Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 11342 |
| ensemblid | ENSG00000082996.20 |
| hgncid | 10057 |
| symbol | RNF13 |
| name | ring finger protein 13 |
| refseq_nuc | NM_183381.3 |
| refseq_prot | NP_899237.1 |
| ensembl_nuc | ENST00000392894.8 |
| ensembl_prot | ENSP00000376628.3 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 149813215 |
| end | 149962139 |
| strand | + |
| ver | v1.2 |
| region | chr3:149813215-149962139 |
| region5000 | chr3:149808215-149967139 |
| regionname0 | RNF13_chr3_149813215_149962139 |
| regionname5000 | RNF13_chr3_149808215_149967139 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 381 | 270 | 73 | 62 | 89 | 16 | 28 | 70 | RNF13_chr3_149808215_149967139 | RNF13 | copy fasta | chr3 | 149808215 | 149967139 |
| a0002 | 0/0 | 381 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | copy fasta | chr3 | 149808215 | 149967139 |
| a0003 | 0/0 | 381 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | copy fasta | chr3 | 149808215 | 149967139 |
| a0004 | 0/0 | 381 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | copy fasta | chr3 | 149808215 | 149967139 |
| a0005 | 0/0 | 381 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | copy fasta | chr3 | 149808215 | 149967139 |
| a0006 | 0/0 | 381 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | copy fasta | chr3 | 149808215 | 149967139 |
| a0007 | 0/0 | 381 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | copy fasta | chr3 | 149808215 | 149967139 |
| chapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 1146 | 164 | 27 | 46 | 61 | 11 | 18 | RNF13_chr3_149808215_149967139 | RNF13 | copy fasta | chr3 | 149808215 | 149967139 | |
| c0002 | 1/0 | 1146 | 106 | 46 | 16 | 28 | 5 | 10 | RNF13_chr3_149808215_149967139 | RNF13 | copy fasta | chr3 | 149808215 | 149967139 | |
| c0003 | 0/0 | 1146 | 3 | 3 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | copy fasta | chr3 | 149808215 | 149967139 | |
| c0004 | 0/0 | 1146 | 2 | 2 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | copy fasta | chr3 | 149808215 | 149967139 | |
| c0005 | 0/0 | 1146 | 2 | 2 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | copy fasta | chr3 | 149808215 | 149967139 | |
| c0006 | 0/0 | 1146 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | copy fasta | chr3 | 149808215 | 149967139 | |
| c0007 | 0/0 | 1146 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | copy fasta | chr3 | 149808215 | 149967139 | |
| c0008 | 0/0 | 1146 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | copy fasta | chr3 | 149808215 | 149967139 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 1192 | 177 | 33 | 45 | 73 | 9 | 16 | RNF13_chr3_149808215_149967139 | RNF13 | copy fasta | chr3 | 149808215 | 149967139 |
| t0002 | 1/0 | 1191 | 45 | 16 | 7 | 12 | 4 | 5 | RNF13_chr3_149808215_149967139 | RNF13 | copy fasta | chr3 | 149808215 | 149967139 |
| t0003 | 0/0 | 1191 | 23 | 9 | 6 | 4 | 2 | 2 | RNF13_chr3_149808215_149967139 | RNF13 | copy fasta | chr3 | 149808215 | 149967139 |
| t0004 | 0/0 | 1191 | 8 | 4 | 2 | 0 | 0 | 2 | RNF13_chr3_149808215_149967139 | RNF13 | copy fasta | chr3 | 149808215 | 149967139 |
| t0005 | 0/0 | 1191 | 8 | 6 | 2 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | copy fasta | chr3 | 149808215 | 149967139 |
| t0006 | 0/0 | 1189 | 8 | 8 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | copy fasta | chr3 | 149808215 | 149967139 |
| t0007 | 0/0 | 1189 | 3 | 3 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | copy fasta | chr3 | 149808215 | 149967139 |
| t0008 | 0/0 | 1191 | 2 | 2 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | copy fasta | chr3 | 149808215 | 149967139 |
| t0009 | 0/0 | 1192 | 1 | 0 | 0 | 0 | 0 | 1 | RNF13_chr3_149808215_149967139 | RNF13 | copy fasta | chr3 | 149808215 | 149967139 |
| t0010 | 0/0 | 1193 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | copy fasta | chr3 | 149808215 | 149967139 |
| t0011 | 0/0 | 1192 | 1 | 0 | 0 | 0 | 0 | 1 | RNF13_chr3_149808215_149967139 | RNF13 | copy fasta | chr3 | 149808215 | 149967139 |
| t0012 | 0/0 | 1190 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | copy fasta | chr3 | 149808215 | 149967139 |
| t0013 | 0/0 | 1192 | 1 | 0 | 0 | 0 | 1 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | copy fasta | chr3 | 149808215 | 149967139 |
| t0014 | 0/0 | 1192 | 1 | 0 | 0 | 0 | 0 | 1 | RNF13_chr3_149808215_149967139 | RNF13 | copy fasta | chr3 | 149808215 | 149967139 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0195 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0270 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1146 | 164 | 27 | 46 | 61 | 11 | 18 | RNF13_chr3_149808215_149967139 | RNF13 | copy fasta | chr3 | 149808215 | 149967139 | |
| a0001c0002 | 1/0 | 1146 | 106 | 46 | 16 | 28 | 5 | 10 | RNF13_chr3_149808215_149967139 | RNF13 | copy fasta | chr3 | 149808215 | 149967139 | |
| a0002c0003 | 0/0 | 1146 | 3 | 3 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | copy fasta | chr3 | 149808215 | 149967139 | |
| a0003c0004 | 0/0 | 1146 | 2 | 2 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | copy fasta | chr3 | 149808215 | 149967139 | |
| a0004c0005 | 0/0 | 1146 | 2 | 2 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | copy fasta | chr3 | 149808215 | 149967139 | |
| a0005c0006 | 0/0 | 1146 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | copy fasta | chr3 | 149808215 | 149967139 | |
| a0006c0007 | 0/0 | 1146 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | copy fasta | chr3 | 149808215 | 149967139 | |
| a0007c0008 | 0/0 | 1146 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | copy fasta | chr3 | 149808215 | 149967139 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 2337 | 158 | 26 | 45 | 61 | 9 | 16 | RNF13_chr3_149808215_149967139 | RNF13 | copy fasta | chr3 | 149808215 | 149967139 |
| a0001c0001t0002 | 0/0 | 2336 | 2 | 0 | 1 | 0 | 1 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | copy fasta | chr3 | 149808215 | 149967139 |
| a0001c0001t0011 | 0/0 | 2337 | 1 | 0 | 0 | 0 | 0 | 1 | RNF13_chr3_149808215_149967139 | RNF13 | copy fasta | chr3 | 149808215 | 149967139 |
| a0001c0001t0012 | 0/0 | 2335 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | copy fasta | chr3 | 149808215 | 149967139 |
| a0001c0001t0013 | 0/0 | 2337 | 1 | 0 | 0 | 0 | 1 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | copy fasta | chr3 | 149808215 | 149967139 |
| a0001c0001t0014 | 0/0 | 2337 | 1 | 0 | 0 | 0 | 0 | 1 | RNF13_chr3_149808215_149967139 | RNF13 | copy fasta | chr3 | 149808215 | 149967139 |
| a0001c0002t0001 | 0/0 | 2337 | 12 | 1 | 0 | 11 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | copy fasta | chr3 | 149808215 | 149967139 |
| a0001c0002t0002 | 1/0 | 2336 | 42 | 15 | 6 | 12 | 3 | 5 | RNF13_chr3_149808215_149967139 | RNF13 | copy fasta | chr3 | 149808215 | 149967139 |
| a0001c0002t0003 | 0/0 | 2336 | 23 | 9 | 6 | 4 | 2 | 2 | RNF13_chr3_149808215_149967139 | RNF13 | copy fasta | chr3 | 149808215 | 149967139 |
| a0001c0002t0004 | 0/0 | 2336 | 8 | 4 | 2 | 0 | 0 | 2 | RNF13_chr3_149808215_149967139 | RNF13 | copy fasta | chr3 | 149808215 | 149967139 |
| a0001c0002t0005 | 0/0 | 2336 | 8 | 6 | 2 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | copy fasta | chr3 | 149808215 | 149967139 |
| a0001c0002t0006 | 0/0 | 2334 | 8 | 8 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | copy fasta | chr3 | 149808215 | 149967139 |
| a0001c0002t0007 | 0/0 | 2334 | 3 | 3 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | copy fasta | chr3 | 149808215 | 149967139 |
| a0001c0002t0009 | 0/0 | 2337 | 1 | 0 | 0 | 0 | 0 | 1 | RNF13_chr3_149808215_149967139 | RNF13 | copy fasta | chr3 | 149808215 | 149967139 |
| a0001c0002t0010 | 0/0 | 2338 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | copy fasta | chr3 | 149808215 | 149967139 |
| a0002c0003t0001 | 0/0 | 2337 | 3 | 3 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | copy fasta | chr3 | 149808215 | 149967139 |
| a0003c0004t0008 | 0/0 | 2336 | 2 | 2 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | copy fasta | chr3 | 149808215 | 149967139 |
| a0004c0005t0001 | 0/0 | 2337 | 2 | 2 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | copy fasta | chr3 | 149808215 | 149967139 |
| a0005c0006t0001 | 0/0 | 2337 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | copy fasta | chr3 | 149808215 | 149967139 |
| a0006c0007t0001 | 0/0 | 2337 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | copy fasta | chr3 | 149808215 | 149967139 |
| a0007c0008t0002 | 0/0 | 2336 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | copy fasta | chr3 | 149808215 | 149967139 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0195 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0011g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0012g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0013g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0001t0014g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0002t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0002t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0002t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0002t0002g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0002t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0002t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0002t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0002t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0002t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0002t0002g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0002t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0002t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0002t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0002t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0002t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0002t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0002t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0002t0002g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0002t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0002t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0002t0002g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0002t0002g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0002t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0002t0002g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0002t0002g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0002t0002g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0002t0002g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0002t0002g0270 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0002t0002g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0002t0002g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0002t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0002t0002g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0002t0002g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0002t0002g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0002t0002g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0002t0002g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0002t0002g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0002t0003g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0002t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0002t0003g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0002t0003g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0002t0003g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0002t0003g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0002t0003g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0002t0003g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0002t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0002t0003g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0002t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0002t0003g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0002t0003g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0002t0003g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0002t0003g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0002t0003g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0002t0003g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0002t0003g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0002t0003g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0002t0003g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0002t0003g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0002t0003g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0002t0003g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0002t0004g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0002t0004g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0002t0004g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0002t0004g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0002t0004g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0002t0004g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0002t0004g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0002t0004g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0002t0005g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0002t0005g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0002t0005g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0002t0005g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0002t0005g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0002t0005g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0002t0005g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0002t0005g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0002t0006g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0002t0006g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0002t0006g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0002t0006g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0002t0006g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0002t0006g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0002t0006g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0002t0006g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0002t0007g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0002t0007g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0002t0007g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0002t0009g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0001c0002t0010g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0002c0003t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0002c0003t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0002c0003t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0003c0004t0008g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0003c0004t0008g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0004c0005t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0004c0005t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0005c0006t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0006c0007t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| a0007c0008t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0174 | EUR | GBR | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG00099 | hp2 | a0001 | c0002 | t0002 | g0275 | EUR | GBR | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0139 | EUR | GBR | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG00140 | hp2 | a0001 | c0002 | t0002 | g0279 | EUR | GBR | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0157 | EUR | FIN | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG00280 | hp2 | a0001 | c0002 | t0003 | g0258 | EUR | FIN | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0083 | EUR | FIN | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0119 | EUR | FIN | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | CHS | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | CHS | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | CHS | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG00609 | hp2 | a0001 | c0002 | t0001 | g0033 | EAS | CHS | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | CHS | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | CHS | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG00639 | hp1 | a0001 | c0002 | t0005 | g0203 | AMR | PUR | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0219 | AMR | PUR | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG00642 | hp2 | a0001 | c0002 | t0005 | g0202 | AMR | PUR | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG00733 | hp1 | a0001 | c0002 | t0002 | g0277 | AMR | PUR | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG00735 | hp1 | a0001 | c0002 | t0004 | g0018 | AMR | PUR | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG00741 | hp1 | a0001 | c0002 | t0002 | g0011 | AMR | PUR | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG01071 | hp1 | a0001 | c0002 | t0003 | g0109 | AMR | PUR | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG01074 | hp2 | a0001 | c0002 | t0003 | g0085 | AMR | PUR | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG01099 | hp2 | a0001 | c0002 | t0003 | g0096 | AMR | PUR | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG01106 | hp1 | a0001 | c0002 | t0003 | g0259 | AMR | PUR | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0194 | AMR | PUR | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG01243 | hp1 | a0001 | c0002 | t0003 | g0262 | AMR | PUR | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG01243 | hp2 | a0001 | c0002 | t0004 | g0019 | AMR | PUR | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | CLM | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG01255 | hp2 | a0001 | c0002 | t0002 | g0040 | AMR | CLM | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | CLM | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | CLM | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | CLM | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | CLM | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | CLM | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | CLM | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | CLM | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG01358 | hp2 | a0001 | c0002 | t0002 | g0043 | AMR | CLM | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | CLM | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | CLM | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG01433 | hp1 | a0001 | c0002 | t0003 | g0087 | AMR | CLM | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | CLM | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG01496 | hp1 | a0001 | c0002 | t0002 | g0248 | AMR | CLM | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0188 | AMR | CLM | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0143 | EUR | IBS | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0267 | EUR | IBS | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0078 | EUR | IBS | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG01516 | hp2 | a0001 | c0002 | t0002 | g0278 | EUR | IBS | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0077 | EUR | IBS | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0164 | EUR | IBS | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | ACB | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG01891 | hp2 | a0001 | c0002 | t0005 | g0205 | AFR | ACB | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | PEL | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | PEL | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PEL | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | PEL | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | PEL | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PEL | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PEL | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PEL | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG02027 | hp1 | a0001 | c0002 | t0002 | g0047 | EAS | KHV | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | KHV | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | KHV | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | KHV | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG02074 | hp1 | a0001 | c0002 | t0003 | g0124 | EAS | KHV | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | KHV | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | KHV | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | KHV | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | KHV | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG02129 | hp2 | a0005 | c0006 | t0001 | g0178 | EAS | KHV | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG02145 | hp1 | a0001 | c0002 | t0003 | g0256 | AFR | ACB | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG02145 | hp2 | a0001 | c0002 | t0002 | g0268 | AFR | ACB | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG02257 | hp1 | a0001 | c0002 | t0005 | g0209 | AFR | ACB | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | ACB | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG02258 | hp1 | a0001 | c0002 | t0006 | g0007 | AFR | ACB | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | ACB | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PEL | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0224 | AMR | PEL | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG02280 | hp1 | a0001 | c0002 | t0003 | g0261 | AFR | ACB | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | ACB | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PEL | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | PEL | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | PEL | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0228 | AMR | PEL | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | KHV | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | KHV | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG02572 | hp1 | a0001 | c0002 | t0005 | g0207 | AFR | GWD | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG02572 | hp2 | a0001 | c0002 | t0002 | g0246 | AFR | GWD | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG02615 | hp1 | a0001 | c0002 | t0002 | g0240 | AFR | GWD | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG02615 | hp2 | a0001 | c0002 | t0006 | g0005 | AFR | GWD | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG02622 | hp1 | a0001 | c0002 | t0004 | g0021 | AFR | GWD | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | GWD | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG02630 | hp1 | a0001 | c0002 | t0004 | g0013 | AFR | GWD | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG02630 | hp2 | a0001 | c0002 | t0006 | g0009 | AFR | GWD | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | GWD | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG02647 | hp2 | a0001 | c0002 | t0005 | g0204 | AFR | GWD | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0066 | SAS | PJL | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0197 | SAS | PJL | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG02698 | hp2 | a0001 | c0002 | t0003 | g0264 | SAS | PJL | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG02717 | hp1 | a0001 | c0002 | t0003 | g0092 | AFR | GWD | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG02717 | hp2 | a0001 | c0002 | t0007 | g0252 | AFR | GWD | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG02723 | hp1 | a0001 | c0002 | t0002 | g0266 | AFR | GWD | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG02723 | hp2 | a0001 | c0001 | t0012 | g0206 | AFR | GWD | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG02738 | hp2 | a0001 | c0001 | t0011 | g0226 | SAS | PJL | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG02809 | hp1 | a0001 | c0002 | t0003 | g0257 | AFR | GWD | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG02809 | hp2 | a0001 | c0002 | t0002 | g0247 | AFR | GWD | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG02818 | hp1 | a0001 | c0002 | t0002 | g0272 | AFR | GWD | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | GWD | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG02886 | hp1 | a0001 | c0002 | t0003 | g0093 | AFR | GWD | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG02886 | hp2 | a0001 | c0002 | t0002 | g0242 | AFR | GWD | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG02896 | hp1 | a0001 | c0002 | t0006 | g0237 | AFR | GWD | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | GWD | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | ESN | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG02922 | hp2 | a0004 | c0005 | t0001 | g0081 | AFR | ESN | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG02965 | hp1 | a0001 | c0002 | t0002 | g0020 | AFR | ESN | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | ESN | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG02970 | hp1 | a0001 | c0002 | t0003 | g0263 | AFR | ESN | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | ESN | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG02976 | hp1 | a0001 | c0002 | t0003 | g0260 | AFR | ESN | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG02976 | hp2 | a0002 | c0003 | t0001 | g0004 | AFR | ESN | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0225 | SAS | PJL | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG03041 | hp1 | a0002 | c0003 | t0001 | g0003 | AFR | GWD | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG03041 | hp2 | a0001 | c0002 | t0006 | g0236 | AFR | GWD | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG03098 | hp1 | a0003 | c0004 | t0008 | g0200 | AFR | MSL | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | MSL | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG03130 | hp1 | a0001 | c0002 | t0007 | g0250 | AFR | ESN | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG03130 | hp2 | a0002 | c0003 | t0001 | g0002 | AFR | ESN | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG03139 | hp1 | a0001 | c0002 | t0002 | g0012 | AFR | ESN | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG03139 | hp2 | a0004 | c0005 | t0001 | g0080 | AFR | ESN | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG03195 | hp1 | a0001 | c0002 | t0002 | g0273 | AFR | ESN | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0239 | AFR | ESN | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG03209 | hp1 | a0001 | c0002 | t0005 | g0208 | AFR | MSL | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG03209 | hp2 | a0001 | c0002 | t0002 | g0244 | AFR | MSL | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG03239 | hp1 | a0001 | c0001 | t0014 | g0133 | SAS | PJL | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0057 | SAS | PJL | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG03453 | hp1 | a0001 | c0002 | t0003 | g0091 | AFR | MSL | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG03453 | hp2 | a0001 | c0002 | t0002 | g0269 | AFR | MSL | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG03486 | hp1 | a0001 | c0002 | t0006 | g0008 | AFR | MSL | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG03486 | hp2 | a0001 | c0002 | t0002 | g0265 | AFR | MSL | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG03491 | hp1 | a0001 | c0002 | t0002 | g0052 | SAS | PJL | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG03492 | hp1 | a0001 | c0002 | t0002 | g0053 | SAS | PJL | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG03516 | hp1 | a0001 | c0002 | t0002 | g0241 | AFR | ESN | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | ESN | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG03540 | hp1 | a0001 | c0002 | t0004 | g0014 | AFR | GWD | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | GWD | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | MSL | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG03579 | hp2 | a0001 | c0002 | t0006 | g0006 | AFR | MSL | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG03710 | hp1 | a0001 | c0002 | t0004 | g0017 | SAS | PJL | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG03710 | hp2 | a0001 | c0002 | t0002 | g0276 | SAS | PJL | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | BEB | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0116 | SAS | BEB | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG03834 | hp1 | a0001 | c0002 | t0004 | g0016 | SAS | BEB | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0173 | SAS | BEB | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG03927 | hp1 | a0001 | c0002 | t0002 | g0031 | SAS | BEB | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0220 | SAS | BEB | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG03942 | hp1 | a0001 | c0002 | t0002 | g0044 | SAS | BEB | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0117 | SAS | BEB | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0042 | SAS | STU | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG04115 | hp2 | a0001 | c0002 | t0003 | g0098 | SAS | STU | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG04184 | hp1 | a0001 | c0002 | t0009 | g0121 | SAS | BEB | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0062 | SAS | BEB | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| NA18522 | hp1 | a0001 | c0002 | t0007 | g0249 | AFR | YRI | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| NA18522 | hp2 | a0001 | c0002 | t0002 | g0274 | AFR | YRI | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | CHB | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | CHB | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| NA18906 | hp1 | a0006 | c0007 | t0001 | g0071 | AFR | YRI | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| NA18906 | hp2 | a0003 | c0004 | t0008 | g0199 | AFR | YRI | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| NA18943 | hp2 | a0001 | c0002 | t0001 | g0029 | EAS | JPT | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| NA18950 | hp2 | a0001 | c0002 | t0010 | g0038 | EAS | JPT | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| NA18953 | hp1 | a0001 | c0002 | t0001 | g0051 | EAS | JPT | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| NA18961 | hp1 | a0001 | c0002 | t0002 | g0222 | EAS | JPT | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| NA18961 | hp2 | a0001 | c0002 | t0002 | g0046 | EAS | JPT | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| NA18972 | hp2 | a0001 | c0002 | t0002 | g0025 | EAS | JPT | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| NA18973 | hp2 | a0001 | c0002 | t0002 | g0030 | EAS | JPT | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| NA18975 | hp1 | a0001 | c0002 | t0002 | g0045 | EAS | JPT | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| NA18981 | hp1 | a0001 | c0002 | t0001 | g0035 | EAS | JPT | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| NA18988 | hp1 | a0001 | c0002 | t0001 | g0049 | EAS | JPT | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| NA18989 | hp2 | a0001 | c0002 | t0002 | g0034 | EAS | JPT | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| NA18998 | hp2 | a0001 | c0002 | t0002 | g0041 | EAS | JPT | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| NA18999 | hp2 | a0001 | c0002 | t0003 | g0255 | EAS | JPT | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| NA19011 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| NA19030 | hp1 | a0001 | c0002 | t0005 | g0210 | AFR | LWK | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | LWK | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | LWK | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| NA19043 | hp2 | a0001 | c0002 | t0001 | g0251 | AFR | LWK | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| NA19058 | hp2 | a0001 | c0002 | t0002 | g0227 | EAS | JPT | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| NA19062 | hp1 | a0001 | c0002 | t0001 | g0032 | EAS | JPT | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| NA19064 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| NA19065 | hp1 | a0001 | c0002 | t0001 | g0048 | EAS | JPT | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| NA19070 | hp1 | a0001 | c0002 | t0002 | g0039 | EAS | JPT | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| NA19077 | hp2 | a0001 | c0002 | t0003 | g0086 | EAS | JPT | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| NA19083 | hp1 | a0001 | c0002 | t0001 | g0037 | EAS | JPT | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| NA19084 | hp2 | a0001 | c0002 | t0001 | g0050 | EAS | JPT | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| NA19086 | hp1 | a0001 | c0002 | t0002 | g0026 | EAS | JPT | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| NA19089 | hp1 | a0001 | c0002 | t0002 | g0036 | EAS | JPT | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| NA19090 | hp1 | a0001 | c0002 | t0003 | g0101 | EAS | JPT | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | YRI | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | YRI | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| NA20129 | hp1 | a0001 | c0002 | t0003 | g0238 | AFR | ASW | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | ASW | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| NA20805 | hp1 | a0001 | c0002 | t0003 | g0254 | EUR | TSI | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| NA20805 | hp2 | a0001 | c0001 | t0013 | g0158 | EUR | TSI | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG01123 | hp1 | a0001 | c0002 | t0002 | g0271 | AMR | CLM | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | CLM | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG02109 | hp1 | a0001 | c0002 | t0006 | g0253 | AFR | ACB | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG02109 | hp2 | a0007 | c0008 | t0002 | g0243 | AFR | ACB | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | ACB | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | ACB | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | MSL | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | MSL | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | USA | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| NA20300 | hp2 | a0001 | c0002 | t0004 | g0023 | AFR | USA | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0195 | REF | REF | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| homoSapiens_grch38 | hp1 | a0001 | c0002 | t0002 | g0270 | REF | REF | RNF13_chr3_149808215_149967139 | RNF13 | chr3 | 149808215 | 149967139 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:149846087 | G | A | 1 | a0005 | 1 | HG02129.hp2 | missense_variant | MODERATE | c.61G>A | p.Val21Ile | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 2/10 | 216/2336 | 61/1146 | 21/381 | chr3 | 149846087 | ||
| chr3:149872116 | G | C | 1 | a0006 | 1 | NA18906.hp1 | missense_variant | MODERATE | c.283G>C | p.Val95Leu | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/10 | 438/2336 | 283/1146 | 95/381 | chr3 | 149872116 | ||
| chr3:149902141 | A | G | 1 | a0004 | 2 | HG02922.hp2 HG03139.hp2 |
missense_variant | MODERATE | c.479A>G | p.Asp160Gly | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 6/10 | 634/2336 | 479/1146 | 160/381 | chr3 | 149902141 | ||
| chr3:149911994 | G | A | 1 | a0002 | 3 | HG02976.hp2 HG03041.hp1 HG03130.hp2 |
missense_variant | MODERATE | c.517G>A | p.Val173Ile | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 7/10 | 672/2336 | 517/1146 | 173/381 | chr3 | 149911994 | ||
| chr3:149921182 | C | T | 1 | a0003 | 2 | HG03098.hp1 NA18906.hp2 |
missense_variant | MODERATE | c.655C>T | p.Arg219Cys | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/10 | 810/2336 | 655/1146 | 219/381 | chr3 | 149921182 | ||
| chr3:149921183 | G | A | 1 | a0007 | 1 | HG02109.hp2 | missense_variant | MODERATE | c.656G>A | p.Arg219His | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/10 | 811/2336 | 656/1146 | 219/381 | chr3 | 149921183 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:149960747 | C | T | 5 | a0001c0001a0002c0003a0004c0005others(2): Show | 171 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(168): Show |
synonymous_variant | LOW | c.789C>T | p.His263His | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 10/10 | 944/2336 | 789/1146 | 263/381 | chr3 | 149960747 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:149813224 | T | G | 1 | a0003c0004t0008 | 2 | HG03098.hp1 NA18906.hp2 |
5_prime_UTR_variant | MODIFIER | c.-146T>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/10 | 32803 | chr3 | 149813224 | |||||
| chr3:149813231 | C | T | 1 | a0001c0001t0014 | 1 | HG03239.hp1 | 5_prime_UTR_variant | MODIFIER | c.-139C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/10 | 32796 | chr3 | 149813231 | |||||
| chr3:149813233 | C | G | 1 | a0001c0001t0013 | 1 | NA20805.hp2 | 5_prime_UTR_variant | MODIFIER | c.-137C>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/10 | 32794 | chr3 | 149813233 | |||||
| chr3:149813252 | TGG | T | 3 | a0001c0001t0012a0001c0002t0005a0001c0002t0006 | 17 | HG00639.hp1 HG00642.hp2 HG01891.hp2 others(14): Show |
5_prime_UTR_variant | MODIFIER | c.-114_-113delGG | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/10 | 32770 | INFO_REALIGN_3_PRIME | chr3 | 149813252 | ||||
| chr3:149961227 | T | G | 2 | a0001c0002t0004a0001c0002t0009 | 9 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*123T>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 10/10 | 123 | chr3 | 149961227 | |||||
| chr3:149961343 | GAA | G | 1 | a0001c0002t0007 | 3 | HG02717.hp2 HG03130.hp1 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*241_*242delAA | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 10/10 | 241 | INFO_REALIGN_3_PRIME | chr3 | 149961343 | ||||
| chr3:149961361 | T | TA | 11 | a0001c0001t0001a0001c0001t0011a0001c0001t0012others(8): Show | 182 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(179): Show |
3_prime_UTR_variant | MODIFIER | c.*270dupA | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 10/10 | 271 | INFO_REALIGN_3_PRIME | chr3 | 149961361 | ||||
| chr3:149961361 | T | TAA | 2 | a0001c0002t0005a0001c0002t0010 | 9 | HG00639.hp1 HG00642.hp2 HG01891.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*269_*270dupAA | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 10/10 | 271 | INFO_REALIGN_3_PRIME | chr3 | 149961361 | ||||
| chr3:149961458 | C | T | 1 | a0001c0002t0003 | 23 | HG00280.hp2 HG01071.hp1 HG01074.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*354C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 10/10 | 354 | chr3 | 149961458 | |||||
| chr3:149961559 | A | C | 1 | a0001c0001t0011 | 1 | HG02738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*455A>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 10/10 | 455 | chr3 | 149961559 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:149813390 | T | G | 269 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0022others(266): Show | 270 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.-17+37T>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149813390 | ||||||
| chr3:149813516 | G | A | 8 | a0001c0002t0006g0005a0001c0002t0006g0006a0001c0002t0006g0007others(5): Show | 8 | HG02258.hp1 HG02615.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.-17+163G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149813516 | ||||||
| chr3:149813541 | G | T | 2 | a0001c0002t0002g0268a0001c0002t0002g0269 | 2 | HG02145.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-17+188G>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149813541 | ||||||
| chr3:149813596 | G | A | 1 | a0001c0001t0001g0010 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-17+243G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149813596 | ||||||
| chr3:149813723 | T | A | 1 | a0001c0002t0002g0011 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-17+370T>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149813723 | ||||||
| chr3:149813745 | A | G | 1 | a0001c0001t0001g0267 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-17+392A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149813745 | ||||||
| chr3:149813752 | G | A | 1 | a0001c0002t0002g0012 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-17+399G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149813752 | ||||||
| chr3:149814129 | C | G | 2 | a0001c0002t0002g0265a0001c0002t0002g0266 | 2 | HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-17+776C>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149814129 | ||||||
| chr3:149814239 | G | A | 11 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0002t0002g0020others(8): Show | 11 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.-17+886G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149814239 | ||||||
| chr3:149814284 | T | G | 1 | a0001c0001t0001g0024 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.-17+931T>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149814284 | ||||||
| chr3:149814353 | G | T | 13 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0002t0002g0020others(10): Show | 13 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-17+1000G>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149814353 | ||||||
| chr3:149814421 | A | G | 239 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0022others(236): Show | 239 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.-17+1068A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149814421 | ||||||
| chr3:149814664 | C | T | 5 | a0001c0002t0006g0005a0001c0002t0006g0006a0001c0002t0006g0007others(2): Show | 5 | HG02258.hp1 HG02615.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.-17+1311C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149814664 | ||||||
| chr3:149814709 | A | C | 1 | a0001c0002t0002g0011 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-17+1356A>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149814709 | ||||||
| chr3:149814794 | G | A | 1 | a0001c0001t0001g0054 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-17+1441G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149814794 | ||||||
| chr3:149814933 | GT | G | 16 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0001t0001g0055others(13): Show | 16 | HG00735.hp1 HG01070.hp2 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.-17+1593delT | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 149814933 | |||||
| chr3:149815039 | T | C | 150 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0054others(147): Show | 150 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.-17+1686T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149815039 | ||||||
| chr3:149815121 | G | A | 40 | a0001c0001t0001g0198a0001c0001t0001g0201a0001c0001t0001g0211others(37): Show | 40 | HG00544.hp2 HG00639.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.-17+1768G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149815121 | ||||||
| chr3:149815275 | G | A | 2 | a0001c0002t0002g0025a0001c0002t0002g0026 | 2 | NA18972.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.-17+1922G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149815275 | ||||||
| chr3:149815441 | G | A | 28 | a0001c0001t0001g0055a0001c0001t0001g0057a0001c0001t0001g0058others(25): Show | 28 | HG00323.hp1 HG00741.hp2 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.-17+2088G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149815441 | ||||||
| chr3:149815481 | G | C | 2 | a0001c0001t0001g0239a0001c0002t0003g0238 | 2 | HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-17+2128G>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149815481 | ||||||
| chr3:149815605 | A | G | 1 | a0001c0002t0003g0264 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-17+2252A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149815605 | ||||||
| chr3:149815862 | G | A | 1 | a0001c0001t0001g0198 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.-17+2509G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149815862 | ||||||
| chr3:149815931 | C | G | 13 | a0001c0001t0001g0239a0001c0002t0003g0238a0001c0002t0003g0254others(10): Show | 13 | HG00280.hp2 HG01106.hp1 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.-17+2578C>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149815931 | ||||||
| chr3:149815961 | T | C | 1 | a0001c0001t0001g0084 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-17+2608T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149815961 | ||||||
| chr3:149815978 | G | A | 11 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0002t0002g0020others(8): Show | 11 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.-17+2625G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149815978 | ||||||
| chr3:149816019 | A | C | 1 | a0001c0001t0001g0197 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-17+2666A>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149816019 | ||||||
| chr3:149816064 | A | AT | 87 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0056others(84): Show | 87 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.-17+2727dupT | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 149816064 | |||||
| chr3:149816322 | G | A | 2 | a0001c0001t0001g0116a0001c0001t0001g0117 | 2 | HG03831.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.-17+2969G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149816322 | ||||||
| chr3:149816488 | G | A | 9 | a0001c0001t0001g0245a0001c0002t0002g0240a0001c0002t0002g0241others(6): Show | 9 | HG01496.hp1 HG02109.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.-17+3135G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149816488 | ||||||
| chr3:149816910 | A | G | 2 | a0001c0002t0006g0236a0001c0002t0006g0237 | 2 | HG02896.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-17+3557A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149816910 | ||||||
| chr3:149817299 | T | G | 1 | a0001c0002t0002g0012 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-17+3946T>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149817299 | ||||||
| chr3:149817697 | C | T | 13 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0002t0002g0020others(10): Show | 13 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-17+4344C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149817697 | ||||||
| chr3:149817755 | T | G | 1 | a0001c0002t0002g0268 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-17+4402T>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149817755 | ||||||
| chr3:149817882 | G | C | 2 | a0003c0004t0008g0199a0003c0004t0008g0200 | 2 | HG03098.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-17+4529G>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149817882 | ||||||
| chr3:149817910 | GA | G | 13 | a0001c0001t0001g0239a0001c0002t0003g0238a0001c0002t0003g0254others(10): Show | 13 | HG00280.hp2 HG01106.hp1 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.-17+4562delA | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 149817910 | |||||
| chr3:149817957 | C | T | 1 | a0001c0001t0001g0115 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-17+4604C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149817957 | ||||||
| chr3:149818207 | T | A | 13 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0002t0002g0020others(10): Show | 13 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-17+4854T>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149818207 | ||||||
| chr3:149818394 | G | A | 11 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0002t0002g0020others(8): Show | 11 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.-17+5041G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149818394 | ||||||
| chr3:149818422 | G | A | 3 | a0001c0002t0003g0254a0001c0002t0003g0255a0001c0002t0003g0264 | 3 | HG02698.hp2 NA18999.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-17+5069G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149818422 | ||||||
| chr3:149818710 | G | A | 2 | a0001c0001t0001g0027a0001c0001t0001g0028 | 2 | HG02080.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.-17+5357G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149818710 | ||||||
| chr3:149818897 | C | T | 2 | a0001c0002t0002g0052a0001c0002t0002g0053 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-17+5544C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149818897 | ||||||
| chr3:149819172 | A | G | 2 | a0001c0002t0002g0265a0001c0002t0002g0266 | 2 | HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-17+5819A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149819172 | ||||||
| chr3:149819435 | A | ATAGT | 13 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0002t0002g0020others(10): Show | 13 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-17+6084_-17+6085i others(6): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 149819435 | |||||
| chr3:149819438 | CTCACTT | C | 19 | a0001c0001t0001g0239a0001c0002t0003g0238a0001c0002t0003g0254others(16): Show | 19 | HG00280.hp2 HG01106.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.-17+6089_-17+6094d others(8): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 149819438 | |||||
| chr3:149819716 | A | C | 1 | a0001c0001t0001g0196 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-17+6363A>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149819716 | ||||||
| chr3:149819849 | G | T | 1 | a0001c0001t0001g0083 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-17+6496G>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149819849 | ||||||
| chr3:149819924 | T | C | 6 | a0001c0002t0006g0005a0001c0002t0006g0006a0001c0002t0006g0007others(3): Show | 6 | HG02109.hp1 HG02258.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-17+6571T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149819924 | ||||||
| chr3:149819990 | T | A | 150 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0054others(147): Show | 150 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.-17+6637T>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149819990 | ||||||
| chr3:149820049 | T | C | 3 | a0001c0002t0003g0085a0001c0002t0003g0086a0001c0002t0003g0087 | 3 | HG01074.hp2 HG01433.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.-17+6696T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149820049 | ||||||
| chr3:149820161 | C | T | 9 | a0001c0001t0001g0245a0001c0002t0002g0240a0001c0002t0002g0241others(6): Show | 9 | HG01496.hp1 HG02109.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.-17+6808C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149820161 | ||||||
| chr3:149820652 | A | C | 2 | a0001c0002t0002g0268a0001c0002t0002g0269 | 2 | HG02145.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-17+7299A>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149820652 | ||||||
| chr3:149820671 | C | T | 2 | a0001c0002t0002g0052a0001c0002t0002g0053 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-17+7318C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149820671 | ||||||
| chr3:149820672 | G | A | 11 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0002t0002g0020others(8): Show | 11 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.-17+7319G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149820672 | ||||||
| chr3:149820693 | A | G | 11 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0002t0002g0020others(8): Show | 11 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.-17+7340A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149820693 | ||||||
| chr3:149820976 | T | C | 1 | a0001c0001t0001g0057 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-17+7623T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149820976 | ||||||
| chr3:149821048 | A | G | 2 | a0001c0002t0002g0052a0001c0002t0002g0053 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-17+7695A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149821048 | ||||||
| chr3:149821253 | G | A | 2 | a0003c0004t0008g0199a0003c0004t0008g0200 | 2 | HG03098.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-17+7900G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149821253 | ||||||
| chr3:149821378 | A | C | 21 | a0001c0001t0001g0239a0001c0002t0003g0238a0001c0002t0003g0254others(18): Show | 21 | HG00280.hp2 HG01106.hp1 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17+8025A>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149821378 | ||||||
| chr3:149821401 | G | A | 1 | a0001c0001t0001g0118 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.-17+8048G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149821401 | ||||||
| chr3:149821508 | C | G | 1 | a0001c0001t0001g0082 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-17+8155C>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149821508 | ||||||
| chr3:149821614 | AT | A | 238 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0022others(235): Show | 238 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.-17+8271delT | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 149821614 | |||||
| chr3:149821804 | C | T | 2 | a0001c0002t0002g0265a0001c0002t0002g0266 | 2 | HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-17+8451C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149821804 | ||||||
| chr3:149821916 | T | G | 4 | a0001c0002t0001g0251a0001c0002t0007g0249a0001c0002t0007g0250others(1): Show | 4 | HG02717.hp2 HG03130.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.-17+8563T>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149821916 | ||||||
| chr3:149821991 | C | A | 2 | a0001c0002t0004g0013a0001c0002t0004g0014 | 2 | HG02630.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-17+8638C>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149821991 | ||||||
| chr3:149822002 | A | G | 1 | a0001c0001t0001g0114 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-17+8649A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149822002 | ||||||
| chr3:149822169 | A | G | 2 | a0001c0001t0001g0194a0001c0001t0001g0195 | 2 | HG01192.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-17+8816A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149822169 | ||||||
| chr3:149822470 | C | T | 11 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0002t0002g0020others(8): Show | 11 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.-17+9117C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149822470 | ||||||
| chr3:149822607 | A | G | 1 | a0001c0001t0001g0267 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-17+9254A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149822607 | ||||||
| chr3:149822678 | C | T | 22 | a0001c0001t0001g0233a0001c0001t0001g0239a0001c0002t0003g0238others(19): Show | 22 | HG00280.hp2 HG01106.hp1 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.-17+9325C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149822678 | ||||||
| chr3:149822917 | A | C | 2 | a0003c0004t0008g0199a0003c0004t0008g0200 | 2 | HG03098.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-17+9564A>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149822917 | ||||||
| chr3:149822938 | T | C | 1 | a0001c0002t0002g0030 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.-17+9585T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149822938 | ||||||
| chr3:149823033 | G | A | 1 | a0001c0001t0001g0088 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-17+9680G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149823033 | ||||||
| chr3:149823420 | T | G | 2 | a0001c0002t0002g0268a0001c0002t0002g0269 | 2 | HG02145.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-17+10067T>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149823420 | ||||||
| chr3:149823465 | A | T | 1 | a0001c0001t0001g0114 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-17+10112A>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149823465 | ||||||
| chr3:149823483 | A | T | 3 | a0001c0001t0001g0082a0004c0005t0001g0080a0004c0005t0001g0081 | 3 | HG02922.hp2 HG03139.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-17+10130A>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149823483 | ||||||
| chr3:149823571 | A | G | 2 | a0001c0002t0002g0265a0001c0002t0002g0266 | 2 | HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-17+10218A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149823571 | ||||||
| chr3:149823613 | T | C | 1 | a0001c0001t0001g0119 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-17+10260T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149823613 | ||||||
| chr3:149823655 | A | G | 5 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(2): Show | 5 | HG00323.hp1 HG01192.hp1 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.-17+10302A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149823655 | ||||||
| chr3:149823980 | G | A | 1 | a0002c0003t0001g0002 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-17+10627G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149823980 | ||||||
| chr3:149824116 | A | G | 9 | a0001c0001t0001g0245a0001c0002t0002g0240a0001c0002t0002g0241others(6): Show | 9 | HG01496.hp1 HG02109.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.-17+10763A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149824116 | ||||||
| chr3:149824235 | G | A | 1 | a0001c0001t0001g0201 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.-17+10882G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149824235 | ||||||
| chr3:149824286 | A | C | 2 | a0001c0002t0002g0265a0001c0002t0002g0266 | 2 | HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-17+10933A>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149824286 | ||||||
| chr3:149824431 | A | G | 1 | a0001c0001t0001g0196 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-17+11078A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149824431 | ||||||
| chr3:149824617 | G | GT | 5 | a0001c0001t0001g0075a0001c0001t0001g0110a0001c0001t0001g0111others(2): Show | 5 | HG02293.hp1 HG02896.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.-17+11273dupT | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 149824617 | |||||
| chr3:149824681 | G | A | 3 | a0001c0002t0002g0031a0001c0002t0002g0052a0001c0002t0002g0053 | 3 | HG03491.hp1 HG03492.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.-17+11328G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149824681 | ||||||
| chr3:149824789 | A | G | 2 | a0001c0002t0002g0265a0001c0002t0002g0266 | 2 | HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-17+11436A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149824789 | ||||||
| chr3:149824961 | AT | A | 13 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0002t0002g0020others(10): Show | 13 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-17+11624delT | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 149824961 | |||||
| chr3:149825108 | G | A | 1 | a0001c0002t0002g0240 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-17+11755G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149825108 | ||||||
| chr3:149825182 | C | CT | 13 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0002t0002g0020others(10): Show | 13 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-17+11841dupT | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 149825182 | |||||
| chr3:149825315 | C | T | 86 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0056others(83): Show | 86 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.-17+11962C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149825315 | ||||||
| chr3:149825364 | A | G | 1 | a0001c0002t0003g0109 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.-17+12011A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149825364 | ||||||
| chr3:149825509 | G | A | 2 | a0001c0002t0002g0265a0001c0002t0002g0266 | 2 | HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-17+12156G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149825509 | ||||||
| chr3:149825578 | A | G | 239 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0022others(236): Show | 239 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.-17+12225A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149825578 | ||||||
| chr3:149825712 | A | G | 1 | a0001c0001t0001g0193 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-17+12359A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149825712 | ||||||
| chr3:149825997 | A | G | 2 | a0003c0004t0008g0199a0003c0004t0008g0200 | 2 | HG03098.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-17+12644A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149825997 | ||||||
| chr3:149826006 | T | A | 11 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0002t0002g0020others(8): Show | 11 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.-17+12653T>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149826006 | ||||||
| chr3:149826083 | G | A | 6 | a0001c0001t0001g0054a0001c0001t0001g0089a0001c0001t0001g0090others(3): Show | 6 | HG02647.hp1 HG02717.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-17+12730G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149826083 | ||||||
| chr3:149826089 | C | G | 2 | a0001c0002t0002g0278a0001c0002t0002g0279 | 2 | HG00140.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.-17+12736C>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149826089 | ||||||
| chr3:149826153 | G | A | 238 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0022others(235): Show | 238 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.-17+12800G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149826153 | ||||||
| chr3:149826412 | G | C | 1 | a0001c0001t0001g0010 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-17+13059G>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149826412 | ||||||
| chr3:149826550 | G | A | 1 | a0001c0001t0001g0084 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-17+13197G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149826550 | ||||||
| chr3:149826571 | A | C | 59 | a0001c0001t0001g0198a0001c0001t0001g0201a0001c0001t0001g0211others(56): Show | 59 | HG00280.hp2 HG00544.hp2 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.-17+13218A>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149826571 | ||||||
| chr3:149826582 | A | G | 1 | a0001c0002t0001g0051 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-17+13229A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149826582 | ||||||
| chr3:149827038 | A | G | 2 | a0001c0002t0006g0236a0001c0002t0006g0237 | 2 | HG02896.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-17+13685A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149827038 | ||||||
| chr3:149827184 | T | C | 1 | a0001c0001t0001g0120 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-17+13831T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149827184 | ||||||
| chr3:149827249 | T | C | 1 | a0001c0001t0001g0094 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-17+13896T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149827249 | ||||||
| chr3:149827704 | A | G | 1 | a0001c0002t0002g0277 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-17+14351A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149827704 | ||||||
| chr3:149827939 | ATCTC | A | 4 | a0001c0001t0001g0089a0001c0002t0002g0265a0001c0002t0002g0266others(1): Show | 4 | HG02723.hp1 HG02970.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-17+14590_-17+1459 others(8): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 149827939 | |||||
| chr3:149827947 | A | AT | 8 | a0001c0001t0001g0108a0001c0001t0001g0119a0001c0001t0001g0190others(5): Show | 8 | HG00323.hp2 HG00544.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.-17+14610dupT | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 149827947 | |||||
| chr3:149827947 | A | C | 1 | a0001c0001t0001g0088 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-17+14594A>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149827947 | ||||||
| chr3:149827947 | AT | A | 6 | a0001c0001t0001g0058a0001c0001t0001g0122a0001c0001t0001g0123others(3): Show | 6 | HG01070.hp1 HG01074.hp2 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.-17+14610delT | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 149827947 | |||||
| chr3:149828106 | T | C | 1 | a0001c0001t0001g0196 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-17+14753T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149828106 | ||||||
| chr3:149828108 | G | A | 1 | a0001c0001t0001g0088 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-17+14755G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149828108 | ||||||
| chr3:149828154 | T | C | 2 | a0001c0002t0002g0268a0001c0002t0002g0269 | 2 | HG02145.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-17+14801T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149828154 | ||||||
| chr3:149828449 | C | A | 1 | a0001c0002t0007g0249 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-17+15096C>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149828449 | ||||||
| chr3:149828493 | A | G | 2 | a0001c0001t0001g0073a0001c0001t0001g0074 | 2 | HG01993.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-17+15140A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149828493 | ||||||
| chr3:149828745 | A | G | 6 | a0001c0002t0006g0005a0001c0002t0006g0006a0001c0002t0006g0007others(3): Show | 6 | HG02109.hp1 HG02258.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-17+15392A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149828745 | ||||||
| chr3:149828756 | C | T | 11 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0002t0002g0020others(8): Show | 11 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.-17+15403C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149828756 | ||||||
| chr3:149828977 | T | C | 1 | a0001c0002t0003g0124 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-17+15624T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149828977 | ||||||
| chr3:149829153 | G | T | 13 | a0001c0001t0001g0239a0001c0002t0003g0238a0001c0002t0003g0254others(10): Show | 13 | HG00280.hp2 HG01106.hp1 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.-17+15800G>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149829153 | ||||||
| chr3:149829202 | C | T | 1 | a0001c0001t0001g0189 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-17+15849C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149829202 | ||||||
| chr3:149829244 | C | T | 11 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0002t0002g0020others(8): Show | 11 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.-17+15891C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149829244 | ||||||
| chr3:149829311 | G | A | 3 | a0001c0002t0007g0249a0001c0002t0007g0250a0001c0002t0007g0252 | 3 | HG02717.hp2 HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-17+15958G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149829311 | ||||||
| chr3:149829337 | C | T | 2 | a0001c0002t0002g0268a0001c0002t0002g0269 | 2 | HG02145.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-17+15984C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149829337 | ||||||
| chr3:149829338 | G | A | 11 | a0001c0001t0012g0206a0001c0002t0005g0202a0001c0002t0005g0203others(8): Show | 11 | HG00639.hp1 HG00642.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.-17+15985G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149829338 | ||||||
| chr3:149829654 | CTAT | C | 3 | a0001c0002t0001g0048a0001c0002t0001g0049a0001c0002t0001g0050 | 3 | NA18988.hp1 NA19065.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.-17+16306_-17+1630 others(7): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 149829654 | |||||
| chr3:149829690 | T | C | 1 | a0001c0002t0001g0251 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-16-16321T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149829690 | ||||||
| chr3:149829697 | C | T | 1 | a0001c0001t0002g0188 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-16-16314C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149829697 | ||||||
| chr3:149829738 | G | A | 2 | a0001c0002t0002g0265a0001c0002t0002g0266 | 2 | HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-16-16273G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149829738 | ||||||
| chr3:149830116 | A | G | 11 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0002t0002g0020others(8): Show | 11 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.-16-15895A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149830116 | ||||||
| chr3:149830200 | G | A | 1 | a0001c0002t0002g0012 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-16-15811G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149830200 | ||||||
| chr3:149830701 | A | G | 1 | a0001c0001t0001g0231 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-16-15310A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149830701 | ||||||
| chr3:149830791 | C | T | 6 | a0001c0002t0006g0005a0001c0002t0006g0006a0001c0002t0006g0007others(3): Show | 6 | HG02109.hp1 HG02258.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-16-15220C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149830791 | ||||||
| chr3:149830792 | T | G | 6 | a0001c0002t0006g0005a0001c0002t0006g0006a0001c0002t0006g0007others(3): Show | 6 | HG02109.hp1 HG02258.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-16-15219T>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149830792 | ||||||
| chr3:149830804 | C | T | 6 | a0001c0002t0006g0005a0001c0002t0006g0006a0001c0002t0006g0007others(3): Show | 6 | HG02109.hp1 HG02258.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-16-15207C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149830804 | ||||||
| chr3:149830809 | T | C | 6 | a0001c0002t0006g0005a0001c0002t0006g0006a0001c0002t0006g0007others(3): Show | 6 | HG02109.hp1 HG02258.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-16-15202T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149830809 | ||||||
| chr3:149830912 | T | C | 1 | a0001c0001t0001g0125 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-16-15099T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149830912 | ||||||
| chr3:149830992 | G | A | 11 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0002t0002g0020others(8): Show | 11 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.-16-15019G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149830992 | ||||||
| chr3:149831007 | G | A | 77 | a0001c0001t0001g0055a0001c0001t0001g0057a0001c0001t0001g0058others(74): Show | 77 | HG00323.hp1 HG00544.hp2 HG00621.hp2 others(74): Show |
intron_variant | MODIFIER | c.-16-15004G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149831007 | ||||||
| chr3:149831105 | G | T | 27 | a0001c0001t0001g0198a0001c0001t0001g0201a0001c0001t0001g0211others(24): Show | 27 | HG00544.hp2 HG00639.hp2 HG01978.hp1 others(24): Show |
intron_variant | MODIFIER | c.-16-14906G>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149831105 | ||||||
| chr3:149831110 | G | A | 1 | a0001c0002t0002g0241 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-16-14901G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149831110 | ||||||
| chr3:149831217 | G | A | 1 | a0001c0001t0001g0126 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-16-14794G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149831217 | ||||||
| chr3:149831228 | C | T | 3 | a0001c0002t0007g0249a0001c0002t0007g0250a0001c0002t0007g0252 | 3 | HG02717.hp2 HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-16-14783C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149831228 | ||||||
| chr3:149831354 | A | T | 1 | a0001c0001t0001g0187 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-16-14657A>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149831354 | ||||||
| chr3:149831369 | C | T | 1 | a0001c0001t0001g0186 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-16-14642C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149831369 | ||||||
| chr3:149831494 | C | A | 13 | a0001c0002t0001g0001a0001c0002t0001g0029a0001c0002t0001g0032others(10): Show | 14 | HG00609.hp2 NA18943.hp2 NA18950.hp2 others(11): Show |
intron_variant | MODIFIER | c.-16-14517C>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149831494 | ||||||
| chr3:149831550 | C | A | 3 | a0002c0003t0001g0002a0002c0003t0001g0003a0002c0003t0001g0004 | 3 | HG02976.hp2 HG03041.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-16-14461C>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149831550 | ||||||
| chr3:149831563 | A | G | 1 | a0003c0004t0008g0200 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-16-14448A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149831563 | ||||||
| chr3:149831682 | G | A | 2 | a0001c0002t0002g0268a0001c0002t0002g0269 | 2 | HG02145.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-16-14329G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149831682 | ||||||
| chr3:149831739 | G | T | 1 | a0001c0001t0001g0196 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-16-14272G>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149831739 | ||||||
| chr3:149831911 | T | A | 1 | a0001c0001t0002g0188 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-16-14100T>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149831911 | ||||||
| chr3:149832165 | A | G | 11 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0002t0002g0020others(8): Show | 11 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.-16-13846A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149832165 | ||||||
| chr3:149832301 | A | C | 11 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0002t0002g0020others(8): Show | 11 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.-16-13710A>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149832301 | ||||||
| chr3:149832315 | G | A | 9 | a0001c0001t0001g0245a0001c0002t0002g0240a0001c0002t0002g0241others(6): Show | 9 | HG01496.hp1 HG02109.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.-16-13696G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149832315 | ||||||
| chr3:149832445 | G | C | 1 | a0001c0001t0001g0075 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-16-13566G>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149832445 | ||||||
| chr3:149832466 | A | G | 2 | a0003c0004t0008g0199a0003c0004t0008g0200 | 2 | HG03098.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-16-13545A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149832466 | ||||||
| chr3:149832633 | T | A | 27 | a0001c0001t0001g0198a0001c0001t0001g0201a0001c0001t0001g0211others(24): Show | 27 | HG00544.hp2 HG00639.hp2 HG01978.hp1 others(24): Show |
intron_variant | MODIFIER | c.-16-13378T>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149832633 | ||||||
| chr3:149832649 | C | T | 276 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0022others(273): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.-16-13362C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149832649 | ||||||
| chr3:149832668 | A | G | 1 | a0001c0002t0010g0038 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-16-13343A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149832668 | ||||||
| chr3:149832924 | T | C | 9 | a0001c0001t0001g0245a0001c0002t0002g0240a0001c0002t0002g0241others(6): Show | 9 | HG01496.hp1 HG02109.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.-16-13087T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149832924 | ||||||
| chr3:149832933 | T | C | 1 | a0001c0001t0001g0122 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-16-13078T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149832933 | ||||||
| chr3:149833044 | G | C | 9 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(6): Show | 9 | HG00323.hp1 HG01123.hp2 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.-16-12967G>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149833044 | ||||||
| chr3:149833118 | C | CT | 195 | a0001c0001t0001g0010a0001c0001t0001g0054a0001c0001t0001g0055others(192): Show | 195 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.-16-12874dupT | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 149833118 | |||||
| chr3:149833118 | C | CTCTTTTT others(2): Show |
9 | a0001c0001t0001g0015a0001c0002t0002g0020a0001c0002t0004g0013others(6): Show | 9 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.-16-12892_-16-1289 others(13): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 149833118 | |||||
| chr3:149833118 | C | CTCTTTTT others(3): Show |
2 | a0001c0001t0001g0022a0001c0002t0004g0023 | 2 | HG03492.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-16-12892_-16-1289 others(14): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 149833118 | |||||
| chr3:149833118 | C | CTT | 22 | a0001c0001t0001g0062a0001c0001t0001g0094a0001c0001t0001g0115others(19): Show | 22 | HG00280.hp2 HG00741.hp1 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.-16-12875_-16-1287 others(6): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 149833118 | |||||
| chr3:149833715 | C | A | 2 | a0001c0001t0001g0132a0001c0001t0014g0133 | 2 | HG01106.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.-16-12296C>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149833715 | ||||||
| chr3:149833717 | G | A | 11 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0002t0002g0020others(8): Show | 11 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.-16-12294G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149833717 | ||||||
| chr3:149833791 | G | A | 2 | a0001c0002t0002g0265a0001c0002t0002g0266 | 2 | HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-16-12220G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149833791 | ||||||
| chr3:149834094 | C | T | 6 | a0001c0002t0006g0005a0001c0002t0006g0006a0001c0002t0006g0007others(3): Show | 6 | HG02109.hp1 HG02258.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-16-11917C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149834094 | ||||||
| chr3:149834135 | T | G | 2 | a0001c0002t0002g0265a0001c0002t0002g0266 | 2 | HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-16-11876T>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149834135 | ||||||
| chr3:149834224 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-16-11787C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149834224 | ||||||
| chr3:149834455 | A | C | 13 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0002t0002g0020others(10): Show | 13 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-16-11556A>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149834455 | ||||||
| chr3:149834801 | C | T | 4 | a0001c0002t0002g0020a0001c0002t0004g0019a0001c0002t0004g0021others(1): Show | 4 | HG01243.hp2 HG02622.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.-16-11210C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149834801 | ||||||
| chr3:149834871 | C | T | 3 | a0001c0002t0003g0091a0001c0002t0003g0092a0001c0002t0003g0093 | 3 | HG02717.hp1 HG02886.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-16-11140C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149834871 | ||||||
| chr3:149834872 | G | A | 11 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0002t0002g0020others(8): Show | 11 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.-16-11139G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149834872 | ||||||
| chr3:149834999 | A | T | 1 | a0001c0001t0001g0054 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-16-11012A>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149834999 | ||||||
| chr3:149835431 | C | G | 2 | a0001c0001t0001g0183a0001c0002t0003g0124 | 2 | HG00609.hp1 HG02074.hp1 |
intron_variant | MODIFIER | c.-16-10580C>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149835431 | ||||||
| chr3:149835439 | T | C | 238 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0022others(235): Show | 238 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.-16-10572T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149835439 | ||||||
| chr3:149835633 | T | TTG | 103 | a0001c0001t0001g0010a0001c0001t0001g0027a0001c0001t0001g0056others(100): Show | 103 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.-16-10346_-16-1034 others(6): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 149835633 | |||||
| chr3:149835633 | T | TTGTG | 35 | a0001c0001t0001g0024a0001c0001t0001g0063a0001c0001t0001g0110others(32): Show | 35 | HG00140.hp1 HG00621.hp1 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.-16-10348_-16-1034 others(8): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 149835633 | |||||
| chr3:149835633 | T | TTGTGTG | 19 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0135others(16): Show | 19 | HG00544.hp1 HG00639.hp1 HG00642.hp2 others(16): Show |
intron_variant | MODIFIER | c.-16-10350_-16-1034 others(10): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 149835633 | |||||
| chr3:149835633 | T | TTGTGTGT others(3): Show |
3 | a0001c0002t0004g0013a0001c0002t0004g0014a0001c0002t0004g0018 | 3 | HG00735.hp1 HG02630.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-16-10354_-16-1034 others(14): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 149835633 | |||||
| chr3:149835633 | T | TTGTGTGT others(5): Show |
1 | a0001c0002t0004g0017 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-16-10356_-16-1034 others(16): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 149835633 | |||||
| chr3:149835633 | T | TTGTGTGT others(7): Show |
1 | a0001c0002t0004g0016 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-16-10358_-16-1034 others(18): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 149835633 | |||||
| chr3:149835633 | T | TTGTGTGT others(9): Show |
3 | a0001c0002t0002g0020a0001c0002t0004g0019a0001c0002t0004g0021 | 3 | HG01243.hp2 HG02622.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.-16-10360_-16-1034 others(20): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 149835633 | |||||
| chr3:149835633 | T | TTGTGTGT others(11): Show |
2 | a0001c0001t0001g0015a0001c0002t0004g0023 | 2 | HG02738.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-16-10362_-16-1034 others(22): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 149835633 | |||||
| chr3:149835633 | TTG | T | 2 | a0001c0001t0001g0182a0001c0002t0002g0248 | 2 | HG01496.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.-16-10346_-16-1034 others(6): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 149835633 | |||||
| chr3:149835665 | G | GTGTGTGT others(11): Show |
1 | a0003c0004t0008g0200 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-16-10345_-16-1034 others(22): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 149835665 | |||||
| chr3:149835665 | G | GTGTGTGT others(7): Show |
1 | a0003c0004t0008g0199 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-16-10345_-16-1034 others(18): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 149835665 | |||||
| chr3:149835665 | G | T | 1 | a0001c0001t0001g0233 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.-16-10346G>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149835665 | ||||||
| chr3:149835667 | T | G | 4 | a0001c0001t0001g0134a0001c0001t0001g0233a0003c0004t0008g0199others(1): Show | 4 | HG03098.hp1 NA18906.hp2 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.-16-10344T>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149835667 | ||||||
| chr3:149835727 | G | C | 1 | a0001c0002t0001g0032 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-16-10284G>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149835727 | ||||||
| chr3:149835842 | GTGGGATT others(16): Show |
G | 2 | a0001c0002t0002g0045a0001c0002t0002g0046 | 2 | NA18961.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.-16-10154_-16-1013 others(27): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 149835842 | |||||
| chr3:149835851 | C | A | 2 | a0001c0002t0002g0265a0001c0002t0002g0266 | 2 | HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-16-10160C>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149835851 | ||||||
| chr3:149835857 | C | A | 1 | a0001c0002t0001g0251 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-16-10154C>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149835857 | ||||||
| chr3:149835857 | C | CCCCAGTA others(16): Show |
2 | a0001c0002t0002g0265a0001c0002t0002g0266 | 2 | HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-16-10108_-16-1008 others(27): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 149835857 | |||||
| chr3:149835857 | CCCCAGTA others(16): Show |
C | 22 | a0001c0001t0001g0153a0001c0001t0012g0206a0001c0002t0002g0039others(19): Show | 22 | HG00639.hp1 HG00642.hp2 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.-16-10108_-16-1008 others(27): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 149835857 | |||||
| chr3:149835857 | CCCCAGTA others(39): Show |
C | 13 | a0001c0001t0001g0239a0001c0002t0003g0238a0001c0002t0003g0254others(10): Show | 13 | HG00280.hp2 HG01106.hp1 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.-16-10131_-16-1008 others(50): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 149835857 | |||||
| chr3:149835869 | G | T | 1 | a0001c0001t0001g0152 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-16-10142G>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149835869 | ||||||
| chr3:149835903 | T | C | 1 | a0001c0001t0001g0211 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-16-10108T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149835903 | ||||||
| chr3:149835921 | T | C | 1 | a0001c0001t0001g0062 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-16-10090T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149835921 | ||||||
| chr3:149836058 | T | A | 2 | a0001c0001t0001g0055a0001c0001t0001g0100 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.-16-9953T>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149836058 | ||||||
| chr3:149836181 | T | C | 5 | a0001c0002t0005g0202a0001c0002t0005g0203a0001c0002t0005g0204others(2): Show | 5 | HG00639.hp1 HG00642.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.-16-9830T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149836181 | ||||||
| chr3:149836223 | C | A | 2 | a0001c0002t0002g0052a0001c0002t0002g0053 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-16-9788C>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149836223 | ||||||
| chr3:149836230 | A | T | 2 | a0001c0002t0003g0258a0001c0002t0003g0259 | 2 | HG00280.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.-16-9781A>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149836230 | ||||||
| chr3:149836428 | A | G | 182 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0054others(179): Show | 182 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.-16-9583A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149836428 | ||||||
| chr3:149836434 | A | G | 19 | a0001c0001t0001g0010a0001c0001t0001g0116a0001c0001t0001g0117others(16): Show | 19 | HG00544.hp1 HG01433.hp2 HG02056.hp2 others(16): Show |
intron_variant | MODIFIER | c.-16-9577A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149836434 | ||||||
| chr3:149836528 | G | A | 2 | a0001c0002t0002g0265a0001c0002t0002g0266 | 2 | HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-16-9483G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149836528 | ||||||
| chr3:149836555 | CTGTT | C | 3 | a0002c0003t0001g0002a0002c0003t0001g0003a0002c0003t0001g0004 | 3 | HG02976.hp2 HG03041.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-16-9452_-16-9449d others(6): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 149836555 | |||||
| chr3:149836782 | A | G | 1 | a0001c0001t0001g0211 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-16-9229A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149836782 | ||||||
| chr3:149837011 | G | A | 2 | a0001c0002t0006g0236a0001c0002t0006g0237 | 2 | HG02896.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-16-9000G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149837011 | ||||||
| chr3:149837268 | G | A | 1 | a0001c0002t0002g0040 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-16-8743G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149837268 | ||||||
| chr3:149837313 | G | T | 2 | a0001c0002t0002g0268a0001c0002t0002g0269 | 2 | HG02145.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-16-8698G>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149837313 | ||||||
| chr3:149837508 | C | G | 2 | a0001c0002t0004g0017a0001c0002t0004g0018 | 2 | HG00735.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.-16-8503C>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149837508 | ||||||
| chr3:149837700 | TCCCTCCC others(194): Show |
T | 1 | a0001c0002t0003g0238 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-16-8310_-16-8110d others(2): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149837700 | ||||||
| chr3:149837794 | C | T | 13 | a0001c0001t0001g0055a0001c0001t0001g0094a0001c0001t0001g0099others(10): Show | 13 | HG01167.hp2 HG01169.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.-16-8217C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149837794 | ||||||
| chr3:149837827 | AG | A | 11 | a0001c0001t0012g0206a0001c0002t0005g0202a0001c0002t0005g0203others(8): Show | 11 | HG00639.hp1 HG00642.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.-16-8183delG | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149837827 | ||||||
| chr3:149837830 | C | T | 11 | a0001c0001t0012g0206a0001c0002t0005g0202a0001c0002t0005g0203others(8): Show | 11 | HG00639.hp1 HG00642.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.-16-8181C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149837830 | ||||||
| chr3:149837865 | A | G | 1 | a0001c0001t0001g0230 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.-16-8146A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149837865 | ||||||
| chr3:149837903 | G | A | 1 | a0001c0002t0003g0238 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-16-8108G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149837903 | ||||||
| chr3:149837962 | T | G | 9 | a0001c0001t0001g0245a0001c0002t0002g0240a0001c0002t0002g0241others(6): Show | 9 | HG01496.hp1 HG02109.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.-16-8049T>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149837962 | ||||||
| chr3:149838049 | A | T | 177 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0054others(174): Show | 177 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.-16-7962A>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149838049 | ||||||
| chr3:149838275 | T | C | 2 | a0001c0001t0001g0089a0001c0001t0001g0090 | 2 | HG02647.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.-16-7736T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149838275 | ||||||
| chr3:149838282 | G | A | 1 | a0001c0001t0001g0070 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-16-7729G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149838282 | ||||||
| chr3:149838443 | G | A | 11 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0002t0002g0020others(8): Show | 11 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.-16-7568G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149838443 | ||||||
| chr3:149838453 | A | T | 1 | a0001c0001t0001g0054 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-16-7558A>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149838453 | ||||||
| chr3:149838603 | C | T | 2 | a0001c0002t0002g0265a0001c0002t0002g0266 | 2 | HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-16-7408C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149838603 | ||||||
| chr3:149839603 | TACTC | T | 177 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0054others(174): Show | 177 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.-16-6403_-16-6400d others(6): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 149839603 | |||||
| chr3:149839702 | G | A | 13 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0002t0002g0020others(10): Show | 13 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-16-6309G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149839702 | ||||||
| chr3:149840027 | T | C | 1 | a0001c0001t0001g0089 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-16-5984T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149840027 | ||||||
| chr3:149840056 | A | G | 4 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0112others(1): Show | 4 | HG02896.hp2 HG02922.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-16-5955A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149840056 | ||||||
| chr3:149840094 | C | T | 13 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0002t0002g0020others(10): Show | 13 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-16-5917C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149840094 | ||||||
| chr3:149840095 | G | A | 1 | a0001c0001t0001g0070 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-16-5916G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149840095 | ||||||
| chr3:149840180 | G | A | 1 | a0001c0002t0002g0011 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-16-5831G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149840180 | ||||||
| chr3:149840262 | C | T | 9 | a0001c0001t0001g0245a0001c0002t0002g0240a0001c0002t0002g0241others(6): Show | 9 | HG01496.hp1 HG02109.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.-16-5749C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149840262 | ||||||
| chr3:149840390 | TAC | T | 8 | a0001c0001t0001g0088a0001c0001t0001g0097a0001c0002t0003g0085others(5): Show | 8 | HG00621.hp2 HG01071.hp1 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.-16-5619_-16-5618d others(4): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 149840390 | |||||
| chr3:149840463 | G | C | 2 | a0001c0001t0001g0102a0001c0001t0001g0103 | 2 | HG01891.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-16-5548G>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149840463 | ||||||
| chr3:149840476 | T | A | 1 | a0001c0001t0001g0054 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-16-5535T>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149840476 | ||||||
| chr3:149840522 | C | T | 1 | a0001c0002t0007g0252 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-16-5489C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149840522 | ||||||
| chr3:149840545 | C | T | 1 | a0005c0006t0001g0178 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-16-5466C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149840545 | ||||||
| chr3:149840601 | C | T | 240 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0022others(237): Show | 240 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.-16-5410C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149840601 | ||||||
| chr3:149840609 | C | T | 11 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0002t0002g0020others(8): Show | 11 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.-16-5402C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149840609 | ||||||
| chr3:149840725 | T | C | 240 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0022others(237): Show | 240 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.-16-5286T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149840725 | ||||||
| chr3:149840800 | A | G | 6 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0134others(3): Show | 6 | HG00544.hp1 NA18965.hp1 NA18975.hp2 others(3): Show |
intron_variant | MODIFIER | c.-16-5211A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149840800 | ||||||
| chr3:149840800 | A | T | 2 | a0003c0004t0008g0199a0003c0004t0008g0200 | 2 | HG03098.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-16-5211A>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149840800 | ||||||
| chr3:149840801 | G | A | 6 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0134others(3): Show | 6 | HG00544.hp1 NA18965.hp1 NA18975.hp2 others(3): Show |
intron_variant | MODIFIER | c.-16-5210G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149840801 | ||||||
| chr3:149840802 | A | T | 6 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0134others(3): Show | 6 | HG00544.hp1 NA18965.hp1 NA18975.hp2 others(3): Show |
intron_variant | MODIFIER | c.-16-5209A>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149840802 | ||||||
| chr3:149841034 | A | G | 9 | a0001c0001t0001g0245a0001c0002t0002g0240a0001c0002t0002g0241others(6): Show | 9 | HG01496.hp1 HG02109.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.-16-4977A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149841034 | ||||||
| chr3:149841337 | A | G | 2 | a0001c0001t0001g0060a0001c0001t0001g0061 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.-16-4674A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149841337 | ||||||
| chr3:149841434 | A | G | 2 | a0001c0002t0002g0268a0001c0002t0002g0269 | 2 | HG02145.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-16-4577A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149841434 | ||||||
| chr3:149841490 | C | T | 1 | a0001c0002t0005g0208 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-16-4521C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149841490 | ||||||
| chr3:149841587 | A | G | 13 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0002t0002g0020others(10): Show | 13 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-16-4424A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149841587 | ||||||
| chr3:149841649 | C | T | 13 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0002t0002g0020others(10): Show | 13 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-16-4362C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149841649 | ||||||
| chr3:149841673 | G | A | 3 | a0001c0002t0003g0254a0001c0002t0003g0255a0001c0002t0003g0264 | 3 | HG02698.hp2 NA18999.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-16-4338G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149841673 | ||||||
| chr3:149841713 | G | A | 1 | a0002c0003t0001g0003 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-16-4298G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149841713 | ||||||
| chr3:149841818 | C | T | 2 | a0001c0002t0002g0268a0001c0002t0002g0269 | 2 | HG02145.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-16-4193C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149841818 | ||||||
| chr3:149841881 | C | T | 1 | a0001c0001t0001g0072 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-16-4130C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149841881 | ||||||
| chr3:149841922 | A | G | 13 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0002t0002g0020others(10): Show | 13 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-16-4089A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149841922 | ||||||
| chr3:149842982 | A | G | 6 | a0001c0002t0006g0005a0001c0002t0006g0006a0001c0002t0006g0007others(3): Show | 6 | HG02109.hp1 HG02258.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-16-3029A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149842982 | ||||||
| chr3:149843591 | G | A | 13 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0002t0002g0020others(10): Show | 13 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-16-2420G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149843591 | ||||||
| chr3:149843747 | G | T | 11 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0002t0002g0020others(8): Show | 11 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.-16-2264G>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149843747 | ||||||
| chr3:149843957 | C | G | 11 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0002t0002g0020others(8): Show | 11 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.-16-2054C>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149843957 | ||||||
| chr3:149844299 | G | A | 3 | a0001c0001t0001g0097a0001c0002t0003g0096a0001c0002t0003g0109 | 3 | HG01071.hp1 HG01099.hp2 HG02074.hp2 |
intron_variant | MODIFIER | c.-16-1712G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149844299 | ||||||
| chr3:149844350 | G | A | 2 | a0001c0002t0002g0265a0001c0002t0002g0266 | 2 | HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-16-1661G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149844350 | ||||||
| chr3:149844427 | A | G | 2 | a0003c0004t0008g0199a0003c0004t0008g0200 | 2 | HG03098.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-16-1584A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149844427 | ||||||
| chr3:149844500 | C | G | 1 | a0001c0001t0001g0229 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-16-1511C>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149844500 | ||||||
| chr3:149844835 | A | T | 1 | a0001c0002t0001g0251 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-16-1176A>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149844835 | ||||||
| chr3:149844857 | A | G | 1 | a0001c0002t0004g0014 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-16-1154A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149844857 | ||||||
| chr3:149845034 | T | C | 178 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0054others(175): Show | 178 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.-16-977T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149845034 | ||||||
| chr3:149845143 | G | A | 1 | a0001c0001t0001g0179 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-16-868G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149845143 | ||||||
| chr3:149845165 | C | G | 2 | a0001c0002t0002g0265a0001c0002t0002g0266 | 2 | HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-16-846C>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149845165 | ||||||
| chr3:149845450 | C | T | 13 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0002t0002g0020others(10): Show | 13 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-16-561C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149845450 | ||||||
| chr3:149845463 | A | C | 1 | a0001c0002t0003g0124 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-16-548A>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149845463 | ||||||
| chr3:149845536 | A | G | 2 | a0003c0004t0008g0199a0003c0004t0008g0200 | 2 | HG03098.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-16-475A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149845536 | ||||||
| chr3:149845551 | T | C | 11 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0002t0002g0020others(8): Show | 11 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.-16-460T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149845551 | ||||||
| chr3:149845653 | A | G | 1 | a0001c0001t0001g0196 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-16-358A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149845653 | ||||||
| chr3:149845693 | A | G | 1 | a0001c0001t0001g0125 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-16-318A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 1/9 | chr3 | 149845693 | ||||||
| chr3:149846181 | TAAAG | T | 9 | a0001c0001t0001g0123a0001c0001t0001g0126a0001c0001t0001g0138others(6): Show | 9 | HG00621.hp1 HG02559.hp2 NA18747.hp1 others(6): Show |
intron_variant | MODIFIER | c.114+45_114+48delGA others(2): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr3 | 149846181 | |||||
| chr3:149846288 | A | G | 237 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0022others(234): Show | 237 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.114+148A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 2/9 | chr3 | 149846288 | ||||||
| chr3:149846621 | A | T | 2 | a0001c0002t0006g0008a0001c0002t0006g0009 | 2 | HG02630.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.114+481A>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 2/9 | chr3 | 149846621 | ||||||
| chr3:149846628 | C | T | 1 | a0001c0001t0001g0069 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.114+488C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 2/9 | chr3 | 149846628 | ||||||
| chr3:149847060 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.114+920G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 2/9 | chr3 | 149847060 | ||||||
| chr3:149847170 | A | G | 1 | a0001c0002t0007g0250 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.114+1030A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 2/9 | chr3 | 149847170 | ||||||
| chr3:149847706 | C | A | 9 | a0001c0001t0001g0245a0001c0002t0002g0240a0001c0002t0002g0241others(6): Show | 9 | HG01496.hp1 HG02109.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.114+1566C>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 2/9 | chr3 | 149847706 | ||||||
| chr3:149847784 | C | T | 8 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(5): Show | 8 | HG00099.hp1 HG01346.hp2 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.114+1644C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 2/9 | chr3 | 149847784 | ||||||
| chr3:149848018 | C | T | 11 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0002t0002g0020others(8): Show | 11 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.114+1878C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 2/9 | chr3 | 149848018 | ||||||
| chr3:149848195 | A | G | 182 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0054others(179): Show | 182 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.114+2055A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 2/9 | chr3 | 149848195 | ||||||
| chr3:149848200 | C | CA | 6 | a0001c0002t0006g0005a0001c0002t0006g0006a0001c0002t0006g0007others(3): Show | 6 | HG02109.hp1 HG02258.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.114+2070dupA | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr3 | 149848200 | |||||
| chr3:149848333 | A | C | 1 | a0001c0002t0003g0124 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.114+2193A>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 2/9 | chr3 | 149848333 | ||||||
| chr3:149848359 | G | T | 1 | a0001c0001t0001g0228 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.114+2219G>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 2/9 | chr3 | 149848359 | ||||||
| chr3:149848374 | C | T | 1 | a0001c0001t0014g0133 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.114+2234C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 2/9 | chr3 | 149848374 | ||||||
| chr3:149848683 | C | G | 1 | a0001c0001t0001g0054 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.114+2543C>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 2/9 | chr3 | 149848683 | ||||||
| chr3:149848730 | GT | G | 11 | a0001c0001t0012g0206a0001c0002t0005g0202a0001c0002t0005g0203others(8): Show | 11 | HG00639.hp1 HG00642.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.114+2598delT | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr3 | 149848730 | |||||
| chr3:149848799 | G | A | 2 | a0001c0002t0006g0236a0001c0002t0006g0237 | 2 | HG02896.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.114+2659G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 2/9 | chr3 | 149848799 | ||||||
| chr3:149849160 | G | A | 13 | a0001c0001t0001g0239a0001c0002t0003g0238a0001c0002t0003g0254others(10): Show | 13 | HG00280.hp2 HG01106.hp1 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.114+3020G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 2/9 | chr3 | 149849160 | ||||||
| chr3:149849370 | AT | A | 13 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0002t0002g0020others(10): Show | 13 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.115-3144delT | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr3 | 149849370 | |||||
| chr3:149849424 | A | G | 1 | a0001c0001t0001g0197 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.115-3092A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 2/9 | chr3 | 149849424 | ||||||
| chr3:149849612 | A | G | 238 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0022others(235): Show | 238 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.115-2904A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 2/9 | chr3 | 149849612 | ||||||
| chr3:149849630 | C | T | 2 | a0001c0002t0002g0265a0001c0002t0002g0266 | 2 | HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.115-2886C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 2/9 | chr3 | 149849630 | ||||||
| chr3:149849713 | T | C | 11 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0002t0002g0020others(8): Show | 11 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.115-2803T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 2/9 | chr3 | 149849713 | ||||||
| chr3:149849844 | A | G | 1 | a0001c0001t0001g0173 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.115-2672A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 2/9 | chr3 | 149849844 | ||||||
| chr3:149849982 | A | AT | 5 | a0001c0002t0006g0236a0001c0002t0006g0237a0002c0003t0001g0002others(2): Show | 5 | HG02896.hp1 HG03041.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.115-2519dupT | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr3 | 149849982 | |||||
| chr3:149850695 | G | C | 13 | a0001c0001t0001g0239a0001c0002t0003g0238a0001c0002t0003g0254others(10): Show | 13 | HG00280.hp2 HG01106.hp1 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.115-1821G>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 2/9 | chr3 | 149850695 | ||||||
| chr3:149850847 | C | T | 2 | a0003c0004t0008g0199a0003c0004t0008g0200 | 2 | HG03098.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.115-1669C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 2/9 | chr3 | 149850847 | ||||||
| chr3:149851020 | A | G | 2 | a0001c0002t0002g0265a0001c0002t0002g0266 | 2 | HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.115-1496A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 2/9 | chr3 | 149851020 | ||||||
| chr3:149851066 | C | T | 6 | a0001c0001t0001g0150a0001c0001t0001g0169a0001c0001t0001g0170others(3): Show | 6 | HG02523.hp1 NA18950.hp1 NA18998.hp1 others(3): Show |
intron_variant | MODIFIER | c.115-1450C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 2/9 | chr3 | 149851066 | ||||||
| chr3:149851080 | A | G | 2 | a0001c0002t0006g0236a0001c0002t0006g0237 | 2 | HG02896.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.115-1436A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 2/9 | chr3 | 149851080 | ||||||
| chr3:149851098 | A | G | 13 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0002t0002g0020others(10): Show | 13 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.115-1418A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 2/9 | chr3 | 149851098 | ||||||
| chr3:149851129 | A | G | 2 | a0003c0004t0008g0199a0003c0004t0008g0200 | 2 | HG03098.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.115-1387A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 2/9 | chr3 | 149851129 | ||||||
| chr3:149851329 | G | C | 15 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0002t0002g0020others(12): Show | 15 | HG00735.hp1 HG01243.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.115-1187G>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 2/9 | chr3 | 149851329 | ||||||
| chr3:149851434 | C | T | 27 | a0001c0001t0001g0024a0001c0001t0001g0084a0001c0001t0001g0118others(24): Show | 27 | HG00609.hp1 HG00621.hp1 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.115-1082C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 2/9 | chr3 | 149851434 | ||||||
| chr3:149851584 | A | G | 1 | a0001c0001t0001g0072 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.115-932A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 2/9 | chr3 | 149851584 | ||||||
| chr3:149851841 | T | C | 1 | a0001c0001t0001g0214 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.115-675T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 2/9 | chr3 | 149851841 | ||||||
| chr3:149851998 | T | C | 11 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0002t0002g0020others(8): Show | 11 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.115-518T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 2/9 | chr3 | 149851998 | ||||||
| chr3:149852265 | T | C | 2 | a0003c0004t0008g0199a0003c0004t0008g0200 | 2 | HG03098.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.115-251T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 2/9 | chr3 | 149852265 | ||||||
| chr3:149852342 | T | C | 2 | a0001c0002t0004g0013a0001c0002t0004g0014 | 2 | HG02630.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.115-174T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 2/9 | chr3 | 149852342 | ||||||
| chr3:149852413 | T | A | 2 | a0001c0001t0001g0153a0005c0006t0001g0178 | 2 | HG02056.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.115-103T>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 2/9 | chr3 | 149852413 | ||||||
| chr3:149852934 | T | C | 1 | a0001c0001t0001g0212 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.195+338T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149852934 | ||||||
| chr3:149853159 | A | G | 11 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0002t0002g0020others(8): Show | 11 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.195+563A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149853159 | ||||||
| chr3:149853453 | AG | A | 4 | a0001c0001t0001g0056a0001c0001t0001g0102a0001c0001t0001g0180others(1): Show | 4 | HG01070.hp2 HG01891.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.195+860delG | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr3 | 149853453 | |||||
| chr3:149853454 | GGGA | G | 8 | a0001c0001t0001g0110a0001c0001t0001g0116a0001c0001t0001g0125others(5): Show | 8 | HG01192.hp2 HG01515.hp2 HG02056.hp1 others(5): Show |
intron_variant | MODIFIER | c.195+860_195+862del others(3): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr3 | 149853454 | |||||
| chr3:149853455 | G | GAGA | 8 | a0001c0001t0001g0042a0001c0001t0001g0189a0001c0002t0001g0029others(5): Show | 8 | HG00609.hp2 HG02080.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.195+859_195+860ins others(3): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149853455 | ||||||
| chr3:149853455 | G | GGA | 27 | a0001c0001t0001g0027a0001c0001t0001g0068a0001c0001t0001g0099others(24): Show | 28 | HG00099.hp2 HG00733.hp1 HG01175.hp1 others(25): Show |
intron_variant | MODIFIER | c.195+904_195+905dup others(2): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr3 | 149853455 | |||||
| chr3:149853455 | G | GGAGA | 15 | a0001c0001t0001g0028a0001c0001t0001g0075a0001c0001t0001g0090others(12): Show | 15 | HG01106.hp1 HG02027.hp1 HG02080.hp2 others(12): Show |
intron_variant | MODIFIER | c.195+902_195+905dup others(4): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr3 | 149853455 | |||||
| chr3:149853455 | G | GGAGAGA | 4 | a0001c0001t0001g0120a0001c0002t0002g0031a0001c0002t0002g0039others(1): Show | 4 | HG03927.hp1 NA18998.hp2 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.195+900_195+905dup others(6): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr3 | 149853455 | |||||
| chr3:149853455 | G | GGAGAGAG others(3): Show |
1 | a0001c0002t0001g0251 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.195+896_195+905dup others(10): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr3 | 149853455 | |||||
| chr3:149853455 | G | GGAGAGAG others(9): Show |
1 | a0001c0002t0003g0255 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.195+890_195+905dup others(16): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr3 | 149853455 | |||||
| chr3:149853455 | G | GGAGAGAG others(15): Show |
1 | a0001c0002t0003g0264 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.195+884_195+905dup others(22): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr3 | 149853455 | |||||
| chr3:149853455 | GGA | G | 44 | a0001c0001t0001g0010a0001c0001t0001g0066a0001c0001t0001g0070others(41): Show | 44 | HG00280.hp2 HG00621.hp2 HG01071.hp1 others(41): Show |
intron_variant | MODIFIER | c.195+904_195+905del others(2): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr3 | 149853455 | |||||
| chr3:149853455 | GGAGA | G | 73 | a0001c0001t0001g0055a0001c0001t0001g0065a0001c0001t0001g0072others(70): Show | 73 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.195+902_195+905del others(4): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr3 | 149853455 | |||||
| chr3:149853455 | GGAGAGA | G | 7 | a0001c0001t0001g0024a0001c0001t0001g0138a0001c0001t0001g0156others(4): Show | 7 | HG00733.hp2 HG02698.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.195+900_195+905del others(6): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr3 | 149853455 | |||||
| chr3:149853455 | GGAGAGAG others(1): Show |
G | 9 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0126others(6): Show | 9 | HG01169.hp2 HG01256.hp1 HG01516.hp1 others(6): Show |
intron_variant | MODIFIER | c.195+898_195+905del others(8): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr3 | 149853455 | |||||
| chr3:149853455 | GGAGAGAG others(3): Show |
G | 13 | a0001c0001t0001g0057a0001c0001t0001g0059a0001c0001t0001g0060others(10): Show | 13 | HG00323.hp1 HG00741.hp2 HG01123.hp2 others(10): Show |
intron_variant | MODIFIER | c.195+896_195+905del others(10): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr3 | 149853455 | |||||
| chr3:149853455 | GGAGAGAG others(5): Show |
G | 11 | a0001c0001t0001g0082a0001c0001t0001g0245a0001c0002t0002g0240others(8): Show | 11 | HG02109.hp2 HG02572.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.195+894_195+905del others(12): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr3 | 149853455 | |||||
| chr3:149853455 | GGAGAGAG others(7): Show |
G | 3 | a0001c0001t0001g0058a0001c0002t0002g0265a0001c0002t0002g0266 | 3 | HG01070.hp1 HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.195+892_195+905del others(14): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr3 | 149853455 | |||||
| chr3:149853463 | A | AGG | 11 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0002t0002g0020others(8): Show | 11 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.195+868_195+869ins others(2): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr3 | 149853463 | |||||
| chr3:149853473 | A | G | 2 | a0001c0002t0002g0265a0001c0002t0002g0266 | 2 | HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.195+877A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149853473 | ||||||
| chr3:149853474 | G | C | 11 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0002t0002g0020others(8): Show | 11 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.195+878G>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149853474 | ||||||
| chr3:149853510 | T | A | 1 | a0001c0001t0001g0099 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.195+914T>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149853510 | ||||||
| chr3:149853552 | T | A | 9 | a0001c0001t0001g0245a0001c0002t0002g0240a0001c0002t0002g0241others(6): Show | 9 | HG01496.hp1 HG02109.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.195+956T>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149853552 | ||||||
| chr3:149853688 | ATTC | A | 177 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0054others(174): Show | 177 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.195+1098_195+1100d others(5): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr3 | 149853688 | |||||
| chr3:149853705 | A | G | 13 | a0001c0001t0001g0055a0001c0001t0001g0094a0001c0001t0001g0099others(10): Show | 13 | HG01167.hp2 HG01169.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.195+1109A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149853705 | ||||||
| chr3:149853834 | C | CT | 13 | a0001c0001t0001g0176a0001c0001t0001g0245a0001c0002t0001g0032others(10): Show | 13 | HG01496.hp1 HG02109.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.195+1258dupT | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr3 | 149853834 | |||||
| chr3:149853834 | C | CTTT | 11 | a0001c0001t0001g0239a0001c0002t0003g0238a0001c0002t0003g0254others(8): Show | 11 | HG00280.hp2 HG01106.hp1 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.195+1256_195+1258d others(5): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr3 | 149853834 | |||||
| chr3:149853834 | CT | C | 7 | a0001c0001t0001g0055a0001c0001t0001g0067a0001c0001t0001g0154others(4): Show | 7 | HG01167.hp2 HG01169.hp2 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.195+1258delT | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr3 | 149853834 | |||||
| chr3:149853923 | G | A | 3 | a0001c0001t0001g0082a0004c0005t0001g0080a0004c0005t0001g0081 | 3 | HG02922.hp2 HG03139.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.195+1327G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149853923 | ||||||
| chr3:149853962 | G | A | 1 | a0001c0001t0001g0070 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.195+1366G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149853962 | ||||||
| chr3:149854222 | T | TA | 7 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0112others(4): Show | 7 | HG02896.hp2 HG02922.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.195+1635dupA | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr3 | 149854222 | |||||
| chr3:149854566 | T | C | 2 | a0001c0002t0002g0268a0001c0002t0002g0269 | 2 | HG02145.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.195+1970T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149854566 | ||||||
| chr3:149854606 | T | C | 3 | a0001c0002t0002g0031a0001c0002t0002g0052a0001c0002t0002g0053 | 3 | HG03491.hp1 HG03492.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.195+2010T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149854606 | ||||||
| chr3:149854731 | A | G | 11 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0002t0002g0020others(8): Show | 11 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.195+2135A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149854731 | ||||||
| chr3:149855090 | A | G | 2 | a0001c0001t0001g0136a0001c0001t0001g0137 | 2 | NA18965.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.195+2494A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149855090 | ||||||
| chr3:149855524 | AAT | A | 9 | a0001c0001t0012g0206a0001c0002t0005g0202a0001c0002t0005g0203others(6): Show | 9 | HG00639.hp1 HG00642.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.195+2935_195+2936d others(4): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr3 | 149855524 | |||||
| chr3:149855592 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.195+2996G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149855592 | ||||||
| chr3:149855679 | T | A | 1 | a0001c0001t0001g0154 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.195+3083T>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149855679 | ||||||
| chr3:149855833 | G | A | 275 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0022others(272): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.195+3237G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149855833 | ||||||
| chr3:149856034 | T | C | 1 | a0001c0001t0001g0072 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.195+3438T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149856034 | ||||||
| chr3:149856119 | C | CA | 7 | a0001c0001t0001g0056a0001c0001t0001g0162a0001c0001t0001g0168others(4): Show | 7 | HG01070.hp2 HG01071.hp2 HG01358.hp2 others(4): Show |
intron_variant | MODIFIER | c.195+3536dupA | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr3 | 149856119 | |||||
| chr3:149856133 | C | T | 13 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0002t0002g0020others(10): Show | 13 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.195+3537C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149856133 | ||||||
| chr3:149856145 | T | G | 3 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0075 | 3 | HG01175.hp1 HG01975.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.195+3549T>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149856145 | ||||||
| chr3:149856234 | T | C | 1 | a0001c0002t0002g0011 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.195+3638T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149856234 | ||||||
| chr3:149856339 | A | G | 11 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0002t0002g0020others(8): Show | 11 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.195+3743A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149856339 | ||||||
| chr3:149856444 | C | CT | 12 | a0001c0001t0001g0015a0001c0001t0001g0239a0001c0002t0003g0238others(9): Show | 12 | HG01243.hp1 HG02145.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.195+3865dupT | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr3 | 149856444 | |||||
| chr3:149856444 | CT | C | 97 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0054others(94): Show | 97 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.195+3865delT | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr3 | 149856444 | |||||
| chr3:149856643 | A | G | 9 | a0001c0001t0001g0245a0001c0002t0002g0240a0001c0002t0002g0241others(6): Show | 9 | HG01496.hp1 HG02109.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.195+4047A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149856643 | ||||||
| chr3:149856694 | C | T | 1 | a0001c0002t0003g0087 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.195+4098C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149856694 | ||||||
| chr3:149856809 | T | C | 239 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0022others(236): Show | 239 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.195+4213T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149856809 | ||||||
| chr3:149856820 | C | T | 1 | a0001c0001t0001g0123 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.195+4224C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149856820 | ||||||
| chr3:149856973 | C | G | 1 | a0001c0001t0001g0151 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.195+4377C>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149856973 | ||||||
| chr3:149857264 | C | T | 1 | a0001c0001t0001g0229 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.195+4668C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149857264 | ||||||
| chr3:149857558 | G | C | 28 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(25): Show | 28 | HG00323.hp1 HG00741.hp2 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.195+4962G>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149857558 | ||||||
| chr3:149857739 | A | G | 1 | a0001c0001t0001g0125 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.195+5143A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149857739 | ||||||
| chr3:149857778 | G | A | 14 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0002t0002g0020others(11): Show | 14 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.195+5182G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149857778 | ||||||
| chr3:149857824 | A | G | 13 | a0001c0001t0001g0239a0001c0002t0003g0238a0001c0002t0003g0254others(10): Show | 13 | HG00280.hp2 HG01106.hp1 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.195+5228A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149857824 | ||||||
| chr3:149858019 | G | A | 1 | a0001c0001t0001g0104 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.195+5423G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149858019 | ||||||
| chr3:149858162 | C | G | 1 | a0001c0001t0001g0125 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.195+5566C>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149858162 | ||||||
| chr3:149858673 | G | A | 19 | a0001c0001t0001g0239a0001c0002t0003g0238a0001c0002t0003g0254others(16): Show | 19 | HG00280.hp2 HG01106.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.195+6077G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149858673 | ||||||
| chr3:149858958 | A | T | 1 | a0001c0002t0002g0276 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.195+6362A>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149858958 | ||||||
| chr3:149859094 | T | C | 6 | a0001c0002t0002g0020a0001c0002t0004g0013a0001c0002t0004g0014others(3): Show | 6 | HG01243.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.195+6498T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149859094 | ||||||
| chr3:149859174 | G | T | 237 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0022others(234): Show | 237 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.195+6578G>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149859174 | ||||||
| chr3:149859362 | C | T | 177 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0054others(174): Show | 177 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.195+6766C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149859362 | ||||||
| chr3:149859496 | GACAC | G | 13 | a0001c0001t0001g0055a0001c0001t0001g0094a0001c0001t0001g0099others(10): Show | 13 | HG01167.hp2 HG01169.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.195+6910_195+6913d others(6): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr3 | 149859496 | |||||
| chr3:149859499 | A | G | 2 | a0001c0001t0001g0136a0001c0001t0001g0137 | 2 | NA18965.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.195+6903A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149859499 | ||||||
| chr3:149859500 | C | T | 5 | a0001c0002t0005g0202a0001c0002t0005g0203a0001c0002t0005g0204others(2): Show | 5 | HG00639.hp1 HG00642.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.195+6904C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149859500 | ||||||
| chr3:149859621 | T | A | 1 | a0001c0001t0001g0115 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.195+7025T>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149859621 | ||||||
| chr3:149859861 | T | TA | 11 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0002t0002g0020others(8): Show | 11 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.195+7266dupA | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr3 | 149859861 | |||||
| chr3:149860033 | G | A | 1 | a0001c0001t0001g0072 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.195+7437G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149860033 | ||||||
| chr3:149860256 | T | TA | 15 | a0001c0001t0001g0057a0001c0001t0001g0082a0001c0001t0001g0099others(12): Show | 15 | HG01074.hp2 HG01515.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.195+7675dupA | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr3 | 149860256 | |||||
| chr3:149860256 | T | TAA | 7 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0186others(4): Show | 7 | HG00639.hp2 HG02818.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.195+7674_195+7675d others(4): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr3 | 149860256 | |||||
| chr3:149860269 | AAATAT | A | 10 | a0001c0001t0001g0239a0001c0002t0003g0254a0001c0002t0003g0255others(7): Show | 10 | HG00280.hp2 HG01106.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.195+7675_195+7679d others(7): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr3 | 149860269 | |||||
| chr3:149860269 | AAATATAT | A | 7 | a0001c0001t0001g0245a0001c0002t0002g0240a0001c0002t0002g0242others(4): Show | 7 | HG01496.hp1 HG02572.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.195+7675_195+7681d others(9): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr3 | 149860269 | |||||
| chr3:149860270 | A | AAAAAAAA others(22): Show |
4 | a0001c0002t0002g0020a0001c0002t0004g0013a0001c0002t0004g0019others(1): Show | 4 | HG01243.hp2 HG02630.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.195+7675_195+7676i others(31): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr3 | 149860270 | |||||
| chr3:149860270 | A | AAAAAAAA others(24): Show |
1 | a0001c0002t0004g0021 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.195+7675_195+7676i others(33): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr3 | 149860270 | |||||
| chr3:149860270 | A | AAAAAAAA others(22): Show |
2 | a0001c0002t0004g0014a0001c0002t0004g0018 | 2 | HG00735.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.195+7675_195+7676i others(31): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr3 | 149860270 | |||||
| chr3:149860270 | A | AAAAAAAA others(26): Show |
1 | a0001c0002t0004g0017 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.195+7675_195+7676i others(35): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr3 | 149860270 | |||||
| chr3:149860270 | A | AAAAAAAA others(18): Show |
2 | a0001c0001t0001g0015a0001c0001t0001g0022 | 2 | HG02738.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.195+7675_195+7676i others(27): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr3 | 149860270 | |||||
| chr3:149860270 | A | AAAAAAAA others(20): Show |
1 | a0001c0002t0004g0016 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.195+7675_195+7676i others(29): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr3 | 149860270 | |||||
| chr3:149860270 | A | AAAATATA others(5): Show |
1 | a0001c0001t0001g0090 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.195+7675_195+7676i others(14): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr3 | 149860270 | |||||
| chr3:149860270 | A | AAAATATA others(9): Show |
1 | a0001c0002t0002g0265 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.195+7675_195+7676i others(18): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr3 | 149860270 | |||||
| chr3:149860270 | A | AAATATAT others(8): Show |
1 | a0001c0002t0002g0266 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.195+7675_195+7676i others(17): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr3 | 149860270 | |||||
| chr3:149860270 | A | T | 2 | a0001c0002t0001g0001a0001c0002t0002g0012 | 3 | HG03139.hp1 NA19011.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.195+7674A>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149860270 | ||||||
| chr3:149860270 | AAT | A | 28 | a0001c0001t0001g0056a0001c0001t0001g0073a0001c0001t0001g0074others(25): Show | 28 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(25): Show |
intron_variant | MODIFIER | c.195+7704_195+7705d others(4): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr3 | 149860270 | |||||
| chr3:149860270 | AATATATA others(3): Show |
A | 1 | a0003c0004t0008g0200 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.195+7696_195+7705d others(12): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr3 | 149860270 | |||||
| chr3:149860271 | AT | A | 113 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0055others(110): Show | 113 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.195+7676delT | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149860271 | ||||||
| chr3:149860272 | T | A | 44 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0072others(41): Show | 44 | HG00099.hp1 HG00639.hp1 HG00642.hp2 others(41): Show |
intron_variant | MODIFIER | c.195+7676T>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149860272 | ||||||
| chr3:149860274 | T | A | 134 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0056others(131): Show | 134 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.195+7678T>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149860274 | ||||||
| chr3:149860276 | T | A | 91 | a0001c0001t0001g0024a0001c0001t0001g0056a0001c0001t0001g0073others(88): Show | 91 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.195+7680T>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149860276 | ||||||
| chr3:149860278 | T | A | 10 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0012g0206others(7): Show | 10 | HG00639.hp1 HG00642.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.195+7682T>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149860278 | ||||||
| chr3:149860300 | T | A | 14 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0002t0001g0037others(11): Show | 14 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.195+7704T>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149860300 | ||||||
| chr3:149860662 | T | C | 2 | a0001c0001t0001g0175a0001c0001t0001g0177 | 2 | HG01433.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.195+8066T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149860662 | ||||||
| chr3:149860697 | T | C | 2 | a0001c0001t0001g0094a0001c0001t0001g0115 | 2 | HG02280.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.195+8101T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149860697 | ||||||
| chr3:149861207 | A | T | 5 | a0001c0001t0001g0119a0001c0001t0001g0143a0001c0001t0001g0163others(2): Show | 5 | HG00323.hp2 HG01175.hp2 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.195+8611A>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149861207 | ||||||
| chr3:149861319 | T | C | 13 | a0001c0001t0001g0239a0001c0002t0003g0238a0001c0002t0003g0254others(10): Show | 13 | HG00280.hp2 HG01106.hp1 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.195+8723T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149861319 | ||||||
| chr3:149861325 | C | T | 2 | a0001c0001t0001g0058a0001c0001t0001g0063 | 2 | HG01070.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.195+8729C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149861325 | ||||||
| chr3:149861788 | G | A | 2 | a0001c0001t0001g0056a0001c0001t0001g0162 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.195+9192G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149861788 | ||||||
| chr3:149861968 | A | G | 3 | a0001c0002t0007g0249a0001c0002t0007g0250a0001c0002t0007g0252 | 3 | HG02717.hp2 HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.195+9372A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149861968 | ||||||
| chr3:149861989 | T | C | 56 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0001t0001g0239others(53): Show | 56 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.195+9393T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149861989 | ||||||
| chr3:149862217 | T | C | 3 | a0001c0002t0005g0205a0001c0002t0005g0207a0001c0002t0005g0208 | 3 | HG01891.hp2 HG02572.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.195+9621T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149862217 | ||||||
| chr3:149862426 | T | C | 9 | a0001c0001t0001g0245a0001c0002t0002g0240a0001c0002t0002g0241others(6): Show | 9 | HG01496.hp1 HG02109.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.196-9603T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149862426 | ||||||
| chr3:149862738 | G | A | 26 | a0001c0001t0001g0142a0001c0001t0001g0201a0001c0001t0001g0211others(23): Show | 26 | HG00544.hp2 HG00639.hp2 HG01978.hp1 others(23): Show |
intron_variant | MODIFIER | c.196-9291G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149862738 | ||||||
| chr3:149862928 | T | A | 1 | a0001c0001t0002g0174 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.196-9101T>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149862928 | ||||||
| chr3:149863411 | G | C | 11 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0002t0002g0020others(8): Show | 11 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.196-8618G>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149863411 | ||||||
| chr3:149863525 | G | A | 1 | a0001c0002t0001g0048 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.196-8504G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149863525 | ||||||
| chr3:149863538 | C | A | 3 | a0001c0001t0001g0131a0001c0001t0001g0184a0001c0001t0001g0185 | 3 | HG01952.hp1 HG01975.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.196-8491C>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149863538 | ||||||
| chr3:149863764 | T | C | 11 | a0001c0001t0012g0206a0001c0002t0005g0202a0001c0002t0005g0203others(8): Show | 11 | HG00639.hp1 HG00642.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.196-8265T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149863764 | ||||||
| chr3:149863864 | A | G | 11 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0002t0002g0020others(8): Show | 11 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.196-8165A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149863864 | ||||||
| chr3:149863882 | G | C | 1 | a0001c0002t0003g0101 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.196-8147G>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149863882 | ||||||
| chr3:149863967 | T | A | 2 | a0001c0001t0001g0224a0001c0001t0001g0228 | 2 | HG02273.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.196-8062T>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149863967 | ||||||
| chr3:149864008 | A | AT | 9 | a0001c0002t0002g0030a0001c0002t0002g0031a0001c0002t0002g0041others(6): Show | 9 | HG01123.hp1 HG01516.hp2 HG02027.hp1 others(6): Show |
intron_variant | MODIFIER | c.196-7989dupT | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr3 | 149864008 | |||||
| chr3:149864008 | AT | A | 20 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0001t0001g0197others(17): Show | 20 | HG00099.hp2 HG00735.hp1 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.196-7989delT | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr3 | 149864008 | |||||
| chr3:149864008 | ATT | A | 45 | a0001c0001t0001g0059a0001c0001t0001g0062a0001c0001t0001g0065others(42): Show | 45 | HG00140.hp1 HG00621.hp1 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.196-7990_196-7989d others(4): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr3 | 149864008 | |||||
| chr3:149864008 | ATTT | A | 145 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0054others(142): Show | 145 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.196-7991_196-7989d others(5): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr3 | 149864008 | |||||
| chr3:149864008 | ATTTT | A | 19 | a0001c0001t0001g0057a0001c0001t0001g0060a0001c0001t0001g0072others(16): Show | 19 | HG00280.hp2 HG00323.hp2 HG01106.hp1 others(16): Show |
intron_variant | MODIFIER | c.196-7992_196-7989d others(6): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr3 | 149864008 | |||||
| chr3:149864008 | ATTTTT | A | 9 | a0001c0001t0012g0206a0001c0002t0005g0202a0001c0002t0005g0203others(6): Show | 9 | HG00639.hp1 HG00642.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.196-7993_196-7989d others(7): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr3 | 149864008 | |||||
| chr3:149864056 | T | TTGTAGTA | 2 | a0001c0002t0006g0236a0001c0002t0006g0237 | 2 | HG02896.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.196-7971_196-7965d others(9): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr3 | 149864056 | |||||
| chr3:149864140 | G | A | 1 | a0001c0002t0003g0256 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.196-7889G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149864140 | ||||||
| chr3:149864173 | G | T | 9 | a0001c0001t0001g0245a0001c0002t0002g0240a0001c0002t0002g0241others(6): Show | 9 | HG01496.hp1 HG02109.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.196-7856G>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149864173 | ||||||
| chr3:149864279 | T | C | 13 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0002t0002g0020others(10): Show | 13 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.196-7750T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149864279 | ||||||
| chr3:149864525 | C | T | 1 | a0001c0001t0011g0226 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.196-7504C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149864525 | ||||||
| chr3:149864575 | T | C | 13 | a0001c0001t0001g0239a0001c0002t0003g0238a0001c0002t0003g0254others(10): Show | 13 | HG00280.hp2 HG01106.hp1 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.196-7454T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149864575 | ||||||
| chr3:149864705 | G | A | 11 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0002t0002g0020others(8): Show | 11 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.196-7324G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149864705 | ||||||
| chr3:149864716 | T | C | 9 | a0001c0001t0012g0206a0001c0002t0005g0202a0001c0002t0005g0203others(6): Show | 9 | HG00639.hp1 HG00642.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.196-7313T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149864716 | ||||||
| chr3:149864856 | C | G | 2 | a0001c0002t0002g0265a0001c0002t0002g0266 | 2 | HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.196-7173C>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149864856 | ||||||
| chr3:149864899 | C | T | 1 | a0001c0002t0002g0272 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.196-7130C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149864899 | ||||||
| chr3:149865149 | T | G | 2 | a0001c0001t0001g0155a0001c0001t0001g0159 | 2 | HG01099.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.196-6880T>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149865149 | ||||||
| chr3:149865215 | T | C | 1 | a0001c0001t0001g0225 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.196-6814T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149865215 | ||||||
| chr3:149865329 | G | GAT | 34 | a0001c0001t0001g0239a0001c0001t0012g0206a0001c0002t0002g0012others(31): Show | 34 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.196-6679_196-6678d others(4): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr3 | 149865329 | |||||
| chr3:149865329 | G | GATAT | 55 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0088others(52): Show | 55 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.196-6681_196-6678d others(6): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr3 | 149865329 | |||||
| chr3:149865329 | G | GATATAT | 85 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0056others(82): Show | 85 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.196-6683_196-6678d others(8): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr3 | 149865329 | |||||
| chr3:149865329 | G | GATATATA others(1): Show |
31 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0063others(28): Show | 31 | HG00280.hp1 HG00544.hp1 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.196-6685_196-6678d others(10): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr3 | 149865329 | |||||
| chr3:149865329 | G | GATATATA others(3): Show |
11 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0073others(8): Show | 11 | HG00323.hp2 HG01167.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.196-6687_196-6678d others(12): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr3 | 149865329 | |||||
| chr3:149865329 | G | GATATATA others(5): Show |
2 | a0001c0001t0001g0058a0001c0001t0001g0163 | 2 | HG01070.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.196-6689_196-6678d others(14): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr3 | 149865329 | |||||
| chr3:149865329 | G | GATATATA others(7): Show |
3 | a0001c0001t0001g0125a0001c0002t0002g0265a0001c0002t0002g0266 | 3 | HG02056.hp1 HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.196-6691_196-6678d others(16): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr3 | 149865329 | |||||
| chr3:149865335 | T | TATAC | 3 | a0001c0002t0003g0085a0001c0002t0003g0086a0001c0002t0003g0087 | 3 | HG01074.hp2 HG01433.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.196-6691_196-6690i others(6): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr3 | 149865335 | |||||
| chr3:149865343 | T | TATATATA others(20): Show |
3 | a0001c0001t0001g0015a0001c0002t0004g0017a0001c0002t0004g0018 | 3 | HG00735.hp1 HG02738.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.196-6678_196-6677i others(29): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr3 | 149865343 | |||||
| chr3:149865343 | T | TATATATA others(22): Show |
1 | a0001c0002t0004g0021 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.196-6678_196-6677i others(31): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr3 | 149865343 | |||||
| chr3:149865343 | T | TATATATA others(24): Show |
4 | a0001c0002t0002g0020a0001c0002t0004g0013a0001c0002t0004g0014others(1): Show | 4 | HG01243.hp2 HG02630.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.196-6678_196-6677i others(33): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr3 | 149865343 | |||||
| chr3:149865343 | T | TATATATA others(26): Show |
1 | a0001c0002t0004g0023 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.196-6678_196-6677i others(35): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr3 | 149865343 | |||||
| chr3:149865343 | T | TATATATA others(28): Show |
1 | a0001c0002t0004g0016 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.196-6678_196-6677i others(37): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr3 | 149865343 | |||||
| chr3:149865394 | T | C | 2 | a0001c0002t0002g0268a0001c0002t0002g0269 | 2 | HG02145.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.196-6635T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149865394 | ||||||
| chr3:149865436 | T | A | 6 | a0001c0002t0006g0005a0001c0002t0006g0006a0001c0002t0006g0007others(3): Show | 6 | HG02109.hp1 HG02258.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.196-6593T>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149865436 | ||||||
| chr3:149865489 | A | T | 2 | a0001c0001t0001g0186a0001c0001t0001g0213 | 2 | NA18747.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.196-6540A>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149865489 | ||||||
| chr3:149865490 | G | C | 2 | a0001c0001t0001g0186a0001c0001t0001g0213 | 2 | NA18747.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.196-6539G>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149865490 | ||||||
| chr3:149865491 | A | T | 2 | a0001c0001t0001g0186a0001c0001t0001g0213 | 2 | NA18747.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.196-6538A>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149865491 | ||||||
| chr3:149865650 | T | A | 3 | a0001c0002t0002g0272a0001c0002t0002g0273a0001c0002t0002g0274 | 3 | HG02818.hp1 HG03195.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.196-6379T>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149865650 | ||||||
| chr3:149865849 | G | A | 1 | a0001c0001t0001g0022 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.196-6180G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149865849 | ||||||
| chr3:149866014 | T | C | 1 | a0001c0002t0002g0227 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.196-6015T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149866014 | ||||||
| chr3:149866049 | T | G | 11 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0002t0002g0020others(8): Show | 11 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.196-5980T>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149866049 | ||||||
| chr3:149866383 | C | T | 9 | a0001c0002t0002g0240a0001c0002t0002g0241a0001c0002t0002g0246others(6): Show | 9 | HG01074.hp2 HG01433.hp1 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.196-5646C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149866383 | ||||||
| chr3:149866424 | C | A | 1 | a0001c0001t0001g0090 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.196-5605C>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149866424 | ||||||
| chr3:149866428 | G | T | 8 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(5): Show | 8 | HG00099.hp1 HG01346.hp2 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.196-5601G>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149866428 | ||||||
| chr3:149866457 | A | G | 32 | a0001c0001t0001g0239a0001c0001t0012g0206a0001c0002t0003g0238others(29): Show | 32 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(29): Show |
intron_variant | MODIFIER | c.196-5572A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149866457 | ||||||
| chr3:149866687 | C | T | 11 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0002t0002g0020others(8): Show | 11 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.196-5342C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149866687 | ||||||
| chr3:149866799 | G | A | 2 | a0001c0002t0003g0258a0001c0002t0003g0259 | 2 | HG00280.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.196-5230G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149866799 | ||||||
| chr3:149866875 | T | C | 13 | a0001c0001t0001g0239a0001c0002t0003g0238a0001c0002t0003g0254others(10): Show | 13 | HG00280.hp2 HG01106.hp1 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.196-5154T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149866875 | ||||||
| chr3:149866923 | G | C | 87 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0056others(84): Show | 87 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.196-5106G>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149866923 | ||||||
| chr3:149866970 | G | A | 1 | a0005c0006t0001g0178 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.196-5059G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149866970 | ||||||
| chr3:149867235 | C | T | 1 | a0001c0002t0002g0276 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.196-4794C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149867235 | ||||||
| chr3:149867404 | T | C | 3 | a0001c0001t0001g0156a0001c0001t0001g0160a0001c0001t0001g0173 | 3 | HG00733.hp2 HG00735.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.196-4625T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149867404 | ||||||
| chr3:149867524 | C | T | 1 | a0001c0001t0001g0267 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.196-4505C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149867524 | ||||||
| chr3:149867888 | C | T | 174 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0054others(171): Show | 174 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.196-4141C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149867888 | ||||||
| chr3:149867907 | C | T | 11 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0002t0002g0020others(8): Show | 11 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.196-4122C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149867907 | ||||||
| chr3:149867965 | G | T | 7 | a0001c0001t0001g0054a0001c0001t0001g0089a0001c0001t0001g0090others(4): Show | 7 | HG02622.hp2 HG02647.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.196-4064G>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149867965 | ||||||
| chr3:149867974 | G | A | 1 | a0001c0001t0001g0123 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.196-4055G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149867974 | ||||||
| chr3:149867983 | T | C | 2 | a0001c0002t0006g0236a0001c0002t0006g0237 | 2 | HG02896.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.196-4046T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149867983 | ||||||
| chr3:149868245 | A | G | 1 | a0001c0002t0002g0030 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.196-3784A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149868245 | ||||||
| chr3:149868313 | A | AT | 6 | a0001c0002t0006g0005a0001c0002t0006g0006a0001c0002t0006g0007others(3): Show | 6 | HG02109.hp1 HG02258.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.196-3707dupT | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr3 | 149868313 | |||||
| chr3:149868555 | C | T | 2 | a0001c0001t0001g0146a0001c0001t0001g0166 | 2 | HG01978.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.196-3474C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149868555 | ||||||
| chr3:149868589 | C | A | 1 | a0001c0002t0002g0030 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.196-3440C>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149868589 | ||||||
| chr3:149868775 | C | A | 1 | a0001c0001t0001g0193 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.196-3254C>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149868775 | ||||||
| chr3:149868928 | C | T | 2 | a0001c0001t0001g0126a0001c0001t0001g0176 | 2 | NA18747.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.196-3101C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149868928 | ||||||
| chr3:149869014 | A | G | 1 | a0001c0001t0001g0175 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.196-3015A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149869014 | ||||||
| chr3:149869325 | G | A | 11 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0002t0002g0020others(8): Show | 11 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.196-2704G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149869325 | ||||||
| chr3:149869328 | G | A | 1 | a0001c0002t0004g0014 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.196-2701G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149869328 | ||||||
| chr3:149869333 | C | T | 87 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0056others(84): Show | 87 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.196-2696C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149869333 | ||||||
| chr3:149869371 | T | C | 2 | a0001c0002t0002g0265a0001c0002t0002g0266 | 2 | HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.196-2658T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149869371 | ||||||
| chr3:149869462 | C | T | 2 | a0001c0002t0002g0268a0001c0002t0002g0269 | 2 | HG02145.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.196-2567C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149869462 | ||||||
| chr3:149869756 | C | G | 2 | a0001c0001t0001g0132a0001c0001t0014g0133 | 2 | HG01106.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.196-2273C>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149869756 | ||||||
| chr3:149870182 | A | C | 1 | a0001c0002t0001g0033 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.196-1847A>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149870182 | ||||||
| chr3:149870182 | A | G | 1 | a0001c0001t0001g0102 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.196-1847A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149870182 | ||||||
| chr3:149870292 | C | T | 2 | a0001c0002t0002g0265a0001c0002t0002g0266 | 2 | HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.196-1737C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149870292 | ||||||
| chr3:149870302 | G | C | 3 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0190 | 3 | HG00544.hp1 NA18975.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.196-1727G>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149870302 | ||||||
| chr3:149870421 | G | A | 13 | a0001c0001t0001g0239a0001c0002t0003g0238a0001c0002t0003g0254others(10): Show | 13 | HG00280.hp2 HG01106.hp1 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.196-1608G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149870421 | ||||||
| chr3:149870449 | C | T | 9 | a0001c0001t0001g0245a0001c0002t0002g0240a0001c0002t0002g0241others(6): Show | 9 | HG01496.hp1 HG02109.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.196-1580C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149870449 | ||||||
| chr3:149870600 | G | A | 2 | a0001c0001t0001g0217a0001c0001t0001g0231 | 2 | HG01978.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.196-1429G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149870600 | ||||||
| chr3:149870628 | A | T | 2 | a0001c0002t0006g0236a0001c0002t0006g0237 | 2 | HG02896.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.196-1401A>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149870628 | ||||||
| chr3:149870690 | C | T | 15 | a0001c0001t0001g0055a0001c0001t0001g0094a0001c0001t0001g0099others(12): Show | 15 | HG00609.hp1 HG01167.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.196-1339C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149870690 | ||||||
| chr3:149870885 | A | C | 2 | a0001c0002t0002g0265a0001c0002t0002g0266 | 2 | HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.196-1144A>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149870885 | ||||||
| chr3:149870885 | A | G | 1 | a0001c0001t0001g0181 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.196-1144A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149870885 | ||||||
| chr3:149871035 | A | AT | 35 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0001t0001g0115others(32): Show | 35 | HG00735.hp1 HG01243.hp1 HG01361.hp1 others(32): Show |
intron_variant | MODIFIER | c.196-972dupT | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr3 | 149871035 | |||||
| chr3:149871042 | T | C | 2 | a0003c0004t0008g0199a0003c0004t0008g0200 | 2 | HG03098.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.196-987T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149871042 | ||||||
| chr3:149871064 | C | T | 11 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0002t0002g0020others(8): Show | 11 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.196-965C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149871064 | ||||||
| chr3:149871080 | C | T | 2 | a0001c0002t0002g0265a0001c0002t0002g0266 | 2 | HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.196-949C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149871080 | ||||||
| chr3:149871124 | T | C | 2 | a0001c0002t0002g0265a0001c0002t0002g0266 | 2 | HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.196-905T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149871124 | ||||||
| chr3:149871425 | C | T | 1 | a0001c0001t0001g0072 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.196-604C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149871425 | ||||||
| chr3:149871450 | A | G | 56 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0001t0001g0239others(53): Show | 56 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.196-579A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149871450 | ||||||
| chr3:149871731 | A | T | 3 | a0001c0002t0003g0091a0001c0002t0003g0092a0001c0002t0003g0093 | 3 | HG02717.hp1 HG02886.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.196-298A>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149871731 | ||||||
| chr3:149871740 | C | A | 13 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0002t0002g0020others(10): Show | 13 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.196-289C>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149871740 | ||||||
| chr3:149871807 | T | C | 2 | a0001c0002t0002g0265a0001c0002t0002g0266 | 2 | HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.196-222T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149871807 | ||||||
| chr3:149871891 | T | C | 2 | a0001c0001t0001g0194a0001c0001t0001g0195 | 2 | HG01192.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.196-138T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149871891 | ||||||
| chr3:149871918 | T | C | 1 | a0001c0001t0001g0267 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.196-111T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 3/9 | chr3 | 149871918 | ||||||
| chr3:149872187 | A | G | 1 | a0001c0001t0001g0072 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.321+33A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149872187 | ||||||
| chr3:149872426 | C | A | 11 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0002t0002g0020others(8): Show | 11 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.321+272C>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149872426 | ||||||
| chr3:149872561 | A | G | 3 | a0001c0002t0007g0249a0001c0002t0007g0250a0001c0002t0007g0252 | 3 | HG02717.hp2 HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.321+407A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149872561 | ||||||
| chr3:149872570 | C | T | 2 | a0001c0002t0002g0265a0001c0002t0002g0266 | 2 | HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.321+416C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149872570 | ||||||
| chr3:149872810 | C | G | 7 | a0001c0001t0001g0054a0001c0001t0001g0089a0001c0001t0001g0090others(4): Show | 7 | HG02622.hp2 HG02647.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.321+656C>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149872810 | ||||||
| chr3:149872810 | C | T | 25 | a0001c0001t0001g0024a0001c0001t0001g0084a0001c0001t0001g0118others(22): Show | 25 | HG00609.hp1 HG00621.hp1 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.321+656C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149872810 | ||||||
| chr3:149873258 | G | A | 2 | a0003c0004t0008g0199a0003c0004t0008g0200 | 2 | HG03098.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.321+1104G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149873258 | ||||||
| chr3:149873341 | A | G | 1 | a0001c0002t0002g0227 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.321+1187A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149873341 | ||||||
| chr3:149873557 | C | A | 2 | a0001c0002t0003g0255a0001c0002t0003g0264 | 2 | HG02698.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.321+1403C>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149873557 | ||||||
| chr3:149873884 | T | A | 9 | a0001c0001t0001g0245a0001c0002t0002g0240a0001c0002t0002g0241others(6): Show | 9 | HG01496.hp1 HG02109.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.321+1730T>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149873884 | ||||||
| chr3:149874066 | G | A | 1 | a0001c0002t0003g0254 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.321+1912G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149874066 | ||||||
| chr3:149874173 | T | C | 2 | a0001c0002t0002g0265a0001c0002t0002g0266 | 2 | HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.321+2019T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149874173 | ||||||
| chr3:149874190 | G | A | 237 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0022others(234): Show | 237 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.321+2036G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149874190 | ||||||
| chr3:149874620 | A | T | 3 | a0001c0001t0001g0082a0004c0005t0001g0080a0004c0005t0001g0081 | 3 | HG02922.hp2 HG03139.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.321+2466A>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149874620 | ||||||
| chr3:149874666 | C | T | 1 | a0001c0001t0001g0196 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.321+2512C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149874666 | ||||||
| chr3:149874837 | C | T | 2 | a0001c0002t0002g0265a0001c0002t0002g0266 | 2 | HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.321+2683C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149874837 | ||||||
| chr3:149874933 | A | G | 1 | a0001c0001t0001g0120 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.321+2779A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149874933 | ||||||
| chr3:149875124 | G | A | 13 | a0001c0001t0001g0239a0001c0002t0003g0238a0001c0002t0003g0254others(10): Show | 13 | HG00280.hp2 HG01106.hp1 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.321+2970G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149875124 | ||||||
| chr3:149875402 | G | A | 2 | a0001c0002t0002g0268a0001c0002t0002g0269 | 2 | HG02145.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.321+3248G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149875402 | ||||||
| chr3:149875424 | C | A | 4 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106others(1): Show | 4 | HG02965.hp2 HG03516.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.321+3270C>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149875424 | ||||||
| chr3:149875492 | A | G | 2 | a0001c0002t0002g0265a0001c0002t0002g0266 | 2 | HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.321+3338A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149875492 | ||||||
| chr3:149875695 | C | T | 2 | a0001c0001t0001g0134a0001c0001t0001g0198 | 2 | NA19004.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.321+3541C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149875695 | ||||||
| chr3:149875849 | C | T | 2 | a0001c0002t0006g0236a0001c0002t0006g0237 | 2 | HG02896.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.321+3695C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149875849 | ||||||
| chr3:149875897 | A | AAAATATA others(98): Show |
76 | a0001c0001t0001g0055a0001c0001t0001g0057a0001c0001t0001g0058others(73): Show | 76 | HG00323.hp1 HG00544.hp2 HG00621.hp2 others(73): Show |
intron_variant | MODIFIER | c.321+3746_321+3747i others(107): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr3 | 149875897 | |||||
| chr3:149875897 | A | AAAATATA others(99): Show |
160 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0022others(157): Show | 160 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.321+3746_321+3747i others(108): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr3 | 149875897 | |||||
| chr3:149875897 | A | AAAATATA others(99): Show |
3 | a0002c0003t0001g0002a0002c0003t0001g0003a0002c0003t0001g0004 | 3 | HG02976.hp2 HG03041.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.321+3746_321+3747i others(108): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr3 | 149875897 | |||||
| chr3:149875913 | G | A | 2 | a0001c0002t0002g0265a0001c0002t0002g0266 | 2 | HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.321+3759G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149875913 | ||||||
| chr3:149876303 | A | G | 1 | a0001c0001t0001g0024 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.321+4149A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149876303 | ||||||
| chr3:149876578 | C | A | 1 | a0004c0005t0001g0081 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.321+4424C>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149876578 | ||||||
| chr3:149876578 | C | T | 3 | a0001c0001t0001g0118a0001c0001t0001g0146a0001c0001t0001g0166 | 3 | HG01978.hp2 HG02293.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.321+4424C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149876578 | ||||||
| chr3:149876764 | A | G | 1 | a0001c0001t0001g0186 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.321+4610A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149876764 | ||||||
| chr3:149876771 | C | CT | 33 | a0001c0001t0001g0116a0001c0001t0001g0125a0001c0001t0001g0129others(30): Show | 33 | HG01978.hp2 HG02056.hp1 HG02109.hp1 others(30): Show |
intron_variant | MODIFIER | c.321+4641dupT | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr3 | 149876771 | |||||
| chr3:149876771 | C | CTT | 7 | a0001c0001t0001g0130a0001c0001t0001g0228a0001c0002t0002g0242others(4): Show | 7 | HG01346.hp2 HG02300.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.321+4640_321+4641d others(4): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr3 | 149876771 | |||||
| chr3:149876771 | CT | C | 10 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0001t0001g0055others(7): Show | 10 | HG01099.hp2 HG01167.hp1 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.321+4641delT | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr3 | 149876771 | |||||
| chr3:149876771 | CTTTTTTT others(3): Show |
C | 2 | a0001c0002t0002g0265a0001c0002t0002g0266 | 2 | HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.321+4632_321+4641d others(12): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr3 | 149876771 | |||||
| chr3:149876771 | CTTTTTTT others(6): Show |
C | 1 | a0001c0002t0006g0009 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.321+4629_321+4641d others(15): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr3 | 149876771 | |||||
| chr3:149876882 | A | G | 1 | a0001c0002t0001g0251 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.321+4728A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149876882 | ||||||
| chr3:149876925 | C | T | 1 | a0001c0002t0002g0030 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.321+4771C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149876925 | ||||||
| chr3:149876981 | T | C | 9 | a0001c0001t0001g0088a0001c0001t0001g0097a0001c0002t0003g0085others(6): Show | 9 | HG00621.hp2 HG01071.hp1 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.321+4827T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149876981 | ||||||
| chr3:149877026 | C | T | 1 | a0001c0001t0001g0125 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.321+4872C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149877026 | ||||||
| chr3:149877059 | C | A | 15 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(12): Show | 15 | HG00323.hp1 HG00741.hp2 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.321+4905C>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149877059 | ||||||
| chr3:149877303 | G | A | 6 | a0001c0001t0001g0054a0001c0001t0001g0089a0001c0001t0001g0090others(3): Show | 6 | HG02647.hp1 HG02717.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.321+5149G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149877303 | ||||||
| chr3:149877472 | C | CT | 27 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0001t0001g0066others(24): Show | 27 | HG00735.hp1 HG01243.hp2 HG01496.hp1 others(24): Show |
intron_variant | MODIFIER | c.321+5338dupT | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr3 | 149877472 | |||||
| chr3:149877472 | CT | C | 31 | a0001c0001t0001g0056a0001c0001t0001g0060a0001c0001t0001g0061others(28): Show | 31 | HG00280.hp2 HG01070.hp2 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.321+5338delT | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr3 | 149877472 | |||||
| chr3:149877665 | A | G | 2 | a0001c0001t0001g0153a0005c0006t0001g0178 | 2 | HG02056.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.321+5511A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149877665 | ||||||
| chr3:149877740 | A | G | 2 | a0001c0002t0006g0236a0001c0002t0006g0237 | 2 | HG02896.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.321+5586A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149877740 | ||||||
| chr3:149877887 | A | C | 1 | a0001c0001t0001g0064 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.321+5733A>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149877887 | ||||||
| chr3:149878128 | C | A | 13 | a0001c0001t0001g0055a0001c0001t0001g0094a0001c0001t0001g0099others(10): Show | 13 | HG01167.hp2 HG01169.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.321+5974C>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149878128 | ||||||
| chr3:149878541 | C | T | 1 | a0001c0001t0001g0231 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.321+6387C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149878541 | ||||||
| chr3:149878573 | A | G | 1 | a0001c0002t0002g0227 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.321+6419A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149878573 | ||||||
| chr3:149878630 | T | C | 9 | a0001c0001t0001g0245a0001c0002t0002g0240a0001c0002t0002g0241others(6): Show | 9 | HG01496.hp1 HG02109.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.321+6476T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149878630 | ||||||
| chr3:149878637 | C | G | 9 | a0001c0001t0012g0206a0001c0002t0005g0202a0001c0002t0005g0203others(6): Show | 9 | HG00639.hp1 HG00642.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.321+6483C>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149878637 | ||||||
| chr3:149879064 | A | G | 1 | a0001c0002t0006g0253 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.321+6910A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149879064 | ||||||
| chr3:149879133 | T | G | 2 | a0001c0002t0002g0265a0001c0002t0002g0266 | 2 | HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.321+6979T>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149879133 | ||||||
| chr3:149879173 | T | C | 239 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0022others(236): Show | 239 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.321+7019T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149879173 | ||||||
| chr3:149879209 | A | G | 2 | a0001c0002t0002g0268a0001c0002t0002g0269 | 2 | HG02145.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.321+7055A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149879209 | ||||||
| chr3:149879307 | A | AT | 204 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0022others(201): Show | 204 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.321+7171dupT | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr3 | 149879307 | |||||
| chr3:149879307 | A | ATT | 18 | a0001c0001t0001g0168a0001c0001t0001g0177a0001c0001t0001g0239others(15): Show | 18 | HG00280.hp2 HG01106.hp1 HG01433.hp2 others(15): Show |
intron_variant | MODIFIER | c.321+7170_321+7171d others(4): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr3 | 149879307 | |||||
| chr3:149879386 | C | T | 2 | a0001c0002t0002g0265a0001c0002t0002g0266 | 2 | HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.321+7232C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149879386 | ||||||
| chr3:149879693 | G | A | 13 | a0001c0001t0001g0055a0001c0001t0001g0094a0001c0001t0001g0099others(10): Show | 13 | HG01167.hp2 HG01169.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.321+7539G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149879693 | ||||||
| chr3:149879763 | A | G | 1 | a0001c0002t0002g0040 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.321+7609A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149879763 | ||||||
| chr3:149880054 | A | C | 1 | a0001c0002t0001g0251 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.321+7900A>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149880054 | ||||||
| chr3:149880087 | G | A | 4 | a0001c0002t0001g0251a0001c0002t0007g0249a0001c0002t0007g0250others(1): Show | 4 | HG02717.hp2 HG03130.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.321+7933G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149880087 | ||||||
| chr3:149880141 | T | C | 2 | a0003c0004t0008g0199a0003c0004t0008g0200 | 2 | HG03098.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.321+7987T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149880141 | ||||||
| chr3:149880857 | A | G | 1 | a0001c0002t0003g0257 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.321+8703A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149880857 | ||||||
| chr3:149881062 | T | G | 1 | a0001c0002t0003g0098 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.321+8908T>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149881062 | ||||||
| chr3:149881339 | G | GT | 11 | a0001c0001t0012g0206a0001c0002t0005g0202a0001c0002t0005g0203others(8): Show | 11 | HG00639.hp1 HG00642.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.321+9194dupT | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr3 | 149881339 | |||||
| chr3:149881365 | C | G | 1 | a0001c0002t0003g0098 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.321+9211C>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149881365 | ||||||
| chr3:149881541 | G | C | 13 | a0001c0001t0001g0239a0001c0002t0003g0238a0001c0002t0003g0254others(10): Show | 13 | HG00280.hp2 HG01106.hp1 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.321+9387G>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149881541 | ||||||
| chr3:149881710 | A | G | 9 | a0001c0001t0001g0245a0001c0002t0002g0240a0001c0002t0002g0241others(6): Show | 9 | HG01496.hp1 HG02109.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.321+9556A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149881710 | ||||||
| chr3:149881728 | C | G | 11 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0002t0002g0020others(8): Show | 11 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.321+9574C>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149881728 | ||||||
| chr3:149881875 | T | A | 2 | a0003c0004t0008g0199a0003c0004t0008g0200 | 2 | HG03098.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.321+9721T>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149881875 | ||||||
| chr3:149881995 | C | T | 177 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0054others(174): Show | 177 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.321+9841C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149881995 | ||||||
| chr3:149882039 | A | G | 237 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0022others(234): Show | 237 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.321+9885A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149882039 | ||||||
| chr3:149882062 | T | G | 1 | a0001c0001t0001g0157 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.321+9908T>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149882062 | ||||||
| chr3:149882276 | G | A | 11 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0002t0002g0020others(8): Show | 11 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.321+10122G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149882276 | ||||||
| chr3:149882282 | G | A | 2 | a0001c0002t0002g0265a0001c0002t0002g0266 | 2 | HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.321+10128G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149882282 | ||||||
| chr3:149882324 | C | T | 3 | a0001c0002t0003g0085a0001c0002t0003g0086a0001c0002t0003g0087 | 3 | HG01074.hp2 HG01433.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.321+10170C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149882324 | ||||||
| chr3:149882325 | G | A | 1 | a0001c0002t0003g0109 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.321+10171G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149882325 | ||||||
| chr3:149882778 | A | C | 1 | a0004c0005t0001g0081 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.321+10624A>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149882778 | ||||||
| chr3:149883020 | C | G | 3 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079 | 3 | HG01192.hp1 HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.321+10866C>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149883020 | ||||||
| chr3:149883146 | T | C | 2 | a0001c0002t0002g0265a0001c0002t0002g0266 | 2 | HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.321+10992T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149883146 | ||||||
| chr3:149883602 | G | A | 1 | a0001c0001t0001g0216 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.321+11448G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149883602 | ||||||
| chr3:149883695 | T | G | 2 | a0001c0001t0001g0194a0001c0001t0001g0195 | 2 | HG01192.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.321+11541T>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149883695 | ||||||
| chr3:149883773 | A | G | 1 | a0001c0001t0001g0108 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.321+11619A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149883773 | ||||||
| chr3:149883790 | G | A | 239 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0022others(236): Show | 239 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.321+11636G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149883790 | ||||||
| chr3:149883858 | C | T | 2 | a0001c0002t0007g0249a0001c0002t0007g0250 | 2 | HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.322-11615C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149883858 | ||||||
| chr3:149884124 | C | T | 1 | a0001c0001t0001g0042 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.322-11349C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149884124 | ||||||
| chr3:149884357 | C | A | 1 | a0001c0002t0002g0272 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.322-11116C>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149884357 | ||||||
| chr3:149884397 | A | G | 1 | a0001c0001t0001g0118 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.322-11076A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149884397 | ||||||
| chr3:149884753 | C | T | 2 | a0001c0001t0001g0126a0001c0001t0001g0176 | 2 | NA18747.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.322-10720C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149884753 | ||||||
| chr3:149884813 | C | A | 1 | a0001c0001t0001g0196 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.322-10660C>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149884813 | ||||||
| chr3:149884866 | GT | G | 13 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0002t0002g0020others(10): Show | 13 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.322-10597delT | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr3 | 149884866 | |||||
| chr3:149885164 | A | G | 6 | a0001c0002t0006g0005a0001c0002t0006g0006a0001c0002t0006g0007others(3): Show | 6 | HG02109.hp1 HG02258.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.322-10309A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149885164 | ||||||
| chr3:149885183 | C | G | 3 | a0001c0002t0002g0030a0001c0002t0002g0039a0001c0002t0002g0041 | 3 | NA18973.hp2 NA18998.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.322-10290C>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149885183 | ||||||
| chr3:149885259 | T | G | 1 | a0001c0002t0005g0209 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.322-10214T>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149885259 | ||||||
| chr3:149885401 | G | GT | 11 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0002t0002g0020others(8): Show | 11 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.322-10064dupT | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr3 | 149885401 | |||||
| chr3:149885469 | A | C | 13 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0002t0002g0020others(10): Show | 13 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.322-10004A>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149885469 | ||||||
| chr3:149885562 | A | G | 33 | a0001c0001t0001g0239a0001c0001t0012g0206a0001c0002t0002g0011others(30): Show | 33 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.322-9911A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149885562 | ||||||
| chr3:149885570 | A | T | 1 | a0001c0002t0001g0251 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.322-9903A>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149885570 | ||||||
| chr3:149885594 | A | G | 2 | a0001c0002t0002g0265a0001c0002t0002g0266 | 2 | HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.322-9879A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149885594 | ||||||
| chr3:149885739 | G | T | 13 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0002t0002g0020others(10): Show | 13 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.322-9734G>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149885739 | ||||||
| chr3:149885764 | G | T | 3 | a0001c0002t0003g0091a0001c0002t0003g0092a0001c0002t0003g0093 | 3 | HG02717.hp1 HG02886.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.322-9709G>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149885764 | ||||||
| chr3:149885953 | C | T | 2 | a0001c0002t0002g0265a0001c0002t0002g0266 | 2 | HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.322-9520C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149885953 | ||||||
| chr3:149886327 | G | A | 11 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0002t0002g0020others(8): Show | 11 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.322-9146G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149886327 | ||||||
| chr3:149886408 | T | C | 6 | a0001c0002t0006g0005a0001c0002t0006g0006a0001c0002t0006g0007others(3): Show | 6 | HG02109.hp1 HG02258.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.322-9065T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149886408 | ||||||
| chr3:149886431 | T | C | 1 | a0001c0001t0001g0107 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.322-9042T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149886431 | ||||||
| chr3:149886466 | C | A | 1 | a0001c0002t0002g0034 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.322-9007C>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149886466 | ||||||
| chr3:149886529 | C | T | 4 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0112others(1): Show | 4 | HG02896.hp2 HG02922.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.322-8944C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149886529 | ||||||
| chr3:149886553 | T | C | 2 | a0003c0004t0008g0199a0003c0004t0008g0200 | 2 | HG03098.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.322-8920T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149886553 | ||||||
| chr3:149886780 | G | A | 2 | a0001c0002t0002g0265a0001c0002t0002g0266 | 2 | HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.322-8693G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149886780 | ||||||
| chr3:149887012 | C | T | 239 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0022others(236): Show | 239 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.322-8461C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149887012 | ||||||
| chr3:149887130 | C | T | 1 | a0001c0002t0001g0037 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.322-8343C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149887130 | ||||||
| chr3:149887288 | G | C | 2 | a0001c0002t0002g0278a0001c0002t0002g0279 | 2 | HG00140.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.322-8185G>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149887288 | ||||||
| chr3:149887362 | A | G | 2 | a0001c0002t0002g0265a0001c0002t0002g0266 | 2 | HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.322-8111A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149887362 | ||||||
| chr3:149887446 | A | G | 13 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0002t0002g0020others(10): Show | 13 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.322-8027A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149887446 | ||||||
| chr3:149887567 | T | G | 9 | a0001c0001t0001g0245a0001c0002t0002g0240a0001c0002t0002g0241others(6): Show | 9 | HG01496.hp1 HG02109.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.322-7906T>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149887567 | ||||||
| chr3:149887582 | G | A | 9 | a0001c0001t0001g0245a0001c0002t0002g0240a0001c0002t0002g0241others(6): Show | 9 | HG01496.hp1 HG02109.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.322-7891G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149887582 | ||||||
| chr3:149887886 | T | A | 6 | a0001c0002t0006g0005a0001c0002t0006g0006a0001c0002t0006g0007others(3): Show | 6 | HG02109.hp1 HG02258.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.322-7587T>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149887886 | ||||||
| chr3:149887952 | G | C | 5 | a0001c0001t0001g0150a0001c0001t0001g0169a0001c0001t0001g0171others(2): Show | 5 | HG02523.hp1 NA18950.hp1 NA18998.hp1 others(2): Show |
intron_variant | MODIFIER | c.322-7521G>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149887952 | ||||||
| chr3:149887978 | C | T | 1 | a0001c0001t0001g0099 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.322-7495C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149887978 | ||||||
| chr3:149888072 | G | C | 1 | a0001c0001t0001g0157 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.322-7401G>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149888072 | ||||||
| chr3:149888079 | G | C | 6 | a0001c0002t0006g0005a0001c0002t0006g0006a0001c0002t0006g0007others(3): Show | 6 | HG02109.hp1 HG02258.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.322-7394G>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149888079 | ||||||
| chr3:149888312 | T | C | 11 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0002t0002g0020others(8): Show | 11 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.322-7161T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149888312 | ||||||
| chr3:149888995 | G | A | 11 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0002t0002g0020others(8): Show | 11 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.322-6478G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149888995 | ||||||
| chr3:149889064 | G | A | 3 | a0002c0003t0001g0002a0002c0003t0001g0003a0002c0003t0001g0004 | 3 | HG02976.hp2 HG03041.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.322-6409G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149889064 | ||||||
| chr3:149889096 | G | A | 1 | a0007c0008t0002g0243 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.322-6377G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149889096 | ||||||
| chr3:149889286 | A | AGTGT | 5 | a0001c0001t0012g0206a0001c0002t0005g0205a0001c0002t0005g0207others(2): Show | 5 | HG01891.hp2 HG02572.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.322-6185_322-6182d others(6): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr3 | 149889286 | |||||
| chr3:149889286 | A | AGTGTGT | 3 | a0001c0002t0005g0202a0001c0002t0005g0203a0001c0002t0005g0204 | 3 | HG00639.hp1 HG00642.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.322-6182_322-6181i others(8): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr3 | 149889286 | |||||
| chr3:149889286 | A | AGTGTGTG others(3): Show |
1 | a0001c0002t0005g0209 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.322-6182_322-6181i others(12): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr3 | 149889286 | |||||
| chr3:149889292 | C | CGT | 14 | a0001c0001t0001g0042a0001c0001t0001g0090a0001c0001t0001g0194others(11): Show | 14 | HG00735.hp1 HG01192.hp2 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.322-6148_322-6147d others(4): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr3 | 149889292 | |||||
| chr3:149889292 | C | CGTGT | 18 | a0001c0001t0001g0022a0001c0001t0001g0125a0001c0001t0001g0127others(15): Show | 18 | HG01358.hp2 HG01496.hp1 HG02056.hp1 others(15): Show |
intron_variant | MODIFIER | c.322-6150_322-6147d others(6): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr3 | 149889292 | |||||
| chr3:149889292 | C | CGTGTGT | 61 | a0001c0001t0001g0015a0001c0001t0001g0057a0001c0001t0001g0084others(58): Show | 61 | HG00099.hp1 HG00140.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.322-6152_322-6147d others(8): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr3 | 149889292 | |||||
| chr3:149889292 | C | CGTGTGTG others(1): Show |
43 | a0001c0001t0001g0024a0001c0001t0001g0056a0001c0001t0001g0065others(40): Show | 43 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(40): Show |
intron_variant | MODIFIER | c.322-6154_322-6147d others(10): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr3 | 149889292 | |||||
| chr3:149889292 | C | CGTGTGTG others(3): Show |
35 | a0001c0001t0001g0010a0001c0001t0001g0058a0001c0001t0001g0059others(32): Show | 35 | HG00323.hp1 HG00544.hp2 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.322-6156_322-6147d others(12): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr3 | 149889292 | |||||
| chr3:149889292 | C | CGTGTGTG others(5): Show |
42 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0063others(39): Show | 42 | HG00639.hp2 HG01099.hp2 HG01167.hp2 others(39): Show |
intron_variant | MODIFIER | c.322-6158_322-6147d others(14): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr3 | 149889292 | |||||
| chr3:149889292 | C | CGTGTGTG others(7): Show |
14 | a0001c0001t0001g0067a0001c0001t0001g0094a0001c0001t0001g0104others(11): Show | 14 | HG01975.hp2 HG01978.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.322-6160_322-6147d others(16): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr3 | 149889292 | |||||
| chr3:149889292 | C | CGTGTGTG others(9): Show |
2 | a0001c0001t0001g0233a0001c0002t0002g0227 | 2 | NA18973.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.322-6162_322-6147d others(18): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr3 | 149889292 | |||||
| chr3:149889292 | C | CGTGTGTG others(11): Show |
2 | a0001c0002t0006g0236a0001c0002t0006g0237 | 2 | HG02896.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.322-6164_322-6147d others(20): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr3 | 149889292 | |||||
| chr3:149889292 | C | T | 9 | a0001c0001t0012g0206a0001c0002t0005g0202a0001c0002t0005g0203others(6): Show | 9 | HG00639.hp1 HG00642.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.322-6181C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149889292 | ||||||
| chr3:149889293 | G | A | 1 | a0001c0002t0002g0040 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.322-6180G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149889293 | ||||||
| chr3:149889327 | C | T | 2 | a0001c0002t0006g0236a0001c0002t0006g0237 | 2 | HG02896.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.322-6146C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149889327 | ||||||
| chr3:149889335 | T | C | 13 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0002t0002g0020others(10): Show | 13 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.322-6138T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149889335 | ||||||
| chr3:149889366 | G | A | 1 | a0001c0002t0002g0043 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.322-6107G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149889366 | ||||||
| chr3:149889385 | A | G | 2 | a0001c0002t0002g0268a0001c0002t0002g0269 | 2 | HG02145.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.322-6088A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149889385 | ||||||
| chr3:149889477 | G | T | 1 | a0001c0001t0001g0099 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.322-5996G>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149889477 | ||||||
| chr3:149889599 | G | T | 1 | a0001c0001t0001g0119 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.322-5874G>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149889599 | ||||||
| chr3:149889606 | A | G | 1 | a0001c0002t0002g0012 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.322-5867A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149889606 | ||||||
| chr3:149889627 | T | C | 1 | a0001c0001t0001g0183 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.322-5846T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149889627 | ||||||
| chr3:149889653 | A | AT | 13 | a0001c0001t0001g0149a0001c0001t0011g0226a0001c0001t0012g0206others(10): Show | 13 | HG00639.hp1 HG00642.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.322-5801dupT | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr3 | 149889653 | |||||
| chr3:149889693 | C | T | 3 | a0001c0002t0002g0011a0001c0002t0006g0236a0001c0002t0006g0237 | 3 | HG00741.hp1 HG02896.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.322-5780C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149889693 | ||||||
| chr3:149889748 | G | A | 9 | a0001c0001t0001g0245a0001c0002t0002g0240a0001c0002t0002g0241others(6): Show | 9 | HG01496.hp1 HG02109.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.322-5725G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149889748 | ||||||
| chr3:149889800 | G | A | 13 | a0001c0001t0001g0239a0001c0002t0003g0238a0001c0002t0003g0254others(10): Show | 13 | HG00280.hp2 HG01106.hp1 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.322-5673G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149889800 | ||||||
| chr3:149889880 | T | G | 2 | a0003c0004t0008g0199a0003c0004t0008g0200 | 2 | HG03098.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.322-5593T>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149889880 | ||||||
| chr3:149890000 | C | T | 1 | a0001c0001t0012g0206 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.322-5473C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149890000 | ||||||
| chr3:149890183 | C | T | 2 | a0001c0002t0002g0268a0001c0002t0002g0269 | 2 | HG02145.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.322-5290C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149890183 | ||||||
| chr3:149890432 | C | A | 2 | a0001c0001t0001g0142a0001c0001t0001g0212 | 2 | NA18942.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.322-5041C>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149890432 | ||||||
| chr3:149890484 | T | C | 38 | a0001c0001t0001g0056a0001c0001t0001g0119a0001c0001t0001g0125others(35): Show | 38 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(35): Show |
intron_variant | MODIFIER | c.322-4989T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149890484 | ||||||
| chr3:149890541 | A | G | 2 | a0001c0002t0002g0265a0001c0002t0002g0266 | 2 | HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.322-4932A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149890541 | ||||||
| chr3:149890710 | T | C | 1 | a0001c0002t0002g0039 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.322-4763T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149890710 | ||||||
| chr3:149890759 | G | A | 1 | a0001c0002t0002g0275 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.322-4714G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149890759 | ||||||
| chr3:149891161 | C | G | 1 | a0001c0001t0001g0089 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.322-4312C>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149891161 | ||||||
| chr3:149891561 | A | G | 1 | a0001c0001t0001g0267 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.322-3912A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149891561 | ||||||
| chr3:149891563 | G | A | 15 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0002t0002g0020others(12): Show | 15 | HG00735.hp1 HG01243.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.322-3910G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149891563 | ||||||
| chr3:149891609 | T | C | 2 | a0001c0002t0002g0265a0001c0002t0002g0266 | 2 | HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.322-3864T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149891609 | ||||||
| chr3:149891738 | CTG | C | 9 | a0001c0001t0001g0245a0001c0002t0002g0240a0001c0002t0002g0241others(6): Show | 9 | HG01496.hp1 HG02109.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.322-3732_322-3731d others(4): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr3 | 149891738 | |||||
| chr3:149892080 | A | G | 1 | a0001c0002t0002g0011 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.322-3393A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149892080 | ||||||
| chr3:149892132 | T | C | 1 | a0001c0001t0001g0157 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.322-3341T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149892132 | ||||||
| chr3:149892399 | G | A | 8 | a0001c0001t0001g0024a0001c0001t0001g0123a0001c0001t0001g0138others(5): Show | 8 | HG00621.hp1 HG02559.hp2 NA18747.hp1 others(5): Show |
intron_variant | MODIFIER | c.322-3074G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149892399 | ||||||
| chr3:149892426 | T | C | 9 | a0001c0001t0012g0206a0001c0002t0005g0202a0001c0002t0005g0203others(6): Show | 9 | HG00639.hp1 HG00642.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.322-3047T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149892426 | ||||||
| chr3:149892463 | G | A | 1 | a0001c0002t0001g0251 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.322-3010G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149892463 | ||||||
| chr3:149892490 | G | T | 7 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0112others(4): Show | 7 | HG02896.hp2 HG02922.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.322-2983G>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149892490 | ||||||
| chr3:149892594 | C | T | 2 | a0003c0004t0008g0199a0003c0004t0008g0200 | 2 | HG03098.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.322-2879C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149892594 | ||||||
| chr3:149892832 | G | A | 13 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0002t0002g0020others(10): Show | 13 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.322-2641G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149892832 | ||||||
| chr3:149893060 | G | A | 3 | a0001c0001t0001g0135a0001c0001t0001g0149a0001c0001t0001g0179 | 3 | NA18995.hp2 NA19062.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.322-2413G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149893060 | ||||||
| chr3:149893065 | C | G | 4 | a0001c0001t0001g0057a0001c0001t0001g0064a0001c0001t0001g0069others(1): Show | 4 | HG00741.hp2 HG01167.hp1 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.322-2408C>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149893065 | ||||||
| chr3:149893093 | A | G | 2 | a0001c0002t0002g0268a0001c0002t0002g0269 | 2 | HG02145.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.322-2380A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149893093 | ||||||
| chr3:149893133 | A | G | 238 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0022others(235): Show | 238 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.322-2340A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149893133 | ||||||
| chr3:149893330 | G | A | 4 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0112others(1): Show | 4 | HG02896.hp2 HG02922.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.322-2143G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149893330 | ||||||
| chr3:149893425 | A | C | 1 | a0001c0002t0002g0041 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.322-2048A>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149893425 | ||||||
| chr3:149893586 | A | G | 1 | a0001c0001t0001g0088 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.322-1887A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149893586 | ||||||
| chr3:149893631 | A | G | 1 | a0001c0002t0001g0035 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.322-1842A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149893631 | ||||||
| chr3:149893858 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.322-1615G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149893858 | ||||||
| chr3:149893954 | A | G | 3 | a0001c0002t0007g0249a0001c0002t0007g0250a0001c0002t0007g0252 | 3 | HG02717.hp2 HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.322-1519A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149893954 | ||||||
| chr3:149894017 | A | G | 239 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0022others(236): Show | 239 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.322-1456A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149894017 | ||||||
| chr3:149894276 | T | G | 13 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0002t0002g0020others(10): Show | 13 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.322-1197T>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149894276 | ||||||
| chr3:149894299 | A | G | 2 | a0001c0002t0002g0265a0001c0002t0002g0266 | 2 | HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.322-1174A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149894299 | ||||||
| chr3:149894385 | C | T | 1 | a0001c0001t0001g0063 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.322-1088C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149894385 | ||||||
| chr3:149894588 | C | T | 1 | a0001c0002t0003g0238 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.322-885C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149894588 | ||||||
| chr3:149895122 | A | G | 13 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0002t0002g0020others(10): Show | 13 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.322-351A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149895122 | ||||||
| chr3:149895140 | A | T | 1 | a0001c0001t0001g0148 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.322-333A>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149895140 | ||||||
| chr3:149895206 | T | C | 8 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(5): Show | 8 | HG00099.hp1 HG01346.hp2 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.322-267T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149895206 | ||||||
| chr3:149895248 | G | T | 2 | a0001c0002t0002g0273a0001c0002t0002g0274 | 2 | HG03195.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.322-225G>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | chr3 | 149895248 | ||||||
| chr3:149895445 | AT | A | 61 | a0001c0001t0001g0042a0001c0001t0001g0235a0001c0001t0001g0245others(58): Show | 62 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.322-10delT | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr3 | 149895445 | |||||
| chr3:149895445 | ATT | A | 214 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0022others(211): Show | 214 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.322-11_322-10delTT | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr3 | 149895445 | |||||
| chr3:149895851 | A | G | 2 | a0001c0002t0002g0268a0001c0002t0002g0269 | 2 | HG02145.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.409+291A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 5/9 | chr3 | 149895851 | ||||||
| chr3:149895908 | A | G | 2 | a0001c0002t0002g0268a0001c0002t0002g0269 | 2 | HG02145.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.409+348A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 5/9 | chr3 | 149895908 | ||||||
| chr3:149895911 | C | T | 238 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0022others(235): Show | 238 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.409+351C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 5/9 | chr3 | 149895911 | ||||||
| chr3:149896259 | G | A | 1 | a0001c0001t0001g0172 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.409+699G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 5/9 | chr3 | 149896259 | ||||||
| chr3:149896418 | C | T | 2 | a0001c0001t0001g0073a0001c0001t0001g0074 | 2 | HG01993.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.409+858C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 5/9 | chr3 | 149896418 | ||||||
| chr3:149896483 | AT | A | 9 | a0001c0001t0001g0245a0001c0002t0002g0240a0001c0002t0002g0241others(6): Show | 9 | HG01496.hp1 HG02109.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.409+936delT | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr3 | 149896483 | |||||
| chr3:149896505 | G | C | 1 | a0001c0001t0001g0075 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.409+945G>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 5/9 | chr3 | 149896505 | ||||||
| chr3:149896543 | G | A | 2 | a0001c0002t0002g0268a0001c0002t0002g0269 | 2 | HG02145.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.409+983G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 5/9 | chr3 | 149896543 | ||||||
| chr3:149896635 | A | G | 1 | a0001c0001t0001g0072 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.409+1075A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 5/9 | chr3 | 149896635 | ||||||
| chr3:149896759 | G | A | 1 | a0001c0002t0002g0275 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.409+1199G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 5/9 | chr3 | 149896759 | ||||||
| chr3:149896839 | T | A | 2 | a0001c0002t0002g0045a0001c0002t0002g0046 | 2 | NA18961.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.409+1279T>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 5/9 | chr3 | 149896839 | ||||||
| chr3:149896996 | T | G | 2 | a0001c0001t0001g0070a0006c0007t0001g0071 | 2 | HG01255.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.409+1436T>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 5/9 | chr3 | 149896996 | ||||||
| chr3:149897311 | A | T | 11 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0002t0002g0020others(8): Show | 11 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.409+1751A>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 5/9 | chr3 | 149897311 | ||||||
| chr3:149897376 | T | A | 1 | a0001c0001t0001g0217 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.409+1816T>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 5/9 | chr3 | 149897376 | ||||||
| chr3:149897654 | C | T | 6 | a0001c0002t0006g0005a0001c0002t0006g0006a0001c0002t0006g0007others(3): Show | 6 | HG02109.hp1 HG02258.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.409+2094C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 5/9 | chr3 | 149897654 | ||||||
| chr3:149897744 | A | T | 19 | a0001c0001t0001g0056a0001c0001t0001g0119a0001c0001t0001g0125others(16): Show | 19 | HG00140.hp1 HG00323.hp2 HG00642.hp1 others(16): Show |
intron_variant | MODIFIER | c.409+2184A>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 5/9 | chr3 | 149897744 | ||||||
| chr3:149898135 | C | G | 177 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0054others(174): Show | 177 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.409+2575C>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 5/9 | chr3 | 149898135 | ||||||
| chr3:149898495 | C | G | 2 | a0001c0001t0001g0144a0001c0001t0001g0145 | 2 | NA18963.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.409+2935C>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 5/9 | chr3 | 149898495 | ||||||
| chr3:149898612 | G | T | 237 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0024others(234): Show | 237 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.409+3052G>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 5/9 | chr3 | 149898612 | ||||||
| chr3:149898652 | G | A | 14 | a0001c0001t0001g0142a0001c0001t0001g0201a0001c0001t0001g0212others(11): Show | 14 | HG02273.hp2 HG02300.hp2 HG02523.hp2 others(11): Show |
intron_variant | MODIFIER | c.409+3092G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 5/9 | chr3 | 149898652 | ||||||
| chr3:149898774 | A | G | 1 | a0001c0002t0009g0121 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.409+3214A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 5/9 | chr3 | 149898774 | ||||||
| chr3:149898984 | C | A | 1 | a0001c0001t0001g0182 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.410-3088C>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 5/9 | chr3 | 149898984 | ||||||
| chr3:149899216 | C | A | 1 | a0001c0002t0002g0036 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.410-2856C>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 5/9 | chr3 | 149899216 | ||||||
| chr3:149899358 | A | G | 2 | a0003c0004t0008g0199a0003c0004t0008g0200 | 2 | HG03098.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.410-2714A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 5/9 | chr3 | 149899358 | ||||||
| chr3:149899360 | A | C | 2 | a0003c0004t0008g0199a0003c0004t0008g0200 | 2 | HG03098.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.410-2712A>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 5/9 | chr3 | 149899360 | ||||||
| chr3:149899444 | G | A | 1 | a0001c0002t0002g0269 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.410-2628G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 5/9 | chr3 | 149899444 | ||||||
| chr3:149899481 | T | TA | 8 | a0001c0001t0001g0105a0001c0001t0001g0110a0001c0001t0001g0111others(5): Show | 8 | HG02896.hp2 HG02922.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.410-2582dupA | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr3 | 149899481 | |||||
| chr3:149899482 | A | T | 1 | a0001c0002t0006g0253 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.410-2590A>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 5/9 | chr3 | 149899482 | ||||||
| chr3:149899501 | A | G | 1 | a0001c0002t0002g0031 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.410-2571A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 5/9 | chr3 | 149899501 | ||||||
| chr3:149900224 | G | A | 1 | a0001c0002t0002g0247 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.410-1848G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 5/9 | chr3 | 149900224 | ||||||
| chr3:149900355 | C | G | 2 | a0001c0002t0002g0265a0001c0002t0002g0266 | 2 | HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.410-1717C>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 5/9 | chr3 | 149900355 | ||||||
| chr3:149900426 | T | TA | 7 | a0001c0001t0001g0097a0001c0001t0001g0144a0001c0001t0001g0145others(4): Show | 7 | HG00609.hp1 HG01361.hp1 HG02074.hp2 others(4): Show |
intron_variant | MODIFIER | c.410-1635dupA | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr3 | 149900426 | |||||
| chr3:149900637 | T | C | 10 | a0001c0001t0001g0015a0001c0002t0002g0020a0001c0002t0004g0013others(7): Show | 10 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.410-1435T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 5/9 | chr3 | 149900637 | ||||||
| chr3:149900830 | C | T | 1 | a0001c0002t0002g0273 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.410-1242C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 5/9 | chr3 | 149900830 | ||||||
| chr3:149900875 | A | G | 238 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0024others(235): Show | 238 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.410-1197A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 5/9 | chr3 | 149900875 | ||||||
| chr3:149900887 | C | T | 9 | a0001c0001t0001g0245a0001c0002t0002g0240a0001c0002t0002g0241others(6): Show | 9 | HG01496.hp1 HG02109.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.410-1185C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 5/9 | chr3 | 149900887 | ||||||
| chr3:149901173 | A | G | 13 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0002t0002g0020others(10): Show | 13 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.410-899A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 5/9 | chr3 | 149901173 | ||||||
| chr3:149901188 | C | G | 13 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0002t0002g0020others(10): Show | 13 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.410-884C>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 5/9 | chr3 | 149901188 | ||||||
| chr3:149901211 | C | G | 2 | a0001c0001t0001g0194a0001c0001t0001g0195 | 2 | HG01192.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.410-861C>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 5/9 | chr3 | 149901211 | ||||||
| chr3:149901386 | C | T | 2 | a0001c0001t0001g0060a0001c0001t0001g0061 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.410-686C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 5/9 | chr3 | 149901386 | ||||||
| chr3:149901414 | G | A | 1 | a0001c0002t0003g0264 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.410-658G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 5/9 | chr3 | 149901414 | ||||||
| chr3:149902012 | A | AAGTT | 13 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0002t0002g0020others(10): Show | 13 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.410-59_410-58insGT others(2): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr3 | 149902012 | |||||
| chr3:149902619 | A | C | 1 | a0001c0002t0002g0040 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.500+457A>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 6/9 | chr3 | 149902619 | ||||||
| chr3:149902696 | C | G | 1 | a0001c0002t0002g0031 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.500+534C>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 6/9 | chr3 | 149902696 | ||||||
| chr3:149902791 | G | T | 2 | a0001c0002t0002g0265a0001c0002t0002g0266 | 2 | HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.500+629G>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 6/9 | chr3 | 149902791 | ||||||
| chr3:149902935 | A | G | 1 | a0001c0002t0002g0012 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.500+773A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 6/9 | chr3 | 149902935 | ||||||
| chr3:149902998 | G | T | 1 | a0001c0002t0002g0012 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.500+836G>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 6/9 | chr3 | 149902998 | ||||||
| chr3:149903163 | G | A | 1 | a0002c0003t0001g0004 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.500+1001G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 6/9 | chr3 | 149903163 | ||||||
| chr3:149903333 | T | G | 9 | a0001c0001t0012g0206a0001c0002t0005g0202a0001c0002t0005g0203others(6): Show | 9 | HG00639.hp1 HG00642.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.500+1171T>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 6/9 | chr3 | 149903333 | ||||||
| chr3:149903515 | A | T | 9 | a0001c0001t0012g0206a0001c0002t0005g0202a0001c0002t0005g0203others(6): Show | 9 | HG00639.hp1 HG00642.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.500+1353A>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 6/9 | chr3 | 149903515 | ||||||
| chr3:149903653 | C | T | 1 | a0001c0002t0001g0251 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.500+1491C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 6/9 | chr3 | 149903653 | ||||||
| chr3:149903681 | G | A | 15 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(12): Show | 15 | HG00323.hp1 HG00741.hp2 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.500+1519G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 6/9 | chr3 | 149903681 | ||||||
| chr3:149903812 | A | G | 1 | a0001c0002t0004g0017 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.500+1650A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 6/9 | chr3 | 149903812 | ||||||
| chr3:149903933 | GTCTA | G | 3 | a0001c0002t0002g0012a0001c0002t0002g0265a0001c0002t0002g0266 | 3 | HG02723.hp1 HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.500+1775_500+1778d others(6): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr3 | 149903933 | |||||
| chr3:149903937 | A | ATCTG | 41 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(38): Show | 41 | HG00323.hp1 HG00621.hp2 HG00741.hp2 others(38): Show |
intron_variant | MODIFIER | c.500+1807_500+1810d others(6): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr3 | 149903937 | |||||
| chr3:149903937 | A | G | 2 | a0001c0002t0001g0032a0001c0002t0002g0011 | 2 | HG00741.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.500+1775A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 6/9 | chr3 | 149903937 | ||||||
| chr3:149903937 | ATCTG | A | 8 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(5): Show | 8 | HG00140.hp1 HG00642.hp1 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.500+1807_500+1810d others(6): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr3 | 149903937 | |||||
| chr3:149903937 | ATCTGTCT others(5): Show |
A | 3 | a0002c0003t0001g0002a0002c0003t0001g0003a0002c0003t0001g0004 | 3 | HG02976.hp2 HG03041.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.500+1799_500+1810d others(14): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr3 | 149903937 | |||||
| chr3:149904058 | C | T | 1 | a0001c0001t0001g0115 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.500+1896C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 6/9 | chr3 | 149904058 | ||||||
| chr3:149904410 | T | C | 9 | a0001c0001t0001g0245a0001c0002t0002g0240a0001c0002t0002g0241others(6): Show | 9 | HG01496.hp1 HG02109.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.500+2248T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 6/9 | chr3 | 149904410 | ||||||
| chr3:149904467 | G | C | 3 | a0001c0001t0001g0084a0001c0001t0001g0167a0001c0001t0001g0168 | 3 | NA19064.hp2 NA19070.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.500+2305G>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 6/9 | chr3 | 149904467 | ||||||
| chr3:149904529 | A | G | 1 | a0001c0001t0001g0054 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.500+2367A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 6/9 | chr3 | 149904529 | ||||||
| chr3:149904748 | TCCTCTCC others(21): Show |
T | 9 | a0001c0001t0001g0245a0001c0002t0002g0240a0001c0002t0002g0241others(6): Show | 9 | HG01496.hp1 HG02109.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.500+2587_500+2614d others(30): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 6/9 | chr3 | 149904748 | ||||||
| chr3:149904788 | T | C | 177 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0054others(174): Show | 177 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.500+2626T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 6/9 | chr3 | 149904788 | ||||||
| chr3:149905001 | T | C | 3 | a0001c0001t0001g0235a0001c0002t0002g0222a0001c0002t0002g0227 | 3 | NA18961.hp1 NA18972.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.500+2839T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 6/9 | chr3 | 149905001 | ||||||
| chr3:149905007 | T | G | 11 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0002t0002g0020others(8): Show | 11 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.500+2845T>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 6/9 | chr3 | 149905007 | ||||||
| chr3:149905021 | G | A | 5 | a0001c0002t0005g0202a0001c0002t0005g0203a0001c0002t0005g0204others(2): Show | 5 | HG00639.hp1 HG00642.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.500+2859G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 6/9 | chr3 | 149905021 | ||||||
| chr3:149905084 | A | T | 1 | a0001c0002t0003g0101 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.500+2922A>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 6/9 | chr3 | 149905084 | ||||||
| chr3:149905158 | A | G | 2 | a0001c0002t0006g0236a0001c0002t0006g0237 | 2 | HG02896.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.500+2996A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 6/9 | chr3 | 149905158 | ||||||
| chr3:149905289 | G | A | 2 | a0001c0002t0002g0268a0001c0002t0002g0269 | 2 | HG02145.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.500+3127G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 6/9 | chr3 | 149905289 | ||||||
| chr3:149905413 | G | GT | 9 | a0001c0001t0001g0088a0001c0002t0003g0085a0001c0002t0003g0086others(6): Show | 9 | HG00621.hp2 HG01071.hp1 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.500+3257dupT | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr3 | 149905413 | |||||
| chr3:149905746 | T | C | 1 | a0001c0001t0001g0211 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.500+3584T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 6/9 | chr3 | 149905746 | ||||||
| chr3:149906002 | G | A | 13 | a0001c0001t0012g0206a0001c0002t0002g0020a0001c0002t0004g0019others(10): Show | 13 | HG00639.hp1 HG00642.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.500+3840G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 6/9 | chr3 | 149906002 | ||||||
| chr3:149906283 | CTTT | C | 13 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0002t0002g0020others(10): Show | 13 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.500+4128_500+4130d others(5): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr3 | 149906283 | |||||
| chr3:149906288 | T | A | 3 | a0001c0002t0002g0275a0001c0002t0002g0276a0001c0002t0002g0277 | 3 | HG00099.hp2 HG00733.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.500+4126T>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 6/9 | chr3 | 149906288 | ||||||
| chr3:149906329 | TTTTA | T | 11 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0002t0002g0020others(8): Show | 11 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.500+4171_500+4174d others(6): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr3 | 149906329 | |||||
| chr3:149906439 | T | C | 86 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0056others(83): Show | 86 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.500+4277T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 6/9 | chr3 | 149906439 | ||||||
| chr3:149906618 | G | A | 2 | a0001c0001t0001g0089a0001c0001t0001g0090 | 2 | HG02647.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.500+4456G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 6/9 | chr3 | 149906618 | ||||||
| chr3:149906645 | C | CT | 169 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0054others(166): Show | 169 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(166): Show |
intron_variant | MODIFIER | c.500+4507dupT | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr3 | 149906645 | |||||
| chr3:149906645 | C | CTT | 6 | a0001c0001t0001g0068a0001c0001t0001g0075a0001c0001t0001g0125others(3): Show | 6 | HG00099.hp1 HG01175.hp1 HG02056.hp1 others(3): Show |
intron_variant | MODIFIER | c.500+4506_500+4507d others(4): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr3 | 149906645 | |||||
| chr3:149906645 | CT | C | 26 | a0001c0001t0001g0022a0001c0001t0012g0206a0001c0002t0002g0020others(23): Show | 26 | HG00642.hp2 HG00735.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.500+4507delT | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr3 | 149906645 | |||||
| chr3:149906730 | C | A | 2 | a0001c0001t0001g0055a0001c0001t0001g0100 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.500+4568C>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 6/9 | chr3 | 149906730 | ||||||
| chr3:149906879 | C | G | 86 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0056others(83): Show | 86 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.500+4717C>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 6/9 | chr3 | 149906879 | ||||||
| chr3:149906900 | G | C | 2 | a0001c0002t0002g0265a0001c0002t0002g0266 | 2 | HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.500+4738G>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 6/9 | chr3 | 149906900 | ||||||
| chr3:149907043 | T | C | 3 | a0001c0002t0003g0091a0001c0002t0003g0092a0001c0002t0003g0093 | 3 | HG02717.hp1 HG02886.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.500+4881T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 6/9 | chr3 | 149907043 | ||||||
| chr3:149907052 | A | G | 21 | a0001c0001t0001g0010a0001c0001t0001g0116a0001c0001t0001g0117others(18): Show | 21 | HG00544.hp1 HG01192.hp2 HG01433.hp2 others(18): Show |
intron_variant | MODIFIER | c.500+4890A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 6/9 | chr3 | 149907052 | ||||||
| chr3:149907180 | T | C | 9 | a0001c0001t0012g0206a0001c0002t0005g0202a0001c0002t0005g0203others(6): Show | 9 | HG00639.hp1 HG00642.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.501-4798T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 6/9 | chr3 | 149907180 | ||||||
| chr3:149907639 | C | T | 1 | a0001c0001t0001g0153 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.501-4339C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 6/9 | chr3 | 149907639 | ||||||
| chr3:149908007 | T | A | 239 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0022others(236): Show | 239 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.501-3971T>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 6/9 | chr3 | 149908007 | ||||||
| chr3:149908384 | A | G | 1 | a0001c0001t0002g0188 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.501-3594A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 6/9 | chr3 | 149908384 | ||||||
| chr3:149908643 | G | A | 86 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0056others(83): Show | 86 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.501-3335G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 6/9 | chr3 | 149908643 | ||||||
| chr3:149908752 | T | C | 238 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0022others(235): Show | 238 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.501-3226T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 6/9 | chr3 | 149908752 | ||||||
| chr3:149908915 | A | C | 1 | a0001c0002t0002g0011 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.501-3063A>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 6/9 | chr3 | 149908915 | ||||||
| chr3:149908993 | A | G | 1 | a0001c0001t0001g0213 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.501-2985A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 6/9 | chr3 | 149908993 | ||||||
| chr3:149909102 | G | A | 4 | a0001c0002t0001g0251a0001c0002t0007g0249a0001c0002t0007g0250others(1): Show | 4 | HG02717.hp2 HG03130.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.501-2876G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 6/9 | chr3 | 149909102 | ||||||
| chr3:149909152 | T | C | 1 | a0001c0001t0001g0054 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.501-2826T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 6/9 | chr3 | 149909152 | ||||||
| chr3:149909212 | A | G | 1 | a0001c0001t0001g0152 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.501-2766A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 6/9 | chr3 | 149909212 | ||||||
| chr3:149909277 | C | CT | 26 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0001t0001g0066others(23): Show | 26 | HG00735.hp1 HG01243.hp2 HG01496.hp1 others(23): Show |
intron_variant | MODIFIER | c.501-2686dupT | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr3 | 149909277 | |||||
| chr3:149909361 | G | A | 3 | a0001c0002t0002g0011a0001c0002t0006g0236a0001c0002t0006g0237 | 3 | HG00741.hp1 HG02896.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.501-2617G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 6/9 | chr3 | 149909361 | ||||||
| chr3:149909365 | C | T | 1 | a0001c0001t0001g0195 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.501-2613C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 6/9 | chr3 | 149909365 | ||||||
| chr3:149909442 | A | AT | 202 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0024others(199): Show | 202 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.501-2516dupT | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr3 | 149909442 | |||||
| chr3:149909442 | A | ATT | 30 | a0001c0001t0001g0022a0001c0001t0001g0102a0001c0001t0001g0103others(27): Show | 30 | HG00735.hp1 HG01496.hp1 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.501-2517_501-2516d others(4): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr3 | 149909442 | |||||
| chr3:149909505 | A | G | 278 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0022others(275): Show | 279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.501-2473A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 6/9 | chr3 | 149909505 | ||||||
| chr3:149909542 | C | T | 1 | a0001c0001t0001g0102 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.501-2436C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 6/9 | chr3 | 149909542 | ||||||
| chr3:149909571 | G | T | 4 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(1): Show | 4 | HG01123.hp2 HG01256.hp2 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.501-2407G>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 6/9 | chr3 | 149909571 | ||||||
| chr3:149909596 | A | G | 3 | a0001c0002t0003g0091a0001c0002t0003g0092a0001c0002t0003g0093 | 3 | HG02717.hp1 HG02886.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.501-2382A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 6/9 | chr3 | 149909596 | ||||||
| chr3:149909710 | C | T | 9 | a0001c0001t0001g0245a0001c0002t0002g0240a0001c0002t0002g0241others(6): Show | 9 | HG01496.hp1 HG02109.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.501-2268C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 6/9 | chr3 | 149909710 | ||||||
| chr3:149909783 | G | A | 10 | a0001c0002t0003g0260a0001c0002t0003g0261a0001c0002t0003g0262others(7): Show | 10 | HG01243.hp1 HG02109.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.501-2195G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 6/9 | chr3 | 149909783 | ||||||
| chr3:149909952 | G | GA | 152 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0054others(149): Show | 152 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.501-2015dupA | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr3 | 149909952 | |||||
| chr3:149909952 | G | GAA | 9 | a0001c0001t0012g0206a0001c0002t0005g0202a0001c0002t0005g0203others(6): Show | 9 | HG00639.hp1 HG00642.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.501-2016_501-2015d others(4): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr3 | 149909952 | |||||
| chr3:149909952 | GA | G | 9 | a0001c0001t0001g0245a0001c0002t0002g0240a0001c0002t0002g0241others(6): Show | 9 | HG01496.hp1 HG02109.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.501-2015delA | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr3 | 149909952 | |||||
| chr3:149910013 | A | G | 1 | a0001c0001t0001g0245 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.501-1965A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 6/9 | chr3 | 149910013 | ||||||
| chr3:149910320 | G | T | 8 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(5): Show | 8 | HG00099.hp1 HG01346.hp2 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.501-1658G>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 6/9 | chr3 | 149910320 | ||||||
| chr3:149910555 | A | G | 3 | a0001c0002t0007g0249a0001c0002t0007g0250a0001c0002t0007g0252 | 3 | HG02717.hp2 HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.501-1423A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 6/9 | chr3 | 149910555 | ||||||
| chr3:149910993 | G | A | 6 | a0001c0002t0006g0005a0001c0002t0006g0006a0001c0002t0006g0007others(3): Show | 6 | HG02109.hp1 HG02258.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.501-985G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 6/9 | chr3 | 149910993 | ||||||
| chr3:149911232 | G | A | 1 | a0001c0001t0001g0119 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.501-746G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 6/9 | chr3 | 149911232 | ||||||
| chr3:149911323 | G | A | 239 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0022others(236): Show | 239 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.501-655G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 6/9 | chr3 | 149911323 | ||||||
| chr3:149911389 | G | A | 85 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0056others(82): Show | 85 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.501-589G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 6/9 | chr3 | 149911389 | ||||||
| chr3:149912165 | C | T | 3 | a0001c0001t0001g0156a0001c0001t0001g0160a0001c0001t0001g0173 | 3 | HG00733.hp2 HG00735.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.606+82C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 7/9 | chr3 | 149912165 | ||||||
| chr3:149912292 | G | T | 13 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0002t0002g0020others(10): Show | 13 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.606+209G>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 7/9 | chr3 | 149912292 | ||||||
| chr3:149912713 | A | G | 1 | a0001c0001t0001g0185 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.606+630A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 7/9 | chr3 | 149912713 | ||||||
| chr3:149912788 | G | A | 2 | a0001c0002t0002g0278a0001c0002t0002g0279 | 2 | HG00140.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.606+705G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 7/9 | chr3 | 149912788 | ||||||
| chr3:149913032 | C | G | 1 | a0001c0001t0001g0054 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.606+949C>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 7/9 | chr3 | 149913032 | ||||||
| chr3:149913326 | G | A | 1 | a0001c0002t0002g0012 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.606+1243G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 7/9 | chr3 | 149913326 | ||||||
| chr3:149913620 | A | G | 1 | a0001c0001t0001g0090 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.606+1537A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 7/9 | chr3 | 149913620 | ||||||
| chr3:149913666 | G | C | 3 | a0001c0002t0002g0011a0001c0002t0006g0236a0001c0002t0006g0237 | 3 | HG00741.hp1 HG02896.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.606+1583G>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 7/9 | chr3 | 149913666 | ||||||
| chr3:149913685 | G | A | 1 | a0001c0001t0001g0066 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.606+1602G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 7/9 | chr3 | 149913685 | ||||||
| chr3:149913774 | A | G | 1 | a0001c0001t0001g0213 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.606+1691A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 7/9 | chr3 | 149913774 | ||||||
| chr3:149914061 | T | G | 2 | a0001c0002t0002g0265a0001c0002t0002g0266 | 2 | HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.606+1978T>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 7/9 | chr3 | 149914061 | ||||||
| chr3:149914367 | A | G | 2 | a0001c0001t0001g0155a0001c0001t0001g0159 | 2 | HG01099.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.606+2284A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 7/9 | chr3 | 149914367 | ||||||
| chr3:149914450 | T | C | 1 | a0001c0001t0001g0123 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.606+2367T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 7/9 | chr3 | 149914450 | ||||||
| chr3:149914482 | G | T | 2 | a0001c0002t0002g0265a0001c0002t0002g0266 | 2 | HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.606+2399G>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 7/9 | chr3 | 149914482 | ||||||
| chr3:149914538 | C | T | 1 | a0001c0001t0001g0193 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.606+2455C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 7/9 | chr3 | 149914538 | ||||||
| chr3:149914650 | C | T | 177 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0054others(174): Show | 177 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.606+2567C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 7/9 | chr3 | 149914650 | ||||||
| chr3:149914657 | G | A | 1 | a0001c0002t0006g0005 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.606+2574G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 7/9 | chr3 | 149914657 | ||||||
| chr3:149914662 | C | A | 3 | a0001c0001t0001g0245a0001c0002t0002g0242a0001c0002t0002g0244 | 3 | HG02818.hp2 HG02886.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.606+2579C>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 7/9 | chr3 | 149914662 | ||||||
| chr3:149914662 | C | T | 3 | a0001c0002t0006g0005a0001c0002t0006g0006a0001c0002t0006g0007 | 3 | HG02258.hp1 HG02615.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.606+2579C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 7/9 | chr3 | 149914662 | ||||||
| chr3:149914726 | GCCT | G | 13 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0002t0002g0020others(10): Show | 13 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.606+2644_606+2646d others(5): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 7/9 | chr3 | 149914726 | ||||||
| chr3:149914770 | T | C | 2 | a0003c0004t0008g0199a0003c0004t0008g0200 | 2 | HG03098.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.606+2687T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 7/9 | chr3 | 149914770 | ||||||
| chr3:149915026 | G | A | 1 | a0001c0002t0002g0011 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.606+2943G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 7/9 | chr3 | 149915026 | ||||||
| chr3:149915035 | A | G | 9 | a0001c0001t0001g0245a0001c0002t0002g0240a0001c0002t0002g0241others(6): Show | 9 | HG01496.hp1 HG02109.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.606+2952A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 7/9 | chr3 | 149915035 | ||||||
| chr3:149915247 | T | A | 1 | a0001c0001t0001g0196 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.606+3164T>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 7/9 | chr3 | 149915247 | ||||||
| chr3:149915303 | G | T | 1 | a0001c0001t0001g0136 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.606+3220G>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 7/9 | chr3 | 149915303 | ||||||
| chr3:149915304 | T | A | 1 | a0001c0001t0001g0136 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.606+3221T>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 7/9 | chr3 | 149915304 | ||||||
| chr3:149915354 | T | C | 2 | a0001c0001t0001g0194a0001c0001t0001g0195 | 2 | HG01192.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.606+3271T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 7/9 | chr3 | 149915354 | ||||||
| chr3:149915671 | A | G | 1 | a0001c0001t0001g0123 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.606+3588A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 7/9 | chr3 | 149915671 | ||||||
| chr3:149915771 | C | T | 13 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0002t0002g0020others(10): Show | 13 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.606+3688C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 7/9 | chr3 | 149915771 | ||||||
| chr3:149915965 | A | G | 1 | a0001c0002t0002g0012 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.606+3882A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 7/9 | chr3 | 149915965 | ||||||
| chr3:149915968 | T | G | 2 | a0001c0001t0001g0126a0001c0001t0001g0176 | 2 | NA18747.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.606+3885T>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 7/9 | chr3 | 149915968 | ||||||
| chr3:149915992 | TTATGTTG others(2): Show |
T | 9 | a0001c0001t0001g0245a0001c0002t0002g0240a0001c0002t0002g0241others(6): Show | 9 | HG01496.hp1 HG02109.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.606+3913_606+3921d others(11): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr3 | 149915992 | |||||
| chr3:149916086 | GT | G | 13 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0002t0002g0020others(10): Show | 13 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.606+4015delT | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr3 | 149916086 | |||||
| chr3:149916098 | T | A | 1 | a0001c0001t0001g0232 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.606+4015T>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 7/9 | chr3 | 149916098 | ||||||
| chr3:149916421 | A | G | 1 | a0001c0002t0002g0011 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.606+4338A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 7/9 | chr3 | 149916421 | ||||||
| chr3:149916458 | C | T | 1 | a0001c0002t0003g0101 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.606+4375C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 7/9 | chr3 | 149916458 | ||||||
| chr3:149916950 | C | T | 2 | a0001c0002t0002g0265a0001c0002t0002g0266 | 2 | HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.607-4184C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 7/9 | chr3 | 149916950 | ||||||
| chr3:149916966 | G | A | 1 | a0001c0002t0002g0012 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.607-4168G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 7/9 | chr3 | 149916966 | ||||||
| chr3:149916975 | T | TA | 8 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0134others(5): Show | 8 | HG00544.hp1 NA18965.hp1 NA18965.hp2 others(5): Show |
intron_variant | MODIFIER | c.607-4158dupA | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr3 | 149916975 | |||||
| chr3:149917158 | G | A | 2 | a0001c0001t0001g0239a0001c0002t0003g0238 | 2 | HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.607-3976G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 7/9 | chr3 | 149917158 | ||||||
| chr3:149917382 | G | A | 11 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0002t0002g0020others(8): Show | 11 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.607-3752G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 7/9 | chr3 | 149917382 | ||||||
| chr3:149917385 | C | T | 1 | a0001c0002t0002g0011 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.607-3749C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 7/9 | chr3 | 149917385 | ||||||
| chr3:149917386 | G | A | 2 | a0003c0004t0008g0199a0003c0004t0008g0200 | 2 | HG03098.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.607-3748G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 7/9 | chr3 | 149917386 | ||||||
| chr3:149917546 | G | A | 1 | a0001c0002t0006g0006 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.607-3588G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 7/9 | chr3 | 149917546 | ||||||
| chr3:149917811 | A | G | 2 | a0001c0002t0002g0268a0001c0002t0002g0269 | 2 | HG02145.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.607-3323A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 7/9 | chr3 | 149917811 | ||||||
| chr3:149917820 | A | T | 1 | a0001c0002t0002g0012 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.607-3314A>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 7/9 | chr3 | 149917820 | ||||||
| chr3:149917917 | C | T | 1 | a0001c0001t0011g0226 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.607-3217C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 7/9 | chr3 | 149917917 | ||||||
| chr3:149917929 | G | A | 1 | a0001c0002t0002g0222 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.607-3205G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 7/9 | chr3 | 149917929 | ||||||
| chr3:149918355 | A | G | 3 | a0002c0003t0001g0002a0002c0003t0001g0003a0002c0003t0001g0004 | 3 | HG02976.hp2 HG03041.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.607-2779A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 7/9 | chr3 | 149918355 | ||||||
| chr3:149918659 | G | C | 13 | a0001c0001t0001g0239a0001c0002t0003g0238a0001c0002t0003g0254others(10): Show | 13 | HG00280.hp2 HG01106.hp1 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.607-2475G>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 7/9 | chr3 | 149918659 | ||||||
| chr3:149918668 | C | T | 177 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0054others(174): Show | 177 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.607-2466C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 7/9 | chr3 | 149918668 | ||||||
| chr3:149918693 | G | GT | 32 | a0001c0001t0001g0061a0001c0001t0001g0132a0001c0001t0001g0139others(29): Show | 32 | HG00140.hp1 HG00280.hp2 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.607-2425dupT | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr3 | 149918693 | |||||
| chr3:149918958 | G | A | 13 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0002t0002g0020others(10): Show | 13 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.607-2176G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 7/9 | chr3 | 149918958 | ||||||
| chr3:149919093 | C | A | 238 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0022others(235): Show | 238 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.607-2041C>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 7/9 | chr3 | 149919093 | ||||||
| chr3:149919098 | G | A | 3 | a0001c0001t0001g0156a0001c0001t0001g0160a0001c0001t0001g0173 | 3 | HG00733.hp2 HG00735.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.607-2036G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 7/9 | chr3 | 149919098 | ||||||
| chr3:149919133 | A | C | 2 | a0001c0002t0006g0236a0001c0002t0006g0237 | 2 | HG02896.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.607-2001A>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 7/9 | chr3 | 149919133 | ||||||
| chr3:149919265 | A | G | 1 | a0001c0002t0002g0240 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.607-1869A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 7/9 | chr3 | 149919265 | ||||||
| chr3:149919358 | A | C | 2 | a0001c0002t0002g0268a0001c0002t0002g0269 | 2 | HG02145.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.607-1776A>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 7/9 | chr3 | 149919358 | ||||||
| chr3:149919539 | A | G | 1 | a0005c0006t0001g0178 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.607-1595A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 7/9 | chr3 | 149919539 | ||||||
| chr3:149919819 | G | T | 3 | a0002c0003t0001g0002a0002c0003t0001g0003a0002c0003t0001g0004 | 3 | HG02976.hp2 HG03041.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.607-1315G>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 7/9 | chr3 | 149919819 | ||||||
| chr3:149919836 | T | C | 4 | a0001c0001t0001g0105a0001c0001t0001g0110a0001c0001t0001g0111others(1): Show | 4 | HG02896.hp2 HG02922.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.607-1298T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 7/9 | chr3 | 149919836 | ||||||
| chr3:149920041 | C | G | 9 | a0001c0001t0001g0245a0001c0002t0002g0240a0001c0002t0002g0241others(6): Show | 9 | HG01496.hp1 HG02109.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.607-1093C>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 7/9 | chr3 | 149920041 | ||||||
| chr3:149920212 | T | C | 1 | a0001c0002t0006g0006 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.607-922T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 7/9 | chr3 | 149920212 | ||||||
| chr3:149920373 | C | A | 181 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0054others(178): Show | 181 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.607-761C>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 7/9 | chr3 | 149920373 | ||||||
| chr3:149920393 | G | A | 1 | a0001c0001t0001g0229 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.607-741G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 7/9 | chr3 | 149920393 | ||||||
| chr3:149920409 | T | C | 1 | a0001c0001t0001g0181 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.607-725T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 7/9 | chr3 | 149920409 | ||||||
| chr3:149920421 | T | TG | 13 | a0001c0001t0001g0239a0001c0002t0003g0238a0001c0002t0003g0254others(10): Show | 13 | HG00280.hp2 HG01106.hp1 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.607-709dupG | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr3 | 149920421 | |||||
| chr3:149920684 | T | C | 2 | a0003c0004t0008g0199a0003c0004t0008g0200 | 2 | HG03098.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.607-450T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 7/9 | chr3 | 149920684 | ||||||
| chr3:149920790 | C | CT | 149 | a0001c0001t0001g0010a0001c0001t0001g0022a0001c0001t0001g0024others(146): Show | 149 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.607-325dupT | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr3 | 149920790 | |||||
| chr3:149920790 | C | CTT | 36 | a0001c0001t0001g0015a0001c0001t0001g0058a0001c0001t0001g0059others(33): Show | 36 | HG00323.hp1 HG00621.hp2 HG00741.hp2 others(33): Show |
intron_variant | MODIFIER | c.607-326_607-325dup others(2): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr3 | 149920790 | |||||
| chr3:149920790 | CT | C | 12 | a0001c0001t0001g0245a0001c0002t0001g0251a0001c0002t0002g0240others(9): Show | 12 | HG01496.hp1 HG02109.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.607-325delT | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr3 | 149920790 | |||||
| chr3:149920994 | A | G | 1 | a0001c0002t0002g0012 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.607-140A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 7/9 | chr3 | 149920994 | ||||||
| chr3:149921295 | A | C | 1 | a0001c0002t0002g0039 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.700+68A>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149921295 | ||||||
| chr3:149921317 | T | C | 1 | a0001c0001t0001g0117 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.700+90T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149921317 | ||||||
| chr3:149921350 | G | C | 1 | a0001c0002t0009g0121 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.700+123G>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149921350 | ||||||
| chr3:149921357 | T | C | 1 | a0001c0002t0002g0248 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.700+130T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149921357 | ||||||
| chr3:149921464 | C | G | 11 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0002t0002g0020others(8): Show | 11 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.700+237C>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149921464 | ||||||
| chr3:149921543 | C | T | 1 | a0001c0002t0004g0018 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.700+316C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149921543 | ||||||
| chr3:149921701 | T | C | 9 | a0001c0001t0001g0245a0001c0002t0002g0240a0001c0002t0002g0241others(6): Show | 9 | HG01496.hp1 HG02109.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.700+474T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149921701 | ||||||
| chr3:149921909 | C | A | 2 | a0001c0002t0003g0255a0001c0002t0003g0264 | 2 | HG02698.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.700+682C>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149921909 | ||||||
| chr3:149922010 | G | T | 2 | a0001c0001t0001g0239a0001c0002t0003g0238 | 2 | HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.700+783G>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149922010 | ||||||
| chr3:149922059 | C | T | 2 | a0001c0002t0002g0278a0001c0002t0002g0279 | 2 | HG00140.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.700+832C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149922059 | ||||||
| chr3:149922061 | C | T | 5 | a0001c0001t0001g0119a0001c0001t0001g0143a0001c0001t0001g0163others(2): Show | 5 | HG00323.hp2 HG01175.hp2 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.700+834C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149922061 | ||||||
| chr3:149922098 | C | T | 1 | a0001c0001t0001g0147 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.700+871C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149922098 | ||||||
| chr3:149922757 | A | G | 1 | a0001c0002t0002g0045 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.700+1530A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149922757 | ||||||
| chr3:149922842 | C | T | 2 | a0001c0002t0006g0236a0001c0002t0006g0237 | 2 | HG02896.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.700+1615C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149922842 | ||||||
| chr3:149923256 | T | G | 2 | a0001c0001t0001g0015a0001c0002t0003g0101 | 2 | HG02738.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.700+2029T>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149923256 | ||||||
| chr3:149923413 | C | G | 3 | a0001c0001t0001g0156a0001c0001t0001g0160a0001c0001t0001g0173 | 3 | HG00733.hp2 HG00735.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.700+2186C>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149923413 | ||||||
| chr3:149923659 | A | G | 238 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0022others(235): Show | 238 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.700+2432A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149923659 | ||||||
| chr3:149923764 | C | CA | 22 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0001t0001g0062others(19): Show | 22 | HG00735.hp1 HG01071.hp1 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.700+2556dupA | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr3 | 149923764 | |||||
| chr3:149923935 | A | T | 1 | a0001c0002t0002g0039 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.700+2708A>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149923935 | ||||||
| chr3:149923970 | A | C | 2 | a0001c0001t0001g0042a0001c0002t0002g0044 | 2 | HG03942.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.700+2743A>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149923970 | ||||||
| chr3:149923999 | G | A | 11 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0002t0002g0020others(8): Show | 11 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.700+2772G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149923999 | ||||||
| chr3:149924014 | T | A | 1 | a0001c0001t0001g0173 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.700+2787T>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149924014 | ||||||
| chr3:149924108 | G | A | 2 | a0001c0002t0002g0265a0001c0002t0002g0266 | 2 | HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.700+2881G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149924108 | ||||||
| chr3:149924386 | G | A | 1 | a0001c0002t0002g0279 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.700+3159G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149924386 | ||||||
| chr3:149924478 | T | G | 1 | a0001c0001t0001g0076 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.700+3251T>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149924478 | ||||||
| chr3:149924659 | G | A | 2 | a0003c0004t0008g0199a0003c0004t0008g0200 | 2 | HG03098.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.700+3432G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149924659 | ||||||
| chr3:149924733 | A | G | 1 | a0001c0002t0002g0269 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.700+3506A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149924733 | ||||||
| chr3:149925010 | T | G | 1 | a0001c0002t0002g0012 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.700+3783T>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149925010 | ||||||
| chr3:149925080 | G | A | 2 | a0001c0002t0002g0268a0001c0002t0002g0269 | 2 | HG02145.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.700+3853G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149925080 | ||||||
| chr3:149925104 | G | T | 2 | a0002c0003t0001g0002a0002c0003t0001g0004 | 2 | HG02976.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.700+3877G>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149925104 | ||||||
| chr3:149925258 | G | A | 1 | a0001c0001t0001g0201 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.700+4031G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149925258 | ||||||
| chr3:149925399 | A | G | 9 | a0001c0001t0001g0245a0001c0002t0002g0240a0001c0002t0002g0241others(6): Show | 9 | HG01496.hp1 HG02109.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.700+4172A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149925399 | ||||||
| chr3:149925456 | C | T | 11 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0002t0002g0020others(8): Show | 11 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.700+4229C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149925456 | ||||||
| chr3:149925601 | C | T | 13 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0002t0002g0020others(10): Show | 13 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.700+4374C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149925601 | ||||||
| chr3:149925677 | G | T | 13 | a0001c0001t0001g0055a0001c0001t0001g0094a0001c0001t0001g0099others(10): Show | 13 | HG01167.hp2 HG01169.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.700+4450G>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149925677 | ||||||
| chr3:149925725 | C | T | 2 | a0003c0004t0008g0199a0003c0004t0008g0200 | 2 | HG03098.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.700+4498C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149925725 | ||||||
| chr3:149925987 | C | T | 2 | a0001c0002t0003g0255a0001c0002t0003g0264 | 2 | HG02698.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.700+4760C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149925987 | ||||||
| chr3:149926001 | C | T | 1 | a0001c0002t0002g0222 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.700+4774C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149926001 | ||||||
| chr3:149926322 | T | C | 1 | a0001c0001t0001g0196 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.700+5095T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149926322 | ||||||
| chr3:149926336 | C | T | 1 | a0001c0001t0001g0185 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.700+5109C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149926336 | ||||||
| chr3:149926431 | C | T | 2 | a0001c0002t0002g0265a0001c0002t0002g0266 | 2 | HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.700+5204C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149926431 | ||||||
| chr3:149926496 | C | T | 262 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0022others(259): Show | 262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.700+5269C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149926496 | ||||||
| chr3:149926836 | G | T | 1 | a0001c0002t0002g0026 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.700+5609G>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149926836 | ||||||
| chr3:149926943 | A | G | 1 | a0001c0001t0001g0125 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.700+5716A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149926943 | ||||||
| chr3:149927383 | A | G | 1 | a0001c0001t0001g0090 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.700+6156A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149927383 | ||||||
| chr3:149927667 | G | T | 238 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0022others(235): Show | 238 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.700+6440G>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149927667 | ||||||
| chr3:149927688 | T | C | 1 | a0001c0001t0001g0099 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.700+6461T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149927688 | ||||||
| chr3:149927754 | G | T | 6 | a0001c0002t0006g0005a0001c0002t0006g0006a0001c0002t0006g0007others(3): Show | 6 | HG02109.hp1 HG02258.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.700+6527G>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149927754 | ||||||
| chr3:149927801 | A | G | 4 | a0001c0001t0001g0105a0001c0001t0001g0110a0001c0001t0001g0111others(1): Show | 4 | HG02896.hp2 HG02922.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.700+6574A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149927801 | ||||||
| chr3:149927802 | A | T | 1 | a0001c0002t0003g0098 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.700+6575A>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149927802 | ||||||
| chr3:149928004 | C | CT | 32 | a0001c0001t0001g0024a0001c0001t0001g0028a0001c0001t0001g0055others(29): Show | 32 | HG00140.hp1 HG01167.hp2 HG01169.hp1 others(29): Show |
intron_variant | MODIFIER | c.700+6796dupT | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr3 | 149928004 | |||||
| chr3:149928004 | CT | C | 27 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0001t0001g0177others(24): Show | 27 | HG00280.hp2 HG00639.hp1 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.700+6796delT | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr3 | 149928004 | |||||
| chr3:149928066 | C | T | 1 | a0001c0002t0002g0266 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.700+6839C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149928066 | ||||||
| chr3:149928086 | A | G | 13 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0002t0002g0020others(10): Show | 13 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.700+6859A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149928086 | ||||||
| chr3:149928091 | C | T | 77 | a0001c0001t0001g0055a0001c0001t0001g0057a0001c0001t0001g0058others(74): Show | 77 | HG00323.hp1 HG00544.hp2 HG00621.hp2 others(74): Show |
intron_variant | MODIFIER | c.700+6864C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149928091 | ||||||
| chr3:149928243 | C | T | 1 | a0001c0002t0003g0256 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.700+7016C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149928243 | ||||||
| chr3:149928371 | C | T | 11 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0002t0002g0020others(8): Show | 11 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.700+7144C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149928371 | ||||||
| chr3:149928626 | T | A | 2 | a0001c0002t0002g0278a0001c0002t0002g0279 | 2 | HG00140.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.700+7399T>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149928626 | ||||||
| chr3:149929292 | G | A | 239 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0022others(236): Show | 239 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.700+8065G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149929292 | ||||||
| chr3:149929343 | C | G | 13 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0002t0002g0020others(10): Show | 13 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.700+8116C>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149929343 | ||||||
| chr3:149929350 | G | C | 37 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(34): Show | 37 | HG00323.hp1 HG00621.hp2 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.700+8123G>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149929350 | ||||||
| chr3:149929666 | AGTT | A | 4 | a0001c0002t0001g0251a0001c0002t0007g0249a0001c0002t0007g0250others(1): Show | 4 | HG02717.hp2 HG03130.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.700+8452_700+8454d others(5): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr3 | 149929666 | |||||
| chr3:149929703 | A | G | 2 | a0001c0002t0002g0268a0001c0002t0002g0269 | 2 | HG02145.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.700+8476A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149929703 | ||||||
| chr3:149929941 | C | T | 11 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0002t0002g0020others(8): Show | 11 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.700+8714C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149929941 | ||||||
| chr3:149929994 | C | T | 11 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0002t0002g0020others(8): Show | 11 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.700+8767C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149929994 | ||||||
| chr3:149930126 | A | G | 2 | a0001c0002t0002g0265a0001c0002t0002g0266 | 2 | HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.700+8899A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149930126 | ||||||
| chr3:149930305 | T | C | 1 | a0001c0001t0001g0234 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.700+9078T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149930305 | ||||||
| chr3:149930317 | C | T | 9 | a0001c0001t0012g0206a0001c0002t0005g0202a0001c0002t0005g0203others(6): Show | 9 | HG00639.hp1 HG00642.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.700+9090C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149930317 | ||||||
| chr3:149930322 | C | T | 1 | a0001c0001t0001g0191 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.700+9095C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149930322 | ||||||
| chr3:149930432 | G | A | 2 | a0001c0002t0006g0236a0001c0002t0006g0237 | 2 | HG02896.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.700+9205G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149930432 | ||||||
| chr3:149930724 | G | A | 1 | a0001c0002t0002g0227 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.700+9497G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149930724 | ||||||
| chr3:149930766 | G | A | 2 | a0001c0001t0001g0223a0001c0001t0001g0230 | 2 | NA18941.hp2 NA18943.hp1 |
intron_variant | MODIFIER | c.700+9539G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149930766 | ||||||
| chr3:149930907 | A | C | 13 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0002t0002g0020others(10): Show | 13 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.700+9680A>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149930907 | ||||||
| chr3:149930979 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.700+9752C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149930979 | ||||||
| chr3:149931138 | A | C | 1 | a0001c0001t0001g0180 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.700+9911A>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149931138 | ||||||
| chr3:149931148 | C | T | 1 | a0001c0002t0002g0011 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.700+9921C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149931148 | ||||||
| chr3:149931276 | C | T | 1 | a0001c0001t0001g0184 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.700+10049C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149931276 | ||||||
| chr3:149931582 | T | C | 6 | a0001c0002t0002g0240a0001c0002t0002g0241a0001c0002t0002g0246others(3): Show | 6 | HG01496.hp1 HG02109.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.700+10355T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149931582 | ||||||
| chr3:149931718 | C | T | 2 | a0001c0002t0003g0258a0001c0002t0003g0259 | 2 | HG00280.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.700+10491C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149931718 | ||||||
| chr3:149931884 | C | A | 1 | a0001c0002t0002g0222 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.700+10657C>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149931884 | ||||||
| chr3:149931921 | C | T | 12 | a0001c0001t0001g0239a0001c0002t0003g0238a0001c0002t0003g0254others(9): Show | 12 | HG00280.hp2 HG01106.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.700+10694C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149931921 | ||||||
| chr3:149932016 | G | GT | 13 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0002t0002g0020others(10): Show | 13 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.700+10798dupT | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr3 | 149932016 | |||||
| chr3:149932025 | T | A | 1 | a0001c0001t0001g0099 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.700+10798T>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149932025 | ||||||
| chr3:149932099 | G | C | 1 | a0001c0001t0001g0090 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.700+10872G>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149932099 | ||||||
| chr3:149932224 | T | C | 86 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0056others(83): Show | 86 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.700+10997T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149932224 | ||||||
| chr3:149932234 | A | T | 1 | a0001c0001t0001g0054 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.700+11007A>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149932234 | ||||||
| chr3:149932350 | T | A | 1 | a0001c0001t0001g0232 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.700+11123T>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149932350 | ||||||
| chr3:149932390 | A | G | 2 | a0001c0002t0002g0268a0001c0002t0002g0269 | 2 | HG02145.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.700+11163A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149932390 | ||||||
| chr3:149932866 | T | G | 1 | a0001c0001t0001g0148 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.700+11639T>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149932866 | ||||||
| chr3:149933028 | C | G | 2 | a0001c0002t0002g0278a0001c0002t0002g0279 | 2 | HG00140.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.700+11801C>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149933028 | ||||||
| chr3:149933263 | C | CT | 5 | a0001c0001t0001g0065a0001c0002t0002g0268a0001c0002t0002g0269others(2): Show | 5 | HG01952.hp2 HG02145.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.700+12050dupT | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr3 | 149933263 | |||||
| chr3:149933277 | TA | T | 20 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0001t0001g0245others(17): Show | 20 | HG00735.hp1 HG01243.hp2 HG01496.hp1 others(17): Show |
intron_variant | MODIFIER | c.700+12053delA | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr3 | 149933277 | |||||
| chr3:149933278 | A | T | 218 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0054others(215): Show | 218 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.700+12051A>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149933278 | ||||||
| chr3:149933427 | G | A | 1 | a0001c0001t0001g0066 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.700+12200G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149933427 | ||||||
| chr3:149933515 | T | C | 1 | a0001c0001t0013g0158 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.700+12288T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149933515 | ||||||
| chr3:149933585 | CT | C | 90 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0056others(87): Show | 90 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.700+12374delT | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr3 | 149933585 | |||||
| chr3:149933734 | C | T | 6 | a0001c0002t0006g0005a0001c0002t0006g0006a0001c0002t0006g0007others(3): Show | 6 | HG02109.hp1 HG02258.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.700+12507C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149933734 | ||||||
| chr3:149933772 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.700+12545C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149933772 | ||||||
| chr3:149933830 | C | T | 2 | a0001c0002t0002g0265a0001c0002t0002g0266 | 2 | HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.700+12603C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149933830 | ||||||
| chr3:149934370 | ATTTC | A | 5 | a0001c0002t0003g0254a0001c0002t0003g0255a0001c0002t0003g0256others(2): Show | 5 | HG02145.hp1 HG02698.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.700+13149_700+1315 others(8): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr3 | 149934370 | |||||
| chr3:149934777 | C | T | 1 | a0001c0001t0001g0180 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.700+13550C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149934777 | ||||||
| chr3:149935591 | A | G | 2 | a0001c0001t0001g0073a0001c0001t0001g0074 | 2 | HG01993.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.700+14364A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149935591 | ||||||
| chr3:149935605 | A | T | 1 | a0001c0002t0002g0040 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.700+14378A>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149935605 | ||||||
| chr3:149935656 | C | A | 2 | a0001c0001t0001g0194a0001c0001t0001g0195 | 2 | HG01192.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.700+14429C>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149935656 | ||||||
| chr3:149935669 | T | C | 2 | a0001c0002t0006g0236a0001c0002t0006g0237 | 2 | HG02896.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.700+14442T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149935669 | ||||||
| chr3:149935716 | C | A | 11 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0002t0002g0020others(8): Show | 11 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.700+14489C>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149935716 | ||||||
| chr3:149935899 | T | C | 22 | a0001c0001t0001g0094a0001c0001t0001g0239a0001c0002t0003g0238others(19): Show | 22 | HG00280.hp2 HG01106.hp1 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.700+14672T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149935899 | ||||||
| chr3:149935949 | G | A | 1 | a0001c0001t0001g0125 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.700+14722G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149935949 | ||||||
| chr3:149936673 | C | A | 3 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079 | 3 | HG01192.hp1 HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.700+15446C>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149936673 | ||||||
| chr3:149937394 | C | T | 1 | a0001c0001t0001g0187 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.700+16167C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149937394 | ||||||
| chr3:149937610 | A | G | 1 | a0001c0001t0001g0193 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.700+16383A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149937610 | ||||||
| chr3:149937683 | G | A | 1 | a0001c0002t0001g0251 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.700+16456G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149937683 | ||||||
| chr3:149937915 | T | C | 3 | a0002c0003t0001g0002a0002c0003t0001g0003a0002c0003t0001g0004 | 3 | HG02976.hp2 HG03041.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.700+16688T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149937915 | ||||||
| chr3:149938163 | A | G | 1 | a0001c0002t0002g0012 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.700+16936A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149938163 | ||||||
| chr3:149938172 | T | A | 6 | a0001c0001t0001g0054a0001c0001t0001g0089a0001c0001t0001g0090others(3): Show | 6 | HG02647.hp1 HG02717.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.700+16945T>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149938172 | ||||||
| chr3:149938338 | C | T | 9 | a0001c0001t0012g0206a0001c0002t0005g0202a0001c0002t0005g0203others(6): Show | 9 | HG00639.hp1 HG00642.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.700+17111C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149938338 | ||||||
| chr3:149938490 | T | A | 1 | a0002c0003t0001g0003 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.700+17263T>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149938490 | ||||||
| chr3:149938764 | T | G | 21 | a0001c0001t0001g0054a0001c0001t0001g0089a0001c0001t0001g0090others(18): Show | 21 | HG01496.hp1 HG01891.hp1 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.700+17537T>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149938764 | ||||||
| chr3:149939046 | G | A | 2 | a0001c0002t0002g0265a0001c0002t0002g0266 | 2 | HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.700+17819G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149939046 | ||||||
| chr3:149939287 | A | C | 1 | a0001c0001t0001g0054 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.700+18060A>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149939287 | ||||||
| chr3:149939290 | A | G | 1 | a0001c0001t0001g0054 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.700+18063A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149939290 | ||||||
| chr3:149939521 | T | C | 2 | a0001c0002t0002g0265a0001c0002t0002g0266 | 2 | HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.700+18294T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149939521 | ||||||
| chr3:149939553 | G | A | 1 | a0001c0001t0001g0084 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.700+18326G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149939553 | ||||||
| chr3:149939585 | C | T | 1 | a0001c0001t0001g0106 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.700+18358C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149939585 | ||||||
| chr3:149939840 | G | A | 3 | a0001c0001t0001g0245a0001c0002t0002g0242a0001c0002t0002g0244 | 3 | HG02818.hp2 HG02886.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.700+18613G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149939840 | ||||||
| chr3:149939870 | G | A | 1 | a0001c0001t0001g0111 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.700+18643G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149939870 | ||||||
| chr3:149939871 | C | T | 1 | a0001c0001t0001g0192 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.700+18644C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149939871 | ||||||
| chr3:149940453 | T | C | 9 | a0001c0001t0012g0206a0001c0002t0005g0202a0001c0002t0005g0203others(6): Show | 9 | HG00639.hp1 HG00642.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.700+19226T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149940453 | ||||||
| chr3:149940817 | G | C | 1 | a0001c0002t0002g0246 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.701-19239G>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149940817 | ||||||
| chr3:149940995 | G | A | 2 | a0001c0002t0002g0265a0001c0002t0002g0266 | 2 | HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.701-19061G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149940995 | ||||||
| chr3:149941162 | G | T | 9 | a0001c0001t0001g0245a0001c0002t0002g0240a0001c0002t0002g0241others(6): Show | 9 | HG01496.hp1 HG02109.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.701-18894G>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149941162 | ||||||
| chr3:149941384 | G | C | 1 | a0006c0007t0001g0071 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.701-18672G>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149941384 | ||||||
| chr3:149941530 | G | GT | 6 | a0001c0002t0002g0047a0001c0002t0002g0273a0001c0002t0002g0278others(3): Show | 6 | HG01516.hp2 HG02027.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.701-18505dupT | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr3 | 149941530 | |||||
| chr3:149941530 | GTT | G | 9 | a0001c0001t0001g0022a0001c0002t0002g0020a0001c0002t0004g0013others(6): Show | 9 | HG00735.hp1 HG02622.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.701-18506_701-1850 others(6): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr3 | 149941530 | |||||
| chr3:149941541 | T | G | 222 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0027others(219): Show | 222 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.701-18515T>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149941541 | ||||||
| chr3:149941659 | C | T | 85 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0056others(82): Show | 85 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.701-18397C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149941659 | ||||||
| chr3:149941889 | A | ATATT | 3 | a0001c0002t0002g0012a0001c0002t0002g0041a0003c0004t0008g0200 | 3 | HG03098.hp1 HG03139.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.701-18140_701-1813 others(8): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr3 | 149941889 | |||||
| chr3:149941889 | A | ATATTTAT others(1): Show |
16 | a0001c0002t0003g0258a0001c0002t0003g0259a0001c0002t0003g0260others(13): Show | 16 | HG00280.hp2 HG01106.hp1 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.701-18144_701-1813 others(12): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr3 | 149941889 | |||||
| chr3:149941889 | A | ATATTTAT others(5): Show |
148 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0022others(145): Show | 148 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.701-18148_701-1813 others(16): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr3 | 149941889 | |||||
| chr3:149941889 | A | ATATTTAT others(9): Show |
49 | a0001c0001t0001g0027a0001c0001t0001g0058a0001c0001t0001g0059others(46): Show | 49 | HG00323.hp1 HG00544.hp2 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.701-18152_701-1813 others(20): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr3 | 149941889 | |||||
| chr3:149941889 | A | ATATTTAT others(13): Show |
17 | a0001c0001t0001g0028a0001c0001t0001g0054a0001c0001t0001g0055others(14): Show | 17 | HG01167.hp2 HG01169.hp1 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.701-18156_701-1813 others(24): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr3 | 149941889 | |||||
| chr3:149942129 | T | C | 1 | a0001c0001t0013g0158 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.701-17927T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149942129 | ||||||
| chr3:149942242 | T | C | 7 | a0001c0001t0001g0105a0001c0001t0001g0110a0001c0001t0001g0111others(4): Show | 7 | HG02896.hp2 HG02922.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.701-17814T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149942242 | ||||||
| chr3:149942382 | G | A | 2 | a0001c0002t0003g0256a0001c0002t0003g0257 | 2 | HG02145.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.701-17674G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149942382 | ||||||
| chr3:149942688 | A | C | 40 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0057others(37): Show | 40 | HG00323.hp1 HG00621.hp2 HG00741.hp2 others(37): Show |
intron_variant | MODIFIER | c.701-17368A>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149942688 | ||||||
| chr3:149942816 | A | G | 11 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0002t0002g0020others(8): Show | 11 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.701-17240A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149942816 | ||||||
| chr3:149942938 | T | C | 1 | a0001c0001t0001g0180 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.701-17118T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149942938 | ||||||
| chr3:149943035 | A | T | 2 | a0001c0002t0002g0268a0001c0002t0002g0269 | 2 | HG02145.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.701-17021A>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149943035 | ||||||
| chr3:149943079 | T | G | 9 | a0001c0001t0012g0206a0001c0002t0005g0202a0001c0002t0005g0203others(6): Show | 9 | HG00639.hp1 HG00642.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.701-16977T>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149943079 | ||||||
| chr3:149943220 | CT | C | 21 | a0001c0001t0001g0075a0001c0001t0001g0154a0001c0001t0001g0176others(18): Show | 21 | HG00280.hp2 HG01106.hp1 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.701-16821delT | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr3 | 149943220 | |||||
| chr3:149943308 | C | G | 11 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0002t0002g0020others(8): Show | 11 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.701-16748C>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149943308 | ||||||
| chr3:149943542 | C | A | 1 | a0001c0002t0002g0011 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.701-16514C>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149943542 | ||||||
| chr3:149943559 | C | T | 1 | a0001c0002t0002g0044 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.701-16497C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149943559 | ||||||
| chr3:149943652 | C | T | 1 | a0001c0002t0002g0246 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.701-16404C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149943652 | ||||||
| chr3:149943810 | CT | C | 9 | a0001c0001t0012g0206a0001c0002t0005g0202a0001c0002t0005g0203others(6): Show | 9 | HG00639.hp1 HG00642.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.701-16235delT | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr3 | 149943810 | |||||
| chr3:149943815 | T | C | 2 | a0001c0002t0002g0268a0001c0002t0002g0269 | 2 | HG02145.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.701-16241T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149943815 | ||||||
| chr3:149943854 | C | T | 1 | a0001c0001t0001g0015 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.701-16202C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149943854 | ||||||
| chr3:149943874 | C | A | 3 | a0001c0002t0003g0091a0001c0002t0003g0092a0001c0002t0003g0093 | 3 | HG02717.hp1 HG02886.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.701-16182C>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149943874 | ||||||
| chr3:149943919 | G | A | 1 | a0001c0002t0006g0253 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.701-16137G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149943919 | ||||||
| chr3:149944008 | A | G | 1 | a0001c0001t0001g0054 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.701-16048A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149944008 | ||||||
| chr3:149944060 | TGTTTG | T | 11 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0002t0002g0020others(8): Show | 11 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.701-15991_701-1598 others(9): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr3 | 149944060 | |||||
| chr3:149944083 | T | C | 11 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0002t0002g0020others(8): Show | 11 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.701-15973T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149944083 | ||||||
| chr3:149944096 | A | T | 11 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0002t0002g0020others(8): Show | 11 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.701-15960A>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149944096 | ||||||
| chr3:149944338 | T | A | 1 | a0001c0001t0001g0120 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.701-15718T>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149944338 | ||||||
| chr3:149944344 | T | G | 2 | a0001c0002t0002g0268a0001c0002t0002g0269 | 2 | HG02145.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.701-15712T>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149944344 | ||||||
| chr3:149944438 | A | T | 241 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0022others(238): Show | 241 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.701-15618A>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149944438 | ||||||
| chr3:149944563 | G | A | 1 | a0001c0001t0001g0148 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.701-15493G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149944563 | ||||||
| chr3:149944634 | C | T | 2 | a0003c0004t0008g0199a0003c0004t0008g0200 | 2 | HG03098.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.701-15422C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149944634 | ||||||
| chr3:149944753 | C | G | 3 | a0001c0002t0007g0249a0001c0002t0007g0250a0001c0002t0007g0252 | 3 | HG02717.hp2 HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.701-15303C>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149944753 | ||||||
| chr3:149944852 | G | T | 39 | a0001c0001t0001g0056a0001c0001t0001g0119a0001c0001t0001g0125others(36): Show | 39 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(36): Show |
intron_variant | MODIFIER | c.701-15204G>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149944852 | ||||||
| chr3:149944853 | C | G | 39 | a0001c0001t0001g0056a0001c0001t0001g0119a0001c0001t0001g0125others(36): Show | 39 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(36): Show |
intron_variant | MODIFIER | c.701-15203C>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149944853 | ||||||
| chr3:149944910 | C | T | 2 | a0001c0002t0002g0268a0001c0002t0002g0269 | 2 | HG02145.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.701-15146C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149944910 | ||||||
| chr3:149944950 | G | A | 19 | a0001c0001t0001g0239a0001c0002t0003g0238a0001c0002t0003g0254others(16): Show | 19 | HG00280.hp2 HG01106.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.701-15106G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149944950 | ||||||
| chr3:149945111 | G | C | 1 | a0001c0001t0002g0188 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.701-14945G>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149945111 | ||||||
| chr3:149945132 | T | C | 1 | a0007c0008t0002g0243 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.701-14924T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149945132 | ||||||
| chr3:149945163 | G | T | 1 | a0001c0001t0001g0079 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.701-14893G>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149945163 | ||||||
| chr3:149945189 | A | G | 2 | a0001c0002t0002g0265a0001c0002t0002g0266 | 2 | HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.701-14867A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149945189 | ||||||
| chr3:149945323 | C | A | 3 | a0001c0002t0007g0249a0001c0002t0007g0250a0001c0002t0007g0252 | 3 | HG02717.hp2 HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.701-14733C>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149945323 | ||||||
| chr3:149945337 | C | T | 3 | a0001c0001t0001g0104a0001c0001t0001g0107a0001c0001t0001g0112 | 3 | HG02965.hp2 HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.701-14719C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149945337 | ||||||
| chr3:149945408 | A | G | 1 | a0001c0001t0001g0189 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.701-14648A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149945408 | ||||||
| chr3:149945425 | C | T | 3 | a0001c0002t0002g0011a0003c0004t0008g0199a0003c0004t0008g0200 | 3 | HG00741.hp1 HG03098.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.701-14631C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149945425 | ||||||
| chr3:149945556 | T | C | 1 | a0001c0001t0001g0168 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.701-14500T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149945556 | ||||||
| chr3:149945591 | T | G | 1 | a0001c0001t0001g0064 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.701-14465T>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149945591 | ||||||
| chr3:149945684 | C | T | 1 | a0002c0003t0001g0003 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.701-14372C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149945684 | ||||||
| chr3:149945755 | T | A | 226 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0027others(223): Show | 226 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.701-14301T>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149945755 | ||||||
| chr3:149945756 | C | G | 226 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0027others(223): Show | 226 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.701-14300C>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149945756 | ||||||
| chr3:149945862 | T | C | 1 | a0001c0001t0001g0094 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.701-14194T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149945862 | ||||||
| chr3:149946211 | A | G | 1 | a0001c0002t0002g0040 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.701-13845A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149946211 | ||||||
| chr3:149946439 | A | G | 3 | a0001c0002t0003g0091a0001c0002t0003g0092a0001c0002t0003g0093 | 3 | HG02717.hp1 HG02886.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.701-13617A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149946439 | ||||||
| chr3:149946658 | C | T | 1 | a0001c0001t0001g0144 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.701-13398C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149946658 | ||||||
| chr3:149946822 | C | G | 1 | a0001c0001t0001g0157 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.701-13234C>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149946822 | ||||||
| chr3:149947026 | G | T | 3 | a0001c0002t0007g0249a0001c0002t0007g0250a0001c0002t0007g0252 | 3 | HG02717.hp2 HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.701-13030G>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149947026 | ||||||
| chr3:149947128 | A | G | 2 | a0001c0002t0006g0236a0001c0002t0006g0237 | 2 | HG02896.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.701-12928A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149947128 | ||||||
| chr3:149947407 | C | CT | 9 | a0001c0002t0002g0011a0001c0002t0002g0045a0001c0002t0002g0046others(6): Show | 9 | HG00642.hp2 HG00741.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.701-12635dupT | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr3 | 149947407 | |||||
| chr3:149947427 | C | T | 9 | a0001c0001t0012g0206a0001c0002t0005g0202a0001c0002t0005g0203others(6): Show | 9 | HG00639.hp1 HG00642.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.701-12629C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149947427 | ||||||
| chr3:149947492 | G | C | 241 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0022others(238): Show | 241 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.701-12564G>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149947492 | ||||||
| chr3:149947631 | C | G | 6 | a0001c0001t0001g0150a0001c0001t0001g0169a0001c0001t0001g0170others(3): Show | 6 | HG02523.hp1 NA18950.hp1 NA18998.hp1 others(3): Show |
intron_variant | MODIFIER | c.701-12425C>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149947631 | ||||||
| chr3:149947689 | C | T | 1 | a0001c0002t0001g0251 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.701-12367C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149947689 | ||||||
| chr3:149947984 | C | G | 2 | a0001c0001t0001g0155a0001c0001t0001g0159 | 2 | HG01099.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.701-12072C>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149947984 | ||||||
| chr3:149948012 | C | T | 1 | a0001c0002t0002g0271 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.701-12044C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149948012 | ||||||
| chr3:149948217 | G | A | 2 | a0001c0001t0001g0146a0001c0001t0001g0166 | 2 | HG01978.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.701-11839G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149948217 | ||||||
| chr3:149948239 | G | A | 9 | a0001c0001t0012g0206a0001c0002t0005g0202a0001c0002t0005g0203others(6): Show | 9 | HG00639.hp1 HG00642.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.701-11817G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149948239 | ||||||
| chr3:149948264 | A | G | 2 | a0001c0002t0002g0268a0001c0002t0002g0269 | 2 | HG02145.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.701-11792A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149948264 | ||||||
| chr3:149948306 | A | G | 1 | a0001c0001t0001g0064 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.701-11750A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149948306 | ||||||
| chr3:149948420 | G | A | 3 | a0001c0002t0007g0249a0001c0002t0007g0250a0001c0002t0007g0252 | 3 | HG02717.hp2 HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.701-11636G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149948420 | ||||||
| chr3:149948633 | A | C | 241 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0022others(238): Show | 241 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.701-11423A>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149948633 | ||||||
| chr3:149949227 | G | A | 1 | a0001c0001t0001g0028 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.701-10829G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149949227 | ||||||
| chr3:149949328 | A | AC | 3 | a0001c0001t0001g0216a0001c0002t0002g0011a0001c0002t0002g0268 | 3 | HG00741.hp1 HG02145.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.701-10726dupC | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr3 | 149949328 | |||||
| chr3:149949342 | G | T | 1 | a0001c0001t0001g0196 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.701-10714G>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149949342 | ||||||
| chr3:149949429 | C | CT | 8 | a0001c0001t0001g0201a0001c0001t0001g0233a0001c0002t0002g0012others(5): Show | 8 | HG02717.hp2 HG02723.hp1 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.701-10613dupT | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr3 | 149949429 | |||||
| chr3:149949429 | CTTT | C | 10 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0002t0002g0020others(7): Show | 10 | HG00735.hp1 HG02622.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.701-10615_701-1061 others(7): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr3 | 149949429 | |||||
| chr3:149949639 | C | A | 80 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0055others(77): Show | 80 | HG00323.hp1 HG00544.hp2 HG00621.hp2 others(77): Show |
intron_variant | MODIFIER | c.701-10417C>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149949639 | ||||||
| chr3:149949983 | G | A | 2 | a0001c0002t0002g0268a0001c0002t0002g0269 | 2 | HG02145.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.701-10073G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149949983 | ||||||
| chr3:149950229 | G | A | 174 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0027others(171): Show | 174 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.701-9827G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149950229 | ||||||
| chr3:149950285 | C | G | 5 | a0001c0002t0002g0265a0001c0002t0002g0266a0001c0002t0007g0249others(2): Show | 5 | HG02717.hp2 HG02723.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.701-9771C>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149950285 | ||||||
| chr3:149950285 | CTGTT | C | 179 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0027others(176): Show | 179 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.701-9767_701-9764d others(6): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr3 | 149950285 | |||||
| chr3:149950287 | G | A | 15 | a0001c0001t0001g0245a0001c0002t0002g0240a0001c0002t0002g0241others(12): Show | 15 | HG01496.hp1 HG02109.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.701-9769G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149950287 | ||||||
| chr3:149950316 | C | T | 6 | a0001c0002t0006g0005a0001c0002t0006g0006a0001c0002t0006g0007others(3): Show | 6 | HG02109.hp1 HG02258.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.701-9740C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149950316 | ||||||
| chr3:149950362 | T | A | 1 | a0001c0001t0001g0072 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.701-9694T>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149950362 | ||||||
| chr3:149950423 | G | C | 3 | a0002c0003t0001g0002a0002c0003t0001g0003a0002c0003t0001g0004 | 3 | HG02976.hp2 HG03041.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.701-9633G>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149950423 | ||||||
| chr3:149950599 | T | C | 275 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0022others(272): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.701-9457T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149950599 | ||||||
| chr3:149950641 | AT | A | 9 | a0001c0001t0012g0206a0001c0002t0005g0202a0001c0002t0005g0203others(6): Show | 9 | HG00639.hp1 HG00642.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.701-9401delT | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr3 | 149950641 | |||||
| chr3:149950698 | A | G | 6 | a0001c0002t0006g0005a0001c0002t0006g0006a0001c0002t0006g0007others(3): Show | 6 | HG02109.hp1 HG02258.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.701-9358A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149950698 | ||||||
| chr3:149950844 | C | G | 5 | a0001c0002t0002g0265a0001c0002t0002g0266a0001c0002t0007g0249others(2): Show | 5 | HG02717.hp2 HG02723.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.701-9212C>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149950844 | ||||||
| chr3:149951052 | A | G | 2 | a0001c0001t0001g0107a0001c0001t0001g0112 | 2 | HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.701-9004A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149951052 | ||||||
| chr3:149951098 | A | G | 9 | a0001c0001t0012g0206a0001c0002t0005g0202a0001c0002t0005g0203others(6): Show | 9 | HG00639.hp1 HG00642.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.701-8958A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149951098 | ||||||
| chr3:149951276 | T | C | 16 | a0001c0001t0001g0119a0001c0001t0001g0132a0001c0001t0001g0139others(13): Show | 16 | HG00140.hp1 HG00323.hp2 HG00642.hp1 others(13): Show |
intron_variant | MODIFIER | c.701-8780T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149951276 | ||||||
| chr3:149951545 | T | G | 2 | a0001c0002t0002g0268a0001c0002t0002g0269 | 2 | HG02145.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.701-8511T>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149951545 | ||||||
| chr3:149951628 | G | A | 4 | a0001c0001t0001g0239a0001c0002t0003g0238a0001c0002t0003g0258others(1): Show | 4 | HG00280.hp2 HG01106.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.701-8428G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149951628 | ||||||
| chr3:149951699 | G | T | 2 | a0001c0002t0002g0265a0001c0002t0002g0266 | 2 | HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.701-8357G>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149951699 | ||||||
| chr3:149952097 | G | C | 2 | a0001c0002t0002g0265a0001c0002t0002g0266 | 2 | HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.701-7959G>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149952097 | ||||||
| chr3:149952391 | A | G | 1 | a0001c0002t0002g0012 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.701-7665A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149952391 | ||||||
| chr3:149952420 | G | A | 1 | a0001c0001t0001g0223 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.701-7636G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149952420 | ||||||
| chr3:149952493 | A | C | 3 | a0001c0002t0007g0249a0001c0002t0007g0250a0001c0002t0007g0252 | 3 | HG02717.hp2 HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.701-7563A>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149952493 | ||||||
| chr3:149952605 | C | CTT | 6 | a0001c0002t0006g0005a0001c0002t0006g0006a0001c0002t0006g0007others(3): Show | 6 | HG02109.hp1 HG02258.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.701-7441_701-7440d others(4): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr3 | 149952605 | |||||
| chr3:149952612 | T | A | 1 | a0001c0001t0001g0059 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.701-7444T>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149952612 | ||||||
| chr3:149952639 | G | A | 191 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0027others(188): Show | 191 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.701-7417G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149952639 | ||||||
| chr3:149953114 | A | AT | 15 | a0001c0001t0001g0245a0001c0002t0002g0240a0001c0002t0002g0241others(12): Show | 15 | HG01496.hp1 HG02109.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.701-6930dupT | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr3 | 149953114 | |||||
| chr3:149953114 | AT | A | 9 | a0001c0001t0012g0206a0001c0002t0005g0202a0001c0002t0005g0203others(6): Show | 9 | HG00639.hp1 HG00642.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.701-6930delT | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr3 | 149953114 | |||||
| chr3:149953116 | T | C | 2 | a0001c0002t0006g0236a0001c0002t0006g0237 | 2 | HG02896.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.701-6940T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149953116 | ||||||
| chr3:149953135 | T | C | 2 | a0001c0002t0002g0265a0001c0002t0002g0266 | 2 | HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.701-6921T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149953135 | ||||||
| chr3:149953352 | A | G | 2 | a0003c0004t0008g0199a0003c0004t0008g0200 | 2 | HG03098.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.701-6704A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149953352 | ||||||
| chr3:149953623 | C | A | 2 | a0001c0001t0001g0070a0006c0007t0001g0071 | 2 | HG01255.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.701-6433C>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149953623 | ||||||
| chr3:149953637 | T | G | 3 | a0001c0001t0001g0084a0001c0001t0001g0167a0001c0001t0001g0168 | 3 | NA19064.hp2 NA19070.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.701-6419T>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149953637 | ||||||
| chr3:149954105 | A | T | 1 | a0001c0001t0001g0221 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.701-5951A>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149954105 | ||||||
| chr3:149954131 | G | A | 1 | a0001c0001t0001g0175 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.701-5925G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149954131 | ||||||
| chr3:149954352 | A | G | 69 | a0001c0001t0001g0055a0001c0001t0001g0072a0001c0001t0001g0082others(66): Show | 69 | HG00280.hp1 HG00280.hp2 HG00621.hp2 others(66): Show |
intron_variant | MODIFIER | c.701-5704A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149954352 | ||||||
| chr3:149954403 | T | A | 6 | a0001c0002t0005g0202a0001c0002t0005g0203a0001c0002t0005g0204others(3): Show | 6 | HG00639.hp1 HG00642.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.701-5653T>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149954403 | ||||||
| chr3:149954800 | T | C | 1 | a0001c0001t0001g0095 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.701-5256T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149954800 | ||||||
| chr3:149955423 | C | T | 1 | a0001c0002t0003g0093 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.701-4633C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149955423 | ||||||
| chr3:149955537 | A | G | 1 | a0001c0001t0001g0083 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.701-4519A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149955537 | ||||||
| chr3:149955815 | C | T | 9 | a0001c0002t0004g0013a0001c0002t0004g0014a0001c0002t0004g0016others(6): Show | 9 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.701-4241C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149955815 | ||||||
| chr3:149955951 | A | G | 1 | a0001c0002t0002g0040 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.701-4105A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149955951 | ||||||
| chr3:149956043 | C | T | 9 | a0001c0002t0004g0013a0001c0002t0004g0014a0001c0002t0004g0016others(6): Show | 9 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.701-4013C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149956043 | ||||||
| chr3:149956099 | A | C | 14 | a0001c0002t0002g0240a0001c0002t0002g0241a0001c0002t0002g0242others(11): Show | 14 | HG01496.hp1 HG02109.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.701-3957A>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149956099 | ||||||
| chr3:149956462 | G | T | 9 | a0001c0002t0004g0013a0001c0002t0004g0014a0001c0002t0004g0016others(6): Show | 9 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.701-3594G>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149956462 | ||||||
| chr3:149956567 | C | T | 2 | a0001c0001t0001g0155a0001c0001t0001g0159 | 2 | HG01099.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.701-3489C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149956567 | ||||||
| chr3:149956568 | A | G | 26 | a0001c0001t0001g0054a0001c0001t0001g0225a0001c0002t0003g0085others(23): Show | 26 | HG00280.hp2 HG01071.hp1 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.701-3488A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149956568 | ||||||
| chr3:149956609 | T | C | 2 | a0001c0002t0002g0222a0001c0002t0002g0227 | 2 | NA18961.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.701-3447T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149956609 | ||||||
| chr3:149956682 | T | C | 9 | a0001c0002t0004g0013a0001c0002t0004g0014a0001c0002t0004g0016others(6): Show | 9 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.701-3374T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149956682 | ||||||
| chr3:149956728 | C | G | 1 | a0001c0001t0001g0139 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.701-3328C>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149956728 | ||||||
| chr3:149956844 | G | T | 9 | a0001c0001t0001g0024a0001c0001t0001g0123a0001c0001t0001g0126others(6): Show | 9 | HG00621.hp1 HG02559.hp2 NA18747.hp2 others(6): Show |
intron_variant | MODIFIER | c.701-3212G>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149956844 | ||||||
| chr3:149956950 | T | G | 1 | a0001c0001t0001g0022 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.701-3106T>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149956950 | ||||||
| chr3:149957048 | T | C | 1 | a0001c0002t0001g0033 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.701-3008T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149957048 | ||||||
| chr3:149957231 | G | A | 1 | a0001c0002t0001g0251 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.701-2825G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149957231 | ||||||
| chr3:149957236 | A | G | 8 | a0001c0002t0002g0240a0001c0002t0002g0241a0001c0002t0002g0242others(5): Show | 8 | HG01496.hp1 HG02109.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.701-2820A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149957236 | ||||||
| chr3:149957331 | T | C | 5 | a0001c0002t0002g0011a0001c0002t0002g0012a0001c0002t0006g0236others(2): Show | 5 | HG00741.hp1 HG02896.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.701-2725T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149957331 | ||||||
| chr3:149957397 | G | A | 1 | a0001c0002t0006g0253 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.701-2659G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149957397 | ||||||
| chr3:149957398 | C | CT | 105 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0022others(102): Show | 106 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.701-2649dupT | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr3 | 149957398 | |||||
| chr3:149957458 | T | G | 5 | a0001c0002t0002g0265a0001c0002t0002g0266a0001c0002t0007g0249others(2): Show | 5 | HG02717.hp2 HG02723.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.701-2598T>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149957458 | ||||||
| chr3:149957637 | G | A | 1 | a0001c0001t0001g0182 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.701-2419G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149957637 | ||||||
| chr3:149957740 | C | G | 1 | a0003c0004t0008g0200 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.701-2316C>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149957740 | ||||||
| chr3:149957767 | C | T | 1 | a0001c0002t0002g0265 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.701-2289C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149957767 | ||||||
| chr3:149957885 | T | C | 9 | a0001c0002t0004g0013a0001c0002t0004g0014a0001c0002t0004g0016others(6): Show | 9 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.701-2171T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149957885 | ||||||
| chr3:149957952 | A | G | 2 | a0001c0002t0002g0052a0001c0002t0002g0053 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.701-2104A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149957952 | ||||||
| chr3:149957962 | A | G | 2 | a0001c0002t0002g0265a0001c0002t0002g0266 | 2 | HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.701-2094A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149957962 | ||||||
| chr3:149958102 | A | G | 1 | a0001c0002t0001g0251 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.701-1954A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149958102 | ||||||
| chr3:149958262 | C | A | 1 | a0001c0001t0013g0158 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.701-1794C>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149958262 | ||||||
| chr3:149958272 | G | A | 31 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0057others(28): Show | 31 | HG00323.hp1 HG00741.hp2 HG01070.hp1 others(28): Show |
intron_variant | MODIFIER | c.701-1784G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149958272 | ||||||
| chr3:149958314 | C | T | 9 | a0001c0002t0004g0013a0001c0002t0004g0014a0001c0002t0004g0016others(6): Show | 9 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.701-1742C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149958314 | ||||||
| chr3:149958882 | G | A | 3 | a0001c0002t0002g0020a0001c0002t0002g0268a0001c0002t0002g0269 | 3 | HG02145.hp2 HG02965.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.701-1174G>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149958882 | ||||||
| chr3:149958892 | T | G | 2 | a0001c0001t0001g0223a0001c0001t0001g0230 | 2 | NA18941.hp2 NA18943.hp1 |
intron_variant | MODIFIER | c.701-1164T>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149958892 | ||||||
| chr3:149958908 | A | C | 4 | a0001c0001t0012g0206a0002c0003t0001g0002a0002c0003t0001g0003others(1): Show | 4 | HG02723.hp2 HG02976.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.701-1148A>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149958908 | ||||||
| chr3:149959117 | G | C | 24 | a0001c0002t0003g0085a0001c0002t0003g0086a0001c0002t0003g0087others(21): Show | 24 | HG00280.hp2 HG01071.hp1 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.701-939G>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149959117 | ||||||
| chr3:149959311 | AAAAC | A | 3 | a0001c0002t0002g0020a0001c0002t0002g0268a0001c0002t0002g0269 | 3 | HG02145.hp2 HG02965.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.701-721_701-718del others(4): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr3 | 149959311 | |||||
| chr3:149959408 | TATG | T | 180 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0022others(177): Show | 180 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.701-645_701-643del others(3): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr3 | 149959408 | |||||
| chr3:149959639 | T | C | 23 | a0001c0002t0003g0085a0001c0002t0003g0086a0001c0002t0003g0087others(20): Show | 23 | HG00280.hp2 HG01071.hp1 HG01074.hp2 others(20): Show |
intron_variant | MODIFIER | c.701-417T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149959639 | ||||||
| chr3:149959643 | A | G | 3 | a0001c0002t0002g0020a0001c0002t0002g0268a0001c0002t0002g0269 | 3 | HG02145.hp2 HG02965.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.701-413A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149959643 | ||||||
| chr3:149959664 | ATAGT | A | 3 | a0001c0002t0002g0020a0001c0002t0002g0268a0001c0002t0002g0269 | 3 | HG02145.hp2 HG02965.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.701-389_701-386del others(4): Show |
RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr3 | 149959664 | |||||
| chr3:149959726 | A | G | 1 | a0001c0001t0001g0084 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.701-330A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149959726 | ||||||
| chr3:149960048 | G | C | 4 | a0001c0001t0001g0114a0001c0001t0001g0196a0001c0001t0001g0239others(1): Show | 4 | HG02622.hp2 HG03139.hp2 HG03195.hp2 others(1): Show |
splice_region_variant&intron_variant | LOW | c.701-8G>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 8/9 | chr3 | 149960048 | ||||||
| chr3:149960150 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.781+14C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 9/9 | chr3 | 149960150 | ||||||
| chr3:149960313 | C | T | 6 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0134others(3): Show | 6 | HG00544.hp1 NA18965.hp1 NA18975.hp2 others(3): Show |
intron_variant | MODIFIER | c.781+177C>T | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 9/9 | chr3 | 149960313 | ||||||
| chr3:149960341 | CA | C | 8 | a0001c0002t0002g0240a0001c0002t0002g0241a0001c0002t0002g0242others(5): Show | 8 | HG01496.hp1 HG02109.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.781+206delA | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 9/9 | chr3 | 149960341 | ||||||
| chr3:149960546 | T | C | 228 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0022others(225): Show | 229 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.782-194T>C | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 9/9 | chr3 | 149960546 | ||||||
| chr3:149960601 | T | A | 1 | a0001c0002t0002g0041 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.782-139T>A | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 9/9 | chr3 | 149960601 | ||||||
| chr3:149960641 | CAT | C | 3 | a0001c0002t0002g0020a0001c0002t0002g0268a0001c0002t0002g0269 | 3 | HG02145.hp2 HG02965.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.782-98_782-97delAT | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 9/9 | chr3 | 149960641 | ||||||
| chr3:149960688 | A | G | 2 | a0001c0001t0001g0082a0004c0005t0001g0081 | 2 | HG02922.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.782-52A>G | RNF13 | ENSG00000082996.20 | transcript | ENST00000392894.8 | protein_coding | 9/9 | chr3 | 149960688 |