Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 10180 |
| ensemblid | ENSG00000004534.15 |
| hgncid | 9903 |
| symbol | RBM6 |
| name | RNA binding motif protein 6 |
| refseq_nuc | NM_005777.3 |
| refseq_prot | NP_005768.1 |
| ensembl_nuc | ENST00000266022.9 |
| ensembl_prot | ENSP00000266022.4 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 49940150 |
| end | 50077249 |
| strand | + |
| ver | v1.2 |
| region | chr3:49940150-50077249 |
| region5000 | chr3:49935150-50082249 |
| regionname0 | RBM6_chr3_49940150_50077249 |
| regionname5000 | RBM6_chr3_49935150_50082249 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1123 | 203 | 83 | 44 | 47 | 11 | 16 | 34 | RBM6_chr3_49935150_50082249 | RBM6 | MWGDS others(1118): Show |
chr3 | 49935150 | 50082249 |
| a0002 | 0/0 | 1123 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | MWGDS others(1118): Show |
chr3 | 49935150 | 50082249 |
| a0003 | 0/0 | 1123 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | MWGDS others(1118): Show |
chr3 | 49935150 | 50082249 |
| a0004 | 0/0 | 1123 | 3 | 0 | 0 | 3 | 0 | 0 | 2 | RBM6_chr3_49935150_50082249 | RBM6 | MWGDS others(1118): Show |
chr3 | 49935150 | 50082249 |
| a0005 | 0/0 | 1123 | 2 | 0 | 1 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | MWGDS others(1118): Show |
chr3 | 49935150 | 50082249 |
| a0006 | 0/0 | 1123 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | MWGDS others(1118): Show |
chr3 | 49935150 | 50082249 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 3369 | 116 | 59 | 18 | 26 | 5 | 8 | RBM6_chr3_49935150_50082249 | RBM6 | ATGTG others(3364): Show |
chr3 | 49935150 | 50082249 | ||
| a0001c0002 | 1/1 | 3369 | 66 | 15 | 19 | 20 | 5 | 5 | RBM6_chr3_49935150_50082249 | RBM6 | ATGTG others(3364): Show |
chr3 | 49935150 | 50082249 | ||
| a0001c0003 | 0/0 | 3369 | 15 | 4 | 7 | 0 | 1 | 3 | RBM6_chr3_49935150_50082249 | RBM6 | ATGTG others(3364): Show |
chr3 | 49935150 | 50082249 | ||
| a0001c0005 | 0/0 | 3369 | 4 | 4 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | ATGTG others(3364): Show |
chr3 | 49935150 | 50082249 | ||
| a0001c0010 | 0/0 | 3369 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | ATGTG others(3364): Show |
chr3 | 49935150 | 50082249 | ||
| a0001c0011 | 0/0 | 3369 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | ATGTG others(3364): Show |
chr3 | 49935150 | 50082249 | ||
| a0002c0004 | 0/0 | 3369 | 6 | 6 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | ATGTG others(3364): Show |
chr3 | 49935150 | 50082249 | ||
| a0003c0007 | 0/0 | 3369 | 3 | 0 | 3 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | ATGTG others(3364): Show |
chr3 | 49935150 | 50082249 | ||
| a0004c0006 | 0/0 | 3369 | 3 | 0 | 0 | 3 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | ATGTG others(3364): Show |
chr3 | 49935150 | 50082249 | ||
| a0005c0008 | 0/0 | 3369 | 2 | 0 | 1 | 0 | 1 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | ATGTG others(3364): Show |
chr3 | 49935150 | 50082249 | ||
| a0006c0009 | 0/0 | 3369 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | ATGTG others(3364): Show |
chr3 | 49935150 | 50082249 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3630 | 114 | 59 | 17 | 26 | 5 | 7 | RBM6_chr3_49935150_50082249 | RBM6 | CCGGT others(3625): Show |
chr3 | 49935150 | 50082249 |
| a0001c0001t0002 | 0/0 | 3630 | 1 | 0 | 1 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | CCGGT others(3625): Show |
chr3 | 49935150 | 50082249 |
| a0001c0001t0003 | 0/0 | 3630 | 1 | 0 | 0 | 0 | 0 | 1 | RBM6_chr3_49935150_50082249 | RBM6 | CCGGT others(3625): Show |
chr3 | 49935150 | 50082249 |
| a0001c0002t0001 | 1/1 | 3630 | 66 | 15 | 19 | 20 | 5 | 5 | RBM6_chr3_49935150_50082249 | RBM6 | CCGGT others(3625): Show |
chr3 | 49935150 | 50082249 |
| a0001c0003t0001 | 0/0 | 3630 | 15 | 4 | 7 | 0 | 1 | 3 | RBM6_chr3_49935150_50082249 | RBM6 | CCGGT others(3625): Show |
chr3 | 49935150 | 50082249 |
| a0001c0005t0001 | 0/0 | 3630 | 4 | 4 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | CCGGT others(3625): Show |
chr3 | 49935150 | 50082249 |
| a0001c0010t0001 | 0/0 | 3630 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | CCGGT others(3625): Show |
chr3 | 49935150 | 50082249 |
| a0001c0011t0001 | 0/0 | 3630 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | CCGGT others(3625): Show |
chr3 | 49935150 | 50082249 |
| a0002c0004t0001 | 0/0 | 3630 | 6 | 6 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | CCGGT others(3625): Show |
chr3 | 49935150 | 50082249 |
| a0003c0007t0001 | 0/0 | 3630 | 3 | 0 | 3 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | CCGGT others(3625): Show |
chr3 | 49935150 | 50082249 |
| a0004c0006t0001 | 0/0 | 3630 | 3 | 0 | 0 | 3 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | CCGGT others(3625): Show |
chr3 | 49935150 | 50082249 |
| a0005c0008t0001 | 0/0 | 3630 | 2 | 0 | 1 | 0 | 1 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | CCGGT others(3625): Show |
chr3 | 49935150 | 50082249 |
| a0006c0009t0001 | 0/0 | 3630 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | CCGGT others(3625): Show |
chr3 | 49935150 | 50082249 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0002g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0002t0001g0045 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0002t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0002t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0002t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0002t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0002t0001g0162 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0002t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0002t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0002t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0002t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0002t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0002t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0002t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0002t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0002t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0002t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0002t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0002t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0002t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0002t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0002t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0002t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0002t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0002t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0002t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0002t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0002t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0002t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0002t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0002t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0002t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0002t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0002t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0002t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0002t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0002t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0003t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0003t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0003t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0003t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0003t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0003t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0003t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0003t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0003t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0003t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0003t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0003t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0003t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0003t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0003t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0005t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0005t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0005t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0005t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0010t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0011t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0002c0004t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0002c0004t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0002c0004t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0002c0004t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0002c0004t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0002c0004t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0003c0007t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0003c0007t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0003c0007t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0004c0006t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0004c0006t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0004c0006t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0005c0008t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0005c0008t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0006c0009t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0002 | t0001 | g0170 | EUR | GBR | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0052 | EUR | GBR | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0117 | EUR | FIN | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG00323 | hp2 | a0001 | c0002 | t0001 | g0159 | EUR | FIN | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG00597 | hp1 | a0001 | c0002 | t0001 | g0186 | EAS | CHS | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | CHS | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG00609 | hp2 | a0001 | c0002 | t0001 | g0155 | EAS | CHS | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG00639 | hp1 | a0001 | c0003 | t0001 | g0028 | AMR | PUR | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG00639 | hp2 | a0001 | c0002 | t0001 | g0156 | AMR | PUR | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG00738 | hp2 | a0001 | c0002 | t0001 | g0192 | AMR | PUR | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG01069 | hp1 | a0001 | c0002 | t0001 | g0158 | AMR | PUR | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG01069 | hp2 | a0001 | c0002 | t0001 | g0177 | AMR | PUR | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG01070 | hp1 | a0001 | c0003 | t0001 | g0032 | AMR | PUR | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG01070 | hp2 | a0001 | c0002 | t0001 | g0191 | AMR | PUR | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG01071 | hp1 | a0001 | c0002 | t0001 | g0161 | AMR | PUR | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG01071 | hp2 | a0001 | c0003 | t0001 | g0031 | AMR | PUR | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0188 | AMR | PUR | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG01099 | hp1 | a0001 | c0002 | t0001 | g0189 | AMR | PUR | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG01099 | hp2 | a0001 | c0003 | t0001 | g0027 | AMR | PUR | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0019 | AMR | PUR | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG01109 | hp2 | a0001 | c0003 | t0001 | g0010 | AMR | PUR | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG01167 | hp1 | a0001 | c0002 | t0001 | g0172 | AMR | PUR | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG01167 | hp2 | a0001 | c0002 | t0001 | g0199 | AMR | PUR | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG01175 | hp1 | a0001 | c0002 | t0001 | g0200 | AMR | PUR | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG01175 | hp2 | a0003 | c0007 | t0001 | g0203 | AMR | PUR | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG01192 | hp1 | a0001 | c0002 | t0001 | g0210 | AMR | PUR | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | CLM | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG01255 | hp2 | a0001 | c0002 | t0001 | g0206 | AMR | CLM | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG01256 | hp1 | a0001 | c0002 | t0001 | g0175 | AMR | CLM | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | CLM | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | CLM | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG01257 | hp2 | a0003 | c0007 | t0001 | g0171 | AMR | CLM | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG01346 | hp1 | a0005 | c0008 | t0001 | g0042 | AMR | CLM | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG01346 | hp2 | a0001 | c0002 | t0001 | g0163 | AMR | CLM | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG01496 | hp1 | a0001 | c0003 | t0001 | g0073 | AMR | CLM | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | CLM | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG01516 | hp1 | a0001 | c0002 | t0001 | g0153 | EUR | IBS | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0060 | EUR | IBS | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG01517 | hp1 | a0001 | c0003 | t0001 | g0030 | EUR | IBS | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG01517 | hp2 | a0001 | c0002 | t0001 | g0154 | EUR | IBS | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | ACB | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | ACB | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | ACB | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | ACB | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG01934 | hp1 | a0003 | c0007 | t0001 | g0173 | AMR | PEL | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG01934 | hp2 | a0001 | c0002 | t0001 | g0184 | AMR | PEL | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0201 | AMR | PEL | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | PEL | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG02004 | hp1 | a0001 | c0002 | t0001 | g0176 | AMR | PEL | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | KHV | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG02027 | hp2 | a0001 | c0002 | t0001 | g0152 | EAS | KHV | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0209 | AFR | ACB | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | ACB | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | KHV | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG02074 | hp2 | a0001 | c0002 | t0001 | g0149 | EAS | KHV | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | KHV | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG02145 | hp1 | a0001 | c0003 | t0001 | g0029 | AFR | ACB | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG02145 | hp2 | a0001 | c0002 | t0001 | g0181 | AFR | ACB | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG02155 | hp1 | a0001 | c0002 | t0001 | g0178 | EAS | CDX | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | CDX | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | ACB | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG02257 | hp2 | a0001 | c0002 | t0001 | g0214 | AFR | ACB | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG02258 | hp1 | a0001 | c0002 | t0001 | g0208 | AFR | ACB | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG02258 | hp2 | a0001 | c0005 | t0001 | g0102 | AFR | ACB | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | ACB | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | ACB | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG02572 | hp2 | a0002 | c0004 | t0001 | g0138 | AFR | GWD | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | GWD | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | GWD | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG02717 | hp2 | a0001 | c0005 | t0001 | g0106 | AFR | GWD | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG02735 | hp2 | a0001 | c0001 | t0003 | g0116 | SAS | PJL | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG02809 | hp1 | a0001 | c0005 | t0001 | g0105 | AFR | GWD | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | GWD | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG02818 | hp1 | a0001 | c0002 | t0001 | g0194 | AFR | GWD | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | GWD | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG02886 | hp1 | a0001 | c0003 | t0001 | g0066 | AFR | GWD | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | GWD | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG02895 | hp2 | a0002 | c0004 | t0001 | g0141 | AFR | GWD | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | GWD | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | GWD | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG02897 | hp1 | a0002 | c0004 | t0001 | g0107 | AFR | GWD | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | GWD | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | ESN | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG02922 | hp2 | a0002 | c0004 | t0001 | g0140 | AFR | ESN | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | ESN | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG02965 | hp2 | a0001 | c0002 | t0001 | g0211 | AFR | ESN | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | ESN | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG02970 | hp2 | a0001 | c0002 | t0001 | g0183 | AFR | ESN | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | ESN | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG02976 | hp2 | a0001 | c0002 | t0001 | g0197 | AFR | ESN | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | GWD | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG03041 | hp2 | a0006 | c0009 | t0001 | g0119 | AFR | GWD | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG03098 | hp1 | a0001 | c0002 | t0001 | g0202 | AFR | MSL | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | ESN | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | ESN | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | ESN | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | ESN | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | ESN | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | ESN | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG03225 | hp1 | a0001 | c0002 | t0001 | g0195 | AFR | MSL | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | MSL | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG03453 | hp1 | a0002 | c0004 | t0001 | g0133 | AFR | MSL | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG03486 | hp1 | a0001 | c0002 | t0001 | g0212 | AFR | MSL | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG03486 | hp2 | a0001 | c0011 | t0001 | g0213 | AFR | MSL | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | GWD | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | MSL | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG03831 | hp1 | a0001 | c0003 | t0001 | g0076 | SAS | BEB | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0051 | SAS | BEB | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG03834 | hp1 | a0001 | c0003 | t0001 | g0083 | SAS | BEB | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG03834 | hp2 | a0001 | c0002 | t0001 | g0190 | SAS | BEB | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG03927 | hp1 | a0001 | c0002 | t0001 | g0185 | SAS | BEB | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0025 | SAS | BEB | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG04184 | hp1 | a0001 | c0002 | t0001 | g0150 | SAS | BEB | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | BEB | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | STU | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG04199 | hp2 | a0001 | c0003 | t0001 | g0033 | SAS | STU | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0048 | SAS | STU | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG04204 | hp2 | a0001 | c0002 | t0001 | g0196 | SAS | STU | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| NA18522 | hp1 | a0001 | c0002 | t0001 | g0182 | AFR | YRI | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | YRI | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| NA18612 | hp1 | a0004 | c0006 | t0001 | g0070 | EAS | CHB | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | CHB | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | YRI | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | YRI | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| NA18952 | hp2 | a0001 | c0002 | t0001 | g0205 | EAS | JPT | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| NA18960 | hp2 | a0001 | c0002 | t0001 | g0165 | EAS | JPT | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| NA18962 | hp1 | a0001 | c0010 | t0001 | g0069 | EAS | JPT | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| NA18962 | hp2 | a0001 | c0002 | t0001 | g0174 | EAS | JPT | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| NA18965 | hp2 | a0001 | c0002 | t0001 | g0167 | EAS | JPT | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| NA18971 | hp1 | a0001 | c0002 | t0001 | g0166 | EAS | JPT | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| NA18982 | hp1 | a0001 | c0002 | t0001 | g0168 | EAS | JPT | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| NA18983 | hp2 | a0001 | c0002 | t0001 | g0204 | EAS | JPT | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| NA18986 | hp1 | a0001 | c0002 | t0001 | g0207 | EAS | JPT | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| NA18995 | hp1 | a0001 | c0002 | t0001 | g0169 | EAS | JPT | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| NA18998 | hp2 | a0001 | c0002 | t0001 | g0160 | EAS | JPT | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | LWK | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | LWK | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| NA19043 | hp1 | a0001 | c0002 | t0001 | g0151 | AFR | LWK | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| NA19043 | hp2 | a0001 | c0005 | t0001 | g0103 | AFR | LWK | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| NA19057 | hp1 | a0001 | c0002 | t0001 | g0179 | EAS | JPT | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| NA19057 | hp2 | a0004 | c0006 | t0001 | g0009 | EAS | JPT | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| NA19063 | hp2 | a0004 | c0006 | t0001 | g0072 | EAS | JPT | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| NA19066 | hp2 | a0001 | c0002 | t0001 | g0164 | EAS | JPT | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| NA19080 | hp2 | a0001 | c0002 | t0001 | g0180 | EAS | JPT | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| NA19082 | hp2 | a0001 | c0002 | t0001 | g0187 | EAS | JPT | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| NA19085 | hp1 | a0001 | c0002 | t0001 | g0111 | EAS | JPT | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | YRI | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | YRI | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| NA20129 | hp1 | a0001 | c0002 | t0001 | g0198 | AFR | ASW | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | ASW | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0047 | EUR | TSI | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| NA20752 | hp2 | a0001 | c0002 | t0001 | g0215 | EUR | TSI | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| NA20805 | hp1 | a0005 | c0008 | t0001 | g0217 | EUR | TSI | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0056 | EUR | TSI | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0041 | SAS | GIH | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| NA20905 | hp2 | a0001 | c0002 | t0001 | g0157 | SAS | GIH | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG01123 | hp1 | a0001 | c0002 | t0001 | g0193 | AMR | CLM | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG01123 | hp2 | a0001 | c0003 | t0001 | g0071 | AMR | CLM | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | ACB | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG02109 | hp2 | a0001 | c0003 | t0001 | g0064 | AFR | ACB | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | ACB | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | MSL | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG03471 | hp2 | a0001 | c0002 | t0001 | g0216 | AFR | MSL | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG06807 | hp1 | a0002 | c0004 | t0001 | g0139 | AFR | USA | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG06807 | hp2 | a0001 | c0003 | t0001 | g0063 | AFR | USA | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | USA | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | USA | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | LWK | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | LWK | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0162 | REF | REF | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0001 | g0045 | REF | REF | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:49968483 | C | T | 1 | a0005 | 2 | HG01346.hp1 NA20805.hp1 |
missense_variant | MODERATE | c.1058C>T | p.Ser353Phe | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 3/21 | 1200/3630 | 1058/3372 | 353/1123 | chr3 | 49968483 | |||
| chr3:49968593 | G | A | 1 | a0002 | 6 | HG02572.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
missense_variant | MODERATE | c.1168G>A | p.Gly390Ser | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 3/21 | 1310/3630 | 1168/3372 | 390/1123 | chr3 | 49968593 | |||
| chr3:50059680 | A | G | 1 | a0003 | 3 | HG01175.hp2 HG01257.hp2 HG01934.hp1 |
missense_variant | MODERATE | c.2162A>G | p.Asn721Ser | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 11/21 | 2304/3630 | 2162/3372 | 721/1123 | chr3 | 50059680 | |||
| chr3:50062067 | A | G | 1 | a0004 | 3 | NA18612.hp1 NA19057.hp2 NA19063.hp2 |
missense_variant | MODERATE | c.2545A>G | p.Lys849Glu | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 15/21 | 2687/3630 | 2545/3372 | 849/1123 | chr3 | 50062067 | |||
| chr3:50070483 | G | A | 1 | a0006 | 1 | HG03041.hp2 | missense_variant | MODERATE | c.3047G>A | p.Arg1016His | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 19/21 | 3189/3630 | 3047/3372 | 1016/1123 | chr3 | 50070483 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:50057780 | C | T | 1 | a0001c0011 | 1 | HG03486.hp2 | synonymous_variant | LOW | c.1746C>T | p.Ser582Ser | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 9/21 | 1888/3630 | 1746/3372 | 582/1123 | chr3 | 50057780 | |||
| chr3:50065072 | C | T | 1 | a0001c0005 | 4 | HG02258.hp2 HG02717.hp2 HG02809.hp1 others(1): Show |
synonymous_variant | LOW | c.2628C>T | p.Asp876Asp | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 16/21 | 2770/3630 | 2628/3372 | 876/1123 | chr3 | 50065072 | |||
| chr3:50066484 | G | A | 2 | a0001c0003 a0004c0006 |
18 | HG00639.hp1 HG01070.hp1 HG01071.hp2 others(15): Show |
synonymous_variant | LOW | c.2925G>A | p.Gln975Gln | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 17/21 | 3067/3630 | 2925/3372 | 975/1123 | chr3 | 50066484 | |||
| chr3:50077017 | C | A | 1 | a0001c0010 | 1 | NA18962.hp1 | synonymous_variant | LOW | c.3256C>A | p.Arg1086Arg | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 21/21 | 3398/3630 | 3256/3372 | 1086/1123 | chr3 | 50077017 | |||
| chr3:50077082 | C | T | 8 | a0001c0001 a0001c0003 a0001c0005 others(5): Show |
148 | HG00140.hp2 HG00323.hp1 HG00597.hp2 others(145): Show |
synonymous_variant | LOW | c.3321C>T | p.Tyr1107Tyr | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 21/21 | 3463/3630 | 3321/3372 | 1107/1123 | chr3 | 50077082 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:49962588 | C | T | 1 | a0001c0001t0003 | 1 | HG02735.hp2 | 5_prime_UTR_variant | MODIFIER | c.-54C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 2/21 | 54 | chr3 | 49962588 | ||||||
| chr3:50077216 | A | G | 1 | a0001c0001t0002 | 1 | HG01106.hp1 | 3_prime_UTR_variant | MODIFIER | c.*83A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 21/21 | 83 | chr3 | 50077216 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:49940319 | C | T | 1 | a0001c0001t0001g0218 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-67+94C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49940319 | |||||||
| chr3:49940353 | G | A | 8 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(5): Show |
8 | HG02486.hp2 HG02559.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.-67+128G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49940353 | |||||||
| chr3:49940548 | C | T | 1 | a0005c0008t0001g0217 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-67+323C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49940548 | |||||||
| chr3:49940636 | C | T | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
130 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.-67+411C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49940636 | |||||||
| chr3:49940890 | C | CT | 45 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(42): Show |
45 | HG01074.hp1 HG01081.hp1 HG01192.hp2 others(42): Show |
intron_variant | MODIFIER | c.-67+685dupT | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 49940890 | ||||||
| chr3:49940890 | C | CTT | 5 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 others(2): Show |
5 | HG01884.hp1 HG02257.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.-67+684_-67+685dup others(2): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 49940890 | ||||||
| chr3:49940890 | C | CTTTT | 31 | a0001c0002t0001g0149 a0001c0002t0001g0150 a0001c0002t0001g0151 others(28): Show |
31 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.-67+682_-67+685dup others(4): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 49940890 | ||||||
| chr3:49940890 | C | CTTTTT | 30 | a0001c0002t0001g0181 a0001c0002t0001g0182 a0001c0002t0001g0183 others(27): Show |
30 | HG00597.hp1 HG00738.hp2 HG01070.hp2 others(27): Show |
intron_variant | MODIFIER | c.-67+681_-67+685dup others(5): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 49940890 | ||||||
| chr3:49940890 | C | CTTTTTT | 6 | a0001c0002t0001g0211 a0001c0002t0001g0212 a0001c0002t0001g0214 others(3): Show |
6 | HG02257.hp2 HG02965.hp2 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.-67+680_-67+685dup others(6): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 49940890 | ||||||
| chr3:49940890 | CT | C | 8 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(5): Show |
8 | HG01109.hp1 HG02622.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.-67+685delT | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 49940890 | ||||||
| chr3:49941038 | C | T | 1 | a0001c0001t0001g0143 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-67+813C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49941038 | |||||||
| chr3:49941640 | C | CA | 26 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(23): Show |
26 | HG00597.hp2 HG01106.hp1 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.-67+1445dupA | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 49941640 | ||||||
| chr3:49941640 | C | CAAAAA | 7 | a0001c0001t0001g0007 a0001c0001t0001g0127 a0001c0001t0001g0128 others(4): Show |
7 | HG01891.hp2 HG02451.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.-67+1441_-67+1445d others(7): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 49941640 | ||||||
| chr3:49941640 | C | CAAAAAA | 8 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(5): Show |
8 | HG02486.hp1 HG02486.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.-67+1440_-67+1445d others(8): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 49941640 | ||||||
| chr3:49941640 | C | CAAAAAAA others(1): Show |
7 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 others(4): Show |
7 | HG02622.hp2 HG02647.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.-67+1438_-67+1445d others(10): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 49941640 | ||||||
| chr3:49941640 | C | CAAAAAAA others(3): Show |
1 | a0001c0001t0001g0001 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-67+1436_-67+1445d others(12): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 49941640 | ||||||
| chr3:49941640 | C | CAAAAAAA others(4): Show |
1 | a0006c0009t0001g0119 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-67+1435_-67+1445d others(13): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 49941640 | ||||||
| chr3:49941640 | CAAAAAAA others(1): Show |
C | 17 | a0001c0001t0001g0095 a0001c0001t0001g0108 a0001c0001t0001g0109 others(14): Show |
17 | HG00597.hp1 HG01106.hp2 HG01934.hp2 others(14): Show |
intron_variant | MODIFIER | c.-67+1438_-67+1445d others(10): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 49941640 | ||||||
| chr3:49941640 | CAAAAAAA others(2): Show |
C | 64 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0098 others(61): Show |
64 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.-67+1437_-67+1445d others(11): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 49941640 | ||||||
| chr3:49941640 | CAAAAAAA others(3): Show |
C | 5 | a0001c0001t0001g0117 a0001c0002t0001g0208 a0001c0002t0001g0209 others(2): Show |
5 | HG00323.hp1 HG01192.hp1 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.-67+1436_-67+1445d others(12): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 49941640 | ||||||
| chr3:49941640 | CAAAAAAA others(8): Show |
C | 1 | a0001c0001t0001g0075 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-67+1431_-67+1445d others(17): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 49941640 | ||||||
| chr3:49941654 | A | C | 1 | a0001c0001t0001g0118 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-67+1429A>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49941654 | |||||||
| chr3:49941657 | A | C | 1 | a0001c0001t0001g0074 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-67+1432A>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49941657 | |||||||
| chr3:49941741 | T | C | 9 | a0001c0003t0001g0010 a0001c0003t0001g0027 a0001c0003t0001g0028 others(6): Show |
9 | HG00639.hp1 HG01070.hp1 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.-67+1516T>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49941741 | |||||||
| chr3:49941764 | C | T | 15 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(12): Show |
15 | HG01891.hp2 HG02486.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.-67+1539C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49941764 | |||||||
| chr3:49941772 | T | C | 19 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(16): Show |
19 | HG00323.hp1 HG01106.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.-67+1547T>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49941772 | |||||||
| chr3:49941938 | CA | C | 61 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(58): Show |
61 | HG00323.hp1 HG01106.hp2 HG01109.hp1 others(58): Show |
intron_variant | MODIFIER | c.-67+1725delA | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 49941938 | ||||||
| chr3:49941982 | C | T | 1 | a0001c0001t0001g0026 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.-67+1757C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49941982 | |||||||
| chr3:49942024 | C | T | 6 | a0002c0004t0001g0107 a0002c0004t0001g0133 a0002c0004t0001g0138 others(3): Show |
6 | HG02572.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-67+1799C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49942024 | |||||||
| chr3:49942058 | G | A | 1 | a0006c0009t0001g0119 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-67+1833G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49942058 | |||||||
| chr3:49942098 | C | CA | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(114): Show |
117 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(114): Show |
intron_variant | MODIFIER | c.-67+1886dupA | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 49942098 | ||||||
| chr3:49942098 | C | CAA | 7 | a0001c0002t0001g0111 a0002c0004t0001g0107 a0002c0004t0001g0133 others(4): Show |
7 | HG02572.hp2 HG02895.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.-67+1885_-67+1886d others(4): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 49942098 | ||||||
| chr3:49942256 | G | A | 1 | a0001c0001t0001g0011 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-67+2031G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49942256 | |||||||
| chr3:49942271 | C | T | 17 | a0001c0001t0001g0104 a0001c0001t0001g0120 a0001c0001t0001g0121 others(14): Show |
17 | HG01243.hp1 HG01884.hp2 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.-67+2046C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49942271 | |||||||
| chr3:49942272 | G | A | 1 | a0001c0001t0003g0116 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-67+2047G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49942272 | |||||||
| chr3:49942294 | C | T | 15 | a0001c0003t0001g0010 a0001c0003t0001g0027 a0001c0003t0001g0028 others(12): Show |
15 | HG00639.hp1 HG01070.hp1 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.-67+2069C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49942294 | |||||||
| chr3:49942313 | C | G | 1 | a0001c0001t0001g0101 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-67+2088C>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49942313 | |||||||
| chr3:49942413 | C | T | 1 | a0001c0003t0001g0073 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-67+2188C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49942413 | |||||||
| chr3:49942438 | G | A | 1 | a0001c0001t0001g0034 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-67+2213G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49942438 | |||||||
| chr3:49942438 | G | T | 2 | a0001c0001t0001g0094 a0001c0010t0001g0069 |
2 | NA18962.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.-67+2213G>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49942438 | |||||||
| chr3:49942496 | C | CA | 36 | a0001c0001t0001g0035 a0001c0002t0001g0149 a0001c0002t0001g0151 others(33): Show |
36 | HG00738.hp2 HG01070.hp2 HG01081.hp2 others(33): Show |
intron_variant | MODIFIER | c.-67+2288dupA | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 49942496 | ||||||
| chr3:49942496 | CA | C | 18 | a0001c0001t0001g0034 a0001c0001t0001g0082 a0001c0001t0001g0093 others(15): Show |
18 | HG01106.hp2 HG01109.hp1 HG01256.hp2 others(15): Show |
intron_variant | MODIFIER | c.-67+2288delA | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 49942496 | ||||||
| chr3:49942785 | A | G | 1 | a0006c0009t0001g0119 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-67+2560A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49942785 | |||||||
| chr3:49943105 | G | T | 8 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(5): Show |
8 | HG02486.hp2 HG02559.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.-67+2880G>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49943105 | |||||||
| chr3:49943163 | C | T | 166 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(163): Show |
166 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.-67+2938C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49943163 | |||||||
| chr3:49943311 | A | AT | 18 | a0001c0001t0001g0035 a0001c0001t0001g0104 a0001c0001t0001g0120 others(15): Show |
18 | HG01243.hp1 HG01884.hp2 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.-67+3095dupT | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 49943311 | ||||||
| chr3:49943320 | T | C | 1 | a0001c0002t0001g0155 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-67+3095T>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49943320 | |||||||
| chr3:49943387 | C | T | 19 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(16): Show |
19 | HG00323.hp1 HG01106.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.-67+3162C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49943387 | |||||||
| chr3:49943627 | A | G | 17 | a0001c0001t0001g0104 a0001c0001t0001g0120 a0001c0001t0001g0121 others(14): Show |
17 | HG01243.hp1 HG01884.hp2 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.-67+3402A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49943627 | |||||||
| chr3:49944148 | T | C | 1 | a0001c0001t0003g0116 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-67+3923T>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49944148 | |||||||
| chr3:49944357 | A | G | 1 | a0001c0002t0001g0149 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-67+4132A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49944357 | |||||||
| chr3:49944474 | C | CT | 21 | a0001c0001t0001g0025 a0001c0001t0001g0060 a0001c0001t0001g0067 others(18): Show |
21 | HG00738.hp1 HG01074.hp1 HG01106.hp2 others(18): Show |
intron_variant | MODIFIER | c.-67+4267dupT | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 49944474 | ||||||
| chr3:49944474 | C | CTT | 17 | a0001c0001t0001g0104 a0001c0001t0001g0120 a0001c0001t0001g0121 others(14): Show |
17 | HG01243.hp1 HG01884.hp2 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.-67+4266_-67+4267d others(4): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 49944474 | ||||||
| chr3:49944474 | CT | C | 9 | a0001c0001t0001g0036 a0001c0001t0001g0112 a0001c0001t0001g0145 others(6): Show |
9 | HG01496.hp1 HG01884.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.-67+4267delT | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 49944474 | ||||||
| chr3:49944474 | CTT | C | 62 | a0001c0002t0001g0111 a0001c0002t0001g0149 a0001c0002t0001g0150 others(59): Show |
62 | HG00140.hp1 HG00323.hp2 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.-67+4266_-67+4267d others(4): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 49944474 | ||||||
| chr3:49944505 | C | T | 1 | a0001c0001t0001g0075 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-67+4280C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49944505 | |||||||
| chr3:49944765 | C | T | 1 | a0001c0002t0001g0178 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-67+4540C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49944765 | |||||||
| chr3:49944801 | T | A | 14 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(11): Show |
14 | HG00323.hp1 HG01106.hp2 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.-67+4576T>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49944801 | |||||||
| chr3:49944883 | A | AT | 27 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(24): Show |
27 | HG00639.hp1 HG00738.hp1 HG01070.hp1 others(24): Show |
intron_variant | MODIFIER | c.-67+4669dupT | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 49944883 | ||||||
| chr3:49944915 | C | T | 3 | a0001c0002t0001g0153 a0001c0002t0001g0154 a0001c0002t0001g0214 |
3 | HG01516.hp1 HG01517.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.-67+4690C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49944915 | |||||||
| chr3:49944946 | G | A | 34 | a0001c0002t0001g0111 a0001c0002t0001g0149 a0001c0002t0001g0150 others(31): Show |
34 | HG00140.hp1 HG00323.hp2 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.-67+4721G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49944946 | |||||||
| chr3:49945002 | G | C | 15 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(12): Show |
15 | HG01891.hp2 HG02486.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.-67+4777G>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49945002 | |||||||
| chr3:49945170 | C | T | 1 | a0001c0001t0001g0126 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-67+4945C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49945170 | |||||||
| chr3:49945176 | A | AT | 20 | a0001c0001t0001g0011 a0001c0001t0001g0059 a0001c0001t0001g0078 others(17): Show |
20 | HG00738.hp2 HG01070.hp2 HG01081.hp2 others(17): Show |
intron_variant | MODIFIER | c.-67+4971dupT | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 49945176 | ||||||
| chr3:49945176 | A | ATT | 53 | a0001c0002t0001g0111 a0001c0002t0001g0149 a0001c0002t0001g0150 others(50): Show |
53 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(50): Show |
intron_variant | MODIFIER | c.-67+4970_-67+4971d others(4): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 49945176 | ||||||
| chr3:49945176 | A | ATTT | 7 | a0001c0002t0001g0186 a0001c0002t0001g0202 a0001c0002t0001g0208 others(4): Show |
7 | HG00597.hp1 HG01192.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.-67+4969_-67+4971d others(5): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 49945176 | ||||||
| chr3:49945176 | AT | A | 6 | a0001c0001t0001g0012 a0001c0001t0001g0036 a0001c0001t0001g0061 others(3): Show |
6 | HG01168.hp2 HG02809.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.-67+4971delT | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 49945176 | ||||||
| chr3:49945332 | C | T | 68 | a0001c0001t0001g0145 a0001c0002t0001g0111 a0001c0002t0001g0149 others(65): Show |
68 | HG00140.hp1 HG00323.hp2 HG00597.hp1 others(65): Show |
intron_variant | MODIFIER | c.-67+5107C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49945332 | |||||||
| chr3:49945492 | A | G | 1 | a0006c0009t0001g0119 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-67+5267A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49945492 | |||||||
| chr3:49945749 | G | A | 1 | a0001c0001t0001g0082 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-67+5524G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49945749 | |||||||
| chr3:49945881 | C | CA | 25 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0013 others(22): Show |
25 | HG00323.hp1 HG00597.hp1 HG01981.hp2 others(22): Show |
intron_variant | MODIFIER | c.-67+5681dupA | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 49945881 | ||||||
| chr3:49945881 | C | CAA | 11 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(8): Show |
11 | HG01106.hp2 HG02572.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.-67+5680_-67+5681d others(4): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 49945881 | ||||||
| chr3:49945881 | CA | C | 6 | a0001c0001t0001g0022 a0001c0001t0001g0058 a0001c0001t0001g0086 others(3): Show |
6 | HG01070.hp1 HG01081.hp1 HG02129.hp2 others(3): Show |
intron_variant | MODIFIER | c.-67+5681delA | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 49945881 | ||||||
| chr3:49945881 | CAAAAAAA | C | 34 | a0001c0002t0001g0151 a0001c0002t0001g0152 a0001c0002t0001g0153 others(31): Show |
34 | HG00738.hp2 HG01069.hp2 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.-67+5675_-67+5681d others(9): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 49945881 | ||||||
| chr3:49946028 | G | A | 1 | a0001c0002t0001g0215 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-67+5803G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49946028 | |||||||
| chr3:49946055 | C | A | 1 | a0001c0001t0001g0120 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-67+5830C>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49946055 | |||||||
| chr3:49946187 | G | A | 1 | a0001c0001t0001g0039 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-67+5962G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49946187 | |||||||
| chr3:49946236 | A | G | 9 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(6): Show |
9 | HG02486.hp2 HG02559.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.-67+6011A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49946236 | |||||||
| chr3:49946245 | C | CT | 15 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(12): Show |
15 | HG01891.hp2 HG02486.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.-67+6032dupT | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 49946245 | ||||||
| chr3:49946681 | G | A | 2 | a0001c0001t0001g0108 a0001c0001t0001g0109 |
2 | HG02647.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-67+6456G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49946681 | |||||||
| chr3:49946731 | C | T | 1 | a0005c0008t0001g0217 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-67+6506C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49946731 | |||||||
| chr3:49946848 | G | GT | 6 | a0001c0001t0001g0036 a0001c0001t0001g0059 a0001c0001t0001g0079 others(3): Show |
6 | HG01192.hp1 HG01256.hp1 HG02004.hp1 others(3): Show |
intron_variant | MODIFIER | c.-67+6636dupT | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 49946848 | ||||||
| chr3:49947081 | CA | C | 28 | a0001c0001t0001g0021 a0001c0001t0001g0036 a0001c0001t0001g0096 others(25): Show |
28 | HG00597.hp1 HG00639.hp2 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.-67+6877delA | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 49947081 | ||||||
| chr3:49947081 | CAA | C | 63 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(60): Show |
63 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(60): Show |
intron_variant | MODIFIER | c.-67+6876_-67+6877d others(4): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 49947081 | ||||||
| chr3:49947081 | CAAA | C | 34 | a0001c0001t0001g0114 a0001c0002t0001g0151 a0001c0002t0001g0152 others(31): Show |
34 | HG00738.hp2 HG01069.hp2 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.-67+6875_-67+6877d others(5): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 49947081 | ||||||
| chr3:49947109 | G | A | 2 | a0002c0004t0001g0138 a0002c0004t0001g0140 |
2 | HG02572.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-67+6884G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49947109 | |||||||
| chr3:49947262 | AG | A | 32 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0020 others(29): Show |
32 | HG01071.hp2 HG01099.hp2 HG01123.hp2 others(29): Show |
intron_variant | MODIFIER | c.-67+7052delG | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 49947262 | ||||||
| chr3:49947262 | AGG | A | 35 | a0001c0001t0001g0008 a0001c0001t0001g0014 a0001c0001t0001g0024 others(32): Show |
35 | HG00140.hp2 HG00639.hp1 HG00738.hp1 others(32): Show |
intron_variant | MODIFIER | c.-67+7051_-67+7052d others(4): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 49947262 | ||||||
| chr3:49947262 | AGGG | A | 24 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(21): Show |
24 | HG01106.hp2 HG01168.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.-67+7050_-67+7052d others(5): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 49947262 | ||||||
| chr3:49947262 | AGGGG | A | 26 | a0001c0001t0001g0026 a0001c0001t0001g0095 a0001c0001t0001g0096 others(23): Show |
26 | HG00323.hp1 HG01109.hp1 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.-67+7049_-67+7052d others(6): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 49947262 | ||||||
| chr3:49947266 | G | C | 10 | a0001c0001t0001g0067 a0001c0001t0001g0080 a0001c0001t0001g0081 others(7): Show |
10 | HG01074.hp1 HG01243.hp2 HG02735.hp1 others(7): Show |
intron_variant | MODIFIER | c.-67+7041G>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49947266 | |||||||
| chr3:49947272 | GGGGGGT | G | 26 | a0001c0002t0001g0111 a0001c0002t0001g0150 a0001c0002t0001g0155 others(23): Show |
26 | HG00140.hp1 HG00609.hp2 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.-67+7048_-67+7053d others(8): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49947272 | |||||||
| chr3:49947274 | GGGGT | G | 18 | a0001c0002t0001g0151 a0001c0002t0001g0153 a0001c0002t0001g0154 others(15): Show |
18 | HG01069.hp2 HG01081.hp2 HG01099.hp1 others(15): Show |
intron_variant | MODIFIER | c.-67+7050_-67+7053d others(6): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49947274 | |||||||
| chr3:49947275 | GGGT | G | 14 | a0001c0002t0001g0152 a0001c0002t0001g0182 a0001c0002t0001g0183 others(11): Show |
14 | HG00738.hp2 HG01192.hp1 HG01934.hp2 others(11): Show |
intron_variant | MODIFIER | c.-67+7051_-67+7053d others(5): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49947275 | |||||||
| chr3:49947277 | G | T | 15 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(12): Show |
15 | HG01891.hp2 HG02486.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.-67+7052G>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49947277 | |||||||
| chr3:49947315 | A | G | 4 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0132 others(1): Show |
4 | HG01891.hp2 HG02970.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-67+7090A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49947315 | |||||||
| chr3:49947346 | C | A | 1 | a0001c0001t0001g0040 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-67+7121C>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49947346 | |||||||
| chr3:49947559 | T | C | 2 | a0001c0001t0001g0086 a0001c0001t0001g0087 |
2 | HG01081.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.-67+7334T>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49947559 | |||||||
| chr3:49947707 | C | T | 1 | a0001c0001t0001g0038 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-67+7482C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49947707 | |||||||
| chr3:49948353 | C | G | 3 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0020 |
3 | HG02559.hp1 HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-67+8128C>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49948353 | |||||||
| chr3:49948420 | A | G | 14 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(11): Show |
14 | HG00323.hp1 HG01106.hp2 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.-67+8195A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49948420 | |||||||
| chr3:49948464 | C | T | 6 | a0002c0004t0001g0107 a0002c0004t0001g0133 a0002c0004t0001g0138 others(3): Show |
6 | HG02572.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-67+8239C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49948464 | |||||||
| chr3:49948479 | C | A | 6 | a0002c0004t0001g0107 a0002c0004t0001g0133 a0002c0004t0001g0138 others(3): Show |
6 | HG02572.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-67+8254C>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49948479 | |||||||
| chr3:49948651 | G | A | 1 | a0006c0009t0001g0119 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-67+8426G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49948651 | |||||||
| chr3:49948672 | A | G | 1 | a0001c0001t0001g0136 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-67+8447A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49948672 | |||||||
| chr3:49948685 | T | C | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
130 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.-67+8460T>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49948685 | |||||||
| chr3:49948710 | CAAAAAAG others(6964): Show |
C | 5 | a0001c0002t0001g0179 a0001c0002t0001g0180 a0001c0002t0001g0187 others(2): Show |
5 | NA18952.hp2 NA18983.hp2 NA19057.hp1 others(2): Show |
intron_variant | MODIFIER | c.-67+8490_-66-6891d others(2): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 49948710 | ||||||
| chr3:49948717 | GA | G | 23 | a0001c0001t0001g0036 a0001c0001t0001g0104 a0001c0001t0001g0120 others(20): Show |
23 | HG01243.hp1 HG01884.hp2 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.-67+8506delA | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 49948717 | ||||||
| chr3:49948785 | C | T | 2 | a0002c0004t0001g0107 a0002c0004t0001g0141 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-67+8560C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49948785 | |||||||
| chr3:49948827 | A | AT | 21 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(18): Show |
21 | HG00639.hp1 HG01099.hp2 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.-67+8623dupT | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 49948827 | ||||||
| chr3:49948827 | AT | A | 73 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(70): Show |
73 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.-67+8623delT | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 49948827 | ||||||
| chr3:49948987 | G | A | 1 | a0006c0009t0001g0119 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-67+8762G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49948987 | |||||||
| chr3:49949024 | T | G | 1 | a0001c0002t0001g0177 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-67+8799T>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49949024 | |||||||
| chr3:49949159 | G | T | 1 | a0001c0001t0001g0084 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.-67+8934G>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49949159 | |||||||
| chr3:49949608 | T | C | 1 | a0001c0010t0001g0069 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.-67+9383T>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49949608 | |||||||
| chr3:49949621 | T | A | 4 | a0001c0005t0001g0102 a0001c0005t0001g0103 a0001c0005t0001g0105 others(1): Show |
4 | HG02258.hp2 HG02717.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.-67+9396T>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49949621 | |||||||
| chr3:49949679 | A | G | 1 | a0001c0002t0001g0199 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-67+9454A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49949679 | |||||||
| chr3:49949740 | C | T | 1 | a0001c0001t0001g0022 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-67+9515C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49949740 | |||||||
| chr3:49949919 | C | G | 1 | a0006c0009t0001g0119 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-67+9694C>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49949919 | |||||||
| chr3:49950042 | C | T | 34 | a0001c0002t0001g0151 a0001c0002t0001g0152 a0001c0002t0001g0153 others(31): Show |
34 | HG00738.hp2 HG01069.hp2 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.-67+9817C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49950042 | |||||||
| chr3:49950151 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-67+9926G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49950151 | |||||||
| chr3:49950469 | G | A | 9 | a0001c0001t0001g0067 a0001c0001t0001g0080 a0001c0001t0001g0081 others(6): Show |
9 | HG01074.hp1 HG01243.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.-67+10244G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49950469 | |||||||
| chr3:49950475 | G | T | 1 | a0003c0007t0001g0173 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-67+10250G>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49950475 | |||||||
| chr3:49950530 | G | A | 1 | a0001c0001t0001g0025 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-67+10305G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49950530 | |||||||
| chr3:49950632 | G | A | 79 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(76): Show |
79 | HG00140.hp1 HG00323.hp2 HG00597.hp1 others(76): Show |
intron_variant | MODIFIER | c.-67+10407G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49950632 | |||||||
| chr3:49951333 | G | A | 6 | a0002c0004t0001g0107 a0002c0004t0001g0133 a0002c0004t0001g0138 others(3): Show |
6 | HG02572.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-67+11108G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49951333 | |||||||
| chr3:49951395 | A | ATG | 14 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(11): Show |
14 | HG01891.hp2 HG02486.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.-66-11166_-66-1116 others(6): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 49951395 | ||||||
| chr3:49951696 | G | GTTA | 3 | a0001c0001t0001g0035 a0001c0001t0001g0058 a0001c0001t0001g0078 |
3 | HG01981.hp2 NA18960.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.-66-10859_-66-1085 others(7): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 49951696 | ||||||
| chr3:49951720 | T | A | 2 | a0001c0003t0001g0071 a0001c0003t0001g0073 |
2 | HG01123.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.-66-10856T>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49951720 | |||||||
| chr3:49951722 | T | G | 124 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(121): Show |
124 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.-66-10854T>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49951722 | |||||||
| chr3:49951937 | G | A | 1 | a0001c0001t0001g0114 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-66-10639G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49951937 | |||||||
| chr3:49952057 | C | T | 19 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(16): Show |
19 | HG00323.hp1 HG01106.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.-66-10519C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49952057 | |||||||
| chr3:49952127 | C | T | 6 | a0002c0004t0001g0107 a0002c0004t0001g0133 a0002c0004t0001g0138 others(3): Show |
6 | HG02572.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-66-10449C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49952127 | |||||||
| chr3:49952158 | C | A | 3 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 |
3 | HG02257.hp1 HG02451.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.-66-10418C>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49952158 | |||||||
| chr3:49952340 | A | G | 17 | a0001c0001t0001g0104 a0001c0001t0001g0120 a0001c0001t0001g0121 others(14): Show |
17 | HG01243.hp1 HG01884.hp2 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.-66-10236A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49952340 | |||||||
| chr3:49952417 | C | G | 6 | a0002c0004t0001g0107 a0002c0004t0001g0133 a0002c0004t0001g0138 others(3): Show |
6 | HG02572.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-66-10159C>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49952417 | |||||||
| chr3:49952502 | GT | G | 120 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(117): Show |
120 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.-66-10059delT | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 49952502 | ||||||
| chr3:49952522 | C | T | 15 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(12): Show |
15 | HG01891.hp2 HG02486.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.-66-10054C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49952522 | |||||||
| chr3:49952837 | A | G | 14 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(11): Show |
14 | HG00323.hp1 HG01106.hp2 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.-66-9739A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49952837 | |||||||
| chr3:49952899 | G | T | 10 | a0001c0001t0001g0104 a0001c0001t0001g0120 a0001c0001t0001g0121 others(7): Show |
10 | HG01243.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.-66-9677G>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49952899 | |||||||
| chr3:49952986 | G | A | 1 | a0001c0003t0001g0071 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-66-9590G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49952986 | |||||||
| chr3:49952996 | C | A | 1 | a0001c0002t0001g0152 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-66-9580C>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49952996 | |||||||
| chr3:49953064 | C | CT | 124 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(121): Show |
124 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.-66-9503dupT | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 49953064 | ||||||
| chr3:49953120 | A | G | 1 | a0006c0009t0001g0119 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-66-9456A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49953120 | |||||||
| chr3:49953126 | G | A | 14 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(11): Show |
14 | HG00323.hp1 HG01106.hp2 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.-66-9450G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49953126 | |||||||
| chr3:49953222 | A | AT | 103 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(100): Show |
103 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.-66-9339dupT | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 49953222 | ||||||
| chr3:49953451 | C | T | 14 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(11): Show |
14 | HG00323.hp1 HG01106.hp2 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.-66-9125C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49953451 | |||||||
| chr3:49953523 | C | CT | 30 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(27): Show |
30 | HG00597.hp1 HG00639.hp1 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.-66-9038dupT | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 49953523 | ||||||
| chr3:49953548 | T | C | 2 | a0001c0002t0001g0151 a0001c0002t0001g0195 |
2 | HG03225.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-66-9028T>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49953548 | |||||||
| chr3:49953548 | T | G | 7 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(4): Show |
7 | HG02486.hp2 HG02559.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.-66-9028T>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49953548 | |||||||
| chr3:49953627 | C | T | 34 | a0001c0002t0001g0151 a0001c0002t0001g0152 a0001c0002t0001g0153 others(31): Show |
34 | HG00738.hp2 HG01069.hp2 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.-66-8949C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49953627 | |||||||
| chr3:49953734 | G | T | 64 | a0001c0001t0001g0145 a0001c0002t0001g0111 a0001c0002t0001g0149 others(61): Show |
64 | HG00140.hp1 HG00323.hp2 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.-66-8842G>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49953734 | |||||||
| chr3:49953829 | T | C | 1 | a0001c0001t0001g0092 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-66-8747T>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49953829 | |||||||
| chr3:49953992 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-66-8584C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49953992 | |||||||
| chr3:49953994 | A | G | 34 | a0001c0002t0001g0151 a0001c0002t0001g0152 a0001c0002t0001g0153 others(31): Show |
34 | HG00738.hp2 HG01069.hp2 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.-66-8582A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49953994 | |||||||
| chr3:49954107 | G | A | 19 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(16): Show |
19 | HG00323.hp1 HG01106.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.-66-8469G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49954107 | |||||||
| chr3:49954137 | G | GA | 11 | a0001c0001t0001g0074 a0001c0001t0001g0118 a0001c0001t0001g0129 others(8): Show |
11 | HG01123.hp2 HG01496.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.-66-8425dupA | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 49954137 | ||||||
| chr3:49954137 | G | GAA | 8 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(5): Show |
8 | HG02486.hp2 HG02559.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.-66-8426_-66-8425d others(4): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 49954137 | ||||||
| chr3:49954137 | GA | G | 6 | a0002c0004t0001g0107 a0002c0004t0001g0133 a0002c0004t0001g0138 others(3): Show |
6 | HG02572.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-66-8425delA | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 49954137 | ||||||
| chr3:49954151 | AT | A | 7 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0099 others(4): Show |
7 | HG01109.hp1 HG02622.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.-66-8422delT | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 49954151 | ||||||
| chr3:49954152 | T | A | 12 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0108 others(9): Show |
12 | HG00323.hp1 HG01106.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.-66-8424T>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49954152 | |||||||
| chr3:49954354 | T | C | 16 | a0001c0001t0001g0104 a0001c0001t0001g0120 a0001c0001t0001g0121 others(13): Show |
16 | HG01243.hp1 HG01884.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.-66-8222T>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49954354 | |||||||
| chr3:49954418 | C | T | 1 | a0001c0001t0001g0051 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-66-8158C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49954418 | |||||||
| chr3:49954419 | G | A | 8 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(5): Show |
8 | HG00738.hp1 HG01168.hp1 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.-66-8157G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49954419 | |||||||
| chr3:49954427 | G | A | 1 | a0001c0011t0001g0213 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-66-8149G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49954427 | |||||||
| chr3:49954439 | CA | C | 17 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0095 others(14): Show |
17 | HG01106.hp2 HG01109.hp1 HG02622.hp1 others(14): Show |
intron_variant | MODIFIER | c.-66-8117delA | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 49954439 | ||||||
| chr3:49954644 | G | A | 1 | a0001c0001t0001g0078 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-66-7932G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49954644 | |||||||
| chr3:49954980 | C | T | 2 | a0001c0001t0001g0108 a0001c0001t0001g0109 |
2 | HG02647.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-66-7596C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49954980 | |||||||
| chr3:49955045 | C | T | 14 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(11): Show |
14 | HG00323.hp1 HG01106.hp2 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.-66-7531C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49955045 | |||||||
| chr3:49955055 | G | A | 1 | a0001c0002t0001g0196 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-66-7521G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49955055 | |||||||
| chr3:49955067 | G | A | 6 | a0002c0004t0001g0107 a0002c0004t0001g0133 a0002c0004t0001g0138 others(3): Show |
6 | HG02572.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-66-7509G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49955067 | |||||||
| chr3:49955089 | T | G | 1 | a0001c0002t0001g0177 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-66-7487T>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49955089 | |||||||
| chr3:49955160 | C | CT | 95 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(92): Show |
95 | HG00140.hp2 HG00323.hp1 HG00597.hp2 others(92): Show |
intron_variant | MODIFIER | c.-66-7392dupT | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 49955160 | ||||||
| chr3:49955160 | C | CTT | 55 | a0001c0001t0001g0051 a0001c0001t0001g0055 a0001c0001t0001g0058 others(52): Show |
55 | HG00140.hp1 HG00323.hp2 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.-66-7393_-66-7392d others(4): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 49955160 | ||||||
| chr3:49955160 | C | CTTT | 12 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(9): Show |
12 | HG01884.hp2 HG02451.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.-66-7394_-66-7392d others(5): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 49955160 | ||||||
| chr3:49955160 | C | CTTTTT | 28 | a0001c0002t0001g0151 a0001c0002t0001g0152 a0001c0002t0001g0153 others(25): Show |
28 | HG00738.hp2 HG01069.hp2 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.-66-7396_-66-7392d others(7): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 49955160 | ||||||
| chr3:49955160 | C | CTTTTTT | 5 | a0001c0002t0001g0188 a0001c0002t0001g0194 a0001c0002t0001g0198 others(2): Show |
5 | HG01081.hp2 HG01192.hp1 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.-66-7397_-66-7392d others(8): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 49955160 | ||||||
| chr3:49955201 | C | G | 6 | a0001c0001t0001g0118 a0001c0001t0001g0129 a0001c0001t0001g0130 others(3): Show |
6 | HG01891.hp2 HG02970.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.-66-7375C>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49955201 | |||||||
| chr3:49955201 | CTGTTGCC others(224): Show |
C | 1 | a0001c0001t0001g0040 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-66-7349_-66-7119d others(2): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 49955201 | ||||||
| chr3:49955289 | A | G | 1 | a0001c0001t0001g0047 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-66-7287A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49955289 | |||||||
| chr3:49955345 | AT | A | 104 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(101): Show |
104 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.-66-7224delT | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 49955345 | ||||||
| chr3:49955397 | T | C | 8 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(5): Show |
8 | HG02486.hp2 HG02559.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.-66-7179T>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49955397 | |||||||
| chr3:49955492 | G | A | 1 | a0001c0002t0001g0170 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-66-7084G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49955492 | |||||||
| chr3:49955522 | C | T | 6 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0127 others(3): Show |
6 | HG01884.hp2 HG02451.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.-66-7054C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49955522 | |||||||
| chr3:49955758 | T | G | 109 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(106): Show |
109 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.-66-6818T>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49955758 | |||||||
| chr3:49955844 | G | GTCTCTC | 4 | a0001c0002t0001g0181 a0001c0002t0001g0208 a0001c0002t0001g0209 others(1): Show |
4 | HG02055.hp1 HG02145.hp2 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.-66-6720_-66-6715d others(8): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 49955844 | ||||||
| chr3:49955860 | C | CTCTCTG | 26 | a0001c0002t0001g0151 a0001c0002t0001g0152 a0001c0002t0001g0153 others(23): Show |
26 | HG00738.hp2 HG01069.hp2 HG01070.hp2 others(23): Show |
intron_variant | MODIFIER | c.-66-6715_-66-6714i others(8): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 49955860 | ||||||
| chr3:49955860 | C | CTG | 52 | a0001c0001t0001g0057 a0001c0001t0001g0095 a0001c0001t0001g0096 others(49): Show |
52 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.-66-6692_-66-6691d others(4): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 49955860 | ||||||
| chr3:49955860 | C | CTGTG | 11 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0099 others(8): Show |
11 | HG01109.hp1 HG02258.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.-66-6694_-66-6691d others(6): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 49955860 | ||||||
| chr3:49955862 | G | C | 8 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(5): Show |
8 | HG02486.hp2 HG02559.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.-66-6714G>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49955862 | |||||||
| chr3:49955886 | A | G | 98 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(95): Show |
98 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.-66-6690A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49955886 | |||||||
| chr3:49956029 | T | A | 34 | a0001c0002t0001g0151 a0001c0002t0001g0152 a0001c0002t0001g0153 others(31): Show |
34 | HG00738.hp2 HG01069.hp2 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.-66-6547T>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49956029 | |||||||
| chr3:49956140 | A | G | 6 | a0002c0004t0001g0107 a0002c0004t0001g0133 a0002c0004t0001g0138 others(3): Show |
6 | HG02572.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-66-6436A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49956140 | |||||||
| chr3:49956307 | C | T | 6 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0127 others(3): Show |
6 | HG01884.hp2 HG02451.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.-66-6269C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49956307 | |||||||
| chr3:49956328 | C | CT | 27 | a0001c0001t0001g0011 a0001c0001t0001g0014 a0001c0001t0001g0018 others(24): Show |
27 | HG00140.hp2 HG00738.hp1 HG01071.hp2 others(24): Show |
intron_variant | MODIFIER | c.-66-6224dupT | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 49956328 | ||||||
| chr3:49956328 | CT | C | 99 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(96): Show |
99 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.-66-6224delT | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 49956328 | ||||||
| chr3:49956328 | CTT | C | 6 | a0002c0004t0001g0107 a0002c0004t0001g0133 a0002c0004t0001g0138 others(3): Show |
6 | HG02572.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-66-6225_-66-6224d others(4): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 49956328 | ||||||
| chr3:49956328 | CTTTTTTT others(4): Show |
C | 4 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0132 others(1): Show |
4 | HG01891.hp2 HG02970.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-66-6234_-66-6224d others(13): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 49956328 | ||||||
| chr3:49956358 | G | A | 1 | a0001c0001t0001g0041 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-66-6218G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49956358 | |||||||
| chr3:49956532 | A | G | 1 | a0001c0002t0001g0172 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-66-6044A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49956532 | |||||||
| chr3:49956597 | G | C | 2 | a0001c0001t0001g0002 a0001c0001t0001g0004 |
2 | HG02486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-66-5979G>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49956597 | |||||||
| chr3:49956654 | A | AT | 6 | a0002c0004t0001g0107 a0002c0004t0001g0133 a0002c0004t0001g0138 others(3): Show |
6 | HG02572.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-66-5916dupT | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 49956654 | ||||||
| chr3:49956866 | T | C | 3 | a0001c0002t0001g0156 a0001c0002t0001g0163 a0001c0002t0001g0175 |
3 | HG00639.hp2 HG01256.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.-66-5710T>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49956866 | |||||||
| chr3:49956912 | G | T | 1 | a0001c0001t0001g0085 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-66-5664G>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49956912 | |||||||
| chr3:49956916 | C | T | 2 | a0001c0001t0001g0011 a0001c0001t0001g0041 |
2 | HG04184.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.-66-5660C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49956916 | |||||||
| chr3:49956945 | G | A | 1 | a0001c0001t0001g0037 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-66-5631G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49956945 | |||||||
| chr3:49957009 | G | T | 8 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(5): Show |
8 | HG00738.hp1 HG01168.hp1 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.-66-5567G>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49957009 | |||||||
| chr3:49957125 | A | C | 1 | a0001c0002t0001g0185 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-66-5451A>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49957125 | |||||||
| chr3:49957184 | A | G | 3 | a0001c0001t0001g0017 a0001c0001t0001g0040 a0001c0001t0001g0085 |
3 | HG02004.hp2 NA18965.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.-66-5392A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49957184 | |||||||
| chr3:49957450 | G | T | 1 | a0001c0001t0001g0137 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-66-5126G>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49957450 | |||||||
| chr3:49957460 | A | G | 1 | a0001c0002t0001g0201 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-66-5116A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49957460 | |||||||
| chr3:49957835 | C | CT | 94 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(91): Show |
94 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.-66-4727dupT | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 49957835 | ||||||
| chr3:49957838 | T | TC | 2 | a0001c0001t0001g0118 a0001c0001t0001g0129 |
2 | NA18906.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-66-4738_-66-4737i others(3): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49957838 | |||||||
| chr3:49958051 | T | G | 6 | a0002c0004t0001g0107 a0002c0004t0001g0133 a0002c0004t0001g0138 others(3): Show |
6 | HG02572.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-66-4525T>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49958051 | |||||||
| chr3:49958079 | C | T | 1 | a0001c0001t0001g0128 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-66-4497C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49958079 | |||||||
| chr3:49958085 | T | C | 129 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(126): Show |
129 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.-66-4491T>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49958085 | |||||||
| chr3:49958170 | A | G | 2 | a0001c0001t0001g0055 a0001c0001t0001g0056 |
2 | HG02109.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.-66-4406A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49958170 | |||||||
| chr3:49958221 | C | T | 1 | a0001c0002t0001g0201 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-66-4355C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49958221 | |||||||
| chr3:49958270 | A | G | 2 | a0001c0001t0001g0124 a0001c0001t0001g0136 |
2 | HG01884.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.-66-4306A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49958270 | |||||||
| chr3:49958279 | G | T | 7 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0099 others(4): Show |
7 | HG01109.hp1 HG02622.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.-66-4297G>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49958279 | |||||||
| chr3:49958291 | C | T | 1 | a0001c0002t0001g0192 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-66-4285C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49958291 | |||||||
| chr3:49958401 | A | AAAAAC | 3 | a0003c0007t0001g0171 a0003c0007t0001g0173 a0003c0007t0001g0203 |
3 | HG01175.hp2 HG01257.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.-66-4160_-66-4156d others(7): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 49958401 | ||||||
| chr3:49958441 | C | T | 2 | a0001c0001t0001g0011 a0001c0002t0001g0174 |
2 | HG04184.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.-66-4135C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49958441 | |||||||
| chr3:49958469 | G | C | 1 | a0001c0001t0001g0126 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-66-4107G>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49958469 | |||||||
| chr3:49958573 | C | CA | 3 | a0001c0001t0001g0136 a0001c0002t0001g0149 a0001c0002t0001g0185 |
3 | HG01884.hp2 HG02074.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.-66-3998dupA | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 49958573 | ||||||
| chr3:49958579 | C | A | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
130 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.-66-3997C>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49958579 | |||||||
| chr3:49958620 | G | A | 68 | a0001c0002t0001g0111 a0001c0002t0001g0149 a0001c0002t0001g0150 others(65): Show |
68 | HG00140.hp1 HG00323.hp2 HG00597.hp1 others(65): Show |
intron_variant | MODIFIER | c.-66-3956G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49958620 | |||||||
| chr3:49958750 | C | CA | 9 | a0001c0001t0001g0095 a0001c0001t0001g0110 a0001c0001t0001g0115 others(6): Show |
9 | HG00323.hp1 HG01106.hp2 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.-66-3812dupA | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 49958750 | ||||||
| chr3:49958782 | C | CT | 86 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(83): Show |
86 | HG00140.hp1 HG00323.hp2 HG00597.hp1 others(83): Show |
intron_variant | MODIFIER | c.-66-3775dupT | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 49958782 | ||||||
| chr3:49958782 | C | CTT | 11 | a0001c0001t0001g0007 a0001c0002t0001g0149 a0001c0002t0001g0150 others(8): Show |
11 | HG01257.hp2 HG01934.hp1 HG01934.hp2 others(8): Show |
intron_variant | MODIFIER | c.-66-3776_-66-3775d others(4): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 49958782 | ||||||
| chr3:49958992 | A | G | 2 | a0001c0002t0001g0191 a0001c0002t0001g0200 |
2 | HG01070.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.-66-3584A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49958992 | |||||||
| chr3:49959188 | C | CT | 27 | a0001c0001t0001g0013 a0001c0001t0001g0051 a0001c0001t0001g0062 others(24): Show |
27 | HG00140.hp1 HG00597.hp1 HG01167.hp1 others(24): Show |
intron_variant | MODIFIER | c.-66-3370dupT | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 49959188 | ||||||
| chr3:49959294 | T | C | 1 | a0001c0001t0001g0135 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-66-3282T>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49959294 | |||||||
| chr3:49959309 | C | A | 1 | a0001c0001t0001g0052 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-66-3267C>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49959309 | |||||||
| chr3:49959355 | A | AT | 13 | a0001c0001t0001g0050 a0001c0001t0001g0092 a0001c0001t0001g0094 others(10): Show |
13 | HG01891.hp2 HG02074.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.-66-3204dupT | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 49959355 | ||||||
| chr3:49959491 | G | T | 68 | a0001c0002t0001g0111 a0001c0002t0001g0149 a0001c0002t0001g0150 others(65): Show |
68 | HG00140.hp1 HG00323.hp2 HG00597.hp1 others(65): Show |
intron_variant | MODIFIER | c.-66-3085G>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49959491 | |||||||
| chr3:49959571 | G | GT | 45 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(42): Show |
45 | HG00597.hp1 HG00609.hp1 HG01106.hp1 others(42): Show |
intron_variant | MODIFIER | c.-66-2988dupT | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 49959571 | ||||||
| chr3:49959571 | G | GTT | 20 | a0001c0001t0001g0001 a0001c0001t0001g0095 a0001c0001t0001g0096 others(17): Show |
20 | HG00323.hp1 HG01106.hp2 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.-66-2989_-66-2988d others(4): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 49959571 | ||||||
| chr3:49959571 | GT | G | 6 | a0001c0001t0001g0023 a0001c0001t0001g0062 a0001c0001t0001g0065 others(3): Show |
6 | HG00738.hp1 HG01168.hp1 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.-66-2988delT | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 49959571 | ||||||
| chr3:49959631 | T | C | 109 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(106): Show |
109 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.-66-2945T>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49959631 | |||||||
| chr3:49959760 | C | CG | 4 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0132 others(1): Show |
4 | HG01891.hp2 HG02970.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-66-2812dupG | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 49959760 | ||||||
| chr3:49959760 | C | T | 35 | a0001c0002t0001g0151 a0001c0002t0001g0152 a0001c0002t0001g0153 others(32): Show |
35 | HG00738.hp2 HG01069.hp2 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.-66-2816C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49959760 | |||||||
| chr3:49959864 | G | T | 1 | a0001c0001t0001g0143 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-66-2712G>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49959864 | |||||||
| chr3:49960141 | C | T | 1 | a0001c0001t0001g0084 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.-66-2435C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49960141 | |||||||
| chr3:49960530 | G | A | 103 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(100): Show |
103 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.-66-2046G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49960530 | |||||||
| chr3:49960849 | C | T | 126 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(123): Show |
126 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.-66-1727C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49960849 | |||||||
| chr3:49960910 | C | CT | 12 | a0001c0001t0001g0129 a0001c0001t0002g0019 a0001c0002t0001g0209 others(9): Show |
12 | HG01106.hp1 HG01175.hp2 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.-66-1647dupT | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 49960910 | ||||||
| chr3:49960910 | CT | C | 5 | a0001c0001t0001g0088 a0001c0001t0001g0112 a0001c0001t0001g0118 others(2): Show |
5 | HG02896.hp2 HG03041.hp2 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.-66-1647delT | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 49960910 | ||||||
| chr3:49961025 | C | T | 1 | a0001c0001t0001g0118 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-66-1551C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49961025 | |||||||
| chr3:49961055 | A | G | 1 | a0001c0001t0001g0109 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-66-1521A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49961055 | |||||||
| chr3:49961163 | C | T | 3 | a0001c0001t0001g0062 a0001c0001t0001g0065 a0001c0001t0001g0068 |
3 | HG00738.hp1 HG01257.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.-66-1413C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49961163 | |||||||
| chr3:49961653 | G | A | 68 | a0001c0002t0001g0111 a0001c0002t0001g0149 a0001c0002t0001g0150 others(65): Show |
68 | HG00140.hp1 HG00323.hp2 HG00597.hp1 others(65): Show |
intron_variant | MODIFIER | c.-66-923G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49961653 | |||||||
| chr3:49961656 | G | A | 1 | a0001c0002t0001g0186 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-66-920G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49961656 | |||||||
| chr3:49961672 | G | A | 6 | a0001c0001t0001g0118 a0001c0001t0001g0129 a0001c0001t0001g0130 others(3): Show |
6 | HG01891.hp2 HG02970.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.-66-904G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49961672 | |||||||
| chr3:49961697 | G | C | 1 | a0001c0001t0001g0145 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-66-879G>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49961697 | |||||||
| chr3:49961718 | G | A | 1 | a0001c0002t0001g0156 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-66-858G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49961718 | |||||||
| chr3:49961777 | C | T | 14 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(11): Show |
14 | HG00323.hp1 HG01106.hp2 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.-66-799C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49961777 | |||||||
| chr3:49961799 | T | TA | 19 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(16): Show |
19 | HG01106.hp2 HG01109.hp1 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.-66-762dupA | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 49961799 | ||||||
| chr3:49961799 | TA | T | 7 | a0001c0001t0001g0037 a0001c0001t0001g0084 a0001c0001t0001g0086 others(4): Show |
7 | HG00323.hp2 HG01081.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.-66-762delA | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 49961799 | ||||||
| chr3:49961910 | C | T | 1 | a0001c0002t0001g0182 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-66-666C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49961910 | |||||||
| chr3:49961973 | C | G | 17 | a0001c0001t0001g0104 a0001c0001t0001g0120 a0001c0001t0001g0121 others(14): Show |
17 | HG01243.hp1 HG01884.hp2 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.-66-603C>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49961973 | |||||||
| chr3:49962025 | G | A | 1 | a0006c0009t0001g0119 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-66-551G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49962025 | |||||||
| chr3:49962029 | G | A | 1 | a0001c0002t0001g0170 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-66-547G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49962029 | |||||||
| chr3:49962150 | T | TA | 18 | a0001c0001t0001g0053 a0001c0001t0001g0104 a0001c0001t0001g0120 others(15): Show |
18 | HG01243.hp1 HG01884.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.-66-408dupA | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 49962150 | ||||||
| chr3:49962150 | T | TAA | 6 | a0002c0004t0001g0107 a0002c0004t0001g0133 a0002c0004t0001g0138 others(3): Show |
6 | HG02572.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-66-409_-66-408dup others(2): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 49962150 | ||||||
| chr3:49962150 | TA | T | 82 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(79): Show |
82 | HG00140.hp1 HG00323.hp2 HG00597.hp1 others(79): Show |
intron_variant | MODIFIER | c.-66-408delA | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 49962150 | ||||||
| chr3:49962175 | C | G | 1 | a0001c0002t0001g0152 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-66-401C>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49962175 | |||||||
| chr3:49962311 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-66-265C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49962311 | |||||||
| chr3:49962325 | GC | G | 19 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(16): Show |
19 | HG00323.hp1 HG01106.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.-66-250delC | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49962325 | |||||||
| chr3:49962363 | C | T | 1 | a0001c0002t0001g0201 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-66-213C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49962363 | |||||||
| chr3:49962410 | C | A | 1 | a0001c0001t0001g0084 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.-66-166C>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49962410 | |||||||
| chr3:49962431 | C | CA | 27 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(24): Show |
27 | HG00323.hp1 HG01106.hp2 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.-66-133dupA | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr3 | 49962431 | ||||||
| chr3:49962487 | G | A | 3 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 |
3 | HG02257.hp1 HG02451.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.-66-89G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49962487 | |||||||
| chr3:49963149 | C | G | 1 | a0006c0009t0001g0119 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.44+464C>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 2/20 | chr3 | 49963149 | |||||||
| chr3:49963320 | G | A | 14 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(11): Show |
14 | HG00323.hp1 HG01106.hp2 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.44+635G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 2/20 | chr3 | 49963320 | |||||||
| chr3:49963640 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.44+955G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 2/20 | chr3 | 49963640 | |||||||
| chr3:49963719 | A | G | 19 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(16): Show |
19 | HG00323.hp1 HG01106.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.44+1034A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 2/20 | chr3 | 49963719 | |||||||
| chr3:49963754 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.44+1069C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 2/20 | chr3 | 49963754 | |||||||
| chr3:49963912 | T | G | 14 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(11): Show |
14 | HG00323.hp1 HG01106.hp2 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.44+1227T>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 2/20 | chr3 | 49963912 | |||||||
| chr3:49963960 | G | T | 9 | a0001c0003t0001g0010 a0001c0003t0001g0027 a0001c0003t0001g0028 others(6): Show |
9 | HG00639.hp1 HG01070.hp1 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.44+1275G>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 2/20 | chr3 | 49963960 | |||||||
| chr3:49963992 | C | T | 14 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(11): Show |
14 | HG00323.hp1 HG01106.hp2 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.44+1307C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 2/20 | chr3 | 49963992 | |||||||
| chr3:49964196 | C | T | 15 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(12): Show |
15 | HG01891.hp2 HG02486.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.44+1511C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 2/20 | chr3 | 49964196 | |||||||
| chr3:49964577 | A | G | 8 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(5): Show |
8 | HG02486.hp2 HG02559.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.44+1892A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 2/20 | chr3 | 49964577 | |||||||
| chr3:49964757 | G | A | 1 | a0001c0001t0001g0126 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.44+2072G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 2/20 | chr3 | 49964757 | |||||||
| chr3:49964812 | T | C | 109 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(106): Show |
109 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.44+2127T>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 2/20 | chr3 | 49964812 | |||||||
| chr3:49965364 | T | G | 3 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 |
3 | HG02257.hp1 HG02451.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.45-2106T>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 2/20 | chr3 | 49965364 | |||||||
| chr3:49965602 | G | A | 2 | a0001c0001t0001g0147 a0001c0001t0001g0148 |
2 | HG02257.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.45-1868G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 2/20 | chr3 | 49965602 | |||||||
| chr3:49965620 | A | G | 1 | a0001c0001t0001g0129 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.45-1850A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 2/20 | chr3 | 49965620 | |||||||
| chr3:49965669 | CA | C | 5 | a0001c0001t0001g0061 a0001c0001t0001g0086 a0001c0002t0001g0187 others(2): Show |
5 | HG01070.hp2 HG01081.hp1 NA18952.hp2 others(2): Show |
intron_variant | MODIFIER | c.45-1787delA | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr3 | 49965669 | ||||||
| chr3:49965781 | A | G | 6 | a0002c0004t0001g0107 a0002c0004t0001g0133 a0002c0004t0001g0138 others(3): Show |
6 | HG02572.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.45-1689A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 2/20 | chr3 | 49965781 | |||||||
| chr3:49965813 | C | T | 109 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(106): Show |
109 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.45-1657C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 2/20 | chr3 | 49965813 | |||||||
| chr3:49965852 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.45-1618C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 2/20 | chr3 | 49965852 | |||||||
| chr3:49965858 | G | T | 1 | a0001c0001t0001g0115 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.45-1612G>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 2/20 | chr3 | 49965858 | |||||||
| chr3:49965872 | A | T | 19 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(16): Show |
19 | HG00323.hp1 HG01106.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.45-1598A>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 2/20 | chr3 | 49965872 | |||||||
| chr3:49965873 | C | T | 1 | a0006c0009t0001g0119 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.45-1597C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 2/20 | chr3 | 49965873 | |||||||
| chr3:49965890 | C | T | 19 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(16): Show |
19 | HG00323.hp1 HG01106.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.45-1580C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 2/20 | chr3 | 49965890 | |||||||
| chr3:49965895 | A | T | 19 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(16): Show |
19 | HG00323.hp1 HG01106.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.45-1575A>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 2/20 | chr3 | 49965895 | |||||||
| chr3:49965910 | G | C | 7 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0089 others(4): Show |
7 | HG01074.hp1 HG01243.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.45-1560G>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 2/20 | chr3 | 49965910 | |||||||
| chr3:49966141 | GAGAA | G | 10 | a0001c0001t0001g0104 a0001c0001t0001g0120 a0001c0001t0001g0121 others(7): Show |
10 | HG01243.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.45-1323_45-1320del others(4): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr3 | 49966141 | ||||||
| chr3:49966153 | G | A | 34 | a0001c0002t0001g0151 a0001c0002t0001g0152 a0001c0002t0001g0153 others(31): Show |
34 | HG00738.hp2 HG01069.hp2 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.45-1317G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 2/20 | chr3 | 49966153 | |||||||
| chr3:49966199 | G | C | 34 | a0001c0002t0001g0111 a0001c0002t0001g0149 a0001c0002t0001g0150 others(31): Show |
34 | HG00140.hp1 HG00323.hp2 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.45-1271G>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 2/20 | chr3 | 49966199 | |||||||
| chr3:49966429 | T | C | 1 | a0001c0001t0001g0074 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.45-1041T>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 2/20 | chr3 | 49966429 | |||||||
| chr3:49966465 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.45-1005G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 2/20 | chr3 | 49966465 | |||||||
| chr3:49966776 | G | A | 103 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(100): Show |
103 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.45-694G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 2/20 | chr3 | 49966776 | |||||||
| chr3:49967017 | G | C | 7 | a0001c0001t0001g0104 a0001c0001t0001g0121 a0001c0001t0001g0122 others(4): Show |
7 | HG01243.hp1 HG02622.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.45-453G>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 2/20 | chr3 | 49967017 | |||||||
| chr3:49967131 | A | C | 1 | a0001c0002t0001g0186 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.45-339A>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 2/20 | chr3 | 49967131 | |||||||
| chr3:49967194 | G | C | 1 | a0001c0001t0001g0005 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.45-276G>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 2/20 | chr3 | 49967194 | |||||||
| chr3:49968770 | C | CT | 45 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0021 others(42): Show |
45 | HG00140.hp1 HG00323.hp1 HG00597.hp1 others(42): Show |
intron_variant | MODIFIER | c.1323+50dupT | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr3 | 49968770 | ||||||
| chr3:49968770 | C | CTT | 17 | a0001c0001t0001g0058 a0001c0001t0001g0096 a0001c0001t0001g0097 others(14): Show |
17 | HG00323.hp2 HG01257.hp2 HG01934.hp1 others(14): Show |
intron_variant | MODIFIER | c.1323+49_1323+50dup others(2): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr3 | 49968770 | ||||||
| chr3:49968770 | C | CTTTT | 6 | a0001c0001t0001g0118 a0001c0001t0001g0130 a0001c0001t0001g0131 others(3): Show |
6 | HG02451.hp2 HG02723.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1323+47_1323+50dup others(4): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr3 | 49968770 | ||||||
| chr3:49968770 | C | CTTTTT | 6 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(3): Show |
6 | HG01891.hp2 HG02257.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1323+46_1323+50dup others(5): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr3 | 49968770 | ||||||
| chr3:49968770 | C | CTTTTTT | 5 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(2): Show |
5 | HG02486.hp2 HG02572.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1323+45_1323+50dup others(6): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr3 | 49968770 | ||||||
| chr3:49968770 | C | CTTTTTTT others(3): Show |
1 | a0001c0001t0001g0145 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1323+41_1323+50dup others(10): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr3 | 49968770 | ||||||
| chr3:49968770 | CT | C | 11 | a0001c0001t0001g0120 a0001c0001t0001g0124 a0001c0001t0001g0125 others(8): Show |
11 | HG02486.hp1 HG02809.hp2 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.1323+50delT | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr3 | 49968770 | ||||||
| chr3:49968770 | CTTTTTTT others(2): Show |
C | 12 | a0001c0001t0001g0104 a0001c0001t0001g0121 a0001c0001t0001g0122 others(9): Show |
12 | HG01243.hp1 HG01981.hp1 HG02027.hp2 others(9): Show |
intron_variant | MODIFIER | c.1323+42_1323+50del others(9): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr3 | 49968770 | ||||||
| chr3:49968770 | CTTTTTTT others(3): Show |
C | 28 | a0001c0002t0001g0151 a0001c0002t0001g0153 a0001c0002t0001g0154 others(25): Show |
28 | HG00738.hp2 HG01069.hp2 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.1323+41_1323+50del others(10): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr3 | 49968770 | ||||||
| chr3:49968770 | CTTTTTTT others(4): Show |
C | 1 | a0001c0002t0001g0198 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1323+40_1323+50del others(11): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr3 | 49968770 | ||||||
| chr3:49968776 | T | TC | 3 | a0001c0002t0001g0156 a0001c0002t0001g0163 a0001c0002t0001g0175 |
3 | HG00639.hp2 HG01256.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.1323+28_1323+29ins others(1): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 3/20 | chr3 | 49968776 | |||||||
| chr3:49968957 | C | T | 1 | a0001c0002t0001g0155 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1323+209C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 3/20 | chr3 | 49968957 | |||||||
| chr3:49968970 | C | CT | 109 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(106): Show |
109 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.1323+235dupT | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr3 | 49968970 | ||||||
| chr3:49969181 | T | C | 15 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(12): Show |
15 | HG01891.hp2 HG02486.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.1323+433T>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 3/20 | chr3 | 49969181 | |||||||
| chr3:49969242 | C | G | 1 | a0001c0001t0001g0096 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1323+494C>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 3/20 | chr3 | 49969242 | |||||||
| chr3:49969259 | G | A | 6 | a0002c0004t0001g0107 a0002c0004t0001g0133 a0002c0004t0001g0138 others(3): Show |
6 | HG02572.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1323+511G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 3/20 | chr3 | 49969259 | |||||||
| chr3:49969316 | C | T | 1 | a0001c0002t0001g0152 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1323+568C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 3/20 | chr3 | 49969316 | |||||||
| chr3:49969324 | G | GT | 21 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(18): Show |
21 | HG01109.hp2 HG01175.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.1323+593dupT | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr3 | 49969324 | ||||||
| chr3:49969329 | T | G | 1 | a0001c0001t0001g0021 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1323+581T>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 3/20 | chr3 | 49969329 | |||||||
| chr3:49969341 | T | C | 1 | a0001c0001t0001g0095 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1323+593T>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 3/20 | chr3 | 49969341 | |||||||
| chr3:49969441 | G | A | 1 | a0001c0001t0001g0023 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1323+693G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 3/20 | chr3 | 49969441 | |||||||
| chr3:49969469 | ATATATAT others(13): Show |
A | 1 | a0001c0001t0001g0041 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1323+741_1323+760d others(22): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr3 | 49969469 | ||||||
| chr3:49969475 | A | G | 2 | a0003c0007t0001g0171 a0003c0007t0001g0203 |
2 | HG01175.hp2 HG01257.hp2 |
intron_variant | MODIFIER | c.1323+727A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 3/20 | chr3 | 49969475 | |||||||
| chr3:49969495 | A | G | 1 | a0006c0009t0001g0119 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1323+747A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 3/20 | chr3 | 49969495 | |||||||
| chr3:49969880 | C | T | 1 | a0001c0001t0001g0052 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1323+1132C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 3/20 | chr3 | 49969880 | |||||||
| chr3:49969940 | G | GT | 6 | a0001c0001t0001g0012 a0001c0001t0001g0034 a0001c0005t0001g0102 others(3): Show |
6 | HG01168.hp2 HG01256.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1323+1203dupT | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr3 | 49969940 | ||||||
| chr3:49969974 | C | T | 2 | a0001c0001t0001g0108 a0001c0001t0001g0109 |
2 | HG02647.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1323+1226C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 3/20 | chr3 | 49969974 | |||||||
| chr3:49970004 | G | A | 23 | a0001c0001t0001g0104 a0001c0001t0001g0120 a0001c0001t0001g0121 others(20): Show |
23 | HG01243.hp1 HG01884.hp2 HG02451.hp1 others(20): Show |
intron_variant | MODIFIER | c.1323+1256G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 3/20 | chr3 | 49970004 | |||||||
| chr3:49970086 | G | A | 1 | a0001c0001t0001g0099 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1323+1338G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 3/20 | chr3 | 49970086 | |||||||
| chr3:49970564 | A | G | 1 | a0001c0001t0001g0020 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1324-1495A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 3/20 | chr3 | 49970564 | |||||||
| chr3:49970612 | C | T | 1 | a0001c0001t0001g0047 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1324-1447C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 3/20 | chr3 | 49970612 | |||||||
| chr3:49970685 | T | C | 18 | a0001c0003t0001g0010 a0001c0003t0001g0027 a0001c0003t0001g0028 others(15): Show |
18 | HG00639.hp1 HG01070.hp1 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.1324-1374T>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 3/20 | chr3 | 49970685 | |||||||
| chr3:49971082 | C | T | 3 | a0001c0001t0001g0077 a0001c0001t0001g0086 a0001c0001t0001g0087 |
3 | HG01081.hp1 HG01192.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.1324-977C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 3/20 | chr3 | 49971082 | |||||||
| chr3:49971133 | A | G | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
130 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.1324-926A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 3/20 | chr3 | 49971133 | |||||||
| chr3:49971190 | T | TGGGAGGC others(10): Show |
34 | a0001c0002t0001g0111 a0001c0002t0001g0149 a0001c0002t0001g0150 others(31): Show |
34 | HG00140.hp1 HG00323.hp2 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.1324-852_1324-836d others(19): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr3 | 49971190 | ||||||
| chr3:49971200 | A | G | 2 | a0001c0001t0001g0108 a0001c0001t0001g0109 |
2 | HG02647.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1324-859A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 3/20 | chr3 | 49971200 | |||||||
| chr3:49971267 | G | GA | 17 | a0001c0001t0001g0015 a0001c0001t0001g0025 a0001c0001t0001g0055 others(14): Show |
17 | HG00597.hp2 HG00639.hp2 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.1324-776dupA | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr3 | 49971267 | ||||||
| chr3:49971340 | G | T | 1 | a0001c0002t0001g0195 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1324-719G>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 3/20 | chr3 | 49971340 | |||||||
| chr3:49971431 | C | T | 68 | a0001c0002t0001g0111 a0001c0002t0001g0149 a0001c0002t0001g0150 others(65): Show |
68 | HG00140.hp1 HG00323.hp2 HG00597.hp1 others(65): Show |
intron_variant | MODIFIER | c.1324-628C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 3/20 | chr3 | 49971431 | |||||||
| chr3:49971475 | C | G | 8 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(5): Show |
8 | HG02486.hp2 HG02559.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1324-584C>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 3/20 | chr3 | 49971475 | |||||||
| chr3:49971494 | G | A | 2 | a0001c0001t0001g0108 a0001c0001t0001g0109 |
2 | HG02647.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1324-565G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 3/20 | chr3 | 49971494 | |||||||
| chr3:49971576 | C | T | 2 | a0001c0001t0001g0108 a0001c0001t0001g0109 |
2 | HG02647.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1324-483C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 3/20 | chr3 | 49971576 | |||||||
| chr3:49971725 | C | T | 6 | a0002c0004t0001g0107 a0002c0004t0001g0133 a0002c0004t0001g0138 others(3): Show |
6 | HG02572.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1324-334C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 3/20 | chr3 | 49971725 | |||||||
| chr3:49971743 | T | C | 103 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(100): Show |
103 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.1324-316T>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 3/20 | chr3 | 49971743 | |||||||
| chr3:49972201 | C | A | 1 | a0001c0001t0001g0096 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1413+53C>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 4/20 | chr3 | 49972201 | |||||||
| chr3:49973045 | G | C | 1 | a0001c0001t0001g0075 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1413+897G>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 4/20 | chr3 | 49973045 | |||||||
| chr3:49973138 | G | T | 84 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(81): Show |
84 | HG00140.hp1 HG00323.hp2 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.1413+990G>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 4/20 | chr3 | 49973138 | |||||||
| chr3:49973308 | A | G | 2 | a0002c0004t0001g0107 a0002c0004t0001g0141 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1413+1160A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 4/20 | chr3 | 49973308 | |||||||
| chr3:49973391 | A | G | 1 | a0006c0009t0001g0119 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1413+1243A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 4/20 | chr3 | 49973391 | |||||||
| chr3:49973404 | G | A | 6 | a0002c0004t0001g0107 a0002c0004t0001g0133 a0002c0004t0001g0138 others(3): Show |
6 | HG02572.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1413+1256G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 4/20 | chr3 | 49973404 | |||||||
| chr3:49973584 | C | CT | 7 | a0001c0001t0001g0008 a0001c0001t0001g0046 a0001c0001t0001g0075 others(4): Show |
7 | HG01255.hp2 HG02155.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1413+1455dupT | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr3 | 49973584 | ||||||
| chr3:49973588 | T | C | 34 | a0001c0002t0001g0111 a0001c0002t0001g0149 a0001c0002t0001g0150 others(31): Show |
34 | HG00140.hp1 HG00323.hp2 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.1413+1440T>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 4/20 | chr3 | 49973588 | |||||||
| chr3:49973662 | T | C | 109 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(106): Show |
109 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.1413+1514T>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 4/20 | chr3 | 49973662 | |||||||
| chr3:49973668 | C | G | 14 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(11): Show |
14 | HG00323.hp1 HG01106.hp2 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1413+1520C>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 4/20 | chr3 | 49973668 | |||||||
| chr3:49973692 | T | TG | 19 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(16): Show |
19 | HG00323.hp1 HG01106.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.1413+1544_1413+154 others(5): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 4/20 | chr3 | 49973692 | |||||||
| chr3:49973693 | C | A | 19 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(16): Show |
19 | HG00323.hp1 HG01106.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.1413+1545C>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 4/20 | chr3 | 49973693 | |||||||
| chr3:49973694 | T | A | 19 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(16): Show |
19 | HG00323.hp1 HG01106.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.1413+1546T>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 4/20 | chr3 | 49973694 | |||||||
| chr3:49973697 | T | A | 3 | a0001c0001t0001g0125 a0001c0001t0001g0127 a0001c0001t0001g0135 |
3 | HG02451.hp1 HG03130.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1413+1549T>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 4/20 | chr3 | 49973697 | |||||||
| chr3:49973886 | TTTTG | T | 69 | a0001c0001t0001g0145 a0001c0002t0001g0111 a0001c0002t0001g0149 others(66): Show |
69 | HG00140.hp1 HG00323.hp2 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.1414-1413_1414-141 others(8): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr3 | 49973886 | ||||||
| chr3:49973999 | A | T | 1 | a0001c0001t0001g0145 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1414-1324A>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 4/20 | chr3 | 49973999 | |||||||
| chr3:49974107 | T | C | 109 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(106): Show |
109 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.1414-1216T>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 4/20 | chr3 | 49974107 | |||||||
| chr3:49974334 | G | A | 1 | a0001c0001t0001g0143 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1414-989G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 4/20 | chr3 | 49974334 | |||||||
| chr3:49974373 | A | AT | 15 | a0001c0001t0001g0104 a0001c0001t0001g0120 a0001c0001t0001g0121 others(12): Show |
15 | HG01243.hp1 HG02055.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.1414-934dupT | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr3 | 49974373 | ||||||
| chr3:49974391 | A | G | 4 | a0002c0004t0001g0133 a0002c0004t0001g0138 a0002c0004t0001g0139 others(1): Show |
4 | HG02572.hp2 HG02922.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1414-932A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 4/20 | chr3 | 49974391 | |||||||
| chr3:49974673 | A | AT | 13 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(10): Show |
13 | HG02257.hp1 HG02486.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.1414-620dupT | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr3 | 49974673 | ||||||
| chr3:49974673 | AT | A | 82 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0014 others(79): Show |
82 | HG00140.hp2 HG00609.hp1 HG00639.hp1 others(79): Show |
intron_variant | MODIFIER | c.1414-620delT | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr3 | 49974673 | ||||||
| chr3:49974673 | ATT | A | 12 | a0001c0001t0001g0012 a0001c0001t0001g0023 a0001c0001t0001g0038 others(9): Show |
12 | HG01070.hp1 HG01099.hp2 HG01168.hp1 others(9): Show |
intron_variant | MODIFIER | c.1414-621_1414-620d others(4): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr3 | 49974673 | ||||||
| chr3:49974673 | ATTTTTTT | A | 9 | a0001c0002t0001g0150 a0001c0002t0001g0196 a0001c0002t0001g0197 others(6): Show |
9 | HG01167.hp2 HG01175.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1414-626_1414-620d others(9): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr3 | 49974673 | ||||||
| chr3:49974673 | ATTTTTTT others(1): Show |
A | 56 | a0001c0002t0001g0111 a0001c0002t0001g0149 a0001c0002t0001g0151 others(53): Show |
56 | HG00140.hp1 HG00323.hp2 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.1414-627_1414-620d others(10): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr3 | 49974673 | ||||||
| chr3:49974842 | A | G | 1 | a0001c0002t0001g0185 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1414-481A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 4/20 | chr3 | 49974842 | |||||||
| chr3:49974953 | C | G | 1 | a0001c0001t0001g0039 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1414-370C>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 4/20 | chr3 | 49974953 | |||||||
| chr3:49974972 | C | A | 1 | a0001c0001t0001g0060 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1414-351C>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 4/20 | chr3 | 49974972 | |||||||
| chr3:49975005 | A | AT | 19 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(16): Show |
19 | HG00323.hp1 HG01106.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.1414-302dupT | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr3 | 49975005 | ||||||
| chr3:49975037 | C | G | 19 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(16): Show |
19 | HG00323.hp1 HG01106.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.1414-286C>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 4/20 | chr3 | 49975037 | |||||||
| chr3:49975293 | A | G | 1 | a0001c0001t0001g0145 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1414-30A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 4/20 | chr3 | 49975293 | |||||||
| chr3:49975532 | A | T | 3 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 |
3 | HG02257.hp1 HG02451.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1483+140A>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49975532 | |||||||
| chr3:49976036 | A | G | 14 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(11): Show |
14 | HG00323.hp1 HG01106.hp2 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1483+644A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49976036 | |||||||
| chr3:49976289 | A | G | 10 | a0001c0002t0001g0181 a0001c0002t0001g0197 a0001c0002t0001g0198 others(7): Show |
10 | HG01167.hp2 HG02055.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.1483+897A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49976289 | |||||||
| chr3:49976486 | G | A | 7 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0099 others(4): Show |
7 | HG01109.hp1 HG02622.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1483+1094G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49976486 | |||||||
| chr3:49976681 | G | A | 34 | a0001c0002t0001g0111 a0001c0002t0001g0149 a0001c0002t0001g0150 others(31): Show |
34 | HG00140.hp1 HG00323.hp2 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.1483+1289G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49976681 | |||||||
| chr3:49976856 | A | G | 4 | a0001c0005t0001g0102 a0001c0005t0001g0103 a0001c0005t0001g0105 others(1): Show |
4 | HG02258.hp2 HG02717.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1483+1464A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49976856 | |||||||
| chr3:49976998 | T | C | 2 | a0001c0001t0001g0147 a0001c0001t0001g0148 |
2 | HG02257.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1483+1606T>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49976998 | |||||||
| chr3:49977043 | G | A | 1 | a0001c0001t0001g0048 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1483+1651G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49977043 | |||||||
| chr3:49977054 | C | T | 1 | a0001c0001t0001g0048 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1483+1662C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49977054 | |||||||
| chr3:49977063 | G | A | 14 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(11): Show |
14 | HG00323.hp1 HG01106.hp2 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1483+1671G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49977063 | |||||||
| chr3:49977381 | G | A | 7 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(4): Show |
7 | HG02486.hp2 HG02559.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1483+1989G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49977381 | |||||||
| chr3:49977609 | A | G | 3 | a0001c0001t0001g0024 a0001c0001t0001g0061 a0001c0001t0001g0079 |
3 | HG02027.hp1 NA18984.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.1483+2217A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49977609 | |||||||
| chr3:49977959 | A | G | 1 | a0001c0005t0001g0103 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1483+2567A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49977959 | |||||||
| chr3:49978025 | G | A | 6 | a0001c0001t0001g0118 a0001c0001t0001g0129 a0001c0001t0001g0130 others(3): Show |
6 | HG01891.hp2 HG02970.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1483+2633G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49978025 | |||||||
| chr3:49978064 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1483+2672G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49978064 | |||||||
| chr3:49978221 | G | A | 1 | a0001c0002t0001g0207 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1483+2829G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49978221 | |||||||
| chr3:49978416 | C | G | 2 | a0001c0001t0001g0011 a0001c0001t0001g0041 |
2 | HG04184.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1483+3024C>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49978416 | |||||||
| chr3:49978655 | C | T | 6 | a0002c0004t0001g0107 a0002c0004t0001g0133 a0002c0004t0001g0138 others(3): Show |
6 | HG02572.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1483+3263C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49978655 | |||||||
| chr3:49978672 | C | G | 1 | a0001c0002t0001g0150 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1483+3280C>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49978672 | |||||||
| chr3:49978801 | T | C | 1 | a0001c0002t0001g0183 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1483+3409T>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49978801 | |||||||
| chr3:49978850 | A | G | 6 | a0002c0004t0001g0107 a0002c0004t0001g0133 a0002c0004t0001g0138 others(3): Show |
6 | HG02572.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1483+3458A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49978850 | |||||||
| chr3:49979087 | A | G | 2 | a0001c0001t0001g0108 a0001c0001t0001g0109 |
2 | HG02647.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1483+3695A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49979087 | |||||||
| chr3:49979122 | A | C | 1 | a0001c0001t0001g0021 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1483+3730A>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49979122 | |||||||
| chr3:49979438 | G | GT | 25 | a0001c0001t0001g0011 a0001c0001t0001g0039 a0001c0001t0001g0059 others(22): Show |
25 | HG00609.hp1 HG01243.hp1 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.1483+4064dupT | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr3 | 49979438 | ||||||
| chr3:49979438 | GT | G | 8 | a0001c0001t0001g0018 a0001c0002t0001g0172 a0002c0004t0001g0107 others(5): Show |
8 | HG01167.hp1 HG02572.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1483+4064delT | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr3 | 49979438 | ||||||
| chr3:49979439 | T | G | 4 | a0001c0005t0001g0102 a0001c0005t0001g0103 a0001c0005t0001g0105 others(1): Show |
4 | HG02258.hp2 HG02717.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1483+4047T>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49979439 | |||||||
| chr3:49979532 | C | T | 1 | a0001c0001t0001g0118 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1483+4140C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49979532 | |||||||
| chr3:49979818 | A | G | 1 | a0001c0001t0001g0126 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1483+4426A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49979818 | |||||||
| chr3:49979878 | C | T | 4 | a0001c0005t0001g0102 a0001c0005t0001g0103 a0001c0005t0001g0105 others(1): Show |
4 | HG02258.hp2 HG02717.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1483+4486C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49979878 | |||||||
| chr3:49979960 | C | T | 1 | a0001c0001t0001g0016 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1483+4568C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49979960 | |||||||
| chr3:49980009 | T | A | 1 | a0001c0001t0001g0145 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1483+4617T>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49980009 | |||||||
| chr3:49980045 | A | G | 126 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(123): Show |
126 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.1483+4653A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49980045 | |||||||
| chr3:49980064 | G | A | 8 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(5): Show |
8 | HG02486.hp2 HG02559.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1483+4672G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49980064 | |||||||
| chr3:49980398 | T | C | 1 | a0002c0004t0001g0133 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1483+5006T>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49980398 | |||||||
| chr3:49980581 | G | A | 6 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0127 others(3): Show |
6 | HG01884.hp2 HG02451.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1483+5189G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49980581 | |||||||
| chr3:49980619 | G | A | 4 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0132 others(1): Show |
4 | HG01891.hp2 HG02970.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1483+5227G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49980619 | |||||||
| chr3:49980740 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1483+5348C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49980740 | |||||||
| chr3:49980761 | T | TA | 66 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0002t0001g0111 others(63): Show |
66 | HG00140.hp1 HG00323.hp2 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.1483+5388dupA | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr3 | 49980761 | ||||||
| chr3:49981152 | T | G | 109 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(106): Show |
109 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.1483+5760T>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49981152 | |||||||
| chr3:49981988 | A | G | 3 | a0002c0004t0001g0133 a0002c0004t0001g0138 a0002c0004t0001g0140 |
3 | HG02572.hp2 HG02922.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1483+6596A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49981988 | |||||||
| chr3:49982001 | A | G | 1 | a0001c0001t0001g0115 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1483+6609A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49982001 | |||||||
| chr3:49982262 | C | CT | 10 | a0001c0001t0001g0024 a0001c0001t0001g0039 a0001c0001t0001g0078 others(7): Show |
10 | HG00609.hp1 HG01175.hp2 HG01517.hp2 others(7): Show |
intron_variant | MODIFIER | c.1483+6898dupT | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr3 | 49982262 | ||||||
| chr3:49982262 | C | CTTTT | 5 | a0001c0001t0001g0124 a0001c0001t0001g0127 a0001c0001t0001g0128 others(2): Show |
5 | HG01884.hp2 HG02451.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1483+6895_1483+689 others(8): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr3 | 49982262 | ||||||
| chr3:49982262 | C | CTTTTTTT others(1): Show |
6 | a0001c0001t0001g0104 a0001c0001t0001g0121 a0001c0001t0001g0123 others(3): Show |
6 | HG02622.hp2 HG02895.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1483+6891_1483+689 others(12): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr3 | 49982262 | ||||||
| chr3:49982262 | C | CTTTTTTT others(3): Show |
1 | a0001c0001t0001g0122 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1483+6889_1483+689 others(14): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr3 | 49982262 | ||||||
| chr3:49982262 | CT | C | 22 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(19): Show |
22 | HG00597.hp1 HG01070.hp2 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.1483+6898delT | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr3 | 49982262 | ||||||
| chr3:49982262 | CTT | C | 7 | a0002c0004t0001g0107 a0002c0004t0001g0133 a0002c0004t0001g0138 others(4): Show |
7 | HG02572.hp2 HG02895.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.1483+6897_1483+689 others(6): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr3 | 49982262 | ||||||
| chr3:49982262 | CTTTTTTT others(3): Show |
C | 1 | a0001c0002t0001g0155 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1483+6889_1483+689 others(14): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr3 | 49982262 | ||||||
| chr3:49982266 | T | TC | 3 | a0001c0001t0001g0099 a0001c0001t0001g0110 a0001c0001t0001g0114 |
3 | HG01106.hp2 HG03041.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1483+6874_1483+687 others(5): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49982266 | |||||||
| chr3:49982267 | T | C | 11 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(8): Show |
11 | HG00323.hp1 HG01109.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.1483+6875T>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49982267 | |||||||
| chr3:49982272 | T | C | 3 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 |
3 | HG02257.hp1 HG02451.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1483+6880T>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49982272 | |||||||
| chr3:49982424 | G | T | 2 | a0001c0003t0001g0071 a0001c0003t0001g0073 |
2 | HG01123.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.1483+7032G>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49982424 | |||||||
| chr3:49982464 | G | A | 19 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(16): Show |
19 | HG00323.hp1 HG01106.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.1483+7072G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49982464 | |||||||
| chr3:49983004 | G | A | 68 | a0001c0002t0001g0111 a0001c0002t0001g0149 a0001c0002t0001g0150 others(65): Show |
68 | HG00140.hp1 HG00323.hp2 HG00597.hp1 others(65): Show |
intron_variant | MODIFIER | c.1483+7612G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49983004 | |||||||
| chr3:49983280 | A | G | 1 | a0001c0002t0001g0199 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1483+7888A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49983280 | |||||||
| chr3:49983393 | G | A | 3 | a0002c0004t0001g0133 a0002c0004t0001g0138 a0002c0004t0001g0140 |
3 | HG02572.hp2 HG02922.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1483+8001G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49983393 | |||||||
| chr3:49983458 | G | GA | 19 | a0001c0002t0001g0152 a0001c0002t0001g0153 a0001c0002t0001g0154 others(16): Show |
19 | HG00738.hp2 HG01069.hp2 HG01070.hp2 others(16): Show |
intron_variant | MODIFIER | c.1483+8076dupA | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr3 | 49983458 | ||||||
| chr3:49983619 | G | A | 2 | a0001c0001t0001g0147 a0001c0001t0001g0148 |
2 | HG02257.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1483+8227G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49983619 | |||||||
| chr3:49983842 | C | T | 3 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 |
3 | HG02257.hp1 HG02451.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1483+8450C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49983842 | |||||||
| chr3:49983863 | C | T | 2 | a0001c0001t0001g0051 a0001c0001t0001g0059 |
2 | HG02055.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.1483+8471C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49983863 | |||||||
| chr3:49984054 | C | G | 213 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(210): Show |
213 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(210): Show |
intron_variant | MODIFIER | c.1483+8662C>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49984054 | |||||||
| chr3:49984226 | G | A | 19 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(16): Show |
19 | HG00323.hp1 HG01106.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.1483+8834G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49984226 | |||||||
| chr3:49984585 | GACATC | G | 19 | a0001c0001t0001g0021 a0001c0001t0001g0026 a0001c0001t0001g0039 others(16): Show |
19 | HG00140.hp2 HG00609.hp1 HG01516.hp2 others(16): Show |
intron_variant | MODIFIER | c.1483+9219_1483+922 others(9): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr3 | 49984585 | ||||||
| chr3:49984596 | A | ACATCGCA others(13): Show |
1 | a0001c0001t0001g0014 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1483+9208_1483+920 others(24): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr3 | 49984596 | ||||||
| chr3:49984601 | A | ACATCG | 2 | a0001c0001t0001g0013 a0001c0001t0001g0065 |
2 | HG01496.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1483+9213_1483+921 others(9): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr3 | 49984601 | ||||||
| chr3:49984601 | A | ACATCGCA others(13): Show |
1 | a0001c0001t0001g0020 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1483+9213_1483+921 others(24): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr3 | 49984601 | ||||||
| chr3:49984601 | A | G | 1 | a0001c0001t0001g0014 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1483+9209A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49984601 | |||||||
| chr3:49984601 | ACATCACA others(8): Show |
A | 1 | a0001c0001t0001g0034 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1483+9214_1483+922 others(19): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr3 | 49984601 | ||||||
| chr3:49984606 | A | ACATCG | 2 | a0001c0001t0001g0062 a0001c0001t0001g0068 |
2 | HG00738.hp1 HG01257.hp1 |
intron_variant | MODIFIER | c.1483+9218_1483+921 others(9): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr3 | 49984606 | ||||||
| chr3:49984606 | A | ACATCGCA others(3): Show |
1 | a0001c0001t0001g0053 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1483+9218_1483+921 others(14): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr3 | 49984606 | ||||||
| chr3:49984606 | A | G | 6 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0020 others(3): Show |
6 | HG01496.hp2 HG02027.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.1483+9214A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49984606 | |||||||
| chr3:49984606 | ACATCACA others(3): Show |
A | 2 | a0001c0001t0001g0094 a0001c0010t0001g0069 |
2 | NA18962.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.1483+9219_1483+922 others(14): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr3 | 49984606 | ||||||
| chr3:49984611 | A | G | 12 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0020 others(9): Show |
12 | HG00738.hp1 HG01257.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.1483+9219A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49984611 | |||||||
| chr3:49984611 | ACATCG | A | 52 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0017 others(49): Show |
52 | HG00639.hp1 HG01070.hp1 HG01071.hp2 others(49): Show |
intron_variant | MODIFIER | c.1483+9268_1483+927 others(9): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr3 | 49984611 | ||||||
| chr3:49984611 | ACATCGCA others(3): Show |
A | 19 | a0001c0001t0001g0006 a0001c0001t0001g0041 a0001c0001t0001g0104 others(16): Show |
19 | HG01243.hp1 HG01884.hp2 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.1483+9263_1483+927 others(14): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr3 | 49984611 | ||||||
| chr3:49984611 | ACATCGCA others(8): Show |
A | 24 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(21): Show |
24 | HG01123.hp1 HG02055.hp1 HG02145.hp2 others(21): Show |
intron_variant | MODIFIER | c.1483+9258_1483+927 others(19): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr3 | 49984611 | ||||||
| chr3:49984611 | ACATCGCA others(13): Show |
A | 12 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 others(9): Show |
12 | HG00738.hp2 HG01081.hp2 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.1483+9253_1483+927 others(24): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr3 | 49984611 | ||||||
| chr3:49984611 | ACATCGCA others(18): Show |
A | 36 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(33): Show |
36 | HG00323.hp1 HG01069.hp2 HG01070.hp2 others(33): Show |
intron_variant | MODIFIER | c.1483+9248_1483+927 others(29): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr3 | 49984611 | ||||||
| chr3:49984611 | ACATCGCA others(23): Show |
A | 31 | a0001c0002t0001g0111 a0001c0002t0001g0149 a0001c0002t0001g0150 others(28): Show |
31 | HG00140.hp1 HG00323.hp2 HG00597.hp1 others(28): Show |
intron_variant | MODIFIER | c.1483+9243_1483+927 others(34): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr3 | 49984611 | ||||||
| chr3:49984611 | ACATCGCA others(28): Show |
A | 3 | a0001c0002t0001g0152 a0001c0002t0001g0182 a0001c0002t0001g0184 |
3 | HG01934.hp2 HG02027.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1483+9238_1483+927 others(39): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr3 | 49984611 | ||||||
| chr3:49984616 | G | A | 1 | a0001c0001t0001g0118 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1483+9224G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49984616 | |||||||
| chr3:49984621 | G | A | 9 | a0001c0001t0001g0051 a0001c0001t0001g0059 a0001c0001t0001g0118 others(6): Show |
9 | HG01891.hp2 HG02055.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1483+9229G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49984621 | |||||||
| chr3:49984626 | G | A | 23 | a0001c0001t0001g0006 a0001c0001t0001g0104 a0001c0001t0001g0118 others(20): Show |
23 | HG01243.hp1 HG01884.hp2 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.1483+9234G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49984626 | |||||||
| chr3:49984631 | G | A | 28 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(25): Show |
28 | HG01123.hp1 HG01891.hp2 HG02055.hp1 others(25): Show |
intron_variant | MODIFIER | c.1483+9239G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49984631 | |||||||
| chr3:49984636 | G | A | 54 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(51): Show |
54 | HG00738.hp2 HG01081.hp2 HG01099.hp1 others(51): Show |
intron_variant | MODIFIER | c.1483+9244G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49984636 | |||||||
| chr3:49984641 | G | A | 75 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(72): Show |
75 | HG00323.hp1 HG00738.hp2 HG01069.hp2 others(72): Show |
intron_variant | MODIFIER | c.1483+9249G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49984641 | |||||||
| chr3:49984646 | G | A | 106 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(103): Show |
106 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.1483+9254G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49984646 | |||||||
| chr3:49984650 | C | T | 17 | a0001c0001t0001g0104 a0001c0001t0001g0120 a0001c0001t0001g0121 others(14): Show |
17 | HG01243.hp1 HG01884.hp2 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.1483+9258C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49984650 | |||||||
| chr3:49984650 | CGCATCGC others(8): Show |
C | 1 | a0001c0001t0001g0077 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1483+9264_1483+927 others(19): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr3 | 49984650 | ||||||
| chr3:49984651 | G | A | 109 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(106): Show |
109 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.1483+9259G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49984651 | |||||||
| chr3:49984656 | G | A | 109 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(106): Show |
109 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.1483+9264G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49984656 | |||||||
| chr3:49984661 | G | A | 109 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(106): Show |
109 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.1483+9269G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49984661 | |||||||
| chr3:49984671 | A | G | 1 | a0001c0001t0001g0020 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1483+9279A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49984671 | |||||||
| chr3:49984676 | A | G | 1 | a0001c0001t0001g0020 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1483+9284A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49984676 | |||||||
| chr3:49984833 | G | C | 1 | a0001c0001t0001g0120 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1483+9441G>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49984833 | |||||||
| chr3:49984859 | G | A | 126 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(123): Show |
126 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.1483+9467G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49984859 | |||||||
| chr3:49985306 | A | T | 1 | a0001c0001t0001g0120 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1483+9914A>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49985306 | |||||||
| chr3:49985335 | C | T | 1 | a0001c0001t0001g0054 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1483+9943C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49985335 | |||||||
| chr3:49985493 | T | C | 131 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(128): Show |
131 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.1483+10101T>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49985493 | |||||||
| chr3:49985707 | C | T | 4 | a0001c0005t0001g0102 a0001c0005t0001g0103 a0001c0005t0001g0105 others(1): Show |
4 | HG02258.hp2 HG02717.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1483+10315C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49985707 | |||||||
| chr3:49985901 | T | C | 213 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(210): Show |
213 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(210): Show |
intron_variant | MODIFIER | c.1483+10509T>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49985901 | |||||||
| chr3:49986005 | A | G | 19 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(16): Show |
19 | HG00323.hp1 HG01106.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.1483+10613A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49986005 | |||||||
| chr3:49986329 | T | C | 2 | a0001c0001t0001g0086 a0001c0001t0001g0087 |
2 | HG01081.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1483+10937T>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49986329 | |||||||
| chr3:49986436 | A | T | 2 | a0001c0001t0001g0038 a0004c0006t0001g0072 |
2 | NA19063.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.1483+11044A>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49986436 | |||||||
| chr3:49986459 | G | A | 2 | a0001c0003t0001g0064 a0001c0003t0001g0066 |
2 | HG02109.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1483+11067G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49986459 | |||||||
| chr3:49986463 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1483+11071C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49986463 | |||||||
| chr3:49986594 | CA | C | 92 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(89): Show |
92 | HG00140.hp1 HG00323.hp2 HG00597.hp1 others(89): Show |
intron_variant | MODIFIER | c.1483+11217delA | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr3 | 49986594 | ||||||
| chr3:49986600 | A | C | 1 | a0001c0002t0001g0178 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1483+11208A>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49986600 | |||||||
| chr3:49986605 | A | C | 100 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(97): Show |
100 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.1483+11213A>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49986605 | |||||||
| chr3:49986694 | CTT | C | 6 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0127 others(3): Show |
6 | HG01884.hp2 HG02451.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1483+11306_1483+11 others(8): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr3 | 49986694 | ||||||
| chr3:49986744 | CT | C | 3 | a0001c0003t0001g0030 a0001c0003t0001g0076 a0001c0003t0001g0083 |
3 | HG01517.hp1 HG03831.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1483+11354delT | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr3 | 49986744 | ||||||
| chr3:49986780 | T | C | 6 | a0002c0004t0001g0107 a0002c0004t0001g0133 a0002c0004t0001g0138 others(3): Show |
6 | HG02572.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1483+11388T>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49986780 | |||||||
| chr3:49986893 | C | G | 6 | a0002c0004t0001g0107 a0002c0004t0001g0133 a0002c0004t0001g0138 others(3): Show |
6 | HG02572.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1483+11501C>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49986893 | |||||||
| chr3:49986973 | G | A | 1 | a0001c0001t0001g0094 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1483+11581G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49986973 | |||||||
| chr3:49987105 | C | G | 2 | a0002c0004t0001g0107 a0002c0004t0001g0141 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1483+11713C>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49987105 | |||||||
| chr3:49987135 | C | T | 34 | a0001c0002t0001g0111 a0001c0002t0001g0149 a0001c0002t0001g0150 others(31): Show |
34 | HG00140.hp1 HG00323.hp2 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.1483+11743C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49987135 | |||||||
| chr3:49987325 | G | T | 126 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(123): Show |
126 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.1483+11933G>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49987325 | |||||||
| chr3:49987573 | T | C | 68 | a0001c0002t0001g0111 a0001c0002t0001g0149 a0001c0002t0001g0150 others(65): Show |
68 | HG00140.hp1 HG00323.hp2 HG00597.hp1 others(65): Show |
intron_variant | MODIFIER | c.1484-11867T>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49987573 | |||||||
| chr3:49987593 | G | A | 1 | a0001c0003t0001g0076 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1484-11847G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49987593 | |||||||
| chr3:49987595 | A | G | 109 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(106): Show |
109 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.1484-11845A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49987595 | |||||||
| chr3:49987646 | C | CT | 6 | a0002c0004t0001g0107 a0002c0004t0001g0133 a0002c0004t0001g0138 others(3): Show |
6 | HG02572.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1484-11784dupT | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr3 | 49987646 | ||||||
| chr3:49987725 | G | A | 4 | a0001c0001t0001g0023 a0001c0001t0001g0062 a0001c0001t0001g0065 others(1): Show |
4 | HG00738.hp1 HG01168.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.1484-11715G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49987725 | |||||||
| chr3:49987748 | C | T | 19 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(16): Show |
19 | HG00323.hp1 HG01106.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.1484-11692C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49987748 | |||||||
| chr3:49988097 | A | G | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
130 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.1484-11343A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49988097 | |||||||
| chr3:49988596 | A | C | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
130 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.1484-10844A>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49988596 | |||||||
| chr3:49988701 | G | A | 4 | a0001c0005t0001g0102 a0001c0005t0001g0103 a0001c0005t0001g0105 others(1): Show |
4 | HG02258.hp2 HG02717.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1484-10739G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49988701 | |||||||
| chr3:49988717 | C | T | 4 | a0001c0005t0001g0102 a0001c0005t0001g0103 a0001c0005t0001g0105 others(1): Show |
4 | HG02258.hp2 HG02717.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1484-10723C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49988717 | |||||||
| chr3:49988955 | GA | G | 69 | a0001c0001t0001g0145 a0001c0002t0001g0111 a0001c0002t0001g0149 others(66): Show |
69 | HG00140.hp1 HG00323.hp2 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.1484-10476delA | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr3 | 49988955 | ||||||
| chr3:49989047 | A | AT | 8 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0098 others(5): Show |
8 | HG01109.hp1 HG02622.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1484-10383dupT | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr3 | 49989047 | ||||||
| chr3:49989057 | T | A | 3 | a0001c0003t0001g0063 a0001c0003t0001g0064 a0001c0003t0001g0066 |
3 | HG02109.hp2 HG02886.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1484-10383T>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49989057 | |||||||
| chr3:49989226 | A | G | 1 | a0001c0001t0001g0123 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1484-10214A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49989226 | |||||||
| chr3:49989854 | C | T | 1 | a0006c0009t0001g0119 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1484-9586C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49989854 | |||||||
| chr3:49989991 | C | T | 1 | a0001c0011t0001g0213 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1484-9449C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49989991 | |||||||
| chr3:49990136 | T | C | 1 | a0006c0009t0001g0119 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1484-9304T>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49990136 | |||||||
| chr3:49990259 | A | G | 2 | a0001c0001t0001g0147 a0001c0001t0001g0148 |
2 | HG02257.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1484-9181A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49990259 | |||||||
| chr3:49990282 | C | T | 1 | a0001c0001t0001g0082 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1484-9158C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49990282 | |||||||
| chr3:49990341 | C | T | 109 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(106): Show |
109 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.1484-9099C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49990341 | |||||||
| chr3:49990481 | C | T | 1 | a0001c0001t0001g0035 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1484-8959C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49990481 | |||||||
| chr3:49990513 | G | T | 1 | a0001c0002t0001g0155 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1484-8927G>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49990513 | |||||||
| chr3:49990709 | T | C | 1 | a0001c0001t0001g0145 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1484-8731T>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49990709 | |||||||
| chr3:49990813 | G | A | 17 | a0001c0001t0001g0104 a0001c0001t0001g0120 a0001c0001t0001g0121 others(14): Show |
17 | HG01243.hp1 HG01884.hp2 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.1484-8627G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49990813 | |||||||
| chr3:49990952 | G | A | 126 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(123): Show |
126 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.1484-8488G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49990952 | |||||||
| chr3:49991295 | C | T | 3 | a0001c0003t0001g0063 a0001c0003t0001g0064 a0001c0003t0001g0066 |
3 | HG02109.hp2 HG02886.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1484-8145C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49991295 | |||||||
| chr3:49991393 | C | T | 1 | a0001c0001t0001g0001 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1484-8047C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49991393 | |||||||
| chr3:49991918 | C | CTTTAT | 42 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(39): Show |
42 | HG01106.hp1 HG01167.hp2 HG01243.hp1 others(39): Show |
intron_variant | MODIFIER | c.1484-7494_1484-749 others(9): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr3 | 49991918 | ||||||
| chr3:49991918 | C | CTTTATTT others(3): Show |
6 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0118 others(3): Show |
6 | HG02257.hp1 HG02451.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1484-7499_1484-749 others(14): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr3 | 49991918 | ||||||
| chr3:49991918 | C | CTTTATTT others(8): Show |
14 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(11): Show |
14 | HG00323.hp1 HG01106.hp2 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1484-7504_1484-749 others(19): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr3 | 49991918 | ||||||
| chr3:49991918 | CTTTATTT others(3): Show |
C | 7 | a0001c0001t0001g0060 a0002c0004t0001g0107 a0002c0004t0001g0133 others(4): Show |
7 | HG01516.hp2 HG02572.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1484-7499_1484-749 others(14): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr3 | 49991918 | ||||||
| chr3:49991953 | T | G | 14 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(11): Show |
14 | HG00323.hp1 HG01106.hp2 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1484-7487T>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49991953 | |||||||
| chr3:49993114 | G | A | 8 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0098 others(5): Show |
8 | HG01109.hp1 HG02622.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1484-6326G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49993114 | |||||||
| chr3:49993115 | C | A | 8 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0098 others(5): Show |
8 | HG01109.hp1 HG02622.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1484-6325C>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49993115 | |||||||
| chr3:49993146 | A | C | 8 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0098 others(5): Show |
8 | HG01109.hp1 HG02622.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1484-6294A>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49993146 | |||||||
| chr3:49993162 | T | G | 3 | a0001c0002t0001g0164 a0001c0002t0001g0174 a0001c0002t0001g0207 |
3 | NA18962.hp2 NA18986.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.1484-6278T>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49993162 | |||||||
| chr3:49993374 | G | C | 1 | a0005c0008t0001g0217 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1484-6066G>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49993374 | |||||||
| chr3:49993425 | C | T | 68 | a0001c0002t0001g0111 a0001c0002t0001g0149 a0001c0002t0001g0150 others(65): Show |
68 | HG00140.hp1 HG00323.hp2 HG00597.hp1 others(65): Show |
intron_variant | MODIFIER | c.1484-6015C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49993425 | |||||||
| chr3:49993567 | G | A | 14 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(11): Show |
14 | HG00323.hp1 HG01106.hp2 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1484-5873G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49993567 | |||||||
| chr3:49993687 | T | G | 1 | a0006c0009t0001g0119 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1484-5753T>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49993687 | |||||||
| chr3:49993703 | T | TA | 36 | a0001c0001t0001g0145 a0001c0002t0001g0111 a0001c0002t0001g0149 others(33): Show |
36 | HG00140.hp1 HG00323.hp2 HG00597.hp1 others(33): Show |
intron_variant | MODIFIER | c.1484-5726dupA | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr3 | 49993703 | ||||||
| chr3:49993703 | TA | T | 9 | a0001c0001t0001g0088 a0001c0001t0001g0104 a0001c0001t0001g0121 others(6): Show |
9 | HG01243.hp1 HG02622.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.1484-5726delA | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr3 | 49993703 | ||||||
| chr3:49993754 | G | A | 1 | a0001c0001t0001g0218 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1484-5686G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49993754 | |||||||
| chr3:49993772 | G | A | 1 | a0001c0003t0001g0063 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1484-5668G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49993772 | |||||||
| chr3:49993814 | C | T | 1 | a0001c0001t0001g0101 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1484-5626C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49993814 | |||||||
| chr3:49994407 | C | T | 34 | a0001c0002t0001g0151 a0001c0002t0001g0152 a0001c0002t0001g0153 others(31): Show |
34 | HG00738.hp2 HG01069.hp2 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.1484-5033C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49994407 | |||||||
| chr3:49994475 | C | T | 1 | a0001c0002t0001g0111 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1484-4965C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49994475 | |||||||
| chr3:49994575 | T | G | 69 | a0001c0001t0001g0145 a0001c0002t0001g0111 a0001c0002t0001g0149 others(66): Show |
69 | HG00140.hp1 HG00323.hp2 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.1484-4865T>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49994575 | |||||||
| chr3:49994669 | G | GGGGTGTG others(3): Show |
2 | a0001c0002t0001g0179 a0001c0002t0001g0180 |
2 | NA19057.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.1484-4770_1484-476 others(14): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr3 | 49994669 | ||||||
| chr3:49994669 | G | GGGGTGTG others(5): Show |
29 | a0001c0002t0001g0149 a0001c0002t0001g0150 a0001c0002t0001g0155 others(26): Show |
29 | HG00140.hp1 HG00323.hp2 HG00597.hp1 others(26): Show |
intron_variant | MODIFIER | c.1484-4770_1484-476 others(16): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr3 | 49994669 | ||||||
| chr3:49994669 | G | GGGGTGTG others(7): Show |
2 | a0001c0002t0001g0111 a0001c0002t0001g0157 |
2 | NA19085.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1484-4770_1484-476 others(18): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr3 | 49994669 | ||||||
| chr3:49994669 | G | GGGGTGTG others(17): Show |
1 | a0001c0001t0001g0118 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1484-4770_1484-476 others(28): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr3 | 49994669 | ||||||
| chr3:49994669 | G | GGT | 3 | a0001c0001t0001g0040 a0001c0001t0001g0137 a0005c0008t0001g0042 |
3 | HG01346.hp1 HG02818.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.1484-4746_1484-474 others(6): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr3 | 49994669 | ||||||
| chr3:49994669 | G | GGTGTGTG others(3): Show |
30 | a0001c0001t0001g0108 a0001c0002t0001g0151 a0001c0002t0001g0152 others(27): Show |
30 | HG00738.hp2 HG01069.hp2 HG01070.hp2 others(27): Show |
intron_variant | MODIFIER | c.1484-4754_1484-474 others(14): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr3 | 49994669 | ||||||
| chr3:49994669 | G | GGTGTGTG others(5): Show |
9 | a0001c0001t0001g0101 a0001c0001t0001g0109 a0001c0001t0001g0146 others(6): Show |
9 | HG02055.hp1 HG02257.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1484-4756_1484-474 others(16): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr3 | 49994669 | ||||||
| chr3:49994669 | G | GGTGTGTG others(9): Show |
17 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(14): Show |
17 | HG00323.hp1 HG01109.hp1 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.1484-4760_1484-474 others(20): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr3 | 49994669 | ||||||
| chr3:49994669 | G | GGTGTGTG others(11): Show |
9 | a0001c0001t0001g0110 a0001c0001t0001g0130 a0001c0001t0001g0131 others(6): Show |
9 | HG01106.hp2 HG01891.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.1484-4762_1484-474 others(22): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr3 | 49994669 | ||||||
| chr3:49994669 | G | GGTGTGTG others(13): Show |
3 | a0001c0001t0001g0001 a0001c0001t0001g0114 a0001c0001t0003g0116 |
3 | HG02735.hp2 HG03453.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1484-4764_1484-474 others(24): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr3 | 49994669 | ||||||
| chr3:49994669 | G | GGTGTGTG others(15): Show |
3 | a0002c0004t0001g0133 a0002c0004t0001g0138 a0002c0004t0001g0140 |
3 | HG02572.hp2 HG02922.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1484-4766_1484-474 others(26): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr3 | 49994669 | ||||||
| chr3:49994671 | T | G | 2 | a0001c0001t0001g0016 a0001c0002t0001g0207 |
2 | NA18952.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.1484-4769T>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49994671 | |||||||
| chr3:49994695 | T | TGTGTGTG others(6): Show |
1 | a0001c0002t0001g0207 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1484-4745_1484-474 others(17): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49994695 | |||||||
| chr3:49994700 | C | T | 69 | a0001c0001t0001g0145 a0001c0002t0001g0111 a0001c0002t0001g0149 others(66): Show |
69 | HG00140.hp1 HG00323.hp2 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.1484-4740C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49994700 | |||||||
| chr3:49994757 | A | AG | 5 | a0001c0002t0001g0165 a0001c0002t0001g0166 a0001c0002t0001g0167 others(2): Show |
5 | NA18960.hp2 NA18965.hp2 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.1484-4682dupG | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr3 | 49994757 | ||||||
| chr3:49995146 | A | G | 1 | a0006c0009t0001g0119 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1484-4294A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49995146 | |||||||
| chr3:49995266 | TA | T | 125 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(122): Show |
125 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(122): Show |
intron_variant | MODIFIER | c.1484-4165delA | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr3 | 49995266 | ||||||
| chr3:49995412 | C | T | 6 | a0002c0004t0001g0107 a0002c0004t0001g0133 a0002c0004t0001g0138 others(3): Show |
6 | HG02572.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1484-4028C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49995412 | |||||||
| chr3:49995545 | C | CA | 5 | a0001c0001t0001g0082 a0001c0001t0001g0085 a0001c0002t0001g0165 others(2): Show |
5 | HG02735.hp1 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1484-3879dupA | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr3 | 49995545 | ||||||
| chr3:49995795 | T | C | 83 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(80): Show |
83 | HG00140.hp1 HG00323.hp2 HG00597.hp1 others(80): Show |
intron_variant | MODIFIER | c.1484-3645T>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49995795 | |||||||
| chr3:49995839 | T | C | 1 | a0001c0001t0001g0018 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1484-3601T>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49995839 | |||||||
| chr3:49996959 | G | A | 1 | a0001c0001t0001g0097 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1484-2481G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49996959 | |||||||
| chr3:49997040 | A | G | 1 | a0006c0009t0001g0119 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1484-2400A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49997040 | |||||||
| chr3:49997056 | A | G | 6 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0127 others(3): Show |
6 | HG01884.hp2 HG02451.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1484-2384A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49997056 | |||||||
| chr3:49997179 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1484-2261C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49997179 | |||||||
| chr3:49997204 | T | G | 10 | a0001c0002t0001g0153 a0001c0002t0001g0154 a0001c0002t0001g0188 others(7): Show |
10 | HG00738.hp2 HG01081.hp2 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.1484-2236T>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49997204 | |||||||
| chr3:49997407 | C | T | 6 | a0002c0004t0001g0107 a0002c0004t0001g0133 a0002c0004t0001g0138 others(3): Show |
6 | HG02572.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1484-2033C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49997407 | |||||||
| chr3:49997822 | T | C | 1 | a0001c0001t0001g0129 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1484-1618T>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49997822 | |||||||
| chr3:49997876 | G | A | 1 | a0001c0002t0001g0196 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1484-1564G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49997876 | |||||||
| chr3:49997890 | T | C | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
130 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.1484-1550T>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49997890 | |||||||
| chr3:49997989 | T | C | 1 | a0001c0001t0001g0039 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1484-1451T>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49997989 | |||||||
| chr3:49998109 | C | T | 126 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(123): Show |
126 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.1484-1331C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49998109 | |||||||
| chr3:49998189 | G | A | 2 | a0001c0001t0001g0108 a0001c0001t0001g0109 |
2 | HG02647.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1484-1251G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49998189 | |||||||
| chr3:49998668 | A | G | 1 | a0001c0001t0001g0039 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1484-772A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49998668 | |||||||
| chr3:49999037 | C | CT | 5 | a0001c0001t0001g0130 a0001c0001t0001g0146 a0001c0001t0001g0147 others(2): Show |
5 | HG02145.hp1 HG02257.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1484-386dupT | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr3 | 49999037 | ||||||
| chr3:49999037 | CT | C | 9 | a0001c0001t0001g0004 a0001c0001t0001g0054 a0001c0001t0001g0101 others(6): Show |
9 | HG02486.hp2 HG02572.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1484-386delT | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr3 | 49999037 | ||||||
| chr3:49999054 | T | C | 3 | a0001c0002t0001g0164 a0001c0002t0001g0174 a0001c0002t0001g0207 |
3 | NA18962.hp2 NA18986.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.1484-386T>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49999054 | |||||||
| chr3:49999139 | C | G | 2 | a0001c0001t0001g0012 a0001c0001t0001g0034 |
2 | HG01168.hp2 HG01256.hp2 |
intron_variant | MODIFIER | c.1484-301C>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49999139 | |||||||
| chr3:49999690 | C | G | 126 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(123): Show |
126 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.1557+177C>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 49999690 | |||||||
| chr3:49999769 | GA | G | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
130 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.1557+270delA | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 49999769 | ||||||
| chr3:49999967 | A | AG | 6 | a0001c0001t0001g0118 a0001c0001t0001g0129 a0001c0001t0001g0130 others(3): Show |
6 | HG01891.hp2 HG02970.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1557+458dupG | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 49999967 | ||||||
| chr3:50000110 | C | T | 15 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(12): Show |
15 | HG01891.hp2 HG02486.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.1557+597C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50000110 | |||||||
| chr3:50000176 | T | C | 8 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(5): Show |
8 | HG02486.hp2 HG02559.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1557+663T>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50000176 | |||||||
| chr3:50000335 | GTT | G | 6 | a0001c0001t0001g0118 a0001c0001t0001g0129 a0001c0001t0001g0130 others(3): Show |
6 | HG01891.hp2 HG02970.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1557+831_1557+832d others(4): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50000335 | ||||||
| chr3:50000346 | CT | C | 35 | a0001c0002t0001g0111 a0001c0002t0001g0149 a0001c0002t0001g0150 others(32): Show |
35 | HG00140.hp1 HG00323.hp2 HG00597.hp1 others(32): Show |
intron_variant | MODIFIER | c.1557+848delT | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50000346 | ||||||
| chr3:50000370 | CACTGCCT others(2): Show |
C | 15 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(12): Show |
15 | HG01891.hp2 HG02486.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.1557+861_1557+869d others(11): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50000370 | ||||||
| chr3:50000445 | A | T | 1 | a0001c0001t0001g0001 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1557+932A>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50000445 | |||||||
| chr3:50000507 | A | G | 126 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(123): Show |
126 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.1557+994A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50000507 | |||||||
| chr3:50000996 | G | A | 4 | a0001c0001t0001g0024 a0001c0001t0001g0061 a0001c0001t0001g0079 others(1): Show |
4 | HG02027.hp1 NA18984.hp1 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.1557+1483G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50000996 | |||||||
| chr3:50001134 | A | G | 1 | a0001c0001t0001g0145 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1557+1621A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50001134 | |||||||
| chr3:50001231 | G | A | 88 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(85): Show |
88 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.1557+1718G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50001231 | |||||||
| chr3:50001647 | C | T | 1 | a0001c0001t0001g0001 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1557+2134C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50001647 | |||||||
| chr3:50001690 | A | G | 2 | a0001c0001t0001g0108 a0001c0001t0001g0109 |
2 | HG02647.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1557+2177A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50001690 | |||||||
| chr3:50001870 | A | G | 19 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(16): Show |
19 | HG00323.hp1 HG01106.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.1557+2357A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50001870 | |||||||
| chr3:50002041 | G | A | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
130 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.1557+2528G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50002041 | |||||||
| chr3:50002149 | G | GT | 2 | a0001c0002t0001g0199 a0001c0002t0001g0211 |
2 | HG01167.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1557+2637dupT | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50002149 | ||||||
| chr3:50002198 | C | G | 19 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(16): Show |
19 | HG00323.hp1 HG01106.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.1557+2685C>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50002198 | |||||||
| chr3:50002264 | CT | C | 28 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(25): Show |
28 | HG00323.hp1 HG01069.hp2 HG01081.hp2 others(25): Show |
intron_variant | MODIFIER | c.1557+2766delT | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50002264 | ||||||
| chr3:50002437 | T | G | 17 | a0001c0001t0001g0104 a0001c0001t0001g0120 a0001c0001t0001g0121 others(14): Show |
17 | HG01243.hp1 HG01884.hp2 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.1557+2924T>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50002437 | |||||||
| chr3:50002505 | G | A | 1 | a0001c0010t0001g0069 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1557+2992G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50002505 | |||||||
| chr3:50002761 | T | A | 88 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(85): Show |
88 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.1557+3248T>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50002761 | |||||||
| chr3:50002859 | ATAAAG | A | 4 | a0001c0001t0001g0104 a0001c0001t0001g0121 a0001c0001t0001g0122 others(1): Show |
4 | HG02622.hp2 HG02647.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1557+3351_1557+335 others(9): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50002859 | ||||||
| chr3:50003139 | T | C | 1 | a0001c0001t0001g0023 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1557+3626T>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50003139 | |||||||
| chr3:50003155 | A | T | 1 | a0006c0009t0001g0119 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1557+3642A>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50003155 | |||||||
| chr3:50003156 | T | A | 1 | a0006c0009t0001g0119 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1557+3643T>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50003156 | |||||||
| chr3:50003308 | TA | T | 17 | a0001c0001t0001g0079 a0001c0001t0001g0120 a0001c0001t0001g0122 others(14): Show |
17 | HG01069.hp1 HG01243.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.1557+3819delA | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50003308 | ||||||
| chr3:50003308 | TAA | T | 139 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(136): Show |
139 | HG00140.hp2 HG00597.hp2 HG00609.hp1 others(136): Show |
intron_variant | MODIFIER | c.1557+3818_1557+381 others(6): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50003308 | ||||||
| chr3:50003308 | TAAA | T | 26 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(23): Show |
26 | HG00323.hp1 HG01099.hp2 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.1557+3817_1557+381 others(7): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50003308 | ||||||
| chr3:50003460 | G | A | 1 | a0001c0001t0001g0114 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1557+3947G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50003460 | |||||||
| chr3:50003497 | C | T | 1 | a0001c0001t0001g0067 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1557+3984C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50003497 | |||||||
| chr3:50003682 | G | A | 1 | a0001c0002t0001g0177 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1557+4169G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50003682 | |||||||
| chr3:50003735 | G | C | 1 | a0001c0001t0001g0046 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1557+4222G>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50003735 | |||||||
| chr3:50003880 | C | T | 113 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(110): Show |
113 | HG00140.hp2 HG00597.hp2 HG00609.hp1 others(110): Show |
intron_variant | MODIFIER | c.1557+4367C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50003880 | |||||||
| chr3:50004306 | T | TC | 13 | a0001c0001t0001g0142 a0001c0002t0001g0149 a0001c0002t0001g0150 others(10): Show |
13 | HG01123.hp1 HG01192.hp1 HG01517.hp2 others(10): Show |
intron_variant | MODIFIER | c.1557+4801dupC | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50004306 | ||||||
| chr3:50004310 | C | CT | 126 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(123): Show |
126 | HG00140.hp2 HG00323.hp1 HG00597.hp2 others(123): Show |
intron_variant | MODIFIER | c.1557+4797_1557+479 others(5): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50004310 | |||||||
| chr3:50004394 | G | T | 19 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(16): Show |
19 | HG00323.hp1 HG01106.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.1557+4881G>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50004394 | |||||||
| chr3:50004474 | A | AT | 55 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(52): Show |
55 | HG00323.hp1 HG01106.hp2 HG01109.hp1 others(52): Show |
intron_variant | MODIFIER | c.1557+4980dupT | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50004474 | ||||||
| chr3:50004564 | C | T | 1 | a0001c0001t0001g0016 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1557+5051C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50004564 | |||||||
| chr3:50004683 | G | A | 1 | a0001c0001t0001g0048 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1557+5170G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50004683 | |||||||
| chr3:50004739 | C | G | 1 | a0001c0002t0001g0178 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1557+5226C>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50004739 | |||||||
| chr3:50004779 | C | T | 6 | a0001c0001t0001g0118 a0001c0001t0001g0129 a0001c0001t0001g0130 others(3): Show |
6 | HG01891.hp2 HG02970.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1557+5266C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50004779 | |||||||
| chr3:50004810 | G | T | 6 | a0001c0003t0001g0010 a0001c0003t0001g0027 a0001c0003t0001g0028 others(3): Show |
6 | HG00639.hp1 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1557+5297G>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50004810 | |||||||
| chr3:50004836 | T | C | 1 | a0001c0001t0001g0145 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1557+5323T>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50004836 | |||||||
| chr3:50005059 | C | G | 2 | a0001c0001t0001g0108 a0001c0001t0001g0109 |
2 | HG02647.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1557+5546C>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50005059 | |||||||
| chr3:50005223 | GTGA | G | 2 | a0001c0001t0001g0118 a0001c0001t0001g0129 |
2 | NA18906.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1557+5713_1557+571 others(7): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50005223 | ||||||
| chr3:50005225 | G | A | 14 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(11): Show |
14 | HG00323.hp1 HG01106.hp2 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1557+5712G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50005225 | |||||||
| chr3:50005257 | C | G | 182 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(179): Show |
182 | HG00140.hp2 HG00323.hp1 HG00597.hp2 others(179): Show |
intron_variant | MODIFIER | c.1557+5744C>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50005257 | |||||||
| chr3:50005292 | T | A | 14 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(11): Show |
14 | HG00323.hp1 HG01106.hp2 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1557+5779T>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50005292 | |||||||
| chr3:50005495 | C | CA | 53 | a0001c0001t0001g0038 a0001c0001t0001g0074 a0001c0001t0001g0108 others(50): Show |
53 | HG00140.hp1 HG00639.hp1 HG00738.hp2 others(50): Show |
intron_variant | MODIFIER | c.1557+5998dupA | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50005495 | ||||||
| chr3:50005778 | A | G | 3 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 |
3 | HG02257.hp1 HG02451.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1557+6265A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50005778 | |||||||
| chr3:50005908 | A | T | 132 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(129): Show |
132 | HG00140.hp2 HG00323.hp1 HG00597.hp2 others(129): Show |
intron_variant | MODIFIER | c.1557+6395A>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50005908 | |||||||
| chr3:50006107 | C | T | 5 | a0001c0001t0001g0095 a0001c0001t0001g0110 a0001c0001t0001g0115 others(2): Show |
5 | HG00323.hp1 HG01106.hp2 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.1557+6594C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50006107 | |||||||
| chr3:50006144 | C | CT | 15 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0146 others(12): Show |
15 | HG01517.hp1 HG02055.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.1557+6649dupT | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50006144 | ||||||
| chr3:50006144 | CT | C | 11 | a0001c0001t0001g0044 a0001c0001t0001g0082 a0001c0001t0001g0124 others(8): Show |
11 | HG01070.hp2 HG01167.hp1 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.1557+6649delT | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50006144 | ||||||
| chr3:50006221 | C | T | 148 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(145): Show |
148 | HG00140.hp2 HG00323.hp1 HG00597.hp2 others(145): Show |
intron_variant | MODIFIER | c.1557+6708C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50006221 | |||||||
| chr3:50006261 | G | C | 6 | a0002c0004t0001g0107 a0002c0004t0001g0133 a0002c0004t0001g0138 others(3): Show |
6 | HG02572.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1557+6748G>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50006261 | |||||||
| chr3:50006469 | A | G | 1 | a0006c0009t0001g0119 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1557+6956A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50006469 | |||||||
| chr3:50006573 | T | A | 34 | a0001c0002t0001g0151 a0001c0002t0001g0152 a0001c0002t0001g0153 others(31): Show |
34 | HG00738.hp2 HG01069.hp2 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.1557+7060T>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50006573 | |||||||
| chr3:50006584 | G | T | 1 | a0006c0009t0001g0119 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1557+7071G>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50006584 | |||||||
| chr3:50006780 | A | C | 15 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(12): Show |
15 | HG01891.hp2 HG02486.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.1557+7267A>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50006780 | |||||||
| chr3:50006833 | T | C | 4 | a0001c0005t0001g0102 a0001c0005t0001g0103 a0001c0005t0001g0105 others(1): Show |
4 | HG02258.hp2 HG02717.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1557+7320T>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50006833 | |||||||
| chr3:50006881 | G | A | 19 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(16): Show |
19 | HG00323.hp1 HG01106.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.1557+7368G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50006881 | |||||||
| chr3:50006931 | C | CA | 8 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0127 others(5): Show |
8 | HG01884.hp2 HG02451.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.1557+7433dupA | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50006931 | ||||||
| chr3:50007058 | G | C | 1 | a0001c0002t0001g0196 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1557+7545G>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50007058 | |||||||
| chr3:50007062 | A | G | 1 | a0001c0002t0001g0204 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1557+7549A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50007062 | |||||||
| chr3:50007113 | C | G | 4 | a0001c0005t0001g0102 a0001c0005t0001g0103 a0001c0005t0001g0105 others(1): Show |
4 | HG02258.hp2 HG02717.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1557+7600C>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50007113 | |||||||
| chr3:50007183 | G | C | 1 | a0001c0002t0001g0176 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1557+7670G>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50007183 | |||||||
| chr3:50007189 | G | GT | 42 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(39): Show |
42 | HG00140.hp2 HG01106.hp2 HG01192.hp2 others(39): Show |
intron_variant | MODIFIER | c.1557+7693dupT | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50007189 | ||||||
| chr3:50007223 | G | A | 1 | a0001c0002t0001g0185 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1557+7710G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50007223 | |||||||
| chr3:50007343 | C | T | 1 | a0001c0011t0001g0213 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1557+7830C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50007343 | |||||||
| chr3:50007380 | T | G | 9 | a0001c0003t0001g0010 a0001c0003t0001g0027 a0001c0003t0001g0028 others(6): Show |
9 | HG00639.hp1 HG01070.hp1 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.1557+7867T>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50007380 | |||||||
| chr3:50007407 | G | A | 19 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(16): Show |
19 | HG00323.hp1 HG01106.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.1557+7894G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50007407 | |||||||
| chr3:50007434 | T | C | 4 | a0001c0005t0001g0102 a0001c0005t0001g0103 a0001c0005t0001g0105 others(1): Show |
4 | HG02258.hp2 HG02717.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1557+7921T>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50007434 | |||||||
| chr3:50007657 | T | C | 1 | a0001c0001t0001g0145 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1557+8144T>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50007657 | |||||||
| chr3:50007724 | G | A | 6 | a0002c0004t0001g0107 a0002c0004t0001g0133 a0002c0004t0001g0138 others(3): Show |
6 | HG02572.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1557+8211G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50007724 | |||||||
| chr3:50007755 | G | A | 2 | a0001c0003t0001g0071 a0001c0003t0001g0073 |
2 | HG01123.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.1557+8242G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50007755 | |||||||
| chr3:50008546 | C | CT | 15 | a0001c0001t0001g0104 a0001c0001t0001g0120 a0001c0001t0001g0121 others(12): Show |
15 | HG01243.hp1 HG02027.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.1557+9059dupT | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50008546 | ||||||
| chr3:50008546 | C | CTT | 12 | a0001c0001t0001g0095 a0001c0001t0001g0097 a0001c0001t0001g0098 others(9): Show |
12 | HG00323.hp1 HG01109.hp1 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.1557+9058_1557+905 others(6): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50008546 | ||||||
| chr3:50008546 | CT | C | 109 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(106): Show |
109 | HG00140.hp2 HG00597.hp2 HG00609.hp1 others(106): Show |
intron_variant | MODIFIER | c.1557+9059delT | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50008546 | ||||||
| chr3:50008546 | CTT | C | 8 | a0001c0001t0001g0058 a0001c0001t0001g0127 a0001c0001t0001g0128 others(5): Show |
8 | HG01099.hp2 HG01884.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.1557+9058_1557+905 others(6): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50008546 | ||||||
| chr3:50008546 | CTTTTTTT others(4): Show |
C | 1 | a0006c0009t0001g0119 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1557+9049_1557+905 others(15): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50008546 | ||||||
| chr3:50008613 | G | T | 86 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(83): Show |
86 | HG00140.hp2 HG00597.hp2 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.1557+9100G>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50008613 | |||||||
| chr3:50008629 | A | G | 1 | a0001c0002t0001g0156 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1557+9116A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50008629 | |||||||
| chr3:50008631 | G | A | 90 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(87): Show |
90 | HG00140.hp2 HG00597.hp2 HG00609.hp1 others(87): Show |
intron_variant | MODIFIER | c.1557+9118G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50008631 | |||||||
| chr3:50008679 | G | A | 34 | a0001c0002t0001g0151 a0001c0002t0001g0152 a0001c0002t0001g0153 others(31): Show |
34 | HG00738.hp2 HG01069.hp2 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.1557+9166G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50008679 | |||||||
| chr3:50008697 | G | A | 15 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(12): Show |
15 | HG01891.hp2 HG02486.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.1557+9184G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50008697 | |||||||
| chr3:50008840 | C | T | 17 | a0001c0001t0001g0104 a0001c0001t0001g0120 a0001c0001t0001g0121 others(14): Show |
17 | HG01243.hp1 HG01884.hp2 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.1557+9327C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50008840 | |||||||
| chr3:50008841 | G | A | 1 | a0001c0001t0001g0114 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1557+9328G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50008841 | |||||||
| chr3:50009037 | T | C | 10 | a0001c0001t0001g0104 a0001c0001t0001g0120 a0001c0001t0001g0121 others(7): Show |
10 | HG01243.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1557+9524T>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50009037 | |||||||
| chr3:50009071 | C | T | 3 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 |
3 | HG02257.hp1 HG02451.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1557+9558C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50009071 | |||||||
| chr3:50009176 | G | A | 5 | a0001c0002t0001g0165 a0001c0002t0001g0166 a0001c0002t0001g0167 others(2): Show |
5 | NA18960.hp2 NA18965.hp2 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.1557+9663G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50009176 | |||||||
| chr3:50009429 | A | C | 1 | a0001c0001t0001g0145 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1557+9916A>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50009429 | |||||||
| chr3:50009688 | G | A | 3 | a0001c0001t0001g0104 a0001c0001t0001g0121 a0001c0001t0001g0122 |
3 | HG02647.hp2 HG02895.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1557+10175G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50009688 | |||||||
| chr3:50009701 | GT | G | 34 | a0001c0002t0001g0151 a0001c0002t0001g0152 a0001c0002t0001g0153 others(31): Show |
34 | HG00738.hp2 HG01069.hp2 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.1557+10189delT | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50009701 | |||||||
| chr3:50009853 | T | C | 1 | a0001c0001t0001g0054 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1557+10340T>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50009853 | |||||||
| chr3:50009971 | C | T | 90 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(87): Show |
90 | HG00140.hp2 HG00597.hp2 HG00609.hp1 others(87): Show |
intron_variant | MODIFIER | c.1557+10458C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50009971 | |||||||
| chr3:50009981 | C | T | 1 | a0001c0001t0001g0005 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1557+10468C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50009981 | |||||||
| chr3:50010104 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1557+10591C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50010104 | |||||||
| chr3:50010291 | A | T | 1 | a0001c0001t0001g0134 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1557+10778A>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50010291 | |||||||
| chr3:50010350 | G | C | 6 | a0001c0002t0001g0197 a0001c0002t0001g0198 a0001c0002t0001g0199 others(3): Show |
6 | HG01167.hp2 HG02965.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1557+10837G>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50010350 | |||||||
| chr3:50010583 | A | T | 1 | a0001c0001t0001g0096 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1557+11070A>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50010583 | |||||||
| chr3:50010785 | C | T | 1 | a0001c0001t0001g0129 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1557+11272C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50010785 | |||||||
| chr3:50010881 | C | T | 8 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(5): Show |
8 | HG02486.hp2 HG02559.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1557+11368C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50010881 | |||||||
| chr3:50010900 | C | CA | 42 | a0001c0001t0001g0075 a0001c0001t0001g0108 a0001c0001t0001g0109 others(39): Show |
42 | HG00140.hp1 HG00597.hp1 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.1557+11411dupA | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50010900 | ||||||
| chr3:50010900 | C | CAA | 116 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(113): Show |
116 | HG00140.hp2 HG00597.hp2 HG00639.hp1 others(113): Show |
intron_variant | MODIFIER | c.1557+11410_1557+11 others(8): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50010900 | ||||||
| chr3:50010900 | C | CAAA | 31 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(28): Show |
31 | HG00609.hp1 HG00738.hp1 HG01192.hp2 others(28): Show |
intron_variant | MODIFIER | c.1557+11409_1557+11 others(9): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50010900 | ||||||
| chr3:50010900 | C | CAAAA | 5 | a0001c0001t0001g0003 a0001c0005t0001g0102 a0001c0005t0001g0103 others(2): Show |
5 | HG02258.hp2 HG02559.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1557+11408_1557+11 others(10): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50010900 | ||||||
| chr3:50010914 | A | G | 1 | a0001c0001t0001g0099 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1557+11401A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50010914 | |||||||
| chr3:50011038 | G | T | 2 | a0001c0001t0001g0118 a0001c0001t0001g0129 |
2 | NA18906.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1557+11525G>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50011038 | |||||||
| chr3:50011127 | T | G | 1 | a0001c0002t0001g0208 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1557+11614T>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50011127 | |||||||
| chr3:50011217 | C | T | 1 | a0006c0009t0001g0119 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1557+11704C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50011217 | |||||||
| chr3:50011233 | G | T | 1 | a0001c0002t0001g0215 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1557+11720G>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50011233 | |||||||
| chr3:50011258 | G | T | 2 | a0001c0001t0001g0108 a0001c0001t0001g0109 |
2 | HG02647.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1557+11745G>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50011258 | |||||||
| chr3:50011375 | C | T | 8 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(5): Show |
8 | HG02486.hp2 HG02559.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1557+11862C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50011375 | |||||||
| chr3:50011409 | AG | A | 17 | a0001c0001t0001g0104 a0001c0001t0001g0120 a0001c0001t0001g0121 others(14): Show |
17 | HG01243.hp1 HG01884.hp2 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.1557+11898delG | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50011409 | ||||||
| chr3:50011618 | C | G | 14 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(11): Show |
14 | HG00323.hp1 HG01106.hp2 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1557+12105C>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50011618 | |||||||
| chr3:50011839 | C | CT | 27 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(24): Show |
27 | HG00639.hp1 HG01070.hp1 HG01071.hp2 others(24): Show |
intron_variant | MODIFIER | c.1557+12339dupT | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50011839 | ||||||
| chr3:50011839 | CT | C | 22 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(19): Show |
22 | HG00323.hp1 HG01106.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1557+12339delT | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50011839 | ||||||
| chr3:50011847 | T | C | 7 | a0001c0001t0001g0104 a0001c0001t0001g0121 a0001c0001t0001g0122 others(4): Show |
7 | HG01243.hp1 HG02622.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1557+12334T>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50011847 | |||||||
| chr3:50011866 | T | G | 86 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(83): Show |
86 | HG00140.hp2 HG00597.hp2 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.1557+12353T>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50011866 | |||||||
| chr3:50011954 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1557+12441C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50011954 | |||||||
| chr3:50012525 | G | T | 132 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(129): Show |
132 | HG00140.hp2 HG00323.hp1 HG00597.hp2 others(129): Show |
intron_variant | MODIFIER | c.1557+13012G>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50012525 | |||||||
| chr3:50012738 | C | CT | 7 | a0001c0001t0001g0059 a0001c0001t0001g0079 a0001c0001t0001g0081 others(4): Show |
7 | HG01243.hp2 HG02027.hp1 HG02027.hp2 others(4): Show |
intron_variant | MODIFIER | c.1557+13246dupT | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50012738 | ||||||
| chr3:50012738 | CT | C | 57 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(54): Show |
57 | HG00323.hp1 HG00323.hp2 HG01069.hp1 others(54): Show |
intron_variant | MODIFIER | c.1557+13246delT | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50012738 | ||||||
| chr3:50012816 | C | G | 6 | a0001c0001t0001g0118 a0001c0001t0001g0129 a0001c0001t0001g0130 others(3): Show |
6 | HG01891.hp2 HG02970.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1557+13303C>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50012816 | |||||||
| chr3:50012894 | C | A | 15 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(12): Show |
15 | HG01891.hp2 HG02486.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.1557+13381C>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50012894 | |||||||
| chr3:50012971 | G | A | 1 | a0001c0002t0001g0211 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1557+13458G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50012971 | |||||||
| chr3:50013156 | G | A | 1 | a0001c0001t0001g0016 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1557+13643G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50013156 | |||||||
| chr3:50013484 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1557+13971G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50013484 | |||||||
| chr3:50013980 | A | G | 1 | a0001c0001t0001g0038 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1557+14467A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50013980 | |||||||
| chr3:50014076 | A | G | 3 | a0001c0002t0001g0208 a0001c0002t0001g0209 a0001c0002t0001g0216 |
3 | HG02055.hp1 HG02258.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1557+14563A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50014076 | |||||||
| chr3:50014197 | G | T | 1 | a0001c0001t0001g0120 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1557+14684G>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50014197 | |||||||
| chr3:50014727 | G | T | 1 | a0001c0001t0003g0116 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1557+15214G>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50014727 | |||||||
| chr3:50014917 | C | T | 3 | a0001c0002t0001g0199 a0001c0002t0001g0211 a0001c0002t0001g0212 |
3 | HG01167.hp2 HG02965.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1557+15404C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50014917 | |||||||
| chr3:50015046 | C | CA | 5 | a0001c0002t0001g0164 a0001c0002t0001g0169 a0001c0002t0001g0186 others(2): Show |
5 | HG00597.hp1 HG01175.hp2 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.1557+15558dupA | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50015046 | ||||||
| chr3:50015046 | CA | C | 62 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(59): Show |
62 | HG00639.hp2 HG00738.hp2 HG01070.hp2 others(59): Show |
intron_variant | MODIFIER | c.1557+15558delA | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50015046 | ||||||
| chr3:50015046 | CAA | C | 105 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(102): Show |
105 | HG00140.hp2 HG00597.hp2 HG00609.hp1 others(102): Show |
intron_variant | MODIFIER | c.1557+15557_1557+15 others(8): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50015046 | ||||||
| chr3:50015046 | CAAA | C | 6 | a0001c0001t0001g0055 a0002c0004t0001g0107 a0002c0004t0001g0133 others(3): Show |
6 | HG02109.hp1 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1557+15556_1557+15 others(9): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50015046 | ||||||
| chr3:50015076 | T | G | 2 | a0001c0002t0001g0197 a0001c0002t0001g0198 |
2 | HG02976.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1557+15563T>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50015076 | |||||||
| chr3:50015296 | C | G | 107 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(104): Show |
107 | HG00140.hp2 HG00597.hp2 HG00609.hp1 others(104): Show |
intron_variant | MODIFIER | c.1557+15783C>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50015296 | |||||||
| chr3:50015401 | T | C | 132 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(129): Show |
132 | HG00140.hp2 HG00323.hp1 HG00597.hp2 others(129): Show |
intron_variant | MODIFIER | c.1557+15888T>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50015401 | |||||||
| chr3:50015433 | T | TATTA | 14 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(11): Show |
14 | HG00323.hp1 HG01106.hp2 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1557+15920_1557+15 others(10): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50015433 | |||||||
| chr3:50015434 | T | A | 163 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(160): Show |
163 | HG00140.hp2 HG00597.hp2 HG00609.hp1 others(160): Show |
intron_variant | MODIFIER | c.1557+15921T>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50015434 | |||||||
| chr3:50015435 | T | A | 2 | a0001c0001t0001g0108 a0001c0001t0001g0109 |
2 | HG02647.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1557+15922T>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50015435 | |||||||
| chr3:50015436 | T | A | 12 | a0001c0001t0001g0095 a0001c0001t0001g0097 a0001c0001t0001g0098 others(9): Show |
12 | HG00323.hp1 HG01106.hp2 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1557+15923T>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50015436 | |||||||
| chr3:50015437 | T | A | 138 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(135): Show |
138 | HG00140.hp2 HG00597.hp2 HG00609.hp1 others(135): Show |
intron_variant | MODIFIER | c.1557+15924T>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50015437 | |||||||
| chr3:50015440 | T | A | 21 | a0001c0001t0001g0104 a0001c0001t0001g0120 a0001c0001t0001g0121 others(18): Show |
21 | HG00738.hp2 HG01081.hp2 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.1557+15927T>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50015440 | |||||||
| chr3:50015492 | G | A | 1 | a0001c0001t0001g0022 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1557+15979G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50015492 | |||||||
| chr3:50015494 | G | T | 1 | a0001c0001t0001g0022 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1557+15981G>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50015494 | |||||||
| chr3:50015578 | G | A | 2 | a0001c0001t0001g0112 a0001c0001t0001g0113 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1557+16065G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50015578 | |||||||
| chr3:50015593 | G | A | 1 | a0006c0009t0001g0119 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1557+16080G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50015593 | |||||||
| chr3:50015678 | T | C | 132 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(129): Show |
132 | HG00140.hp2 HG00323.hp1 HG00597.hp2 others(129): Show |
intron_variant | MODIFIER | c.1557+16165T>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50015678 | |||||||
| chr3:50016081 | C | G | 14 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(11): Show |
14 | HG00323.hp1 HG01106.hp2 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1557+16568C>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50016081 | |||||||
| chr3:50016230 | C | T | 1 | a0001c0001t0001g0057 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1557+16717C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50016230 | |||||||
| chr3:50016280 | C | CT | 5 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0146 others(2): Show |
5 | HG02257.hp1 HG02451.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1557+16773dupT | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50016280 | ||||||
| chr3:50016335 | C | T | 1 | a0001c0002t0001g0204 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1557+16822C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50016335 | |||||||
| chr3:50016469 | T | C | 1 | a0001c0002t0001g0183 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1557+16956T>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50016469 | |||||||
| chr3:50016504 | GT | G | 101 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(98): Show |
101 | HG00140.hp2 HG00323.hp2 HG00597.hp2 others(98): Show |
intron_variant | MODIFIER | c.1557+17004delT | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50016504 | ||||||
| chr3:50016730 | C | T | 2 | a0002c0004t0001g0107 a0002c0004t0001g0141 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1557+17217C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50016730 | |||||||
| chr3:50016805 | G | A | 4 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0132 others(1): Show |
4 | HG01891.hp2 HG02970.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1557+17292G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50016805 | |||||||
| chr3:50016824 | G | GT | 64 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(61): Show |
64 | HG00140.hp1 HG00738.hp2 HG01069.hp2 others(61): Show |
intron_variant | MODIFIER | c.1557+17330dupT | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50016824 | ||||||
| chr3:50016824 | G | GTT | 31 | a0001c0001t0001g0002 a0001c0001t0001g0095 a0001c0001t0001g0097 others(28): Show |
31 | HG00323.hp1 HG01167.hp2 HG01255.hp2 others(28): Show |
intron_variant | MODIFIER | c.1557+17329_1557+17 others(8): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50016824 | ||||||
| chr3:50016824 | G | GTTT | 5 | a0001c0001t0001g0096 a0001c0001t0001g0098 a0001c0001t0001g0100 others(2): Show |
5 | HG01106.hp2 HG01109.hp1 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.1557+17328_1557+17 others(9): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50016824 | ||||||
| chr3:50016827 | T | TTG | 10 | a0001c0001t0001g0079 a0001c0003t0001g0010 a0001c0003t0001g0027 others(7): Show |
10 | HG00639.hp1 HG01070.hp1 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.1557+17315_1557+17 others(8): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50016827 | ||||||
| chr3:50016828 | T | TG | 76 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(73): Show |
76 | HG00140.hp2 HG00597.hp2 HG00609.hp1 others(73): Show |
intron_variant | MODIFIER | c.1557+17315_1557+17 others(7): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50016828 | |||||||
| chr3:50016935 | C | T | 4 | a0001c0005t0001g0102 a0001c0005t0001g0103 a0001c0005t0001g0105 others(1): Show |
4 | HG02258.hp2 HG02717.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1557+17422C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50016935 | |||||||
| chr3:50017073 | A | G | 2 | a0001c0002t0001g0199 a0001c0002t0001g0211 |
2 | HG01167.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1557+17560A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50017073 | |||||||
| chr3:50017328 | C | T | 6 | a0001c0001t0001g0118 a0001c0001t0001g0129 a0001c0001t0001g0130 others(3): Show |
6 | HG01891.hp2 HG02970.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1557+17815C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50017328 | |||||||
| chr3:50017334 | G | C | 2 | a0001c0001t0001g0056 a0001c0003t0001g0064 |
2 | HG02109.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1557+17821G>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50017334 | |||||||
| chr3:50017430 | C | T | 1 | a0001c0001t0001g0052 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1557+17917C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50017430 | |||||||
| chr3:50017448 | T | C | 2 | a0001c0001t0001g0108 a0001c0001t0001g0109 |
2 | HG02647.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1557+17935T>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50017448 | |||||||
| chr3:50017449 | G | T | 2 | a0001c0001t0001g0108 a0001c0001t0001g0109 |
2 | HG02647.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1557+17936G>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50017449 | |||||||
| chr3:50017474 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1557+17961C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50017474 | |||||||
| chr3:50017559 | A | G | 1 | a0001c0001t0001g0090 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1557+18046A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50017559 | |||||||
| chr3:50017663 | C | T | 1 | a0001c0005t0001g0102 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1557+18150C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50017663 | |||||||
| chr3:50017925 | A | G | 4 | a0001c0002t0001g0177 a0001c0002t0001g0191 a0001c0002t0001g0200 others(1): Show |
4 | HG01069.hp2 HG01070.hp2 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.1557+18412A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50017925 | |||||||
| chr3:50017971 | T | C | 2 | a0002c0004t0001g0138 a0002c0004t0001g0140 |
2 | HG02572.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1557+18458T>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50017971 | |||||||
| chr3:50018527 | A | G | 1 | a0001c0001t0001g0118 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1557+19014A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50018527 | |||||||
| chr3:50018581 | G | GT | 22 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(19): Show |
22 | HG00609.hp2 HG01175.hp1 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.1557+19098dupT | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50018581 | ||||||
| chr3:50018581 | GT | G | 35 | a0001c0001t0001g0021 a0001c0001t0001g0024 a0001c0001t0001g0026 others(32): Show |
35 | HG00609.hp1 HG00738.hp1 HG01255.hp1 others(32): Show |
intron_variant | MODIFIER | c.1557+19098delT | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50018581 | ||||||
| chr3:50018581 | GTT | G | 74 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0015 others(71): Show |
74 | HG00140.hp2 HG00597.hp2 HG01070.hp1 others(71): Show |
intron_variant | MODIFIER | c.1557+19097_1557+19 others(8): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50018581 | ||||||
| chr3:50018581 | GTTT | G | 16 | a0001c0001t0001g0017 a0001c0001t0001g0080 a0001c0001t0001g0088 others(13): Show |
16 | HG00323.hp1 HG00639.hp1 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.1557+19096_1557+19 others(9): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50018581 | ||||||
| chr3:50018581 | GTTTT | G | 5 | a0001c0001t0001g0067 a0001c0001t0001g0110 a0001c0001t0001g0114 others(2): Show |
5 | HG01106.hp2 HG02735.hp2 NA18612.hp2 others(2): Show |
intron_variant | MODIFIER | c.1557+19095_1557+19 others(10): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50018581 | ||||||
| chr3:50018581 | GTTTTT | G | 5 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0146 others(2): Show |
5 | HG02257.hp1 HG02451.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1557+19094_1557+19 others(11): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50018581 | ||||||
| chr3:50018594 | T | G | 4 | a0002c0004t0001g0133 a0002c0004t0001g0138 a0002c0004t0001g0139 others(1): Show |
4 | HG02572.hp2 HG02922.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1557+19081T>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50018594 | |||||||
| chr3:50018595 | T | G | 1 | a0001c0001t0001g0054 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1557+19082T>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50018595 | |||||||
| chr3:50018596 | T | G | 3 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 |
3 | HG02257.hp1 HG02451.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1557+19083T>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50018596 | |||||||
| chr3:50018601 | T | G | 3 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 |
3 | HG02257.hp1 HG02451.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1557+19088T>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50018601 | |||||||
| chr3:50018609 | T | C | 1 | a0001c0003t0001g0073 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1557+19096T>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50018609 | |||||||
| chr3:50018634 | C | CACCA | 3 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 |
3 | HG02257.hp1 HG02451.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1557+19121_1557+19 others(10): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50018634 | |||||||
| chr3:50018685 | A | C | 3 | a0001c0001t0001g0055 a0001c0003t0001g0063 a0001c0003t0001g0066 |
3 | HG02109.hp1 HG02886.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1557+19172A>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50018685 | |||||||
| chr3:50018832 | G | A | 15 | a0001c0003t0001g0010 a0001c0003t0001g0027 a0001c0003t0001g0028 others(12): Show |
15 | HG00639.hp1 HG01070.hp1 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.1557+19319G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50018832 | |||||||
| chr3:50018971 | G | T | 1 | a0001c0001t0001g0129 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1557+19458G>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50018971 | |||||||
| chr3:50019045 | T | A | 21 | a0001c0001t0001g0075 a0001c0001t0001g0094 a0001c0001t0001g0095 others(18): Show |
21 | HG00323.hp1 HG01106.hp2 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.1557+19532T>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50019045 | |||||||
| chr3:50019049 | T | A | 1 | a0001c0001t0003g0116 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1557+19536T>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50019049 | |||||||
| chr3:50019301 | C | T | 6 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0127 others(3): Show |
6 | HG01884.hp2 HG02451.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1557+19788C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50019301 | |||||||
| chr3:50019604 | C | T | 5 | a0001c0002t0001g0197 a0001c0002t0001g0198 a0001c0002t0001g0199 others(2): Show |
5 | HG01167.hp2 HG02965.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1557+20091C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50019604 | |||||||
| chr3:50019809 | T | A | 2 | a0001c0002t0001g0179 a0001c0002t0001g0180 |
2 | NA19057.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.1557+20296T>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50019809 | |||||||
| chr3:50019860 | T | C | 2 | a0001c0001t0001g0061 a0001c0001t0001g0084 |
2 | NA18984.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.1557+20347T>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50019860 | |||||||
| chr3:50019955 | G | C | 1 | a0001c0002t0001g0210 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1557+20442G>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50019955 | |||||||
| chr3:50020067 | T | C | 182 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(179): Show |
182 | HG00140.hp2 HG00323.hp1 HG00597.hp2 others(179): Show |
intron_variant | MODIFIER | c.1557+20554T>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50020067 | |||||||
| chr3:50020855 | G | A | 1 | a0001c0001t0001g0022 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1557+21342G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50020855 | |||||||
| chr3:50021140 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1557+21627G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50021140 | |||||||
| chr3:50021177 | G | T | 211 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(208): Show |
211 | HG00140.hp2 HG00323.hp1 HG00597.hp1 others(208): Show |
intron_variant | MODIFIER | c.1557+21664G>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50021177 | |||||||
| chr3:50021218 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1557+21705G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50021218 | |||||||
| chr3:50021244 | G | A | 6 | a0001c0001t0001g0118 a0001c0001t0001g0129 a0001c0001t0001g0130 others(3): Show |
6 | HG01891.hp2 HG02970.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1557+21731G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50021244 | |||||||
| chr3:50021405 | C | T | 6 | a0002c0004t0001g0107 a0002c0004t0001g0133 a0002c0004t0001g0138 others(3): Show |
6 | HG02572.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1557+21892C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50021405 | |||||||
| chr3:50021468 | C | T | 4 | a0001c0005t0001g0102 a0001c0005t0001g0103 a0001c0005t0001g0105 others(1): Show |
4 | HG02258.hp2 HG02717.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1557+21955C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50021468 | |||||||
| chr3:50021740 | C | CTT | 37 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(34): Show |
37 | HG00597.hp2 HG01070.hp1 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.1557+22256_1557+22 others(8): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50021740 | ||||||
| chr3:50021740 | C | CTTT | 33 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(30): Show |
33 | HG00140.hp2 HG01106.hp1 HG01168.hp1 others(30): Show |
intron_variant | MODIFIER | c.1557+22255_1557+22 others(9): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50021740 | ||||||
| chr3:50021740 | C | CTTTT | 6 | a0001c0001t0001g0006 a0001c0001t0001g0024 a0001c0001t0001g0061 others(3): Show |
6 | HG01255.hp1 HG02027.hp1 NA18522.hp2 others(3): Show |
intron_variant | MODIFIER | c.1557+22254_1557+22 others(10): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50021740 | ||||||
| chr3:50021740 | C | CTTTTT | 6 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(3): Show |
6 | HG00609.hp1 HG01891.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1557+22253_1557+22 others(11): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50021740 | ||||||
| chr3:50021740 | CT | C | 39 | a0001c0001t0001g0124 a0001c0001t0001g0129 a0001c0001t0001g0145 others(36): Show |
39 | HG00323.hp2 HG00597.hp1 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.1557+22257delT | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50021740 | ||||||
| chr3:50021740 | CTT | C | 34 | a0001c0001t0001g0096 a0001c0001t0001g0110 a0001c0001t0001g0114 others(31): Show |
34 | HG00738.hp2 HG01069.hp2 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.1557+22256_1557+22 others(8): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50021740 | ||||||
| chr3:50021740 | CTTT | C | 17 | a0001c0001t0001g0095 a0001c0001t0001g0097 a0001c0001t0001g0098 others(14): Show |
17 | HG00323.hp1 HG01109.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.1557+22255_1557+22 others(9): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50021740 | ||||||
| chr3:50021740 | CTTTTTTT others(5): Show |
C | 4 | a0002c0004t0001g0133 a0002c0004t0001g0138 a0002c0004t0001g0139 others(1): Show |
4 | HG02572.hp2 HG02922.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1557+22246_1557+22 others(18): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50021740 | ||||||
| chr3:50021740 | CTTTTTTT others(6): Show |
C | 2 | a0002c0004t0001g0107 a0002c0004t0001g0141 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1557+22245_1557+22 others(19): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50021740 | ||||||
| chr3:50021906 | T | C | 113 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(110): Show |
113 | HG00140.hp2 HG00597.hp2 HG00609.hp1 others(110): Show |
intron_variant | MODIFIER | c.1557+22393T>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50021906 | |||||||
| chr3:50022218 | G | A | 19 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(16): Show |
19 | HG00323.hp1 HG01106.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.1557+22705G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50022218 | |||||||
| chr3:50022325 | T | C | 113 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(110): Show |
113 | HG00140.hp2 HG00597.hp2 HG00609.hp1 others(110): Show |
intron_variant | MODIFIER | c.1557+22812T>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50022325 | |||||||
| chr3:50022335 | C | CT | 10 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(7): Show |
10 | HG01243.hp1 HG02004.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.1557+22834dupT | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50022335 | ||||||
| chr3:50022433 | T | C | 113 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(110): Show |
113 | HG00140.hp2 HG00597.hp2 HG00609.hp1 others(110): Show |
intron_variant | MODIFIER | c.1557+22920T>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50022433 | |||||||
| chr3:50022483 | A | C | 4 | a0001c0005t0001g0102 a0001c0005t0001g0103 a0001c0005t0001g0105 others(1): Show |
4 | HG02258.hp2 HG02717.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1557+22970A>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50022483 | |||||||
| chr3:50022549 | C | T | 6 | a0002c0004t0001g0107 a0002c0004t0001g0133 a0002c0004t0001g0138 others(3): Show |
6 | HG02572.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1557+23036C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50022549 | |||||||
| chr3:50022575 | C | G | 1 | a0001c0001t0001g0058 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1557+23062C>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50022575 | |||||||
| chr3:50022576 | T | C | 1 | a0001c0001t0001g0058 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1557+23063T>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50022576 | |||||||
| chr3:50022625 | T | A | 1 | a0001c0001t0001g0145 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1557+23112T>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50022625 | |||||||
| chr3:50022888 | C | A | 1 | a0001c0001t0001g0082 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1557+23375C>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50022888 | |||||||
| chr3:50022899 | G | C | 107 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(104): Show |
107 | HG00140.hp2 HG00597.hp2 HG00609.hp1 others(104): Show |
intron_variant | MODIFIER | c.1557+23386G>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50022899 | |||||||
| chr3:50023241 | C | A | 1 | a0001c0001t0001g0018 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1557+23728C>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50023241 | |||||||
| chr3:50023391 | C | T | 6 | a0002c0004t0001g0107 a0002c0004t0001g0133 a0002c0004t0001g0138 others(3): Show |
6 | HG02572.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1557+23878C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50023391 | |||||||
| chr3:50023410 | A | G | 4 | a0001c0005t0001g0102 a0001c0005t0001g0103 a0001c0005t0001g0105 others(1): Show |
4 | HG02258.hp2 HG02717.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1557+23897A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50023410 | |||||||
| chr3:50023546 | A | G | 19 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(16): Show |
19 | HG00323.hp1 HG01106.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.1557+24033A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50023546 | |||||||
| chr3:50023577 | C | T | 7 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0099 others(4): Show |
7 | HG01109.hp1 HG02622.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1557+24064C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50023577 | |||||||
| chr3:50023645 | A | G | 19 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(16): Show |
19 | HG00323.hp1 HG01106.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.1557+24132A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50023645 | |||||||
| chr3:50023655 | A | AT | 109 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(106): Show |
109 | HG00140.hp2 HG00323.hp1 HG00597.hp2 others(106): Show |
intron_variant | MODIFIER | c.1557+24162dupT | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50023655 | ||||||
| chr3:50023655 | A | ATT | 8 | a0001c0001t0001g0025 a0001c0001t0001g0048 a0001c0001t0001g0087 others(5): Show |
8 | HG01192.hp2 HG02257.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1557+24161_1557+24 others(8): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50023655 | ||||||
| chr3:50023925 | G | C | 1 | a0001c0001t0001g0145 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1558-24320G>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50023925 | |||||||
| chr3:50024233 | A | G | 6 | a0002c0004t0001g0107 a0002c0004t0001g0133 a0002c0004t0001g0138 others(3): Show |
6 | HG02572.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1558-24012A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50024233 | |||||||
| chr3:50024385 | T | C | 6 | a0002c0004t0001g0107 a0002c0004t0001g0133 a0002c0004t0001g0138 others(3): Show |
6 | HG02572.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1558-23860T>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50024385 | |||||||
| chr3:50024393 | A | G | 1 | a0006c0009t0001g0119 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1558-23852A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50024393 | |||||||
| chr3:50024420 | G | T | 19 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(16): Show |
19 | HG00323.hp1 HG01106.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.1558-23825G>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50024420 | |||||||
| chr3:50024484 | CT | C | 19 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(16): Show |
19 | HG00323.hp1 HG01106.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.1558-23758delT | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50024484 | ||||||
| chr3:50024528 | C | A | 2 | a0001c0001t0001g0056 a0001c0003t0001g0064 |
2 | HG02109.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1558-23717C>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50024528 | |||||||
| chr3:50024549 | T | A | 1 | a0001c0001t0001g0058 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1558-23696T>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50024549 | |||||||
| chr3:50024604 | G | C | 1 | a0001c0011t0001g0213 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1558-23641G>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50024604 | |||||||
| chr3:50024676 | G | A | 6 | a0002c0004t0001g0107 a0002c0004t0001g0133 a0002c0004t0001g0138 others(3): Show |
6 | HG02572.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1558-23569G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50024676 | |||||||
| chr3:50024759 | C | T | 10 | a0001c0001t0001g0104 a0001c0001t0001g0120 a0001c0001t0001g0121 others(7): Show |
10 | HG01243.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1558-23486C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50024759 | |||||||
| chr3:50024898 | G | A | 6 | a0002c0004t0001g0107 a0002c0004t0001g0133 a0002c0004t0001g0138 others(3): Show |
6 | HG02572.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1558-23347G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50024898 | |||||||
| chr3:50025001 | A | C | 1 | a0001c0001t0001g0018 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1558-23244A>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50025001 | |||||||
| chr3:50025004 | C | A | 148 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(145): Show |
148 | HG00140.hp2 HG00323.hp1 HG00597.hp2 others(145): Show |
intron_variant | MODIFIER | c.1558-23241C>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50025004 | |||||||
| chr3:50025080 | G | GT | 8 | a0001c0001t0001g0034 a0001c0001t0001g0114 a0001c0001t0001g0118 others(5): Show |
8 | HG01256.hp2 HG01891.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.1558-23154dupT | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50025080 | ||||||
| chr3:50025080 | GT | G | 5 | a0001c0001t0001g0059 a0001c0001t0001g0146 a0001c0001t0001g0147 others(2): Show |
5 | HG02055.hp2 HG02257.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1558-23154delT | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50025080 | ||||||
| chr3:50025091 | T | C | 2 | a0001c0001t0001g0108 a0001c0001t0001g0109 |
2 | HG02647.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1558-23154T>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50025091 | |||||||
| chr3:50025338 | A | G | 1 | a0003c0007t0001g0173 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1558-22907A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50025338 | |||||||
| chr3:50025445 | G | A | 34 | a0001c0002t0001g0151 a0001c0002t0001g0152 a0001c0002t0001g0153 others(31): Show |
34 | HG00738.hp2 HG01069.hp2 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.1558-22800G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50025445 | |||||||
| chr3:50025587 | AT | A | 15 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(12): Show |
15 | HG01081.hp2 HG01099.hp1 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.1558-22639delT | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50025587 | ||||||
| chr3:50025591 | T | TTTTTTTT others(265): Show |
3 | a0001c0001t0001g0013 a0001c0001t0001g0059 a0005c0008t0001g0042 |
3 | HG01346.hp1 HG02055.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1558-22639_1558-22 others(278): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50025591 | ||||||
| chr3:50025592 | T | TTTTTTTT others(262): Show |
3 | a0001c0001t0001g0038 a0001c0003t0001g0032 a0004c0006t0001g0072 |
3 | HG01070.hp1 NA19063.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.1558-22639_1558-22 others(275): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50025592 | ||||||
| chr3:50025592 | T | TTTTTTTT others(263): Show |
67 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0015 others(64): Show |
67 | HG00140.hp2 HG00597.hp2 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.1558-22639_1558-22 others(276): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50025592 | ||||||
| chr3:50025592 | T | TTTTTTTT others(264): Show |
15 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0036 others(12): Show |
15 | HG01109.hp2 HG01192.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.1558-22639_1558-22 others(277): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50025592 | ||||||
| chr3:50025592 | T | TTTTTTTT others(265): Show |
2 | a0001c0001t0001g0014 a0001c0003t0001g0028 |
2 | HG00639.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1558-22639_1558-22 others(278): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50025592 | ||||||
| chr3:50025625 | A | G | 1 | a0001c0001t0001g0145 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1558-22620A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50025625 | |||||||
| chr3:50026320 | G | T | 182 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(179): Show |
182 | HG00140.hp2 HG00323.hp1 HG00597.hp2 others(179): Show |
intron_variant | MODIFIER | c.1558-21925G>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50026320 | |||||||
| chr3:50026379 | G | A | 3 | a0002c0004t0001g0133 a0002c0004t0001g0138 a0002c0004t0001g0140 |
3 | HG02572.hp2 HG02922.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1558-21866G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50026379 | |||||||
| chr3:50026381 | C | G | 1 | a0001c0001t0001g0120 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1558-21864C>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50026381 | |||||||
| chr3:50026383 | C | CT | 12 | a0001c0001t0001g0087 a0001c0002t0001g0154 a0001c0002t0001g0179 others(9): Show |
12 | HG01192.hp2 HG01517.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.1558-21848dupT | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50026383 | ||||||
| chr3:50026514 | G | A | 6 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0127 others(3): Show |
6 | HG01884.hp2 HG02451.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1558-21731G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50026514 | |||||||
| chr3:50026657 | A | T | 1 | a0001c0001t0001g0048 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1558-21588A>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50026657 | |||||||
| chr3:50026781 | C | T | 3 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 |
3 | HG02257.hp1 HG02451.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1558-21464C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50026781 | |||||||
| chr3:50026782 | G | A | 4 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0132 others(1): Show |
4 | HG01891.hp2 HG02970.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1558-21463G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50026782 | |||||||
| chr3:50026890 | C | G | 1 | a0004c0006t0001g0072 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1558-21355C>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50026890 | |||||||
| chr3:50026901 | C | CA | 34 | a0001c0001t0001g0001 a0001c0001t0001g0095 a0001c0001t0001g0096 others(31): Show |
34 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.1558-21322dupA | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50026901 | ||||||
| chr3:50026901 | C | CAA | 7 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(4): Show |
7 | HG00323.hp1 HG01106.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1558-21323_1558-21 others(8): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50026901 | ||||||
| chr3:50026901 | CAAAAAAA others(4): Show |
C | 86 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(83): Show |
86 | HG00140.hp2 HG00597.hp2 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.1558-21332_1558-21 others(17): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50026901 | ||||||
| chr3:50026991 | G | A | 91 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(88): Show |
91 | HG00140.hp2 HG00597.hp2 HG00609.hp1 others(88): Show |
intron_variant | MODIFIER | c.1558-21254G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50026991 | |||||||
| chr3:50027197 | G | T | 19 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(16): Show |
19 | HG00323.hp1 HG01106.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.1558-21048G>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50027197 | |||||||
| chr3:50027323 | A | T | 1 | a0001c0001t0001g0126 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1558-20922A>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50027323 | |||||||
| chr3:50027434 | T | C | 90 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(87): Show |
90 | HG00140.hp2 HG00597.hp2 HG00609.hp1 others(87): Show |
intron_variant | MODIFIER | c.1558-20811T>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50027434 | |||||||
| chr3:50027436 | C | T | 1 | a0001c0001t0001g0146 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1558-20809C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50027436 | |||||||
| chr3:50027595 | A | G | 1 | a0001c0001t0001g0090 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1558-20650A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50027595 | |||||||
| chr3:50027756 | G | A | 2 | a0001c0002t0001g0151 a0001c0002t0001g0195 |
2 | HG03225.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1558-20489G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50027756 | |||||||
| chr3:50027797 | A | G | 1 | a0001c0001t0001g0016 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1558-20448A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50027797 | |||||||
| chr3:50027841 | G | A | 31 | a0001c0002t0001g0151 a0001c0002t0001g0152 a0001c0002t0001g0153 others(28): Show |
31 | HG00738.hp2 HG01069.hp2 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.1558-20404G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50027841 | |||||||
| chr3:50027973 | A | G | 1 | a0001c0002t0001g0183 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1558-20272A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50027973 | |||||||
| chr3:50028008 | T | C | 1 | a0001c0001t0001g0145 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1558-20237T>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50028008 | |||||||
| chr3:50028064 | GT | G | 113 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(110): Show |
113 | HG00140.hp2 HG00597.hp2 HG00609.hp1 others(110): Show |
intron_variant | MODIFIER | c.1558-20168delT | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50028064 | ||||||
| chr3:50028310 | G | A | 4 | a0001c0005t0001g0102 a0001c0005t0001g0103 a0001c0005t0001g0105 others(1): Show |
4 | HG02258.hp2 HG02717.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1558-19935G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50028310 | |||||||
| chr3:50028362 | G | A | 2 | a0004c0006t0001g0009 a0004c0006t0001g0070 |
2 | NA18612.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.1558-19883G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50028362 | |||||||
| chr3:50028902 | G | C | 6 | a0001c0001t0001g0118 a0001c0001t0001g0129 a0001c0001t0001g0130 others(3): Show |
6 | HG01891.hp2 HG02970.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1558-19343G>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50028902 | |||||||
| chr3:50029319 | G | T | 1 | a0001c0001t0001g0146 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1558-18926G>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50029319 | |||||||
| chr3:50029483 | C | T | 1 | a0001c0003t0001g0076 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1558-18762C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50029483 | |||||||
| chr3:50029548 | T | G | 1 | a0006c0009t0001g0119 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1558-18697T>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50029548 | |||||||
| chr3:50029561 | C | T | 9 | a0001c0001t0001g0104 a0001c0001t0001g0120 a0001c0001t0001g0121 others(6): Show |
9 | HG01243.hp1 HG02622.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.1558-18684C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50029561 | |||||||
| chr3:50029865 | T | A | 132 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(129): Show |
132 | HG00140.hp2 HG00323.hp1 HG00597.hp2 others(129): Show |
intron_variant | MODIFIER | c.1558-18380T>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50029865 | |||||||
| chr3:50029889 | G | T | 2 | a0001c0002t0001g0151 a0001c0002t0001g0195 |
2 | HG03225.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1558-18356G>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50029889 | |||||||
| chr3:50029917 | T | C | 31 | a0001c0002t0001g0151 a0001c0002t0001g0152 a0001c0002t0001g0153 others(28): Show |
31 | HG00738.hp2 HG01069.hp2 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.1558-18328T>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50029917 | |||||||
| chr3:50030070 | A | G | 1 | a0006c0009t0001g0119 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1558-18175A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50030070 | |||||||
| chr3:50030205 | C | T | 5 | a0001c0001t0001g0095 a0001c0001t0001g0110 a0001c0001t0001g0115 others(2): Show |
5 | HG00323.hp1 HG01106.hp2 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.1558-18040C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50030205 | |||||||
| chr3:50030215 | C | T | 1 | a0001c0001t0001g0115 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1558-18030C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50030215 | |||||||
| chr3:50030286 | T | TA | 19 | a0001c0001t0001g0145 a0001c0002t0001g0151 a0001c0002t0001g0155 others(16): Show |
19 | HG00609.hp2 HG00639.hp2 HG01167.hp2 others(16): Show |
intron_variant | MODIFIER | c.1558-17932dupA | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50030286 | ||||||
| chr3:50030286 | TA | T | 13 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(10): Show |
13 | HG00323.hp2 HG02559.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.1558-17932delA | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50030286 | ||||||
| chr3:50030286 | TAAA | T | 24 | a0001c0001t0001g0014 a0001c0001t0001g0088 a0001c0001t0001g0104 others(21): Show |
24 | HG01243.hp1 HG01891.hp2 HG02257.hp1 others(21): Show |
intron_variant | MODIFIER | c.1558-17934_1558-17 others(9): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50030286 | ||||||
| chr3:50030286 | TAAAA | T | 48 | a0001c0001t0001g0013 a0001c0001t0001g0038 a0001c0001t0001g0043 others(45): Show |
48 | HG00323.hp1 HG00639.hp1 HG00738.hp1 others(45): Show |
intron_variant | MODIFIER | c.1558-17935_1558-17 others(10): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50030286 | ||||||
| chr3:50030286 | TAAAAA | T | 62 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0015 others(59): Show |
62 | HG00140.hp2 HG00597.hp2 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.1558-17936_1558-17 others(11): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50030286 | ||||||
| chr3:50030313 | AT | A | 2 | a0001c0001t0001g0002 a0001c0001t0001g0004 |
2 | HG02486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1558-17931delT | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50030313 | |||||||
| chr3:50030465 | T | A | 4 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0132 others(1): Show |
4 | HG01891.hp2 HG02970.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1558-17780T>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50030465 | |||||||
| chr3:50030494 | C | T | 2 | a0005c0008t0001g0042 a0005c0008t0001g0217 |
2 | HG01346.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1558-17751C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50030494 | |||||||
| chr3:50030537 | A | G | 1 | a0001c0001t0001g0145 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1558-17708A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50030537 | |||||||
| chr3:50030684 | A | C | 8 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(5): Show |
8 | HG02486.hp2 HG02559.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1558-17561A>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50030684 | |||||||
| chr3:50030982 | A | G | 1 | a0001c0001t0001g0047 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1558-17263A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50030982 | |||||||
| chr3:50031295 | C | T | 1 | a0001c0002t0001g0196 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1558-16950C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50031295 | |||||||
| chr3:50031552 | C | T | 1 | a0001c0001t0001g0001 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1558-16693C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50031552 | |||||||
| chr3:50031599 | A | G | 18 | a0001c0002t0001g0152 a0001c0002t0001g0153 a0001c0002t0001g0154 others(15): Show |
18 | HG00738.hp2 HG01069.hp2 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.1558-16646A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50031599 | |||||||
| chr3:50031703 | C | A | 2 | a0002c0004t0001g0107 a0002c0004t0001g0141 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1558-16542C>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50031703 | |||||||
| chr3:50031924 | G | A | 19 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(16): Show |
19 | HG00323.hp1 HG01106.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.1558-16321G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50031924 | |||||||
| chr3:50031945 | G | A | 1 | a0001c0001t0001g0126 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1558-16300G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50031945 | |||||||
| chr3:50032019 | G | T | 86 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(83): Show |
86 | HG00140.hp2 HG00597.hp2 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.1558-16226G>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50032019 | |||||||
| chr3:50032171 | G | A | 6 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(3): Show |
6 | HG02486.hp2 HG02559.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1558-16074G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50032171 | |||||||
| chr3:50032318 | T | TA | 9 | a0001c0001t0001g0067 a0001c0001t0001g0080 a0001c0001t0001g0081 others(6): Show |
9 | HG01243.hp2 HG02735.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.1558-15919dupA | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50032318 | ||||||
| chr3:50032330 | A | G | 1 | a0001c0001t0001g0026 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1558-15915A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50032330 | |||||||
| chr3:50032344 | C | T | 1 | a0001c0001t0001g0146 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1558-15901C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50032344 | |||||||
| chr3:50032482 | C | CA | 19 | a0001c0001t0001g0047 a0001c0001t0001g0052 a0001c0001t0001g0060 others(16): Show |
19 | HG00140.hp2 HG01106.hp1 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.1558-15745dupA | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50032482 | ||||||
| chr3:50032482 | C | CAA | 16 | a0001c0001t0001g0104 a0001c0001t0001g0120 a0001c0001t0001g0121 others(13): Show |
16 | HG01243.hp1 HG01884.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.1558-15746_1558-15 others(8): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50032482 | ||||||
| chr3:50032789 | T | C | 1 | a0001c0001t0001g0034 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1558-15456T>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50032789 | |||||||
| chr3:50032846 | A | G | 132 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(129): Show |
132 | HG00140.hp2 HG00323.hp1 HG00597.hp2 others(129): Show |
intron_variant | MODIFIER | c.1558-15399A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50032846 | |||||||
| chr3:50032939 | C | T | 2 | a0002c0004t0001g0138 a0002c0004t0001g0140 |
2 | HG02572.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1558-15306C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50032939 | |||||||
| chr3:50033330 | A | C | 86 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(83): Show |
86 | HG00140.hp2 HG00597.hp2 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.1558-14915A>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50033330 | |||||||
| chr3:50033410 | A | T | 5 | a0001c0001t0001g0012 a0001c0001t0001g0023 a0001c0001t0001g0062 others(2): Show |
5 | HG00738.hp1 HG01168.hp1 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.1558-14835A>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50033410 | |||||||
| chr3:50033420 | A | G | 148 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(145): Show |
148 | HG00140.hp2 HG00323.hp1 HG00597.hp2 others(145): Show |
intron_variant | MODIFIER | c.1558-14825A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50033420 | |||||||
| chr3:50033846 | A | C | 147 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(144): Show |
147 | HG00140.hp2 HG00323.hp1 HG00597.hp2 others(144): Show |
intron_variant | MODIFIER | c.1558-14399A>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50033846 | |||||||
| chr3:50033848 | G | T | 2 | a0001c0001t0001g0124 a0001c0001t0001g0136 |
2 | HG01884.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.1558-14397G>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50033848 | |||||||
| chr3:50033893 | G | A | 4 | a0001c0005t0001g0102 a0001c0005t0001g0103 a0001c0005t0001g0105 others(1): Show |
4 | HG02258.hp2 HG02717.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1558-14352G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50033893 | |||||||
| chr3:50034090 | C | CT | 5 | a0001c0002t0001g0177 a0001c0002t0001g0194 a0001c0002t0001g0200 others(2): Show |
5 | HG01069.hp2 HG01175.hp1 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.1558-14137dupT | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50034090 | ||||||
| chr3:50034090 | CT | C | 137 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(134): Show |
137 | HG00140.hp2 HG00323.hp1 HG00597.hp2 others(134): Show |
intron_variant | MODIFIER | c.1558-14137delT | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50034090 | ||||||
| chr3:50034134 | C | T | 1 | a0002c0004t0001g0138 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1558-14111C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50034134 | |||||||
| chr3:50034244 | G | A | 132 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(129): Show |
132 | HG00140.hp2 HG00323.hp1 HG00597.hp2 others(129): Show |
intron_variant | MODIFIER | c.1558-14001G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50034244 | |||||||
| chr3:50034532 | C | T | 2 | a0001c0001t0001g0056 a0001c0003t0001g0064 |
2 | HG02109.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1558-13713C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50034532 | |||||||
| chr3:50034618 | G | A | 15 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(12): Show |
15 | HG01891.hp2 HG02486.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.1558-13627G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50034618 | |||||||
| chr3:50034687 | G | C | 2 | a0001c0001t0001g0118 a0001c0001t0001g0129 |
2 | NA18906.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1558-13558G>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50034687 | |||||||
| chr3:50034719 | A | C | 148 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(145): Show |
148 | HG00140.hp2 HG00323.hp1 HG00597.hp2 others(145): Show |
intron_variant | MODIFIER | c.1558-13526A>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50034719 | |||||||
| chr3:50034995 | C | CCCTCTCC others(3): Show |
107 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(104): Show |
107 | HG00140.hp2 HG00597.hp2 HG00609.hp1 others(104): Show |
intron_variant | MODIFIER | c.1558-13238_1558-13 others(16): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50034995 | ||||||
| chr3:50035159 | A | T | 1 | a0001c0002t0001g0181 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1558-13086A>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50035159 | |||||||
| chr3:50035480 | A | G | 10 | a0001c0001t0001g0104 a0001c0001t0001g0120 a0001c0001t0001g0121 others(7): Show |
10 | HG01243.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1558-12765A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50035480 | |||||||
| chr3:50035554 | T | C | 148 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(145): Show |
148 | HG00140.hp2 HG00323.hp1 HG00597.hp2 others(145): Show |
intron_variant | MODIFIER | c.1558-12691T>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50035554 | |||||||
| chr3:50035613 | C | T | 107 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(104): Show |
107 | HG00140.hp2 HG00597.hp2 HG00609.hp1 others(104): Show |
intron_variant | MODIFIER | c.1558-12632C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50035613 | |||||||
| chr3:50035660 | C | T | 1 | a0001c0001t0001g0039 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1558-12585C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50035660 | |||||||
| chr3:50035712 | C | T | 2 | a0001c0002t0001g0182 a0001c0002t0001g0184 |
2 | HG01934.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1558-12533C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50035712 | |||||||
| chr3:50035766 | A | T | 2 | a0001c0001t0001g0137 a0001c0002t0001g0186 |
2 | HG00597.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1558-12479A>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50035766 | |||||||
| chr3:50035766 | AT | A | 8 | a0001c0001t0001g0118 a0001c0001t0001g0121 a0001c0001t0001g0129 others(5): Show |
8 | HG00323.hp2 HG01891.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1558-12467delT | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50035766 | ||||||
| chr3:50035767 | T | A | 12 | a0001c0001t0001g0015 a0001c0001t0001g0022 a0001c0001t0001g0046 others(9): Show |
12 | HG00597.hp2 HG01884.hp1 HG02074.hp1 others(9): Show |
intron_variant | MODIFIER | c.1558-12478T>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50035767 | |||||||
| chr3:50036207 | T | C | 19 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(16): Show |
19 | HG00323.hp1 HG01106.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.1558-12038T>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50036207 | |||||||
| chr3:50036482 | C | T | 1 | a0001c0001t0001g0021 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1558-11763C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50036482 | |||||||
| chr3:50036522 | T | TA | 6 | a0002c0004t0001g0107 a0002c0004t0001g0133 a0002c0004t0001g0138 others(3): Show |
6 | HG02572.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1558-11711dupA | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50036522 | ||||||
| chr3:50036565 | A | G | 4 | a0001c0005t0001g0102 a0001c0005t0001g0103 a0001c0005t0001g0105 others(1): Show |
4 | HG02258.hp2 HG02717.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1558-11680A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50036565 | |||||||
| chr3:50036867 | C | G | 6 | a0002c0004t0001g0107 a0002c0004t0001g0133 a0002c0004t0001g0138 others(3): Show |
6 | HG02572.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1558-11378C>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50036867 | |||||||
| chr3:50036944 | G | C | 19 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(16): Show |
19 | HG00323.hp1 HG01106.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.1558-11301G>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50036944 | |||||||
| chr3:50036967 | G | T | 5 | a0001c0001t0001g0095 a0001c0001t0001g0110 a0001c0001t0001g0115 others(2): Show |
5 | HG00323.hp1 HG01106.hp2 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.1558-11278G>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50036967 | |||||||
| chr3:50037005 | C | G | 17 | a0001c0001t0001g0104 a0001c0001t0001g0120 a0001c0001t0001g0121 others(14): Show |
17 | HG01243.hp1 HG01884.hp2 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.1558-11240C>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50037005 | |||||||
| chr3:50037208 | G | T | 148 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(145): Show |
148 | HG00140.hp2 HG00323.hp1 HG00597.hp2 others(145): Show |
intron_variant | MODIFIER | c.1558-11037G>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50037208 | |||||||
| chr3:50037340 | A | G | 132 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(129): Show |
132 | HG00140.hp2 HG00323.hp1 HG00597.hp2 others(129): Show |
intron_variant | MODIFIER | c.1558-10905A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50037340 | |||||||
| chr3:50037750 | C | T | 1 | a0001c0002t0001g0187 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1558-10495C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50037750 | |||||||
| chr3:50037767 | G | A | 6 | a0002c0004t0001g0107 a0002c0004t0001g0133 a0002c0004t0001g0138 others(3): Show |
6 | HG02572.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1558-10478G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50037767 | |||||||
| chr3:50037818 | C | A | 2 | a0001c0001t0001g0108 a0001c0001t0001g0109 |
2 | HG02647.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1558-10427C>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50037818 | |||||||
| chr3:50037819 | C | CT | 6 | a0001c0001t0001g0081 a0001c0001t0001g0088 a0001c0002t0001g0185 others(3): Show |
6 | HG01243.hp2 HG02055.hp1 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1558-10407dupT | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50037819 | ||||||
| chr3:50037819 | CT | C | 47 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(44): Show |
47 | HG00323.hp1 HG00323.hp2 HG01106.hp2 others(44): Show |
intron_variant | MODIFIER | c.1558-10407delT | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50037819 | ||||||
| chr3:50037870 | G | A | 2 | a0005c0008t0001g0042 a0005c0008t0001g0217 |
2 | HG01346.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1558-10375G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50037870 | |||||||
| chr3:50038061 | A | G | 1 | a0001c0002t0001g0176 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1558-10184A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50038061 | |||||||
| chr3:50038078 | T | C | 6 | a0002c0004t0001g0107 a0002c0004t0001g0133 a0002c0004t0001g0138 others(3): Show |
6 | HG02572.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1558-10167T>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50038078 | |||||||
| chr3:50038147 | C | T | 1 | a0001c0002t0001g0210 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1558-10098C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50038147 | |||||||
| chr3:50038416 | A | C | 1 | a0001c0001t0001g0058 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1558-9829A>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50038416 | |||||||
| chr3:50038656 | C | A | 6 | a0002c0004t0001g0107 a0002c0004t0001g0133 a0002c0004t0001g0138 others(3): Show |
6 | HG02572.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1558-9589C>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50038656 | |||||||
| chr3:50038750 | G | A | 1 | a0001c0001t0001g0006 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1558-9495G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50038750 | |||||||
| chr3:50038751 | T | G | 7 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(4): Show |
7 | HG02486.hp2 HG02559.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1558-9494T>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50038751 | |||||||
| chr3:50039102 | GA | G | 132 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(129): Show |
132 | HG00140.hp2 HG00323.hp1 HG00597.hp2 others(129): Show |
intron_variant | MODIFIER | c.1558-9136delA | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50039102 | ||||||
| chr3:50039128 | A | G | 7 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(4): Show |
7 | HG02486.hp2 HG02559.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1558-9117A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50039128 | |||||||
| chr3:50039193 | TCCA | T | 17 | a0001c0001t0001g0104 a0001c0001t0001g0120 a0001c0001t0001g0121 others(14): Show |
17 | HG01243.hp1 HG01884.hp2 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.1558-9048_1558-904 others(7): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50039193 | ||||||
| chr3:50039301 | A | G | 132 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(129): Show |
132 | HG00140.hp2 HG00323.hp1 HG00597.hp2 others(129): Show |
intron_variant | MODIFIER | c.1558-8944A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50039301 | |||||||
| chr3:50039364 | C | T | 1 | a0001c0011t0001g0213 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1558-8881C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50039364 | |||||||
| chr3:50039482 | A | AC | 13 | a0001c0002t0001g0161 a0001c0002t0001g0170 a0001c0002t0001g0176 others(10): Show |
13 | HG00140.hp1 HG01071.hp1 HG01167.hp2 others(10): Show |
intron_variant | MODIFIER | c.1558-8749dupC | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50039482 | ||||||
| chr3:50039482 | AC | A | 26 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0002t0001g0111 others(23): Show |
26 | HG00639.hp2 HG00738.hp2 HG01069.hp2 others(23): Show |
intron_variant | MODIFIER | c.1558-8749delC | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50039482 | ||||||
| chr3:50039482 | ACC | A | 17 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(14): Show |
17 | HG00609.hp1 HG00609.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.1558-8750_1558-874 others(6): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50039482 | ||||||
| chr3:50039482 | ACCC | A | 119 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(116): Show |
119 | HG00140.hp2 HG00323.hp1 HG00597.hp2 others(116): Show |
intron_variant | MODIFIER | c.1558-8751_1558-874 others(7): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50039482 | ||||||
| chr3:50039486 | C | G | 6 | a0001c0001t0001g0011 a0001c0001t0001g0025 a0001c0001t0001g0039 others(3): Show |
6 | HG00609.hp1 HG02027.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.1558-8759C>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50039486 | |||||||
| chr3:50039487 | C | G | 101 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(98): Show |
101 | HG00140.hp2 HG00597.hp2 HG00639.hp1 others(98): Show |
intron_variant | MODIFIER | c.1558-8758C>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50039487 | |||||||
| chr3:50039840 | T | G | 1 | a0001c0001t0001g0046 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1558-8405T>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50039840 | |||||||
| chr3:50039866 | A | G | 1 | a0001c0001t0001g0041 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1558-8379A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50039866 | |||||||
| chr3:50040168 | C | T | 1 | a0001c0002t0001g0172 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1558-8077C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50040168 | |||||||
| chr3:50040371 | G | A | 107 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(104): Show |
107 | HG00140.hp2 HG00597.hp2 HG00609.hp1 others(104): Show |
intron_variant | MODIFIER | c.1558-7874G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50040371 | |||||||
| chr3:50040445 | CA | C | 12 | a0001c0001t0001g0096 a0001c0001t0001g0098 a0001c0001t0001g0101 others(9): Show |
12 | HG01081.hp2 HG01934.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.1558-7773delA | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50040445 | ||||||
| chr3:50040445 | CAA | C | 11 | a0001c0001t0001g0097 a0001c0001t0001g0125 a0001c0001t0001g0127 others(8): Show |
11 | HG00639.hp2 HG01256.hp1 HG01346.hp2 others(8): Show |
intron_variant | MODIFIER | c.1558-7774_1558-777 others(6): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50040445 | ||||||
| chr3:50040445 | CAAAAAA | C | 11 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(8): Show |
11 | HG02258.hp2 HG02486.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1558-7778_1558-777 others(10): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50040445 | ||||||
| chr3:50040445 | CAAAAAAA others(3): Show |
C | 2 | a0001c0001t0001g0108 a0001c0001t0001g0109 |
2 | HG02647.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1558-7782_1558-777 others(14): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50040445 | ||||||
| chr3:50040460 | AAAAAAAA others(6): Show |
A | 4 | a0001c0001t0001g0055 a0001c0003t0001g0063 a0001c0003t0001g0066 others(1): Show |
4 | HG01496.hp1 HG02109.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1558-7783_1558-777 others(17): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50040460 | ||||||
| chr3:50040461 | A | T | 1 | a0001c0001t0001g0129 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1558-7784A>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50040461 | |||||||
| chr3:50040461 | AAAAAAAA others(7): Show |
A | 1 | a0004c0006t0001g0009 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1558-7782_1558-776 others(18): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50040461 | ||||||
| chr3:50040462 | AAAAAAAA others(4): Show |
A | 1 | a0001c0001t0001g0058 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1558-7781_1558-777 others(15): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50040462 | ||||||
| chr3:50040462 | AAAAAAAA others(6): Show |
A | 4 | a0001c0003t0001g0033 a0001c0003t0001g0071 a0004c0006t0001g0070 others(1): Show |
4 | HG01123.hp2 HG04199.hp2 NA18612.hp1 others(1): Show |
intron_variant | MODIFIER | c.1558-7781_1558-776 others(17): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50040462 | ||||||
| chr3:50040463 | A | T | 1 | a0001c0001t0001g0129 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1558-7782A>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50040463 | |||||||
| chr3:50040463 | AAAAAAAA others(3): Show |
A | 4 | a0001c0001t0001g0035 a0001c0001t0001g0146 a0001c0001t0001g0147 others(1): Show |
4 | HG02257.hp1 HG02451.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1558-7780_1558-777 others(14): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50040463 | ||||||
| chr3:50040463 | AAAAAAAA others(7): Show |
A | 17 | a0001c0001t0001g0014 a0001c0001t0001g0020 a0001c0001t0001g0024 others(14): Show |
17 | HG01074.hp2 HG01243.hp2 HG02027.hp1 others(14): Show |
intron_variant | MODIFIER | c.1558-7780_1558-776 others(18): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50040463 | ||||||
| chr3:50040464 | AAAAAAAA others(4): Show |
A | 15 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0026 others(12): Show |
15 | HG00597.hp2 HG01081.hp1 HG01192.hp2 others(12): Show |
intron_variant | MODIFIER | c.1558-7779_1558-776 others(15): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50040464 | ||||||
| chr3:50040464 | AAAAAAAA others(6): Show |
A | 14 | a0001c0001t0001g0012 a0001c0001t0001g0023 a0001c0001t0001g0048 others(11): Show |
14 | HG00639.hp1 HG01070.hp1 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.1558-7779_1558-776 others(17): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50040464 | ||||||
| chr3:50040465 | A | T | 2 | a0001c0001t0001g0096 a0001c0001t0001g0129 |
2 | HG03195.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1558-7780A>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50040465 | |||||||
| chr3:50040465 | AAAAAAAA others(3): Show |
A | 2 | a0001c0001t0001g0034 a0001c0001t0002g0019 |
2 | HG01106.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.1558-7778_1558-776 others(14): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50040465 | ||||||
| chr3:50040465 | AAAAAAAA others(5): Show |
A | 2 | a0001c0001t0001g0011 a0001c0001t0001g0074 |
2 | HG04184.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.1558-7778_1558-776 others(16): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50040465 | ||||||
| chr3:50040465 | AAAAAAAA others(7): Show |
A | 22 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0018 others(19): Show |
22 | HG00140.hp2 HG00609.hp1 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.1558-7778_1558-776 others(18): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50040465 | ||||||
| chr3:50040466 | AAAAAAAT others(4): Show |
A | 1 | a0001c0001t0001g0038 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1558-7777_1558-776 others(15): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50040466 | ||||||
| chr3:50040466 | AAAAAAAT others(6): Show |
A | 1 | a0001c0001t0001g0051 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1558-7777_1558-776 others(17): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50040466 | ||||||
| chr3:50040467 | A | AT | 23 | a0001c0001t0001g0115 a0001c0001t0001g0130 a0001c0001t0001g0131 others(20): Show |
23 | HG00738.hp2 HG01070.hp2 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.1558-7778_1558-777 others(5): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50040467 | |||||||
| chr3:50040467 | A | ATAT | 4 | a0001c0001t0001g0110 a0001c0001t0003g0116 a0001c0002t0001g0181 others(1): Show |
4 | HG01106.hp2 HG02145.hp2 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.1558-7778_1558-777 others(7): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50040467 | |||||||
| chr3:50040467 | A | T | 9 | a0001c0001t0001g0096 a0001c0001t0001g0114 a0001c0001t0001g0118 others(6): Show |
9 | HG01192.hp1 HG02970.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.1558-7778A>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50040467 | |||||||
| chr3:50040469 | A | AT | 5 | a0001c0002t0001g0150 a0001c0002t0001g0155 a0001c0002t0001g0157 others(2): Show |
5 | HG00609.hp2 HG01069.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.1558-7776_1558-777 others(5): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50040469 | |||||||
| chr3:50040469 | A | ATAT | 2 | a0001c0002t0001g0158 a0001c0002t0001g0196 |
2 | HG01069.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1558-7776_1558-777 others(7): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50040469 | |||||||
| chr3:50040469 | A | T | 54 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(51): Show |
54 | HG00323.hp1 HG00738.hp2 HG01070.hp2 others(51): Show |
intron_variant | MODIFIER | c.1558-7776A>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50040469 | |||||||
| chr3:50040469 | AAAATAT | A | 6 | a0001c0001t0001g0104 a0001c0001t0001g0121 a0001c0001t0001g0122 others(3): Show |
6 | HG01243.hp1 HG02647.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1558-7774_1558-776 others(10): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50040469 | ||||||
| chr3:50040471 | A | AT | 2 | a0001c0002t0001g0153 a0001c0002t0001g0185 |
2 | HG01516.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.1558-7774_1558-777 others(5): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50040471 | |||||||
| chr3:50040471 | A | ATAT | 3 | a0001c0002t0001g0169 a0003c0007t0001g0171 a0003c0007t0001g0203 |
3 | HG01175.hp2 HG01257.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.1558-7774_1558-777 others(7): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50040471 | |||||||
| chr3:50040471 | A | T | 87 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(84): Show |
87 | HG00323.hp1 HG00323.hp2 HG00609.hp2 others(84): Show |
intron_variant | MODIFIER | c.1558-7774A>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50040471 | |||||||
| chr3:50040489 | T | C | 14 | a0001c0001t0001g0218 a0001c0002t0001g0151 a0001c0002t0001g0181 others(11): Show |
14 | HG01167.hp2 HG02055.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.1558-7756T>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50040489 | |||||||
| chr3:50040489 | TATATACA others(5): Show |
T | 1 | a0001c0001t0001g0124 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1558-7754_1558-774 others(16): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50040489 | ||||||
| chr3:50040491 | T | C | 50 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(47): Show |
50 | HG00738.hp2 HG01069.hp2 HG01070.hp2 others(47): Show |
intron_variant | MODIFIER | c.1558-7754T>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50040491 | |||||||
| chr3:50040491 | T | TAC | 4 | a0001c0002t0001g0152 a0001c0002t0001g0154 a0001c0002t0001g0210 others(1): Show |
4 | HG01192.hp1 HG01517.hp2 HG02027.hp2 others(1): Show |
intron_variant | MODIFIER | c.1558-7753_1558-775 others(6): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50040491 | ||||||
| chr3:50040493 | T | C | 110 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(107): Show |
110 | HG00597.hp2 HG00738.hp2 HG01069.hp1 others(107): Show |
intron_variant | MODIFIER | c.1558-7752T>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50040493 | |||||||
| chr3:50040493 | T | TACACACA others(1): Show |
3 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0142 |
3 | HG01891.hp2 HG03130.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1558-7735_1558-772 others(12): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50040493 | ||||||
| chr3:50040493 | T | TATAC | 3 | a0001c0001t0001g0095 a0001c0002t0001g0159 a0001c0002t0001g0161 |
3 | HG00323.hp2 HG01071.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.1558-7751_1558-775 others(8): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50040493 | ||||||
| chr3:50040493 | T | TATATATA others(9): Show |
1 | a0006c0009t0001g0119 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1558-7751_1558-775 others(20): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50040493 | ||||||
| chr3:50040493 | TACAC | T | 2 | a0001c0001t0001g0012 a0001c0001t0001g0023 |
2 | HG01168.hp1 HG01168.hp2 |
intron_variant | MODIFIER | c.1558-7731_1558-772 others(8): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50040493 | ||||||
| chr3:50040495 | C | T | 5 | a0001c0001t0001g0022 a0001c0002t0001g0156 a0001c0002t0001g0163 others(2): Show |
5 | HG00639.hp2 HG01255.hp2 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.1558-7750C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50040495 | |||||||
| chr3:50040741 | C | T | 4 | a0001c0005t0001g0102 a0001c0005t0001g0103 a0001c0005t0001g0105 others(1): Show |
4 | HG02258.hp2 HG02717.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1558-7504C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50040741 | |||||||
| chr3:50040788 | T | C | 132 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(129): Show |
132 | HG00140.hp2 HG00323.hp1 HG00597.hp2 others(129): Show |
intron_variant | MODIFIER | c.1558-7457T>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50040788 | |||||||
| chr3:50040833 | C | T | 1 | a0001c0002t0001g0210 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1558-7412C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50040833 | |||||||
| chr3:50041108 | C | T | 107 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(104): Show |
107 | HG00140.hp2 HG00597.hp2 HG00609.hp1 others(104): Show |
intron_variant | MODIFIER | c.1558-7137C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50041108 | |||||||
| chr3:50041177 | A | T | 1 | a0001c0001t0001g0109 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1558-7068A>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50041177 | |||||||
| chr3:50041197 | C | T | 8 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(5): Show |
8 | HG02486.hp2 HG02559.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1558-7048C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50041197 | |||||||
| chr3:50041459 | G | C | 1 | a0001c0001t0001g0145 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1558-6786G>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50041459 | |||||||
| chr3:50042245 | C | T | 1 | a0001c0002t0001g0196 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1558-6000C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50042245 | |||||||
| chr3:50042276 | G | A | 16 | a0001c0001t0001g0104 a0001c0001t0001g0120 a0001c0001t0001g0121 others(13): Show |
16 | HG01243.hp1 HG01884.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.1558-5969G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50042276 | |||||||
| chr3:50042741 | C | G | 19 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(16): Show |
19 | HG00323.hp1 HG01106.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.1558-5504C>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50042741 | |||||||
| chr3:50042745 | C | CT | 4 | a0001c0005t0001g0102 a0001c0005t0001g0103 a0001c0005t0001g0105 others(1): Show |
4 | HG02258.hp2 HG02717.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1558-5492dupT | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50042745 | ||||||
| chr3:50042753 | T | A | 17 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(14): Show |
17 | HG01884.hp1 HG01891.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.1558-5492T>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50042753 | |||||||
| chr3:50042754 | A | T | 6 | a0001c0002t0001g0176 a0001c0002t0001g0185 a0001c0005t0001g0102 others(3): Show |
6 | HG02004.hp1 HG02258.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1558-5491A>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50042754 | |||||||
| chr3:50043006 | A | G | 113 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(110): Show |
113 | HG00140.hp2 HG00597.hp2 HG00609.hp1 others(110): Show |
intron_variant | MODIFIER | c.1558-5239A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50043006 | |||||||
| chr3:50043224 | C | T | 1 | a0001c0001t0001g0013 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1558-5021C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50043224 | |||||||
| chr3:50043241 | C | T | 5 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0146 others(2): Show |
5 | HG02257.hp1 HG02451.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1558-5004C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50043241 | |||||||
| chr3:50043316 | C | G | 3 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 |
3 | HG02257.hp1 HG02451.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1558-4929C>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50043316 | |||||||
| chr3:50043336 | A | G | 3 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 |
3 | HG02257.hp1 HG02451.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1558-4909A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50043336 | |||||||
| chr3:50043340 | C | G | 19 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(16): Show |
19 | HG00323.hp1 HG01106.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.1558-4905C>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50043340 | |||||||
| chr3:50043340 | C | T | 2 | a0002c0004t0001g0107 a0002c0004t0001g0141 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1558-4905C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50043340 | |||||||
| chr3:50043487 | C | CA | 128 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(125): Show |
128 | HG00140.hp2 HG00597.hp2 HG00609.hp1 others(125): Show |
intron_variant | MODIFIER | c.1558-4746dupA | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50043487 | ||||||
| chr3:50043487 | C | CAA | 13 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0098 others(10): Show |
13 | HG01109.hp1 HG02257.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.1558-4747_1558-474 others(6): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50043487 | ||||||
| chr3:50043487 | C | CAAA | 6 | a0001c0001t0001g0095 a0001c0001t0001g0110 a0001c0001t0001g0114 others(3): Show |
6 | HG00323.hp1 HG01106.hp2 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.1558-4748_1558-474 others(7): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50043487 | ||||||
| chr3:50043509 | A | G | 2 | a0001c0001t0001g0086 a0001c0001t0001g0087 |
2 | HG01081.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1558-4736A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50043509 | |||||||
| chr3:50043539 | TAC | T | 3 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 |
3 | HG02257.hp1 HG02451.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1558-4704_1558-470 others(6): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50043539 | ||||||
| chr3:50043573 | T | C | 1 | a0001c0001t0001g0137 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1558-4672T>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50043573 | |||||||
| chr3:50043647 | G | A | 1 | a0001c0001t0001g0129 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1558-4598G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50043647 | |||||||
| chr3:50043674 | T | C | 148 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(145): Show |
148 | HG00140.hp2 HG00323.hp1 HG00597.hp2 others(145): Show |
intron_variant | MODIFIER | c.1558-4571T>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50043674 | |||||||
| chr3:50043881 | C | CT | 8 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0132 others(5): Show |
8 | HG01255.hp2 HG01346.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.1558-4347dupT | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50043881 | ||||||
| chr3:50043881 | CT | C | 106 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(103): Show |
106 | HG00140.hp2 HG00597.hp2 HG00609.hp1 others(103): Show |
intron_variant | MODIFIER | c.1558-4347delT | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50043881 | ||||||
| chr3:50043993 | G | T | 1 | a0006c0009t0001g0119 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1558-4252G>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50043993 | |||||||
| chr3:50044005 | C | T | 1 | a0001c0001t0001g0129 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1558-4240C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50044005 | |||||||
| chr3:50044100 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1558-4145C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50044100 | |||||||
| chr3:50044188 | C | T | 6 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0127 others(3): Show |
6 | HG01884.hp2 HG02451.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1558-4057C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50044188 | |||||||
| chr3:50044569 | G | A | 6 | a0002c0004t0001g0107 a0002c0004t0001g0133 a0002c0004t0001g0138 others(3): Show |
6 | HG02572.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1558-3676G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50044569 | |||||||
| chr3:50045027 | T | G | 1 | a0001c0001t0001g0035 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1558-3218T>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50045027 | |||||||
| chr3:50045200 | T | C | 15 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(12): Show |
15 | HG01891.hp2 HG02486.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.1558-3045T>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50045200 | |||||||
| chr3:50045284 | G | A | 1 | a0001c0001t0001g0052 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1558-2961G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50045284 | |||||||
| chr3:50045362 | G | C | 1 | a0006c0009t0001g0119 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1558-2883G>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50045362 | |||||||
| chr3:50045481 | C | G | 148 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(145): Show |
148 | HG00140.hp2 HG00323.hp1 HG00597.hp2 others(145): Show |
intron_variant | MODIFIER | c.1558-2764C>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50045481 | |||||||
| chr3:50045882 | A | G | 2 | a0001c0001t0001g0055 a0001c0003t0001g0066 |
2 | HG02109.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1558-2363A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50045882 | |||||||
| chr3:50046366 | G | A | 6 | a0002c0004t0001g0107 a0002c0004t0001g0133 a0002c0004t0001g0138 others(3): Show |
6 | HG02572.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1558-1879G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50046366 | |||||||
| chr3:50046460 | T | C | 1 | a0001c0003t0001g0066 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1558-1785T>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50046460 | |||||||
| chr3:50046511 | G | A | 1 | a0001c0002t0001g0215 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1558-1734G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50046511 | |||||||
| chr3:50046583 | G | GA | 13 | a0001c0001t0001g0013 a0001c0001t0001g0054 a0001c0001t0001g0094 others(10): Show |
13 | HG01106.hp2 HG01109.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1558-1644dupA | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50046583 | ||||||
| chr3:50046583 | GA | G | 9 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(6): Show |
9 | HG02486.hp2 HG02559.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1558-1644delA | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr3 | 50046583 | ||||||
| chr3:50047000 | C | T | 3 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 |
3 | HG02257.hp1 HG02451.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1558-1245C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50047000 | |||||||
| chr3:50047022 | T | C | 18 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(15): Show |
18 | HG00323.hp1 HG01106.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.1558-1223T>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50047022 | |||||||
| chr3:50047325 | C | T | 1 | a0001c0002t0001g0185 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1558-920C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50047325 | |||||||
| chr3:50047628 | G | A | 1 | a0001c0001t0001g0005 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1558-617G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50047628 | |||||||
| chr3:50047644 | C | T | 1 | a0001c0001t0001g0118 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1558-601C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50047644 | |||||||
| chr3:50047648 | C | T | 3 | a0003c0007t0001g0171 a0003c0007t0001g0173 a0003c0007t0001g0203 |
3 | HG01175.hp2 HG01257.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.1558-597C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50047648 | |||||||
| chr3:50047720 | A | G | 34 | a0001c0002t0001g0151 a0001c0002t0001g0152 a0001c0002t0001g0153 others(31): Show |
34 | HG00738.hp2 HG01069.hp2 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.1558-525A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50047720 | |||||||
| chr3:50048002 | C | T | 6 | a0002c0004t0001g0107 a0002c0004t0001g0133 a0002c0004t0001g0138 others(3): Show |
6 | HG02572.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1558-243C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50048002 | |||||||
| chr3:50048048 | C | G | 3 | a0001c0002t0001g0158 a0001c0002t0001g0159 a0001c0002t0001g0161 |
3 | HG00323.hp2 HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1558-197C>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50048048 | |||||||
| chr3:50048229 | G | C | 1 | a0001c0001t0001g0022 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1558-16G>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50048229 | |||||||
| chr3:50048353 | G | A | 15 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(12): Show |
15 | HG01891.hp2 HG02486.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.1632+34G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 7/20 | chr3 | 50048353 | |||||||
| chr3:50048495 | A | G | 7 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0099 others(4): Show |
7 | HG01109.hp1 HG02622.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1632+176A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 7/20 | chr3 | 50048495 | |||||||
| chr3:50049301 | G | T | 1 | a0001c0002t0001g0175 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1632+982G>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 7/20 | chr3 | 50049301 | |||||||
| chr3:50049399 | G | A | 4 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0132 others(1): Show |
4 | HG01891.hp2 HG02970.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1632+1080G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 7/20 | chr3 | 50049399 | |||||||
| chr3:50049720 | G | A | 1 | a0001c0001t0001g0018 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1632+1401G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 7/20 | chr3 | 50049720 | |||||||
| chr3:50049756 | C | T | 6 | a0002c0004t0001g0107 a0002c0004t0001g0133 a0002c0004t0001g0138 others(3): Show |
6 | HG02572.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1632+1437C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 7/20 | chr3 | 50049756 | |||||||
| chr3:50049832 | A | ACTAT | 147 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(144): Show |
147 | HG00140.hp2 HG00323.hp1 HG00597.hp2 others(144): Show |
intron_variant | MODIFIER | c.1632+1516_1632+151 others(8): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr3 | 50049832 | ||||||
| chr3:50049888 | A | G | 1 | a0001c0001t0001g0018 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1632+1569A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 7/20 | chr3 | 50049888 | |||||||
| chr3:50050196 | A | T | 2 | a0001c0001t0001g0002 a0001c0001t0001g0004 |
2 | HG02486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1632+1877A>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 7/20 | chr3 | 50050196 | |||||||
| chr3:50050272 | C | T | 17 | a0001c0001t0001g0104 a0001c0001t0001g0120 a0001c0001t0001g0121 others(14): Show |
17 | HG01243.hp1 HG01884.hp2 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.1632+1953C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 7/20 | chr3 | 50050272 | |||||||
| chr3:50050292 | G | A | 2 | a0001c0001t0001g0110 a0001c0001t0001g0117 |
2 | HG00323.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.1632+1973G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 7/20 | chr3 | 50050292 | |||||||
| chr3:50050320 | T | C | 1 | a0001c0011t0001g0213 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1632+2001T>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 7/20 | chr3 | 50050320 | |||||||
| chr3:50050444 | A | G | 1 | a0001c0001t0001g0109 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1632+2125A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 7/20 | chr3 | 50050444 | |||||||
| chr3:50050514 | A | G | 2 | a0001c0001t0001g0051 a0001c0001t0001g0059 |
2 | HG02055.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.1632+2195A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 7/20 | chr3 | 50050514 | |||||||
| chr3:50050635 | A | G | 1 | a0001c0001t0001g0099 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1632+2316A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 7/20 | chr3 | 50050635 | |||||||
| chr3:50050685 | C | T | 1 | a0001c0001t0001g0134 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1632+2366C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 7/20 | chr3 | 50050685 | |||||||
| chr3:50050740 | C | T | 6 | a0002c0004t0001g0107 a0002c0004t0001g0133 a0002c0004t0001g0138 others(3): Show |
6 | HG02572.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1632+2421C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 7/20 | chr3 | 50050740 | |||||||
| chr3:50050833 | T | C | 113 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(110): Show |
113 | HG00140.hp2 HG00597.hp2 HG00609.hp1 others(110): Show |
intron_variant | MODIFIER | c.1632+2514T>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 7/20 | chr3 | 50050833 | |||||||
| chr3:50050843 | G | T | 1 | a0001c0001t0001g0145 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1632+2524G>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 7/20 | chr3 | 50050843 | |||||||
| chr3:50050868 | G | A | 19 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(16): Show |
19 | HG00323.hp1 HG01106.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.1632+2549G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 7/20 | chr3 | 50050868 | |||||||
| chr3:50051047 | A | G | 1 | a0001c0001t0001g0128 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1632+2728A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 7/20 | chr3 | 50051047 | |||||||
| chr3:50051510 | A | G | 132 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(129): Show |
132 | HG00140.hp2 HG00323.hp1 HG00597.hp2 others(129): Show |
intron_variant | MODIFIER | c.1633-2825A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 7/20 | chr3 | 50051510 | |||||||
| chr3:50052209 | C | A | 1 | a0001c0001t0001g0016 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1633-2126C>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 7/20 | chr3 | 50052209 | |||||||
| chr3:50052257 | G | T | 86 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(83): Show |
86 | HG00140.hp2 HG00597.hp2 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.1633-2078G>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 7/20 | chr3 | 50052257 | |||||||
| chr3:50052837 | C | T | 15 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(12): Show |
15 | HG01891.hp2 HG02486.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.1633-1498C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 7/20 | chr3 | 50052837 | |||||||
| chr3:50052983 | AGGGGTGT others(3): Show |
A | 1 | a0001c0002t0001g0172 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1633-1351_1633-134 others(14): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 7/20 | chr3 | 50052983 | |||||||
| chr3:50052986 | G | GGT | 10 | a0001c0001t0001g0090 a0001c0001t0001g0096 a0001c0001t0001g0097 others(7): Show |
10 | HG00597.hp1 HG01074.hp1 HG01256.hp1 others(7): Show |
intron_variant | MODIFIER | c.1633-1300_1633-129 others(6): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr3 | 50052986 | ||||||
| chr3:50052986 | G | GGTGT | 4 | a0001c0001t0001g0074 a0001c0002t0001g0187 a0001c0002t0001g0204 others(1): Show |
4 | HG04199.hp1 NA18952.hp2 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.1633-1302_1633-129 others(8): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr3 | 50052986 | ||||||
| chr3:50052986 | G | GGTGTGTG others(3): Show |
1 | a0001c0001t0001g0125 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1633-1308_1633-129 others(14): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr3 | 50052986 | ||||||
| chr3:50052986 | GGT | G | 36 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(33): Show |
36 | HG00323.hp2 HG00597.hp2 HG00609.hp2 others(33): Show |
intron_variant | MODIFIER | c.1633-1300_1633-129 others(6): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr3 | 50052986 | ||||||
| chr3:50052986 | GGTGT | G | 27 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(24): Show |
27 | HG00738.hp1 HG01109.hp1 HG01257.hp1 others(24): Show |
intron_variant | MODIFIER | c.1633-1302_1633-129 others(8): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr3 | 50052986 | ||||||
| chr3:50052986 | GGTGTGT | G | 45 | a0001c0001t0001g0012 a0001c0001t0001g0018 a0001c0001t0001g0024 others(42): Show |
45 | HG00140.hp2 HG00323.hp1 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.1633-1304_1633-129 others(10): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr3 | 50052986 | ||||||
| chr3:50052986 | GGTGTGTG others(1): Show |
G | 19 | a0001c0001t0001g0016 a0001c0001t0001g0025 a0001c0001t0001g0026 others(16): Show |
19 | HG02055.hp1 HG02145.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.1633-1306_1633-129 others(12): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr3 | 50052986 | ||||||
| chr3:50052986 | GGTGTGTG others(3): Show |
G | 33 | a0001c0001t0001g0123 a0001c0002t0001g0151 a0001c0002t0001g0152 others(30): Show |
33 | HG00738.hp2 HG01070.hp2 HG01081.hp2 others(30): Show |
intron_variant | MODIFIER | c.1633-1308_1633-129 others(14): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr3 | 50052986 | ||||||
| chr3:50052986 | GGTGTGTG others(5): Show |
G | 6 | a0001c0001t0001g0143 a0001c0002t0001g0197 a0001c0002t0001g0198 others(3): Show |
6 | HG01167.hp2 HG02965.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1633-1310_1633-129 others(16): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr3 | 50052986 | ||||||
| chr3:50052986 | GGTGTGTG others(7): Show |
G | 1 | a0001c0011t0001g0213 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1633-1312_1633-129 others(18): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr3 | 50052986 | ||||||
| chr3:50052986 | GGTGTGTG others(11): Show |
G | 1 | a0001c0001t0001g0053 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1633-1316_1633-129 others(22): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr3 | 50052986 | ||||||
| chr3:50052986 | GGTGTGTG others(19): Show |
G | 1 | a0001c0001t0001g0147 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1633-1324_1633-129 others(30): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr3 | 50052986 | ||||||
| chr3:50052986 | GGTGTGTG others(23): Show |
G | 1 | a0001c0001t0001g0118 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1633-1328_1633-129 others(34): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr3 | 50052986 | ||||||
| chr3:50052996 | T | G | 1 | a0001c0002t0001g0172 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1633-1339T>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 7/20 | chr3 | 50052996 | |||||||
| chr3:50053033 | GTGT | G | 2 | a0001c0001t0001g0056 a0001c0002t0001g0185 |
2 | HG03927.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1633-1300_1633-129 others(7): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr3 | 50053033 | ||||||
| chr3:50053101 | G | C | 2 | a0002c0004t0001g0107 a0002c0004t0001g0141 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1633-1234G>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 7/20 | chr3 | 50053101 | |||||||
| chr3:50053139 | TGAG | T | 6 | a0002c0004t0001g0107 a0002c0004t0001g0133 a0002c0004t0001g0138 others(3): Show |
6 | HG02572.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1633-1192_1633-119 others(7): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr3 | 50053139 | ||||||
| chr3:50053201 | A | G | 2 | a0001c0001t0001g0124 a0001c0001t0001g0136 |
2 | HG01884.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.1633-1134A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 7/20 | chr3 | 50053201 | |||||||
| chr3:50053522 | A | T | 4 | a0001c0005t0001g0102 a0001c0005t0001g0103 a0001c0005t0001g0105 others(1): Show |
4 | HG02258.hp2 HG02717.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1633-813A>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 7/20 | chr3 | 50053522 | |||||||
| chr3:50053536 | G | GA | 11 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(8): Show |
11 | HG02451.hp1 HG02486.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1633-786dupA | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr3 | 50053536 | ||||||
| chr3:50053591 | T | G | 1 | a0001c0003t0001g0033 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1633-744T>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 7/20 | chr3 | 50053591 | |||||||
| chr3:50053769 | T | G | 1 | a0001c0001t0001g0137 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1633-566T>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 7/20 | chr3 | 50053769 | |||||||
| chr3:50053896 | G | C | 2 | a0001c0002t0001g0153 a0001c0002t0001g0154 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1633-439G>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 7/20 | chr3 | 50053896 | |||||||
| chr3:50054509 | T | C | 2 | a0005c0008t0001g0042 a0005c0008t0001g0217 |
2 | HG01346.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1693+114T>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 8/20 | chr3 | 50054509 | |||||||
| chr3:50054624 | G | A | 1 | a0001c0001t0001g0118 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1693+229G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 8/20 | chr3 | 50054624 | |||||||
| chr3:50054793 | G | A | 90 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(87): Show |
90 | HG00140.hp2 HG00597.hp2 HG00609.hp1 others(87): Show |
intron_variant | MODIFIER | c.1693+398G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 8/20 | chr3 | 50054793 | |||||||
| chr3:50054894 | G | C | 8 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(5): Show |
8 | HG02486.hp2 HG02559.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1693+499G>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 8/20 | chr3 | 50054894 | |||||||
| chr3:50055117 | C | T | 8 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(5): Show |
8 | HG02486.hp2 HG02559.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1693+722C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 8/20 | chr3 | 50055117 | |||||||
| chr3:50055249 | G | A | 1 | a0001c0001t0001g0218 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1693+854G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 8/20 | chr3 | 50055249 | |||||||
| chr3:50055298 | C | T | 1 | a0006c0009t0001g0119 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1693+903C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 8/20 | chr3 | 50055298 | |||||||
| chr3:50055776 | G | A | 148 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(145): Show |
148 | HG00140.hp2 HG00323.hp1 HG00597.hp2 others(145): Show |
intron_variant | MODIFIER | c.1693+1381G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 8/20 | chr3 | 50055776 | |||||||
| chr3:50056474 | T | C | 1 | a0001c0001t0001g0099 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1694-1254T>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 8/20 | chr3 | 50056474 | |||||||
| chr3:50056583 | C | T | 9 | a0001c0001t0001g0043 a0001c0001t0001g0067 a0001c0001t0001g0080 others(6): Show |
9 | HG01074.hp2 HG01243.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.1694-1145C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 8/20 | chr3 | 50056583 | |||||||
| chr3:50056701 | A | G | 1 | a0001c0001t0001g0120 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1694-1027A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 8/20 | chr3 | 50056701 | |||||||
| chr3:50056838 | T | A | 14 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(11): Show |
14 | HG00323.hp1 HG01106.hp2 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1694-890T>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 8/20 | chr3 | 50056838 | |||||||
| chr3:50057167 | T | C | 1 | a0001c0001t0001g0145 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1694-561T>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 8/20 | chr3 | 50057167 | |||||||
| chr3:50057512 | C | T | 2 | a0001c0001t0001g0036 a0001c0001t0001g0038 |
2 | NA18986.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.1694-216C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 8/20 | chr3 | 50057512 | |||||||
| chr3:50057587 | C | CA | 28 | a0001c0001t0001g0008 a0001c0001t0001g0034 a0001c0001t0001g0095 others(25): Show |
28 | HG00323.hp1 HG01106.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.1694-119dupA | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr3 | 50057587 | ||||||
| chr3:50057587 | C | CAA | 92 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(89): Show |
92 | HG00140.hp2 HG00597.hp2 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.1694-120_1694-119d others(4): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr3 | 50057587 | ||||||
| chr3:50057587 | C | CAAA | 15 | a0001c0001t0001g0011 a0001c0001t0001g0021 a0001c0001t0001g0038 others(12): Show |
15 | HG01074.hp2 HG01106.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.1694-121_1694-119d others(5): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr3 | 50057587 | ||||||
| chr3:50057670 | C | CT | 8 | a0001c0001t0001g0036 a0001c0001t0001g0038 a0001c0001t0001g0044 others(5): Show |
8 | NA18612.hp1 NA18945.hp2 NA18960.hp1 others(5): Show |
intron_variant | MODIFIER | c.1694-43dupT | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr3 | 50057670 | ||||||
| chr3:50057670 | CT | C | 19 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(16): Show |
19 | HG00323.hp1 HG01106.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.1694-43delT | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr3 | 50057670 | ||||||
| chr3:50057676 | T | C | 16 | a0001c0001t0001g0104 a0001c0001t0001g0120 a0001c0001t0001g0121 others(13): Show |
16 | HG01243.hp1 HG01884.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.1694-52T>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 8/20 | chr3 | 50057676 | |||||||
| chr3:50058055 | T | C | 2 | a0001c0003t0001g0071 a0001c0003t0001g0073 |
2 | HG01123.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.1969+52T>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 9/20 | chr3 | 50058055 | |||||||
| chr3:50058108 | T | G | 1 | a0001c0001t0001g0126 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1969+105T>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 9/20 | chr3 | 50058108 | |||||||
| chr3:50058258 | A | G | 6 | a0001c0001t0001g0095 a0001c0001t0001g0110 a0001c0001t0001g0114 others(3): Show |
6 | HG00323.hp1 HG01106.hp2 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.1970-144A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 9/20 | chr3 | 50058258 | |||||||
| chr3:50058315 | T | TA | 6 | a0002c0004t0001g0107 a0002c0004t0001g0133 a0002c0004t0001g0138 others(3): Show |
6 | HG02572.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1970-81dupA | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chr3 | 50058315 | ||||||
| chr3:50058603 | C | T | 3 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 |
3 | HG02257.hp1 HG02451.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.2130+41C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 10/20 | chr3 | 50058603 | |||||||
| chr3:50058848 | G | A | 1 | a0002c0004t0001g0133 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2130+286G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 10/20 | chr3 | 50058848 | |||||||
| chr3:50058915 | C | CA | 5 | a0001c0001t0001g0094 a0001c0001t0001g0100 a0001c0001t0001g0114 others(2): Show |
5 | HG01109.hp1 HG01981.hp1 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.2130+371dupA | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr3 | 50058915 | ||||||
| chr3:50059563 | G | A | 1 | a0006c0009t0001g0119 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2131-86G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 10/20 | chr3 | 50059563 | |||||||
| chr3:50059886 | C | A | 90 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(87): Show |
90 | HG00140.hp2 HG00597.hp2 HG00609.hp1 others(87): Show |
intron_variant | MODIFIER | c.2228+140C>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 11/20 | chr3 | 50059886 | |||||||
| chr3:50059897 | C | T | 1 | a0001c0001t0001g0021 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2228+151C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 11/20 | chr3 | 50059897 | |||||||
| chr3:50059933 | G | A | 14 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(11): Show |
14 | HG00323.hp1 HG01106.hp2 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.2228+187G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 11/20 | chr3 | 50059933 | |||||||
| chr3:50060513 | C | T | 6 | a0002c0004t0001g0107 a0002c0004t0001g0133 a0002c0004t0001g0138 others(3): Show |
6 | HG02572.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.2229-443C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 11/20 | chr3 | 50060513 | |||||||
| chr3:50060563 | C | T | 4 | a0001c0005t0001g0102 a0001c0005t0001g0103 a0001c0005t0001g0105 others(1): Show |
4 | HG02258.hp2 HG02717.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.2229-393C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 11/20 | chr3 | 50060563 | |||||||
| chr3:50060591 | CAA | C | 131 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(128): Show |
131 | HG00140.hp2 HG00323.hp1 HG00597.hp2 others(128): Show |
intron_variant | MODIFIER | c.2229-353_2229-352d others(4): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr3 | 50060591 | ||||||
| chr3:50060679 | A | G | 148 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(145): Show |
148 | HG00140.hp2 HG00323.hp1 HG00597.hp2 others(145): Show |
intron_variant | MODIFIER | c.2229-277A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 11/20 | chr3 | 50060679 | |||||||
| chr3:50060753 | C | CA | 108 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(105): Show |
108 | HG00597.hp2 HG00609.hp1 HG00639.hp1 others(105): Show |
intron_variant | MODIFIER | c.2229-180dupA | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr3 | 50060753 | ||||||
| chr3:50060753 | C | CAA | 9 | a0001c0001t0001g0018 a0001c0001t0001g0052 a0001c0001t0001g0061 others(6): Show |
9 | HG00140.hp2 HG01081.hp1 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.2229-181_2229-180d others(4): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr3 | 50060753 | ||||||
| chr3:50060904 | G | A | 9 | a0001c0001t0001g0043 a0001c0001t0001g0067 a0001c0001t0001g0080 others(6): Show |
9 | HG01074.hp2 HG01243.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.2229-52G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 11/20 | chr3 | 50060904 | |||||||
| chr3:50061377 | C | A | 2 | a0002c0004t0001g0138 a0002c0004t0001g0140 |
2 | HG02572.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.2354-85C>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 13/20 | chr3 | 50061377 | |||||||
| chr3:50061560 | C | CT | 15 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(12): Show |
15 | HG01168.hp1 HG01168.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.2439+37dupT | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr3 | 50061560 | ||||||
| chr3:50061560 | C | CTT | 72 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(69): Show |
72 | HG00140.hp2 HG00597.hp2 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.2439+36_2439+37dup others(2): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr3 | 50061560 | ||||||
| chr3:50061560 | C | CTTT | 29 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0022 others(26): Show |
29 | HG01071.hp2 HG01074.hp1 HG01074.hp2 others(26): Show |
intron_variant | MODIFIER | c.2439+35_2439+37dup others(3): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr3 | 50061560 | ||||||
| chr3:50061560 | CT | C | 62 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(59): Show |
62 | HG00140.hp1 HG00323.hp1 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.2439+37delT | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr3 | 50061560 | ||||||
| chr3:50061560 | CTT | C | 5 | a0001c0002t0001g0159 a0001c0002t0001g0165 a0001c0002t0001g0168 others(2): Show |
5 | HG00323.hp2 HG02965.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.2439+36_2439+37del others(2): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr3 | 50061560 | ||||||
| chr3:50062240 | A | C | 2 | a0001c0002t0001g0150 a0001c0002t0001g0157 |
2 | HG04184.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.2586+132A>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 15/20 | chr3 | 50062240 | |||||||
| chr3:50062242 | C | T | 1 | a0001c0001t0001g0099 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2586+134C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 15/20 | chr3 | 50062242 | |||||||
| chr3:50062282 | A | T | 1 | a0001c0001t0001g0074 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2586+174A>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 15/20 | chr3 | 50062282 | |||||||
| chr3:50062421 | T | C | 2 | a0001c0001t0001g0108 a0001c0001t0001g0109 |
2 | HG02647.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.2586+313T>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 15/20 | chr3 | 50062421 | |||||||
| chr3:50062502 | C | CA | 19 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(16): Show |
19 | HG01106.hp2 HG01109.hp2 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.2586+410dupA | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr3 | 50062502 | ||||||
| chr3:50062516 | A | C | 5 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0146 others(2): Show |
5 | HG02257.hp1 HG02451.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.2586+408A>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 15/20 | chr3 | 50062516 | |||||||
| chr3:50062633 | A | G | 19 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(16): Show |
19 | HG00323.hp1 HG01106.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.2586+525A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 15/20 | chr3 | 50062633 | |||||||
| chr3:50062755 | C | A | 132 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(129): Show |
132 | HG00140.hp2 HG00323.hp1 HG00597.hp2 others(129): Show |
intron_variant | MODIFIER | c.2586+647C>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 15/20 | chr3 | 50062755 | |||||||
| chr3:50062892 | CT | C | 85 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(82): Show |
85 | HG00140.hp2 HG00597.hp2 HG00609.hp1 others(82): Show |
intron_variant | MODIFIER | c.2586+801delT | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr3 | 50062892 | ||||||
| chr3:50063034 | C | T | 6 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0127 others(3): Show |
6 | HG01884.hp2 HG02451.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.2586+926C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 15/20 | chr3 | 50063034 | |||||||
| chr3:50063239 | T | C | 2 | a0001c0001t0001g0118 a0001c0001t0001g0129 |
2 | NA18906.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2586+1131T>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 15/20 | chr3 | 50063239 | |||||||
| chr3:50063595 | C | CA | 10 | a0001c0001t0001g0011 a0001c0001t0001g0018 a0001c0001t0001g0104 others(7): Show |
10 | HG02622.hp2 HG02647.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.2587-1420dupA | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr3 | 50063595 | ||||||
| chr3:50064035 | G | A | 34 | a0001c0002t0001g0151 a0001c0002t0001g0152 a0001c0002t0001g0153 others(31): Show |
34 | HG00738.hp2 HG01069.hp2 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.2587-996G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 15/20 | chr3 | 50064035 | |||||||
| chr3:50064089 | C | T | 2 | a0001c0001t0001g0011 a0001c0001t0001g0041 |
2 | HG04184.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.2587-942C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 15/20 | chr3 | 50064089 | |||||||
| chr3:50064204 | T | C | 4 | a0001c0001t0001g0023 a0001c0001t0001g0062 a0001c0001t0001g0065 others(1): Show |
4 | HG00738.hp1 HG01168.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.2587-827T>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 15/20 | chr3 | 50064204 | |||||||
| chr3:50064295 | TGTGTGTT others(6): Show |
T | 1 | a0001c0001t0001g0034 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.2587-735_2587-723d others(15): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 15/20 | chr3 | 50064295 | |||||||
| chr3:50064672 | C | G | 2 | a0001c0002t0001g0165 a0001c0002t0001g0166 |
2 | NA18960.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.2587-359C>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 15/20 | chr3 | 50064672 | |||||||
| chr3:50064733 | A | G | 1 | a0004c0006t0001g0070 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2587-298A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 15/20 | chr3 | 50064733 | |||||||
| chr3:50064797 | C | G | 4 | a0001c0005t0001g0102 a0001c0005t0001g0103 a0001c0005t0001g0105 others(1): Show |
4 | HG02258.hp2 HG02717.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.2587-234C>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 15/20 | chr3 | 50064797 | |||||||
| chr3:50064821 | C | T | 3 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 |
3 | HG02257.hp1 HG02451.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.2587-210C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 15/20 | chr3 | 50064821 | |||||||
| chr3:50064916 | C | T | 1 | a0001c0001t0001g0048 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2587-115C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 15/20 | chr3 | 50064916 | |||||||
| chr3:50065013 | T | C | 8 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(5): Show |
8 | HG00738.hp1 HG01168.hp1 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.2587-18T>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 15/20 | chr3 | 50065013 | |||||||
| chr3:50065169 | G | C | 1 | a0001c0001t0001g0129 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2682+43G>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 16/20 | chr3 | 50065169 | |||||||
| chr3:50065248 | G | C | 3 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 |
3 | HG02257.hp1 HG02451.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.2682+122G>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 16/20 | chr3 | 50065248 | |||||||
| chr3:50065383 | A | G | 1 | a0001c0001t0001g0098 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2682+257A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 16/20 | chr3 | 50065383 | |||||||
| chr3:50065390 | G | A | 15 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(12): Show |
15 | HG01891.hp2 HG02486.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.2682+264G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 16/20 | chr3 | 50065390 | |||||||
| chr3:50065910 | T | G | 2 | a0001c0001t0001g0051 a0001c0001t0001g0059 |
2 | HG02055.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.2683-332T>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 16/20 | chr3 | 50065910 | |||||||
| chr3:50066120 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2683-122G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 16/20 | chr3 | 50066120 | |||||||
| chr3:50066136 | T | C | 2 | a0001c0001t0001g0062 a0001c0001t0001g0068 |
2 | HG00738.hp1 HG01257.hp1 |
intron_variant | MODIFIER | c.2683-106T>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 16/20 | chr3 | 50066136 | |||||||
| chr3:50066179 | A | G | 4 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0132 others(1): Show |
4 | HG01891.hp2 HG02970.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.2683-63A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 16/20 | chr3 | 50066179 | |||||||
| chr3:50066203 | G | A | 6 | a0002c0004t0001g0107 a0002c0004t0001g0133 a0002c0004t0001g0138 others(3): Show |
6 | HG02572.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.2683-39G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 16/20 | chr3 | 50066203 | |||||||
| chr3:50066549 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2943+47C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 17/20 | chr3 | 50066549 | |||||||
| chr3:50066765 | T | C | 6 | a0001c0001t0001g0118 a0001c0001t0001g0129 a0001c0001t0001g0130 others(3): Show |
6 | HG01891.hp2 HG02970.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.2943+263T>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 17/20 | chr3 | 50066765 | |||||||
| chr3:50066831 | A | AAAAACAA others(3): Show |
148 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(145): Show |
148 | HG00140.hp2 HG00323.hp1 HG00597.hp2 others(145): Show |
intron_variant | MODIFIER | c.2943+340_2943+349d others(12): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr3 | 50066831 | ||||||
| chr3:50066874 | G | A | 19 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(16): Show |
19 | HG00323.hp1 HG01106.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.2943+372G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 17/20 | chr3 | 50066874 | |||||||
| chr3:50067186 | C | CA | 30 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0024 others(27): Show |
30 | HG00597.hp2 HG00609.hp2 HG01175.hp1 others(27): Show |
intron_variant | MODIFIER | c.2943+710dupA | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr3 | 50067186 | ||||||
| chr3:50067186 | CA | C | 15 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(12): Show |
15 | HG01891.hp2 HG02486.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.2943+710delA | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr3 | 50067186 | ||||||
| chr3:50067275 | A | G | 14 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(11): Show |
14 | HG00323.hp1 HG01106.hp2 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.2943+773A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 17/20 | chr3 | 50067275 | |||||||
| chr3:50067297 | C | T | 1 | a0001c0001t0001g0144 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2943+795C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 17/20 | chr3 | 50067297 | |||||||
| chr3:50067440 | C | G | 19 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(16): Show |
19 | HG00323.hp1 HG01106.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.2943+938C>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 17/20 | chr3 | 50067440 | |||||||
| chr3:50067658 | C | T | 1 | a0001c0002t0001g0190 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2944-1032C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 17/20 | chr3 | 50067658 | |||||||
| chr3:50068079 | A | T | 17 | a0001c0001t0001g0104 a0001c0001t0001g0120 a0001c0001t0001g0121 others(14): Show |
17 | HG01243.hp1 HG01884.hp2 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.2944-611A>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 17/20 | chr3 | 50068079 | |||||||
| chr3:50068167 | G | A | 1 | a0005c0008t0001g0217 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2944-523G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 17/20 | chr3 | 50068167 | |||||||
| chr3:50068364 | A | G | 1 | a0001c0001t0001g0135 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2944-326A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 17/20 | chr3 | 50068364 | |||||||
| chr3:50069131 | A | G | 1 | a0001c0001t0001g0025 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.3018+367A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 18/20 | chr3 | 50069131 | |||||||
| chr3:50069241 | G | A | 3 | a0001c0002t0001g0158 a0001c0002t0001g0159 a0001c0002t0001g0161 |
3 | HG00323.hp2 HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.3018+477G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 18/20 | chr3 | 50069241 | |||||||
| chr3:50069433 | G | A | 3 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 |
3 | HG02257.hp1 HG02451.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.3018+669G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 18/20 | chr3 | 50069433 | |||||||
| chr3:50069507 | C | CA | 90 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(87): Show |
90 | HG00597.hp2 HG00609.hp1 HG00639.hp1 others(87): Show |
intron_variant | MODIFIER | c.3018+761dupA | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr3 | 50069507 | ||||||
| chr3:50069507 | C | CAAAAAA | 16 | a0001c0001t0001g0104 a0001c0001t0001g0120 a0001c0001t0001g0121 others(13): Show |
16 | HG01243.hp1 HG01884.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.3018+756_3018+761d others(8): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr3 | 50069507 | ||||||
| chr3:50069546 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3018+782C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 18/20 | chr3 | 50069546 | |||||||
| chr3:50069786 | T | C | 131 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(128): Show |
131 | HG00140.hp2 HG00323.hp1 HG00597.hp2 others(128): Show |
intron_variant | MODIFIER | c.3019-669T>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 18/20 | chr3 | 50069786 | |||||||
| chr3:50069803 | G | A | 1 | a0001c0001t0001g0008 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3019-652G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 18/20 | chr3 | 50069803 | |||||||
| chr3:50069901 | T | G | 6 | a0002c0004t0001g0107 a0002c0004t0001g0133 a0002c0004t0001g0138 others(3): Show |
6 | HG02572.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.3019-554T>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 18/20 | chr3 | 50069901 | |||||||
| chr3:50070079 | G | A | 107 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(104): Show |
107 | HG00140.hp2 HG00597.hp2 HG00609.hp1 others(104): Show |
intron_variant | MODIFIER | c.3019-376G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 18/20 | chr3 | 50070079 | |||||||
| chr3:50070095 | A | G | 1 | a0001c0001t0001g0145 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3019-360A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 18/20 | chr3 | 50070095 | |||||||
| chr3:50070236 | T | C | 17 | a0001c0001t0001g0104 a0001c0001t0001g0120 a0001c0001t0001g0121 others(14): Show |
17 | HG01243.hp1 HG01884.hp2 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.3019-219T>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 18/20 | chr3 | 50070236 | |||||||
| chr3:50070755 | C | T | 14 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(11): Show |
14 | HG00323.hp1 HG01106.hp2 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.3116+203C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 19/20 | chr3 | 50070755 | |||||||
| chr3:50070973 | T | C | 3 | a0001c0002t0001g0153 a0001c0002t0001g0154 a0001c0002t0001g0214 |
3 | HG01516.hp1 HG01517.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.3116+421T>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 19/20 | chr3 | 50070973 | |||||||
| chr3:50071001 | T | C | 6 | a0002c0004t0001g0107 a0002c0004t0001g0133 a0002c0004t0001g0138 others(3): Show |
6 | HG02572.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.3116+449T>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 19/20 | chr3 | 50071001 | |||||||
| chr3:50071160 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.3116+608G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 19/20 | chr3 | 50071160 | |||||||
| chr3:50071252 | A | T | 2 | a0001c0001t0001g0051 a0001c0001t0001g0059 |
2 | HG02055.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.3116+700A>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 19/20 | chr3 | 50071252 | |||||||
| chr3:50071277 | C | A | 1 | a0001c0003t0001g0073 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.3116+725C>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 19/20 | chr3 | 50071277 | |||||||
| chr3:50071359 | C | A | 148 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(145): Show |
148 | HG00140.hp2 HG00323.hp1 HG00597.hp2 others(145): Show |
intron_variant | MODIFIER | c.3116+807C>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 19/20 | chr3 | 50071359 | |||||||
| chr3:50071515 | G | GAGTC | 34 | a0001c0002t0001g0151 a0001c0002t0001g0152 a0001c0002t0001g0153 others(31): Show |
34 | HG00738.hp2 HG01069.hp2 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.3116+964_3116+967d others(6): Show |
RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr3 | 50071515 | ||||||
| chr3:50071611 | T | C | 19 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(16): Show |
19 | HG00323.hp1 HG01106.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.3116+1059T>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 19/20 | chr3 | 50071611 | |||||||
| chr3:50071634 | C | G | 1 | a0001c0002t0001g0204 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.3116+1082C>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 19/20 | chr3 | 50071634 | |||||||
| chr3:50071640 | A | T | 113 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(110): Show |
113 | HG00140.hp2 HG00597.hp2 HG00609.hp1 others(110): Show |
intron_variant | MODIFIER | c.3116+1088A>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 19/20 | chr3 | 50071640 | |||||||
| chr3:50071961 | G | A | 14 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(11): Show |
14 | HG00323.hp1 HG01106.hp2 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.3116+1409G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 19/20 | chr3 | 50071961 | |||||||
| chr3:50072083 | C | CA | 28 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0036 others(25): Show |
28 | HG01243.hp1 HG01255.hp2 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.3116+1553dupA | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr3 | 50072083 | ||||||
| chr3:50072083 | CA | C | 21 | a0001c0001t0001g0012 a0001c0001t0001g0058 a0001c0001t0001g0095 others(18): Show |
21 | HG00323.hp1 HG01106.hp2 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.3116+1553delA | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr3 | 50072083 | ||||||
| chr3:50072101 | A | G | 15 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(12): Show |
15 | HG01891.hp2 HG02486.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.3116+1549A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 19/20 | chr3 | 50072101 | |||||||
| chr3:50072409 | C | CA | 18 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(15): Show |
18 | HG00323.hp1 HG01106.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.3116+1869dupA | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr3 | 50072409 | ||||||
| chr3:50072435 | A | T | 6 | a0002c0004t0001g0107 a0002c0004t0001g0133 a0002c0004t0001g0138 others(3): Show |
6 | HG02572.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.3116+1883A>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 19/20 | chr3 | 50072435 | |||||||
| chr3:50072869 | C | G | 1 | a0001c0001t0001g0014 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.3116+2317C>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 19/20 | chr3 | 50072869 | |||||||
| chr3:50073056 | C | T | 1 | a0002c0004t0001g0139 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.3117-2145C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 19/20 | chr3 | 50073056 | |||||||
| chr3:50073731 | C | T | 2 | a0001c0002t0001g0151 a0001c0002t0001g0195 |
2 | HG03225.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.3117-1470C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 19/20 | chr3 | 50073731 | |||||||
| chr3:50073743 | C | T | 8 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(5): Show |
8 | HG02486.hp2 HG02559.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.3117-1458C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 19/20 | chr3 | 50073743 | |||||||
| chr3:50073846 | C | CT | 105 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(102): Show |
105 | HG00140.hp2 HG00597.hp2 HG00609.hp1 others(102): Show |
intron_variant | MODIFIER | c.3117-1343dupT | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr3 | 50073846 | ||||||
| chr3:50073846 | CT | C | 14 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(11): Show |
14 | HG01891.hp2 HG02486.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.3117-1343delT | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr3 | 50073846 | ||||||
| chr3:50073936 | G | A | 1 | a0001c0001t0001g0020 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.3117-1265G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 19/20 | chr3 | 50073936 | |||||||
| chr3:50074131 | C | A | 1 | a0001c0001t0001g0108 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.3117-1070C>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 19/20 | chr3 | 50074131 | |||||||
| chr3:50074308 | G | C | 6 | a0002c0004t0001g0107 a0002c0004t0001g0133 a0002c0004t0001g0138 others(3): Show |
6 | HG02572.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.3117-893G>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 19/20 | chr3 | 50074308 | |||||||
| chr3:50074623 | G | A | 1 | a0001c0002t0001g0194 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3117-578G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 19/20 | chr3 | 50074623 | |||||||
| chr3:50074710 | T | A | 1 | a0001c0002t0001g0155 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.3117-491T>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 19/20 | chr3 | 50074710 | |||||||
| chr3:50074751 | C | T | 4 | a0001c0005t0001g0102 a0001c0005t0001g0103 a0001c0005t0001g0105 others(1): Show |
4 | HG02258.hp2 HG02717.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.3117-450C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 19/20 | chr3 | 50074751 | |||||||
| chr3:50075111 | G | A | 1 | a0001c0011t0001g0213 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3117-90G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 19/20 | chr3 | 50075111 | |||||||
| chr3:50075152 | G | A | 14 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(11): Show |
14 | HG00323.hp1 HG01106.hp2 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.3117-49G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 19/20 | chr3 | 50075152 | |||||||
| chr3:50075565 | T | C | 19 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(16): Show |
19 | HG00323.hp1 HG01106.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.3246+235T>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 20/20 | chr3 | 50075565 | |||||||
| chr3:50075571 | T | C | 182 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(179): Show |
182 | HG00140.hp2 HG00323.hp1 HG00597.hp2 others(179): Show |
intron_variant | MODIFIER | c.3246+241T>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 20/20 | chr3 | 50075571 | |||||||
| chr3:50075585 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3246+255G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 20/20 | chr3 | 50075585 | |||||||
| chr3:50075601 | A | G | 90 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(87): Show |
90 | HG00140.hp2 HG00597.hp2 HG00609.hp1 others(87): Show |
intron_variant | MODIFIER | c.3246+271A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 20/20 | chr3 | 50075601 | |||||||
| chr3:50075602 | G | A | 1 | a0001c0001t0001g0034 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.3246+272G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 20/20 | chr3 | 50075602 | |||||||
| chr3:50075913 | T | C | 19 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(16): Show |
19 | HG00323.hp1 HG01106.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.3246+583T>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 20/20 | chr3 | 50075913 | |||||||
| chr3:50075925 | C | A | 3 | a0001c0001t0001g0024 a0001c0001t0001g0079 a0001c0001t0001g0084 |
3 | HG02027.hp1 NA18984.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.3246+595C>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 20/20 | chr3 | 50075925 | |||||||
| chr3:50076264 | C | A | 6 | a0002c0004t0001g0107 a0002c0004t0001g0133 a0002c0004t0001g0138 others(3): Show |
6 | HG02572.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.3247-744C>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 20/20 | chr3 | 50076264 | |||||||
| chr3:50076265 | G | A | 1 | a0001c0001t0001g0129 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3247-743G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 20/20 | chr3 | 50076265 | |||||||
| chr3:50076451 | G | A | 2 | a0001c0002t0001g0191 a0001c0002t0001g0200 |
2 | HG01070.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.3247-557G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 20/20 | chr3 | 50076451 | |||||||
| chr3:50076476 | G | A | 1 | a0006c0009t0001g0119 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.3247-532G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 20/20 | chr3 | 50076476 | |||||||
| chr3:50076661 | G | A | 1 | a0001c0001t0001g0077 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.3247-347G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 20/20 | chr3 | 50076661 | |||||||
| chr3:50076684 | G | A | 1 | a0006c0009t0001g0119 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.3247-324G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 20/20 | chr3 | 50076684 | |||||||
| chr3:50076747 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3247-261G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 20/20 | chr3 | 50076747 | |||||||
| chr3:50076954 | G | A | 1 | a0001c0001t0001g0082 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.3247-54G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 20/20 | chr3 | 50076954 | |||||||
| chr3:50076986 | A | T | 1 | a0001c0010t0001g0069 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.3247-22A>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 20/20 | chr3 | 50076986 |