944 | GGCGGAGCTTGCAGT[A/G]AGCCGAGATCGCACC | 51667 |
rs560149904 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | NUB1 | GRCh38.p7 | 7:151339794 | TTCTTGCCCCATACA[A/G]GCCTTGAATTCAGCA | 51667 |
rs560169555 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151366271 | GAAATCAGCTGGGCC[A/G]TTAGAGCCTGGTGCT | 51667 |
rs560200496 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NUB1 | GRCh38.p7 | 7:151373030 | GCCTGTGGAGTCTGG[C/T]TCCACAATGATGATG | 51667 |
rs560340137 | snp | G/T | | | upstream-variant-2KB | NUB1 | GRCh38.p7 | 7:151341372 | AGCCGCTGGTTTAGG[G/T]AAGGGGTCCAGCCTA | 51667 |
rs560345739 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151359743 | GATCGCACCACTGCC[C/G]TCCAGCCTGGACGAC | 51667 |
rs560352284 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151346483 | CCAAAAGTACCAAGC[C/T]GTGATTAGACACTTG | 51667 |
rs560470994 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151359346 | TACTTGGGAGGCTGA[A/G]GCAGGAGAATGGTGT | 51667 |
rs560532049 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | NUB1 | GRCh38.p7 | 7:151341531 | CCTGGAAGACTGAGC[A/C]TGGGGTGGCGTTGGA | 51667 |
rs560563423 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151353299 | ACTGAGGAAGGTCCA[G/T]TGTGGCTGTGTGTGG | 51667 |
rs560872295 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151360578 | GATGATTATTCCTCA[A/G]ATCCGTTGTTTAAGA | 51667 |
rs560945376 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | NUB1 | GRCh38.p7 | 7:151340067 | TCTGACTTCGCTTTC[C/T]GGCTTTTCTAGTTGT | 51667 |
rs560981812 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | NUB1 | GRCh38.p7 | 7:151372475 | TTGGATGTTAGGTGC[A/G]CTTCTTAGCCTTTTG | 51667 |
rs561005069 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151372972 | TCTTCATCCCTGGAG[A/T]TGTTTCCAGCAGCCA | 51667 |
rs561016268 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NUB1 | GRCh38.p7 | 7:151366223 | CTGCTGCCACGAATA[C/T]GGAGTCAAATTTTGC | 51667 |
rs561020191 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151358803 | GGCGCGGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 51667 |
rs561039294 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | NUB1, WDR86 | GRCh38.p7 | 7:151378430 | CGATGGAAATAAAAG[A/G]TGGGAAATATATTCA | 51667 |
rs561127147 | in-del | -/AAAAAAAAAAAAAAAA | 0.499137 | 0.0207489 | intron-variant | NUB1 | GRCh38.p7 | 7:151344181 | GTGAGACTCCCTCTC[-/AAAAAAAAAAAAAAAA]AAAAAAAAAAAAAAA | 51667 |
rs561133081 | snp | C/T | | | upstream-variant-2KB | NUB1 | GRCh38.p7 | 7:151341647 | CCGCGGTAACCACGC[C/T]CACACAACCGTATCC | 51667 |
rs561159433 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151345682 | TTTTTCAGGCATATA[G/T]TTTTAATACCATCAC | 51667 |
rs561187397 | snp | A/C | | | intron-variant | NUB1 | GRCh38.p7 | 7:151359874 | AAGTAGAATCCAGAT[A/C]AGTGGATACGAAAAT | 51667 |
rs561253141 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151352689 | CTCAAGCCATCCTCC[C/G]ACCTTGGCCTCCCAG | 51667 |
rs561358255 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151359255 | CATCCTGGCTAACAC[A/G]GTGAAACCCTGTCTC | 51667 |
rs561364240 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151374775 | GAGAAGCATATCGAA[G/T]CCTCAGTAGGGCAGG | 51667 |
rs561372399 | snp | C/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151363620 | ATGAAAACTATAAAC[C/G]CCCAGATGCAATGAC | 51667 |
rs561463946 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151367586 | TGGTTTGGATTTCTG[C/T]ATACTTCTCTGCTGA | 51667 |
rs561465632 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NUB1 | GRCh38.p7 | 7:151359971 | GGCTTCAGTATTTAA[A/G]TGAAATAAAGCTTTA | 51667 |
rs561519546 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151365483 | CATGCAGGAGATGGA[A/G]AAGTTCGGCCACATG | 51667 |
rs561675803 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151354857 | AAGCAATCCTCCCAC[C/G]TCAGCTTCCCACTGA | 51667 |
rs561717824 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | NUB1, WDR86 | GRCh38.p7 | 7:151377858 | GTAAAATACGCCCCC[A/G]AAATTCAAGATTGAG | 51667 |
rs561826173 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151354219 | TGACCCTTTTTGGGG[A/G]GCCCTGTTCCTATAT | 51667 |
rs561898111 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | NUB1 | GRCh38.p7 | 7:151341696 | GCCTTGGCCCCGCCC[A/G]CAACCCTCTTTCCAA | 51667 |
rs561964757 | snp | A/C | | | missense | NUB1 | GRCh38.p7 | 7:151375904 | CAATCCTGAAACCGA[A/C]AACCGTCAAGAAAGT | 51667 |
rs561987357 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NUB1 | GRCh38.p7 | 7:151369085 | CGATCTTGGCTCACT[A/G]CAAGCTCCGCCTCCC | 51667 |
rs562050061 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151376127 | GGCAGGGGAGGCCTC[C/G]TTGGAAAGCAGGAAA | 51667 |
rs562096378 | snp | A/G | 1.95414e-05 | 0.00312575 | missense | NUB1 | GRCh38.p7 | 7:151366961 | TGCAGAGAGCTGCTG[A/G]ACACAGTGGATAACT | 51667 |
rs562109494 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151356294 | GGTTTTTTAGTTGCT[C/T]TATGTTGGAAGTGTT | 51667 |
rs562153507 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151376565 | AGTCGGCTGTCCACT[C/T]GTATGGCTGACGGGG | 51667 |
rs562257448 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151366362 | TCATCAGCTGAGGCA[C/T]TCATAGTACGTAGGG | 51667 |
rs562385070 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151369652 | AATATGTTCTGCAGT[A/G]AAAGAACTGAGGTCT | 51667 |
rs562445001 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | NUB1 | GRCh38.p7 | 7:151353024 | GAAGTTTACTAAAAT[-/A]AAAATGTAAAGCAGA | 51667 |
rs562528887 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | NUB1 | GRCh38.p7 | 7:151355559 | GGGCCTGTAGTCCCA[C/G]CTCCTCGGGAGGCTG | 51667 |
rs562568264 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | NUB1 | GRCh38.p7 | 7:151344981 | TCCAGCCTGGGCGAC[-/A]AGAGCGAGACTCCGT | 51667 |
rs562627594 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151359857 | TCTGAATAGAATATT[A/T]GAAGTAGAATCCAGA | 51667 |
rs562665612 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151354060 | GCCACAAGGATAGTC[G/T]ACATTTTCTTGAATA | 51667 |
rs562710220 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NUB1 | GRCh38.p7 | 7:151346595 | GCCTGCATAATGAAA[A/C]TTCCATACAAACCCC | 51667 |
rs562896072 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151342442 | GCAATGATCGATTCA[C/T]TACAAAAGTGAAAGT | 51667 |
rs562907036 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NUB1 | GRCh38.p7 | 7:151348961 | GGACTGCAGTGTAAC[A/G]GGGCGACCTCCACTC | 51667 |
rs562919407 | in-del | -/GGCACCTCCTTCCTGCCCCACG | 0.00119737 | 0.0244387 | intron-variant | NUB1 | GRCh38.p7 | 7:151373845 | TGGCGGGGCTGGCGA[-/GGCACCTCCTTCCTGCCCCACG]GGCATCTCACTTCCA | 51667 |
rs562932954 | snp | C/G | 0.00478085 | 0.0486577 | upstream-variant-2KB | NUB1 | GRCh38.p7 | 7:151341629 | CCCCGTCGCGGCTCC[C/G]CCCCGCGGTAACCAC | 51667 |
rs562998459 | snp | G/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151362372 | GTAAGCCAAATAGAA[G/T]GCAGATGGAGGAAAC | 51667 |
rs563023791 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151369528 | ATCATAGAAACAAGT[A/T]GTATTATATTATGAA | 51667 |
rs563173539 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NUB1 | GRCh38.p7 | 7:151376095 | CCACCTCAGAGGCCA[C/T]CCACGCAGTAACAGA | 51667 |
rs563246591 | snp | C/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151369610 | AAACCTTAGAATTTT[C/G]GAGTTGGAAGCATCC | 51667 |
rs563253585 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NUB1 | GRCh38.p7 | 7:151344324 | TATATATTTATTATT[A/G]TTTTGAGACGGAGTC | 51667 |
rs563259150 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151347762 | TCGCGCCCAATCTAT[A/G]CTCATATCTATAAAG | 51667 |
rs563293211 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151363800 | TTTTATTTTTTCAGA[C/T]GGAGTCTCACTCTGT | 51667 |
rs563341041 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151372830 | CTGAGAGGTAGAGCA[C/T]GTAATGGGGGCATGA | 51667 |
rs563455241 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NUB1 | GRCh38.p7 | 7:151362926 | TGGTAGTCACAGGGC[A/G]TCAAATAGAGTCTTC | 51667 |
rs563455276 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151371703 | CTCGGAGTTCCAACG[C/T]TCTAGGTATGAGCAT | 51667 |
rs563611222 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | NUB1, WDR86 | GRCh38.p7 | 7:151377678 | ATCTCTGCCAGGGTG[C/T]CACATGGGTTCCTGT | 51667 |
rs563697488 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151355036 | GGTGTGAACCACCAC[A/G]CCCTGCTGGTCTTTG | 51667 |
rs563854738 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NUB1 | GRCh38.p7 | 7:151357909 | GCCACTGCGCCCGGC[C/T]GGATTAAAGTTGTTT | 51667 |
rs563856433 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151375470 | AAAATAACCCTACTA[C/T]CTGCCTGACATTTTA | 51667 |
rs563871912 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | NUB1 | GRCh38.p7 | 7:151344866 | TTAGCCGGGCGTGGT[A/G]GCGCATGCCTGTAAT | 51667 |
rs563920176 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NUB1 | GRCh38.p7 | 7:151373072 | CTAAGAGATGAGGCC[A/G]CTTTCCTGCTGTGGG | 51667 |
rs563998036 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NUB1 | GRCh38.p7 | 7:151357438 | CCCTTGGGGGCCTCT[A/G]TAGCAGCATTCTGGA | 51667 |
rs564036595 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151350411 | CCGCTAGACCAAGGT[C/T]TGCTAAGTAACGAGG | 51667 |
rs564160613 | snp | C/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151350450 | GGGCACTGGAGTTAC[C/G]GCTAGACGAGGGAGC | 51667 |
rs564189998 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151370626 | TATACATGTGCCATG[C/T]TGGTGCGCTGCACCC | 51667 |
rs564310482 | in-del | -/TA | 0.00119737 | 0.0244387 | intron-variant | NUB1 | GRCh38.p7 | 7:151361650 | CCCAAGATAATACTG[-/TA]TATACTCCCAGAAGA | 51667 |
rs564433238 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NUB1 | GRCh38.p7 | 7:151369727 | TCTTGCCAAAACAAG[A/C]AGTTGGTACTAGATT | 51667 |
rs564482459 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151357383 | CCCGCCTCGGCCTCC[C/T]GAAGTTCTGGGATTA | 51667 |
rs564648517 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151363545 | GTCCCTGGAAAGGCA[A/G]ACATGTGGGACAGAA | 51667 |
rs564907929 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | NUB1, WDR86 | GRCh38.p7 | 7:151377797 | CACACCAGGTCGCAG[A/C]AAATGGCTTCAGCCT | 51667 |
rs565148941 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | NUB1, WDR86 | GRCh38.p7 | 7:151378405 | GTCATTCTTTTTAAA[C/T]GGATGATACCGATGG | 51667 |
rs565187594 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151372328 | AATGTTCTCACATGT[A/G]TTTACATGATTAAAA | 51667 |
rs565235544 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151352621 | CTAATTTTTAAAAAT[G/T]TTTTGTAGAGATAGG | 51667 |
rs565259577 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NUB1 | GRCh38.p7 | 7:151358787 | AATTGTTTTGGGGCC[A/G]GGCGCGGTGGCTCAC | 51667 |
rs565365873 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | NUB1 | GRCh38.p7 | 7:151340005 | CTGGAATATCAAGTC[C/T]CCCCATTCTTGCCTC | 51667 |
rs565392084 | snp | A/C | | | intron-variant | NUB1 | GRCh38.p7 | 7:151343986 | GGAGATTGAGACCAT[A/C]CTGGCCAACACGGTG | 51667 |
rs565492857 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151347709 | GAGCAATCCTCTCAC[C/T]TTGCCTTCCAAAGTG | 51667 |
rs565582446 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151363024 | GAACAGTACCCTTAA[C/G]TTACCGTTTTCAAAT | 51667 |
rs565584670 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NUB1 | GRCh38.p7 | 7:151356652 | TTTCCTCATACTCTT[C/T]CCCTGTTCTATAATT | 51667 |
rs565607579 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151343358 | TTTGAACTTTCTTTT[A/T]AAAAATATTTGTTTA | 51667 |
rs565663262 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151344174 | CGACAGAGTGAGACT[C/T]CCTCTCAAAAAAAAA | 51667 |
rs565774211 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151342913 | CTCCTGACCTCAGGT[A/G]ATCCACTGGCCTCGG | 51667 |
rs565929752 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | NUB1, WDR86 | GRCh38.p7 | 7:151378138 | AGTTCGCTGTGTGTC[A/G]GCTCCAGCAGTAACC | 51667 |
rs566093151 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151344523 | GATAGGGCTTCACCA[C/T]GTTGACCAGGCTGGT | 51667 |
rs566248634 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NUB1 | GRCh38.p7 | 7:151344616 | GCCACCACACCCATC[C/T]GAAAATATTTATTAT | 51667 |
rs566419468 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NUB1 | GRCh38.p7 | 7:151372607 | AAAGACTCCTGCTGG[C/T]ATGTGTGGTTGGGGT | 51667 |
rs566519873 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151358398 | CTGCAGATGGGTACC[A/G]GTCCGTGGCTTGTTA | 51667 |
rs566535675 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151364392 | CACCACTGCACTCCA[G/T]CCTGGAGGAGAGAGC | 51667 |
rs566592043 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NUB1 | GRCh38.p7 | 7:151345027 | AAGAAGTTCACGACT[C/T]GAGGGATTTATCTTT | 51667 |
rs566611804 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151356413 | CCTGTGCTTTTCAGC[A/G]CATTAGTACAAAATG | 51667 |
rs566756599 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151358952 | CGCCTGTAGTCCCAG[C/G]TACTCGGGAGGCTGA | 51667 |
rs566823643 | in-del | -/AGAA | | | intron-variant | NUB1 | GRCh38.p7 | 7:151366542 | GAAAGAAAGAAAGAA[-/AGAA]CGTTGCTCTGGCCCA | 51667 |
rs566869257 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151373581 | GGCCCTGGAGTCCTT[G/T]CTCCCCAGGCTGTGG | 51667 |
rs566895626 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151369912 | CGTGGTTGTTTGCCT[A/G]CCTGATGCCAGAGAG | 51667 |
rs566908091 | snp | C/T | 0.000700231 | 0.0186983 | intron-variant | NUB1 | GRCh38.p7 | 7:151374347 | GCTCACTCCTATGGG[C/T]TGCCCCGTCATCCGG | 51667 |
rs566960973 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151345759 | TGGAACAGTATTGGT[A/G]CCAGTAAGTAATTGC | 51667 |
rs567027210 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151366552 | AAGAAAGAACGTTGC[C/T]CTGGCCCAGGTGATG | 51667 |
rs567061290 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NUB1 | GRCh38.p7 | 7:151359633 | AAATACGAAATTAGC[C/T]GGGCATGGTGGCTCA | 51667 |
rs567124347 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151359397 | GCAGTGAGTCGAGAT[C/T]GCGCCACTGCACTCC | 51667 |
rs567144070 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NUB1 | GRCh38.p7 | 7:151374801 | GCAGGTGCTGCGCTG[C/T]GTCTCAGCAGCTTGG | 51667 |
rs567206484 | snp | A/G | | | upstream-variant-2KB | NUB1 | GRCh38.p7 | 7:151341579 | TCGCCCCACACGGCC[A/G]CATCCTCGCCCAGCC | 51667 |
rs567303417 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151351787 | AGTGAGTGATACAAG[C/G]AGGAGACACCTGGTA | 51667 |
rs567310794 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151364105 | GGCCTAAAATTTTTA[C/T]GTTAAATAAATATTA | 51667 |
rs567334871 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NUB1 | GRCh38.p7 | 7:151371201 | AAGCAACAACAACAA[A/C]AAAAAACCCAAAATG | 51667 |
rs567373393 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | NUB1 | GRCh38.p7 | 7:151371939 | CTCAAAACTCCTGGG[G/T]TCAAGCAGTCCTCCC | 51667 |
rs567447130 | in-del | -/AT | 0.00119737 | 0.0244387 | intron-variant | NUB1 | GRCh38.p7 | 7:151345098 | TTAAGAAATAGAAAC[-/AT]GTAATAATCCTTGCT | 51667 |
rs567532484 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151357785 | TGGCTAATTTTTGTA[C/T]TTTTAGTAGAGACGG | 51667 |
rs567547752 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NUB1 | GRCh38.p7 | 7:151364776 | CCGCCTCGGCCTCCC[A/T]AAGTGCTGGGATTAC | 51667 |
rs567562727 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151359034 | CGCGCCACTGCACTC[C/T]AGCCTGGAAGACAGA | 51667 |
rs567568853 | snp | C/G/T | | | upstream-variant-2KB | NUB1 | GRCh38.p7 | 7:151340112 | TTGGTCTACTGCAAG[C/G/T]TGCTCCATCACACCT | 51667 |
rs567569114 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151350722 | ATTATACTGGAACAA[C/T]TTGTGCCCTCGGTCT | 51667 |
rs567581556 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151358367 | ACCTTTATCACAGGG[G/T]TTCCCACCCCACAGG | 51667 |
rs567648976 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime | NUB1, WDR86 | GRCh38.p7 | 7:151378792 | TTTGGCTAACAAATC[A/G]CTGTCCTGCGCTTGG | 51667 |
rs567751284 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151371805 | CTGGAGGGCAGTGGC[A/G]TGATTATGGCTCACT | 51667 |
rs567753534 | snp | A/C/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151350572 | GCCTGGTTTTTCCTA[A/C/G]GTTATAATTGTAGAA | 51667 |
rs567834939 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151373243 | TTAACTTTGTTGAAA[A/G]CTTTCTGTCTCCTTG | 51667 |
rs567852914 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NUB1 | GRCh38.p7 | 7:151344397 | CTCACTACAACCTCT[C/G]CCTCCTGGATTCAAG | 51667 |
rs567952492 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon, intron-variant | NUB1 | GRCh38.p7 | 7:151374189 | GGGCTACTCCACGCA[C/T]GCGGCCCAGCAGGTA | 51667 |
rs568021573 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151346723 | GACCCTTCCAGACCT[C/T]GCCTTAGTACCTCTT | 51667 |
rs568025607 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151373351 | CCCCTTTTTAAATGA[C/T]ATTTTTATGGGGATA | 51667 |
rs568187789 | in-del | -/AA | 0.0325976 | 0.123435 | intron-variant | NUB1 | GRCh38.p7 | 7:151363752 | AGCTAACCTTTCTTG[-/AA]AAAAGTTAGGTAAGT | 51667 |
rs568331056 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | NUB1 | GRCh38.p7 | 7:151341164 | AGTAAGAGATTAACA[A/G]CAATAACTGATAATA | 51667 |
rs568511451 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151360856 | TGCCCATACTAGTCT[C/T]AAACTCCTGGGCTCA | 51667 |
rs568512906 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NUB1 | GRCh38.p7 | 7:151375758 | AGCAGAGGACGGCGG[A/G]GTCTGCCTAGCACAT | 51667 |
rs568549899 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151368227 | TAGAGGTGAGCCAGG[A/C]CGGAGCAGTGAGCAG | 51667 |
rs568639951 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NUB1 | GRCh38.p7 | 7:151347744 | GATTACAGGCATGAG[C/T]CATCGCGCCCAATCT | 51667 |
rs568644496 | snp | A/G | | | missense, utr-variant-5-prime | NUB1 | GRCh38.p7 | 7:151351482 | GAGAACTGAGGTCCA[A/G]GTAAGTATCTGTGTG | 51667 |
rs568681518 | snp | G/T | 0.145305 | 0.227022 | intron-variant | NUB1 | GRCh38.p7 | 7:151348568 | TGTTTTTTGCTTTTT[G/T]CTTTTTTTTTTTTTT | 51667 |
rs569147660 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151345963 | TCATCAGAAATGATA[C/T]TGTATGTAAGTGATG | 51667 |
rs569168725 | snp | A/C | | | intron-variant | NUB1 | GRCh38.p7 | 7:151356832 | AAGTGATTCTCCTGC[A/C]TCAGCCTCCTGAGTA | 51667 |
rs569341955 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NUB1 | GRCh38.p7 | 7:151374420 | GCTGCGTGAGGCCAC[C/G]TGAGGCCCCATGCTC | 51667 |
rs569349296 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151342828 | GGATGGCATCTTTTT[A/T]AAAATTTTTTATTTG | 51667 |
rs569373264 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151374871 | TGAGAGACAAACTCA[C/G]AGCACACGTGGTGAG | 51667 |
rs569385276 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151354429 | AAAAAAATCCAGCTA[C/G]TTTTCCAGAAATGTG | 51667 |
rs569423872 | snp | G/T | 0 | 0 | intron-variant | NUB1 | GRCh38.p7 | 7:151347641 | ATATTTTTAGTTTTT[G/T]TAGAGACGGGGTTTC | 51667 |
rs569466322 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151353733 | AGACCAGTTAGCTAC[C/T]GCAGCCATCCATACA | 51667 |
rs569473729 | snp | A/C | | | intron-variant | NUB1 | GRCh38.p7 | 7:151354583 | TTTGGCTAATTTATT[A/C]ATGGAGCCAGCTTTT | 51667 |
rs569546839 | snp | C/G | 0.000231054 | 0.0107459 | synonymous-codon | NUB1 | GRCh38.p7 | 7:151367887 | GAAAGAGAAGGTACT[C/G]TTTCTAAGACTCTAC | 51667 |
rs569549691 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NUB1 | GRCh38.p7 | 7:151360657 | AGAGTCTCACTCTGT[C/T]ACCCAGGCTGGAATG | 51667 |
rs569555629 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151361546 | ACTATGATGCAGACA[C/T]ATTCAACATTTGAAA | 51667 |
rs569557666 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NUB1 | GRCh38.p7 | 7:151369815 | CATGTATGTTACCTC[A/G]TTTCCCTTTTTGCTA | 51667 |
rs569619405 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151369254 | CTCAAGTGATGCGCC[C/T]ACCTCAGTTTCCCAA | 51667 |
rs569715126 | snp | G/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151346217 | GGGTCCTAGTTCTTC[G/T]GTTTCTTCTGTTCCA | 51667 |
rs569784928 | snp | A/C | | | intron-variant | NUB1 | GRCh38.p7 | 7:151364804 | TACAAGCGTGAGCCA[A/C]TGTGCCTGGCCAGGA | 51667 |
rs569811850 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151367202 | CTGTTAAAGTATTTG[A/T]ACTACTGCCAGAAGG | 51667 |
rs569851979 | snp | C/T | 4.17388e-05 | 0.00456812 | intron-variant | NUB1 | GRCh38.p7 | 7:151376594 | GGGTGGCAGAAGAGG[C/T]GCCAGGGGCTGATGC | 51667 |
rs569896195 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151376288 | TGTATCCCAAGTGAC[A/G]GCTCTGTCCACATTT | 51667 |
rs569922715 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151376380 | TGAGGCTGGTGTGGC[A/G]CCCTGCTCTCAGCCC | 51667 |
rs570011200 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151349496 | CTGATCCTTTCTAGC[A/G]TGTGAACGTTGAGAA | 51667 |
rs570074423 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151373713 | CACCGCGTGCAGAAG[C/T]TCTCCTACCCGGTTC | 51667 |
rs570150473 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151356449 | TCTCACTGTCCTGGA[A/G]CAGTGACTTTCAACA | 51667 |
rs570258597 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | NUB1 | GRCh38.p7 | 7:151377432 | CTGGCCTGGCGCAGG[A/C]CGTTCCATCTGCCTC | 51667 |
rs570336421 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151343992 | TGAGACCATCCTGGC[C/T]AACACGGTGAAACCC | 51667 |
rs570590279 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151368380 | CTGTGGCTGCATGCC[A/G]TTGACTTCGACTTCA | 51667 |
rs570806928 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151362181 | TACATTAACATGTCC[A/G]GTAAGTGGTAGGTAT | 51667 |
rs570866526 | snp | A/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151351323 | TTTTTAACAGTGAAC[A/T]CAGTTTATATCCTCT | 51667 |
rs570897119 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NUB1 | GRCh38.p7 | 7:151369100 | GCAAGCTCCGCCTCC[C/T]GGGTTCAAGCAATTC | 51667 |
rs570936141 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151361237 | ATGAGTTGCTTCACT[A/G]TCACCCTCCAAAGGT | 51667 |
rs570959192 | snp | C/T | | | missense | NUB1 | GRCh38.p7 | 7:151376746 | GAGGAAGCCTGCCTC[C/T]CGAGCTGCCGCTGTC | 51667 |
rs571022556 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151374802 | CAGGTGCTGCGCTGC[A/G]TCTCAGCAGCTTGGC | 51667 |
rs571041917 | snp | A/C | | | intron-variant | NUB1 | GRCh38.p7 | 7:151373822 | CCATCCTGATGCCGG[A/C]TGGTGGATGGCGGGG | 51667 |
rs571065366 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151343503 | AACTCATATTTTTTC[C/T]ACTCTCTAGAACTTG | 51667 |
rs571132462 | snp | C/G | | | upstream-variant-2KB | NUB1 | GRCh38.p7 | 7:151340432 | GGTTTTATAAGCATA[C/G]GGTAATGACGCATGA | 51667 |
rs571174453 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151348720 | AGCTGGGCCTACAGG[C/T]ACACGCCACCATGCC | 51667 |
rs571331739 | snp | A/G | 0.000399281 | 0.0141238 | missense | NUB1 | GRCh38.p7 | 7:151376748 | GGAAGCCTGCCTCCC[A/G]AGCTGCCGCTGTCGC | 51667 |
rs571345707 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151344877 | TGGTGGCGCATGCCT[A/G]TAATCCCAGTGAGTA | 51667 |
rs571444243 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151362968 | GCCTCAGCACTAGGG[A/C]ATAATTTGGTTTCAC | 51667 |
rs571476546 | in-del | -/GCGGCC/GCGGCGGCC | 0.00436845 | 0.0465438 | upstream-variant-2KB, utr-variant-5-prime | NUB1 | GRCh38.p7 | 7:151341732 | GCGGCGGCGGCGGCG[-/GCGGCC/GCGGCGGCC]CGAAGGCGACAGCGG | 51667 |
rs571531495 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151357105 | CACTGCAGCCTTAAC[C/T]TCCTGGGCTTGAGCG | 51667 |
rs571571627 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151360431 | AATTGACCTTTCCTC[C/T]CTGTAAAGAAAAGAA | 51667 |
rs571816121 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime | NUB1, WDR86 | GRCh38.p7 | 7:151378634 | TGCCGCACGCCAAGC[A/G]GGGCTGGGGTGCATC | 51667 |
rs571973855 | snp | G/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151357431 | ACCCAGCCCCTTGGG[G/T]GCCTCTATAGCAGCA | 51667 |
rs571977318 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NUB1 | GRCh38.p7 | 7:151369325 | AACTTGTCTTTTTCA[A/G]TTGGATCATTTTTCA | 51667 |
rs571982066 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151354888 | GTAGCTAGGACCACA[A/G]GTGCATACCACCATG | 51667 |
rs572011969 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | NUB1, WDR86 | GRCh38.p7 | 7:151377759 | GCTGTGGGGCATAAC[A/G]ATGAGGCGCTGGCCT | 51667 |
rs572018778 | snp | A/G | 0.000148562 | 0.00861735 | missense | NUB1 | GRCh38.p7 | 7:151355845 | CAATCTGAAGAGGAC[A/G]CGAGGAAAAACTTCC | 51667 |
rs572144476 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NUB1 | GRCh38.p7 | 7:151343682 | TAGACAGCTCCATCG[C/T]GGTACATACTTCTCT | 51667 |
rs572144717 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151367639 | TGTCTGGAGGCTGGT[A/G]CCCTGACACTGACTC | 51667 |
rs572159852 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NUB1 | GRCh38.p7 | 7:151348883 | CCCAGTCTCAAATAA[A/G]TGTTTTCACTTTTTC | 51667 |
rs572361424 | snp | C/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, downstream-variant-500B | NUB1, WDR86 | GRCh38.p7 | 7:151377527 | GGTCCTGTAGAACAG[C/G]GGTCCTGGGGAAGGT | 51667 |
rs572400263 | in-del | -/TCTTT | 0.00119737 | 0.0244387 | intron-variant | NUB1 | GRCh38.p7 | 7:151342528 | TATTAATGAGTTTCG[-/TCTTT]TCTTAGTTACAATGT | 51667 |
rs572551138 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NUB1 | GRCh38.p7 | 7:151371511 | CCAAGACTGGCTCAG[A/G]CCTGTGGCAAGAGAT | 51667 |
rs572589223 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NUB1 | GRCh38.p7 | 7:151363455 | ACAGAGAAAAGGCTA[A/G]AAAAAAAAAAAAATG | 51667 |
rs572598242 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151362770 | CCTTTTGAGTCTTCT[C/G]CTCAGTAATGATCAG | 51667 |
rs572601771 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | NUB1, WDR86 | GRCh38.p7 | 7:151377793 | GGGCCACACCAGGTC[A/G]CAGCAAATGGCTTCA | 51667 |
rs572660235 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151370490 | CTTTACTATTACTCC[A/G]CTACCAGTAAGAATT | 51667 |
rs572739345 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151362180 | ATACATTAACATGTC[C/T]GGTAAGTGGTAGGTA | 51667 |
rs572756794 | in-del | -/AAA | 0.00159617 | 0.0282053 | intron-variant | NUB1 | GRCh38.p7 | 7:151365757 | ACGAAATTAGAAATG[-/AAA]TTGAGAGAGATGAAA | 51667 |
rs572923740 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151350859 | AGTCCAAATGTCCAT[C/G]AACAGATGAAGGGAT | 51667 |
rs572938533 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NUB1 | GRCh38.p7 | 7:151358723 | ATTATGCGAACATTT[A/G]AATTGAAAAATCTAA | 51667 |
rs572984430 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151350254 | GGGAGACGTTTAGGC[C/T]TCTGGATGGCTGTGG | 51667 |
rs572986051 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NUB1 | GRCh38.p7 | 7:151357857 | TCAGGTGATCCACCC[A/G]CCTCGGCCTCCCAAA | 51667 |
rs573069578 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151344855 | AAATATGAAAATTAG[C/G]CGGGCGTGGTGGCGC | 51667 |
rs573223886 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151365786 | AAATAAATATAAAAA[C/T]ACTGCTGTGATACAT | 51667 |
rs573398855 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151355361 | TACCAATTATGTGGC[A/G]TGATGGTATGCAGGA | 51667 |
rs573545457 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NUB1 | GRCh38.p7 | 7:151344774 | TGAGACCAAGGTGGG[C/T]GGATCACTTGAGGTC | 51667 |
rs573598198 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151357142 | CCGCCTCCGCCTTCT[A/G]GGTAGCTGGGACTGC | 51667 |
rs573745647 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151362627 | TCAGGTTACGGGGCA[G/T]GGAGGGCAAACCCAG | 51667 |
rs573783925 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151363319 | CACATTAGAATGTAA[C/G]AGATGAAAAGTACAA | 51667 |
rs573834093 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NUB1 | GRCh38.p7 | 7:151350066 | CCCTTGTAGGTAGAC[A/G]AGGCGGAGAGAGAGG | 51667 |
rs573916372 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151359908 | CTAATGAAAGCAAAG[A/G/T]GCCAAGTGCTGGTTA | 51667 |
rs574001796 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NUB1 | GRCh38.p7 | 7:151358495 | TCAGATCAGCGGCGG[C/T]ATTAGAGTCTTAGGA | 51667 |
rs574196055 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NUB1 | GRCh38.p7 | 7:151351999 | TTTCATCTCCTTGTA[C/T]GTTTTAAAATGGTGT | 51667 |
rs574226063 | in-del | -/GGGCCG | 0.0103295 | 0.0711199 | intron-variant | NUB1 | GRCh38.p7 | 7:151341987 | GCCATGCGTGGAGCT[-/GGGCCG]GGGCCGGGGCCGGGG | 51667 |
rs574467505 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NUB1 | GRCh38.p7 | 7:151344941 | GGGGGCGGAGCTTGC[A/C]GTGAGCCGAGATCGC | 51667 |
rs574569506 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NUB1 | GRCh38.p7 | 7:151374540 | GCAGCAGAGTTTAGT[A/G]AAACAGGCAGTTTCC | 51667 |
rs574698046 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151346300 | TATTGTTACAGTCTC[C/T]TGGTTTAGAAACTAG | 51667 |
rs574930827 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151353764 | AGCACTGTAGCCCAC[G/T]GGTTTCCAGTGCGTT | 51667 |
rs574976099 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NUB1 | GRCh38.p7 | 7:151342017 | GCCGGGGCCGGGAGC[A/G]GTGGGCCGGGCTTCG | 51667 |
rs574993337 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NUB1 | GRCh38.p7 | 7:151360292 | GCTTTAAGGAAGATG[A/G]CCCAGACTATACAGA | 51667 |
rs574995266 | in-del | -/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151370098 | TGAAAAGCTGAGTTC[-/T]TTTTTTTTTTTTTAT | 51667 |
rs575014745 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151342544 | CTTTTCTTAGTTACA[A/G]TGTGAAACATTGTAT | 51667 |
rs575026894 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151374921 | AGGAGGCAGGGGGCT[A/G]GCTGTGTGGAGGCAG | 51667 |
rs575093786 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151347121 | TAAAAAAGTATTTAT[A/T]ATATATATTCTAGGT | 51667 |
rs575396213 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NUB1 | GRCh38.p7 | 7:151344861 | GAAAATTAGCCGGGC[A/G]TGGTGGCGCATGCCT | 51667 |
rs575425325 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NUB1 | GRCh38.p7 | 7:151351906 | TTTCAGGCTGTTGGC[A/C]CATCTGTAAAACACA | 51667 |
rs575480575 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | NUB1 | GRCh38.p7 | 7:151340808 | ATTAAAGATCTATTG[G/T]TTTTTATTGATTCAT | 51667 |
rs575516304 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151346199 | AGGTGACAAACTGTA[A/T]TAGGGTCCTAGTTCT | 51667 |
rs575540648 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151373604 | GGCTGTGGGGGGCGG[A/G]TCACCAGCTTTGGCA | 51667 |
rs575636393 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151359692 | TGAGGCAGGAGAATC[G/T]CTTGAACCCAGGAGG | 51667 |
rs575660391 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NUB1 | GRCh38.p7 | 7:151367577 | TCTGATACCTGGTTT[A/G]GATTTCTGCATACTT | 51667 |
rs575728236 | snp | A/G | | | intron-variant, utr-variant-5-prime | NUB1 | GRCh38.p7 | 7:151352142 | ACACACATGCGTAGA[A/G]GACCCTGTGGATCAG | 51667 |
rs575729911 | in-del | -/T | 0.461212 | 0.133752 | intron-variant | NUB1 | GRCh38.p7 | 7:151365891 | CAAAATTAAAGTCCT[-/T]TTTTTTTTTATTCCA | 51667 |
rs575743150 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | NUB1 | GRCh38.p7 | 7:151341431 | GGTCCCGACCCTTCC[C/G]CCAGCCTCTTTCAAG | 51667 |
rs575776682 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NUB1 | GRCh38.p7 | 7:151365910 | TTTTTTATTCCATGC[A/G]TATTTTGATAGGCAG | 51667 |
rs575813634 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151366615 | TTAAAGCATGGTCTT[C/T]CCCGTATTTGCTGAG | 51667 |
rs575848776 | snp | A/G | 0.00033184 | 0.0128767 | intron-variant | NUB1 | GRCh38.p7 | 7:151352213 | AGGTAGATTTTCTCC[A/G]GATGTGCAACTAGGG | 51667 |
rs575935129 | snp | A/G | 0.368119 | 0.220336 | intron-variant | NUB1 | GRCh38.p7 | 7:151360996 | GTGTTGCTCAGGCTG[A/G]TCTTGAACTCCTGGA | 51667 |
rs576036765 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151369868 | AAAAAAGCAGCCTCA[A/G]GGGTATTTGGATGGG | 51667 |
rs576154847 | snp | C/T | 0.0023933 | 0.0345097 | downstream-variant-500B, utr-variant-3-prime | NUB1, WDR86 | GRCh38.p7 | 7:151378920 | GAGCCGCAGAGGAAG[C/T]CGGCTGTGGAGGCAG | 51667 |
rs576464087 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151371781 | CAGAGCCTTGCTCTC[C/T]TGTCCAGGCTGGAGG | 51667 |
rs576546661 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151367790 | AGACCAAGGGAATGA[C/T]AGAGATGAGTATTAT | 51667 |
rs576551925 | snp | A/G | 4.311e-05 | 0.00464253 | synonymous-codon | NUB1 | GRCh38.p7 | 7:151376783 | AGACTCTTTGTCCCC[A/G]CCAGCCACGTCCCCT | 51667 |
rs576590123 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151365636 | TCTCAAAGGCAGGTT[C/T]TCAGGCTGAGCCGTA | 51667 |
rs576636705 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | NUB1 | GRCh38.p7 | 7:151376555 | TAAACATGAGAGTCG[C/G]CTGTCCACTCGTATG | 51667 |
rs576646426 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151348823 | CAAGTGATGCGCCTG[C/T]CTCGGCCTCCCAAAG | 51667 |
rs576691695 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | NUB1 | GRCh38.p7 | 7:151375010 | CTTAGGTTGTGCACG[C/T]GCTGGGGGCGGGGCT | 51667 |
rs576739478 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151370325 | AACTCCTGACCTCAA[G/T]TGATCCTCCCGCCTT | 51667 |
rs577029669 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151366843 | AATATATACCAAGAA[C/T]GGGGAAAGAATTCCA | 51667 |
rs577063981 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151359755 | GCCCTCCAGCCTGGA[C/T]GACAGAATGAGACTC | 51667 |
rs577069643 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151367454 | ATGCAGAAAATAGAC[A/G]TTTCAGCAGTAATGG | 51667 |
rs577115978 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | NUB1 | GRCh38.p7 | 7:151341552 | TGGCGTTGGACACCA[A/G]CTCCCAGGTCCTCGC | 51667 |
rs577219257 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151349309 | TCAAATAAATTGTTG[C/T]TGTTTGGAAAGTTAC | 51667 |
rs577261149 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151347785 | CTATAAAGTTTTCCA[A/G]CTTCACTTTTATCAT | 51667 |
rs577403550 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151347234 | TTCCTCTTTTCCTAC[A/G]TAACTATTAAAAAAA | 51667 |
rs577427102 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151354543 | TTATTTGCATCTTTG[A/G]CATAATTTTTGTTAG | 51667 |
rs577463709 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NUB1 | GRCh38.p7 | 7:151343766 | GGAAGTTCAGAGTCC[A/T]GTGTTGTGGGTGGAA | 51667 |
rs577538742 | snp | C/G | 1.71749e-05 | 0.00293038 | intron-variant | NUB1 | GRCh38.p7 | 7:151368913 | TCACATGCCCTAGCT[C/G]TCTTGGGTATGAAAG | 51667 |
rs577604861 | snp | A/C/G | 5.13152e-05 | 0.00506512 | missense | NUB1 | GRCh38.p7 | 7:151355891 | AGCAAAATGAGGCCA[A/C/G]ACTCAAAGAAAAACA | 51667 |
rs577640976 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151371599 | ACACCTCAGGGAGGG[A/G]TAGAATGGGTGCTGG | 51667 |
rs577645314 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | NUB1, WDR86 | GRCh38.p7 | 7:151378207 | CCAGTGGGAGTTCCT[C/T]CCAGCCCCAGGACCA | 51667 |
rs577667942 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151361701 | TTTCCATTGGTCAGT[A/G]CCTTTGGGTTCTAAG | 51667 |
rs577727459 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151344163 | TCTAGCCTGGGCGAC[A/T]GAGTGAGACTCCCTC | 51667 |
rs577775947 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151369456 | AAACAAAATTGTTTT[C/T]TCATGAGGTCATTAT | 51667 |
rs577814740 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NUB1 | GRCh38.p7 | 7:151370050 | CTTTGGGTCTTGCTA[C/T]AGAAGTCAATGAGTA | 51667 |
rs577835608 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151356750 | GAGACGGAGTTTTGC[C/T]CTTGTTGCTCAGGCT | 51667 |
rs577879168 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151372138 | TCGGCATGGCCAGGC[C/T]GTGAGACGTAGCCTT | 51667 |
rs578075635 | in-del | -/AAAG | 0.0598883 | 0.16235 | intron-variant | NUB1 | GRCh38.p7 | 7:151366523 | CAATGATTCTTAAAG[-/AAAG]AAAGAAAGAAAGAAA | 51667 |
rs578138914 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NUB1 | GRCh38.p7 | 7:151357895 | GATTACAGGCATGAG[A/C]CACTGCGCCCGGCCG | 51667 |
rs745351577 | snp | C/T | 1.67804e-05 | 0.00289653 | missense | NUB1 | GRCh38.p7 | 7:151356158 | TGGATCCAGAAATGA[C/T]ACCGTACTTAGACAT | 51667 |
rs745373677 | in-del | -/TTTTTT | | | intron-variant | NUB1 | GRCh38.p7 | 7:151348570 | TTTTTTGCTTTTTGC[-/TTTTTT]TTTTTTTTTTTTTTT | 51667 |
rs745390870 | snp | C/T | 6.1864e-05 | 0.00556131 | synonymous-codon | NUB1 | GRCh38.p7 | 7:151377075 | CTCAACAGACGAAGA[C/T]ATGGAGACAGAGGCC | 51667 |
rs745541978 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151348712 | CCCCAAGTAGCTGGG[C/T]CTACAGGCACACGCC | 51667 |
rs745569456 | snp | A/T | 1.70003e-05 | 0.00291545 | utr-variant-3-prime | NUB1 | GRCh38.p7 | 7:151377250 | AGAAATAGCGCTAAT[A/T]TTCTGCTTATAAATG | 51667 |
rs745712676 | snp | A/C | | | upstream-variant-2KB | NUB1 | GRCh38.p7 | 7:151341162 | ACAGTAAGAGATTAA[A/C]AGCAATAACTGATAA | 51667 |
rs745798767 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151372253 | CAGTACTCACTGTCA[C/T]TGATTTGATCTACTT | 51667 |
rs745819236 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151374405 | CCAGCCCAGACACAG[A/G]CTGCGTGAGGCCACG | 51667 |
rs745872738 | snp | A/G | 1.65608e-05 | 0.00287752 | missense | NUB1 | GRCh38.p7 | 7:151375902 | TCCAATCCTGAAACC[A/G]ACAACCGTCAAGAAA | 51667 |
rs745882037 | in-del | -/CCAC | 1.66125e-05 | 0.00288201 | frameshift-variant | NUB1 | GRCh38.p7 | 7:151368861 | ACGTGGATCATGCGG[-/CCAC]CCACTCATATTACCA | 51667 |
rs745901303 | snp | A/G | | | upstream-variant-2KB | NUB1 | GRCh38.p7 | 7:151340729 | AGGCGAATCAGATTG[A/G]TCTGGTGCGGTTATA | 51667 |
rs745903814 | snp | A/G | 3.54114e-05 | 0.00420766 | intron-variant | NUB1 | GRCh38.p7 | 7:151376611 | CCAGGGGCTGATGCT[A/G]TGACCCCTGCGCTCT | 51667 |
rs745961599 | snp | A/G | 0.000116121 | 0.00761886 | synonymous-codon | NUB1 | GRCh38.p7 | 7:151376675 | CGTGGCCGAAGCTGC[A/G]CTGAGAGTGTTCAGA | 51667 |
rs746168856 | snp | C/T | 1.65446e-05 | 0.00287612 | intron-variant | NUB1 | GRCh38.p7 | 7:151366893 | CAAATGCTAAAAATG[C/T]TTCAAATGCTGCTTG | 51667 |
rs746192993 | snp | A/G | | | upstream-variant-2KB | NUB1 | GRCh38.p7 | 7:151339837 | ATTTCCCCCTACATC[A/G]CTGTGTTGGTTTTGT | 51667 |
rs746201939 | snp | A/G | 1.72534e-05 | 0.00293708 | intron-variant | NUB1 | GRCh38.p7 | 7:151368700 | GCTTTAAGTATTGCC[A/G]TGGTTACATGATTCT | 51667 |
rs746234176 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151371159 | TTCCACCCAACAGAT[A/G]TTGTTAGTTACGATG | 51667 |
rs746255446 | snp | C/T | 1.90936e-05 | 0.00308973 | intron-variant | NUB1 | GRCh38.p7 | 7:151351491 | GGTCCAAGTAAGTAT[C/T]TGTGTGCTCTGTGTC | 51667 |
rs746257071 | snp | C/T | 1.65778e-05 | 0.002879 | synonymous-codon | NUB1 | GRCh38.p7 | 7:151368782 | TCCATCAAAAGTGGA[C/T]AATTTGTTGCAGTTG | 51667 |
rs746393998 | snp | C/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151345216 | TGGAGCTCATTTAAA[C/G]CATAGTAATTTATAT | 51667 |
rs746451600 | snp | C/T | | | upstream-variant-2KB | NUB1 | GRCh38.p7 | 7:151341065 | TTACATACACACACA[C/T]ATATATATACTATAT | 51667 |
rs746469984 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151344859 | ATGAAAATTAGCCGG[A/G]CGTGGTGGCGCATGC | 51667 |
rs746470056 | snp | A/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151367385 | GTGATCACCCTGACC[A/T]GGAGAGAGCTGCTGA | 51667 |
rs746497859 | snp | A/G | 8.43505e-05 | 0.0064937 | synonymous-codon, intron-variant | NUB1 | GRCh38.p7 | 7:151374192 | CTACTCCACGCACGC[A/G]GCCCAGCAGGTACTC | 51667 |
rs746511747 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151372249 | AGTGCAGTACTCACT[A/G]TCATTGATTTGATCT | 51667 |
rs746673936 | in-del | -/AGCTTGG | 4.97006e-05 | 0.00498476 | intron-variant | NUB1 | GRCh38.p7 | 7:151375969 | GGCCTTTGTGCCCTC[-/AGCTTGG]ACAGCCTCGGGTGGG | 51667 |
rs746800245 | snp | C/T | 8.38399e-05 | 0.00647402 | intron-variant | NUB1 | GRCh38.p7 | 7:151345486 | TTTTCTTTTAAGACA[C/T]CAATAATTAGCAGCA | 51667 |
rs746811662 | snp | A/C | 1.66158e-05 | 0.0028823 | missense, utr-variant-5-prime | NUB1 | GRCh38.p7 | 7:151349119 | AATGCTGTGAAAATG[A/C]AGTAGAAAAGGTAAT | 51667 |
rs746844068 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151351227 | TGGTGCCACGCTGCC[A/G]CCCCCTTGAGGACGT | 51667 |
rs746857650 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151366075 | GACTTGAGACCTAGA[C/T]TGGCATTAGGAATTT | 51667 |
rs746968071 | snp | A/G | | | intron-variant, utr-variant-5-prime | NUB1 | GRCh38.p7 | 7:151352137 | ATGCAACACACATGC[A/G]TAGAAGACCCTGTGG | 51667 |
rs746972274 | snp | C/T | | | upstream-variant-2KB | NUB1 | GRCh38.p7 | 7:151340315 | TAGAAGCCAACACCA[C/T]GGCACGGGCTTTTGA | 51667 |
rs746977497 | snp | A/C/T | 5.1675e-05 | 0.00508284 | intron-variant | NUB1 | GRCh38.p7 | 7:151368915 | ACATGCCCTAGCTCT[A/C/T]TTGGGTATGAAAGAA | 51667 |
rs747040612 | snp | A/G | 3.68501e-05 | 0.00429228 | missense, utr-variant-5-prime | NUB1 | GRCh38.p7 | 7:151351449 | ACTTGTTGGAGACCC[A/G]ATTGCACATCACTGG | 51667 |
rs747143137 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151342178 | AAATGCTATACTTGA[A/G]TCGTAACACTCCGAG | 51667 |
rs747181440 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151346457 | AGATAGCTTCAGGAT[A/G]GGGCTGGTCACCAAA | 51667 |
rs747196172 | snp | A/C | | | utr-variant-3-prime | NUB1, WDR86 | GRCh38.p7 | 7:151378178 | GCGCCACGCACTCCT[A/C]TGTAGATGTGTGCCC | 51667 |
rs747202423 | in-del | -/T | 1.67649e-05 | 0.0028952 | intron-variant | NUB1 | GRCh38.p7 | 7:151349271 | AATTTGAGTAGGCAC[-/T]TAATGTCCAGTTAGT | 51667 |
rs747202728 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151362696 | TGGGCTTGCAGGAGG[C/T]CAAGGAGGTGAGAGG | 51667 |
rs747327476 | in-del | -/TTG | | | intron-variant | NUB1 | GRCh38.p7 | 7:151360034 | GATTGAGTTATGATC[-/TTG]TTTTCATTTTTTTTA | 51667 |
rs747335922 | snp | C/G/T | 0.000132111 | 0.00812659 | missense, synonymous-codon | NUB1 | GRCh38.p7 | 7:151377069 | TAGTGCCTCAACAGA[C/G/T]GAAGACATGGAGACA | 51667 |
rs747387276 | snp | C/T | 5.03233e-05 | 0.00501589 | utr-variant-3-prime | NUB1 | GRCh38.p7 | 7:151377234 | AAACTAAATAATGAA[C/T]AGAAATAGCGCTAAT | 51667 |
rs747391038 | snp | A/G | 4.37111e-05 | 0.00467479 | missense | NUB1 | GRCh38.p7 | 7:151367870 | TTTTAGGGAAATTGT[A/G]GGAAAGAGAAGGTAC | 51667 |
rs747419598 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151369070 | TGGAGTGCAGTGGCA[C/T]GATCTTGGCTCACTG | 51667 |
rs747498571 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151354933 | TATTTTCTGTGGAGA[C/T]GGGGTCCACTGTGTT | 51667 |
rs747528101 | in-del | -/A | | | intron-variant | NUB1 | GRCh38.p7 | 7:151346369 | GTTCCTGGCAGAGCC[-/A]AAACTCTTGGGATTT | 51667 |
rs747542758 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151371085 | CTGAAGTTAAAAGCC[C/T]TTGGAGAAAATGCAA | 51667 |
rs747619837 | snp | A/C | 3.31488e-05 | 0.00407103 | synonymous-codon | NUB1 | GRCh38.p7 | 7:151368827 | GGAAGCCCGGCTTGG[A/C]CTGAGGGCGTGTGAT | 51667 |
rs747672865 | snp | C/T | 8.52958e-05 | 0.00652998 | intron-variant | NUB1 | GRCh38.p7 | 7:151368905 | ACCCACTTTCACATG[C/T]CCTAGCTCTCTTGGG | 51667 |
rs747679136 | snp | C/G | | | upstream-variant-2KB | NUB1 | GRCh38.p7 | 7:151340061 | ATGTTTTCTGACTTC[C/G]CTTTCTGGCTTTTCT | 51667 |
rs747703327 | snp | A/C | 1.67837e-05 | 0.00289682 | missense, utr-variant-5-prime | NUB1 | GRCh38.p7 | 7:151352852 | GAAAATTATATCAAA[A/C]TTGTCATAAATAAGA | 51667 |
rs747731158 | in-del | -/TTTAA | | | intron-variant | NUB1 | GRCh38.p7 | 7:151370535 | TTATTTATTTTTTCC[-/TTTAA]TTTTATTTTATTATT | 51667 |
rs747818989 | snp | C/T | 3.40315e-05 | 0.00412488 | missense, utr-variant-5-prime | NUB1 | GRCh38.p7 | 7:151355797 | GAACAAGGCGTGGCT[C/T]ACAATGTGAAAGCGA | 51667 |
rs747921061 | snp | A/G | 4.95025e-05 | 0.00497482 | intron-variant | NUB1 | GRCh38.p7 | 7:151360289 | CCAGCTTTAAGGAAG[A/G]TGGCCCAGACTATAC | 51667 |
rs747963811 | snp | C/T | 1.73658e-05 | 0.00294662 | stop-gained, utr-variant-5-prime | NUB1 | GRCh38.p7 | 7:151345371 | CAAAAGAAATATCTT[C/T]AAGCAAAATTGACCC | 51667 |
rs747996917 | in-del | -/ACC | 1.66751e-05 | 0.00288744 | intron-variant | NUB1 | GRCh38.p7 | 7:151355953 | CTGGCAAAGAGAGGT[-/ACC]CAGAGCTCTGGGCTT | 51667 |
rs748016928 | snp | A/G | 2.22536e-05 | 0.00333561 | missense, utr-variant-5-prime | NUB1 | GRCh38.p7 | 7:151345465 | TTGGTTTGGCATTAA[A/G]GGTATTTTTCTTTTA | 51667 |
rs748049930 | in-del | -/AG | 7.49372e-05 | 0.0061207 | frameshift-variant, intron-variant | NUB1 | GRCh38.p7 | 7:151374126 | AAGGAAGGAGGAAAA[-/AG]AGAAGAAAAGACGCC | 51667 |
rs748119731 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151353266 | TTATGTCAGAGCACT[A/G]TGGTGTGAATTTGAG | 51667 |
rs748142399 | snp | C/T | 6.09849e-05 | 0.00552166 | intron-variant | NUB1 | GRCh38.p7 | 7:151367846 | TTTTATCCTTTTTTT[C/T]TTCAATAATTTTAGG | 51667 |
rs748174614 | in-del | -/GCAGAG | | | intron-variant | NUB1 | GRCh38.p7 | 7:151353357 | AGGATGGAGGGGCAA[-/GCAGAG]GCCACACTGTGAATT | 51667 |
rs748245389 | snp | A/C | 1.66084e-05 | 0.00288165 | missense | NUB1 | GRCh38.p7 | 7:151368760 | TCTTTAAAGAGCTAT[A/C]TATTGATCCATCAAA | 51667 |
rs748404521 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151343325 | CTAATTCTTGTCCCC[A/G]CACTGACATAAAATA | 51667 |
rs748464039 | snp | A/C | | | intron-variant | NUB1 | GRCh38.p7 | 7:151360788 | CACAGGTGCACATCA[A/C]CATGCCCAGATAATT | 51667 |
rs748472096 | in-del | -/C | | | intron-variant | NUB1 | GRCh38.p7 | 7:151343815 | TGCCTAATTTTGTGT[-/C]CTTTGCCTGAGTCAT | 51667 |
rs748530591 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151348685 | GGTTCAAGCGATTCT[C/T]CTGCCTCAGCCCCCC | 51667 |
rs748635158 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151367467 | ACATTTCAGCAGTAA[C/T]GGTTTACGTGAATGA | 51667 |
rs748744095 | snp | A/T | 1.65875e-05 | 0.00287984 | missense | NUB1 | GRCh38.p7 | 7:151367057 | GATGCAGAAAAAAAA[A/T]TAAACTTGGCCCAGA | 51667 |
rs748754266 | snp | A/G | 0.000115334 | 0.00759299 | utr-variant-3-prime | NUB1 | GRCh38.p7 | 7:151377268 | CTGCTTATAAATGCT[A/G]TCATTATGAAAAGGC | 51667 |
rs748805805 | snp | C/T | 2.31147e-05 | 0.00339953 | intron-variant | NUB1 | GRCh38.p7 | 7:151345331 | GGAGTTTTATTAATG[C/T]ATTGTTTTGCTTTCA | 51667 |
rs748818873 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151349907 | CACTACCACCTAGAC[A/G]CGGAAACCGGTAGTG | 51667 |
rs748834149 | snp | A/C | 1.70461e-05 | 0.00291938 | intron-variant | NUB1 | GRCh38.p7 | 7:151368719 | TTACATGATTCTTAC[A/C]TTTCCCTGTCTCTAG | 51667 |
rs748940516 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151348185 | TGGGGAGGAACCATA[A/G]TGACTTTGCTCTCAG | 51667 |
rs748947781 | snp | A/G | 1.65704e-05 | 0.00287836 | synonymous-codon | NUB1 | GRCh38.p7 | 7:151368800 | TTTGTTGCAGTTGGG[A/G]TTTACTGCCCAGGAA | 51667 |
rs748950547 | snp | G/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151350822 | TCATAGCAACACTAT[G/T]CAGTAGCTGAGAGAT | 51667 |
rs749093560 | snp | A/C/T | 3.35814e-05 | 0.00409753 | stop-gained, synonymous-codon | NUB1 | GRCh38.p7 | 7:151356165 | AGAAATGACACCGTA[A/C/T]TTAGACATAGCTAAC | 51667 |
rs749100558 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151368209 | CTCACTCATCTTGCC[A/G]TCTAGAGGTGAGCCA | 51667 |
rs749132094 | snp | C/T | 6.62526e-05 | 0.00575516 | stop-gained | NUB1 | GRCh38.p7 | 7:151375941 | CAGGAAAACATTGAC[C/T]GAGTGAGTGACAGGC | 51667 |
rs749280139 | in-del | -/CTT | 1.88734e-05 | 0.00307187 | cds-indel, utr-variant-5-prime | NUB1 | GRCh38.p7 | 7:151351434 | ACAGGATAGGAAAAA[-/CTT]CTTGTTGGAGACCCG | 51667 |
rs749287363 | snp | A/T | 4.62952e-05 | 0.00481097 | intron-variant | NUB1 | GRCh38.p7 | 7:151360113 | TATATTTTAAAGTGA[A/T]GTTTTTTAAATTTGT | 51667 |
rs749340809 | in-del | -/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151375191 | CAGTACTTTTGTAAC[-/T]ATGTACATGTATATT | 51667 |
rs749349890 | snp | C/G/T | 5.324e-05 | 0.00515923 | intron-variant | NUB1 | GRCh38.p7 | 7:151366913 | AATGCTGCTTGGCAG[C/G/T]GATGTCACTGTCCTT | 51667 |
rs749390873 | snp | C/G | 1.66322e-05 | 0.00288371 | missense | NUB1 | GRCh38.p7 | 7:151367024 | TACTTCCGCCTGGAA[C/G]AGCTGGAATGCCTTG | 51667 |
rs749421176 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151367440 | TTTGCAAGATGTAAA[C/T]GCAGAAAATAGACAT | 51667 |
rs749451383 | snp | C/T | | | downstream-variant-500B, utr-variant-3-prime | NUB1, WDR86 | GRCh38.p7 | 7:151378633 | ATGCCGCACGCCAAG[C/T]GGGGCTGGGGTGCAT | 51667 |
rs749584437 | snp | A/G | 1.67973e-05 | 0.00289799 | missense, utr-variant-5-prime | NUB1 | GRCh38.p7 | 7:151352828 | ATAGCTGAAACCTTT[A/G]GACTTCAAGAAAATT | 51667 |
rs749682596 | snp | G/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151358600 | GACCTGAGGTAGAAT[G/T]TTTTCACCCTGAAAC | 51667 |
rs749682838 | snp | C/T | 1.65798e-05 | 0.00287917 | missense, utr-variant-5-prime | NUB1 | GRCh38.p7 | 7:151355777 | TTATAGGGAAAACCC[C/T]TGAAGAACAAGGCGT | 51667 |
rs749723770 | snp | C/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151344712 | TTATGTTAAACTAGC[C/G]AAAGTATGAGAGAAT | 51667 |
rs749735837 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151347679 | TGCCCAGGTTGGTCT[C/T]GAAGTCCTGGGCTTG | 51667 |
rs749857425 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151343029 | GCTTGGCTCCAGTAA[C/T]CAGCCTGTGAAATTA | 51667 |
rs749901667 | snp | C/T | 0.000149092 | 0.00863271 | intron-variant | NUB1 | GRCh38.p7 | 7:151375973 | TTTGTGCCCTCAGCT[C/T]GGACAGCCTCGGGTG | 51667 |
rs749922815 | snp | C/G | 4.53186e-05 | 0.00475996 | intron-variant | NUB1 | GRCh38.p7 | 7:151356272 | GATTTGTTGTCAGGG[C/G]AGAGGTGGTTTTTTA | 51667 |
rs749954813 | snp | A/G | 7.35592e-05 | 0.00606417 | missense | NUB1 | GRCh38.p7 | 7:151376643 | CCCTAGTTGGTGTAC[A/G]TGGGTTTTGATGCAC | 51667 |
rs749975721 | snp | C/T | 7.9186e-05 | 0.0062918 | intron-variant | NUB1 | GRCh38.p7 | 7:151345310 | TAACATTTTAAAATG[C/T]GATGTGGAGTTTTAT | 51667 |
rs749991383 | snp | C/T | 5.79828e-05 | 0.00538405 | synonymous-codon | NUB1 | GRCh38.p7 | 7:151376729 | GACCCTTGCTCACAA[C/T]GGAGGAAGCCTGCCT | 51667 |
rs750007094 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151355005 | TGCCTCAGCCTGCCA[A/G]AGTACTGAGATTACA | 51667 |
rs750008703 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | NUB1, WDR86 | GRCh38.p7 | 7:151377766 | GGCATAACGATGAGG[C/T]GCTGGCCTTGGGGGC | 51667 |
rs750025708 | snp | A/G/T | 7.62973e-05 | 0.00617608 | intron-variant | NUB1 | GRCh38.p7 | 7:151360254 | ATATTTCTGGTAGGC[A/G/T]CTTTTGTACTTGGTG | 51667 |
rs750067194 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | NUB1, WDR86 | GRCh38.p7 | 7:151377682 | CTGCCAGGGTGCCAC[A/G]TGGGTTCCTGTGCCA | 51667 |
rs750115836 | snp | A/C | | | intron-variant | NUB1 | GRCh38.p7 | 7:151362777 | AGTCTTCTGCTCAGT[A/C]ATGATCAGCACATGT | 51667 |
rs750217394 | snp | A/C | 0.000139655 | 0.00835512 | intron-variant | NUB1 | GRCh38.p7 | 7:151367988 | GAAAAGTAAAGTTGT[A/C]ACCAATTTTCACCTC | 51667 |
rs750272481 | snp | C/T | 0.000156605 | 0.00884748 | intron-variant | NUB1 | GRCh38.p7 | 7:151351414 | TTTTACTTTGTCTTA[C/T]TTTTAACAGGATAGG | 51667 |
rs750308434 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151353863 | AGCCTTGCTTTCCAG[C/T]GTCATCTCTAGCAAT | 51667 |
rs750404174 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151364305 | AGGCGCCTGTAGTCC[C/T]AGCTACTTGAGAGGC | 51667 |
rs750410461 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151362642 | GGGAGGGCAAACCCA[A/G]GCAGAGCCTTGTGCT | 51667 |
rs750437658 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151358492 | CTGTCAGATCAGCGG[C/T]GGCATTAGAGTCTTA | 51667 |
rs750478189 | snp | C/T | 1.67525e-05 | 0.00289413 | intron-variant | NUB1 | GRCh38.p7 | 7:151355743 | AATGGCTTTTTAAAA[C/T]AATAGGCAGTTCTGA | 51667 |
rs750533197 | snp | C/G | 1.78755e-05 | 0.00298955 | missense | NUB1 | GRCh38.p7 | 7:151355872 | TTCCAGTTAGAGGAA[C/G]AGGAGCAAAATGAGG | 51667 |
rs750784903 | snp | A/G | 1.74759e-05 | 0.00295595 | synonymous-codon, utr-variant-5-prime | NUB1 | GRCh38.p7 | 7:151345427 | ACTTTGGAAACCTCC[A/G]TATACAGATGAAAAT | 51667 |
rs751020213 | snp | A/G | 1.6566e-05 | 0.00287797 | intron-variant | NUB1 | GRCh38.p7 | 7:151351394 | ATGGGTTAAATTCAA[A/G]TACGTTTTACTTTGT | 51667 |
rs751159565 | snp | G/T | 1.65652e-05 | 0.0028779 | intron-variant | NUB1 | GRCh38.p7 | 7:151375962 | AGTGACAGGCCTTTG[G/T]GCCCTCAGCTTGGAC | 51667 |
rs751190930 | snp | A/G | 1.68007e-05 | 0.00289828 | synonymous-codon | NUB1 | GRCh38.p7 | 7:151356138 | TACAGCAGCAGAGAC[A/G]GTGGTGGATCCAGAA | 51667 |
rs751323095 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151348163 | GAGATACTCATCTGG[A/G]TTTTTTTGGGGAGGA | 51667 |
rs751325033 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151347394 | CTCCAGCCTGGGCAA[C/T]GTAGTGAGACCCCGT | 51667 |
rs751349118 | in-del | -/TGT | | | intron-variant | NUB1 | GRCh38.p7 | 7:151375386 | AATGGAAGTACTGAG[-/TGT]TGTTGGAAAGGAAAG | 51667 |
rs751381088 | snp | A/G | 1.7257e-05 | 0.00293738 | intron-variant | NUB1 | GRCh38.p7 | 7:151376843 | TGAGGGCCGCATTGA[A/G]AGCAAAGTGTCTTCA | 51667 |
rs751384706 | snp | A/G | 9.16632e-05 | 0.00676928 | missense | NUB1 | GRCh38.p7 | 7:151367955 | ATGTAGAGGCTTATG[A/G]GTATCTTAACAAGGT | 51667 |
rs751404399 | snp | C/T | 1.71264e-05 | 0.00292624 | intron-variant | NUB1 | GRCh38.p7 | 7:151367142 | TATGTTCCTGGAATT[C/T]ATCTTATGTCTCGTT | 51667 |
rs751445697 | snp | C/G | 1.6577e-05 | 0.00287893 | missense, utr-variant-5-prime | NUB1 | GRCh38.p7 | 7:151349211 | GGAATTGCTACAATC[C/G]AGGTGTTTTTACCAC | 51667 |
rs751472376 | snp | C/T | 1.72228e-05 | 0.00293447 | intron-variant | NUB1 | GRCh38.p7 | 7:151367149 | CTGGAATTCATCTTA[C/T]GTCTCGTTGAGTCCA | 51667 |
rs751620768 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151344145 | GAGATTGTACCACTG[C/T]ACTCTAGCCTGGGCG | 51667 |
rs751621170 | snp | A/T | 1.66059e-05 | 0.00288144 | stop-gained | NUB1 | GRCh38.p7 | 7:151368761 | CTTTAAAGAGCTATA[A/T]ATTGATCCATCAAAA | 51667 |
rs751622861 | snp | G/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151366702 | CCTGGGGCAAGTGGT[G/T]GTAAGCTTTGATTCC | 51667 |
rs751672594 | snp | C/T | 3.3216e-05 | 0.00407515 | missense | NUB1 | GRCh38.p7 | 7:151368859 | GGAACGTGGATCATG[C/T]GGCCACTCATATTAC | 51667 |
rs751675231 | snp | G/T | 1.72773e-05 | 0.00293911 | intron-variant | NUB1 | GRCh38.p7 | 7:151352907 | GCAAAGTATGCATAA[G/T]TTTTTAATGAACCAA | 51667 |
rs751745651 | in-del | -/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151364522 | TCAAATGGGATTTAA[-/T]TTTTTGTTGTTGTTG | 51667 |
rs751961573 | snp | C/T | 2.11396e-05 | 0.00325106 | intron-variant | NUB1 | GRCh38.p7 | 7:151356263 | CTGTTCTTAGATTTG[C/T]TGTCAGGGCAGAGGT | 51667 |
rs752011644 | snp | G/T | 0.000211707 | 0.0102863 | intron-variant, utr-variant-5-prime | NUB1 | GRCh38.p7 | 7:151341864 | GAGGACACGGCGGCC[G/T]AGTGTCCTCGACCCC | 51667 |
rs752053676 | snp | G/T | 1.70243e-05 | 0.00291751 | missense, utr-variant-5-prime | NUB1 | GRCh38.p7 | 7:151345405 | TTTTAAGGGAAGACA[G/T]GATTCAACTTTGGAA | 51667 |
rs752084197 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151351692 | AGACTTGCAAGCACT[A/G]TTTCCTGGTGTAACT | 51667 |
rs752135788 | snp | C/G | 1.67041e-05 | 0.00288994 | missense | NUB1 | GRCh38.p7 | 7:151367105 | TACGGAGAAAATCAT[C/G]AGAGACTGGTCCACA | 51667 |
rs752140621 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151349877 | TAGAAGAAAAGACAG[C/T]TGGGCCCGGAGGACC | 51667 |
rs752193946 | snp | C/T | 6.6778e-05 | 0.00577793 | synonymous-codon, utr-variant-5-prime | NUB1 | GRCh38.p7 | 7:151349081 | TTGATAGGACCTTGC[C/T]AAGCAGTACTCTGAC | 51667 |
rs752319631 | snp | A/G | | | upstream-variant-2KB | NUB1 | GRCh38.p7 | 7:151339708 | ACCCTAGCAGATCTC[A/G]GACTCGAATCTTTGT | 51667 |
rs752405570 | snp | A/G | 2.31806e-05 | 0.00340437 | missense | NUB1 | GRCh38.p7 | 7:151376670 | GCACTCGTGGCCGAA[A/G]CTGCGCTGAGAGTGT | 51667 |
rs752472598 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151376527 | GGGCCATGGTGCACA[C/T]GCCGGGAGCTCTTAA | 51667 |
rs752559659 | snp | C/T | 7.23825e-05 | 0.00601548 | synonymous-codon | NUB1 | GRCh38.p7 | 7:151376757 | CCTCCCGAGCTGCCG[C/T]TGTCGCCAGAAGACT | 51667 |
rs752654396 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151347232 | TCTTCCTCTTTTCCT[A/G]CGTAACTATTAAAAA | 51667 |
rs752759189 | snp | A/C | | | intron-variant | NUB1 | GRCh38.p7 | 7:151370494 | ACTATTACTCCACTA[A/C]CAGTAAGAATTTATT | 51667 |
rs752797838 | snp | A/T | 1.66776e-05 | 0.00288765 | missense | NUB1 | GRCh38.p7 | 7:151368745 | TCTAGGCACGTCAGC[A/T]CTTTAAAGAGCTATA | 51667 |
rs752819162 | snp | A/C | 0.000209008 | 0.0102206 | missense, upstream-variant-2KB | NUB1 | GRCh38.p7 | 7:151341777 | CTGGCCTCACCCGGA[A/C]TGAAAACAAACGGCG | 51667 |
rs752841653 | snp | C/T | 8.35038e-05 | 0.00646103 | intron-variant | NUB1 | GRCh38.p7 | 7:151368004 | ACCAATTTTCACCTC[C/T]TTTTAAAAAACATTC | 51667 |
rs752877333 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151344940 | AGGGGGCGGAGCTTG[C/T]AGTGAGCCGAGATCG | 51667 |
rs752897618 | snp | A/C | 1.90239e-05 | 0.00308408 | missense, utr-variant-5-prime | NUB1 | GRCh38.p7 | 7:151351430 | TTTTAACAGGATAGG[A/C]AAAACTTGTTGGAGA | 51667 |
rs752982511 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151371777 | GAGACAGAGCCTTGC[C/T]CTCTTGTCCAGGCTG | 51667 |
rs753007493 | snp | G/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151343683 | AGACAGCTCCATCGC[G/T]GTACATACTTCTCTG | 51667 |
rs753052890 | in-del | -/CG | 1.65751e-05 | 0.00287876 | frameshift-variant, utr-variant-5-prime | NUB1 | GRCh38.p7 | 7:151349210 | GGGAATTGCTACAAT[-/CG]AGGTGTTTTTACCAC | 51667 |
rs753089925 | snp | A/G | 1.65688e-05 | 0.00287821 | intron-variant | NUB1 | GRCh38.p7 | 7:151375805 | TGTCTGAATGTGTGA[A/G]GAGTTCTTAGTGATG | 51667 |
rs753202128 | snp | C/T | 1.98159e-05 | 0.00314763 | intron-variant | NUB1 | GRCh38.p7 | 7:151356249 | GAGAAATGTGTGGCC[C/T]GTTCTTAGATTTGTT | 51667 |
rs753249469 | in-del | -/TT | 0.000108021 | 0.00734837 | intron-variant | NUB1 | GRCh38.p7 | 7:151367855 | TTTTTTCTTCAATAA[-/TT]TTAGGGAAATTGTGG | 51667 |
rs753281855 | snp | G/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151354572 | AGATTTGTGTATTTG[G/T]CTAATTTATTCATGG | 51667 |
rs753315256 | snp | A/T | 1.84459e-05 | 0.00303688 | stop-gained, utr-variant-5-prime | NUB1 | GRCh38.p7 | 7:151345443 | TATACAGATGAAAAT[A/T]AAAAAGTTGGTTTGG | 51667 |
rs753320871 | snp | C/G | 1.96539e-05 | 0.00313473 | intron-variant | NUB1 | GRCh38.p7 | 7:151360263 | GTAGGCGCTTTTGTA[C/G]TTGGTGAACACCAGC | 51667 |
rs753322816 | snp | C/G/T | 6.81687e-05 | 0.00583778 | synonymous-codon | NUB1 | GRCh38.p7 | 7:151376747 | AGGAAGCCTGCCTCC[C/G/T]GAGCTGCCGCTGTCG | 51667 |
rs753334894 | snp | C/T | | | utr-variant-3-prime | NUB1 | GRCh38.p7 | 7:151377416 | GGGGAAGAAGCTTCC[C/T]CTGGCCTGGCGCAGG | 51667 |
rs753359149 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151345859 | ACAATTGCTCCTTTT[C/T]CCCCCAGTTTTTTTG | 51667 |
rs753380109 | snp | C/T | 5.10035e-05 | 0.00504967 | synonymous-codon | NUB1 | GRCh38.p7 | 7:151366981 | AGTGGATAACTACGC[C/T]GTCCTCCAGCTGGAT | 51667 |
rs753413124 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151365812 | TACATTTTTCTTGCC[A/G]CACCCACAACTGGAC | 51667 |
rs753416781 | snp | A/G | | | downstream-variant-500B, utr-variant-3-prime | NUB1, WDR86 | GRCh38.p7 | 7:151378719 | AGCTGAGGTGACGCG[A/G]AGTCTCAGCCTCATT | 51667 |
rs753477025 | snp | A/T | 0.000169624 | 0.00920777 | intron-variant | NUB1 | GRCh38.p7 | 7:151349037 | TTGCCTTTTTTTTTT[A/T]AAGTCAGTATTGCAT | 51667 |
rs753512364 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151374014 | CTTTGCCTGGAAATG[C/T]GGAGAATCCTGCAGA | 51667 |
rs753604792 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151369936 | CAGAGAGGGAGTGGA[C/T]TCGTGGGTTCATTCC | 51667 |
rs753675058 | snp | C/T | 0.000162562 | 0.00901413 | intron-variant, utr-variant-5-prime | NUB1 | GRCh38.p7 | 7:151352162 | CTGTGGATCAGCCCC[C/T]GCTATGGGCTTCTCC | 51667 |
rs753744541 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151355354 | ATATTTTTACCAATT[A/G]TGTGGCGTGATGGTA | 51667 |
rs753937993 | snp | C/T | 1.68724e-05 | 0.00290446 | intron-variant | NUB1 | GRCh38.p7 | 7:151355998 | GCTGCTTGGGGGCAG[C/T]ACTGGATCACACAGT | 51667 |
rs753961182 | snp | C/G | 0.000115413 | 0.00759562 | intron-variant | NUB1 | GRCh38.p7 | 7:151377008 | GTCCCCAGGACAATC[C/G]TCACATAATTCACTT | 51667 |
rs754074426 | snp | C/T | 4.72601e-05 | 0.00486084 | synonymous-codon | NUB1 | GRCh38.p7 | 7:151377147 | CTATCTTGACTCAAC[C/T]CTGGAAGATGAAGAA | 51667 |
rs754113393 | snp | C/T | | | upstream-variant-2KB | NUB1 | GRCh38.p7 | 7:151341563 | ACCAACTCCCAGGTC[C/T]TCGCCCCACACGGCC | 51667 |
rs754140884 | snp | A/C | | | intron-variant | NUB1 | GRCh38.p7 | 7:151369549 | ATATTATGAAAGCAC[A/C]GGTTAAAAAACTATA | 51667 |
rs754174937 | snp | A/C/T | 0.000416976 | 0.0144341 | synonymous-codon, intron-variant | NUB1 | GRCh38.p7 | 7:151374147 | GAAAAGACGCCGCCT[A/C/T]GAGAACATCAGGTTT | 51667 |
rs754194881 | snp | C/T | 1.66746e-05 | 0.00288739 | missense | NUB1 | GRCh38.p7 | 7:151368874 | CGGCCACTCATATTA[C/T]CAACCGCAGAGAGGT | 51667 |
rs754227832 | snp | A/T | 1.74275e-05 | 0.00295186 | missense | NUB1 | GRCh38.p7 | 7:151355882 | AGGAAGAGGAGCAAA[A/T]TGAGGCCAAACTCAA | 51667 |
rs754245726 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151342763 | CCCTGGAGTGTCTGA[C/T]ACGCACTGGGTTTGT | 51667 |
rs754263396 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151367308 | ATCTGGCTGTCTCTC[C/T]TACTTAGCGTGTGAG | 51667 |
rs754293616 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151375241 | TAAATTTTTATTTGA[A/G]TATCATCTAGTTCGT | 51667 |
rs754388896 | in-del | -/TT | 0.0242388 | 0.107387 | intron-variant | NUB1 | GRCh38.p7 | 7:151349027 | TTTCTATATTTTGCC[-/TT]TTTTTTTTTAAGTCA | 51667 |
rs754390945 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151360335 | GCCCTTGAGACTGCA[A/G]ACTTTCATCTACAAC | 51667 |
rs754414640 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151376457 | TTGAGTCTTCCAAGC[C/T]CCCTTCCAGGTTGCT | 51667 |
rs754431483 | snp | C/T | 3.88259e-05 | 0.00440584 | missense, utr-variant-5-prime | NUB1 | GRCh38.p7 | 7:151345450 | ATGAAAATAAAAAAG[C/T]TGGTTTGGCATTAAA | 51667 |
rs754455794 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151364835 | TTTAATTTTTTGAAA[A/G]CTAGGCTCAGTAGAT | 51667 |
rs754455918 | snp | A/G | | | downstream-variant-500B, utr-variant-3-prime | NUB1, WDR86 | GRCh38.p7 | 7:151378842 | TTCCCAGCTGTTTTT[A/G]GCCATCATAGAAGCA | 51667 |
rs754474978 | in-del | -/TTA | | | intron-variant | NUB1 | GRCh38.p7 | 7:151370505 | ACTACCAGTAAGAAT[-/TTA]TTATTTTTATTTTTA | 51667 |
rs754735642 | snp | A/G | 1.65756e-05 | 0.00287881 | intron-variant | NUB1 | GRCh38.p7 | 7:151375990 | GACAGCCTCGGGTGG[A/G]GTTGCTTGGGGTAAC | 51667 |
rs754857275 | snp | C/T | 2.31618e-05 | 0.00340299 | synonymous-codon | NUB1 | GRCh38.p7 | 7:151376666 | TGATGCACTCGTGGC[C/T]GAAGCTGCGCTGAGA | 51667 |
rs754942454 | snp | C/T | 0.000109679 | 0.00740456 | intron-variant | NUB1 | GRCh38.p7 | 7:151377021 | TCCTCACATAATTCA[C/T]TTACTCCTGCGGTAT | 51667 |
rs754945852 | snp | A/G | 6.0347e-05 | 0.00549271 | intron-variant | NUB1 | GRCh38.p7 | 7:151360269 | GCTTTTGTACTTGGT[A/G]AACACCAGCTTTAAG | 51667 |
rs754970195 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | NUB1, WDR86 | GRCh38.p7 | 7:151377857 | AGTAAAATACGCCCC[C/T]GAAATTCAAGATTGA | 51667 |
rs755078414 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151349517 | ACGTTGAGAAATAAT[A/G]GGGAATAAAGGATTC | 51667 |
rs755190386 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151368522 | CCAGCCTCTTACCTC[A/G]TGTTGTGCTGTGGCT | 51667 |
rs755210246 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151369939 | AGAGGGAGTGGATTC[A/G]TGGGTTCATTCCGTG | 51667 |
rs755214893 | snp | A/G | 4.49408e-05 | 0.00474008 | synonymous-codon | NUB1 | GRCh38.p7 | 7:151377177 | AATTATTATTGCAGA[A/G]TACCTATCCTATGTA | 51667 |
rs755233146 | snp | C/T | 5.25058e-05 | 0.00512349 | intron-variant | NUB1 | GRCh38.p7 | 7:151367162 | TATGTCTCGTTGAGT[C/T]CATTTCTAGCATTTG | 51667 |
rs755236400 | snp | C/T | 0.000151412 | 0.0086996 | synonymous-codon, utr-variant-5-prime | NUB1 | GRCh38.p7 | 7:151355790 | CCTTGAAGAACAAGG[C/T]GTGGCTCACAATGTG | 51667 |
rs755245218 | snp | G/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151342411 | ATGTATACTTGAAAA[G/T]GTGTGGCTAAATGTA | 51667 |
rs755249565 | in-del | -/CTC | | | intron-variant | NUB1 | GRCh38.p7 | 7:151342898 | CAGGCTGGTCTTGAA[-/CTC]CTGACCTCAGGTGAT | 51667 |
rs755265674 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151354676 | GTATGAGGAAACTGA[A/G]TCCTAGAAGATAGGT | 51667 |
rs755288080 | snp | C/G | 0.000147091 | 0.00857461 | intron-variant | NUB1 | GRCh38.p7 | 7:151367990 | AAAGTAAAGTTGTAA[C/G]CAATTTTCACCTCCT | 51667 |
rs755371750 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151375243 | AATTTTTATTTGAAT[A/G]TCATCTAGTTCGTTT | 51667 |
rs755400034 | snp | G/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151360444 | TCCCTGTAAAGAAAA[G/T]AATTTTCAAGCAGGT | 51667 |
rs755455220 | snp | G/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151348457 | ATCACAGTCACATAA[G/T]TCATAGCCCACCCTT | 51667 |
rs755497424 | snp | A/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151352470 | TTTTTTAGAGACAGG[A/T]TCTTGCTCTGTCACC | 51667 |
rs755558168 | snp | C/G/T | 3.26536e-05 | 0.00404051 | missense | NUB1 | GRCh38.p7 | 7:151376743 | ACGGAGGAAGCCTGC[C/G/T]TCCCGAGCTGCCGCT | 51667 |
rs755709114 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151373723 | AGAAGCTCTCCTACC[C/T]GGTTCCTACCTGGTT | 51667 |
rs755726490 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151372001 | GTGTGAGCCACTGCA[C/T]CCAGCCTTTAATACA | 51667 |
rs755753090 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | NUB1, WDR86 | GRCh38.p7 | 7:151377776 | TGAGGCGCTGGCCTT[A/G]GGGGCCACACCAGGT | 51667 |
rs755784108 | snp | A/G | 0.000496077 | 0.0157414 | intron-variant | NUB1 | GRCh38.p7 | 7:151345311 | AACATTTTAAAATGC[A/G]ATGTGGAGTTTTATT | 51667 |
rs755863594 | snp | C/T | | | upstream-variant-2KB | NUB1 | GRCh38.p7 | 7:151339869 | TCCCCAGCAGTGGCC[C/T]TCTGTGGTCTCAAAG | 51667 |
rs755920687 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151359304 | AAAAATTAGCCAGGC[A/G]TGGTGGTGGGTACCT | 51667 |
rs755922221 | snp | A/T | 1.93257e-05 | 0.00310845 | splice-acceptor-variant | NUB1 | GRCh38.p7 | 7:151351422 | TGTCTTATTTTTAAC[A/T]GGATAGGAAAAACTT | 51667 |
rs755942732 | snp | A/C | | | intron-variant | NUB1 | GRCh38.p7 | 7:151368327 | GAGAGAGTCCAGAGC[A/C]GGCCACTGGAGAGAT | 51667 |
rs756127614 | snp | G/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151355318 | TGCTTAACAGTGACA[G/T]AGTTACAACCAAATG | 51667 |
rs756180372 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151347659 | GAGACGGGGTTTCAC[C/T]TTGTTGCCCAGGTTG | 51667 |
rs756209898 | in-del | -/A | 1.67363e-05 | 0.00289272 | frameshift-variant | NUB1 | GRCh38.p7 | 7:151368881 | CATATTACCAACCGC[-/A]AGAGAGGTACCCACT | 51667 |
rs756235462 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151348250 | CAATCTTCTTTTTTT[C/T]CTCAATTCTAAAGCT | 51667 |
rs756364002 | snp | A/G | 1.65767e-05 | 0.00287891 | missense | NUB1 | GRCh38.p7 | 7:151368783 | CCATCAAAAGTGGAC[A/G]ATTTGTTGCAGTTGG | 51667 |
rs756395362 | snp | C/T | 4.02309e-05 | 0.00448485 | synonymous-codon | NUB1 | GRCh38.p7 | 7:151376775 | TCGCCAGAAGACTCT[C/T]TGTCCCCGCCAGCCA | 51667 |
rs756432557 | snp | A/T | 0.000867453 | 0.020808 | intron-variant | NUB1 | GRCh38.p7 | 7:151376853 | ATTGAGAGCAAAGTG[A/T]CTTCAGAAGCCAACA | 51667 |
rs756467047 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151367278 | TATATTTATAAAGTG[C/T]TCAATGTTTTACAAA | 51667 |
rs756483791 | snp | C/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151372091 | ATCTGAGAAAAGCAA[C/G]AGCTGTAGAAACGGA | 51667 |
rs756498126 | snp | A/G | | | upstream-variant-2KB | NUB1 | GRCh38.p7 | 7:151340931 | GAAAGCAGCAACAGG[A/G]AACGAAAAACGGATT | 51667 |
rs756594711 | snp | C/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151358551 | ATGTGAGGGATCTAG[C/G]CTGTGCACTCCTGAT | 51667 |
rs756654420 | snp | C/T | 3.32984e-05 | 0.00408021 | intron-variant | NUB1 | GRCh38.p7 | 7:151355756 | AATAATAGGCAGTTC[C/T]GATTTTTATAGGGAA | 51667 |
rs756736464 | snp | C/G | 1.65611e-05 | 0.00287755 | missense | NUB1 | GRCh38.p7 | 7:151375884 | ATGTGGTGGTTAAAT[C/G]ATTCCAATCCTGAAA | 51667 |
rs756805331 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151342996 | GCATCTCTGAGTACC[A/G]CATCAGCCTTTCAAA | 51667 |
rs756911047 | snp | G/T | 2.14595e-05 | 0.00327556 | intron-variant | NUB1 | GRCh38.p7 | 7:151356265 | GTTCTTAGATTTGTT[G/T]TCAGGGCAGAGGTGG | 51667 |
rs756967796 | snp | A/G | 1.67897e-05 | 0.00289733 | missense | NUB1 | GRCh38.p7 | 7:151356142 | GCAGCAGAGACAGTG[A/G]TGGATCCAGAAATGA | 51667 |
rs756969837 | snp | A/C | | | intron-variant | NUB1 | GRCh38.p7 | 7:151375824 | TTCTTAGTGATGGGT[A/C]AAGGGTGTTCCTGTG | 51667 |
rs756976417 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151366121 | CTTAAAATTAGTCAC[C/T]TTGATGGCTGTCTTT | 51667 |
rs757021231 | in-del | -/A | | | frameshift-variant, intron-variant | NUB1 | GRCh38.p7 | 7:151374197 | CCACGCACGCGGCCC[-/A]GCAGGTACTCCACGC | 51667 |
rs757025223 | snp | A/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151360824 | GTATTTGTTGTAGAG[A/T]TGAGGTTTCACTATG | 51667 |
rs757028706 | snp | A/G | 1.6601e-05 | 0.00288101 | synonymous-codon, utr-variant-5-prime | NUB1 | GRCh38.p7 | 7:151349129 | AAATGAAGTAGAAAA[A/G]GTAATAGAAGAAATA | 51667 |
rs757055272 | snp | A/G | | | upstream-variant-2KB | NUB1 | GRCh38.p7 | 7:151341687 | GCTGGCTTCGCCTTG[A/G]CCCCGCCCACAACCC | 51667 |
rs757137843 | snp | A/G/T | 3.31561e-05 | 0.0040715 | missense, utr-variant-5-prime | NUB1 | GRCh38.p7 | 7:151349212 | GAATTGCTACAATCG[A/G/T]GGTGTTTTTACCACC | 51667 |
rs757151062 | in-del | -/TA | | | utr-variant-3-prime, downstream-variant-500B | NUB1, WDR86 | GRCh38.p7 | 7:151377884 | TTGAGTGTCAGGCTT[-/TA]TATATATTCAGCATT | 51667 |
rs757175374 | snp | C/T | | | upstream-variant-2KB | NUB1 | GRCh38.p7 | 7:151340511 | GACCCTGCCATGGGG[C/T]GACACCAGGGCTTGA | 51667 |
rs757176212 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151367172 | TGAGTCCATTTCTAG[C/T]ATTTGTGTTTATTCC | 51667 |
rs757185192 | in-del | -/C | | | upstream-variant-2KB | NUB1 | GRCh38.p7 | 7:151340662 | TACGTGCGAAACCTT[-/C]CATCTGGGAGTCCAT | 51667 |
rs757236027 | snp | C/G | 0.000167856 | 0.00915967 | intron-variant | NUB1 | GRCh38.p7 | 7:151352223 | TCTCCGGATGTGCAA[C/G]TAGGGCTTCCTGTTC | 51667 |
rs757382068 | in-del | -/AT | 0.000154779 | 0.00879576 | intron-variant | NUB1 | GRCh38.p7 | 7:151368708 | TATTGCCGTGGTTAC[-/AT]GATTCTTACATTTCC | 51667 |
rs757409116 | in-del | -/A | 3.21321e-05 | 0.00400812 | intron-variant | NUB1 | GRCh38.p7 | 7:151351376 | CAGGGTAATCTCTCC[-/A]AAATGGGTTAAATTC | 51667 |
rs757457727 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151347385 | GCCACTGCACTCCAG[C/T]CTGGGCAACGTAGTG | 51667 |
rs757530513 | snp | C/G | 2.31398e-05 | 0.00340138 | missense | NUB1 | GRCh38.p7 | 7:151376671 | CACTCGTGGCCGAAG[C/G]TGCGCTGAGAGTGTT | 51667 |
rs757690469 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151367321 | TCTTACTTAGCGTGT[A/G]AGCATTTAGCCCAAA | 51667 |
rs757714668 | in-del | -/TTTT | | | intron-variant | NUB1 | GRCh38.p7 | 7:151357184 | ACCATGTCCAGCTAA[-/TTTT]TTTTTTTTTTTTTTT | 51667 |
rs757742051 | snp | C/T | | | upstream-variant-2KB | NUB1 | GRCh38.p7 | 7:151339733 | CTTTGTTTTGCAAGT[C/T]TATCAAAAACTTCTG | 51667 |
rs757751931 | snp | C/T | 3.45955e-05 | 0.00415891 | intron-variant | NUB1 | GRCh38.p7 | 7:151368698 | AAGCTTTAAGTATTG[C/T]CGTGGTTACATGATT | 51667 |
rs757804913 | snp | A/T | 1.65952e-05 | 0.00288051 | missense | NUB1 | GRCh38.p7 | 7:151368767 | AGAGCTATATATTGA[A/T]CCATCAAAAGTGGAC | 51667 |
rs757864153 | snp | A/G | 0.000132551 | 0.00813991 | synonymous-codon, utr-variant-5-prime | NUB1 | GRCh38.p7 | 7:151349195 | CAATTATAGAACAAC[A/G]GGAATTGCTACAATC | 51667 |
rs757868688 | snp | C/T | | | upstream-variant-2KB | NUB1 | GRCh38.p7 | 7:151340726 | AAAAGGCGAATCAGA[C/T]TGGTCTGGTGCGGTT | 51667 |
rs757870044 | snp | A/G | 3.32088e-05 | 0.00407471 | missense | NUB1 | GRCh38.p7 | 7:151367081 | GCCCAGAAATGCTTT[A/G]AAAATTGTTACGGAG | 51667 |
rs757870487 | snp | A/G | | | intron-variant, utr-variant-5-prime | NUB1 | GRCh38.p7 | 7:151352106 | AGGGCTGTCAGGGGT[A/G]GATTCAGGAAGTGGC | 51667 |
rs758075453 | snp | G/T | 3.6322e-05 | 0.00426142 | missense | NUB1 | GRCh38.p7 | 7:151376758 | CTCCCGAGCTGCCGC[G/T]GTCGCCAGAAGACTC | 51667 |
rs758078093 | snp | C/G | | | upstream-variant-2KB | NUB1 | GRCh38.p7 | 7:151341616 | CCGCTTAGCTCCGCC[C/G]CGTCGCGGCTCCGCC | 51667 |
rs758140717 | in-del | -/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151354322 | TCCCCCCACCCTTGC[-/T]TTTTTTTTTTTTTTT | 51667 |
rs758147290 | snp | A/G | | | utr-variant-3-prime | NUB1, WDR86 | GRCh38.p7 | 7:151378165 | AACCGTCCTCACTGC[A/G]CCACGCACTCCTCTG | 51667 |
rs758155456 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151376039 | AGGACTGGGGGAGTC[C/T]GTGCTGAAACCTTGG | 51667 |
rs758167207 | snp | A/G | 1.68244e-05 | 0.00290033 | synonymous-codon | NUB1 | GRCh38.p7 | 7:151355907 | ACTCAAAGAAAAACA[A/G]ATTCAGAGGACCAAG | 51667 |
rs758189583 | snp | A/C | | | intron-variant | NUB1 | GRCh38.p7 | 7:151373699 | CTGGAAGGCCTTCCC[A/C]CCGCGTGCAGAAGCT | 51667 |
rs758253660 | in-del | -/C | | | intron-variant | NUB1 | GRCh38.p7 | 7:151343909 | TAGTAGGGCCAGGCG[-/C]GGTGGCTCAGGCCTG | 51667 |
rs758263960 | snp | G/T | 5.04961e-05 | 0.00502449 | synonymous-codon | NUB1 | GRCh38.p7 | 7:151366993 | CGCCGTCCTCCAGCT[G/T]GATATAGTGTGGTGT | 51667 |
rs758266380 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151347233 | CTTCCTCTTTTCCTA[C/T]GTAACTATTAAAAAA | 51667 |
rs758381553 | snp | C/G | 1.66687e-05 | 0.00288688 | missense, utr-variant-5-prime | NUB1 | GRCh38.p7 | 7:151349094 | GCTAAGCAGTACTCT[C/G]ACAGACTAGAATGCT | 51667 |
rs758387875 | snp | C/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151365938 | CAGGACAGGAAGCTT[C/G]AGGCCATGTGGATTT | 51667 |
rs758401549 | snp | C/T | | | intron-variant, utr-variant-5-prime | NUB1 | GRCh38.p7 | 7:151341961 | GGAGCGGCCGCGGGG[C/T]GGGGGTGAGCAGCCA | 51667 |
rs758548468 | snp | A/G | 0.00014871 | 0.00862165 | missense, utr-variant-5-prime | NUB1 | GRCh38.p7 | 7:151351442 | AGGAAAAACTTGTTG[A/G]AGACCCGATTGCACA | 51667 |
rs758604419 | snp | A/C | | | intron-variant | NUB1 | GRCh38.p7 | 7:151355537 | AATTAACTGGGTGTG[A/C]TGGCATGGGCCTGTA | 51667 |
rs758643365 | snp | C/T | 3.32193e-05 | 0.00407536 | missense | NUB1 | GRCh38.p7 | 7:151368759 | CTCTTTAAAGAGCTA[C/T]ATATTGATCCATCAA | 51667 |
rs758700522 | snp | G/T | 0.00024947 | 0.0111657 | intron-variant, utr-variant-5-prime | NUB1 | GRCh38.p7 | 7:151352169 | TCAGCCCCCGCTATG[G/T]GCTTCTCCAGGGAGA | 51667 |
rs758741209 | in-del | -/TTAT | | | intron-variant | NUB1 | GRCh38.p7 | 7:151354474 | TTTTAGTTCACAATA[-/TTAT]TTGTTATTTTAAAAT | 51667 |
rs758822715 | in-del | -/AG | 1.65787e-05 | 0.00287907 | frameshift-variant, utr-variant-5-prime | NUB1 | GRCh38.p7 | 7:151349217 | CTACAATCGAGGTGT[-/AG]TTTTACCACCAAGAC | 51667 |
rs758873667 | in-del | -/CTGTTT | 3.90282e-05 | 0.0044173 | cds-indel | NUB1 | GRCh38.p7 | 7:151367885 | GGGAAAGAGAAGGTA[-/CTGTTT]CTAAGACTCTACTTA | 51667 |
rs758876935 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151370878 | TGTTTTAAAATGAGA[C/T]CATTTGGAAAACAGT | 51667 |
rs758879339 | snp | A/C | 8.36995e-05 | 0.0064686 | synonymous-codon | NUB1 | GRCh38.p7 | 7:151377048 | GTATTTTATTGTAGG[A/C]ACCTCTAGTGCCTCA | 51667 |
rs758922717 | snp | C/G | 6.8764e-05 | 0.00586321 | intron-variant | NUB1 | GRCh38.p7 | 7:151376831 | GTCTGAGGTCTTTGA[C/G]GGCCGCATTGAGAGC | 51667 |
rs758923260 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151349669 | GTGGGGTCACCTCCT[C/T]TCATTGCCATGGCCA | 51667 |
rs758936687 | snp | G/T | 1.6636e-05 | 0.00288405 | missense | NUB1 | GRCh38.p7 | 7:151377200 | CCTATGTAGAAAATA[G/T]GAAGTCAGCAACAAA | 51667 |
rs759035713 | in-del | -/TGTG | 2.60305e-05 | 0.00360757 | frameshift-variant | NUB1 | GRCh38.p7 | 7:151376712 | TCCAGCTGGCCGCCC[-/TGTG]AGACCCTTGCTCACA | 51667 |
rs759055331 | snp | A/G | 1.66418e-05 | 0.00288455 | missense | NUB1 | GRCh38.p7 | 7:151367096 | AAAAATTGTTACGGA[A/G]AAAATCATCAGAGAC | 51667 |
rs759092557 | in-del | -/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151362003 | TATAATGAGCTTCCA[-/T]TATACACTCATAACT | 51667 |
rs759105997 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151347144 | TTCTAGGTTTTAAAA[A/G]GTATGTATATAAATA | 51667 |
rs759321968 | snp | A/T | | | upstream-variant-2KB | NUB1 | GRCh38.p7 | 7:151340403 | TCTGTCTCCTTGAGC[A/T]TGGGGCTGGGTTGGG | 51667 |
rs759344356 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151371665 | CTATCGGAGCTTTAG[A/G]TGAGCAAGAGAAATC | 51667 |
rs759495494 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151356595 | TAGGGAAACTGTGTC[A/G]TTTGGGAAAAGTCCA | 51667 |
rs759548225 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151358223 | GTGATCCGCCTGCCT[C/T]GGCCTCCCAAAGTGC | 51667 |
rs759624297 | snp | A/G | 3.81323e-05 | 0.00436631 | intron-variant | NUB1 | GRCh38.p7 | 7:151356236 | AAGTAAGTACTATGA[A/G]AAATGTGTGGCCTGT | 51667 |
rs759707983 | in-del | -/AAG | | | cds-indel | NUB1 | GRCh38.p7 | 7:151352864 | AAAATTGTCATAAAT[-/AAG]AAGCAACTACAACTA | 51667 |
rs759827071 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151354251 | TTCTGTTCTTCCTAC[C/T]CACCTGTGGTGTTTT | 51667 |
rs759885139 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151342789 | TTTGTAACACTCCTT[C/T]GTCCTTCTGTCAAGT | 51667 |
rs759938232 | snp | A/C | | | intron-variant | NUB1 | GRCh38.p7 | 7:151343601 | AGCGCTGTGCTACAC[A/C]TGCCAGCTGCCTTAC | 51667 |
rs760013425 | snp | C/T | 3.30792e-05 | 0.00406675 | intron-variant | NUB1 | GRCh38.p7 | 7:151356093 | CATAACTGTTTAACA[C/T]TGAGTTCATGGAGGT | 51667 |
rs760021147 | in-del | -/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151361237 | TGAGTTGCTTCACTA[-/T]TCACCCTCCAAAGGT | 51667 |
rs760076279 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151376476 | TTCCAGGTTGCTCTA[C/T]GCTCACATTGCACAG | 51667 |
rs760102115 | in-del | -/A | 1.66037e-05 | 0.00288125 | frameshift-variant | NUB1 | GRCh38.p7 | 7:151367049 | GCCTTGATGATGCAG[-/A]AAAAAAATTAAACTT | 51667 |
rs760109106 | snp | C/T | | | utr-variant-3-prime | NUB1 | GRCh38.p7 | 7:151377289 | ATGAAAAGGCTAATG[C/T]AGCTCTTTCTGTTCT | 51667 |
rs760120083 | snp | G/T | 2.34359e-05 | 0.00342307 | missense | NUB1 | GRCh38.p7 | 7:151376654 | GTACATGGGTTTTGA[G/T]GCACTCGTGGCCGAA | 51667 |
rs760133472 | snp | A/G | | | utr-variant-3-prime | NUB1 | GRCh38.p7 | 7:151377427 | TTCCTCTGGCCTGGC[A/G]CAGGCCGTTCCATCT | 51667 |
rs760162334 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151375597 | ATGCTGCTTCCACCT[A/G]CTCTCCATCCCTTCC | 51667 |
rs760193471 | in-del | -/T | 0.000458001 | 0.0151258 | intron-variant | NUB1 | GRCh38.p7 | 7:151360114 | TATTTTAAAGTGATG[-/T]TTTTTTAAATTTGTA | 51667 |
rs760247047 | snp | A/C | | | intron-variant | NUB1 | GRCh38.p7 | 7:151343452 | ATGTGGAATACTGGC[A/C]CTCAATAGAAGAAAG | 51667 |
rs760262898 | snp | A/G | | | downstream-variant-500B, utr-variant-3-prime | NUB1, WDR86 | GRCh38.p7 | 7:151378627 | TGAAAGATGCCGCAC[A/G]CCAAGCGGGGCTGGG | 51667 |
rs760271994 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151345813 | TCTTGGCTCATTCTC[A/G]GTCCTCCTTGCTATC | 51667 |
rs760277126 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151346891 | TCAGACAAAAGTATG[A/G]GTAACCTGGGGACCA | 51667 |
rs760302609 | in-del | -/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151349027 | TTTCTATATTTTGCC[-/T]TTTTTTTTTTAAGTC | 51667 |
rs760309446 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151358040 | GAGTGCAGTGGCACA[A/G]TCTTGGCTCACTGCA | 51667 |
rs760449157 | snp | A/C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151350189 | GCCAGGTGTACAGAG[A/C/T]GGAACATGAAAGTGA | 51667 |
rs760525423 | snp | A/G | 3.31532e-05 | 0.0040713 | synonymous-codon | NUB1 | GRCh38.p7 | 7:151368836 | GCTTGGCCTGAGGGC[A/G]TGTGATGGGAACGTG | 51667 |
rs760548354 | snp | A/C | 0.000162298 | 0.00900682 | intron-variant, utr-variant-5-prime | NUB1 | GRCh38.p7 | 7:151352128 | GGAAGTGGCATGCAA[A/C]ACACATGCGTAGAAG | 51667 |
rs760642250 | snp | G/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151369733 | CAAAACAAGAAGTTG[G/T]TACTAGATTATCTCA | 51667 |
rs760694280 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151371422 | CCATAATCTGTGTCC[C/T]AGAATCCTCAGGGAA | 51667 |
rs760743811 | snp | C/T | 1.67195e-05 | 0.00289127 | intron-variant | NUB1 | GRCh38.p7 | 7:151355977 | TCTGGGCTTGTCACC[C/T]ACTCAGCTGCTTGGG | 51667 |
rs760755061 | snp | A/G | 6.81872e-05 | 0.00583858 | intron-variant | NUB1 | GRCh38.p7 | 7:151352892 | AACTAGGTATGTATG[A/G]CAAAGTATGCATAAT | 51667 |
rs760758471 | snp | A/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151362343 | CTCTTTTCATAAAGG[A/T]AATCAGCAGTAATGT | 51667 |
rs760759430 | snp | C/T | 0.000145254 | 0.0085209 | intron-variant | NUB1 | GRCh38.p7 | 7:151374353 | TCCTATGGGCTGCCC[C/T]GTCATCCGGATCTGA | 51667 |
rs760890940 | snp | C/G | 3.31538e-05 | 0.00407134 | missense, utr-variant-5-prime | NUB1 | GRCh38.p7 | 7:151349213 | AATTGCTACAATCGA[C/G]GTGTTTTTACCACCA | 51667 |
rs760941638 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151369298 | CAGGTGTGAGCCACC[A/G]CGCCTGGCCGAAACT | 51667 |
rs760942466 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151352552 | GGTTCAAGCAATCCT[C/T]CTACCCAAACCTCCC | 51667 |
rs760943699 | snp | C/T | 1.73222e-05 | 0.00294292 | synonymous-codon | NUB1 | GRCh38.p7 | 7:151356204 | CAGATCAATCAGAAT[C/T]CCCCCATCAGAAAGA | 51667 |
rs760953748 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151363613 | CAGTTTGATGAAAAC[C/T]ATAAACCCCCAGATG | 51667 |
rs760956893 | snp | C/T | 1.65795e-05 | 0.00287914 | missense, utr-variant-5-prime | NUB1 | GRCh38.p7 | 7:151349155 | AAATACGTTGCAAGG[C/T]AATTGAGCGTGGAAC | 51667 |
rs761056796 | snp | G/T | 0.00018707 | 0.00966954 | intron-variant | NUB1 | GRCh38.p7 | 7:151349023 | CCCTTTTCTATATTT[G/T]GCCTTTTTTTTTTTA | 51667 |
rs761186009 | snp | C/T | 0.000162933 | 0.0090244 | intron-variant | NUB1 | GRCh38.p7 | 7:151352074 | GATTTTTCTCATTTC[C/T]TTCTTTGGTCTACAT | 51667 |
rs761247957 | snp | C/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151356735 | TGTTTTTTTGTTTTT[C/G]AGACGGAGTTTTGCT | 51667 |
rs761252363 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151358474 | CCGCCTGAGCTCCAC[C/T]TCCTGTCAGATCAGC | 51667 |
rs761278385 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151371259 | TGGGATTTATTGGCC[A/G]TTTACTTGTAAAAAG | 51667 |
rs761385889 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151369481 | CATTATTAAAGTTGG[A/G]GATTGCATCCTTGCC | 51667 |
rs761437151 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151355146 | AGGAGAGGTGTGTTA[C/T]ACTTTCTCATTTTCC | 51667 |
rs761462744 | in-del | -/CGA | 0.000407415 | 0.0142668 | upstream-variant-2KB, utr-variant-5-prime | NUB1 | GRCh38.p7 | 7:151341730 | CGGCGGCGGCGGCGG[-/CGA]CGCGAAGGCGACAGC | 51667 |
rs761481482 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151343758 | TCCATGACGGAAGTT[C/T]AGAGTCCAGTGTTGT | 51667 |
rs761551992 | snp | A/G | 1.65762e-05 | 0.00287886 | missense, utr-variant-5-prime | NUB1 | GRCh38.p7 | 7:151349164 | GCAAGGCAATTGAGC[A/G]TGGAACAGGAAATGA | 51667 |
rs761563968 | snp | A/C | 2.90229e-05 | 0.00380928 | intron-variant | NUB1 | GRCh38.p7 | 7:151376625 | TGTGACCCCTGCGCT[A/C]TCCCCTAGTTGGTGT | 51667 |
rs761638513 | snp | C/T | 4.86299e-05 | 0.00493078 | synonymous-codon | NUB1 | GRCh38.p7 | 7:151377135 | GCATGAGGAAGACTA[C/T]CTTGACTCAACTCTG | 51667 |
rs761672527 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151368096 | TCCGTGCACAGGAGA[C/T]GTTGAACCAGAAACA | 51667 |
rs761680100 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151364278 | TACAAAAAATTAGCC[A/G]GGCATGGTGGCAGGC | 51667 |
rs761836755 | snp | C/G | 4.78023e-05 | 0.00488865 | missense | NUB1 | GRCh38.p7 | 7:151367960 | GAGGCTTATGAGTAT[C/G]TTAACAAGGTAAGAA | 51667 |
rs761857903 | snp | C/T | 2.9616e-05 | 0.003848 | intron-variant | NUB1 | GRCh38.p7 | 7:151351397 | GGTTAAATTCAAGTA[C/T]GTTTTACTTTGTCTT | 51667 |
rs761887512 | snp | C/T | 1.68009e-05 | 0.00289831 | missense | NUB1 | GRCh38.p7 | 7:151368736 | TTCCCTGTCTCTAGG[C/T]ACGTCAGCTCTTTAA | 51667 |
rs761929936 | in-del | -/T | | | utr-variant-3-prime | NUB1 | GRCh38.p7 | 7:151377462 | CCAGGTCTGCGTCCC[-/T]TAACCCCTTCCCCAG | 51667 |
rs761978324 | snp | A/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151374783 | TATCGAATCCTCAGT[A/T]GGGCAGGTGCTGCGC | 51667 |
rs761996881 | in-del | -/TTT | | | intron-variant | NUB1 | GRCh38.p7 | 7:151357185 | CCATGTCCAGCTAAT[-/TTT]TTTTTTTTTTTTTTT | 51667 |
rs762016820 | snp | A/G | 8.3212e-05 | 0.00644973 | synonymous-codon, intron-variant | NUB1 | GRCh38.p7 | 7:151374099 | TGTTTTCCTAAAGGA[A/G]CTGGCCCAAATAAGG | 51667 |
rs762024757 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151342254 | CTATTTAATGACAAG[A/G]CACTTGATTTTCTCG | 51667 |
rs762030419 | snp | A/G | 0.000270023 | 0.0116163 | synonymous-codon | NUB1 | GRCh38.p7 | 7:151376735 | TGCTCACAACGGAGG[A/G]AGCCTGCCTCCCGAG | 51667 |
rs762031213 | snp | C/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151376152 | AGGAAAACTGGGGAA[C/G]TGTCAGGAAGTTCTC | 51667 |
rs762068196 | snp | G/T | 4.76406e-05 | 0.00488037 | intron-variant | NUB1 | GRCh38.p7 | 7:151374331 | TCCAGCATCCTCCCG[G/T]GCTCACTCCTATGGG | 51667 |
rs762070082 | snp | A/G | 4.1165e-05 | 0.00453661 | synonymous-codon | NUB1 | GRCh38.p7 | 7:151355847 | ATCTGAAGAGGACGC[A/G]AGGAAAAACTTCCAG | 51667 |
rs762087814 | snp | C/T | 2.47338e-05 | 0.00351657 | intron-variant | NUB1 | GRCh38.p7 | 7:151366922 | TGGCAGTGATGTCAC[C/T]GTCCTTCTCTTTCCA | 51667 |
rs762186923 | snp | A/G | 1.78058e-05 | 0.00298372 | missense | NUB1 | GRCh38.p7 | 7:151360231 | CCATGTCTGTTGGAC[A/G]CTGACAAATATTTCT | 51667 |
rs762272216 | snp | C/T | 1.71322e-05 | 0.00292674 | missense, utr-variant-5-prime | NUB1 | GRCh38.p7 | 7:151345414 | AAGACAGGATTCAAC[C/T]TTGGAAACCTCCATA | 51667 |
rs762319114 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151351813 | TGGTACTCACTAGCT[C/T]ATTAGTTTTGAATTA | 51667 |
rs762332598 | snp | C/T | 8.9658e-05 | 0.00669484 | missense | NUB1 | GRCh38.p7 | 7:151367951 | AATGATGTAGAGGCT[C/T]ATGAGTATCTTAACA | 51667 |
rs762413820 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151352457 | TAAAAAATATTTATT[C/T]TTTAGAGACAGGATC | 51667 |
rs762465043 | snp | C/G | 3.36417e-05 | 0.00410119 | intron-variant | NUB1 | GRCh38.p7 | 7:151349279 | GTAGGCACTAATGTC[C/G]AGTTAGTGATGAGGT | 51667 |
rs762483043 | snp | C/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151358837 | TGGGAGGCCGAGGTG[C/G]GTGGATCACAAGATC | 51667 |
rs762608475 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151346412 | GCATGATAGGAGCAA[C/T]CTTTGTGCTCATGAG | 51667 |
rs762695389 | snp | C/G | 1.66804e-05 | 0.00288789 | intron-variant | NUB1 | GRCh38.p7 | 7:151355966 | GTACCCAGAGCTCTG[C/G]GCTTGTCACCCACTC | 51667 |
rs762697140 | in-del | -/TA | | | intron-variant | NUB1 | GRCh38.p7 | 7:151350137 | ATCAAAGACGTTAAT[-/TA]ACTTTCACTTTCTGC | 51667 |
rs762724175 | snp | C/T | 1.97136e-05 | 0.00313949 | intron-variant | NUB1 | GRCh38.p7 | 7:151351514 | TCTGTGTCCTAGGTG[C/T]TCTGGGCCTTTTTAC | 51667 |
rs762800121 | snp | A/C | | | intron-variant | NUB1 | GRCh38.p7 | 7:151358353 | GATCTTTTTGGAAAA[A/C]CTTTATCACAGGGGT | 51667 |
rs762825564 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151348127 | GATGCTGAATTTTGG[C/T]GATTTCAGATTTTTA | 51667 |
rs762947697 | snp | A/G | 0.000227834 | 0.0106708 | intron-variant | NUB1 | GRCh38.p7 | 7:151376836 | AGGTCTTTGAGGGCC[A/G]CATTGAGAGCAAAGT | 51667 |
rs762954435 | snp | A/G | 3.3953e-05 | 0.00412011 | intron-variant | NUB1 | GRCh38.p7 | 7:151345499 | CATCAATAATTAGCA[A/G]CATTATAAATCTCCT | 51667 |
rs762979215 | snp | C/T | | | upstream-variant-2KB | NUB1 | GRCh38.p7 | 7:151340594 | CTGCTTTGATCTGAG[C/T]ACTCAGGTTCCGCCC | 51667 |
rs763057927 | snp | A/C | 1.70351e-05 | 0.00291843 | synonymous-codon, utr-variant-5-prime | NUB1 | GRCh38.p7 | 7:151345395 | TTGACCCAGTTTTTA[A/C]GGGAAGACAGGATTC | 51667 |
rs763115611 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151351543 | ACATTGGCTTATTTG[A/G]TCCTCTGTGAGCGTC | 51667 |
rs763134389 | snp | C/T | 4.97682e-05 | 0.00498815 | synonymous-codon | NUB1 | GRCh38.p7 | 7:151368848 | GGCGTGTGATGGGAA[C/T]GTGGATCATGCGGCC | 51667 |
rs763141743 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151353716 | CATGAGTTGACTTGG[A/G]GAGACCAGTTAGCTA | 51667 |
rs763243180 | snp | G/T | 4.14156e-05 | 0.00455039 | intron-variant | NUB1 | GRCh38.p7 | 7:151345514 | GCATTATAAATCTCC[G/T]TGGTAAATAAGATTC | 51667 |
rs763256170 | snp | A/G | | | upstream-variant-2KB | NUB1 | GRCh38.p7 | 7:151341247 | GGCAGAGCTCCCTAG[A/G]CCTTGTGGTCCCTAG | 51667 |
rs763364783 | snp | C/T | 3.31296e-05 | 0.00406985 | intron-variant | NUB1 | GRCh38.p7 | 7:151375956 | CGAGTGAGTGACAGG[C/T]CTTTGTGCCCTCAGC | 51667 |
rs763416103 | snp | C/T | 2.01367e-05 | 0.003173 | intron-variant | NUB1 | GRCh38.p7 | 7:151356253 | AATGTGTGGCCTGTT[C/T]TTAGATTTGTTGTCA | 51667 |
rs763418062 | snp | C/G | 3.2386e-05 | 0.00402392 | intron-variant | NUB1 | GRCh38.p7 | 7:151376618 | CTGATGCTGTGACCC[C/G]TGCGCTCTCCCCTAG | 51667 |
rs763469751 | snp | C/T | | | utr-variant-3-prime | NUB1, WDR86 | GRCh38.p7 | 7:151378443 | AGGTGGGAAATATAT[C/T]CAAAAATTGTCACCC | 51667 |
rs763561253 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151365706 | GTGTCTGCGTGCACA[C/T]GTGTGTAAAACATGG | 51667 |
rs763614004 | snp | A/G | 1.71914e-05 | 0.0029318 | missense | NUB1 | GRCh38.p7 | 7:151360198 | TTCCTGAAAAGAAAA[A/G]AATATGGAATAGCCT | 51667 |
rs763671505 | snp | C/G/T | 1.65652e-05 | 0.0028779 | intron-variant | NUB1 | GRCh38.p7 | 7:151375960 | TGAGTGACAGGCCTT[C/G/T]GTGCCCTCAGCTTGG | 51667 |
rs763676621 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151343458 | AATACTGGCCCTCAA[C/T]AGAAGAAAGAAATTT | 51667 |
rs763725549 | snp | A/T | 1.65693e-05 | 0.00287826 | intron-variant | NUB1 | GRCh38.p7 | 7:151351388 | TCCAAAATGGGTTAA[A/T]TTCAAGTACGTTTTA | 51667 |
rs763805739 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151355060 | GTCTTTGCTTTTAAC[C/T]GTGACAGACTGCAGT | 51667 |
rs763909078 | snp | A/G | 0.000289537 | 0.0120285 | intron-variant | NUB1 | GRCh38.p7 | 7:151367136 | TAAAAGTATGTTCCT[A/G]GAATTCATCTTATGT | 51667 |
rs763934198 | in-del | -/GTC | | | utr-variant-3-prime, cds-indel | NUB1, WDR86 | GRCh38.p7 | 7:151378390 | GATGGGAATCTTCTT[-/GTC]ATTCTTTTTAAACGG | 51667 |
rs763960622 | snp | C/T | 0.000165741 | 0.00910182 | synonymous-codon, utr-variant-5-prime | NUB1 | GRCh38.p7 | 7:151349210 | GGGAATTGCTACAAT[C/T]GAGGTGTTTTTACCA | 51667 |
rs763975105 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151359514 | CCGGGCACCGTGGCT[C/T]ACGCCTGTAATCCCA | 51667 |
rs764022598 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151348156 | TAGATTAGAGATACT[C/T]ATCTGGATTTTTTTG | 51667 |
rs764104380 | snp | A/C | 3.32613e-05 | 0.00407793 | missense | NUB1 | GRCh38.p7 | 7:151367952 | ATGATGTAGAGGCTT[A/C]TGAGTATCTTAACAA | 51667 |
rs764136389 | snp | A/G | 6.65104e-05 | 0.00576635 | missense | NUB1 | GRCh38.p7 | 7:151367093 | TTTAAAAATTGTTAC[A/G]GAGAAAATCATCAGA | 51667 |
rs764161493 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151371868 | CCTGCCAAGAGCTCT[C/T]GGCTGATTTTTATTT | 51667 |
rs764274039 | snp | A/G | 6.63592e-05 | 0.00575979 | missense | NUB1 | GRCh38.p7 | 7:151368849 | GCGTGTGATGGGAAC[A/G]TGGATCATGCGGCCA | 51667 |
rs764284550 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151373007 | GTTCTGCCTGCTCCT[A/G]CTGTGGGGCCTGTGG | 51667 |
rs764370286 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151369308 | CCACCGCGCCTGGCC[A/G]AAACTTGTCTTTTTC | 51667 |
rs764399884 | snp | A/C | 1.72552e-05 | 0.00293723 | intron-variant | NUB1 | GRCh38.p7 | 7:151352905 | TGGCAAAGTATGCAT[A/C]ATTTTTTAATGAACC | 51667 |
rs764532360 | in-del | -/G | 5.32779e-05 | 0.00516102 | frameshift-variant | NUB1 | GRCh38.p7 | 7:151367968 | TGAGTATCTTAACAA[-/G]GTAAGAAAAGTAAAG | 51667 |
rs764620219 | snp | A/G | 2.02936e-05 | 0.00318534 | intron-variant | NUB1 | GRCh38.p7 | 7:151356256 | GTGTGGCCTGTTCTT[A/G]GATTTGTTGTCAGGG | 51667 |
rs764676132 | snp | A/G | | | downstream-variant-500B, utr-variant-3-prime | NUB1, WDR86 | GRCh38.p7 | 7:151378922 | GCCGCAGAGGAAGCC[A/G]GCTGTGGAGGCAGTT | 51667 |
rs764677148 | snp | A/G | 0.000200381 | 0.0100075 | missense, utr-variant-5-prime | NUB1 | GRCh38.p7 | 7:151341831 | TGCTGGTCGCGGCGG[A/G]AGTGGCGTGGCGCAG | 51667 |
rs764677489 | snp | C/T | 3.48432e-05 | 0.00417377 | missense | NUB1 | GRCh38.p7 | 7:151360217 | ATGGAATAGCCTTGC[C/T]ATGTCTGTTGGACGC | 51667 |
rs764729614 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151365906 | TTTTTTTTTTATTCC[A/G]TGCATATTTTGATAG | 51667 |
rs764730381 | snp | C/G | 1.70191e-05 | 0.00291706 | missense, utr-variant-5-prime | NUB1 | GRCh38.p7 | 7:151345398 | ACCCAGTTTTTAAGG[C/G]AAGACAGGATTCAAC | 51667 |
rs764797402 | snp | A/G | 1.67354e-05 | 0.00289265 | splice-acceptor-variant | NUB1 | GRCh38.p7 | 7:151349071 | CTGATTTTTCTTGAT[A/G]GGACCTTGCTAAGCA | 51667 |
rs764799304 | snp | A/G | 3.33695e-05 | 0.00408456 | missense | NUB1 | GRCh38.p7 | 7:151367103 | GTTACGGAGAAAATC[A/G]TCAGAGACTGGTCCA | 51667 |
rs764850600 | snp | A/G | 1.65704e-05 | 0.00287836 | synonymous-codon, utr-variant-5-prime | NUB1 | GRCh38.p7 | 7:151349189 | AAATGACAATTATAG[A/G]ACAACGGGAATTGCT | 51667 |
rs764903481 | snp | A/G | 1.67933e-05 | 0.00289765 | intron-variant | NUB1 | GRCh38.p7 | 7:151349276 | TGAGTAGGCACTAAT[A/G]TCCAGTTAGTGATGA | 51667 |
rs764909690 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151367553 | TCAAAATCCTGCTGA[C/T]GCAGACTCTCTGATA | 51667 |
rs764971533 | snp | C/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151356740 | TTTTGTTTTTGAGAC[C/G]GAGTTTTGCTCTTGT | 51667 |
rs765161331 | snp | C/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151358258 | ATTACAGGTGTGAGC[C/G]ACTGTGCCCGGCCAA | 51667 |
rs765166900 | snp | A/G | 0.000242043 | 0.0109983 | utr-variant-5-prime, upstream-variant-2KB | NUB1 | GRCh38.p7 | 7:151341765 | GCGGGGGCGGGGCTG[A/G]CCTCACCCGGAATGA | 51667 |
rs765176567 | snp | C/T | 3.38708e-05 | 0.00411512 | synonymous-codon | NUB1 | GRCh38.p7 | 7:151366984 | GGATAACTACGCCGT[C/T]CTCCAGCTGGATATA | 51667 |
rs765220574 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151362638 | GGCAGGGAGGGCAAA[C/T]CCAGGCAGAGCCTTG | 51667 |
rs765234879 | snp | C/G | 6.82326e-05 | 0.00584052 | intron-variant | NUB1 | GRCh38.p7 | 7:151376833 | CTGAGGTCTTTGAGG[C/G]CCGCATTGAGAGCAA | 51667 |
rs765334399 | snp | A/C | 1.81618e-05 | 0.0030134 | intron-variant | NUB1 | GRCh38.p7 | 7:151368000 | TGTAACCAATTTTCA[A/C]CTCCTTTTAAAAAAC | 51667 |
rs765335468 | snp | G/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151347216 | GTTAACATAGGTATA[G/T]TCTTCCTCTTTTCCT | 51667 |
rs765427234 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151371746 | AATGTAAAACAATTC[A/G]TTCATGTTTTTGTTT | 51667 |
rs765439644 | snp | A/G | | | upstream-variant-2KB | NUB1 | GRCh38.p7 | 7:151340450 | TAATGACGCATGATC[A/G]GATTAGATTTTGCGA | 51667 |
rs765510234 | snp | C/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151349576 | GACACAGCACAGAAG[C/G]CTTCATCCTTTTCCT | 51667 |
rs765511814 | in-del | -/A | | | intron-variant | NUB1 | GRCh38.p7 | 7:151353126 | GATAAAATGTTAGAG[-/A]ATGGAATGTAAGGTG | 51667 |
rs765512622 | snp | C/T | 1.67396e-05 | 0.00289301 | synonymous-codon | NUB1 | GRCh38.p7 | 7:151368740 | CTGTCTCTAGGCACG[C/T]CAGCTCTTTAAAGAG | 51667 |
rs765563191 | snp | A/C | | | intron-variant | NUB1 | GRCh38.p7 | 7:151373185 | CCGTCCTCGCTGCTG[A/C]TGATGGTGGGGCTGG | 51667 |
rs765635760 | in-del | -/TTTT | 7.44131e-05 | 0.00609926 | intron-variant | NUB1 | GRCh38.p7 | 7:151349027 | TTTCTATATTTTGCC[-/TTTT]TTTTTTTAAGTCAGT | 51667 |
rs765689677 | snp | C/G | 1.93977e-05 | 0.00311424 | intron-variant | NUB1 | GRCh38.p7 | 7:151356243 | TACTATGAGAAATGT[C/G]TGGCCTGTTCTTAGA | 51667 |
rs765700897 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151376546 | GGGAGCTCTTAAACA[C/T]GAGAGTCGGCTGTCC | 51667 |
rs765701624 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151349524 | GAAATAATGGGGAAT[A/G]AAGGATTCCCAAGTT | 51667 |
rs765746262 | snp | A/G | 1.7249e-05 | 0.0029367 | intron-variant | NUB1 | GRCh38.p7 | 7:151356101 | TTTAACATTGAGTTC[A/G]TGGAGGTCCTTTTGG | 51667 |
rs765756101 | snp | A/C | 0.000212202 | 0.0102983 | intron-variant | NUB1 | GRCh38.p7 | 7:151374396 | TCCTGGGCTCCAGCC[A/C]AGACACAGGCTGCGT | 51667 |
rs765773488 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151358843 | GCCGAGGTGGGTGGA[C/T]CACAAGATCAGGAGA | 51667 |
rs765781504 | in-del | -/T/TT | 0.0242388 | 0.107387 | intron-variant | NUB1 | GRCh38.p7 | 7:151349026 | TTTCTATATTTTGCC[-/T/TT]TTTTTTTTTTTAAGT | 51667 |
rs765823269 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151362621 | GAAGTTTCAGGTTAC[A/G]GGGCAGGGAGGGCAA | 51667 |
rs765825472 | snp | A/G | | | utr-variant-3-prime | NUB1 | GRCh38.p7 | 7:151377458 | GCCTCCCAGGTCTGC[A/G]TCCCTAACCCCTTCC | 51667 |
rs765828784 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151345835 | CTTGCTATCATCATC[C/T]GCTGTGAAACAATTG | 51667 |
rs765882810 | snp | G/T | | | utr-variant-3-prime, downstream-variant-500B | NUB1, WDR86 | GRCh38.p7 | 7:151377790 | TGGGGGCCACACCAG[G/T]TCGCAGCAAATGGCT | 51667 |
rs765902728 | in-del | -/T | 0.000134508 | 0.00819975 | intron-variant | NUB1 | GRCh38.p7 | 7:151367838 | AAGGCAATTTTATCC[-/T]TTTTTTTCTTCAATA | 51667 |
rs765929736 | snp | C/T | 3.30934e-05 | 0.00406763 | synonymous-codon | NUB1 | GRCh38.p7 | 7:151376744 | CGGAGGAAGCCTGCC[C/T]CCCGAGCTGCCGCTG | 51667 |
rs765941059 | in-del | -/CTT | 0.000120991 | 0.00777693 | intron-variant | NUB1 | GRCh38.p7 | 7:151366926 | AGTGATGTCACTGTC[-/CTT]CTCTTTCCAGTGAGT | 51667 |
rs766309549 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151369793 | ATAGAAGTCTCTAGA[A/G]TCTTCACATGTATGT | 51667 |
rs766360748 | snp | A/C | | | intron-variant | NUB1 | GRCh38.p7 | 7:151355319 | GCTTAACAGTGACAT[A/C]GTTACAACCAAATGT | 51667 |
rs766403674 | snp | C/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151371524 | AGGCCTGTGGCAAGA[C/G]ATAGAGGGTTGCCAC | 51667 |
rs766433588 | snp | C/T | 1.68196e-05 | 0.00289992 | intron-variant | NUB1 | GRCh38.p7 | 7:151355995 | TCAGCTGCTTGGGGG[C/T]AGCACTGGATCACAC | 51667 |
rs766485245 | in-del | -/T | 5.19953e-05 | 0.00509852 | intron-variant | NUB1 | GRCh38.p7 | 7:151368686 | CACTTTGTATTAAGC[-/T]TTTAAGTATTGCCGT | 51667 |
rs766543694 | snp | C/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151364499 | TTCTGTTAAATAACC[C/G]ACTTAAGCTCAAATG | 51667 |
rs766657793 | snp | C/G | 1.72764e-05 | 0.00293903 | intron-variant | NUB1 | GRCh38.p7 | 7:151377000 | CGTGCAGTGTCCCCA[C/G]GACAATCCTCACATA | 51667 |
rs766732524 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151342761 | CTCCCTGGAGTGTCT[A/G]ACACGCACTGGGTTT | 51667 |
rs766737107 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151352390 | GTCAGTTGAAATCCT[A/G]GGTGTTTCTGATAAA | 51667 |
rs766785484 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151375206 | TATGTACATGTATAT[C/T]TAACATATACGTTAA | 51667 |
rs766790483 | snp | G/T | | | upstream-variant-2KB | NUB1 | GRCh38.p7 | 7:151341559 | GGACACCAACTCCCA[G/T]GTCCTCGCCCCACAC | 51667 |
rs766835947 | snp | A/G | 0.00031351 | 0.0125163 | intron-variant | NUB1 | GRCh38.p7 | 7:151360262 | GGTAGGCGCTTTTGT[A/G]CTTGGTGAACACCAG | 51667 |
rs766861799 | snp | C/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151375305 | GAAATTCTGAATATT[C/G]GAAGGGACTGATGGG | 51667 |
rs766868195 | snp | A/G | 0.000141004 | 0.00839536 | missense, intron-variant | NUB1 | GRCh38.p7 | 7:151374143 | AGAAGAAAAGACGCC[A/G]CCTCGAGAACATCAG | 51667 |
rs766919101 | snp | A/C | 1.76157e-05 | 0.00296775 | missense | NUB1 | GRCh38.p7 | 7:151355878 | TTAGAGGAAGAGGAG[A/C]AAAATGAGGCCAAAC | 51667 |
rs767033870 | snp | C/T | 2.76071e-05 | 0.00371521 | intron-variant | NUB1 | GRCh38.p7 | 7:151376629 | ACCCCTGCGCTCTCC[C/T]CTAGTTGGTGTACAT | 51667 |
rs767089160 | snp | C/T | 3.80626e-05 | 0.00436232 | intron-variant | NUB1 | GRCh38.p7 | 7:151360253 | AATATTTCTGGTAGG[C/T]GCTTTTGTACTTGGT | 51667 |
rs767101044 | snp | C/T | 1.65685e-05 | 0.00287819 | intron-variant | NUB1 | GRCh38.p7 | 7:151375971 | CCTTTGTGCCCTCAG[C/T]TTGGACAGCCTCGGG | 51667 |
rs767256399 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151345544 | CTGAATTGTCAGGCA[C/T]GACCATATAAACTTT | 51667 |
rs767277631 | snp | A/T | 1.65734e-05 | 0.00287862 | missense, utr-variant-5-prime | NUB1 | GRCh38.p7 | 7:151349175 | GAGCGTGGAACAGGA[A/T]ATGACAATTATAGAA | 51667 |
rs767478410 | snp | A/C | 1.68114e-05 | 0.00289921 | missense | NUB1 | GRCh38.p7 | 7:151367966 | TATGAGTATCTTAAC[A/C]AGGTAAGAAAAGTAA | 51667 |
rs767529911 | snp | C/G/T | 0.000100621 | 0.00709236 | missense | NUB1 | GRCh38.p7 | 7:151368738 | CCCTGTCTCTAGGCA[C/G/T]GTCAGCTCTTTAAAG | 51667 |
rs767582674 | snp | G/T | 0.000162747 | 0.00901926 | intron-variant | NUB1 | GRCh38.p7 | 7:151352082 | TCATTTCCTTCTTTG[G/T]TCTACATCAGGGCTG | 51667 |
rs767606066 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151368668 | CTAATTTCTTTTAGG[C/T]TTTCACTTTGTATTA | 51667 |
rs767639484 | snp | A/G | 7.39672e-05 | 0.00608097 | synonymous-codon, intron-variant | NUB1 | GRCh38.p7 | 7:151374129 | GAAGGAGGAAAAAGA[A/G]AAGAAAAGACGCCGC | 51667 |
rs767641411 | snp | A/G | 3.62463e-05 | 0.00425698 | intron-variant | NUB1 | GRCh38.p7 | 7:151352931 | GAACCAAATATAGAA[A/G]TAATGACTTCCCTTT | 51667 |
rs767792732 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151348189 | GAGGAACCATAATGA[C/T]TTTGCTCTCAGTAAT | 51667 |
rs767845855 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151352536 | GCAACCTCAAACTCG[C/T]GGTTCAAGCAATCCT | 51667 |
rs767849806 | in-del | -/GAACAGGGGTCCTGTA | | | utr-variant-3-prime, downstream-variant-500B | NUB1, WDR86 | GRCh38.p7 | 7:151377505 | CCCCGAAACAGGAAG[-/GAACAGGGGTCCTGTA]GAACAGGGGTCCTGG | 51667 |
rs767947887 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151351816 | TACTCACTAGCTCAT[C/T]AGTTTTGAATTACTA | 51667 |
rs767962500 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151373268 | TCCTTGTTGGGAAAA[C/T]AATGAGGTTGGATTA | 51667 |
rs768059524 | snp | C/T | 1.73111e-05 | 0.00294198 | missense, utr-variant-5-prime | NUB1 | GRCh38.p7 | 7:151345423 | TTCAACTTTGGAAAC[C/T]TCCATATACAGATGA | 51667 |
rs768112767 | snp | A/G | 0.000114541 | 0.00756686 | intron-variant | NUB1 | GRCh38.p7 | 7:151345508 | TTAGCAGCATTATAA[A/G]TCTCCTTGGTAAATA | 51667 |
rs768116050 | snp | C/T | 1.70095e-05 | 0.00291625 | intron-variant | NUB1 | GRCh38.p7 | 7:151368723 | ATGATTCTTACATTT[C/T]CCTGTCTCTAGGCAC | 51667 |
rs768169061 | snp | G/T | 3.96786e-05 | 0.00445396 | intron-variant | NUB1 | GRCh38.p7 | 7:151351515 | CTGTGTCCTAGGTGC[G/T]CTGGGCCTTTTTACA | 51667 |
rs768196473 | snp | A/G | | | upstream-variant-2KB | NUB1 | GRCh38.p7 | 7:151341467 | TGGAGAAACAAAGCC[A/G]GGATCCATTTCCTCT | 51667 |
rs768299400 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151369354 | CACATGCTGCAGTCT[C/T]CTTAGTTTTGTTTCC | 51667 |
rs768328041 | snp | C/G | 4.97146e-05 | 0.00498546 | missense | NUB1 | GRCh38.p7 | 7:151368819 | ACTGCCCAGGAAGCC[C/G]GGCTTGGCCTGAGGG | 51667 |
rs768385156 | snp | C/T | 1.67809e-05 | 0.00289658 | synonymous-codon, utr-variant-5-prime | NUB1 | GRCh38.p7 | 7:151352833 | TGAAACCTTTGGACT[C/T]CAAGAAAATTATATC | 51667 |
rs768412160 | in-del | -/GTGCTCTGTGTCCTAG | 1.90863e-05 | 0.00308914 | intron-variant | NUB1 | GRCh38.p7 | 7:151351495 | CAAGTAAGTATCTGT[-/GTGCTCTGTGTCCTAG]GTGCTCTGGGCCTTT | 51667 |
rs768414205 | snp | C/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151362038 | TTCTGCAGTTATAAA[C/G]ACATGGTTGATCTTC | 51667 |
rs768418010 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151364111 | AAATTTTTATGTTAA[A/G]TAAATATTAATTTCA | 51667 |
rs768517587 | snp | A/C | 8.30117e-05 | 0.00644197 | missense | NUB1 | GRCh38.p7 | 7:151377049 | TATTTTATTGTAGGA[A/C]CCTCTAGTGCCTCAA | 51667 |
rs768566097 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151343195 | TTGCTGTGATAAGCC[A/G]TTTGTCAGTGCTTGA | 51667 |
rs768596305 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151367443 | GCAAGATGTAAATGC[A/G]GAAAATAGACATTTC | 51667 |
rs768636175 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151376326 | TACACGCGTTAGCAC[A/G]CCTGTATGCTGTGGC | 51667 |
rs768788847 | snp | A/G | 6.64993e-05 | 0.00576587 | missense | NUB1 | GRCh38.p7 | 7:151367025 | ACTTCCGCCTGGAAC[A/G]GCTGGAATGCCTTGA | 51667 |
rs768788923 | snp | A/C | 3.45811e-05 | 0.00415805 | intron-variant | NUB1 | GRCh38.p7 | 7:151345501 | TCAATAATTAGCAGC[A/C]TTATAAATCTCCTTG | 51667 |
rs768814090 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151343366 | TTCTTTTAAAAAATA[C/T]TTGTTTATGAAATAC | 51667 |
rs768909845 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151374690 | CTTTTCAAAGAACCC[C/T]TCAGGAGTGACAGCA | 51667 |
rs768960744 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151353149 | GTAAGGTGTGCTGAG[C/T]GTAAGATGCCAGTTC | 51667 |
rs768984925 | snp | A/G | 1.65853e-05 | 0.00287964 | missense, utr-variant-5-prime | NUB1 | GRCh38.p7 | 7:151349146 | TAATAGAAGAAATAC[A/G]TTGCAAGGCAATTGA | 51667 |
rs769013443 | snp | G/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151342134 | GTTTGGGGAGAGAAA[G/T]GAATAAATATGTCTA | 51667 |
rs769166188 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151347699 | TCCTGGGCTTGAGCA[A/G]TCCTCTCACCTTGCC | 51667 |
rs769223407 | snp | C/T | 8.91822e-05 | 0.00667706 | missense | NUB1 | GRCh38.p7 | 7:151376791 | TGTCCCCGCCAGCCA[C/T]GTCCCCTTCTGACTC | 51667 |
rs769226428 | snp | C/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151358534 | CCTATTGTGAACTGG[C/G]CATGTGAGGGATCTA | 51667 |
rs769329255 | snp | G/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151361607 | AGTTAACAAATTTAG[G/T]GTTAACTTCTTTTCT | 51667 |
rs769380206 | in-del | -/TTG | | | intron-variant | NUB1 | GRCh38.p7 | 7:151349303 | ATGAGGTCAAATAAA[-/TTG]TTGTTGTTTGGAAAG | 51667 |
rs769395832 | in-del | -/G | 7.12581e-05 | 0.00596858 | utr-variant-3-prime | NUB1 | GRCh38.p7 | 7:151377241 | TAATGAACAGAAATA[-/G]GCGCTAATTTTCTGC | 51667 |
rs769468400 | snp | A/C | 0.000101158 | 0.00711118 | utr-variant-3-prime | NUB1 | GRCh38.p7 | 7:151377259 | GCTAATTTTCTGCTT[A/C]TAAATGCTATCATTA | 51667 |
rs769514835 | snp | C/G | 5.78665e-05 | 0.00537865 | missense, intron-variant | NUB1 | GRCh38.p7 | 7:151374238 | AACTTGGATGAGGCC[C/G]TGAAGGTAGCAGCTC | 51667 |
rs769519458 | snp | A/T | 3.43253e-05 | 0.00414264 | intron-variant | NUB1 | GRCh38.p7 | 7:151368709 | ATTGCCGTGGTTACA[A/T]GATTCTTACATTTCC | 51667 |
rs769526817 | snp | G/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151348752 | AGCTAATTTTTGTAT[G/T]TAAGTAGTTATGGGG | 51667 |
rs769599084 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151366214 | GGGTTCAGCCTGCTG[C/T]CACGAATACGGAGTC | 51667 |
rs769682291 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151359623 | TCTCTACTAAAAATA[C/T]GAAATTAGCCGGGCA | 51667 |
rs769759492 | snp | A/C | 3.33461e-05 | 0.00408313 | intron-variant | NUB1 | GRCh38.p7 | 7:151355961 | GAGAGGTACCCAGAG[A/C]TCTGGGCTTGTCACC | 51667 |
rs769774850 | snp | A/G | | | missense | NUB1 | GRCh38.p7 | 7:151355851 | GAAGAGGACGCGAGG[A/G]AAAACTTCCAGTTAG | 51667 |
rs769845670 | snp | C/T | 3.43625e-05 | 0.00414488 | synonymous-codon | NUB1 | GRCh38.p7 | 7:151360186 | AAGGGCAGAGCTTTC[C/T]TGAAAAGAAAAGAAT | 51667 |
rs769891606 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151353434 | TTATAACTTGGTGAC[A/G]GGGGAGGTTGTGCTG | 51667 |
rs769932747 | snp | C/T | 4.9028e-05 | 0.00495092 | synonymous-codon | NUB1 | GRCh38.p7 | 7:151376696 | AGTGTTCAGAGGCAA[C/T]GTCCAGCTGGCCGCC | 51667 |
rs769950657 | snp | C/T | 2.95059e-05 | 0.00384085 | intron-variant | NUB1 | GRCh38.p7 | 7:151345490 | CTTTTAAGACATCAA[C/T]AATTAGCAGCATTAT | 51667 |
rs770045325 | snp | A/G/T | 3.41025e-05 | 0.0041292 | missense, utr-variant-5-prime | NUB1 | GRCh38.p7 | 7:151345389 | GCAAAATTGACCCAG[A/G/T]TTTTAAGGGAAGACA | 51667 |
rs770067248 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151375131 | GGGAGTCCACCCTGC[C/T]TTTGCCTCTTATCCC | 51667 |
rs770078059 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151343046 | AGCCTGTGAAATTAC[C/T]GTCCCCCAGTGGGGA | 51667 |
rs770087630 | snp | C/G | 1.92066e-05 | 0.00309886 | intron-variant | NUB1 | GRCh38.p7 | 7:151351500 | AAGTATCTGTGTGCT[C/G]TGTGTCCTAGGTGCT | 51667 |
rs770124540 | snp | A/G | | | synonymous-codon | NUB1 | GRCh38.p7 | 7:151355880 | AGAGGAAGAGGAGCA[A/G]AATGAGGCCAAACTC | 51667 |
rs770128174 | snp | C/G | 2.81996e-05 | 0.00375486 | intron-variant | NUB1 | GRCh38.p7 | 7:151366904 | AATGTTTCAAATGCT[C/G]CTTGGCAGTGATGTC | 51667 |
rs770271564 | snp | G/T | 1.69318e-05 | 0.00290957 | splice-acceptor-variant | NUB1 | GRCh38.p7 | 7:151352811 | TGGTTTTATTTTACA[G/T]AATAGCTGAAACCTT | 51667 |
rs770296285 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151346657 | GGTGAACACATCCAC[A/G]TGTCGGGATGTACAC | 51667 |
rs770361126 | snp | A/G | | | upstream-variant-2KB | NUB1 | GRCh38.p7 | 7:151341152 | TTTATTAGGCACAGT[A/G]AGAGATTAACAGCAA | 51667 |
rs770429500 | in-del | -/C | 6.82932e-05 | 0.00584311 | intron-variant | NUB1 | GRCh38.p7 | 7:151376614 | GGGCTGATGCTGTGA[-/C]CCCCTGCGCTCTCCC | 51667 |
rs770495796 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151373820 | GCCCATCCTGATGCC[A/G]GATGGTGGATGGCGG | 51667 |
rs770508441 | snp | A/G | 1.66774e-05 | 0.00288763 | splice-donor-variant | NUB1 | GRCh38.p7 | 7:151355951 | TACTGGCAAAGAGAG[A/G]TACCCAGAGCTCTGG | 51667 |
rs770550090 | snp | G/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151347829 | GTCATAAATTTATGC[G/T]TACACCATAATTTTT | 51667 |
rs770586255 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151358125 | GGACTACAGTGCACG[C/T]CACCATGCCCAGCTA | 51667 |
rs770755897 | snp | G/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151348186 | GGGGAGGAACCATAA[G/T]GACTTTGCTCTCAGT | 51667 |
rs770882357 | snp | A/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151346416 | GATAGGAGCAACCTT[A/T]GTGCTCATGAGGCTT | 51667 |
rs770935329 | in-del | -/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151374079 | AACTTGGGATGGGAC[-/T]TTGCTGTTTTCCTAA | 51667 |
rs770935477 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151368229 | GAGGTGAGCCAGGCC[A/G]GAGCAGTGAGCAGCC | 51667 |
rs771027468 | snp | A/G | 5.46284e-05 | 0.00522601 | synonymous-codon | NUB1 | GRCh38.p7 | 7:151355817 | TGTGAAAGCGATGGT[A/G]CTTGAACTAAAACAA | 51667 |
rs771093682 | snp | C/T | 2.04121e-05 | 0.00319463 | missense | NUB1 | GRCh38.p7 | 7:151360144 | ATTTTTTCCTAGGCC[C/T]TTATGTTAGCTATGG | 51667 |
rs771159791 | snp | A/C | 1.74363e-05 | 0.0029526 | synonymous-codon | NUB1 | GRCh38.p7 | 7:151356207 | ATCAATCAGAATTCC[A/C]CCATCAGAAAGAAAA | 51667 |
rs771162382 | snp | A/G | | | utr-variant-3-prime | NUB1 | GRCh38.p7 | 7:151377341 | GTCCTCTTTGGGTGT[A/G]GGAGGGGGTGGGCAG | 51667 |
rs771219728 | snp | C/T | | | utr-variant-3-prime | NUB1, WDR86 | GRCh38.p7 | 7:151378206 | CCCAGTGGGAGTTCC[C/T]TCCAGCCCCAGGACC | 51667 |
rs771245533 | snp | A/C | | | downstream-variant-500B, utr-variant-3-prime | NUB1, WDR86 | GRCh38.p7 | 7:151378826 | AGGCGTGTCTTCTAG[A/C]TTCCCAGCTGTTTTT | 51667 |
rs771247849 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151365251 | GGATGACATGTACCC[C/T]TCTAATATGAGACCT | 51667 |
rs771303901 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151369101 | CAAGCTCCGCCTCCC[A/G]GGTTCAAGCAATTCT | 51667 |
rs771341081 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151344816 | ACCAGCCTGGCCAAC[A/G]TGGCGAAACCCCGTC | 51667 |
rs771357338 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151371120 | AAAAACCAGTGTATA[C/T]AGTGCAGTTGATCCT | 51667 |
rs771359012 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151354935 | TTTTCTGTGGAGACG[A/G]GGTCCACTGTGTTGC | 51667 |
rs771511644 | snp | A/G | 1.86027e-05 | 0.00304976 | missense, utr-variant-5-prime | NUB1 | GRCh38.p7 | 7:151351476 | CTGGCAGAGAACTGA[A/G]GTCCAAGTAAGTATC | 51667 |
rs771638796 | snp | A/G | 3.37081e-05 | 0.00410523 | synonymous-codon, utr-variant-5-prime | NUB1 | GRCh38.p7 | 7:151352875 | AAATAAGAAGCAACT[A/G]CAACTAGGTATGTAT | 51667 |
rs771642955 | snp | A/T | 1.71572e-05 | 0.00292888 | intron-variant | NUB1 | GRCh38.p7 | 7:151368912 | TTCACATGCCCTAGC[A/T]CTCTTGGGTATGAAA | 51667 |
rs771680495 | snp | A/C | | | intron-variant | NUB1 | GRCh38.p7 | 7:151357965 | TTGAGTTATCAGTAG[A/C]TTGATGTTTGTCTTT | 51667 |
rs771766696 | snp | A/G | 9.07839e-05 | 0.00673674 | missense | NUB1 | GRCh38.p7 | 7:151376736 | GCTCACAACGGAGGA[A/G]GCCTGCCTCCCGAGC | 51667 |
rs771800731 | snp | A/T | 1.73366e-05 | 0.00294415 | missense, utr-variant-5-prime | NUB1 | GRCh38.p7 | 7:151345372 | AAAAGAAATATCTTC[A/T]AGCAAAATTGACCCA | 51667 |
rs771833370 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151363385 | TGCAGAATAGACACT[A/G]TAGAAGAGAAGATTA | 51667 |
rs771840879 | snp | C/T | 3.1792e-05 | 0.00398685 | missense, utr-variant-5-prime | NUB1 | GRCh38.p7 | 7:151355804 | GCGTGGCTCACAATG[C/T]GAAAGCGATGGTGCT | 51667 |
rs771853626 | in-del | -/G | 3.35177e-05 | 0.00409362 | intron-variant | NUB1 | GRCh38.p7 | 7:151355990 | CCCACTCAGCTGCTT[-/G]GGGGCAGCACTGGAT | 51667 |
rs771874076 | in-del | -/A | 1.67242e-05 | 0.00289168 | frameshift-variant, intron-variant | NUB1 | GRCh38.p7 | 7:151374166 | AACATCAGGTTTCTG[-/A]AAGGGATGGGCTACT | 51667 |
rs771983382 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151374615 | TTTGGCATTAAAATT[C/T]TAAATGTAAGTATCT | 51667 |
rs771994920 | snp | G/T | 4.7112e-05 | 0.00485323 | intron-variant | NUB1 | GRCh38.p7 | 7:151345470 | TTGGCATTAAAGGTA[G/T]TTTTCTTTTAAGACA | 51667 |
rs772017032 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151350664 | ATAATCATATCTATA[A/G]TCTATTTCTAGTGTA | 51667 |
rs772021685 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151354850 | CAGGTGCAAGCAATC[C/T]TCCCACCTCAGCTTC | 51667 |
rs772054194 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151351089 | TGGTTGCCAGGGGCT[A/G]GGGGGCAAAGGGGAG | 51667 |
rs772066789 | snp | A/G | | | upstream-variant-2KB | NUB1 | GRCh38.p7 | 7:151340738 | AGATTGGTCTGGTGC[A/G]GTTATACAGTTATTA | 51667 |
rs772128778 | snp | A/G | 5.00747e-05 | 0.00500348 | intron-variant | NUB1 | GRCh38.p7 | 7:151349247 | CTAAAAAAAGTGAGT[A/G]ATTTCCCTAAATTTG | 51667 |
rs772155977 | snp | A/G | 1.65762e-05 | 0.00287886 | synonymous-codon | NUB1 | GRCh38.p7 | 7:151368833 | CCGGCTTGGCCTGAG[A/G]GCGTGTGATGGGAAC | 51667 |
rs772248122 | snp | C/G | 0.000139208 | 0.00834174 | intron-variant | NUB1 | GRCh38.p7 | 7:151374345 | GGGCTCACTCCTATG[C/G]GCTGCCCCGTCATCC | 51667 |
rs772303473 | snp | G/T | 4.96824e-05 | 0.00498385 | missense | NUB1 | GRCh38.p7 | 7:151375923 | CGTCAAGAAAGTCCT[G/T]CCCAGGAAAACATTG | 51667 |
rs772432398 | snp | C/G | 1.6588e-05 | 0.00287988 | missense | NUB1 | GRCh38.p7 | 7:151367062 | AGAAAAAAAATTAAA[C/G]TTGGCCCAGAAATGC | 51667 |
rs772477333 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151358267 | GTGAGCCACTGTGCC[C/T]GGCCAATGTTTGTCT | 51667 |
rs772521464 | snp | C/T | 3.3432e-05 | 0.00408838 | missense | NUB1 | GRCh38.p7 | 7:151368879 | ACTCATATTACCAAC[C/T]GCAGAGAGGTACCCA | 51667 |
rs772536569 | snp | C/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151348700 | CCTGCCTCAGCCCCC[C/G]AAGTAGCTGGGCCTA | 51667 |
rs772571783 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151367475 | GCAGTAATGGTTTAC[A/G]TGAATGAGTCACAGC | 51667 |
rs772663530 | snp | C/T | 1.65872e-05 | 0.00287981 | intron-variant | NUB1 | GRCh38.p7 | 7:151367855 | TTTTTTCTTCAATAA[C/T]TTTAGGGAAATTGTG | 51667 |
rs772702621 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151353307 | AGGTCCAGTGTGGCT[A/G]TGTGTGGAGAATGAG | 51667 |
rs772784632 | snp | C/T | 3.15204e-05 | 0.00396979 | synonymous-codon | NUB1 | GRCh38.p7 | 7:151376739 | CACAACGGAGGAAGC[C/T]TGCCTCCCGAGCTGC | 51667 |
rs772810327 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151371293 | AGAAGTAGGATAGGT[C/T]TCAGGGTTAGGTGAT | 51667 |
rs772840703 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151363507 | GGCACAATTTCAGGC[A/G]GCCTAAAATGCATGT | 51667 |
rs772841054 | snp | C/G | 1.68792e-05 | 0.00290505 | missense, utr-variant-5-prime | NUB1 | GRCh38.p7 | 7:151352879 | AAGAAGCAACTACAA[C/G]TAGGTATGTATGGCA | 51667 |
rs772897382 | in-del | -/TAACTGTT | 1.73525e-05 | 0.0029455 | intron-variant | NUB1 | GRCh38.p7 | 7:151356080 | AGGCTGTCATCATCA[-/TAACTGTT]TAACATTGAGTTCAT | 51667 |
rs772900393 | snp | A/G | 3.15303e-05 | 0.00397041 | synonymous-codon, utr-variant-5-prime | NUB1 | GRCh38.p7 | 7:151355805 | CGTGGCTCACAATGT[A/G]AAAGCGATGGTGCTT | 51667 |
rs772949363 | in-del | -/C | 4.96923e-05 | 0.00498434 | intron-variant | NUB1 | GRCh38.p7 | 7:151375834 | TGGGTAAAGGGTGTT[-/C]CTGTGTGTTTTAGAT | 51667 |
rs773004384 | snp | A/C | | | intron-variant | NUB1 | GRCh38.p7 | 7:151350097 | ACAGCTTACGTCATT[A/C]TTTCTTCTATGCTCT | 51667 |
rs773050525 | in-del | -/TCCTGGGCATCTATTTA | | | intron-variant | NUB1 | GRCh38.p7 | 7:151362250 | AGAAAGTTTTTTTTT[-/TCCTGGGCATCTATTTA]TCCTGGGCATCTATT | 51667 |
rs773118178 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151342561 | GTGAAACATTGTATG[A/G]CATGCATGAAACTTT | 51667 |
rs773136010 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151368063 | TTTGTGACTTGTGAG[A/G]AACATGCCTGTGCTT | 51667 |
rs773184512 | snp | C/T | | | upstream-variant-2KB | NUB1 | GRCh38.p7 | 7:151340137 | ACACCTGAGCGTGGA[C/T]ATTCAATTTCCTGAT | 51667 |
rs773217308 | in-del | -/CTCTGTTGCCATTCTC | | | intron-variant | NUB1 | GRCh38.p7 | 7:151357218 | TGAGATGGAGTCTCG[-/CTCTGTTGCCATTCTC]CTGCTTCAGCCTCCT | 51667 |
rs773223853 | snp | C/T | 1.65767e-05 | 0.00287891 | missense | NUB1 | GRCh38.p7 | 7:151368835 | GGCTTGGCCTGAGGG[C/T]GTGTGATGGGAACGT | 51667 |
rs773293109 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151354854 | TGCAAGCAATCCTCC[C/T]ACCTCAGCTTCCCAC | 51667 |
rs773348013 | snp | G/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151343487 | TTATCTTGGTAATAT[G/T]AACTCATATTTTTTC | 51667 |
rs773360882 | snp | A/G | 3.34169e-05 | 0.00408746 | intron-variant | NUB1 | GRCh38.p7 | 7:151355974 | AGCTCTGGGCTTGTC[A/G]CCCACTCAGCTGCTT | 51667 |
rs773425506 | snp | A/G | 1.65619e-05 | 0.00287762 | synonymous-codon | NUB1 | GRCh38.p7 | 7:151375928 | AGAAAGTCCTTCCCA[A/G]GAAAACATTGACCGA | 51667 |
rs773431480 | snp | A/G | 2.16551e-05 | 0.00329045 | missense | NUB1 | GRCh38.p7 | 7:151366940 | CCTTCTCTTTCCAGT[A/G]AGTGTTGCAGAGAGC | 51667 |
rs773544371 | in-del | -/A | | | intron-variant | NUB1 | GRCh38.p7 | 7:151364441 | CAAAAACAAAAAAAA[-/A]CAAAAAAAAAAACAA | 51667 |
rs773550729 | snp | C/T | 5.07627e-05 | 0.00503774 | synonymous-codon | NUB1 | GRCh38.p7 | 7:151376807 | GTCCCCTTCTGACTC[C/T]GCAGGTAGGTCTGAG | 51667 |
rs773662843 | snp | C/G | 1.65938e-05 | 0.00288039 | missense | NUB1 | GRCh38.p7 | 7:151367077 | CTTGGCCCAGAAATG[C/G]TTTAAAAATTGTTAC | 51667 |
rs773823506 | snp | C/T | 8.38638e-05 | 0.00647494 | synonymous-codon, utr-variant-5-prime | NUB1 | GRCh38.p7 | 7:151352842 | TGGACTTCAAGAAAA[C/T]TATATCAAAATTGTC | 51667 |
rs773950857 | snp | C/T | 0.000162933 | 0.0090244 | intron-variant | NUB1 | GRCh38.p7 | 7:151352073 | TGATTTTTCTCATTT[C/T]CTTCTTTGGTCTACA | 51667 |
rs773961375 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151358880 | CCATCCTGGCTAACA[C/T]AATGAAACCCCATCT | 51667 |
rs773984694 | snp | C/T | 1.69017e-05 | 0.00290699 | intron-variant | NUB1 | GRCh38.p7 | 7:151368729 | CTTACATTTCCCTGT[C/T]TCTAGGCACGTCAGC | 51667 |
rs774045236 | snp | G/T | 1.6571e-05 | 0.0028784 | synonymous-codon | NUB1 | GRCh38.p7 | 7:151368821 | TGCCCAGGAAGCCCG[G/T]CTTGGCCTGAGGGCG | 51667 |
rs774094265 | snp | A/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151359762 | AGCCTGGACGACAGA[A/T]TGAGACTCCGTCTCA | 51667 |
rs774096291 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151376067 | TGGCTCCCAGGCTCC[A/G]GGTGTAACCTGCCCA | 51667 |
rs774124571 | snp | G/T | 1.68088e-05 | 0.00289899 | stop-gained | NUB1 | GRCh38.p7 | 7:151356167 | AAATGACACCGTACT[G/T]AGACATAGCTAACCA | 51667 |
rs774149174 | in-del | -/T | 1.72662e-05 | 0.00293817 | intron-variant | NUB1 | GRCh38.p7 | 7:151352907 | GCAAAGTATGCATAA[-/T]TTTTTAATGAACCAA | 51667 |
rs774205846 | snp | A/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151349931 | GGTAGTGGCCCCGAA[A/T]GCCTGGCTGTGCTGT | 51667 |
rs774278941 | snp | A/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151348204 | CTTTGCTCTCAGTAA[A/T]AACTGGTTCCCATCC | 51667 |
rs774339654 | snp | A/G/T | 1.65803e-05 | 0.00287922 | missense, utr-variant-5-prime | NUB1 | GRCh38.p7 | 7:151349154 | GAAATACGTTGCAAG[A/G/T]CAATTGAGCGTGGAA | 51667 |
rs774442171 | snp | C/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151367453 | AATGCAGAAAATAGA[C/G]ATTTCAGCAGTAATG | 51667 |
rs774453405 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151356415 | TGTGCTTTTCAGCGC[A/G]TTAGTACAAAATGTC | 51667 |
rs774468231 | in-del | -/C | | | intron-variant | NUB1 | GRCh38.p7 | 7:151365318 | GGTTTTCTTCTCTCT[-/C]TTTTTTTTTTTTTTG | 51667 |
rs774502088 | snp | C/T | 8.64118e-05 | 0.00657255 | intron-variant | NUB1 | GRCh38.p7 | 7:151374092 | ACTTTGCTGTTTTCC[C/T]AAAGGAACTGGCCCA | 51667 |
rs774554393 | snp | A/G | 6.04906e-05 | 0.00549924 | intron-variant | NUB1 | GRCh38.p7 | 7:151376622 | TGCTGTGACCCCTGC[A/G]CTCTCCCCTAGTTGG | 51667 |
rs774567023 | snp | A/G/T | 7.39214e-05 | 0.00607917 | intron-variant | NUB1 | GRCh38.p7 | 7:151345506 | AATTAGCAGCATTAT[A/G/T]AATCTCCTTGGTAAA | 51667 |
rs774575439 | snp | A/G | | | upstream-variant-2KB | NUB1 | GRCh38.p7 | 7:151341272 | CCCTAGTGGCCGTGG[A/G]CAGCATGGGGGAGGA | 51667 |
rs774577640 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151353225 | AGTGGGGAGGCCATG[A/G]TGGCGTGCGTTCCAG | 51667 |
rs774620409 | snp | A/C/G | 3.31621e-05 | 0.00407188 | missense, utr-variant-5-prime | NUB1 | GRCh38.p7 | 7:151349152 | AAGAAATACGTTGCA[A/C/G]GGCAATTGAGCGTGG | 51667 |
rs774700268 | snp | A/C | | | intron-variant | NUB1 | GRCh38.p7 | 7:151342151 | AATAAATATGTCTAT[A/C]AAAAATTAGCCAAAT | 51667 |
rs774818064 | snp | C/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151361727 | CTAAGTGAACAAGTC[C/G]CAACTTTAACGTACA | 51667 |
rs774885961 | snp | C/T | 3.49241e-05 | 0.00417862 | missense | NUB1 | GRCh38.p7 | 7:151360219 | GGAATAGCCTTGCCA[C/T]GTCTGTTGGACGCTG | 51667 |
rs774939348 | snp | A/G | 2.51651e-05 | 0.0035471 | intron-variant | NUB1 | GRCh38.p7 | 7:151366920 | CTTGGCAGTGATGTC[A/G]CTGTCCTTCTCTTTC | 51667 |
rs774959085 | snp | C/T | 1.71179e-05 | 0.00292552 | intron-variant | NUB1 | GRCh38.p7 | 7:151368714 | CGTGGTTACATGATT[C/T]TTACATTTCCCTGTC | 51667 |
rs775025537 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151363631 | AAACCCCCAGATGCA[A/G]TGACTTTAATGACCC | 51667 |
rs775074804 | snp | C/G | 1.681e-05 | 0.00289909 | intron-variant | NUB1 | GRCh38.p7 | 7:151349278 | AGTAGGCACTAATGT[C/G]CAGTTAGTGATGAGG | 51667 |
rs775096357 | snp | A/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151347958 | ACCTCACATGCAGAT[A/T]CAGATTGAGAGGAGT | 51667 |
rs775098941 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151367610 | CTGCTGACCAGAAGG[A/G]CCACTGTGCTGCATG | 51667 |
rs775107682 | snp | A/G | 8.44202e-05 | 0.00649638 | missense | NUB1 | GRCh38.p7 | 7:151367940 | ATCACAGTGGAAATG[A/G]TGTAGAGGCTTATGA | 51667 |
rs775148364 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151362165 | CATCTTCAGTTCATG[A/G]TACATTAACATGTCC | 51667 |
rs775186179 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151350696 | CTATTCTTATTCTAT[A/G]TATTTTCTTTATTAT | 51667 |
rs775186244 | snp | A/G | 5.00388e-05 | 0.00500169 | intron-variant | NUB1 | GRCh38.p7 | 7:151355965 | GGTACCCAGAGCTCT[A/G]GGCTTGTCACCCACT | 51667 |
rs775228761 | snp | C/T | 7.19968e-05 | 0.00599944 | intron-variant | NUB1 | GRCh38.p7 | 7:151376835 | GAGGTCTTTGAGGGC[C/T]GCATTGAGAGCAAAG | 51667 |
rs775250298 | snp | A/G | 0.000261301 | 0.0114273 | intron-variant | NUB1 | GRCh38.p7 | 7:151374330 | CTCCAGCATCCTCCC[A/G]GGCTCACTCCTATGG | 51667 |
rs775463854 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151359648 | CGGGCATGGTGGCTC[A/G]TGCCTGTAGTCCTAG | 51667 |
rs775484736 | snp | A/T | | | missense | NUB1 | GRCh38.p7 | 7:151368754 | GTCAGCTCTTTAAAG[A/T]GCTATATATTGATCC | 51667 |
rs775621739 | snp | A/C | | | upstream-variant-2KB | NUB1 | GRCh38.p7 | 7:151341186 | CTGATAATAAAATAG[A/C]AGCGTCACTGTTGAG | 51667 |
rs775644802 | in-del | -/AAAAAAAAACAAA | | | intron-variant | NUB1 | GRCh38.p7 | 7:151364433 | CTCAAAAACAAAAAC[-/AAAAAAAAACAAA]AAAAAAAACAAAAAA | 51667 |
rs775673769 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151365515 | CCATTGCTTTCCTGC[A/G]AGTGGCAGGAGAGTC | 51667 |
rs775708320 | snp | A/G | 1.7182e-05 | 0.00293099 | synonymous-codon | NUB1 | GRCh38.p7 | 7:151360188 | GGGCAGAGCTTTCCT[A/G]AAAAGAAAAGAATAT | 51667 |
rs775742048 | snp | A/G | 3.19331e-05 | 0.00399569 | intron-variant | NUB1 | GRCh38.p7 | 7:151345495 | AAGACATCAATAATT[A/G]GCAGCATTATAAATC | 51667 |
rs775772739 | snp | A/G | | | upstream-variant-2KB | NUB1 | GRCh38.p7 | 7:151340551 | ATTCTGGATCTCACC[A/G]TGCAGTGCCCATTTC | 51667 |
rs775853443 | snp | A/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151352378 | GTTTGTGAGTCAGTC[A/T]GTTGAAATCCTGGGT | 51667 |
rs775932810 | in-del | -/AG | 2.07954e-05 | 0.00322448 | frameshift-variant | NUB1 | GRCh38.p7 | 7:151366949 | TCCAGTGAGTGTTGC[-/AG]AGAGCTGCTGGACAC | 51667 |
rs776043345 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151356682 | TTGGGATAGGTAGGC[A/G]GAGGTTTAATCTTAA | 51667 |
rs776062115 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | NUB1, WDR86 | GRCh38.p7 | 7:151377484 | CTTCCCCAGCTTGGT[A/G]TTTTACCCCGAAACA | 51667 |
rs776086533 | snp | A/G | 3.41478e-05 | 0.00413191 | intron-variant | NUB1 | GRCh38.p7 | 7:151376614 | GGGGCTGATGCTGTG[A/G]CCCCTGCGCTCTCCC | 51667 |
rs776090112 | snp | A/G | 1.66112e-05 | 0.00288189 | missense | NUB1 | GRCh38.p7 | 7:151377070 | AGTGCCTCAACAGAC[A/G]AAGACATGGAGACAG | 51667 |
rs776187012 | in-del | -/ATCA | 0.000112899 | 0.00751243 | utr-variant-3-prime | NUB1 | GRCh38.p7 | 7:151377267 | CTGCTTATAAATGCT[-/ATCA]ATCATTATGAAAAGG | 51667 |
rs776219050 | snp | C/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151364249 | ACAGGGCGAAACCCC[C/G]TCTCTACTAAAAATA | 51667 |
rs776332805 | in-del | -/CCC | 2.57384e-05 | 0.00358727 | cds-indel | NUB1 | GRCh38.p7 | 7:151376710 | ACGTCCAGCTGGCCG[-/CCC]AGACCCTTGCTCACA | 51667 |
rs776335624 | snp | C/T | 1.72344e-05 | 0.00293546 | intron-variant | NUB1 | GRCh38.p7 | 7:151368916 | CATGCCCTAGCTCTC[C/T]TGGGTATGAAAGAAC | 51667 |
rs776355288 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151371574 | ACCTGGGGAGCTGGA[A/G]CAGCCTCCCACACCT | 51667 |
rs776384038 | snp | A/G | 2.45474e-05 | 0.0035033 | synonymous-codon | NUB1 | GRCh38.p7 | 7:151355829 | GGTGCTTGAACTAAA[A/G]CAATCTGAAGAGGAC | 51667 |
rs776418002 | snp | A/T | | | upstream-variant-2KB | NUB1 | GRCh38.p7 | 7:151340392 | AAACCCTCAGCTCTG[A/T]CTCCTTGAGCTTGGG | 51667 |
rs776421232 | snp | G/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151347856 | TTTTACGTACTACAT[G/T]GTATTACATTATGAA | 51667 |
rs776474667 | snp | A/G | 1.65836e-05 | 0.0028795 | missense | NUB1 | GRCh38.p7 | 7:151368843 | CTGAGGGCGTGTGAT[A/G]GGAACGTGGATCATG | 51667 |
rs776540115 | snp | C/T | | | upstream-variant-2KB | NUB1 | GRCh38.p7 | 7:151341120 | ATACATACGTACATA[C/T]CTACGATAAAGTTTA | 51667 |
rs776618183 | snp | A/G | 1.87922e-05 | 0.00306525 | intron-variant | NUB1 | GRCh38.p7 | 7:151356232 | AGAAAAGTAAGTACT[A/G]TGAGAAATGTGTGGC | 51667 |
rs776829708 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151363838 | GCTGTAGTGCAGTGA[C/T]GCAATCTTAGTTTAC | 51667 |
rs776845354 | snp | A/G | 1.72901e-05 | 0.0029402 | missense, utr-variant-5-prime | NUB1 | GRCh38.p7 | 7:151345374 | AAGAAATATCTTCAA[A/G]CAAAATTGACCCAGT | 51667 |
rs776867359 | snp | A/T | 1.98932e-05 | 0.00315376 | synonymous-codon | NUB1 | GRCh38.p7 | 7:151360146 | TTTTTCCTAGGCCCT[A/T]ATGTTAGCTATGGGA | 51667 |
rs776937417 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151369196 | TATTTTTAGTAAAGA[C/T]GGGGTTTCACCATGT | 51667 |
rs776980077 | snp | C/T | 3.81905e-05 | 0.00436965 | synonymous-codon | NUB1 | GRCh38.p7 | 7:151367890 | AGAGAAGGTACTGTT[C/T]CTAAGACTCTACTTA | 51667 |
rs776988528 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151354973 | GATCTTGAACTCCGG[A/G]GCTCAAGTGATCCAC | 51667 |
rs777033050 | snp | C/T | 1.67699e-05 | 0.00289563 | intron-variant | NUB1 | GRCh38.p7 | 7:151349269 | CTAAATTTGAGTAGG[C/T]ACTAATGTCCAGTTA | 51667 |
rs777126885 | snp | A/G | 0.000459102 | 0.015144 | intron-variant | NUB1 | GRCh38.p7 | 7:151374361 | GCTGCCCCGTCATCC[A/G]GATCTGAAGGGCAGG | 51667 |
rs777239428 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151345209 | AGAAGTCTGGAGCTC[A/G]TTTAAACCATAGTAA | 51667 |
rs777292983 | snp | A/T | | | missense, utr-variant-5-prime | NUB1 | GRCh38.p7 | 7:151352827 | AATAGCTGAAACCTT[A/T]GGACTTCAAGAAAAT | 51667 |
rs777299071 | snp | C/T | | | upstream-variant-2KB | NUB1 | GRCh38.p7 | 7:151341033 | GCCTGAAACCTCGGA[C/T]AGTACTGCACCCCAT | 51667 |
rs777299926 | in-del | -/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151358799 | GCCGGGCGCGGTGGC[-/T]CACGCCTGTAATCCC | 51667 |
rs777489351 | snp | G/T | 2.37962e-05 | 0.00344928 | intron-variant | NUB1 | GRCh38.p7 | 7:151345471 | TGGCATTAAAGGTAT[G/T]TTTCTTTTAAGACAT | 51667 |
rs777528943 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151373748 | CTGGTTCCTAGAAGA[A/G]AATCCATGCACCTCA | 51667 |
rs777531212 | snp | A/C | 1.67671e-05 | 0.00289539 | synonymous-codon | NUB1 | GRCh38.p7 | 7:151355914 | GAAAAACAAATTCAG[A/C]GGACCAAGAGAGGAC | 51667 |
rs777566750 | snp | A/C | | | intron-variant | NUB1 | GRCh38.p7 | 7:151365996 | TTTTAGTAGAACACC[A/C]ATGAACATAAAGAGA | 51667 |
rs777581395 | snp | C/T | | | utr-variant-3-prime | NUB1, WDR86 | GRCh38.p7 | 7:151378166 | ACCGTCCTCACTGCG[C/T]CACGCACTCCTCTGT | 51667 |
rs777582054 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151372003 | GTGAGCCACTGCACC[C/T]AGCCTTTAATACATA | 51667 |
rs777681977 | snp | C/T | 1.67874e-05 | 0.00289714 | missense | NUB1 | GRCh38.p7 | 7:151366998 | TCCTCCAGCTGGATA[C/T]AGTGTGGTGTTACTT | 51667 |
rs777734039 | snp | A/G | 0.00032457 | 0.012735 | intron-variant, utr-variant-5-prime | NUB1 | GRCh38.p7 | 7:151352120 | TGGATTCAGGAAGTG[A/G]CATGCAACACACATG | 51667 |
rs777847047 | snp | A/C | | | intron-variant | NUB1 | GRCh38.p7 | 7:151344964 | GAGATCGCACCACTG[A/C]ACTCCAGCCTGGGCG | 51667 |
rs777971124 | snp | C/G | 1.84602e-05 | 0.00303805 | missense, utr-variant-5-prime | NUB1 | GRCh38.p7 | 7:151351448 | AACTTGTTGGAGACC[C/G]GATTGCACATCACTG | 51667 |
rs777982120 | snp | A/C | | | intron-variant | NUB1 | GRCh38.p7 | 7:151344602 | GGTTACAGGCCTGAG[A/C]CACCACACCCATCCG | 51667 |
rs778095295 | snp | C/T | 4.58516e-05 | 0.00478787 | synonymous-codon | NUB1 | GRCh38.p7 | 7:151367866 | ATAATTTTAGGGAAA[C/T]TGTGGGAAAGAGAAG | 51667 |
rs778099958 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151346363 | TCCCTGGTTCCTGGC[A/G]GAGCCAAAACTCTTG | 51667 |
rs778126427 | snp | A/C | | | intron-variant | NUB1 | GRCh38.p7 | 7:151344978 | GCACTCCAGCCTGGG[A/C]GACAGAGCGAGACTC | 51667 |
rs778206388 | in-del | -/A | 1.66109e-05 | 0.00288187 | frameshift-variant, utr-variant-5-prime | NUB1 | GRCh38.p7 | 7:151349233 | TTTACCACCAAGACT[-/A]AAAAAAAGTGAGTAA | 51667 |
rs778221502 | snp | A/G | 3.50257e-05 | 0.00418469 | intron-variant | NUB1 | GRCh38.p7 | 7:151368924 | AGCTCTCTTGGGTAT[A/G]AAAGAACAAAAAAAG | 51667 |
rs778351260 | snp | A/G | 1.73096e-05 | 0.00294185 | intron-variant | NUB1 | GRCh38.p7 | 7:151368691 | TTGTATTAAGCTTTA[A/G]GTATTGCCGTGGTTA | 51667 |
rs778359267 | in-del | -/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151362939 | GCGTCAAATAGAGTC[-/T]TCAGAAGGGTGTTGC | 51667 |
rs778416036 | snp | C/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151351868 | ATAGCTTGCTATGAC[C/G]TTCAGCACGGTGTTT | 51667 |
rs778438679 | snp | C/T | 6.62515e-05 | 0.00575512 | missense | NUB1 | GRCh38.p7 | 7:151375936 | CTTCCCAGGAAAACA[C/T]TGACCGAGTGAGTGA | 51667 |
rs778565464 | snp | A/G | 1.65773e-05 | 0.00287895 | intron-variant | NUB1 | GRCh38.p7 | 7:151375991 | ACAGCCTCGGGTGGG[A/G]TTGCTTGGGGTAACC | 51667 |
rs778658366 | snp | C/G | 1.67567e-05 | 0.00289449 | missense | NUB1 | GRCh38.p7 | 7:151368885 | ATTACCAACCGCAGA[C/G]AGGTACCCACTTTCA | 51667 |
rs778726349 | snp | A/T | 1.65748e-05 | 0.00287874 | | | GRCh38.p7 | 7:151360120 | TAAAGTGATGTTTTT[A/T]AAATTTGTATTTTTT | 51667 |
rs778777527 | snp | A/G | 1.76095e-05 | 0.00296723 | synonymous-codon, utr-variant-5-prime | NUB1 | GRCh38.p7 | 7:151345364 | GATGGCACAAAAGAA[A/G]TATCTTCAAGCAAAA | 51667 |
rs778785335 | snp | C/T | 2.14075e-05 | 0.00327159 | intron-variant | NUB1 | GRCh38.p7 | 7:151360279 | TTGGTGAACACCAGC[C/T]TTAAGGAAGATGGCC | 51667 |
rs778818099 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151363022 | CTGAACAGTACCCTT[A/G]ACTTACCGTTTTCAA | 51667 |
rs778838678 | snp | C/G | 5.99239e-05 | 0.00547342 | missense, utr-variant-5-prime | NUB1 | GRCh38.p7 | 7:151345453 | AAAATAAAAAAGTTG[C/G]TTTGGCATTAAAGGT | 51667 |
rs778840390 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151374258 | GGTAGCAGCTCCCTC[A/G]GGGCCTCTGGCCTTG | 51667 |
rs778853589 | snp | C/T | 1.6593e-05 | 0.00288031 | missense | NUB1 | GRCh38.p7 | 7:151367046 | AATGCCTTGATGATG[C/T]AGAAAAAAAATTAAA | 51667 |
rs778891701 | in-del | -/A | 0.00041253 | 0.014356 | intron-variant | NUB1 | GRCh38.p7 | 7:151368932 | TGGGTATGAAAGAAC[-/A]AAAAAAGATAATCCC | 51667 |
rs779045942 | snp | C/T | 1.68258e-05 | 0.00290045 | intron-variant | NUB1 | GRCh38.p7 | 7:151377028 | ATAATTCACTTACTC[C/T]TGCGGTATTTTATTG | 51667 |
rs779190108 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151369952 | TCGTGGGTTCATTCC[A/G]TGGTGAGCAGTCACA | 51667 |
rs779226162 | snp | A/G | 9.09628e-05 | 0.00674338 | synonymous-codon | NUB1 | GRCh38.p7 | 7:151376792 | GTCCCCGCCAGCCAC[A/G]TCCCCTTCTGACTCC | 51667 |
rs779326646 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151355392 | TTAAGAATTCCATTT[C/T]GTCCAGGAGCAAGGC | 51667 |
rs779473734 | snp | C/T | 0.000107336 | 0.00732507 | utr-variant-3-prime | NUB1 | GRCh38.p7 | 7:151377264 | TTTTCTGCTTATAAA[C/T]GCTATCATTATGAAA | 51667 |
rs779485979 | snp | A/G | 2.53367e-05 | 0.00355917 | intron-variant | NUB1 | GRCh38.p7 | 7:151345317 | TTAAAATGCGATGTG[A/G]AGTTTTATTAATGTA | 51667 |
rs779490882 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151376910 | TGGAGACTGAGGGGG[C/T]GTCCCCTGACGTCAC | 51667 |
rs779559895 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151364511 | ACCGACTTAAGCTCA[A/G]ATGGGATTTAATTTT | 51667 |
rs779614971 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151350792 | ATTAATATGTAAAAC[C/T]TCATACATGAATGGT | 51667 |
rs779723174 | snp | C/T | 1.83242e-05 | 0.00302684 | synonymous-codon, utr-variant-5-prime | NUB1 | GRCh38.p7 | 7:151345442 | ATATACAGATGAAAA[C/T]AAAAAAGTTGGTTTG | 51667 |
rs779745894 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151349820 | TTTCTCCTCATGTGC[A/G]GAGACAAGAGATCGT | 51667 |
rs779861111 | snp | C/T | 0.000149037 | 0.00863114 | missense | NUB1 | GRCh38.p7 | 7:151375908 | CCTGAAACCGACAAC[C/T]GTCAAGAAAGTCCTT | 51667 |
rs779873149 | snp | C/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151374632 | AAATGTAAGTATCTA[C/G]TTTTATTTATTTAGT | 51667 |
rs779914273 | snp | A/G | 4.97179e-05 | 0.00498562 | intron-variant | NUB1 | GRCh38.p7 | 7:151375984 | AGCTTGGACAGCCTC[A/G]GGTGGGGTTGCTTGG | 51667 |
rs779929455 | snp | C/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151342052 | GCGCTGGCCGTTCGG[C/G]GCCCTTTGGTTTGCC | 51667 |
rs779938743 | snp | A/T | 1.65611e-05 | 0.00287755 | missense | NUB1 | GRCh38.p7 | 7:151375875 | AATCCTCAGATGTGG[A/T]GGTTAAATGATTCCA | 51667 |
rs779992955 | snp | A/G | 5.03563e-05 | 0.00501753 | synonymous-codon | NUB1 | GRCh38.p7 | 7:151356162 | TCCAGAAATGACACC[A/G]TACTTAGACATAGCT | 51667 |
rs780138748 | snp | G/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151348282 | TCCCTTACAAATAGT[G/T]TTACAACTAGTACCC | 51667 |
rs780143566 | snp | C/G | 0.00011613 | 0.00761914 | missense, utr-variant-5-prime | NUB1 | GRCh38.p7 | 7:151349139 | GAAAAGGTAATAGAA[C/G]AAATACGTTGCAAGG | 51667 |
rs780232718 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151372096 | AGAAAAGCAACAGCT[A/G]TAGAAACGGAGCTCA | 51667 |
rs780318073 | snp | C/T | 4.24187e-05 | 0.00460517 | missense | NUB1 | GRCh38.p7 | 7:151376782 | AAGACTCTTTGTCCC[C/T]GCCAGCCACGTCCCC | 51667 |
rs780328543 | snp | C/T | 1.66382e-05 | 0.00288424 | synonymous-codon | NUB1 | GRCh38.p7 | 7:151368869 | TCATGCGGCCACTCA[C/T]ATTACCAACCGCAGA | 51667 |
rs780381465 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151362651 | AACCCAGGCAGAGCC[C/T]TGTGCTCCCTGGAGT | 51667 |
rs780397383 | in-del | -/TTT/TTTT | | | intron-variant | NUB1 | GRCh38.p7 | 7:151348575 | GCTTTTTGCTTTTTT[-/TTT/TTTT]TTTTTTTTTTTTTTT | 51667 |
rs780426472 | snp | C/T | 1.73288e-05 | 0.00294348 | intron-variant | NUB1 | GRCh38.p7 | 7:151367154 | ATTCATCTTATGTCT[C/T]GTTGAGTCCATTTCT | 51667 |
rs780444121 | snp | A/G | 1.6902e-05 | 0.00290701 | missense, utr-variant-5-prime | NUB1 | GRCh38.p7 | 7:151352813 | GTTTTATTTTACAGA[A/G]TAGCTGAAACCTTTG | 51667 |
rs780459886 | snp | G/T | 1.65701e-05 | 0.00287833 | missense | NUB1 | GRCh38.p7 | 7:151368797 | CAATTTGTTGCAGTT[G/T]GGGTTTACTGCCCAG | 51667 |
rs780472478 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151373542 | GCACTCTGTGGGTTC[C/T]GAATGGAATGACAGG | 51667 |
rs780473457 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151368371 | CACCCAGCGCTGTGG[C/T]TGCATGCCATTGACT | 51667 |
rs780542262 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151347647 | TTAGTTTTTGTAGAG[A/G]CGGGGTTTCACTTTG | 51667 |
rs780578938 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151347670 | TCACTTTGTTGCCCA[A/G]GTTGGTCTTGAAGTC | 51667 |
rs780606514 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151367506 | TCAAGAGCTGTGGCT[C/T]GAGTAAGGATTTTTC | 51667 |
rs780626926 | snp | A/T | 3.35638e-05 | 0.00409643 | missense | NUB1 | GRCh38.p7 | 7:151356146 | CAGAGACAGTGGTGG[A/T]TCCAGAAATGACACC | 51667 |
rs780667005 | snp | C/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151346082 | ATGTACTTCTCTGCT[C/G]TCATTCAGAGTATCC | 51667 |
rs780699843 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151343024 | AAATTGCTTGGCTCC[A/G]GTAACCAGCCTGTGA | 51667 |
rs780740026 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151371654 | AAAGTGAGCTCCTAT[C/T]GGAGCTTTAGATGAG | 51667 |
rs780764405 | snp | G/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151375490 | CTGACATTTTAAGTC[G/T]AGAGGGCATGACGCT | 51667 |
rs780856549 | snp | A/G | 2.25233e-05 | 0.00335576 | intron-variant | NUB1 | GRCh38.p7 | 7:151356270 | TAGATTTGTTGTCAG[A/G]GCAGAGGTGGTTTTT | 51667 |
rs780989244 | snp | G/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151366153 | TCAGTGCTCCTCCTG[G/T]AGCACACTGACTTCT | 51667 |
rs781004670 | snp | A/G | 2.63383e-05 | 0.00362884 | intron-variant | NUB1 | GRCh38.p7 | 7:151345309 | TTAACATTTTAAAAT[A/G]CGATGTGGAGTTTTA | 51667 |
rs781040713 | snp | C/T | 0.000166154 | 0.00911315 | intron-variant | NUB1 | GRCh38.p7 | 7:151352212 | TAGGTAGATTTTCTC[C/T]GGATGTGCAACTAGG | 51667 |
rs781085092 | in-del | -/TTAC | 1.98183e-05 | 0.00314782 | intron-variant | NUB1 | GRCh38.p7 | 7:151351400 | AAATTCAAGTACGTT[-/TTAC]TTACTTTGTCTTATT | 51667 |
rs781173003 | in-del | -/AA | | | utr-variant-3-prime | NUB1, WDR86 | GRCh38.p7 | 7:151378015 | AACTCACTGCTAGCT[-/AA]GAGACCTATCAGAGA | 51667 |
rs781243823 | snp | A/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151376425 | TCCTGAGATGGCTGC[A/T]CCCTGACGCACCCGA | 51667 |
rs781279640 | snp | A/G | 3.05246e-05 | 0.00390658 | intron-variant | NUB1 | GRCh38.p7 | 7:151360296 | TAAGGAAGATGGCCC[A/G]GACTATACAGAACAC | 51667 |
rs781336673 | in-del | -/TA | 1.6623e-05 | 0.00288292 | frameshift-variant | NUB1 | GRCh38.p7 | 7:151368757 | AGCTCTTTAAAGAGC[-/TA]TATATTGATCCATCA | 51667 |
rs781398735 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151362776 | GAGTCTTCTGCTCAG[C/T]AATGATCAGCACATG | 51667 |
rs781515966 | snp | C/T | 4.64792e-05 | 0.00482052 | missense | NUB1 | GRCh38.p7 | 7:151376674 | TCGTGGCCGAAGCTG[C/T]GCTGAGAGTGTTCAG | 51667 |
rs781517665 | in-del | -/TAGATGT | | | intron-variant | NUB1 | GRCh38.p7 | 7:151344221 | AAAAAAAGTAGATGT[-/TAGATGT]GCTGTTAGGCTGTTA | 51667 |
rs781573213 | snp | C/T | 7.45796e-05 | 0.00610608 | missense | NUB1 | GRCh38.p7 | 7:151376761 | CCGAGCTGCCGCTGT[C/T]GCCAGAAGACTCTTT | 51667 |
rs781635987 | snp | A/C | 1.88525e-05 | 0.00307016 | intron-variant | NUB1 | GRCh38.p7 | 7:151351486 | ACTGAGGTCCAAGTA[A/C]GTATCTGTGTGCTCT | 51667 |
rs781637392 | snp | C/T | 1.65814e-05 | 0.00287931 | missense | NUB1 | GRCh38.p7 | 7:151368778 | TTGATCCATCAAAAG[C/T]GGACAATTTGTTGCA | 51667 |
rs781664404 | snp | A/G/T | 0.000110577 | 0.00743479 | missense, utr-variant-5-prime | NUB1 | GRCh38.p7 | 7:151355791 | CTTGAAGAACAAGGC[A/G/T]TGGCTCACAATGTGA | 51667 |
rs781705591 | snp | G/T | | | upstream-variant-2KB | NUB1 | GRCh38.p7 | 7:151339758 | CTTCTGCTTTCAGAG[G/T]CCTTCCATTTACATT | 51667 |
rs781721697 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151372016 | CCCAGCCTTTAATAC[A/G]TAATTATTAAAAGTT | 51667 |
rs796068925 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151344388 | CCATCTCGGCTCACT[A/G]CAACCTCTGCCTCCT | 51667 |
rs796142644 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151367756 | GGACATTTTAATACC[C/T]ATCATGTTGCCCCTC | 51667 |
rs796175697 | snp | A/C | | | intron-variant | NUB1 | GRCh38.p7 | 7:151360978 | TACAGATGGGGTCTC[A/C]CTGTGTTGCTCAGGC | 51667 |
rs796222061 | in-del | AATTATAC/GTTGTAG | | | intron-variant | NUB1 | GRCh38.p7 | 7:151360958 | TTTTTTTTTTTTTTA[AATTATAC/GTTGTAG]GATGGGGTCTCCCTG | 51667 |
rs796296246 | in-del | -/G | | | utr-variant-3-prime | NUB1 | GRCh38.p7 | 7:151377371 | GGGACAAGTCCAGGA[-/G]GGGGTCCCAGGGCCT | 51667 |
rs796389566 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151360971 | TTAATTATACAGATG[A/G]GGTCTCCCTGTGTTG | 51667 |
rs796406208 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151360981 | AGATGGGGTCTCCCT[A/G]TGTTGCTCAGGCTGA | 51667 |
rs796483396 | in-del | -/AGGGTT | | | intron-variant | NUB1 | GRCh38.p7 | 7:151371296 | AGTAGGATAGGTCTC[-/AGGGTT]AGGTGATTCATTCAG | 51667 |
rs796548499 | snp | A/G | | | intron-variant | NUB1 | GRCh38.p7 | 7:151350289 | GCCTGACTAATGTCA[A/G]GCCTTCCACAAGAGG | 51667 |
rs796599923 | multinucleotide-polymorphism | GTA/TTT | | | intron-variant | NUB1 | GRCh38.p7 | 7:151360952 | TTTTTTTTTTTTTTT[GTA/TTT]TTAATTATACAGATG | 51667 |
rs796667260 | in-del | -/AA | | | intron-variant | NUB1 | GRCh38.p7 | 7:151363756 | AACCTTTCTTGAAAA[-/AA]GTTAGGTAAGTTTGG | 51667 |
rs796713445 | snp | G/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151344661 | TCAAGCAAGCTTTTC[G/T]TTATATTTAACTACC | 51667 |
rs796786942 | snp | A/C | | | upstream-variant-2KB | NUB1 | GRCh38.p7 | 7:151339948 | ACACACCAATACAAG[A/C]CACTGCAGACATTAG | 51667 |
rs796894420 | snp | C/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151345645 | TTCATTAATATTTTA[C/T]TCACATGAGGATGTT | 51667 |
rs796925167 | in-del | -/T | | | intron-variant | NUB1 | GRCh38.p7 | 7:151365900 | AAGTCCTTTTTTTTT[-/T]ATTCCATGCATATTT | 51667 |