Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 55298 |
| ensemblid | ENSG00000137522.18 |
| hgncid | 21070 |
| symbol | RNF121 |
| name | ring finger protein 121 |
| refseq_nuc | NM_018320.5 |
| refseq_prot | NP_060790.2 |
| ensembl_nuc | ENST00000361756.8 |
| ensembl_prot | ENSP00000354571.3 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 71929046 |
| end | 71997597 |
| strand | + |
| ver | v1.2 |
| region | chr11:71929046-71997597 |
| region5000 | chr11:71924046-72002597 |
| regionname0 | RNF121_chr11_71929046_71997597 |
| regionname5000 | RNF121_chr11_71924046_72002597 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 327 | 254 | 90 | 38 | 90 | 8 | 26 | 72 | RNF121_chr11_71924046_72002597 | RNF121 | copy fasta | chr11 | 71924046 | 72002597 |
| chapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 984 | 227 | 78 | 35 | 85 | 8 | 19 | RNF121_chr11_71924046_72002597 | RNF121 | copy fasta | chr11 | 71924046 | 72002597 | |
| c0002 | 0/0 | 984 | 14 | 0 | 2 | 5 | 0 | 7 | RNF121_chr11_71924046_72002597 | RNF121 | copy fasta | chr11 | 71924046 | 72002597 | |
| c0003 | 0/0 | 984 | 11 | 10 | 1 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | copy fasta | chr11 | 71924046 | 72002597 | |
| c0004 | 0/0 | 984 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | copy fasta | chr11 | 71924046 | 72002597 | |
| c0005 | 0/0 | 984 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | copy fasta | chr11 | 71924046 | 72002597 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 1297 | 121 | 26 | 26 | 47 | 6 | 15 | RNF121_chr11_71924046_72002597 | RNF121 | copy fasta | chr11 | 71924046 | 72002597 |
| t0002 | 1/0 | 1299 | 51 | 6 | 8 | 30 | 2 | 4 | RNF121_chr11_71924046_72002597 | RNF121 | copy fasta | chr11 | 71924046 | 72002597 |
| t0003 | 0/0 | 1299 | 17 | 15 | 2 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | copy fasta | chr11 | 71924046 | 72002597 |
| t0004 | 0/0 | 1297 | 14 | 14 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | copy fasta | chr11 | 71924046 | 72002597 |
| t0005 | 0/0 | 1297 | 14 | 14 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | copy fasta | chr11 | 71924046 | 72002597 |
| t0006 | 0/0 | 1297 | 13 | 0 | 2 | 5 | 0 | 6 | RNF121_chr11_71924046_72002597 | RNF121 | copy fasta | chr11 | 71924046 | 72002597 |
| t0007 | 0/0 | 1297 | 10 | 10 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | copy fasta | chr11 | 71924046 | 72002597 |
| t0008 | 0/0 | 1299 | 4 | 0 | 0 | 4 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | copy fasta | chr11 | 71924046 | 72002597 |
| t0009 | 0/0 | 1299 | 2 | 1 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | copy fasta | chr11 | 71924046 | 72002597 |
| t0010 | 0/0 | 1301 | 2 | 1 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | copy fasta | chr11 | 71924046 | 72002597 |
| t0011 | 0/0 | 1297 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | copy fasta | chr11 | 71924046 | 72002597 |
| t0012 | 0/0 | 1297 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | copy fasta | chr11 | 71924046 | 72002597 |
| t0013 | 0/0 | 1301 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | copy fasta | chr11 | 71924046 | 72002597 |
| t0014 | 0/0 | 1299 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | copy fasta | chr11 | 71924046 | 72002597 |
| t0015 | 0/0 | 1297 | 1 | 0 | 0 | 0 | 0 | 1 | RNF121_chr11_71924046_72002597 | RNF121 | copy fasta | chr11 | 71924046 | 72002597 |
| t0016 | 0/0 | 1299 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | copy fasta | chr11 | 71924046 | 72002597 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0006 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0045 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0088 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 984 | 227 | 78 | 35 | 85 | 8 | 19 | RNF121_chr11_71924046_72002597 | RNF121 | copy fasta | chr11 | 71924046 | 72002597 | |
| a0001c0002 | 0/0 | 984 | 14 | 0 | 2 | 5 | 0 | 7 | RNF121_chr11_71924046_72002597 | RNF121 | copy fasta | chr11 | 71924046 | 72002597 | |
| a0001c0003 | 0/0 | 984 | 11 | 10 | 1 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | copy fasta | chr11 | 71924046 | 72002597 | |
| a0001c0004 | 0/0 | 984 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | copy fasta | chr11 | 71924046 | 72002597 | |
| a0001c0005 | 0/0 | 984 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | copy fasta | chr11 | 71924046 | 72002597 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 2280 | 121 | 26 | 26 | 47 | 6 | 15 | RNF121_chr11_71924046_72002597 | RNF121 | copy fasta | chr11 | 71924046 | 72002597 |
| a0001c0001t0002 | 1/0 | 2282 | 51 | 6 | 8 | 30 | 2 | 4 | RNF121_chr11_71924046_72002597 | RNF121 | copy fasta | chr11 | 71924046 | 72002597 |
| a0001c0001t0003 | 0/0 | 2282 | 5 | 4 | 1 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | copy fasta | chr11 | 71924046 | 72002597 |
| a0001c0001t0004 | 0/0 | 2280 | 14 | 14 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | copy fasta | chr11 | 71924046 | 72002597 |
| a0001c0001t0005 | 0/0 | 2280 | 13 | 13 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | copy fasta | chr11 | 71924046 | 72002597 |
| a0001c0001t0007 | 0/0 | 2280 | 10 | 10 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | copy fasta | chr11 | 71924046 | 72002597 |
| a0001c0001t0008 | 0/0 | 2282 | 4 | 0 | 0 | 4 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | copy fasta | chr11 | 71924046 | 72002597 |
| a0001c0001t0009 | 0/0 | 2282 | 2 | 1 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | copy fasta | chr11 | 71924046 | 72002597 |
| a0001c0001t0010 | 0/0 | 2284 | 2 | 1 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | copy fasta | chr11 | 71924046 | 72002597 |
| a0001c0001t0011 | 0/0 | 2280 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | copy fasta | chr11 | 71924046 | 72002597 |
| a0001c0001t0012 | 0/0 | 2280 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | copy fasta | chr11 | 71924046 | 72002597 |
| a0001c0001t0013 | 0/0 | 2284 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | copy fasta | chr11 | 71924046 | 72002597 |
| a0001c0001t0014 | 0/0 | 2282 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | copy fasta | chr11 | 71924046 | 72002597 |
| a0001c0001t0016 | 0/0 | 2282 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | copy fasta | chr11 | 71924046 | 72002597 |
| a0001c0002t0006 | 0/0 | 2280 | 13 | 0 | 2 | 5 | 0 | 6 | RNF121_chr11_71924046_72002597 | RNF121 | copy fasta | chr11 | 71924046 | 72002597 |
| a0001c0002t0015 | 0/0 | 2280 | 1 | 0 | 0 | 0 | 0 | 1 | RNF121_chr11_71924046_72002597 | RNF121 | copy fasta | chr11 | 71924046 | 72002597 |
| a0001c0003t0003 | 0/0 | 2282 | 11 | 10 | 1 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | copy fasta | chr11 | 71924046 | 72002597 |
| a0001c0004t0005 | 0/0 | 2280 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | copy fasta | chr11 | 71924046 | 72002597 |
| a0001c0005t0003 | 0/0 | 2282 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | copy fasta | chr11 | 71924046 | 72002597 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0006 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0088 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0002g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0002g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0002g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0002g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0002g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0002g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0002g0045 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0003g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0003g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0003g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0003g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0003g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0004g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0004g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0004g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0004g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0004g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0004g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0004g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0004g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0004g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0004g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0004g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0004g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0004g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0004g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0005g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0005g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0005g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0005g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0005g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0005g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0005g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0005g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0005g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0005g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0005g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0005g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0005g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0007g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0007g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0007g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0007g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0007g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0007g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0007g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0008g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0008g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0008g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0008g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0009g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0009g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0010g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0010g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0011g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0012g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0013g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0014g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0001t0016g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0002t0006g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0002t0006g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0002t0006g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0002t0006g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0002t0006g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0002t0006g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0002t0006g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0002t0006g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0002t0006g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0002t0006g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0002t0006g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0002t0006g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0002t0006g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0002t0015g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0003t0003g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0003t0003g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0003t0003g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0003t0003g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0003t0003g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0003t0003g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0003t0003g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0003t0003g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0003t0003g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0003t0003g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0004t0005g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| a0001c0005t0003g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0031 | EUR | GBR | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0113 | EUR | GBR | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0108 | EUR | FIN | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0086 | EUR | FIN | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0026 | EUR | FIN | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0172 | EUR | FIN | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | CHS | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | CHS | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | CHS | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | CHS | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | CHS | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG00621 | hp2 | a0001 | c0001 | t0008 | g0029 | EAS | CHS | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0038 | EAS | CHS | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | CHS | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG00738 | hp1 | a0001 | c0002 | t0006 | g0223 | AMR | PUR | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG01074 | hp1 | a0001 | c0003 | t0003 | g0215 | AMR | PUR | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0053 | AMR | PUR | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0035 | AMR | PUR | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | CLM | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0245 | AMR | CLM | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | CLM | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0061 | AMR | CLM | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0023 | AMR | CLM | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | CLM | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PEL | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | PEL | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PEL | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG01975 | hp2 | a0001 | c0002 | t0006 | g0227 | AMR | PEL | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | PEL | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PEL | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG02004 | hp1 | a0001 | c0001 | t0003 | g0095 | AMR | PEL | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PEL | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0059 | EAS | KHV | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | KHV | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | KHV | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG02074 | hp2 | a0001 | c0001 | t0010 | g0055 | EAS | KHV | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG02083 | hp1 | a0001 | c0001 | t0012 | g0089 | EAS | KHV | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | KHV | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG02145 | hp1 | a0001 | c0001 | t0005 | g0241 | AFR | ACB | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0019 | AFR | ACB | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | PEL | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PEL | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | CDX | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | CDX | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG02258 | hp1 | a0001 | c0001 | t0007 | g0001 | AFR | ACB | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | ACB | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0044 | AMR | PEL | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | PEL | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG02280 | hp2 | a0001 | c0004 | t0005 | g0221 | AFR | ACB | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | PEL | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0046 | AMR | PEL | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PEL | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0051 | AMR | PEL | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | ACB | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG02451 | hp2 | a0001 | c0001 | t0004 | g0163 | AFR | ACB | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0158 | SAS | PJL | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | GWD | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG02615 | hp2 | a0001 | c0001 | t0007 | g0015 | AFR | GWD | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG02622 | hp1 | a0001 | c0001 | t0004 | g0170 | AFR | GWD | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | GWD | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG02630 | hp1 | a0001 | c0001 | t0007 | g0067 | AFR | GWD | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | GWD | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | GWD | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG02647 | hp2 | a0001 | c0001 | t0004 | g0161 | AFR | GWD | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0056 | SAS | PJL | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG02683 | hp2 | a0001 | c0002 | t0015 | g0229 | SAS | PJL | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG02717 | hp1 | a0001 | c0001 | t0007 | g0016 | AFR | GWD | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG02717 | hp2 | a0001 | c0001 | t0007 | g0002 | AFR | GWD | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG02723 | hp1 | a0001 | c0001 | t0014 | g0236 | AFR | GWD | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG02723 | hp2 | a0001 | c0001 | t0005 | g0201 | AFR | GWD | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG02735 | hp1 | a0001 | c0002 | t0006 | g0231 | SAS | PJL | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0210 | SAS | PJL | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0157 | SAS | PJL | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG02738 | hp2 | a0001 | c0002 | t0006 | g0234 | SAS | PJL | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0240 | AFR | GWD | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG02809 | hp2 | a0001 | c0003 | t0003 | g0214 | AFR | GWD | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG02818 | hp1 | a0001 | c0003 | t0003 | g0218 | AFR | GWD | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | GWD | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0022 | AFR | GWD | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG02886 | hp2 | a0001 | c0003 | t0003 | g0216 | AFR | GWD | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG02895 | hp1 | a0001 | c0001 | t0004 | g0069 | AFR | GWD | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG02895 | hp2 | a0001 | c0001 | t0003 | g0244 | AFR | GWD | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0239 | AFR | GWD | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG02896 | hp2 | a0001 | c0001 | t0005 | g0200 | AFR | GWD | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG02897 | hp1 | a0001 | c0001 | t0004 | g0070 | AFR | GWD | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG02897 | hp2 | a0001 | c0001 | t0005 | g0202 | AFR | GWD | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | ESN | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | ESN | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG02965 | hp1 | a0001 | c0003 | t0003 | g0211 | AFR | ESN | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | ESN | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG02970 | hp1 | a0001 | c0001 | t0003 | g0237 | AFR | ESN | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG02970 | hp2 | a0001 | c0001 | t0004 | g0169 | AFR | ESN | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG02976 | hp1 | a0001 | c0001 | t0005 | g0207 | AFR | ESN | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG02976 | hp2 | a0001 | c0001 | t0004 | g0166 | AFR | ESN | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0036 | SAS | PJL | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG03041 | hp1 | a0001 | c0001 | t0007 | g0014 | AFR | GWD | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG03041 | hp2 | a0001 | c0001 | t0005 | g0203 | AFR | GWD | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | MSL | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG03098 | hp2 | a0001 | c0001 | t0005 | g0206 | AFR | MSL | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | ESN | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG03130 | hp2 | a0001 | c0005 | t0003 | g0220 | AFR | ESN | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG03139 | hp1 | a0001 | c0003 | t0003 | g0008 | AFR | ESN | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | ESN | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | ESN | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG03195 | hp2 | a0001 | c0001 | t0004 | g0164 | AFR | ESN | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG03209 | hp1 | a0001 | c0001 | t0005 | g0205 | AFR | MSL | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG03225 | hp1 | a0001 | c0001 | t0005 | g0208 | AFR | MSL | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG03225 | hp2 | a0001 | c0001 | t0010 | g0021 | AFR | MSL | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0072 | SAS | PJL | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG03239 | hp2 | a0001 | c0002 | t0006 | g0230 | SAS | PJL | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG03453 | hp1 | a0001 | c0001 | t0004 | g0167 | AFR | MSL | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG03453 | hp2 | a0001 | c0001 | t0005 | g0242 | AFR | MSL | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG03486 | hp1 | a0001 | c0001 | t0007 | g0001 | AFR | MSL | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | MSL | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0150 | SAS | PJL | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0173 | SAS | PJL | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0154 | SAS | PJL | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG03516 | hp1 | a0001 | c0001 | t0005 | g0243 | AFR | ESN | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | ESN | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | GWD | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0024 | AFR | GWD | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG03579 | hp1 | a0001 | c0001 | t0004 | g0124 | AFR | MSL | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | MSL | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG03831 | hp1 | a0001 | c0002 | t0006 | g0224 | SAS | BEB | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0159 | SAS | BEB | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0034 | SAS | BEB | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0084 | SAS | BEB | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | BEB | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0062 | SAS | BEB | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG04115 | hp1 | a0001 | c0002 | t0006 | g0232 | SAS | STU | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0175 | SAS | STU | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | STU | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG04204 | hp2 | a0001 | c0002 | t0006 | g0228 | SAS | STU | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0018 | AFR | YRI | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| NA18522 | hp2 | a0001 | c0001 | t0004 | g0162 | AFR | YRI | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | CHB | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | CHB | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | YRI | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| NA18906 | hp2 | a0001 | c0001 | t0013 | g0238 | AFR | YRI | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| NA18980 | hp2 | a0001 | c0001 | t0009 | g0140 | EAS | JPT | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| NA18981 | hp2 | a0001 | c0002 | t0006 | g0225 | EAS | JPT | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| NA18986 | hp2 | a0001 | c0002 | t0006 | g0222 | EAS | JPT | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| NA18995 | hp1 | a0001 | c0002 | t0006 | g0233 | EAS | JPT | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| NA18997 | hp2 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| NA19007 | hp2 | a0001 | c0001 | t0016 | g0033 | EAS | JPT | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| NA19011 | hp1 | a0001 | c0001 | t0008 | g0037 | EAS | JPT | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| NA19030 | hp1 | a0001 | c0001 | t0005 | g0204 | AFR | LWK | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| NA19030 | hp2 | a0001 | c0003 | t0003 | g0217 | AFR | LWK | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| NA19043 | hp1 | a0001 | c0001 | t0004 | g0075 | AFR | LWK | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| NA19043 | hp2 | a0001 | c0001 | t0011 | g0137 | AFR | LWK | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| NA19056 | hp2 | a0001 | c0002 | t0006 | g0235 | EAS | JPT | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| NA19064 | hp1 | a0001 | c0001 | t0008 | g0043 | EAS | JPT | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| NA19072 | hp1 | a0001 | c0001 | t0008 | g0012 | EAS | JPT | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| NA19077 | hp1 | a0001 | c0002 | t0006 | g0226 | EAS | JPT | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| NA19078 | hp2 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| NA19240 | hp1 | a0001 | c0001 | t0007 | g0001 | AFR | YRI | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | YRI | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| NA20129 | hp1 | a0001 | c0001 | t0004 | g0165 | AFR | ASW | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ASW | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0097 | EUR | TSI | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0151 | EUR | TSI | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | CLM | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0066 | AMR | CLM | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG02109 | hp1 | a0001 | c0001 | t0007 | g0013 | AFR | ACB | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | ACB | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG02486 | hp1 | a0001 | c0003 | t0003 | g0213 | AFR | ACB | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG02486 | hp2 | a0001 | c0001 | t0009 | g0081 | AFR | ACB | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG02559 | hp1 | a0001 | c0003 | t0003 | g0219 | AFR | ACB | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | ACB | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG03471 | hp1 | a0001 | c0001 | t0007 | g0002 | AFR | MSL | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG03471 | hp2 | a0001 | c0003 | t0003 | g0008 | AFR | MSL | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0020 | AFR | USA | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| HG06807 | hp2 | a0001 | c0003 | t0003 | g0212 | AFR | USA | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0017 | AFR | USA | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| NA20300 | hp2 | a0001 | c0001 | t0004 | g0168 | AFR | USA | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| NA21309 | hp1 | a0001 | c0001 | t0005 | g0209 | AFR | LWK | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | LWK | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0088 | REF | REF | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0045 | REF | REF | RNF121_chr11_71924046_72002597 | RNF121 | chr11 | 71924046 | 72002597 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:71960759 | C | T | 1 | a0001c0005 | 1 | HG03130.hp2 | synonymous_variant | LOW | c.111C>T | p.His37His | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/9 | 127/2282 | 111/984 | 37/327 | chr11 | 71960759 | ||
| chr11:71990705 | A | G | 2 | a0001c0003a0001c0005 | 12 | HG01074.hp1 HG02486.hp1 HG02559.hp1 others(9): Show |
synonymous_variant | LOW | c.615A>G | p.Ala205Ala | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 6/9 | 631/2282 | 615/984 | 205/327 | chr11 | 71990705 | ||
| chr11:71990717 | G | A | 1 | a0001c0002 | 14 | HG00738.hp1 HG01975.hp2 HG02683.hp2 others(11): Show |
splice_region_variant&synonymous_variant | LOW | c.627G>A | p.Gly209Gly | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 6/9 | 643/2282 | 627/984 | 209/327 | chr11 | 71990717 | ||
| chr11:71995498 | A | G | 2 | a0001c0002a0001c0004 | 15 | HG00738.hp1 HG01975.hp2 HG02280.hp2 others(12): Show |
synonymous_variant | LOW | c.810A>G | p.Gln270Gln | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 8/9 | 826/2282 | 810/984 | 270/327 | chr11 | 71995498 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:71996419 | T | C | 14 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(11): Show | 186 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(183): Show |
3_prime_UTR_variant | MODIFIER | c.*104T>C | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 9/9 | 104 | chr11 | 71996419 | |||||
| chr11:71996420 | G | T | 2 | a0001c0002t0006a0001c0002t0015 | 14 | HG00738.hp1 HG01975.hp2 HG02683.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*105G>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 9/9 | 105 | chr11 | 71996420 | |||||
| chr11:71996443 | T | C | 15 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(12): Show | 196 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(193): Show |
3_prime_UTR_variant | MODIFIER | c.*128T>C | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 9/9 | 128 | chr11 | 71996443 | |||||
| chr11:71996471 | A | G | 1 | a0001c0001t0014 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*156A>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 9/9 | 156 | chr11 | 71996471 | |||||
| chr11:71996762 | G | A | 1 | a0001c0001t0011 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*447G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 9/9 | 447 | chr11 | 71996762 | |||||
| chr11:71996772 | C | T | 1 | a0001c0001t0014 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*457C>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 9/9 | 457 | chr11 | 71996772 | |||||
| chr11:71996773 | G | A | 1 | a0001c0001t0012 | 1 | HG02083.hp1 | 3_prime_UTR_variant | MODIFIER | c.*458G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 9/9 | 458 | chr11 | 71996773 | |||||
| chr11:71996967 | G | A | 5 | a0001c0001t0001a0001c0001t0004a0001c0001t0009others(2): Show | 139 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(136): Show |
3_prime_UTR_variant | MODIFIER | c.*652G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 9/9 | 652 | chr11 | 71996967 | |||||
| chr11:71996997 | C | A | 1 | a0001c0002t0015 | 1 | HG02683.hp2 | 3_prime_UTR_variant | MODIFIER | c.*682C>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 9/9 | 682 | chr11 | 71996997 | |||||
| chr11:71997154 | G | A | 2 | a0001c0002t0006a0001c0002t0015 | 14 | HG00738.hp1 HG01975.hp2 HG02683.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*839G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 9/9 | 839 | chr11 | 71997154 | |||||
| chr11:71997203 | C | CGT | 2 | a0001c0001t0010a0001c0001t0013 | 3 | HG02074.hp2 HG03225.hp2 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*911_*912dupGT | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 9/9 | 913 | INFO_REALIGN_3_PRIME | chr11 | 71997203 | ||||
| chr11:71997203 | CGT | C | 9 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(6): Show | 175 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(172): Show |
3_prime_UTR_variant | MODIFIER | c.*911_*912delGT | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 9/9 | 911 | INFO_REALIGN_3_PRIME | chr11 | 71997203 | ||||
| chr11:71997369 | G | A | 1 | a0001c0001t0016 | 1 | NA19007.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1054G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 9/9 | 1054 | chr11 | 71997369 | |||||
| chr11:71997411 | C | T | 1 | a0001c0001t0004 | 14 | HG02451.hp2 HG02622.hp1 HG02647.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1096C>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 9/9 | 1096 | chr11 | 71997411 | |||||
| chr11:71997482 | G | T | 2 | a0001c0001t0008a0001c0001t0016 | 5 | HG00621.hp2 NA19007.hp2 NA19011.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1167G>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 9/9 | 1167 | chr11 | 71997482 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:71929258 | C | T | 1 | a0001c0001t0001g0245 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.63+134C>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71929258 | ||||||
| chr11:71929434 | T | A | 1 | a0001c0001t0001g0009 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.63+310T>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71929434 | ||||||
| chr11:71929554 | G | A | 1 | a0001c0001t0002g0010 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.63+430G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71929554 | ||||||
| chr11:71929610 | A | G | 9 | a0001c0001t0003g0237a0001c0001t0003g0239a0001c0001t0003g0240others(6): Show | 9 | HG02145.hp1 HG02723.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.63+486A>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71929610 | ||||||
| chr11:71929704 | C | G | 15 | a0001c0002t0006g0222a0001c0002t0006g0223a0001c0002t0006g0224others(12): Show | 15 | HG00738.hp1 HG01975.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.63+580C>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71929704 | ||||||
| chr11:71929766 | G | T | 1 | a0001c0005t0003g0220 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.63+642G>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71929766 | ||||||
| chr11:71929914 | A | T | 1 | a0001c0002t0006g0235 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.63+790A>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71929914 | ||||||
| chr11:71929940 | A | G | 11 | a0001c0003t0003g0008a0001c0003t0003g0211a0001c0003t0003g0212others(8): Show | 12 | HG01074.hp1 HG02486.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.63+816A>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71929940 | ||||||
| chr11:71929953 | T | G | 1 | a0001c0001t0001g0011 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.63+829T>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71929953 | ||||||
| chr11:71930047 | A | T | 184 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(181): Show | 187 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.63+923A>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71930047 | ||||||
| chr11:71930100 | A | G | 8 | a0001c0003t0003g0008a0001c0003t0003g0213a0001c0003t0003g0214others(5): Show | 9 | HG01074.hp1 HG02486.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.63+976A>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71930100 | ||||||
| chr11:71930210 | G | A | 184 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(181): Show | 187 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.63+1086G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71930210 | ||||||
| chr11:71930255 | A | G | 1 | a0001c0001t0001g0210 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.63+1131A>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71930255 | ||||||
| chr11:71930416 | G | A | 1 | a0001c0001t0007g0067 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.63+1292G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71930416 | ||||||
| chr11:71930422 | G | A | 1 | a0001c0001t0007g0067 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.63+1298G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71930422 | ||||||
| chr11:71930490 | A | G | 10 | a0001c0001t0005g0200a0001c0001t0005g0201a0001c0001t0005g0202others(7): Show | 10 | HG02723.hp2 HG02896.hp2 HG02897.hp2 others(7): Show |
intron_variant | MODIFIER | c.63+1366A>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71930490 | ||||||
| chr11:71930542 | AG | A | 125 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(122): Show | 127 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.63+1419delG | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71930542 | ||||||
| chr11:71930553 | G | A | 15 | a0001c0002t0006g0222a0001c0002t0006g0223a0001c0002t0006g0224others(12): Show | 15 | HG00738.hp1 HG01975.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.63+1429G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71930553 | ||||||
| chr11:71930609 | A | T | 8 | a0001c0003t0003g0008a0001c0003t0003g0213a0001c0003t0003g0214others(5): Show | 9 | HG01074.hp1 HG02486.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.63+1485A>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71930609 | ||||||
| chr11:71930888 | A | G | 1 | a0001c0001t0002g0066 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.63+1764A>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71930888 | ||||||
| chr11:71930993 | C | T | 168 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(165): Show | 171 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.63+1869C>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71930993 | ||||||
| chr11:71931081 | A | G | 9 | a0001c0001t0003g0237a0001c0001t0003g0239a0001c0001t0003g0240others(6): Show | 9 | HG02145.hp1 HG02723.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.63+1957A>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71931081 | ||||||
| chr11:71931106 | A | G | 11 | a0001c0003t0003g0008a0001c0003t0003g0211a0001c0003t0003g0212others(8): Show | 12 | HG01074.hp1 HG02486.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.63+1982A>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71931106 | ||||||
| chr11:71931212 | C | T | 168 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(165): Show | 171 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.63+2088C>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71931212 | ||||||
| chr11:71931264 | A | G | 1 | a0001c0001t0001g0186 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.63+2140A>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71931264 | ||||||
| chr11:71931376 | T | G | 1 | a0001c0001t0008g0012 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.63+2252T>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71931376 | ||||||
| chr11:71931377 | G | T | 1 | a0001c0001t0008g0012 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.63+2253G>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71931377 | ||||||
| chr11:71931478 | G | A | 190 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(187): Show | 196 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(193): Show |
intron_variant | MODIFIER | c.63+2354G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71931478 | ||||||
| chr11:71931530 | C | G | 157 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(154): Show | 159 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.63+2406C>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71931530 | ||||||
| chr11:71931581 | A | G | 1 | a0001c0003t0003g0212 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.63+2457A>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71931581 | ||||||
| chr11:71931616 | C | T | 1 | a0001c0001t0001g0199 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.63+2492C>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71931616 | ||||||
| chr11:71931633 | C | T | 1 | a0001c0001t0007g0067 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.63+2509C>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71931633 | ||||||
| chr11:71931656 | C | T | 3 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0198 | 3 | HG02451.hp1 HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.63+2532C>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71931656 | ||||||
| chr11:71931661 | T | A | 1 | a0001c0001t0008g0012 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.63+2537T>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71931661 | ||||||
| chr11:71931847 | A | G | 3 | a0001c0003t0003g0211a0001c0003t0003g0212a0001c0005t0003g0220 | 3 | HG02965.hp1 HG03130.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.63+2723A>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71931847 | ||||||
| chr11:71932294 | A | C | 3 | a0001c0001t0007g0014a0001c0001t0007g0015a0001c0001t0007g0016 | 3 | HG02615.hp2 HG02717.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.63+3170A>C | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71932294 | ||||||
| chr11:71932387 | G | A | 4 | a0001c0001t0005g0200a0001c0001t0005g0201a0001c0001t0005g0202others(1): Show | 4 | HG02723.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+3263G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71932387 | ||||||
| chr11:71932912 | G | A | 198 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(195): Show | 204 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(201): Show |
intron_variant | MODIFIER | c.63+3788G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71932912 | ||||||
| chr11:71932958 | C | T | 3 | a0001c0001t0007g0014a0001c0001t0007g0015a0001c0001t0007g0016 | 3 | HG02615.hp2 HG02717.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.63+3834C>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71932958 | ||||||
| chr11:71933068 | A | C | 1 | a0001c0001t0001g0185 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.63+3944A>C | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71933068 | ||||||
| chr11:71933148 | G | A | 13 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189others(10): Show | 13 | HG01243.hp2 HG02451.hp1 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.63+4024G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71933148 | ||||||
| chr11:71933202 | A | T | 1 | a0001c0001t0002g0065 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.63+4078A>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71933202 | ||||||
| chr11:71933258 | G | A | 1 | a0001c0001t0001g0068 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.63+4134G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71933258 | ||||||
| chr11:71933278 | T | C | 15 | a0001c0002t0006g0222a0001c0002t0006g0223a0001c0002t0006g0224others(12): Show | 15 | HG00738.hp1 HG01975.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.63+4154T>C | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71933278 | ||||||
| chr11:71933287 | A | G | 181 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(178): Show | 184 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.63+4163A>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71933287 | ||||||
| chr11:71933288 | T | G | 2 | a0001c0001t0004g0069a0001c0001t0004g0070 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.63+4164T>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71933288 | ||||||
| chr11:71933291 | A | G | 2 | a0001c0001t0004g0069a0001c0001t0004g0070 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.63+4167A>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71933291 | ||||||
| chr11:71933292 | T | G | 2 | a0001c0001t0004g0069a0001c0001t0004g0070 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.63+4168T>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71933292 | ||||||
| chr11:71933324 | G | A | 1 | a0001c0001t0001g0071 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.63+4200G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71933324 | ||||||
| chr11:71933651 | T | G | 1 | a0001c0004t0005g0221 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.63+4527T>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71933651 | ||||||
| chr11:71933701 | G | A | 1 | a0001c0001t0002g0025 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.63+4577G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71933701 | ||||||
| chr11:71933993 | A | G | 3 | a0001c0001t0007g0001a0001c0001t0007g0002a0001c0001t0007g0013 | 6 | HG02109.hp1 HG02258.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.63+4869A>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71933993 | ||||||
| chr11:71934013 | T | G | 15 | a0001c0002t0006g0222a0001c0002t0006g0223a0001c0002t0006g0224others(12): Show | 15 | HG00738.hp1 HG01975.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.63+4889T>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71934013 | ||||||
| chr11:71934118 | T | C | 15 | a0001c0002t0006g0222a0001c0002t0006g0223a0001c0002t0006g0224others(12): Show | 15 | HG00738.hp1 HG01975.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.63+4994T>C | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71934118 | ||||||
| chr11:71934570 | T | C | 1 | a0001c0004t0005g0221 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.63+5446T>C | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71934570 | ||||||
| chr11:71934609 | A | C | 14 | a0001c0002t0006g0222a0001c0002t0006g0223a0001c0002t0006g0224others(11): Show | 14 | HG00738.hp1 HG01975.hp2 HG02683.hp2 others(11): Show |
intron_variant | MODIFIER | c.63+5485A>C | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71934609 | ||||||
| chr11:71934695 | T | G | 2 | a0001c0001t0001g0072a0001c0001t0001g0073 | 2 | HG03239.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.63+5571T>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71934695 | ||||||
| chr11:71934736 | A | G | 1 | a0001c0001t0001g0184 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.63+5612A>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71934736 | ||||||
| chr11:71934757 | A | C | 168 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(165): Show | 171 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.63+5633A>C | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71934757 | ||||||
| chr11:71934834 | C | G | 5 | a0001c0001t0001g0011a0001c0001t0001g0180a0001c0001t0001g0181others(2): Show | 5 | HG01192.hp1 HG02273.hp2 HG02293.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+5710C>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71934834 | ||||||
| chr11:71934938 | ATTC | A | 137 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(134): Show | 139 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.63+5817_63+5819del others(3): Show |
RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 71934938 | |||||
| chr11:71934938 | ATTCT | A | 11 | a0001c0001t0001g0074a0001c0001t0001g0185a0001c0001t0005g0200others(8): Show | 11 | HG02723.hp2 HG02896.hp2 HG02897.hp2 others(8): Show |
intron_variant | MODIFIER | c.63+5817_63+5820del others(4): Show |
RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 71934938 | |||||
| chr11:71934941 | CTT | C | 20 | a0001c0001t0003g0237a0001c0001t0003g0239a0001c0001t0003g0240others(17): Show | 21 | HG01074.hp1 HG02145.hp1 HG02486.hp1 others(18): Show |
intron_variant | MODIFIER | c.63+5837_63+5838del others(2): Show |
RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 71934941 | |||||
| chr11:71934942 | T | C | 137 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(134): Show | 139 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.63+5818T>C | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71934942 | ||||||
| chr11:71934943 | T | C | 11 | a0001c0001t0001g0074a0001c0001t0001g0185a0001c0001t0005g0200others(8): Show | 11 | HG02723.hp2 HG02896.hp2 HG02897.hp2 others(8): Show |
intron_variant | MODIFIER | c.63+5819T>C | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71934943 | ||||||
| chr11:71935099 | G | A | 1 | a0001c0002t0006g0235 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.63+5975G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71935099 | ||||||
| chr11:71935152 | C | T | 1 | a0001c0005t0003g0220 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.63+6028C>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71935152 | ||||||
| chr11:71935375 | T | C | 1 | a0001c0001t0002g0026 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.63+6251T>C | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71935375 | ||||||
| chr11:71935490 | G | T | 14 | a0001c0002t0006g0222a0001c0002t0006g0223a0001c0002t0006g0224others(11): Show | 14 | HG00738.hp1 HG01975.hp2 HG02683.hp2 others(11): Show |
intron_variant | MODIFIER | c.63+6366G>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71935490 | ||||||
| chr11:71935591 | T | A | 15 | a0001c0002t0006g0222a0001c0002t0006g0223a0001c0002t0006g0224others(12): Show | 15 | HG00738.hp1 HG01975.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.63+6467T>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71935591 | ||||||
| chr11:71935846 | C | CT | 12 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0174others(9): Show | 12 | HG00323.hp2 HG01175.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.63+6743dupT | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 71935846 | |||||
| chr11:71935846 | CT | C | 16 | a0001c0002t0006g0222a0001c0002t0006g0223a0001c0002t0006g0224others(13): Show | 16 | HG00738.hp1 HG01975.hp2 HG02683.hp2 others(13): Show |
intron_variant | MODIFIER | c.63+6743delT | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 71935846 | |||||
| chr11:71935846 | CTT | C | 7 | a0001c0003t0003g0008a0001c0003t0003g0213a0001c0003t0003g0214others(4): Show | 8 | HG01074.hp1 HG02486.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.63+6742_63+6743del others(2): Show |
RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 71935846 | |||||
| chr11:71935852 | T | C | 1 | a0001c0001t0001g0184 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.63+6728T>C | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71935852 | ||||||
| chr11:71935972 | T | C | 3 | a0001c0001t0007g0001a0001c0001t0007g0002a0001c0001t0007g0013 | 6 | HG02109.hp1 HG02258.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.63+6848T>C | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71935972 | ||||||
| chr11:71936032 | A | G | 1 | a0001c0001t0002g0061 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.63+6908A>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71936032 | ||||||
| chr11:71936038 | A | G | 1 | a0001c0001t0002g0060 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.63+6914A>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71936038 | ||||||
| chr11:71936040 | G | C | 1 | a0001c0001t0004g0075 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.63+6916G>C | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71936040 | ||||||
| chr11:71936106 | C | A | 1 | a0001c0001t0001g0076 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.63+6982C>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71936106 | ||||||
| chr11:71936107 | A | G | 1 | a0001c0001t0001g0076 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.63+6983A>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71936107 | ||||||
| chr11:71936118 | A | T | 1 | a0001c0001t0002g0024 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.63+6994A>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71936118 | ||||||
| chr11:71936408 | T | TAAG | 198 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(195): Show | 204 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(201): Show |
intron_variant | MODIFIER | c.63+7285_63+7286ins others(3): Show |
RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 71936408 | |||||
| chr11:71936424 | C | G | 15 | a0001c0002t0006g0222a0001c0002t0006g0223a0001c0002t0006g0224others(12): Show | 15 | HG00738.hp1 HG01975.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.63+7300C>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71936424 | ||||||
| chr11:71936443 | G | A | 15 | a0001c0002t0006g0222a0001c0002t0006g0223a0001c0002t0006g0224others(12): Show | 15 | HG00738.hp1 HG01975.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.63+7319G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71936443 | ||||||
| chr11:71936510 | C | G | 4 | a0001c0001t0005g0200a0001c0001t0005g0201a0001c0001t0005g0202others(1): Show | 4 | HG02723.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+7386C>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71936510 | ||||||
| chr11:71936568 | G | T | 1 | a0001c0001t0001g0171 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.63+7444G>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71936568 | ||||||
| chr11:71936615 | C | T | 9 | a0001c0001t0003g0237a0001c0001t0003g0239a0001c0001t0003g0240others(6): Show | 9 | HG02145.hp1 HG02723.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.63+7491C>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71936615 | ||||||
| chr11:71936712 | T | A | 14 | a0001c0002t0006g0222a0001c0002t0006g0223a0001c0002t0006g0224others(11): Show | 14 | HG00738.hp1 HG01975.hp2 HG02683.hp2 others(11): Show |
intron_variant | MODIFIER | c.63+7588T>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71936712 | ||||||
| chr11:71936830 | T | TG | 184 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(181): Show | 187 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.63+7706_63+7707ins others(1): Show |
RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71936830 | ||||||
| chr11:71936904 | C | G | 13 | a0001c0001t0004g0069a0001c0001t0004g0070a0001c0001t0004g0075others(10): Show | 13 | HG02451.hp2 HG02622.hp1 HG02647.hp2 others(10): Show |
intron_variant | MODIFIER | c.63+7780C>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71936904 | ||||||
| chr11:71936933 | T | C | 1 | a0001c0003t0003g0213 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.63+7809T>C | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71936933 | ||||||
| chr11:71937098 | A | G | 1 | a0001c0001t0007g0067 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.63+7974A>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71937098 | ||||||
| chr11:71937123 | G | A | 157 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(154): Show | 159 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.63+7999G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71937123 | ||||||
| chr11:71937182 | G | A | 1 | a0001c0001t0001g0077 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.63+8058G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71937182 | ||||||
| chr11:71937248 | G | A | 1 | a0001c0001t0001g0078 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.63+8124G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71937248 | ||||||
| chr11:71937313 | T | C | 1 | a0001c0001t0002g0027 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.63+8189T>C | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71937313 | ||||||
| chr11:71937387 | A | C | 34 | a0001c0001t0001g0011a0001c0001t0001g0071a0001c0001t0001g0074others(31): Show | 34 | HG00738.hp2 HG01106.hp2 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.63+8263A>C | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71937387 | ||||||
| chr11:71937390 | G | T | 14 | a0001c0002t0006g0222a0001c0002t0006g0223a0001c0002t0006g0224others(11): Show | 14 | HG00738.hp1 HG01975.hp2 HG02683.hp2 others(11): Show |
intron_variant | MODIFIER | c.63+8266G>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71937390 | ||||||
| chr11:71937587 | A | G | 1 | a0001c0001t0002g0027 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.63+8463A>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71937587 | ||||||
| chr11:71937631 | G | C | 15 | a0001c0002t0006g0222a0001c0002t0006g0223a0001c0002t0006g0224others(12): Show | 15 | HG00738.hp1 HG01975.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.63+8507G>C | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71937631 | ||||||
| chr11:71937661 | T | C | 2 | a0001c0001t0005g0204a0001c0001t0005g0205 | 2 | HG03209.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.63+8537T>C | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71937661 | ||||||
| chr11:71937898 | T | C | 1 | a0001c0001t0002g0028 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.63+8774T>C | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71937898 | ||||||
| chr11:71937920 | G | C | 148 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(145): Show | 150 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.63+8796G>C | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71937920 | ||||||
| chr11:71937930 | T | C | 1 | a0001c0001t0007g0067 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.63+8806T>C | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71937930 | ||||||
| chr11:71938237 | A | G | 1 | a0001c0003t0003g0213 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.63+9113A>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71938237 | ||||||
| chr11:71938299 | G | A | 1 | a0001c0001t0001g0079 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.63+9175G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71938299 | ||||||
| chr11:71938306 | G | A | 190 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(187): Show | 196 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(193): Show |
intron_variant | MODIFIER | c.63+9182G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71938306 | ||||||
| chr11:71938314 | A | AT | 8 | a0001c0001t0002g0010a0001c0001t0002g0058a0001c0001t0002g0059others(5): Show | 8 | HG02056.hp1 HG02630.hp1 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.63+9213dupT | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 71938314 | |||||
| chr11:71938314 | A | ATT | 33 | a0001c0001t0001g0072a0001c0001t0001g0082a0001c0001t0001g0083others(30): Show | 34 | HG01074.hp1 HG01109.hp1 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.63+9212_63+9213dup others(2): Show |
RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 71938314 | |||||
| chr11:71938314 | A | ATTT | 94 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(91): Show | 96 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.63+9211_63+9213dup others(3): Show |
RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 71938314 | |||||
| chr11:71938314 | A | ATTTT | 29 | a0001c0001t0001g0126a0001c0001t0001g0127a0001c0001t0001g0128others(26): Show | 29 | HG00609.hp2 HG01358.hp1 HG01934.hp1 others(26): Show |
intron_variant | MODIFIER | c.63+9210_63+9213dup others(4): Show |
RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 71938314 | |||||
| chr11:71938314 | ATTTTTTT others(4): Show |
A | 9 | a0001c0001t0003g0237a0001c0001t0003g0239a0001c0001t0003g0240others(6): Show | 9 | HG02145.hp1 HG02723.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.63+9203_63+9213del others(11): Show |
RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 71938314 | |||||
| chr11:71938351 | G | A | 1 | a0001c0001t0001g0186 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.63+9227G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71938351 | ||||||
| chr11:71938969 | A | T | 1 | a0001c0001t0001g0186 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.63+9845A>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71938969 | ||||||
| chr11:71939007 | C | T | 1 | a0001c0001t0002g0057 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.63+9883C>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71939007 | ||||||
| chr11:71939063 | C | A | 4 | a0001c0001t0001g0080a0001c0001t0001g0126a0001c0001t0001g0127others(1): Show | 4 | NA18747.hp1 NA18950.hp2 NA18981.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+9939C>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71939063 | ||||||
| chr11:71939195 | T | C | 184 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(181): Show | 187 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.63+10071T>C | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71939195 | ||||||
| chr11:71939322 | T | C | 125 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(122): Show | 127 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.63+10198T>C | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71939322 | ||||||
| chr11:71939407 | C | T | 1 | a0001c0001t0007g0067 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.63+10283C>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71939407 | ||||||
| chr11:71939471 | T | C | 1 | a0001c0001t0008g0029 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.63+10347T>C | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71939471 | ||||||
| chr11:71939536 | A | G | 1 | a0001c0001t0001g0160 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.63+10412A>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71939536 | ||||||
| chr11:71939806 | T | TAA | 2 | a0001c0001t0007g0002a0001c0001t0007g0013 | 3 | HG02109.hp1 HG02717.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.63+10682_63+10683i others(4): Show |
RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71939806 | ||||||
| chr11:71939872 | A | G | 14 | a0001c0002t0006g0222a0001c0002t0006g0223a0001c0002t0006g0224others(11): Show | 14 | HG00738.hp1 HG01975.hp2 HG02683.hp2 others(11): Show |
intron_variant | MODIFIER | c.63+10748A>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71939872 | ||||||
| chr11:71940023 | G | A | 1 | a0001c0001t0001g0126 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.63+10899G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71940023 | ||||||
| chr11:71940459 | C | T | 14 | a0001c0002t0006g0222a0001c0002t0006g0223a0001c0002t0006g0224others(11): Show | 14 | HG00738.hp1 HG01975.hp2 HG02683.hp2 others(11): Show |
intron_variant | MODIFIER | c.63+11335C>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71940459 | ||||||
| chr11:71940473 | G | C | 1 | a0001c0001t0007g0067 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.63+11349G>C | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71940473 | ||||||
| chr11:71940479 | G | A | 8 | a0001c0003t0003g0008a0001c0003t0003g0213a0001c0003t0003g0214others(5): Show | 9 | HG01074.hp1 HG02486.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.63+11355G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71940479 | ||||||
| chr11:71940656 | A | G | 1 | a0001c0001t0007g0067 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.63+11532A>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71940656 | ||||||
| chr11:71940674 | A | G | 1 | a0001c0001t0001g0245 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.63+11550A>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71940674 | ||||||
| chr11:71940736 | A | G | 11 | a0001c0003t0003g0008a0001c0003t0003g0211a0001c0003t0003g0212others(8): Show | 12 | HG01074.hp1 HG02486.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.63+11612A>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71940736 | ||||||
| chr11:71940915 | G | C | 137 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(134): Show | 139 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.63+11791G>C | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71940915 | ||||||
| chr11:71940945 | T | C | 1 | a0001c0001t0001g0129 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.63+11821T>C | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71940945 | ||||||
| chr11:71940949 | A | C | 3 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0183 | 3 | HG01192.hp1 HG02273.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.63+11825A>C | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71940949 | ||||||
| chr11:71940961 | G | A | 1 | a0001c0001t0001g0084 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.63+11837G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71940961 | ||||||
| chr11:71940978 | A | G | 3 | a0001c0001t0007g0001a0001c0001t0007g0002a0001c0001t0007g0013 | 6 | HG02109.hp1 HG02258.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.63+11854A>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71940978 | ||||||
| chr11:71941016 | A | G | 15 | a0001c0001t0001g0123a0001c0001t0004g0069a0001c0001t0004g0070others(12): Show | 15 | HG02451.hp2 HG02622.hp1 HG02647.hp2 others(12): Show |
intron_variant | MODIFIER | c.63+11892A>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71941016 | ||||||
| chr11:71941035 | A | G | 1 | a0001c0001t0002g0056 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.63+11911A>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71941035 | ||||||
| chr11:71941175 | G | A | 15 | a0001c0002t0006g0222a0001c0002t0006g0223a0001c0002t0006g0224others(12): Show | 15 | HG00738.hp1 HG01975.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.63+12051G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71941175 | ||||||
| chr11:71941265 | G | A | 1 | a0001c0001t0001g0172 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.63+12141G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71941265 | ||||||
| chr11:71941427 | C | T | 1 | a0001c0001t0002g0059 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.63+12303C>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71941427 | ||||||
| chr11:71941439 | G | A | 168 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(165): Show | 171 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.63+12315G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71941439 | ||||||
| chr11:71941930 | A | AT | 5 | a0001c0001t0002g0054a0001c0001t0002g0059a0001c0001t0002g0062others(2): Show | 5 | HG02056.hp1 HG02074.hp2 HG03942.hp2 others(2): Show |
intron_variant | MODIFIER | c.63+12826dupT | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 71941930 | |||||
| chr11:71941930 | AT | A | 166 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(163): Show | 169 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.63+12826delT | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 71941930 | |||||
| chr11:71941956 | G | A | 1 | a0001c0004t0005g0221 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.63+12832G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71941956 | ||||||
| chr11:71942010 | G | A | 3 | a0001c0001t0005g0206a0001c0001t0005g0207a0001c0001t0005g0209 | 3 | HG02976.hp1 HG03098.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.63+12886G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71942010 | ||||||
| chr11:71942229 | G | A | 1 | a0001c0001t0001g0130 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.63+13105G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71942229 | ||||||
| chr11:71942240 | G | A | 7 | a0001c0003t0003g0008a0001c0003t0003g0213a0001c0003t0003g0214others(4): Show | 8 | HG01074.hp1 HG02486.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.63+13116G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71942240 | ||||||
| chr11:71942423 | T | G | 3 | a0001c0003t0003g0211a0001c0003t0003g0212a0001c0005t0003g0220 | 3 | HG02965.hp1 HG03130.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.63+13299T>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71942423 | ||||||
| chr11:71942485 | G | A | 1 | a0001c0005t0003g0220 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.63+13361G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71942485 | ||||||
| chr11:71942503 | C | G | 1 | a0001c0001t0007g0067 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.63+13379C>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71942503 | ||||||
| chr11:71942537 | C | T | 2 | a0001c0001t0002g0022a0001c0001t0002g0023 | 2 | HG01433.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.63+13413C>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71942537 | ||||||
| chr11:71942616 | T | A | 1 | a0001c0005t0003g0220 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.63+13492T>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71942616 | ||||||
| chr11:71942678 | C | T | 1 | a0001c0001t0001g0122 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.63+13554C>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71942678 | ||||||
| chr11:71942679 | G | A | 9 | a0001c0001t0003g0237a0001c0001t0003g0239a0001c0001t0003g0240others(6): Show | 9 | HG02145.hp1 HG02723.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.63+13555G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71942679 | ||||||
| chr11:71942772 | G | GTA | 3 | a0001c0001t0005g0242a0001c0003t0003g0211a0001c0003t0003g0212 | 3 | HG02965.hp1 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.63+13665_63+13666d others(4): Show |
RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 71942772 | |||||
| chr11:71942783 | T | TAGATATA others(17): Show |
6 | a0001c0002t0006g0228a0001c0002t0006g0230a0001c0002t0006g0231others(3): Show | 6 | HG02683.hp2 HG02735.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.63+13660_63+13661i others(26): Show |
RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 71942783 | |||||
| chr11:71942787 | T | TAG | 147 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(144): Show | 149 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.63+13664_63+13665i others(4): Show |
RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 71942787 | |||||
| chr11:71942791 | G | C | 1 | a0001c0001t0001g0141 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.63+13667G>C | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71942791 | ||||||
| chr11:71942791 | G | T | 8 | a0001c0002t0006g0222a0001c0002t0006g0223a0001c0002t0006g0224others(5): Show | 8 | HG00738.hp1 HG01975.hp2 HG03831.hp1 others(5): Show |
intron_variant | MODIFIER | c.63+13667G>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71942791 | ||||||
| chr11:71942802 | G | A | 8 | a0001c0002t0006g0222a0001c0002t0006g0223a0001c0002t0006g0224others(5): Show | 8 | HG00738.hp1 HG01975.hp2 HG03831.hp1 others(5): Show |
intron_variant | MODIFIER | c.63+13678G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71942802 | ||||||
| chr11:71942803 | T | TACAC | 28 | a0001c0001t0002g0010a0001c0001t0002g0017a0001c0001t0002g0018others(25): Show | 28 | HG00099.hp1 HG00323.hp1 HG00558.hp2 others(25): Show |
intron_variant | MODIFIER | c.63+13697_63+13700d others(6): Show |
RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 71942803 | |||||
| chr11:71942803 | T | TACACAA | 162 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(159): Show | 165 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.63+13684_63+13685i others(8): Show |
RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 71942803 | |||||
| chr11:71942803 | T | TACACAAA others(1): Show |
5 | a0001c0001t0001g0142a0001c0001t0001g0178a0001c0001t0007g0001others(2): Show | 8 | HG02109.hp1 HG02258.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.63+13684_63+13685i others(10): Show |
RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 71942803 | |||||
| chr11:71942803 | T | TACACACA others(3): Show |
1 | a0001c0001t0007g0015 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.63+13691_63+13700d others(12): Show |
RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 71942803 | |||||
| chr11:71942803 | T | TATATATA others(25): Show |
1 | a0001c0002t0006g0222 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.63+13680_63+13681i others(34): Show |
RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 71942803 | |||||
| chr11:71942803 | T | TATATATA others(19): Show |
1 | a0001c0002t0006g0223 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.63+13680_63+13681i others(28): Show |
RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 71942803 | |||||
| chr11:71942803 | T | TATATATA others(29): Show |
1 | a0001c0002t0006g0224 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.63+13680_63+13681i others(38): Show |
RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 71942803 | |||||
| chr11:71942803 | T | TATATATA others(31): Show |
2 | a0001c0002t0006g0225a0001c0002t0006g0233 | 2 | NA18981.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.63+13680_63+13681i others(40): Show |
RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 71942803 | |||||
| chr11:71942803 | T | TATATATA others(25): Show |
1 | a0001c0002t0006g0235 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.63+13680_63+13681i others(34): Show |
RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 71942803 | |||||
| chr11:71942803 | T | TATATATA others(33): Show |
1 | a0001c0002t0006g0226 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.63+13680_63+13681i others(42): Show |
RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 71942803 | |||||
| chr11:71942803 | T | TATATATA others(27): Show |
1 | a0001c0002t0006g0227 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.63+13680_63+13681i others(36): Show |
RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 71942803 | |||||
| chr11:71942805 | C | CACAA | 12 | a0001c0001t0003g0237a0001c0001t0003g0239a0001c0001t0003g0240others(9): Show | 12 | HG02145.hp1 HG02723.hp1 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.63+13684_63+13685i others(6): Show |
RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 71942805 | |||||
| chr11:71942825 | T | C | 15 | a0001c0001t0007g0067a0001c0002t0006g0222a0001c0002t0006g0223others(12): Show | 15 | HG00738.hp1 HG01975.hp2 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.63+13701T>C | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71942825 | ||||||
| chr11:71942853 | G | C | 15 | a0001c0002t0006g0222a0001c0002t0006g0223a0001c0002t0006g0224others(12): Show | 15 | HG00738.hp1 HG01975.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.63+13729G>C | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71942853 | ||||||
| chr11:71942933 | T | G | 11 | a0001c0003t0003g0008a0001c0003t0003g0211a0001c0003t0003g0212others(8): Show | 12 | HG01074.hp1 HG02486.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.63+13809T>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71942933 | ||||||
| chr11:71942966 | A | G | 125 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(122): Show | 127 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.63+13842A>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71942966 | ||||||
| chr11:71943084 | G | A | 183 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(180): Show | 186 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.63+13960G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71943084 | ||||||
| chr11:71943097 | G | A | 184 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(181): Show | 187 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.63+13973G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71943097 | ||||||
| chr11:71943352 | C | T | 2 | a0001c0001t0002g0020a0001c0001t0010g0021 | 2 | HG03225.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.64-13875C>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71943352 | ||||||
| chr11:71943500 | C | T | 1 | a0001c0005t0003g0220 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.64-13727C>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71943500 | ||||||
| chr11:71943735 | A | G | 1 | a0001c0001t0001g0195 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.64-13492A>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71943735 | ||||||
| chr11:71943947 | G | A | 1 | a0001c0004t0005g0221 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.64-13280G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71943947 | ||||||
| chr11:71943989 | G | A | 1 | a0001c0001t0001g0085 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.64-13238G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71943989 | ||||||
| chr11:71944243 | G | T | 15 | a0001c0002t0006g0222a0001c0002t0006g0223a0001c0002t0006g0224others(12): Show | 15 | HG00738.hp1 HG01975.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.64-12984G>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71944243 | ||||||
| chr11:71944272 | G | A | 2 | a0001c0003t0003g0211a0001c0003t0003g0212 | 2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.64-12955G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71944272 | ||||||
| chr11:71944327 | T | C | 184 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(181): Show | 187 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.64-12900T>C | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71944327 | ||||||
| chr11:71944362 | A | G | 3 | a0001c0001t0005g0241a0001c0001t0005g0242a0001c0001t0005g0243 | 3 | HG02145.hp1 HG03453.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.64-12865A>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71944362 | ||||||
| chr11:71944459 | G | A | 15 | a0001c0002t0006g0222a0001c0002t0006g0223a0001c0002t0006g0224others(12): Show | 15 | HG00738.hp1 HG01975.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.64-12768G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71944459 | ||||||
| chr11:71944558 | G | A | 2 | a0001c0001t0001g0086a0001c0001t0001g0210 | 2 | HG00280.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.64-12669G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71944558 | ||||||
| chr11:71944720 | C | T | 1 | a0001c0001t0002g0053 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.64-12507C>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71944720 | ||||||
| chr11:71944801 | A | G | 138 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(135): Show | 140 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.64-12426A>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71944801 | ||||||
| chr11:71944886 | C | T | 10 | a0001c0001t0005g0200a0001c0001t0005g0201a0001c0001t0005g0202others(7): Show | 10 | HG02723.hp2 HG02896.hp2 HG02897.hp2 others(7): Show |
intron_variant | MODIFIER | c.64-12341C>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71944886 | ||||||
| chr11:71944997 | G | GT | 6 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0154others(3): Show | 6 | HG02280.hp2 HG03239.hp1 HG03492.hp1 others(3): Show |
intron_variant | MODIFIER | c.64-12219dupT | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 71944997 | |||||
| chr11:71945076 | C | T | 1 | a0001c0001t0004g0170 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.64-12151C>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71945076 | ||||||
| chr11:71945081 | G | A | 15 | a0001c0002t0006g0222a0001c0002t0006g0223a0001c0002t0006g0224others(12): Show | 15 | HG00738.hp1 HG01975.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.64-12146G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71945081 | ||||||
| chr11:71945160 | A | T | 183 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(180): Show | 186 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.64-12067A>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71945160 | ||||||
| chr11:71945659 | A | G | 168 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(165): Show | 171 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.64-11568A>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71945659 | ||||||
| chr11:71945798 | T | TA | 183 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(180): Show | 186 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.64-11421dupA | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 71945798 | |||||
| chr11:71945921 | T | A | 138 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(135): Show | 140 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.64-11306T>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71945921 | ||||||
| chr11:71946112 | AAAAAGAA others(3): Show |
A | 1 | a0001c0001t0002g0059 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.64-11095_64-11086d others(12): Show |
RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 71946112 | |||||
| chr11:71946116 | AG | A | 6 | a0001c0002t0006g0228a0001c0002t0006g0230a0001c0002t0006g0231others(3): Show | 6 | HG02683.hp2 HG02735.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-11110delG | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71946116 | ||||||
| chr11:71946117 | G | A | 178 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(175): Show | 181 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(178): Show |
intron_variant | MODIFIER | c.64-11110G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71946117 | ||||||
| chr11:71946145 | C | T | 9 | a0001c0001t0003g0237a0001c0001t0003g0239a0001c0001t0003g0240others(6): Show | 9 | HG02145.hp1 HG02723.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.64-11082C>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71946145 | ||||||
| chr11:71946417 | A | G | 3 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0024 | 3 | HG02145.hp2 HG03540.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.64-10810A>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71946417 | ||||||
| chr11:71946428 | G | A | 15 | a0001c0002t0006g0222a0001c0002t0006g0223a0001c0002t0006g0224others(12): Show | 15 | HG00738.hp1 HG01975.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.64-10799G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71946428 | ||||||
| chr11:71946514 | C | G | 1 | a0001c0004t0005g0221 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.64-10713C>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71946514 | ||||||
| chr11:71946565 | G | A | 1 | a0001c0001t0007g0067 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.64-10662G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71946565 | ||||||
| chr11:71946647 | G | GT | 10 | a0001c0001t0001g0129a0001c0001t0001g0184a0001c0003t0003g0008others(7): Show | 11 | HG01074.hp1 HG02056.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.64-10564dupT | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 71946647 | |||||
| chr11:71946665 | G | A | 15 | a0001c0002t0006g0222a0001c0002t0006g0223a0001c0002t0006g0224others(12): Show | 15 | HG00738.hp1 HG01975.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.64-10562G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71946665 | ||||||
| chr11:71946867 | C | CT | 18 | a0001c0001t0001g0186a0001c0001t0002g0010a0001c0001t0002g0026others(15): Show | 21 | HG00323.hp1 HG02074.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.64-10340dupT | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 71946867 | |||||
| chr11:71946867 | C | CTT | 126 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(123): Show | 128 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.64-10341_64-10340d others(4): Show |
RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 71946867 | |||||
| chr11:71946867 | C | CTTT | 12 | a0001c0001t0001g0080a0001c0001t0001g0083a0001c0001t0001g0122others(9): Show | 12 | HG01109.hp1 HG01978.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.64-10342_64-10340d others(5): Show |
RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 71946867 | |||||
| chr11:71946867 | C | CTTTTT | 12 | a0001c0002t0006g0222a0001c0002t0006g0223a0001c0002t0006g0226others(9): Show | 12 | HG00738.hp1 HG01975.hp2 HG02683.hp2 others(9): Show |
intron_variant | MODIFIER | c.64-10344_64-10340d others(7): Show |
RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 71946867 | |||||
| chr11:71946867 | CT | C | 5 | a0001c0001t0002g0018a0001c0001t0002g0031a0001c0001t0005g0200others(2): Show | 5 | HG00099.hp1 HG02896.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.64-10340delT | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 71946867 | |||||
| chr11:71947017 | G | A | 8 | a0001c0003t0003g0008a0001c0003t0003g0213a0001c0003t0003g0214others(5): Show | 9 | HG01074.hp1 HG02486.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.64-10210G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71947017 | ||||||
| chr11:71947257 | G | A | 4 | a0001c0001t0003g0237a0001c0001t0003g0239a0001c0001t0013g0238others(1): Show | 4 | HG02723.hp1 HG02896.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.64-9970G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71947257 | ||||||
| chr11:71947279 | CG | C | 4 | a0001c0001t0005g0200a0001c0001t0005g0201a0001c0001t0005g0202others(1): Show | 4 | HG02723.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.64-9946delG | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 71947279 | |||||
| chr11:71947342 | A | T | 2 | a0001c0001t0002g0018a0001c0001t0002g0019 | 2 | HG02145.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.64-9885A>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71947342 | ||||||
| chr11:71947483 | C | CA | 167 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(164): Show | 170 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.64-9732dupA | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 71947483 | |||||
| chr11:71947887 | T | C | 1 | a0001c0001t0001g0173 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.64-9340T>C | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71947887 | ||||||
| chr11:71948373 | G | A | 1 | a0001c0001t0001g0143 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.64-8854G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71948373 | ||||||
| chr11:71948463 | T | C | 15 | a0001c0002t0006g0222a0001c0002t0006g0223a0001c0002t0006g0224others(12): Show | 15 | HG00738.hp1 HG01975.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.64-8764T>C | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71948463 | ||||||
| chr11:71948513 | C | CA | 59 | a0001c0001t0001g0071a0001c0001t0001g0073a0001c0001t0001g0074others(56): Show | 59 | HG00738.hp2 HG01106.hp1 HG01106.hp2 others(56): Show |
intron_variant | MODIFIER | c.64-8688dupA | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 71948513 | |||||
| chr11:71948513 | C | CAA | 7 | a0001c0001t0001g0011a0001c0001t0001g0127a0001c0001t0001g0131others(4): Show | 7 | HG02293.hp1 HG02738.hp1 HG03516.hp2 others(4): Show |
intron_variant | MODIFIER | c.64-8689_64-8688dup others(2): Show |
RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 71948513 | |||||
| chr11:71948513 | CA | C | 24 | a0001c0001t0001g0119a0001c0001t0002g0017a0001c0001t0002g0018others(21): Show | 25 | HG01074.hp1 HG01975.hp1 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.64-8688delA | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 71948513 | |||||
| chr11:71948513 | CAA | C | 10 | a0001c0001t0007g0001a0001c0001t0007g0002a0001c0001t0007g0014others(7): Show | 13 | HG02258.hp1 HG02615.hp2 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.64-8689_64-8688del others(2): Show |
RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 71948513 | |||||
| chr11:71948513 | CAAA | C | 14 | a0001c0001t0007g0067a0001c0002t0006g0222a0001c0002t0006g0223others(11): Show | 14 | HG00738.hp1 HG01975.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.64-8690_64-8688del others(3): Show |
RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 71948513 | |||||
| chr11:71948513 | CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0001g0120 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.64-8700_64-8688del others(13): Show |
RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 71948513 | |||||
| chr11:71948945 | GT | G | 183 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(180): Show | 186 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.64-8279delT | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 71948945 | |||||
| chr11:71949004 | T | C | 1 | a0001c0001t0002g0028 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.64-8223T>C | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71949004 | ||||||
| chr11:71949156 | G | T | 14 | a0001c0002t0006g0222a0001c0002t0006g0223a0001c0002t0006g0224others(11): Show | 14 | HG00738.hp1 HG01975.hp2 HG02683.hp2 others(11): Show |
intron_variant | MODIFIER | c.64-8071G>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71949156 | ||||||
| chr11:71949157 | C | T | 14 | a0001c0002t0006g0222a0001c0002t0006g0223a0001c0002t0006g0224others(11): Show | 14 | HG00738.hp1 HG01975.hp2 HG02683.hp2 others(11): Show |
intron_variant | MODIFIER | c.64-8070C>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71949157 | ||||||
| chr11:71949158 | C | A | 10 | a0001c0001t0005g0200a0001c0001t0005g0201a0001c0001t0005g0202others(7): Show | 10 | HG02723.hp2 HG02896.hp2 HG02897.hp2 others(7): Show |
intron_variant | MODIFIER | c.64-8069C>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71949158 | ||||||
| chr11:71949345 | A | G | 1 | a0001c0001t0001g0130 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.64-7882A>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71949345 | ||||||
| chr11:71949409 | C | A | 2 | a0001c0003t0003g0211a0001c0003t0003g0212 | 2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.64-7818C>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71949409 | ||||||
| chr11:71949495 | A | G | 6 | a0001c0002t0006g0228a0001c0002t0006g0230a0001c0002t0006g0231others(3): Show | 6 | HG02683.hp2 HG02735.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-7732A>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71949495 | ||||||
| chr11:71949696 | T | C | 1 | a0001c0001t0001g0125 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.64-7531T>C | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71949696 | ||||||
| chr11:71949863 | G | T | 1 | a0001c0001t0001g0118 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.64-7364G>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71949863 | ||||||
| chr11:71950007 | A | G | 1 | a0001c0001t0001g0082 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.64-7220A>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71950007 | ||||||
| chr11:71950014 | A | AAC | 14 | a0001c0001t0001g0073a0001c0001t0001g0117a0001c0001t0001g0150others(11): Show | 15 | HG01074.hp1 HG02486.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.64-7195_64-7194dup others(2): Show |
RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 71950014 | |||||
| chr11:71950014 | A | AACAC | 2 | a0001c0003t0003g0211a0001c0003t0003g0212 | 2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.64-7197_64-7194dup others(4): Show |
RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 71950014 | |||||
| chr11:71950039 | C | T | 1 | a0001c0002t0006g0224 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.64-7188C>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71950039 | ||||||
| chr11:71950269 | A | G | 1 | a0001c0001t0001g0132 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.64-6958A>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71950269 | ||||||
| chr11:71950499 | G | A | 15 | a0001c0002t0006g0222a0001c0002t0006g0223a0001c0002t0006g0224others(12): Show | 15 | HG00738.hp1 HG01975.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.64-6728G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71950499 | ||||||
| chr11:71950547 | G | A | 1 | a0001c0003t0003g0215 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.64-6680G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71950547 | ||||||
| chr11:71950552 | C | G | 1 | a0001c0001t0001g0135 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.64-6675C>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71950552 | ||||||
| chr11:71950644 | T | C | 15 | a0001c0002t0006g0222a0001c0002t0006g0223a0001c0002t0006g0224others(12): Show | 15 | HG00738.hp1 HG01975.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.64-6583T>C | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71950644 | ||||||
| chr11:71950766 | C | T | 15 | a0001c0002t0006g0222a0001c0002t0006g0223a0001c0002t0006g0224others(12): Show | 15 | HG00738.hp1 HG01975.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.64-6461C>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71950766 | ||||||
| chr11:71950789 | A | G | 1 | a0001c0001t0001g0116 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.64-6438A>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71950789 | ||||||
| chr11:71950836 | T | C | 5 | a0001c0001t0001g0187a0001c0001t0001g0189a0001c0001t0001g0190others(2): Show | 5 | HG01243.hp2 HG02630.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.64-6391T>C | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71950836 | ||||||
| chr11:71950863 | A | G | 1 | a0001c0001t0008g0029 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.64-6364A>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71950863 | ||||||
| chr11:71950906 | A | C | 2 | a0001c0001t0005g0207a0001c0001t0005g0209 | 2 | HG02976.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.64-6321A>C | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71950906 | ||||||
| chr11:71950949 | G | C | 2 | a0001c0001t0001g0074a0001c0001t0001g0142 | 2 | HG03017.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.64-6278G>C | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71950949 | ||||||
| chr11:71950988 | G | A | 2 | a0001c0001t0001g0087a0001c0001t0001g0094 | 2 | HG02258.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.64-6239G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71950988 | ||||||
| chr11:71951048 | A | C | 1 | a0001c0001t0007g0067 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.64-6179A>C | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71951048 | ||||||
| chr11:71951209 | C | CAA | 165 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(162): Show | 168 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.64-6006_64-6005dup others(2): Show |
RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 71951209 | |||||
| chr11:71951239 | G | A | 14 | a0001c0002t0006g0222a0001c0002t0006g0223a0001c0002t0006g0224others(11): Show | 14 | HG00738.hp1 HG01975.hp2 HG02683.hp2 others(11): Show |
intron_variant | MODIFIER | c.64-5988G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71951239 | ||||||
| chr11:71951294 | A | C | 3 | a0001c0001t0005g0206a0001c0001t0005g0207a0001c0001t0005g0209 | 3 | HG02976.hp1 HG03098.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.64-5933A>C | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71951294 | ||||||
| chr11:71951313 | A | T | 2 | a0001c0001t0001g0086a0001c0001t0001g0210 | 2 | HG00280.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.64-5914A>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71951313 | ||||||
| chr11:71951573 | C | T | 2 | a0001c0001t0001g0115a0001c0001t0001g0134 | 2 | HG01934.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.64-5654C>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71951573 | ||||||
| chr11:71951638 | TA | T | 19 | a0001c0001t0001g0121a0001c0001t0002g0018a0001c0001t0002g0024others(16): Show | 19 | HG00738.hp1 HG01975.hp2 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.64-5571delA | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 71951638 | |||||
| chr11:71952020 | T | A | 3 | a0001c0001t0005g0241a0001c0001t0005g0242a0001c0001t0005g0243 | 3 | HG02145.hp1 HG03453.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.64-5207T>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71952020 | ||||||
| chr11:71952116 | C | T | 15 | a0001c0002t0006g0222a0001c0002t0006g0223a0001c0002t0006g0224others(12): Show | 15 | HG00738.hp1 HG01975.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.64-5111C>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71952116 | ||||||
| chr11:71952170 | G | C | 1 | a0001c0004t0005g0221 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.64-5057G>C | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71952170 | ||||||
| chr11:71952179 | C | T | 1 | a0001c0001t0007g0015 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.64-5048C>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71952179 | ||||||
| chr11:71952287 | G | A | 5 | a0001c0001t0001g0011a0001c0001t0001g0180a0001c0001t0001g0181others(2): Show | 5 | HG01192.hp1 HG02273.hp2 HG02293.hp1 others(2): Show |
intron_variant | MODIFIER | c.64-4940G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71952287 | ||||||
| chr11:71952429 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.64-4798C>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71952429 | ||||||
| chr11:71952450 | T | A | 1 | a0001c0001t0002g0059 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.64-4777T>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71952450 | ||||||
| chr11:71952691 | C | T | 1 | a0001c0001t0001g0183 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.64-4536C>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71952691 | ||||||
| chr11:71952807 | C | CA | 165 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(162): Show | 168 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.64-4409dupA | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 71952807 | |||||
| chr11:71952859 | A | G | 8 | a0001c0002t0006g0222a0001c0002t0006g0223a0001c0002t0006g0224others(5): Show | 8 | HG00738.hp1 HG01975.hp2 HG03831.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-4368A>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71952859 | ||||||
| chr11:71952902 | A | G | 1 | a0001c0004t0005g0221 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.64-4325A>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71952902 | ||||||
| chr11:71952969 | G | A | 3 | a0001c0001t0005g0241a0001c0001t0005g0242a0001c0001t0005g0243 | 3 | HG02145.hp1 HG03453.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.64-4258G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71952969 | ||||||
| chr11:71953420 | A | G | 1 | a0001c0001t0001g0149 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.64-3807A>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71953420 | ||||||
| chr11:71953449 | T | A | 183 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(180): Show | 186 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.64-3778T>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71953449 | ||||||
| chr11:71953497 | A | G | 1 | a0001c0001t0001g0133 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.64-3730A>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71953497 | ||||||
| chr11:71953580 | ACAAGCTC others(1): Show |
A | 15 | a0001c0002t0006g0222a0001c0002t0006g0223a0001c0002t0006g0224others(12): Show | 15 | HG00738.hp1 HG01975.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.64-3644_64-3637del others(8): Show |
RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 71953580 | |||||
| chr11:71954157 | C | G | 1 | a0001c0001t0010g0055 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.64-3070C>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71954157 | ||||||
| chr11:71954424 | G | A | 13 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189others(10): Show | 13 | HG01243.hp2 HG02451.hp1 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.64-2803G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71954424 | ||||||
| chr11:71954727 | T | C | 1 | a0001c0004t0005g0221 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.64-2500T>C | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71954727 | ||||||
| chr11:71954992 | A | G | 1 | a0001c0001t0001g0131 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.64-2235A>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71954992 | ||||||
| chr11:71955087 | G | A | 15 | a0001c0002t0006g0222a0001c0002t0006g0223a0001c0002t0006g0224others(12): Show | 15 | HG00738.hp1 HG01975.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.64-2140G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71955087 | ||||||
| chr11:71955110 | G | A | 1 | a0001c0001t0007g0067 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.64-2117G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71955110 | ||||||
| chr11:71955437 | C | T | 10 | a0001c0001t0005g0200a0001c0001t0005g0201a0001c0001t0005g0202others(7): Show | 10 | HG02723.hp2 HG02896.hp2 HG02897.hp2 others(7): Show |
intron_variant | MODIFIER | c.64-1790C>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71955437 | ||||||
| chr11:71955488 | A | G | 15 | a0001c0002t0006g0222a0001c0002t0006g0223a0001c0002t0006g0224others(12): Show | 15 | HG00738.hp1 HG01975.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.64-1739A>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71955488 | ||||||
| chr11:71955554 | A | G | 1 | a0001c0001t0001g0151 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.64-1673A>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71955554 | ||||||
| chr11:71955698 | A | T | 1 | a0001c0001t0009g0081 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.64-1529A>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71955698 | ||||||
| chr11:71955717 | A | G | 1 | a0001c0001t0001g0148 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.64-1510A>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71955717 | ||||||
| chr11:71956095 | G | T | 168 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(165): Show | 171 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.64-1132G>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71956095 | ||||||
| chr11:71956415 | C | T | 178 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(175): Show | 181 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(178): Show |
intron_variant | MODIFIER | c.64-812C>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71956415 | ||||||
| chr11:71956461 | C | T | 1 | a0001c0001t0005g0205 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.64-766C>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71956461 | ||||||
| chr11:71956558 | C | T | 124 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(121): Show | 126 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.64-669C>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71956558 | ||||||
| chr11:71956810 | TCTC | T | 5 | a0001c0001t0001g0006a0001c0001t0001g0088a0001c0001t0001g0096others(2): Show | 6 | HG02300.hp1 HG02602.hp1 HG02602.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-412_64-410delTC others(1): Show |
RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 71956810 | |||||
| chr11:71956828 | C | T | 15 | a0001c0002t0006g0222a0001c0002t0006g0223a0001c0002t0006g0224others(12): Show | 15 | HG00738.hp1 HG01975.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.64-399C>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71956828 | ||||||
| chr11:71956943 | T | C | 167 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(164): Show | 170 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.64-284T>C | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71956943 | ||||||
| chr11:71956987 | C | T | 4 | a0001c0001t0001g0078a0001c0001t0001g0092a0001c0001t0001g0093others(1): Show | 4 | HG00673.hp2 HG01074.hp2 HG01106.hp1 others(1): Show |
intron_variant | MODIFIER | c.64-240C>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 1/8 | chr11 | 71956987 | ||||||
| chr11:71957316 | CT | C | 182 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(179): Show | 185 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.101+54delT | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 71957316 | |||||
| chr11:71957379 | CGGTAGGA others(2): Show |
C | 11 | a0001c0003t0003g0008a0001c0003t0003g0211a0001c0003t0003g0212others(8): Show | 12 | HG01074.hp1 HG02486.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.101+119_101+127del others(9): Show |
RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 71957379 | |||||
| chr11:71957456 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.101+192C>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 2/8 | chr11 | 71957456 | ||||||
| chr11:71957570 | G | C | 1 | a0001c0001t0001g0098 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.101+306G>C | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 2/8 | chr11 | 71957570 | ||||||
| chr11:71957635 | T | C | 1 | a0001c0004t0005g0221 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.101+371T>C | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 2/8 | chr11 | 71957635 | ||||||
| chr11:71957712 | A | G | 1 | a0001c0001t0001g0182 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.101+448A>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 2/8 | chr11 | 71957712 | ||||||
| chr11:71957820 | G | A | 183 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(180): Show | 186 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.101+556G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 2/8 | chr11 | 71957820 | ||||||
| chr11:71957895 | A | C | 13 | a0001c0001t0004g0069a0001c0001t0004g0070a0001c0001t0004g0075others(10): Show | 13 | HG02451.hp2 HG02622.hp1 HG02647.hp2 others(10): Show |
intron_variant | MODIFIER | c.101+631A>C | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 2/8 | chr11 | 71957895 | ||||||
| chr11:71958034 | A | C | 8 | a0001c0003t0003g0008a0001c0003t0003g0213a0001c0003t0003g0214others(5): Show | 9 | HG01074.hp1 HG02486.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.101+770A>C | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 2/8 | chr11 | 71958034 | ||||||
| chr11:71958196 | C | T | 167 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(164): Show | 170 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.101+932C>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 2/8 | chr11 | 71958196 | ||||||
| chr11:71958262 | C | T | 2 | a0001c0001t0007g0014a0001c0001t0007g0016 | 2 | HG02717.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.101+998C>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 2/8 | chr11 | 71958262 | ||||||
| chr11:71958441 | G | T | 167 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(164): Show | 170 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.101+1177G>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 2/8 | chr11 | 71958441 | ||||||
| chr11:71958542 | T | G | 1 | a0001c0001t0001g0171 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.101+1278T>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 2/8 | chr11 | 71958542 | ||||||
| chr11:71958880 | A | C | 1 | a0001c0001t0004g0165 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.101+1616A>C | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 2/8 | chr11 | 71958880 | ||||||
| chr11:71958919 | A | G | 1 | a0001c0001t0001g0079 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.101+1655A>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 2/8 | chr11 | 71958919 | ||||||
| chr11:71958998 | T | C | 168 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(165): Show | 171 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.101+1734T>C | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 2/8 | chr11 | 71958998 | ||||||
| chr11:71959176 | C | T | 168 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(165): Show | 171 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.102-1574C>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 2/8 | chr11 | 71959176 | ||||||
| chr11:71959217 | G | A | 1 | a0001c0003t0003g0217 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.102-1533G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 2/8 | chr11 | 71959217 | ||||||
| chr11:71959532 | G | C | 138 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(135): Show | 140 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.102-1218G>C | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 2/8 | chr11 | 71959532 | ||||||
| chr11:71959637 | C | CT | 11 | a0001c0001t0001g0112a0001c0001t0003g0237a0001c0001t0003g0239others(8): Show | 11 | HG02145.hp1 HG02723.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.102-1097dupT | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 71959637 | |||||
| chr11:71959637 | CT | C | 10 | a0001c0001t0001g0143a0001c0003t0003g0008a0001c0003t0003g0213others(7): Show | 11 | HG01074.hp1 HG02486.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.102-1097delT | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 71959637 | |||||
| chr11:71959675 | G | A | 138 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(135): Show | 140 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.102-1075G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 2/8 | chr11 | 71959675 | ||||||
| chr11:71959697 | G | A | 2 | a0001c0001t0005g0201a0001c0001t0005g0203 | 2 | HG02723.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.102-1053G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 2/8 | chr11 | 71959697 | ||||||
| chr11:71959797 | G | A | 9 | a0001c0001t0003g0237a0001c0001t0003g0239a0001c0001t0003g0240others(6): Show | 9 | HG02145.hp1 HG02723.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.102-953G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 2/8 | chr11 | 71959797 | ||||||
| chr11:71959851 | A | C | 1 | a0001c0004t0005g0221 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.102-899A>C | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 2/8 | chr11 | 71959851 | ||||||
| chr11:71959872 | G | A | 2 | a0001c0001t0002g0041a0001c0001t0002g0042 | 2 | NA18950.hp1 NA18951.hp2 |
intron_variant | MODIFIER | c.102-878G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 2/8 | chr11 | 71959872 | ||||||
| chr11:71960120 | C | T | 138 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(135): Show | 140 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.102-630C>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 2/8 | chr11 | 71960120 | ||||||
| chr11:71960399 | A | C | 9 | a0001c0001t0003g0237a0001c0001t0003g0239a0001c0001t0003g0240others(6): Show | 9 | HG02145.hp1 HG02723.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.102-351A>C | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 2/8 | chr11 | 71960399 | ||||||
| chr11:71960434 | C | G | 8 | a0001c0003t0003g0008a0001c0003t0003g0213a0001c0003t0003g0214others(5): Show | 9 | HG01074.hp1 HG02486.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.102-316C>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 2/8 | chr11 | 71960434 | ||||||
| chr11:71960646 | G | C | 15 | a0001c0002t0006g0222a0001c0002t0006g0223a0001c0002t0006g0224others(12): Show | 15 | HG00738.hp1 HG01975.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.102-104G>C | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 2/8 | chr11 | 71960646 | ||||||
| chr11:71960937 | G | C | 1 | a0001c0001t0007g0067 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.243+46G>C | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71960937 | ||||||
| chr11:71961090 | C | T | 3 | a0001c0001t0001g0147a0001c0001t0001g0150a0001c0001t0001g0154 | 3 | HG01106.hp2 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.243+199C>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71961090 | ||||||
| chr11:71961133 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.243+242G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71961133 | ||||||
| chr11:71961286 | T | A | 1 | a0001c0001t0001g0077 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.243+395T>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71961286 | ||||||
| chr11:71961390 | A | G | 1 | a0001c0001t0001g0132 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.243+499A>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71961390 | ||||||
| chr11:71961635 | A | G | 10 | a0001c0001t0005g0200a0001c0001t0005g0201a0001c0001t0005g0202others(7): Show | 10 | HG02723.hp2 HG02896.hp2 HG02897.hp2 others(7): Show |
intron_variant | MODIFIER | c.243+744A>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71961635 | ||||||
| chr11:71961718 | G | A | 2 | a0001c0001t0007g0014a0001c0001t0007g0016 | 2 | HG02717.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.243+827G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71961718 | ||||||
| chr11:71961966 | A | AT | 153 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(150): Show | 156 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.243+1094dupT | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 71961966 | |||||
| chr11:71961966 | A | ATT | 9 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0118others(6): Show | 9 | HG00099.hp2 HG02615.hp1 HG02738.hp1 others(6): Show |
intron_variant | MODIFIER | c.243+1093_243+1094d others(4): Show |
RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 71961966 | |||||
| chr11:71961966 | A | ATTT | 8 | a0001c0001t0003g0237a0001c0001t0003g0239a0001c0001t0003g0240others(5): Show | 8 | HG02145.hp1 HG02723.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.243+1092_243+1094d others(5): Show |
RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 71961966 | |||||
| chr11:71961999 | G | A | 14 | a0001c0002t0006g0222a0001c0002t0006g0223a0001c0002t0006g0224others(11): Show | 14 | HG00738.hp1 HG01975.hp2 HG02683.hp2 others(11): Show |
intron_variant | MODIFIER | c.243+1108G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71961999 | ||||||
| chr11:71962253 | C | T | 8 | a0001c0003t0003g0008a0001c0003t0003g0213a0001c0003t0003g0214others(5): Show | 9 | HG01074.hp1 HG02486.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.243+1362C>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71962253 | ||||||
| chr11:71962255 | C | T | 14 | a0001c0002t0006g0222a0001c0002t0006g0223a0001c0002t0006g0224others(11): Show | 14 | HG00738.hp1 HG01975.hp2 HG02683.hp2 others(11): Show |
intron_variant | MODIFIER | c.243+1364C>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71962255 | ||||||
| chr11:71962473 | A | T | 1 | a0001c0001t0007g0067 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.243+1582A>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71962473 | ||||||
| chr11:71962597 | A | G | 1 | a0001c0001t0005g0205 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.243+1706A>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71962597 | ||||||
| chr11:71962686 | C | G | 168 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(165): Show | 171 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.243+1795C>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71962686 | ||||||
| chr11:71962866 | T | A | 2 | a0001c0001t0001g0086a0001c0001t0001g0210 | 2 | HG00280.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.243+1975T>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71962866 | ||||||
| chr11:71962886 | T | A | 183 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(180): Show | 186 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.243+1995T>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71962886 | ||||||
| chr11:71963195 | A | C | 1 | a0001c0001t0001g0126 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.243+2304A>C | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71963195 | ||||||
| chr11:71963255 | T | A | 1 | a0001c0001t0007g0067 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.243+2364T>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71963255 | ||||||
| chr11:71963308 | T | C | 183 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(180): Show | 186 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.243+2417T>C | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71963308 | ||||||
| chr11:71963624 | A | C | 1 | a0001c0001t0001g0115 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.243+2733A>C | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71963624 | ||||||
| chr11:71963628 | A | AT | 9 | a0001c0001t0005g0200a0001c0001t0005g0201a0001c0001t0005g0202others(6): Show | 9 | HG02723.hp2 HG02896.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.243+2737_243+2738i others(3): Show |
RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71963628 | ||||||
| chr11:71963745 | G | T | 1 | a0001c0001t0001g0097 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.243+2854G>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71963745 | ||||||
| chr11:71963830 | G | T | 3 | a0001c0001t0007g0001a0001c0001t0007g0002a0001c0001t0007g0013 | 6 | HG02109.hp1 HG02258.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.243+2939G>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71963830 | ||||||
| chr11:71963891 | G | A | 167 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(164): Show | 170 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.243+3000G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71963891 | ||||||
| chr11:71964118 | A | G | 1 | a0001c0001t0001g0133 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.243+3227A>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71964118 | ||||||
| chr11:71964142 | A | C | 4 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0030others(1): Show | 6 | HG00609.hp1 NA18947.hp1 NA18969.hp1 others(3): Show |
intron_variant | MODIFIER | c.243+3251A>C | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71964142 | ||||||
| chr11:71964252 | G | A | 15 | a0001c0002t0006g0222a0001c0002t0006g0223a0001c0002t0006g0224others(12): Show | 15 | HG00738.hp1 HG01975.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.243+3361G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71964252 | ||||||
| chr11:71964287 | T | A | 1 | a0001c0001t0005g0208 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.243+3396T>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71964287 | ||||||
| chr11:71964440 | T | TAGAG | 220 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(217): Show | 226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.243+3550_243+3553d others(6): Show |
RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 71964440 | |||||
| chr11:71964567 | C | T | 1 | a0001c0001t0001g0193 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.243+3676C>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71964567 | ||||||
| chr11:71964623 | G | A | 15 | a0001c0002t0006g0222a0001c0002t0006g0223a0001c0002t0006g0224others(12): Show | 15 | HG00738.hp1 HG01975.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.243+3732G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71964623 | ||||||
| chr11:71964631 | C | T | 1 | a0001c0001t0003g0244 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.243+3740C>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71964631 | ||||||
| chr11:71964699 | G | A | 1 | a0001c0005t0003g0220 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.243+3808G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71964699 | ||||||
| chr11:71964800 | A | G | 183 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(180): Show | 186 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.243+3909A>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71964800 | ||||||
| chr11:71965254 | A | AT | 13 | a0001c0002t0006g0223a0001c0002t0006g0224a0001c0002t0006g0225others(10): Show | 13 | HG00738.hp1 HG01975.hp2 HG02683.hp2 others(10): Show |
intron_variant | MODIFIER | c.243+4381dupT | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 71965254 | |||||
| chr11:71965254 | AT | A | 166 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(163): Show | 169 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.243+4381delT | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 71965254 | |||||
| chr11:71965437 | G | A | 1 | a0001c0002t0006g0227 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.243+4546G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71965437 | ||||||
| chr11:71965520 | A | G | 6 | a0001c0001t0003g0237a0001c0001t0003g0239a0001c0001t0003g0240others(3): Show | 6 | HG02723.hp1 HG02809.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.243+4629A>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71965520 | ||||||
| chr11:71965580 | A | G | 15 | a0001c0002t0006g0222a0001c0002t0006g0223a0001c0002t0006g0224others(12): Show | 15 | HG00738.hp1 HG01975.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.243+4689A>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71965580 | ||||||
| chr11:71965613 | T | G | 9 | a0001c0001t0005g0200a0001c0001t0005g0201a0001c0001t0005g0202others(6): Show | 9 | HG02723.hp2 HG02896.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.243+4722T>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71965613 | ||||||
| chr11:71965628 | G | A | 3 | a0001c0001t0007g0001a0001c0001t0007g0002a0001c0001t0007g0013 | 6 | HG02109.hp1 HG02258.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.243+4737G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71965628 | ||||||
| chr11:71965807 | A | G | 1 | a0001c0001t0002g0031 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.243+4916A>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71965807 | ||||||
| chr11:71965986 | C | G | 168 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(165): Show | 171 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.243+5095C>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71965986 | ||||||
| chr11:71966001 | A | G | 15 | a0001c0002t0006g0222a0001c0002t0006g0223a0001c0002t0006g0224others(12): Show | 15 | HG00738.hp1 HG01975.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.243+5110A>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71966001 | ||||||
| chr11:71966064 | G | C | 6 | a0001c0002t0006g0228a0001c0002t0006g0230a0001c0002t0006g0231others(3): Show | 6 | HG02683.hp2 HG02735.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.243+5173G>C | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71966064 | ||||||
| chr11:71966069 | G | A | 9 | a0001c0001t0003g0237a0001c0001t0003g0239a0001c0001t0003g0240others(6): Show | 9 | HG02145.hp1 HG02723.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.243+5178G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71966069 | ||||||
| chr11:71966205 | G | A | 155 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(152): Show | 157 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.243+5314G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71966205 | ||||||
| chr11:71966298 | T | G | 15 | a0001c0002t0006g0222a0001c0002t0006g0223a0001c0002t0006g0224others(12): Show | 15 | HG00738.hp1 HG01975.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.243+5407T>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71966298 | ||||||
| chr11:71966301 | G | A | 14 | a0001c0002t0006g0222a0001c0002t0006g0223a0001c0002t0006g0224others(11): Show | 14 | HG00738.hp1 HG01975.hp2 HG02683.hp2 others(11): Show |
intron_variant | MODIFIER | c.243+5410G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71966301 | ||||||
| chr11:71966306 | G | A | 15 | a0001c0002t0006g0222a0001c0002t0006g0223a0001c0002t0006g0224others(12): Show | 15 | HG00738.hp1 HG01975.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.243+5415G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71966306 | ||||||
| chr11:71966384 | C | G | 2 | a0001c0001t0001g0087a0001c0001t0001g0094 | 2 | HG02258.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.243+5493C>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71966384 | ||||||
| chr11:71966405 | G | A | 3 | a0001c0001t0007g0001a0001c0001t0007g0002a0001c0001t0007g0013 | 6 | HG02109.hp1 HG02258.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.243+5514G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71966405 | ||||||
| chr11:71966541 | G | C | 1 | a0001c0004t0005g0221 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.243+5650G>C | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71966541 | ||||||
| chr11:71966567 | A | T | 9 | a0001c0001t0003g0237a0001c0001t0003g0239a0001c0001t0003g0240others(6): Show | 9 | HG02145.hp1 HG02723.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.243+5676A>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71966567 | ||||||
| chr11:71966570 | C | T | 15 | a0001c0002t0006g0222a0001c0002t0006g0223a0001c0002t0006g0224others(12): Show | 15 | HG00738.hp1 HG01975.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.243+5679C>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71966570 | ||||||
| chr11:71966674 | G | C | 1 | a0001c0001t0001g0182 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.243+5783G>C | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71966674 | ||||||
| chr11:71966870 | GT | G | 165 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(162): Show | 167 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.243+5991delT | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 71966870 | |||||
| chr11:71966887 | C | T | 13 | a0001c0001t0004g0069a0001c0001t0004g0070a0001c0001t0004g0075others(10): Show | 13 | HG02451.hp2 HG02622.hp1 HG02647.hp2 others(10): Show |
intron_variant | MODIFIER | c.243+5996C>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71966887 | ||||||
| chr11:71966903 | C | T | 1 | a0001c0001t0004g0164 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.243+6012C>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71966903 | ||||||
| chr11:71966904 | A | G | 189 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(186): Show | 195 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(192): Show |
intron_variant | MODIFIER | c.243+6013A>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71966904 | ||||||
| chr11:71966912 | C | T | 167 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(164): Show | 170 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.243+6021C>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71966912 | ||||||
| chr11:71966966 | G | A | 1 | a0001c0001t0005g0204 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.243+6075G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71966966 | ||||||
| chr11:71967017 | A | G | 182 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(179): Show | 185 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.243+6126A>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71967017 | ||||||
| chr11:71967026 | C | T | 15 | a0001c0002t0006g0222a0001c0002t0006g0223a0001c0002t0006g0224others(12): Show | 15 | HG00738.hp1 HG01975.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.243+6135C>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71967026 | ||||||
| chr11:71967037 | A | G | 1 | a0001c0001t0001g0131 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.243+6146A>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71967037 | ||||||
| chr11:71967072 | C | T | 167 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(164): Show | 170 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.243+6181C>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71967072 | ||||||
| chr11:71967117 | C | T | 15 | a0001c0001t0001g0079a0001c0002t0006g0222a0001c0002t0006g0223others(12): Show | 15 | HG00738.hp1 HG01975.hp2 HG02683.hp2 others(12): Show |
intron_variant | MODIFIER | c.243+6226C>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71967117 | ||||||
| chr11:71967161 | G | A | 1 | a0001c0001t0007g0067 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.243+6270G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71967161 | ||||||
| chr11:71967167 | G | A | 9 | a0001c0001t0003g0237a0001c0001t0003g0239a0001c0001t0003g0240others(6): Show | 9 | HG02145.hp1 HG02723.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.243+6276G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71967167 | ||||||
| chr11:71967339 | G | T | 1 | a0001c0004t0005g0221 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.243+6448G>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71967339 | ||||||
| chr11:71967340 | G | T | 183 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(180): Show | 186 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.243+6449G>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71967340 | ||||||
| chr11:71967341 | T | A | 1 | a0001c0001t0004g0167 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.243+6450T>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71967341 | ||||||
| chr11:71967349 | G | GT | 129 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0068others(126): Show | 131 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.243+6476dupT | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 71967349 | |||||
| chr11:71967349 | G | GTT | 8 | a0001c0001t0001g0011a0001c0001t0001g0117a0001c0001t0001g0121others(5): Show | 8 | HG01106.hp2 HG02293.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.243+6475_243+6476d others(4): Show |
RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 71967349 | |||||
| chr11:71967349 | G | T | 3 | a0001c0001t0005g0204a0001c0002t0006g0225a0001c0002t0006g0226 | 3 | NA18981.hp2 NA19030.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.243+6458G>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71967349 | ||||||
| chr11:71967355 | T | G | 8 | a0001c0003t0003g0008a0001c0003t0003g0213a0001c0003t0003g0214others(5): Show | 9 | HG01074.hp1 HG02486.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.243+6464T>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71967355 | ||||||
| chr11:71967357 | T | G | 1 | a0001c0002t0015g0229 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.243+6466T>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71967357 | ||||||
| chr11:71967358 | T | TG | 3 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0135 | 3 | NA18950.hp2 NA19091.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.243+6467_243+6468i others(3): Show |
RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71967358 | ||||||
| chr11:71967629 | G | T | 6 | a0001c0003t0003g0008a0001c0003t0003g0214a0001c0003t0003g0215others(3): Show | 7 | HG01074.hp1 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.243+6738G>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71967629 | ||||||
| chr11:71967875 | A | T | 2 | a0001c0003t0003g0211a0001c0003t0003g0212 | 2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.243+6984A>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71967875 | ||||||
| chr11:71968068 | C | CT | 155 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(152): Show | 158 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.243+7188dupT | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 71968068 | |||||
| chr11:71968068 | C | CTT | 9 | a0001c0001t0003g0237a0001c0001t0003g0239a0001c0001t0003g0240others(6): Show | 9 | HG02145.hp1 HG02723.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.243+7187_243+7188d others(4): Show |
RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 71968068 | |||||
| chr11:71968151 | C | T | 15 | a0001c0002t0006g0222a0001c0002t0006g0223a0001c0002t0006g0224others(12): Show | 15 | HG00738.hp1 HG01975.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.243+7260C>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71968151 | ||||||
| chr11:71968163 | G | A | 8 | a0001c0003t0003g0008a0001c0003t0003g0213a0001c0003t0003g0214others(5): Show | 9 | HG01074.hp1 HG02486.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.243+7272G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71968163 | ||||||
| chr11:71968330 | G | A | 168 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(165): Show | 171 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.243+7439G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71968330 | ||||||
| chr11:71968475 | C | T | 1 | a0001c0005t0003g0220 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.243+7584C>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71968475 | ||||||
| chr11:71968525 | G | A | 1 | a0001c0001t0002g0020 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.243+7634G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71968525 | ||||||
| chr11:71968575 | G | A | 7 | a0001c0001t0005g0200a0001c0001t0005g0201a0001c0001t0005g0202others(4): Show | 7 | HG02723.hp2 HG02896.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.243+7684G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71968575 | ||||||
| chr11:71968888 | C | CT | 53 | a0001c0001t0001g0011a0001c0001t0001g0071a0001c0001t0001g0077others(50): Show | 56 | HG00673.hp2 HG00738.hp2 HG01074.hp2 others(53): Show |
intron_variant | MODIFIER | c.243+8012dupT | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 71968888 | |||||
| chr11:71968888 | C | CTT | 78 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(75): Show | 80 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.243+8011_243+8012d others(4): Show |
RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 71968888 | |||||
| chr11:71968892 | T | C | 1 | a0001c0001t0002g0026 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.243+8001T>C | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71968892 | ||||||
| chr11:71968940 | C | T | 1 | a0001c0001t0001g0194 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.243+8049C>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71968940 | ||||||
| chr11:71969107 | G | A | 1 | a0001c0001t0001g0155 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.243+8216G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71969107 | ||||||
| chr11:71969544 | C | T | 184 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(181): Show | 187 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.243+8653C>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71969544 | ||||||
| chr11:71969689 | G | A | 15 | a0001c0002t0006g0222a0001c0002t0006g0223a0001c0002t0006g0224others(12): Show | 15 | HG00738.hp1 HG01975.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.243+8798G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71969689 | ||||||
| chr11:71969711 | C | T | 168 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(165): Show | 171 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.243+8820C>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71969711 | ||||||
| chr11:71969874 | C | T | 183 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(180): Show | 186 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.243+8983C>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71969874 | ||||||
| chr11:71969958 | C | T | 1 | a0001c0001t0001g0085 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.243+9067C>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71969958 | ||||||
| chr11:71970107 | T | C | 190 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(187): Show | 196 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(193): Show |
intron_variant | MODIFIER | c.243+9216T>C | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71970107 | ||||||
| chr11:71970154 | T | C | 1 | a0001c0001t0001g0085 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.243+9263T>C | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71970154 | ||||||
| chr11:71970308 | G | T | 2 | a0001c0001t0002g0048a0001c0001t0002g0064 | 2 | NA18994.hp1 NA18997.hp2 |
intron_variant | MODIFIER | c.243+9417G>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71970308 | ||||||
| chr11:71970407 | T | C | 1 | a0001c0001t0001g0155 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.243+9516T>C | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71970407 | ||||||
| chr11:71970473 | C | T | 9 | a0001c0001t0003g0237a0001c0001t0003g0239a0001c0001t0003g0240others(6): Show | 9 | HG02145.hp1 HG02723.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.243+9582C>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71970473 | ||||||
| chr11:71970597 | C | T | 8 | a0001c0001t0002g0028a0001c0003t0003g0008a0001c0003t0003g0213others(5): Show | 9 | HG01074.hp1 HG02486.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.243+9706C>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71970597 | ||||||
| chr11:71970700 | G | A | 2 | a0001c0001t0005g0204a0001c0001t0005g0205 | 2 | HG03209.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.243+9809G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71970700 | ||||||
| chr11:71970807 | A | G | 2 | a0001c0001t0005g0201a0001c0001t0005g0203 | 2 | HG02723.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.243+9916A>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71970807 | ||||||
| chr11:71970818 | A | T | 9 | a0001c0001t0003g0237a0001c0001t0003g0239a0001c0001t0003g0240others(6): Show | 9 | HG02145.hp1 HG02723.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.243+9927A>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71970818 | ||||||
| chr11:71970859 | A | G | 14 | a0001c0002t0006g0222a0001c0002t0006g0223a0001c0002t0006g0224others(11): Show | 14 | HG00738.hp1 HG01975.hp2 HG02683.hp2 others(11): Show |
intron_variant | MODIFIER | c.243+9968A>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71970859 | ||||||
| chr11:71971134 | G | A | 13 | a0001c0001t0004g0069a0001c0001t0004g0070a0001c0001t0004g0075others(10): Show | 13 | HG02451.hp2 HG02622.hp1 HG02647.hp2 others(10): Show |
intron_variant | MODIFIER | c.243+10243G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71971134 | ||||||
| chr11:71971396 | A | C | 9 | a0001c0001t0003g0237a0001c0001t0003g0239a0001c0001t0003g0240others(6): Show | 9 | HG02145.hp1 HG02723.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.243+10505A>C | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71971396 | ||||||
| chr11:71971558 | A | G | 1 | a0001c0001t0001g0085 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.243+10667A>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71971558 | ||||||
| chr11:71971592 | AAGAC | A | 7 | a0001c0003t0003g0008a0001c0003t0003g0213a0001c0003t0003g0214others(4): Show | 8 | HG01074.hp1 HG02486.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.243+10704_243+1070 others(8): Show |
RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 71971592 | |||||
| chr11:71971926 | G | T | 1 | a0001c0001t0005g0209 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.244-10835G>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71971926 | ||||||
| chr11:71972061 | T | G | 3 | a0001c0001t0007g0001a0001c0001t0007g0002a0001c0001t0007g0013 | 6 | HG02109.hp1 HG02258.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.244-10700T>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71972061 | ||||||
| chr11:71972130 | A | G | 1 | a0001c0004t0005g0221 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.244-10631A>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71972130 | ||||||
| chr11:71972185 | G | C | 168 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(165): Show | 171 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.244-10576G>C | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71972185 | ||||||
| chr11:71972363 | C | T | 3 | a0001c0001t0007g0014a0001c0001t0007g0015a0001c0001t0007g0016 | 3 | HG02615.hp2 HG02717.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.244-10398C>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71972363 | ||||||
| chr11:71972568 | G | C | 1 | a0001c0001t0001g0118 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.244-10193G>C | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71972568 | ||||||
| chr11:71972598 | T | C | 1 | a0001c0001t0001g0100 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.244-10163T>C | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71972598 | ||||||
| chr11:71973042 | C | T | 1 | a0001c0002t0006g0227 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.244-9719C>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71973042 | ||||||
| chr11:71973090 | G | A | 3 | a0001c0001t0001g0147a0001c0001t0001g0150a0001c0001t0001g0154 | 3 | HG01106.hp2 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.244-9671G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71973090 | ||||||
| chr11:71973134 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.244-9627C>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71973134 | ||||||
| chr11:71973388 | G | A | 2 | a0001c0001t0005g0204a0001c0001t0005g0205 | 2 | HG03209.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.244-9373G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71973388 | ||||||
| chr11:71973552 | C | T | 3 | a0001c0001t0002g0027a0001c0001t0002g0038a0001c0001t0002g0039 | 3 | HG00558.hp2 HG00673.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.244-9209C>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71973552 | ||||||
| chr11:71973575 | T | G | 125 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(122): Show | 127 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.244-9186T>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71973575 | ||||||
| chr11:71973874 | G | A | 10 | a0001c0001t0005g0200a0001c0001t0005g0201a0001c0001t0005g0202others(7): Show | 10 | HG02723.hp2 HG02896.hp2 HG02897.hp2 others(7): Show |
intron_variant | MODIFIER | c.244-8887G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71973874 | ||||||
| chr11:71974011 | G | A | 1 | a0001c0001t0001g0171 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.244-8750G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71974011 | ||||||
| chr11:71974069 | G | A | 10 | a0001c0001t0005g0200a0001c0001t0005g0201a0001c0001t0005g0202others(7): Show | 10 | HG02723.hp2 HG02896.hp2 HG02897.hp2 others(7): Show |
intron_variant | MODIFIER | c.244-8692G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71974069 | ||||||
| chr11:71974131 | C | T | 3 | a0001c0003t0003g0211a0001c0003t0003g0212a0001c0005t0003g0220 | 3 | HG02965.hp1 HG03130.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.244-8630C>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71974131 | ||||||
| chr11:71974237 | A | G | 220 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(217): Show | 226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.244-8524A>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71974237 | ||||||
| chr11:71974266 | A | C | 15 | a0001c0002t0006g0222a0001c0002t0006g0223a0001c0002t0006g0224others(12): Show | 15 | HG00738.hp1 HG01975.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.244-8495A>C | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71974266 | ||||||
| chr11:71974383 | A | G | 183 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(180): Show | 186 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.244-8378A>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71974383 | ||||||
| chr11:71974518 | A | G | 1 | a0001c0001t0001g0115 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.244-8243A>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71974518 | ||||||
| chr11:71974527 | A | G | 1 | a0001c0001t0001g0184 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.244-8234A>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71974527 | ||||||
| chr11:71974640 | G | A | 1 | a0001c0001t0001g0115 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.244-8121G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71974640 | ||||||
| chr11:71974668 | CA | C | 156 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(153): Show | 158 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.244-8092delA | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71974668 | ||||||
| chr11:71974805 | T | C | 15 | a0001c0002t0006g0222a0001c0002t0006g0223a0001c0002t0006g0224others(12): Show | 15 | HG00738.hp1 HG01975.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.244-7956T>C | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71974805 | ||||||
| chr11:71974960 | G | A | 1 | a0001c0002t0006g0228 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.244-7801G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71974960 | ||||||
| chr11:71975113 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.244-7648G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71975113 | ||||||
| chr11:71975331 | A | G | 6 | a0001c0002t0006g0228a0001c0002t0006g0230a0001c0002t0006g0231others(3): Show | 6 | HG02683.hp2 HG02735.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.244-7430A>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71975331 | ||||||
| chr11:71975360 | C | T | 3 | a0001c0001t0001g0007a0001c0001t0001g0087a0001c0001t0001g0094 | 4 | HG02258.hp2 HG02280.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.244-7401C>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71975360 | ||||||
| chr11:71975665 | C | T | 1 | a0001c0001t0001g0185 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.244-7096C>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71975665 | ||||||
| chr11:71975755 | A | G | 1 | a0001c0001t0004g0170 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.244-7006A>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71975755 | ||||||
| chr11:71975941 | A | T | 7 | a0001c0003t0003g0008a0001c0003t0003g0213a0001c0003t0003g0214others(4): Show | 8 | HG01074.hp1 HG02486.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.244-6820A>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71975941 | ||||||
| chr11:71975971 | A | G | 1 | a0001c0005t0003g0220 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.244-6790A>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71975971 | ||||||
| chr11:71975993 | C | G | 1 | a0001c0001t0005g0204 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.244-6768C>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71975993 | ||||||
| chr11:71976193 | G | A | 1 | a0001c0001t0005g0208 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.244-6568G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71976193 | ||||||
| chr11:71976251 | T | C | 1 | a0001c0001t0001g0101 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.244-6510T>C | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71976251 | ||||||
| chr11:71976328 | T | A | 9 | a0001c0001t0003g0237a0001c0001t0003g0239a0001c0001t0003g0240others(6): Show | 9 | HG02145.hp1 HG02723.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.244-6433T>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71976328 | ||||||
| chr11:71976345 | C | CT | 11 | a0001c0001t0002g0005a0001c0001t0002g0019a0001c0001t0002g0050others(8): Show | 12 | HG00609.hp1 HG02109.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.244-6388dupT | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 71976345 | |||||
| chr11:71976345 | CT | C | 135 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0011others(132): Show | 137 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.244-6388delT | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 71976345 | |||||
| chr11:71976345 | CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0001g0098 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.244-6400_244-6388d others(15): Show |
RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 71976345 | |||||
| chr11:71976345 | CTTTTTTT others(9): Show |
C | 1 | a0001c0001t0001g0130 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.244-6403_244-6388d others(18): Show |
RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 71976345 | |||||
| chr11:71976442 | G | A | 4 | a0001c0001t0001g0130a0001c0001t0001g0136a0001c0001t0009g0081others(1): Show | 4 | HG02486.hp2 HG03195.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.244-6319G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71976442 | ||||||
| chr11:71976495 | G | A | 106 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005others(103): Show | 113 | HG00099.hp1 HG00323.hp1 HG00558.hp2 others(110): Show |
intron_variant | MODIFIER | c.244-6266G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71976495 | ||||||
| chr11:71976600 | T | C | 1 | a0001c0004t0005g0221 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.244-6161T>C | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71976600 | ||||||
| chr11:71976604 | T | C | 76 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005others(73): Show | 82 | HG00099.hp1 HG00323.hp1 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.244-6157T>C | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71976604 | ||||||
| chr11:71976748 | A | C | 61 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005others(58): Show | 67 | HG00099.hp1 HG00323.hp1 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.244-6013A>C | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71976748 | ||||||
| chr11:71977205 | G | A | 9 | a0001c0001t0003g0237a0001c0001t0003g0239a0001c0001t0003g0240others(6): Show | 9 | HG02145.hp1 HG02723.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.244-5556G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71977205 | ||||||
| chr11:71977301 | G | A | 60 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005others(57): Show | 66 | HG00099.hp1 HG00323.hp1 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.244-5460G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71977301 | ||||||
| chr11:71977934 | G | A | 9 | a0001c0001t0003g0237a0001c0001t0003g0239a0001c0001t0003g0240others(6): Show | 9 | HG02145.hp1 HG02723.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.244-4827G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71977934 | ||||||
| chr11:71977977 | G | A | 1 | a0001c0001t0002g0056 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.244-4784G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71977977 | ||||||
| chr11:71978070 | A | G | 1 | a0001c0001t0002g0018 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.244-4691A>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71978070 | ||||||
| chr11:71978196 | C | T | 3 | a0001c0001t0005g0206a0001c0001t0005g0207a0001c0001t0005g0209 | 3 | HG02976.hp1 HG03098.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.244-4565C>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71978196 | ||||||
| chr11:71978473 | G | A | 10 | a0001c0001t0005g0200a0001c0001t0005g0201a0001c0001t0005g0202others(7): Show | 10 | HG02723.hp2 HG02896.hp2 HG02897.hp2 others(7): Show |
intron_variant | MODIFIER | c.244-4288G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71978473 | ||||||
| chr11:71978495 | A | G | 168 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(165): Show | 171 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.244-4266A>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71978495 | ||||||
| chr11:71978553 | A | T | 183 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(180): Show | 186 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.244-4208A>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71978553 | ||||||
| chr11:71978558 | A | G | 1 | a0001c0001t0001g0128 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.244-4203A>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71978558 | ||||||
| chr11:71978650 | C | T | 2 | a0001c0003t0003g0211a0001c0003t0003g0212 | 2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.244-4111C>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71978650 | ||||||
| chr11:71979195 | T | C | 3 | a0001c0001t0001g0147a0001c0001t0001g0150a0001c0001t0001g0154 | 3 | HG01106.hp2 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.244-3566T>C | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71979195 | ||||||
| chr11:71979241 | C | T | 15 | a0001c0002t0006g0222a0001c0002t0006g0223a0001c0002t0006g0224others(12): Show | 15 | HG00738.hp1 HG01975.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.244-3520C>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71979241 | ||||||
| chr11:71979450 | T | C | 1 | a0001c0001t0001g0186 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.244-3311T>C | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71979450 | ||||||
| chr11:71979486 | C | T | 1 | a0001c0001t0003g0095 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.244-3275C>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71979486 | ||||||
| chr11:71979618 | A | G | 2 | a0001c0003t0003g0211a0001c0003t0003g0212 | 2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.244-3143A>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71979618 | ||||||
| chr11:71979950 | C | T | 5 | a0001c0001t0001g0187a0001c0001t0001g0189a0001c0001t0001g0190others(2): Show | 5 | HG01243.hp2 HG02630.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.244-2811C>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71979950 | ||||||
| chr11:71980142 | TC | T | 3 | a0001c0003t0003g0211a0001c0003t0003g0212a0001c0003t0003g0219 | 3 | HG02559.hp1 HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.244-2618delC | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71980142 | ||||||
| chr11:71980350 | CT | C | 226 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(223): Show | 234 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.244-2399delT | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 71980350 | |||||
| chr11:71980350 | CTT | C | 18 | a0001c0001t0001g0180a0001c0001t0003g0237a0001c0001t0003g0239others(15): Show | 19 | HG01074.hp1 HG02145.hp1 HG02486.hp1 others(16): Show |
intron_variant | MODIFIER | c.244-2400_244-2399d others(4): Show |
RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 71980350 | |||||
| chr11:71980377 | C | T | 15 | a0001c0002t0006g0222a0001c0002t0006g0223a0001c0002t0006g0224others(12): Show | 15 | HG00738.hp1 HG01975.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.244-2384C>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71980377 | ||||||
| chr11:71980816 | T | C | 1 | a0001c0001t0002g0059 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.244-1945T>C | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71980816 | ||||||
| chr11:71980900 | G | A | 183 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(180): Show | 186 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.244-1861G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71980900 | ||||||
| chr11:71980982 | A | G | 15 | a0001c0002t0006g0222a0001c0002t0006g0223a0001c0002t0006g0224others(12): Show | 15 | HG00738.hp1 HG01975.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.244-1779A>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71980982 | ||||||
| chr11:71981201 | A | C | 14 | a0001c0002t0006g0222a0001c0002t0006g0223a0001c0002t0006g0224others(11): Show | 14 | HG00738.hp1 HG01975.hp2 HG02683.hp2 others(11): Show |
intron_variant | MODIFIER | c.244-1560A>C | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71981201 | ||||||
| chr11:71981215 | A | AT | 138 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(135): Show | 140 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.244-1538dupT | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 71981215 | |||||
| chr11:71981350 | G | A | 1 | a0001c0004t0005g0221 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.244-1411G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71981350 | ||||||
| chr11:71981433 | T | G | 2 | a0001c0001t0007g0014a0001c0001t0007g0016 | 2 | HG02717.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.244-1328T>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71981433 | ||||||
| chr11:71981437 | T | A | 15 | a0001c0002t0006g0222a0001c0002t0006g0223a0001c0002t0006g0224others(12): Show | 15 | HG00738.hp1 HG01975.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.244-1324T>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71981437 | ||||||
| chr11:71981438 | T | A | 183 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(180): Show | 186 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.244-1323T>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71981438 | ||||||
| chr11:71981525 | A | T | 2 | a0001c0001t0002g0041a0001c0001t0002g0042 | 2 | NA18950.hp1 NA18951.hp2 |
intron_variant | MODIFIER | c.244-1236A>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71981525 | ||||||
| chr11:71981582 | A | G | 1 | a0001c0001t0009g0140 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.244-1179A>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71981582 | ||||||
| chr11:71981583 | T | C | 7 | a0001c0003t0003g0008a0001c0003t0003g0213a0001c0003t0003g0214others(4): Show | 8 | HG01074.hp1 HG02486.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.244-1178T>C | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71981583 | ||||||
| chr11:71981595 | C | T | 14 | a0001c0002t0006g0222a0001c0002t0006g0223a0001c0002t0006g0224others(11): Show | 14 | HG00738.hp1 HG01975.hp2 HG02683.hp2 others(11): Show |
intron_variant | MODIFIER | c.244-1166C>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71981595 | ||||||
| chr11:71981750 | C | G | 1 | a0001c0002t0006g0225 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.244-1011C>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71981750 | ||||||
| chr11:71981795 | T | C | 1 | a0001c0001t0001g0102 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.244-966T>C | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71981795 | ||||||
| chr11:71981987 | C | T | 1 | a0001c0001t0001g0114 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.244-774C>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71981987 | ||||||
| chr11:71982295 | C | T | 2 | a0001c0001t0001g0109a0001c0001t0001g0156 | 2 | NA19007.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.244-466C>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71982295 | ||||||
| chr11:71982335 | C | CA | 5 | a0001c0001t0001g0130a0001c0001t0002g0032a0001c0001t0002g0052others(2): Show | 5 | HG00621.hp2 HG02074.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.244-407dupA | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 71982335 | |||||
| chr11:71982335 | C | CAA | 14 | a0001c0001t0007g0067a0001c0002t0006g0222a0001c0002t0006g0223others(11): Show | 14 | HG00738.hp1 HG01975.hp2 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.244-408_244-407dup others(2): Show |
RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 71982335 | |||||
| chr11:71982335 | C | CAAAA | 13 | a0001c0001t0001g0007a0001c0001t0001g0078a0001c0001t0001g0094others(10): Show | 14 | HG00099.hp2 HG01074.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.244-410_244-407dup others(4): Show |
RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 71982335 | |||||
| chr11:71982335 | C | CAAAAA | 142 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0011others(139): Show | 144 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(141): Show |
intron_variant | MODIFIER | c.244-411_244-407dup others(5): Show |
RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 71982335 | |||||
| chr11:71982335 | C | CAAAAAA | 9 | a0001c0001t0001g0079a0001c0001t0001g0098a0001c0001t0001g0131others(6): Show | 9 | HG01175.hp1 HG03130.hp2 HG03209.hp1 others(6): Show |
intron_variant | MODIFIER | c.244-412_244-407dup others(6): Show |
RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 71982335 | |||||
| chr11:71982382 | T | C | 2 | a0001c0001t0004g0162a0001c0001t0004g0168 | 2 | NA18522.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.244-379T>C | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71982382 | ||||||
| chr11:71982399 | G | A | 1 | a0001c0001t0001g0131 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.244-362G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71982399 | ||||||
| chr11:71982422 | C | T | 1 | a0001c0001t0002g0053 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.244-339C>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71982422 | ||||||
| chr11:71982423 | G | A | 14 | a0001c0002t0006g0222a0001c0002t0006g0223a0001c0002t0006g0224others(11): Show | 14 | HG00738.hp1 HG01975.hp2 HG02683.hp2 others(11): Show |
intron_variant | MODIFIER | c.244-338G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 3/8 | chr11 | 71982423 | ||||||
| chr11:71982985 | A | G | 1 | a0001c0001t0001g0123 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.398+70A>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 4/8 | chr11 | 71982985 | ||||||
| chr11:71983078 | C | T | 1 | a0001c0001t0003g0244 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.398+163C>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 4/8 | chr11 | 71983078 | ||||||
| chr11:71983599 | C | T | 183 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(180): Show | 186 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.398+684C>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 4/8 | chr11 | 71983599 | ||||||
| chr11:71984308 | G | A | 1 | a0001c0001t0002g0017 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.398+1393G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 4/8 | chr11 | 71984308 | ||||||
| chr11:71984316 | G | A | 4 | a0001c0001t0005g0200a0001c0001t0005g0201a0001c0001t0005g0202others(1): Show | 4 | HG02723.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.398+1401G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 4/8 | chr11 | 71984316 | ||||||
| chr11:71984328 | G | A | 4 | a0001c0001t0001g0076a0001c0001t0001g0082a0001c0001t0001g0107others(1): Show | 4 | HG02074.hp1 NA18951.hp1 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.398+1413G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 4/8 | chr11 | 71984328 | ||||||
| chr11:71984480 | C | A | 183 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(180): Show | 186 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.398+1565C>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 4/8 | chr11 | 71984480 | ||||||
| chr11:71984632 | A | G | 184 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(181): Show | 187 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.398+1717A>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 4/8 | chr11 | 71984632 | ||||||
| chr11:71984745 | A | AT | 5 | a0001c0001t0002g0010a0001c0001t0002g0022a0001c0001t0002g0041others(2): Show | 5 | HG00621.hp2 HG02886.hp1 NA18951.hp2 others(2): Show |
intron_variant | MODIFIER | c.398+1855dupT | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 71984745 | |||||
| chr11:71984745 | A | ATTTT | 7 | a0001c0001t0005g0200a0001c0001t0005g0201a0001c0001t0005g0202others(4): Show | 7 | HG02280.hp2 HG02723.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.398+1852_398+1855d others(6): Show |
RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 71984745 | |||||
| chr11:71984745 | AT | A | 10 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0024others(7): Show | 13 | HG02109.hp1 HG02145.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.398+1855delT | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 71984745 | |||||
| chr11:71984745 | ATTT | A | 19 | a0001c0001t0001g0009a0001c0001t0001g0079a0001c0001t0001g0087others(16): Show | 19 | HG02148.hp2 HG02622.hp1 HG02622.hp2 others(16): Show |
intron_variant | MODIFIER | c.398+1853_398+1855d others(5): Show |
RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 71984745 | |||||
| chr11:71984745 | ATTTT | A | 122 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(119): Show | 124 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.398+1852_398+1855d others(6): Show |
RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 71984745 | |||||
| chr11:71984745 | ATTTTTTT | A | 21 | a0001c0002t0006g0222a0001c0002t0006g0223a0001c0002t0006g0225others(18): Show | 22 | HG00738.hp1 HG01074.hp1 HG01975.hp2 others(19): Show |
intron_variant | MODIFIER | c.398+1849_398+1855d others(9): Show |
RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 71984745 | |||||
| chr11:71984833 | C | T | 3 | a0001c0001t0007g0014a0001c0001t0007g0015a0001c0001t0007g0016 | 3 | HG02615.hp2 HG02717.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.398+1918C>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 4/8 | chr11 | 71984833 | ||||||
| chr11:71984839 | G | A | 2 | a0001c0001t0001g0086a0001c0001t0001g0210 | 2 | HG00280.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.398+1924G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 4/8 | chr11 | 71984839 | ||||||
| chr11:71984938 | T | TA | 137 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(134): Show | 139 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.398+2024dupA | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 71984938 | |||||
| chr11:71984947 | G | A | 1 | a0001c0001t0001g0078 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.398+2032G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 4/8 | chr11 | 71984947 | ||||||
| chr11:71984990 | C | T | 1 | a0001c0001t0001g0083 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.399-2014C>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 4/8 | chr11 | 71984990 | ||||||
| chr11:71985014 | T | C | 1 | a0001c0001t0014g0236 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.399-1990T>C | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 4/8 | chr11 | 71985014 | ||||||
| chr11:71985164 | G | C | 243 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(240): Show | 252 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.399-1840G>C | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 4/8 | chr11 | 71985164 | ||||||
| chr11:71985214 | A | G | 2 | a0001c0003t0003g0211a0001c0003t0003g0212 | 2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.399-1790A>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 4/8 | chr11 | 71985214 | ||||||
| chr11:71985497 | T | A | 243 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(240): Show | 252 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.399-1507T>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 4/8 | chr11 | 71985497 | ||||||
| chr11:71985821 | A | C | 1 | a0001c0001t0002g0062 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.399-1183A>C | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 4/8 | chr11 | 71985821 | ||||||
| chr11:71985943 | A | G | 1 | a0001c0001t0001g0113 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.399-1061A>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 4/8 | chr11 | 71985943 | ||||||
| chr11:71986010 | A | G | 1 | a0001c0001t0002g0027 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.399-994A>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 4/8 | chr11 | 71986010 | ||||||
| chr11:71986024 | T | C | 1 | a0001c0004t0005g0221 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.399-980T>C | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 4/8 | chr11 | 71986024 | ||||||
| chr11:71986034 | G | C | 1 | a0001c0002t0006g0230 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.399-970G>C | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 4/8 | chr11 | 71986034 | ||||||
| chr11:71986203 | A | G | 7 | a0001c0003t0003g0008a0001c0003t0003g0213a0001c0003t0003g0214others(4): Show | 8 | HG01074.hp1 HG02486.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.399-801A>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 4/8 | chr11 | 71986203 | ||||||
| chr11:71986328 | T | C | 1 | a0001c0001t0001g0190 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.399-676T>C | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 4/8 | chr11 | 71986328 | ||||||
| chr11:71986542 | T | C | 168 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(165): Show | 171 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.399-462T>C | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 4/8 | chr11 | 71986542 | ||||||
| chr11:71986568 | C | G | 1 | a0001c0002t0006g0235 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.399-436C>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 4/8 | chr11 | 71986568 | ||||||
| chr11:71986684 | G | A | 8 | a0001c0003t0003g0008a0001c0003t0003g0213a0001c0003t0003g0214others(5): Show | 9 | HG01074.hp1 HG02486.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.399-320G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 4/8 | chr11 | 71986684 | ||||||
| chr11:71986769 | CA | C | 171 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(168): Show | 174 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.399-215delA | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 71986769 | |||||
| chr11:71986785 | A | G | 1 | a0001c0001t0007g0067 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.399-219A>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 4/8 | chr11 | 71986785 | ||||||
| chr11:71986786 | A | G | 5 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0030others(2): Show | 7 | HG00609.hp1 HG02559.hp1 NA18947.hp1 others(4): Show |
intron_variant | MODIFIER | c.399-218A>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 4/8 | chr11 | 71986786 | ||||||
| chr11:71986787 | A | G | 1 | a0001c0001t0001g0112 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.399-217A>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 4/8 | chr11 | 71986787 | ||||||
| chr11:71987198 | A | G | 3 | a0001c0001t0007g0001a0001c0001t0007g0002a0001c0001t0007g0013 | 6 | HG02109.hp1 HG02258.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.506+87A>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 5/8 | chr11 | 71987198 | ||||||
| chr11:71987270 | G | T | 2 | a0001c0001t0002g0049a0001c0001t0002g0052 | 2 | NA18967.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.506+159G>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 5/8 | chr11 | 71987270 | ||||||
| chr11:71987492 | A | C | 1 | a0001c0001t0007g0067 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.506+381A>C | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 5/8 | chr11 | 71987492 | ||||||
| chr11:71987494 | G | A | 1 | a0001c0001t0001g0092 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.506+383G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 5/8 | chr11 | 71987494 | ||||||
| chr11:71987670 | G | A | 2 | a0001c0003t0003g0211a0001c0003t0003g0212 | 2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.506+559G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 5/8 | chr11 | 71987670 | ||||||
| chr11:71987691 | A | G | 1 | a0001c0001t0001g0176 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.506+580A>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 5/8 | chr11 | 71987691 | ||||||
| chr11:71987755 | G | A | 182 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(179): Show | 185 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.506+644G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 5/8 | chr11 | 71987755 | ||||||
| chr11:71987792 | A | G | 183 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(180): Show | 186 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.506+681A>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 5/8 | chr11 | 71987792 | ||||||
| chr11:71987818 | T | C | 15 | a0001c0002t0006g0222a0001c0002t0006g0223a0001c0002t0006g0224others(12): Show | 15 | HG00738.hp1 HG01975.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.506+707T>C | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 5/8 | chr11 | 71987818 | ||||||
| chr11:71987872 | T | C | 184 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(181): Show | 187 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.506+761T>C | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 5/8 | chr11 | 71987872 | ||||||
| chr11:71987884 | G | A | 2 | a0001c0001t0001g0098a0001c0001t0001g0103 | 2 | NA18993.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.506+773G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 5/8 | chr11 | 71987884 | ||||||
| chr11:71987964 | G | A | 5 | a0001c0001t0001g0090a0001c0001t0001g0143a0001c0001t0001g0148others(2): Show | 5 | NA18969.hp2 NA18983.hp1 NA18997.hp1 others(2): Show |
intron_variant | MODIFIER | c.506+853G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 5/8 | chr11 | 71987964 | ||||||
| chr11:71988172 | G | A | 15 | a0001c0002t0006g0222a0001c0002t0006g0223a0001c0002t0006g0224others(12): Show | 15 | HG00738.hp1 HG01975.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.506+1061G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 5/8 | chr11 | 71988172 | ||||||
| chr11:71988297 | G | T | 2 | a0001c0003t0003g0211a0001c0003t0003g0212 | 2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.506+1186G>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 5/8 | chr11 | 71988297 | ||||||
| chr11:71988379 | G | A | 1 | a0001c0001t0001g0111 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.506+1268G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 5/8 | chr11 | 71988379 | ||||||
| chr11:71988640 | T | TA | 153 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(150): Show | 155 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.506+1544dupA | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr11 | 71988640 | |||||
| chr11:71988652 | A | AG | 14 | a0001c0002t0006g0222a0001c0002t0006g0223a0001c0002t0006g0224others(11): Show | 14 | HG00738.hp1 HG01975.hp2 HG02683.hp2 others(11): Show |
intron_variant | MODIFIER | c.506+1541_506+1542i others(3): Show |
RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 5/8 | chr11 | 71988652 | ||||||
| chr11:71988799 | G | C | 9 | a0001c0001t0003g0237a0001c0001t0003g0239a0001c0001t0003g0240others(6): Show | 9 | HG02145.hp1 HG02723.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.506+1688G>C | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 5/8 | chr11 | 71988799 | ||||||
| chr11:71988823 | G | A | 1 | a0001c0004t0005g0221 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.506+1712G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 5/8 | chr11 | 71988823 | ||||||
| chr11:71989070 | T | TTTTG | 147 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0011others(144): Show | 148 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.507-1499_507-1496d others(6): Show |
RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr11 | 71989070 | |||||
| chr11:71989070 | TTTTG | T | 18 | a0001c0001t0001g0007a0001c0001t0003g0237a0001c0001t0003g0239others(15): Show | 19 | HG00738.hp1 HG01975.hp2 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.507-1499_507-1496d others(6): Show |
RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr11 | 71989070 | |||||
| chr11:71989289 | G | A | 1 | a0001c0001t0002g0038 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.507-1308G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 5/8 | chr11 | 71989289 | ||||||
| chr11:71989468 | G | A | 3 | a0001c0002t0006g0225a0001c0002t0006g0226a0001c0002t0006g0233 | 3 | NA18981.hp2 NA18995.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.507-1129G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 5/8 | chr11 | 71989468 | ||||||
| chr11:71989520 | G | A | 147 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(144): Show | 149 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.507-1077G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 5/8 | chr11 | 71989520 | ||||||
| chr11:71989862 | T | C | 184 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(181): Show | 187 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.507-735T>C | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 5/8 | chr11 | 71989862 | ||||||
| chr11:71990000 | C | T | 13 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189others(10): Show | 13 | HG01243.hp2 HG02451.hp1 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.507-597C>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 5/8 | chr11 | 71990000 | ||||||
| chr11:71990115 | T | C | 48 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0068others(45): Show | 49 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(46): Show |
intron_variant | MODIFIER | c.507-482T>C | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 5/8 | chr11 | 71990115 | ||||||
| chr11:71990321 | A | G | 167 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(164): Show | 170 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.507-276A>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 5/8 | chr11 | 71990321 | ||||||
| chr11:71990374 | G | A | 1 | a0001c0001t0002g0030 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.507-223G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 5/8 | chr11 | 71990374 | ||||||
| chr11:71990421 | G | A | 1 | a0001c0001t0001g0180 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.507-176G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 5/8 | chr11 | 71990421 | ||||||
| chr11:71990456 | G | C | 15 | a0001c0002t0006g0222a0001c0002t0006g0223a0001c0002t0006g0224others(12): Show | 15 | HG00738.hp1 HG01975.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.507-141G>C | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 5/8 | chr11 | 71990456 | ||||||
| chr11:71990477 | G | A | 183 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(180): Show | 186 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.507-120G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 5/8 | chr11 | 71990477 | ||||||
| chr11:71990486 | C | T | 14 | a0001c0002t0006g0222a0001c0002t0006g0223a0001c0002t0006g0224others(11): Show | 14 | HG00738.hp1 HG01975.hp2 HG02683.hp2 others(11): Show |
intron_variant | MODIFIER | c.507-111C>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 5/8 | chr11 | 71990486 | ||||||
| chr11:71991090 | A | G | 1 | a0001c0001t0001g0135 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.627+373A>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 6/8 | chr11 | 71991090 | ||||||
| chr11:71991092 | G | A | 167 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(164): Show | 170 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.627+375G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 6/8 | chr11 | 71991092 | ||||||
| chr11:71991191 | AC | A | 3 | a0001c0001t0002g0034a0001c0001t0002g0036a0001c0001t0002g0062 | 3 | HG03017.hp2 HG03927.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.627+476delC | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr11 | 71991191 | |||||
| chr11:71991202 | T | C | 1 | a0001c0001t0001g0106 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.627+485T>C | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 6/8 | chr11 | 71991202 | ||||||
| chr11:71991236 | T | TA | 135 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(132): Show | 137 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.627+529dupA | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr11 | 71991236 | |||||
| chr11:71991299 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.627+582G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 6/8 | chr11 | 71991299 | ||||||
| chr11:71991385 | A | G | 184 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(181): Show | 187 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.627+668A>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 6/8 | chr11 | 71991385 | ||||||
| chr11:71991954 | C | CA | 12 | a0001c0001t0001g0098a0001c0001t0001g0100a0001c0001t0001g0103others(9): Show | 12 | HG01175.hp2 HG01192.hp2 HG02056.hp1 others(9): Show |
intron_variant | MODIFIER | c.627+1251dupA | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr11 | 71991954 | |||||
| chr11:71991954 | CA | C | 15 | a0001c0002t0006g0222a0001c0002t0006g0223a0001c0002t0006g0224others(12): Show | 15 | HG00738.hp1 HG01975.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.627+1251delA | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr11 | 71991954 | |||||
| chr11:71992245 | T | G | 5 | a0001c0001t0001g0078a0001c0001t0001g0092a0001c0001t0001g0093others(2): Show | 5 | HG00673.hp2 HG01074.hp2 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.627+1528T>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 6/8 | chr11 | 71992245 | ||||||
| chr11:71992437 | G | A | 3 | a0001c0001t0001g0147a0001c0001t0001g0150a0001c0001t0001g0154 | 3 | HG01106.hp2 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.627+1720G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 6/8 | chr11 | 71992437 | ||||||
| chr11:71992466 | CT | C | 3 | a0001c0001t0001g0007a0001c0001t0001g0087a0001c0001t0001g0094 | 4 | HG02258.hp2 HG02280.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.627+1752delT | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr11 | 71992466 | |||||
| chr11:71992469 | T | C | 2 | a0001c0001t0001g0102a0001c0001t0001g0110 | 2 | HG00558.hp1 HG00621.hp1 |
intron_variant | MODIFIER | c.627+1752T>C | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 6/8 | chr11 | 71992469 | ||||||
| chr11:71992571 | C | A | 1 | a0001c0001t0001g0179 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.627+1854C>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 6/8 | chr11 | 71992571 | ||||||
| chr11:71992689 | A | G | 14 | a0001c0002t0006g0222a0001c0002t0006g0223a0001c0002t0006g0224others(11): Show | 14 | HG00738.hp1 HG01975.hp2 HG02683.hp2 others(11): Show |
intron_variant | MODIFIER | c.627+1972A>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 6/8 | chr11 | 71992689 | ||||||
| chr11:71992701 | C | T | 3 | a0001c0001t0007g0014a0001c0001t0007g0015a0001c0001t0007g0016 | 3 | HG02615.hp2 HG02717.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.627+1984C>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 6/8 | chr11 | 71992701 | ||||||
| chr11:71992803 | G | A | 182 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(179): Show | 185 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.628-1916G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 6/8 | chr11 | 71992803 | ||||||
| chr11:71992834 | AT | A | 6 | a0001c0002t0006g0228a0001c0002t0006g0230a0001c0002t0006g0231others(3): Show | 6 | HG02683.hp2 HG02735.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.628-1875delT | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr11 | 71992834 | |||||
| chr11:71992834 | ATTTT | A | 167 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(164): Show | 170 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.628-1878_628-1875d others(6): Show |
RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr11 | 71992834 | |||||
| chr11:71992889 | G | A | 182 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(179): Show | 185 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.628-1830G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 6/8 | chr11 | 71992889 | ||||||
| chr11:71993095 | G | T | 11 | a0001c0003t0003g0008a0001c0003t0003g0211a0001c0003t0003g0212others(8): Show | 12 | HG01074.hp1 HG02486.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.628-1624G>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 6/8 | chr11 | 71993095 | ||||||
| chr11:71993114 | T | C | 4 | a0001c0001t0001g0077a0001c0001t0001g0098a0001c0001t0001g0103others(1): Show | 4 | NA18971.hp1 NA18993.hp2 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.628-1605T>C | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 6/8 | chr11 | 71993114 | ||||||
| chr11:71993264 | A | G | 15 | a0001c0002t0006g0222a0001c0002t0006g0223a0001c0002t0006g0224others(12): Show | 15 | HG00738.hp1 HG01975.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.628-1455A>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 6/8 | chr11 | 71993264 | ||||||
| chr11:71993301 | T | A | 11 | a0001c0003t0003g0008a0001c0003t0003g0211a0001c0003t0003g0212others(8): Show | 12 | HG01074.hp1 HG02486.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.628-1418T>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 6/8 | chr11 | 71993301 | ||||||
| chr11:71993380 | C | T | 7 | a0001c0003t0003g0008a0001c0003t0003g0213a0001c0003t0003g0214others(4): Show | 8 | HG01074.hp1 HG02486.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.628-1339C>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 6/8 | chr11 | 71993380 | ||||||
| chr11:71993476 | T | TTGTCTC | 182 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(179): Show | 185 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.628-1241_628-1240i others(8): Show |
RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr11 | 71993476 | |||||
| chr11:71993495 | G | A | 1 | a0001c0001t0005g0208 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.628-1224G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 6/8 | chr11 | 71993495 | ||||||
| chr11:71993533 | A | T | 1 | a0001c0001t0001g0184 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.628-1186A>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 6/8 | chr11 | 71993533 | ||||||
| chr11:71993575 | C | T | 3 | a0001c0001t0007g0001a0001c0001t0007g0002a0001c0001t0007g0013 | 6 | HG02109.hp1 HG02258.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.628-1144C>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 6/8 | chr11 | 71993575 | ||||||
| chr11:71993841 | C | CT | 6 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0002g0050others(3): Show | 9 | HG02109.hp1 HG02258.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.628-861dupT | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr11 | 71993841 | |||||
| chr11:71993841 | CT | C | 20 | a0001c0001t0001g0107a0001c0001t0001g0150a0001c0001t0001g0153others(17): Show | 20 | HG00738.hp1 HG01975.hp2 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.628-861delT | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr11 | 71993841 | |||||
| chr11:71993873 | G | C | 9 | a0001c0001t0003g0237a0001c0001t0003g0239a0001c0001t0003g0240others(6): Show | 9 | HG02145.hp1 HG02723.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.628-846G>C | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 6/8 | chr11 | 71993873 | ||||||
| chr11:71993993 | A | T | 3 | a0001c0003t0003g0211a0001c0003t0003g0212a0001c0003t0003g0219 | 3 | HG02559.hp1 HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.628-726A>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 6/8 | chr11 | 71993993 | ||||||
| chr11:71994083 | G | A | 183 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(180): Show | 186 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.628-636G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 6/8 | chr11 | 71994083 | ||||||
| chr11:71994119 | C | T | 2 | a0001c0001t0002g0022a0001c0001t0002g0023 | 2 | HG01433.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.628-600C>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 6/8 | chr11 | 71994119 | ||||||
| chr11:71994122 | C | G | 2 | a0001c0001t0002g0031a0001c0001t0003g0095 | 2 | HG00099.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.628-597C>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 6/8 | chr11 | 71994122 | ||||||
| chr11:71994383 | A | G | 8 | a0001c0001t0004g0069a0001c0001t0004g0070a0001c0001t0004g0161others(5): Show | 8 | HG02451.hp2 HG02647.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.628-336A>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 6/8 | chr11 | 71994383 | ||||||
| chr11:71994468 | G | A | 13 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189others(10): Show | 13 | HG01243.hp2 HG02451.hp1 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.628-251G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 6/8 | chr11 | 71994468 | ||||||
| chr11:71994541 | T | G | 2 | a0001c0001t0002g0050a0001c0001t0002g0063 | 2 | NA18979.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.628-178T>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 6/8 | chr11 | 71994541 | ||||||
| chr11:71994560 | T | C | 1 | a0001c0002t0006g0222 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.628-159T>C | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 6/8 | chr11 | 71994560 | ||||||
| chr11:71994610 | C | T | 2 | a0001c0003t0003g0211a0001c0003t0003g0212 | 2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.628-109C>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 6/8 | chr11 | 71994610 | ||||||
| chr11:71994622 | G | A | 1 | a0001c0003t0003g0213 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.628-97G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 6/8 | chr11 | 71994622 | ||||||
| chr11:71994935 | C | G | 1 | a0001c0001t0002g0060 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.761+83C>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 7/8 | chr11 | 71994935 | ||||||
| chr11:71995051 | G | A | 2 | a0001c0001t0001g0158a0001c0001t0001g0174 | 2 | HG01255.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.761+199G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 7/8 | chr11 | 71995051 | ||||||
| chr11:71995140 | G | A | 9 | a0001c0001t0003g0237a0001c0001t0003g0239a0001c0001t0003g0240others(6): Show | 9 | HG02145.hp1 HG02723.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.761+288G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 7/8 | chr11 | 71995140 | ||||||
| chr11:71995286 | C | A | 15 | a0001c0002t0006g0222a0001c0002t0006g0223a0001c0002t0006g0224others(12): Show | 15 | HG00738.hp1 HG01975.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.762-164C>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 7/8 | chr11 | 71995286 | ||||||
| chr11:71995409 | C | T | 15 | a0001c0002t0006g0222a0001c0002t0006g0223a0001c0002t0006g0224others(12): Show | 15 | HG00738.hp1 HG01975.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.762-41C>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 7/8 | chr11 | 71995409 | ||||||
| chr11:71995615 | C | A | 1 | a0001c0001t0002g0024 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.863+64C>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 8/8 | chr11 | 71995615 | ||||||
| chr11:71995700 | G | A | 15 | a0001c0002t0006g0222a0001c0002t0006g0223a0001c0002t0006g0224others(12): Show | 15 | HG00738.hp1 HG01975.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.863+149G>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 8/8 | chr11 | 71995700 | ||||||
| chr11:71995712 | C | A | 4 | a0001c0001t0001g0173a0001c0001t0001g0175a0001c0001t0001g0176others(1): Show | 4 | HG01243.hp1 HG01255.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.863+161C>A | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 8/8 | chr11 | 71995712 | ||||||
| chr11:71995762 | C | T | 1 | a0001c0001t0001g0142 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.863+211C>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 8/8 | chr11 | 71995762 | ||||||
| chr11:71996056 | C | T | 15 | a0001c0002t0006g0222a0001c0002t0006g0223a0001c0002t0006g0224others(12): Show | 15 | HG00738.hp1 HG01975.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.864-139C>T | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 8/8 | chr11 | 71996056 | ||||||
| chr11:71996103 | A | G | 1 | a0001c0001t0001g0091 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.864-92A>G | RNF121 | ENSG00000137522.18 | transcript | ENST00000361756.8 | protein_coding | 8/8 | chr11 | 71996103 |