Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 5939 |
|---|---|
| ensemblid | ENSG00000076067.14 |
| hgncid | 9909 |
| symbol | RBMS2 |
| name | RNA binding motif single stranded interacting protein 2 |
| refseq_nuc | NM_002898.4 |
| refseq_prot | NP_002889.1 |
| ensembl_nuc | ENST00000262031.10 |
| ensembl_prot | ENSP00000262031.5 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 56521820 |
| end | 56596193 |
| strand | + |
| ver | v1.2 |
| region | chr12:56521820-56596193 |
| region5000 | chr12:56516820-56601193 |
| regionname0 | RBMS2_chr12_56521820_56596193 |
| regionname5000 | RBMS2_chr12_56516820_56601193 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 407 | 280 | 88 | 54 | 94 | 12 | 30 | 62 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 1224 | 167 | 34 | 36 | 69 | 7 | 21 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| c0002 | 1/1 | 1224 | 105 | 49 | 16 | 24 | 5 | 9 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| c0003 | 0/0 | 1224 | 4 | 4 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| c0004 | 0/0 | 1224 | 3 | 1 | 2 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| c0005 | 0/0 | 1224 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 7264 | 62 | 3 | 17 | 29 | 4 | 9 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| t0002 | 0/0 | 7265 | 37 | 4 | 8 | 20 | 2 | 3 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| t0003 | 0/0 | 7264 | 35 | 4 | 7 | 19 | 3 | 2 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| t0004 | 0/0 | 7264 | 7 | 7 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| t0005 | 0/0 | 7264 | 5 | 5 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| t0006 | 0/0 | 7264 | 5 | 5 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| t0007 | 0/0 | 7264 | 5 | 5 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| t0008 | 0/0 | 7264 | 4 | 0 | 0 | 1 | 0 | 3 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| t0009 | 0/0 | 7264 | 4 | 0 | 3 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| t0010 | 0/0 | 7262 | 4 | 4 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| t0011 | 0/0 | 7262 | 4 | 4 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| t0012 | 0/0 | 7264 | 4 | 4 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| t0013 | 0/0 | 7264 | 3 | 3 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| t0014 | 0/0 | 7265 | 3 | 0 | 0 | 0 | 0 | 3 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| t0015 | 0/0 | 7265 | 3 | 1 | 2 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| t0016 | 0/0 | 7264 | 3 | 0 | 0 | 1 | 0 | 2 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| t0017 | 0/0 | 7264 | 3 | 3 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| t0018 | 0/0 | 7264 | 3 | 1 | 2 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| t0019 | 0/0 | 7264 | 3 | 0 | 1 | 2 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| t0020 | 0/0 | 7262 | 3 | 3 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| t0021 | 0/0 | 7262 | 3 | 2 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| t0022 | 0/0 | 7261 | 3 | 0 | 0 | 0 | 3 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| t0023 | 0/0 | 7255 | 2 | 2 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| t0024 | 0/0 | 7265 | 2 | 0 | 0 | 2 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| t0025 | 0/0 | 7265 | 2 | 0 | 0 | 2 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| t0026 | 0/0 | 7264 | 2 | 2 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| t0027 | 0/0 | 7264 | 2 | 0 | 2 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| t0028 | 0/0 | 7264 | 2 | 0 | 0 | 2 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| t0029 | 0/0 | 7264 | 2 | 0 | 0 | 2 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| t0030 | 0/0 | 7265 | 2 | 1 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| t0031 | 0/0 | 7264 | 2 | 0 | 2 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| t0032 | 0/0 | 7265 | 2 | 0 | 0 | 1 | 0 | 1 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| t0033 | 0/0 | 7264 | 2 | 2 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| t0034 | 0/0 | 7254 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| t0035 | 0/0 | 7252 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| t0036 | 0/0 | 7254 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| t0037 | 0/0 | 7254 | 1 | 0 | 0 | 0 | 0 | 1 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| t0038 | 0/0 | 7264 | 1 | 0 | 0 | 0 | 0 | 1 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| t0039 | 0/0 | 7265 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| t0040 | 0/0 | 7264 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| t0041 | 0/0 | 7265 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| t0042 | 0/0 | 7265 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| t0043 | 0/0 | 7262 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| t0044 | 0/0 | 7264 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| t0045 | 0/0 | 7265 | 1 | 0 | 0 | 0 | 0 | 1 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| t0046 | 0/0 | 7264 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| t0047 | 0/0 | 7264 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| t0048 | 0/0 | 7264 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| t0049 | 0/0 | 7264 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| t0050 | 0/0 | 7264 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| t0051 | 0/0 | 7264 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| t0052 | 0/0 | 7262 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| t0053 | 0/0 | 7265 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| t0054 | 0/0 | 7264 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| t0055 | 0/0 | 7264 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| t0056 | 0/0 | 7264 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| t0057 | 0/0 | 7264 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| t0058 | 0/0 | 7264 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| t0059 | 0/0 | 7264 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| t0060 | 0/0 | 7264 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| t0061 | 0/0 | 7264 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| t0062 | 0/0 | 7264 | 1 | 0 | 0 | 0 | 0 | 1 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| t0063 | 0/0 | 7264 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| t0064 | 0/0 | 7264 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| t0065 | 0/0 | 7265 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| t0066 | 0/0 | 7264 | 1 | 0 | 0 | 0 | 0 | 1 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| t0067 | 0/1 | 7264 | 1 | 0 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| t0068 | 0/0 | 7264 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| t0069 | 0/0 | 7264 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| t0070 | 0/0 | 7264 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| t0071 | 0/0 | 7264 | 1 | 0 | 0 | 0 | 0 | 1 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| t0072 | 0/0 | 7265 | 1 | 0 | 0 | 0 | 0 | 1 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| t0073 | 0/0 | 7264 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| t0074 | 0/0 | 7264 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| t0075 | 0/0 | 7264 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| t0076 | 0/0 | 7264 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| t0077 | 0/0 | 7264 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| t0078 | 1/0 | 7265 | 1 | 0 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| t0079 | 0/0 | 7264 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| t0080 | 0/0 | 7254 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| t0081 | 0/0 | 7264 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| t0082 | 0/0 | 7264 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| t0083 | 0/0 | 7262 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| t0084 | 0/0 | 7264 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| t0085 | 0/0 | 7264 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0007 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0183 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0207 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1224 | 167 | 34 | 36 | 69 | 7 | 21 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| a0001c0002 | 1/1 | 1224 | 105 | 49 | 16 | 24 | 5 | 9 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| a0001c0003 | 0/0 | 1224 | 4 | 4 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| a0001c0004 | 0/0 | 1224 | 3 | 1 | 2 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| a0001c0005 | 0/0 | 1224 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 8487 | 48 | 3 | 13 | 22 | 2 | 8 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| a0001c0001t0002 | 0/0 | 8488 | 18 | 1 | 3 | 10 | 2 | 2 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| a0001c0001t0003 | 0/0 | 8487 | 20 | 2 | 2 | 15 | 0 | 1 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| a0001c0001t0005 | 0/0 | 8487 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| a0001c0001t0006 | 0/0 | 8487 | 2 | 2 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| a0001c0001t0007 | 0/0 | 8487 | 3 | 3 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| a0001c0001t0008 | 0/0 | 8487 | 2 | 0 | 0 | 0 | 0 | 2 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| a0001c0001t0009 | 0/0 | 8487 | 2 | 0 | 2 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| a0001c0001t0010 | 0/0 | 8485 | 2 | 2 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| a0001c0001t0011 | 0/0 | 8485 | 2 | 2 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| a0001c0001t0012 | 0/0 | 8487 | 2 | 2 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| a0001c0001t0014 | 0/0 | 8488 | 2 | 0 | 0 | 0 | 0 | 2 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| a0001c0001t0015 | 0/0 | 8488 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| a0001c0001t0016 | 0/0 | 8487 | 3 | 0 | 0 | 1 | 0 | 2 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| a0001c0001t0017 | 0/0 | 8487 | 2 | 2 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| a0001c0001t0018 | 0/0 | 8487 | 3 | 1 | 2 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| a0001c0001t0019 | 0/0 | 8487 | 3 | 0 | 1 | 2 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| a0001c0001t0020 | 0/0 | 8485 | 3 | 3 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| a0001c0001t0021 | 0/0 | 8485 | 3 | 2 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| a0001c0001t0022 | 0/0 | 8484 | 3 | 0 | 0 | 0 | 3 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| a0001c0001t0024 | 0/0 | 8488 | 2 | 0 | 0 | 2 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| a0001c0001t0025 | 0/0 | 8488 | 2 | 0 | 0 | 2 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| a0001c0001t0027 | 0/0 | 8487 | 2 | 0 | 2 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| a0001c0001t0028 | 0/0 | 8487 | 2 | 0 | 0 | 2 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| a0001c0001t0029 | 0/0 | 8487 | 2 | 0 | 0 | 2 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| a0001c0001t0030 | 0/0 | 8488 | 2 | 1 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| a0001c0001t0031 | 0/0 | 8487 | 2 | 0 | 2 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| a0001c0001t0032 | 0/0 | 8488 | 1 | 0 | 0 | 0 | 0 | 1 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| a0001c0001t0035 | 0/0 | 8475 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| a0001c0001t0036 | 0/0 | 8477 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| a0001c0001t0037 | 0/0 | 8477 | 1 | 0 | 0 | 0 | 0 | 1 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| a0001c0001t0039 | 0/0 | 8488 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| a0001c0001t0040 | 0/0 | 8487 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| a0001c0001t0041 | 0/0 | 8488 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| a0001c0001t0042 | 0/0 | 8488 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| a0001c0001t0044 | 0/0 | 8487 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| a0001c0001t0046 | 0/0 | 8487 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| a0001c0001t0052 | 0/0 | 8485 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| a0001c0001t0053 | 0/0 | 8488 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| a0001c0001t0056 | 0/0 | 8487 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| a0001c0001t0057 | 0/0 | 8487 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| a0001c0001t0058 | 0/0 | 8487 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| a0001c0001t0059 | 0/0 | 8487 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| a0001c0001t0060 | 0/0 | 8487 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| a0001c0001t0061 | 0/0 | 8487 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| a0001c0001t0064 | 0/0 | 8487 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| a0001c0001t0065 | 0/0 | 8488 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| a0001c0001t0066 | 0/0 | 8487 | 1 | 0 | 0 | 0 | 0 | 1 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| a0001c0001t0068 | 0/0 | 8487 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| a0001c0001t0069 | 0/0 | 8487 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| a0001c0001t0070 | 0/0 | 8487 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| a0001c0001t0071 | 0/0 | 8487 | 1 | 0 | 0 | 0 | 0 | 1 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| a0001c0001t0074 | 0/0 | 8487 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| a0001c0001t0077 | 0/0 | 8487 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| a0001c0001t0080 | 0/0 | 8477 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| a0001c0002t0001 | 0/0 | 8487 | 14 | 0 | 4 | 7 | 2 | 1 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| a0001c0002t0002 | 0/0 | 8488 | 17 | 3 | 3 | 10 | 0 | 1 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| a0001c0002t0003 | 0/0 | 8487 | 15 | 2 | 5 | 4 | 3 | 1 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| a0001c0002t0004 | 0/0 | 8487 | 7 | 7 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| a0001c0002t0005 | 0/0 | 8487 | 4 | 4 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| a0001c0002t0006 | 0/0 | 8487 | 2 | 2 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| a0001c0002t0007 | 0/0 | 8487 | 2 | 2 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| a0001c0002t0008 | 0/0 | 8487 | 2 | 0 | 0 | 1 | 0 | 1 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| a0001c0002t0009 | 0/0 | 8487 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| a0001c0002t0010 | 0/0 | 8485 | 2 | 2 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| a0001c0002t0011 | 0/0 | 8485 | 2 | 2 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| a0001c0002t0012 | 0/0 | 8487 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| a0001c0002t0013 | 0/0 | 8487 | 3 | 3 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| a0001c0002t0014 | 0/0 | 8488 | 1 | 0 | 0 | 0 | 0 | 1 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| a0001c0002t0015 | 0/0 | 8488 | 2 | 0 | 2 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| a0001c0002t0017 | 0/0 | 8487 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| a0001c0002t0023 | 0/0 | 8478 | 2 | 2 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| a0001c0002t0026 | 0/0 | 8487 | 2 | 2 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| a0001c0002t0032 | 0/0 | 8488 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| a0001c0002t0033 | 0/0 | 8487 | 2 | 2 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| a0001c0002t0034 | 0/0 | 8477 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| a0001c0002t0038 | 0/0 | 8487 | 1 | 0 | 0 | 0 | 0 | 1 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| a0001c0002t0043 | 0/0 | 8485 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| a0001c0002t0045 | 0/0 | 8488 | 1 | 0 | 0 | 0 | 0 | 1 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| a0001c0002t0047 | 0/0 | 8487 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| a0001c0002t0048 | 0/0 | 8487 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| a0001c0002t0049 | 0/0 | 8487 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| a0001c0002t0050 | 0/0 | 8487 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| a0001c0002t0054 | 0/0 | 8487 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| a0001c0002t0055 | 0/0 | 8487 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| a0001c0002t0062 | 0/0 | 8487 | 1 | 0 | 0 | 0 | 0 | 1 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| a0001c0002t0063 | 0/0 | 8487 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| a0001c0002t0067 | 0/1 | 8487 | 1 | 0 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| a0001c0002t0072 | 0/0 | 8488 | 1 | 0 | 0 | 0 | 0 | 1 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| a0001c0002t0076 | 0/0 | 8487 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| a0001c0002t0078 | 1/0 | 8488 | 1 | 0 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| a0001c0002t0079 | 0/0 | 8487 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| a0001c0002t0081 | 0/0 | 8487 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| a0001c0002t0082 | 0/0 | 8487 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| a0001c0002t0083 | 0/0 | 8485 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| a0001c0002t0084 | 0/0 | 8487 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| a0001c0002t0085 | 0/0 | 8487 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| a0001c0003t0006 | 0/0 | 8487 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| a0001c0003t0051 | 0/0 | 8487 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| a0001c0003t0073 | 0/0 | 8487 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| a0001c0003t0075 | 0/0 | 8487 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| a0001c0004t0002 | 0/0 | 8488 | 2 | 0 | 2 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| a0001c0004t0012 | 0/0 | 8487 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| a0001c0005t0009 | 0/0 | 8487 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | copy fasta | chr12 | 56516820 | 56601193 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0002g0007 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0002g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0003g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0003g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0003g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0003g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0003g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0003g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0003g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0005g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0006g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0006g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0007g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0007g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0007g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0008g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0008g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0009g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0009g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0010g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0010g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0011g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0011g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0012g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0012g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0014g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0014g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0015g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0016g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0016g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0016g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0017g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0017g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0018g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0018g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0018g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0019g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0019g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0019g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0020g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0020g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0020g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0021g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0021g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0021g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0022g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0022g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0022g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0024g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0024g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0025g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0025g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0027g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0027g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0028g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0028g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0029g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0029g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0030g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0030g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0031g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0031g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0032g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0035g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0036g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0037g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0039g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0040g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0041g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0042g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0044g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0046g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0052g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0053g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0056g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0057g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0058g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0059g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0060g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0061g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0064g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0065g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0066g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0068g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0069g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0070g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0071g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0074g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0077g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0001t0080g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0002t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0002t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0002t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0002t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0002t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0002t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0002t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0002t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0002t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0002t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0002t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0002t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0002t0002g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0002t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0002t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0002t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0002t0002g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0002t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0002t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0002t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0002t0003g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0002t0003g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0002t0003g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0002t0003g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0002t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0002t0003g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0002t0003g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0002t0003g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0002t0003g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0002t0003g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0002t0003g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0002t0003g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0002t0003g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0002t0004g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0002t0004g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0002t0004g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0002t0004g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0002t0004g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0002t0004g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0002t0004g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0002t0005g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0002t0005g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0002t0005g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0002t0005g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0002t0006g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0002t0006g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0002t0007g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0002t0007g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0002t0008g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0002t0008g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0002t0009g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0002t0010g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0002t0010g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0002t0011g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0002t0011g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0002t0012g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0002t0013g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0002t0013g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0002t0014g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0002t0015g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0002t0015g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0002t0017g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0002t0023g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0002t0023g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0002t0026g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0002t0026g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0002t0032g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0002t0033g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0002t0033g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0002t0034g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0002t0038g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0002t0043g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0002t0045g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0002t0047g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0002t0048g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0002t0049g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0002t0050g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0002t0054g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0002t0055g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0002t0062g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0002t0063g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0002t0067g0183 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0002t0072g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0002t0076g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0002t0078g0207 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0002t0079g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0002t0081g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0002t0082g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0002t0083g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0002t0084g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0002t0085g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0003t0006g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0003t0051g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0003t0073g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0003t0075g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0004t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0004t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0004t0012g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| a0001c0005t0009g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0022 | EUR | GBR | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG00099 | hp2 | a0001 | c0002 | t0001 | g0269 | EUR | GBR | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG00140 | hp1 | a0001 | c0002 | t0001 | g0270 | EUR | GBR | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG00140 | hp2 | a0001 | c0001 | t0022 | g0041 | EUR | GBR | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG00544 | hp1 | a0001 | c0002 | t0001 | g0265 | EAS | CHS | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG00544 | hp2 | a0001 | c0001 | t0069 | g0221 | EAS | CHS | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG00558 | hp1 | a0001 | c0001 | t0042 | g0138 | EAS | CHS | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG00558 | hp2 | a0001 | c0001 | t0065 | g0062 | EAS | CHS | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0129 | EAS | CHS | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0055 | EAS | CHS | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG00621 | hp2 | a0001 | c0002 | t0003 | g0277 | EAS | CHS | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG00639 | hp1 | a0001 | c0001 | t0053 | g0020 | AMR | PUR | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG00642 | hp2 | a0001 | c0002 | t0015 | g0267 | AMR | PUR | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG00735 | hp2 | a0001 | c0002 | t0003 | g0240 | AMR | PUR | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG01071 | hp1 | a0001 | c0002 | t0003 | g0247 | AMR | PUR | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG01071 | hp2 | a0001 | c0001 | t0027 | g0065 | AMR | PUR | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG01099 | hp1 | a0001 | c0001 | t0003 | g0271 | AMR | PUR | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0050 | AMR | PUR | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG01106 | hp1 | a0001 | c0002 | t0003 | g0250 | AMR | PUR | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG01106 | hp2 | a0001 | c0002 | t0015 | g0246 | AMR | PUR | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG01109 | hp2 | a0001 | c0001 | t0021 | g0189 | AMR | PUR | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG01167 | hp1 | a0001 | c0004 | t0002 | g0197 | AMR | PUR | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0075 | AMR | PUR | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0127 | AMR | PUR | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG01168 | hp2 | a0001 | c0001 | t0031 | g0078 | AMR | PUR | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG01169 | hp1 | a0001 | c0004 | t0002 | g0196 | AMR | PUR | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG01169 | hp2 | a0001 | c0001 | t0031 | g0049 | AMR | PUR | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG01243 | hp1 | a0001 | c0001 | t0080 | g0097 | AMR | PUR | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG01243 | hp2 | a0001 | c0002 | t0003 | g0234 | AMR | PUR | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG01255 | hp1 | a0001 | c0002 | t0002 | g0260 | AMR | CLM | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | CLM | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG01256 | hp2 | a0001 | c0001 | t0003 | g0166 | AMR | CLM | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | CLM | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG01257 | hp2 | a0001 | c0002 | t0076 | g0030 | AMR | CLM | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG01358 | hp1 | a0001 | c0001 | t0009 | g0090 | AMR | CLM | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG01358 | hp2 | a0001 | c0001 | t0018 | g0086 | AMR | CLM | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG01361 | hp1 | a0001 | c0002 | t0002 | g0211 | AMR | CLM | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG01361 | hp2 | a0001 | c0002 | t0001 | g0278 | AMR | CLM | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG01433 | hp1 | a0001 | c0001 | t0018 | g0188 | AMR | CLM | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG01433 | hp2 | a0001 | c0001 | t0044 | g0026 | AMR | CLM | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG01515 | hp1 | a0001 | c0002 | t0003 | g0253 | EUR | IBS | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG01515 | hp2 | a0001 | c0001 | t0022 | g0053 | EUR | IBS | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG01516 | hp1 | a0001 | c0002 | t0003 | g0242 | EUR | IBS | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0135 | EUR | IBS | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG01517 | hp1 | a0001 | c0001 | t0022 | g0068 | EUR | IBS | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG01517 | hp2 | a0001 | c0002 | t0003 | g0252 | EUR | IBS | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG01884 | hp1 | a0001 | c0002 | t0033 | g0217 | AFR | ACB | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG01884 | hp2 | a0001 | c0002 | t0063 | g0146 | AFR | ACB | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG01891 | hp1 | a0001 | c0002 | t0005 | g0108 | AFR | ACB | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG01891 | hp2 | a0001 | c0001 | t0017 | g0179 | AFR | ACB | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG01928 | hp1 | a0001 | c0002 | t0001 | g0276 | AMR | PEL | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG01934 | hp1 | a0001 | c0001 | t0070 | g0088 | AMR | PEL | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG01943 | hp2 | a0001 | c0002 | t0003 | g0248 | AMR | PEL | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG01952 | hp2 | a0001 | c0002 | t0002 | g0085 | AMR | PEL | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG01978 | hp1 | a0001 | c0001 | t0019 | g0139 | AMR | PEL | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0275 | AMR | PEL | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG02004 | hp1 | a0001 | c0001 | t0077 | g0013 | AMR | PEL | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | PEL | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG02055 | hp1 | a0001 | c0002 | t0055 | g0235 | AFR | ACB | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG02055 | hp2 | a0001 | c0002 | t0081 | g0102 | AFR | ACB | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0165 | EAS | KHV | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG02056 | hp2 | a0001 | c0002 | t0002 | g0255 | EAS | KHV | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG02071 | hp1 | a0001 | c0001 | t0003 | g0219 | EAS | KHV | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG02071 | hp2 | a0001 | c0001 | t0030 | g0040 | EAS | KHV | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG02074 | hp1 | a0001 | c0002 | t0002 | g0076 | EAS | KHV | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG02074 | hp2 | a0001 | c0002 | t0054 | g0120 | EAS | KHV | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | KHV | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0079 | EAS | KHV | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG02083 | hp1 | a0001 | c0002 | t0003 | g0116 | EAS | KHV | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | KHV | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG02135 | hp1 | a0001 | c0002 | t0001 | g0245 | EAS | KHV | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG02135 | hp2 | a0001 | c0001 | t0060 | g0059 | EAS | KHV | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG02145 | hp1 | a0001 | c0002 | t0017 | g0093 | AFR | ACB | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG02145 | hp2 | a0001 | c0002 | t0010 | g0123 | AFR | ACB | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG02148 | hp1 | a0001 | c0001 | t0061 | g0016 | AMR | PEL | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG02148 | hp2 | a0001 | c0001 | t0009 | g0136 | AMR | PEL | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG02155 | hp1 | a0001 | c0001 | t0058 | g0220 | EAS | CDX | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG02155 | hp2 | a0001 | c0001 | t0003 | g0066 | EAS | CDX | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG02165 | hp1 | a0001 | c0002 | t0001 | g0119 | EAS | CDX | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG02165 | hp2 | a0001 | c0001 | t0056 | g0019 | EAS | CDX | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG02257 | hp1 | a0001 | c0002 | t0034 | g0100 | AFR | ACB | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG02257 | hp2 | a0001 | c0003 | t0073 | g0094 | AFR | ACB | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG02258 | hp1 | a0001 | c0002 | t0003 | g0238 | AFR | ACB | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG02258 | hp2 | a0001 | c0002 | t0079 | g0212 | AFR | ACB | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG02273 | hp1 | a0001 | c0001 | t0039 | g0143 | AMR | PEL | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG02273 | hp2 | a0001 | c0002 | t0009 | g0017 | AMR | PEL | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG02280 | hp1 | a0001 | c0002 | t0043 | g0279 | AFR | ACB | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | ACB | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG02293 | hp1 | a0001 | c0001 | t0064 | g0126 | AMR | PEL | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG02293 | hp2 | a0001 | c0002 | t0001 | g0272 | AMR | PEL | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG02300 | hp1 | a0001 | c0001 | t0027 | g0028 | AMR | PEL | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG02523 | hp1 | a0001 | c0002 | t0003 | g0048 | EAS | KHV | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG02523 | hp2 | a0001 | c0001 | t0003 | g0035 | EAS | KHV | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG02572 | hp1 | a0001 | c0001 | t0020 | g0112 | AFR | GWD | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG02572 | hp2 | a0001 | c0002 | t0005 | g0109 | AFR | GWD | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0176 | SAS | PJL | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG02602 | hp2 | a0001 | c0001 | t0032 | g0047 | SAS | PJL | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG02615 | hp1 | a0001 | c0002 | t0007 | g0203 | AFR | GWD | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG02615 | hp2 | a0001 | c0001 | t0007 | g0162 | AFR | GWD | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG02622 | hp1 | a0001 | c0003 | t0075 | g0231 | AFR | GWD | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG02622 | hp2 | a0001 | c0002 | t0005 | g0150 | AFR | GWD | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG02630 | hp1 | a0001 | c0002 | t0011 | g0124 | AFR | GWD | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG02630 | hp2 | a0001 | c0001 | t0007 | g0152 | AFR | GWD | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG02647 | hp1 | a0001 | c0003 | t0006 | g0233 | AFR | GWD | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG02647 | hp2 | a0001 | c0001 | t0035 | g0098 | AFR | GWD | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG02683 | hp1 | a0001 | c0001 | t0008 | g0061 | SAS | PJL | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG02683 | hp2 | a0001 | c0002 | t0062 | g0254 | SAS | PJL | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | PJL | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG02698 | hp2 | a0001 | c0002 | t0001 | g0256 | SAS | PJL | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG02717 | hp1 | a0001 | c0002 | t0023 | g0209 | AFR | GWD | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG02717 | hp2 | a0001 | c0002 | t0004 | g0206 | AFR | GWD | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG02723 | hp1 | a0001 | c0001 | t0068 | g0158 | AFR | GWD | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0141 | AFR | GWD | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG02735 | hp1 | a0001 | c0001 | t0014 | g0198 | SAS | PJL | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0052 | SAS | PJL | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG02809 | hp1 | a0001 | c0002 | t0047 | g0091 | AFR | GWD | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG02809 | hp2 | a0001 | c0001 | t0020 | g0111 | AFR | GWD | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG02886 | hp1 | a0001 | c0002 | t0011 | g0204 | AFR | GWD | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG02886 | hp2 | a0001 | c0001 | t0036 | g0096 | AFR | GWD | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG02895 | hp1 | a0001 | c0002 | t0026 | g0208 | AFR | GWD | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG02895 | hp2 | a0001 | c0002 | t0083 | g0104 | AFR | GWD | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG02896 | hp1 | a0001 | c0002 | t0007 | g0214 | AFR | GWD | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG02896 | hp2 | a0001 | c0002 | t0004 | g0223 | AFR | GWD | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG02897 | hp1 | a0001 | c0002 | t0026 | g0205 | AFR | GWD | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG02897 | hp2 | a0001 | c0002 | t0004 | g0224 | AFR | GWD | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG02922 | hp1 | a0001 | c0001 | t0074 | g0155 | AFR | ESN | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG02922 | hp2 | a0001 | c0002 | t0013 | g0001 | AFR | ESN | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG02965 | hp1 | a0001 | c0001 | t0012 | g0156 | AFR | ESN | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG02965 | hp2 | a0001 | c0002 | t0004 | g0215 | AFR | ESN | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG02970 | hp1 | a0001 | c0002 | t0013 | g0001 | AFR | ESN | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG02970 | hp2 | a0001 | c0001 | t0021 | g0167 | AFR | ESN | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG02976 | hp1 | a0001 | c0002 | t0023 | g0099 | AFR | ESN | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG02976 | hp2 | a0001 | c0002 | t0048 | g0106 | AFR | ESN | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG03041 | hp1 | a0001 | c0001 | t0018 | g0187 | AFR | GWD | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG03041 | hp2 | a0001 | c0001 | t0017 | g0230 | AFR | GWD | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG03098 | hp1 | a0001 | c0002 | t0003 | g0200 | AFR | MSL | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG03098 | hp2 | a0001 | c0002 | t0010 | g0194 | AFR | MSL | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG03130 | hp1 | a0001 | c0001 | t0011 | g0159 | AFR | ESN | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG03130 | hp2 | a0001 | c0002 | t0033 | g0210 | AFR | ESN | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG03139 | hp1 | a0001 | c0003 | t0051 | g0191 | AFR | ESN | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG03139 | hp2 | a0001 | c0001 | t0007 | g0122 | AFR | ESN | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG03195 | hp1 | a0001 | c0002 | t0006 | g0092 | AFR | ESN | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG03195 | hp2 | a0001 | c0004 | t0012 | g0195 | AFR | ESN | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG03209 | hp1 | a0001 | c0002 | t0006 | g0202 | AFR | MSL | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG03209 | hp2 | a0001 | c0001 | t0020 | g0113 | AFR | MSL | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG03225 | hp1 | a0001 | c0001 | t0012 | g0114 | AFR | MSL | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG03225 | hp2 | a0001 | c0002 | t0005 | g0236 | AFR | MSL | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG03453 | hp1 | a0001 | c0001 | t0011 | g0201 | AFR | MSL | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG03453 | hp2 | a0001 | c0001 | t0005 | g0229 | AFR | MSL | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG03486 | hp1 | a0001 | c0001 | t0003 | g0128 | AFR | MSL | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG03486 | hp2 | a0001 | c0002 | t0085 | g0103 | AFR | MSL | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG03491 | hp1 | a0001 | c0002 | t0008 | g0239 | SAS | PJL | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0173 | SAS | PJL | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG03516 | hp1 | a0001 | c0002 | t0082 | g0105 | AFR | ESN | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG03516 | hp2 | a0001 | c0002 | t0050 | g0218 | AFR | ESN | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG03579 | hp1 | a0001 | c0001 | t0046 | g0087 | AFR | MSL | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG03579 | hp2 | a0001 | c0002 | t0002 | g0232 | AFR | MSL | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG03654 | hp1 | a0001 | c0001 | t0066 | g0182 | SAS | PJL | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG03654 | hp2 | a0001 | c0001 | t0037 | g0095 | SAS | PJL | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG03688 | hp1 | a0001 | c0001 | t0014 | g0264 | SAS | STU | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG03688 | hp2 | a0001 | c0002 | t0038 | g0262 | SAS | STU | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG03831 | hp1 | a0001 | c0002 | t0072 | g0259 | SAS | BEB | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG03831 | hp2 | a0001 | c0001 | t0008 | g0181 | SAS | BEB | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0144 | SAS | BEB | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG03834 | hp2 | a0001 | c0002 | t0003 | g0268 | SAS | BEB | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0051 | SAS | BEB | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG03927 | hp2 | a0001 | c0001 | t0071 | g0192 | SAS | BEB | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG04115 | hp1 | a0001 | c0001 | t0016 | g0193 | SAS | STU | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG04115 | hp2 | a0001 | c0002 | t0045 | g0261 | SAS | STU | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0190 | SAS | BEB | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG04184 | hp2 | a0001 | c0001 | t0016 | g0082 | SAS | BEB | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG04204 | hp1 | a0001 | c0002 | t0002 | g0243 | SAS | STU | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0070 | SAS | STU | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0149 | SAS | STU | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG04228 | hp2 | a0001 | c0002 | t0014 | g0168 | SAS | STU | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| NA18522 | hp1 | a0001 | c0002 | t0012 | g0226 | AFR | YRI | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| NA18522 | hp2 | a0001 | c0001 | t0010 | g0225 | AFR | YRI | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| NA18612 | hp1 | a0001 | c0001 | t0057 | g0089 | EAS | CHB | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| NA18612 | hp2 | a0001 | c0001 | t0003 | g0064 | EAS | CHB | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| NA18747 | hp1 | a0001 | c0001 | t0003 | g0161 | EAS | CHB | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | CHB | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| NA18906 | hp1 | a0001 | c0001 | t0010 | g0227 | AFR | YRI | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| NA18906 | hp2 | a0001 | c0002 | t0049 | g0213 | AFR | YRI | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| NA18940 | hp2 | a0001 | c0002 | t0002 | g0257 | EAS | JPT | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| NA18942 | hp1 | a0001 | c0001 | t0025 | g0175 | EAS | JPT | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| NA18942 | hp2 | a0001 | c0001 | t0003 | g0057 | EAS | JPT | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| NA18944 | hp1 | a0001 | c0001 | t0019 | g0018 | EAS | JPT | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| NA18944 | hp2 | a0001 | c0002 | t0003 | g0241 | EAS | JPT | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| NA18947 | hp2 | a0001 | c0002 | t0002 | g0244 | EAS | JPT | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| NA18951 | hp1 | a0001 | c0001 | t0029 | g0074 | EAS | JPT | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| NA18954 | hp1 | a0001 | c0005 | t0009 | g0134 | EAS | JPT | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| NA18954 | hp2 | a0001 | c0001 | t0040 | g0011 | EAS | JPT | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| NA18960 | hp2 | a0001 | c0001 | t0003 | g0164 | EAS | JPT | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| NA18963 | hp1 | a0001 | c0002 | t0001 | g0249 | EAS | JPT | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| NA18963 | hp2 | a0001 | c0002 | t0002 | g0058 | EAS | JPT | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| NA18964 | hp1 | a0001 | c0002 | t0001 | g0263 | EAS | JPT | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| NA18966 | hp1 | a0001 | c0002 | t0032 | g0266 | EAS | JPT | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| NA18971 | hp1 | a0001 | c0002 | t0002 | g0274 | EAS | JPT | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| NA18973 | hp1 | a0001 | c0002 | t0001 | g0258 | EAS | JPT | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| NA18975 | hp2 | a0001 | c0001 | t0019 | g0039 | EAS | JPT | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| NA18987 | hp1 | a0001 | c0001 | t0016 | g0037 | EAS | JPT | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| NA18987 | hp2 | a0001 | c0001 | t0024 | g0171 | EAS | JPT | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| NA18990 | hp1 | a0001 | c0001 | t0003 | g0042 | EAS | JPT | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| NA18998 | hp2 | a0001 | c0002 | t0002 | g0237 | EAS | JPT | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| NA19000 | hp1 | a0001 | c0001 | t0024 | g0148 | EAS | JPT | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| NA19000 | hp2 | a0001 | c0001 | t0028 | g0027 | EAS | JPT | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| NA19007 | hp2 | a0001 | c0002 | t0001 | g0273 | EAS | JPT | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| NA19009 | hp1 | a0001 | c0001 | t0003 | g0163 | EAS | JPT | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| NA19010 | hp1 | a0001 | c0001 | t0041 | g0184 | EAS | JPT | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| NA19010 | hp2 | a0001 | c0001 | t0003 | g0222 | EAS | JPT | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| NA19011 | hp1 | a0001 | c0001 | t0025 | g0080 | EAS | JPT | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| NA19012 | hp1 | a0001 | c0001 | t0003 | g0071 | EAS | JPT | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| NA19030 | hp1 | a0001 | c0002 | t0004 | g0216 | AFR | LWK | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| NA19030 | hp2 | a0001 | c0002 | t0002 | g0185 | AFR | LWK | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0174 | AFR | LWK | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| NA19043 | hp2 | a0001 | c0002 | t0084 | g0107 | AFR | LWK | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| NA19057 | hp1 | a0001 | c0002 | t0002 | g0115 | EAS | JPT | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| NA19057 | hp2 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| NA19063 | hp2 | a0001 | c0001 | t0029 | g0083 | EAS | JPT | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| NA19065 | hp2 | a0001 | c0002 | t0008 | g0251 | EAS | JPT | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| NA19066 | hp2 | a0001 | c0001 | t0003 | g0063 | EAS | JPT | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| NA19070 | hp1 | a0001 | c0001 | t0059 | g0060 | EAS | JPT | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| NA19070 | hp2 | a0001 | c0001 | t0003 | g0131 | EAS | JPT | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| NA19079 | hp1 | a0001 | c0002 | t0002 | g0118 | EAS | JPT | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| NA19085 | hp1 | a0001 | c0001 | t0028 | g0032 | EAS | JPT | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| NA19085 | hp2 | a0001 | c0002 | t0002 | g0117 | EAS | JPT | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| NA19240 | hp1 | a0001 | c0002 | t0002 | g0084 | AFR | YRI | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| NA19240 | hp2 | a0001 | c0001 | t0052 | g0069 | AFR | YRI | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0145 | EUR | TSI | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0007 | EUR | TSI | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | GIH | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0029 | SAS | GIH | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG02559 | hp1 | a0001 | c0002 | t0004 | g0186 | AFR | ACB | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG02559 | hp2 | a0001 | c0002 | t0013 | g0199 | AFR | ACB | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG03471 | hp1 | a0001 | c0001 | t0021 | g0147 | AFR | MSL | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG03471 | hp2 | a0001 | c0001 | t0006 | g0180 | AFR | MSL | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG06807 | hp1 | a0001 | c0002 | t0004 | g0228 | AFR | USA | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | USA | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| NA20300 | hp1 | a0001 | c0001 | t0030 | g0044 | AFR | USA | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| NA20300 | hp2 | a0001 | c0001 | t0015 | g0172 | AFR | USA | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| NA21309 | hp1 | a0001 | c0001 | t0006 | g0157 | AFR | LWK | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | LWK | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0067 | g0183 | REF | REF | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| homoSapiens_grch38 | hp1 | a0001 | c0002 | t0078 | g0207 | REF | REF | RBMS2_chr12_56516820_56601193 | RBMS2 | chr12 | 56516820 | 56601193 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:56562429
|
T | C | 2 | a0001c0001a0001c0005 | 168 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(165): Show |
synonymous_variant | LOW | c.79T>C | p.Leu27Leu | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 2/14 | 283/8488 | 79/1224 | 27/407 | chr12 | 56562429 | ||
| chr12:56587586
|
C | G | 1 | a0001c0004 | 3 | HG01167.hp1 HG01169.hp1 HG03195.hp2 |
synonymous_variant | LOW | c.984C>G | p.Pro328Pro | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 11/14 | 1188/8488 | 984/1224 | 328/407 | chr12 | 56587586 | ||
| chr12:56588329
|
C | T | 1 | a0001c0003 | 4 | HG02257.hp2 HG02622.hp1 HG02647.hp1 others(1): Show |
synonymous_variant | LOW | c.1098C>T | p.Tyr366Tyr | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 12/14 | 1302/8488 | 1098/1224 | 366/407 | chr12 | 56588329 | ||
| chr12:56588967
|
C | T | 1 | a0001c0005 | 1 | NA18954.hp1 | synonymous_variant | LOW | c.1179C>T | p.Asp393Asp | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 13/14 | 1383/8488 | 1179/1224 | 393/407 | chr12 | 56588967 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:56521840
|
C | T | 5 | a0001c0002t0081a0001c0002t0082a0001c0002t0083others(2): Show | 5 | HG02055.hp2 HG02895.hp2 HG03486.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-184C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/14 | 184 | chr12 | 56521840 | |||||
| chr12:56521861
|
C | T | 1 | a0001c0001t0080 | 1 | HG01243.hp1 | 5_prime_UTR_variant | MODIFIER | c.-163C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/14 | 163 | chr12 | 56521861 | |||||
| chr12:56521977
|
TTCTCTCT others(3): Show |
T | 6 | a0001c0001t0035a0001c0001t0036a0001c0001t0037others(3): Show | 7 | HG01243.hp1 HG02257.hp1 HG02647.hp2 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-36_-27delTCTCTCTC others(2): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/14 | 27 | INFO_REALIGN_3_PRIME | chr12 | 56521977 | ||||
| chr12:56521998
|
G | A | 102 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(99): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
5_prime_UTR_variant | MODIFIER | c.-26G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/14 | 26 | chr12 | 56521998 | |||||
| chr12:56589162
|
G | A | 1 | a0001c0001t0024 | 2 | NA18987.hp2 NA19000.hp1 |
3_prime_UTR_variant | MODIFIER | c.*29G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 14/14 | 150 | chr12 | 56589162 | |||||
| chr12:56589458
|
A | T | 1 | a0001c0001t0077 | 1 | HG02004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*325A>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 14/14 | 446 | chr12 | 56589458 | |||||
| chr12:56589468
|
C | T | 69 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(66): Show | 192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
3_prime_UTR_variant | MODIFIER | c.*335C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 14/14 | 456 | chr12 | 56589468 | |||||
| chr12:56589497
|
G | A | 1 | a0001c0003t0051 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*364G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 14/14 | 485 | chr12 | 56589497 | |||||
| chr12:56589640
|
A | G | 69 | a0001c0001t0002a0001c0001t0005a0001c0001t0006others(66): Show | 139 | HG00140.hp2 HG00558.hp1 HG00597.hp1 others(136): Show |
3_prime_UTR_variant | MODIFIER | c.*507A>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 14/14 | 628 | chr12 | 56589640 | |||||
| chr12:56589641
|
T | C | 26 | a0001c0001t0002a0001c0001t0009a0001c0001t0014others(23): Show | 68 | HG00558.hp1 HG00597.hp1 HG00642.hp2 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*508T>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 14/14 | 629 | chr12 | 56589641 | |||||
| chr12:56589663
|
T | C | 1 | a0001c0001t0046 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*530T>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 14/14 | 651 | chr12 | 56589663 | |||||
| chr12:56589958
|
A | G | 1 | a0001c0001t0069 | 1 | HG00544.hp2 | 3_prime_UTR_variant | MODIFIER | c.*825A>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 14/14 | 946 | chr12 | 56589958 | |||||
| chr12:56590034
|
C | T | 1 | a0001c0002t0038 | 1 | HG03688.hp2 | 3_prime_UTR_variant | MODIFIER | c.*901C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 14/14 | 1022 | chr12 | 56590034 | |||||
| chr12:56590261
|
G | A | 7 | a0001c0001t0010a0001c0001t0020a0001c0001t0021others(4): Show | 13 | HG01109.hp2 HG02145.hp2 HG02572.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1128G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 14/14 | 1249 | chr12 | 56590261 | |||||
| chr12:56590290
|
C | T | 1 | a0001c0001t0068 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1157C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 14/14 | 1278 | chr12 | 56590290 | |||||
| chr12:56590822
|
C | T | 51 | a0001c0001t0001a0001c0001t0003a0001c0001t0007others(48): Show | 165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
3_prime_UTR_variant | MODIFIER | c.*1689C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 14/14 | 1810 | chr12 | 56590822 | |||||
| chr12:56590967
|
C | T | 8 | a0001c0001t0010a0001c0001t0020a0001c0001t0021others(5): Show | 14 | HG01109.hp2 HG02145.hp2 HG02280.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1834C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 14/14 | 1955 | chr12 | 56590967 | |||||
| chr12:56591169
|
G | C | 1 | a0001c0001t0046 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2036G>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 14/14 | 2157 | chr12 | 56591169 | |||||
| chr12:56591316
|
C | T | 2 | a0001c0001t0011a0001c0002t0011 | 4 | HG02630.hp1 HG02886.hp1 HG03130.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2183C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 14/14 | 2304 | chr12 | 56591316 | |||||
| chr12:56591381
|
G | A | 5 | a0001c0002t0004a0001c0002t0026a0001c0002t0033others(2): Show | 13 | HG01884.hp1 HG02257.hp1 HG02257.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2248G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 14/14 | 2369 | chr12 | 56591381 | |||||
| chr12:56591393
|
G | A | 1 | a0001c0002t0054 | 1 | HG02074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2260G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 14/14 | 2381 | chr12 | 56591393 | |||||
| chr12:56591673
|
G | A | 1 | a0001c0001t0027 | 2 | HG01071.hp2 HG02300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2540G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 14/14 | 2661 | chr12 | 56591673 | |||||
| chr12:56591774
|
C | A | 25 | a0001c0001t0002a0001c0001t0009a0001c0001t0010others(22): Show | 68 | HG00597.hp1 HG00639.hp1 HG01099.hp2 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*2641C>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 14/14 | 2762 | chr12 | 56591774 | |||||
| chr12:56591776
|
A | C | 9 | a0001c0001t0006a0001c0001t0019a0001c0001t0036others(6): Show | 13 | HG01978.hp1 HG02258.hp2 HG02647.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2643A>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 14/14 | 2764 | chr12 | 56591776 | |||||
| chr12:56591899
|
G | A | 1 | a0001c0002t0033 | 2 | HG01884.hp1 HG03130.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2766G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 14/14 | 2887 | chr12 | 56591899 | |||||
| chr12:56592218
|
T | C | 1 | a0001c0001t0020 | 3 | HG02572.hp1 HG02809.hp2 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3085T>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 14/14 | 3206 | chr12 | 56592218 | |||||
| chr12:56592499
|
G | A | 1 | a0001c0001t0056 | 1 | HG02165.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3366G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 14/14 | 3487 | chr12 | 56592499 | |||||
| chr12:56592667
|
T | C | 1 | a0001c0003t0075 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3534T>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 14/14 | 3655 | chr12 | 56592667 | |||||
| chr12:56592702
|
G | A | 5 | a0001c0001t0022a0001c0001t0037a0001c0001t0044others(2): Show | 7 | HG00140.hp2 HG01243.hp1 HG01433.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3569G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 14/14 | 3690 | chr12 | 56592702 | |||||
| chr12:56592730
|
C | T | 1 | a0001c0002t0082 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3597C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 14/14 | 3718 | chr12 | 56592730 | |||||
| chr12:56592882
|
C | T | 1 | a0001c0001t0066 | 1 | HG03654.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3749C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 14/14 | 3870 | chr12 | 56592882 | |||||
| chr12:56593146
|
G | T | 2 | a0001c0001t0014a0001c0002t0014 | 3 | HG02735.hp1 HG03688.hp1 HG04228.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4013G>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 14/14 | 4134 | chr12 | 56593146 | |||||
| chr12:56593286
|
G | C | 20 | a0001c0001t0001a0001c0001t0008a0001c0001t0016others(17): Show | 89 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(86): Show |
3_prime_UTR_variant | MODIFIER | c.*4153G>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 14/14 | 4274 | chr12 | 56593286 | |||||
| chr12:56593395
|
A | G | 55 | a0001c0001t0002a0001c0001t0007a0001c0001t0009others(52): Show | 113 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(110): Show |
3_prime_UTR_variant | MODIFIER | c.*4262A>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 14/14 | 4383 | chr12 | 56593395 | |||||
| chr12:56593784
|
T | C | 1 | a0001c0001t0028 | 2 | NA19000.hp2 NA19085.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4651T>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 14/14 | 4772 | chr12 | 56593784 | |||||
| chr12:56593944
|
A | G | 1 | a0001c0001t0031 | 2 | HG01168.hp2 HG01169.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4811A>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 14/14 | 4932 | chr12 | 56593944 | |||||
| chr12:56593989
|
T | C | 1 | a0001c0001t0039 | 1 | HG02273.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4856T>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 14/14 | 4977 | chr12 | 56593989 | |||||
| chr12:56594026
|
C | G | 3 | a0001c0001t0007a0001c0002t0007a0001c0002t0050 | 6 | HG02615.hp1 HG02615.hp2 HG02630.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4893C>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 14/14 | 5014 | chr12 | 56594026 | |||||
| chr12:56594207
|
T | C | 1 | a0001c0002t0076 | 1 | HG01257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5074T>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 14/14 | 5195 | chr12 | 56594207 | |||||
| chr12:56594320
|
A | G | 1 | a0001c0001t0061 | 1 | HG02148.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5187A>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 14/14 | 5308 | chr12 | 56594320 | |||||
| chr12:56594424
|
C | A | 1 | a0001c0002t0062 | 1 | HG02683.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5291C>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 14/14 | 5412 | chr12 | 56594424 | |||||
| chr12:56594515
|
C | G | 1 | a0001c0001t0060 | 1 | HG02135.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5382C>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 14/14 | 5503 | chr12 | 56594515 | |||||
| chr12:56594558
|
C | A | 64 | a0001c0001t0002a0001c0001t0005a0001c0001t0006others(61): Show | 133 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(130): Show |
3_prime_UTR_variant | MODIFIER | c.*5425C>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 14/14 | 5546 | chr12 | 56594558 | |||||
| chr12:56594821
|
G | A | 2 | a0001c0001t0070a0001c0002t0063 | 2 | HG01884.hp2 HG01934.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5688G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 14/14 | 5809 | chr12 | 56594821 | |||||
| chr12:56594972
|
T | C | 1 | a0001c0002t0047 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5839T>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 14/14 | 5960 | chr12 | 56594972 | |||||
| chr12:56594972
|
TAC | T | 10 | a0001c0001t0010a0001c0001t0011a0001c0001t0020others(7): Show | 18 | HG01109.hp2 HG02145.hp2 HG02280.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*5841_*5842delCA | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 14/14 | 5962 | INFO_REALIGN_3_PRIME | chr12 | 56594972 | ||||
| chr12:56594976
|
G | C | 1 | a0001c0002t0047 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5843G>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 14/14 | 5964 | chr12 | 56594976 | |||||
| chr12:56594978
|
G | C | 1 | a0001c0002t0047 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5845G>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 14/14 | 5966 | chr12 | 56594978 | |||||
| chr12:56594980
|
T | A | 1 | a0001c0002t0047 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5847T>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 14/14 | 5968 | chr12 | 56594980 | |||||
| chr12:56594983
|
C | T | 1 | a0001c0002t0047 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5850C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 14/14 | 5971 | chr12 | 56594983 | |||||
| chr12:56595063
|
T | C | 1 | a0001c0001t0057 | 1 | NA18612.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5930T>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 14/14 | 6051 | chr12 | 56595063 | |||||
| chr12:56595318
|
C | T | 1 | a0001c0001t0077 | 1 | HG02004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6185C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 14/14 | 6306 | chr12 | 56595318 | |||||
| chr12:56595433
|
ACTT | A | 1 | a0001c0001t0022 | 3 | HG00140.hp2 HG01515.hp2 HG01517.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6306_*6308delTCT | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 14/14 | 6427 | INFO_REALIGN_3_PRIME | chr12 | 56595433 | ||||
| chr12:56595568
|
C | CT | 20 | a0001c0001t0002a0001c0001t0014a0001c0001t0015others(17): Show | 60 | HG00558.hp1 HG00558.hp2 HG00597.hp1 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*6447dupT | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 14/14 | 6569 | INFO_REALIGN_3_PRIME | chr12 | 56595568 | ||||
| chr12:56595654
|
A | G | 1 | a0001c0001t0059 | 1 | NA19070.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6521A>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 14/14 | 6642 | chr12 | 56595654 | |||||
| chr12:56595760
|
C | G | 1 | a0001c0001t0029 | 2 | NA18951.hp1 NA19063.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6627C>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 14/14 | 6748 | chr12 | 56595760 | |||||
| chr12:56595824
|
C | T | 1 | a0001c0001t0064 | 1 | HG02293.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6691C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 14/14 | 6812 | chr12 | 56595824 | |||||
| chr12:56595945
|
GT | G | 102 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(99): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
3_prime_UTR_variant | MODIFIER | c.*6820delT | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 14/14 | 6941 | INFO_REALIGN_3_PRIME | chr12 | 56595945 | ||||
| chr12:56595954
|
A | T | 1 | a0001c0001t0058 | 1 | HG02155.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6821A>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 14/14 | 6942 | chr12 | 56595954 | |||||
| chr12:56595956
|
TCAACAAC others(56): Show |
T | 1 | a0001c0001t0058 | 1 | HG02155.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6824_*6886delCAAC others(59): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 14/14 | 6945 | chr12 | 56595956 | |||||
| chr12:56596024
|
T | TTTTTTTT others(55): Show |
1 | a0001c0001t0058 | 1 | HG02155.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6892_*6893insTTTT others(58): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 14/14 | 7014 | INFO_REALIGN_3_PRIME | chr12 | 56596024 | ||||
| chr12:56596026
|
C | T | 1 | a0001c0001t0058 | 1 | HG02155.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6893C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 14/14 | 7014 | chr12 | 56596026 | |||||
| chr12:56596028
|
C | G | 1 | a0001c0001t0058 | 1 | HG02155.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6895C>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 14/14 | 7016 | chr12 | 56596028 | |||||
| chr12:56596030
|
A | G | 1 | a0001c0001t0058 | 1 | HG02155.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6897A>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 14/14 | 7018 | chr12 | 56596030 | |||||
| chr12:56596031
|
G | T | 1 | a0001c0001t0058 | 1 | HG02155.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6898G>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 14/14 | 7019 | chr12 | 56596031 | |||||
| chr12:56596032
|
A | T | 1 | a0001c0001t0058 | 1 | HG02155.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6899A>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 14/14 | 7020 | chr12 | 56596032 | |||||
| chr12:56596033
|
C | T | 1 | a0001c0001t0058 | 1 | HG02155.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6900C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 14/14 | 7021 | chr12 | 56596033 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:56522830
|
T | C | 82 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(79): Show | 82 | HG00099.hp1 HG00140.hp2 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.66+741T>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56522830 | ||||||
| chr12:56522858
|
T | C | 1 | a0001c0002t0002g0084 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.66+769T>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56522858 | ||||||
| chr12:56522969
|
A | C | 1 | a0001c0002t0043g0279 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.66+880A>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56522969 | ||||||
| chr12:56523132
|
G | A | 1 | a0001c0001t0001g0002 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.66+1043G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56523132 | ||||||
| chr12:56523503
|
G | T | 7 | a0001c0002t0001g0272a0001c0002t0001g0273a0001c0002t0001g0275others(4): Show | 7 | HG00621.hp2 HG01361.hp2 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.66+1414G>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56523503 | ||||||
| chr12:56523581
|
C | A | 1 | a0001c0002t0002g0085 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.66+1492C>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56523581 | ||||||
| chr12:56523606
|
C | T | 44 | a0001c0001t0003g0271a0001c0001t0014g0264a0001c0002t0001g0245others(41): Show | 44 | HG00099.hp2 HG00140.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.66+1517C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56523606 | ||||||
| chr12:56523941
|
T | C | 1 | a0001c0001t0018g0086 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.66+1852T>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56523941 | ||||||
| chr12:56524187
|
A | C | 1 | a0001c0002t0055g0235 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.66+2098A>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56524187 | ||||||
| chr12:56524284
|
C | A | 1 | a0001c0001t0046g0087 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.66+2195C>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56524284 | ||||||
| chr12:56524347
|
T | C | 3 | a0001c0001t0009g0090a0001c0001t0057g0089a0001c0001t0070g0088 | 3 | HG01358.hp1 HG01934.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.66+2258T>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56524347 | ||||||
| chr12:56524393
|
C | T | 12 | a0001c0001t0005g0229a0001c0001t0010g0225a0001c0001t0010g0227others(9): Show | 12 | HG01243.hp2 HG02622.hp1 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.66+2304C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56524393 | ||||||
| chr12:56524422
|
CT | C | 153 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(150): Show | 153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.66+2346delT | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56524422 | |||||
| chr12:56524449
|
G | A | 44 | a0001c0001t0003g0271a0001c0001t0014g0264a0001c0002t0001g0245others(41): Show | 44 | HG00099.hp2 HG00140.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.66+2360G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56524449 | ||||||
| chr12:56524476
|
G | A | 1 | a0001c0002t0055g0235 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.66+2387G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56524476 | ||||||
| chr12:56524666
|
T | C | 12 | a0001c0001t0005g0229a0001c0001t0010g0225a0001c0001t0010g0227others(9): Show | 12 | HG01243.hp2 HG02622.hp1 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.66+2577T>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56524666 | ||||||
| chr12:56524782
|
T | C | 160 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(157): Show | 160 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(157): Show |
intron_variant | MODIFIER | c.66+2693T>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56524782 | ||||||
| chr12:56524814
|
G | T | 3 | a0001c0002t0023g0099a0001c0002t0034g0100a0001c0002t0055g0235 | 3 | HG02055.hp1 HG02257.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.66+2725G>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56524814 | ||||||
| chr12:56524862
|
G | A | 1 | a0001c0002t0005g0109 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.66+2773G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56524862 | ||||||
| chr12:56524876
|
C | T | 4 | a0001c0001t0003g0219a0001c0001t0003g0222a0001c0001t0058g0220others(1): Show | 4 | HG00544.hp2 HG02071.hp1 HG02155.hp1 others(1): Show |
intron_variant | MODIFIER | c.66+2787C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56524876 | ||||||
| chr12:56525013
|
C | A | 1 | a0001c0001t0001g0110 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.66+2924C>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56525013 | ||||||
| chr12:56525050
|
T | G | 86 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(83): Show | 86 | HG00099.hp1 HG00140.hp2 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.66+2961T>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56525050 | ||||||
| chr12:56525284
|
C | G | 4 | a0001c0002t0002g0232a0001c0002t0003g0234a0001c0003t0006g0233others(1): Show | 4 | HG01243.hp2 HG02622.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.66+3195C>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56525284 | ||||||
| chr12:56525325
|
G | A | 3 | a0001c0001t0020g0111a0001c0001t0020g0112a0001c0001t0020g0113 | 3 | HG02572.hp1 HG02809.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.66+3236G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56525325 | ||||||
| chr12:56525403
|
G | T | 1 | a0001c0002t0050g0218 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.66+3314G>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56525403 | ||||||
| chr12:56525612
|
C | A | 1 | a0001c0001t0012g0114 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.66+3523C>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56525612 | ||||||
| chr12:56525971
|
A | G | 1 | a0001c0002t0055g0235 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.66+3882A>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56525971 | ||||||
| chr12:56526293
|
T | C | 2 | a0001c0002t0004g0223a0001c0002t0004g0224 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.66+4204T>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56526293 | ||||||
| chr12:56526320
|
T | TAAATA | 6 | a0001c0002t0002g0232a0001c0002t0003g0234a0001c0002t0004g0223others(3): Show | 6 | HG01243.hp2 HG02622.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.66+4250_66+4254dup others(5): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56526320 | |||||
| chr12:56526320
|
T | TAAATAAA others(8): Show |
6 | a0001c0001t0005g0229a0001c0001t0010g0225a0001c0001t0010g0227others(3): Show | 6 | HG03041.hp2 HG03453.hp2 HG06807.hp1 others(3): Show |
intron_variant | MODIFIER | c.66+4240_66+4254dup others(15): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56526320 | |||||
| chr12:56526601
|
G | A | 1 | a0001c0001t0001g0003 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.66+4512G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56526601 | ||||||
| chr12:56526618
|
T | G | 90 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(87): Show | 90 | HG00099.hp1 HG00140.hp2 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.66+4529T>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56526618 | ||||||
| chr12:56526668
|
T | TA | 245 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(242): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.66+4595dupA | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56526668 | |||||
| chr12:56526727
|
A | G | 1 | a0001c0001t0002g0079 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.66+4638A>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56526727 | ||||||
| chr12:56526812
|
C | T | 2 | a0001c0002t0017g0093a0001c0003t0073g0094 | 2 | HG02145.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.66+4723C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56526812 | ||||||
| chr12:56526817
|
A | G | 1 | a0001c0002t0055g0235 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.66+4728A>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56526817 | ||||||
| chr12:56527155
|
T | C | 44 | a0001c0001t0003g0271a0001c0001t0014g0264a0001c0002t0001g0245others(41): Show | 44 | HG00099.hp2 HG00140.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.66+5066T>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56527155 | ||||||
| chr12:56527520
|
G | A | 44 | a0001c0001t0003g0271a0001c0001t0014g0264a0001c0002t0001g0245others(41): Show | 44 | HG00099.hp2 HG00140.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.66+5431G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56527520 | ||||||
| chr12:56527634
|
A | G | 44 | a0001c0001t0003g0271a0001c0001t0014g0264a0001c0002t0001g0245others(41): Show | 44 | HG00099.hp2 HG00140.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.66+5545A>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56527634 | ||||||
| chr12:56527646
|
A | G | 1 | a0001c0002t0005g0109 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.66+5557A>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56527646 | ||||||
| chr12:56527752
|
A | AC | 30 | a0001c0001t0001g0077a0001c0001t0001g0110a0001c0001t0001g0190others(27): Show | 30 | HG00099.hp2 HG00140.hp1 HG00544.hp1 others(27): Show |
intron_variant | MODIFIER | c.66+5670dupC | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56527752 | |||||
| chr12:56528006
|
T | C | 1 | a0001c0002t0010g0194 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.66+5917T>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56528006 | ||||||
| chr12:56528025
|
G | A | 1 | a0001c0002t0055g0235 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.66+5936G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56528025 | ||||||
| chr12:56528182
|
C | T | 87 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(84): Show | 87 | HG00099.hp1 HG00140.hp2 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.66+6093C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56528182 | ||||||
| chr12:56528249
|
C | CA | 157 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(154): Show | 157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): Show |
intron_variant | MODIFIER | c.66+6175dupA | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56528249 | |||||
| chr12:56528249
|
C | CAA | 8 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0002t0017g0093others(5): Show | 8 | HG00735.hp1 HG01952.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.66+6174_66+6175dup others(2): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56528249 | |||||
| chr12:56528346
|
G | T | 1 | a0001c0001t0002g0073 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.66+6257G>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56528346 | ||||||
| chr12:56528444
|
A | G | 4 | a0001c0002t0081g0102a0001c0002t0082g0105a0001c0002t0083g0104others(1): Show | 4 | HG02055.hp2 HG02895.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.66+6355A>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56528444 | ||||||
| chr12:56528455
|
TC | T | 5 | a0001c0002t0004g0215a0001c0002t0004g0216a0001c0002t0007g0214others(2): Show | 5 | HG02280.hp1 HG02896.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.66+6367delC | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56528455 | ||||||
| chr12:56528686
|
G | A | 2 | a0001c0002t0023g0099a0001c0002t0034g0100 | 2 | HG02257.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.66+6597G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56528686 | ||||||
| chr12:56528702
|
G | A | 1 | a0001c0002t0081g0102 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.66+6613G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56528702 | ||||||
| chr12:56528745
|
T | C | 3 | a0001c0004t0002g0196a0001c0004t0002g0197a0001c0004t0012g0195 | 3 | HG01167.hp1 HG01169.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.66+6656T>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56528745 | ||||||
| chr12:56528793
|
G | A | 1 | a0001c0002t0002g0085 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.66+6704G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56528793 | ||||||
| chr12:56528991
|
G | A | 1 | a0001c0001t0002g0007 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.66+6902G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56528991 | ||||||
| chr12:56529054
|
G | C | 253 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(250): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.66+6965G>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56529054 | ||||||
| chr12:56529127
|
C | T | 1 | a0001c0001t0001g0072 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.66+7038C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56529127 | ||||||
| chr12:56529206
|
A | G | 87 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(84): Show | 87 | HG00099.hp1 HG00140.hp2 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.66+7117A>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56529206 | ||||||
| chr12:56529221
|
A | G | 253 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(250): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.66+7132A>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56529221 | ||||||
| chr12:56529266
|
T | C | 8 | a0001c0002t0002g0084a0001c0002t0005g0108a0001c0002t0048g0106others(5): Show | 8 | HG01891.hp1 HG02055.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.66+7177T>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56529266 | ||||||
| chr12:56529451
|
C | A | 3 | a0001c0001t0009g0090a0001c0001t0057g0089a0001c0001t0070g0088 | 3 | HG01358.hp1 HG01934.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.66+7362C>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56529451 | ||||||
| chr12:56529563
|
CAACAACA others(8): Show |
C | 1 | a0001c0001t0046g0087 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.66+7489_66+7503del others(15): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56529563 | |||||
| chr12:56529630
|
G | A | 3 | a0001c0001t0007g0122a0001c0002t0010g0123a0001c0002t0011g0124 | 3 | HG02145.hp2 HG02630.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.66+7541G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56529630 | ||||||
| chr12:56529671
|
A | T | 2 | a0001c0001t0005g0229a0001c0001t0017g0230 | 2 | HG03041.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.66+7582A>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56529671 | ||||||
| chr12:56529678
|
C | T | 1 | a0001c0001t0046g0087 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.66+7589C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56529678 | ||||||
| chr12:56529811
|
A | G | 8 | a0001c0002t0002g0084a0001c0002t0005g0108a0001c0002t0048g0106others(5): Show | 8 | HG01891.hp1 HG02055.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.66+7722A>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56529811 | ||||||
| chr12:56529886
|
T | G | 2 | a0001c0002t0004g0223a0001c0002t0004g0224 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.66+7797T>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56529886 | ||||||
| chr12:56530006
|
C | G | 3 | a0001c0001t0020g0111a0001c0001t0020g0112a0001c0001t0020g0113 | 3 | HG02572.hp1 HG02809.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.66+7917C>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56530006 | ||||||
| chr12:56530081
|
T | A | 2 | a0001c0002t0005g0236a0001c0002t0038g0262 | 2 | HG03225.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.66+7992T>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56530081 | ||||||
| chr12:56530129
|
A | C | 2 | a0001c0001t0018g0187a0001c0001t0018g0188 | 2 | HG01433.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.66+8040A>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56530129 | ||||||
| chr12:56530146
|
G | C | 50 | a0001c0001t0003g0271a0001c0001t0014g0264a0001c0002t0001g0119others(47): Show | 50 | HG00099.hp2 HG00140.hp1 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.66+8057G>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56530146 | ||||||
| chr12:56530174
|
C | T | 3 | a0001c0001t0009g0090a0001c0001t0057g0089a0001c0001t0070g0088 | 3 | HG01358.hp1 HG01934.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.66+8085C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56530174 | ||||||
| chr12:56530253
|
G | A | 100 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(97): Show | 100 | HG00099.hp1 HG00140.hp2 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.66+8164G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56530253 | ||||||
| chr12:56530332
|
G | A | 49 | a0001c0001t0003g0271a0001c0001t0014g0264a0001c0002t0001g0119others(46): Show | 49 | HG00099.hp2 HG00140.hp1 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.66+8243G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56530332 | ||||||
| chr12:56530350
|
C | CT | 28 | a0001c0001t0001g0170a0001c0001t0001g0173a0001c0001t0001g0176others(25): Show | 28 | HG01109.hp1 HG01358.hp2 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.66+8289dupT | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56530350 | |||||
| chr12:56530350
|
CT | C | 118 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(115): Show | 118 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(115): Show |
intron_variant | MODIFIER | c.66+8289delT | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56530350 | |||||
| chr12:56530350
|
CTT | C | 15 | a0001c0001t0001g0010a0001c0001t0002g0009a0001c0001t0005g0229others(12): Show | 15 | HG02055.hp1 HG02132.hp2 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.66+8288_66+8289del others(2): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56530350 | |||||
| chr12:56530350
|
CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0001g0008 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.66+8278_66+8289del others(12): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56530350 | |||||
| chr12:56530545
|
A | G | 14 | a0001c0001t0005g0229a0001c0001t0010g0225a0001c0001t0010g0227others(11): Show | 14 | HG01243.hp2 HG02145.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.66+8456A>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56530545 | ||||||
| chr12:56530552
|
G | T | 1 | a0001c0002t0004g0215 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.66+8463G>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56530552 | ||||||
| chr12:56530603
|
T | C | 1 | a0001c0002t0005g0109 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.66+8514T>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56530603 | ||||||
| chr12:56530605
|
C | G | 50 | a0001c0001t0003g0271a0001c0001t0014g0264a0001c0002t0001g0119others(47): Show | 50 | HG00099.hp2 HG00140.hp1 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.66+8516C>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56530605 | ||||||
| chr12:56530663
|
A | T | 100 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(97): Show | 100 | HG00099.hp1 HG00140.hp2 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.66+8574A>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56530663 | ||||||
| chr12:56531010
|
C | T | 4 | a0001c0001t0003g0063a0001c0001t0003g0064a0001c0001t0003g0071others(1): Show | 4 | HG00558.hp2 NA18612.hp2 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.66+8921C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56531010 | ||||||
| chr12:56531168
|
T | G | 1 | a0001c0001t0018g0086 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.66+9079T>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56531168 | ||||||
| chr12:56531555
|
G | A | 8 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0012others(5): Show | 8 | HG00735.hp1 HG01928.hp2 HG01934.hp2 others(5): Show |
intron_variant | MODIFIER | c.66+9466G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56531555 | ||||||
| chr12:56531599
|
C | T | 4 | a0001c0001t0035g0098a0001c0001t0036g0096a0001c0001t0037g0095others(1): Show | 4 | HG01243.hp1 HG02647.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.66+9510C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56531599 | ||||||
| chr12:56531624
|
G | A | 1 | a0001c0001t0021g0189 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.66+9535G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56531624 | ||||||
| chr12:56531734
|
G | A | 1 | a0001c0002t0005g0236 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.66+9645G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56531734 | ||||||
| chr12:56531747
|
G | A | 100 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(97): Show | 100 | HG00099.hp1 HG00140.hp2 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.66+9658G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56531747 | ||||||
| chr12:56531757
|
G | T | 1 | a0001c0001t0002g0007 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.66+9668G>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56531757 | ||||||
| chr12:56531816
|
C | CA | 66 | a0001c0001t0003g0271a0001c0001t0005g0229a0001c0001t0010g0225others(63): Show | 66 | HG00099.hp2 HG00140.hp1 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.66+9744dupA | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56531816 | |||||
| chr12:56531941
|
C | T | 2 | a0001c0002t0023g0099a0001c0002t0034g0100 | 2 | HG02257.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.66+9852C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56531941 | ||||||
| chr12:56531942
|
G | A | 4 | a0001c0001t0035g0098a0001c0001t0036g0096a0001c0001t0037g0095others(1): Show | 4 | HG01243.hp1 HG02647.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.66+9853G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56531942 | ||||||
| chr12:56531970
|
C | T | 3 | a0001c0001t0001g0070a0001c0001t0008g0061a0001c0001t0016g0082 | 3 | HG02683.hp1 HG04184.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.66+9881C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56531970 | ||||||
| chr12:56532179
|
G | A | 100 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(97): Show | 100 | HG00099.hp1 HG00140.hp2 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.66+10090G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56532179 | ||||||
| chr12:56532259
|
T | A | 2 | a0001c0002t0004g0223a0001c0002t0004g0224 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.66+10170T>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56532259 | ||||||
| chr12:56532473
|
T | C | 100 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(97): Show | 100 | HG00099.hp1 HG00140.hp2 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.66+10384T>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56532473 | ||||||
| chr12:56532484
|
G | A | 92 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(89): Show | 92 | HG00099.hp1 HG00140.hp2 HG00558.hp2 others(89): Show |
intron_variant | MODIFIER | c.66+10395G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56532484 | ||||||
| chr12:56532519
|
G | A | 1 | a0001c0002t0003g0268 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.66+10430G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56532519 | ||||||
| chr12:56532533
|
ACT | A | 100 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(97): Show | 100 | HG00099.hp1 HG00140.hp2 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.66+10447_66+10448d others(4): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56532533 | |||||
| chr12:56532568
|
T | TA | 100 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(97): Show | 100 | HG00099.hp1 HG00140.hp2 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.66+10488dupA | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56532568 | |||||
| chr12:56532698
|
A | C | 1 | a0001c0001t0059g0060 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.66+10609A>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56532698 | ||||||
| chr12:56532769
|
A | G | 1 | a0001c0002t0014g0168 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.66+10680A>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56532769 | ||||||
| chr12:56532881
|
C | G | 100 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(97): Show | 100 | HG00099.hp1 HG00140.hp2 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.66+10792C>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56532881 | ||||||
| chr12:56532921
|
TTTTTA | T | 87 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(84): Show | 87 | HG00099.hp1 HG00140.hp2 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.66+10857_66+10861d others(7): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56532921 | |||||
| chr12:56532958
|
T | C | 2 | a0001c0002t0005g0108a0001c0002t0048g0106 | 2 | HG01891.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.66+10869T>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56532958 | ||||||
| chr12:56532997
|
C | T | 1 | a0001c0001t0021g0167 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.66+10908C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56532997 | ||||||
| chr12:56533001
|
C | A | 1 | a0001c0001t0056g0019 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.66+10912C>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56533001 | ||||||
| chr12:56533026
|
C | A | 100 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(97): Show | 100 | HG00099.hp1 HG00140.hp2 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.66+10937C>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56533026 | ||||||
| chr12:56533039
|
A | G | 1 | a0001c0002t0055g0235 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.66+10950A>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56533039 | ||||||
| chr12:56533049
|
C | T | 1 | a0001c0001t0003g0166 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.66+10960C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56533049 | ||||||
| chr12:56533391
|
G | A | 3 | a0001c0001t0009g0090a0001c0001t0057g0089a0001c0001t0070g0088 | 3 | HG01358.hp1 HG01934.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.66+11302G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56533391 | ||||||
| chr12:56533408
|
C | CT | 21 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0012others(18): Show | 21 | HG00621.hp1 HG00735.hp1 HG01928.hp2 others(18): Show |
intron_variant | MODIFIER | c.66+11344dupT | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56533408 | |||||
| chr12:56533408
|
C | CTTTTT | 11 | a0001c0001t0005g0229a0001c0001t0010g0225a0001c0001t0010g0227others(8): Show | 11 | HG02257.hp2 HG02258.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.66+11340_66+11344d others(7): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56533408 | |||||
| chr12:56533408
|
C | CTTTTTT | 40 | a0001c0001t0001g0101a0001c0001t0002g0169a0001c0001t0003g0271others(37): Show | 40 | HG00544.hp1 HG00735.hp2 HG01071.hp1 others(37): Show |
intron_variant | MODIFIER | c.66+11339_66+11344d others(8): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56533408 | |||||
| chr12:56533408
|
C | CTTTTTTT | 59 | a0001c0001t0001g0004a0001c0001t0001g0130a0001c0001t0001g0132others(56): Show | 59 | HG00558.hp1 HG00597.hp1 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.66+11338_66+11344d others(9): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56533408 | |||||
| chr12:56533408
|
C | CTTTTTTT others(1): Show |
32 | a0001c0001t0001g0110a0001c0001t0001g0151a0001c0001t0001g0153others(29): Show | 32 | HG00544.hp2 HG00639.hp2 HG01109.hp2 others(29): Show |
intron_variant | MODIFIER | c.66+11337_66+11344d others(10): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56533408 | |||||
| chr12:56533408
|
C | CTTTTTTT others(2): Show |
7 | a0001c0001t0001g0121a0001c0001t0003g0163a0001c0001t0003g0164others(4): Show | 7 | HG01361.hp1 HG02615.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.66+11336_66+11344d others(11): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56533408 | |||||
| chr12:56533408
|
C | CTTTTTTT others(3): Show |
1 | a0001c0001t0002g0165 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.66+11335_66+11344d others(12): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56533408 | |||||
| chr12:56533408
|
C | CTTTTTTT others(6): Show |
1 | a0001c0002t0079g0212 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.66+11332_66+11344d others(15): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56533408 | |||||
| chr12:56533408
|
CT | C | 7 | a0001c0001t0001g0022a0001c0001t0003g0021a0001c0001t0008g0061others(4): Show | 7 | HG00099.hp1 HG00639.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.66+11344delT | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56533408 | |||||
| chr12:56533408
|
CTTTTTT | C | 19 | a0001c0001t0011g0201a0001c0002t0001g0256a0001c0002t0001g0269others(16): Show | 20 | HG00099.hp2 HG00140.hp1 HG01169.hp1 others(17): Show |
intron_variant | MODIFIER | c.66+11339_66+11344d others(8): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56533408 | |||||
| chr12:56533537
|
T | G | 4 | a0001c0002t0081g0102a0001c0002t0082g0105a0001c0002t0083g0104others(1): Show | 4 | HG02055.hp2 HG02895.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.66+11448T>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56533537 | ||||||
| chr12:56533556
|
T | C | 100 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(97): Show | 100 | HG00099.hp1 HG00140.hp2 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.66+11467T>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56533556 | ||||||
| chr12:56533560
|
C | T | 100 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(97): Show | 100 | HG00099.hp1 HG00140.hp2 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.66+11471C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56533560 | ||||||
| chr12:56533635
|
C | T | 1 | a0001c0001t0001g0004 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.66+11546C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56533635 | ||||||
| chr12:56533667
|
T | C | 2 | a0001c0001t0018g0187a0001c0001t0018g0188 | 2 | HG01433.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.66+11578T>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56533667 | ||||||
| chr12:56533853
|
G | A | 100 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(97): Show | 100 | HG00099.hp1 HG00140.hp2 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.66+11764G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56533853 | ||||||
| chr12:56533897
|
T | C | 100 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(97): Show | 100 | HG00099.hp1 HG00140.hp2 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.66+11808T>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56533897 | ||||||
| chr12:56534046
|
G | A | 100 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(97): Show | 100 | HG00099.hp1 HG00140.hp2 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.66+11957G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56534046 | ||||||
| chr12:56534056
|
G | C | 2 | a0001c0002t0023g0099a0001c0002t0034g0100 | 2 | HG02257.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.66+11967G>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56534056 | ||||||
| chr12:56534188
|
A | G | 1 | a0001c0002t0004g0228 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.66+12099A>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56534188 | ||||||
| chr12:56534192
|
AT | A | 100 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(97): Show | 100 | HG00099.hp1 HG00140.hp2 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.66+12109delT | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56534192 | |||||
| chr12:56534285
|
T | C | 14 | a0001c0001t0005g0229a0001c0001t0010g0225a0001c0001t0010g0227others(11): Show | 14 | HG01243.hp2 HG02145.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.66+12196T>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56534285 | ||||||
| chr12:56534491
|
G | A | 8 | a0001c0002t0002g0084a0001c0002t0005g0108a0001c0002t0048g0106others(5): Show | 8 | HG01891.hp1 HG02055.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.66+12402G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56534491 | ||||||
| chr12:56534512
|
C | A | 3 | a0001c0001t0007g0122a0001c0002t0010g0123a0001c0002t0011g0124 | 3 | HG02145.hp2 HG02630.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.66+12423C>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56534512 | ||||||
| chr12:56534704
|
C | A | 1 | a0001c0002t0005g0236 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.66+12615C>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56534704 | ||||||
| chr12:56534742
|
C | T | 1 | a0001c0001t0060g0059 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.66+12653C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56534742 | ||||||
| chr12:56534772
|
G | T | 1 | a0001c0001t0002g0079 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.66+12683G>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56534772 | ||||||
| chr12:56534774
|
A | T | 166 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(163): Show | 166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.66+12685A>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56534774 | ||||||
| chr12:56534829
|
C | G | 100 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(97): Show | 100 | HG00099.hp1 HG00140.hp2 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.66+12740C>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56534829 | ||||||
| chr12:56534866
|
C | T | 2 | a0001c0001t0022g0053a0001c0001t0022g0068 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.66+12777C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56534866 | ||||||
| chr12:56534989
|
T | C | 3 | a0001c0001t0001g0170a0001c0001t0024g0148a0001c0001t0024g0171 | 3 | NA18987.hp2 NA19000.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.66+12900T>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56534989 | ||||||
| chr12:56534993
|
T | C | 100 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(97): Show | 100 | HG00099.hp1 HG00140.hp2 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.66+12904T>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56534993 | ||||||
| chr12:56535030
|
A | G | 45 | a0001c0001t0003g0271a0001c0001t0014g0264a0001c0002t0001g0119others(42): Show | 45 | HG00544.hp1 HG00621.hp2 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.66+12941A>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56535030 | ||||||
| chr12:56535047
|
C | T | 100 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(97): Show | 100 | HG00099.hp1 HG00140.hp2 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.66+12958C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56535047 | ||||||
| chr12:56535142
|
G | A | 87 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(84): Show | 87 | HG00099.hp1 HG00140.hp2 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.66+13053G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56535142 | ||||||
| chr12:56535265
|
T | A | 1 | a0001c0002t0005g0236 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.66+13176T>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56535265 | ||||||
| chr12:56535376
|
T | C | 100 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(97): Show | 100 | HG00099.hp1 HG00140.hp2 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.66+13287T>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56535376 | ||||||
| chr12:56535383
|
T | C | 100 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(97): Show | 100 | HG00099.hp1 HG00140.hp2 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.66+13294T>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56535383 | ||||||
| chr12:56535494
|
C | CA | 87 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(84): Show | 87 | HG00099.hp1 HG00140.hp2 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.66+13425dupA | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56535494 | |||||
| chr12:56535494
|
C | CAA | 50 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0054others(47): Show | 50 | HG00099.hp2 HG00140.hp1 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.66+13424_66+13425d others(4): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56535494 | |||||
| chr12:56535494
|
C | CAAA | 6 | a0001c0002t0001g0272a0001c0002t0001g0275a0001c0002t0001g0276others(3): Show | 6 | HG01928.hp1 HG01978.hp2 HG02293.hp2 others(3): Show |
intron_variant | MODIFIER | c.66+13423_66+13425d others(5): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56535494 | |||||
| chr12:56535494
|
C | CAAAAAAA others(3): Show |
2 | a0001c0001t0009g0090a0001c0001t0057g0089 | 2 | HG01358.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.66+13416_66+13425d others(12): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56535494 | |||||
| chr12:56535494
|
C | CAAAAAAA others(4): Show |
3 | a0001c0001t0070g0088a0001c0002t0023g0099a0001c0002t0034g0100 | 3 | HG01934.hp1 HG02257.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.66+13415_66+13425d others(13): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56535494 | |||||
| chr12:56535494
|
CAAAA | C | 8 | a0001c0002t0002g0084a0001c0002t0005g0108a0001c0002t0048g0106others(5): Show | 8 | HG01891.hp1 HG02055.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.66+13422_66+13425d others(6): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56535494 | |||||
| chr12:56535560
|
C | T | 92 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(89): Show | 92 | HG00099.hp1 HG00140.hp2 HG00558.hp2 others(89): Show |
intron_variant | MODIFIER | c.66+13471C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56535560 | ||||||
| chr12:56535580
|
T | C | 100 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(97): Show | 100 | HG00099.hp1 HG00140.hp2 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.66+13491T>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56535580 | ||||||
| chr12:56535663
|
A | G | 92 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(89): Show | 92 | HG00099.hp1 HG00140.hp2 HG00558.hp2 others(89): Show |
intron_variant | MODIFIER | c.66+13574A>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56535663 | ||||||
| chr12:56535735
|
T | C | 100 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(97): Show | 100 | HG00099.hp1 HG00140.hp2 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.66+13646T>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56535735 | ||||||
| chr12:56535910
|
C | T | 49 | a0001c0001t0003g0271a0001c0002t0001g0119a0001c0002t0001g0245others(46): Show | 49 | HG00099.hp2 HG00140.hp1 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.66+13821C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56535910 | ||||||
| chr12:56535919
|
T | A | 100 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(97): Show | 100 | HG00099.hp1 HG00140.hp2 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.66+13830T>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56535919 | ||||||
| chr12:56535933
|
A | G | 1 | a0001c0002t0002g0255 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.66+13844A>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56535933 | ||||||
| chr12:56536052
|
T | C | 100 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(97): Show | 100 | HG00099.hp1 HG00140.hp2 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.66+13963T>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56536052 | ||||||
| chr12:56536060
|
G | A | 100 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(97): Show | 100 | HG00099.hp1 HG00140.hp2 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.66+13971G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56536060 | ||||||
| chr12:56536070
|
G | A | 1 | a0001c0002t0023g0209 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.66+13981G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56536070 | ||||||
| chr12:56536200
|
C | CA | 64 | a0001c0001t0001g0110a0001c0001t0001g0130a0001c0001t0001g0132others(61): Show | 64 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.66+14139dupA | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56536200 | |||||
| chr12:56536200
|
C | CAA | 6 | a0001c0001t0005g0229a0001c0002t0002g0257a0001c0002t0038g0262others(3): Show | 6 | HG02257.hp2 HG02622.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.66+14138_66+14139d others(4): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56536200 | |||||
| chr12:56536200
|
C | CAAAAAAA others(3): Show |
1 | a0001c0001t0007g0122 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.66+14130_66+14139d others(12): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56536200 | |||||
| chr12:56536200
|
C | CAAAAAAA others(4): Show |
2 | a0001c0002t0010g0123a0001c0002t0011g0124 | 2 | HG02145.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.66+14129_66+14139d others(13): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56536200 | |||||
| chr12:56536200
|
CA | C | 15 | a0001c0001t0001g0004a0001c0001t0001g0121a0001c0001t0001g0142others(12): Show | 15 | HG01891.hp2 HG02132.hp1 HG02273.hp1 others(12): Show |
intron_variant | MODIFIER | c.66+14139delA | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56536200 | |||||
| chr12:56536200
|
CAAA | C | 10 | a0001c0001t0021g0147a0001c0001t0021g0189a0001c0002t0002g0185others(7): Show | 10 | HG01109.hp2 HG01884.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.66+14137_66+14139d others(5): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56536200 | |||||
| chr12:56536200
|
CAAAAAA | C | 21 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0023others(18): Show | 21 | HG00558.hp2 HG00642.hp1 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.66+14134_66+14139d others(8): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56536200 | |||||
| chr12:56536200
|
CAAAAAAA | C | 70 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(67): Show | 70 | HG00099.hp1 HG00140.hp2 HG00597.hp2 others(67): Show |
intron_variant | MODIFIER | c.66+14133_66+14139d others(9): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56536200 | |||||
| chr12:56536232
|
C | T | 4 | a0001c0001t0035g0098a0001c0001t0036g0096a0001c0001t0037g0095others(1): Show | 4 | HG01243.hp1 HG02647.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.66+14143C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56536232 | ||||||
| chr12:56536261
|
G | A | 253 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(250): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.66+14172G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56536261 | ||||||
| chr12:56536285
|
C | T | 105 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(102): Show | 105 | HG00099.hp1 HG00140.hp2 HG00558.hp2 others(102): Show |
intron_variant | MODIFIER | c.66+14196C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56536285 | ||||||
| chr12:56536320
|
C | T | 1 | a0001c0002t0055g0235 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.66+14231C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56536320 | ||||||
| chr12:56536521
|
C | T | 9 | a0001c0001t0009g0090a0001c0001t0035g0098a0001c0001t0036g0096others(6): Show | 9 | HG01243.hp1 HG01358.hp1 HG01934.hp1 others(6): Show |
intron_variant | MODIFIER | c.66+14432C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56536521 | ||||||
| chr12:56536527
|
TCTTTTC | T | 9 | a0001c0001t0009g0090a0001c0001t0035g0098a0001c0001t0036g0096others(6): Show | 9 | HG01243.hp1 HG01358.hp1 HG01934.hp1 others(6): Show |
intron_variant | MODIFIER | c.66+14439_66+14444d others(8): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56536527 | ||||||
| chr12:56536531
|
TTC | T | 14 | a0001c0001t0021g0147a0001c0001t0021g0189a0001c0002t0002g0084others(11): Show | 14 | HG01109.hp2 HG01884.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.66+14448_66+14449d others(4): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56536531 | |||||
| chr12:56536565
|
T | C | 120 | a0001c0001t0001g0004a0001c0001t0001g0029a0001c0001t0001g0052others(117): Show | 120 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(117): Show |
intron_variant | MODIFIER | c.66+14476T>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56536565 | ||||||
| chr12:56536599
|
A | G | 166 | a0001c0001t0001g0004a0001c0001t0001g0101a0001c0001t0001g0110others(163): Show | 166 | HG00099.hp2 HG00140.hp1 HG00544.hp1 others(163): Show |
intron_variant | MODIFIER | c.66+14510A>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56536599 | ||||||
| chr12:56536646
|
C | T | 1 | a0001c0001t0001g0012 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.66+14557C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56536646 | ||||||
| chr12:56536691
|
C | T | 2 | a0001c0001t0024g0148a0001c0001t0024g0171 | 2 | NA18987.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.66+14602C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56536691 | ||||||
| chr12:56536813
|
C | A | 1 | a0001c0002t0001g0249 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.66+14724C>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56536813 | ||||||
| chr12:56536922
|
C | CT | 10 | a0001c0001t0010g0227a0001c0001t0046g0087a0001c0001t0070g0088others(7): Show | 10 | HG01243.hp2 HG01934.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.66+14849dupT | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56536922 | |||||
| chr12:56537001
|
A | G | 7 | a0001c0001t0011g0201a0001c0002t0006g0202a0001c0002t0026g0205others(4): Show | 7 | HG01167.hp1 HG01169.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.66+14912A>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56537001 | ||||||
| chr12:56537109
|
C | T | 2 | a0001c0002t0023g0099a0001c0002t0034g0100 | 2 | HG02257.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.66+15020C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56537109 | ||||||
| chr12:56537208
|
G | A | 83 | a0001c0001t0001g0101a0001c0001t0001g0110a0001c0001t0001g0130others(80): Show | 83 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(80): Show |
intron_variant | MODIFIER | c.66+15119G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56537208 | ||||||
| chr12:56537444
|
A | G | 167 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(164): Show | 167 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(164): Show |
intron_variant | MODIFIER | c.66+15355A>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56537444 | ||||||
| chr12:56537450
|
T | C | 167 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(164): Show | 167 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(164): Show |
intron_variant | MODIFIER | c.66+15361T>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56537450 | ||||||
| chr12:56537494
|
C | T | 161 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(158): Show | 161 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(158): Show |
intron_variant | MODIFIER | c.66+15405C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56537494 | ||||||
| chr12:56537619
|
G | A | 167 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(164): Show | 167 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(164): Show |
intron_variant | MODIFIER | c.66+15530G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56537619 | ||||||
| chr12:56537644
|
T | C | 167 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(164): Show | 167 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(164): Show |
intron_variant | MODIFIER | c.66+15555T>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56537644 | ||||||
| chr12:56537752
|
CTA | C | 3 | a0001c0001t0009g0090a0001c0001t0057g0089a0001c0001t0070g0088 | 3 | HG01358.hp1 HG01934.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.66+15665_66+15666d others(4): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56537752 | |||||
| chr12:56537848
|
CT | C | 96 | a0001c0001t0001g0004a0001c0001t0001g0101a0001c0001t0001g0110others(93): Show | 96 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(93): Show |
intron_variant | MODIFIER | c.66+15776delT | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56537848 | |||||
| chr12:56537848
|
CTT | C | 151 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(148): Show | 151 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(148): Show |
intron_variant | MODIFIER | c.66+15775_66+15776d others(4): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56537848 | |||||
| chr12:56537848
|
CTTT | C | 7 | a0001c0001t0001g0072a0001c0002t0001g0263a0001c0002t0002g0237others(4): Show | 7 | HG01255.hp2 HG02572.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.66+15774_66+15776d others(5): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56537848 | |||||
| chr12:56538022
|
TTTTA | T | 157 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(154): Show | 157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): Show |
intron_variant | MODIFIER | c.66+15957_66+15960d others(6): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56538022 | |||||
| chr12:56538085
|
T | G | 1 | a0001c0002t0063g0146 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.66+15996T>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56538085 | ||||||
| chr12:56538150
|
A | C | 160 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(157): Show | 160 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(157): Show |
intron_variant | MODIFIER | c.66+16061A>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56538150 | ||||||
| chr12:56538189
|
T | C | 160 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(157): Show | 160 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(157): Show |
intron_variant | MODIFIER | c.66+16100T>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56538189 | ||||||
| chr12:56538328
|
C | G | 1 | a0001c0001t0003g0161 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.66+16239C>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56538328 | ||||||
| chr12:56538351
|
T | C | 6 | a0001c0002t0002g0260a0001c0002t0003g0238a0001c0002t0003g0240others(3): Show | 6 | HG00735.hp2 HG01071.hp1 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.66+16262T>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56538351 | ||||||
| chr12:56538388
|
C | T | 4 | a0001c0001t0035g0098a0001c0001t0036g0096a0001c0001t0037g0095others(1): Show | 4 | HG01243.hp1 HG02647.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.66+16299C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56538388 | ||||||
| chr12:56538447
|
C | T | 1 | a0001c0001t0058g0220 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.66+16358C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56538447 | ||||||
| chr12:56538466
|
CT | C | 79 | a0001c0001t0001g0004a0001c0001t0001g0101a0001c0001t0001g0130others(76): Show | 79 | HG00544.hp2 HG00597.hp1 HG00639.hp2 others(76): Show |
intron_variant | MODIFIER | c.66+16404delT | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56538466 | |||||
| chr12:56538466
|
CTTTTTT | C | 28 | a0001c0001t0003g0055a0001c0001t0021g0147a0001c0001t0021g0189others(25): Show | 28 | HG00621.hp1 HG01109.hp2 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.66+16399_66+16404d others(8): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56538466 | |||||
| chr12:56538466
|
CTTTTTTT | C | 125 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(122): Show | 125 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(122): Show |
intron_variant | MODIFIER | c.66+16398_66+16404d others(9): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56538466 | |||||
| chr12:56538466
|
CTTTTTTT others(1): Show |
C | 6 | a0001c0001t0001g0023a0001c0001t0035g0098a0001c0001t0036g0096others(3): Show | 6 | HG01243.hp1 HG01256.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.66+16397_66+16404d others(10): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56538466 | |||||
| chr12:56538519
|
A | G | 158 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(155): Show | 158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
intron_variant | MODIFIER | c.66+16430A>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56538519 | ||||||
| chr12:56538576
|
G | T | 158 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(155): Show | 158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
intron_variant | MODIFIER | c.66+16487G>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56538576 | ||||||
| chr12:56538626
|
C | T | 157 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(154): Show | 157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): Show |
intron_variant | MODIFIER | c.66+16537C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56538626 | ||||||
| chr12:56538639
|
GC | G | 14 | a0001c0002t0002g0084a0001c0002t0002g0185a0001c0002t0003g0200others(11): Show | 14 | HG01884.hp2 HG01891.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.66+16553delC | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56538639 | |||||
| chr12:56538671
|
A | G | 158 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(155): Show | 158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
intron_variant | MODIFIER | c.66+16582A>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56538671 | ||||||
| chr12:56538672
|
C | G | 158 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(155): Show | 158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
intron_variant | MODIFIER | c.66+16583C>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56538672 | ||||||
| chr12:56538766
|
C | T | 1 | a0001c0001t0021g0167 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.66+16677C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56538766 | ||||||
| chr12:56538770
|
G | A | 154 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(151): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.66+16681G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56538770 | ||||||
| chr12:56538862
|
T | C | 2 | a0001c0002t0004g0223a0001c0002t0004g0224 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.66+16773T>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56538862 | ||||||
| chr12:56538987
|
G | GTTGT | 94 | a0001c0001t0001g0004a0001c0001t0001g0101a0001c0001t0001g0110others(91): Show | 94 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.66+16900_66+16903d others(6): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56538987 | |||||
| chr12:56539009
|
G | T | 1 | a0001c0002t0005g0109 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.66+16920G>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56539009 | ||||||
| chr12:56539015
|
C | CT | 5 | a0001c0001t0001g0110a0001c0001t0001g0145a0001c0001t0001g0177others(2): Show | 5 | HG01109.hp1 HG01884.hp1 HG02056.hp1 others(2): Show |
intron_variant | MODIFIER | c.66+16944dupT | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56539015 | |||||
| chr12:56539015
|
CTTTTTTT | C | 150 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(147): Show | 150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
intron_variant | MODIFIER | c.66+16938_66+16944d others(9): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56539015 | |||||
| chr12:56539053
|
G | T | 154 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(151): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.66+16964G>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56539053 | ||||||
| chr12:56539118
|
C | A | 1 | a0001c0001t0001g0151 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.66+17029C>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56539118 | ||||||
| chr12:56539229
|
C | G | 153 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(150): Show | 153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.66+17140C>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56539229 | ||||||
| chr12:56539378
|
T | C | 79 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(76): Show | 79 | HG00099.hp1 HG00140.hp2 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.66+17289T>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56539378 | ||||||
| chr12:56539417
|
C | T | 1 | a0001c0002t0001g0256 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.66+17328C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56539417 | ||||||
| chr12:56539449
|
C | A | 154 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(151): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.66+17360C>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56539449 | ||||||
| chr12:56539460
|
G | T | 154 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(151): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.66+17371G>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56539460 | ||||||
| chr12:56539505
|
T | C | 1 | a0001c0001t0037g0095 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.66+17416T>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56539505 | ||||||
| chr12:56539632
|
A | G | 154 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(151): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.66+17543A>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56539632 | ||||||
| chr12:56539637
|
A | C | 3 | a0001c0002t0003g0200a0001c0002t0012g0226a0001c0002t0055g0235 | 3 | HG02055.hp1 HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.66+17548A>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56539637 | ||||||
| chr12:56539867
|
G | A | 154 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(151): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.66+17778G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56539867 | ||||||
| chr12:56539938
|
G | A | 153 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(150): Show | 153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.66+17849G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56539938 | ||||||
| chr12:56540001
|
T | C | 19 | a0001c0002t0002g0084a0001c0002t0002g0232a0001c0002t0003g0200others(16): Show | 19 | HG01884.hp2 HG01891.hp1 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.66+17912T>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56540001 | ||||||
| chr12:56540061
|
C | T | 1 | a0001c0002t0002g0185 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.66+17972C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56540061 | ||||||
| chr12:56540215
|
C | T | 3 | a0001c0002t0003g0234a0001c0003t0006g0233a0001c0003t0075g0231 | 3 | HG01243.hp2 HG02622.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.66+18126C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56540215 | ||||||
| chr12:56540228
|
G | A | 2 | a0001c0002t0010g0123a0001c0002t0011g0124 | 2 | HG02145.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.66+18139G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56540228 | ||||||
| chr12:56540270
|
A | G | 19 | a0001c0002t0002g0084a0001c0002t0002g0232a0001c0002t0003g0200others(16): Show | 19 | HG01884.hp2 HG01891.hp1 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.66+18181A>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56540270 | ||||||
| chr12:56540336
|
T | G | 19 | a0001c0002t0002g0084a0001c0002t0002g0232a0001c0002t0003g0200others(16): Show | 19 | HG01884.hp2 HG01891.hp1 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.66+18247T>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56540336 | ||||||
| chr12:56540364
|
T | C | 4 | a0001c0002t0010g0123a0001c0002t0011g0124a0001c0002t0017g0093others(1): Show | 4 | HG02145.hp1 HG02145.hp2 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.66+18275T>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56540364 | ||||||
| chr12:56540413
|
T | G | 1 | a0001c0001t0002g0141 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.66+18324T>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56540413 | ||||||
| chr12:56540432
|
G | A | 1 | a0001c0002t0023g0209 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.66+18343G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56540432 | ||||||
| chr12:56540463
|
A | G | 11 | a0001c0002t0002g0084a0001c0002t0002g0232a0001c0002t0004g0186others(8): Show | 11 | HG01884.hp2 HG01891.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.66+18374A>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56540463 | ||||||
| chr12:56540600
|
G | A | 19 | a0001c0001t0011g0201a0001c0002t0004g0206a0001c0002t0004g0215others(16): Show | 20 | HG01167.hp1 HG01169.hp1 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.66+18511G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56540600 | ||||||
| chr12:56540677
|
G | A | 1 | a0001c0001t0002g0075 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.66+18588G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56540677 | ||||||
| chr12:56540705
|
A | G | 8 | a0001c0002t0002g0232a0001c0002t0004g0186a0001c0002t0063g0146others(5): Show | 8 | HG01884.hp2 HG02055.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.66+18616A>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56540705 | ||||||
| chr12:56540974
|
A | G | 251 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(248): Show | 251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.66+18885A>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56540974 | ||||||
| chr12:56541100
|
C | CA | 10 | a0001c0001t0002g0079a0001c0001t0016g0082a0001c0002t0002g0085others(7): Show | 10 | HG01106.hp1 HG01952.hp2 HG02080.hp2 others(7): Show |
intron_variant | MODIFIER | c.66+19026dupA | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56541100 | |||||
| chr12:56541100
|
C | CAA | 6 | a0001c0001t0032g0047a0001c0001t0036g0096a0001c0001t0037g0095others(3): Show | 6 | HG01243.hp1 HG02280.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.66+19025_66+19026d others(4): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56541100 | |||||
| chr12:56541100
|
C | CAAA | 77 | a0001c0001t0001g0004a0001c0001t0001g0101a0001c0001t0001g0110others(74): Show | 77 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.66+19024_66+19026d others(5): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56541100 | |||||
| chr12:56541100
|
C | CAAAA | 10 | a0001c0001t0003g0128a0001c0001t0003g0163a0001c0001t0003g0222others(7): Show | 10 | HG01358.hp2 HG01433.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.66+19023_66+19026d others(6): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56541100 | |||||
| chr12:56541115
|
A | C | 1 | a0001c0002t0003g0247 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.66+19026A>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56541115 | ||||||
| chr12:56541125
|
C | T | 2 | a0001c0002t0010g0123a0001c0002t0011g0124 | 2 | HG02145.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.66+19036C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56541125 | ||||||
| chr12:56541144
|
T | C | 153 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(150): Show | 153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.66+19055T>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56541144 | ||||||
| chr12:56541233
|
C | T | 5 | a0001c0001t0032g0047a0001c0001t0035g0098a0001c0001t0036g0096others(2): Show | 5 | HG01243.hp1 HG02602.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.66+19144C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56541233 | ||||||
| chr12:56541246
|
T | C | 1 | a0001c0001t0052g0069 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.66+19157T>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56541246 | ||||||
| chr12:56541570
|
A | G | 1 | a0001c0002t0055g0235 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.66+19481A>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56541570 | ||||||
| chr12:56541618
|
T | A | 153 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(150): Show | 153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.66+19529T>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56541618 | ||||||
| chr12:56541629
|
A | G | 93 | a0001c0001t0001g0004a0001c0001t0001g0101a0001c0001t0001g0110others(90): Show | 93 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.66+19540A>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56541629 | ||||||
| chr12:56541868
|
G | A | 98 | a0001c0001t0001g0004a0001c0001t0001g0101a0001c0001t0001g0110others(95): Show | 98 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.66+19779G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56541868 | ||||||
| chr12:56541908
|
A | G | 3 | a0001c0002t0003g0234a0001c0003t0006g0233a0001c0003t0075g0231 | 3 | HG01243.hp2 HG02622.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.66+19819A>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56541908 | ||||||
| chr12:56542037
|
A | C | 2 | a0001c0002t0003g0200a0001c0002t0055g0235 | 2 | HG02055.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.66+19948A>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56542037 | ||||||
| chr12:56542059
|
A | AT | 249 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(246): Show | 249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.66+19978dupT | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56542059 | |||||
| chr12:56542236
|
C | CT | 148 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(145): Show | 148 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(145): Show |
intron_variant | MODIFIER | c.66+20156dupT | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56542236 | |||||
| chr12:56542261
|
C | T | 1 | a0001c0001t0001g0023 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.67-20156C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56542261 | ||||||
| chr12:56542265
|
A | T | 5 | a0001c0001t0032g0047a0001c0001t0035g0098a0001c0001t0036g0096others(2): Show | 5 | HG01243.hp1 HG02602.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.67-20152A>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56542265 | ||||||
| chr12:56542354
|
C | T | 1 | a0001c0001t0009g0090 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.67-20063C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56542354 | ||||||
| chr12:56542355
|
G | A | 5 | a0001c0002t0005g0109a0001c0002t0010g0123a0001c0002t0011g0124others(2): Show | 5 | HG02145.hp1 HG02145.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.67-20062G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56542355 | ||||||
| chr12:56542355
|
G | T | 14 | a0001c0002t0002g0084a0001c0002t0002g0232a0001c0002t0003g0200others(11): Show | 14 | HG01884.hp2 HG01891.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.67-20062G>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56542355 | ||||||
| chr12:56542413
|
T | TA | 251 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(248): Show | 251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.67-20003dupA | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56542413 | |||||
| chr12:56542478
|
T | A | 1 | a0001c0001t0003g0174 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.67-19939T>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56542478 | ||||||
| chr12:56542479
|
T | A | 43 | a0001c0001t0001g0031a0001c0001t0001g0170a0001c0001t0001g0190others(40): Show | 43 | HG00544.hp2 HG00597.hp1 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.67-19938T>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56542479 | ||||||
| chr12:56542480
|
T | A | 239 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(236): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.67-19937T>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56542480 | ||||||
| chr12:56542480
|
T | TA | 4 | a0001c0002t0010g0123a0001c0002t0011g0124a0001c0002t0017g0093others(1): Show | 4 | HG02145.hp1 HG02145.hp2 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.67-19932dupA | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56542480 | |||||
| chr12:56542481
|
A | T | 3 | a0001c0002t0005g0109a0001c0002t0033g0210a0001c0002t0033g0217 | 3 | HG01884.hp1 HG02572.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.67-19936A>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56542481 | ||||||
| chr12:56542512
|
T | C | 2 | a0001c0001t0019g0018a0001c0001t0028g0032 | 2 | NA18944.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.67-19905T>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56542512 | ||||||
| chr12:56542530
|
CT | C | 249 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(246): Show | 249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.67-19875delT | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56542530 | |||||
| chr12:56542552
|
CT | C | 12 | a0001c0002t0001g0272a0001c0002t0001g0275a0001c0002t0001g0276others(9): Show | 12 | HG01361.hp2 HG01928.hp1 HG01978.hp2 others(9): Show |
intron_variant | MODIFIER | c.67-19850delT | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56542552 | |||||
| chr12:56542639
|
C | T | 4 | a0001c0002t0002g0232a0001c0002t0004g0186a0001c0002t0063g0146others(1): Show | 4 | HG01884.hp2 HG02559.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.67-19778C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56542639 | ||||||
| chr12:56542886
|
C | G | 2 | a0001c0002t0023g0099a0001c0002t0034g0100 | 2 | HG02257.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.67-19531C>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56542886 | ||||||
| chr12:56543047
|
A | G | 2 | a0001c0002t0023g0099a0001c0002t0034g0100 | 2 | HG02257.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.67-19370A>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56543047 | ||||||
| chr12:56543074
|
G | A | 2 | a0001c0001t0001g0052a0001c0001t0027g0065 | 2 | HG01071.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.67-19343G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56543074 | ||||||
| chr12:56543190
|
C | T | 251 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(248): Show | 251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.67-19227C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56543190 | ||||||
| chr12:56543239
|
T | C | 2 | a0001c0002t0033g0210a0001c0002t0033g0217 | 2 | HG01884.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.67-19178T>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56543239 | ||||||
| chr12:56543280
|
C | T | 2 | a0001c0001t0035g0098a0001c0001t0036g0096 | 2 | HG02647.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.67-19137C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56543280 | ||||||
| chr12:56543416
|
CAG | C | 93 | a0001c0001t0001g0004a0001c0001t0001g0101a0001c0001t0001g0110others(90): Show | 93 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.67-18997_67-18996d others(4): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56543416 | |||||
| chr12:56543421
|
A | T | 3 | a0001c0001t0001g0110a0001c0001t0001g0132a0001c0001t0001g0137 | 3 | NA18940.hp1 NA18947.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.67-18996A>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56543421 | ||||||
| chr12:56543445
|
A | G | 2 | a0001c0002t0005g0108a0001c0002t0048g0106 | 2 | HG01891.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.67-18972A>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56543445 | ||||||
| chr12:56543479
|
T | C | 251 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(248): Show | 251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.67-18938T>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56543479 | ||||||
| chr12:56543508
|
C | T | 2 | a0001c0002t0003g0200a0001c0002t0055g0235 | 2 | HG02055.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.67-18909C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56543508 | ||||||
| chr12:56543511
|
C | CT | 12 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(9): Show | 12 | HG00642.hp1 HG00735.hp1 HG01928.hp2 others(9): Show |
intron_variant | MODIFIER | c.67-18890dupT | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56543511 | |||||
| chr12:56543592
|
A | T | 3 | a0001c0002t0003g0234a0001c0003t0006g0233a0001c0003t0075g0231 | 3 | HG01243.hp2 HG02622.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.67-18825A>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56543592 | ||||||
| chr12:56543824
|
C | T | 1 | a0001c0001t0002g0144 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.67-18593C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56543824 | ||||||
| chr12:56543874
|
G | T | 5 | a0001c0002t0004g0206a0001c0002t0011g0204a0001c0002t0013g0001others(2): Show | 6 | HG02559.hp2 HG02717.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.67-18543G>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56543874 | ||||||
| chr12:56544218
|
A | G | 15 | a0001c0001t0001g0004a0001c0001t0001g0121a0001c0001t0001g0142others(12): Show | 15 | HG01099.hp1 HG01109.hp1 HG02132.hp1 others(12): Show |
intron_variant | MODIFIER | c.67-18199A>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56544218 | ||||||
| chr12:56544219
|
T | A | 1 | a0001c0001t0002g0033 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.67-18198T>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56544219 | ||||||
| chr12:56544330
|
G | T | 8 | a0001c0001t0001g0170a0001c0001t0002g0129a0001c0001t0003g0219others(5): Show | 8 | HG00544.hp2 HG00597.hp1 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.67-18087G>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56544330 | ||||||
| chr12:56544523
|
G | C | 251 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(248): Show | 251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.67-17894G>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56544523 | ||||||
| chr12:56544537
|
C | T | 2 | a0001c0002t0010g0123a0001c0002t0011g0124 | 2 | HG02145.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.67-17880C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56544537 | ||||||
| chr12:56544599
|
T | G | 153 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(150): Show | 153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.67-17818T>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56544599 | ||||||
| chr12:56544609
|
G | A | 5 | a0001c0002t0005g0109a0001c0002t0010g0123a0001c0002t0011g0124others(2): Show | 5 | HG02145.hp1 HG02145.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.67-17808G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56544609 | ||||||
| chr12:56544753
|
A | G | 5 | a0001c0002t0005g0109a0001c0002t0010g0123a0001c0002t0011g0124others(2): Show | 5 | HG02145.hp1 HG02145.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.67-17664A>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56544753 | ||||||
| chr12:56544754
|
A | ATT | 86 | a0001c0001t0001g0004a0001c0001t0001g0034a0001c0001t0001g0070others(83): Show | 86 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(83): Show |
intron_variant | MODIFIER | c.67-17651_67-17650d others(4): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56544754 | |||||
| chr12:56544754
|
A | ATTT | 133 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(130): Show | 133 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.67-17652_67-17650d others(5): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56544754 | |||||
| chr12:56544754
|
A | ATTTT | 26 | a0001c0001t0001g0003a0001c0001t0001g0046a0001c0001t0002g0050others(23): Show | 26 | HG00140.hp1 HG00642.hp2 HG01099.hp2 others(23): Show |
intron_variant | MODIFIER | c.67-17653_67-17650d others(6): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56544754 | |||||
| chr12:56544768
|
C | T | 246 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(243): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.67-17649C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56544768 | ||||||
| chr12:56544786
|
A | G | 1 | a0001c0001t0003g0174 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.67-17631A>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56544786 | ||||||
| chr12:56544793
|
C | T | 132 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(129): Show | 132 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(129): Show |
intron_variant | MODIFIER | c.67-17624C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56544793 | ||||||
| chr12:56544857
|
G | A | 2 | a0001c0002t0004g0216a0001c0002t0050g0218 | 2 | HG03516.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.67-17560G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56544857 | ||||||
| chr12:56544917
|
G | A | 251 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(248): Show | 251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.67-17500G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56544917 | ||||||
| chr12:56544919
|
A | G | 98 | a0001c0001t0001g0004a0001c0001t0001g0101a0001c0001t0001g0110others(95): Show | 98 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.67-17498A>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56544919 | ||||||
| chr12:56545075
|
C | T | 8 | a0001c0002t0002g0232a0001c0002t0004g0186a0001c0002t0063g0146others(5): Show | 8 | HG01884.hp2 HG02055.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.67-17342C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56545075 | ||||||
| chr12:56545157
|
A | G | 1 | a0001c0002t0007g0214 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.67-17260A>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56545157 | ||||||
| chr12:56545315
|
C | T | 3 | a0001c0001t0001g0170a0001c0001t0024g0148a0001c0001t0024g0171 | 3 | NA18987.hp2 NA19000.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.67-17102C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56545315 | ||||||
| chr12:56545555
|
C | G | 2 | a0001c0002t0010g0123a0001c0002t0011g0124 | 2 | HG02145.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.67-16862C>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56545555 | ||||||
| chr12:56545809
|
T | C | 251 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(248): Show | 251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.67-16608T>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56545809 | ||||||
| chr12:56545909
|
T | C | 1 | a0001c0002t0038g0262 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.67-16508T>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56545909 | ||||||
| chr12:56545938
|
T | TTC | 6 | a0001c0002t0002g0084a0001c0002t0005g0108a0001c0002t0010g0123others(3): Show | 6 | HG01891.hp1 HG02145.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.67-16478_67-16477i others(4): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56545938 | |||||
| chr12:56545939
|
T | TC | 242 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(239): Show | 242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.67-16478_67-16477i others(3): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56545939 | ||||||
| chr12:56545940
|
T | C | 3 | a0001c0001t0001g0029a0001c0001t0002g0127a0001c0001t0031g0049 | 3 | HG01168.hp1 HG01169.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.67-16477T>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56545940 | ||||||
| chr12:56546276
|
G | C | 3 | a0001c0001t0032g0047a0001c0001t0037g0095a0001c0001t0080g0097 | 3 | HG01243.hp1 HG02602.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.67-16141G>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56546276 | ||||||
| chr12:56546307
|
T | C | 3 | a0001c0002t0003g0234a0001c0003t0006g0233a0001c0003t0075g0231 | 3 | HG01243.hp2 HG02622.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.67-16110T>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56546307 | ||||||
| chr12:56546339
|
A | ATACATTA others(46): Show |
1 | a0001c0001t0007g0152 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.67-16061_67-16060i others(55): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56546339 | |||||
| chr12:56546339
|
A | ATACATTA others(23): Show |
89 | a0001c0001t0001g0004a0001c0001t0001g0101a0001c0001t0001g0110others(86): Show | 89 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.67-16067_67-16038d others(32): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56546339 | |||||
| chr12:56546339
|
A | ATACATTA others(83): Show |
1 | a0001c0002t0003g0234 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.67-16038_67-16037i others(92): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56546339 | |||||
| chr12:56546339
|
A | ATACATTA others(113): Show |
2 | a0001c0003t0006g0233a0001c0003t0075g0231 | 2 | HG02622.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.67-16038_67-16037i others(122): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56546339 | |||||
| chr12:56546339
|
ATACATTA others(23): Show |
A | 2 | a0001c0002t0006g0092a0001c0002t0047g0091 | 2 | HG02809.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.67-16067_67-16038d others(32): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56546339 | |||||
| chr12:56546348
|
AAATATAA others(5): Show |
A | 1 | a0001c0002t0009g0017 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.67-16062_67-16051d others(14): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56546348 | |||||
| chr12:56546488
|
CA | C | 132 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(129): Show | 132 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(129): Show |
intron_variant | MODIFIER | c.67-15923delA | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56546488 | |||||
| chr12:56546623
|
G | A | 1 | a0001c0002t0067g0183 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.67-15794G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56546623 | ||||||
| chr12:56546812
|
G | A | 2 | a0001c0002t0006g0092a0001c0002t0047g0091 | 2 | HG02809.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.67-15605G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56546812 | ||||||
| chr12:56546875
|
C | T | 1 | a0001c0002t0076g0030 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.67-15542C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56546875 | ||||||
| chr12:56547072
|
G | A | 1 | a0001c0002t0002g0058 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.67-15345G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56547072 | ||||||
| chr12:56547077
|
C | T | 1 | a0001c0001t0006g0180 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.67-15340C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56547077 | ||||||
| chr12:56547115
|
C | T | 3 | a0001c0002t0003g0234a0001c0003t0006g0233a0001c0003t0075g0231 | 3 | HG01243.hp2 HG02622.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.67-15302C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56547115 | ||||||
| chr12:56547241
|
C | G | 251 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(248): Show | 251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.67-15176C>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56547241 | ||||||
| chr12:56547355
|
G | GA | 10 | a0001c0001t0001g0110a0001c0001t0001g0160a0001c0001t0001g0190others(7): Show | 10 | HG01433.hp1 HG02056.hp1 HG02071.hp1 others(7): Show |
intron_variant | MODIFIER | c.67-15056dupA | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56547355 | |||||
| chr12:56547362
|
C | A | 93 | a0001c0001t0001g0004a0001c0001t0001g0101a0001c0001t0001g0110others(90): Show | 93 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.67-15055C>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56547362 | ||||||
| chr12:56547368
|
T | C | 251 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(248): Show | 251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.67-15049T>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56547368 | ||||||
| chr12:56547577
|
C | A | 2 | a0001c0002t0023g0099a0001c0002t0034g0100 | 2 | HG02257.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.67-14840C>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56547577 | ||||||
| chr12:56547652
|
C | CT | 78 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(75): Show | 78 | HG00099.hp1 HG00140.hp2 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.67-14750dupT | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56547652 | |||||
| chr12:56547765
|
C | T | 93 | a0001c0001t0001g0004a0001c0001t0001g0101a0001c0001t0001g0110others(90): Show | 93 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.67-14652C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56547765 | ||||||
| chr12:56547836
|
A | G | 251 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(248): Show | 251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.67-14581A>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56547836 | ||||||
| chr12:56547950
|
C | A | 93 | a0001c0001t0001g0004a0001c0001t0001g0101a0001c0001t0001g0110others(90): Show | 93 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.67-14467C>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56547950 | ||||||
| chr12:56548082
|
G | A | 1 | a0001c0002t0084g0107 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.67-14335G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56548082 | ||||||
| chr12:56548151
|
A | G | 2 | a0001c0002t0017g0093a0001c0003t0073g0094 | 2 | HG02145.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.67-14266A>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56548151 | ||||||
| chr12:56548231
|
G | A | 3 | a0001c0002t0003g0234a0001c0003t0006g0233a0001c0003t0075g0231 | 3 | HG01243.hp2 HG02622.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.67-14186G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56548231 | ||||||
| chr12:56548437
|
ACT | A | 153 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(150): Show | 153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.67-13977_67-13976d others(4): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56548437 | |||||
| chr12:56548771
|
A | G | 251 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(248): Show | 251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.67-13646A>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56548771 | ||||||
| chr12:56548872
|
G | C | 251 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(248): Show | 251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.67-13545G>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56548872 | ||||||
| chr12:56548971
|
C | T | 3 | a0001c0002t0004g0186a0001c0002t0063g0146a0001c0003t0051g0191 | 3 | HG01884.hp2 HG02559.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.67-13446C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56548971 | ||||||
| chr12:56549067
|
C | T | 2 | a0001c0002t0023g0099a0001c0002t0034g0100 | 2 | HG02257.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.67-13350C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56549067 | ||||||
| chr12:56549119
|
C | T | 153 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(150): Show | 153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.67-13298C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56549119 | ||||||
| chr12:56549290
|
G | A | 12 | a0001c0001t0005g0229a0001c0001t0006g0157a0001c0001t0007g0122others(9): Show | 12 | HG02615.hp2 HG02630.hp2 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.67-13127G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56549290 | ||||||
| chr12:56549580
|
G | T | 2 | a0001c0002t0004g0223a0001c0002t0004g0224 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.67-12837G>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56549580 | ||||||
| chr12:56549749
|
A | G | 251 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(248): Show | 251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.67-12668A>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56549749 | ||||||
| chr12:56549826
|
G | A | 1 | a0001c0001t0001g0054 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.67-12591G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56549826 | ||||||
| chr12:56549863
|
A | G | 132 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(129): Show | 132 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(129): Show |
intron_variant | MODIFIER | c.67-12554A>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56549863 | ||||||
| chr12:56549935
|
A | G | 11 | a0001c0002t0002g0084a0001c0002t0002g0232a0001c0002t0004g0186others(8): Show | 11 | HG01884.hp2 HG01891.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.67-12482A>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56549935 | ||||||
| chr12:56549940
|
C | T | 3 | a0001c0001t0001g0003a0001c0001t0001g0045a0001c0001t0001g0072 | 3 | HG01255.hp2 HG02004.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.67-12477C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56549940 | ||||||
| chr12:56550014
|
G | A | 2 | a0001c0002t0004g0223a0001c0002t0004g0224 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.67-12403G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56550014 | ||||||
| chr12:56550028
|
C | A | 277 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(274): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.67-12389C>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56550028 | ||||||
| chr12:56550034
|
A | G | 1 | a0001c0001t0002g0135 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.67-12383A>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56550034 | ||||||
| chr12:56550056
|
T | C | 93 | a0001c0001t0001g0004a0001c0001t0001g0101a0001c0001t0001g0110others(90): Show | 93 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.67-12361T>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56550056 | ||||||
| chr12:56550073
|
A | G | 251 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(248): Show | 251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.67-12344A>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56550073 | ||||||
| chr12:56550525
|
C | A | 8 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(5): Show | 8 | HG00642.hp1 HG00735.hp1 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.67-11892C>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56550525 | ||||||
| chr12:56550584
|
G | A | 1 | a0001c0001t0001g0151 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.67-11833G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56550584 | ||||||
| chr12:56550849
|
T | A | 148 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(145): Show | 148 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(145): Show |
intron_variant | MODIFIER | c.67-11568T>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56550849 | ||||||
| chr12:56550853
|
T | A | 85 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(82): Show | 85 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.67-11564T>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56550853 | ||||||
| chr12:56550854
|
A | T | 1 | a0001c0001t0001g0022 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.67-11563A>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56550854 | ||||||
| chr12:56551133
|
G | A | 3 | a0001c0002t0003g0234a0001c0003t0006g0233a0001c0003t0075g0231 | 3 | HG01243.hp2 HG02622.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.67-11284G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56551133 | ||||||
| chr12:56551133
|
GA | G | 95 | a0001c0001t0001g0004a0001c0001t0001g0101a0001c0001t0001g0110others(92): Show | 95 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(92): Show |
intron_variant | MODIFIER | c.67-11274delA | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56551133 | |||||
| chr12:56551134
|
A | G | 3 | a0001c0002t0003g0234a0001c0003t0006g0233a0001c0003t0075g0231 | 3 | HG01243.hp2 HG02622.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.67-11283A>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56551134 | ||||||
| chr12:56551565
|
G | T | 1 | a0001c0002t0002g0243 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.67-10852G>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56551565 | ||||||
| chr12:56551610
|
G | A | 5 | a0001c0001t0002g0141a0001c0001t0003g0128a0001c0001t0021g0147others(2): Show | 5 | HG01109.hp2 HG02723.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.67-10807G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56551610 | ||||||
| chr12:56551646
|
CAAGTT | C | 98 | a0001c0001t0001g0004a0001c0001t0001g0101a0001c0001t0001g0110others(95): Show | 98 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.67-10767_67-10763d others(7): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56551646 | |||||
| chr12:56551685
|
G | C | 1 | a0001c0001t0001g0190 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.67-10732G>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56551685 | ||||||
| chr12:56551908
|
C | G | 11 | a0001c0002t0002g0084a0001c0002t0002g0232a0001c0002t0004g0186others(8): Show | 11 | HG01884.hp2 HG01891.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.67-10509C>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56551908 | ||||||
| chr12:56552037
|
G | A | 1 | a0001c0001t0037g0095 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.67-10380G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56552037 | ||||||
| chr12:56552231
|
T | C | 2 | a0001c0002t0023g0099a0001c0002t0034g0100 | 2 | HG02257.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.67-10186T>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56552231 | ||||||
| chr12:56552456
|
A | G | 79 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(76): Show | 79 | HG00099.hp1 HG00140.hp2 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.67-9961A>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56552456 | ||||||
| chr12:56552649
|
A | G | 246 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(243): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.67-9768A>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56552649 | ||||||
| chr12:56552912
|
A | G | 2 | a0001c0001t0002g0125a0001c0001t0003g0131 | 2 | NA18990.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.67-9505A>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56552912 | ||||||
| chr12:56552922
|
C | CT | 5 | a0001c0002t0010g0123a0001c0002t0011g0124a0001c0002t0049g0213others(2): Show | 5 | HG01169.hp1 HG02145.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.67-9471dupT | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56552922 | |||||
| chr12:56552922
|
CT | C | 23 | a0001c0001t0001g0043a0001c0001t0001g0110a0001c0001t0001g0154others(20): Show | 23 | HG00639.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.67-9471delT | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56552922 | |||||
| chr12:56552922
|
CTT | C | 210 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(207): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.67-9472_67-9471del others(2): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56552922 | |||||
| chr12:56552922
|
CTTT | C | 9 | a0001c0001t0001g0190a0001c0001t0003g0066a0001c0001t0020g0111others(6): Show | 9 | HG01515.hp2 HG02055.hp1 HG02155.hp2 others(6): Show |
intron_variant | MODIFIER | c.67-9473_67-9471del others(3): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56552922 | |||||
| chr12:56553034
|
T | G | 14 | a0001c0002t0002g0084a0001c0002t0002g0232a0001c0002t0003g0200others(11): Show | 14 | HG01884.hp2 HG01891.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.67-9383T>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56553034 | ||||||
| chr12:56553238
|
G | A | 1 | a0001c0002t0002g0185 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.67-9179G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56553238 | ||||||
| chr12:56553298
|
T | C | 1 | a0001c0001t0002g0075 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.67-9119T>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56553298 | ||||||
| chr12:56553366
|
T | A | 1 | a0001c0001t0021g0167 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.67-9051T>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56553366 | ||||||
| chr12:56553397
|
C | A | 1 | a0001c0003t0051g0191 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.67-9020C>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56553397 | ||||||
| chr12:56553462
|
A | G | 251 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(248): Show | 251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.67-8955A>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56553462 | ||||||
| chr12:56553612
|
G | C | 12 | a0001c0001t0005g0229a0001c0001t0006g0157a0001c0001t0007g0122others(9): Show | 12 | HG02615.hp2 HG02630.hp2 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.67-8805G>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56553612 | ||||||
| chr12:56553696
|
G | C | 1 | a0001c0002t0008g0239 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.67-8721G>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56553696 | ||||||
| chr12:56553751
|
G | T | 1 | a0001c0002t0005g0236 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.67-8666G>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56553751 | ||||||
| chr12:56553781
|
A | G | 1 | a0001c0001t0060g0059 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.67-8636A>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56553781 | ||||||
| chr12:56553826
|
GT | G | 14 | a0001c0002t0002g0084a0001c0002t0003g0234a0001c0002t0003g0268others(11): Show | 14 | HG01243.hp2 HG01891.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.67-8575delT | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56553826 | |||||
| chr12:56553826
|
GTT | G | 142 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(139): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(139): Show |
intron_variant | MODIFIER | c.67-8576_67-8575del others(2): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56553826 | |||||
| chr12:56554252
|
A | G | 2 | a0001c0001t0002g0169a0001c0001t0025g0080 | 2 | NA18951.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.67-8165A>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56554252 | ||||||
| chr12:56554969
|
A | G | 1 | a0001c0002t0005g0109 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.67-7448A>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56554969 | ||||||
| chr12:56555002
|
C | A | 92 | a0001c0001t0001g0004a0001c0001t0001g0101a0001c0001t0001g0110others(89): Show | 92 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(89): Show |
intron_variant | MODIFIER | c.67-7415C>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56555002 | ||||||
| chr12:56555036
|
C | T | 2 | a0001c0001t0031g0049a0001c0001t0031g0078 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.67-7381C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56555036 | ||||||
| chr12:56555072
|
T | TA | 249 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(246): Show | 249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.67-7335dupA | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56555072 | |||||
| chr12:56555225
|
T | C | 17 | a0001c0002t0002g0084a0001c0002t0002g0232a0001c0002t0002g0243others(14): Show | 17 | HG01884.hp2 HG01891.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.67-7192T>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56555225 | ||||||
| chr12:56555314
|
C | T | 15 | a0001c0002t0002g0084a0001c0002t0002g0232a0001c0002t0003g0200others(12): Show | 15 | HG01884.hp2 HG01891.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.67-7103C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56555314 | ||||||
| chr12:56555386
|
T | G | 17 | a0001c0002t0002g0084a0001c0002t0002g0232a0001c0002t0002g0243others(14): Show | 17 | HG01884.hp2 HG01891.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.67-7031T>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56555386 | ||||||
| chr12:56555387
|
A | C | 17 | a0001c0002t0002g0084a0001c0002t0002g0232a0001c0002t0002g0243others(14): Show | 17 | HG01884.hp2 HG01891.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.67-7030A>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56555387 | ||||||
| chr12:56555440
|
C | CA | 27 | a0001c0001t0001g0002a0001c0001t0002g0009a0001c0001t0005g0229others(24): Show | 27 | HG00558.hp1 HG00597.hp2 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.67-6961dupA | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56555440 | |||||
| chr12:56555548
|
A | G | 5 | a0001c0001t0032g0047a0001c0001t0035g0098a0001c0001t0036g0096others(2): Show | 5 | HG01243.hp1 HG02602.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.67-6869A>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56555548 | ||||||
| chr12:56556046
|
T | TA | 19 | a0001c0001t0029g0083a0001c0002t0002g0084a0001c0002t0002g0232others(16): Show | 19 | HG01884.hp2 HG01891.hp1 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.67-6357dupA | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56556046 | |||||
| chr12:56556056
|
A | G | 5 | a0001c0001t0032g0047a0001c0001t0035g0098a0001c0001t0036g0096others(2): Show | 5 | HG01243.hp1 HG02602.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.67-6361A>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56556056 | ||||||
| chr12:56556288
|
T | G | 2 | a0001c0002t0010g0123a0001c0002t0011g0124 | 2 | HG02145.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.67-6129T>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56556288 | ||||||
| chr12:56556376
|
C | CT | 14 | a0001c0001t0003g0042a0001c0001t0021g0189a0001c0001t0025g0080others(11): Show | 14 | HG00621.hp2 HG01109.hp2 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.67-6025dupT | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56556376 | |||||
| chr12:56556408
|
C | T | 1 | a0001c0001t0035g0098 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.67-6009C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56556408 | ||||||
| chr12:56556522
|
C | T | 250 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(247): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.67-5895C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56556522 | ||||||
| chr12:56556578
|
G | A | 1 | a0001c0002t0003g0200 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.67-5839G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56556578 | ||||||
| chr12:56556601
|
C | A | 3 | a0001c0002t0003g0200a0001c0002t0012g0226a0001c0002t0055g0235 | 3 | HG02055.hp1 HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.67-5816C>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56556601 | ||||||
| chr12:56556918
|
T | C | 3 | a0001c0002t0005g0109a0001c0002t0017g0093a0001c0003t0073g0094 | 3 | HG02145.hp1 HG02257.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.67-5499T>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56556918 | ||||||
| chr12:56557276
|
G | A | 1 | a0001c0002t0014g0168 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.67-5141G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56557276 | ||||||
| chr12:56557348
|
C | A | 1 | a0001c0001t0037g0095 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.67-5069C>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56557348 | ||||||
| chr12:56557435
|
G | A | 131 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(128): Show |
intron_variant | MODIFIER | c.67-4982G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56557435 | ||||||
| chr12:56557726
|
T | TTTTTC | 3 | a0001c0002t0005g0109a0001c0002t0017g0093a0001c0003t0073g0094 | 3 | HG02145.hp1 HG02257.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.67-4676_67-4672dup others(5): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56557726 | |||||
| chr12:56557741
|
C | T | 4 | a0001c0001t0006g0180a0001c0001t0011g0159a0001c0001t0011g0201others(1): Show | 4 | HG01891.hp2 HG03130.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.67-4676C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56557741 | ||||||
| chr12:56557741
|
CT | C | 18 | a0001c0001t0003g0066a0001c0001t0053g0020a0001c0002t0002g0084others(15): Show | 18 | HG00639.hp1 HG01884.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.67-4662delT | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56557741 | |||||
| chr12:56557805
|
G | C | 249 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(246): Show | 249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.67-4612G>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56557805 | ||||||
| chr12:56557965
|
C | T | 1 | a0001c0002t0002g0243 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.67-4452C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56557965 | ||||||
| chr12:56557986
|
G | A | 18 | a0001c0002t0004g0206a0001c0002t0004g0215a0001c0002t0004g0216others(15): Show | 19 | HG01167.hp1 HG01169.hp1 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.67-4431G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56557986 | ||||||
| chr12:56557987
|
C | T | 132 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(129): Show | 132 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(129): Show |
intron_variant | MODIFIER | c.67-4430C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56557987 | ||||||
| chr12:56557999
|
A | G | 2 | a0001c0002t0010g0123a0001c0002t0011g0124 | 2 | HG02145.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.67-4418A>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56557999 | ||||||
| chr12:56558038
|
C | CT | 6 | a0001c0001t0002g0075a0001c0002t0005g0109a0001c0002t0010g0194others(3): Show | 6 | HG01167.hp2 HG02257.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.67-4355dupT | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56558038 | |||||
| chr12:56558038
|
CT | C | 134 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(131): Show | 134 | HG00099.hp2 HG00140.hp1 HG00544.hp1 others(131): Show |
intron_variant | MODIFIER | c.67-4355delT | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56558038 | |||||
| chr12:56558038
|
CTT | C | 91 | a0001c0001t0001g0004a0001c0001t0001g0023a0001c0001t0001g0101others(88): Show | 91 | HG00544.hp2 HG00558.hp1 HG00639.hp1 others(88): Show |
intron_variant | MODIFIER | c.67-4356_67-4355del others(2): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56558038 | |||||
| chr12:56558038
|
CTTT | C | 5 | a0001c0001t0001g0052a0001c0001t0001g0121a0001c0001t0003g0161others(2): Show | 5 | HG01934.hp1 HG02735.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.67-4357_67-4355del others(3): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56558038 | |||||
| chr12:56558038
|
CTTTTTTT others(5): Show |
C | 1 | a0001c0002t0017g0093 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.67-4366_67-4355del others(12): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56558038 | |||||
| chr12:56558098
|
G | A | 1 | a0001c0003t0006g0233 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.67-4319G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56558098 | ||||||
| chr12:56558205
|
G | A | 1 | a0001c0002t0002g0243 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.67-4212G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56558205 | ||||||
| chr12:56558238
|
G | A | 2 | a0001c0002t0023g0099a0001c0002t0034g0100 | 2 | HG02257.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.67-4179G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56558238 | ||||||
| chr12:56558273
|
C | T | 1 | a0001c0002t0006g0092 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.67-4144C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56558273 | ||||||
| chr12:56558288
|
C | T | 124 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(121): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.67-4129C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56558288 | ||||||
| chr12:56558297
|
C | CGGCCTCC others(294): Show |
1 | a0001c0002t0003g0234 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.67-4083_67-4082ins others(301): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56558297 | |||||
| chr12:56558297
|
C | CGGCCTCC others(295): Show |
3 | a0001c0002t0048g0106a0001c0003t0006g0233a0001c0003t0075g0231 | 3 | HG02622.hp1 HG02647.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.67-4083_67-4082ins others(302): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56558297 | |||||
| chr12:56558297
|
C | CGGCCTCC others(296): Show |
1 | a0001c0002t0005g0109 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.67-4083_67-4082ins others(303): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56558297 | |||||
| chr12:56558297
|
C | CGGCCTCC others(297): Show |
12 | a0001c0001t0001g0023a0001c0001t0008g0061a0001c0002t0002g0084others(9): Show | 12 | HG01256.hp1 HG01884.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.67-4083_67-4082ins others(304): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56558297 | |||||
| chr12:56558297
|
C | CGGCCTCC others(298): Show |
1 | a0001c0001t0002g0009 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.67-4083_67-4082ins others(305): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56558297 | |||||
| chr12:56558297
|
C | CGGCCTCC others(298): Show |
1 | a0001c0002t0002g0243 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.67-4083_67-4082ins others(305): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56558297 | |||||
| chr12:56558297
|
C | CGGCCTCC others(298): Show |
114 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(111): Show | 114 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(111): Show |
intron_variant | MODIFIER | c.67-4083_67-4082ins others(305): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56558297 | |||||
| chr12:56558297
|
C | CGGCCTCC others(298): Show |
2 | a0001c0001t0001g0052a0001c0001t0053g0020 | 2 | HG00639.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.67-4083_67-4082ins others(305): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56558297 | |||||
| chr12:56558297
|
C | CGGCCTCC others(299): Show |
15 | a0001c0001t0001g0003a0001c0001t0001g0043a0001c0001t0001g0070others(12): Show | 15 | HG01099.hp2 HG01106.hp1 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.67-4083_67-4082ins others(306): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56558297 | |||||
| chr12:56558297
|
C | CGGCCTCC others(300): Show |
1 | a0001c0001t0019g0139 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.67-4083_67-4082ins others(307): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56558297 | |||||
| chr12:56558297
|
C | CGGCCTCC others(300): Show |
1 | a0001c0002t0001g0245 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.67-4083_67-4082ins others(307): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56558297 | |||||
| chr12:56558297
|
C | CGGCCTCC others(302): Show |
59 | a0001c0001t0001g0101a0001c0001t0001g0110a0001c0001t0001g0121others(56): Show | 59 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.67-4083_67-4082ins others(309): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56558297 | |||||
| chr12:56558297
|
C | CGGCCTCC others(303): Show |
31 | a0001c0001t0001g0004a0001c0001t0001g0151a0001c0001t0001g0153others(28): Show | 31 | HG00597.hp1 HG01099.hp1 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.67-4083_67-4082ins others(310): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56558297 | |||||
| chr12:56558297
|
C | CGGCCTCC others(304): Show |
3 | a0001c0001t0001g0140a0001c0001t0007g0152a0001c0001t0008g0181 | 3 | HG02280.hp2 HG02630.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.67-4083_67-4082ins others(311): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56558297 | |||||
| chr12:56558297
|
C | CGGCCTCC others(305): Show |
2 | a0001c0002t0010g0123a0001c0002t0011g0124 | 2 | HG02145.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.67-4083_67-4082ins others(312): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56558297 | |||||
| chr12:56558309
|
G | GTGCTGGG others(298): Show |
2 | a0001c0002t0017g0093a0001c0003t0073g0094 | 2 | HG02145.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.67-4083_67-4082ins others(305): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56558309 | |||||
| chr12:56558500
|
G | T | 8 | a0001c0002t0001g0272a0001c0002t0001g0273a0001c0002t0001g0275others(5): Show | 8 | HG00621.hp2 HG01361.hp2 HG01928.hp1 others(5): Show |
intron_variant | MODIFIER | c.67-3917G>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56558500 | ||||||
| chr12:56558567
|
TCTTTCC | T | 3 | a0001c0002t0003g0200a0001c0002t0012g0226a0001c0002t0055g0235 | 3 | HG02055.hp1 HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.67-3849_67-3844del others(6): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56558567 | ||||||
| chr12:56558576
|
C | T | 3 | a0001c0002t0003g0200a0001c0002t0012g0226a0001c0002t0055g0235 | 3 | HG02055.hp1 HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.67-3841C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56558576 | ||||||
| chr12:56558584
|
T | C | 3 | a0001c0002t0003g0200a0001c0002t0012g0226a0001c0002t0055g0235 | 3 | HG02055.hp1 HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.67-3833T>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56558584 | ||||||
| chr12:56558590
|
C | CT | 64 | a0001c0002t0001g0119a0001c0002t0001g0245a0001c0002t0001g0249others(61): Show | 64 | HG00099.hp2 HG00140.hp1 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.67-3811dupT | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56558590 | |||||
| chr12:56558590
|
C | CTT | 18 | a0001c0001t0032g0047a0001c0001t0035g0098a0001c0001t0036g0096others(15): Show | 18 | HG01243.hp1 HG01243.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.67-3812_67-3811dup others(2): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56558590 | |||||
| chr12:56558590
|
C | CTTT | 10 | a0001c0001t0001g0036a0001c0001t0001g0137a0001c0001t0002g0075others(7): Show | 10 | HG01167.hp2 HG01169.hp2 HG02155.hp2 others(7): Show |
intron_variant | MODIFIER | c.67-3813_67-3811dup others(3): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56558590 | |||||
| chr12:56558590
|
C | CTTTT | 146 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(143): Show | 146 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(143): Show |
intron_variant | MODIFIER | c.67-3814_67-3811dup others(4): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56558590 | |||||
| chr12:56558590
|
C | CTTTTT | 7 | a0001c0001t0001g0145a0001c0001t0001g0177a0001c0001t0009g0136others(4): Show | 7 | HG01109.hp1 HG01433.hp1 HG02148.hp2 others(4): Show |
intron_variant | MODIFIER | c.67-3815_67-3811dup others(5): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56558590 | |||||
| chr12:56558770
|
AT | A | 169 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(166): Show | 169 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(166): Show |
intron_variant | MODIFIER | c.67-3637delT | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56558770 | |||||
| chr12:56558780
|
T | A | 3 | a0001c0002t0008g0239a0001c0002t0045g0261a0001c0002t0072g0259 | 3 | HG03491.hp1 HG03831.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.67-3637T>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56558780 | ||||||
| chr12:56558862
|
T | C | 1 | a0001c0002t0017g0093 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.67-3555T>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56558862 | ||||||
| chr12:56558880
|
T | G | 248 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(245): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.67-3537T>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56558880 | ||||||
| chr12:56558979
|
C | T | 2 | a0001c0002t0002g0084a0001c0002t0084g0107 | 2 | NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.67-3438C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56558979 | ||||||
| chr12:56559094
|
G | A | 250 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(247): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.67-3323G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56559094 | ||||||
| chr12:56559186
|
A | AT | 31 | a0001c0001t0001g0101a0001c0001t0001g0110a0001c0001t0001g0130others(28): Show | 31 | HG00558.hp1 HG00639.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.67-3221dupT | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56559186 | |||||
| chr12:56559203
|
A | G | 251 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(248): Show | 251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.67-3214A>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56559203 | ||||||
| chr12:56559218
|
T | C | 251 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(248): Show | 251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.67-3199T>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56559218 | ||||||
| chr12:56559236
|
G | A | 2 | a0001c0002t0010g0123a0001c0002t0011g0124 | 2 | HG02145.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.67-3181G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56559236 | ||||||
| chr12:56559242
|
C | T | 2 | a0001c0002t0017g0093a0001c0003t0073g0094 | 2 | HG02145.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.67-3175C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56559242 | ||||||
| chr12:56559331
|
G | A | 1 | a0001c0002t0006g0202 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.67-3086G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56559331 | ||||||
| chr12:56559647
|
C | T | 2 | a0001c0002t0005g0108a0001c0002t0048g0106 | 2 | HG01891.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.67-2770C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56559647 | ||||||
| chr12:56559668
|
G | A | 1 | a0001c0001t0001g0015 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.67-2749G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56559668 | ||||||
| chr12:56559710
|
G | A | 2 | a0001c0002t0017g0093a0001c0003t0073g0094 | 2 | HG02145.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.67-2707G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56559710 | ||||||
| chr12:56559786
|
C | G | 278 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(275): Show | 279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.67-2631C>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56559786 | ||||||
| chr12:56559787
|
G | C | 278 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(275): Show | 279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.67-2630G>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56559787 | ||||||
| chr12:56559850
|
CA | C | 22 | a0001c0002t0002g0211a0001c0002t0004g0206a0001c0002t0004g0215others(19): Show | 23 | HG01167.hp1 HG01257.hp2 HG01361.hp1 others(20): Show |
intron_variant | MODIFIER | c.67-2542delA | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56559850 | |||||
| chr12:56559850
|
CAA | C | 15 | a0001c0002t0001g0245a0001c0002t0001g0263a0001c0002t0001g0275others(12): Show | 15 | HG01169.hp1 HG01361.hp2 HG01978.hp2 others(12): Show |
intron_variant | MODIFIER | c.67-2543_67-2542del others(2): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56559850 | |||||
| chr12:56559850
|
CAAA | C | 55 | a0001c0002t0001g0119a0001c0002t0001g0249a0001c0002t0001g0256others(52): Show | 55 | HG00099.hp2 HG00140.hp1 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.67-2544_67-2542del others(3): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56559850 | |||||
| chr12:56559850
|
CAAAA | C | 14 | a0001c0001t0008g0181a0001c0002t0002g0084a0001c0002t0002g0232others(11): Show | 14 | HG01884.hp2 HG02055.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.67-2545_67-2542del others(4): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56559850 | |||||
| chr12:56559850
|
CAAAAA | C | 6 | a0001c0001t0001g0005a0001c0001t0001g0110a0001c0001t0001g0137others(3): Show | 6 | HG01099.hp2 HG01952.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.67-2546_67-2542del others(5): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56559850 | |||||
| chr12:56559850
|
CAAAAAA | C | 160 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(157): Show | 160 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(157): Show |
intron_variant | MODIFIER | c.67-2547_67-2542del others(6): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56559850 | |||||
| chr12:56559895
|
CT | C | 84 | a0001c0001t0001g0012a0001c0001t0001g0137a0001c0001t0001g0190others(81): Show | 84 | HG00099.hp2 HG00140.hp1 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.67-2505delT | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56559895 | |||||
| chr12:56559895
|
CTT | C | 163 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(160): Show | 163 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(160): Show |
intron_variant | MODIFIER | c.67-2506_67-2505del others(2): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56559895 | |||||
| chr12:56559899
|
T | C | 1 | a0001c0002t0002g0243 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.67-2518T>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56559899 | ||||||
| chr12:56559981
|
G | T | 2 | a0001c0002t0017g0093a0001c0003t0073g0094 | 2 | HG02145.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.67-2436G>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56559981 | ||||||
| chr12:56559986
|
CCAGGTT | C | 169 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(166): Show | 169 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(166): Show |
intron_variant | MODIFIER | c.67-2428_67-2423del others(6): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56559986 | |||||
| chr12:56560048
|
C | G | 1 | a0001c0002t0003g0248 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.67-2369C>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56560048 | ||||||
| chr12:56560052
|
G | A | 7 | a0001c0002t0002g0232a0001c0002t0004g0186a0001c0002t0081g0102others(4): Show | 7 | HG02055.hp2 HG02559.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.67-2365G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56560052 | ||||||
| chr12:56560132
|
T | C | 169 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(166): Show | 169 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(166): Show |
intron_variant | MODIFIER | c.67-2285T>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56560132 | ||||||
| chr12:56560260
|
A | AT | 7 | a0001c0001t0014g0264a0001c0001t0032g0047a0001c0001t0035g0098others(4): Show | 7 | HG01243.hp1 HG01884.hp2 HG02602.hp2 others(4): Show |
intron_variant | MODIFIER | c.67-2143dupT | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56560260 | |||||
| chr12:56560260
|
AT | A | 60 | a0001c0001t0003g0161a0001c0002t0001g0119a0001c0002t0001g0245others(57): Show | 60 | HG00099.hp2 HG00140.hp1 HG00544.hp1 others(57): Show |
intron_variant | MODIFIER | c.67-2143delT | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56560260 | |||||
| chr12:56560280
|
G | A | 7 | a0001c0002t0002g0232a0001c0002t0004g0186a0001c0002t0081g0102others(4): Show | 7 | HG02055.hp2 HG02559.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.67-2137G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56560280 | ||||||
| chr12:56560325
|
C | T | 163 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(160): Show | 163 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(160): Show |
intron_variant | MODIFIER | c.67-2092C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56560325 | ||||||
| chr12:56560326
|
G | A | 3 | a0001c0002t0003g0200a0001c0002t0012g0226a0001c0002t0055g0235 | 3 | HG02055.hp1 HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.67-2091G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56560326 | ||||||
| chr12:56560359
|
C | T | 1 | a0001c0002t0002g0211 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.67-2058C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56560359 | ||||||
| chr12:56560553
|
C | T | 3 | a0001c0001t0002g0178a0001c0001t0019g0039a0001c0001t0040g0011 | 3 | NA18954.hp2 NA18975.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.67-1864C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56560553 | ||||||
| chr12:56560833
|
G | C | 5 | a0001c0002t0001g0272a0001c0002t0001g0275a0001c0002t0001g0276others(2): Show | 5 | HG01361.hp2 HG01928.hp1 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.67-1584G>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56560833 | ||||||
| chr12:56561094
|
T | A | 1 | a0001c0005t0009g0134 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.67-1323T>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56561094 | ||||||
| chr12:56561134
|
A | G | 3 | a0001c0002t0003g0234a0001c0003t0006g0233a0001c0003t0075g0231 | 3 | HG01243.hp2 HG02622.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.67-1283A>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56561134 | ||||||
| chr12:56561537
|
C | T | 1 | a0001c0002t0004g0228 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.67-880C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56561537 | ||||||
| chr12:56561580
|
C | T | 7 | a0001c0002t0002g0232a0001c0002t0004g0186a0001c0002t0081g0102others(4): Show | 7 | HG02055.hp2 HG02559.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.67-837C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56561580 | ||||||
| chr12:56561673
|
A | AT | 24 | a0001c0001t0001g0008a0001c0001t0001g0036a0001c0001t0002g0067others(21): Show | 24 | HG00642.hp1 HG01361.hp1 HG02145.hp1 others(21): Show |
intron_variant | MODIFIER | c.67-728dupT | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56561673 | |||||
| chr12:56561673
|
AT | A | 25 | a0001c0001t0001g0004a0001c0001t0001g0121a0001c0001t0001g0142others(22): Show | 25 | HG01109.hp1 HG01243.hp2 HG02083.hp1 others(22): Show |
intron_variant | MODIFIER | c.67-728delT | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56561673 | |||||
| chr12:56561707
|
G | A | 1 | a0001c0001t0071g0192 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.67-710G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56561707 | ||||||
| chr12:56561732
|
G | T | 11 | a0001c0002t0002g0084a0001c0002t0002g0243a0001c0002t0005g0108others(8): Show | 11 | HG01891.hp1 HG02145.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.67-685G>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56561732 | ||||||
| chr12:56561765
|
CCCT | C | 59 | a0001c0001t0005g0229a0001c0001t0006g0157a0001c0001t0007g0122others(56): Show | 59 | HG00544.hp1 HG00621.hp2 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.67-648_67-646delCC others(1): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56561765 | |||||
| chr12:56561766
|
CCT | C | 97 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0023others(94): Show | 97 | HG00099.hp2 HG00140.hp1 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.67-649_67-648delTC | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 56561766 | |||||
| chr12:56561767
|
CT | C | 77 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(74): Show | 77 | HG00099.hp1 HG00140.hp2 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.67-649delT | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56561767 | ||||||
| chr12:56561768
|
T | C | 16 | a0001c0001t0001g0010a0001c0001t0001g0077a0001c0001t0002g0051others(13): Show | 16 | HG01891.hp1 HG02055.hp2 HG02071.hp2 others(13): Show |
intron_variant | MODIFIER | c.67-649T>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56561768 | ||||||
| chr12:56561771
|
T | C | 11 | a0001c0001t0005g0229a0001c0001t0006g0157a0001c0001t0007g0122others(8): Show | 11 | HG02615.hp2 HG02630.hp2 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.67-646T>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56561771 | ||||||
| chr12:56561772
|
T | C | 1 | a0001c0001t0012g0114 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.67-645T>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56561772 | ||||||
| chr12:56561817
|
G | A | 1 | a0001c0002t0014g0168 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.67-600G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56561817 | ||||||
| chr12:56561846
|
C | T | 3 | a0001c0002t0006g0202a0001c0002t0026g0205a0001c0002t0026g0208 | 3 | HG02895.hp1 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.67-571C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56561846 | ||||||
| chr12:56561927
|
C | A | 13 | a0001c0002t0002g0232a0001c0002t0003g0200a0001c0002t0003g0234others(10): Show | 13 | HG01243.hp2 HG02055.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.67-490C>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56561927 | ||||||
| chr12:56562051
|
G | A | 58 | a0001c0002t0001g0119a0001c0002t0001g0245a0001c0002t0001g0249others(55): Show | 58 | HG00099.hp2 HG00140.hp1 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.67-366G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56562051 | ||||||
| chr12:56562242
|
T | A | 1 | a0001c0002t0005g0150 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.67-175T>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 1/13 | chr12 | 56562242 | ||||||
| chr12:56562658
|
G | A | 5 | a0001c0001t0032g0047a0001c0001t0035g0098a0001c0001t0036g0096others(2): Show | 5 | HG01243.hp1 HG02602.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.233+75G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 2/13 | chr12 | 56562658 | ||||||
| chr12:56562707
|
T | C | 2 | a0001c0002t0004g0223a0001c0002t0004g0224 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.233+124T>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 2/13 | chr12 | 56562707 | ||||||
| chr12:56562897
|
C | T | 3 | a0001c0002t0003g0200a0001c0002t0012g0226a0001c0002t0055g0235 | 3 | HG02055.hp1 HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.233+314C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 2/13 | chr12 | 56562897 | ||||||
| chr12:56562914
|
A | G | 168 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(165): Show | 168 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(165): Show |
intron_variant | MODIFIER | c.233+331A>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 2/13 | chr12 | 56562914 | ||||||
| chr12:56562980
|
G | A | 1 | a0001c0001t0003g0042 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.233+397G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 2/13 | chr12 | 56562980 | ||||||
| chr12:56562991
|
C | T | 16 | a0001c0001t0001g0004a0001c0001t0001g0056a0001c0001t0001g0121others(13): Show | 16 | HG01099.hp1 HG01109.hp1 HG02132.hp1 others(13): Show |
intron_variant | MODIFIER | c.233+408C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 2/13 | chr12 | 56562991 | ||||||
| chr12:56563008
|
A | G | 1 | a0001c0002t0063g0146 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.233+425A>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 2/13 | chr12 | 56563008 | ||||||
| chr12:56563017
|
G | A | 5 | a0001c0002t0001g0256a0001c0002t0001g0269a0001c0002t0001g0270others(2): Show | 5 | HG00099.hp2 HG00140.hp1 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.233+434G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 2/13 | chr12 | 56563017 | ||||||
| chr12:56563101
|
C | T | 5 | a0001c0002t0001g0256a0001c0002t0001g0269a0001c0002t0001g0270others(2): Show | 5 | HG00099.hp2 HG00140.hp1 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.233+518C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 2/13 | chr12 | 56563101 | ||||||
| chr12:56563232
|
C | T | 11 | a0001c0002t0002g0084a0001c0002t0002g0243a0001c0002t0005g0108others(8): Show | 11 | HG01891.hp1 HG02145.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.233+649C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 2/13 | chr12 | 56563232 | ||||||
| chr12:56563235
|
A | G | 2 | a0001c0002t0003g0200a0001c0002t0055g0235 | 2 | HG02055.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.233+652A>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 2/13 | chr12 | 56563235 | ||||||
| chr12:56563384
|
C | T | 10 | a0001c0002t0002g0232a0001c0002t0003g0200a0001c0002t0004g0186others(7): Show | 10 | HG02055.hp1 HG02055.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.233+801C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 2/13 | chr12 | 56563384 | ||||||
| chr12:56563808
|
T | C | 2 | a0001c0002t0010g0123a0001c0002t0011g0124 | 2 | HG02145.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.233+1225T>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 2/13 | chr12 | 56563808 | ||||||
| chr12:56563871
|
G | T | 3 | a0001c0002t0003g0234a0001c0003t0006g0233a0001c0003t0075g0231 | 3 | HG01243.hp2 HG02622.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.233+1288G>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 2/13 | chr12 | 56563871 | ||||||
| chr12:56563990
|
TA | T | 4 | a0001c0001t0006g0180a0001c0001t0011g0159a0001c0001t0011g0201others(1): Show | 4 | HG01891.hp2 HG03130.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.233+1410delA | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 56563990 | |||||
| chr12:56564046
|
T | A | 1 | a0001c0002t0002g0243 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.233+1463T>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 2/13 | chr12 | 56564046 | ||||||
| chr12:56564108
|
G | C | 252 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(249): Show | 252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.233+1525G>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 2/13 | chr12 | 56564108 | ||||||
| chr12:56564122
|
T | G | 2 | a0001c0002t0004g0186a0001c0003t0051g0191 | 2 | HG02559.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.233+1539T>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 2/13 | chr12 | 56564122 | ||||||
| chr12:56564201
|
C | T | 174 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(171): Show | 174 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(171): Show |
intron_variant | MODIFIER | c.233+1618C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 2/13 | chr12 | 56564201 | ||||||
| chr12:56564609
|
C | T | 1 | a0001c0002t0002g0115 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.233+2026C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 2/13 | chr12 | 56564609 | ||||||
| chr12:56564663
|
T | C | 231 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(228): Show | 232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.233+2080T>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 2/13 | chr12 | 56564663 | ||||||
| chr12:56564739
|
C | A | 2 | a0001c0002t0004g0186a0001c0003t0051g0191 | 2 | HG02559.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.233+2156C>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 2/13 | chr12 | 56564739 | ||||||
| chr12:56564823
|
A | T | 1 | a0001c0001t0029g0083 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.233+2240A>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 2/13 | chr12 | 56564823 | ||||||
| chr12:56564854
|
G | A | 1 | a0001c0001t0027g0065 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.233+2271G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 2/13 | chr12 | 56564854 | ||||||
| chr12:56564889
|
T | A | 219 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(216): Show | 220 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(217): Show |
intron_variant | MODIFIER | c.233+2306T>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 2/13 | chr12 | 56564889 | ||||||
| chr12:56564906
|
A | G | 8 | a0001c0001t0001g0170a0001c0001t0002g0129a0001c0001t0003g0219others(5): Show | 8 | HG00544.hp2 HG00597.hp1 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.233+2323A>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 2/13 | chr12 | 56564906 | ||||||
| chr12:56565121
|
A | G | 2 | a0001c0002t0017g0093a0001c0003t0073g0094 | 2 | HG02145.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.233+2538A>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 2/13 | chr12 | 56565121 | ||||||
| chr12:56565602
|
G | C | 8 | a0001c0001t0001g0170a0001c0001t0002g0129a0001c0001t0003g0219others(5): Show | 8 | HG00544.hp2 HG00597.hp1 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.233+3019G>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 2/13 | chr12 | 56565602 | ||||||
| chr12:56565805
|
T | G | 1 | a0001c0001t0029g0083 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.234-3170T>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 2/13 | chr12 | 56565805 | ||||||
| chr12:56565896
|
G | A | 1 | a0001c0002t0005g0236 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.234-3079G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 2/13 | chr12 | 56565896 | ||||||
| chr12:56566196
|
T | C | 1 | a0001c0002t0001g0256 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.234-2779T>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 2/13 | chr12 | 56566196 | ||||||
| chr12:56566484
|
T | C | 6 | a0001c0001t0001g0151a0001c0002t0001g0256a0001c0002t0001g0269others(3): Show | 6 | HG00099.hp2 HG00140.hp1 HG02698.hp2 others(3): Show |
intron_variant | MODIFIER | c.234-2491T>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 2/13 | chr12 | 56566484 | ||||||
| chr12:56566496
|
C | A | 1 | a0001c0001t0029g0083 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.234-2479C>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 2/13 | chr12 | 56566496 | ||||||
| chr12:56566547
|
G | A | 2 | a0001c0002t0004g0216a0001c0002t0050g0218 | 2 | HG03516.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.234-2428G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 2/13 | chr12 | 56566547 | ||||||
| chr12:56566749
|
C | T | 2 | a0001c0002t0002g0084a0001c0002t0084g0107 | 2 | NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.234-2226C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 2/13 | chr12 | 56566749 | ||||||
| chr12:56566914
|
C | A | 2 | a0001c0002t0001g0270a0001c0002t0067g0183 | 2 | HG00140.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.234-2061C>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 2/13 | chr12 | 56566914 | ||||||
| chr12:56566982
|
T | A | 58 | a0001c0001t0002g0165a0001c0001t0006g0180a0001c0001t0012g0114others(55): Show | 58 | HG00544.hp1 HG00621.hp2 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.234-1993T>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 2/13 | chr12 | 56566982 | ||||||
| chr12:56567258
|
G | A | 1 | a0001c0002t0002g0243 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.234-1717G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 2/13 | chr12 | 56567258 | ||||||
| chr12:56567381
|
A | G | 250 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(247): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.234-1594A>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 2/13 | chr12 | 56567381 | ||||||
| chr12:56567385
|
CA | C | 58 | a0001c0001t0001g0173a0001c0001t0002g0165a0001c0001t0006g0180others(55): Show | 58 | HG00544.hp1 HG00621.hp2 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.234-1577delA | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 56567385 | |||||
| chr12:56567435
|
G | C | 8 | a0001c0001t0005g0229a0001c0001t0006g0157a0001c0001t0010g0225others(5): Show | 8 | HG02922.hp1 HG02965.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.234-1540G>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 2/13 | chr12 | 56567435 | ||||||
| chr12:56567557
|
C | G | 1 | a0001c0001t0074g0155 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.234-1418C>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 2/13 | chr12 | 56567557 | ||||||
| chr12:56567557
|
C | T | 33 | a0001c0001t0001g0151a0001c0001t0001g0170a0001c0001t0001g0190others(30): Show | 33 | HG00099.hp2 HG00140.hp1 HG00544.hp2 others(30): Show |
intron_variant | MODIFIER | c.234-1418C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 2/13 | chr12 | 56567557 | ||||||
| chr12:56567749
|
T | C | 1 | a0001c0001t0012g0156 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.234-1226T>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 2/13 | chr12 | 56567749 | ||||||
| chr12:56567756
|
A | G | 8 | a0001c0001t0007g0152a0001c0001t0007g0162a0001c0002t0003g0234others(5): Show | 8 | HG01243.hp2 HG02145.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.234-1219A>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 2/13 | chr12 | 56567756 | ||||||
| chr12:56567783
|
T | C | 1 | a0001c0002t0063g0146 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.234-1192T>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 2/13 | chr12 | 56567783 | ||||||
| chr12:56567788
|
A | G | 1 | a0001c0002t0005g0236 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.234-1187A>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 2/13 | chr12 | 56567788 | ||||||
| chr12:56567828
|
T | C | 250 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(247): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.234-1147T>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 2/13 | chr12 | 56567828 | ||||||
| chr12:56567904
|
A | G | 1 | a0001c0001t0030g0044 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.234-1071A>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 2/13 | chr12 | 56567904 | ||||||
| chr12:56567920
|
T | A | 1 | a0001c0001t0029g0083 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.234-1055T>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 2/13 | chr12 | 56567920 | ||||||
| chr12:56568014
|
T | A | 1 | a0001c0001t0029g0083 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.234-961T>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 2/13 | chr12 | 56568014 | ||||||
| chr12:56568148
|
C | T | 139 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(136): Show | 139 | HG00099.hp1 HG00140.hp2 HG00558.hp1 others(136): Show |
intron_variant | MODIFIER | c.234-827C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 2/13 | chr12 | 56568148 | ||||||
| chr12:56568156
|
A | T | 1 | a0001c0001t0053g0020 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.234-819A>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 2/13 | chr12 | 56568156 | ||||||
| chr12:56568534
|
TTTTTC | T | 5 | a0001c0001t0009g0090a0001c0001t0070g0088a0001c0002t0001g0119others(2): Show | 5 | HG01358.hp1 HG01934.hp1 HG02074.hp2 others(2): Show |
intron_variant | MODIFIER | c.234-436_234-432del others(5): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 56568534 | |||||
| chr12:56568619
|
C | T | 1 | a0001c0001t0065g0062 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.234-356C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 2/13 | chr12 | 56568619 | ||||||
| chr12:56568841
|
T | C | 2 | a0001c0002t0047g0091a0001c0002t0048g0106 | 2 | HG02809.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.234-134T>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 2/13 | chr12 | 56568841 | ||||||
| chr12:56569156
|
G | A | 2 | a0001c0001t0021g0147a0001c0001t0021g0189 | 2 | HG01109.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.292+123G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 3/13 | chr12 | 56569156 | ||||||
| chr12:56569160
|
T | C | 1 | a0001c0002t0005g0236 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.292+127T>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 3/13 | chr12 | 56569160 | ||||||
| chr12:56569475
|
C | T | 248 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(245): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.293-424C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 3/13 | chr12 | 56569475 | ||||||
| chr12:56569578
|
G | A | 11 | a0001c0001t0007g0152a0001c0001t0007g0162a0001c0001t0021g0167others(8): Show | 11 | HG01243.hp2 HG02145.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.293-321G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 3/13 | chr12 | 56569578 | ||||||
| chr12:56569592
|
T | G | 1 | a0001c0001t0002g0127 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.293-307T>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 3/13 | chr12 | 56569592 | ||||||
| chr12:56569600
|
G | A | 262 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(259): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.293-299G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 3/13 | chr12 | 56569600 | ||||||
| chr12:56570171
|
A | G | 1 | a0001c0001t0002g0127 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.384+181A>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 4/13 | chr12 | 56570171 | ||||||
| chr12:56570368
|
G | A | 2 | a0001c0002t0002g0243a0001c0003t0073g0094 | 2 | HG02257.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.384+378G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 4/13 | chr12 | 56570368 | ||||||
| chr12:56570382
|
A | C | 1 | a0001c0001t0029g0083 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.384+392A>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 4/13 | chr12 | 56570382 | ||||||
| chr12:56570516
|
A | G | 7 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0012others(4): Show | 7 | HG00735.hp1 HG01928.hp2 HG01934.hp2 others(4): Show |
intron_variant | MODIFIER | c.384+526A>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 4/13 | chr12 | 56570516 | ||||||
| chr12:56570563
|
C | T | 3 | a0001c0001t0032g0047a0001c0001t0037g0095a0001c0001t0080g0097 | 3 | HG01243.hp1 HG02602.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.384+573C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 4/13 | chr12 | 56570563 | ||||||
| chr12:56570573
|
T | C | 1 | a0001c0002t0017g0093 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.384+583T>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 4/13 | chr12 | 56570573 | ||||||
| chr12:56570662
|
G | C | 1 | a0001c0001t0003g0271 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.384+672G>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 4/13 | chr12 | 56570662 | ||||||
| chr12:56570664
|
A | G | 1 | a0001c0001t0003g0271 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.384+674A>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 4/13 | chr12 | 56570664 | ||||||
| chr12:56570678
|
C | T | 1 | a0001c0001t0003g0064 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.384+688C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 4/13 | chr12 | 56570678 | ||||||
| chr12:56570723
|
A | G | 1 | a0001c0001t0003g0166 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.384+733A>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 4/13 | chr12 | 56570723 | ||||||
| chr12:56570858
|
T | G | 1 | a0001c0001t0029g0083 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.385-840T>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 4/13 | chr12 | 56570858 | ||||||
| chr12:56570887
|
C | T | 1 | a0001c0001t0001g0130 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.385-811C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 4/13 | chr12 | 56570887 | ||||||
| chr12:56570946
|
C | A | 149 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(146): Show | 149 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(146): Show |
intron_variant | MODIFIER | c.385-752C>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 4/13 | chr12 | 56570946 | ||||||
| chr12:56571222
|
T | C | 248 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(245): Show | 249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.385-476T>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 4/13 | chr12 | 56571222 | ||||||
| chr12:56571945
|
C | T | 1 | a0001c0002t0002g0237 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.542+90C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 5/13 | chr12 | 56571945 | ||||||
| chr12:56571985
|
G | GGTAAGTC others(22): Show |
1 | a0001c0001t0029g0083 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.542+132_542+160dup others(29): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr12 | 56571985 | |||||
| chr12:56572017
|
G | A | 1 | a0001c0001t0001g0101 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.542+162G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 5/13 | chr12 | 56572017 | ||||||
| chr12:56572160
|
A | G | 5 | a0001c0001t0007g0152a0001c0001t0007g0162a0001c0001t0035g0098others(2): Show | 5 | HG02615.hp2 HG02630.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.542+305A>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 5/13 | chr12 | 56572160 | ||||||
| chr12:56572257
|
G | A | 3 | a0001c0001t0002g0141a0001c0002t0023g0099a0001c0002t0034g0100 | 3 | HG02257.hp1 HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.542+402G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 5/13 | chr12 | 56572257 | ||||||
| chr12:56572269
|
A | G | 76 | a0001c0001t0001g0133a0001c0001t0001g0151a0001c0001t0001g0160others(73): Show | 76 | HG00099.hp2 HG00140.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.542+414A>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 5/13 | chr12 | 56572269 | ||||||
| chr12:56572288
|
C | CA | 29 | a0001c0001t0001g0121a0001c0001t0001g0190a0001c0001t0002g0051others(26): Show | 29 | HG00544.hp2 HG01884.hp2 HG01978.hp1 others(26): Show |
intron_variant | MODIFIER | c.542+453dupA | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr12 | 56572288 | |||||
| chr12:56572288
|
CA | C | 68 | a0001c0001t0001g0151a0001c0001t0001g0160a0001c0001t0001g0170others(65): Show | 68 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.542+453delA | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr12 | 56572288 | |||||
| chr12:56572288
|
CAA | C | 10 | a0001c0001t0001g0133a0001c0002t0002g0243a0001c0002t0003g0234others(7): Show | 10 | HG01243.hp2 HG02145.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.542+452_542+453del others(2): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr12 | 56572288 | |||||
| chr12:56572420
|
G | A | 7 | a0001c0002t0003g0234a0001c0002t0005g0109a0001c0002t0017g0093others(4): Show | 7 | HG01243.hp2 HG02145.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.542+565G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 5/13 | chr12 | 56572420 | ||||||
| chr12:56572544
|
G | A | 1 | a0001c0002t0063g0146 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.542+689G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 5/13 | chr12 | 56572544 | ||||||
| chr12:56572799
|
G | A | 1 | a0001c0001t0037g0095 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.542+944G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 5/13 | chr12 | 56572799 | ||||||
| chr12:56573056
|
C | CT | 85 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(82): Show | 85 | HG00099.hp1 HG00140.hp2 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.542+1217dupT | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr12 | 56573056 | |||||
| chr12:56573056
|
CT | C | 5 | a0001c0001t0035g0098a0001c0002t0002g0243a0001c0002t0004g0223others(2): Show | 5 | HG02257.hp2 HG02647.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.542+1217delT | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr12 | 56573056 | |||||
| chr12:56573059
|
T | C | 1 | a0001c0003t0073g0094 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.542+1204T>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 5/13 | chr12 | 56573059 | ||||||
| chr12:56573247
|
C | T | 1 | a0001c0001t0001g0023 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.542+1392C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 5/13 | chr12 | 56573247 | ||||||
| chr12:56573324
|
A | G | 5 | a0001c0002t0001g0256a0001c0002t0001g0269a0001c0002t0001g0270others(2): Show | 5 | HG00099.hp2 HG00140.hp1 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.542+1469A>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 5/13 | chr12 | 56573324 | ||||||
| chr12:56573345
|
C | T | 155 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(152): Show | 155 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(152): Show |
intron_variant | MODIFIER | c.542+1490C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 5/13 | chr12 | 56573345 | ||||||
| chr12:56573476
|
C | CA | 14 | a0001c0001t0003g0161a0001c0001t0007g0122a0001c0001t0010g0227others(11): Show | 15 | HG02055.hp1 HG02145.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.542+1647dupA | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr12 | 56573476 | |||||
| chr12:56573476
|
CA | C | 125 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(122): Show | 125 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.542+1647delA | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr12 | 56573476 | |||||
| chr12:56573476
|
CAAA | C | 21 | a0001c0001t0001g0151a0001c0001t0002g0165a0001c0001t0006g0157others(18): Show | 21 | HG00099.hp2 HG00140.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.542+1645_542+1647d others(5): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr12 | 56573476 | |||||
| chr12:56573476
|
CAAAA | C | 53 | a0001c0001t0001g0133a0001c0001t0001g0160a0001c0001t0001g0170others(50): Show | 53 | HG00544.hp1 HG00597.hp1 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.542+1644_542+1647d others(6): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr12 | 56573476 | |||||
| chr12:56573751
|
C | CT | 21 | a0001c0001t0001g0151a0001c0001t0006g0157a0001c0001t0008g0181others(18): Show | 21 | HG00099.hp2 HG00140.hp1 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.542+1913dupT | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr12 | 56573751 | |||||
| chr12:56573751
|
CT | C | 13 | a0001c0001t0001g0052a0001c0001t0016g0037a0001c0001t0021g0167others(10): Show | 13 | HG01243.hp2 HG01884.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.542+1913delT | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr12 | 56573751 | |||||
| chr12:56573897
|
A | G | 10 | a0001c0001t0021g0167a0001c0002t0002g0243a0001c0002t0003g0234others(7): Show | 10 | HG01243.hp2 HG02145.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.542+2042A>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 5/13 | chr12 | 56573897 | ||||||
| chr12:56574051
|
G | A | 3 | a0001c0001t0021g0147a0001c0001t0021g0189a0001c0002t0084g0107 | 3 | HG01109.hp2 HG03471.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.542+2196G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 5/13 | chr12 | 56574051 | ||||||
| chr12:56574158
|
A | T | 1 | a0001c0001t0021g0167 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.542+2303A>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 5/13 | chr12 | 56574158 | ||||||
| chr12:56574198
|
G | A | 3 | a0001c0001t0021g0147a0001c0001t0021g0189a0001c0002t0084g0107 | 3 | HG01109.hp2 HG03471.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.542+2343G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 5/13 | chr12 | 56574198 | ||||||
| chr12:56574707
|
C | A | 3 | a0001c0001t0021g0147a0001c0001t0021g0189a0001c0002t0084g0107 | 3 | HG01109.hp2 HG03471.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.542+2852C>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 5/13 | chr12 | 56574707 | ||||||
| chr12:56574725
|
A | G | 1 | a0001c0001t0001g0005 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.542+2870A>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 5/13 | chr12 | 56574725 | ||||||
| chr12:56574839
|
A | G | 1 | a0001c0002t0063g0146 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.542+2984A>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 5/13 | chr12 | 56574839 | ||||||
| chr12:56574919
|
C | T | 1 | a0001c0002t0083g0104 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.542+3064C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 5/13 | chr12 | 56574919 | ||||||
| chr12:56574937
|
A | G | 1 | a0001c0001t0006g0180 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.542+3082A>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 5/13 | chr12 | 56574937 | ||||||
| chr12:56575009
|
G | A | 1 | a0001c0002t0012g0226 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.542+3154G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 5/13 | chr12 | 56575009 | ||||||
| chr12:56575163
|
C | T | 4 | a0001c0001t0001g0145a0001c0001t0001g0177a0001c0001t0009g0136others(1): Show | 4 | HG01109.hp1 HG02148.hp2 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.542+3308C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 5/13 | chr12 | 56575163 | ||||||
| chr12:56575279
|
CA | C | 74 | a0001c0001t0001g0133a0001c0001t0001g0151a0001c0001t0001g0160others(71): Show | 74 | HG00099.hp2 HG00140.hp1 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.542+3432delA | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr12 | 56575279 | |||||
| chr12:56575436
|
C | T | 1 | a0001c0002t0063g0146 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.542+3581C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 5/13 | chr12 | 56575436 | ||||||
| chr12:56575470
|
C | T | 2 | a0001c0002t0005g0150a0001c0002t0010g0194 | 2 | HG02622.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.542+3615C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 5/13 | chr12 | 56575470 | ||||||
| chr12:56575497
|
C | G | 48 | a0001c0001t0001g0133a0001c0001t0001g0160a0001c0001t0001g0170others(45): Show | 48 | HG00544.hp1 HG00597.hp1 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.542+3642C>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 5/13 | chr12 | 56575497 | ||||||
| chr12:56575538
|
C | T | 9 | a0001c0001t0001g0151a0001c0001t0006g0157a0001c0001t0012g0156others(6): Show | 9 | HG01243.hp1 HG01891.hp1 HG02602.hp2 others(6): Show |
intron_variant | MODIFIER | c.542+3683C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 5/13 | chr12 | 56575538 | ||||||
| chr12:56575554
|
C | T | 1 | a0001c0003t0073g0094 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.542+3699C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 5/13 | chr12 | 56575554 | ||||||
| chr12:56575562
|
C | A | 1 | a0001c0002t0002g0115 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.542+3707C>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 5/13 | chr12 | 56575562 | ||||||
| chr12:56575762
|
C | T | 5 | a0001c0002t0003g0234a0001c0002t0005g0109a0001c0002t0017g0093others(2): Show | 5 | HG01243.hp2 HG02145.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.542+3907C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 5/13 | chr12 | 56575762 | ||||||
| chr12:56575898
|
G | GA | 9 | a0001c0001t0001g0151a0001c0001t0006g0157a0001c0001t0012g0156others(6): Show | 9 | HG01243.hp1 HG01891.hp1 HG02602.hp2 others(6): Show |
intron_variant | MODIFIER | c.542+4056dupA | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr12 | 56575898 | |||||
| chr12:56575909
|
A | T | 1 | a0001c0001t0059g0060 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.542+4054A>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 5/13 | chr12 | 56575909 | ||||||
| chr12:56575925
|
C | T | 2 | a0001c0001t0003g0063a0001c0001t0003g0071 | 2 | NA19012.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.542+4070C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 5/13 | chr12 | 56575925 | ||||||
| chr12:56576229
|
C | T | 1 | a0001c0002t0002g0185 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.542+4374C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 5/13 | chr12 | 56576229 | ||||||
| chr12:56576289
|
A | T | 1 | a0001c0001t0003g0161 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.542+4434A>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 5/13 | chr12 | 56576289 | ||||||
| chr12:56576545
|
G | C | 1 | a0001c0002t0002g0085 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.543-4639G>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 5/13 | chr12 | 56576545 | ||||||
| chr12:56576591
|
T | A | 3 | a0001c0004t0002g0196a0001c0004t0002g0197a0001c0004t0012g0195 | 3 | HG01167.hp1 HG01169.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.543-4593T>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 5/13 | chr12 | 56576591 | ||||||
| chr12:56576872
|
C | G | 1 | a0001c0001t0001g0160 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.543-4312C>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 5/13 | chr12 | 56576872 | ||||||
| chr12:56577035
|
C | CA | 24 | a0001c0001t0001g0006a0001c0001t0001g0151a0001c0001t0006g0157others(21): Show | 24 | HG00099.hp2 HG00140.hp1 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.543-4129dupA | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr12 | 56577035 | |||||
| chr12:56577035
|
C | CAA | 7 | a0001c0001t0006g0180a0001c0001t0080g0097a0001c0002t0004g0186others(4): Show | 7 | HG01243.hp1 HG02559.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.543-4130_543-4129d others(4): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr12 | 56577035 | |||||
| chr12:56577145
|
C | T | 9 | a0001c0001t0021g0167a0001c0002t0003g0234a0001c0002t0005g0109others(6): Show | 9 | HG01243.hp2 HG01884.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.543-4039C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 5/13 | chr12 | 56577145 | ||||||
| chr12:56577155
|
G | A | 5 | a0001c0002t0001g0256a0001c0002t0001g0269a0001c0002t0001g0270others(2): Show | 5 | HG00099.hp2 HG00140.hp1 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.543-4029G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 5/13 | chr12 | 56577155 | ||||||
| chr12:56577360
|
G | A | 4 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0045others(1): Show | 4 | HG00642.hp1 HG01255.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.543-3824G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 5/13 | chr12 | 56577360 | ||||||
| chr12:56577398
|
C | T | 2 | a0001c0001t0006g0180a0001c0002t0006g0092 | 2 | HG03195.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.543-3786C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 5/13 | chr12 | 56577398 | ||||||
| chr12:56577437
|
A | G | 8 | a0001c0001t0021g0167a0001c0002t0003g0234a0001c0002t0005g0109others(5): Show | 8 | HG01243.hp2 HG02145.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.543-3747A>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 5/13 | chr12 | 56577437 | ||||||
| chr12:56577456
|
A | AATT | 41 | a0001c0001t0001g0029a0001c0001t0001g0056a0001c0001t0001g0170others(38): Show | 41 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(38): Show |
intron_variant | MODIFIER | c.543-3694_543-3692d others(5): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr12 | 56577456 | |||||
| chr12:56577456
|
A | AATTATT | 8 | a0001c0001t0001g0121a0001c0001t0001g0176a0001c0001t0021g0167others(5): Show | 8 | HG02155.hp1 HG02602.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.543-3697_543-3692d others(8): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr12 | 56577456 | |||||
| chr12:56577456
|
A | AATTATTA others(2): Show |
5 | a0001c0001t0006g0180a0001c0001t0020g0112a0001c0002t0002g0084others(2): Show | 5 | HG02257.hp2 HG02572.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.543-3700_543-3692d others(11): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr12 | 56577456 | |||||
| chr12:56577456
|
A | AATTATTA others(8): Show |
1 | a0001c0002t0005g0236 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.543-3706_543-3692d others(17): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr12 | 56577456 | |||||
| chr12:56577456
|
AATT | A | 15 | a0001c0001t0007g0152a0001c0001t0007g0162a0001c0001t0035g0098others(12): Show | 15 | HG01243.hp2 HG01884.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.543-3694_543-3692d others(5): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr12 | 56577456 | |||||
| chr12:56577456
|
AATTATT | A | 22 | a0001c0001t0001g0151a0001c0001t0006g0157a0001c0001t0011g0159others(19): Show | 22 | HG00099.hp2 HG00140.hp1 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.543-3697_543-3692d others(8): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr12 | 56577456 | |||||
| chr12:56577510
|
G | A | 1 | a0001c0001t0001g0056 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.543-3674G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 5/13 | chr12 | 56577510 | ||||||
| chr12:56577722
|
G | A | 1 | a0001c0001t0003g0057 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.543-3462G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 5/13 | chr12 | 56577722 | ||||||
| chr12:56577722
|
G | T | 2 | a0001c0001t0021g0147a0001c0001t0021g0189 | 2 | HG01109.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.543-3462G>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 5/13 | chr12 | 56577722 | ||||||
| chr12:56577734
|
G | T | 235 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(232): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.543-3450G>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 5/13 | chr12 | 56577734 | ||||||
| chr12:56577758
|
T | C | 7 | a0001c0001t0011g0159a0001c0001t0011g0201a0001c0001t0017g0179others(4): Show | 7 | HG01109.hp2 HG01891.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.543-3426T>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 5/13 | chr12 | 56577758 | ||||||
| chr12:56577759
|
G | T | 7 | a0001c0001t0011g0159a0001c0001t0011g0201a0001c0001t0017g0179others(4): Show | 7 | HG01109.hp2 HG01891.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.543-3425G>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 5/13 | chr12 | 56577759 | ||||||
| chr12:56577922
|
A | G | 1 | a0001c0001t0003g0057 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.543-3262A>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 5/13 | chr12 | 56577922 | ||||||
| chr12:56577956
|
A | AGGATTAC others(2538): Show |
1 | a0001c0001t0002g0050 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.543-2805_543-2804i others(2547): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr12 | 56577956 | |||||
| chr12:56578248
|
C | T | 1 | a0001c0001t0001g0031 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.543-2936C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 5/13 | chr12 | 56578248 | ||||||
| chr12:56578380
|
C | T | 153 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(150): Show | 153 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(150): Show |
intron_variant | MODIFIER | c.543-2804C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 5/13 | chr12 | 56578380 | ||||||
| chr12:56578719
|
C | G | 1 | a0001c0001t0003g0219 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.543-2465C>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 5/13 | chr12 | 56578719 | ||||||
| chr12:56579072
|
C | A | 153 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(150): Show | 153 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(150): Show |
intron_variant | MODIFIER | c.543-2112C>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 5/13 | chr12 | 56579072 | ||||||
| chr12:56579072
|
C | T | 1 | a0001c0002t0002g0274 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.543-2112C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 5/13 | chr12 | 56579072 | ||||||
| chr12:56579219
|
C | T | 5 | a0001c0001t0012g0114a0001c0002t0081g0102a0001c0002t0082g0105others(2): Show | 5 | HG02055.hp2 HG02895.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.543-1965C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 5/13 | chr12 | 56579219 | ||||||
| chr12:56579359
|
G | A | 47 | a0001c0001t0001g0133a0001c0001t0001g0160a0001c0001t0001g0170others(44): Show | 47 | HG00544.hp1 HG00597.hp1 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.543-1825G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 5/13 | chr12 | 56579359 | ||||||
| chr12:56579589
|
G | A | 47 | a0001c0001t0001g0133a0001c0001t0001g0160a0001c0001t0001g0170others(44): Show | 47 | HG00544.hp1 HG00597.hp1 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.543-1595G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 5/13 | chr12 | 56579589 | ||||||
| chr12:56579633
|
C | CA | 16 | a0001c0001t0001g0151a0001c0001t0006g0157a0001c0001t0012g0156others(13): Show | 16 | HG00099.hp2 HG00140.hp1 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.543-1535dupA | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr12 | 56579633 | |||||
| chr12:56579669
|
A | G | 2 | a0001c0002t0002g0243a0001c0003t0073g0094 | 2 | HG02257.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.543-1515A>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 5/13 | chr12 | 56579669 | ||||||
| chr12:56580037
|
C | A | 1 | a0001c0001t0001g0024 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.543-1147C>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 5/13 | chr12 | 56580037 | ||||||
| chr12:56580134
|
T | C | 168 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(165): Show | 168 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(165): Show |
intron_variant | MODIFIER | c.543-1050T>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 5/13 | chr12 | 56580134 | ||||||
| chr12:56580177
|
C | T | 1 | a0001c0002t0003g0248 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.543-1007C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 5/13 | chr12 | 56580177 | ||||||
| chr12:56580215
|
A | G | 4 | a0001c0002t0001g0256a0001c0002t0001g0269a0001c0002t0001g0270others(1): Show | 4 | HG00099.hp2 HG00140.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.543-969A>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 5/13 | chr12 | 56580215 | ||||||
| chr12:56580230
|
C | CT | 14 | a0001c0001t0001g0015a0001c0001t0001g0046a0001c0001t0001g0077others(11): Show | 14 | HG01884.hp2 HG01928.hp2 HG01978.hp1 others(11): Show |
intron_variant | MODIFIER | c.543-934dupT | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr12 | 56580230 | |||||
| chr12:56580230
|
C | CTT | 44 | a0001c0001t0001g0133a0001c0001t0001g0160a0001c0001t0001g0170others(41): Show | 44 | HG00544.hp1 HG00597.hp1 HG00621.hp2 others(41): Show |
intron_variant | MODIFIER | c.543-935_543-934dup others(2): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr12 | 56580230 | |||||
| chr12:56580230
|
C | CTTTT | 7 | a0001c0001t0011g0159a0001c0001t0017g0179a0001c0001t0021g0167others(4): Show | 7 | HG01109.hp2 HG01891.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.543-937_543-934dup others(4): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr12 | 56580230 | |||||
| chr12:56580230
|
CT | C | 10 | a0001c0001t0001g0151a0001c0001t0002g0141a0001c0001t0006g0157others(7): Show | 10 | HG01243.hp1 HG01891.hp1 HG02602.hp2 others(7): Show |
intron_variant | MODIFIER | c.543-934delT | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr12 | 56580230 | |||||
| chr12:56580389
|
C | A | 1 | a0001c0001t0003g0128 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.543-795C>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 5/13 | chr12 | 56580389 | ||||||
| chr12:56580512
|
C | T | 1 | a0001c0001t0001g0015 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.543-672C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 5/13 | chr12 | 56580512 | ||||||
| chr12:56580581
|
G | A | 1 | a0001c0002t0002g0185 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.543-603G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 5/13 | chr12 | 56580581 | ||||||
| chr12:56581001
|
A | G | 157 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(154): Show | 157 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(154): Show |
intron_variant | MODIFIER | c.543-183A>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 5/13 | chr12 | 56581001 | ||||||
| chr12:56581101
|
C | T | 1 | a0001c0002t0063g0146 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.543-83C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 5/13 | chr12 | 56581101 | ||||||
| chr12:56581131
|
G | A | 14 | a0001c0001t0001g0151a0001c0001t0006g0157a0001c0001t0012g0156others(11): Show | 14 | HG00099.hp2 HG00140.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.543-53G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 5/13 | chr12 | 56581131 | ||||||
| chr12:56581161
|
C | T | 1 | a0001c0002t0005g0236 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.543-23C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 5/13 | chr12 | 56581161 | ||||||
| chr12:56581677
|
G | A | 1 | a0001c0001t0001g0002 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.733-156G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 7/13 | chr12 | 56581677 | ||||||
| chr12:56581895
|
A | C | 2 | a0001c0001t0003g0063a0001c0001t0003g0071 | 2 | NA19012.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.779+16A>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 8/13 | chr12 | 56581895 | ||||||
| chr12:56582538
|
C | G | 3 | a0001c0001t0021g0147a0001c0001t0021g0189a0001c0002t0084g0107 | 3 | HG01109.hp2 HG03471.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.873+386C>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 9/13 | chr12 | 56582538 | ||||||
| chr12:56582868
|
C | T | 3 | a0001c0001t0006g0180a0001c0002t0005g0236a0001c0002t0006g0092 | 3 | HG03195.hp1 HG03225.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.873+716C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 9/13 | chr12 | 56582868 | ||||||
| chr12:56582909
|
A | G | 1 | a0001c0002t0050g0218 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.873+757A>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 9/13 | chr12 | 56582909 | ||||||
| chr12:56582970
|
A | G | 1 | a0001c0002t0002g0185 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.873+818A>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 9/13 | chr12 | 56582970 | ||||||
| chr12:56583112
|
G | A | 1 | a0001c0001t0071g0192 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.873+960G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 9/13 | chr12 | 56583112 | ||||||
| chr12:56583200
|
C | T | 2 | a0001c0002t0047g0091a0001c0002t0048g0106 | 2 | HG02809.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.873+1048C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 9/13 | chr12 | 56583200 | ||||||
| chr12:56583252
|
A | G | 1 | a0001c0002t0001g0263 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.873+1100A>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 9/13 | chr12 | 56583252 | ||||||
| chr12:56583349
|
C | A | 1 | a0001c0001t0003g0042 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.873+1197C>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 9/13 | chr12 | 56583349 | ||||||
| chr12:56583385
|
G | A | 16 | a0001c0001t0005g0229a0001c0001t0006g0157a0001c0001t0012g0114others(13): Show | 16 | HG01243.hp1 HG01891.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.873+1233G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 9/13 | chr12 | 56583385 | ||||||
| chr12:56583654
|
CA | C | 237 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(234): Show | 237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.873+1513delA | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr12 | 56583654 | |||||
| chr12:56583855
|
C | G | 1 | a0001c0001t0029g0074 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.873+1703C>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 9/13 | chr12 | 56583855 | ||||||
| chr12:56584131
|
A | G | 5 | a0001c0002t0002g0185a0001c0003t0006g0233a0001c0003t0051g0191others(2): Show | 5 | HG02257.hp2 HG02622.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.873+1979A>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 9/13 | chr12 | 56584131 | ||||||
| chr12:56584303
|
C | T | 3 | a0001c0001t0001g0145a0001c0001t0001g0177a0001c0001t0009g0136 | 3 | HG01109.hp1 HG02148.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.873+2151C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 9/13 | chr12 | 56584303 | ||||||
| chr12:56584387
|
G | A | 160 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(157): Show | 160 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(157): Show |
intron_variant | MODIFIER | c.873+2235G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 9/13 | chr12 | 56584387 | ||||||
| chr12:56584464
|
A | G | 1 | a0001c0002t0005g0109 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.873+2312A>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 9/13 | chr12 | 56584464 | ||||||
| chr12:56584559
|
G | A | 1 | a0001c0001t0003g0057 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.874-2290G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 9/13 | chr12 | 56584559 | ||||||
| chr12:56584610
|
G | C | 245 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(242): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.874-2239G>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 9/13 | chr12 | 56584610 | ||||||
| chr12:56584764
|
G | A | 3 | a0001c0001t0003g0149a0001c0001t0019g0139a0001c0002t0001g0256 | 3 | HG01978.hp1 HG02698.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.874-2085G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 9/13 | chr12 | 56584764 | ||||||
| chr12:56584822
|
C | CT | 18 | a0001c0001t0001g0145a0001c0001t0001g0177a0001c0001t0005g0229others(15): Show | 18 | HG01109.hp1 HG01243.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.874-2009dupT | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr12 | 56584822 | |||||
| chr12:56584854
|
G | A | 2 | a0001c0002t0047g0091a0001c0002t0048g0106 | 2 | HG02809.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.874-1995G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 9/13 | chr12 | 56584854 | ||||||
| chr12:56584996
|
T | C | 3 | a0001c0001t0021g0167a0001c0002t0004g0223a0001c0002t0004g0224 | 3 | HG02896.hp2 HG02897.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.874-1853T>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 9/13 | chr12 | 56584996 | ||||||
| chr12:56585015
|
G | A | 1 | a0001c0002t0002g0185 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.874-1834G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 9/13 | chr12 | 56585015 | ||||||
| chr12:56585070
|
A | G | 41 | a0001c0001t0001g0133a0001c0001t0001g0160a0001c0001t0001g0170others(38): Show | 41 | HG00597.hp1 HG00621.hp2 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.874-1779A>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 9/13 | chr12 | 56585070 | ||||||
| chr12:56585181
|
C | CT | 16 | a0001c0001t0005g0229a0001c0001t0006g0157a0001c0001t0012g0114others(13): Show | 16 | HG01243.hp1 HG01891.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.874-1667dupT | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr12 | 56585181 | |||||
| chr12:56585321
|
T | C | 2 | a0001c0001t0001g0054a0001c0002t0001g0249 | 2 | NA18963.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.874-1528T>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 9/13 | chr12 | 56585321 | ||||||
| chr12:56585760
|
T | C | 1 | a0001c0001t0060g0059 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.874-1089T>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 9/13 | chr12 | 56585760 | ||||||
| chr12:56586012
|
G | A | 2 | a0001c0001t0001g0145a0001c0001t0001g0177 | 2 | HG01109.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.874-837G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 9/13 | chr12 | 56586012 | ||||||
| chr12:56586055
|
A | G | 6 | a0001c0001t0007g0152a0001c0001t0007g0162a0001c0001t0035g0098others(3): Show | 6 | HG02615.hp2 HG02630.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.874-794A>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 9/13 | chr12 | 56586055 | ||||||
| chr12:56586056
|
C | T | 4 | a0001c0001t0007g0122a0001c0002t0004g0215a0001c0002t0007g0203others(1): Show | 4 | HG02615.hp1 HG02896.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.874-793C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 9/13 | chr12 | 56586056 | ||||||
| chr12:56586124
|
T | G | 1 | a0001c0002t0003g0234 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.874-725T>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 9/13 | chr12 | 56586124 | ||||||
| chr12:56586149
|
A | G | 1 | a0001c0001t0001g0038 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.874-700A>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 9/13 | chr12 | 56586149 | ||||||
| chr12:56586160
|
C | G | 1 | a0001c0002t0012g0226 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.874-689C>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 9/13 | chr12 | 56586160 | ||||||
| chr12:56586193
|
A | G | 1 | a0001c0002t0017g0093 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.874-656A>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 9/13 | chr12 | 56586193 | ||||||
| chr12:56586484
|
G | C | 1 | a0001c0002t0002g0115 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.874-365G>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 9/13 | chr12 | 56586484 | ||||||
| chr12:56586536
|
TAGAG | T | 6 | a0001c0001t0003g0128a0001c0001t0020g0111a0001c0001t0020g0112others(3): Show | 6 | HG02572.hp1 HG02809.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.874-309_874-306del others(4): Show |
RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr12 | 56586536 | |||||
| chr12:56586605
|
G | A | 1 | a0001c0002t0004g0216 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.874-244G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 9/13 | chr12 | 56586605 | ||||||
| chr12:56586614
|
G | A | 1 | a0001c0001t0021g0167 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.874-235G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 9/13 | chr12 | 56586614 | ||||||
| chr12:56587053
|
G | T | 1 | a0001c0001t0036g0096 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.951+127G>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 10/13 | chr12 | 56587053 | ||||||
| chr12:56587064
|
G | A | 2 | a0001c0002t0047g0091a0001c0002t0048g0106 | 2 | HG02809.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.951+138G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 10/13 | chr12 | 56587064 | ||||||
| chr12:56587267
|
C | CA | 6 | a0001c0002t0007g0203a0001c0002t0007g0214a0001c0003t0006g0233others(3): Show | 6 | HG02257.hp2 HG02615.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.952-273dupA | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr12 | 56587267 | |||||
| chr12:56587284
|
C | A | 1 | a0001c0001t0046g0087 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.952-270C>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 10/13 | chr12 | 56587284 | ||||||
| chr12:56587495
|
T | C | 2 | a0001c0002t0047g0091a0001c0002t0048g0106 | 2 | HG02809.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.952-59T>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 10/13 | chr12 | 56587495 | ||||||
| chr12:56587725
|
C | A | 5 | a0001c0001t0001g0004a0001c0001t0009g0090a0001c0001t0056g0019others(2): Show | 5 | HG01358.hp1 HG01934.hp1 HG02074.hp2 others(2): Show |
intron_variant | MODIFIER | c.1062+61C>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 11/13 | chr12 | 56587725 | ||||||
| chr12:56587911
|
C | T | 2 | a0001c0002t0047g0091a0001c0002t0048g0106 | 2 | HG02809.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1062+247C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 11/13 | chr12 | 56587911 | ||||||
| chr12:56587914
|
A | G | 27 | a0001c0001t0001g0177a0001c0001t0010g0225a0001c0001t0010g0227others(24): Show | 28 | HG00099.hp2 HG00140.hp1 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.1062+250A>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 11/13 | chr12 | 56587914 | ||||||
| chr12:56587947
|
C | G | 4 | a0001c0003t0006g0233a0001c0003t0051g0191a0001c0003t0073g0094others(1): Show | 4 | HG02257.hp2 HG02622.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.1062+283C>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 11/13 | chr12 | 56587947 | ||||||
| chr12:56588090
|
G | A | 1 | a0001c0001t0021g0167 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1063-204G>A | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 11/13 | chr12 | 56588090 | ||||||
| chr12:56588100
|
C | T | 1 | a0001c0002t0045g0261 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1063-194C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 11/13 | chr12 | 56588100 | ||||||
| chr12:56588179
|
A | G | 1 | a0001c0001t0015g0172 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1063-115A>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 11/13 | chr12 | 56588179 | ||||||
| chr12:56588254
|
A | G | 2 | a0001c0002t0047g0091a0001c0002t0048g0106 | 2 | HG02809.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1063-40A>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 11/13 | chr12 | 56588254 | ||||||
| chr12:56588381
|
G | C | 2 | a0001c0001t0002g0169a0001c0001t0025g0080 | 2 | NA18951.hp2 NA19011.hp1 |
splice_region_variant&intron_variant | LOW | c.1143+7G>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 12/13 | chr12 | 56588381 | ||||||
| chr12:56588428
|
G | C | 1 | a0001c0002t0002g0257 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1143+54G>C | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 12/13 | chr12 | 56588428 | ||||||
| chr12:56588506
|
C | T | 268 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(265): Show | 269 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(266): Show |
intron_variant | MODIFIER | c.1143+132C>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 12/13 | chr12 | 56588506 | ||||||
| chr12:56588627
|
A | G | 2 | a0001c0001t0001g0153a0001c0001t0066g0182 | 2 | HG02698.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.1143+253A>G | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 12/13 | chr12 | 56588627 | ||||||
| chr12:56589094
|
G | T | 1 | a0001c0002t0007g0214 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.*7-46G>T | RBMS2 | ENSG00000076067.14 | transcript | ENST00000262031.10 | protein_coding | 13/13 | chr12 | 56589094 |