Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| 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 | copy fasta | chr3 | 49935150 | 50082249 |
| a0002 | 0/0 | 1123 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | copy fasta | chr3 | 49935150 | 50082249 |
| a0003 | 0/0 | 1123 | 3 | 0 | 0 | 3 | 0 | 0 | 2 | RBM6_chr3_49935150_50082249 | RBM6 | copy fasta | chr3 | 49935150 | 50082249 |
| a0004 | 0/0 | 1123 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | copy fasta | chr3 | 49935150 | 50082249 |
| a0005 | 0/0 | 1123 | 2 | 0 | 1 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | copy fasta | chr3 | 49935150 | 50082249 |
| a0006 | 0/0 | 1123 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | copy fasta | chr3 | 49935150 | 50082249 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 3372 | 116 | 59 | 18 | 26 | 5 | 8 | RBM6_chr3_49935150_50082249 | RBM6 | copy fasta | chr3 | 49935150 | 50082249 |
| c0002 | 1/1 | 3372 | 66 | 15 | 19 | 20 | 5 | 5 | RBM6_chr3_49935150_50082249 | RBM6 | copy fasta | chr3 | 49935150 | 50082249 |
| c0003 | 0/0 | 3372 | 15 | 4 | 7 | 0 | 1 | 3 | RBM6_chr3_49935150_50082249 | RBM6 | copy fasta | chr3 | 49935150 | 50082249 |
| c0004 | 0/0 | 3372 | 6 | 6 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | copy fasta | chr3 | 49935150 | 50082249 |
| c0005 | 0/0 | 3372 | 4 | 4 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | copy fasta | chr3 | 49935150 | 50082249 |
| c0006 | 0/0 | 3372 | 3 | 0 | 0 | 3 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | copy fasta | chr3 | 49935150 | 50082249 |
| c0007 | 0/0 | 3372 | 3 | 0 | 3 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | copy fasta | chr3 | 49935150 | 50082249 |
| c0008 | 0/0 | 3372 | 2 | 0 | 1 | 0 | 1 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | copy fasta | chr3 | 49935150 | 50082249 |
| c0009 | 0/0 | 3372 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | copy fasta | chr3 | 49935150 | 50082249 |
| c0010 | 0/0 | 3372 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | copy fasta | chr3 | 49935150 | 50082249 |
| c0011 | 0/0 | 3372 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | copy fasta | chr3 | 49935150 | 50082249 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 259 | 216 | 90 | 47 | 50 | 12 | 15 | RBM6_chr3_49935150_50082249 | RBM6 | copy fasta | chr3 | 49935150 | 50082249 |
| t0002 | 0/0 | 259 | 1 | 0 | 1 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | copy fasta | chr3 | 49935150 | 50082249 |
| t0003 | 0/0 | 259 | 1 | 0 | 0 | 0 | 0 | 1 | RBM6_chr3_49935150_50082249 | RBM6 | copy fasta | chr3 | 49935150 | 50082249 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0042 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0165 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 3372 | 116 | 59 | 18 | 26 | 5 | 8 | RBM6_chr3_49935150_50082249 | RBM6 | copy fasta | chr3 | 49935150 | 50082249 |
| a0001c0002 | 1/1 | 3372 | 66 | 15 | 19 | 20 | 5 | 5 | RBM6_chr3_49935150_50082249 | RBM6 | copy fasta | chr3 | 49935150 | 50082249 |
| a0001c0003 | 0/0 | 3372 | 15 | 4 | 7 | 0 | 1 | 3 | RBM6_chr3_49935150_50082249 | RBM6 | copy fasta | chr3 | 49935150 | 50082249 |
| a0001c0005 | 0/0 | 3372 | 4 | 4 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | copy fasta | chr3 | 49935150 | 50082249 |
| a0001c0010 | 0/0 | 3372 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | copy fasta | chr3 | 49935150 | 50082249 |
| a0001c0011 | 0/0 | 3372 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | copy fasta | chr3 | 49935150 | 50082249 |
| a0002c0004 | 0/0 | 3372 | 6 | 6 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | copy fasta | chr3 | 49935150 | 50082249 |
| a0003c0006 | 0/0 | 3372 | 3 | 0 | 0 | 3 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | copy fasta | chr3 | 49935150 | 50082249 |
| a0004c0007 | 0/0 | 3372 | 3 | 0 | 3 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | copy fasta | chr3 | 49935150 | 50082249 |
| a0005c0008 | 0/0 | 3372 | 2 | 0 | 1 | 0 | 1 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | copy fasta | chr3 | 49935150 | 50082249 |
| a0006c0009 | 0/0 | 3372 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | copy fasta | 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 | copy fasta | chr3 | 49935150 | 50082249 |
| a0001c0001t0002 | 0/0 | 3630 | 1 | 0 | 1 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | copy fasta | chr3 | 49935150 | 50082249 |
| a0001c0001t0003 | 0/0 | 3630 | 1 | 0 | 0 | 0 | 0 | 1 | RBM6_chr3_49935150_50082249 | RBM6 | copy fasta | chr3 | 49935150 | 50082249 |
| a0001c0002t0001 | 1/1 | 3630 | 66 | 15 | 19 | 20 | 5 | 5 | RBM6_chr3_49935150_50082249 | RBM6 | copy fasta | chr3 | 49935150 | 50082249 |
| a0001c0003t0001 | 0/0 | 3630 | 15 | 4 | 7 | 0 | 1 | 3 | RBM6_chr3_49935150_50082249 | RBM6 | copy fasta | chr3 | 49935150 | 50082249 |
| a0001c0005t0001 | 0/0 | 3630 | 4 | 4 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | copy fasta | chr3 | 49935150 | 50082249 |
| a0001c0010t0001 | 0/0 | 3630 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | copy fasta | chr3 | 49935150 | 50082249 |
| a0001c0011t0001 | 0/0 | 3630 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | copy fasta | chr3 | 49935150 | 50082249 |
| a0002c0004t0001 | 0/0 | 3630 | 6 | 6 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | copy fasta | chr3 | 49935150 | 50082249 |
| a0003c0006t0001 | 0/0 | 3630 | 3 | 0 | 0 | 3 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | copy fasta | chr3 | 49935150 | 50082249 |
| a0004c0007t0001 | 0/0 | 3630 | 3 | 0 | 3 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | copy fasta | chr3 | 49935150 | 50082249 |
| a0005c0008t0001 | 0/0 | 3630 | 2 | 0 | 1 | 0 | 1 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | copy fasta | chr3 | 49935150 | 50082249 |
| a0006c0009t0001 | 0/0 | 3630 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | copy fasta | 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 | 1 | 0 | 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 | 0 | 1 | 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 |
| a0001c0001t0001g0019 | 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 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| 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 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 0 | 0 | 0 | 1 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 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 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 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 | 1 | 0 | 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 | 0 | 1 | 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 |
| a0001c0001t0002g0020 | 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 |
| a0001c0002t0001g0042 | 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 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0002t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 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 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0002t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0002t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 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 | 1 | 0 | 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 | 0 | 1 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0002t0001g0184 | 0/0 | 1 | 1 | 0 | 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 | 1 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0001c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 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 | 0 | 1 | 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 |
| a0001c0003t0001g0070 | 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 |
| a0003c0006t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0003c0006t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0003c0006t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0004c0007t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0004c0007t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0004c0007t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| a0005c0008t0001g0041 | 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 | g0166 | EUR | GBR | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0055 | 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 | g0160 | 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 | g0016 | 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 | g0031 | 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 | g0189 | AMR | PUR | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG01069 | hp1 | a0001 | c0002 | t0001 | g0159 | 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 | g0188 | 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 | g0028 | AMR | PUR | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0091 | 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 | g0192 | AMR | PUR | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG01099 | hp1 | a0001 | c0002 | t0001 | g0190 | AMR | PUR | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG01099 | hp2 | a0001 | c0003 | t0001 | g0029 | AMR | PUR | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0020 | 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 | g0201 | AMR | PUR | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0024 | 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 | g0199 | AMR | PUR | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG01175 | hp2 | a0004 | 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 | g0136 | 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 | g0065 | AMR | CLM | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG01257 | hp2 | a0004 | c0007 | t0001 | g0171 | AMR | CLM | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG01346 | hp1 | a0005 | c0008 | t0001 | g0041 | AMR | CLM | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG01346 | hp2 | a0001 | c0002 | t0001 | g0167 | 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 | g0062 | 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 | g0135 | AFR | ACB | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | ACB | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | ACB | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG01934 | hp1 | a0004 | c0007 | t0001 | g0173 | AMR | PEL | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG01934 | hp2 | a0001 | c0002 | t0001 | g0183 | AMR | PEL | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0200 | 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 | g0015 | 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 | g0151 | EAS | KHV | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0208 | 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 | g0045 | 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 | g0027 | 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 | g0044 | 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 | g0209 | 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 | g0128 | 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 | g0121 | 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 | g0127 | AFR | GWD | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG02818 | hp1 | a0001 | c0002 | t0001 | g0195 | 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 | g0122 | 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 | g0098 | AFR | ESN | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG02922 | hp2 | a0002 | c0004 | t0001 | g0139 | AFR | ESN | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0090 | 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 | g0129 | AFR | ESN | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG02970 | hp2 | a0001 | c0002 | t0001 | g0182 | 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 | g0198 | 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 | g0134 | 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 | g0097 | AFR | ESN | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0092 | 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 | g0194 | 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 | g0004 | 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 | g0053 | 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 | g0191 | 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 | g0047 | SAS | STU | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG04204 | hp2 | a0001 | c0002 | t0001 | g0197 | SAS | STU | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| NA18522 | hp1 | a0001 | c0002 | t0001 | g0184 | AFR | YRI | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | YRI | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| NA18612 | hp1 | a0003 | c0006 | t0001 | g0071 | 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 | g0130 | AFR | YRI | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0132 | 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 | g0052 | EAS | JPT | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0017 | 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 | g0163 | 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 | g0084 | EAS | JPT | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| NA18965 | hp2 | a0001 | c0002 | t0001 | g0164 | EAS | JPT | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| NA18971 | hp1 | a0001 | c0002 | t0001 | g0169 | 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 | g0162 | EAS | JPT | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0051 | 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 | g0085 | 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 | g0170 | 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 | g0158 | 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 | g0152 | 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 | a0003 | 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 | a0003 | c0006 | t0001 | g0072 | EAS | JPT | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| NA19066 | hp2 | a0001 | c0002 | t0001 | g0168 | 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 | g0054 | EAS | JPT | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0088 | 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 | g0196 | AFR | ASW | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | ASW | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0049 | 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 | g0048 | EUR | TSI | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0046 | 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 | g0070 | AMR | CLM | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0050 | 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 | g0006 | AFR | ACB | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0019 | 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 | g0140 | 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 | hp1 | a0001 | c0002 | t0001 | g0165 | REF | REF | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| homoSapiens_grch38 | hp1 | a0001 | c0002 | t0001 | g0042 | REF | REF | RBM6_chr3_49935150_50082249 | RBM6 | chr3 | 49935150 | 50082249 |
| 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 | a0004 | 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 | a0003 | 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 |
| 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 | a0001c0003a0003c0006 | 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 | a0001c0001a0001c0003a0001c0005others(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 |
| 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 |
| 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | 131 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(128): Show | 131 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(128): 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 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(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 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0146others(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 | 32 | a0001c0002t0001g0149a0001c0002t0001g0150a0001c0002t0001g0151others(29): Show | 32 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(29): 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 | a0001c0002t0001g0181a0001c0002t0001g0182a0001c0002t0001g0183others(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 | a0001c0002t0001g0211a0001c0002t0001g0212a0001c0002t0001g0214others(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 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(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 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(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 | a0001c0001t0001g0007a0001c0001t0001g0127a0001c0001t0001g0128others(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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(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 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(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 | a0001c0001t0001g0095a0001c0001t0001g0108a0001c0001t0001g0109others(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 | 65 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0098others(62): Show | 65 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(62): 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 | a0001c0001t0001g0117a0001c0002t0001g0208a0001c0002t0001g0209others(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 | a0001c0003t0001g0010a0001c0003t0001g0027a0001c0003t0001g0028others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0002c0004t0001g0107a0002c0004t0001g0133a0002c0004t0001g0138others(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 | 118 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(115): Show | 118 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(115): 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 | a0001c0002t0001g0111a0002c0004t0001g0107a0002c0004t0001g0133others(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 | a0001c0001t0001g0104a0001c0001t0001g0120a0001c0001t0001g0121others(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 | a0001c0003t0001g0010a0001c0003t0001g0027a0001c0003t0001g0028others(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 | a0001c0001t0001g0094a0001c0010t0001g0069 | 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 | a0001c0001t0001g0035a0001c0002t0001g0149a0001c0002t0001g0151others(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 | a0001c0001t0001g0034a0001c0001t0001g0082a0001c0001t0001g0093others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | 167 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(164): Show | 167 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(164): 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 | a0001c0001t0001g0035a0001c0001t0001g0104a0001c0001t0001g0120others(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 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(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 | a0001c0001t0001g0104a0001c0001t0001g0120a0001c0001t0001g0121others(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 | a0001c0001t0001g0025a0001c0001t0001g0060a0001c0001t0001g0067others(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 | a0001c0001t0001g0104a0001c0001t0001g0120a0001c0001t0001g0121others(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 | a0001c0001t0001g0036a0001c0001t0001g0112a0001c0001t0001g0145others(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 | 63 | a0001c0002t0001g0111a0001c0002t0001g0149a0001c0002t0001g0150others(60): Show | 63 | HG00140.hp1 HG00323.hp2 HG00597.hp1 others(60): 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 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(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 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(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 | a0001c0002t0001g0153a0001c0002t0001g0154a0001c0002t0001g0214 | 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 | 35 | a0001c0002t0001g0111a0001c0002t0001g0149a0001c0002t0001g0150others(32): Show | 35 | HG00140.hp1 HG00323.hp2 HG00597.hp1 others(32): 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0001c0001t0001g0011a0001c0001t0001g0059a0001c0001t0001g0078others(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 | 54 | a0001c0002t0001g0111a0001c0002t0001g0149a0001c0002t0001g0150others(51): Show | 54 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(51): 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 | a0001c0002t0001g0186a0001c0002t0001g0202a0001c0002t0001g0208others(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 | a0001c0001t0001g0012a0001c0001t0001g0036a0001c0001t0001g0061others(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 | 69 | a0001c0001t0001g0145a0001c0002t0001g0111a0001c0002t0001g0149others(66): Show | 69 | HG00140.hp1 HG00323.hp2 HG00597.hp1 others(66): 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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0013others(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 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(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 | a0001c0001t0001g0022a0001c0001t0001g0058a0001c0001t0001g0086others(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 | a0001c0002t0001g0151a0001c0002t0001g0152a0001c0002t0001g0153others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0001c0001t0001g0108a0001c0001t0001g0109 | 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 | a0001c0001t0001g0036a0001c0001t0001g0059a0001c0001t0001g0079others(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 | a0001c0001t0001g0021a0001c0001t0001g0036a0001c0001t0001g0096others(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 | 64 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(61): Show | 64 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(61): 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 | a0001c0001t0001g0114a0001c0002t0001g0151a0001c0002t0001g0152others(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 | a0002c0004t0001g0138a0002c0004t0001g0139 | 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 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0019others(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 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0023others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0001c0001t0001g0026a0001c0001t0001g0095a0001c0001t0001g0096others(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 | a0001c0001t0001g0067a0001c0001t0001g0080a0001c0001t0001g0081others(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 | 27 | a0001c0002t0001g0111a0001c0002t0001g0150a0001c0002t0001g0155others(24): Show | 27 | HG00140.hp1 HG00609.hp2 HG00639.hp2 others(24): 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 | a0001c0002t0001g0152a0001c0002t0001g0153a0001c0002t0001g0154others(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 | a0001c0002t0001g0151a0001c0002t0001g0182a0001c0002t0001g0183others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0132others(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 | a0001c0001t0001g0086a0001c0001t0001g0087 | 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 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0019 | 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 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(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 | a0002c0004t0001g0107a0002c0004t0001g0133a0002c0004t0001g0138others(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 | a0002c0004t0001g0107a0002c0004t0001g0133a0002c0004t0001g0138others(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 | a0001c0001t0001g0135 | 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 | 131 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(128): Show | 131 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(128): 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 | a0001c0002t0001g0179a0001c0002t0001g0180a0001c0002t0001g0187others(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 | a0001c0001t0001g0036a0001c0001t0001g0104a0001c0001t0001g0120others(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 | a0002c0004t0001g0107a0002c0004t0001g0141 | 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 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0011others(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 | 74 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(71): Show | 74 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(71): 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 | a0001c0001t0001g0085 | 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 | a0001c0005t0001g0102a0001c0005t0001g0103a0001c0005t0001g0105others(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 | a0001c0002t0001g0201 | 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 | a0001c0002t0001g0151a0001c0002t0001g0152a0001c0002t0001g0153others(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 | a0001c0001t0001g0067a0001c0001t0001g0080a0001c0001t0001g0081others(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 | a0004c0007t0001g0173 | 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 | 80 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(77): Show | 80 | HG00140.hp1 HG00323.hp2 HG00597.hp1 others(77): 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 | a0002c0004t0001g0107a0002c0004t0001g0133a0002c0004t0001g0138others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0001c0001t0001g0035a0001c0001t0001g0058a0001c0001t0001g0078 | 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 | a0001c0003t0001g0070a0001c0003t0001g0073 | 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 | 125 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(122): Show | 125 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(122): 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 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(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 | a0002c0004t0001g0107a0002c0004t0001g0133a0002c0004t0001g0138others(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 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148 | 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 | a0001c0001t0001g0104a0001c0001t0001g0120a0001c0001t0001g0121others(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 | a0002c0004t0001g0107a0002c0004t0001g0133a0002c0004t0001g0138others(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 | 121 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(118): Show | 121 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(118): 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(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 | a0001c0001t0001g0104a0001c0001t0001g0120a0001c0001t0001g0121others(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 | a0001c0003t0001g0070 | 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 | a0001c0002t0001g0151 | 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 | 125 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(122): Show | 125 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(122): 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 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(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 | 104 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(101): Show | 104 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(101): 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 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0001c0002t0001g0152a0001c0002t0001g0194 | 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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(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 | a0001c0002t0001g0151a0001c0002t0001g0152a0001c0002t0001g0153others(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 | 65 | a0001c0001t0001g0145a0001c0002t0001g0111a0001c0002t0001g0149others(62): Show | 65 | HG00140.hp1 HG00323.hp2 HG00597.hp1 others(62): 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 | a0001c0001t0001g0088 | 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 | a0001c0002t0001g0151a0001c0002t0001g0152a0001c0002t0001g0153others(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 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(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 | a0001c0001t0001g0074a0001c0001t0001g0118a0001c0001t0001g0129others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0002c0004t0001g0107a0002c0004t0001g0133a0002c0004t0001g0138others(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 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099others(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 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0108others(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 | a0001c0001t0001g0104a0001c0001t0001g0120a0001c0001t0001g0121others(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 | a0001c0001t0001g0053 | 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 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(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 | a0001c0001t0001g0082a0001c0001t0001g0085a0001c0001t0001g0095others(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 | a0001c0001t0001g0108a0001c0001t0001g0109 | 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 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(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 | a0001c0002t0001g0197 | 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 | a0002c0004t0001g0107a0002c0004t0001g0133a0002c0004t0001g0138others(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 | 96 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0016others(93): Show | 96 | HG00140.hp2 HG00323.hp1 HG00597.hp2 others(93): 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 | a0001c0001t0001g0050a0001c0001t0001g0053a0001c0001t0001g0058others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0001c0002t0001g0151a0001c0002t0001g0152a0001c0002t0001g0153others(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 | a0001c0002t0001g0192a0001c0002t0001g0195a0001c0002t0001g0196others(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 | a0001c0001t0001g0118a0001c0001t0001g0129a0001c0001t0001g0130others(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 | a0001c0001t0001g0049 | 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 | 105 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(102): Show | 105 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(102): 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0001c0002t0001g0166 | 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 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0127others(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 | 110 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(107): Show | 110 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(107): 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 | a0001c0002t0001g0181a0001c0002t0001g0208a0001c0002t0001g0209others(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 | a0001c0002t0001g0151a0001c0002t0001g0152a0001c0002t0001g0153others(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 | 53 | a0001c0001t0001g0057a0001c0001t0001g0095a0001c0001t0001g0096others(50): Show | 53 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(50): 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 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099others(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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(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 | 99 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(96): Show | 99 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(96): 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 | a0001c0002t0001g0151a0001c0002t0001g0152a0001c0002t0001g0153others(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 | a0002c0004t0001g0107a0002c0004t0001g0133a0002c0004t0001g0138others(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 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0127others(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 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0018others(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 | 100 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(97): Show | 100 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(97): 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 | a0002c0004t0001g0107a0002c0004t0001g0133a0002c0004t0001g0138others(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 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0132others(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 | a0001c0001t0001g0046 | 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 | a0001c0001t0001g0002a0001c0001t0001g0006 | 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 | a0002c0004t0001g0107a0002c0004t0001g0133a0002c0004t0001g0138others(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 | a0001c0002t0001g0156a0001c0002t0001g0167a0001c0002t0001g0175 | 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 | a0001c0001t0001g0084 | 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 | a0001c0001t0001g0011a0001c0001t0001g0046 | 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 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(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 | a0001c0001t0001g0015a0001c0001t0001g0040a0001c0001t0001g0084 | 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 | a0001c0002t0001g0200 | 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 | 95 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(92): Show | 95 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(92): 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 | a0001c0001t0001g0118a0001c0001t0001g0130 | 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 | a0002c0004t0001g0107a0002c0004t0001g0133a0002c0004t0001g0138others(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 | a0001c0001t0001g0127 | 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 | 130 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(127): Show | 130 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(127): 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 | a0001c0001t0001g0048a0001c0001t0001g0050 | 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 | a0001c0002t0001g0200 | 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 | a0001c0001t0001g0124a0001c0001t0001g0135 | 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 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099others(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 | a0001c0002t0001g0189 | 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 | a0004c0007t0001g0171a0004c0007t0001g0173a0004c0007t0001g0203 | 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 | a0001c0001t0001g0011a0001c0002t0001g0174 | 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 | a0001c0001t0001g0135a0001c0002t0001g0149a0001c0002t0001g0185 | 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 | 131 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(128): Show | 131 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.-66-3997C>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49958579 | ||||||
| chr3:49958620
|
G | A | 69 | a0001c0002t0001g0111a0001c0002t0001g0149a0001c0002t0001g0150others(66): Show | 69 | HG00140.hp1 HG00323.hp2 HG00597.hp1 others(66): 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 | a0001c0001t0001g0095a0001c0001t0001g0110a0001c0001t0001g0115others(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 | 87 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(84): Show | 87 | HG00140.hp1 HG00323.hp2 HG00597.hp1 others(84): 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 | a0001c0001t0001g0007a0001c0002t0001g0149a0001c0002t0001g0150others(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 | a0001c0002t0001g0188a0001c0002t0001g0199 | 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 | a0001c0001t0001g0013a0001c0001t0001g0053a0001c0001t0001g0065others(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 | a0001c0001t0001g0134 | 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 | a0001c0001t0001g0055 | 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 | a0001c0001t0001g0045a0001c0001t0001g0088a0001c0001t0001g0094others(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 | 69 | a0001c0002t0001g0111a0001c0002t0001g0149a0001c0002t0001g0150others(66): Show | 69 | HG00140.hp1 HG00323.hp2 HG00597.hp1 others(66): 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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(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 | a0001c0001t0001g0001a0001c0001t0001g0095a0001c0001t0001g0096others(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 | a0001c0001t0001g0024a0001c0001t0001g0062a0001c0001t0001g0065others(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 | 110 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(107): Show | 110 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(107): 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 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0132others(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 | a0001c0002t0001g0151a0001c0002t0001g0152a0001c0002t0001g0153others(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 | a0001c0001t0001g0085 | 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 | 104 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(101): Show | 104 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.-66-2046G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 1/20 | chr3 | 49960530 | ||||||
| chr3:49960849
|
C | T | 127 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(124): Show | 127 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(124): 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 | a0001c0001t0001g0130a0001c0001t0002g0020a0001c0002t0001g0208others(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 | a0001c0001t0001g0089a0001c0001t0001g0112a0001c0001t0001g0118others(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 | a0001c0001t0001g0062a0001c0001t0001g0065a0001c0001t0001g0068 | 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 | 69 | a0001c0002t0001g0111a0001c0002t0001g0149a0001c0002t0001g0150others(66): Show | 69 | HG00140.hp1 HG00323.hp2 HG00597.hp1 others(66): 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 | a0001c0001t0001g0118a0001c0001t0001g0129a0001c0001t0001g0130others(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 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(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 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(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 | a0001c0001t0001g0037a0001c0001t0001g0085a0001c0001t0001g0086others(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 | a0001c0002t0001g0184 | 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 | a0001c0001t0001g0104a0001c0001t0001g0120a0001c0001t0001g0121others(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 | a0001c0002t0001g0166 | 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 | a0001c0001t0001g0056a0001c0001t0001g0104a0001c0001t0001g0120others(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 | a0002c0004t0001g0107a0002c0004t0001g0133a0002c0004t0001g0138others(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 | 83 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(80): Show | 83 | HG00140.hp1 HG00323.hp2 HG00597.hp1 others(80): 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 | a0001c0002t0001g0151 | 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 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(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 | a0001c0002t0001g0200 | 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 | a0001c0001t0001g0085 | 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148 | 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 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(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 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(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 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(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 | a0001c0003t0001g0010a0001c0003t0001g0027a0001c0003t0001g0028others(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 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | 110 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(107): Show | 110 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(107): 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 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148 | 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 | a0001c0001t0001g0147a0001c0001t0001g0148 | 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 | a0001c0001t0001g0130 | 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 | a0001c0001t0001g0061a0001c0001t0001g0086a0001c0002t0001g0187others(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 | a0002c0004t0001g0107a0002c0004t0001g0133a0002c0004t0001g0138others(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 | 110 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(107): Show | 110 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(107): 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 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(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 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(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 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(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 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0088others(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 | a0001c0001t0001g0104a0001c0001t0001g0120a0001c0001t0001g0121others(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 | a0001c0002t0001g0151a0001c0002t0001g0152a0001c0002t0001g0153others(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 | 35 | a0001c0002t0001g0111a0001c0002t0001g0149a0001c0002t0001g0150others(32): Show | 35 | HG00140.hp1 HG00323.hp2 HG00597.hp1 others(32): 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 | 104 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(101): Show | 104 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(101): 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 | a0001c0001t0001g0104a0001c0001t0001g0121a0001c0001t0001g0122others(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 | a0001c0001t0001g0004 | 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 | 46 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0021others(43): Show | 46 | HG00140.hp1 HG00323.hp1 HG00597.hp1 others(43): 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 | a0001c0001t0001g0058a0001c0001t0001g0096a0001c0001t0001g0097others(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 | a0001c0001t0001g0118a0001c0001t0001g0129a0001c0001t0001g0132others(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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(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 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(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 | a0001c0001t0001g0120a0001c0001t0001g0124a0001c0001t0001g0125others(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 | a0001c0001t0001g0104a0001c0001t0001g0121a0001c0001t0001g0122others(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 | a0001c0002t0001g0152a0001c0002t0001g0153a0001c0002t0001g0154others(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 | a0001c0002t0001g0196 | 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 | a0001c0002t0001g0156a0001c0002t0001g0167a0001c0002t0001g0175 | 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 | 110 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(107): Show | 110 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(107): 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0002c0004t0001g0107a0002c0004t0001g0133a0002c0004t0001g0138others(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 | a0001c0002t0001g0151 | 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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(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 | a0001c0001t0001g0024 | 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 | a0001c0001t0001g0046 | 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 | a0004c0007t0001g0171a0004c0007t0001g0203 | 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 | a0001c0001t0001g0055 | 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 | a0001c0001t0001g0012a0001c0001t0001g0034a0001c0005t0001g0102others(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 | a0001c0001t0001g0108a0001c0001t0001g0109 | 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 | a0001c0001t0001g0104a0001c0001t0001g0120a0001c0001t0001g0121others(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 | a0001c0001t0001g0019 | 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 | a0001c0001t0001g0049 | 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 | a0001c0003t0001g0010a0001c0003t0001g0027a0001c0003t0001g0028others(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 | a0001c0001t0001g0077a0001c0001t0001g0086a0001c0001t0001g0087 | 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 | 131 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(128): Show | 131 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(128): 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 |
35 | a0001c0002t0001g0111a0001c0002t0001g0149a0001c0002t0001g0150others(32): Show | 35 | HG00140.hp1 HG00323.hp2 HG00597.hp1 others(32): 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 | a0001c0001t0001g0108a0001c0001t0001g0109 | 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 | a0001c0001t0001g0016a0001c0001t0001g0025a0001c0001t0001g0050others(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 | a0001c0002t0001g0194 | 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 | 69 | a0001c0002t0001g0111a0001c0002t0001g0149a0001c0002t0001g0150others(66): Show | 69 | HG00140.hp1 HG00323.hp2 HG00597.hp1 others(66): 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0001c0001t0001g0108a0001c0001t0001g0109 | 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 | a0001c0001t0001g0108a0001c0001t0001g0109 | 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 | a0002c0004t0001g0107a0002c0004t0001g0133a0002c0004t0001g0138others(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 | 104 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(101): Show | 104 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(101): 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 | 85 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(82): Show | 85 | HG00140.hp1 HG00323.hp2 HG00597.hp1 others(82): 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 | a0002c0004t0001g0107a0002c0004t0001g0141 | 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 | a0002c0004t0001g0107a0002c0004t0001g0133a0002c0004t0001g0138others(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 | a0001c0001t0001g0008a0001c0001t0001g0044a0001c0001t0001g0075others(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 | 35 | a0001c0002t0001g0111a0001c0002t0001g0149a0001c0002t0001g0150others(32): Show | 35 | HG00140.hp1 HG00323.hp2 HG00597.hp1 others(32): Show |
intron_variant | MODIFIER | c.1413+1440T>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 4/20 | chr3 | 49973588 | ||||||
| chr3:49973662
|
T | C | 110 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(107): Show | 110 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(107): 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 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(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 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(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 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(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 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(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 | a0001c0001t0001g0125a0001c0001t0001g0128a0001c0001t0001g0134 | 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 | 70 | a0001c0001t0001g0145a0001c0002t0001g0111a0001c0002t0001g0149others(67): Show | 70 | HG00140.hp1 HG00323.hp2 HG00597.hp1 others(67): 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 | 110 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(107): Show | 110 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(107): 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 | a0001c0001t0001g0104a0001c0001t0001g0120a0001c0001t0001g0121others(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 | a0002c0004t0001g0133a0002c0004t0001g0138a0002c0004t0001g0139others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0014others(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 | a0001c0001t0001g0012a0001c0001t0001g0024a0001c0001t0001g0038others(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 | a0001c0002t0001g0150a0001c0002t0001g0196a0001c0002t0001g0197others(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 | 57 | a0001c0002t0001g0111a0001c0002t0001g0149a0001c0002t0001g0151others(54): Show | 57 | HG00140.hp1 HG00323.hp2 HG00597.hp1 others(54): 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 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(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 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(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 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148 | 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 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(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 | a0001c0002t0001g0181a0001c0002t0001g0196a0001c0002t0001g0198others(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 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099others(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 | 35 | a0001c0002t0001g0111a0001c0002t0001g0149a0001c0002t0001g0150others(32): Show | 35 | HG00140.hp1 HG00323.hp2 HG00597.hp1 others(32): 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 | a0001c0005t0001g0102a0001c0005t0001g0103a0001c0005t0001g0105others(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 | a0001c0001t0001g0147a0001c0001t0001g0148 | 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 | a0001c0001t0001g0047 | 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 | a0001c0001t0001g0047 | 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 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(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 | a0001c0001t0001g0023a0001c0001t0001g0061a0001c0001t0001g0079 | 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 | a0001c0001t0001g0118a0001c0001t0001g0129a0001c0001t0001g0130others(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 | a0001c0001t0001g0011a0001c0001t0001g0046 | 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 | a0002c0004t0001g0107a0002c0004t0001g0133a0002c0004t0001g0138others(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 | a0001c0002t0001g0182 | 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 | a0002c0004t0001g0107a0002c0004t0001g0133a0002c0004t0001g0138others(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 | a0001c0001t0001g0108a0001c0001t0001g0109 | 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 | a0001c0001t0001g0011a0001c0001t0001g0039a0001c0001t0001g0059others(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 | a0001c0001t0001g0018a0001c0002t0001g0172a0002c0004t0001g0107others(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 | a0001c0005t0001g0102a0001c0005t0001g0103a0001c0005t0001g0105others(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 | a0001c0005t0001g0102a0001c0005t0001g0103a0001c0005t0001g0105others(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 | a0001c0001t0001g0017 | 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 | 127 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(124): Show | 127 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(124): 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0127others(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 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0132others(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 | 67 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0002t0001g0111others(64): Show | 67 | HG00140.hp1 HG00323.hp2 HG00597.hp1 others(64): 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 | 110 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(107): Show | 110 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(107): 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 | a0002c0004t0001g0133a0002c0004t0001g0138a0002c0004t0001g0139 | 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 | a0001c0001t0001g0023a0001c0001t0001g0039a0001c0001t0001g0078others(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 | a0001c0001t0001g0124a0001c0001t0001g0127a0001c0001t0001g0128others(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 | a0001c0001t0001g0104a0001c0001t0001g0122a0001c0001t0001g0123others(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 | a0001c0001t0001g0121 | 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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(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 | a0002c0004t0001g0107a0002c0004t0001g0133a0002c0004t0001g0138others(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 | a0001c0001t0001g0099a0001c0001t0001g0110a0001c0001t0001g0114 | 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 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(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 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148 | 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 | a0001c0003t0001g0070a0001c0003t0001g0073 | 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 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(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 | 69 | a0001c0002t0001g0111a0001c0002t0001g0149a0001c0002t0001g0150others(66): Show | 69 | HG00140.hp1 HG00323.hp2 HG00597.hp1 others(66): 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 | a0001c0002t0001g0201 | 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 | a0002c0004t0001g0133a0002c0004t0001g0138a0002c0004t0001g0139 | 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 | a0001c0002t0001g0151a0001c0002t0001g0153a0001c0002t0001g0154others(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 | a0001c0001t0001g0147a0001c0001t0001g0148 | 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 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148 | 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 | a0001c0001t0001g0053a0001c0001t0001g0059 | 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 | 214 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(211): Show | 214 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(211): 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 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(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 | a0001c0001t0001g0021a0001c0001t0001g0026a0001c0001t0001g0039others(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 | a0001c0001t0001g0013a0001c0001t0001g0062 | 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 | a0001c0001t0001g0019 | 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 | a0001c0001t0001g0065a0001c0001t0001g0068 | 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 | a0001c0001t0001g0056 | 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 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0019others(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 | a0001c0001t0001g0094a0001c0010t0001g0069 | 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 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0019others(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 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0017others(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 | a0001c0001t0001g0005a0001c0001t0001g0046a0001c0001t0001g0104others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148others(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 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(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 | 32 | a0001c0002t0001g0111a0001c0002t0001g0149a0001c0002t0001g0150others(29): Show | 32 | HG00140.hp1 HG00323.hp2 HG00597.hp1 others(29): 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 | a0001c0002t0001g0151a0001c0002t0001g0183a0001c0002t0001g0184 | 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 | a0001c0001t0001g0053a0001c0001t0001g0059a0001c0001t0001g0118others(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 | a0001c0001t0001g0005a0001c0001t0001g0104a0001c0001t0001g0118others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | 107 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(104): Show | 107 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(104): 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 | a0001c0001t0001g0104a0001c0001t0001g0120a0001c0001t0001g0121others(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 | 110 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(107): Show | 110 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.1483+9259G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49984651 | ||||||
| chr3:49984656
|
G | A | 110 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(107): Show | 110 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.1483+9264G>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49984656 | ||||||
| chr3:49984661
|
G | A | 110 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(107): Show | 110 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(107): 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 | a0001c0001t0001g0019 | 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 | a0001c0001t0001g0019 | 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 | 127 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(124): Show | 127 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(124): 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 | a0001c0001t0001g0051 | 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 | 132 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(129): Show | 132 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(129): 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 | a0001c0005t0001g0102a0001c0005t0001g0103a0001c0005t0001g0105others(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 | 214 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(211): Show | 214 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(211): 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 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(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 | a0001c0001t0001g0086a0001c0001t0001g0087 | 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 | a0001c0001t0001g0038a0003c0006t0001g0072 | 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 | a0001c0003t0001g0064a0001c0003t0001g0066 | 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 | ||||||
| chr3:49986556
|
A | C | 217 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(214): Show | 217 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.1483+11164A>C | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49986556 | ||||||
| chr3:49986594
|
CA | C | 93 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(90): Show | 93 | HG00140.hp1 HG00323.hp2 HG00597.hp1 others(90): 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 | 101 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(98): Show | 101 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(98): 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 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0127others(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 | a0001c0003t0001g0030a0001c0003t0001g0076a0001c0003t0001g0083 | 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 | a0002c0004t0001g0107a0002c0004t0001g0133a0002c0004t0001g0138others(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 | a0002c0004t0001g0107a0002c0004t0001g0133a0002c0004t0001g0138others(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 | a0002c0004t0001g0107a0002c0004t0001g0141 | 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 | 35 | a0001c0002t0001g0111a0001c0002t0001g0149a0001c0002t0001g0150others(32): Show | 35 | HG00140.hp1 HG00323.hp2 HG00597.hp1 others(32): Show |
intron_variant | MODIFIER | c.1483+11743C>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49987135 | ||||||
| chr3:49987325
|
G | T | 127 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(124): Show | 127 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(124): Show |
intron_variant | MODIFIER | c.1483+11933G>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49987325 | ||||||
| chr3:49987573
|
T | C | 69 | a0001c0002t0001g0111a0001c0002t0001g0149a0001c0002t0001g0150others(66): Show | 69 | HG00140.hp1 HG00323.hp2 HG00597.hp1 others(66): 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 | 110 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(107): Show | 110 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(107): 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 | a0002c0004t0001g0107a0002c0004t0001g0133a0002c0004t0001g0138others(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 | a0001c0001t0001g0024a0001c0001t0001g0062a0001c0001t0001g0065others(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 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(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 | 131 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(128): Show | 131 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.1484-11343A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49988097 | ||||||
| chr3:49988596
|
A | C | 131 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(128): Show | 131 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(128): 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 | a0001c0005t0001g0102a0001c0005t0001g0103a0001c0005t0001g0105others(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 | a0001c0005t0001g0102a0001c0005t0001g0103a0001c0005t0001g0105others(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 | 70 | a0001c0001t0001g0145a0001c0002t0001g0111a0001c0002t0001g0149others(67): Show | 70 | HG00140.hp1 HG00323.hp2 HG00597.hp1 others(67): 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 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0098others(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 | a0001c0003t0001g0063a0001c0003t0001g0064a0001c0003t0001g0066 | 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 | ||||||
| chr3:49989264
|
A | G | 1 | a0001c0002t0001g0165 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1484-10176A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 5/20 | chr3 | 49989264 | ||||||
| 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 | a0001c0001t0001g0147a0001c0001t0001g0148 | 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 | 110 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(107): Show | 110 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(107): 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 | a0001c0001t0001g0104a0001c0001t0001g0120a0001c0001t0001g0121others(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 | 127 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(124): Show | 127 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(124): 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 | a0001c0003t0001g0063a0001c0003t0001g0064a0001c0003t0001g0066 | 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0118others(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 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(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 | a0001c0001t0001g0060a0002c0004t0001g0107a0002c0004t0001g0133others(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 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(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 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0098others(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 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0098others(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 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0098others(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 | a0001c0002t0001g0168a0001c0002t0001g0174a0001c0002t0001g0207 | 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 | 69 | a0001c0002t0001g0111a0001c0002t0001g0149a0001c0002t0001g0150others(66): Show | 69 | HG00140.hp1 HG00323.hp2 HG00597.hp1 others(66): 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 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(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 | 37 | a0001c0001t0001g0145a0001c0002t0001g0111a0001c0002t0001g0149others(34): Show | 37 | HG00140.hp1 HG00323.hp2 HG00597.hp1 others(34): 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 | a0001c0001t0001g0089a0001c0001t0001g0104a0001c0001t0001g0121others(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 | a0001c0002t0001g0151a0001c0002t0001g0152a0001c0002t0001g0153others(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 | 70 | a0001c0001t0001g0145a0001c0002t0001g0111a0001c0002t0001g0149others(67): Show | 70 | HG00140.hp1 HG00323.hp2 HG00597.hp1 others(67): 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 | a0001c0002t0001g0179a0001c0002t0001g0180 | 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 | a0001c0002t0001g0149a0001c0002t0001g0150a0001c0002t0001g0155others(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 | a0001c0002t0001g0111a0001c0002t0001g0157 | 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(9): Show |
1 | a0001c0002t0001g0165 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1484-4770_1484-476 others(20): 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 | a0001c0001t0001g0040a0001c0001t0001g0137a0005c0008t0001g0041 | 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 | a0001c0001t0001g0108a0001c0002t0001g0151a0001c0002t0001g0152others(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 | a0001c0001t0001g0101a0001c0001t0001g0109a0001c0001t0001g0146others(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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(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 | a0001c0001t0001g0110a0001c0001t0001g0129a0001c0001t0001g0131others(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 | a0001c0001t0001g0001a0001c0001t0001g0114a0001c0001t0003g0116 | 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 | a0002c0004t0001g0133a0002c0004t0001g0138a0002c0004t0001g0139 | 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 | a0001c0001t0001g0017a0001c0002t0001g0207 | 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 | 70 | a0001c0001t0001g0145a0001c0002t0001g0111a0001c0002t0001g0149others(67): Show | 70 | HG00140.hp1 HG00323.hp2 HG00597.hp1 others(67): 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 | a0001c0002t0001g0162a0001c0002t0001g0163a0001c0002t0001g0164others(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 | 126 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(123): Show | 126 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(123): 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 | a0002c0004t0001g0107a0002c0004t0001g0133a0002c0004t0001g0138others(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 | 6 | a0001c0001t0001g0082a0001c0001t0001g0084a0001c0002t0001g0163others(3): Show | 6 | HG02735.hp1 HG02895.hp2 HG02897.hp1 others(3): 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 | 84 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(81): Show | 84 | HG00140.hp1 HG00323.hp2 HG00597.hp1 others(81): 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 | a0001c0001t0001g0098 | 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 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0127others(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 | a0001c0002t0001g0153a0001c0002t0001g0154a0001c0002t0001g0189others(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 | a0002c0004t0001g0107a0002c0004t0001g0133a0002c0004t0001g0138others(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 | a0001c0001t0001g0130 | 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 | a0001c0002t0001g0197 | 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 | 131 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(128): Show | 131 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(128): 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 | 127 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(124): Show | 127 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(124): 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 | a0001c0001t0001g0108a0001c0001t0001g0109 | 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 | a0001c0001t0001g0129a0001c0001t0001g0146a0001c0001t0001g0147others(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 | a0001c0001t0001g0006a0001c0001t0001g0051a0001c0001t0001g0101others(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 | a0001c0002t0001g0168a0001c0002t0001g0174a0001c0002t0001g0207 | 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 | a0001c0001t0001g0012a0001c0001t0001g0034 | 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 | 127 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(124): Show | 127 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(124): Show |
intron_variant | MODIFIER | c.1557+177C>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 49999690 | ||||||
| chr3:49999769
|
GA | G | 131 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(128): Show | 131 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(128): 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 | a0001c0001t0001g0118a0001c0001t0001g0129a0001c0001t0001g0130others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0001c0001t0001g0118a0001c0001t0001g0129a0001c0001t0001g0130others(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 | 36 | a0001c0002t0001g0111a0001c0002t0001g0149a0001c0002t0001g0150others(33): Show | 36 | HG00140.hp1 HG00323.hp2 HG00597.hp1 others(33): 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | 127 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(124): Show | 127 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(124): 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 | a0001c0001t0001g0023a0001c0001t0001g0061a0001c0001t0001g0079others(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 | 89 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(86): Show | 89 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(86): 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 | a0001c0001t0001g0108a0001c0001t0001g0109 | 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 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(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 | 131 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(128): Show | 131 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(128): 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 | a0001c0002t0001g0201a0001c0002t0001g0211 | 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 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(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 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(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 | a0001c0001t0001g0104a0001c0001t0001g0120a0001c0001t0001g0121others(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 | 89 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(86): Show | 89 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(86): 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 | a0001c0001t0001g0104a0001c0001t0001g0121a0001c0001t0001g0122others(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 | a0001c0001t0001g0024 | 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 | a0001c0001t0001g0079a0001c0001t0001g0120a0001c0001t0001g0121others(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 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0001c0001t0001g0044 | 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 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(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 | a0001c0001t0001g0142a0001c0002t0001g0149a0001c0002t0001g0150others(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 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(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 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0001c0001t0001g0017 | 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 | a0001c0001t0001g0047 | 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 | a0001c0001t0001g0118a0001c0001t0001g0129a0001c0001t0001g0130others(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 | a0001c0003t0001g0010a0001c0003t0001g0027a0001c0003t0001g0028others(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 | a0001c0001t0001g0108a0001c0001t0001g0109 | 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 | a0001c0001t0001g0118a0001c0001t0001g0130 | 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 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(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 | a0001c0001t0001g0038a0001c0001t0001g0074a0001c0001t0001g0108others(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 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148 | 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 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(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 | a0001c0001t0001g0095a0001c0001t0001g0110a0001c0001t0001g0115others(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 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0146others(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 | a0001c0001t0001g0052a0001c0001t0001g0082a0001c0001t0001g0124others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0002c0004t0001g0107a0002c0004t0001g0133a0002c0004t0001g0138others(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 | a0001c0002t0001g0151a0001c0002t0001g0152a0001c0002t0001g0153others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0001c0005t0001g0102a0001c0005t0001g0103a0001c0005t0001g0105others(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 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(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 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0127others(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 | a0001c0002t0001g0197 | 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 | a0001c0005t0001g0102a0001c0005t0001g0103a0001c0005t0001g0105others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0001c0003t0001g0010a0001c0003t0001g0027a0001c0003t0001g0028others(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 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(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 | a0001c0005t0001g0102a0001c0005t0001g0103a0001c0005t0001g0105others(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 | a0002c0004t0001g0107a0002c0004t0001g0133a0002c0004t0001g0138others(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 | a0001c0003t0001g0070a0001c0003t0001g0073 | 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 | a0001c0001t0001g0104a0001c0001t0001g0120a0001c0001t0001g0121others(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 | a0001c0001t0001g0095a0001c0001t0001g0097a0001c0001t0001g0098others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0001c0001t0001g0058a0001c0001t0001g0127a0001c0001t0001g0128others(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 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(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 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(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 | a0001c0002t0001g0151a0001c0002t0001g0152a0001c0002t0001g0153others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0001c0001t0001g0104a0001c0001t0001g0120a0001c0001t0001g0121others(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 | a0001c0001t0001g0104a0001c0001t0001g0120a0001c0001t0001g0121others(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 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148 | 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 | a0001c0002t0001g0162a0001c0002t0001g0163a0001c0002t0001g0164others(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 | a0001c0001t0001g0104a0001c0001t0001g0121a0001c0001t0001g0122 | 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 | a0001c0002t0001g0151a0001c0002t0001g0152a0001c0002t0001g0153others(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 | a0001c0001t0001g0051 | 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 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(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 | a0001c0001t0001g0004 | 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 | a0001c0001t0001g0136 | 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 | a0001c0002t0001g0196a0001c0002t0001g0198a0001c0002t0001g0201others(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 | a0001c0001t0001g0130 | 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0001c0001t0001g0075a0001c0001t0001g0108a0001c0001t0001g0109others(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 | 117 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(114): Show | 117 | HG00140.hp2 HG00597.hp2 HG00639.hp1 others(114): 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 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0011others(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 | a0001c0001t0001g0003a0001c0005t0001g0102a0001c0005t0001g0103others(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 | a0001c0001t0001g0118a0001c0001t0001g0130 | 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 | a0001c0002t0001g0209 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1557+11614T>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50011127 | ||||||
| chr3:50011186
|
C | A | 1 | a0001c0002t0001g0165 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1557+11673C>A | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50011186 | ||||||
| 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 | a0001c0001t0001g0108a0001c0001t0001g0109 | 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0001c0001t0001g0104a0001c0001t0001g0120a0001c0001t0001g0121others(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 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(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 | a0001c0001t0001g0104a0001c0001t0001g0121a0001c0001t0001g0122others(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 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(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 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(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 | a0001c0001t0001g0059a0001c0001t0001g0079a0001c0001t0001g0081others(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 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(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 | a0001c0001t0001g0118a0001c0001t0001g0129a0001c0001t0001g0130others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0001c0001t0001g0017 | 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 | a0001c0002t0001g0208a0001c0002t0001g0209a0001c0002t0001g0216 | 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 | a0001c0002t0001g0201a0001c0002t0001g0211a0001c0002t0001g0212 | 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 | a0001c0002t0001g0168a0001c0002t0001g0170a0001c0002t0001g0186others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(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 | a0001c0001t0001g0050a0002c0004t0001g0107a0002c0004t0001g0133others(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 | a0001c0002t0001g0196a0001c0002t0001g0198 | 2 | HG02976.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1557+15563T>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50015076 | ||||||
| chr3:50015151
|
A | G | 217 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(214): Show | 217 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.1557+15638A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50015151 | ||||||
| chr3:50015296
|
C | G | 107 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(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 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(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 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(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 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(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 | a0001c0001t0001g0108a0001c0001t0001g0109 | 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 | a0001c0001t0001g0095a0001c0001t0001g0097a0001c0001t0001g0098others(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 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(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 | a0001c0001t0001g0104a0001c0001t0001g0120a0001c0001t0001g0122others(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 | a0001c0001t0001g0112a0001c0001t0001g0113 | 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 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(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 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(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 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0146others(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 | a0001c0002t0001g0182 | 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0002c0004t0001g0107a0002c0004t0001g0141 | 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 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0132others(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 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(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 | a0001c0001t0001g0002a0001c0001t0001g0095a0001c0001t0001g0098others(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 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0100others(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 | a0001c0001t0001g0079a0001c0003t0001g0010a0001c0003t0001g0027others(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 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(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 | a0001c0005t0001g0102a0001c0005t0001g0103a0001c0005t0001g0105others(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 | a0001c0002t0001g0201a0001c0002t0001g0211 | 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 | a0001c0001t0001g0118a0001c0001t0001g0129a0001c0001t0001g0130others(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 | a0001c0001t0001g0048a0001c0003t0001g0064 | 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 | a0001c0001t0001g0055 | 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 | a0001c0001t0001g0108a0001c0001t0001g0109 | 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 | a0001c0001t0001g0108a0001c0001t0001g0109 | 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 | a0001c0001t0001g0091 | 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 | a0001c0002t0001g0177a0001c0002t0001g0188a0001c0002t0001g0199others(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 | a0002c0004t0001g0138a0002c0004t0001g0139 | 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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(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 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0026others(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 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0016others(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 | a0001c0001t0001g0015a0001c0001t0001g0080a0001c0001t0001g0088others(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 | a0001c0001t0001g0067a0001c0001t0001g0110a0001c0001t0001g0114others(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 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0146others(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 | a0002c0004t0001g0133a0002c0004t0001g0138a0002c0004t0001g0139others(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 | a0001c0001t0001g0051 | 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 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148 | 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 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148 | 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 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148 | 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 | a0001c0001t0001g0050a0001c0003t0001g0063a0001c0003t0001g0066 | 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 | a0001c0003t0001g0010a0001c0003t0001g0027a0001c0003t0001g0028others(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 | a0001c0001t0001g0130 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1557+19458G>T | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50018971 | ||||||
| chr3:50019002
|
C | G | 1 | a0001c0002t0001g0165 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1557+19489C>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 6/20 | chr3 | 50019002 | ||||||
| chr3:50019045
|
T | A | 21 | a0001c0001t0001g0075a0001c0001t0001g0094a0001c0001t0001g0095others(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 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0127others(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 | a0001c0002t0001g0196a0001c0002t0001g0198a0001c0002t0001g0201others(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 | a0001c0002t0001g0179a0001c0002t0001g0180 | 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 | a0001c0001t0001g0061a0001c0001t0001g0085 | 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0001c0001t0001g0118a0001c0001t0001g0129a0001c0001t0001g0130others(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 | a0002c0004t0001g0107a0002c0004t0001g0133a0002c0004t0001g0138others(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 | a0001c0005t0001g0102a0001c0005t0001g0103a0001c0005t0001g0105others(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 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(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 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(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 | a0001c0001t0001g0005a0001c0001t0001g0023a0001c0001t0001g0061others(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 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(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 | 40 | a0001c0001t0001g0124a0001c0001t0001g0130a0001c0001t0001g0145others(37): Show | 40 | HG00323.hp2 HG00597.hp1 HG00639.hp2 others(37): 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 | a0001c0001t0001g0096a0001c0001t0001g0110a0001c0001t0001g0114others(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 | a0001c0001t0001g0095a0001c0001t0001g0097a0001c0001t0001g0098others(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 | a0002c0004t0001g0133a0002c0004t0001g0138a0002c0004t0001g0139others(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 | a0002c0004t0001g0107a0002c0004t0001g0141 | 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 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(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 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(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 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(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 | a0001c0005t0001g0102a0001c0005t0001g0103a0001c0005t0001g0105others(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 | a0002c0004t0001g0107a0002c0004t0001g0133a0002c0004t0001g0138others(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 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(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 | a0002c0004t0001g0107a0002c0004t0001g0133a0002c0004t0001g0138others(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 | a0001c0005t0001g0102a0001c0005t0001g0103a0001c0005t0001g0105others(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 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(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 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099others(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 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(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 | 110 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(107): Show | 110 | HG00140.hp2 HG00323.hp1 HG00597.hp2 others(107): 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 | a0001c0001t0001g0025a0001c0001t0001g0047a0001c0001t0001g0087others(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 | a0002c0004t0001g0107a0002c0004t0001g0133a0002c0004t0001g0138others(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 | a0002c0004t0001g0107a0002c0004t0001g0133a0002c0004t0001g0138others(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 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(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 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(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 | a0001c0001t0001g0048a0001c0003t0001g0064 | 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 | a0002c0004t0001g0107a0002c0004t0001g0133a0002c0004t0001g0138others(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 | a0001c0001t0001g0104a0001c0001t0001g0120a0001c0001t0001g0121others(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 | a0002c0004t0001g0107a0002c0004t0001g0133a0002c0004t0001g0138others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0001c0001t0001g0034a0001c0001t0001g0114a0001c0001t0001g0118others(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 | a0001c0001t0001g0059a0001c0001t0001g0146a0001c0001t0001g0147others(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 | a0001c0001t0001g0108a0001c0001t0001g0109 | 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 | a0004c0007t0001g0173 | 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 | a0001c0002t0001g0151a0001c0002t0001g0152a0001c0002t0001g0153others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0001c0001t0001g0013a0001c0001t0001g0059a0005c0008t0001g0041 | 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 | a0001c0001t0001g0038a0001c0003t0001g0032a0003c0006t0001g0072 | 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 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0015others(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 | a0001c0001t0001g0019a0001c0001t0001g0025a0001c0001t0001g0036others(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 | a0001c0001t0001g0014a0001c0003t0001g0031 | 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0002c0004t0001g0133a0002c0004t0001g0138a0002c0004t0001g0139 | 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 | a0001c0001t0001g0087a0001c0002t0001g0154a0001c0002t0001g0179others(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 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0127others(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 | a0001c0001t0001g0047 | 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 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148 | 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 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0132others(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 | a0003c0006t0001g0072 | 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 | a0001c0001t0001g0001a0001c0001t0001g0095a0001c0001t0001g0096others(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 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(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 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(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 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(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 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(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 | a0001c0001t0001g0091 | 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 | a0001c0002t0001g0152a0001c0002t0001g0194 | 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 | a0001c0001t0001g0017 | 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 | a0001c0002t0001g0151a0001c0002t0001g0152a0001c0002t0001g0153others(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 | a0001c0002t0001g0182 | 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 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(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 | a0001c0005t0001g0102a0001c0005t0001g0103a0001c0005t0001g0105others(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 | a0003c0006t0001g0009a0003c0006t0001g0071 | 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 | a0001c0001t0001g0118a0001c0001t0001g0129a0001c0001t0001g0130others(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 | a0001c0001t0001g0104a0001c0001t0001g0120a0001c0001t0001g0121others(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 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(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 | a0001c0002t0001g0152a0001c0002t0001g0194 | 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 | a0001c0002t0001g0151a0001c0002t0001g0152a0001c0002t0001g0153others(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 | a0001c0001t0001g0095a0001c0001t0001g0110a0001c0001t0001g0115others(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 | a0001c0001t0001g0145a0001c0002t0001g0152a0001c0002t0001g0155others(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 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(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 | a0001c0001t0001g0014a0001c0001t0001g0089a0001c0001t0001g0104others(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 | a0001c0001t0001g0013a0001c0001t0001g0038a0001c0001t0001g0043others(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 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0015others(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 | a0001c0001t0001g0002a0001c0001t0001g0006 | 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 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0132others(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 | a0005c0008t0001g0041a0005c0008t0001g0217 | 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0001c0001t0001g0049 | 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 | a0001c0002t0001g0197 | 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 | a0001c0002t0001g0151a0001c0002t0001g0153a0001c0002t0001g0154others(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 | a0002c0004t0001g0107a0002c0004t0001g0141 | 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 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(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 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(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 | a0001c0001t0001g0067a0001c0001t0001g0080a0001c0001t0001g0081others(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 | a0001c0001t0001g0049a0001c0001t0001g0055a0001c0001t0001g0060others(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 | a0001c0001t0001g0104a0001c0001t0001g0120a0001c0001t0001g0121others(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 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(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 | a0002c0004t0001g0138a0002c0004t0001g0139 | 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 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(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 | a0001c0001t0001g0012a0001c0001t0001g0024a0001c0001t0001g0062others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0001c0001t0001g0124a0001c0001t0001g0135 | 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 | a0001c0005t0001g0102a0001c0005t0001g0103a0001c0005t0001g0105others(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 | a0001c0002t0001g0177a0001c0002t0001g0195a0001c0002t0001g0199others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(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 | a0001c0001t0001g0048a0001c0003t0001g0064 | 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0001c0001t0001g0118a0001c0001t0001g0130 | 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(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 | a0001c0001t0001g0104a0001c0001t0001g0120a0001c0001t0001g0121others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(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 | a0001c0002t0001g0183a0001c0002t0001g0184 | 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 | a0001c0001t0001g0137a0001c0002t0001g0186 | 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 | a0001c0001t0001g0118a0001c0001t0001g0122a0001c0001t0001g0129others(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 | a0001c0001t0001g0016a0001c0001t0001g0022a0001c0001t0001g0044others(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 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(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 | a0002c0004t0001g0107a0002c0004t0001g0133a0002c0004t0001g0138others(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 | a0001c0005t0001g0102a0001c0005t0001g0103a0001c0005t0001g0105others(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 | a0002c0004t0001g0107a0002c0004t0001g0133a0002c0004t0001g0138others(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 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(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 | a0001c0001t0001g0095a0001c0001t0001g0110a0001c0001t0001g0115others(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 | a0001c0001t0001g0104a0001c0001t0001g0120a0001c0001t0001g0121others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(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 | a0002c0004t0001g0107a0002c0004t0001g0133a0002c0004t0001g0138others(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 | a0001c0001t0001g0108a0001c0001t0001g0109 | 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 | 7 | a0001c0001t0001g0081a0001c0001t0001g0089a0001c0002t0001g0165others(4): Show | 7 | HG01243.hp2 HG02055.hp1 HG03486.hp2 others(4): 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0005c0008t0001g0041a0005c0008t0001g0217 | 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 | a0002c0004t0001g0107a0002c0004t0001g0133a0002c0004t0001g0138others(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 | a0002c0004t0001g0107a0002c0004t0001g0133a0002c0004t0001g0138others(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 | a0001c0001t0001g0005 | 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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(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 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(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 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(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 | a0001c0001t0001g0104a0001c0001t0001g0120a0001c0001t0001g0121others(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 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(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 | a0001c0002t0001g0161a0001c0002t0001g0166a0001c0002t0001g0176others(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 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0002t0001g0111others(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 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(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 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(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 | a0001c0001t0001g0011a0001c0001t0001g0025a0001c0001t0001g0039others(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 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(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 | a0001c0001t0001g0044 | 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 | a0001c0001t0001g0046 | 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 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(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 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0101others(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 | a0001c0001t0001g0098a0001c0001t0001g0125a0001c0001t0001g0127others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0001c0001t0001g0108a0001c0001t0001g0109 | 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 | a0001c0001t0001g0050a0001c0003t0001g0063a0001c0003t0001g0066others(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 | a0001c0001t0001g0130 | 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 | a0003c0006t0001g0009 | 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 | a0001c0003t0001g0033a0001c0003t0001g0070a0003c0006t0001g0071others(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 | a0001c0001t0001g0130 | 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 | a0001c0001t0001g0035a0001c0001t0001g0146a0001c0001t0001g0147others(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 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0001g0023others(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 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0026others(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 | a0001c0001t0001g0012a0001c0001t0001g0024a0001c0001t0001g0047others(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 | a0001c0001t0001g0096a0001c0001t0001g0130 | 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 | a0001c0001t0001g0034a0001c0001t0002g0020 | 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 | a0001c0001t0001g0011a0001c0001t0001g0074 | 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 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0018others(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 | a0001c0001t0001g0053 | 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 | a0001c0001t0001g0115a0001c0001t0001g0129a0001c0001t0001g0131others(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 | a0001c0001t0001g0110a0001c0001t0003g0116a0001c0002t0001g0181others(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 | a0001c0001t0001g0096a0001c0001t0001g0114a0001c0001t0001g0118others(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 | a0001c0002t0001g0150a0001c0002t0001g0155a0001c0002t0001g0157others(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 | a0001c0002t0001g0159a0001c0002t0001g0197 | 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0001c0001t0001g0104a0001c0001t0001g0121a0001c0001t0001g0122others(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 | a0001c0002t0001g0153a0001c0002t0001g0185 | 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 | a0001c0002t0001g0170a0004c0007t0001g0171a0004c0007t0001g0203 | 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0001c0001t0001g0218a0001c0002t0001g0152a0001c0002t0001g0181others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0001c0002t0001g0151a0001c0002t0001g0154a0001c0002t0001g0210others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0142 | 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 | a0001c0001t0001g0095a0001c0002t0001g0160a0001c0002t0001g0161 | 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 | a0001c0001t0001g0012a0001c0001t0001g0024 | 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 | a0001c0001t0001g0022a0001c0002t0001g0156a0001c0002t0001g0167others(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 | a0001c0005t0001g0102a0001c0005t0001g0103a0001c0005t0001g0105others(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 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(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 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0001c0002t0001g0197 | 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 | a0001c0001t0001g0104a0001c0001t0001g0120a0001c0001t0001g0121others(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 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(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 | a0001c0005t0001g0102a0001c0005t0001g0103a0001c0005t0001g0105others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0001c0002t0001g0176a0001c0002t0001g0185a0001c0005t0001g0102others(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 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(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 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0146others(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 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148 | 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 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148 | 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 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(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 | a0002c0004t0001g0107a0002c0004t0001g0141 | 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0098others(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 | a0001c0001t0001g0095a0001c0001t0001g0110a0001c0001t0001g0114others(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 | a0001c0001t0001g0086a0001c0001t0001g0087 | 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 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148 | 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 | a0001c0001t0001g0130 | 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0132others(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 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(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 | a0001c0001t0001g0130 | 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 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0127others(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 | a0002c0004t0001g0107a0002c0004t0001g0133a0002c0004t0001g0138others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0001c0001t0001g0055 | 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0001c0001t0001g0050a0001c0003t0001g0066 | 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 | a0002c0004t0001g0107a0002c0004t0001g0133a0002c0004t0001g0138others(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 | a0001c0001t0001g0013a0001c0001t0001g0051a0001c0001t0001g0094others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148 | 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 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(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 | a0001c0001t0001g0004 | 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 | a0004c0007t0001g0171a0004c0007t0001g0173a0004c0007t0001g0203 | 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 | a0001c0002t0001g0151a0001c0002t0001g0152a0001c0002t0001g0153others(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 | a0002c0004t0001g0107a0002c0004t0001g0133a0002c0004t0001g0138others(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 | a0001c0002t0001g0159a0001c0002t0001g0160a0001c0002t0001g0161 | 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099others(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 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0132others(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 | a0002c0004t0001g0107a0002c0004t0001g0133a0002c0004t0001g0138others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0001c0001t0001g0002a0001c0001t0001g0006 | 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 | a0001c0001t0001g0104a0001c0001t0001g0120a0001c0001t0001g0121others(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 | a0001c0001t0001g0110a0001c0001t0001g0117 | 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 | a0001c0001t0001g0053a0001c0001t0001g0059 | 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 | a0001c0001t0001g0136 | 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 | a0002c0004t0001g0107a0002c0004t0001g0133a0002c0004t0001g0138others(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 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(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 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(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 | a0001c0001t0001g0127 | 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 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(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 | a0001c0001t0001g0017 | 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 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0001c0001t0001g0091a0001c0001t0001g0096a0001c0001t0001g0098others(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 | 5 | a0001c0001t0001g0074a0001c0002t0001g0165a0001c0002t0001g0187others(2): Show | 5 | HG04199.hp1 NA18952.hp2 NA18983.hp2 others(2): 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 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0023others(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 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0026others(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 | a0001c0001t0001g0123a0001c0002t0001g0151a0001c0002t0001g0152others(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 | a0001c0001t0001g0143a0001c0002t0001g0196a0001c0002t0001g0198others(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 | a0001c0001t0001g0056 | 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 | a0001c0001t0001g0048a0001c0002t0001g0185 | 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 | a0002c0004t0001g0107a0002c0004t0001g0141 | 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 | a0002c0004t0001g0107a0002c0004t0001g0133a0002c0004t0001g0138others(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 | a0001c0001t0001g0124a0001c0001t0001g0135 | 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 | a0001c0005t0001g0102a0001c0005t0001g0103a0001c0005t0001g0105others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0001c0002t0001g0153a0001c0002t0001g0154 | 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 | a0005c0008t0001g0041a0005c0008t0001g0217 | 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 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | ||||||
| chr3:50055725
|
A | G | 1 | a0001c0002t0001g0165 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1693+1330A>G | RBM6 | ENSG00000004534.15 | transcript | ENST00000266022.9 | protein_coding | 8/20 | chr3 | 50055725 | ||||||
| chr3:50055776
|
G | A | 148 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0001c0001t0001g0043a0001c0001t0001g0067a0001c0001t0001g0080others(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 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(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 | a0001c0001t0001g0036a0001c0001t0001g0038 | 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 | a0001c0001t0001g0008a0001c0001t0001g0034a0001c0001t0001g0095others(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 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(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 | a0001c0001t0001g0011a0001c0001t0001g0021a0001c0001t0001g0038others(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 | a0001c0001t0001g0036a0001c0001t0001g0038a0001c0001t0001g0051others(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 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(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 | a0001c0001t0001g0104a0001c0001t0001g0120a0001c0001t0001g0121others(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 | a0001c0003t0001g0070a0001c0003t0001g0073 | 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 | a0001c0001t0001g0095a0001c0001t0001g0110a0001c0001t0001g0114others(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 | a0002c0004t0001g0107a0002c0004t0001g0133a0002c0004t0001g0138others(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 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148 | 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 | a0001c0001t0001g0094a0001c0001t0001g0100a0001c0001t0001g0114others(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 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(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 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(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 | a0002c0004t0001g0107a0002c0004t0001g0133a0002c0004t0001g0138others(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 | a0001c0005t0001g0102a0001c0005t0001g0103a0001c0005t0001g0105others(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 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0001c0001t0001g0018a0001c0001t0001g0055a0001c0001t0001g0061others(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 | a0001c0001t0001g0043a0001c0001t0001g0067a0001c0001t0001g0080others(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 | a0002c0004t0001g0138a0002c0004t0001g0139 | 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0022others(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 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(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 | a0001c0002t0001g0160a0001c0002t0001g0162a0001c0002t0001g0163others(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 | a0001c0002t0001g0150a0001c0002t0001g0157 | 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 | a0001c0001t0001g0108a0001c0001t0001g0109 | 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 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(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 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0146others(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 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(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 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(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 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(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 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0127others(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 | a0001c0001t0001g0118a0001c0001t0001g0130 | 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 | a0001c0001t0001g0011a0001c0001t0001g0018a0001c0001t0001g0104others(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 | a0001c0002t0001g0151a0001c0002t0001g0152a0001c0002t0001g0153others(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 | a0001c0001t0001g0011a0001c0001t0001g0046 | 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 | a0001c0001t0001g0024a0001c0001t0001g0062a0001c0001t0001g0065others(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 | a0001c0002t0001g0163a0001c0002t0001g0169 | 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 | a0003c0006t0001g0071 | 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 | a0001c0005t0001g0102a0001c0005t0001g0103a0001c0005t0001g0105others(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 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148 | 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 | a0001c0001t0001g0047 | 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 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(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 | a0001c0001t0001g0130 | 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 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148 | 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 | a0001c0001t0001g0097 | 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0001c0001t0001g0053a0001c0001t0001g0059 | 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 | a0001c0001t0001g0065a0001c0001t0001g0068 | 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 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0132others(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 | a0002c0004t0001g0107a0002c0004t0001g0133a0002c0004t0001g0138others(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 | a0001c0001t0001g0118a0001c0001t0001g0129a0001c0001t0001g0130others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(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 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0023others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(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 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(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 | a0001c0002t0001g0191 | 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 | a0001c0001t0001g0104a0001c0001t0001g0120a0001c0001t0001g0121others(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 | a0001c0001t0001g0134 | 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 | a0001c0002t0001g0159a0001c0002t0001g0160a0001c0002t0001g0161 | 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 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148 | 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 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(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 | a0001c0001t0001g0104a0001c0001t0001g0120a0001c0001t0001g0121others(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 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(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 | a0002c0004t0001g0107a0002c0004t0001g0133a0002c0004t0001g0138others(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 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(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 | a0001c0001t0001g0104a0001c0001t0001g0120a0001c0001t0001g0121others(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 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(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 | a0001c0002t0001g0153a0001c0002t0001g0154a0001c0002t0001g0214 | 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 | a0002c0004t0001g0107a0002c0004t0001g0133a0002c0004t0001g0138others(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 | a0001c0001t0001g0053a0001c0001t0001g0059 | 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0001c0002t0001g0151a0001c0002t0001g0152a0001c0002t0001g0153others(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 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(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 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(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 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(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 | a0001c0001t0001g0019a0001c0001t0001g0025a0001c0001t0001g0036others(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 | a0001c0001t0001g0012a0001c0001t0001g0058a0001c0001t0001g0095others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(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 | a0002c0004t0001g0107a0002c0004t0001g0133a0002c0004t0001g0138others(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 | a0002c0004t0001g0140 | 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 | a0001c0002t0001g0152a0001c0002t0001g0194 | 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0001c0001t0001g0019 | 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 | a0002c0004t0001g0107a0002c0004t0001g0133a0002c0004t0001g0138others(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 | a0001c0002t0001g0195 | 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 | a0001c0005t0001g0102a0001c0005t0001g0103a0001c0005t0001g0105others(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 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(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 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(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 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(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 | a0001c0001t0001g0023a0001c0001t0001g0079a0001c0001t0001g0085 | 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 | a0002c0004t0001g0107a0002c0004t0001g0133a0002c0004t0001g0138others(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 | a0001c0001t0001g0130 | 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 | a0001c0002t0001g0188a0001c0002t0001g0199 | 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 |