SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs563689090 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:429462 | AATTCCCGACCGCAG[C/G]TGATCCACCTGCCTC | 10616 |
rs563858860 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RBCK1 | GRCh38.p7 | 20:425271 | CCACCTCGGCCTCCC[A/G]AAGTGCTAGGATTAC | 10616 |
rs563877438 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:423165 | TTAGCCGGGTGTGGT[A/G]GCGCATGCCTGTAAT | 10616 |
rs563878445 | snp | C/G | 0.15698 | 0.23205 | intron-variant | RBCK1 | GRCh38.p7 | 20:419872 | GGCAGTGACCCTGCA[C/G]CTGGCTGTGACCCTG | 10616 |
rs564128498 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:413220 | GGAAATACAAGTTCT[C/T]CAACTTTTGTTCTTT | 10616 |
rs564263812 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:412433 | TCAAGTGATTCTCCT[A/G]CCCCAGCCTCCTGAG | 10616 |
rs564432077 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:418526 | GGCGCCCGCCACCAC[A/G/T]CCCGGCTAATTTTTT | 10616 |
rs564496882 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:430162 | TTCCCGGATCTAGGC[A/G]TGGGTAGACTGAGTG | 10616 |
rs564497908 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RBCK1 | GRCh38.p7 | 20:419163 | AGCATTTATCGGTGG[A/G]ATAGGGACCCTGACC | 10616 |
rs564542978 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:408521 | GCCCAGTGCGGACCT[A/G]TCTCGGCGCCCGCTG | 10616 |
rs564681004 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:425244 | TTGAACTCCTGACCT[C/T]AGGTGATCCACCCAC | 10616 |
rs564711971 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RBCK1 | GRCh38.p7 | 20:414955 | TATTTTGCTCTGTCA[A/G]TTCATTGATAGTTGA | 10616 |
rs564804447 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:409184 | CCTCTGTGTTCTCCA[A/G]ACAAAACCCAGAGGC | 10616 |
rs564936469 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | RBCK1 | GRCh38.p7 | 20:420178 | TCCTACTCCTGACCT[C/G]TTCCCTCTCGGGCTG | 10616 |
rs564946730 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:421140 | CTCATTGGACGCCCG[C/T]GAAAACCTACGAGGT | 10616 |
rs564965259 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RBCK1 | GRCh38.p7 | 20:414302 | CTGTAGTCCCAGCTA[C/T]TTGAGAGGCTGAGAT | 10616 |
rs565073300 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:425872 | CCTCGTGATGCGCCC[A/G]CCTCGGCCTCCCAGA | 10616 |
rs565143763 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RBCK1 | GRCh38.p7 | 20:411610 | CTGACCTCGTGATCC[A/G]CCCGCCTATGCCTCC | 10616 |
rs565329577 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:413410 | TTGAGATATCTACTT[A/C]TTGAAATGATTGCTT | 10616 |
rs565412752 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:416242 | CTCACTGCACGGTCC[A/G]CCTCCCGGGTTCACA | 10616 |
rs565520412 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:410282 | GGATGTTAGGCCTTA[C/T]ACAACAGAAGAAAAC | 10616 |
rs565521326 | snp | C/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:423503 | GGATAGAACATATTC[C/T]TACAAAAAAAATTAC | 10616 |
rs565657779 | snp | A/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:424797 | CCTGGAGCCCACTGG[A/G]GTTGATGTGAGTCTC | 10616 |
rs565813341 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:431077 | AGTTGACTTGTCAGT[C/T]CATCTGTGGTAGAAT | 10616 |
rs565886268 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RBCK1 | GRCh38.p7 | 20:419021 | GCTGATGTTTCCTCC[A/G]GAGTGGATCAAGTCA | 10616 |
rs566078466 | snp | A/G | 0.000798403 | 0.0199641 | stop-gained, synonymous-codon, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:419695 | GGAGCGAGCGCGCCT[A/G]GCGGGCGAGGAGGAG | 10616 |
rs566081614 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:425111 | CGCCTCCCGGGTTCA[C/T]GCCATTCTCCTGCCT | 10616 |
rs566093412 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:414469 | ATGCATTTATAGTAT[A/G]TAAGTTAAAATTAAG | 10616 |
rs566405879 | snp | C/T | 0.00835141 | 0.0640778 | upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:407832 | TGGGTGAGCAGGCGC[C/T]GGGCTCGCAGGGCGC | 10616 |
rs566615418 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RBCK1 | GRCh38.p7 | 20:421300 | CCCTCTACCTTTCGC[C/T]GCCCGGGCTCCTGCA | 10616 |
rs566673783 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:416361 | GAGACGGGTTTTCAC[C/T]GTGTTAGCCAGGATG | 10616 |
rs566719769 | in-del | -/AG | 0.00119737 | 0.0244387 | intron-variant | RBCK1 | GRCh38.p7 | 20:424833 | ATGGTCAAGTGTGAC[-/AG]AGAGAAGGAGGCAGG | 10616 |
rs566720318 | in-del | -/C | 0.00636936 | 0.0560724 | upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:407907 | CCTCCAGCCCCGGCT[-/C]CCGGCGCCGACTCCT | 10616 |
rs566732515 | snp | C/T | | | intron-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:429253 | TTTTTTGAAACGGAG[C/T]TTCACTCTTGTTGCC | 10616 |
rs566912235 | snp | A/G | | | missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:427443 | TTGAGGATGATGTCA[A/G]TGAGTTCACCTGCCC | 10616 |
rs567076038 | snp | A/C/G | 0.00197889 | 0.0313931 | intron-variant | RBCK1 | GRCh38.p7 | 20:419789 | GGGGAGGTGTAGGCC[A/C/G]GGAAGGGAGACACCT | 10616 |
rs567140864 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | RBCK1 | GRCh38.p7 | 20:420273 | CGACCCCGGTCCTAC[A/G]CCTTAGCCCTACCCC | 10616 |
rs567141022 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:415275 | CAGGAGGCTGAGGTG[A/G]GAGGGTCACCTCAGT | 10616 |
rs567411576 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:425904 | TGTTCAGATTACAGG[C/T]GTGATCCATCATTCC | 10616 |
rs567412824 | snp | C/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:416582 | CCATACCCTAAATGA[C/T]CTCTGTTTCCTTTGG | 10616 |
rs567490108 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:425368 | ACACAATAAAATGTA[C/T]TCATTGTAAGTATGC | 10616 |
rs567542235 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:409467 | GGATCGCAATCTGAC[A/T]TTTTTTTTTTTTCTT | 10616 |
rs567647759 | snp | A/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:425424 | ACTCTCGTAACCACC[A/T]ACCACTGTTACATAT | 10616 |
rs567784507 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RBCK1 | GRCh38.p7 | 20:426952 | CAACCCAGCCTCCCA[A/G]GCAGCTGGGACTACA | 10616 |
rs567982151 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:422655 | GGCAACATGGCAAAA[A/C]ATATTCAAAAAATAG | 10616 |
rs568005329 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:421962 | CAGGGTGGAGGCCTT[A/G]GTGATGGGTTGGTGA | 10616 |
rs568042309 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:426586 | ATGTGCCACGTTTTC[C/T]TTATAGGATACTAGT | 10616 |
rs568105659 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:421557 | AAATGCTACATACAG[C/T]ACATTAAGAGACAAC | 10616 |
rs568251181 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RBCK1 | GRCh38.p7 | 20:411512 | AGCTGGGACTACAGG[C/T]GCCCGCCACCACGCC | 10616 |
rs568266212 | snp | A/C/G | 0.00239369 | 0.0345212 | intron-variant | RBCK1 | GRCh38.p7 | 20:418493 | CCTGCCTCAGCCTCC[A/C/G]GAGTAGCTGGGACTA | 10616 |
rs568390660 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | RBCK1 | GRCh38.p7 | 20:410686 | CTGTGCTCCAGGAGA[C/T]TTAAACTCAATGCTG | 10616 |
rs568512214 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:423830 | CTGGTGGGTCAGCCG[C/T]GGTGGCCTGGTTTAT | 10616 |
rs568714524 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:429190 | ATGGGCCATATCCAA[A/C]CCAGCACCTGAATTT | 10616 |
rs568820415 | snp | A/G | 4.97129e-05 | 0.00498538 | utr-variant-5-prime, missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:417796 | GGCAGCGGCTGGCAC[A/G]AGACCAGGAGACCCT | 10616 |
rs568890918 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:421410 | GGGAACACAGACCCG[A/C]TCACCACAGCGGACC | 10616 |
rs568956631 | snp | A/G | 6.75105e-05 | 0.00580954 | utr-variant-5-prime, intron-variant, synonymous-codon, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:410014 | TGAGGTCTCCCCAAC[A/G]CAGGACATCAGGTGA | 10616 |
rs568959526 | in-del | -/C | 0.00159617 | 0.0282053 | intron-variant | RBCK1 | GRCh38.p7 | 20:418609 | TCCTGACTTTGTGAT[-/C]CGCCCGCCTCGGCCT | 10616 |
rs568996651 | in-del | -/C | 0.0037417 | 0.0430912 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:408726 | CCCAGGAGGCACGGT[-/C]CCCCCCAGGGGGATG | 10616 |
rs569027636 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, missense, utr-variant-5-prime, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:417245 | GAGAAGACAGAAGAG[A/G]TTGGAGAGGTCAGGG | 10616 |
rs569089434 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:416408 | CTCGTGATCCACCCA[C/T]CTCGGCCTCCCAAAG | 10616 |
rs569126908 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:423230 | CTTGAACCCCGGAGG[C/T]GGAGGTTGTGGTGAA | 10616 |
rs569130647 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:418295 | ATGTTTCAGACCTAC[A/C]GAAAAGTTGCTAAAT | 10616 |
rs569207010 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | RBCK1 | GRCh38.p7 | 20:421844 | TTCTGAGATAGACTC[C/T]AGGGGCCAGATGGAT | 10616 |
rs569310074 | snp | A/G | 0.00029818 | 0.0122066 | intron-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:429109 | GGTGAGTCTTTGCTC[A/G]TGGTGGTGTGGAGAG | 10616 |
rs569446432 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:418444 | CACAATCTCGGCTCA[C/T]TGCAAGCTCCGACTC | 10616 |
rs569558323 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:412562 | ACCTCAGGTGATCCA[C/T]CCACCTTGGCCTTTC | 10616 |
rs569685597 | snp | A/C | | | upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:406866 | ACATATGGAGCCTCC[A/C]TTATGTGTTTGGAAC | 10616 |
rs570093249 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:430298 | AGCGCTCGGCTGTGG[A/G]GGCAGTCTCTGCACT | 10616 |
rs570145825 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:414369 | GTGAGCCATGATCAT[G/T]CCTGAGTGACAAGGT | 10616 |
rs570164908 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:407703 | GAGCCTGCCAGGCCT[A/G]GATTCAAACCTCGGC | 10616 |
rs570201504 | snp | C/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:418577 | GTTTCACCGTGTTAG[C/T]CAGGATGGTCTCGAT | 10616 |
rs570391132 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | RBCK1 | GRCh38.p7 | 20:418648 | GCTGGGATTACAGGC[A/G]TGAGCCACCACGCCC | 10616 |
rs570517854 | in-del | -/GCCATGACCCCAGCACCCTA | 0.00557542 | 0.0525036 | intron-variant, frameshift-variant | RBCK1 | GRCh38.p7 | 20:420036 | ACACGAGTATGGCTG[-/GCCATGACCCCAGCACCCTA]GCCATGACCCCAGCA | 10616 |
rs570820620 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:429645 | CTTTGGAGCACAGCC[A/G]TGTTCATTCATTCAC | 10616 |
rs570881424 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:423922 | ACCAGCAGGCTGCCC[A/G]GGCCTTCTCATGTCA | 10616 |
rs570894442 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:407591 | AAATTAAAGCGGCGC[A/G]TGAGGCAGACGAATG | 10616 |
rs570954124 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | RBCK1 | GRCh38.p7 | 20:418620 | TGATCCGCCCGCCTC[A/G/T]GCCTCCCAAAGTGCT | 10616 |
rs570968202 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:413616 | TACAATGTCAGCCAC[A/C]ATCTTGCTACTAAAG | 10616 |
rs570980213 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:406665 | GTGAGCCATGATCAC[C/G]CCACTGCACTCCAGC | 10616 |
rs571004344 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:429217 | ATTTGTACAGCTCCC[A/G]AGGTAAGAATTTTTT | 10616 |
rs571067836 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:425142 | CAGCCTCCCAAGTAG[C/T]TGGGACTAGAGGCGC | 10616 |
rs571132743 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | RBCK1 | GRCh38.p7 | 20:425307 | TGAGCCACCGTGCCC[A/G/T]GCCAGATATGATTTT | 10616 |
rs571159196 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | RBCK1 | GRCh38.p7 | 20:418576 | GGTTTCACCGTGTTA[A/C/G]CCAGGATGGTCTCGA | 10616 |
rs571199765 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:424377 | CCAAAACATGGCAGC[C/T]GAGGCCCAAATGGGA | 10616 |
rs571247381 | in-del | -/T | 0.00953873 | 0.0683987 | intron-variant | RBCK1 | GRCh38.p7 | 20:426066 | TACTAGTTTGTTTAA[-/T]TTTTTATTTTTTATT | 10616 |
rs571253146 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:431092 | CCATCTGTGGTAGAA[A/T]GAGGCTGTGACTGAG | 10616 |
rs571330210 | snp | C/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:426759 | CACCACCATCCACCT[C/T]CAGAACTTTTAGAAA | 10616 |
rs571442642 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:419737 | GTACCAGCAGGTGGG[C/T]GGGAAAGTCCCTGGA | 10616 |
rs571878697 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:409385 | TCCTTCAGGTCTTAG[C/T]TTCAGTGTTACCCCC | 10616 |
rs571929416 | snp | C/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:426928 | CCTTCTGGGCTCAAG[C/T]GATCCTCACAACCCA | 10616 |
rs571951673 | snp | C/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:421397 | ACCCCTGAATGTGGG[C/G]AACACAGACCCGCTC | 10616 |
rs571996386 | snp | A/C/T | 0.016246 | 0.0887035 | intron-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:429453 | CTGGTCTCAAATTCC[A/C/T]GACCGCAGGTGATCC | 10616 |
rs572008958 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:429835 | TGGCACATACTGACT[C/G]TGTGATTAGGCTGCC | 10616 |
rs572110482 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RBCK1 | GRCh38.p7 | 20:424131 | TGGAGTCACCACTCC[A/G]CCAGTCTGTCACAGC | 10616 |
rs572166090 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:418524 | CAGGCGCCCGCCACC[A/G]CGCCCGGCTAATTTT | 10616 |
rs572353750 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:423730 | CAATTCTCTGGATAC[C/T]GAGGGATGACTATAA | 10616 |
rs572421706 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | RBCK1 | GRCh38.p7 | 20:413829 | ATAGTTTACTTAGCT[A/G]TTACATTAATTAATA | 10616 |
rs572425397 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:418587 | GTTAGCCAGGATGGT[A/C]TCGATCTCCTGACTT | 10616 |
rs572489984 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:407006 | AGACAGTAATAGATG[C/T]TGAGAAGAAAAAATG | 10616 |
rs572529282 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:414913 | TGTGGTAAACTTTTA[A/G]AGTCTTTGCATGTTT | 10616 |
rs572613033 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:413098 | ATTGACCATAAATGT[C/G]AGTGCTTATTTCTGG | 10616 |
rs572676357 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RBCK1 | GRCh38.p7 | 20:422901 | TGTGACCACAAGTCA[G/T]ATATTTAACCTCTCT | 10616 |
rs572834973 | snp | A/C | 0.00119737 | 0.0244387 | upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:406861 | ATTCAACATATGGAG[A/C]CTCCATTATGTGTTT | 10616 |
rs572901110 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RBCK1 | GRCh38.p7 | 20:425172 | CACACCGCCATGCCC[A/G]GCTAATTTTTGTATT | 10616 |
rs572960429 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:431364 | GGTTGTCCATCCTAT[G/T]TTCTCGTCTCAAGCA | 10616 |
rs573249266 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RBCK1 | GRCh38.p7 | 20:426654 | TTCTTTTCTTTATTG[A/T]GAGAAAATAGACATA | 10616 |
rs573318245 | snp | C/T | | | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:408438 | GGACTTGGAACGCCC[C/T]GGCTGGGTGGTGTCC | 10616 |
rs573348550 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:421631 | GTAGCCCCAGAGCAG[A/G]GACCGGAAGGCCTGC | 10616 |
rs573410772 | snp | C/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:428085 | GTAAACAGGTCTGGA[C/G]CCTGGTCTCAGACTC | 10616 |
rs573457767 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:414658 | ATGCTTTGCCTCTAG[A/G]TTGATTCTAAAAGTG | 10616 |
rs573641082 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:414157 | TCACGCTGGGCATGG[C/T]GGCTCAGCACTTTGG | 10616 |
rs573658689 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:430528 | CCTTGCTTGCTGTAG[C/G]GTTGTAGGGGCCCTG | 10616 |
rs573670138 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RBCK1 | GRCh38.p7 | 20:430045 | GGGGGCCTGTTGCTA[C/T]GTTCAGGTAGACTTT | 10616 |
rs573902704 | in-del | -/TG | 0.00953873 | 0.0683987 | intron-variant | RBCK1 | GRCh38.p7 | 20:426205 | CAAGCATTTATCCTT[-/TG]TGTTACAGACAATCC | 10616 |
rs574074446 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:407759 | CAAACAGAGCCTTCG[C/T]TTATTCATGTGCAAA | 10616 |
rs574107194 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:408925 | TCAGTTTCCTCCTTT[C/G]GTACCTGCTGGCTTC | 10616 |
rs574127850 | snp | G/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:424030 | TTGACACTGTCCCAT[G/T]GGCCAAAGCAAGTCC | 10616 |
rs574141365 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RBCK1 | GRCh38.p7 | 20:426168 | AATAATCACATCATG[A/G]AGAATGGGGAATCCA | 10616 |
rs574254155 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:425734 | CGGGTTCAAACGATT[C/G]TCCTGCCTCAGCCTC | 10616 |
rs574386864 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:410142 | CTGGCTTCTAACCCT[A/T]GTTATGTCATTAATC | 10616 |
rs574405779 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:407799 | GGACCGGGCCTGCCC[C/T]GAGGTATGCCTGAGG | 10616 |
rs574468909 | snp | A/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:418056 | GAGGACCCTATCCAA[A/G]TGGGGAAGAGAGGAC | 10616 |
rs574491137 | snp | C/T | | | intron-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:429298 | ATAGCACAATCTCAG[C/T]TCACTGCAACCTCTG | 10616 |
rs574530238 | snp | A/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:416237 | CTTGGCTCACTGCAC[A/G]GTCCGCCTCCCGGGT | 10616 |
rs574560739 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:421057 | CAGTCCCACCCCCGG[C/G]AATGCAGCTTAATCA | 10616 |
rs574630043 | snp | C/G | | | upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:406560 | GCAACATGACCAAAC[C/G]CTGTCTCTACAAAAA | 10616 |
rs574705326 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RBCK1 | GRCh38.p7 | 20:412031 | GGTCATACAGTAACT[C/G]TATGTTACTTTTTGA | 10616 |
rs574826808 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:427055 | TCTCAGGCTGGTCTG[A/T]AACTCTTGGCCTCAA | 10616 |
rs574835647 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:411167 | TCTTTCACTTAGGAT[C/T]GTTTTCGAGATTCAT | 10616 |
rs574916931 | snp | C/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:412573 | TCCACCCACCTTGGC[C/T]TTTCCAAAGTGTTGG | 10616 |
rs575115866 | snp | G/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:414985 | ACTGGGTATTCAAAT[G/T]GTTTACCTGAAGAAT | 10616 |
rs575270448 | snp | A/G | 0.0715223 | 0.175059 | intron-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:420690 | CACCCCCCACCCCCC[A/G]TCCCCCAGCCCCACC | 10616 |
rs575319203 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | RBCK1 | GRCh38.p7 | 20:415993 | AGCTGCCCCTATGAC[C/G]CAAACACCTCCCACC | 10616 |
rs575392530 | snp | C/T | 8.27986e-05 | 0.0064337 | utr-variant-5-prime, missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:417584 | ATCTGGCTCACAGTG[C/T]GCCCTGATATGACAG | 10616 |
rs575457871 | snp | A/C | 0.158302 | 0.232576 | intron-variant | RBCK1 | GRCh38.p7 | 20:419867 | CTGCTGGCAGTGACC[A/C]TGCACCTGGCTGTGA | 10616 |
rs575507403 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:431417 | CAGTATTTACTAGAA[C/T]CCACTCTGTGCTGGT | 10616 |
rs575531945 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:409624 | GCTTGTTGGATAAAT[C/G]AATAGAAATATGAGG | 10616 |
rs575578439 | snp | G/T | 1.66319e-05 | 0.00288369 | missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:422209 | ACCTACTCGTGCTCG[G/T]GCAAGCTGCTGGAGA | 10616 |
rs575744845 | snp | A/C | | | intron-variant | RBCK1 | GRCh38.p7 | 20:416955 | GGTAGCACTACTGCA[A/C]TCCAGCCTGGGCCAC | 10616 |
rs576091696 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RBCK1 | GRCh38.p7 | 20:411596 | ATGGTCTCCATCTCC[C/T]GACCTCGTGATCCGC | 10616 |
rs576124423 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:429311 | AGCTCACTGCAACCT[C/T]TGCCTTCCGGGTTCA | 10616 |
rs576272262 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:423085 | CGGGTGGATCACCTG[A/G]GGTCGGGAATTCGAG | 10616 |
rs576290053 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:428764 | TCATGTCAGGAAGAG[C/T]GTCTGGGTGGAGGGT | 10616 |
rs576692090 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:406134 | TTTTAGTAGAGACAG[C/G]GTTTCACCATGTTGG | 10616 |
rs576699481 | in-del | -/CTCT | 0.00835141 | 0.0640778 | intron-variant | RBCK1 | GRCh38.p7 | 20:426229 | GACAATCCAGTTAAC[-/CTCT]CTTAGTTATTATAAA | 10616 |
rs576903629 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | RBCK1 | GRCh38.p7 | 20:410760 | AACATTAGTGTCTAT[C/T]GTTATTTTTTGACTG | 10616 |
rs577066591 | snp | C/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:414660 | GCTTTGCCTCTAGGT[C/T]GATTCTAAAAGTGTA | 10616 |
rs577067705 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | RBCK1 | GRCh38.p7 | 20:418408 | GAGTCTCGCTCTGTC[G/T]CCCAGGCTGGAGTGC | 10616 |
rs577077393 | snp | C/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:416674 | CAAGAAAGTTAAAAC[C/G]ACTTTCTCTGGAATA | 10616 |
rs577192276 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | RBCK1 | GRCh38.p7 | 20:418507 | CGGAGTAGCTGGGAC[G/T]ACAGGCGCCCGCCAC | 10616 |
rs577269743 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RBCK1 | GRCh38.p7 | 20:423369 | GTTGTTAGCGCTTAC[C/T]GTGTAACAAATCACT | 10616 |
rs577498437 | snp | A/C | 6.62866e-05 | 0.00575664 | utr-variant-3-prime, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:430458 | GGGGCCACATGCTGA[A/C]CCAGCCCCACATCCA | 10616 |
rs577720734 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:418659 | AGGCGTGAGCCACCA[C/T]GCCCAACCCACATTT | 10616 |
rs577781018 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:414102 | CATACAAAAAAAAAA[A/C]AGAAAAATCCCTGGG | 10616 |
rs578035608 | snp | C/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:423737 | CTGGATACCGAGGGA[C/T]GACTATAATTTGGGC | 10616 |
rs578069523 | snp | C/G | 0.00755907 | 0.0610114 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:408217 | GTCCGCCGCCGCCGG[C/G]TAGCCGGGCAGTGGA | 10616 |
rs578170337 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:407166 | TGGCAGGTGCAAAGG[C/T]CTTAGGGCGGGAGTG | 10616 |
rs578195999 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RBCK1 | GRCh38.p7 | 20:425251 | CCTGACCTCAGGTGA[G/T]CCACCCACCTCGGCC | 10616 |
rs587777561 | snp | C/T | | | intron-variant, stop-gained, nc-transcript-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:420904 | GAGGGGAACTACCTG[C/T]AGCACGTCCAGCTGG | 10616 |
rs727503762 | snp | C/T | | | synonymous-codon, stop-gained, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:419439 | GAACCCGGACGGGGG[C/T]AGCCAGATGCAGTGC | 10616 |
rs727503763 | in-del | -/CT | | | utr-variant-5-prime, intron-variant, frameshift-variant, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:409979 | GAGCAACGGGTGCCC[-/CT]GAGTGTGCAACTGAA | 10616 |
rs727503764 | in-del | -/AGTG | | | intron-variant, frameshift-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:421010 | CCGTGGTGCTGCGTG[-/AGTG]TCTGCACACCTTCTG | 10616 |
rs727503765 | snp | G/T | | | synonymous-codon, stop-gained, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:419702 | GCGCGCCTGGCGGGC[G/T]AGGAGGAGGCGCTGC | 10616 |
rs730880329 | in-del | -/GGCG | | | frameshift-variant, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:419702 | CGCGCCTGGCGGGCG[-/GGCG]AGGAGGAGGCGCTGC | 10616 |
rs730880330 | in-del | -/GACGAGG | | | frameshift-variant, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:419678 | ACCAGCCCGACGAGG[-/GACGAGG]AGGAGCGAGCGCGCC | 10616 |
rs745348866 | snp | A/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:419257 | GAGGATAGGGGGAGG[A/G]TCTGCCTGGCTGGCT | 10616 |
rs745439922 | snp | C/T | | | upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:407214 | GACCCAGCAGGTCAA[C/T]GGGACTTGAGTGGAA | 10616 |
rs745440701 | snp | A/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:421260 | AGCCTAGACGTGAGC[A/G]CAGGCGTGGGGGGAG | 10616 |
rs745473198 | in-del | -/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:416596 | ATCTCTGTTTCCTTT[-/G]GGGTCGGTTCTGTTT | 10616 |
rs745494014 | snp | C/G | 5.16062e-05 | 0.00507942 | intron-variant, missense, utr-variant-5-prime, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:417282 | CAGATCATGGAGGCC[C/G]TCGTGTGCTGCCACG | 10616 |
rs745578097 | snp | A/G | 0.000133621 | 0.00817269 | intron-variant | RBCK1 | GRCh38.p7 | 20:417373 | GGAAGAAGCATGGGT[A/G]GGGCCTACCCCAGAC | 10616 |
rs745658376 | snp | G/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:419139 | GTTTTGAAGCTCAAA[G/T]GACATAGAAGCATTT | 10616 |
rs745790249 | snp | C/T | 3.33378e-05 | 0.00408262 | intron-variant | RBCK1 | GRCh38.p7 | 20:427511 | GGGCCTGCAGGGACT[C/T]CCCCCACCTAGTCAC | 10616 |
rs745803854 | snp | C/T | 4.04032e-05 | 0.00449444 | intron-variant | RBCK1 | GRCh38.p7 | 20:417943 | AAGGTGAGGCTCTGC[C/T]CTGAGCACCGCCGGA | 10616 |
rs745843150 | snp | A/G | 1.68878e-05 | 0.00290579 | intron-variant | RBCK1 | GRCh38.p7 | 20:419314 | GACCAAGTGGGCCGC[A/G]TGGAACCACCACCCT | 10616 |
rs745858969 | snp | A/T | 1.65847e-05 | 0.0028796 | utr-variant-5-prime, intron-variant, missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:409935 | GCGGGGATGAACAGG[A/T]GGCAATGAAGTGTGC | 10616 |
rs745861091 | snp | A/C | | | intron-variant | RBCK1 | GRCh38.p7 | 20:428839 | CTGGCAGAGCCACAC[A/C]GGAGAGACTCCACAG | 10616 |
rs745894381 | snp | G/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:416829 | TAGTGAGACCCTGTC[G/T]CTACAAAAACTTAAA | 10616 |
rs746101066 | snp | G/T | 1.72561e-05 | 0.0029373 | intron-variant | RBCK1 | GRCh38.p7 | 20:422109 | TGATCCTAACTCTTT[G/T]CCCCTCCCCTCCCCT | 10616 |
rs746145296 | snp | C/T | 1.6625e-05 | 0.00288309 | intron-variant | RBCK1 | GRCh38.p7 | 20:417700 | CTCCTCTGGCCCTCC[C/T]TTCCCACTCTCCCTC | 10616 |
rs746197240 | snp | C/G | 4.96997e-05 | 0.00498472 | utr-variant-5-prime, missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:417801 | CGGCTGGCACGAGAC[C/G]AGGAGACCCTGCACT | 10616 |
rs746250041 | snp | A/G | 2.49106e-05 | 0.00352912 | intron-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:408825 | TTCCGGTGGGAAGTG[A/G]GCCCCGCAGGACCTG | 10616 |
rs746252621 | in-del | -/CTAA | 6.97739e-05 | 0.00590611 | intron-variant | RBCK1 | GRCh38.p7 | 20:422099 | GGGGTTCCTATGATC[-/CTAA]CTCTTTTCCCCTCCC | 10616 |
rs746367898 | snp | C/T | 0.000109308 | 0.00739201 | intron-variant | RBCK1 | GRCh38.p7 | 20:428637 | TTTAAGTTCTGGGAT[C/T]CAGGTGGGGGCTGGG | 10616 |
rs746380962 | snp | A/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:412601 | TGGGATTACAGGCAT[A/G]AGCCACTGCACCCGG | 10616 |
rs746385953 | snp | C/T | 6.90262e-05 | 0.00587438 | synonymous-codon, nc-transcript-variant, utr-variant-3-prime | RBCK1 | GRCh38.p7 | 20:428998 | CCCCCAGTGCCAGAT[C/T]GTGGTACAGAAGAAG | 10616 |
rs746398460 | snp | A/G | 5.07138e-05 | 0.00503531 | synonymous-codon, missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:419558 | ACCCTCTGCTCCCAG[A/G]TGGGCTGGCAGTGCC | 10616 |
rs746398718 | snp | A/G | | | upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:407286 | GGAGGCAATTTGCGA[A/G]CCCTGGGACAGATCT | 10616 |
rs746636151 | snp | C/T | 2.29439e-05 | 0.00338695 | intron-variant | RBCK1 | GRCh38.p7 | 20:419537 | CTGCCCAGTCGGGCT[C/T]ACAGCACCCTCTGCT | 10616 |
rs746640446 | in-del | -/CCCGCCCCGTGGC | 0.00016682 | 0.00913137 | intron-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:420839 | CCCCCGAGGCCCTGA[-/CCCGCCCCGTGGC]CCCGCCCCGTGGCCC | 10616 |
rs746683237 | snp | G/T | | | splice-acceptor-variant | RBCK1 | GRCh38.p7 | 20:427312 | CATGGTGTGTTGGCA[G/T]CTCCTGACCCCTGAG | 10616 |
rs746706038 | snp | A/C | 1.74397e-05 | 0.00295289 | intron-variant, utr-variant-3-prime | RBCK1 | GRCh38.p7 | 20:410570 | AGAACTGATTCCCAC[A/C]GCTACAGTTCAGCTT | 10616 |
rs746724862 | snp | C/G | 0.000235641 | 0.0108519 | missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:419674 | CTCATACCAGCCCGA[C/G]GAGGAGGAGCGAGCG | 10616 |
rs746763063 | snp | C/T | 1.71082e-05 | 0.00292469 | intron-variant, missense, utr-variant-5-prime, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:417272 | AGGGAGGTGCCAGAT[C/T]ATGGAGGCCCTCGTG | 10616 |
rs746777664 | snp | A/C/G | 7.04399e-05 | 0.00593422 | intron-variant | RBCK1 | GRCh38.p7 | 20:428453 | GCTTCTTAACCCCCT[A/C/G]AGGAACCTTCTTACC | 10616 |
rs746915677 | snp | A/G | 1.66142e-05 | 0.00288216 | synonymous-codon, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:422220 | CTCGGGCAAGCTGCT[A/G]GAGAGGGAGATCAAG | 10616 |
rs746970150 | snp | A/G | 4.97971e-05 | 0.0049896 | missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:417829 | ACTCCCATGGGGTGC[A/G]GCAGAATGGGGACAG | 10616 |
rs747055775 | snp | A/G | 1.84698e-05 | 0.00303884 | intron-variant | RBCK1 | GRCh38.p7 | 20:410055 | GCTGGCCTGAACCCA[A/G]GGGACAGCAGGACAG | 10616 |
rs747105184 | snp | A/C | 1.74096e-05 | 0.00295034 | intron-variant, synonymous-codon | RBCK1 | GRCh38.p7 | 20:410484 | GAAGGGAAGAAAGAC[A/C]CCCCTCCACACTCTT | 10616 |
rs747135242 | snp | A/C | 1.79056e-05 | 0.00299207 | intron-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:429130 | GTGTGGAGAGGGTGC[A/C]CTTGTGGGCTTTGCC | 10616 |
rs747231064 | snp | C/T | 3.32358e-05 | 0.00407637 | synonymous-codon, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:430367 | CCCAGGAGACACCAG[C/T]GGGGGCTGCCGCTGC | 10616 |
rs747304144 | in-del | -/A | | | intron-variant | RBCK1 | GRCh38.p7 | 20:413917 | AAGAGACAAATCACC[-/A]AAAAAAAAAAAAAAA | 10616 |
rs747311134 | snp | C/T | 1.77461e-05 | 0.00297871 | intron-variant | RBCK1 | GRCh38.p7 | 20:422076 | GAGGGATGGAGTCCC[C/T]AGTGAAGGGGGTTCC | 10616 |
rs747325324 | in-del | -/C | 0.0037417 | 0.0430912 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:408725 | CCCAGGAGGCACGGT[-/C]CCCCCCCAGGGGGAT | 10616 |
rs747372112 | snp | C/T | | | upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:407620 | TGCAAACTTCACCAA[C/T]AGCTCAACGAAAAGA | 10616 |
rs747538597 | snp | C/T | 1.66335e-05 | 0.00288383 | intron-variant | RBCK1 | GRCh38.p7 | 20:417688 | TGCTTCCTCTCTCTC[C/T]TCTGGCCCTCCCTTC | 10616 |
rs747595621 | snp | C/T | | | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:408713 | GGAGGTAGCATTTCC[C/T]AGGAGGCACGGTCCC | 10616 |
rs747669456 | snp | A/G | 2.25894e-05 | 0.00336068 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:408701 | CCCAGGCGACCCGGA[A/G]GTAGCATTTCCCAGG | 10616 |
rs747694919 | snp | G/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:424735 | CCACCCCAGCCAAGG[G/T]GCATTATGCTGGGGC | 10616 |
rs747748267 | snp | G/T | 1.67041e-05 | 0.00288994 | intron-variant | RBCK1 | GRCh38.p7 | 20:427522 | GACTCCCCCCACCTA[G/T]TCACTGTCATCTTGC | 10616 |
rs747760608 | in-del | -/A | 0.000653516 | 0.0180646 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:408714 | GAGGTAGCATTTCCC[-/A]GGAGGCACGGTCCCC | 10616 |
rs747821371 | snp | C/G/T | 0.000142577 | 0.00844226 | missense, synonymous-codon, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:419433 | CCCCAGGAACCCGGA[C/G/T]GGGGGCAGCCAGATG | 10616 |
rs747884624 | snp | C/T | 2.06056e-05 | 0.00320973 | intron-variant | RBCK1 | GRCh38.p7 | 20:419518 | GCCCCTCCCTTGCCT[C/T]ACCCTGCCCAGTCGG | 10616 |
rs747884739 | snp | C/G | 1.74005e-05 | 0.00294957 | intron-variant, missense | RBCK1 | GRCh38.p7 | 20:410497 | ACACCCCTCCACACT[C/G]TTCTAAAGAGCATAG | 10616 |
rs748085439 | snp | C/G | 6.96585e-05 | 0.00590122 | intron-variant, missense | RBCK1 | GRCh38.p7 | 20:410556 | AATTCCTGTGGACCA[C/G]AACTGATTCCCACAG | 10616 |
rs748103840 | snp | A/G | | | upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:406970 | CCCAGAATAACATAA[A/G]TAAGTAAAACATGCT | 10616 |
rs748158080 | snp | A/G | 1.82191e-05 | 0.00301815 | missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:417919 | GGGAGCGGCAGCTGC[A/G]GATGCTGGAAGGTGA | 10616 |
rs748205397 | snp | C/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:424600 | GCAGCCCCATTTTTC[C/T]CTGTTGTCTCTGGGT | 10616 |
rs748244437 | in-del | -/AG | | | intron-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:409781 | CAGGAAGACAGAGAA[-/AG]AGCAGCACACACAAA | 10616 |
rs748269306 | in-del | -/CCCTGCACCTGGCTGTG | | | intron-variant | RBCK1 | GRCh38.p7 | 20:419883 | TGCACCTGGCTGTGA[-/CCCTGCACCTGGCTGTG]ACCTGCCCTCTCTCA | 10616 |
rs748270197 | in-del | -/TAAT | | | intron-variant | RBCK1 | GRCh38.p7 | 20:422103 | TCCTATGATCCTAAC[-/TAAT]TCTTTTCCCCTCCCC | 10616 |
rs748296986 | snp | G/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:425529 | AATTTTTCTAAAGAT[G/T]ATTACAAATCTCAAT | 10616 |
rs748386516 | snp | G/T | 0.000132716 | 0.00814497 | utr-variant-5-prime, intron-variant, missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:409927 | AGTGGCGGGCGGGGA[G/T]GAACAGGTGGCAATG | 10616 |
rs748388237 | snp | A/G | 0.000265025 | 0.0115083 | intron-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:429120 | GCTCGTGGTGGTGTG[A/G]AGAGGGTGCCCTTGT | 10616 |
rs748477851 | snp | C/T | 1.66466e-05 | 0.00288496 | intron-variant | RBCK1 | GRCh38.p7 | 20:430344 | TCTCTTCCTCCCATC[C/T]TCTAGGGCCCAGGAG | 10616 |
rs748682825 | snp | A/C | 1.73857e-05 | 0.00294831 | intron-variant, missense, nc-transcript-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:420937 | CAGAGGAGCCTGGTG[A/C]TGAACACGGAGCCCG | 10616 |
rs748703915 | snp | C/T | | | intron-variant, utr-variant-3-prime | RBCK1 | GRCh38.p7 | 20:420333 | ACAGACATTGATCCC[C/T]GAGTGCTCCCCATTC | 10616 |
rs748710681 | in-del | -/T | | | intron-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:429492 | GGCCTCCCAAAGTGC[-/T]TAGGATTACAGGCGT | 10616 |
rs748728239 | snp | C/G | 4.45206e-05 | 0.00471787 | intron-variant | RBCK1 | GRCh38.p7 | 20:417390 | GGCCTACCCCAGACT[C/G]GGGTTTGTGTGTGTG | 10616 |
rs748777760 | snp | A/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:429779 | AGAGGACAGCAAGTA[A/G]AGGTTCGATCTGGAG | 10616 |
rs748867323 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:430853 | TCTTGCTAACCTGTT[C/G]AGAGCCAGGAAGGAG | 10616 |
rs749049083 | snp | C/G/T | 3.36957e-05 | 0.0041045 | intron-variant | RBCK1 | GRCh38.p7 | 20:419335 | CCACCACCCTTTAAC[C/G/T]CTCCTCCACAGATCT | 10616 |
rs749184826 | snp | C/T | 4.96956e-05 | 0.00498451 | missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:430377 | ACCAGCGGGGGCTGC[C/T]GCTGCAGGGTAAATG | 10616 |
rs749237300 | snp | A/G | 1.99229e-05 | 0.00315611 | intron-variant | RBCK1 | GRCh38.p7 | 20:410070 | AGGGACAGCAGGACA[A/G]GATATTCTTGCCTGT | 10616 |
rs749423940 | snp | A/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:415503 | GCTTTTTACAATTGG[A/T]TTCTTCAAATCAGGA | 10616 |
rs749518640 | snp | A/C | 3.31645e-05 | 0.00407199 | utr-variant-5-prime, missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:417819 | GAGACCCTGCACTCC[A/C]ATGGGGTGCGGCAGA | 10616 |
rs749518835 | snp | A/G | 1.78302e-05 | 0.00298577 | missense, synonymous-codon, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:417911 | GCTGCAGCGGGAGCG[A/G]CAGCTGCGGATGCTG | 10616 |
rs749566927 | in-del | -/AT | | | intron-variant | RBCK1 | GRCh38.p7 | 20:423304 | ACTCCGTCTGAAAAT[-/AT]ATATATATATATATT | 10616 |
rs749576109 | snp | A/C/T | 3.34025e-05 | 0.00408661 | utr-variant-5-prime, intron-variant, synonymous-codon, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:409921 | CCGAGCAGTGGCGGG[A/C/T]GGGGATGAACAGGTG | 10616 |
rs749774741 | snp | A/G | | | intron-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:409698 | TGAGGAGGAGTGGGG[A/G]ATATTAGAGAACCCC | 10616 |
rs749795892 | snp | G/T | 0.000192709 | 0.00981415 | missense, synonymous-codon, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:419689 | CGAGGAGGAGCGAGC[G/T]CGCCTGGCGGGCGAG | 10616 |
rs749797934 | in-del | -/TTTA | | | intron-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:410867 | TTTTCTTAAAACAGT[-/TTTA]TTTATTTATTTATCC | 10616 |
rs749801662 | snp | C/T | 1.74382e-05 | 0.00295276 | intron-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:429103 | CCCTGGGGTGAGTCT[C/T]TGCTCGTGGTGGTGT | 10616 |
rs749846041 | snp | A/C | 3.41262e-05 | 0.00413061 | intron-variant, missense, utr-variant-5-prime, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:417293 | GGCCCTCGTGTGCTG[A/C]CACGAGTTGATTCTA | 10616 |
rs749891698 | snp | C/T | 1.72442e-05 | 0.00293629 | synonymous-codon, nc-transcript-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:429088 | GGGCCCACGCTGGGG[C/T]CCTGGGGTGAGTCTT | 10616 |
rs750051203 | snp | A/G | 3.35723e-05 | 0.00409695 | intron-variant | RBCK1 | GRCh38.p7 | 20:430314 | GGCAGTCTCTGCACT[A/G]CGCTGACATTCTCTT | 10616 |
rs750120857 | snp | A/G | 1.77369e-05 | 0.00297795 | intron-variant, missense, nc-transcript-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:420881 | CCCAGCGGAAGCAGC[A/G]GCAGCAGGAGGGGAA | 10616 |
rs750138837 | snp | C/G/T | 4.97107e-05 | 0.00498531 | utr-variant-5-prime, missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:417555 | TGGAGGATGCTCAGA[C/G/T]GCACACCGTCACCAT | 10616 |
rs750180114 | snp | A/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:422993 | ATTACAGTAGAGGAT[A/G]TGTGTATAGAATTCA | 10616 |
rs750244391 | snp | A/G | 1.66294e-05 | 0.00288347 | intron-variant | RBCK1 | GRCh38.p7 | 20:417648 | CGGAGGGCGACACTG[A/G]GGTGAAGGCTCTCCC | 10616 |
rs750260363 | snp | C/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:421686 | CCTGTTGGAGGAGAC[C/T]GAGGAGGTCTCTTGG | 10616 |
rs750411276 | snp | G/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:427197 | TACATGAAGAAAAGA[G/T]CCTGGGGCTGGGTTG | 10616 |
rs750426473 | snp | A/T | 5.51678e-05 | 0.00525175 | intron-variant | RBCK1 | GRCh38.p7 | 20:428474 | CCTTCTTACCTTGAG[A/T]CCCTCACCCGCTACA | 10616 |
rs750427179 | snp | C/G | 0.000137744 | 0.00829778 | missense, synonymous-codon, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:419638 | CTGCCGGGCGCGCCC[C/G]GAGGCCTACCAGGTC | 10616 |
rs750472732 | snp | C/G | 1.74054e-05 | 0.00294998 | intron-variant, missense | RBCK1 | GRCh38.p7 | 20:410548 | CTTCCGTTAATTCCT[C/G]TGGACCAGAACTGAT | 10616 |
rs750479524 | snp | C/T | 1.73954e-05 | 0.00294913 | intron-variant | RBCK1 | GRCh38.p7 | 20:417215 | CTTCTGGTGGTTTCA[C/T]TAAGGAGCAGGGGAG | 10616 |
rs750491290 | snp | A/G | | | intron-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:429409 | TTTTGTATTTTTAGG[A/G]GAGACGGGGTTTCTC | 10616 |
rs750519863 | snp | C/T | | | intron-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:429520 | CGTGAGCCACCGGGC[C/T]GCAAGAATGTTCTTT | 10616 |
rs750664557 | snp | A/G | 1.66471e-05 | 0.00288501 | synonymous-codon, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:422202 | TGACAACACCTACTC[A/G]TGCTCGGGCAAGCTG | 10616 |
rs750705670 | snp | C/T | | | upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:406447 | AGAACAGCAGTTAGA[C/T]TGACAGGTGATGATA | 10616 |
rs750764272 | snp | C/G | 3.38335e-05 | 0.00411286 | intron-variant | RBCK1 | GRCh38.p7 | 20:427268 | TCAAGGGTCATATGT[C/G]AGGTGTTCTGAATCC | 10616 |
rs750834643 | snp | G/T | 1.74946e-05 | 0.00295753 | missense, synonymous-codon, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:417905 | TCAGGAGCTGCAGCG[G/T]GAGCGGCAGCTGCGG | 10616 |
rs750877383 | snp | A/G | 0.000313038 | 0.0125068 | synonymous-codon, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:427447 | GGATGATGTCAATGA[A/G]TTCACCTGCCCTGTG | 10616 |
rs750989488 | snp | C/G | 2.08862e-05 | 0.00323151 | intron-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:408803 | AGGCTGGAGGTGGCT[C/G]GGGAACTTCCGGTGG | 10616 |
rs751005507 | snp | C/T | 1.67022e-05 | 0.00288978 | utr-variant-5-prime, intron-variant, stop-gained, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:409907 | GCCCTGAGCCTCACC[C/T]GAGCAGTGGCGGGCG | 10616 |
rs751009844 | snp | C/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:427737 | TTCACAATGGAGCCC[C/T]GACCCTGGGCCAGTC | 10616 |
rs751068368 | snp | C/T | 8.67401e-05 | 0.00658502 | synonymous-codon, missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:417903 | CCTCAGGAGCTGCAG[C/T]GGGAGCGGCAGCTGC | 10616 |
rs751085793 | snp | A/C | 1.66944e-05 | 0.0028891 | utr-variant-5-prime, intron-variant, missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:409901 | GAAATGGCCCTGAGC[A/C]TCACCCGAGCAGTGG | 10616 |
rs751182894 | in-del | -/CCA | 1.65855e-05 | 0.00287967 | utr-variant-3-prime, nc-transcript-variant, cds-indel | RBCK1 | GRCh38.p7 | 20:430465 | CATGCTGACCCAGCC[-/CCA]CATCCACATTCTGTT | 10616 |
rs751222067 | snp | C/G | | | intron-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:410938 | TTTTAGTATATTCAA[C/G]GTTGTGCAACCATTG | 10616 |
rs751232933 | snp | A/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:424160 | GCGTTATGTGTGTCT[A/G]CATACGTGTGTGCTT | 10616 |
rs751274254 | snp | A/G | 1.73637e-05 | 0.00294644 | missense, synonymous-codon, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:419731 | GCGTCAGTACCAGCA[A/G]GTGGGCGGGAAAGTC | 10616 |
rs751384381 | snp | C/T | 1.88525e-05 | 0.00307016 | intron-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:420847 | GGCCCTGACCCGCCC[C/T]GTGGCCCCGCCCCGT | 10616 |
rs751413155 | snp | A/G | | | upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:406163 | GGCCAGGCTGGTCTC[A/G]AACTCCTGACCTCAA | 10616 |
rs751414000 | snp | A/G | 4.5634e-05 | 0.00477649 | intron-variant | RBCK1 | GRCh38.p7 | 20:417365 | CTAATAAAGGAAGAA[A/G]CATGGGTGGGGCCTA | 10616 |
rs751464992 | snp | A/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:429566 | TGAAAAAATACCAGA[A/T]GATGACTATTTTGTG | 10616 |
rs751523688 | snp | A/G | 2.22948e-05 | 0.0033387 | missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:428567 | ACGATGTGGCTGCCC[A/G]GCAGACGACAGAGAT | 10616 |
rs751554744 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:430550 | GGGGCCCTGCCTGCA[C/T]TGCGGTTGTCCACGG | 10616 |
rs751582683 | snp | G/T | 1.66106e-05 | 0.00288184 | utr-variant-5-prime, missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:417533 | CTCTGCAGGCTGTGG[G/T]TGAGCGTGGAGGATG | 10616 |
rs751606144 | snp | C/T | 1.91137e-05 | 0.00309136 | intron-variant | RBCK1 | GRCh38.p7 | 20:419499 | CCTCAGTATCCTCTT[C/T]TGTGCCCCTCCCTTG | 10616 |
rs751621844 | snp | A/C | 8.70269e-05 | 0.0065959 | synonymous-codon, missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:419400 | CCTCTGGAGCCAGGC[A/C]CCCCAAAGCCCGGGG | 10616 |
rs751653272 | snp | C/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:419000 | TTTTTTTGGCGGGGG[C/T]TGGGGGCTGATGTTT | 10616 |
rs751677840 | snp | C/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:413854 | TTAATAAAACATGAG[C/T]GCTGAAAGAGTTGTT | 10616 |
rs751730438 | snp | C/G | | | upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:407682 | TCTGGGTAAGGGCGG[C/G]TTCCTGAGCCTGCCA | 10616 |
rs751741194 | snp | C/G | | | intron-variant, utr-variant-3-prime | RBCK1 | GRCh38.p7 | 20:420155 | CGCCGTGACCTCACC[C/G]TGGACTCTCCTACTC | 10616 |
rs751743040 | snp | C/T | 1.6574e-05 | 0.00287867 | utr-variant-3-prime, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:430459 | GGGCCACATGCTGAC[C/T]CAGCCCCACATCCAC | 10616 |
rs751771346 | snp | A/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:421934 | CCAGAGAATCAGAGC[A/G]GCAGTATGGAGGCAG | 10616 |
rs751813159 | in-del | -/CG | 5.07292e-05 | 0.00503607 | intron-variant, frameshift-variant, utr-variant-5-prime, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:417284 | GATCATGGAGGCCCT[-/CG]TGTGCTGCCACGAGT | 10616 |
rs751840773 | snp | A/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:425200 | ATTTTCAGTACAGAC[A/G]AGTTTTCACCATGTT | 10616 |
rs751901388 | snp | C/T | 1.76281e-05 | 0.0029688 | intron-variant, utr-variant-3-prime | RBCK1 | GRCh38.p7 | 20:410611 | TGTATAGCCAAGATA[C/T]TCAGCTAGAATTCAG | 10616 |
rs752017752 | snp | C/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:426459 | ACATGTAATGTTTGT[C/T]TGTCTGTGCCTGGCT | 10616 |
rs752060848 | in-del | -/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:418940 | AAAGACTTGGCATTC[-/T]GCTGTCATGTCTCAG | 10616 |
rs752086794 | in-del | -/G | 0.00054301 | 0.0164685 | intron-variant | RBCK1 | GRCh38.p7 | 20:417965 | ACCGCCGGACCCAGC[-/G]GGGGCCCTGGACTCA | 10616 |
rs752107228 | snp | C/T | 1.66524e-05 | 0.00288547 | intron-variant | RBCK1 | GRCh38.p7 | 20:417669 | AGGCTCTCCCTTTCA[C/T]TCCTGCTTCCTCTCT | 10616 |
rs752143985 | snp | C/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:418520 | ACTACAGGCGCCCGC[C/T]ACCACGCCCGGCTAA | 10616 |
rs752151838 | snp | A/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:411957 | GAACATTTGTGTCCA[A/G]CTTTTTGTGTGGACA | 10616 |
rs752153553 | snp | A/C/G | 3.31209e-05 | 0.00406935 | utr-variant-5-prime, missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:417787 | GGGTGATTGGGCAGC[A/C/G]GCTGGCACGAGACCA | 10616 |
rs752211933 | snp | G/T | 1.67567e-05 | 0.00289449 | missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:422163 | CCGCAACAGCCAGGA[G/T]GCGGAGGTCTCCTGC | 10616 |
rs752266924 | snp | C/G | 1.65559e-05 | 0.00287709 | utr-variant-5-prime, missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:417770 | ACCAGTCTTGCAGCA[C/G]TGGGTGATTGGGCAG | 10616 |
rs752416716 | snp | A/G | 1.97276e-05 | 0.0031406 | utr-variant-5-prime, synonymous-codon, missense, nc-transcript-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:408769 | CCAGATGGACGAGAA[A/G]ACCAAGAAAGGTGGG | 10616 |
rs752502262 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:430664 | CCCCAGCCTTAAACA[C/T]AGCCCCTGGCCAGAG | 10616 |
rs752577528 | snp | C/T | 0.000124355 | 0.00788429 | intron-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:421040 | TCTGCAGGTGCGGCC[C/T]CCAGTCCCACCCCCG | 10616 |
rs752666659 | snp | G/T | 1.66877e-05 | 0.00288852 | synonymous-codon, missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:419657 | GCCTACCAGGTCCCC[G/T]CCTCATACCAGCCCG | 10616 |
rs752707150 | snp | C/T | 1.65924e-05 | 0.00288027 | intron-variant | RBCK1 | GRCh38.p7 | 20:427501 | CTGCAAGGTGGGGCC[C/T]GCAGGGACTCCCCCC | 10616 |
rs752710558 | in-del | -/TC | 0.000369972 | 0.0135959 | intron-variant | RBCK1 | GRCh38.p7 | 20:430304 | CGGCTGTGGGGGCAG[-/TC]TCTGCACTGCGCTGA | 10616 |
rs752770129 | snp | C/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:421635 | CCCCAGAGCAGGGAC[C/T]GGAAGGCCTGCTGTA | 10616 |
rs752901453 | snp | A/G | 1.69037e-05 | 0.00290716 | intron-variant | RBCK1 | GRCh38.p7 | 20:419305 | ATGGGTGTGGACCAA[A/G]TGGGCCGCGTGGAAC | 10616 |
rs752958560 | snp | C/G | 1.72124e-05 | 0.00293359 | missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:419391 | CCGCGGGGCCCTCTG[C/G]AGCCAGGCCCCCCAA | 10616 |
rs752967988 | snp | C/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:415322 | GCAGTGAGCCAAGAT[C/G]ATGCCACTACACTCC | 10616 |
rs753012580 | snp | A/T | 6.95737e-05 | 0.00589763 | intron-variant, synonymous-codon | RBCK1 | GRCh38.p7 | 20:410532 | AAAATTGTACACACT[A/T]CTTCCGTTAATTCCT | 10616 |
rs753018967 | snp | C/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:414267 | AATAAAAAAAATTAG[C/T]CAGGCTGGGTGGCAC | 10616 |
rs753060133 | snp | C/T | 1.74753e-05 | 0.0029559 | intron-variant, stop-gained | RBCK1 | GRCh38.p7 | 20:410449 | CATTCCAGCTCCATC[C/T]AGCCATCACATCACA | 10616 |
rs753192749 | snp | C/T | 1.73372e-05 | 0.0029442 | intron-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:421041 | CTGCAGGTGCGGCCC[C/T]CAGTCCCACCCCCGG | 10616 |
rs753193765 | snp | C/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:417461 | AATATGTACATGTCT[C/G]TAGCCGGTGGCTGAG | 10616 |
rs753347152 | snp | A/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:413593 | ACTGGCGTTTCCTTT[A/G]TAAAATGTACAATGT | 10616 |
rs753350673 | snp | A/C | 1.65504e-05 | 0.00287662 | utr-variant-3-prime, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:430435 | ACTGCCACTGAGCTA[A/C]AGATGGTGGGGCCAC | 10616 |
rs753438644 | snp | A/C | | | intron-variant | RBCK1 | GRCh38.p7 | 20:415020 | AGAGCATTTTCTGGA[A/C]TGCTTTTAAATAAAT | 10616 |
rs753472058 | snp | C/T | 1.65644e-05 | 0.00287783 | utr-variant-5-prime, missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:417561 | ATGCTCAGATGCACA[C/T]CGTCACCATCTGGCT | 10616 |
rs753501481 | in-del | -/TTTA | | | intron-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:410870 | CTTAAAACAGTTTTA[-/TTTA]TTTATTTATTTATCC | 10616 |
rs753505499 | in-del | -/AG | 2.96687e-05 | 0.00385143 | intron-variant | RBCK1 | GRCh38.p7 | 20:428603 | AGGTGAGGCTGGGAC[-/AG]GGCCGAGGCCTAGGG | 10616 |
rs753512153 | snp | A/G | 0.000197064 | 0.00992437 | intron-variant, synonymous-codon, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:421011 | CGTGGTGCTGCGTGA[A/G]TGTCTGCACACCTTC | 10616 |
rs753525234 | snp | G/T | 1.66391e-05 | 0.00288431 | intron-variant | RBCK1 | GRCh38.p7 | 20:417658 | CACTGGGGTGAAGGC[G/T]CTCCCTTTCACTCCT | 10616 |
rs753580819 | snp | A/C | 2.30253e-05 | 0.00339295 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:408692 | CCCGCCTCTCCCAGG[A/C]GACCCGGAGGTAGCA | 10616 |
rs753580979 | snp | C/T | 4.9943e-05 | 0.0049969 | utr-variant-5-prime, synonymous-codon, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:417752 | TCTGGACTATGGCTT[C/T]CCACCAGTCTTGCAG | 10616 |
rs753624249 | snp | C/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:421784 | AGTGAGGAGTTGGGA[C/T]TTGTTCTGGGTAGGA | 10616 |
rs753724294 | in-del | -/GTTT | 4.35587e-05 | 0.00466663 | intron-variant | RBCK1 | GRCh38.p7 | 20:417393 | CTACCCCAGACTGGG[-/GTTT]GTGTGTGTGTGTGTG | 10616 |
rs753800040 | snp | A/C | 2.30902e-05 | 0.00339773 | missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:428576 | CTGCCCGGCAGACGA[A/C]AGAGATGCTGAAGGT | 10616 |
rs753858607 | snp | C/T | 0.000138191 | 0.00831122 | intron-variant | RBCK1 | GRCh38.p7 | 20:419509 | CTCTTCTGTGCCCCT[C/T]CCTTGCCTCACCCTG | 10616 |
rs753863690 | snp | A/C | | | intron-variant | RBCK1 | GRCh38.p7 | 20:419046 | AAGTCACTGTTTTGG[A/C]AGGACCGCCTCAGCG | 10616 |
rs753888011 | snp | C/T | 1.90911e-05 | 0.00308953 | intron-variant, synonymous-codon, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:428945 | CCAGCACCTGCCCCA[C/T]TCCAGGTGATGCTGC | 10616 |
rs753918686 | snp | A/C | 8.61698e-05 | 0.00656334 | intron-variant, missense, utr-variant-5-prime, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:417340 | ATTGGAGGGGCCTAA[A/C]TGGTGGGTTCTAATA | 10616 |
rs754010675 | snp | A/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:428058 | ATCTCAAAAGTTGAA[A/G]GTGAGGAGCCGGTAA | 10616 |
rs754061330 | snp | C/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:416694 | TCTCTGGAATAATAC[C/T]ATGTAGATTTAAATC | 10616 |
rs754143920 | snp | A/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:416916 | ATGGGAAGAGCCCAG[A/G]AGGTTGATACTGCAG | 10616 |
rs754190543 | snp | C/G | 1.66012e-05 | 0.00288103 | intron-variant | RBCK1 | GRCh38.p7 | 20:417979 | CGGGGGCCCTGGACT[C/G]ACTTGAGGGCATAGG | 10616 |
rs754317998 | snp | C/T | 1.67475e-05 | 0.00289369 | intron-variant | RBCK1 | GRCh38.p7 | 20:430321 | TCTGCACTGCGCTGA[C/T]ATTCTCTTCTCTTCC | 10616 |
rs754366884 | snp | C/T | 1.78777e-05 | 0.00298974 | intron-variant | RBCK1 | GRCh38.p7 | 20:410408 | TTCTGCCATTCATTC[C/T]CAGATTCCTCATGGT | 10616 |
rs754511518 | snp | C/T | 0.000118322 | 0.00769071 | intron-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:421035 | CACCTTCTGCAGGTG[C/T]GGCCCCCAGTCCCAC | 10616 |
rs754534278 | snp | C/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:424178 | TACGTGTGTGCTTGC[C/T]GCTGGCGCTCTTCAT | 10616 |
rs754620561 | snp | A/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:412407 | CTCACTGCAACCTCC[A/G]CCTCCCAGGTTCAAG | 10616 |
rs754652689 | snp | A/C | 2.28935e-05 | 0.00338323 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:408695 | GCCTCTCCCAGGCGA[A/C]CCGGAGGTAGCATTT | 10616 |
rs754802788 | snp | A/G | 2.38558e-05 | 0.0034536 | synonymous-codon, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:428517 | GCAGATGAACTGCAA[A/G]GAGTATCAGGAGGAC | 10616 |
rs754823170 | snp | A/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:429574 | TACCAGAAGATGACT[A/G]TTTTGTGACGTGAAA | 10616 |
rs754865819 | in-del | -/GTGA | 1.6563e-05 | 0.00287771 | splice-donor-variant | RBCK1 | GRCh38.p7 | 20:417620 | TCTCTCAAGGACATG[-/GTGA]GTGAGGAGGCGGAGG | 10616 |
rs754873531 | snp | C/G | 1.74102e-05 | 0.00295039 | intron-variant, missense | RBCK1 | GRCh38.p7 | 20:410553 | GTTAATTCCTGTGGA[C/G]CAGAACTGATTCCCA | 10616 |
rs754890674 | snp | C/G | 2.33e-05 | 0.00341313 | missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:428578 | GCCCGGCAGACGACA[C/G]AGATGCTGAAGGTGA | 10616 |
rs754909272 | snp | C/G | 1.99444e-05 | 0.00315781 | intron-variant | RBCK1 | GRCh38.p7 | 20:419510 | TCTTCTGTGCCCCTC[C/G]CTTGCCTCACCCTGC | 10616 |
rs754967314 | snp | C/G | 4.68198e-05 | 0.00483815 | missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:419641 | CCGGGCGCGCCCCGA[C/G]GCCTACCAGGTCCCC | 10616 |
rs755008179 | snp | A/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:419012 | GGGTTGGGGGCTGAT[A/G]TTTCCTCCGGAGTGG | 10616 |
rs755087113 | snp | C/T | 1.66927e-05 | 0.00288895 | intron-variant | RBCK1 | GRCh38.p7 | 20:427297 | CCTGAGCAGCAAGGA[C/T]ATGGTGTGTTGGCAG | 10616 |
rs755142186 | snp | C/G | 1.6577e-05 | 0.00287893 | intron-variant | RBCK1 | GRCh38.p7 | 20:427495 | CCTGCTCTGCAAGGT[C/G]GGGCCTGCAGGGACT | 10616 |
rs755160706 | snp | C/T | 1.66001e-05 | 0.00288094 | intron-variant | RBCK1 | GRCh38.p7 | 20:417981 | GGGGCCCTGGACTCA[C/T]TTGAGGGCATAGGGC | 10616 |
rs755178275 | snp | A/G | 1.80621e-05 | 0.00300512 | missense, synonymous-codon, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:417914 | GCAGCGGGAGCGGCA[A/G]CTGCGGATGCTGGAA | 10616 |
rs755188024 | snp | C/T | | | upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:407715 | CCTGGATTCAAACCT[C/T]GGCTGAGTGGCCTTG | 10616 |
rs755329454 | snp | A/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:430119 | ATGTCTAGAATATGC[A/G]GAGTGGTCAGATCCT | 10616 |
rs755353013 | snp | A/G | 6.73253e-05 | 0.00580156 | utr-variant-5-prime, intron-variant, missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:410012 | CCTGAGGTCTCCCCA[A/G]CGCAGGACATCAGGT | 10616 |
rs755476845 | snp | C/T | 3.54208e-05 | 0.00420822 | intron-variant, synonymous-codon | RBCK1 | GRCh38.p7 | 20:410418 | CATTCCCAGATTCCT[C/T]ATGGTGCAAAATGGC | 10616 |
rs755538520 | in-del | -/A | | | intron-variant | RBCK1 | GRCh38.p7 | 20:430158 | CCTGTTCCCGGATCT[-/A]GGCGTGGGTAGACTG | 10616 |
rs755655378 | snp | C/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:413369 | TGAATCTGTAGATCA[C/T]TGGCCACTTGATTTT | 10616 |
rs755702825 | snp | A/G | 1.67276e-05 | 0.00289197 | intron-variant | RBCK1 | GRCh38.p7 | 20:417380 | GCATGGGTGGGGCCT[A/G]CCCCAGACTGGGGTT | 10616 |
rs755727231 | snp | C/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:428460 | AACCCCCTGAGGAAC[C/T]TTCTTACCTTGAGTC | 10616 |
rs755744736 | snp | A/T | 0.000121396 | 0.00778995 | intron-variant, missense, nc-transcript-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:420884 | AGCGGAAGCAGCAGC[A/T]GCAGGAGGGGAACTA | 10616 |
rs756013920 | snp | C/G/T | 8.82362e-05 | 0.00664163 | missense, synonymous-codon, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:419411 | AGGCCCCCCAAAGCC[C/G/T]GGGGTCCCCCAGGAA | 10616 |
rs756145648 | snp | G/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:423918 | ACCCACCAGCAGGCT[G/T]CCCGGGCCTTCTCAT | 10616 |
rs756148420 | snp | C/T | | | upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:407775 | TTATTCATGTGCAAA[C/T]GGGGCCAAGGACCGG | 10616 |
rs756276470 | snp | C/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:426579 | TGTATATATGTGCCA[C/T]GTTTTCTTTATAGGA | 10616 |
rs756314610 | in-del | -/C | | | frameshift-variant, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:427395 | CTTCAGCTACCATTG[-/C]CAAGACCCCAGATTG | 10616 |
rs756372483 | snp | C/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:415336 | TCATGCCACTACACT[C/T]CATCCTGGGTGACAG | 10616 |
rs756372544 | snp | C/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:427919 | GCTTCTGACTGAATC[C/T]GTGACAGACTAAGGC | 10616 |
rs756397237 | snp | C/G | | | upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:406864 | CAACATATGGAGCCT[C/G]CATTATGTGTTTGGA | 10616 |
rs756454135 | snp | C/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:416417 | CACCCACCTCGGCCT[C/T]CCAAAGTGCTGGGAT | 10616 |
rs756500607 | snp | A/G/T | 3.56565e-05 | 0.00422223 | missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:417910 | AGCTGCAGCGGGAGC[A/G/T]GCAGCTGCGGATGCT | 10616 |
rs756541073 | in-del | -/GGA | | | intron-variant | RBCK1 | GRCh38.p7 | 20:423224 | AATCGCTTGAACCCC[-/GGA]GGAGGCGGAGGTTGT | 10616 |
rs756632208 | snp | C/T | 1.72543e-05 | 0.00293715 | missense, nc-transcript-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:429089 | GGCCCACGCTGGGGC[C/T]CTGGGGTGAGTCTTT | 10616 |
rs756665763 | snp | C/T | 1.66799e-05 | 0.00288785 | utr-variant-5-prime, intron-variant, missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:409905 | TGGCCCTGAGCCTCA[C/T]CCGAGCAGTGGCGGG | 10616 |
rs756720324 | snp | A/C | 1.6649e-05 | 0.00288518 | utr-variant-5-prime, intron-variant, missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:410001 | TGCAACTGAAGCCTG[A/C]GGTCTCCCCAACGCA | 10616 |
rs756811010 | snp | C/G | 0.000117952 | 0.00767869 | synonymous-codon, missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:419675 | TCATACCAGCCCGAC[C/G]AGGAGGAGCGAGCGC | 10616 |
rs756825937 | snp | C/G | 1.73601e-05 | 0.00294614 | synonymous-codon, nc-transcript-variant, utr-variant-3-prime | RBCK1 | GRCh38.p7 | 20:428986 | GGCCATGCGCTGCCC[C/G]CAGTGCCAGATCGTG | 10616 |
rs756845632 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:430629 | GACTTCTCTCCCCTG[C/T]GGCTCCCACCTCTGC | 10616 |
rs756866079 | snp | A/G | 5.41756e-05 | 0.00520431 | intron-variant, missense, utr-variant-5-prime, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:417276 | AGGTGCCAGATCATG[A/G]AGGCCCTCGTGTGCT | 10616 |
rs756866407 | snp | A/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:412266 | CATCTTTTCATGCAC[A/G]TATTTTCTTTGGAGG | 10616 |
rs756904349 | in-del | -/TC | 1.66045e-05 | 0.00288132 | utr-variant-3-prime, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:430477 | GCCCCACATCCACAT[-/TC]TGTTAGAATGTAGCT | 10616 |
rs756942322 | snp | C/G | | | intron-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:421113 | CGTGGGTGGGGCCCT[C/G]TGCTCTGATACCTCA | 10616 |
rs756988921 | snp | C/T | | | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:408310 | CGCCACTTTCACTTT[C/T]TCTTCCGCCGAAGCC | 10616 |
rs757075589 | snp | A/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:418591 | GCCAGGATGGTCTCG[A/G]TCTCCTGACTTTGTG | 10616 |
rs757115540 | snp | C/T | 1.66023e-05 | 0.00288113 | utr-variant-5-prime, synonymous-codon, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:417538 | CAGGCTGTGGGTGAG[C/T]GTGGAGGATGCTCAG | 10616 |
rs757133628 | snp | A/G | 1.67469e-05 | 0.00289364 | intron-variant | RBCK1 | GRCh38.p7 | 20:417367 | AATAAAGGAAGAAGC[A/G]TGGGTGGGGCCTACC | 10616 |
rs757154507 | snp | A/G | | | intron-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:420697 | CACCCCCCATCCCCC[A/G]GCCCCACCCCCATCC | 10616 |
rs757156263 | snp | A/G | 1.6609e-05 | 0.0028817 | intron-variant | RBCK1 | GRCh38.p7 | 20:427505 | AAGGTGGGGCCTGCA[A/G]GGACTCCCCCCACCT | 10616 |
rs757282936 | snp | G/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:428182 | AGGGTCTCACCCTAG[G/T]GGTATAAGGGATTTC | 10616 |
rs757387219 | snp | A/C | 1.7406e-05 | 0.00295003 | intron-variant, missense | RBCK1 | GRCh38.p7 | 20:410486 | AGGGAAGAAAGACAC[A/C]CCTCCACACTCTTCT | 10616 |
rs757419664 | snp | G/T | 1.90885e-05 | 0.00308932 | intron-variant | RBCK1 | GRCh38.p7 | 20:419500 | CTCAGTATCCTCTTC[G/T]GTGCCCCTCCCTTGC | 10616 |
rs757431852 | snp | C/T | 1.65905e-05 | 0.0028801 | utr-variant-3-prime, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:430465 | CATGCTGACCCAGCC[C/T]CACATCCACATTCTG | 10616 |
rs757568224 | snp | C/T | 1.75755e-05 | 0.00296436 | intron-variant | RBCK1 | GRCh38.p7 | 20:422092 | AGTGAAGGGGGTTCC[C/T]ATGATCCTAACTCTT | 10616 |
rs757874797 | snp | A/G/T | 8.74953e-05 | 0.00661373 | missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:417904 | CTCAGGAGCTGCAGC[A/G/T]GGAGCGGCAGCTGCG | 10616 |
rs757924227 | snp | A/G | 2.59683e-05 | 0.00360326 | intron-variant | RBCK1 | GRCh38.p7 | 20:428592 | AGAGATGCTGAAGGT[A/G]AGGCTGGGACAGGGC | 10616 |
rs757942076 | in-del | -/TG | | | intron-variant | RBCK1 | GRCh38.p7 | 20:417397 | CCAGACTGGGGTTTG[-/TG]TGTGTGTGTGTGTGT | 10616 |
rs757958288 | snp | A/G | 2.25405e-05 | 0.00335705 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:408702 | CCAGGCGACCCGGAG[A/G]TAGCATTTCCCAGGA | 10616 |
rs757959297 | snp | A/G | 1.98218e-05 | 0.0031481 | utr-variant-5-prime, synonymous-codon, missense, nc-transcript-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:408775 | GGACGAGAAGACCAA[A/G]AAAGGTGGGCACAGG | 10616 |
rs758001493 | in-del | -/CCCGGGGTCCCCCAGGAA | 1.75271e-05 | 0.00296028 | cds-indel, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:419409 | CCAGGCCCCCCAAAG[-/CCCGGGGTCCCCCAGGAA]CCCGGACGGGGGCAG | 10616 |
rs758176942 | snp | A/G | | | intron-variant, utr-variant-3-prime | RBCK1 | GRCh38.p7 | 20:410652 | GGTAAGGGAAGGGAA[A/G]AGAATGGATACTGTC | 10616 |
rs758386365 | snp | A/G | 6.2903e-05 | 0.00560781 | intron-variant, missense, utr-variant-5-prime, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:417260 | GTTGGAGAGGTCAGG[A/G]AGGTGCCAGATCATG | 10616 |
rs758405216 | snp | A/G | | | utr-variant-5-prime, synonymous-codon, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:417803 | GCTGGCACGAGACCA[A/G]GAGACCCTGCACTCC | 10616 |
rs758443598 | snp | A/G | 4.49327e-05 | 0.00473966 | intron-variant | RBCK1 | GRCh38.p7 | 20:417359 | TGGGTTCTAATAAAG[A/G]AAGAAGCATGGGTGG | 10616 |
rs758447834 | in-del | -/C | 4.97232e-05 | 0.00498589 | utr-variant-3-prime, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:430458 | GGGGCCACATGCTGA[-/C]CCAGCCCCACATCCA | 10616 |
rs758541405 | snp | A/C/T | 8.44667e-05 | 0.00649827 | intron-variant | RBCK1 | GRCh38.p7 | 20:419313 | GGACCAAGTGGGCCG[A/C/T]GTGGAACCACCACCC | 10616 |
rs758588390 | snp | C/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:418946 | TTGGCATTCTGCTGT[C/T]ATGTCTCAGTCCCTT | 10616 |
rs758597425 | snp | A/G | 1.72904e-05 | 0.00294022 | synonymous-codon, missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:419397 | GGCCCTCTGGAGCCA[A/G]GCCCCCCAAAGCCCG | 10616 |
rs758599536 | snp | G/T | 1.75093e-05 | 0.00295877 | intron-variant | RBCK1 | GRCh38.p7 | 20:410033 | GACATCAGGTGAGGA[G/T]TGCATGGCTGGCCTG | 10616 |
rs758654522 | snp | C/T | 1.74528e-05 | 0.00295399 | intron-variant, missense | RBCK1 | GRCh38.p7 | 20:410458 | TCCATCCAGCCATCA[C/T]ATCACAGGAGGAAGG | 10616 |
rs758678392 | snp | A/G | | | upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:406453 | GCAGTTAGATTGACA[A/G]GTGATGATATCTCAA | 10616 |
rs758729708 | snp | A/T | 0.000668226 | 0.0182665 | intron-variant, missense, nc-transcript-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:420947 | TGGTGCTGAACACGG[A/T]GCCCGCCGAGTGCCC | 10616 |
rs758772979 | multinucleotide-polymorphism | CTC/TTT | | | intron-variant | RBCK1 | GRCh38.p7 | 20:418601 | TCTCGATCTCCTGAC[CTC/TTT]GTGATCCGCCCGCCT | 10616 |
rs758798261 | snp | C/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:426281 | GGCTACAGTCTGTTG[C/T]GCTATCAAATACTAG | 10616 |
rs758900894 | snp | A/G | 1.65608e-05 | 0.00287752 | utr-variant-3-prime, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:430444 | GAGCTAAAGATGGTG[A/G]GGCCACATGCTGACC | 10616 |
rs758917306 | snp | C/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:412614 | ATGAGCCACTGCACC[C/T]GGCTGGGTTTATGTT | 10616 |
rs758925514 | snp | A/G | 0.000170111 | 0.009221 | intron-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:421058 | AGTCCCACCCCCGGC[A/G]ATGCAGCTTAATCAA | 10616 |
rs758933742 | snp | A/G | | | upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:406270 | AAATTTGATTGTGAT[A/G]ATGGGTGTACAATTC | 10616 |
rs759020970 | snp | C/T | 1.74561e-05 | 0.00295428 | intron-variant, utr-variant-3-prime | RBCK1 | GRCh38.p7 | 20:410575 | TGATTCCCACAGCTA[C/T]AGTTCAGCTTGAGGG | 10616 |
rs759142159 | snp | A/G | 1.65888e-05 | 0.00287996 | intron-variant | RBCK1 | GRCh38.p7 | 20:422244 | GATCAAGGCGGTAAG[A/G]CCTCAGGGTGGGAGA | 10616 |
rs759203606 | snp | A/G | 5.048e-05 | 0.00502369 | missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:422150 | TGCAGGGCACCATCC[A/G]CAACAGCCAGGAGGC | 10616 |
rs759216580 | snp | A/G | 1.65751e-05 | 0.00287876 | utr-variant-5-prime, synonymous-codon, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:417755 | GGACTATGGCTTCCC[A/G]CCAGTCTTGCAGCAG | 10616 |
rs759244310 | in-del | -/TGG | | | intron-variant | RBCK1 | GRCh38.p7 | 20:417123 | GCAGTACCTGTCTGA[-/TGG]TGGGTTGGTTGAGAG | 10616 |
rs759278003 | snp | C/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:425186 | CAGCTAATTTTTGTA[C/T]TTTCAGTACAGACGA | 10616 |
rs759312313 | snp | C/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:414654 | CTTTATGCTTTGCCT[C/G]TAGGTTGATTCTAAA | 10616 |
rs759350620 | snp | C/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:413274 | AAGTCTCTTGAATTT[C/G]CATATAAATTTTACG | 10616 |
rs759389289 | in-del | -/CTGCCCCAGCCCCGCCCCAGGGCCAGCAC | 2.192e-05 | 0.00331051 | intron-variant | RBCK1 | GRCh38.p7 | 20:428907 | GGCCAGGCTGGGTGA[lengthTooLong]CTGCCCCAGCCCCGC | 10616 |
rs759428679 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:431420 | TATTTACTAGAACCC[A/T]CTCTGTGCTGGTCGG | 10616 |
rs759462242 | snp | A/C | 3.43637e-05 | 0.00414496 | intron-variant, synonymous-codon, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:409861 | CTGTGCTAACTGGCT[A/C]CTGCTGTACTGGCTT | 10616 |
rs759487513 | snp | C/T | | | upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:406170 | CTGGTCTCGAACTCC[C/T]GACCTCAAGTGATCC | 10616 |
rs759491343 | snp | C/T | 1.81269e-05 | 0.00301051 | stop-gained, nc-transcript-variant, utr-variant-3-prime | RBCK1 | GRCh38.p7 | 20:428960 | CTCCAGGTGATGCTG[C/T]AGCAGGGCGAGGCCA | 10616 |
rs759579190 | snp | A/G | 3.40536e-05 | 0.00412621 | missense, nc-transcript-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:429041 | TGGATCCGCTGCACC[A/G]TCTGCCACACCGAGA | 10616 |
rs759632355 | snp | C/G | 1.66604e-05 | 0.00288616 | intron-variant | RBCK1 | GRCh38.p7 | 20:417510 | GCCCATGCTGAGCCC[C/G]TGCTGTTCTCTGCAG | 10616 |
rs759717818 | snp | G/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:418005 | ATAGGGCAAGCAGGG[G/T]CAGAGCCCCTGGGTT | 10616 |
rs759758359 | snp | C/T | 7.12073e-05 | 0.00596646 | intron-variant | RBCK1 | GRCh38.p7 | 20:428451 | CAGCTTCTTAACCCC[C/T]TGAGGAACCTTCTTA | 10616 |
rs759833242 | snp | C/G | 1.65603e-05 | 0.00287747 | utr-variant-5-prime, missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:417614 | GTGGCGTCTCTCAAG[C/G]ACATGGTGAGTGAGG | 10616 |
rs759857468 | snp | C/G | | | intron-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:408868 | GCCAGAAGGGCCTTG[C/G]AGAGGGGGCTTTAGC | 10616 |
rs759942496 | snp | A/C | 2.12479e-05 | 0.00325937 | missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:428552 | CCCTGCGGGCTCAGA[A/C]CGATGTGGCTGCCCG | 10616 |
rs759950149 | in-del | -/TG | 1.75142e-05 | 0.00295919 | intron-variant, utr-variant-3-prime | RBCK1 | GRCh38.p7 | 20:410596 | AGCTTGAGGGGAGAC[-/TG]TATAGCCAAGATATT | 10616 |
rs759984918 | snp | C/T | 1.65531e-05 | 0.00287686 | utr-variant-3-prime, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:430439 | CCACTGAGCTAAAGA[C/T]GGTGGGGCCACATGC | 10616 |
rs760002092 | snp | A/G | 1.70255e-05 | 0.00291761 | missense, synonymous-codon, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:419372 | CAAGGACCTCACGCT[A/G]CAGCCGCGGGGCCCT | 10616 |
rs760007593 | snp | A/C/T | 5.37382e-05 | 0.00518331 | missense, synonymous-codon, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:419460 | GATGCAGTGCCTGAG[A/C/T]CCCCACCGGTAAGCT | 10616 |
rs760200864 | snp | A/C | 0.000180528 | 0.00949903 | intron-variant | RBCK1 | GRCh38.p7 | 20:410400 | TCTCACCATTCTGCC[A/C]TTCATTCCCAGATTC | 10616 |
rs760299554 | snp | A/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:422946 | TCTCTGTTAGAGTCA[A/G]AGTTACAGCTTCTAT | 10616 |
rs760320592 | snp | C/T | 0.000202184 | 0.0100524 | intron-variant, synonymous-codon, nc-transcript-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:420996 | GGCGCCCGGCGAGGC[C/T]GTGGTGCTGCGTGAG | 10616 |
rs760320947 | snp | C/T | 1.65419e-05 | 0.00287588 | synonymous-codon, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:430400 | GGTAAATGGGATTCC[C/T]TGCCACCCAAGCTGT | 10616 |
rs760335895 | snp | C/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:426264 | TGTACAATTAAATTA[C/T]TGGCTACAGTCTGTT | 10616 |
rs760358929 | in-del | -/TTAG | | | intron-variant | RBCK1 | GRCh38.p7 | 20:425568 | TACTGTTTATACCTC[-/TTAG]TTCTAGTTTCTCAGT | 10616 |
rs760395382 | snp | A/G | 1.73939e-05 | 0.00294901 | intron-variant, missense | RBCK1 | GRCh38.p7 | 20:410509 | ACTCTTCTAAAGAGC[A/G]TAGCTCAAAAATTGT | 10616 |
rs760402039 | snp | A/G | | | intron-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:429126 | GGTGGTGTGGAGAGG[A/G]TGCCCTTGTGGGCTT | 10616 |
rs760518647 | snp | A/G | 1.68957e-05 | 0.00290647 | missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:422138 | CTAGGGAGTGCCTGC[A/G]GGGCACCATCCGCAA | 10616 |
rs760559062 | snp | A/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:421717 | TGGCTGGAGCAGAGG[A/G]ATGAAGGGGGTAATC | 10616 |
rs760684684 | snp | A/G | 3.91221e-05 | 0.00442261 | utr-variant-5-prime, synonymous-codon, nc-transcript-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:408753 | GATGGGCACAGCCAC[A/G]CCAGATGGACGAGAA | 10616 |
rs760689114 | snp | C/T | 2.27876e-05 | 0.00337539 | missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:428573 | TGGCTGCCCGGCAGA[C/T]GACAGAGATGCTGAA | 10616 |
rs760819620 | snp | C/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:411849 | CAAATAATAATCTAT[C/T]GTATAGACATATCTC | 10616 |
rs760893792 | snp | C/G | 8.03181e-05 | 0.00633661 | missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:419710 | GGCGGGCGAGGAGGA[C/G]GCGCTGCGTCAGTAC | 10616 |
rs760948890 | snp | A/C | 0.000175886 | 0.00937614 | intron-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:420822 | CCTTCGGGGTCTGAC[A/C]CGCCCCCGAGGCCCT | 10616 |
rs760950144 | snp | C/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:427128 | ACAAGTGTAAGCCAC[C/G]ACACCTGGCCTAAAA | 10616 |
rs760972268 | snp | G/T | 1.66829e-05 | 0.00288811 | intron-variant | RBCK1 | GRCh38.p7 | 20:417501 | CTGGCCAGAGCCCAT[G/T]CTGAGCCCCTGCTGT | 10616 |
rs761051360 | in-del | -/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:416334 | CTAATTTTTTTTTTT[-/G]TATTTTTAGTAGAGA | 10616 |
rs761061665 | snp | A/C | 1.67795e-05 | 0.00289646 | intron-variant | RBCK1 | GRCh38.p7 | 20:427533 | CCTAGTCACTGTCAT[A/C]TTGCCTGGAGCTCAC | 10616 |
rs761116626 | snp | C/G | 3.38032e-05 | 0.00411102 | missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:419361 | GATCTGGGCTTCAAG[C/G]ACCTCACGCTGCAGC | 10616 |
rs761165201 | snp | A/T | 1.64808e-05 | 0.00287057 | synonymous-codon, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:427459 | TGAGTTCACCTGCCC[A/T]GTGTGTTTCCACGTC | 10616 |
rs761214707 | snp | C/T | | | missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:427403 | TACCATTGCAAGACC[C/T]CAGATTGCAAGGGAT | 10616 |
rs761306350 | snp | A/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:418215 | GCCCAGTTTGCTAAA[A/G]TCATAAATTGGGTAT | 10616 |
rs761352463 | snp | A/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:423071 | TTGGGAGGCCAAGGC[A/G]GGTGGATCACCTGAG | 10616 |
rs761481740 | snp | C/T | 1.68049e-05 | 0.00289865 | intron-variant | RBCK1 | GRCh38.p7 | 20:430310 | TGGGGGCAGTCTCTG[C/T]ACTGCGCTGACATTC | 10616 |
rs761523821 | snp | C/T | 1.68536e-05 | 0.00290285 | intron-variant | RBCK1 | GRCh38.p7 | 20:419344 | TTTAACCCTCCTCCA[C/T]AGATCTGGGCTTCAA | 10616 |
rs761524908 | snp | C/T | 1.65416e-05 | 0.00287586 | utr-variant-5-prime, intron-variant, missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:409976 | GCAGAGCAACGGGTG[C/T]CCCTGAGTGTGCAAC | 10616 |
rs761689020 | snp | C/T | | | intron-variant, missense | RBCK1 | GRCh38.p7 | 20:410438 | TGCAAAATGGCCATT[C/T]CAGCTCCATCCAGCC | 10616 |
rs761727859 | snp | C/G | 6.961e-05 | 0.00589917 | intron-variant, synonymous-codon, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:409846 | TCCTGAAAATAAACC[C/G]TGTGCTAACTGGCTC | 10616 |
rs761771581 | snp | A/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:423764 | GGGCTGGACTTACCT[A/G]GATGGTTCTTCTGGT | 10616 |
rs761782681 | snp | A/G | 0.000103141 | 0.00718051 | intron-variant, synonymous-codon, nc-transcript-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:420984 | CTACTCGGTGCTGGC[A/G]CCCGGCGAGGCCGTG | 10616 |
rs761915746 | snp | A/G | 4.43685e-05 | 0.00470981 | missense, synonymous-codon, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:419632 | GATGTGCTGCCGGGC[A/G]CGCCCCGAGGCCTAC | 10616 |
rs761931914 | snp | A/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:412020 | TGGAATTGCTGGGTC[A/T]TACAGTAACTCTATG | 10616 |
rs761973251 | snp | C/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:430272 | GCAGAGGCAAAGGCC[C/T]GGGGTGGGAGAGCGC | 10616 |
rs761976413 | snp | A/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:428484 | TTGAGTCCCTCACCC[A/G]CTACAGGCCATCCAT | 10616 |
rs761995748 | snp | C/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:411613 | ACCTCGTGATCCGCC[C/T]GCCTATGCCTCCCAA | 10616 |
rs762006733 | in-del | -/CC | 1.66346e-05 | 0.00288393 | intron-variant | RBCK1 | GRCh38.p7 | 20:428447 | CTCCCAGCTTCTTAA[-/CC]CCCTGAGGAACCTTC | 10616 |
rs762028720 | snp | C/G/T | 1.98679e-05 | 0.00315175 | intron-variant, missense, synonymous-codon, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:428937 | CCCCAGGGCCAGCAC[C/G/T]TGCCCCACTCCAGGT | 10616 |
rs762051680 | snp | C/T | 1.77118e-05 | 0.00297583 | intron-variant | RBCK1 | GRCh38.p7 | 20:417200 | CGTAGTTAACAACAA[C/T]TTCTGGTGGTTTCAC | 10616 |
rs762064217 | in-del | -/TGCT | 3.54981e-05 | 0.00421281 | intron-variant, frameshift-variant, utr-variant-5-prime, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:417288 | ATGGAGGCCCTCGTG[-/TGCT]GCCACGAGTTGATTC | 10616 |
rs762116740 | snp | C/T | 3.41099e-05 | 0.00412962 | synonymous-codon, nc-transcript-variant, utr-variant-3-prime | RBCK1 | GRCh38.p7 | 20:429037 | CGACTGGATCCGCTG[C/T]ACCGTCTGCCACACC | 10616 |
rs762123098 | snp | A/G/T | 7.03953e-05 | 0.00593234 | missense, synonymous-codon, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:419698 | GCGAGCGCGCCTGGC[A/G/T]GGCGAGGAGGAGGCG | 10616 |
rs762176396 | snp | A/G | 0.000223198 | 0.0105617 | intron-variant, synonymous-codon, utr-variant-5-prime, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:417298 | TCGTGTGCTGCCACG[A/G]GTTGATTCTAAGAGT | 10616 |
rs762197615 | snp | C/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:418650 | TGGGATTACAGGCGT[C/G]AGCCACCACGCCCAA | 10616 |
rs762223633 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:431103 | AGAATGAGGCTGTGA[C/G]TGAGCACTGGGACCT | 10616 |
rs762315366 | snp | C/G/T | 6.13252e-05 | 0.00553704 | missense, synonymous-codon, stop-gained, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:419684 | CCCGACGAGGAGGAG[C/G/T]GAGCGCGCCTGGCGG | 10616 |
rs762332296 | snp | C/T | | | upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:407377 | ACATTTTAACAGGAC[C/T]CTCCGGCAGCTAGGT | 10616 |
rs762390613 | snp | A/G | 1.69063e-05 | 0.00290738 | intron-variant | RBCK1 | GRCh38.p7 | 20:427262 | TAGTGGTCAAGGGTC[A/G]TATGTCAGGTGTTCT | 10616 |
rs762445622 | snp | C/G | 1.64765e-05 | 0.00287019 | missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:427436 | TGCTTCTTTGAGGAT[C/G]ATGTCAATGAGTTCA | 10616 |
rs762539213 | snp | C/T | 2.11997e-05 | 0.00325567 | intron-variant | RBCK1 | GRCh38.p7 | 20:417952 | CTCTGCCCTGAGCAC[C/T]GCCGGACCCAGCGGG | 10616 |
rs762587991 | snp | A/G | 1.65419e-05 | 0.00287588 | utr-variant-5-prime, intron-variant, synonymous-codon, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:409966 | CATCTGGCTGGCAGA[A/G]CAACGGGTGCCCCTG | 10616 |
rs762610925 | snp | A/T | 4.97558e-05 | 0.00498753 | intron-variant | RBCK1 | GRCh38.p7 | 20:422262 | TCAGGGTGGGAGACA[A/T]ACCCCAAGTCCCAAC | 10616 |
rs762636240 | snp | C/G | 1.68738e-05 | 0.00290458 | synonymous-codon, missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:417882 | GCCCGCAACACCTCC[C/G]TCAACCCTCAGGAGC | 10616 |
rs762666056 | snp | C/T | 1.64792e-05 | 0.00287042 | synonymous-codon, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:427384 | AAACCGCAGTGCCTT[C/T]AGCTACCATTGCAAG | 10616 |
rs762693602 | snp | C/T | 1.70041e-05 | 0.00291577 | intron-variant, missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:409871 | TGGCTCCTGCTGTAC[C/T]GGCTTTCAGCAGAGG | 10616 |
rs762696336 | snp | A/G | 1.70012e-05 | 0.00291553 | missense, nc-transcript-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:429050 | TGCACCGTCTGCCAC[A/G]CCGAGATCTGCTGGG | 10616 |
rs762778104 | snp | C/G | 8.56714e-05 | 0.00654434 | missense, synonymous-codon, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:419716 | CGAGGAGGAGGCGCT[C/G]CGTCAGTACCAGCAG | 10616 |
rs762804671 | in-del | -/TTGA | 0.000223231 | 0.0105625 | intron-variant, frameshift-variant, utr-variant-5-prime, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:417300 | GTGTGCTGCCACGAG[-/TTGA]TTCTAAGAGTAGCGT | 10616 |
rs762815954 | in-del | -/AA | | | intron-variant | RBCK1 | GRCh38.p7 | 20:413918 | AAGAGACAAATCACC[-/AA]AAAAAAAAAAAAAAA | 10616 |
rs762880682 | snp | C/T | 1.65943e-05 | 0.00288043 | intron-variant | RBCK1 | GRCh38.p7 | 20:417726 | CCCTCTCTTTGCCCC[C/T]ACCAGGTTTTTCTGG | 10616 |
rs762902250 | snp | C/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:413145 | CATTGAACTATAATA[C/T]ATATCTGCCCTTACG | 10616 |
rs762933371 | snp | G/T | 1.81302e-05 | 0.00301078 | intron-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:429140 | GGTGCCCTTGTGGGC[G/T]TTGCCTTAGAGGAGG | 10616 |
rs762983816 | in-del | -/C | 3.31763e-05 | 0.00407272 | intron-variant | RBCK1 | GRCh38.p7 | 20:422272 | AGACATACCCCAAGT[-/C]CCAACTCCTAAGGAA | 10616 |
rs763071132 | snp | A/G | 2.16088e-05 | 0.00328693 | missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:428557 | CGGGCTCAGAACGAT[A/G]TGGCTGCCCGGCAGA | 10616 |
rs763108374 | in-del | -/CCAGATCATGGAGGCCCTCGTGTGCTGC | 0.0001188 | 0.00770623 | intron-variant, frameshift-variant, utr-variant-5-prime, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:417265 | GAGGTCAGGGAGGTG[-/CCAGATCATGGAGGCCCTCGTGTGCTGC]CCAGATCATGGAGGC | 10616 |
rs763194893 | snp | A/G | 5.4254e-05 | 0.00520807 | intron-variant | RBCK1 | GRCh38.p7 | 20:419476 | CCCCACCGGTAAGCT[A/G]TCCTTGGCCTCAGTA | 10616 |
rs763207809 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:431225 | AAGTCTGCAGAGAAG[A/G]ATGGGCTTAGGGGCG | 10616 |
rs763248858 | snp | C/T | 3.39058e-05 | 0.00411725 | synonymous-codon, missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:419603 | ATCAACAAGCCCACG[C/T]GGCCTGGCTGTGAGA | 10616 |
rs763250873 | snp | C/T | 1.7396e-05 | 0.00294919 | intron-variant, missense | RBCK1 | GRCh38.p7 | 20:410536 | TTGTACACACTTCTT[C/T]CGTTAATTCCTGTGG | 10616 |
rs763261811 | snp | A/G | 1.97584e-05 | 0.00314305 | utr-variant-5-prime, missense, nc-transcript-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:408741 | CCCCCCCAGGGGGAT[A/G]GGCACAGCCACGCCA | 10616 |
rs763357454 | snp | C/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:421365 | CCAGTTTCTGAGTCT[C/T]CTGTCATGGCCCCCC | 10616 |
rs763401410 | snp | A/G | | | intron-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:409777 | TTCACCAGGAAGACA[A/G]AGAAAGCAGCACACA | 10616 |
rs763445513 | snp | A/G | 7.83638e-05 | 0.00625905 | utr-variant-5-prime, missense, synonymous-codon, nc-transcript-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:408762 | AGCCACGCCAGATGG[A/G]CGAGAAGACCAAGAA | 10616 |
rs763450262 | snp | C/G | 1.75823e-05 | 0.00296493 | intron-variant, utr-variant-3-prime | RBCK1 | GRCh38.p7 | 20:410607 | AGACTGTATAGCCAA[C/G]ATATTCAGCTAGAAT | 10616 |
rs763555602 | snp | C/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:426385 | TGGTAAGCATCCTTT[C/T]ACTGTCTGTCCTCAT | 10616 |
rs763562321 | snp | A/G | 5.114e-05 | 0.00505642 | missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:417892 | CCTCCCTCAACCCTC[A/G]GGAGCTGCAGCGGGA | 10616 |
rs763655919 | snp | G/T | 1.65553e-05 | 0.00287705 | utr-variant-5-prime, missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:417779 | GCAGCAGTGGGTGAT[G/T]GGGCAGCGGCTGGCA | 10616 |
rs763710094 | snp | A/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:413584 | CTAACTGGCACTGGC[A/G]TTTCCTTTGTAAAAT | 10616 |
rs763766234 | snp | A/G | 4.37216e-05 | 0.00467535 | intron-variant | RBCK1 | GRCh38.p7 | 20:417953 | TCTGCCCTGAGCACC[A/G]CCGGACCCAGCGGGG | 10616 |
rs763808209 | snp | C/T | 1.81434e-05 | 0.00301187 | intron-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:429142 | TGCCCTTGTGGGCTT[C/T]GCCTTAGAGGAGGGC | 10616 |
rs763822201 | snp | A/G | 3.30803e-05 | 0.00406682 | utr-variant-5-prime, intron-variant, synonymous-codon, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:409969 | CTGGCTGGCAGAGCA[A/G]CGGGTGCCCCTGAGT | 10616 |
rs763860228 | snp | A/C | | | intron-variant, utr-variant-3-prime | RBCK1 | GRCh38.p7 | 20:420353 | GCTCCCCATTCTGAT[A/C]TCACCCCTGGCCCCA | 10616 |
rs763872700 | snp | A/G | 0.00016368 | 0.00904505 | intron-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:420843 | CCGAGGCCCTGACCC[A/G]CCCCGTGGCCCCGCC | 10616 |
rs763912049 | snp | A/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:411558 | ATTTTTAGTAGAGAC[A/G]GGGTTTCGCCGTGTT | 10616 |
rs763971799 | snp | A/G | 0.000180636 | 0.00950186 | missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:419721 | AGGAGGCGCTGCGTC[A/G]GTACCAGCAGGTGGG | 10616 |
rs763994994 | snp | C/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:422740 | GAGTGGGCTGAGGTG[C/G]GAGGATTGCTTGAGC | 10616 |
rs764058033 | snp | A/G | 4.50582e-05 | 0.00474627 | intron-variant | RBCK1 | GRCh38.p7 | 20:417362 | GTTCTAATAAAGGAA[A/G]AAGCATGGGTGGGGC | 10616 |
rs764085122 | snp | A/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:410246 | CTATCTCATAGGGTT[A/G]TTAGGAGGTGTACTG | 10616 |
rs764099682 | in-del | -/TTTC | | | intron-variant | RBCK1 | GRCh38.p7 | 20:422320 | AGCAGACATCTTTCT[-/TTTC]TTTCTTTTTTTTTTT | 10616 |
rs764120025 | snp | A/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:419045 | CAAGTCACTGTTTTG[A/G]CAGGACCGCCTCAGC | 10616 |
rs764150236 | snp | G/T | | | intron-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:409067 | GGGAGACAGACGTCA[G/T]TTGACCTGAGAAGCA | 10616 |
rs764237313 | snp | C/T | 3.67972e-05 | 0.0042892 | intron-variant | RBCK1 | GRCh38.p7 | 20:419485 | TAAGCTGTCCTTGGC[C/T]TCAGTATCCTCTTCT | 10616 |
rs764244683 | snp | C/T | 0.000178317 | 0.00944069 | missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:428566 | AACGATGTGGCTGCC[C/T]GGCAGACGACAGAGA | 10616 |
rs764253450 | in-del | -/AGATCATGGAGGCCCT | 5.76485e-05 | 0.00536851 | intron-variant, frameshift-variant, utr-variant-5-prime, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:417267 | GGTCAGGGAGGTGCC[-/AGATCATGGAGGCCCT]AGATCATGGAGGCCC | 10616 |
rs764259533 | snp | C/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:427172 | TGGAGTTTTTCAACA[C/G]TATGAGGATTACATG | 10616 |
rs764307640 | snp | A/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:427577 | GTGTTCTCCTGGGAA[A/G]GGAGCTGTGACACTG | 10616 |
rs764357407 | snp | A/G | 4.17493e-05 | 0.00456869 | missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:419628 | GTGAGATGTGCTGCC[A/G]GGCGCGCCCCGAGGC | 10616 |
rs764429530 | snp | C/G/T | 6.95826e-05 | 0.00589806 | intron-variant, missense | RBCK1 | GRCh38.p7 | 20:410537 | TGTACACACTTCTTC[C/G/T]GTTAATTCCTGTGGA | 10616 |
rs764486461 | snp | C/T | | | intron-variant, utr-variant-3-prime | RBCK1 | GRCh38.p7 | 20:410609 | ACTGTATAGCCAAGA[C/T]ATTCAGCTAGAATTC | 10616 |
rs764508468 | snp | C/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:418399 | TTTGAGACGGAGTCT[C/T]GCTCTGTCGCCCAGG | 10616 |
rs764573450 | snp | A/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:416608 | TTTGGGGTCGGTTCT[A/G]TTTTTTCATCTTTTC | 10616 |
rs764633980 | snp | G/T | | | upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:406275 | TGATTGTGATGATGG[G/T]TGTACAATTCTGTAA | 10616 |
rs764675755 | snp | A/G | 1.67882e-05 | 0.00289721 | missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:422156 | GCACCATCCGCAACA[A/G]CCAGGAGGCGGAGGT | 10616 |
rs764728866 | snp | C/T | 3.31175e-05 | 0.00406911 | utr-variant-5-prime, missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:417760 | ATGGCTTCCCACCAG[C/T]CTTGCAGCAGTGGGT | 10616 |
rs765000861 | snp | G/T | 1.9645e-05 | 0.00313403 | utr-variant-5-prime, stop-gained, missense, nc-transcript-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:408764 | CCACGCCAGATGGAC[G/T]AGAAGACCAAGAAAG | 10616 |
rs765037868 | snp | A/C | 1.70159e-05 | 0.00291679 | synonymous-codon, nc-transcript-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:429043 | GATCCGCTGCACCGT[A/C]TGCCACACCGAGATC | 10616 |
rs765059864 | snp | G/T | 1.71328e-05 | 0.00292679 | intron-variant, synonymous-codon, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:409864 | TGCTAACTGGCTCCT[G/T]CTGTACTGGCTTTCA | 10616 |
rs765129534 | snp | A/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:423840 | AGCCGCGGTGGCCTG[A/G]TTTATAATGGTCTCA | 10616 |
rs765131022 | snp | A/G | 3.5429e-05 | 0.00420871 | missense, nc-transcript-variant, utr-variant-3-prime | RBCK1 | GRCh38.p7 | 20:428969 | ATGCTGCAGCAGGGC[A/G]AGGCCATGCGCTGCC | 10616 |
rs765191996 | snp | C/T | 6.96173e-05 | 0.00589947 | intron-variant, missense | RBCK1 | GRCh38.p7 | 20:410488 | GGAAGAAAGACACCC[C/T]TCCACACTCTTCTAA | 10616 |
rs765206788 | snp | C/T | 5.04579e-05 | 0.00502259 | missense, synonymous-codon, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:419653 | CGAGGCCTACCAGGT[C/T]CCCGCCTCATACCAG | 10616 |
rs765331664 | snp | C/T | 1.65913e-05 | 0.00288017 | intron-variant | RBCK1 | GRCh38.p7 | 20:427500 | TCTGCAAGGTGGGGC[C/T]TGCAGGGACTCCCCC | 10616 |
rs765389725 | snp | A/C | | | intron-variant | RBCK1 | GRCh38.p7 | 20:413652 | CCTGTGGACCACAAC[A/C]TGGGGGGAATCTCAG | 10616 |
rs765533753 | snp | G/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:419773 | ACCTGCAGACCGCAC[G/T]GGGGAGGTGTAGGCC | 10616 |
rs765582031 | snp | A/G | 1.70778e-05 | 0.00292209 | missense, synonymous-codon, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:419378 | CCTCACGCTGCAGCC[A/G]CGGGGCCCTCTGGAG | 10616 |
rs765631019 | snp | C/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:418656 | TACAGGCGTGAGCCA[C/T]CACGCCCAACCCACA | 10616 |
rs765697612 | snp | C/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:427671 | CCCTGGCCCCACAGA[C/T]GGAGTCCCAGCCCCA | 10616 |
rs765814341 | snp | A/C | 0.000332779 | 0.0128949 | missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:430420 | ACCCAAGCTGTCAGA[A/C]CTGCCACTGAGCTAA | 10616 |
rs765903793 | snp | A/G | 8.39158e-05 | 0.00647695 | intron-variant | RBCK1 | GRCh38.p7 | 20:430316 | CAGTCTCTGCACTGC[A/G]CTGACATTCTCTTCT | 10616 |
rs765956229 | snp | A/G | 0.000100538 | 0.00708935 | intron-variant, missense, nc-transcript-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:420997 | GCGCCCGGCGAGGCC[A/G]TGGTGCTGCGTGAGT | 10616 |
rs765970206 | snp | G/T | 1.79223e-05 | 0.00299346 | intron-variant | RBCK1 | GRCh38.p7 | 20:410406 | CATTCTGCCATTCAT[G/T]CCCAGATTCCTCATG | 10616 |
rs766154575 | snp | G/T | 1.66596e-05 | 0.00288609 | intron-variant | RBCK1 | GRCh38.p7 | 20:417656 | GACACTGGGGTGAAG[G/T]CTCTCCCTTTCACTC | 10616 |
rs766154791 | snp | C/T | 3.37115e-05 | 0.00410543 | synonymous-codon, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:422145 | GTGCCTGCAGGGCAC[C/T]ATCCGCAACAGCCAG | 10616 |
rs766179518 | snp | A/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:412382 | CAGGAGTGCAATGGT[A/G]CAATCTCGGCTCACT | 10616 |
rs766182401 | snp | C/G | 1.95563e-05 | 0.00312694 | utr-variant-5-prime, missense, nc-transcript-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:408754 | ATGGGCACAGCCACG[C/G]CAGATGGACGAGAAG | 10616 |
rs766210330 | snp | C/T | 1.65729e-05 | 0.00287857 | utr-variant-5-prime, synonymous-codon, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:417749 | TTTTCTGGACTATGG[C/T]TTCCCACCAGTCTTG | 10616 |
rs766366513 | snp | A/G | 4.58043e-05 | 0.0047854 | synonymous-codon, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:428574 | GGCTGCCCGGCAGAC[A/G]ACAGAGATGCTGAAG | 10616 |
rs766442885 | in-del | -/A | | | intron-variant | RBCK1 | GRCh38.p7 | 20:418074 | GGGAAGAGAGGACCT[-/A]AGACACATGGGAGGG | 10616 |
rs766493201 | in-del | -/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:414311 | AGCTATTTGAGAGGC[-/T]TGAGATGAGAGGATT | 10616 |
rs766498545 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:430546 | TGTAGGGGCCCTGCC[C/T]GCACTGCGGTTGTCC | 10616 |
rs766562059 | snp | C/T | 1.70194e-05 | 0.00291709 | missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:419712 | CGGGCGAGGAGGAGG[C/T]GCTGCGTCAGTACCA | 10616 |
rs766586383 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:431395 | AGATGGCACAGTATC[A/G]ATTCAGCAGTATTTA | 10616 |
rs766613221 | snp | A/G | 0.000126133 | 0.00794043 | intron-variant, missense, utr-variant-5-prime, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:417332 | GTGGAGCCATTGGAG[A/G]GGCCTAACTGGTGGG | 10616 |
rs766615187 | snp | A/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:413852 | AATTAATAAAACATG[A/T]GCGCTGAAAGAGTTG | 10616 |
rs766618284 | snp | C/T | 1.64917e-05 | 0.00287151 | synonymous-codon, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:427471 | CCCTGTGTGTTTCCA[C/T]GTCAACTGCCTGCTC | 10616 |
rs766660796 | snp | A/G | | | intron-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:408783 | AGACCAAGAAAGGTG[A/G]GCACAGGCTGGAGGT | 10616 |
rs766673147 | snp | A/G | 1.6596e-05 | 0.00288058 | intron-variant | RBCK1 | GRCh38.p7 | 20:417976 | CAGCGGGGGCCCTGG[A/G]CTCACTTGAGGGCAT | 10616 |
rs766686012 | snp | A/C | | | upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:407666 | GAGAGGCAGCGTCGG[A/C]TCTGGGTAAGGGCGG | 10616 |
rs766786444 | snp | C/T | 1.67778e-05 | 0.00289631 | intron-variant | RBCK1 | GRCh38.p7 | 20:427534 | CTAGTCACTGTCATC[C/T]TGCCTGGAGCTCACC | 10616 |
rs766841580 | snp | C/G/T | 6.79849e-05 | 0.00582996 | missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:419368 | GCTTCAAGGACCTCA[C/G/T]GCTGCAGCCGCGGGG | 10616 |
rs766968693 | snp | C/T | | | missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:419416 | CCCCAAAGCCCGGGG[C/T]CCCCCAGGAACCCGG | 10616 |
rs766974386 | snp | C/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:427561 | CACCACACTGCAGTG[C/T]GTGTTCTCCTGGGAA | 10616 |
rs767016233 | snp | A/C | 1.71012e-05 | 0.00292409 | synonymous-codon, nc-transcript-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:429076 | CTGGGTCACCAAGGG[A/C]CCACGCTGGGGCCCT | 10616 |
rs767184087 | snp | C/T | 3.30841e-05 | 0.00406706 | utr-variant-5-prime, intron-variant, missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:409977 | CAGAGCAACGGGTGC[C/T]CCTGAGTGTGCAACT | 10616 |
rs767237519 | snp | C/G | 1.84623e-05 | 0.00303822 | intron-variant | RBCK1 | GRCh38.p7 | 20:410386 | GCTCATATTGTTTCT[C/G]TCACCATTCTGCCAT | 10616 |
rs767298144 | snp | C/T | 0.000143978 | 0.00848341 | intron-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:420860 | CCCGTGGCCCCGCCC[C/T]GTGTGCCCAGCGGAA | 10616 |
rs767320205 | snp | A/G | 1.66147e-05 | 0.0028822 | intron-variant | RBCK1 | GRCh38.p7 | 20:417641 | GAGGAGGCGGAGGGC[A/G]ACACTGGGGTGAAGG | 10616 |
rs767353266 | snp | C/T | 0.000201511 | 0.0100357 | intron-variant, synonymous-codon, nc-transcript-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:420990 | GGTGCTGGCGCCCGG[C/T]GAGGCCGTGGTGCTG | 10616 |
rs767397557 | snp | A/G | 3.31895e-05 | 0.00407353 | utr-variant-5-prime, missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:417539 | AGGCTGTGGGTGAGC[A/G]TGGAGGATGCTCAGA | 10616 |
rs767493935 | snp | C/T | 3.94773e-05 | 0.00444265 | intron-variant | RBCK1 | GRCh38.p7 | 20:419507 | TCCTCTTCTGTGCCC[C/T]TCCCTTGCCTCACCC | 10616 |
rs767654656 | snp | C/T | 8.85661e-05 | 0.00665396 | synonymous-codon, missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:419633 | ATGTGCTGCCGGGCG[C/T]GCCCCGAGGCCTACC | 10616 |
rs767721747 | snp | C/T | | | upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:407740 | GCCTTGGACAGGTCA[C/T]CAACAAACAGAGCCT | 10616 |
rs767790757 | in-del | -/CTTAC | 6.53019e-05 | 0.00571373 | intron-variant | RBCK1 | GRCh38.p7 | 20:428463 | CCCCTGAGGAACCTT[-/CTTAC]CTTGAGTCCCTCACC | 10616 |
rs767798541 | snp | C/T | 1.69032e-05 | 0.00290711 | intron-variant | RBCK1 | GRCh38.p7 | 20:427265 | TGGTCAAGGGTCATA[C/T]GTCAGGTGTTCTGAA | 10616 |
rs767887429 | snp | C/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:427775 | AGTCACAGACTGAAT[C/T]CCAGTCCCACATTGA | 10616 |
rs768006735 | snp | A/G | 1.6477e-05 | 0.00287024 | missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:427442 | TTTGAGGATGATGTC[A/G]ATGAGTTCACCTGCC | 10616 |
rs768072029 | snp | C/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:414113 | AAAAAAGAAAAATCC[C/G]TGGGAAACTCCAATG | 10616 |
rs768386835 | snp | C/T | 1.66893e-05 | 0.00288867 | intron-variant | RBCK1 | GRCh38.p7 | 20:427518 | CAGGGACTCCCCCCA[C/T]CTAGTCACTGTCATC | 10616 |
rs768404116 | snp | C/T | 1.91782e-05 | 0.00309657 | intron-variant | RBCK1 | GRCh38.p7 | 20:410364 | CTGCTCCCGACAGTC[C/T]TCAGAGGCTCATATT | 10616 |
rs768525416 | in-del | -/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:426817 | TTACTTTTCTTTTCC[-/T]TTTTTTTTTTTTTTT | 10616 |
rs768576248 | snp | A/C | | | intron-variant | RBCK1 | GRCh38.p7 | 20:417157 | TAAATGAGTTAATAC[A/C]CATGAAGTGCATTAA | 10616 |
rs768579983 | in-del | -/CAGCCCGACGAGGAGGAGCGA | | | cds-indel, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:419666 | GTCCCCGCCTCATAC[-/CAGCCCGACGAGGAGGAGCGA]GCGCGCCTGGCGGGC | 10616 |
rs768587494 | snp | C/T | 8.70193e-05 | 0.00659561 | intron-variant, synonymous-codon | RBCK1 | GRCh38.p7 | 20:410490 | AAGAAAGACACCCCT[C/T]CACACTCTTCTAAAG | 10616 |
rs768693422 | in-del | -/TGG | 1.6679e-05 | 0.00288777 | intron-variant | RBCK1 | GRCh38.p7 | 20:427299 | TGAGCAGCAAGGACA[-/TGG]TGTGTTGGCAGCTCC | 10616 |
rs768710610 | snp | A/C/G | 6.96844e-05 | 0.00590238 | intron-variant, missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:409845 | CTCCTGAAAATAAAC[A/C/G]CTGTGCTAACTGGCT | 10616 |
rs768716887 | snp | A/G | 2.08197e-05 | 0.00322636 | intron-variant, splice-acceptor-variant | RBCK1 | GRCh38.p7 | 20:428927 | CCCAGCCCCGCCCCA[A/G]GGCCAGCACCTGCCC | 10616 |
rs768765441 | snp | A/G | 1.65946e-05 | 0.00288046 | intron-variant | RBCK1 | GRCh38.p7 | 20:417727 | CCTCTCTTTGCCCCC[A/G]CCAGGTTTTTCTGGA | 10616 |
rs768917282 | snp | A/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:430225 | TCCATCAGGTAGCTG[A/G]GGCTGACCAGGCCAT | 10616 |
rs769108644 | snp | G/T | 6.57441e-05 | 0.00573304 | missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:419691 | AGGAGGAGCGAGCGC[G/T]CCTGGCGGGCGAGGA | 10616 |
rs769199018 | snp | A/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:428743 | GGTGGGACTTAGGCC[A/G]AATGGTCATGTCAGG | 10616 |
rs769222994 | snp | C/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:418631 | CCTCGGCCTCCCAAA[C/G]TGCTGGGATTACAGG | 10616 |
rs769293339 | snp | C/G | | | intron-variant, synonymous-codon, utr-variant-5-prime, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:417265 | AGAGGTCAGGGAGGT[C/G]CCAGATCATGGAGGC | 10616 |
rs769421493 | snp | C/T | 6.63482e-05 | 0.00575931 | intron-variant | RBCK1 | GRCh38.p7 | 20:422246 | TCAAGGCGGTAAGGC[C/T]TCAGGGTGGGAGACA | 10616 |
rs769443911 | snp | C/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:429617 | CCACGTTTCAGTGTC[C/T]GTAGGTAAAGTGCTT | 10616 |
rs769447394 | in-del | -/C | | | intron-variant | RBCK1 | GRCh38.p7 | 20:416693 | TTCTCTGGAATAATA[-/C]CATGTAGATTTAAAT | 10616 |
rs769517890 | snp | A/T | 4.08873e-05 | 0.00452128 | intron-variant | RBCK1 | GRCh38.p7 | 20:417945 | GGTGAGGCTCTGCCC[A/T]GAGCACCGCCGGACC | 10616 |
rs769535158 | in-del | -/ATTA | | | intron-variant | RBCK1 | GRCh38.p7 | 20:413834 | TTACTTAGCTATTAC[-/ATTA]ATTAATAAAACATGA | 10616 |
rs769673523 | snp | A/T | 1.65564e-05 | 0.00287714 | utr-variant-5-prime, intron-variant, synonymous-codon, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:409939 | GGATGAACAGGTGGC[A/T]ATGAAGTGTGCCATC | 10616 |
rs769793981 | snp | C/T | | | upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:407054 | GTGAAATGCTGGATA[C/T]GTGTGTCTGTGAAAT | 10616 |
rs769807324 | snp | C/G | 1.72184e-05 | 0.00293409 | intron-variant | RBCK1 | GRCh38.p7 | 20:422111 | ATCCTAACTCTTTTC[C/G]CCTCCCCTCCCCTAG | 10616 |
rs769870871 | snp | C/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:425547 | TACAAATCTCAATAG[C/G]ACATATACTGTTTAT | 10616 |
rs769906923 | snp | C/T | 0.000207922 | 0.010194 | intron-variant, missense, nc-transcript-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:420974 | GCCCCGTGTGCTACT[C/T]GGTGCTGGCGCCCGG | 10616 |
rs770038981 | snp | C/T | 1.6591e-05 | 0.00288015 | intron-variant | RBCK1 | GRCh38.p7 | 20:417633 | TGGTGAGTGAGGAGG[C/T]GGAGGGCGACACTGG | 10616 |
rs770095642 | snp | C/T | 1.66214e-05 | 0.00288278 | intron-variant | RBCK1 | GRCh38.p7 | 20:417705 | CTGGCCCTCCCTTCC[C/T]ACTCTCCCTCTCTTT | 10616 |
rs770141575 | in-del | -/C | 1.66499e-05 | 0.00288525 | frameshift-variant, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:422201 | TTGACAACACCTACT[-/C]GTGCTCGGGCAAGCT | 10616 |
rs770216625 | snp | G/T | 1.7205e-05 | 0.00293295 | missense, nc-transcript-variant, utr-variant-3-prime | RBCK1 | GRCh38.p7 | 20:429002 | CAGTGCCAGATCGTG[G/T]TACAGAAGAAGGACG | 10616 |
rs770216987 | snp | A/G | 5.24095e-05 | 0.00511879 | intron-variant, utr-variant-3-prime | RBCK1 | GRCh38.p7 | 20:410581 | CCACAGCTACAGTTC[A/G]GCTTGAGGGGAGACT | 10616 |
rs770255844 | snp | C/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:422115 | TAACTCTTTTCCCCT[C/T]CCCTCCCCTAGGGAG | 10616 |
rs770273534 | snp | C/T | | | intron-variant, utr-variant-3-prime | RBCK1 | GRCh38.p7 | 20:420349 | GAGTGCTCCCCATTC[C/T]GATCTCACCCCTGGC | 10616 |
rs770302308 | snp | C/G | 6.21214e-05 | 0.00557287 | missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:419685 | CCGACGAGGAGGAGC[C/G]AGCGCGCCTGGCGGG | 10616 |
rs770331676 | snp | C/G | 5.34602e-05 | 0.00516984 | missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:419451 | GGGCAGCCAGATGCA[C/G]TGCCTGAGCCCCCAC | 10616 |
rs770335016 | snp | A/G | | | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:408714 | GAGGTAGCATTTCCC[A/G]GGAGGCACGGTCCCC | 10616 |
rs770342689 | snp | C/T | 2.54982e-05 | 0.0035705 | intron-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:408830 | GTGGGAAGTGGGCCC[C/T]GCAGGACCTGGCCTT | 10616 |
rs770384791 | snp | A/G | 3.47844e-05 | 0.00417025 | intron-variant, missense | RBCK1 | GRCh38.p7 | 20:410516 | TAAAGAGCATAGCTC[A/G]AAAATTGTACACACT | 10616 |
rs770388757 | snp | C/T | | | upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:407857 | GGGCGCGCTCCTAAC[C/T]CGTCCCCAGCGGCTC | 10616 |
rs770403336 | in-del | -/ATTCAGCTAGA | 1.75987e-05 | 0.00296631 | intron-variant, utr-variant-3-prime | RBCK1 | GRCh38.p7 | 20:410610 | CTGTATAGCCAAGAT[-/ATTCAGCTAGA]ATTCAGGGGTTCGCT | 10616 |
rs770406471 | snp | C/T | 1.65482e-05 | 0.00287643 | intron-variant | RBCK1 | GRCh38.p7 | 20:428614 | GGACAGGGCCGAGGC[C/T]TAGGGATTTTAAGTT | 10616 |
rs770435109 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:430895 | TTGAAAGCACAGCCC[A/G]TCAGGTCCGGCTCTG | 10616 |
rs770513754 | snp | A/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:428657 | TGGGGGCTGGGGGCT[A/T]CCCAGTAAGGGCTGT | 10616 |
rs770514108 | in-del | -/C | | | intron-variant | RBCK1 | GRCh38.p7 | 20:416007 | CCCAAACACCTCCCA[-/C]CAGGCCTCACCTTCA | 10616 |
rs770516014 | snp | A/G | 2.34442e-05 | 0.00342367 | intron-variant | RBCK1 | GRCh38.p7 | 20:419540 | CCCAGTCGGGCTCAC[A/G]GCACCCTCTGCTCCC | 10616 |
rs770571017 | snp | C/T | 5.23473e-05 | 0.00511575 | intron-variant, utr-variant-3-prime | RBCK1 | GRCh38.p7 | 20:410573 | ACTGATTCCCACAGC[C/T]ACAGTTCAGCTTGAG | 10616 |
rs770634114 | in-del | -/C | | | intron-variant | RBCK1 | GRCh38.p7 | 20:419885 | CACCTGGCTGTGACC[-/C]TGCACCTGGCTGTGA | 10616 |
rs770707896 | in-del | -/TT | | | intron-variant | RBCK1 | GRCh38.p7 | 20:425627 | TTGCATGGTGTATTC[-/TT]TTTTTTTTTTTTTTT | 10616 |
rs770729985 | snp | C/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:426086 | TATTTTTTATTTTTG[C/T]GGGTACATAGTTGGT | 10616 |
rs770760430 | snp | A/G | 1.65968e-05 | 0.00288065 | synonymous-codon, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:422235 | GGAGAGGGAGATCAA[A/G]GCGGTAAGGCCTCAG | 10616 |
rs770767944 | in-del | -/AGC | 0.000519953 | 0.0161154 | intron-variant, cds-indel, nc-transcript-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:420875 | CGTGTGCCCAGCGGA[-/AGC]AGCAGCAGCAGGAGG | 10616 |
rs770815337 | snp | A/G | 1.65982e-05 | 0.00288077 | missense, synonymous-codon, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:417830 | CTCCCATGGGGTGCG[A/G]CAGAATGGGGACAGT | 10616 |
rs770866712 | snp | A/G | 1.92636e-05 | 0.00310345 | intron-variant | RBCK1 | GRCh38.p7 | 20:417935 | GATGCTGGAAGGTGA[A/G]GCTCTGCCCTGAGCA | 10616 |
rs770910595 | snp | A/T | 1.73135e-05 | 0.00294218 | intron-variant, missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:409853 | AATAAACCCTGTGCT[A/T]ACTGGCTCCTGCTGT | 10616 |
rs770973545 | snp | A/G | 4.97665e-05 | 0.00498806 | missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:430368 | CCAGGAGACACCAGC[A/G]GGGGCTGCCGCTGCA | 10616 |
rs771012579 | snp | C/T | 1.799e-05 | 0.00299911 | intron-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:429133 | TGGAGAGGGTGCCCT[C/T]GTGGGCTTTGCCTTA | 10616 |
rs771183032 | snp | A/G | 0.000175392 | 0.00936298 | intron-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:420824 | TTCGGGGTCTGACCC[A/G]CCCCCGAGGCCCTGA | 10616 |
rs771238122 | snp | C/G | 1.71064e-05 | 0.00292454 | intron-variant, synonymous-codon, nc-transcript-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:420963 | GCCCGCCGAGTGCCC[C/G]GTGTGCTACTCGGTG | 10616 |
rs771323030 | snp | C/T | 6.37261e-05 | 0.00564437 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:408720 | GCATTTCCCAGGAGG[C/T]ACGGTCCCCCCCAGG | 10616 |
rs771360977 | snp | C/T | 2.11329e-05 | 0.00325054 | missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:428542 | GAGGACCTGGCCCTG[C/T]GGGCTCAGAACGATG | 10616 |
rs771379970 | snp | C/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:411391 | TTTTTCTTTGAGATG[C/G]GAGTCTCACTCTGTC | 10616 |
rs771450771 | in-del | -/G | 2.01114e-05 | 0.00317101 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:408733 | GCACGGTCCCCCCCA[-/G]GGGGGATGGGCACAG | 10616 |
rs771475938 | snp | C/G | 1.67273e-05 | 0.00289195 | intron-variant | RBCK1 | GRCh38.p7 | 20:427526 | CCCCCCACCTAGTCA[C/G]TGTCATCTTGCCTGG | 10616 |
rs771489690 | snp | C/T | 1.6628e-05 | 0.00288335 | intron-variant | RBCK1 | GRCh38.p7 | 20:417696 | CTCTCTCCTCTGGCC[C/T]TCCCTTCCCACTCTC | 10616 |
rs771565452 | snp | C/T | | | upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:407235 | TTGAGTGGAATGAGG[C/T]AGGGGCAGGGCAGTC | 10616 |
rs771656345 | in-del | -/CA | | | utr-variant-3-prime, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:430873 | CCAGGAAGGAGACTG[-/CA]CAGTTTTGAAAGCAC | 10616 |
rs771658713 | snp | A/G | 2.21437e-05 | 0.00332737 | missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:428528 | GCAAGGAGTATCAGG[A/G]GGACCTGGCCCTGCG | 10616 |
rs771665704 | snp | G/T | | | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:408529 | CGGACCTGTCTCGGC[G/T]CCCGCTGCCCTCTCA | 10616 |
rs771753077 | snp | A/C | 1.68846e-05 | 0.00290552 | stop-gained, missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:419357 | CACAGATCTGGGCTT[A/C]AAGGACCTCACGCTG | 10616 |
rs771777007 | snp | C/T | | | intron-variant, utr-variant-3-prime | RBCK1 | GRCh38.p7 | 20:420584 | CCTTCCGTGGCTACC[C/T]GGCCGGCCTCCCCTC | 10616 |
rs771779681 | in-del | -/T | 0.000229509 | 0.0107099 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:408724 | TCCCAGGAGGCACGG[-/T]TCCCCCCCAGGGGGA | 10616 |
rs771819021 | snp | C/T | 1.65477e-05 | 0.00287638 | synonymous-codon, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:430391 | CCGCTGCAGGGTAAA[C/T]GGGATTCCTTGCCAC | 10616 |
rs771854201 | snp | A/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:415693 | TATTAGACCACTCTA[A/G]CATTGCTACAAAGAA | 10616 |
rs771863730 | snp | G/T | 1.73993e-05 | 0.00294947 | intron-variant, missense | RBCK1 | GRCh38.p7 | 20:410498 | CACCCCTCCACACTC[G/T]TCTAAAGAGCATAGC | 10616 |
rs771919744 | snp | A/G | | | intron-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:410979 | TTTTAGAACATTTTC[A/G]TCATCCTGTAAAGAA | 10616 |
rs771925464 | snp | A/G | 1.69856e-05 | 0.00291419 | synonymous-codon, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:422127 | CCTCCCCTCCCCTAG[A/G]GAGTGCCTGCAGGGC | 10616 |
rs771998529 | snp | G/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:426961 | CTCCCAAGCAGCTGG[G/T]ACTACAGGTGTGAGC | 10616 |
rs772007051 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:431004 | GAGGAAATGAATGTC[C/G]TGGCCTGGGACTCTA | 10616 |
rs772059478 | snp | A/C | 1.74178e-05 | 0.00295103 | intron-variant, missense | RBCK1 | GRCh38.p7 | 20:410559 | TCCTGTGGACCAGAA[A/C]TGATTCCCACAGCTA | 10616 |
rs772107907 | snp | A/G | 1.65872e-05 | 0.00287981 | utr-variant-5-prime, intron-variant, missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:409928 | GTGGCGGGCGGGGAT[A/G]AACAGGTGGCAATGA | 10616 |
rs772116091 | snp | A/G | 7.02469e-05 | 0.00592609 | synonymous-codon, missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:419699 | CGAGCGCGCCTGGCG[A/G]GCGAGGAGGAGGCGC | 10616 |
rs772294784 | snp | A/G | 1.70502e-05 | 0.00291972 | missense, nc-transcript-variant, utr-variant-3-prime | RBCK1 | GRCh38.p7 | 20:429038 | GACTGGATCCGCTGC[A/G]CCGTCTGCCACACCG | 10616 |
rs772376156 | snp | C/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:422637 | GAGTTCCAGACCAAC[C/T]TGGGCAACATGGCAA | 10616 |
rs772386160 | snp | C/G | 1.77574e-05 | 0.00297966 | intron-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:429124 | GTGGTGGTGTGGAGA[C/G]GGTGCCCTTGTGGGC | 10616 |
rs772407882 | snp | A/G | 3.31181e-05 | 0.00406914 | utr-variant-5-prime, missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:417585 | TCTGGCTCACAGTGC[A/G]CCCTGATATGACAGT | 10616 |
rs772467629 | snp | A/C | | | intron-variant | RBCK1 | GRCh38.p7 | 20:410127 | CTGGCTTCAGGAGGC[A/C]TGGCTTCTAACCCTA | 10616 |
rs772526815 | snp | G/T | 1.66971e-05 | 0.00288934 | intron-variant | RBCK1 | GRCh38.p7 | 20:417495 | GGACCCCTGGCCAGA[G/T]CCCATGCTGAGCCCC | 10616 |
rs772546224 | snp | A/T | 2.15329e-05 | 0.00328116 | missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:428534 | AGTATCAGGAGGACC[A/T]GGCCCTGCGGGCTCA | 10616 |
rs772730205 | snp | C/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:418283 | TTAACTTCTGAAATG[C/T]TTCAGACCTACAGAA | 10616 |
rs772796019 | snp | A/G | 3.37815e-05 | 0.0041097 | missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:419359 | CAGATCTGGGCTTCA[A/G]GGACCTCACGCTGCA | 10616 |
rs772823151 | snp | C/T | 0.000117557 | 0.00766582 | intron-variant, missense, utr-variant-5-prime, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:417266 | GAGGTCAGGGAGGTG[C/T]CAGATCATGGAGGCC | 10616 |
rs772851007 | in-del | -/A | | | intron-variant | RBCK1 | GRCh38.p7 | 20:415368 | GTGAGACCCTGTCTC[-/A]AAAAAAAACAAAAAC | 10616 |
rs772853220 | snp | C/T | 5.4776e-05 | 0.00523307 | intron-variant | RBCK1 | GRCh38.p7 | 20:410393 | TTGTTTCTCTCACCA[C/T]TCTGCCATTCATTCC | 10616 |
rs772910589 | snp | A/G | 1.65449e-05 | 0.00287614 | missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:430393 | GCTGCAGGGTAAATG[A/G]GATTCCTTGCCACCC | 10616 |
rs773000565 | snp | C/G | 3.38771e-05 | 0.00411551 | missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:422132 | CCTCCCCTAGGGAGT[C/G]CCTGCAGGGCACCAT | 10616 |
rs773053894 | snp | A/G | 1.73942e-05 | 0.00294903 | intron-variant, missense | RBCK1 | GRCh38.p7 | 20:410507 | ACACTCTTCTAAAGA[A/G]CATAGCTCAAAAATT | 10616 |
rs773087121 | snp | C/G | 1.65894e-05 | 0.00288 | intron-variant | RBCK1 | GRCh38.p7 | 20:417729 | TCTCTTTGCCCCCAC[C/G]AGGTTTTTCTGGACT | 10616 |
rs773247812 | snp | A/C | 3.31708e-05 | 0.00407238 | utr-variant-5-prime, intron-variant, missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:409929 | TGGCGGGCGGGGATG[A/C]ACAGGTGGCAATGAA | 10616 |
rs773313826 | snp | C/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:414375 | CATGATCATGCCTGA[C/G]TGACAAGGTGAAACC | 10616 |
rs773426974 | snp | A/G | 1.66852e-05 | 0.0028883 | intron-variant | RBCK1 | GRCh38.p7 | 20:417499 | CCCTGGCCAGAGCCC[A/G]TGCTGAGCCCCTGCT | 10616 |
rs773433863 | in-del | -/GG | | | intron-variant | RBCK1 | GRCh38.p7 | 20:413653 | TGTGGACCACAACAT[-/GG]GGGGGGAATCTCAGG | 10616 |
rs773437115 | snp | A/C | 0.000159859 | 0.00893891 | synonymous-codon, missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:419709 | TGGCGGGCGAGGAGG[A/C]GGCGCTGCGTCAGTA | 10616 |
rs773490697 | snp | G/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:421343 | TCAGCCTCGCTGTGG[G/T]CATCTGCCAGTTTCT | 10616 |
rs773550251 | snp | A/G | 7.93997e-05 | 0.00630028 | intron-variant, missense, utr-variant-5-prime, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:417317 | GATTCTAAGAGTAGC[A/G]TGGAGCCATTGGAGG | 10616 |
rs773582638 | snp | A/T | 1.95635e-05 | 0.00312752 | utr-variant-5-prime, missense, nc-transcript-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:408758 | GCACAGCCACGCCAG[A/T]TGGACGAGAAGACCA | 10616 |
rs773666900 | snp | C/T | | | upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:407640 | CAACGAAAAGACAGA[C/T]GGTGACCGCTGAGAG | 10616 |
rs773801372 | snp | C/T | | | intron-variant, utr-variant-3-prime | RBCK1 | GRCh38.p7 | 20:410697 | GAGACTTAAACTCAA[C/T]GCTGAAACACTTTGC | 10616 |
rs773805974 | snp | A/G | 1.67503e-05 | 0.00289393 | intron-variant | RBCK1 | GRCh38.p7 | 20:427531 | CACCTAGTCACTGTC[A/G]TCTTGCCTGGAGCTC | 10616 |
rs773881698 | snp | A/C | | | intron-variant | RBCK1 | GRCh38.p7 | 20:419206 | GGATGCCCACTTGGC[A/C]AGATGGAAGCTGGAG | 10616 |
rs773934109 | snp | A/G | 6.61748e-05 | 0.00575178 | utr-variant-5-prime, intron-variant, missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:409971 | GGCTGGCAGAGCAAC[A/G]GGTGCCCCTGAGTGT | 10616 |
rs773938926 | snp | C/T | | | upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:406091 | AGGATTACAGATGTC[C/T]GCCACCACACCTGGC | 10616 |
rs773953891 | snp | A/G | 1.64768e-05 | 0.00287021 | synonymous-codon, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:427432 | ATGGTGCTTCTTTGA[A/G]GATGATGTCAATGAG | 10616 |
rs774006712 | snp | A/T | 1.67019e-05 | 0.00288975 | intron-variant | RBCK1 | GRCh38.p7 | 20:427521 | GGACTCCCCCCACCT[A/T]GTCACTGTCATCTTG | 10616 |
rs774063569 | snp | C/G | 7.27061e-05 | 0.00602891 | intron-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:429143 | GCCCTTGTGGGCTTT[C/G]CCTTAGAGGAGGGCT | 10616 |
rs774223329 | snp | G/T | 0.000102886 | 0.00717164 | intron-variant, missense, nc-transcript-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:420977 | CCGTGTGCTACTCGG[G/T]GCTGGCGCCCGGCGA | 10616 |
rs774461310 | in-del | -/A | 4.96676e-05 | 0.00498311 | splice-donor-variant | RBCK1 | GRCh38.p7 | 20:427494 | CCTGCTCTGCAAGGT[-/A]GGGGCCTGCAGGGAC | 10616 |
rs774464341 | snp | C/T | 6.6368e-05 | 0.00576017 | synonymous-codon, missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:417828 | CACTCCCATGGGGTG[C/T]GGCAGAATGGGGACA | 10616 |
rs774507518 | snp | A/G | 5.11749e-05 | 0.00505814 | missense, nc-transcript-variant, utr-variant-3-prime | RBCK1 | GRCh38.p7 | 20:429033 | GCTGCGACTGGATCC[A/G]CTGCACCGTCTGCCA | 10616 |
rs774508721 | snp | C/G | 7.98324e-05 | 0.00631742 | intron-variant, missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:428936 | GCCCCAGGGCCAGCA[C/G]CTGCCCCACTCCAGG | 10616 |
rs774520733 | in-del | -/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:425628 | TGCATGGTGTATTCT[-/T]TTTTTTTTTTTTTTT | 10616 |
rs774526046 | snp | A/T | 6.66245e-05 | 0.00577129 | missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:419694 | AGGAGCGAGCGCGCC[A/T]GGCGGGCGAGGAGGA | 10616 |
rs774579373 | snp | A/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:415704 | TCTAGCATTGCTACA[A/G]AGAAATATCTGAGAC | 10616 |
rs774714482 | snp | A/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:421429 | CCACAGCGGACCCTT[A/G]TGGAGCCGCCCCTGG | 10616 |
rs774877187 | snp | A/G | 1.65872e-05 | 0.00287981 | intron-variant | RBCK1 | GRCh38.p7 | 20:422250 | GGCGGTAAGGCCTCA[A/G]GGTGGGAGACATACC | 10616 |
rs774953797 | snp | C/T | 3.51685e-05 | 0.00419321 | intron-variant, synonymous-codon, utr-variant-5-prime, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:417286 | TCATGGAGGCCCTCG[C/T]GTGCTGCCACGAGTT | 10616 |
rs774963165 | snp | C/T | | | intron-variant, synonymous-codon, splice-donor-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:421008 | GGCCGTGGTGCTGCG[C/T]GAGTGTCTGCACACC | 10616 |
rs775013342 | snp | C/T | | | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:408534 | CTGTCTCGGCGCCCG[C/T]TGCCCTCTCACCGCC | 10616 |
rs775234853 | snp | A/G | 1.91635e-05 | 0.00309538 | intron-variant | RBCK1 | GRCh38.p7 | 20:410064 | AACCCAAGGGACAGC[A/G]GGACAGGATATTCTT | 10616 |
rs775281966 | snp | C/G | 1.64795e-05 | 0.00287045 | missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:427377 | TTGCTGAAAACCGCA[C/G]TGCCTTCAGCTACCA | 10616 |
rs775299786 | snp | A/G | 1.65433e-05 | 0.002876 | utr-variant-5-prime, intron-variant, missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:409952 | GCAATGAAGTGTGCC[A/G]TCTGGCTGGCAGAGC | 10616 |
rs775361272 | snp | A/G | | | intron-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:411174 | CTTAGGATCGTTTTC[A/G]AGATTCATCCATGTT | 10616 |
rs775370317 | in-del | -/AAC | 0.000124945 | 0.00790298 | intron-variant | RBCK1 | GRCh38.p7 | 20:417192 | TCTTAGCACGTAGTT[-/AAC]AACAACTTCTGGTGG | 10616 |
rs775470439 | snp | A/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:422639 | GTTCCAGACCAACCT[A/G]GGCAACATGGCAAAA | 10616 |
rs775476361 | snp | G/T | 1.70142e-05 | 0.00291664 | missense, nc-transcript-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:429044 | ATCCGCTGCACCGTC[G/T]GCCACACCGAGATCT | 10616 |
rs775621312 | snp | C/T | 1.71808e-05 | 0.00293089 | intron-variant | RBCK1 | GRCh38.p7 | 20:422113 | CCTAACTCTTTTCCC[C/T]TCCCCTCCCCTAGGG | 10616 |
rs775656819 | snp | C/T | 4.36805e-05 | 0.00467315 | intron-variant | RBCK1 | GRCh38.p7 | 20:428911 | CAGGCTGGGTGACTG[C/T]CCCAGCCCCGCCCCA | 10616 |
rs775672608 | snp | C/T | 1.66167e-05 | 0.00288237 | intron-variant | RBCK1 | GRCh38.p7 | 20:417707 | GGCCCTCCCTTCCCA[C/T]TCTCCCTCTCTTTGC | 10616 |
rs775755546 | snp | A/G | 2.1376e-05 | 0.00326918 | missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:428554 | CTGCGGGCTCAGAAC[A/G]ATGTGGCTGCCCGGC | 10616 |
rs775784249 | snp | A/G | 1.79819e-05 | 0.00299844 | missense, synonymous-codon, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:419468 | GCCTGAGCCCCCACC[A/G]GTAAGCTGTCCTTGG | 10616 |
rs775798243 | snp | A/G | 1.98679e-05 | 0.00315175 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:408738 | GGTCCCCCCCAGGGG[A/G]ATGGGCACAGCCACG | 10616 |
rs775839800 | snp | C/T | 3.34947e-05 | 0.00409221 | missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:419601 | TCATCAACAAGCCCA[C/T]GCGGCCTGGCTGTGA | 10616 |
rs775930866 | snp | C/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:411804 | GTGTGAGCCACCATG[C/T]CCAACCAGAACTTTA | 10616 |
rs776037039 | snp | A/G | 5.23501e-05 | 0.00511589 | intron-variant, utr-variant-3-prime | RBCK1 | GRCh38.p7 | 20:410574 | CTGATTCCCACAGCT[A/G]CAGTTCAGCTTGAGG | 10616 |
rs776039775 | snp | A/G | 1.75072e-05 | 0.00295859 | intron-variant, utr-variant-3-prime | RBCK1 | GRCh38.p7 | 20:410593 | TTCAGCTTGAGGGGA[A/G]ACTGTATAGCCAAGA | 10616 |
rs776087537 | in-del | -/C | 1.65886e-05 | 0.00287993 | intron-variant | RBCK1 | GRCh38.p7 | 20:422264 | AGGGTGGGAGACATA[-/C]CCCAAGTCCCAACTC | 10616 |
rs776253021 | snp | A/G | 3.29832e-05 | 0.00406085 | missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:427338 | CTGAGGATTACCAGC[A/G]ATTTCTAGACCTGGG | 10616 |
rs776512085 | snp | A/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:417186 | AAATAGTCTTAGCAC[A/G]TAGTTAACAACAACT | 10616 |
rs776605379 | snp | G/T | 1.72484e-05 | 0.00293665 | intron-variant, missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:409857 | AACCCTGTGCTAACT[G/T]GCTCCTGCTGTACTG | 10616 |
rs776616165 | snp | A/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:411970 | CAACTTTTTGTGTGG[A/G]CACGTTTTCATTTCT | 10616 |
rs776625184 | snp | A/C | | | intron-variant | RBCK1 | GRCh38.p7 | 20:422845 | TCAAAAAAAGAAAAA[A/C]AAAATTAGTCAGGGA | 10616 |
rs776715261 | snp | C/G | 1.65822e-05 | 0.00287938 | synonymous-codon, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:430370 | AGGAGACACCAGCGG[C/G]GGCTGCCGCTGCAGG | 10616 |
rs776732477 | snp | C/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:424452 | CCCCCTGCCTCTCTC[C/T]TATGCCCCTATTTCT | 10616 |
rs776804827 | snp | A/C/G | 0.000338639 | 0.0130079 | intron-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:420835 | ACCCGCCCCCGAGGC[A/C/G]CTGACCCGCCCCGTG | 10616 |
rs776856644 | snp | C/G/T | 0.000104302 | 0.00722083 | intron-variant, missense, synonymous-codon, nc-transcript-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:420969 | CGAGTGCCCCGTGTG[C/G/T]TACTCGGTGCTGGCG | 10616 |
rs776856738 | snp | A/C | 1.66771e-05 | 0.00288761 | intron-variant | RBCK1 | GRCh38.p7 | 20:417507 | AGAGCCCATGCTGAG[A/C]CCCTGCTGTTCTCTG | 10616 |
rs776899738 | snp | G/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:412937 | TCTTACATTTAGGTC[G/T]TTGGTCCATTTTGAT | 10616 |
rs776939371 | snp | C/T | 0.000361337 | 0.0134364 | intron-variant | RBCK1 | GRCh38.p7 | 20:428449 | CCCAGCTTCTTAACC[C/T]CCTGAGGAACCTTCT | 10616 |
rs776994199 | snp | A/G | 2.10604e-05 | 0.00324496 | missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:428545 | GACCTGGCCCTGCGG[A/G]CTCAGAACGATGTGG | 10616 |
rs777052574 | snp | C/T | 1.65564e-05 | 0.00287714 | utr-variant-5-prime, synonymous-codon, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:417607 | TATGACAGTGGCGTC[C/T]CTCAAGGACATGGTG | 10616 |
rs777077565 | snp | A/C | 2.02247e-05 | 0.00317993 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:408731 | GAGGCACGGTCCCCC[A/C]CAGGGGGATGGGCAC | 10616 |
rs777146424 | snp | G/T | 2.2089e-05 | 0.00332325 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:408708 | GACCCGGAGGTAGCA[G/T]TTCCCAGGAGGCACG | 10616 |
rs777187545 | in-del | -/G | 2.01114e-05 | 0.00317101 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:408734 | GCACGGTCCCCCCCA[-/G]GGGGATGGGCACAGC | 10616 |
rs777259879 | snp | A/G | 5.35776e-05 | 0.00517551 | synonymous-codon, missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:419457 | CCAGATGCAGTGCCT[A/G]AGCCCCCACCGGTAA | 10616 |
rs777394647 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:430695 | GCCTTGCTGGGTGGA[A/G]CCTCTGTGTGACTCC | 10616 |
rs777410845 | in-del | -/C | 6.63361e-05 | 0.00575879 | utr-variant-3-prime, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:430463 | CACATGCTGACCCAG[-/C]CCCACATCCACATTC | 10616 |
rs777448406 | snp | A/G | | | intron-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:421092 | CGCCAATTACGCAGG[A/G]CTGGACGTGGGTGGG | 10616 |
rs777524842 | in-del | -/CCTGGACAGACACCT | 0.000256148 | 0.0113141 | intron-variant | RBCK1 | GRCh38.p7 | 20:419747 | GTGGGCGGGAAAGTC[-/CCTGGACAGACACCT]GCAGACCGCACGGGG | 10616 |
rs777540489 | snp | A/T | 2.19152e-05 | 0.00331015 | intron-variant | RBCK1 | GRCh38.p7 | 20:419528 | TGCCTCACCCTGCCC[A/T]GTCGGGCTCACAGCA | 10616 |
rs777678371 | snp | A/G | 1.74363e-05 | 0.0029526 | intron-variant, utr-variant-3-prime | RBCK1 | GRCh38.p7 | 20:410568 | CCAGAACTGATTCCC[A/G]CAGCTACAGTTCAGC | 10616 |
rs777689889 | snp | C/T | | | utr-variant-5-prime, synonymous-codon, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:417527 | GCTGTTCTCTGCAGG[C/T]TGTGGGTGAGCGTGG | 10616 |
rs777729381 | snp | A/G | | | upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:407059 | ATGCTGGATACGTGT[A/G]TCTGTGAAATTTCAG | 10616 |
rs777854248 | snp | C/G | 3.48584e-05 | 0.00417468 | missense, synonymous-codon, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:419399 | CCCTCTGGAGCCAGG[C/G]CCCCCAAAGCCCGGG | 10616 |
rs777856382 | snp | C/T | 1.75068e-05 | 0.00295857 | intron-variant | RBCK1 | GRCh38.p7 | 20:410034 | ACATCAGGTGAGGAG[C/T]GCATGGCTGGCCTGA | 10616 |
rs777866641 | snp | C/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:426588 | GTGCCACGTTTTCTT[C/T]ATAGGATACTAGTTT | 10616 |
rs777909927 | snp | A/G | 1.7429e-05 | 0.00295199 | intron-variant, missense | RBCK1 | GRCh38.p7 | 20:410467 | CCATCACATCACAGG[A/G]GGAAGGGAAGAAAGA | 10616 |
rs777946763 | snp | C/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:415445 | GAATTCCTTAAAATC[C/T]GCTAATGCCCTGTTT | 10616 |
rs778086791 | snp | C/T | 1.66363e-05 | 0.00288407 | intron-variant | RBCK1 | GRCh38.p7 | 20:417687 | CTGCTTCCTCTCTCT[C/T]CTCTGGCCCTCCCTT | 10616 |
rs778181987 | snp | C/G | 1.6612e-05 | 0.00288196 | missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:430363 | AGGGCCCAGGAGACA[C/G]CAGCGGGGGCTGCCG | 10616 |
rs778228682 | snp | C/T | 1.6557e-05 | 0.00287719 | utr-variant-5-prime, missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:417600 | GCCCTGATATGACAG[C/T]GGCGTCTCTCAAGGA | 10616 |
rs778259648 | snp | C/T | 0.000111303 | 0.00745916 | intron-variant, missense, nc-transcript-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:420950 | TGCTGAACACGGAGC[C/T]CGCCGAGTGCCCCGT | 10616 |
rs778314809 | snp | A/G | 0.000181077 | 0.00951346 | intron-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:421063 | CACCCCCGGCAATGC[A/G]GCTTAATCAAAGCCG | 10616 |
rs778332884 | snp | A/C/G | 4.99674e-05 | 0.00499816 | synonymous-codon, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:422196 | CTTCATTGACAACAC[A/C/G]TACTCGTGCTCGGGC | 10616 |
rs778362577 | snp | A/G | 3.31268e-05 | 0.00406968 | utr-variant-5-prime, missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:417563 | GCTCAGATGCACACC[A/G]TCACCATCTGGCTCA | 10616 |
rs778466733 | snp | C/G | 2.28762e-05 | 0.00338195 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:408697 | CTCTCCCAGGCGACC[C/G]GGAGGTAGCATTTCC | 10616 |
rs778506636 | snp | C/T | 1.66532e-05 | 0.00288554 | intron-variant | RBCK1 | GRCh38.p7 | 20:417663 | GGGTGAAGGCTCTCC[C/T]TTTCACTCCTGCTTC | 10616 |
rs778573818 | snp | A/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:412352 | TTGAGATGGAGTCTC[A/G]CTCTGTCACCCAAGC | 10616 |
rs778585476 | snp | C/T | | | intron-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:409313 | GGCCAAGGCCCTTAC[C/T]CTTCCTTCCACCTGG | 10616 |
rs778602283 | snp | A/T | 1.74017e-05 | 0.00294967 | intron-variant, missense | RBCK1 | GRCh38.p7 | 20:410494 | AAGACACCCCTCCAC[A/T]CTCTTCTAAAGAGCA | 10616 |
rs778603564 | snp | A/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:421874 | TGCAGGGAGCCCAGC[A/G]AGGAGGCTCCTGGAG | 10616 |
rs778615463 | in-del | -/A | | | intron-variant | RBCK1 | GRCh38.p7 | 20:413919 | AGAGACAAATCACCA[-/A]AAAAAAAAAAAAAAA | 10616 |
rs778692739 | snp | A/G | | | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:408454 | GGCTGGGTGGTGTCC[A/G]GGCGTCCTTTCCCCG | 10616 |
rs778770852 | snp | A/G | 7.04068e-05 | 0.00593283 | missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:428519 | AGATGAACTGCAAGG[A/G]GTATCAGGAGGACCT | 10616 |
rs778815783 | snp | G/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:418594 | AGGATGGTCTCGATC[G/T]CCTGACTTTGTGATC | 10616 |
rs778848038 | snp | A/C | 1.7412e-05 | 0.00295055 | intron-variant, missense | RBCK1 | GRCh38.p7 | 20:410554 | TTAATTCCTGTGGAC[A/C]AGAACTGATTCCCAC | 10616 |
rs778879169 | snp | G/T | 2.03436e-05 | 0.00318926 | intron-variant | RBCK1 | GRCh38.p7 | 20:419513 | TCTGTGCCCCTCCCT[G/T]GCCTCACCCTGCCCA | 10616 |
rs778915066 | in-del | -/A | 1.65825e-05 | 0.00287941 | frameshift-variant, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:417819 | AGACCCTGCACTCCC[-/A]ATGGGGTGCGGCAGA | 10616 |
rs778939051 | snp | A/G | 1.66131e-05 | 0.00288206 | intron-variant | RBCK1 | GRCh38.p7 | 20:427308 | AGGACATGGTGTGTT[A/G]GCAGCTCCTGACCCC | 10616 |
rs778995926 | snp | C/T | 3.63511e-05 | 0.00426312 | synonymous-codon, missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:417918 | CGGGAGCGGCAGCTG[C/T]GGATGCTGGAAGGTG | 10616 |
rs779047290 | snp | C/T | 1.69115e-05 | 0.00290782 | intron-variant | RBCK1 | GRCh38.p7 | 20:419301 | CCCCATGGGTGTGGA[C/T]CAAGTGGGCCGCGTG | 10616 |
rs779070748 | snp | A/C | | | intron-variant | RBCK1 | GRCh38.p7 | 20:416799 | GCCAAGAGTTCAAGA[A/C]CAGCTTTGGCAACAT | 10616 |
rs779179077 | snp | C/G | 1.66518e-05 | 0.00288542 | intron-variant | RBCK1 | GRCh38.p7 | 20:430343 | TTCTCTTCCTCCCAT[C/G]CTCTAGGGCCCAGGA | 10616 |
rs779282200 | snp | A/G | 1.76024e-05 | 0.00296663 | intron-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:429114 | GTCTTTGCTCGTGGT[A/G]GTGTGGAGAGGGTGC | 10616 |
rs779329081 | snp | C/T | 1.68752e-05 | 0.00290471 | utr-variant-5-prime, intron-variant, missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:410013 | CTGAGGTCTCCCCAA[C/T]GCAGGACATCAGGTG | 10616 |
rs779337385 | snp | A/T | 3.75777e-05 | 0.00433445 | intron-variant | RBCK1 | GRCh38.p7 | 20:419822 | GCACTGCCGCGCCTC[A/T]CCGTTACTGCCTTGC | 10616 |
rs779422053 | snp | C/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:426135 | CATGAAATACTTTGA[C/T]ACAGGCATGCAATGC | 10616 |
rs779463535 | snp | C/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:422039 | GACTGAGTGAGGCCC[C/G]TGGGGTCAGGCCTTG | 10616 |
rs779511293 | snp | A/G | 0.000248849 | 0.0111518 | intron-variant | RBCK1 | GRCh38.p7 | 20:419777 | GCAGACCGCACGGGG[A/G]AGGTGTAGGCCAGGA | 10616 |
rs779564413 | snp | C/G | 1.67511e-05 | 0.00289401 | intron-variant | RBCK1 | GRCh38.p7 | 20:417384 | GGGTGGGGCCTACCC[C/G]AGACTGGGGTTTGTG | 10616 |
rs779609253 | snp | A/G | | | intron-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:429458 | CTCAAATTCCCGACC[A/G]CAGGTGATCCACCTG | 10616 |
rs779617514 | snp | C/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:417026 | AAATGAATCCTGCCT[C/T]TAACAGTTATTAGTT | 10616 |
rs779621384 | snp | A/G | 9.93888e-05 | 0.00704872 | utr-variant-5-prime, missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:417560 | GATGCTCAGATGCAC[A/G]CCGTCACCATCTGGC | 10616 |
rs779625863 | in-del | -/AAA | | | utr-variant-3-prime, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:430623 | GGCCAGACTTCTCTC[-/AAA]CCCTGCGGCTCCCAC | 10616 |
rs779658812 | snp | C/T | | | intron-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:409481 | CTTTTTTTTTTTTTC[C/T]TGTTAAACTTGTTCA | 10616 |
rs779748318 | snp | C/T | 3.37183e-05 | 0.00410585 | intron-variant | RBCK1 | GRCh38.p7 | 20:419326 | CGCGTGGAACCACCA[C/T]CCTTTAACCCTCCTC | 10616 |
rs779749591 | multinucleotide-polymorphism | CA/TG | | | intron-variant | RBCK1 | GRCh38.p7 | 20:418571 | GACGGGGTTTCACCG[CA/TG]TTAGCCAGGATGGTC | 10616 |
rs779752735 | snp | C/T | | | intron-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:410886 | TTTATTTATTTATCC[C/T]TACAGTTCGACCATT | 10616 |
rs779832262 | snp | A/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:417089 | GTGCCTCACATTTTT[A/G]TCTGTAAAACAGGGA | 10616 |
rs779920679 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:431060 | TGGGAACTGCATCAG[A/G]AAGTTGACTTGTCAG | 10616 |
rs779993422 | snp | G/T | 7.91108e-05 | 0.00628881 | intron-variant, stop-gained, utr-variant-5-prime, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:417239 | AGGGGAGAGAAGACA[G/T]AAGAGGTTGGAGAGG | 10616 |
rs780027024 | snp | C/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:428425 | ACTCCTGCCCTGCAC[C/G]TCACCTCTCCCAGCT | 10616 |
rs780029397 | snp | C/T | 2.90744e-05 | 0.00381266 | synonymous-codon, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:428499 | GCTACAGGCCATCCA[C/T]GAGCAGATGAACTGC | 10616 |
rs780084492 | snp | A/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:419187 | CCTGACCCTGGGGGA[A/G]CCAGGATGCCCACTT | 10616 |
rs780195821 | snp | C/G | 1.65762e-05 | 0.00287886 | utr-variant-5-prime, synonymous-codon, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:417812 | AGACCAGGAGACCCT[C/G]CACTCCCATGGGGTG | 10616 |
rs780216221 | snp | A/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:424337 | GAAATGACCTTCCCA[A/G]ACTTGGGCACTGTGG | 10616 |
rs780338702 | snp | C/T | | | upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:407592 | AATTAAAGCGGCGCA[C/T]GAGGCAGACGAATGC | 10616 |
rs780378188 | snp | A/G | 1.68923e-05 | 0.00290618 | intron-variant | RBCK1 | GRCh38.p7 | 20:427271 | AGGGTCATATGTCAG[A/G]TGTTCTGAATCCTGA | 10616 |
rs780410784 | in-del | -/TG | | | intron-variant | RBCK1 | GRCh38.p7 | 20:429834 | CTGGCACATACTGAC[-/TG]TGTGATTAGGCTGCC | 10616 |
rs780470011 | snp | A/G | 1.73003e-05 | 0.00294106 | synonymous-codon, nc-transcript-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:429094 | ACGCTGGGGCCCTGG[A/G]GTGAGTCTTTGCTCG | 10616 |
rs780494996 | snp | C/T | 5.14064e-05 | 0.00506957 | synonymous-codon, nc-transcript-variant, utr-variant-3-prime | RBCK1 | GRCh38.p7 | 20:429016 | GGTACAGAAGAAGGA[C/T]GGCTGCGACTGGATC | 10616 |
rs780498965 | snp | G/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:425178 | GCCATGCCCAGCTAA[G/T]TTTTGTATTTTCAGT | 10616 |
rs780585893 | snp | A/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:412627 | CCCGGCTGGGTTTAT[A/G]TTTTTATATTGAGTT | 10616 |
rs780587700 | snp | C/T | 0.000117171 | 0.00765324 | utr-variant-5-prime, intron-variant, missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:409917 | TCACCCGAGCAGTGG[C/T]GGGCGGGGATGAACA | 10616 |
rs780599319 | snp | A/T | 6.17799e-05 | 0.00555753 | missense, synonymous-codon, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:419686 | CGACGAGGAGGAGCG[A/T]GCGCGCCTGGCGGGC | 10616 |
rs780624754 | snp | A/C | | | intron-variant | RBCK1 | GRCh38.p7 | 20:427999 | TGACCCCAAACCTAG[A/C]CAGCCCTACCTGATC | 10616 |
rs780632249 | snp | G/T | | | intron-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:420698 | ACCCCCCATCCCCCA[G/T]CCCCACCCCCATCCC | 10616 |
rs780653781 | snp | G/T | 2.04689e-05 | 0.00319907 | intron-variant | RBCK1 | GRCh38.p7 | 20:419769 | AGACACCTGCAGACC[G/T]CACGGGGGAGGTGTA | 10616 |
rs780685911 | snp | C/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:413723 | GAGGCTCTGGGCAAC[C/T]GGCACCTCTCAGACC | 10616 |
rs780692913 | in-del | -/GACACCTGCAGACCGCACGGGGGAG | | | intron-variant | RBCK1 | GRCh38.p7 | 20:419755 | GAAAGTCCCTGGACA[-/GACACCTGCAGACCGCACGGGGGAG]GTGTAGGCCAGGAAG | 10616 |
rs780837404 | snp | C/T | 1.66751e-05 | 0.00288744 | utr-variant-5-prime, intron-variant, synonymous-codon, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:409906 | GGCCCTGAGCCTCAC[C/T]CGAGCAGTGGCGGGC | 10616 |
rs780840283 | snp | C/G | 5.26524e-05 | 0.00513063 | intron-variant, synonymous-codon, utr-variant-5-prime, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:417280 | GCCAGATCATGGAGG[C/G]CCTCGTGTGCTGCCA | 10616 |
rs780849786 | snp | C/G | 8.95776e-05 | 0.00669185 | intron-variant | RBCK1 | GRCh38.p7 | 20:417371 | AAGGAAGAAGCATGG[C/G]TGGGGCCTACCCCAG | 10616 |
rs780854072 | snp | C/T | 1.64953e-05 | 0.00287182 | stop-gained, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:427337 | CCTGAGGATTACCAG[C/T]GATTTCTAGACCTGG | 10616 |
rs780896940 | in-del | -/AA | | | upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:406708 | GTGAAACTCCATCTC[-/AA]AAAAAAAAAAAAAAA | 10616 |
rs780911649 | in-del | -/TGTT | 1.6617e-05 | 0.00288239 | utr-variant-3-prime, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:430478 | CCCACATCCACATTC[-/TGTT]TGTTAGAATGTAGCT | 10616 |
rs780979452 | snp | A/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:429584 | TGACTATTTTGTGAC[A/G]TGAAAATTACATGAA | 10616 |
rs781160269 | snp | A/C | 1.65899e-05 | 0.00288005 | utr-variant-3-prime, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:430468 | GCTGACCCAGCCCCA[A/C]ATCCACATTCTGTTA | 10616 |
rs781249541 | snp | A/T | 1.66618e-05 | 0.00288628 | intron-variant | RBCK1 | GRCh38.p7 | 20:427510 | GGGGCCTGCAGGGAC[A/T]CCCCCCACCTAGTCA | 10616 |
rs781330081 | snp | A/C | 1.74057e-05 | 0.00295001 | intron-variant, synonymous-codon | RBCK1 | GRCh38.p7 | 20:410487 | GGGAAGAAAGACACC[A/C]CTCCACACTCTTCTA | 10616 |
rs781348179 | snp | G/T | | | upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:406822 | AAAAATTATCCCAGA[G/T]GAAGGTCTGAGGTTC | 10616 |
rs781409115 | in-del | -/T | 0.000105502 | 0.00726222 | intron-variant, frameshift-variant, nc-transcript-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:420966 | GCCGAGTGCCCCGTG[-/T]TGCTACTCGGTGCTG | 10616 |
rs781465884 | snp | A/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:426534 | AAATGGCAGGATTGC[A/G]TTCTTTTTTGTGGCC | 10616 |
rs781592121 | snp | C/T | 0.000116534 | 0.00763238 | missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:422201 | TTGACAACACCTACT[C/T]GTGCTCGGGCAAGCT | 10616 |
rs781623894 | snp | A/G | 3.5113e-05 | 0.0041899 | intron-variant | RBCK1 | GRCh38.p7 | 20:422093 | GTGAAGGGGGTTCCT[A/G]TGATCCTAACTCTTT | 10616 |
rs781666908 | snp | C/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:410328 | ACAAATTTGATGGCA[C/G]GGAGTCCAGATAGGG | 10616 |
rs781667012 | snp | G/T | 1.66228e-05 | 0.0028829 | intron-variant | RBCK1 | GRCh38.p7 | 20:417697 | TCTCTCCTCTGGCCC[G/T]CCCTTCCCACTCTCC | 10616 |
rs781693914 | snp | C/T | 4.88914e-05 | 0.00494402 | intron-variant | RBCK1 | GRCh38.p7 | 20:428631 | AGGGATTTTAAGTTC[C/T]GGGATCCAGGTGGGG | 10616 |
rs781737460 | snp | A/G | 0.000232434 | 0.0107779 | intron-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:408814 | GGCTGGGGAACTTCC[A/G]GTGGGAAGTGGGCCC | 10616 |
rs796096279 | in-del | -/TTTTTTTTTTTTTTTTTTT | | | intron-variant | RBCK1 | GRCh38.p7 | 20:426817 | TTACTTTTCTTTTCC[-/TTTTTTTTTTTTTTTTTTT]TTTTTTTTTAGCTAG | 10616 |
rs796170470 | snp | C/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:427822 | AGTCCATAGACTTGG[C/T]CTCTGACCAAACCTG | 10616 |
rs796177243 | snp | C/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:418445 | ACAATCTCGGCTCAC[C/T]GCAAGCTCCGACTCC | 10616 |
rs796229921 | snp | A/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:423831 | TGGTGGGTCAGCCGC[A/G]GTGGCCTGGTTTATA | 10616 |
rs796666596 | snp | C/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:417053 | AGTTGCTTAGTTTGG[C/G]AGAGTCACTGGAACC | 10616 |
rs796794713 | in-del | -/AGTC | | | intron-variant | RBCK1 | GRCh38.p7 | 20:422852 | AAGAAAAAAAAAATT[-/AGTC]AGGGAACTCTGGAGC | 10616 |
rs796963770 | snp | A/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:427001 | GGTTATTTTATTTTT[A/T]AAAAAAATTTTTTGG | 10616 |
rs797004868 | snp | A/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:416301 | GCTGGGACTACAGGC[A/G]CCCGCCACCGTGCCT | 10616 |