SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs7059 | snp | C/T | 0.492153 | 0.0621426 | intron-variant, synonymous-codon | RBCK1 | GRCh38.p7 | 20:410526 | AGCTCAAAAATTGTA[C/T]ACACTTCTTCCGTTA | 10616 |
rs959093 | snp | A/G | 0.306679 | 0.24349 | intron-variant | RBCK1 | GRCh38.p7 | 20:419117 | GGAAGGGCTGGTGTT[A/G]TGCTGGGTTTTGAAG | 10616 |
rs1040755 | snp | A/T | 0.147991 | 0.228242 | intron-variant | RBCK1 | GRCh38.p7 | 20:427609 | TGACATGTAGCTCTA[A/T]GTCATGACCAGCAGG | 10616 |
rs1045368 | snp | A/C | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:430722 | CTCCATACTCCTCCC[A/C]CCACAACACTCATCT | 10616 |
rs1045374 | snp | C/T | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:430755 | CAAACACCAAGCACT[C/T]TCAGCCTCCCCGCCT | 10616 |
rs1045378 | snp | C/T | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:430786 | TCAGCTGTCAGCTTT[C/T]TGGGGCTAACTTCTC | 10616 |
rs1045395 | snp | C/T | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:430908 | CCGTCAGGTCCGGCT[C/T]TGCGTCTCCCTCTCT | 10616 |
rs1047188 | snp | A/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:414105 | ACAAAAAAAAAAAAG[A/G]AAAATCCCTGGGAAA | 10616 |
rs1063146 | snp | A/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:414104 | TACAAAAAAAAAAAA[A/G]AAAAATCCCTGGGAA | 10616 |
rs1129387 | snp | C/T | 0.483272 | 0.0899109 | intron-variant | RBCK1 | GRCh38.p7 | 20:414317 | TTTGAGAGGCTGAGA[C/T]GAGAGGATTATTAGA | 10616 |
rs1358782 | snp | C/T | 0.278399 | 0.248382 | intron-variant | RBCK1 | GRCh38.p7 | 20:413334 | aatccctaccaaaat[C/T]cccagttgttgttgt | 10616 |
rs2057251 | snp | C/T | 0.449726 | 0.150364 | intron-variant | RBCK1 | GRCh38.p7 | 20:422066 | TCACTGGGGACTCCA[C/T]CCCTCACATGGCAAG | 10616 |
rs2273462 | snp | A/G | 0.141934 | 0.225437 | intron-variant | RBCK1 | GRCh38.p7 | 20:428652 | CCAGGTGGGGGCTGG[A/G]GGCTTCCCAGTAAGG | 10616 |
rs2281553 | snp | G/T | 0.00133947 | 0.0258446 | missense, synonymous-codon, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:419713 | GGGCGAGGAGGAGGC[G/T]CTGCGTCAGTACCAG | 10616 |
rs2295493 | snp | A/G | 0.198324 | 0.244601 | intron-variant | RBCK1 | GRCh38.p7 | 20:421796 | GGATTTGTTCTGGGT[A/G]GGATGGGAGTCACTG | 10616 |
rs2295494 | snp | C/T | 0.391583 | 0.206044 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:431129 | GACCTTTCTACCAGA[C/T]GTGGACCCCATGCCC | 10616 |
rs2295495 | snp | A/G | 0.460477 | 0.134905 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:431198 | CAGGACAGGTGGAGT[A/G]TGCAGTGTGTCAAGT | 10616 |
rs2316404 | snp | A/G | 0.47666 | 0.105476 | intron-variant | RBCK1 | GRCh38.p7 | 20:418579 | ttcaccgtgttagcc[A/G]ggatggtctcgatct | 10616 |
rs2316405 | snp | C/T | 0.487995 | 0.0765403 | intron-variant | RBCK1 | GRCh38.p7 | 20:418603 | tcgatctcctgactt[C/T]gtgatccgcccgcct | 10616 |
rs3050691 | snp | A/G | | | upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:406732 | aaaaaaaaaaaaaaa[A/G]GGCTTCCCCAGGCCA | 10616 |
rs3746792 | snp | C/T | 0.49834 | 0.0287645 | intron-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:408812 | GTGGCTGGGGAACTT[C/T]CGGTGGGAAGTGGGC | 10616 |
rs3787563 | snp | C/T | 0.49949 | 0.0159663 | intron-variant | RBCK1 | GRCh38.p7 | 20:424272 | GGGACTCCATTTCCT[C/T]ATCTGAAAAGTGGAC | 10616 |
rs3838059 | in-del | -/C | 0.494976 | 0.0498674 | intron-variant | RBCK1 | GRCh38.p7 | 20:424413 | CACAAAACACATACA[-/C]CAGACCTCCTCTTTA | 10616 |
rs4061743 | snp | C/T | 0.489434 | 0.0719116 | intron-variant | RBCK1 | GRCh38.p7 | 20:418601 | tctcgatctcctgac[C/T]ttgtgatccgcccgc | 10616 |
rs4331586 | snp | A/C | 0.0588605 | 0.161139 | intron-variant, utr-variant-3-prime | RBCK1 | GRCh38.p7 | 20:420540 | CGGCCCCCTTCCTTA[A/C]CTTGCTGCCATTGCT | 10616 |
rs4635591 | snp | A/T | 0.431029 | 0.17242 | intron-variant, utr-variant-3-prime | RBCK1 | GRCh38.p7 | 20:420561 | TGCCATTGCTGTCTC[A/T]CCTGGCGCCTTCCGT | 10616 |
rs4815582 | snp | G/T | 0 | 0 | upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:406835 | GATGAAGGTCTGAGG[G/T]TCattccttcattca | 10616 |
rs4815585 | snp | C/T | 0.44546 | 0.155869 | intron-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:409237 | TGTCCTCAGTCACCC[C/T]GCCATGCTCACTCTA | 10616 |
rs4815586 | snp | C/T | 0.438246 | 0.16451 | intron-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:409340 | CTGGACCACTCTTCC[C/T]CACTGGAGCTTGACA | 10616 |
rs6037593 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | RBCK1 | GRCh38.p7 | 20:413004 | ttcattcttttgcac[A/G]tggatattgagttgt | 10616 |
rs6037611 | snp | C/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:419902 | GCACCTGGCTGTGAC[C/T]TGCCCTCTCTCAAAG | 10616 |
rs6037624 | snp | C/T | 0.0640965 | 0.167152 | intron-variant | RBCK1 | GRCh38.p7 | 20:428648 | GGATCCAGGTGGGGG[C/T]TGGGGGCTTCCCAGT | 10616 |
rs6051833 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:410920 | agtatacagttcaat[A/G]gcttttagtatattc | 10616 |
rs6051879 | snp | C/G | 0.233235 | 0.249437 | intron-variant | RBCK1 | GRCh38.p7 | 20:418153 | ACTCCGTCCAGGCTC[C/G]GGCATTCCCAGCTGT | 10616 |
rs6051883 | snp | A/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:418639 | tcccaaagtgctggg[A/G]ttacaggcgtgagcc | 10616 |
rs6051889 | snp | A/G | 0.15665 | 0.231917 | intron-variant | RBCK1 | GRCh38.p7 | 20:419863 | CATGCTGCTGGCAGT[A/G]ACCCTGCACCTGGCT | 10616 |
rs6051899 | snp | A/G | 0.452719 | 0.146304 | intron-variant | RBCK1 | GRCh38.p7 | 20:421409 | GGGGAACACAGACCC[A/G]CTCACCACAGCGGAC | 10616 |
rs6051900 | snp | C/T | 0.484701 | 0.0861117 | intron-variant | RBCK1 | GRCh38.p7 | 20:421527 | TCGCTGGTTGATGTC[C/T]TTGTGAATTGTGTCA | 10616 |
rs6051905 | snp | C/G | 0.443717 | 0.158031 | intron-variant | RBCK1 | GRCh38.p7 | 20:422277 | TACCCCAAGTCCCAA[C/G]TCCTAAGGAACTGGG | 10616 |
rs6051908 | snp | G/T | 0.436408 | 0.16659 | intron-variant | RBCK1 | GRCh38.p7 | 20:423009 | tgtgtatagaattca[G/T]agtagtacATccagg | 10616 |
rs6051934 | snp | C/T | 0.0763149 | 0.179815 | intron-variant | RBCK1 | GRCh38.p7 | 20:425414 | AACAAATGTAACTCT[C/T]GTAACCACCAACCAC | 10616 |
rs6051935 | snp | C/T | 0.48 | 0.0979796 | intron-variant | RBCK1 | GRCh38.p7 | 20:425626 | TTTGCATGGTGTATT[C/T]TTTTTTTTTTTTTTT | 10616 |
rs6051936 | snp | A/G | 0.259674 | 0.249813 | intron-variant | RBCK1 | GRCh38.p7 | 20:425915 | CAGGCGTGATCCATC[A/G]TTCCTGGCTGGTGCA | 10616 |
rs6051939 | snp | C/T | 0.121717 | 0.214577 | intron-variant | RBCK1 | GRCh38.p7 | 20:426090 | ttttatttttgcggg[C/T]acatagttggtgtat | 10616 |
rs6051941 | snp | C/T | 0.26271 | 0.249677 | intron-variant | RBCK1 | GRCh38.p7 | 20:426232 | AATCCAGTTAACCTC[C/T]CTTAGTTATTATAAA | 10616 |
rs6051942 | snp | C/T | 0.197393 | 0.244402 | intron-variant | RBCK1 | GRCh38.p7 | 20:426415 | TTAGTTCAGTTGTTT[C/T]GATTTTTAGCACCTG | 10616 |
rs6051943 | snp | G/T | 0.0718919 | 0.175435 | intron-variant | RBCK1 | GRCh38.p7 | 20:426464 | TAATGTTTGTTTGTC[G/T]GTGCCTGGCTTATTT | 10616 |
rs6051946 | snp | C/G | 0 | 0 | intron-variant | RBCK1 | GRCh38.p7 | 20:426897 | gtgcatcagtcatgg[C/G]tcactgcatccttga | 10616 |
rs6051947 | snp | G/T | 0.225597 | 0.248806 | intron-variant | RBCK1 | GRCh38.p7 | 20:426906 | tcatggctcactgca[G/T]ccttgaccttctggg | 10616 |
rs6051948 | snp | G/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:426970 | agctgggactacagg[G/T]gtgagcaccacacct | 10616 |
rs6051951 | snp | C/G | 0 | 0 | intron-variant | RBCK1 | GRCh38.p7 | 20:427592 | GGGAGCTGTGACACT[C/G]GCCTGCTGGTCATGA | 10616 |
rs6051953 | snp | A/G | 0.276534 | 0.248588 | intron-variant | RBCK1 | GRCh38.p7 | 20:428007 | AACCTAGACAGCCCT[A/G]CCTGATCCTTCCCCC | 10616 |
rs6051957 | snp | C/T | 0.199564 | 0.24486 | intron-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:429158 | GCCTTAGAGGagggc[C/T]gggaaaactacagcc | 10616 |
rs6051967 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:431250 | GGGGCGGGAGGGGAA[A/G]TCTTGCCACTCCTGC | 10616 |
rs6076510 | snp | A/G | 0.463018 | 0.130857 | upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:407083 | atttcagatggagta[A/G]ctagggaagattttt | 10616 |
rs6076530 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:426765 | catccacctccagaa[C/G/T]ttttAGAAATTCCCC | 10616 |
rs6084349 | snp | A/G | 0.480618 | 0.0965156 | upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:407113 | TGGGTAAAGACCAAA[A/G]TAAAGGGAAGGAGGG | 10616 |
rs6084373 | snp | A/C | 0.479502 | 0.0991411 | intron-variant | RBCK1 | GRCh38.p7 | 20:413941 | AAAAAAAAAAGATTA[A/C]CACTTTTGGGTGAGA | 10616 |
rs6084401 | snp | G/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:423051 | attcctgtaatccca[G/T]cgctttgggaggcca | 10616 |
rs6084402 | snp | G/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:423270 | cgccattgcactcca[G/T]cctgggcaaccagag | 10616 |
rs6084417 | snp | A/G | 0 | 0 | intron-variant | RBCK1 | GRCh38.p7 | 20:430196 | TGGGAGCCCAGAAAA[A/G]GCCTCAGTGACTCTC | 10616 |
rs6084418 | snp | A/G | 0 | 0 | intron-variant | RBCK1 | GRCh38.p7 | 20:430226 | CCATCAGGTAGCTGA[A/G]GCTGACCAGGCCATT | 10616 |
rs6107288 | snp | C/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:414371 | gagccatgatcatgc[C/T]tgagtgacaaggtga | 10616 |
rs6107294 | snp | A/G | 0.49753 | 0.0350569 | intron-variant | RBCK1 | GRCh38.p7 | 20:418658 | caggcgtgagccacc[A/G]cgcccaacccacatt | 10616 |
rs6107298 | snp | C/T | 0.0479149 | 0.147179 | intron-variant | RBCK1 | GRCh38.p7 | 20:423017 | GAATTCATAGTAGTA[C/T]ATccaggcgcagtgg | 10616 |
rs6107299 | snp | C/T | 0.0475351 | 0.146656 | intron-variant | RBCK1 | GRCh38.p7 | 20:423070 | tttgggaggccaagg[C/T]gggtggatcacctga | 10616 |
rs6107300 | snp | C/T | 0.0475351 | 0.146656 | intron-variant | RBCK1 | GRCh38.p7 | 20:423089 | tggatcacctgaggt[C/T]gggaattcgagatca | 10616 |
rs6107302 | snp | A/G | 0.496245 | 0.0431677 | intron-variant | RBCK1 | GRCh38.p7 | 20:423705 | tgggtatctgcaggg[A/G]tcttggaaccaattc | 10616 |
rs6107303 | snp | C/T | 0.480302 | 0.0972668 | intron-variant | RBCK1 | GRCh38.p7 | 20:423763 | tgggctggacttacc[C/T]ggatggttcttctgg | 10616 |
rs6107317 | snp | G/T | 0.0463947 | 0.145069 | utr-variant-3-prime, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:430647 | CTCCCACCTCTGCCT[G/T]ACCCCAGCCTTAAAC | 10616 |
rs6115874 | snp | G/T | 0.0111196 | 0.0737302 | intron-variant | RBCK1 | GRCh38.p7 | 20:412159 | ttgttgtttatcttt[G/T]tgattatagccatcc | 10616 |
rs6115888 | snp | A/C/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:414434 | CCATTGGCTGTACAC[A/C/T]TAGAGACTGGCCAGT | 10616 |
rs6115898 | snp | C/T | 0.47934 | 0.0995154 | intron-variant | RBCK1 | GRCh38.p7 | 20:415178 | CCCATGAGTTCAAAA[C/T]CAGCCTGGGCAACAT | 10616 |
rs6115906 | snp | C/T | 0.294394 | 0.246027 | intron-variant, missense, utr-variant-5-prime, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:417284 | GATCATGGAGGCCCT[C/T]GTGTGCTGCCACGAG | 10616 |
rs6115910 | snp | A/G | 0.040671 | 0.13668 | intron-variant | RBCK1 | GRCh38.p7 | 20:418818 | ttttcttacattact[A/G]ggtataacaatccaa | 10616 |
rs6115915 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | RBCK1 | GRCh38.p7 | 20:419024 | gatgtttcctccgga[A/G]tggatcaagtcactg | 10616 |
rs6115916 | snp | A/G | 0.0337553 | 0.125452 | intron-variant | RBCK1 | GRCh38.p7 | 20:419124 | CTGGTGTTGTGCTGG[A/G]TTTTGAAGCTCAAAG | 10616 |
rs6115919 | snp | C/G | 0.093777 | 0.195178 | intron-variant, utr-variant-3-prime | RBCK1 | GRCh38.p7 | 20:420239 | CTGGACCCTCGCTGC[C/G]CCCTAGGGGGATGAC | 10616 |
rs6115931 | snp | A/T | 0.0310518 | 0.120672 | intron-variant | RBCK1 | GRCh38.p7 | 20:423304 | aactccgtctgaaaa[A/T]aTATATATATATATT | 10616 |
rs6133035 | snp | A/G | 0.462144 | 0.132269 | upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:407171 | ggtgcaaaggcctta[A/G]ggcgggagtgtgtct | 10616 |
rs6139097 | snp | A/G | 0.0240402 | 0.106968 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:408557 | TCACCGCCCCACGCA[A/G]GATCCCGGCCTGGTC | 10616 |
rs6139104 | snp | A/T | 0.19646 | 0.2442 | intron-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:409666 | TGGGAAGGACAAACA[A/T]CCAAATGAGCCTAGT | 10616 |
rs6139108 | snp | A/G | 0 | 0 | intron-variant | RBCK1 | GRCh38.p7 | 20:410267 | aggTGTACTGTATTA[A/G]GATGTTAGGCCTTAT | 10616 |
rs6139109 | snp | C/T | 0.259609 | 0.249815 | intron-variant | RBCK1 | GRCh38.p7 | 20:410381 | CAGAGGCTCATATTG[C/T]TTCTCTCACCATTCT | 10616 |
rs6139113 | snp | C/T | 0.344147 | 0.231595 | intron-variant | RBCK1 | GRCh38.p7 | 20:411639 | cccaatgtgctggga[C/T]tacaggcgtgagcca | 10616 |
rs6139114 | snp | C/G | 0.186737 | 0.241863 | intron-variant | RBCK1 | GRCh38.p7 | 20:411691 | taatttttagaaagt[C/G]tgtagagataaggtc | 10616 |
rs6139116 | snp | A/G | 0.263535 | 0.249633 | intron-variant | RBCK1 | GRCh38.p7 | 20:412130 | tagtttctccacatc[A/G]tctctaatacttgtt | 10616 |
rs6139126 | snp | A/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:415088 | gtcttcaaaaaatta[A/G]gacttggcggggcac | 10616 |
rs6139131 | snp | G/T | | | utr-variant-5-prime, missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:417553 | CGTGGAGGATGCTCA[G/T]ATGCACACCGTCACC | 10616 |
rs6139134 | snp | C/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:418624 | ccgcccgcctcggcc[C/T]cccaaagtgctggga | 10616 |
rs6139146 | snp | A/C | 0 | 0 | intron-variant | RBCK1 | GRCh38.p7 | 20:424621 | GTCTCTGGGTGGTTG[A/C]TGAGGCTCCTTCGCT | 10616 |
rs6139147 | snp | C/T | 0 | 0 | intron-variant | RBCK1 | GRCh38.p7 | 20:424652 | CTGGCCTGGAGAGAC[C/T]TCATGACCAGTCATT | 10616 |
rs7265211 | snp | A/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:418571 | gacggggtttcaccg[A/T]gttagccaggatggt | 10616 |
rs7267656 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | RBCK1 | GRCh38.p7 | 20:412925 | tatggttttagctct[C/T]acatttaggtctttg | 10616 |
rs7354339 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RBCK1 | GRCh38.p7 | 20:421294 | CCCTTCCCCTCTACC[C/T]TTCGCCGCCCGGGCT | 10616 |
rs8116493 | snp | G/T | 0.172674 | 0.237741 | intron-variant | RBCK1 | GRCh38.p7 | 20:416334 | ctaattttttttttt[G/T]tatttttagtagaga | 10616 |
rs8123007 | snp | C/G | 0.120674 | 0.21395 | intron-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:409607 | GTAGAAGCTCAATAA[C/G]TGCTTGTTGGATAAA | 10616 |
rs10611249 | in-del | -/AAT | 0.255503 | 0.249939 | intron-variant, utr-variant-3-prime | RBCK1 | GRCh38.p7 | 20:410738 | GCGTGTTATGCACTC[-/AAT]AATAAACATTAGTGT | 10616 |
rs10706664 | in-del | -/A | 0.481087 | 0.0953875 | intron-variant | RBCK1 | GRCh38.p7 | 20:413918 | AAGAGACAAATCACC[-/A]AAAAAAAAAAAAAAA | 10616 |
rs11473908 | in-del | -/AAAC | | | intron-variant | RBCK1 | GRCh38.p7 | 20:415380 | CTCAAAAAAAACAAA[-/AAAC]AACAAACAAAACCCC | 10616 |
rs11475730 | in-del | -/T | 0.341235 | 0.232758 | intron-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:409467 | GGATCGCAATCTGAC[-/T]TTTTTTTTTTTTCTT | 10616 |
rs11477386 | in-del | -/A | 0 | 0 | intron-variant | RBCK1 | GRCh38.p7 | 20:413935 | AAAAAAAAAAAAAAA[-/A]GATTACCACTTTTGG | 10616 |
rs11480357 | in-del | -/G | 0.496746 | 0.040204 | intron-variant, utr-variant-3-prime | RBCK1 | GRCh38.p7 | 20:420465 | CACCCCTGACGTTGA[-/G]GTGGCTCCACCAGCC | 10616 |
rs11481454 | in-del | -/A | 0 | 0 | intron-variant | RBCK1 | GRCh38.p7 | 20:414091 | TACAAAAAAAAAAAA[-/A]GAAAAATCCCTGGGA | 10616 |
rs11482134 | in-del | -/A | 0.198324 | 0.244601 | upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:407013 | ATAGATGCTGAGAAG[-/A]AAAAAATGAAGCCAG | 10616 |
rs11484235 | in-del | -/C | 0.181978 | 0.240568 | intron-variant | RBCK1 | GRCh38.p7 | 20:413804 | GTTGTATGTGTTATT[-/C]GGTAATAACATAGTT | 10616 |
rs11697052 | snp | A/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:418876 | tggtatccagtctac[A/G]gatcttactcagatt | 10616 |
rs11697821 | snp | C/T | 0.444444 | 0.157135 | intron-variant | RBCK1 | GRCh38.p7 | 20:426746 | gttgtgcaaccatca[C/T]caccatccacctcca | 10616 |
rs11698154 | snp | G/T | 0.244437 | 0.249938 | intron-variant | RBCK1 | GRCh38.p7 | 20:417634 | GGTGAGTGAGGAGGC[G/T]GAGGGCGACACTGGG | 10616 |
rs11905546 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant | RBCK1 | GRCh38.p7 | 20:424303 | AGTTGGGCTTGATTC[A/T]TGGTTTTCAAACTGC | 10616 |
rs11906374 | snp | A/G | 0.45235 | 0.146814 | intron-variant | RBCK1 | GRCh38.p7 | 20:422548 | AAGAATCAGGGACTC[A/G]GCTGGGCGTGGCAGC | 10616 |
rs11906780 | snp | C/T | 0.040671 | 0.13668 | utr-variant-3-prime, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:430598 | CCTTTGTCCTTCCCT[C/T]GGGGCTTGCCGGCCA | 10616 |
rs12625895 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RBCK1 | GRCh38.p7 | 20:426151 | acaggcatgcaatgc[A/G]taataatcacatcat | 10616 |
rs28570506 | snp | A/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:414255 | GTCTCTGCAAAAAAT[A/T]AAAAAAATTAGCCAG | 10616 |
rs34279807 | in-del | -/A | | | utr-variant-3-prime, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:430846 | TGGAACTCTTGCTAA[-/A]CCTGTTCAGAGCCAG | 10616 |
rs34324154 | in-del | -/G | | | utr-variant-3-prime, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:430961 | TTAAAATGGTTTTCC[-/G]GGGAAGGGATGAGTG | 10616 |
rs34892054 | snp | C/T | 0.467439 | 0.123371 | upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:407872 | CCGTCCCCAGCGGCT[C/T]GACGCTGTGGATCCC | 10616 |
rs35073025 | snp | A/C | 0.443598 | 0.158176 | intron-variant, utr-variant-3-prime | RBCK1 | GRCh38.p7 | 20:420228 | GAGAGCCTGGCCTGG[A/C]CCCTCGCTGCGCCCT | 10616 |
rs35467583 | in-del | -/A | 0.434976 | 0.168179 | intron-variant | RBCK1 | GRCh38.p7 | 20:422515 | CCACATCTATGAAGG[-/A]AGGACAGCAGAGTTG | 10616 |
rs35786105 | in-del | -/A | | | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:408278 | CCCCCTCCCAGTCCC[-/A]GCCCCACTTCCGGGG | 10616 |
rs36085908 | in-del | -/G | | | intron-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:411069 | TAGGCAACCACTAAT[-/G]CTACTTTTTATCTCT | 10616 |
rs41279374 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RBCK1 | GRCh38.p7 | 20:430254 | ATTCTTGCAGGAGGA[A/C]CTGCAGAGGCAAAGG | 10616 |
rs41279378 | snp | C/T | 0.0883596 | 0.190715 | utr-variant-3-prime, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:430675 | AACATAGCCCCTGGC[C/T]AGAGGCCTTGCTGGG | 10616 |
rs41279380 | snp | C/G | 0.0659589 | 0.169201 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:431083 | CTTGTCAGTCCATCT[C/G]TGGTAGAATGAGGCT | 10616 |
rs41279382 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:431089 | AGTCCATCTGTGGTA[A/G]AATGAGGCTGTGACT | 10616 |
rs41281892 | snp | A/G | 0.069667 | 0.173147 | utr-variant-5-prime, intron-variant, synonymous-codon, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:410002 | GCAACTGAAGCCTGA[A/G]GTCTCCCCAACGCAG | 10616 |
rs41306771 | snp | A/G | 0.0383715 | 0.133092 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:408636 | CACAGGGCTTGGGCC[A/G]CGCCGGAGGCCACAC | 10616 |
rs55844958 | snp | A/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:414230 | AGCCTGGGCAACATA[A/G]TGAGACCTTGTCTCT | 10616 |
rs56003619 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | RBCK1 | GRCh38.p7 | 20:428724 | GCTGTCACTCCCATC[C/T]GGAGGTGGGACTTAG | 10616 |
rs56140233 | snp | G/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:416312 | AGGCGCCCGCCACCG[G/T]GCCTGGCTAATTTTT | 10616 |
rs56173827 | in-del | -/CAAA | 0 | 0 | intron-variant | RBCK1 | GRCh38.p7 | 20:415390 | ACAAAAACAAACAAA[-/CAAA]ACCCCTCAATACTAT | 10616 |
rs56367061 | snp | A/G | 0.244776 | 0.249945 | intron-variant | RBCK1 | GRCh38.p7 | 20:415512 | AATTGGTTTCTTCAA[A/G]TCAGGAGCCAAACAA | 10616 |
rs56980394 | in-del | -/AAAAAAAAAAAG/AAAAAAAAAG/G | | | upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:406732 | AAAAAAAAAAAAAAA[-/AAAAAAAAAAAG/AAAAAAAAAG/G]GGCTTCCCCAGGCCA | 10616 |
rs57454310 | snp | A/G | 0.287085 | 0.247234 | intron-variant | RBCK1 | GRCh38.p7 | 20:419185 | ACCCTGACCCTGGGG[A/G]AGCCAGGATGCCCAC | 10616 |
rs57957698 | snp | C/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:428702 | GGAGGCTCTGACCTC[C/T]CTTCTGGCTGTCACT | 10616 |
rs58002794 | snp | A/C | 0.0126979 | 0.078662 | intron-variant | RBCK1 | GRCh38.p7 | 20:425158 | TGGGACTAGAGGCGC[A/C]CACCGCCATGCCCAG | 10616 |
rs59905706 | snp | C/T | 0.149665 | 0.228982 | intron-variant | RBCK1 | GRCh38.p7 | 20:423253 | GTGGTGAACTGAGAT[C/T]GCGCCATTGCACTCC | 10616 |
rs60153029 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:409740 | GGGACTTTTAGTCTG[A/G]GTGCTGAAGGATACG | 10616 |
rs60232959 | in-del | -/G | | | upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:406733 | AAAAAAAAAAAAAAG[-/G]GGCTTCCCCAGGCCA | 10616 |
rs60540117 | snp | C/T | 0.0452528 | 0.143452 | intron-variant | RBCK1 | GRCh38.p7 | 20:429605 | ATTACATGAAATCCA[C/T]GTTTCAGTGTCCGTA | 10616 |
rs60590164 | in-del | -/T | 0.262435 | 0.249691 | intron-variant | RBCK1 | GRCh38.p7 | 20:426307 | TTACTCTATTTTTTT[-/T]GTACCAATTTGCCAT | 10616 |
rs60715867 | snp | C/T | 0.297382 | 0.245469 | intron-variant, utr-variant-3-prime | RBCK1 | GRCh38.p7 | 20:420472 | TGACGTTGAGTGGCT[C/T]CACCAGCCCTGGCCC | 10616 |
rs61202599 | in-del | -/T/TTTT | | | intron-variant | RBCK1 | GRCh38.p7 | 20:425644 | TTTTTTTTTTTTTTT[-/T/TTTT]GAGACGAAGTCTCAC | 10616 |
rs62189969 | snp | C/T | 0.5 | 0 | intron-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:429390 | CGCCACCACGCCCGG[C/T]TAGTTTTGTATTTTT | 10616 |
rs62191446 | snp | A/C | | | intron-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:408986 | TGGGCTGGCTCTGTG[A/C]TGAGATGGGGCTAGG | 10616 |
rs62191448 | snp | C/T | 0.00911815 | 0.0669024 | intron-variant | RBCK1 | GRCh38.p7 | 20:417955 | TGCCCTGAGCACCGC[C/T]GGACCCAGCGGGGGC | 10616 |
rs62191449 | snp | A/G | 0.5 | 0 | intron-variant | RBCK1 | GRCh38.p7 | 20:421514 | GAGAATCGGATAATC[A/G]CTGGTTGATGTCTTT | 10616 |
rs66583727 | in-del | -/TTTT | | | intron-variant | RBCK1 | GRCh38.p7 | 20:425641 | TTTTTTTTTTTTTTT[-/TTTT]TTTGAGACGAAGTCT | 10616 |
rs67040509 | snp | C/T | 0.238749 | 0.249747 | intron-variant | RBCK1 | GRCh38.p7 | 20:412091 | TGCACCATTTTACAT[C/T]CCCACCAGCATATAT | 10616 |
rs67470622 | in-del | -/GTGACCCTGCACCTGGCT | 0.499563 | 0.0147699 | intron-variant | RBCK1 | GRCh38.p7 | 20:419861 | ACCATGCTGCTGGCA[-/GTGACCCTGCACCTGGCT]GTGACCCTGCACCTG | 10616 |
rs67707964 | in-del | -/TG | 0.5 | 0 | intron-variant | RBCK1 | GRCh38.p7 | 20:417396 | CCCCAGACTGGGGTT[-/TG]TGTGTGTGTGTGTGT | 10616 |
rs71191941 | in-del | -/G | 0 | 0 | upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:407966 | CCGCCCCCGGCCCCG[-/G]CCCCGCCCCCCGGCC | 10616 |
rs71191942 | in-del | -/T | 0.48692 | 0.0798058 | intron-variant | RBCK1 | GRCh38.p7 | 20:425627 | TTGCATGGTGTATTC[-/T]TTTTTTTTTTTTTTT | 10616 |
rs73567130 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | RBCK1 | GRCh38.p7 | 20:414473 | ATTTATAGTATGTAA[A/G]TTAAAATTAAGTGTT | 10616 |
rs73567132 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | RBCK1 | GRCh38.p7 | 20:418035 | TTTTAGTCAGGGACT[C/T]ACCCAGAGGACCCTA | 10616 |
rs73567137 | snp | A/C | 0.0501905 | 0.150254 | intron-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:421098 | TTACGCAGGGCTGGA[A/C]GTGGGTGGGGCCCTG | 10616 |
rs73567142 | snp | A/C | 0.0260105 | 0.111035 | intron-variant | RBCK1 | GRCh38.p7 | 20:423803 | GGCCTCGCTGATTTC[A/C]CCTGGGCCTGGCTGG | 10616 |
rs73567145 | snp | A/G | 0.0596104 | 0.162024 | intron-variant | RBCK1 | GRCh38.p7 | 20:426267 | ACAATTAAATTATTG[A/G]CTACAGTCTGTTGTG | 10616 |
rs73567146 | snp | C/T | 0.0433465 | 0.140692 | intron-variant | RBCK1 | GRCh38.p7 | 20:427965 | TACCACGTCTCCACC[C/T]GTGTCCTCAACTGAG | 10616 |
rs73611629 | in-del | -/C | | | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:408057 | CCGCCCACCCCGCCT[-/C]GCGGCCCAGCTCCTT | 10616 |
rs73891999 | snp | G/T | 0.0126979 | 0.078662 | intron-variant | RBCK1 | GRCh38.p7 | 20:417450 | GCCTGTGTGCAAATA[G/T]GTACATGTCTGTAGC | 10616 |
rs74271564 | snp | A/G | 0.183886 | 0.241099 | intron-variant | RBCK1 | GRCh38.p7 | 20:424934 | AGAGCAGAAATCAGA[A/G]AGAAAATCACCCACA | 10616 |
rs74666838 | snp | G/T | 0.5 | 0 | intron-variant | RBCK1 | GRCh38.p7 | 20:412339 | TCTTTTTTTTTTTTT[G/T]AGATGGAGTCTCGCT | 10616 |
rs74798178 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RBCK1 | GRCh38.p7 | 20:410320 | TGACGTAAACAAATT[C/T]GATGGCAGGGAGTCC | 10616 |
rs75697241 | snp | A/G | 0.029116 | 0.117091 | utr-variant-3-prime, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:430904 | CAGCCCGTCAGGTCC[A/G]GCTCTGCGTCTCCCT | 10616 |
rs75905519 | snp | C/T | 0.13446 | 0.221699 | intron-variant | RBCK1 | GRCh38.p7 | 20:424373 | CAGGCCAAAACATGG[C/T]AGCCGAGGCCCAAAT | 10616 |
rs76085570 | snp | C/T | 0.0573587 | 0.15934 | intron-variant | RBCK1 | GRCh38.p7 | 20:418190 | TTGGGCAAGGTTGCT[C/T]CTATCTGCTGCCCAG | 10616 |
rs76101251 | snp | C/G | 0.000590279 | 0.0171695 | intron-variant | RBCK1 | GRCh38.p7 | 20:410371 | CGACAGTCCTCAGAG[C/G]CTCATATTGTTTCTC | 10616 |
rs76201975 | snp | A/C | 0.264358 | 0.249587 | intron-variant | RBCK1 | GRCh38.p7 | 20:411618 | GTGATCCGCCCGCCT[A/C]TGCCTCCCAATGTGC | 10616 |
rs76224515 | snp | A/G | 0.00198749 | 0.031461 | intron-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:429138 | AGGGTGCCCTTGTGG[A/G]CTTTGCCTTAGAGGA | 10616 |
rs76389162 | snp | A/T | 0.5 | 0 | intron-variant | RBCK1 | GRCh38.p7 | 20:411371 | ACCACACCCGGCTAA[A/T]TTTTTTTTTCTTTGA | 10616 |
rs76531088 | snp | A/T | 0.5 | 0 | intron-variant | RBCK1 | GRCh38.p7 | 20:427009 | TATTTTTTAAAAAAA[A/T]TTTTTGGTAGAGATG | 10616 |
rs76627701 | snp | C/T | 0.039522 | 0.134904 | intron-variant | RBCK1 | GRCh38.p7 | 20:421233 | CCCAGGCCCACGGCT[C/T]ATGAGAGAAGCAGCC | 10616 |
rs76741385 | snp | G/T | 0.0452528 | 0.143452 | intron-variant | RBCK1 | GRCh38.p7 | 20:412970 | AATTTTTATATAAGG[G/T]GTGAGGTAAGGGTCC | 10616 |
rs76757362 | snp | A/C | 0.5 | 0 | intron-variant | RBCK1 | GRCh38.p7 | 20:414091 | TCGATGTGGTTCATA[A/C]AAAAAAAAAAAAGAA | 10616 |
rs77078232 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RBCK1 | GRCh38.p7 | 20:425905 | GTTCAGATTACAGGC[A/G]TGATCCATCATTCCT | 10616 |
rs77114706 | snp | A/G | 0.5 | 0 | intron-variant, missense | RBCK1 | GRCh38.p7 | 20:410473 | CATCACAGGAGGAAG[A/G]GAAGAAAGACACCCC | 10616 |
rs77178231 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | RBCK1 | GRCh38.p7 | 20:412224 | GATTTGCAATTTCCT[A/G]ACCATTTGATGACAA | 10616 |
rs77218398 | snp | A/G | 0.0810805 | 0.184299 | intron-variant | RBCK1 | GRCh38.p7 | 20:424935 | GAGCAGAAATCAGAG[A/G]GAAAATCACCCACAA | 10616 |
rs77285019 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:411125 | TATAAGTTGAATCAT[A/G]CAATATGTGGCCTTT | 10616 |
rs77307851 | snp | A/T | 0.5 | 0 | intron-variant | RBCK1 | GRCh38.p7 | 20:416321 | CCACCGTGCCTGGCT[A/T]ATTTTTTTTTTTGTA | 10616 |
rs77359014 | snp | C/T | 0.0195453 | 0.096908 | intron-variant, stop-gained, utr-variant-5-prime, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:417296 | CCTCGTGTGCTGCCA[C/T]GAGTTGATTCTAAGA | 10616 |
rs77493687 | snp | A/C | 0.5 | 0 | intron-variant | RBCK1 | GRCh38.p7 | 20:415379 | GTCTCAAAAAAAACA[A/C]AAACAAACAAAACCC | 10616 |
rs77722296 | snp | A/C | 0.0252325 | 0.109451 | intron-variant | RBCK1 | GRCh38.p7 | 20:418240 | GGGTATGACAGTGAT[A/C]GTGATAACTAGTGTT | 10616 |
rs77771230 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | RBCK1 | GRCh38.p7 | 20:415793 | GCATGGTCCTGACAT[C/T]TGCTTGGCTTCTGGG | 10616 |
rs78102847 | snp | A/G | 0.0648419 | 0.167978 | intron-variant | RBCK1 | GRCh38.p7 | 20:428273 | TCAGGAGGCTGAGGT[A/G]TATTTTGCTGTTAGC | 10616 |
rs78237393 | snp | G/T | 0.14933 | 0.228835 | intron-variant | RBCK1 | GRCh38.p7 | 20:424255 | AGTTGTTTCCCTTCT[G/T]TGGGACTCCATTTCC | 10616 |
rs78728494 | snp | G/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:413748 | CAGACCTGCTGTTGG[G/T]TTCTCATCGATGGAC | 10616 |
rs78934224 | snp | A/T | 0.5 | 0 | intron-variant | RBCK1 | GRCh38.p7 | 20:416323 | ACCGTGCCTGGCTAA[A/T]TTTTTTTTTTGTATT | 10616 |
rs79181474 | snp | C/G | 0.00433601 | 0.0463595 | intron-variant | RBCK1 | GRCh38.p7 | 20:422264 | AGGGTGGGAGACATA[C/G]CCCAAGTCCCAACTC | 10616 |
rs79201923 | snp | A/C | 0.5 | 0 | intron-variant | RBCK1 | GRCh38.p7 | 20:415377 | CTGTCTCAAAAAAAA[A/C]AAAAACAAACAAAAC | 10616 |
rs79556700 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | RBCK1 | GRCh38.p7 | 20:413276 | GTCTCTTGAATTTCC[A/G]TATAAATTTTACGAT | 10616 |
rs79572225 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | RBCK1 | GRCh38.p7 | 20:416931 | GAGGTTGATACTGCA[A/G]TGAGCCAAGGTAGCA | 10616 |
rs79669501 | snp | A/G | 0.0524604 | 0.153226 | intron-variant | RBCK1 | GRCh38.p7 | 20:424634 | TGCTGAGGCTCCTTC[A/G]CTCTGGCCTGGAGAG | 10616 |
rs79845007 | snp | A/C | 0.00844233 | 0.0644197 | intron-variant | RBCK1 | GRCh38.p7 | 20:419520 | CCCTCCCTTGCCTCA[A/C]CCTGCCCAGTCGGGC | 10616 |
rs80055441 | snp | C/G | 0.0596104 | 0.162024 | intron-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:409009 | GGGCTAGGGGACTCG[C/G]AGAGGACACAGGGCA | 10616 |
rs80113867 | snp | G/T | 0 | 0 | intron-variant | RBCK1 | GRCh38.p7 | 20:412337 | TATCTTTTTTTTTTT[G/T]TGAGATGGAGTCTCG | 10616 |
rs80337819 | snp | A/G | 0.0861826 | 0.188849 | intron-variant | RBCK1 | GRCh38.p7 | 20:415822 | GGGAGGCCTCAGTGA[A/G]CTTTTACTGAAGCGG | 10616 |
rs80355598 | snp | A/G | 0.0752113 | 0.178743 | intron-variant | RBCK1 | GRCh38.p7 | 20:419119 | AAGGGCTGGTGTTGT[A/G]CTGGGTTTTGAAGCT | 10616 |
rs111269618 | snp | C/T | 0.0733688 | 0.176922 | intron-variant | RBCK1 | GRCh38.p7 | 20:411277 | GGTGCCATCATCGCT[C/T]ACTACAGCCTCAACT | 10616 |
rs111279117 | snp | A/C | | | intron-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:420686 | CCCCCACCCCCCACC[A/C]CCCATCCCCCAGCCC | 10616 |
rs111283441 | snp | A/C/G | 0.000226835 | 0.0106473 | intron-variant, missense, nc-transcript-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:420921 | GCACGTCCAGCTGGA[A/C/G]CAGAGGAGCCTGGTG | 10616 |
rs111379652 | snp | A/T | 0.5 | 0 | intron-variant | RBCK1 | GRCh38.p7 | 20:418443 | GCACAATCTCGGCTC[A/T]CTGCAAGCTCCGACT | 10616 |
rs111583781 | in-del | -/T | 0.5 | 0 | intron-variant | RBCK1 | GRCh38.p7 | 20:425007 | GTATCTCTGGGCAAA[-/T]TTTTTTTTTTTTTTC | 10616 |
rs111665087 | snp | A/T | 0.0170251 | 0.090679 | intron-variant | RBCK1 | GRCh38.p7 | 20:411792 | CTGGGATTACAGGTG[A/T]GAGCCACCATGCCCA | 10616 |
rs111951407 | snp | A/G | 2.04342e-05 | 0.00319636 | intron-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:408790 | GAAAGGTGGGCACAG[A/G]CTGGAGGTGGCTGGG | 10616 |
rs112001097 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RBCK1 | GRCh38.p7 | 20:421307 | CCTTTCGCCGCCCGG[A/G]CTCCTGCAGCCACGC | 10616 |
rs112086441 | snp | C/T | 0.00061623 | 0.0175424 | intron-variant | RBCK1 | GRCh38.p7 | 20:430340 | CTCTTCTCTTCCTCC[C/T]ATCCTCTAGGGCCCA | 10616 |
rs112094149 | snp | A/C | | | splice-acceptor-variant | RBCK1 | GRCh38.p7 | 20:427311 | ACATGGTGTGTTGGC[A/C]GCTCCTGACCCCTGA | 10616 |
rs112157257 | snp | C/T | 0.120326 | 0.21374 | intron-variant | RBCK1 | GRCh38.p7 | 20:411568 | GAGACGGGGTTTCGC[C/T]GTGTTAACCAGGATG | 10616 |
rs112173604 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant | RBCK1 | GRCh38.p7 | 20:412295 | GGTTTGCCTATTCAG[C/G]TCTTTTGCCCATTTT | 10616 |
rs112270470 | snp | A/C | 0.5 | 0 | intron-variant | RBCK1 | GRCh38.p7 | 20:415378 | TGTCTCAAAAAAAAC[A/C]AAAACAAACAAAACC | 10616 |
rs112275709 | snp | A/G | 0.5 | 0 | intron-variant | RBCK1 | GRCh38.p7 | 20:418503 | CCTCCGGAGTAGCTG[A/G]GACTACAGGCGCCCG | 10616 |
rs112445559 | snp | A/T | 0.0558544 | 0.157504 | intron-variant | RBCK1 | GRCh38.p7 | 20:419878 | GACCCTGCACCTGGC[A/T]GTGACCCTGCACCTG | 10616 |
rs112530501 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | RBCK1 | GRCh38.p7 | 20:425876 | GTGATGCGCCCGCCT[C/T]GGCCTCCCAGAGTGT | 10616 |
rs112623441 | in-del | -/A | 0.5 | 0 | intron-variant | RBCK1 | GRCh38.p7 | 20:421796 | GGATTTGTTCTGGGT[-/A]GGATGGGAGTCACTG | 10616 |
rs112669093 | in-del | -/G | 0 | 0 | intron-variant | RBCK1 | GRCh38.p7 | 20:417397 | CCCAGACTGGGGTTT[-/G]TGTGTGTGTGTGTGT | 10616 |
rs112762527 | snp | C/T | 0.5 | 0 | intron-variant | RBCK1 | GRCh38.p7 | 20:418409 | AGTCTCGCTCTGTCG[C/T]CCAGGCTGGAGTGCA | 10616 |
rs112886032 | in-del | -/A | 0.5 | 0 | intron-variant | RBCK1 | GRCh38.p7 | 20:427001 | GTTATTTTATTTTTT[-/A]AAAAAAATTTTTTGG | 10616 |
rs113051328 | snp | A/G | 0.0528381 | 0.153711 | intron-variant | RBCK1 | GRCh38.p7 | 20:423254 | TGGTGAACTGAGATC[A/G]CGCCATTGCACTCCA | 10616 |
rs113232753 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | RBCK1 | GRCh38.p7 | 20:415240 | AGGCATGGTGGTGCG[C/T]CCATCTAGTCCCAGC | 10616 |
rs113233849 | snp | C/T | 0.5 | 0 | intron-variant | RBCK1 | GRCh38.p7 | 20:421225 | CGCCTTACCCCAGGC[C/T]CACGGCTCATGAGAG | 10616 |
rs113434275 | snp | A/G | | | intron-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:420722 | CCATCCCCCACCCCC[A/G]TCCCCCATCCCCCAT | 10616 |
rs113523442 | snp | A/G | 0.5 | 0 | intron-variant | RBCK1 | GRCh38.p7 | 20:416217 | CTGGAGTGCGGTGGC[A/G]CAATCTTGGCTCACT | 10616 |
rs113524043 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RBCK1 | GRCh38.p7 | 20:415239 | TAGGCATGGTGGTGC[A/G]CCCATCTAGTCCCAG | 10616 |
rs113621551 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:418665 | GAGCCACCACGCCCA[A/G]CCCACATTTGCTTTC | 10616 |
rs113703568 | snp | A/T | 0.039522 | 0.134904 | intron-variant | RBCK1 | GRCh38.p7 | 20:426184 | AGAATGGGGAATCCA[A/T]CCCCTCAAGCATTTA | 10616 |
rs113734762 | snp | A/G | 0.5 | 0 | intron-variant | RBCK1 | GRCh38.p7 | 20:418514 | GCTGGGACTACAGGC[A/G]CCCGCCACCACGCCC | 10616 |
rs113794638 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | RBCK1 | GRCh38.p7 | 20:422890 | TGGCCTGGGTGTGTG[A/G]CCACAAGTCAGATAT | 10616 |
rs113928542 | snp | C/T | 0.5 | 0 | intron-variant | RBCK1 | GRCh38.p7 | 20:417702 | CCTCTGGCCCTCCCT[C/T]CCCACTCTCCCTCTC | 10616 |
rs113981218 | snp | C/T | 0.312593 | 0.242037 | intron-variant | RBCK1 | GRCh38.p7 | 20:422567 | GGGCGTGGCAGCTCA[C/T]ACCTGTAATCCCAGC | 10616 |
rs114111862 | snp | A/G | 0.00795532 | 0.062565 | intron-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:409574 | GATTCCAGTTCCTGG[A/G]ACAGTGGGTGGCACA | 10616 |
rs114263153 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | RBCK1 | GRCh38.p7 | 20:424462 | CTCTCCTATGCCCCT[A/G]TTTCTCCTGAGAATG | 10616 |
rs114551330 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | RBCK1 | GRCh38.p7 | 20:421928 | CCTGGACCAGAGAAT[C/G]AGAGCGGCAGTATGG | 10616 |
rs115383867 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:409634 | TAAATGAATAGAAAT[A/G]TGAGGGACCCTGGGA | 10616 |
rs115654037 | snp | C/T | 0.0178098 | 0.0926698 | utr-variant-3-prime, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:430911 | TCAGGTCCGGCTCTG[C/T]GTCTCCCTCTCTGCA | 10616 |
rs115831273 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | RBCK1 | GRCh38.p7 | 20:426509 | ACCTCCAGTTCTTCC[A/G]TGTTGCTGTAAATGG | 10616 |
rs115981754 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:429512 | ATTACAGGCGTGAGC[C/T]ACCGGGCCGCAAGAA | 10616 |
rs116063345 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | RBCK1 | GRCh38.p7 | 20:411732 | GTCTGGGCTGGTCTT[C/G]AACTTCTGGCTTAAG | 10616 |
rs116134788 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RBCK1 | GRCh38.p7 | 20:416513 | CTTTCTGAATGCAGT[A/G]TTTTCCCAAATCTCT | 10616 |
rs116547788 | snp | A/G/T | 0.0333695 | 0.124785 | intron-variant | RBCK1 | GRCh38.p7 | 20:424821 | GAGTCTCAGAAAATG[A/G/T]TCAAGTGTGACAGAG | 10616 |
rs116638933 | snp | A/G | 0.144296 | 0.226554 | intron-variant | RBCK1 | GRCh38.p7 | 20:426325 | TTTTTGTACCAATTT[A/G]CCATCCCCACTCCCC | 10616 |
rs116690465 | snp | C/T | 0.0569829 | 0.158885 | intron-variant | RBCK1 | GRCh38.p7 | 20:416115 | CCGTTTTTCCTGTAA[C/T]TGGTAGTTAGAGATA | 10616 |
rs116708170 | snp | A/C/T | 0.0150606 | 0.0854603 | intron-variant | RBCK1 | GRCh38.p7 | 20:424234 | GGCTGCTGGTGATCT[A/C/T]GAGCAAGTTGTTTCC | 10616 |
rs116763776 | snp | A/G/T | 0.0189856 | 0.0955633 | intron-variant | RBCK1 | GRCh38.p7 | 20:418660 | GGCGTGAGCCACCAC[A/G/T]CCCAACCCACATTTG | 10616 |
rs116903696 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RBCK1 | GRCh38.p7 | 20:410221 | TTTAAAAATCAGACC[A/G]TAACAGTAGCTATCT | 10616 |
rs116940177 | snp | A/C | 0.030278 | 0.119257 | intron-variant | RBCK1 | GRCh38.p7 | 20:429887 | CCATTTCCTCTGTGA[A/C]ATGGAGATGATAGCT | 10616 |
rs116989964 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RBCK1 | GRCh38.p7 | 20:414550 | CGATCCTGATGTCAC[A/G]TTGGATGAGAGAGCT | 10616 |
rs117232119 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RBCK1 | GRCh38.p7 | 20:425975 | TAAAGAAGTGGGATG[A/G]GTACCAAAGGGTCAG | 10616 |
rs117385292 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | RBCK1 | GRCh38.p7 | 20:413103 | CCATAAATGTGAGTG[C/T]TTATTTCTGGACTCT | 10616 |
rs117541850 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | RBCK1 | GRCh38.p7 | 20:423751 | ATGACTATAATTTGG[G/T]CTGGACTTACCTGGA | 10616 |
rs117693373 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:408951 | GCTTCCAGAGCCATC[A/T]TGGGGCCCTGAGAAC | 10616 |
rs117958154 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | RBCK1 | GRCh38.p7 | 20:430068 | TAGACTTTCAGACAG[C/G]TGGAGGCAGAGGAAA | 10616 |
rs117962695 | snp | C/T | 0.0376037 | 0.131863 | intron-variant | RBCK1 | GRCh38.p7 | 20:415123 | GATGATGCTTGTAAT[C/T]CTAGCACTTTGGGAG | 10616 |
rs137898372 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | RBCK1 | GRCh38.p7 | 20:421774 | CGTGAGCAGCAGTGA[A/G]GAGTTGGGATTTGTT | 10616 |
rs138009555 | snp | C/G | 1.78105e-05 | 0.00298412 | missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:419442 | CCCGGACGGGGGCAG[C/G]CAGATGCAGTGCCTG | 10616 |
rs138026431 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | RBCK1 | GRCh38.p7 | 20:418438 | CAGTGGCACAATCTC[A/G]GCTCACTGCAAGCTC | 10616 |
rs138051141 | in-del | -/CAAA | | | intron-variant | RBCK1 | GRCh38.p7 | 20:415387 | AAAACAAAAACAAAC[-/CAAA]AAAACCCCTCAATAC | 10616 |
rs138189091 | snp | C/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:418305 | CCTACAGAAAAGTTG[C/T]TAAATTTTACAAAGT | 10616 |
rs138309125 | snp | A/G | | | intron-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:409118 | TGTCCCCTGCACCTA[A/G]GGTTGTAGAACGGAA | 10616 |
rs138415318 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | RBCK1 | GRCh38.p7 | 20:428044 | GTCCCCGCCGCTTCA[C/T]CTCAAAAGTTGAAGG | 10616 |
rs138458476 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:431314 | GGCAGGTAGATAGTT[C/G]AAGAAGGAACGAAGC | 10616 |
rs138508164 | snp | A/G | 0.00914312 | 0.0669923 | upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:406799 | AAGGGATGTGTTTCC[A/G]GCAAAAGAAAAATTA | 10616 |
rs138518621 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RBCK1 | GRCh38.p7 | 20:427600 | TGACACTGGCCTGCT[A/G]GTCATGACTTAGAGC | 10616 |
rs138588115 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RBCK1 | GRCh38.p7 | 20:415360 | GTGACAGAAGTGAGA[C/T]CCTGTCTCAAAAAAA | 10616 |
rs138707764 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | RBCK1 | GRCh38.p7 | 20:421724 | AGCAGAGGGATGAAG[C/G]GGGTAATCAGAGCAG | 10616 |
rs138806187 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | RBCK1 | GRCh38.p7 | 20:415193 | CCAGCCTGGGCAACA[C/T]AGTGAAACCTTGTCT | 10616 |
rs138999353 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | RBCK1 | GRCh38.p7 | 20:425067 | CCAGGCTGGAGTGCA[A/G]TGGCGCGATCTCAGC | 10616 |
rs139043551 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RBCK1 | GRCh38.p7 | 20:412987 | TGAGGTAAGGGTCCA[A/G]CTTCATTCTTTTGCA | 10616 |
rs139105921 | snp | A/G | 0.00438332 | 0.0466095 | upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:407519 | GGAGGTGAGGGATGA[A/G]ATTCTGCAAGTGGAG | 10616 |
rs139191851 | snp | A/G/T | 8.37649e-05 | 0.00647122 | missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:417871 | ATCTGCTGTCAGCCC[A/G/T]CAACACCTCCCTCAA | 10616 |
rs139219914 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | RBCK1 | GRCh38.p7 | 20:411365 | TGTACCACCACACCC[A/G]GCTAATTTTTTTTTT | 10616 |
rs139240943 | snp | A/G | 1.66308e-05 | 0.00288359 | missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:422210 | CCTACTCGTGCTCGG[A/G]CAAGCTGCTGGAGAG | 10616 |
rs139315417 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:409802 | CACACACAAAGGATC[A/G]CCTCCTTTCCTACCC | 10616 |
rs139366921 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | RBCK1 | GRCh38.p7 | 20:416710 | ATGTAGATTTAAATC[C/G]TGCCTCTGGCTGAAC | 10616 |
rs139638845 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RBCK1 | GRCh38.p7 | 20:423015 | TAGAATTCATAGTAG[C/T]ACATCCAGGCGCAGT | 10616 |
rs139682969 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RBCK1 | GRCh38.p7 | 20:425290 | TGCTAGGATTACAGG[C/T]GTGAGCCACCGTGCC | 10616 |
rs139871143 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:429515 | ACAGGCGTGAGCCAC[C/T]GGGCCGCAAGAATGT | 10616 |
rs139881961 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:410080 | GGACAGGATATTCTT[A/G]CCTGTAGAACAGTTC | 10616 |
rs139915449 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:412617 | AGCCACTGCACCCGG[C/T]TGGGTTTATGTTTTT | 10616 |
rs140133260 | snp | G/T | 0.00914312 | 0.0669923 | intron-variant | RBCK1 | GRCh38.p7 | 20:422730 | GGTCTGGGATGAGTG[G/T]GCTGAGGTGGGAGGA | 10616 |
rs140276089 | snp | A/C | 0.000333409 | 0.0129071 | utr-variant-5-prime, missense, nc-transcript-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:408749 | GGGGGATGGGCACAG[A/C]CACGCCAGATGGACG | 10616 |
rs140285933 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RBCK1 | GRCh38.p7 | 20:416045 | GGATTACAGTTCAAG[A/G]TAAGATTTGGGCAGG | 10616 |
rs140458333 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RBCK1 | GRCh38.p7 | 20:418325 | TTTTACAAAGTAGTA[C/T]ATAAAGAATTCCCAT | 10616 |
rs140516101 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RBCK1 | GRCh38.p7 | 20:411416 | TCTGTCCCCCAGGCT[A/G]GAGTGCAGTGGCGCG | 10616 |
rs140524808 | snp | A/G | 0.00121433 | 0.0246108 | intron-variant | RBCK1 | GRCh38.p7 | 20:419828 | CCGCGCCTCTCCGTT[A/G]CTGCCTTGCCCCTCC | 10616 |
rs140534156 | snp | A/G | 0.000309952 | 0.0124451 | missense, nc-transcript-variant, synonymous-codon | RBCK1 | GRCh38.p7 | 20:428951 | CCTGCCCCACTCCAG[A/G]TGATGCTGCAGCAGG | 10616 |
rs140623224 | in-del | -/TTG | 0.00557542 | 0.0525036 | intron-variant | RBCK1 | GRCh38.p7 | 20:412141 | CATCATCTCTAATAC[-/TTG]TTGTTGTTTATCTTT | 10616 |
rs140639296 | snp | C/T | 0.00358779 | 0.0422022 | upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:406393 | AGAACAGCAGTTAGA[C/T]TGACAGGTGATGATA | 10616 |
rs140794028 | snp | A/G | 0.00279162 | 0.0372561 | utr-variant-3-prime, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:430484 | ATCCACATTCTGTTA[A/G]AATGTAGCTCAGGGA | 10616 |
rs140820323 | snp | A/G | 0.0248432 | 0.108648 | upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:406092 | GGATTACAGATGTCC[A/G]CCACCACACCTGGCT | 10616 |
rs140934287 | snp | A/T | 0.0267878 | 0.112589 | intron-variant | RBCK1 | GRCh38.p7 | 20:423148 | CTACTAAAAATAGAA[A/T]ATTAGCCGGGTGTGG | 10616 |
rs140948810 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:415109 | GGCGGGGCACGATGG[A/C]TGATGCTTGTAATCC | 10616 |
rs141049851 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:413469 | GAAAAATGAGGAAGT[A/T]AACATACTCATCTTC | 10616 |
rs141075596 | in-del | -/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:424872 | AAGTAATGTAGTGGA[-/G]GGTTGTTTTTACAAA | 10616 |
rs141145396 | in-del | -/G | 0.0154538 | 0.0865337 | intron-variant | RBCK1 | GRCh38.p7 | 20:430273 | CAGAGGCAAAGGCCC[-/G]GGGTGGGAGAGCGCT | 10616 |
rs141226853 | in-del | -/A | 0.167809 | 0.236103 | intron-variant | RBCK1 | GRCh38.p7 | 20:424528 | GTTCTGCCCCTGGGG[-/A]AAAAGGGGGAGGCAG | 10616 |
rs141228657 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:412811 | GTCCAGTTAGTCTAT[A/G]TTTTATTTTGTTGTT | 10616 |
rs141268774 | snp | A/G | 0.181659 | 0.240478 | intron-variant | RBCK1 | GRCh38.p7 | 20:418430 | CTGGAGTGCAGTGGC[A/G]CAATCTCGGCTCACT | 10616 |
rs141273274 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RBCK1 | GRCh38.p7 | 20:423921 | CACCAGCAGGCTGCC[C/T]GGGCCTTCTCATGTC | 10616 |
rs141359971 | in-del | -/A | 0.0532157 | 0.154195 | intron-variant | RBCK1 | GRCh38.p7 | 20:422916 | ATATTTAACCTCTCT[-/A]ATGCCTCTATCTCAT | 10616 |
rs141386874 | snp | C/T | 0.00795532 | 0.062565 | intron-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:409338 | ACCTGGACCACTCTT[C/T]CCCACTGGAGCTTGA | 10616 |
rs141609326 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | RBCK1 | GRCh38.p7 | 20:424235 | GCTGCTGGTGATCTC[A/G]AGCAAGTTGTTTCCC | 10616 |
rs141923181 | snp | A/G | 0.000707489 | 0.0187948 | intron-variant | RBCK1 | GRCh38.p7 | 20:428609 | GGCTGGGACAGGGCC[A/G]AGGCCTAGGGATTTT | 10616 |
rs142047924 | snp | A/G | 0.0193772 | 0.0965046 | upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:406179 | AACTCCTGACCTCAA[A/G]TGATCCGCCCACCTC | 10616 |
rs142222146 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | RBCK1 | GRCh38.p7 | 20:425073 | TGGAGTGCAATGGCG[C/G/T]GATCTCAGCCCACTG | 10616 |
rs142258379 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | RBCK1 | GRCh38.p7 | 20:425764 | CCCGAGTAGCTGGGA[C/T]TACAGGCAGATGCCA | 10616 |
rs142287534 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RBCK1 | GRCh38.p7 | 20:427693 | CCAGCCCCAGCCCCA[A/G]ATGGAGCCTCAAACC | 10616 |
rs142486884 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:407176 | AAAGGCCTTAGGGCG[A/G]GAGTGTGTCTGACTT | 10616 |
rs142636828 | snp | C/T | 1.65622e-05 | 0.00287764 | synonymous-codon, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:430379 | CAGCGGGGGCTGCCG[C/T]TGCAGGGTAAATGGG | 10616 |
rs142679585 | snp | A/G | 0.0361258 | 0.12979 | intron-variant | RBCK1 | GRCh38.p7 | 20:418582 | ACCGTGTTAGCCAGG[A/G]TGGTCTCGATCTCCT | 10616 |
rs142740447 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RBCK1 | GRCh38.p7 | 20:421744 | AATCAGAGCAGGATA[A/G]AGAGGTGTTGGGTAC | 10616 |
rs142975858 | snp | A/G/T | 0.000347937 | 0.0131856 | intron-variant, synonymous-codon | RBCK1 | GRCh38.p7 | 20:410538 | GTACACACTTCTTCC[A/G/T]TTAATTCCTGTGGAC | 10616 |
rs143041437 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:427562 | ACCACACTGCAGTGC[A/G]TGTTCTCCTGGGAAG | 10616 |
rs143101005 | snp | A/G | 1.76163e-05 | 0.0029678 | missense, synonymous-codon, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:419414 | CCCCCCAAAGCCCGG[A/G]GTCCCCCAGGAACCC | 10616 |
rs143194967 | snp | C/T | 0.00081484 | 0.0201682 | missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:422207 | ACACCTACTCGTGCT[C/T]GGGCAAGCTGCTGGA | 10616 |
rs143258235 | snp | A/G | 0.0023933 | 0.0345097 | utr-variant-3-prime, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:430511 | GGGAGCTTCGTGGAC[A/G]GCCTTGCTTGCTGTA | 10616 |
rs143497465 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RBCK1 | GRCh38.p7 | 20:424130 | TTGGAGTCACCACTC[C/T]GCCAGTCTGTCACAG | 10616 |
rs143500235 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | RBCK1 | GRCh38.p7 | 20:415888 | AGAGAGAGTTGGTGG[G/T]GAGGTGCCACACTTT | 10616 |
rs143566046 | snp | A/C | 0.0912534 | 0.193131 | intron-variant | RBCK1 | GRCh38.p7 | 20:418456 | TCACTGCAAGCTCCG[A/C]CTCCCGGGTTCACGC | 10616 |
rs143702857 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RBCK1 | GRCh38.p7 | 20:418962 | ATGTCTCAGTCCCTT[A/T]CAAAGAGTCCAGGCC | 10616 |
rs143715500 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | RBCK1 | GRCh38.p7 | 20:414536 | CTGCTGTTCACCAGC[G/T]ATCCTGATGTCACAT | 10616 |
rs143762157 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:422778 | GTAAGGTTGCAGTGA[A/G]CTGTGATTGTGCCAC | 10616 |
rs143804674 | snp | C/G | 0.000182774 | 0.00955792 | utr-variant-5-prime, missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:417531 | TTCTCTGCAGGCTGT[C/G]GGTGAGCGTGGAGGA | 10616 |
rs143871997 | snp | G/T | 1.65737e-05 | 0.00287864 | utr-variant-5-prime, missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:417741 | CACCAGGTTTTTCTG[G/T]ACTATGGCTTCCCAC | 10616 |
rs144018482 | snp | C/T | 6.59228e-05 | 0.00574083 | missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:427373 | TCCATTGCTGAAAAC[C/T]GCAGTGCCTTCAGCT | 10616 |
rs144079511 | snp | A/C | 0.000871399 | 0.0208552 | intron-variant, missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:409844 | GCTCCTGAAAATAAA[A/C]CCTGTGCTAACTGGC | 10616 |
rs144105841 | snp | C/T | 0.000201956 | 0.0100467 | missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:422149 | CTGCAGGGCACCATC[C/T]GCAACAGCCAGGAGG | 10616 |
rs144186082 | snp | G/T | 0.0166335 | 0.0896665 | intron-variant | RBCK1 | GRCh38.p7 | 20:419834 | CTCTCCGTTACTGCC[G/T]TGCCCCTCCCAACCA | 10616 |
rs144261654 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | RBCK1 | GRCh38.p7 | 20:425377 | AATGTACTCATTGTA[A/G]GTATGCAGTCAGGTA | 10616 |
rs144367165 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RBCK1 | GRCh38.p7 | 20:422621 | GATTGCTTGAACCCA[C/T]GAGTTCCAGACCAAC | 10616 |
rs144502558 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RBCK1 | GRCh38.p7 | 20:415712 | TGCTACAAAGAAATA[C/T]CTGAGACTGGGTAAT | 10616 |
rs144508620 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:426043 | CTTTCTCAGTGCTAC[A/G]TACTAGCTTACTAGT | 10616 |
rs144523123 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:429526 | CCACCGGGCCGCAAG[A/T]ATGTTCTTTACATCT | 10616 |
rs144693124 | snp | C/G | 0.184521 | 0.241273 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:408274 | CGGCCCCCCCTCCCA[C/G]TCCCGCCCCACTTCC | 10616 |
rs144851771 | snp | A/C/G | 0.0248576 | 0.108776 | intron-variant | RBCK1 | GRCh38.p7 | 20:418590 | AGCCAGGATGGTCTC[A/C/G]ATCTCCTGACTTTGT | 10616 |
rs144891082 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RBCK1 | GRCh38.p7 | 20:418402 | GAGACGGAGTCTCGC[C/T]CTGTCGCCCAGGCTG | 10616 |
rs144929105 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | RBCK1 | GRCh38.p7 | 20:416125 | TGTAACTGGTAGTTA[A/G]AGATAAAGTTTCAAT | 10616 |
rs145017759 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | RBCK1 | GRCh38.p7 | 20:415141 | AGCACTTTGGGAGGC[C/T]GAGGCAGGTGGACTG | 10616 |
rs145132343 | snp | A/T | 8.28562e-05 | 0.00643593 | utr-variant-5-prime, intron-variant, missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:409990 | GCCCCTGAGTGTGCA[A/T]CTGAAGCCTGAGGTC | 10616 |
rs145329089 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RBCK1 | GRCh38.p7 | 20:417110 | AAAACAGGGATACAG[C/T]AGTACCTGTCTGATG | 10616 |
rs145423115 | snp | C/T | 0.000255992 | 0.0113106 | missense, nc-transcript-variant, utr-variant-3-prime | RBCK1 | GRCh38.p7 | 20:429032 | GGCTGCGACTGGATC[C/T]GCTGCACCGTCTGCC | 10616 |
rs145482638 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RBCK1 | GRCh38.p7 | 20:410214 | TCCTCATTTTAAAAA[C/T]CAGACCGTAACAGTA | 10616 |
rs145674291 | snp | C/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:427947 | GGCCTGACCCTGGCC[C/T]TATACCACGTCTCCA | 10616 |
rs145888638 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | RBCK1 | GRCh38.p7 | 20:421623 | CCAAGGAGGTAGCCC[C/T]AGAGCAGGGACCGGA | 10616 |
rs145893594 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | RBCK1 | GRCh38.p7 | 20:427862 | TTGTCACTTAAGGTG[G/T]TCCCATATTCAGCTC | 10616 |
rs145900772 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:431199 | AGGACAGGTGGAGTG[C/T]GCAGTGTGTCAAGTC | 10616 |
rs145976650 | snp | C/G | 0.00273874 | 0.0369035 | intron-variant | RBCK1 | GRCh38.p7 | 20:410058 | GGCCTGAACCCAAGG[C/G]ACAGCAGGACAGGAT | 10616 |
rs146010777 | snp | C/T | 0.0611083 | 0.163768 | intron-variant | RBCK1 | GRCh38.p7 | 20:412406 | GCTCACTGCAACCTC[C/T]GCCTCCCAGGTTCAA | 10616 |
rs146014721 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:423400 | GCAGGCTCAAAACAA[C/G]AGTCATTTATTCAGC | 10616 |
rs146181107 | snp | A/G/T | 4.9905e-05 | 0.00499504 | synonymous-codon, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:422208 | CACCTACTCGTGCTC[A/G/T]GGCAAGCTGCTGGAG | 10616 |
rs146277718 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:412033 | TCATACAGTAACTCT[A/G]TGTTACTTTTTGAAG | 10616 |
rs146325218 | snp | C/T | 1.67478e-05 | 0.00289372 | synonymous-codon, missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:417870 | TATCTGCTGTCAGCC[C/T]GCAACACCTCCCTCA | 10616 |
rs146338955 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RBCK1 | GRCh38.p7 | 20:422921 | TTAACCTCTCTATGC[C/T]TCTATCTCATCTCTG | 10616 |
rs146442317 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:406084 | AGTAGCTAGGATTAC[A/C]GATGTCCGCCACCAC | 10616 |
rs146561173 | in-del | -/T | | | intron-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:429227 | CTCCCGAGGTAAGAA[-/T]TTTTTTTTTTTTTTT | 10616 |
rs146563252 | snp | G/T | 0.00993419 | 0.0697739 | upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:407508 | ATGGGGCCGGAGGAG[G/T]TGAGGGATGAGATTC | 10616 |
rs146678964 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:430753 | GTCAAACACCAAGCA[C/T]TCTCAGCCTCCCCGC | 10616 |
rs146801967 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RBCK1 | GRCh38.p7 | 20:418011 | CAAGCAGGGGCAGAG[C/T]CCCTGGGTTTTTAGT | 10616 |
rs146804136 | snp | A/G | 0.00305343 | 0.0389537 | intron-variant | RBCK1 | GRCh38.p7 | 20:419734 | TCAGTACCAGCAGGT[A/G]GGCGGGAAAGTCCCT | 10616 |
rs147148511 | in-del | -/AAAC | | | intron-variant | RBCK1 | GRCh38.p7 | 20:415379 | TCTCAAAAAAAACAA[-/AAAC]AAAACAAACAAAACC | 10616 |
rs147148864 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RBCK1 | GRCh38.p7 | 20:415935 | ACGAGGACTCACTAT[A/G]GCGAGAAGTCACTAC | 10616 |
rs147165414 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RBCK1 | GRCh38.p7 | 20:418558 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCGTGT | 10616 |
rs147407444 | snp | A/G | 0.000159876 | 0.00893939 | synonymous-codon, missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:419436 | CAGGAACCCGGACGG[A/G]GGCAGCCAGATGCAG | 10616 |
rs147468187 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:429249 | TTTTTTTTTTGAAAC[A/G]GAGTTTCACTCTTGT | 10616 |
rs147592534 | in-del | -/T/TT | 0.298598 | 0.267364 | intron-variant | RBCK1 | GRCh38.p7 | 20:412325 | TCTTTTTTTTTTTTT[-/T/TT]GAGATGGAGTCTCGC | 10616 |
rs147734042 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:410894 | TTTATCCTTACAGTT[A/C]GACCATTTAAAGTAT | 10616 |
rs147820294 | snp | C/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:423859 | ATAATGGTCTCATCT[C/G]TGATGACTGGGATGA | 10616 |
rs147840431 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RBCK1 | GRCh38.p7 | 20:429713 | GGCCGTATGGCTGCC[C/T]GGCCCAAAATGACTG | 10616 |
rs147871258 | snp | A/T | 0.0103295 | 0.0711199 | intron-variant | RBCK1 | GRCh38.p7 | 20:425840 | CTATGTTGGCCAAGC[A/T]AGTCTTAAACTCCTG | 10616 |
rs147940745 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | RBCK1 | GRCh38.p7 | 20:414035 | TCTAAGTTCTTGCTC[G/T]CTTTAAAGAAGCTGC | 10616 |
rs147946351 | snp | A/G | 0.0345262 | 0.126772 | intron-variant | RBCK1 | GRCh38.p7 | 20:416260 | TCCCGGGTTCACACC[A/G]TTCTCCTGCCTCAAT | 10616 |
rs147982960 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:424220 | CAGGTTCTCTGCCTG[A/G]CTGCTGGTGATCTCG | 10616 |
rs148046322 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | RBCK1 | GRCh38.p7 | 20:421199 | GGAACCTGAGGGAAA[C/G]AGAGGCCCAGCGCCT | 10616 |
rs148082482 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:409008 | GGGGCTAGGGGACTC[G/T]CAGAGGACACAGGGC | 10616 |
rs148091459 | snp | A/G | 0.000231811 | 0.0107634 | utr-variant-5-prime, synonymous-codon, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:417604 | TGATATGACAGTGGC[A/G]TCTCTCAAGGACATG | 10616 |
rs148303409 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:430656 | CTGCCTGACCCCAGC[C/T]TTAAACATAGCCCCT | 10616 |
rs148460290 | snp | C/G | 0.0150606 | 0.0854603 | intron-variant | RBCK1 | GRCh38.p7 | 20:430015 | CTGTCGTTATTAGGG[C/G]TGTGCTCTGGAATTG | 10616 |
rs148685980 | snp | A/G | 0.0031269 | 0.0394166 | synonymous-codon, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:422166 | CAACAGCCAGGAGGC[A/G]GAGGTCTCCTGCCCC | 10616 |
rs148721532 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RBCK1 | GRCh38.p7 | 20:425599 | AGTTTGTAATACTCC[C/T]TCAAGGAATGTTTTG | 10616 |
rs148768187 | snp | C/T | | | utr-variant-5-prime, intron-variant, missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:409998 | GTGTGCAACTGAAGC[C/T]TGAGGTCTCCCCAAC | 10616 |
rs148822498 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RBCK1 | GRCh38.p7 | 20:410358 | GAGGTTCTGCTCCCG[A/G]CAGTCCTCAGAGGCT | 10616 |
rs148969237 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RBCK1 | GRCh38.p7 | 20:414203 | GAATGGCTTGAACTC[A/G]AGTTTAAGACCAGCC | 10616 |
rs148978758 | in-del | -/GT | 0.143959 | 0.226396 | intron-variant | RBCK1 | GRCh38.p7 | 20:426438 | AGCACCTGCAAATAA[-/GT]GAGAACATGTAATGT | 10616 |
rs149008463 | snp | C/T | 0.00212767 | 0.032547 | utr-variant-5-prime, intron-variant, synonymous-codon, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:410008 | GAAGCCTGAGGTCTC[C/T]CCAACGCAGGACATC | 10616 |
rs149038161 | snp | A/G | 0.000232454 | 0.0107784 | intron-variant | RBCK1 | GRCh38.p7 | 20:427309 | GGACATGGTGTGTTG[A/G]CAGCTCCTGACCCCT | 10616 |
rs149132789 | snp | A/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:428739 | CGGAGGTGGGACTTA[A/G]GCCGAATGGTCATGT | 10616 |
rs149174797 | snp | G/T | 0.00239844 | 0.0345466 | intron-variant | RBCK1 | GRCh38.p7 | 20:417506 | CAGAGCCCATGCTGA[G/T]CCCCTGCTGTTCTCT | 10616 |
rs149373416 | snp | A/G | 0.00926535 | 0.0674302 | intron-variant | RBCK1 | GRCh38.p7 | 20:428921 | GACTGCCCCAGCCCC[A/G]CCCCAGGGCCAGCAC | 10616 |
rs149541936 | snp | A/G | 0.00110766 | 0.0235075 | missense, synonymous-codon, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:419629 | TGAGATGTGCTGCCG[A/G]GCGCGCCCCGAGGCC | 10616 |
rs149552051 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | RBCK1 | GRCh38.p7 | 20:411940 | ATAAACAATGCTGCC[A/G]TGAACATTTGTGTCC | 10616 |
rs149600454 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RBCK1 | GRCh38.p7 | 20:425329 | TATGATTTTTTAAGT[C/G]AACTTTACTTAAGTA | 10616 |
rs149653480 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RBCK1 | GRCh38.p7 | 20:421946 | AGCGGCAGTATGGAG[A/G]CAGGGTGGAGGCCTT | 10616 |
rs149689056 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RBCK1 | GRCh38.p7 | 20:410157 | AGTTATGTCATTAAT[C/T]AACTGTGAAATACAG | 10616 |
rs149958100 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RBCK1 | GRCh38.p7 | 20:423225 | AATCGCTTGAACCCC[A/G]GAGGCGGAGGTTGTG | 10616 |
rs150028634 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:416876 | GTGGCATGAGCCTGT[A/G]GTCCCAGCTACTTGG | 10616 |
rs150032325 | snp | A/G | 0.000297039 | 0.0121832 | missense, nc-transcript-variant, utr-variant-3-prime | RBCK1 | GRCh38.p7 | 20:428979 | AGGGCGAGGCCATGC[A/G]CTGCCCCCAGTGCCA | 10616 |
rs150326754 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:426405 | TCTGTCCTCATTAGT[C/T]CAGTTGTTTCGATTT | 10616 |
rs150357183 | snp | A/G | 0.170084 | 0.236883 | intron-variant | RBCK1 | GRCh38.p7 | 20:418432 | GGAGTGCAGTGGCAC[A/G]ATCTCGGCTCACTGC | 10616 |
rs150479871 | snp | C/T | 0.00914312 | 0.0669923 | upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:406499 | AGCATTTTGGGAGGC[C/T]GAGGTGGGCAGATCA | 10616 |
rs150646962 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RBCK1 | GRCh38.p7 | 20:428653 | CAGGTGGGGGCTGGG[A/G]GCTTCCCAGTAAGGG | 10616 |
rs150678322 | snp | A/C/T | 0.00398564 | 0.0444627 | intron-variant | RBCK1 | GRCh38.p7 | 20:418647 | TGCTGGGATTACAGG[A/C/T]GTGAGCCACCACGCC | 10616 |
rs150728406 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:421760 | AGAGGTGTTGGGTAC[A/G]TGAGCAGCAGTGAGG | 10616 |
rs150732300 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RBCK1 | GRCh38.p7 | 20:412855 | TCATATCTAAGAAAT[C/T]GTTGCCTCATCCAAG | 10616 |
rs150785959 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:409356 | CACTGGAGCTTGACA[A/C]GTGCAGCTTCTCCTC | 10616 |
rs150977425 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | RBCK1 | GRCh38.p7 | 20:430146 | TCCTCTCCCTGGCCT[A/G]TTCCCGGATCTAGGC | 10616 |
rs151054127 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RBCK1 | GRCh38.p7 | 20:414637 | TCTAACATAATTAAG[A/G]CCTTTATGCTTTGCC | 10616 |
rs151137857 | snp | C/T | 0.0123036 | 0.0774623 | upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:406286 | ATGGGTGTACAATTC[C/T]GTAAATGTTACTAAA | 10616 |
rs151306710 | snp | C/T | 0.000489732 | 0.0156405 | synonymous-codon, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:428538 | TCAGGAGGACCTGGC[C/T]CTGCGGGCTCAGAAC | 10616 |
rs180745184 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | RBCK1 | GRCh38.p7 | 20:421780 | CAGCAGTGAGGAGTT[C/G]GGATTTGTTCTGGGT | 10616 |
rs180959710 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:425097 | CCCACTGCAAGCTCC[C/G]CCTCCCGGGTTCACG | 10616 |
rs181002053 | snp | G/T | 0.00835141 | 0.0640778 | upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:406497 | CCAGCATTTTGGGAG[G/T]CCGAGGTGGGCAGAT | 10616 |
rs181270406 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RBCK1 | GRCh38.p7 | 20:418407 | GGAGTCTCGCTCTGT[C/T]GCCCAGGCTGGAGTG | 10616 |
rs181295082 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RBCK1 | GRCh38.p7 | 20:424613 | TCTCTGTTGTCTCTG[C/G]GTGGTTGCTGAGGCT | 10616 |
rs181416680 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RBCK1 | GRCh38.p7 | 20:418142 | GGGAGGGGTGGACTC[A/C]GTCCAGGCTCCGGCA | 10616 |
rs181500434 | snp | C/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:425161 | GACTAGAGGCGCACA[C/T]CGCCATGCCCAGCTA | 10616 |
rs181626643 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:408879 | CTTGGAGAGGGGGCT[G/T]TAGCCTGCCCTCCCT | 10616 |
rs181893541 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RBCK1 | GRCh38.p7 | 20:422646 | ACCAACCTGGGCAAC[A/G]TGGCAAAAAATATTC | 10616 |
rs182049875 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RBCK1 | GRCh38.p7 | 20:423376 | GCGCTTACTGTGTAA[C/T]AAATCACTGCAGGCT | 10616 |
rs182084622 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:411851 | AATAATAATCTATTG[C/T]ATAGACATATCTCAT | 10616 |
rs182122386 | snp | G/T | 0.0107246 | 0.0724382 | intron-variant, utr-variant-3-prime | RBCK1 | GRCh38.p7 | 20:420146 | GCTCCACCTCGCCGT[G/T]ACCTCACCCTGGACT | 10616 |
rs182279147 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:428312 | TGACCTTGACTTCAC[C/T]TCCCTGGCGCCAATA | 10616 |
rs182484272 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:409754 | GGGTGCTGAAGGATA[C/T]GTAGGAGTTCACCAG | 10616 |
rs182651308 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | RBCK1 | GRCh38.p7 | 20:413727 | CTCTGGGCAACCGGC[A/C]CCTCTCAGACCTGCT | 10616 |
rs182893185 | snp | A/G/T | 0.00159617 | 0.0282053 | intron-variant | RBCK1 | GRCh38.p7 | 20:418664 | TGAGCCACCACGCCC[A/G/T]ACCCACATTTGCTTT | 10616 |
rs182909015 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | RBCK1 | GRCh38.p7 | 20:418909 | ACCAGTTGTCCCACT[A/G]TTGTCATTTATAGCA | 10616 |
rs182972920 | snp | A/G | 0.0349115 | 0.127424 | intron-variant | RBCK1 | GRCh38.p7 | 20:418518 | GGACTACAGGCGCCC[A/G]CCACCACGCCCGGCT | 10616 |
rs183245609 | snp | A/C/G | 0.00199529 | 0.0315338 | intron-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:429521 | GTGAGCCACCGGGCC[A/C/G]CAAGAATGTTCTTTA | 10616 |
rs183479570 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:410943 | GTATATTCAAGGTTG[G/T]GCAACCATTGCCACA | 10616 |
rs183667937 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | RBCK1 | GRCh38.p7 | 20:419226 | GGAAGCTGGAGGTAC[A/C]CCCAGGGAGGAGGGA | 10616 |
rs183756924 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RBCK1 | GRCh38.p7 | 20:423097 | CTGAGGTCGGGAATT[A/C]GAGATCAGCCTGACT | 10616 |
rs183827371 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:414777 | TTTATGTTTCAAAAC[C/T]CTTATTGCTGGAAGA | 10616 |
rs184068004 | snp | A/G | | | missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:430350 | CCTCCCATCCTCTAG[A/G]GCCCAGGAGACACCA | 10616 |
rs184115019 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:411255 | CTTGTCTAGGTTGAA[A/G/T]TGCAGTGGTGCCATC | 10616 |
rs184310368 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RBCK1 | GRCh38.p7 | 20:424839 | AAGTGTGACAGAGAG[A/G]AGGAGGCAGGGATCA | 10616 |
rs184416997 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RBCK1 | GRCh38.p7 | 20:411647 | GCTGGGACTACAGGC[A/G]TGAGCCACCACACCC | 10616 |
rs184622682 | snp | A/G | 0.000744879 | 0.0192843 | intron-variant, missense, utr-variant-5-prime, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:417227 | TCACTAAGGAGCAGG[A/G]GAGAGAAGACAGAAG | 10616 |
rs184646988 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:423739 | GGATACCGAGGGATG[A/G]CTATAATTTGGGCTG | 10616 |
rs184671150 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:421125 | CCTGTGCTCTGATAC[C/T]TCATTGGACGCCCGC | 10616 |
rs185063324 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:416465 | TGTGCAGGAACTCTT[C/G]CTCATTTTTTGGTTG | 10616 |
rs185351338 | snp | G/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:413297 | ATTTTACGATCAGCT[G/T]GTCTGTTTCTGCAAA | 10616 |
rs185357780 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RBCK1 | GRCh38.p7 | 20:424094 | CACCCAAAAGTGTGG[A/G]ATCGGGGAGACAGAA | 10616 |
rs185358860 | snp | C/G | 0.0123036 | 0.0774623 | intron-variant | RBCK1 | GRCh38.p7 | 20:422349 | TTTTTTGGAGATGGG[C/G]TCTCACTATGTTGTC | 10616 |
rs185607868 | snp | A/C | 0.000200161 | 0.0100023 | intron-variant | RBCK1 | GRCh38.p7 | 20:427516 | TGCAGGGACTCCCCC[A/C]ACCTAGTCACTGTCA | 10616 |
rs185899302 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:418326 | TTTACAAAGTAGTAC[A/G]TAAAGAATTCCCATG | 10616 |
rs185970596 | snp | A/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:414004 | GGGCTCTGTGCTCTG[A/G]TGCTTCAGGAGTGTG | 10616 |
rs186356187 | snp | A/G | 0.039522 | 0.134904 | intron-variant | RBCK1 | GRCh38.p7 | 20:418559 | ATTTTTAGTAGAGAC[A/G]GGGTTTCACCGTGTT | 10616 |
rs186533520 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:422983 | GATTGCAAAGATTAC[A/T]GTAGAGGATATGTGT | 10616 |
rs186644254 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RBCK1 | GRCh38.p7 | 20:423664 | ACTGCACTATTTTAT[A/G]TAAGGGGTTTGAGCA | 10616 |
rs186728931 | snp | A/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:418462 | CAAGCTCCGACTCCC[A/G]GGTTCACGCCATTCT | 10616 |
rs186759136 | snp | A/C/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:409084 | TGACCTGAGAAGCAG[A/C/G]GGTACTTGCCTCTTC | 10616 |
rs186976163 | snp | A/G | 0.0295035 | 0.117819 | intron-variant | RBCK1 | GRCh38.p7 | 20:425163 | CTAGAGGCGCACACC[A/G]CCATGCCCAGCTAAT | 10616 |
rs187050442 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:416381 | TAGCCAGGATGGTCT[C/T]GATCTCCTGACCTCG | 10616 |
rs187063425 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | RBCK1 | GRCh38.p7 | 20:425112 | GCCTCCCGGGTTCAC[A/G]CCATTCTCCTGCCTC | 10616 |
rs187146835 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:409762 | AAGGATACGTAGGAG[G/T]TCACCAGGAAGACAG | 10616 |
rs187287940 | snp | C/T | 0.00318978 | 0.0398085 | upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:406817 | AAAAGAAAAATTATC[C/T]CAGATGAAGGTCTGA | 10616 |
rs187509129 | snp | C/G | | | intron-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:411032 | GTCCTCATCTCTCTA[C/G]CTTTTCCCTAACTCC | 10616 |
rs187564308 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RBCK1 | GRCh38.p7 | 20:419233 | GGAGGTACCCCCAGG[A/G]AGGAGGGAGAGGATA | 10616 |
rs187631651 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RBCK1 | GRCh38.p7 | 20:411852 | ATAATAATCTATTGT[A/G]TAGACATATCTCATT | 10616 |
rs187845241 | snp | C/G | 0.0154538 | 0.0865337 | intron-variant | RBCK1 | GRCh38.p7 | 20:423224 | GAATCGCTTGAACCC[C/G]GGAGGCGGAGGTTGT | 10616 |
rs188039631 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:415106 | CTTGGCGGGGCACGA[C/T]GGATGATGCTTGTAA | 10616 |
rs188217988 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:425074 | GGAGTGCAATGGCGC[G/T]ATCTCAGCCCACTGC | 10616 |
rs188262576 | snp | A/G | 0.00755907 | 0.0610114 | upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:406456 | GTTAGATTGACAGGT[A/G]ATGATATCTCAACAG | 10616 |
rs188363862 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RBCK1 | GRCh38.p7 | 20:418984 | GTCCAGGCCAGTTTC[C/T]TTTTTTTGGCGGGGG | 10616 |
rs188614643 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RBCK1 | GRCh38.p7 | 20:429754 | GAAAAGGTTTGCCCA[C/T]TCCTGCCCTAGAGGA | 10616 |
rs188651695 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RBCK1 | GRCh38.p7 | 20:428352 | GTAAAATGGCTTATG[C/T]ATTACAAAGTGAGGT | 10616 |
rs188751991 | snp | C/T | 0.00636936 | 0.0560724 | utr-variant-3-prime, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:430636 | CTCCCCTGCGGCTCC[C/T]ACCTCTGCCTGACCC | 10616 |
rs188797045 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RBCK1 | GRCh38.p7 | 20:411569 | AGACGGGGTTTCGCC[A/G]TGTTAACCAGGATGG | 10616 |
rs188867784 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:411956 | TGAACATTTGTGTCC[A/C]ACTTTTTGTGTGGAC | 10616 |
rs188914068 | snp | A/G | 1.7517e-05 | 0.00295942 | intron-variant, missense | RBCK1 | GRCh38.p7 | 20:410440 | CAAAATGGCCATTCC[A/G]GCTCCATCCAGCCAT | 10616 |
rs189124784 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RBCK1 | GRCh38.p7 | 20:416601 | TGTTTCCTTTGGGGT[C/T]GGTTCTGTTTTTTCA | 10616 |
rs189170438 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:423755 | CTATAATTTGGGCTG[G/T]ACTTACCTGGATGGT | 10616 |
rs189407509 | snp | C/T | 0.00024842 | 0.0111422 | utr-variant-5-prime, synonymous-codon, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:417562 | TGCTCAGATGCACAC[C/T]GTCACCATCTGGCTC | 10616 |
rs189415929 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RBCK1 | GRCh38.p7 | 20:424244 | GATCTCGAGCAAGTT[A/G]TTTCCCTTCTGTGGG | 10616 |
rs189627680 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:410298 | ACAACAGAAGAAAAC[A/G]GAACAGTGACGTAAA | 10616 |
rs189631772 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:428011 | TAGACAGCCCTACCT[G/T]ATCCTTCCCCCAGGC | 10616 |
rs189671742 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | RBCK1 | GRCh38.p7 | 20:418363 | TCATGTGGGTTTTAC[C/T]ACATGTGCTTTCTTT | 10616 |
rs189945390 | snp | C/G | 0.00398731 | 0.0445001 | intron-variant | RBCK1 | GRCh38.p7 | 20:421268 | CGTGAGCGCAGGCGT[C/G]GGGGGAGACTCCCTT | 10616 |
rs189951094 | snp | C/T | 0.0153248 | 0.0861831 | intron-variant | RBCK1 | GRCh38.p7 | 20:419835 | TCTCCGTTACTGCCT[C/T]GCCCCTCCCAACCAT | 10616 |
rs190025248 | snp | C/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:422411 | ATCATTCATCCTCAG[C/T]CCCCCAGACATTTTT | 10616 |
rs190160917 | snp | C/G/T | 0.00279162 | 0.0372561 | intron-variant | RBCK1 | GRCh38.p7 | 20:413677 | TCTCAGGTCTCACCT[C/G/T]AGACTTGCTGGGTCA | 10616 |
rs190439659 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RBCK1 | GRCh38.p7 | 20:411843 | TATTGCCAAATAATA[A/G]TCTATTGTATAGACA | 10616 |
rs190673583 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:409626 | TTGTTGGATAAATGA[A/G]TAGAAATATGAGGGA | 10616 |
rs190688492 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:425167 | AGGCGCACACCGCCA[C/T]GCCCAGCTAATTTTT | 10616 |
rs190720652 | snp | C/T | 0.116488 | 0.211364 | intron-variant | RBCK1 | GRCh38.p7 | 20:418517 | GGGACTACAGGCGCC[C/T]GCCACCACGCCCGGC | 10616 |
rs191104521 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RBCK1 | GRCh38.p7 | 20:418657 | ACAGGCGTGAGCCAC[C/T]ACGCCCAACCCACAT | 10616 |
rs191217132 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RBCK1 | GRCh38.p7 | 20:414173 | GGCTCAGCACTTTGG[A/G]AGGCTCAGGCAGGAG | 10616 |
rs191286649 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:431434 | CACTCTGTGCTGGTC[A/G]GAGGTTACTAAGACA | 10616 |
rs191446465 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RBCK1 | GRCh38.p7 | 20:423668 | CACTATTTTATATAA[A/G]GGGTTTGAGCATCCA | 10616 |
rs191452909 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | RBCK1 | GRCh38.p7 | 20:423286 | CCTGGGCAACCAGAG[C/T]GAAACTCCGTCTGAA | 10616 |
rs191485435 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | RBCK1 | GRCh38.p7 | 20:423074 | GGAGGCCAAGGCGGG[C/T]GGATCACCTGAGGTC | 10616 |
rs192038698 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:418780 | AAATAATTCAGTGTG[A/C]ATTTCCTTGAAAAGA | 10616 |
rs192040430 | snp | A/C | 0.00358779 | 0.0422022 | upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:407278 | AGAGATCGGGAGGCA[A/C]TTTGCGAGCCCTGGG | 10616 |
rs192080108 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:416095 | ATGGTGTCATTTACT[A/G]TCTCCCGTTTTTCCT | 10616 |
rs192210297 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RBCK1 | GRCh38.p7 | 20:419129 | GTTGTGCTGGGTTTT[C/G]AAGCTCAAAGGACAT | 10616 |
rs192317901 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:411231 | CTTTTTTTTTTTGAC[A/G]TGGGGTCTCTTGTCT | 10616 |
rs192357723 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | RBCK1 | GRCh38.p7 | 20:425151 | AAGTAGCTGGGACTA[C/G]AGGCGCACACCGCCA | 10616 |
rs192514601 | snp | C/G | 0.000426823 | 0.0146024 | intron-variant | RBCK1 | GRCh38.p7 | 20:419541 | CCAGTCGGGCTCACA[C/G]CACCCTCTGCTCCCA | 10616 |
rs192629085 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RBCK1 | GRCh38.p7 | 20:411571 | ACGGGGTTTCGCCGT[A/G]TTAACCAGGATGGTC | 10616 |
rs192709314 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | RBCK1 | GRCh38.p7 | 20:416412 | TGATCCACCCACCTC[A/G]GCCTCCCAAAGTGCT | 10616 |
rs192777750 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RBCK1 | GRCh38.p7 | 20:416772 | GAGGCCAAGGCAGGA[A/G]GATCACTTGAGGCCA | 10616 |
rs192852320 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:423860 | TAATGGTCTCATCTG[G/T]GATGACTGGGATGAC | 10616 |
rs193109887 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | RBCK1 | GRCh38.p7 | 20:410725 | TGCACAATGCCTGGC[A/G]TGTTATGCACTCAAT | 10616 |
rs193264558 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:429248 | TTTTTTTTTTTGAAA[C/T]GGAGTTTCACTCTTG | 10616 |
rs199527581 | in-del | -/C | | | intron-variant | RBCK1 | GRCh38.p7 | 20:419883 | TGCACCTGGCTGTGA[-/C]CCTGCACCTGGCTGT | 10616 |
rs199702405 | snp | A/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:426439 | GCACCTGCAAATAAG[A/T]GAGAACATGTAATGT | 10616 |
rs199774576 | snp | C/T | 0.000263193 | 0.0114685 | intron-variant | RBCK1 | GRCh38.p7 | 20:428461 | ACCCCCTGAGGAACC[C/T]TCTTACCTTGAGTCC | 10616 |
rs199918172 | snp | A/G | 0.000386259 | 0.0138917 | intron-variant | RBCK1 | GRCh38.p7 | 20:430311 | GGGGGCAGTCTCTGC[A/G]CTGCGCTGACATTCT | 10616 |
rs199951498 | in-del | -/C/CTC | 0.00716266 | 0.059414 | intron-variant | RBCK1 | GRCh38.p7 | 20:417040 | CTAACAGTTATTAGT[-/C/CTC]TGCTTAGTTTGGCAG | 10616 |
rs200101786 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:430766 | CACTCTCAGCCTCCC[C/T]GCCTTCAGCTGTCAG | 10616 |
rs200146141 | snp | C/T | 0.00036602 | 0.0135232 | missense, synonymous-codon, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:417848 | GAATGGGGACAGTGC[C/T]TACCTCTATCTGCTG | 10616 |
rs200194918 | in-del | -/AGCCCC | | | intron-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:420697 | CACCCCCCATCCCCC[-/AGCCCC]ACCCCCATCCCCCAC | 10616 |
rs200294099 | in-del | -/T/TTTTTTA/TTTTTTT | 0.270948 | 0.262687 | intron-variant | RBCK1 | GRCh38.p7 | 20:426995 | CACCTGGTTATTTTA[-/T/TTTTTTA/TTTTTTT]TTTTTTAAAAAAATT | 10616 |
rs200408386 | in-del | -/AC/ACT | 0.00716266 | 0.059414 | intron-variant | RBCK1 | GRCh38.p7 | 20:417039 | TCTAACAGTTATTAG[-/AC/ACT]TTGCTTAGTTTGGCA | 10616 |
rs200457271 | snp | C/G | 0.00802484 | 0.0628333 | intron-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:420856 | CCGCCCCGTGGCCCC[C/G]CCCCGTGTGCCCAGC | 10616 |
rs200484492 | snp | C/G | 5.06838e-05 | 0.00503382 | intron-variant | RBCK1 | GRCh38.p7 | 20:427270 | AAGGGTCATATGTCA[C/G]GTGTTCTGAATCCTG | 10616 |
rs200524483 | in-del | -/TGC | | | intron-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:420664 | CAACCTGCCTGCTCC[-/TGC]CCATCCCCCACCCCC | 10616 |
rs200546199 | snp | C/T | 0.000199312 | 0.0099808 | intron-variant | RBCK1 | GRCh38.p7 | 20:417640 | TGAGGAGGCGGAGGG[C/T]GACACTGGGGTGAAG | 10616 |
rs200677519 | in-del | -/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:425623 | GTTTTGCATGGTGTA[-/T]TTCTTTTTTTTTTTT | 10616 |
rs200754266 | in-del | -/TT | 0.00478085 | 0.0486577 | intron-variant | RBCK1 | GRCh38.p7 | 20:414908 | GAAAATGTGGTAAAC[-/TT]TTAGAGTCTTTGCAT | 10616 |
rs200757913 | snp | A/G | 0.000133502 | 0.00816905 | utr-variant-5-prime, intron-variant, missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:409908 | CCCTGAGCCTCACCC[A/G]AGCAGTGGCGGGCGG | 10616 |
rs200793606 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:428602 | AAGGTGAGGCTGGGA[C/G]AGGGCCGAGGCCTAG | 10616 |
rs201030033 | snp | A/G | 0.00129161 | 0.0253798 | synonymous-codon, missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:419678 | TACCAGCCCGACGAG[A/G]AGGAGCGAGCGCGCC | 10616 |
rs201072906 | snp | A/G | 0.000885326 | 0.0210209 | intron-variant | RBCK1 | GRCh38.p7 | 20:417965 | ACCGCCGGACCCAGC[A/G]GGGGCCCTGGACTCA | 10616 |
rs201109999 | in-del | -/C | | | intron-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:420728 | CCCACCCCCGTCCCC[-/C]ATCCCCCATCCCTAC | 10616 |
rs201296265 | in-del | -/TC | 0.102014 | 0.201495 | intron-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:420670 | GCCTGCTCCTGCCCA[-/TC]CCCCACCCCCCACCC | 10616 |
rs201470953 | snp | A/G | 0.000182529 | 0.00955149 | synonymous-codon, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:422238 | GAGGGAGATCAAGGC[A/G]GTAAGGCCTCAGGGT | 10616 |
rs201529134 | snp | A/G | 1.66142e-05 | 0.00288216 | missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:430362 | TAGGGCCCAGGAGAC[A/G]CCAGCGGGGGCTGCC | 10616 |
rs201612261 | in-del | -/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:413802 | CTGTTGTATGTGTTA[-/T]TTGGTAATAACATAG | 10616 |
rs201645896 | snp | C/G | 0.000453361 | 0.0150491 | intron-variant, missense, nc-transcript-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:420922 | CACGTCCAGCTGGAC[C/G]AGAGGAGCCTGGTGC | 10616 |
rs201767592 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RBCK1 | GRCh38.p7 | 20:430046 | GGGGCCTGTTGCTAC[A/G]TTCAGGTAGACTTTC | 10616 |
rs201871116 | in-del | -/C | | | intron-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:420684 | ATCCCCCACCCCCCA[-/C]CCCCCATCCCCCAGC | 10616 |
rs201943000 | snp | G/T | 1.74385e-05 | 0.00295278 | missense, nc-transcript-variant, utr-variant-3-prime | RBCK1 | GRCh38.p7 | 20:428981 | GGCGAGGCCATGCGC[G/T]GCCCCCAGTGCCAGA | 10616 |
rs202028110 | in-del | -/TCCTG | | | intron-variant | RBCK1 | GRCh38.p7 | 20:420661 | TCCCAACCTGCCTGC[-/TCCTG]CCCATCCCCCACCCC | 10616 |
rs202094414 | in-del | -/TG | | | intron-variant | RBCK1 | GRCh38.p7 | 20:417423 | GTGTGTGTGTGTGTG[-/TG]CATGGCCATGTGCCT | 10616 |
rs267605923 | snp | A/G | | | missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:430351 | CTCCCATCCTCTAGG[A/G]CCCAGGAGACACCAG | 10616 |
rs367588385 | snp | A/G | 1.79001e-05 | 0.00299161 | intron-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:429128 | TGGTGTGGAGAGGGT[A/G]CCCTTGTGGGCTTTG | 10616 |
rs367600993 | snp | A/G | 0.000109957 | 0.00741392 | intron-variant, missense, nc-transcript-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:420952 | CTGAACACGGAGCCC[A/G]CCGAGTGCCCCGTGT | 10616 |
rs367646763 | in-del | -/TCCCCCACCCCCCACC | | | intron-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:420670 | GCCTGCTCCTGCCCA[-/TCCCCCACCCCCCACC]CCCCATCCCCCAGCC | 10616 |
rs367754028 | snp | G/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:413771 | CGATGGACCCGATGC[G/T]TCCTAGCAAATGATA | 10616 |
rs367787351 | in-del | -/C | | | intron-variant | RBCK1 | GRCh38.p7 | 20:425626 | TTTGCATGGTGTATT[-/C]TTTTTTTTTTTTTTT | 10616 |
rs367871981 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:411217 | ACAACTTCATTCCCC[C/T]TTTTTTTTTTGACAT | 10616 |
rs367971559 | snp | G/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:421342 | CTCAGCCTCGCTGTG[G/T]GCATCTGCCAGTTTC | 10616 |
rs367992757 | in-del | -/A | | | intron-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:420683 | CATCCCCCACCCCCC[-/A]CCCCCCATCCCCCAG | 10616 |
rs368306179 | snp | A/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:423731 | AATTCTCTGGATACC[A/G]AGGGATGACTATAAT | 10616 |
rs368469345 | snp | G/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:414552 | ATCCTGATGTCACAT[G/T]GGATGAGAGAGCTCC | 10616 |
rs368511092 | snp | A/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:425341 | AGTCAACTTTACTTA[A/T]GTATACTTTGCACAC | 10616 |
rs368544476 | snp | A/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:424166 | TGTGTGTCTGCATAC[A/G]TGTGTGCTTGCCGCT | 10616 |
rs368576987 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RBCK1 | GRCh38.p7 | 20:416033 | CTTCAACACTGAGGA[A/T]TACAGTTCAAGGTAA | 10616 |
rs368582438 | snp | C/T | 6.1149e-05 | 0.00552908 | intron-variant | RBCK1 | GRCh38.p7 | 20:428468 | GAGGAACCTTCTTAC[C/T]TTGAGTCCCTCACCC | 10616 |
rs368668838 | snp | A/C | 0.000348553 | 0.0131968 | intron-variant | RBCK1 | GRCh38.p7 | 20:417954 | CTGCCCTGAGCACCG[A/C]CGGACCCAGCGGGGG | 10616 |
rs368745414 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:430750 | TCTGTCAAACACCAA[A/G]CACTCTCAGCCTCCC | 10616 |
rs368996082 | in-del | -/AG | 0.00914312 | 0.0669923 | intron-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:409782 | CAGGAAGACAGAGAA[-/AG]CAGCACACACAAAGG | 10616 |
rs369017943 | snp | A/C | 6.98788e-05 | 0.00591054 | intron-variant, synonymous-codon, utr-variant-5-prime, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:417250 | GACAGAAGAGGTTGG[A/C]GAGGTCAGGGAGGTG | 10616 |
rs369024234 | snp | A/G | 0.000501195 | 0.0158223 | intron-variant | RBCK1 | GRCh38.p7 | 20:427295 | ATCCTGAGCAGCAAG[A/G]ACATGGTGTGTTGGC | 10616 |
rs369067636 | snp | C/G | | | upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:407966 | CCGCCCCCGGCCCCG[C/G]CCCCGGCCCCCGGCC | 10616 |
rs369079371 | snp | A/G | 1.66043e-05 | 0.00288129 | utr-variant-3-prime, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:430475 | CAGCCCCACATCCAC[A/G]TTCTGTTAGAATGTA | 10616 |
rs369095938 | snp | C/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:417466 | GTACATGTCTGTAGC[C/T]GGTGGCTGAGGCTGG | 10616 |
rs369222089 | in-del | -/GTT | | | intron-variant | RBCK1 | GRCh38.p7 | 20:412149 | CTAATACTTGTTGTT[-/GTT]TATCTTTTTGATTAT | 10616 |
rs369328889 | snp | A/G/T | 0.000243441 | 0.0110304 | intron-variant, synonymous-codon, missense | RBCK1 | GRCh38.p7 | 20:410523 | CATAGCTCAAAAATT[A/G/T]TACACACTTCTTCCG | 10616 |
rs369347857 | snp | A/G | | | upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:407297 | GCGAGCCCTGGGACA[A/G]ATCTCGGATTTTGCT | 10616 |
rs369361019 | snp | A/C/T | 0.010335 | 0.0711961 | intron-variant | RBCK1 | GRCh38.p7 | 20:418513 | AGCTGGGACTACAGG[A/C/T]GCCCGCCACCACGCC | 10616 |
rs369452684 | snp | C/T | 0.000153988 | 0.00877327 | intron-variant | RBCK1 | GRCh38.p7 | 20:417964 | CACCGCCGGACCCAG[C/T]GGGGGCCCTGGACTC | 10616 |
rs369471646 | snp | C/T | 0.000119917 | 0.00774237 | intron-variant | RBCK1 | GRCh38.p7 | 20:422116 | AACTCTTTTCCCCTC[C/T]CCTCCCCTAGGGAGT | 10616 |
rs369696483 | snp | A/C | | | intron-variant | RBCK1 | GRCh38.p7 | 20:417010 | TTAAATCAAGACATA[A/C]AAATGAATCCTGCCT | 10616 |
rs369725341 | snp | G/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:418649 | CTGGGATTACAGGCG[G/T]GAGCCACCACGCCCA | 10616 |
rs369786332 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | RBCK1 | GRCh38.p7 | 20:418589 | TAGCCAGGATGGTCT[C/T]GATCTCCTGACTTTG | 10616 |
rs369877444 | snp | C/T | 1.65556e-05 | 0.00287707 | utr-variant-5-prime, missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:417778 | TGCAGCAGTGGGTGA[C/T]TGGGCAGCGGCTGGC | 10616 |
rs369912362 | snp | C/T | 5.09844e-05 | 0.00504872 | synonymous-codon, nc-transcript-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:429052 | CACCGTCTGCCACAC[C/T]GAGATCTGCTGGGTC | 10616 |
rs370138905 | snp | C/T | 0.000149195 | 0.00863569 | synonymous-codon, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:428553 | CCTGCGGGCTCAGAA[C/T]GATGTGGCTGCCCGG | 10616 |
rs370182004 | in-del | -/C | 0.0213609 | 0.101115 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:408732 | AGGCACGGTCCCCCC[-/C]AGGGGGATGGGCACA | 10616 |
rs370337997 | in-del | -/ACCCTGCACCTGGCTGTG | | | intron-variant | RBCK1 | GRCh38.p7 | 20:419864 | ATGCTGCTGGCAGTG[-/ACCCTGCACCTGGCTGTG]ACCCTGCACCTGGCT | 10616 |
rs370394352 | snp | A/T | | | intron-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:429493 | GGCCTCCCAAAGTGC[A/T]AGGATTACAGGCGTG | 10616 |
rs370397834 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | RBCK1 | GRCh38.p7 | 20:415321 | TGCAGTGAGCCAAGA[A/T]CATGCCACTACACTC | 10616 |
rs370402266 | snp | C/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:424688 | TGTCCCCAGCACCCA[C/T]AGCCATTTGCTTAGA | 10616 |
rs370427697 | snp | C/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:417366 | TAATAAAGGAAGAAG[C/T]ATGGGTGGGGCCTAC | 10616 |
rs370484953 | snp | A/G | 0.000157987 | 0.00888643 | intron-variant, synonymous-codon, nc-transcript-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:420903 | GGAGGGGAACTACCT[A/G]CAGCACGTCCAGCTG | 10616 |
rs370699351 | snp | C/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:423828 | GGCTGGTGGGTCAGC[C/T]GCGGTGGCCTGGTTT | 10616 |
rs370701347 | snp | C/T | | | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:408461 | TGGTGTCCGGGCGTC[C/T]TTTCCCCGCTTCTTC | 10616 |
rs370710091 | in-del | -/TG | | | intron-variant | RBCK1 | GRCh38.p7 | 20:426439 | GCACCTGCAAATAAG[-/TG]AGAACATGTAATGTT | 10616 |
rs370871903 | snp | A/T | | | intron-variant, utr-variant-3-prime | RBCK1 | GRCh38.p7 | 20:420214 | ACCCCTGACTTCCTG[A/T]GAGCCTGGCCTGGAC | 10616 |
rs370963132 | snp | C/G | 0.000132186 | 0.00812867 | missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:427323 | GGCAGCTCCTGACCC[C/G]TGAGGATTACCAGCG | 10616 |
rs370964809 | snp | C/G | | | intron-variant, synonymous-codon | RBCK1 | GRCh38.p7 | 20:419926 | CTCAAAGGTCACCCT[C/G]TGGCTGAGACCCGCT | 10616 |
rs371077650 | snp | A/G | 8.67039e-05 | 0.00658365 | missense, nc-transcript-variant, utr-variant-3-prime | RBCK1 | GRCh38.p7 | 20:428988 | CCATGCGCTGCCCCC[A/G]GTGCCAGATCGTGGT | 10616 |
rs371483995 | snp | C/T | 0.000199112 | 0.00997579 | intron-variant, synonymous-codon, utr-variant-5-prime, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:417316 | TGATTCTAAGAGTAG[C/T]GTGGAGCCATTGGAG | 10616 |
rs371527119 | snp | A/G | 1.65515e-05 | 0.00287671 | missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:430386 | GGCTGCCGCTGCAGG[A/G]TAAATGGGATTCCTT | 10616 |
rs371556646 | snp | C/T | 0.000232786 | 0.0107861 | intron-variant | RBCK1 | GRCh38.p7 | 20:417686 | CCTGCTTCCTCTCTC[C/T]CCTCTGGCCCTCCCT | 10616 |
rs371696823 | snp | C/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:415921 | AACAGCCAGATCTCA[C/T]GAGGACTCACTATGG | 10616 |
rs371735831 | in-del | -/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:426071 | GTTTGTTTAATTTTT[-/T]ATTTTTTATTTTTGC | 10616 |
rs371850464 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RBCK1 | GRCh38.p7 | 20:416102 | CATTTACTATCTCCC[A/G]TTTTTCCTGTAACTG | 10616 |
rs371854549 | snp | A/G | 0.000117953 | 0.00767872 | intron-variant | RBCK1 | GRCh38.p7 | 20:419343 | CTTTAACCCTCCTCC[A/G]CAGATCTGGGCTTCA | 10616 |
rs372045918 | snp | C/T | 6.71456e-05 | 0.00579382 | intron-variant | RBCK1 | GRCh38.p7 | 20:430315 | GCAGTCTCTGCACTG[C/T]GCTGACATTCTCTTC | 10616 |
rs372046457 | snp | C/T | | | intron-variant, missense, utr-variant-5-prime, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:417246 | AGAAGACAGAAGAGG[C/T]TGGAGAGGTCAGGGA | 10616 |
rs372213198 | snp | A/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:421636 | CCCAGAGCAGGGACC[A/G]GAAGGCCTGCTGTAG | 10616 |
rs372371417 | snp | C/T | 9.98752e-05 | 0.00706595 | intron-variant, missense, nc-transcript-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:420995 | TGGCGCCCGGCGAGG[C/T]CGTGGTGCTGCGTGA | 10616 |
rs372404720 | in-del | -/TAA | | | intron-variant, utr-variant-3-prime | RBCK1 | GRCh38.p7 | 20:410743 | TTATGCACTCAATAA[-/TAA]ACATTAGTGTCTATC | 10616 |
rs372540581 | snp | C/T | 8.75726e-05 | 0.00661654 | missense, nc-transcript-variant, utr-variant-3-prime | RBCK1 | GRCh38.p7 | 20:428978 | CAGGGCGAGGCCATG[C/T]GCTGCCCCCAGTGCC | 10616 |
rs372591105 | snp | C/T | 4.97195e-05 | 0.00498571 | utr-variant-5-prime, missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:417808 | CACGAGACCAGGAGA[C/T]CCTGCACTCCCATGG | 10616 |
rs372731662 | snp | C/G | 1.66871e-05 | 0.00288847 | synonymous-codon, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:422181 | GGAGGTCTCCTGCCC[C/G]TTCATTGACAACACC | 10616 |
rs372760165 | snp | C/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:416839 | CTGTCTCTACAAAAA[C/T]TTAAAAAATTAGCCA | 10616 |
rs372810496 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | RBCK1 | GRCh38.p7 | 20:427681 | ACAGACGGAGTCCCA[C/G]CCCCAGCCCCAGATG | 10616 |
rs372845814 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RBCK1 | GRCh38.p7 | 20:424453 | CCCCTGCCTCTCTCC[C/T]ATGCCCCTATTTCTC | 10616 |
rs372883087 | snp | C/G | 0.00398564 | 0.0444627 | upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:407655 | CGGTGACCGCTGAGA[C/G]GCAGCGTCGGATCTG | 10616 |
rs372940635 | in-del | -/GT | | | intron-variant | RBCK1 | GRCh38.p7 | 20:426208 | GCATTTATCCTTTGT[-/GT]TACAGACAATCCAGT | 10616 |
rs372983302 | snp | A/G | 8.77385e-05 | 0.00662281 | missense, nc-transcript-variant, utr-variant-3-prime | RBCK1 | GRCh38.p7 | 20:428975 | CAGCAGGGCGAGGCC[A/G]TGCGCTGCCCCCAGT | 10616 |
rs373020265 | snp | A/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:424120 | CAGAAACAAATTGGA[A/G]TCACCACTCCGCCAG | 10616 |
rs373145383 | snp | A/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:425608 | TACTCCTTCAAGGAA[A/T]GTTTTGCATGGTGTA | 10616 |
rs373282474 | snp | C/T | 1.71164e-05 | 0.00292539 | intron-variant, synonymous-codon, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:409865 | GCTAACTGGCTCCTG[C/T]TGTACTGGCTTTCAG | 10616 |
rs373351177 | snp | A/G | 2.38416e-05 | 0.00345257 | synonymous-codon, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:428580 | CCGGCAGACGACAGA[A/G]ATGCTGAAGGTGAGG | 10616 |
rs373431777 | snp | C/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:411642 | AATGTGCTGGGACTA[C/T]AGGCGTGAGCCACCA | 10616 |
rs373437723 | snp | C/T | | | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:408082 | CTCCTTCCCGCGGCT[C/T]TGCGATGCGGCCCGC | 10616 |
rs373444531 | snp | A/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:426580 | GTATATATGTGCCAC[A/G]TTTTCTTTATAGGAT | 10616 |
rs373488350 | in-del | -/TGTGTGTGTG | | | intron-variant | RBCK1 | GRCh38.p7 | 20:417414 | GTGTGTGTGTGTGTG[-/TGTGTGTGTG]CATGGCCATGTGCCT | 10616 |
rs373808622 | snp | C/T | 0.000161987 | 0.00899818 | intron-variant | RBCK1 | GRCh38.p7 | 20:419772 | CACCTGCAGACCGCA[C/T]GGGGGAGGTGTAGGC | 10616 |
rs374013750 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:409198 | AAACAAAACCCAGAG[A/G]CCCTGGGTGGCCCAC | 10616 |
rs374247283 | snp | A/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:412374 | CACCCAAGCAGGAGT[A/G]CAATGGTGCAATCTC | 10616 |
rs374266902 | in-del | -/AT | | | intron-variant | RBCK1 | GRCh38.p7 | 20:423303 | AAACTCCGTCTGAAA[-/AT]ATATATATATATATT | 10616 |
rs374473934 | snp | C/G/T | 5.01344e-05 | 0.00500651 | intron-variant | RBCK1 | GRCh38.p7 | 20:417485 | GGCTGAGGCTGGACC[C/G/T]CTGGCCAGAGCCCAT | 10616 |
rs374537594 | in-del | -/CTGCACCTGGCTGTGACC | | | intron-variant | RBCK1 | GRCh38.p7 | 20:419885 | CACCTGGCTGTGACC[-/CTGCACCTGGCTGTGACC]TGCCCTCTCTCAAAG | 10616 |
rs374557483 | snp | C/T | | | intron-variant, utr-variant-3-prime | RBCK1 | GRCh38.p7 | 20:420140 | AAGCCTGCTCCACCT[C/T]GCCGTGACCTCACCC | 10616 |
rs374649555 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:416362 | AGACGGGTTTTCACC[A/G]TGTTAGCCAGGATGG | 10616 |
rs374711337 | snp | A/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:413661 | CACAACATGGGGGGA[A/T]TCTCAGGTCTCACCT | 10616 |
rs374741074 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | RBCK1 | GRCh38.p7 | 20:414372 | AGCCATGATCATGCC[C/T]GAGTGACAAGGTGAA | 10616 |
rs374754678 | snp | G/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:428386 | GCCAGTGACTACACC[G/T]AGAGGCATTAAGTGC | 10616 |
rs374789796 | snp | A/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:424349 | CCAGACTTGGGCACT[A/G]TGGGTTCCCAGGCCA | 10616 |
rs374913274 | snp | C/G | 1.66432e-05 | 0.00288467 | intron-variant | RBCK1 | GRCh38.p7 | 20:417659 | ACTGGGGTGAAGGCT[C/G]TCCCTTTCACTCCTG | 10616 |
rs374991295 | snp | C/T | 2.18802e-05 | 0.00330751 | intron-variant | RBCK1 | GRCh38.p7 | 20:428908 | GGCCAGGCTGGGTGA[C/T]TGCCCCAGCCCCGCC | 10616 |
rs375018967 | snp | C/G/T | 0.000336676 | 0.0129703 | missense, synonymous-codon, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:419417 | CCCAAAGCCCGGGGT[C/G/T]CCCCAGGAACCCGGA | 10616 |
rs375030772 | snp | G/T | | | intron-variant, synonymous-codon | RBCK1 | GRCh38.p7 | 20:419932 | GGTCACCCTGTGGCT[G/T]AGACCCGCTCCCTGG | 10616 |
rs375154473 | snp | A/G | 2.32962e-05 | 0.00341285 | synonymous-codon, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:428520 | GATGAACTGCAAGGA[A/G]TATCAGGAGGACCTG | 10616 |
rs375252781 | in-del | -/AACCATGCTGCTGGCAGT | | | intron-variant | RBCK1 | GRCh38.p7 | 20:419862 | CATGCTGCTGGCAGT[-/AACCATGCTGCTGGCAGT]GACCCTGCACCTGGC | 10616 |
rs375409706 | snp | C/G | | | intron-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:410771 | CTATCGTTATTTTTT[C/G]ACTGCTTTTTCATTA | 10616 |
rs375413509 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | RBCK1 | GRCh38.p7 | 20:419472 | GAGCCCCCACCGGTA[A/G]GCTGTCCTTGGCCTC | 10616 |
rs375464941 | snp | C/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:418367 | GTGGGTTTTACCACA[C/T]GTGCTTTCTTTTTTT | 10616 |
rs375598489 | snp | A/G | 2.24454e-05 | 0.00334996 | intron-variant | RBCK1 | GRCh38.p7 | 20:417956 | GCCCTGAGCACCGCC[A/G]GACCCAGCGGGGGCC | 10616 |
rs375635112 | snp | C/T | 1.70504e-05 | 0.00291975 | synonymous-codon, nc-transcript-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:429070 | GATCTGCTGGGTCAC[C/T]AAGGGCCCACGCTGG | 10616 |
rs375670781 | snp | C/T | | | intron-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:429197 | ATATCCAACCCAGCA[C/T]CTGAATTTGTACAGC | 10616 |
rs375909448 | snp | A/C/G/T | 4.9663e-05 | 0.00498291 | utr-variant-3-prime, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:430441 | ACTGAGCTAAAGATG[A/C/G/T]TGGGGCCACATGCTG | 10616 |
rs375997075 | snp | C/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:424476 | TATTTCTCCTGAGAA[C/T]GCTCCCAACTTCACC | 10616 |
rs376006512 | snp | A/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:417002 | TCTTAAAATTAAATC[A/G]AGACATACAAATGAA | 10616 |
rs376043659 | snp | C/T | 8.62701e-05 | 0.00656716 | intron-variant | RBCK1 | GRCh38.p7 | 20:428483 | CTTGAGTCCCTCACC[C/T]GCTACAGGCCATCCA | 10616 |
rs376155806 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | RBCK1 | GRCh38.p7 | 20:425621 | AATGTTTTGCATGGT[A/G]TATTCTTTTTTTTTT | 10616 |
rs376202580 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:430005 | CAGATGGTAGCTGTC[A/G]TTATTAGGGGTGTGC | 10616 |
rs376438608 | snp | C/G | 6.72314e-05 | 0.00579752 | utr-variant-5-prime, intron-variant, missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:409886 | TGGCTTTCAGCAGAG[C/G]AAATGGCCCTGAGCC | 10616 |
rs376787224 | snp | A/G | 0.00197824 | 0.031388 | intron-variant | RBCK1 | GRCh38.p7 | 20:419775 | CTGCAGACCGCACGG[A/G]GGAGGTGTAGGCCAG | 10616 |
rs376791021 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:408849 | GGACCTGGCCTTGCC[C/T]CTGGCCAGAAGGGCC | 10616 |
rs376861314 | snp | A/G | 0.000153988 | 0.00877327 | synonymous-codon, missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:419618 | CGGCCTGGCTGTGAG[A/G]TGTGCTGCCGGGCGC | 10616 |
rs376868018 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:413788 | CCTAGCAAATGATAC[C/T]TGTTGTATGTGTTAT | 10616 |
rs376976830 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RBCK1 | GRCh38.p7 | 20:425286 | AAAGTGCTAGGATTA[C/G]AGGCGTGAGCCACCG | 10616 |
rs377036635 | snp | C/T | | | missense, synonymous-codon, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:419429 | GGTCCCCCAGGAACC[C/T]GGACGGGGGCAGCCA | 10616 |
rs377041529 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:418400 | TTGAGACGGAGTCTC[A/G]CTCTGTCGCCCAGGC | 10616 |
rs377298288 | snp | C/G | 0.000153988 | 0.00877328 | utr-variant-5-prime, missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:417759 | TATGGCTTCCCACCA[C/G]TCTTGCAGCAGTGGG | 10616 |
rs377302535 | snp | G/T | | | upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:406943 | CCCTGCCCTCTAGGA[G/T]AGGAAAACAGACCCA | 10616 |
rs377305490 | snp | C/T | 0.000119796 | 0.00773846 | synonymous-codon, nc-transcript-variant, utr-variant-3-prime | RBCK1 | GRCh38.p7 | 20:429022 | GAAGAAGGACGGCTG[C/T]GACTGGATCCGCTGC | 10616 |
rs377466962 | snp | A/G | 2.46734e-05 | 0.00351228 | synonymous-codon, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:428586 | GACGACAGAGATGCT[A/G]AAGGTGAGGCTGGGA | 10616 |
rs377605009 | snp | A/G | 0.00174024 | 0.0294464 | intron-variant, missense, nc-transcript-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:420896 | AGCAGCAGGAGGGGA[A/G]CTACCTGCAGCACGT | 10616 |
rs377615436 | snp | A/C | 0.000153988 | 0.00877328 | utr-variant-5-prime, missense, nc-transcript-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:408752 | GGATGGGCACAGCCA[A/C]GCCAGATGGACGAGA | 10616 |
rs386811499 | multinucleotide-polymorphism | CTG/GTA | | | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB, cds-indel | RBCK1 | GRCh38.p7 | 20:408217 | GTCCGCCGCCGCCGG[CTG/GTA]GCCGGGCAGTGGAGG | 10616 |
rs386811500 | multinucleotide-polymorphism | ACA/GCG | | | intron-variant | RBCK1 | GRCh38.p7 | 20:418430 | CTGGAGTGCAGTGGC[ACA/GCG]ATCTCGGCTCACTGC | 10616 |
rs386811501 | multinucleotide-polymorphism | GC/TT | | | intron-variant | RBCK1 | GRCh38.p7 | 20:419834 | CTCTCCGTTACTGCC[GC/TT]GCCCCTCCCAACCAT | 10616 |
rs386811502 | multinucleotide-polymorphism | AACCATGCTGCTGGCA/GACCCTGCACCTGGCT | | | intron-variant | RBCK1 | GRCh38.p7 | 20:419863 | CATGCTGCTGGCAGT[lengthTooLong]GTGACCCTGCACCTG | 10616 |
rs386811503 | in-del | A/GACCCTGCACCTGGCTGTG | | | intron-variant | RBCK1 | GRCh38.p7 | 20:419863 | CATGCTGCTGGCAGT[A/GACCCTGCACCTGGCTGTG]ACCCTGCACCTGGCT | 10616 |
rs397760082 | in-del | -/A | | | intron-variant | RBCK1 | GRCh38.p7 | 20:414103 | TACAAAAAAAAAAAA[-/A]GAAAAATCCCTGGGA | 10616 |
rs397826412 | in-del | -/A | | | upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:407019 | GCTGAGAAGAAAAAA[-/A]TGAAGCCAGGAAAGC | 10616 |
rs397841318 | in-del | -/C | | | intron-variant | RBCK1 | GRCh38.p7 | 20:424414 | ACAAAACACATACAC[-/C]AGACCTCCTCTTTAT | 10616 |
rs398035160 | in-del | -/T | 0 | 0 | intron-variant | RBCK1 | GRCh38.p7 | 20:425644 | TTTTTTTTTTTTTTT[-/T]GAGACGAAGTCTCAC | 10616 |
rs527251870 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RBCK1 | GRCh38.p7 | 20:422688 | AGGCGCGGGGGCATG[C/T]GCCTGTAGTCCTAGC | 10616 |
rs527392526 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:428391 | TGACTACACCTAGAG[A/G]CATTAAGTGCCTTTG | 10616 |
rs527442252 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:411794 | GGGATTACAGGTGTG[A/G]GCCACCATGCCCAAC | 10616 |
rs527577878 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:423119 | AGCCTGACTAACATG[C/G]AGAAACCCCATCTCT | 10616 |
rs527633925 | snp | G/T | 0.0111196 | 0.0737302 | intron-variant | RBCK1 | GRCh38.p7 | 20:418421 | TCGCCCAGGCTGGAG[G/T]GCAGTGGCACAATCT | 10616 |
rs527646483 | snp | A/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:418570 | AGACGGGGTTTCACC[A/G]TGTTAGCCAGGATGG | 10616 |
rs527665614 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:413769 | ATCGATGGACCCGAT[A/G]CTTCCTAGCAAATGA | 10616 |
rs528036004 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:406539 | AGGAGTTCAAGACCA[C/G]CCTGGGCAACATGAC | 10616 |
rs528042249 | snp | C/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:411488 | TTCTCCTGCCTCAGC[C/T]TCCCGAGTAGCTGGG | 10616 |
rs528101985 | snp | C/T | | | intron-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:409415 | CTCCCAGAGGCCTCC[C/T]CTGGTCTCCTTAACC | 10616 |
rs528161107 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RBCK1 | GRCh38.p7 | 20:418618 | TGTGATCCGCCCGCC[G/T]CGGCCTCCCAAAGTG | 10616 |
rs528173890 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RBCK1 | GRCh38.p7 | 20:425046 | GATGAAGTCTCACTC[C/T]GTCATCCAGGCTGGA | 10616 |
rs528362770 | snp | A/C | | | intron-variant | RBCK1 | GRCh38.p7 | 20:426504 | TAATGACCTCCAGTT[A/C]TTCCATGTTGCTGTA | 10616 |
rs528404011 | snp | G/T | 0.00358779 | 0.0422022 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:408439 | GACTTGGAACGCCCC[G/T]GCTGGGTGGTGTCCG | 10616 |
rs528441717 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:425824 | TAGAGATGGGGTTTC[A/G]CTATGTTGGCCAAGC | 10616 |
rs528572750 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:425300 | ACAGGCGTGAGCCAC[C/T]GTGCCCAGCCAGATA | 10616 |
rs528639085 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:416161 | AGCAGTCACTTTTTT[C/T]TTTTTTTTTTTTGAG | 10616 |
rs528716290 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:409715 | TATTAGAGAACCCCT[C/G]CCGGAGAAAGGGACT | 10616 |
rs528768828 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | RBCK1 | GRCh38.p7 | 20:420101 | CACCTCAGCTCGGAC[A/C]TCACCCCCACCCGTC | 10616 |
rs528821769 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | RBCK1 | GRCh38.p7 | 20:418604 | CGATCTCCTGACTTT[A/G]TGATCCGCCCGCCTC | 10616 |
rs528886138 | snp | C/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:424685 | ATATGTCCCCAGCAC[C/T]CATAGCCATTTGCTT | 10616 |
rs528956730 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | RBCK1 | GRCh38.p7 | 20:418554 | TTTATATTTTTAGTA[C/G]AGACGGGGTTTCACC | 10616 |
rs529034729 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:407270 | ACGAAGACAGAGATC[A/G]GGAGGCAATTTGCGA | 10616 |
rs529296730 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:425103 | GCAAGCTCCGCCTCC[C/T]GGGTTCACGCCATTC | 10616 |
rs529473960 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:415107 | TTGGCGGGGCACGAT[A/G]GATGATGCTTGTAAT | 10616 |
rs529496478 | snp | C/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:418614 | ACTTTGTGATCCGCC[C/T]GCCTCGGCCTCCCAA | 10616 |
rs529603216 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RBCK1 | GRCh38.p7 | 20:418997 | TCTTTTTTTTGGCGG[A/G]GGTTGGGGGCTGATG | 10616 |
rs529733446 | snp | A/C/G | 3.98678e-05 | 0.0044646 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:408736 | ACGGTCCCCCCCAGG[A/C/G]GGATGGGCACAGCCA | 10616 |
rs529790930 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:415594 | TATTTTTATGCCACT[A/G]GTTTTTTTTTTAAGA | 10616 |
rs529839562 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:409258 | GCTCACTCTACTGGA[A/G]CCCCACTGGCTTCCT | 10616 |
rs530002162 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | RBCK1 | GRCh38.p7 | 20:417008 | AATTAAATCAAGACA[C/T]ACAAATGAATCCTGC | 10616 |
rs530020671 | snp | C/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:415015 | TTTTGAGAGCATTTT[C/T]TGGACTGCTTTTAAA | 10616 |
rs530137240 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RBCK1 | GRCh38.p7 | 20:416317 | CCCGCCACCGTGCCT[A/G]GCTAATTTTTTTTTT | 10616 |
rs530212368 | snp | C/G | | | intron-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:429186 | GCCCATGGGCCATAT[C/G]CAACCCAGCACCTGA | 10616 |
rs530409828 | in-del | -/CCAT | | | intron-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:420671 | CTGCTCCTGCCCATC[-/CCAT]CCCCACCCCCCACCC | 10616 |
rs530484939 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:408615 | CCGCGGGGACAGCGA[A/G]GCACACACAGGGCTT | 10616 |
rs530559902 | snp | A/T | 0.00199481 | 0.0315187 | upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:407613 | AGACGAATGCAAACT[A/T]CACCAATAGCTCAAC | 10616 |
rs530577178 | snp | C/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:413159 | ATATATCTGCCCTTA[C/T]GCCAGTACCACACTA | 10616 |
rs530593516 | snp | A/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:428862 | CTCCACAGCTCTAGA[A/G]GGTCACCACCTTCTC | 10616 |
rs530612161 | in-del | -/TCTCAT | 0.00438332 | 0.0466095 | intron-variant | RBCK1 | GRCh38.p7 | 20:412722 | TTTGCAAAAATTTTC[-/TCTCAT]TCTGTGGATTGTCTT | 10616 |
rs530677897 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:414973 | CATTGATAGTTGACT[A/G]GGTATTCAAATTGTT | 10616 |
rs530780138 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RBCK1 | GRCh38.p7 | 20:415846 | GAAGCGGGAGCAGGC[A/T]CTTCACATGGTGAGA | 10616 |
rs530917281 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:426335 | AATTTGCCATCCCCA[C/T]TCCCCTGCCACGCCT | 10616 |
rs530927820 | snp | A/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:412217 | TGGTTTTGATTTGCA[A/G]TTTCCTAACCATTTG | 10616 |
rs531033984 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:409656 | ACCCTGGGAATGGGA[A/T]GGACAAACAACCAAA | 10616 |
rs531215245 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:416247 | TGCACGGTCCGCCTC[C/T]CGGGTTCACACCATT | 10616 |
rs531364402 | snp | A/T | 6.59055e-05 | 0.00574007 | missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:427400 | AGCTACCATTGCAAG[A/T]CCCCAGATTGCAAGG | 10616 |
rs531750880 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:411789 | GTGCTGGGATTACAG[G/T]TGTGAGCCACCATGC | 10616 |
rs531820543 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:418403 | AGACGGAGTCTCGCT[C/G]TGTCGCCCAGGCTGG | 10616 |
rs531840206 | snp | A/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:416933 | GGTTGATACTGCAGT[A/G]AGCCAAGGTAGCACT | 10616 |
rs532230520 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:410812 | AGGCAATAGTTTTAT[G/T]GTTTCTGATTTTTGG | 10616 |
rs532374024 | snp | C/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:415155 | CTGAGGCAGGTGGAC[C/T]GCTTGAACCCATGAG | 10616 |
rs532442476 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:426466 | ATGTTTGTTTGTCTG[G/T]GCCTGGCTTATTTCA | 10616 |
rs532482744 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:422426 | CCCCCCAGACATTTT[C/T]CAAGAGCTTTGTCCA | 10616 |
rs532542504 | snp | C/T | 2.0219e-05 | 0.00317948 | intron-variant | RBCK1 | GRCh38.p7 | 20:417942 | GAAGGTGAGGCTCTG[C/T]CCTGAGCACCGCCGG | 10616 |
rs532621367 | snp | G/T | 0.00424827 | 0.0458921 | intron-variant | RBCK1 | GRCh38.p7 | 20:417206 | TAACAACAACTTCTG[G/T]TGGTTTCACTAAGGA | 10616 |
rs532857178 | snp | C/T | 6.81327e-05 | 0.00583624 | synonymous-codon, nc-transcript-variant, utr-variant-3-prime | RBCK1 | GRCh38.p7 | 20:429040 | CTGGATCCGCTGCAC[C/T]GTCTGCCACACCGAG | 10616 |
rs532871228 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:429497 | TCCCAAAGTGCTAGG[A/G]TTACAGGCGTGAGCC | 10616 |
rs532915796 | snp | C/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:422806 | CACTGCACTCCAGCC[C/T]GGGCAACAGAGTGAG | 10616 |
rs533062130 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:418529 | GCCCGCCACCACGCC[C/T]GGCTAATTTTTTATA | 10616 |
rs533107699 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:413222 | AAATACAAGTTCTCC[A/G]ACTTTTGTTCTTTTT | 10616 |
rs533185670 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:406307 | TGTTACTAAAAACTA[C/T]TGAATTGTATATTTT | 10616 |
rs533282339 | snp | A/G | 1.67044e-05 | 0.00288997 | intron-variant | RBCK1 | GRCh38.p7 | 20:417476 | GTAGCCGGTGGCTGA[A/G]GCTGGACCCCTGGCC | 10616 |
rs533532292 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:418949 | GCATTCTGCTGTCAT[A/G]TCTCAGTCCCTTTCA | 10616 |
rs533660392 | snp | A/G | 0 | 0 | intron-variant | RBCK1 | GRCh38.p7 | 20:424378 | CAAAACATGGCAGCC[A/G]AGGCCCAAATGGGAG | 10616 |
rs533688894 | snp | C/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:418595 | GGATGGTCTCGATCT[C/T]CTGACTTTGTGATCC | 10616 |
rs533742759 | snp | C/G/T | 4.10366e-05 | 0.00452953 | intron-variant, missense, utr-variant-5-prime, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:417327 | GTAGCGTGGAGCCAT[C/G/T]GGAGGGGCCTAACTG | 10616 |
rs533885560 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:421586 | ACAGGAGTCCTTCCC[A/G]GAGAGGGTGGTCTGG | 10616 |
rs534063272 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | RBCK1 | GRCh38.p7 | 20:410709 | CAATGCTGAAACACT[G/T]TGCACAATGCCTGGC | 10616 |
rs534076855 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:414557 | GATGTCACATTGGAT[C/G]AGAGAGCTCCAGCTG | 10616 |
rs534126526 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | RBCK1 | GRCh38.p7 | 20:411516 | GGGACTACAGGCGCC[C/T]GCCACCACGCCCAGC | 10616 |
rs534214607 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RBCK1 | GRCh38.p7 | 20:415571 | CTTAAGTCCCTTTTA[C/T]TCTCCTCTATTTTTA | 10616 |
rs534218503 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:429202 | CAACCCAGCACCTGA[A/G]TTTGTACAGCTCCCG | 10616 |
rs534376818 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:418562 | TTTAGTAGAGACGGG[A/G]TTTCACCGTGTTAGC | 10616 |
rs534595189 | snp | G/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:428225 | AACTTAAATAAGCTG[G/T]GTGTGGCAGCACATG | 10616 |
rs535166468 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RBCK1 | GRCh38.p7 | 20:418448 | ATCTCGGCTCACTGC[A/G]AGCTCCGACTCCCGG | 10616 |
rs535226172 | snp | C/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:421287 | GGAGACTCCCTTCCC[C/G]TCTACCTTTCGCCGC | 10616 |
rs535321662 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:407868 | TAACCCGTCCCCAGC[G/T]GCTCGACGCTGTGGA | 10616 |
rs535389968 | snp | G/T | 2.62436e-05 | 0.00362231 | intron-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:408831 | TGGGAAGTGGGCCCC[G/T]CAGGACCTGGCCTTG | 10616 |
rs535526859 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:411609 | CCTGACCTCGTGATC[C/T]GCCCGCCTATGCCTC | 10616 |
rs535576881 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RBCK1 | GRCh38.p7 | 20:424117 | AGACAGAAACAAATT[A/G]GAGTCACCACTCCGC | 10616 |
rs535964216 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:418584 | CGTGTTAGCCAGGAT[A/G]GTCTCGATCTCCTGA | 10616 |
rs535986559 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:431220 | GTGTCAAGTCTGCAG[A/C]GAAGGATGGGCTTAG | 10616 |
rs536150596 | snp | C/T | 0.000725953 | 0.0190381 | intron-variant | RBCK1 | GRCh38.p7 | 20:419806 | GAAGGGAGACACCTG[C/T]GCACTGCCGCGCCTC | 10616 |
rs536305640 | snp | G/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:418224 | GCTAAAATCATAAAT[G/T]GGGTATGACAGTGAT | 10616 |
rs536423946 | in-del | -/A | 0.000934621 | 0.0215972 | intron-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:429133 | GGAGAGGGTGCCCTT[-/A]GTGGGCTTTGCCTTA | 10616 |
rs536546935 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:425374 | TAAAATGTACTCATT[C/G]TAAGTATGCAGTCAG | 10616 |
rs536662011 | snp | A/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:425837 | TCACTATGTTGGCCA[A/G]GCTAGTCTTAAACTC | 10616 |
rs536727572 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:406738 | AAAAAAAAAAGGCTT[C/T]CCCAGGCCATTCAAA | 10616 |
rs536799897 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:409537 | CCATAAGGAGAGGGG[C/T]CCTGTTTATAAATCT | 10616 |
rs536886590 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:426600 | CTTTATAGGATACTA[C/G]TTTAATCATGTCTTT | 10616 |
rs537141274 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:419743 | GCAGGTGGGCGGGAA[A/G]GTCCCTGGACAGACA | 10616 |
rs537143723 | snp | C/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:425297 | ATTACAGGCGTGAGC[C/T]ACCGTGCCCAGCCAG | 10616 |
rs537321012 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:409391 | AGGTCTTAGCTTCAG[C/T]GTTACCCCCTCCCAG | 10616 |
rs537605909 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, synonymous-codon | RBCK1 | GRCh38.p7 | 20:410547 | TCTTCCGTTAATTCC[C/T]GTGGACCAGAACTGA | 10616 |
rs537866020 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:421422 | CCGCTCACCACAGCG[A/G]ACCCTTGTGGAGCCG | 10616 |
rs537892511 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:426137 | TGAAATACTTTGATA[C/T]AGGCATGCAATGCGT | 10616 |
rs537903779 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | RBCK1 | GRCh38.p7 | 20:418814 | TCATTTTCTTACATT[-/A]ACTGGGTATAACAAT | 10616 |
rs538125039 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:416411 | GTGATCCACCCACCT[C/G]GGCCTCCCAAAGTGC | 10616 |
rs538152074 | snp | C/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:412428 | CAGGTTCAAGTGATT[C/T]TCCTGCCCCAGCCTC | 10616 |
rs538163573 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:422919 | ATTTAACCTCTCTAT[G/T]CCTCTATCTCATCTC | 10616 |
rs538276619 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RBCK1 | GRCh38.p7 | 20:427955 | CCTGGCCCTATACCA[C/T]GTCTCCACCCGTGTC | 10616 |
rs538669306 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:426013 | TGGGATGGTTGAAAC[A/G]TTATTGCCACATTGC | 10616 |
rs538873682 | snp | G/T | 0.00518109 | 0.0506754 | intron-variant | RBCK1 | GRCh38.p7 | 20:418641 | CCAAAGTGCTGGGAT[G/T]ACAGGCGTGAGCCAC | 10616 |
rs538876684 | snp | A/G | 2.57702e-05 | 0.00358949 | missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:428508 | CATCCATGAGCAGAT[A/G]AACTGCAAGGAGTAT | 10616 |
rs538934053 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:416018 | CCCACCAGGCCTCAC[C/G]TTCAACACTGAGGAT | 10616 |
rs538961301 | snp | A/G | 6.59663e-05 | 0.00574272 | missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:427472 | CCTGTGTGTTTCCAC[A/G]TCAACTGCCTGCTCT | 10616 |
rs538964683 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:427703 | CCCCAGATGGAGCCT[C/T]AAACCTAGGCAGCCC | 10616 |
rs539058982 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:429388 | TGCGCCACCACGCCC[A/G]GCTAGTTTTGTATTT | 10616 |
rs539098181 | snp | C/G | | | intron-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:420771 | TTGCCTGTGGCTGGT[C/G]TGACCCAGCCCTGAC | 10616 |
rs539365501 | in-del | -/A | 0.00318978 | 0.0398085 | intron-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:429461 | AATTCCCGACCGCAG[-/A]GTGATCCACCTGCCT | 10616 |
rs539510245 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, synonymous-codon, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:417529 | TGTTCTCTGCAGGCT[A/G]TGGGTGAGCGTGGAG | 10616 |
rs539750135 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:412979 | ATAAGGTGTGAGGTA[A/G]GGGTCCAGCTTCATT | 10616 |
rs539872930 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RBCK1 | GRCh38.p7 | 20:423958 | GTCTCAAGGTTCCAA[A/G]AGCAGCCATGGGGAG | 10616 |
rs539955441 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:429647 | TTGGAGCACAGCCGT[G/T]TTCATTCATTCACAT | 10616 |
rs539989236 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RBCK1 | GRCh38.p7 | 20:413668 | TGGGGGGAATCTCAG[C/G]TCTCACCTCAGACTT | 10616 |
rs540061976 | snp | C/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:415767 | ACTCAGTTCTGCAGG[C/T]GGTGTAGGAAGCATG | 10616 |
rs540128705 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:418633 | TCGGCCTCCCAAAGT[C/G]CTGGGATTACAGGCG | 10616 |
rs540263731 | snp | A/G/T | 1.6636e-05 | 0.00288405 | intron-variant | RBCK1 | GRCh38.p7 | 20:417649 | GGAGGGCGACACTGG[A/G/T]GTGAAGGCTCTCCCT | 10616 |
rs540389313 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:422328 | TCTTTCTTTTCTTTC[C/T]TTTTTTTTTTTGGAG | 10616 |
rs540441576 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RBCK1 | GRCh38.p7 | 20:412670 | TATTCATTTTAGCTA[A/G]AAGTACTTTATTCAT | 10616 |
rs540465178 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:427223 | GGTTGGAGTTTCTGG[A/G]CTGGGGGCTTTCTGG | 10616 |
rs540509415 | snp | A/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:416249 | CACGGTCCGCCTCCC[A/G]GGTTCACACCATTCT | 10616 |
rs540915003 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:418385 | GCTTTCTTTTTTTTT[G/T]TGAGACGGAGTCTCG | 10616 |
rs541337153 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RBCK1 | GRCh38.p7 | 20:424184 | TGTGCTTGCCGCTGG[C/T]GCTCTTCATGAATTC | 10616 |
rs541510223 | in-del | -/TAT | 0.00318978 | 0.0398085 | intron-variant | RBCK1 | GRCh38.p7 | 20:429572 | ATACCAGAAGATGAC[-/TAT]TATTTTGTGACGTGA | 10616 |
rs541548912 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:406232 | GTAGGTGTGAGCCAC[C/T]ATGCTCAGCCAAAAA | 10616 |
rs541641346 | snp | A/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:419071 | TCAGCGGTGCTCTTG[A/G]GTCCCTCTTGGTGCA | 10616 |
rs541688718 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:431389 | CAAGCAAGATGGCAC[A/G]GTATCGATTCAGCAG | 10616 |
rs541719568 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:428765 | CATGTCAGGAAGAGC[A/G]TCTGGGTGGAGGGTG | 10616 |
rs542131511 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:429376 | GGATTACAGGCATGC[A/G]CCACCACGCCCGGCT | 10616 |
rs542217738 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RBCK1 | GRCh38.p7 | 20:413023 | ATATTGAGTTGTGCC[A/G]GCACTATTTGTTAAG | 10616 |
rs542252619 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:418711 | TCTATATAAAATTAT[A/T]TTTTTTCTGAACCAT | 10616 |
rs542289782 | snp | A/C/T | 0.00159617 | 0.0282053 | intron-variant | RBCK1 | GRCh38.p7 | 20:418525 | AGGCGCCCGCCACCA[A/C/T]GCCCGGCTAATTTTT | 10616 |
rs542354159 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | RBCK1 | GRCh38.p7 | 20:412209 | TCTCACTGTGGTTTT[C/G]ATTTGCAATTTCCTA | 10616 |
rs542354774 | snp | G/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:428170 | TGTTAGGGATGCAGG[G/T]TCTCACCCTAGGGGT | 10616 |
rs542492557 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:406143 | AGACAGGGTTTCACC[A/G]TGTTGGCCAGGCTGG | 10616 |
rs542666766 | snp | C/T | 0.00517822 | 0.0506191 | utr-variant-3-prime, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:430553 | GCCCTGCCTGCACTG[C/T]GGTTGTCCACGGTCA | 10616 |
rs542669029 | snp | A/C | | | upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:406096 | TACAGATGTCCGCCA[A/C]CACACCTGGCTAATT | 10616 |
rs542670138 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:425422 | TAACTCTCGTAACCA[C/T]CAACCACTGTTACAT | 10616 |
rs542778827 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:408290 | TCCCGCCCCACTTCC[A/G]GGGCCGCCACTTTCA | 10616 |
rs542885659 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:421089 | AGCCGCCAATTACGC[A/G]GGGCTGGACGTGGGT | 10616 |
rs542971880 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | RBCK1 | GRCh38.p7 | 20:426183 | GAGAATGGGGAATCC[A/G]TCCCCTCAAGCATTT | 10616 |
rs543264334 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:425751 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGACTA | 10616 |
rs543275589 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:415670 | ATCCATTACCTCTTC[A/G]TGGTATGTATTAGAC | 10616 |
rs543326130 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, missense | RBCK1 | GRCh38.p7 | 20:419954 | GCTCCCTGGCTGTGG[C/T]GCACATCCAGGTTCA | 10616 |
rs543366019 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:413240 | TTTTGTTCTTTTTCA[A/G]TATTGTTTTGGTTAT | 10616 |
rs543382263 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:430008 | ATGGTAGCTGTCGTT[A/G]TTAGGGGTGTGCTCT | 10616 |
rs543518086 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RBCK1 | GRCh38.p7 | 20:430273 | CAGAGGCAAAGGCCC[A/G]GGGTGGGAGAGCGCT | 10616 |
rs543553562 | snp | A/G | 0.00755907 | 0.0610114 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:408219 | CCGCCGCCGCCGGGT[A/G]GCCGGGCAGTGGAGG | 10616 |
rs543554306 | snp | G/T | | | upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:407707 | CTGCCAGGCCTGGAT[G/T]CAAACCTCGGCTGAG | 10616 |
rs543628186 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RBCK1 | GRCh38.p7 | 20:414145 | GCAGGTATAAACTCA[C/T]GCTGGGCATGGCGGC | 10616 |
rs544008312 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | RBCK1 | GRCh38.p7 | 20:425262 | GTGATCCACCCACCT[C/T]GGCCTCCCAAAGTGC | 10616 |
rs544068610 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RBCK1 | GRCh38.p7 | 20:425605 | TAATACTCCTTCAAG[G/T]AATGTTTTGCATGGT | 10616 |
rs544076645 | snp | A/G | | | missense, synonymous-codon, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:419369 | CTTCAAGGACCTCAC[A/G]CTGCAGCCGCGGGGC | 10616 |
rs544159284 | snp | C/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:413232 | TCTCCAACTTTTGTT[C/T]TTTTTCAATATTGTT | 10616 |
rs544211970 | snp | C/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:414987 | TGGGTATTCAAATTG[C/T]TTACCTGAAGAATTT | 10616 |
rs544235364 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RBCK1 | GRCh38.p7 | 20:421735 | GAAGGGGGTAATCAG[A/G]GCAGGATAGAGAGGT | 10616 |
rs544278174 | snp | A/T | 0.15698 | 0.23205 | intron-variant | RBCK1 | GRCh38.p7 | 20:419871 | TGGCAGTGACCCTGC[A/T]CCTGGCTGTGACCCT | 10616 |
rs544310400 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:415584 | TACTCTCCTCTATTT[C/T]TATGCCACTAGTTTT | 10616 |
rs544403878 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:426984 | GTGTGAGCACCACAC[C/G]TGGTTATTTTATTTT | 10616 |
rs544518686 | snp | C/T | 6.62361e-05 | 0.00575445 | utr-variant-5-prime, missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:417603 | CTGATATGACAGTGG[C/T]GTCTCTCAAGGACAT | 10616 |
rs544560978 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:431423 | TTACTAGAACCCACT[C/G]TGTGCTGGTCGGAGG | 10616 |
rs544567357 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:413070 | TAATCATCTTAACCC[G/T]TTTTGGAAATTAATT | 10616 |
rs544731593 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:418828 | TTACTGGGTATAACA[A/G]TCCAACTCAGGAAAC | 10616 |
rs544905735 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:410319 | GTGACGTAAACAAAT[G/T]TGATGGCAGGGAGTC | 10616 |
rs544970910 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:415535 | CCAAACAAGATCTAC[A/C]TGTAGCATTTCTTAC | 10616 |
rs545017655 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:414924 | TTTAGAGTCTTTGCA[C/T]GTTTAAAAATTTCTA | 10616 |
rs545079804 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | RBCK1 | GRCh38.p7 | 20:425241 | GTCTTGAACTCCTGA[C/G]CTCAGGTGATCCACC | 10616 |
rs545105196 | snp | C/T | 5.05932e-05 | 0.00502932 | intron-variant | RBCK1 | GRCh38.p7 | 20:419324 | GCCGCGTGGAACCAC[C/T]ACCCTTTAACCCTCC | 10616 |
rs545301043 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:416647 | GATTTTCCAAACATG[C/T]TGGAGGATCCTCAAG | 10616 |
rs545393831 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:421719 | GCTGGAGCAGAGGGA[C/T]GAAGGGGGTAATCAG | 10616 |
rs545579049 | snp | C/T | | | upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:406297 | ATTCTGTAAATGTTA[C/T]TAAAAACTATTGAAT | 10616 |
rs545638819 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:421134 | TGATACCTCATTGGA[C/T]GCCCGCGAAAACCTA | 10616 |
rs545702012 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:416241 | GCTCACTGCACGGTC[C/T]GCCTCCCGGGTTCAC | 10616 |
rs545713829 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:408494 | ACCTCGGCTGGTCCC[G/T]TTTCCTCCTGCGCCC | 10616 |
rs545737282 | in-del | -/CT | 0.00199481 | 0.0315187 | intron-variant | RBCK1 | GRCh38.p7 | 20:411766 | TCTTCCCACCTCAGC[-/CT]CTCAAAGTGCTGGGA | 10616 |
rs545903451 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RBCK1 | GRCh38.p7 | 20:410251 | TCATAGGGTTGTTAG[G/T]AGGTGTACTGTATTA | 10616 |
rs545999107 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:418401 | TGAGACGGAGTCTCG[C/G]TCTGTCGCCCAGGCT | 10616 |
rs546060934 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:428706 | GCTCTGACCTCCCTT[C/T]TGGCTGTCACTCCCA | 10616 |
rs546230153 | snp | C/T | 2.11182e-05 | 0.00324941 | intron-variant | RBCK1 | GRCh38.p7 | 20:417951 | GCTCTGCCCTGAGCA[C/T]CGCCGGACCCAGCGG | 10616 |
rs546469428 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:412114 | GCATATATGAGGGTT[C/G]TAGTTTCTCCACATC | 10616 |
rs546501497 | snp | A/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:412603 | GGATTACAGGCATGA[A/G]CCACTGCACCCGGCT | 10616 |
rs546711324 | snp | A/G | 3.32281e-05 | 0.0040759 | utr-variant-5-prime, intron-variant, missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:409922 | CGAGCAGTGGCGGGC[A/G]GGGATGAACAGGTGG | 10616 |
rs546752788 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | RBCK1 | GRCh38.p7 | 20:420453 | TTCGTCACTTCCCCA[C/G]CCCTGACGTTGAGTG | 10616 |
rs546838170 | snp | G/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:413746 | CTCAGACCTGCTGTT[G/T]GGTTCTCATCGATGG | 10616 |
rs546843845 | in-del | -/C | 0.00755907 | 0.0610114 | intron-variant | RBCK1 | GRCh38.p7 | 20:421267 | CGTGAGCGCAGGCGT[-/C]GGGGGGAGACTCCCT | 10616 |
rs547058548 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RBCK1 | GRCh38.p7 | 20:428404 | AGGCATTAAGTGCCT[C/T]TGTGGACTCCTGCCC | 10616 |
rs547434173 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | RBCK1 | GRCh38.p7 | 20:414228 | CCAGCCTGGGCAACA[C/T]AGTGAGACCTTGTCT | 10616 |
rs547559557 | snp | A/C | | | intron-variant, utr-variant-3-prime | RBCK1 | GRCh38.p7 | 20:420539 | CCGGCCCCCTTCCTT[A/C]CCTTGCTGCCATTGC | 10616 |
rs547623965 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | RBCK1 | GRCh38.p7 | 20:418424 | CCCAGGCTGGAGTGC[A/G]GTGGCACAATCTCGG | 10616 |
rs547657447 | snp | A/G/T | 0.00159617 | 0.0282053 | intron-variant | RBCK1 | GRCh38.p7 | 20:418575 | GGGTTTCACCGTGTT[A/G/T]GCCAGGATGGTCTCG | 10616 |
rs547664754 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RBCK1 | GRCh38.p7 | 20:411517 | GGACTACAGGCGCCC[A/G]CCACCACGCCCAGCT | 10616 |
rs547732236 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RBCK1 | GRCh38.p7 | 20:415585 | ACTCTCCTCTATTTT[C/T]ATGCCACTAGTTTTT | 10616 |
rs547815925 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RBCK1 | GRCh38.p7 | 20:429615 | ATCCACGTTTCAGTG[C/T]CCGTAGGTAAAGTGC | 10616 |
rs548013102 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RBCK1 | GRCh38.p7 | 20:418619 | GTGATCCGCCCGCCT[C/T]GGCCTCCCAAAGTGC | 10616 |
rs548076519 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:430161 | GTTCCCGGATCTAGG[C/T]GTGGGTAGACTGAGT | 10616 |
rs548272459 | snp | A/C | | | intron-variant | RBCK1 | GRCh38.p7 | 20:418629 | CGCCTCGGCCTCCCA[A/C]AGTGCTGGGATTACA | 10616 |
rs548467650 | in-del | -/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:416155 | TAGTCAGCAGTCACT[-/T]TTTTTTTTTTTTTTT | 10616 |
rs548526459 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RBCK1 | GRCh38.p7 | 20:417991 | ACTCACTTGAGGGCA[A/T]AGGGCAAGCAGGGGC | 10616 |
rs548606452 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:413353 | TTGGTAGGGATTTCA[C/T]TGAATCTGTAGATCA | 10616 |
rs548692022 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RBCK1 | GRCh38.p7 | 20:418611 | CTGACTTTGTGATCC[A/G]CCCGCCTCGGCCTCC | 10616 |
rs548809867 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:423824 | GCCTGGCTGGTGGGT[C/T]AGCCGCGGTGGCCTG | 10616 |
rs548829354 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:424778 | AAAGGGCTGCATGAA[C/T]TTCCCTGGAGCCCAC | 10616 |
rs548958736 | in-del | -/T | 0.00636936 | 0.0560724 | intron-variant | RBCK1 | GRCh38.p7 | 20:418535 | ACCACGCCCGGCTAA[-/T]TTTTTTATATTTTTA | 10616 |
rs549339903 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RBCK1 | GRCh38.p7 | 20:425104 | CAAGCTCCGCCTCCC[A/G]GGTTCACGCCATTCT | 10616 |
rs549369680 | snp | A/C/G | 0.000394282 | 0.014036 | missense, synonymous-codon, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:419671 | CGCCTCATACCAGCC[A/C/G]GACGAGGAGGAGCGA | 10616 |
rs549445505 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:419001 | TTTTTTGGCGGGGGT[C/T]GGGGGCTGATGTTTC | 10616 |
rs549514624 | snp | A/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:422867 | AGTCAGGGAACTCTG[A/G]AGCCTGGTGGCCTGG | 10616 |
rs549551276 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:411911 | CATTTGGGTGTTTCT[A/G]TTTTTTGGCTATTAT | 10616 |
rs549598957 | snp | G/T | | | intron-variant, utr-variant-3-prime | RBCK1 | GRCh38.p7 | 20:420265 | ATGACCCCCGACCCC[G/T]GTCCTACGCCTTAGC | 10616 |
rs549633848 | snp | A/G | 1.9756e-05 | 0.00314287 | utr-variant-5-prime, missense, nc-transcript-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:408743 | CCCCCAGGGGGATGG[A/G]CACAGCCACGCCAGA | 10616 |
rs549656180 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:414404 | CCCTGTCTCAAAGAA[A/G]GAAAGAGAGAAAAGC | 10616 |
rs549828065 | in-del | -/T | | | upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:406637 | AGCTGAGCCCAGGAG[-/T]TTGGAGGCTGTAGTG | 10616 |
rs549865974 | snp | C/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:418437 | GCAGTGGCACAATCT[C/T]GGCTCACTGCAAGCT | 10616 |
rs549956629 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:430847 | TGGAACTCTTGCTAA[C/G]CTGTTCAGAGCCAGG | 10616 |
rs549981055 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:429656 | AGCCGTGTTCATTCA[C/T]TCACATGTTGGCTGT | 10616 |
rs550001016 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:412458 | CCTGAGTAGCTGGAT[C/T]ACAGGTGCCCACCAC | 10616 |
rs550248595 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:424403 | TGGGAGATCCCCACA[A/G]AACACATACACAGAC | 10616 |
rs550357071 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RBCK1 | GRCh38.p7 | 20:415070 | TTAAATACTTTAGTA[C/T]GTGTCTTCAAAAAAT | 10616 |
rs550390300 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:414333 | GAGAGGATTATTAGA[A/C]CCTGGGTGGTTGAGG | 10616 |
rs550458134 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:418640 | CCCAAAGTGCTGGGA[C/T]TACAGGCGTGAGCCA | 10616 |
rs550460441 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RBCK1 | GRCh38.p7 | 20:425089 | GATCTCAGCCCACTG[C/T]AAGCTCCGCCTCCCG | 10616 |
rs550551366 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | RBCK1 | GRCh38.p7 | 20:425902 | AGTGTTCAGATTACA[C/G]GCGTGATCCATCATT | 10616 |
rs550684613 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RBCK1 | GRCh38.p7 | 20:415866 | ACATGGTGAGAGAGG[A/G]AGCAAGAGAGAGAGT | 10616 |
rs550735479 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:425364 | TTGCACACAATAAAA[G/T]GTACTCATTGTAAGT | 10616 |
rs550895061 | snp | A/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:411629 | GCCTATGCCTCCCAA[A/T]GTGCTGGGACTACAG | 10616 |
rs550982004 | snp | C/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:411589 | AACCAGGATGGTCTC[C/G]ATCTCCTGACCTCGT | 10616 |
rs550987081 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:409431 | CTGGTCTCCTTAACC[G/T]GTTTATTTCCCTGCC | 10616 |
rs550987854 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:409792 | GAGAAAGCAGCACAC[A/G]CAAAGGATCGCCTCC | 10616 |
rs551016864 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:413595 | TGGCGTTTCCTTTGT[A/C]AAATGTACAATGTCA | 10616 |
rs551062353 | snp | A/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:426929 | CTTCTGGGCTCAAGC[A/G]ATCCTCACAACCCAG | 10616 |
rs551076176 | snp | A/T | 0.00199481 | 0.0315187 | upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:406577 | TGTCTCTACAAAAAT[A/T]AGCCAGCTGTGGTGG | 10616 |
rs551163913 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:425114 | CTCCCGGGTTCACGC[C/T]ATTCTCCTGCCTCAG | 10616 |
rs551204417 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:414257 | CTCTGCAAAAAATAA[A/G]AAAAATTAGCCAGGC | 10616 |
rs551244404 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:409596 | GGTGGCACACAGTAG[A/G]AGCTCAATAACTGCT | 10616 |
rs551296243 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RBCK1 | GRCh38.p7 | 20:425155 | AGCTGGGACTAGAGG[C/T]GCACACCGCCATGCC | 10616 |
rs551307755 | snp | G/T | | | upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:407239 | GTGGAATGAGGCAGG[G/T]GCAGGGCAGTCAGCT | 10616 |
rs551426221 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RBCK1 | GRCh38.p7 | 20:425301 | CAGGCGTGAGCCACC[A/G]TGCCCAGCCAGATAT | 10616 |
rs551591567 | in-del | -/A | 0.00279162 | 0.0372561 | intron-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:420690 | CACCCCCCACCCCCC[-/A]TCCCCCAGCCCCACC | 10616 |
rs551665998 | in-del | -/C | 0.0166325 | 0.0896639 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:431134 | TCTACCAGATGTGGA[-/C]CCCCATGCCCAGCCT | 10616 |
rs551698533 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | RBCK1 | GRCh38.p7 | 20:426536 | ATGGCAGGATTGCAT[G/T]CTTTTTTGTGGCCGA | 10616 |
rs551784348 | in-del | -/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:430012 | TAGCTGTCGTTATTA[-/G]GGGTGTGCTCTGGAA | 10616 |
rs552054205 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:408847 | CAGGACCTGGCCTTG[C/T]CCCTGGCCAGAAGGG | 10616 |
rs552115645 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:409375 | CAGCTTCTCCTCCTT[C/T]AGGTCTTAGCTTCAG | 10616 |
rs552205283 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:426473 | TTTGTCTGTGCCTGG[C/T]TTATTTCATTTAACA | 10616 |
rs552353906 | snp | A/G | 6.82245e-05 | 0.00584017 | missense, nc-transcript-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:429072 | TCTGCTGGGTCACCA[A/G]GGGCCCACGCTGGGG | 10616 |
rs552355525 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:422895 | TGGGTGTGTGACCAC[A/C]AGTCAGATATTTAAC | 10616 |
rs552376597 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | RBCK1 | GRCh38.p7 | 20:421843 | GTTCTGAGATAGACT[C/T]TAGGGGCCAGATGGA | 10616 |
rs552415974 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RBCK1 | GRCh38.p7 | 20:411939 | TATAAACAATGCTGC[C/T]GTGAACATTTGTGTC | 10616 |
rs552685513 | snp | A/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:413951 | GATTAACACTTTTGG[A/G]TGAGACAGTAGTAAG | 10616 |
rs552789635 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:415937 | GAGGACTCACTATGG[C/T]GAGAAGTCACTACAG | 10616 |
rs553008945 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:409555 | TGTTTATAAATCTCT[A/G]TGGGATTCCAGTTCC | 10616 |
rs553134392 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:431363 | GGGTTGTCCATCCTA[C/T]TTTCTCGTCTCAAGC | 10616 |
rs553141650 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:426623 | ATGTCTTTCCCAACA[A/T]TGCTTATTATTTATG | 10616 |
rs553245482 | in-del | -/TA | 0.00159617 | 0.0282053 | intron-variant | RBCK1 | GRCh38.p7 | 20:412037 | CAGTAACTCTATGTT[-/TA]ACTTTTTGAAGAAAT | 10616 |
rs553415950 | snp | C/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:427146 | ACCTGGCCTAAAATC[C/T]ACTCTTTGAATGGAG | 10616 |
rs553676705 | snp | A/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:425877 | TGATGCGCCCGCCTC[A/G]GCCTCCCAGAGTGTT | 10616 |
rs553870653 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:416550 | GTACTAGTTAGACTT[C/T]ACTGTTGCTTATTGT | 10616 |
rs553879706 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RBCK1 | GRCh38.p7 | 20:418391 | TTTTTTTTTTTGAGA[C/T]GGAGTCTCGCTCTGT | 10616 |
rs553928017 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:412040 | GTAACTCTATGTTAC[C/T]TTTTGAAGAAATGCC | 10616 |
rs554141586 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RBCK1 | GRCh38.p7 | 20:423347 | TGTCACATAGTAAGC[C/T]TTTGTTGTTGTTAGC | 10616 |
rs554199510 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:429203 | AACCCAGCACCTGAA[C/T]TTGTACAGCTCCCGA | 10616 |
rs554413615 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:418494 | CTGCCTCAGCCTCCG[C/G]AGTAGCTGGGACTAC | 10616 |
rs554616141 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RBCK1 | GRCh38.p7 | 20:416139 | AGAGATAAAGTTTCA[A/G]TTAGTCAGCAGTCAC | 10616 |
rs554620017 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:426568 | TAGTACTCCATTGTA[C/T]ATATGTGCCACGTTT | 10616 |
rs554643499 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RBCK1 | GRCh38.p7 | 20:428237 | CTGGGTGTGGCAGCA[C/T]ATGTCAGTGGTCCCA | 10616 |
rs554674208 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, synonymous-codon, nc-transcript-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:420954 | GAACACGGAGCCCGC[C/T]GAGTGCCCCGTGTGC | 10616 |
rs554867432 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | RBCK1 | GRCh38.p7 | 20:410633 | AGAATTCAGGGGTTC[A/G]CTTGGTAAGGGAAGG | 10616 |
rs554956050 | snp | C/T | 0.000165994 | 0.00910877 | intron-variant | RBCK1 | GRCh38.p7 | 20:428608 | AGGCTGGGACAGGGC[C/T]GAGGCCTAGGGATTT | 10616 |
rs554958770 | snp | A/T | | | intron-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:411106 | CTACCTTCTGGAAAT[A/T]CCATATAAGTTGAAT | 10616 |
rs555270855 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RBCK1 | GRCh38.p7 | 20:412440 | ATTCTCCTGCCCCAG[C/T]CTCCTGAGTAGCTGG | 10616 |
rs555398406 | in-del | -/C | 0.00199481 | 0.0315187 | intron-variant | RBCK1 | GRCh38.p7 | 20:421438 | ACCCTTGTGGAGCCG[-/C]CCCTGGGTGACAGGC | 10616 |
rs555531913 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:429785 | CAGCAAGTAAAGGTT[C/T]GATCTGGAGTCAGAG | 10616 |
rs555549704 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RBCK1 | GRCh38.p7 | 20:424575 | GGAGTTCACAGCTCT[A/G]ATATCAGGAGCAGCC | 10616 |
rs555869241 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:418586 | TGTTAGCCAGGATGG[A/T]CTCGATCTCCTGACT | 10616 |
rs555986925 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:406957 | AGAGGAAAACAGACC[C/T]AGAATAACATAAATA | 10616 |
rs556270791 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:431239 | GGATGGGCTTAGGGG[C/T]GGGAGGGGAAGTCTT | 10616 |
rs556392453 | snp | A/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:421223 | AGCGCCTTACCCCAG[A/G]CCCACGGCTCATGAG | 10616 |
rs556583903 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:424028 | ACTTGACACTGTCCC[A/G]TTGGCCAAAGCAAGT | 10616 |
rs557194363 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:408918 | CTCCCCATCAGTTTC[C/T]TCCTTTGGTACCTGC | 10616 |
rs557344635 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:429921 | CTTATCTCAGGCTTG[C/T]TGTCAGAATCAAGTG | 10616 |
rs557382460 | snp | A/C | 0.000798403 | 0.0199641 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:408267 | ATTTTTCCGGCCCCC[A/C]CTCCCAGTCCCGCCC | 10616 |
rs557520771 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:424757 | TGCTGGGGCCAGGTT[A/C]ATGCCAAAGGGCTGC | 10616 |
rs557655392 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:424194 | GCTGGCGCTCTTCAT[C/G]AATTCGTTAGCAGGT | 10616 |
rs557657408 | snp | A/G | 1.65493e-05 | 0.00287652 | synonymous-codon, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:430388 | CTGCCGCTGCAGGGT[A/G]AATGGGATTCCTTGC | 10616 |
rs558136876 | in-del | -/AA | | | intron-variant | RBCK1 | GRCh38.p7 | 20:413934 | AAAAAAAAAAAAAAA[-/AA]GATTAACACTTTTGG | 10616 |
rs558526612 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:415569 | GTCTTAAGTCCCTTT[C/T]ACTCTCCTCTATTTT | 10616 |
rs558649571 | snp | C/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:414960 | TGCTCTGTCAATTCA[C/T]TGATAGTTGACTGGG | 10616 |
rs558689190 | snp | A/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:412181 | TAGCCATCCTAGTAA[A/G]TTTGAAGAGGTATCT | 10616 |
rs558712113 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:425565 | ATATACTGTTTATAC[C/G]TCTTAGTTCTAGTTT | 10616 |
rs558797592 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RBCK1 | GRCh38.p7 | 20:421722 | GGAGCAGAGGGATGA[A/T]GGGGGTAATCAGAGC | 10616 |
rs558799401 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:427786 | GAATCCCAGTCCCAC[A/C]TTGAGCCCTGATCCC | 10616 |
rs559052274 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RBCK1 | GRCh38.p7 | 20:418615 | CTTTGTGATCCGCCC[A/G]CCTCGGCCTCCCAAA | 10616 |
rs559098796 | snp | A/G | 0.00199481 | 0.0315187 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:408305 | GGGGCCGCCACTTTC[A/G]CTTTCTCTTCCGCCG | 10616 |
rs559185379 | snp | A/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:407438 | GCAAGGAGGCCCAGG[A/T]GGAGGCTGGTTCAAG | 10616 |
rs559186597 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant, utr-variant-3-prime | RBCK1 | GRCh38.p7 | 20:420396 | TTGGACCCGGTGCTG[C/T]CCCTGGCCACCCCAC | 10616 |
rs559189292 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RBCK1 | GRCh38.p7 | 20:414859 | CTCCTGTATCAGACT[A/C]ATCTATTTTTGTTTT | 10616 |
rs559212251 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:424950 | AGAAAATCACCCACA[A/C]ACCCAGGAAATCCTC | 10616 |
rs559653039 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RBCK1 | GRCh38.p7 | 20:425291 | GCTAGGATTACAGGC[A/G]TGAGCCACCGTGCCC | 10616 |
rs559822286 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, synonymous-codon | RBCK1 | GRCh38.p7 | 20:420055 | TGACCCCAGCACCCT[A/G]GCCATGACCCCAGCA | 10616 |
rs559975058 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:415702 | ACTCTAGCATTGCTA[C/T]AAAGAAATATCTGAG | 10616 |
rs560063961 | snp | A/G | | | upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:406235 | GGTGTGAGCCACCAT[A/G]CTCAGCCAAAAATGT | 10616 |
rs560253511 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:409704 | GGAGTGGGGAATATT[A/C]GAGAACCCCTCCCGG | 10616 |
rs560382162 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RBCK1 | GRCh38.p7 | 20:411646 | TGCTGGGACTACAGG[C/T]GTGAGCCACCACACC | 10616 |
rs560407701 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:417143 | TTGGTTGAGAGGATT[A/G]AATGAGTTAATACAC | 10616 |
rs560528051 | snp | A/G | 1.65847e-05 | 0.0028796 | missense, synonymous-codon, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:417824 | CCTGCACTCCCATGG[A/G]GTGCGGCAGAATGGG | 10616 |
rs560707588 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:409246 | TCACCCCGCCATGCT[C/T]ACTCTACTGGAGCCC | 10616 |
rs560937638 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RBCK1 | GRCh38.p7 | 20:416310 | ACAGGCGCCCGCCAC[C/T]GTGCCTGGCTAATTT | 10616 |
rs560943976 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:426379 | AGCCTCTGGTAAGCA[A/T]CCTTTTACTGTCTGT | 10616 |
rs560996809 | snp | A/G | | | intron-variant | RBCK1 | GRCh38.p7 | 20:415008 | TGAAGAATTTTGAGA[A/G]CATTTTCTGGACTGC | 10616 |
rs561010669 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:408686 | TGGTCTCCCGCCTCT[C/T]CCAGGCGACCCGGAG | 10616 |
rs561314113 | snp | C/G | | | intron-variant, downstream-variant-500B | RBCK1 | GRCh38.p7 | 20:410830 | TTCTGATTTTTGGTT[C/G]TCTTGGTGGGTCCCA | 10616 |
rs561464973 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:427002 | GTTATTTTATTTTTT[A/G]AAAAAATTTTTTGGT | 10616 |
rs561479240 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:428380 | GGTCCTGCCAGTGAC[C/T]ACACCTAGAGGCATT | 10616 |
rs561740964 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RBCK1 | GRCh38.p7 | 20:428868 | AGCTCTAGAGGGTCA[A/C]CACCTTCTCCCTGCC | 10616 |
rs561745462 | in-del | -/TGG | 0.00199481 | 0.0315187 | intron-variant | RBCK1 | GRCh38.p7 | 20:417124 | GCAGTACCTGTCTGA[-/TGG]GTTGGTTGAGAGGAT | 10616 |
rs561784844 | in-del | -/AAA | 0.480302 | 0.0972668 | upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:406709 | GTGAAACTCCATCTC[-/AAA]AAAAAAAAAAAAAAA | 10616 |
rs561867281 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:411793 | TGGGATTACAGGTGT[G/T]AGCCACCATGCCCAA | 10616 |
rs561869349 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RBCK1 | GRCh38.p7 | 20:418523 | ACAGGCGCCCGCCAC[C/T]ACGCCCGGCTAATTT | 10616 |
rs561883464 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RBCK1 | GRCh38.p7 | 20:418531 | CCGCCACCACGCCCG[A/G]CTAATTTTTTATATT | 10616 |
rs561932073 | snp | C/T | 2.78905e-05 | 0.00373423 | missense, synonymous-codon, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:419575 | GGGCTGGCAGTGCCC[C/T]GGGTGCACCTTCATC | 10616 |
rs561987709 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:406146 | CAGGGTTTCACCATG[C/T]TGGCCAGGCTGGTCT | 10616 |
rs562488006 | snp | A/G | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:427374 | CCATTGCTGAAAACC[A/G]CAGTGCCTTCAGCTA | 10616 |
rs562806967 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:428288 | ATATTTTGCTGTTAG[C/T]ATATGTGATGACCTT | 10616 |
rs562810332 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RBCK1 | GRCh38.p7 | 20:411358 | ACTGGCATGTACCAC[C/T]ACACCCGGCTAATTT | 10616 |
rs562939403 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | RBCK1 | GRCh38.p7 | 20:418542 | CCCGGCTAATTTTTT[A/C]TATTTTTAGTAGAGA | 10616 |
rs563058912 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RBCK1 | GRCh38.p7 | 20:426347 | CCACTCCCCTGCCAC[A/G]CCTCACTACCCTTTG | 10616 |
rs563077504 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:423793 | GTCTGGGCAGGGCCT[C/T]GCTGATTTCACCTGG | 10616 |
rs563108799 | in-del | -/T | | | intron-variant | RBCK1 | GRCh38.p7 | 20:418375 | ACCACATGTGCTTTC[-/T]TTTTTTTTTTTGAGA | 10616 |
rs563326249 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RBCK1 | GRCh38.p7 | 20:414146 | CAGGTATAAACTCAC[A/G]CTGGGCATGGCGGCT | 10616 |
rs563429927 | snp | C/T | | | intron-variant, utr-variant-3-prime | RBCK1 | GRCh38.p7 | 20:410563 | GTGGACCAGAACTGA[C/T]TCCCACAGCTACAGT | 10616 |
rs563486103 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RBCK1 | GRCh38.p7 | 20:406426 | TCAATAAAGCTGTTT[A/G]TAAAAAGAACAGCAG | 10616 |
rs563657453 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RBCK1 | GRCh38.p7 | 20:430885 | CTGCACAGTTTTGAA[A/C]GCACAGCCCGTCAGG | 10616 |