| geneid | 220441 |
|---|---|
| ensemblid | ENSG00000176641.11 |
| hgncid | 26811 |
| symbol | RNF152 |
| name | ring finger protein 152 |
| refseq_nuc | NM_173557.3 |
| refseq_prot | NP_775828.1 |
| ensembl_nuc | ENST00000312828.4 |
| ensembl_prot | ENSP00000316628.3 |
| mane_status | MANE Select |
| chr | chr18 |
| start | 61808067 |
| end | 61893007 |
| strand | - |
| ver | v1.2 |
| region | chr18:61808067-61893007 |
| region5000 | chr18:61803067-61898007 |
| regionname0 | RNF152_chr18_61808067_61893007 |
| regionname5000 | RNF152_chr18_61803067_61898007 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 203 | 308 | 85 | 51 | 128 | 14 | 28 | 96 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0002 | 0/0 | 203 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0003 | 0/0 | 203 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/0 | 612 | 247 | 59 | 43 | 112 | 11 | 21 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| c0002 | 0/0 | 612 | 55 | 24 | 8 | 15 | 2 | 6 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| c0003 | 0/1 | 612 | 3 | 1 | 0 | 0 | 1 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| c0004 | 0/0 | 612 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| c0005 | 0/0 | 612 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| c0006 | 0/0 | 612 | 1 | 0 | 0 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| c0007 | 0/0 | 612 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| c0008 | 0/0 | 612 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 8136 | 46 | 4 | 3 | 37 | 0 | 2 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0002 | 0/0 | 8130 | 22 | 1 | 9 | 6 | 3 | 3 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0003 | 1/0 | 8134 | 16 | 2 | 3 | 7 | 1 | 2 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0004 | 0/0 | 8134 | 13 | 1 | 3 | 5 | 2 | 2 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0005 | 0/0 | 8144 | 11 | 1 | 2 | 5 | 0 | 3 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0006 | 0/0 | 8135 | 10 | 1 | 2 | 6 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0007 | 0/0 | 8131 | 10 | 0 | 1 | 7 | 1 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0008 | 0/0 | 8137 | 6 | 0 | 2 | 3 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0009 | 0/0 | 8130 | 5 | 0 | 0 | 5 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0010 | 0/0 | 8132 | 5 | 4 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0011 | 0/0 | 8134 | 4 | 2 | 1 | 0 | 1 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0012 | 0/0 | 8135 | 4 | 2 | 1 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0013 | 0/0 | 8132 | 4 | 4 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0014 | 0/0 | 8132 | 4 | 3 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0015 | 0/0 | 8145 | 3 | 0 | 1 | 1 | 1 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0016 | 0/0 | 8122 | 3 | 3 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0017 | 0/1 | 8125 | 3 | 1 | 0 | 0 | 1 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0018 | 0/0 | 8130 | 3 | 0 | 3 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0019 | 0/0 | 8135 | 3 | 0 | 2 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0020 | 0/0 | 8137 | 3 | 0 | 0 | 3 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0021 | 0/0 | 8135 | 3 | 0 | 0 | 3 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0022 | 0/0 | 8131 | 3 | 2 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0023 | 0/0 | 8143 | 2 | 1 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0024 | 0/0 | 8147 | 2 | 0 | 0 | 2 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0025 | 0/0 | 8124 | 2 | 2 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0026 | 0/0 | 8140 | 2 | 2 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0027 | 0/0 | 8127 | 2 | 2 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0028 | 0/0 | 8137 | 2 | 2 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0029 | 0/0 | 8131 | 2 | 0 | 1 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0030 | 0/0 | 8136 | 2 | 0 | 0 | 2 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0031 | 0/0 | 8135 | 2 | 0 | 0 | 1 | 1 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0032 | 0/0 | 8138 | 2 | 0 | 0 | 2 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0033 | 0/0 | 8143 | 2 | 0 | 0 | 2 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0034 | 0/0 | 8134 | 2 | 0 | 0 | 0 | 0 | 2 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0035 | 0/0 | 8130 | 2 | 1 | 0 | 0 | 1 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0036 | 0/0 | 8131 | 2 | 0 | 0 | 1 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0037 | 0/0 | 8130 | 2 | 0 | 2 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0038 | 0/0 | 8132 | 2 | 2 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0039 | 0/0 | 8131 | 2 | 2 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0040 | 0/0 | 8130 | 2 | 2 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0041 | 0/0 | 8129 | 2 | 0 | 0 | 0 | 0 | 2 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0042 | 0/0 | 8130 | 2 | 0 | 0 | 2 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0043 | 0/0 | 8136 | 2 | 2 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0044 | 0/0 | 8152 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0045 | 0/0 | 8140 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0046 | 0/0 | 8131 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0047 | 0/0 | 8139 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0048 | 0/0 | 8142 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0049 | 0/0 | 8143 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0050 | 0/0 | 8144 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0051 | 0/0 | 8140 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0052 | 0/0 | 8142 | 1 | 0 | 0 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0053 | 0/0 | 8145 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0054 | 0/0 | 8146 | 1 | 0 | 0 | 0 | 1 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0055 | 0/0 | 8144 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0056 | 0/0 | 8143 | 1 | 0 | 0 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0057 | 0/0 | 8125 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0058 | 0/0 | 8122 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0059 | 0/0 | 8124 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0060 | 0/0 | 8135 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0061 | 0/0 | 8142 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0062 | 0/0 | 8161 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0063 | 0/0 | 8159 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0064 | 0/0 | 8126 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0065 | 0/0 | 8136 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0066 | 0/0 | 8154 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0067 | 0/0 | 8140 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0068 | 0/0 | 8139 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0069 | 0/0 | 8143 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0070 | 0/0 | 8159 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0071 | 0/0 | 8140 | 1 | 0 | 0 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0072 | 0/0 | 8138 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0073 | 0/0 | 8138 | 1 | 0 | 0 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0074 | 0/0 | 8136 | 1 | 0 | 0 | 0 | 1 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0075 | 0/0 | 8129 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0076 | 0/0 | 8132 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0077 | 0/0 | 8134 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0078 | 0/0 | 8135 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0079 | 0/0 | 8136 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0080 | 0/0 | 8136 | 1 | 0 | 0 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0081 | 0/0 | 8136 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0082 | 0/0 | 8137 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0083 | 0/0 | 8133 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0084 | 0/0 | 8134 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0085 | 0/0 | 8134 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0086 | 0/0 | 8136 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0087 | 0/0 | 8134 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0088 | 0/0 | 8134 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0089 | 0/0 | 8135 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0090 | 0/0 | 8136 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0091 | 0/0 | 8137 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0092 | 0/0 | 8137 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0093 | 0/0 | 8133 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0094 | 0/0 | 8134 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0095 | 0/0 | 8135 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0096 | 0/0 | 8137 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0097 | 0/0 | 8456 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0098 | 0/0 | 8131 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0099 | 0/0 | 8127 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0100 | 0/0 | 8131 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0101 | 0/0 | 8130 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0102 | 0/0 | 8133 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0103 | 0/0 | 8130 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0104 | 0/0 | 8133 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0105 | 0/0 | 8131 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0106 | 0/0 | 8130 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0107 | 0/0 | 8131 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0108 | 0/0 | 8135 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0109 | 0/0 | 8131 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0110 | 0/0 | 8137 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0111 | 0/0 | 8128 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0112 | 0/0 | 8131 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0113 | 0/0 | 8130 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0114 | 0/0 | 8130 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0115 | 0/0 | 8131 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0116 | 0/0 | 8133 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0117 | 0/0 | 8133 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0118 | 0/0 | 8135 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0119 | 0/0 | 8135 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0120 | 0/0 | 8134 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0121 | 0/0 | 8130 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0122 | 0/0 | 8135 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0123 | 0/0 | 8128 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0124 | 0/0 | 8134 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0125 | 0/0 | 8128 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0126 | 0/0 | 8136 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| t0127 | 0/0 | 8128 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0004 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0007 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0237 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0268 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0281 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 612 | 247 | 59 | 43 | 112 | 11 | 21 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0002 | 0/0 | 612 | 55 | 24 | 8 | 15 | 2 | 6 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0003 | 0/1 | 612 | 3 | 1 | 0 | 0 | 1 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0004 | 0/0 | 612 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0006 | 0/0 | 612 | 1 | 0 | 0 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0008 | 0/0 | 612 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0002c0005 | 0/0 | 612 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0003c0007 | 0/0 | 612 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 8747 | 45 | 4 | 3 | 37 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0001t0002 | 0/0 | 8741 | 22 | 1 | 9 | 6 | 3 | 3 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0001t0003 | 1/0 | 8745 | 16 | 2 | 3 | 7 | 1 | 2 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0001t0004 | 0/0 | 8745 | 12 | 1 | 3 | 4 | 2 | 2 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0001t0006 | 0/0 | 8746 | 10 | 1 | 2 | 6 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0001t0007 | 0/0 | 8742 | 10 | 0 | 1 | 7 | 1 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0001t0008 | 0/0 | 8748 | 6 | 0 | 2 | 3 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0001t0009 | 0/0 | 8741 | 5 | 0 | 0 | 5 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0001t0010 | 0/0 | 8743 | 5 | 4 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0001t0011 | 0/0 | 8745 | 4 | 2 | 1 | 0 | 1 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0001t0012 | 0/0 | 8746 | 4 | 2 | 1 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0001t0013 | 0/0 | 8743 | 4 | 4 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0001t0014 | 0/0 | 8743 | 4 | 3 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0001t0018 | 0/0 | 8741 | 3 | 0 | 3 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0001t0019 | 0/0 | 8746 | 3 | 0 | 2 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0001t0020 | 0/0 | 8748 | 3 | 0 | 0 | 3 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0001t0021 | 0/0 | 8746 | 3 | 0 | 0 | 3 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0001t0022 | 0/0 | 8742 | 3 | 2 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0001t0029 | 0/0 | 8742 | 2 | 0 | 1 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0001t0030 | 0/0 | 8747 | 2 | 0 | 0 | 2 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0001t0031 | 0/0 | 8746 | 2 | 0 | 0 | 1 | 1 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0001t0032 | 0/0 | 8749 | 2 | 0 | 0 | 2 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0001t0033 | 0/0 | 8754 | 2 | 0 | 0 | 2 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0001t0034 | 0/0 | 8745 | 2 | 0 | 0 | 0 | 0 | 2 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0001t0035 | 0/0 | 8741 | 2 | 1 | 0 | 0 | 1 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0001t0036 | 0/0 | 8742 | 2 | 0 | 0 | 1 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0001t0037 | 0/0 | 8741 | 2 | 0 | 2 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0001t0038 | 0/0 | 8743 | 2 | 2 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0001t0039 | 0/0 | 8742 | 2 | 2 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0001t0040 | 0/0 | 8741 | 2 | 2 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0001t0041 | 0/0 | 8740 | 2 | 0 | 0 | 0 | 0 | 2 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0001t0042 | 0/0 | 8741 | 2 | 0 | 0 | 2 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0001t0043 | 0/0 | 8747 | 2 | 2 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0001t0046 | 0/0 | 8742 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0001t0072 | 0/0 | 8749 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0001t0073 | 0/0 | 8749 | 1 | 0 | 0 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0001t0074 | 0/0 | 8747 | 1 | 0 | 0 | 0 | 1 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0001t0075 | 0/0 | 8740 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0001t0076 | 0/0 | 8743 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0001t0077 | 0/0 | 8745 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0001t0078 | 0/0 | 8746 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0001t0079 | 0/0 | 8747 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0001t0080 | 0/0 | 8747 | 1 | 0 | 0 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0001t0081 | 0/0 | 8747 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0001t0082 | 0/0 | 8748 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0001t0083 | 0/0 | 8744 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0001t0084 | 0/0 | 8745 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0001t0085 | 0/0 | 8745 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0001t0086 | 0/0 | 8747 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0001t0087 | 0/0 | 8745 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0001t0088 | 0/0 | 8745 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0001t0089 | 0/0 | 8746 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0001t0090 | 0/0 | 8747 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0001t0091 | 0/0 | 8748 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0001t0092 | 0/0 | 8748 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0001t0093 | 0/0 | 8744 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0001t0094 | 0/0 | 8745 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0001t0095 | 0/0 | 8746 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0001t0096 | 0/0 | 8748 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0001t0097 | 0/0 | 9067 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0001t0098 | 0/0 | 8742 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0001t0099 | 0/0 | 8738 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0001t0100 | 0/0 | 8742 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0001t0102 | 0/0 | 8744 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0001t0104 | 0/0 | 8744 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0001t0105 | 0/0 | 8742 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0001t0106 | 0/0 | 8741 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0001t0107 | 0/0 | 8742 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0001t0108 | 0/0 | 8746 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0001t0109 | 0/0 | 8742 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0001t0110 | 0/0 | 8748 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0001t0111 | 0/0 | 8739 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0001t0112 | 0/0 | 8742 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0001t0113 | 0/0 | 8741 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0001t0114 | 0/0 | 8741 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0001t0115 | 0/0 | 8742 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0001t0116 | 0/0 | 8744 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0001t0117 | 0/0 | 8744 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0001t0118 | 0/0 | 8746 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0001t0119 | 0/0 | 8746 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0001t0120 | 0/0 | 8745 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0001t0121 | 0/0 | 8741 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0001t0122 | 0/0 | 8746 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0001t0123 | 0/0 | 8739 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0001t0124 | 0/0 | 8745 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0001t0125 | 0/0 | 8739 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0001t0126 | 0/0 | 8747 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0001t0127 | 0/0 | 8739 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0002t0005 | 0/0 | 8755 | 11 | 1 | 2 | 5 | 0 | 3 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0002t0015 | 0/0 | 8756 | 3 | 0 | 1 | 1 | 1 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0002t0016 | 0/0 | 8733 | 3 | 3 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0002t0023 | 0/0 | 8754 | 2 | 1 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0002t0024 | 0/0 | 8758 | 2 | 0 | 0 | 2 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0002t0025 | 0/0 | 8735 | 2 | 2 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0002t0026 | 0/0 | 8751 | 2 | 2 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0002t0027 | 0/0 | 8738 | 2 | 2 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0002t0028 | 0/0 | 8748 | 2 | 2 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0002t0044 | 0/0 | 8763 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0002t0045 | 0/0 | 8751 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0002t0047 | 0/0 | 8750 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0002t0048 | 0/0 | 8753 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0002t0049 | 0/0 | 8754 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0002t0050 | 0/0 | 8755 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0002t0051 | 0/0 | 8751 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0002t0052 | 0/0 | 8753 | 1 | 0 | 0 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0002t0053 | 0/0 | 8756 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0002t0054 | 0/0 | 8757 | 1 | 0 | 0 | 0 | 1 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0002t0055 | 0/0 | 8755 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0002t0056 | 0/0 | 8754 | 1 | 0 | 0 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0002t0057 | 0/0 | 8736 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0002t0058 | 0/0 | 8733 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0002t0059 | 0/0 | 8735 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0002t0060 | 0/0 | 8746 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0002t0061 | 0/0 | 8753 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0002t0062 | 0/0 | 8772 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0002t0063 | 0/0 | 8770 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0002t0064 | 0/0 | 8737 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0002t0065 | 0/0 | 8747 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0002t0066 | 0/0 | 8765 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0002t0067 | 0/0 | 8751 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0002t0068 | 0/0 | 8750 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0002t0069 | 0/0 | 8754 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0002t0071 | 0/0 | 8751 | 1 | 0 | 0 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0003t0017 | 0/1 | 8736 | 3 | 1 | 0 | 0 | 1 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0004t0101 | 0/0 | 8741 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0006t0001 | 0/0 | 8747 | 1 | 0 | 0 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0001c0008t0004 | 0/0 | 8745 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0002c0005t0070 | 0/0 | 8770 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| a0003c0007t0103 | 0/0 | 8741 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | copy fasta | chr18 | 61803067 | 61898007 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0002g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0002g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0002g0007 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0002g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0002g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0002g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0003g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0003g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0003g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0003g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0003g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0003g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0003g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0003g0237 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0003g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0004g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0004g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0004g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0004g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0004g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0004g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0004g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0004g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0004g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0004g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0004g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0004g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0006g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0006g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0006g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0006g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0006g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0006g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0006g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0006g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0006g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0006g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0007g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0007g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0007g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0007g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0007g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0007g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0007g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0007g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0007g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0007g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0008g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0008g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0008g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0008g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0008g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0008g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0009g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0009g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0009g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0009g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0009g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0010g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0010g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0010g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0010g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0010g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0011g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0011g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0011g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0011g0268 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0012g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0012g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0012g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0012g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0013g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0013g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0013g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0013g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0014g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0014g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0014g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0014g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0018g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0018g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0018g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0019g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0019g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0019g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0020g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0020g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0020g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0021g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0021g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0021g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0022g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0022g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0022g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0029g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0029g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0030g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0030g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0031g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0031g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0032g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0032g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0033g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0033g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0034g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0034g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0035g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0035g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0036g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0036g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0037g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0037g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0038g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0038g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0039g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0039g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0040g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0040g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0041g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0041g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0042g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0042g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0043g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0043g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0046g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0072g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0073g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0074g0004 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0075g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0076g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0077g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0078g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0079g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0080g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0081g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0082g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0083g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0084g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0085g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0086g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0087g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0088g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0089g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0090g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0091g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0092g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0093g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0094g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0095g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0096g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0097g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0098g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0099g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0100g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0102g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0104g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0105g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0106g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0107g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0108g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0109g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0110g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0111g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0112g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0113g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0114g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0115g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0116g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0117g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0118g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0119g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0120g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0121g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0122g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0123g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0124g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0125g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0126g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0001t0127g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0002t0005g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0002t0005g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0002t0005g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0002t0005g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0002t0005g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0002t0005g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0002t0005g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0002t0005g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0002t0005g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0002t0005g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0002t0005g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0002t0015g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0002t0015g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0002t0015g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0002t0016g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0002t0016g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0002t0016g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0002t0023g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0002t0023g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0002t0024g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0002t0024g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0002t0025g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0002t0025g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0002t0026g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0002t0026g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0002t0027g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0002t0027g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0002t0028g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0002t0028g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0002t0044g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0002t0045g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0002t0047g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0002t0048g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0002t0049g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0002t0050g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0002t0051g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0002t0052g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0002t0053g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0002t0054g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0002t0055g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0002t0056g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0002t0057g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0002t0058g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0002t0059g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0002t0060g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0002t0061g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0002t0062g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0002t0063g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0002t0064g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0002t0065g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0002t0066g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0002t0067g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0002t0068g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0002t0069g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0002t0071g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0003t0017g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0003t0017g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0003t0017g0281 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0004t0101g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0006t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0001c0008t0004g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0002c0005t0070g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| a0003c0007t0103g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0074 | g0004 | EUR | GBR | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0152 | EUR | GBR | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG00140 | hp1 | a0001 | c0001 | t0007 | g0036 | EUR | GBR | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG00140 | hp2 | a0001 | c0001 | t0011 | g0268 | EUR | GBR | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG00280 | hp1 | a0001 | c0003 | t0017 | g0280 | EUR | FIN | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG00280 | hp2 | a0001 | c0001 | t0004 | g0057 | EUR | FIN | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0015 | EUR | FIN | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG00323 | hp2 | a0001 | c0001 | t0031 | g0101 | EUR | FIN | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | CHS | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG00408 | hp2 | a0001 | c0001 | t0032 | g0193 | EAS | CHS | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG00423 | hp1 | a0001 | c0002 | t0024 | g0308 | EAS | CHS | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG00423 | hp2 | a0001 | c0001 | t0003 | g0149 | EAS | CHS | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | CHS | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | CHS | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG00597 | hp1 | a0001 | c0002 | t0049 | g0013 | EAS | CHS | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG00597 | hp2 | a0001 | c0001 | t0008 | g0087 | EAS | CHS | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | CHS | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | CHS | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG00621 | hp1 | a0001 | c0001 | t0081 | g0244 | EAS | CHS | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG00621 | hp2 | a0001 | c0001 | t0126 | g0040 | EAS | CHS | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG00639 | hp1 | a0001 | c0001 | t0124 | g0234 | AMR | PUR | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG00639 | hp2 | a0001 | c0001 | t0012 | g0239 | AMR | PUR | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0039 | AMR | PUR | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG00735 | hp2 | a0001 | c0002 | t0069 | g0083 | AMR | PUR | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0043 | AMR | PUR | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG00738 | hp2 | a0001 | c0001 | t0006 | g0077 | AMR | PUR | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG00741 | hp1 | a0001 | c0002 | t0005 | g0112 | AMR | PUR | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0026 | AMR | PUR | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG01070 | hp1 | a0001 | c0001 | t0018 | g0250 | AMR | PUR | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG01070 | hp2 | a0003 | c0007 | t0103 | g0269 | AMR | PUR | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0029 | AMR | PUR | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG01071 | hp2 | a0001 | c0001 | t0018 | g0247 | AMR | PUR | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0275 | AMR | PUR | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG01081 | hp2 | a0001 | c0001 | t0114 | g0037 | AMR | PUR | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG01099 | hp1 | a0001 | c0001 | t0094 | g0246 | AMR | PUR | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG01099 | hp2 | a0001 | c0001 | t0121 | g0002 | AMR | PUR | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG01106 | hp1 | a0001 | c0001 | t0087 | g0288 | AMR | PUR | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG01106 | hp2 | a0001 | c0001 | t0006 | g0271 | AMR | PUR | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG01109 | hp1 | a0001 | c0001 | t0014 | g0263 | AMR | PUR | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG01109 | hp2 | a0001 | c0001 | t0004 | g0058 | AMR | PUR | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG01167 | hp1 | a0001 | c0002 | t0005 | g0210 | AMR | PUR | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0038 | AMR | PUR | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0225 | AMR | PUR | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0022 | AMR | PUR | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG01175 | hp1 | a0001 | c0001 | t0019 | g0285 | AMR | PUR | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG01175 | hp2 | a0001 | c0001 | t0046 | g0014 | AMR | PUR | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG01192 | hp1 | a0001 | c0001 | t0019 | g0289 | AMR | PUR | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0012 | AMR | PUR | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG01243 | hp1 | a0001 | c0001 | t0037 | g0270 | AMR | PUR | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG01243 | hp2 | a0001 | c0001 | t0010 | g0146 | AMR | PUR | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG01255 | hp1 | a0001 | c0002 | t0066 | g0258 | AMR | CLM | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG01255 | hp2 | a0001 | c0001 | t0018 | g0249 | AMR | CLM | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0231 | AMR | CLM | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG01258 | hp2 | a0001 | c0002 | t0062 | g0296 | AMR | CLM | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG01261 | hp1 | a0001 | c0002 | t0015 | g0227 | AMR | CLM | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG01261 | hp2 | a0001 | c0001 | t0116 | g0035 | AMR | CLM | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG01346 | hp1 | a0001 | c0001 | t0003 | g0203 | AMR | CLM | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG01346 | hp2 | a0001 | c0001 | t0011 | g0267 | AMR | CLM | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG01433 | hp1 | a0001 | c0001 | t0037 | g0265 | AMR | CLM | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG01433 | hp2 | a0001 | c0001 | t0029 | g0257 | AMR | CLM | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG01517 | hp1 | a0001 | c0002 | t0015 | g0226 | EUR | IBS | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG01517 | hp2 | a0001 | c0001 | t0035 | g0197 | EUR | IBS | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG01884 | hp1 | a0001 | c0001 | t0004 | g0053 | AFR | ACB | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG01884 | hp2 | a0001 | c0002 | t0016 | g0171 | AFR | ACB | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG01928 | hp1 | a0001 | c0001 | t0003 | g0230 | AMR | PEL | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG01928 | hp2 | a0001 | c0001 | t0008 | g0075 | AMR | PEL | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG01934 | hp1 | a0001 | c0002 | t0063 | g0297 | AMR | PEL | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | PEL | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG01943 | hp1 | a0001 | c0001 | t0004 | g0133 | AMR | PEL | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG01943 | hp2 | a0001 | c0001 | t0084 | g0195 | AMR | PEL | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PEL | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG01975 | hp2 | a0001 | c0002 | t0048 | g0196 | AMR | PEL | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0243 | AMR | PEL | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG01981 | hp2 | a0001 | c0001 | t0004 | g0150 | AMR | PEL | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | KHV | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | KHV | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG02027 | hp1 | a0001 | c0001 | t0021 | g0229 | EAS | KHV | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | KHV | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG02055 | hp1 | a0001 | c0001 | t0039 | g0136 | AFR | ACB | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG02055 | hp2 | a0001 | c0001 | t0006 | g0287 | AFR | ACB | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG02071 | hp1 | a0001 | c0008 | t0004 | g0063 | EAS | KHV | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG02071 | hp2 | a0001 | c0001 | t0003 | g0147 | EAS | KHV | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG02080 | hp1 | a0001 | c0002 | t0023 | g0021 | EAS | KHV | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | KHV | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG02083 | hp1 | a0001 | c0001 | t0032 | g0093 | EAS | KHV | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG02083 | hp2 | a0001 | c0001 | t0072 | g0159 | EAS | KHV | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG02129 | hp1 | a0001 | c0001 | t0003 | g0158 | EAS | KHV | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG02129 | hp2 | a0001 | c0001 | t0086 | g0292 | EAS | KHV | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG02132 | hp1 | a0001 | c0001 | t0006 | g0062 | EAS | KHV | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG02132 | hp2 | a0001 | c0001 | t0090 | g0074 | EAS | KHV | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG02135 | hp1 | a0001 | c0001 | t0120 | g0155 | EAS | KHV | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | KHV | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG02145 | hp1 | a0001 | c0002 | t0045 | g0255 | AFR | ACB | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG02145 | hp2 | a0001 | c0001 | t0097 | g0220 | AFR | ACB | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG02155 | hp1 | a0001 | c0002 | t0015 | g0205 | EAS | CDX | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | CDX | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG02257 | hp1 | a0001 | c0002 | t0027 | g0134 | AFR | ACB | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG02257 | hp2 | a0001 | c0002 | t0060 | g0298 | AFR | ACB | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG02258 | hp1 | a0001 | c0001 | t0078 | g0219 | AFR | ACB | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG02258 | hp2 | a0001 | c0002 | t0064 | g0178 | AFR | ACB | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG02280 | hp1 | a0001 | c0002 | t0025 | g0173 | AFR | ACB | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG02280 | hp2 | a0001 | c0002 | t0005 | g0025 | AFR | ACB | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG02451 | hp1 | a0001 | c0001 | t0122 | g0145 | AFR | ACB | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG02451 | hp2 | a0001 | c0002 | t0026 | g0216 | AFR | ACB | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG02523 | hp1 | a0001 | c0002 | t0055 | g0241 | EAS | KHV | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | KHV | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG02572 | hp1 | a0001 | c0001 | t0092 | g0141 | AFR | GWD | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG02572 | hp2 | a0001 | c0001 | t0119 | g0279 | AFR | GWD | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG02602 | hp1 | a0001 | c0001 | t0004 | g0177 | SAS | PJL | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG02602 | hp2 | a0001 | c0001 | t0012 | g0156 | SAS | PJL | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0201 | AFR | GWD | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG02615 | hp2 | a0001 | c0001 | t0014 | g0095 | AFR | GWD | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG02622 | hp1 | a0001 | c0002 | t0028 | g0187 | AFR | GWD | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG02622 | hp2 | a0001 | c0001 | t0012 | g0165 | AFR | GWD | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG02630 | hp1 | a0001 | c0001 | t0043 | g0144 | AFR | GWD | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG02630 | hp2 | a0001 | c0001 | t0040 | g0184 | AFR | GWD | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG02647 | hp1 | a0001 | c0001 | t0038 | g0166 | AFR | GWD | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG02647 | hp2 | a0001 | c0001 | t0109 | g0072 | AFR | GWD | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG02683 | hp1 | a0001 | c0001 | t0004 | g0204 | SAS | PJL | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG02683 | hp2 | a0001 | c0001 | t0041 | g0160 | SAS | PJL | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG02717 | hp1 | a0001 | c0001 | t0104 | g0303 | AFR | GWD | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG02717 | hp2 | a0001 | c0002 | t0059 | g0170 | AFR | GWD | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG02723 | hp1 | a0001 | c0001 | t0013 | g0084 | AFR | GWD | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG02723 | hp2 | a0001 | c0001 | t0003 | g0194 | AFR | GWD | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG02735 | hp1 | a0001 | c0002 | t0056 | g0132 | SAS | PJL | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG02735 | hp2 | a0001 | c0002 | t0005 | g0213 | SAS | PJL | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG02738 | hp1 | a0001 | c0001 | t0034 | g0120 | SAS | PJL | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG02738 | hp2 | a0001 | c0001 | t0006 | g0003 | SAS | PJL | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG02809 | hp1 | a0001 | c0001 | t0125 | g0306 | AFR | GWD | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG02809 | hp2 | a0001 | c0001 | t0012 | g0164 | AFR | GWD | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG02818 | hp1 | a0001 | c0002 | t0016 | g0174 | AFR | GWD | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG02818 | hp2 | a0001 | c0001 | t0118 | g0137 | AFR | GWD | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG02886 | hp1 | a0001 | c0003 | t0017 | g0041 | AFR | GWD | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG02886 | hp2 | a0001 | c0002 | t0025 | g0172 | AFR | GWD | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG02896 | hp1 | a0001 | c0001 | t0107 | g0168 | AFR | GWD | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG02896 | hp2 | a0001 | c0001 | t0013 | g0302 | AFR | GWD | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG02897 | hp1 | a0001 | c0001 | t0075 | g0276 | AFR | GWD | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG02897 | hp2 | a0001 | c0001 | t0013 | g0304 | AFR | GWD | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG02922 | hp1 | a0001 | c0001 | t0110 | g0181 | AFR | ESN | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG02922 | hp2 | a0001 | c0002 | t0057 | g0176 | AFR | ESN | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG02970 | hp1 | a0001 | c0001 | t0079 | g0218 | AFR | ESN | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG02970 | hp2 | a0001 | c0001 | t0022 | g0260 | AFR | ESN | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG02976 | hp1 | a0001 | c0002 | t0058 | g0169 | AFR | ESN | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG02976 | hp2 | a0001 | c0001 | t0043 | g0143 | AFR | ESN | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0009 | SAS | PJL | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0163 | SAS | PJL | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG03041 | hp1 | a0001 | c0001 | t0099 | g0139 | AFR | GWD | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG03041 | hp2 | a0001 | c0001 | t0014 | g0262 | AFR | GWD | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG03098 | hp1 | a0002 | c0005 | t0070 | g0192 | AFR | MSL | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG03098 | hp2 | a0001 | c0004 | t0101 | g0253 | AFR | MSL | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG03130 | hp1 | a0001 | c0001 | t0035 | g0027 | AFR | ESN | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG03130 | hp2 | a0001 | c0001 | t0108 | g0180 | AFR | ESN | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG03139 | hp1 | a0001 | c0001 | t0091 | g0274 | AFR | ESN | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG03139 | hp2 | a0001 | c0001 | t0022 | g0277 | AFR | ESN | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG03195 | hp1 | a0001 | c0001 | t0039 | g0138 | AFR | ESN | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG03195 | hp2 | a0001 | c0001 | t0010 | g0199 | AFR | ESN | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG03453 | hp1 | a0001 | c0002 | t0061 | g0215 | AFR | MSL | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG03453 | hp2 | a0001 | c0001 | t0013 | g0094 | AFR | MSL | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG03486 | hp1 | a0001 | c0001 | t0127 | g0261 | AFR | MSL | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG03486 | hp2 | a0001 | c0002 | t0028 | g0301 | AFR | MSL | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG03516 | hp1 | a0001 | c0001 | t0106 | g0082 | AFR | ESN | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG03516 | hp2 | a0001 | c0001 | t0123 | g0307 | AFR | ESN | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG03540 | hp1 | a0001 | c0002 | t0016 | g0175 | AFR | GWD | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0278 | AFR | GWD | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG03579 | hp1 | a0001 | c0001 | t0010 | g0065 | AFR | MSL | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG03579 | hp2 | a0001 | c0002 | t0065 | g0188 | AFR | MSL | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG03669 | hp1 | a0001 | c0001 | t0036 | g0052 | SAS | PJL | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0202 | SAS | PJL | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0189 | SAS | PJL | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG03704 | hp2 | a0001 | c0001 | t0034 | g0059 | SAS | PJL | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG03710 | hp1 | a0001 | c0002 | t0071 | g0190 | SAS | PJL | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG03710 | hp2 | a0001 | c0001 | t0080 | g0295 | SAS | PJL | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG03831 | hp1 | a0001 | c0002 | t0005 | g0020 | SAS | BEB | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG03831 | hp2 | a0001 | c0001 | t0008 | g0294 | SAS | BEB | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG03834 | hp1 | a0001 | c0001 | t0041 | g0056 | SAS | BEB | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG03834 | hp2 | a0001 | c0002 | t0052 | g0293 | SAS | BEB | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG03942 | hp1 | a0001 | c0001 | t0007 | g0071 | SAS | BEB | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG03942 | hp2 | a0001 | c0001 | t0019 | g0286 | SAS | BEB | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0142 | SAS | STU | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG04115 | hp2 | a0001 | c0001 | t0029 | g0252 | SAS | STU | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG04204 | hp1 | a0001 | c0001 | t0003 | g0153 | SAS | STU | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG04204 | hp2 | a0001 | c0001 | t0073 | g0110 | SAS | STU | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | YRI | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA18522 | hp2 | a0001 | c0001 | t0014 | g0259 | AFR | YRI | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA18906 | hp1 | a0001 | c0002 | t0067 | g0254 | AFR | YRI | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA18906 | hp2 | a0001 | c0002 | t0027 | g0179 | AFR | YRI | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA18939 | hp1 | a0001 | c0002 | t0050 | g0018 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA18942 | hp2 | a0001 | c0001 | t0009 | g0033 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA18943 | hp1 | a0001 | c0001 | t0021 | g0299 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA18943 | hp2 | a0001 | c0001 | t0089 | g0016 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA18944 | hp1 | a0001 | c0001 | t0076 | g0300 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA18945 | hp1 | a0001 | c0002 | t0044 | g0097 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA18945 | hp2 | a0001 | c0001 | t0007 | g0080 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA18946 | hp1 | a0001 | c0001 | t0003 | g0222 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA18946 | hp2 | a0001 | c0001 | t0007 | g0114 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA18947 | hp1 | a0001 | c0001 | t0004 | g0128 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0273 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA18948 | hp1 | a0001 | c0001 | t0006 | g0061 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA18948 | hp2 | a0001 | c0001 | t0093 | g0148 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA18949 | hp1 | a0001 | c0001 | t0009 | g0124 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA18949 | hp2 | a0001 | c0001 | t0082 | g0208 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA18951 | hp1 | a0001 | c0001 | t0095 | g0236 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA18951 | hp2 | a0001 | c0001 | t0096 | g0024 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA18954 | hp2 | a0001 | c0001 | t0006 | g0064 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA18956 | hp2 | a0001 | c0002 | t0005 | g0221 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA18957 | hp1 | a0001 | c0001 | t0003 | g0123 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA18957 | hp2 | a0001 | c0001 | t0006 | g0162 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA18959 | hp1 | a0001 | c0001 | t0030 | g0207 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA18959 | hp2 | a0001 | c0002 | t0005 | g0055 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA18960 | hp2 | a0001 | c0001 | t0036 | g0283 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA18964 | hp2 | a0001 | c0001 | t0113 | g0044 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA18965 | hp1 | a0001 | c0001 | t0042 | g0049 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA18965 | hp2 | a0001 | c0001 | t0008 | g0073 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA18969 | hp2 | a0001 | c0002 | t0053 | g0206 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA18972 | hp1 | a0001 | c0002 | t0005 | g0224 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA18979 | hp2 | a0001 | c0001 | t0004 | g0010 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA18984 | hp1 | a0001 | c0001 | t0006 | g0151 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA18984 | hp2 | a0001 | c0001 | t0007 | g0107 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA18989 | hp2 | a0001 | c0002 | t0024 | g0309 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA18990 | hp2 | a0001 | c0001 | t0030 | g0209 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA18991 | hp1 | a0001 | c0001 | t0033 | g0126 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA18991 | hp2 | a0001 | c0001 | t0033 | g0105 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA18995 | hp1 | a0001 | c0001 | t0020 | g0118 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0272 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA19000 | hp1 | a0001 | c0001 | t0098 | g0034 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA19000 | hp2 | a0001 | c0001 | t0100 | g0130 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA19003 | hp2 | a0001 | c0001 | t0009 | g0023 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA19005 | hp2 | a0001 | c0001 | t0007 | g0161 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA19009 | hp1 | a0001 | c0001 | t0003 | g0235 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA19009 | hp2 | a0001 | c0002 | t0005 | g0030 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA19010 | hp1 | a0001 | c0001 | t0020 | g0088 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA19010 | hp2 | a0001 | c0001 | t0022 | g0282 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA19011 | hp1 | a0001 | c0001 | t0004 | g0154 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA19011 | hp2 | a0001 | c0001 | t0003 | g0232 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA19030 | hp1 | a0001 | c0002 | t0023 | g0256 | AFR | LWK | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA19030 | hp2 | a0001 | c0001 | t0010 | g0200 | AFR | LWK | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA19043 | hp1 | a0001 | c0001 | t0088 | g0191 | AFR | LWK | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA19043 | hp2 | a0001 | c0001 | t0011 | g0135 | AFR | LWK | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA19054 | hp1 | a0001 | c0001 | t0042 | g0048 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA19057 | hp1 | a0001 | c0001 | t0009 | g0031 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA19062 | hp1 | a0001 | c0001 | t0008 | g0167 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA19062 | hp2 | a0001 | c0001 | t0007 | g0081 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA19064 | hp1 | a0001 | c0001 | t0021 | g0233 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA19064 | hp2 | a0001 | c0001 | t0083 | g0129 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA19065 | hp1 | a0001 | c0001 | t0077 | g0045 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA19067 | hp1 | a0001 | c0001 | t0006 | g0017 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA19067 | hp2 | a0001 | c0001 | t0007 | g0113 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA19068 | hp2 | a0001 | c0001 | t0009 | g0032 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA19074 | hp2 | a0001 | c0001 | t0007 | g0111 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA19075 | hp1 | a0001 | c0001 | t0111 | g0228 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA19075 | hp2 | a0001 | c0001 | t0031 | g0011 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA19077 | hp2 | a0001 | c0001 | t0115 | g0212 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA19078 | hp1 | a0001 | c0001 | t0112 | g0042 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA19078 | hp2 | a0001 | c0001 | t0020 | g0078 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA19085 | hp2 | a0001 | c0002 | t0005 | g0019 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA19088 | hp1 | a0001 | c0001 | t0004 | g0085 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA19088 | hp2 | a0001 | c0002 | t0051 | g0223 | EAS | JPT | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA19240 | hp1 | a0001 | c0001 | t0102 | g0305 | AFR | YRI | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA19240 | hp2 | a0001 | c0001 | t0010 | g0198 | AFR | YRI | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA20752 | hp1 | a0001 | c0002 | t0054 | g0214 | EUR | TSI | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA20752 | hp2 | a0001 | c0001 | t0004 | g0242 | EUR | TSI | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0007 | EUR | TSI | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA20805 | hp2 | a0001 | c0001 | t0003 | g0245 | EUR | TSI | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA20905 | hp1 | a0001 | c0002 | t0005 | g0211 | SAS | GIH | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA20905 | hp2 | a0001 | c0006 | t0001 | g0157 | SAS | GIH | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG01123 | hp1 | a0001 | c0001 | t0008 | g0076 | AMR | CLM | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG01123 | hp2 | a0001 | c0001 | t0007 | g0008 | AMR | CLM | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0266 | AFR | ACB | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | ACB | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG02486 | hp1 | a0001 | c0002 | t0026 | g0217 | AFR | ACB | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG02486 | hp2 | a0001 | c0002 | t0068 | g0098 | AFR | ACB | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG02559 | hp1 | a0001 | c0001 | t0040 | g0185 | AFR | ACB | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG02559 | hp2 | a0001 | c0001 | t0117 | g0284 | AFR | ACB | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG03471 | hp1 | a0001 | c0002 | t0047 | g0264 | AFR | MSL | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG03471 | hp2 | a0001 | c0001 | t0011 | g0066 | AFR | MSL | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG06807 | hp1 | a0001 | c0001 | t0105 | g0183 | AFR | USA | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| HG06807 | hp2 | a0001 | c0001 | t0085 | g0140 | AFR | USA | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | USA | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| NA20300 | hp2 | a0001 | c0001 | t0038 | g0182 | AFR | USA | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0003 | t0017 | g0281 | REF | REF | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0003 | g0237 | REF | REF | RNF152_chr18_61803067_61898007 | RNF152 | chr18 | 61803067 | 61898007 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:61816015
|
G | A | 1 | a0002 | 1 | HG03098.hp1 | missense_variant | MODERATE | c.449C>T | p.Ala150Val | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 797/8745 | 449/612 | 150/203 | chr18 | 61816015 | ||
| chr18:61816048
|
T | C | 1 | a0003 | 1 | HG01070.hp2 | missense_variant | MODERATE | c.416A>G | p.Gln139Arg | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 764/8745 | 416/612 | 139/203 | chr18 | 61816048 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:61815969
|
G | C | 1 | a0001c0003 | 3 | HG00280.hp1 HG02886.hp1 homoSapiens_chm13v2.hp1 |
synonymous_variant | LOW | c.495C>G | p.Thr165Thr | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 843/8745 | 495/612 | 165/203 | chr18 | 61815969 | ||
| chr18:61816077
|
G | A | 1 | a0001c0003 | 3 | HG00280.hp1 HG02886.hp1 homoSapiens_chm13v2.hp1 |
synonymous_variant | LOW | c.387C>T | p.Ser129Ser | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 735/8745 | 387/612 | 129/203 | chr18 | 61816077 | ||
| chr18:61816263
|
C | T | 1 | a0001c0006 | 1 | NA20905.hp2 | synonymous_variant | LOW | c.201G>A | p.Ser67Ser | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 549/8745 | 201/612 | 67/203 | chr18 | 61816263 | ||
| chr18:61816275
|
G | T | 1 | a0001c0003 | 3 | HG00280.hp1 HG02886.hp1 homoSapiens_chm13v2.hp1 |
synonymous_variant | LOW | c.189C>A | p.Gly63Gly | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 537/8745 | 189/612 | 63/203 | chr18 | 61816275 | ||
| chr18:61816281
|
A | G | 3 | a0001c0002a0001c0003a0002c0005 | 59 | HG00280.hp1 HG00423.hp1 HG00597.hp1 others(56): Show |
synonymous_variant | LOW | c.183T>C | p.Pro61Pro | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 531/8745 | 183/612 | 61/203 | chr18 | 61816281 | ||
| chr18:61816299
|
G | A | 1 | a0001c0008 | 1 | HG02071.hp1 | synonymous_variant | LOW | c.165C>T | p.Arg55Arg | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 513/8745 | 165/612 | 55/203 | chr18 | 61816299 | ||
| chr18:61816455
|
C | G | 1 | a0001c0004 | 1 | HG03098.hp2 | synonymous_variant | LOW | c.9G>C | p.Thr3Thr | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 357/8745 | 9/612 | 3/203 | chr18 | 61816455 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:61808167
|
C | T | 2 | a0001c0001t0018a0001c0001t0029 | 5 | HG01070.hp1 HG01071.hp2 HG01255.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*7685G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 7685 | chr18 | 61808167 | |||||
| chr18:61808387
|
T | TA | 24 | a0001c0001t0006a0001c0001t0007a0001c0001t0008others(21): Show | 57 | HG00140.hp1 HG00597.hp2 HG00621.hp2 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*7464dupT | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 7464 | chr18 | 61808387 | |||||
| chr18:61808387
|
T | TAAA | 5 | a0001c0002t0023a0001c0002t0047a0001c0002t0048others(2): Show | 6 | HG00597.hp1 HG01975.hp2 HG02080.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*7462_*7464dupTTT | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 7464 | chr18 | 61808387 | |||||
| chr18:61808387
|
T | TAAAA | 10 | a0001c0001t0043a0001c0001t0122a0001c0002t0005others(7): Show | 21 | HG00741.hp1 HG01167.hp1 HG02280.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*7461_*7464dupTTTT | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 7464 | chr18 | 61808387 | |||||
| chr18:61808387
|
T | TAAAAA | 9 | a0001c0002t0015a0001c0002t0024a0001c0002t0026others(6): Show | 14 | HG00423.hp1 HG00735.hp2 HG01261.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*7460_*7464dupTTTT others(1): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 7464 | chr18 | 61808387 | |||||
| chr18:61808387
|
T | TAAAAAAA others(6): Show |
1 | a0001c0002t0066 | 1 | HG01255.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7452_*7464dupTTTT others(9): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 7464 | chr18 | 61808387 | |||||
| chr18:61808387
|
T | TAAAAAAA others(7): Show |
1 | a0002c0005t0070 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7451_*7464dupTTTT others(10): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 7464 | chr18 | 61808387 | |||||
| chr18:61808387
|
T | TAAAAAAA others(14): Show |
2 | a0001c0002t0062a0001c0002t0063 | 2 | HG01258.hp2 HG01934.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7444_*7464dupTTTT others(17): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 7464 | chr18 | 61808387 | |||||
| chr18:61808387
|
T | TAAAAAAA others(15): Show |
1 | a0001c0002t0044 | 1 | NA18945.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7443_*7464dupTTTT others(18): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 7464 | chr18 | 61808387 | |||||
| chr18:61808387
|
TAAA | T | 4 | a0001c0002t0016a0001c0002t0025a0001c0002t0058others(1): Show | 7 | HG01884.hp2 HG02280.hp1 HG02717.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*7462_*7464delTTT | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 7462 | chr18 | 61808387 | |||||
| chr18:61808484
|
A | T | 1 | a0001c0001t0094 | 1 | HG01099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7368T>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 7368 | chr18 | 61808484 | |||||
| chr18:61808543
|
G | A | 9 | a0001c0001t0039a0001c0001t0040a0001c0001t0099others(6): Show | 11 | HG02055.hp1 HG02559.hp1 HG02630.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*7309C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 7309 | chr18 | 61808543 | |||||
| chr18:61808563
|
G | A | 26 | a0001c0001t0043a0001c0001t0122a0001c0002t0005others(23): Show | 43 | HG00423.hp1 HG00597.hp1 HG00735.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*7289C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 7289 | chr18 | 61808563 | |||||
| chr18:61808595
|
A | T | 37 | a0001c0001t0043a0001c0001t0122a0001c0002t0005others(34): Show | 59 | HG00280.hp1 HG00423.hp1 HG00597.hp1 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*7257T>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 7257 | chr18 | 61808595 | |||||
| chr18:61808935
|
C | T | 1 | a0001c0002t0056 | 1 | HG02735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6917G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 6917 | chr18 | 61808935 | |||||
| chr18:61809202
|
T | C | 26 | a0001c0001t0043a0001c0001t0122a0001c0002t0005others(23): Show | 43 | HG00423.hp1 HG00597.hp1 HG00735.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*6650A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 6650 | chr18 | 61809202 | |||||
| chr18:61809236
|
A | G | 37 | a0001c0001t0043a0001c0001t0122a0001c0002t0005others(34): Show | 59 | HG00280.hp1 HG00423.hp1 HG00597.hp1 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*6616T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 6616 | chr18 | 61809236 | |||||
| chr18:61809349
|
G | A | 1 | a0001c0001t0084 | 1 | HG01943.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6503C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 6503 | chr18 | 61809349 | |||||
| chr18:61809425
|
C | A | 1 | a0001c0001t0094 | 1 | HG01099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6427G>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 6427 | chr18 | 61809425 | |||||
| chr18:61809747
|
A | T | 1 | a0001c0001t0042 | 2 | NA18965.hp1 NA19054.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6105T>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 6105 | chr18 | 61809747 | |||||
| chr18:61809856
|
G | GA | 40 | a0001c0001t0002a0001c0001t0007a0001c0001t0009others(37): Show | 92 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(89): Show |
3_prime_UTR_variant | MODIFIER | c.*5995dupT | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 5995 | chr18 | 61809856 | |||||
| chr18:61809856
|
G | GAA | 25 | a0001c0001t0022a0001c0001t0079a0001c0001t0081others(22): Show | 43 | HG00423.hp1 HG00597.hp1 HG00621.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*5994_*5995dupTT | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 5995 | chr18 | 61809856 | |||||
| chr18:61809856
|
GA | G | 9 | a0001c0001t0083a0001c0001t0093a0001c0001t0095others(6): Show | 9 | HG02647.hp2 HG02896.hp1 HG03041.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*5995delT | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 5995 | chr18 | 61809856 | |||||
| chr18:61809856
|
GAAA | G | 4 | a0001c0002t0044a0001c0002t0062a0001c0002t0063others(1): Show | 6 | HG00280.hp1 HG01258.hp2 HG01934.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5993_*5995delTTT | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 5993 | chr18 | 61809856 | |||||
| chr18:61809856
|
GAAAA | G | 6 | a0001c0002t0016a0001c0002t0025a0001c0002t0057others(3): Show | 9 | HG01255.hp1 HG01884.hp2 HG02280.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*5992_*5995delTTTT | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 5992 | chr18 | 61809856 | |||||
| chr18:61809882
|
T | C | 1 | a0001c0001t0104 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5970A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 5970 | chr18 | 61809882 | |||||
| chr18:61810026
|
A | T | 36 | a0001c0001t0043a0001c0001t0122a0001c0002t0005others(33): Show | 58 | HG00280.hp1 HG00423.hp1 HG00597.hp1 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*5826T>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 5826 | chr18 | 61810026 | |||||
| chr18:61810029
|
T | C | 26 | a0001c0001t0043a0001c0001t0122a0001c0002t0005others(23): Show | 43 | HG00423.hp1 HG00597.hp1 HG00735.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*5823A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 5823 | chr18 | 61810029 | |||||
| chr18:61810065
|
C | T | 26 | a0001c0001t0043a0001c0001t0122a0001c0002t0005others(23): Show | 43 | HG00423.hp1 HG00597.hp1 HG00735.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*5787G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 5787 | chr18 | 61810065 | |||||
| chr18:61810180
|
C | G | 3 | a0001c0001t0030a0001c0001t0081a0001c0001t0082 | 4 | HG00621.hp1 NA18949.hp2 NA18959.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5672G>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 5672 | chr18 | 61810180 | |||||
| chr18:61810243
|
A | C | 3 | a0001c0002t0044a0001c0002t0062a0001c0002t0063 | 3 | HG01258.hp2 HG01934.hp1 NA18945.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5609T>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 5609 | chr18 | 61810243 | |||||
| chr18:61810272
|
G | GGT | 33 | a0001c0001t0043a0001c0001t0080a0001c0001t0102others(30): Show | 53 | HG00423.hp1 HG00597.hp1 HG00735.hp2 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*5578_*5579dupAC | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 5579 | chr18 | 61810272 | |||||
| chr18:61810272
|
G | GGTGTGTG others(1): Show |
1 | a0001c0003t0017 | 3 | HG00280.hp1 HG02886.hp1 homoSapiens_chm13v2.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5572_*5579dupACAC others(4): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 5579 | chr18 | 61810272 | |||||
| chr18:61810272
|
G | GGTGTGTG others(3): Show |
2 | a0001c0002t0044a0002c0005t0070 | 2 | HG03098.hp1 NA18945.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5570_*5579dupACAC others(6): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 5579 | chr18 | 61810272 | |||||
| chr18:61810272
|
G | GGTGTGTG others(7): Show |
1 | a0001c0002t0066 | 1 | HG01255.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5566_*5579dupACAC others(10): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 5579 | chr18 | 61810272 | |||||
| chr18:61810272
|
G | GGTGTGTG others(11): Show |
1 | a0001c0002t0063 | 1 | HG01934.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5562_*5579dupACAC others(14): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 5579 | chr18 | 61810272 | |||||
| chr18:61810272
|
G | GGTGTGTG others(13): Show |
1 | a0001c0002t0062 | 1 | HG01258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5560_*5579dupACAC others(16): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 5579 | chr18 | 61810272 | |||||
| chr18:61810272
|
GGTGT | G | 2 | a0001c0001t0014a0001c0001t0127 | 5 | HG01109.hp1 HG02615.hp2 HG03041.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*5576_*5579delACAC | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 5576 | chr18 | 61810272 | |||||
| chr18:61810362
|
T | A | 1 | a0001c0001t0086 | 1 | HG02129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5490A>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 5490 | chr18 | 61810362 | |||||
| chr18:61810516
|
C | T | 1 | a0003c0007t0103 | 1 | HG01070.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5336G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 5336 | chr18 | 61810516 | |||||
| chr18:61810517
|
G | A | 2 | a0001c0001t0102a0001c0001t0104 | 2 | HG02717.hp1 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5335C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 5335 | chr18 | 61810517 | |||||
| chr18:61810580
|
G | A | 1 | a0002c0005t0070 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5272C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 5272 | chr18 | 61810580 | |||||
| chr18:61810582
|
A | C | 3 | a0001c0001t0011a0001c0001t0019a0001c0001t0087 | 8 | HG00140.hp2 HG01106.hp1 HG01175.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*5270T>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 5270 | chr18 | 61810582 | |||||
| chr18:61810648
|
C | CATAA | 2 | a0001c0001t0033a0001c0001t0073 | 3 | HG04204.hp2 NA18991.hp1 NA18991.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5200_*5203dupTTAT | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 5203 | chr18 | 61810648 | |||||
| chr18:61810710
|
G | A | 2 | a0001c0001t0123a0001c0001t0125 | 2 | HG02809.hp1 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5142C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 5142 | chr18 | 61810710 | |||||
| chr18:61810733
|
C | A | 1 | a0001c0002t0071 | 1 | HG03710.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5119G>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 5119 | chr18 | 61810733 | |||||
| chr18:61810807
|
T | C | 4 | a0001c0001t0038a0001c0001t0105a0001c0001t0108others(1): Show | 5 | HG02647.hp1 HG02922.hp1 HG03130.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*5045A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 5045 | chr18 | 61810807 | |||||
| chr18:61810809
|
T | C | 2 | a0001c0001t0037a0003c0007t0103 | 3 | HG01070.hp2 HG01243.hp1 HG01433.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5043A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 5043 | chr18 | 61810809 | |||||
| chr18:61810873
|
TGACA | T | 1 | a0001c0003t0017 | 3 | HG00280.hp1 HG02886.hp1 homoSapiens_chm13v2.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4975_*4978delTGTC | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 4975 | chr18 | 61810873 | |||||
| chr18:61811047
|
C | CA | 28 | a0001c0001t0043a0001c0001t0091a0001c0002t0005others(25): Show | 47 | HG00280.hp1 HG00423.hp1 HG00597.hp1 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*4804dupT | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 4804 | chr18 | 61811047 | |||||
| chr18:61811047
|
CA | C | 24 | a0001c0001t0002a0001c0001t0007a0001c0001t0009others(21): Show | 70 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(67): Show |
3_prime_UTR_variant | MODIFIER | c.*4804delT | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 4804 | chr18 | 61811047 | |||||
| chr18:61811220
|
C | T | 7 | a0001c0001t0039a0001c0001t0040a0001c0001t0099others(4): Show | 9 | HG02055.hp1 HG02559.hp1 HG02630.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*4632G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 4632 | chr18 | 61811220 | |||||
| chr18:61811221
|
A | G | 26 | a0001c0001t0043a0001c0001t0122a0001c0002t0005others(23): Show | 43 | HG00423.hp1 HG00597.hp1 HG00735.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*4631T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 4631 | chr18 | 61811221 | |||||
| chr18:61811256
|
A | G | 1 | a0001c0002t0066 | 1 | HG01255.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4596T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 4596 | chr18 | 61811256 | |||||
| chr18:61811471
|
G | A | 1 | a0001c0001t0104 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4381C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 4381 | chr18 | 61811471 | |||||
| chr18:61811547
|
A | T | 1 | a0001c0001t0090 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4305T>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 4305 | chr18 | 61811547 | |||||
| chr18:61811568
|
A | C | 1 | a0001c0001t0118 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4284T>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 4284 | chr18 | 61811568 | |||||
| chr18:61811611
|
G | C | 1 | a0001c0001t0113 | 1 | NA18964.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4241C>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 4241 | chr18 | 61811611 | |||||
| chr18:61812089
|
T | G | 2 | a0001c0001t0085a0001c0001t0092 | 2 | HG02572.hp1 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3763A>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 3763 | chr18 | 61812089 | |||||
| chr18:61812148
|
G | A | 2 | a0001c0002t0058a0001c0002t0059 | 2 | HG02717.hp2 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3704C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 3704 | chr18 | 61812148 | |||||
| chr18:61812174
|
T | A | 1 | a0002c0005t0070 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3678A>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 3678 | chr18 | 61812174 | |||||
| chr18:61812176
|
G | A | 2 | a0001c0001t0123a0001c0001t0125 | 2 | HG02809.hp1 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3676C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 3676 | chr18 | 61812176 | |||||
| chr18:61812180
|
T | C | 1 | a0001c0001t0114 | 1 | HG01081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3672A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 3672 | chr18 | 61812180 | |||||
| chr18:61812286
|
G | A | 2 | a0001c0001t0111a0001c0001t0115 | 2 | NA19075.hp1 NA19077.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3566C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 3566 | chr18 | 61812286 | |||||
| chr18:61812378
|
C | T | 1 | a0001c0001t0100 | 1 | NA19000.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3474G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 3474 | chr18 | 61812378 | |||||
| chr18:61812593
|
C | G | 4 | a0001c0001t0038a0001c0001t0105a0001c0001t0108others(1): Show | 5 | HG02647.hp1 HG02922.hp1 HG03130.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3259G>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 3259 | chr18 | 61812593 | |||||
| chr18:61812597
|
T | G | 4 | a0001c0001t0038a0001c0001t0105a0001c0001t0108others(1): Show | 5 | HG02647.hp1 HG02922.hp1 HG03130.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3255A>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 3255 | chr18 | 61812597 | |||||
| chr18:61812768
|
C | T | 1 | a0001c0003t0017 | 3 | HG00280.hp1 HG02886.hp1 homoSapiens_chm13v2.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3084G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 3084 | chr18 | 61812768 | |||||
| chr18:61812856
|
CA | C | 36 | a0001c0002t0005a0001c0002t0015a0001c0002t0016others(33): Show | 58 | HG00280.hp1 HG00423.hp1 HG00597.hp1 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*2995delT | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 2995 | chr18 | 61812856 | |||||
| chr18:61812970
|
G | C | 36 | a0001c0002t0005a0001c0002t0015a0001c0002t0016others(33): Show | 58 | HG00280.hp1 HG00423.hp1 HG00597.hp1 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*2882C>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 2882 | chr18 | 61812970 | |||||
| chr18:61812994
|
C | T | 36 | a0001c0002t0005a0001c0002t0015a0001c0002t0016others(33): Show | 58 | HG00280.hp1 HG00423.hp1 HG00597.hp1 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*2858G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 2858 | chr18 | 61812994 | |||||
| chr18:61813239
|
C | A | 1 | a0001c0002t0053 | 1 | NA18969.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2613G>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 2613 | chr18 | 61813239 | |||||
| chr18:61813257
|
T | TTC | 16 | a0001c0001t0001a0001c0001t0008a0001c0001t0014others(13): Show | 71 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*2593_*2594dupGA | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 2594 | chr18 | 61813257 | |||||
| chr18:61813257
|
T | TTCTC | 4 | a0001c0001t0032a0001c0001t0033a0001c0001t0072others(1): Show | 6 | HG00408.hp2 HG02083.hp1 HG02083.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2591_*2594dupGAGA | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 2594 | chr18 | 61813257 | |||||
| chr18:61813257
|
TTC | T | 5 | a0001c0002t0026a0001c0002t0045a0001c0002t0060others(2): Show | 6 | HG02145.hp1 HG02257.hp2 HG02451.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2593_*2594delGA | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 2593 | chr18 | 61813257 | |||||
| chr18:61813257
|
TTCTC | T | 2 | a0001c0002t0025a0001c0002t0059 | 3 | HG02280.hp1 HG02717.hp2 HG02886.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2591_*2594delGAGA | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 2591 | chr18 | 61813257 | |||||
| chr18:61813274
|
TCTCTCA | T | 3 | a0001c0002t0016a0001c0002t0057a0001c0002t0058 | 5 | HG01884.hp2 HG02818.hp1 HG02922.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2572_*2577delTGAG others(2): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 2572 | chr18 | 61813274 | |||||
| chr18:61813274
|
TCTCTCAC others(1): Show |
T | 2 | a0001c0002t0027a0001c0002t0064 | 3 | HG02257.hp1 HG02258.hp2 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2570_*2577delTGTG others(4): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 2570 | chr18 | 61813274 | |||||
| chr18:61813274
|
TCTCTCAC others(3): Show |
T | 3 | a0001c0002t0044a0001c0002t0062a0001c0002t0063 | 3 | HG01258.hp2 HG01934.hp1 NA18945.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2568_*2577delTGTG others(6): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 2568 | chr18 | 61813274 | |||||
| chr18:61813276
|
TCTCACA | T | 2 | a0001c0002t0028a0001c0002t0065 | 3 | HG02622.hp1 HG03486.hp2 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2570_*2575delTGTG others(2): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 2570 | chr18 | 61813276 | |||||
| chr18:61813278
|
T | A | 2 | a0001c0002t0061a0001c0002t0069 | 2 | HG00735.hp2 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2574A>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 2574 | chr18 | 61813278 | |||||
| chr18:61813278
|
T | TCA | 8 | a0001c0001t0074a0001c0002t0005a0001c0002t0015others(5): Show | 21 | HG00099.hp1 HG00741.hp1 HG01167.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*2572_*2573dupTG | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 2573 | chr18 | 61813278 | |||||
| chr18:61813278
|
T | TCACA | 3 | a0001c0002t0024a0001c0002t0054a0001c0002t0055 | 4 | HG00423.hp1 HG02523.hp1 NA18989.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2570_*2573dupTGTG | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 2573 | chr18 | 61813278 | |||||
| chr18:61813278
|
TCA | T | 11 | a0001c0001t0010a0001c0001t0013a0001c0001t0076others(8): Show | 18 | HG01243.hp2 HG01255.hp1 HG01261.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*2572_*2573delTG | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 2572 | chr18 | 61813278 | |||||
| chr18:61813278
|
TCACA | T | 28 | a0001c0001t0002a0001c0001t0007a0001c0001t0009others(25): Show | 75 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*2570_*2573delTGTG | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 2570 | chr18 | 61813278 | |||||
| chr18:61813278
|
TCACACA | T | 7 | a0001c0001t0043a0001c0001t0075a0001c0001t0099others(4): Show | 8 | HG02451.hp1 HG02630.hp1 HG02809.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2568_*2573delTGTG others(2): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 2568 | chr18 | 61813278 | |||||
| chr18:61813278
|
TCACACAC others(3): Show |
T | 1 | a0001c0003t0017 | 3 | HG00280.hp1 HG02886.hp1 homoSapiens_chm13v2.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2564_*2573delTGTG others(6): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 2564 | chr18 | 61813278 | |||||
| chr18:61813280
|
A | T | 39 | a0001c0001t0001a0001c0001t0004a0001c0001t0006others(36): Show | 124 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(121): Show |
3_prime_UTR_variant | MODIFIER | c.*2572T>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 2572 | chr18 | 61813280 | |||||
| chr18:61813282
|
A | T | 32 | a0001c0001t0004a0001c0001t0006a0001c0001t0010others(29): Show | 66 | HG00140.hp2 HG00280.hp2 HG00621.hp1 others(63): Show |
3_prime_UTR_variant | MODIFIER | c.*2570T>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 2570 | chr18 | 61813282 | |||||
| chr18:61813284
|
A | T | 39 | a0001c0001t0002a0001c0001t0007a0001c0001t0009others(36): Show | 90 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(87): Show |
3_prime_UTR_variant | MODIFIER | c.*2568T>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 2568 | chr18 | 61813284 | |||||
| chr18:61813286
|
A | T | 37 | a0001c0001t0002a0001c0001t0007a0001c0001t0009others(34): Show | 88 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(85): Show |
3_prime_UTR_variant | MODIFIER | c.*2566T>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 2566 | chr18 | 61813286 | |||||
| chr18:61813288
|
A | T | 31 | a0001c0001t0002a0001c0001t0007a0001c0001t0009others(28): Show | 78 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*2564T>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 2564 | chr18 | 61813288 | |||||
| chr18:61813309
|
C | A | 14 | a0001c0001t0002a0001c0001t0007a0001c0001t0009others(11): Show | 50 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*2543G>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 2543 | chr18 | 61813309 | |||||
| chr18:61813317
|
T | C | 1 | a0001c0002t0055 | 1 | HG02523.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2535A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 2535 | chr18 | 61813317 | |||||
| chr18:61813321
|
CA | C | 3 | a0001c0002t0026a0001c0002t0060a0001c0002t0061 | 4 | HG02257.hp2 HG02451.hp2 HG02486.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2530delT | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 2530 | chr18 | 61813321 | |||||
| chr18:61813343
|
C | A | 1 | a0001c0003t0017 | 3 | HG00280.hp1 HG02886.hp1 homoSapiens_chm13v2.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2509G>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 2509 | chr18 | 61813343 | |||||
| chr18:61813396
|
C | T | 7 | a0001c0001t0009a0001c0001t0098a0001c0002t0016others(4): Show | 14 | HG01884.hp2 HG02280.hp1 HG02717.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*2456G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 2456 | chr18 | 61813396 | |||||
| chr18:61813512
|
T | TGGGATTG others(313): Show |
1 | a0001c0001t0097 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2339_*2340insGGCC others(316): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 2339 | chr18 | 61813512 | |||||
| chr18:61813688
|
T | C | 1 | a0001c0001t0034 | 2 | HG02738.hp1 HG03704.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2164A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 2164 | chr18 | 61813688 | |||||
| chr18:61813755
|
C | T | 1 | a0001c0001t0074 | 1 | HG00099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2097G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 2097 | chr18 | 61813755 | |||||
| chr18:61813848
|
T | C | 75 | a0001c0001t0002a0001c0001t0007a0001c0001t0009others(72): Show | 146 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(143): Show |
3_prime_UTR_variant | MODIFIER | c.*2004A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 2004 | chr18 | 61813848 | |||||
| chr18:61814007
|
G | C | 3 | a0001c0001t0117a0001c0001t0118a0001c0001t0119 | 3 | HG02559.hp2 HG02572.hp2 HG02818.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1845C>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 1845 | chr18 | 61814007 | |||||
| chr18:61814219
|
C | T | 36 | a0001c0002t0005a0001c0002t0015a0001c0002t0016others(33): Show | 58 | HG00280.hp1 HG00423.hp1 HG00597.hp1 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*1633G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 1633 | chr18 | 61814219 | |||||
| chr18:61814225
|
G | A | 1 | a0001c0002t0056 | 1 | HG02735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1627C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 1627 | chr18 | 61814225 | |||||
| chr18:61814316
|
C | G | 15 | a0001c0002t0005a0001c0002t0015a0001c0002t0023others(12): Show | 29 | HG00423.hp1 HG00597.hp1 HG00741.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*1536G>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 1536 | chr18 | 61814316 | |||||
| chr18:61814398
|
G | C | 1 | a0001c0001t0120 | 1 | HG02135.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1454C>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 1454 | chr18 | 61814398 | |||||
| chr18:61814491
|
G | A | 1 | a0001c0001t0121 | 1 | HG01099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1361C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 1361 | chr18 | 61814491 | |||||
| chr18:61814683
|
C | A | 4 | a0001c0001t0043a0001c0001t0122a0001c0001t0123others(1): Show | 5 | HG02451.hp1 HG02630.hp1 HG02809.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1169G>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 1169 | chr18 | 61814683 | |||||
| chr18:61814734
|
C | T | 1 | a0001c0001t0073 | 1 | HG04204.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1118G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 1118 | chr18 | 61814734 | |||||
| chr18:61814884
|
G | C | 1 | a0001c0002t0071 | 1 | HG03710.hp1 | 3_prime_UTR_variant | MODIFIER | c.*968C>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 968 | chr18 | 61814884 | |||||
| chr18:61814895
|
G | A | 1 | a0001c0001t0010 | 5 | HG01243.hp2 HG03195.hp2 HG03579.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*957C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 957 | chr18 | 61814895 | |||||
| chr18:61814913
|
C | T | 1 | a0001c0001t0072 | 1 | HG02083.hp2 | 3_prime_UTR_variant | MODIFIER | c.*939G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 939 | chr18 | 61814913 | |||||
| chr18:61815050
|
A | G | 37 | a0001c0002t0005a0001c0002t0015a0001c0002t0016others(34): Show | 59 | HG00280.hp1 HG00423.hp1 HG00597.hp1 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*802T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 802 | chr18 | 61815050 | |||||
| chr18:61815053
|
C | T | 1 | a0001c0001t0046 | 1 | HG01175.hp2 | 3_prime_UTR_variant | MODIFIER | c.*799G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 799 | chr18 | 61815053 | |||||
| chr18:61815074
|
T | A | 1 | a0001c0001t0124 | 1 | HG00639.hp1 | 3_prime_UTR_variant | MODIFIER | c.*778A>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 778 | chr18 | 61815074 | |||||
| chr18:61815077
|
G | A | 1 | a0001c0001t0124 | 1 | HG00639.hp1 | 3_prime_UTR_variant | MODIFIER | c.*775C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 775 | chr18 | 61815077 | |||||
| chr18:61815197
|
C | T | 1 | a0001c0002t0045 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*655G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 655 | chr18 | 61815197 | |||||
| chr18:61815685
|
G | A | 1 | a0001c0001t0125 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*167C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 167 | chr18 | 61815685 | |||||
| chr18:61815743
|
G | C | 1 | a0001c0001t0126 | 1 | HG00621.hp2 | 3_prime_UTR_variant | MODIFIER | c.*109C>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 109 | chr18 | 61815743 | |||||
| chr18:61816485
|
G | T | 1 | a0001c0002t0044 | 1 | NA18945.hp1 | 5_prime_UTR_variant | MODIFIER | c.-22C>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 22 | chr18 | 61816485 | |||||
| chr18:61816530
|
G | A | 2 | a0001c0001t0014a0001c0001t0127 | 5 | HG01109.hp1 HG02615.hp2 HG03041.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-67C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 2/2 | 67 | chr18 | 61816530 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:61816612
|
A | G | 1 | a0001c0002t0044g0097 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-135-14T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61816612 | ||||||
| chr18:61816765
|
C | T | 1 | a0001c0002t0066g0258 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-135-167G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61816765 | ||||||
| chr18:61816848
|
C | T | 3 | a0001c0001t0001g0001a0001c0001t0001g0100a0001c0001t0001g0186 | 4 | NA18944.hp2 NA18964.hp1 NA19054.hp2 others(1): Show |
intron_variant | MODIFIER | c.-135-250G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61816848 | ||||||
| chr18:61816969
|
T | C | 87 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(84): Show | 87 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.-135-371A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61816969 | ||||||
| chr18:61817131
|
C | G | 84 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(81): Show | 84 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.-135-533G>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61817131 | ||||||
| chr18:61817173
|
G | A | 3 | a0001c0001t0039g0136a0001c0001t0039g0138a0001c0001t0106g0082 | 3 | HG02055.hp1 HG03195.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-135-575C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61817173 | ||||||
| chr18:61817190
|
T | C | 3 | a0001c0003t0017g0041a0001c0003t0017g0280a0001c0003t0017g0281 | 3 | HG00280.hp1 HG02886.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-135-592A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61817190 | ||||||
| chr18:61817437
|
C | G | 1 | a0001c0001t0106g0082 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-135-839G>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61817437 | ||||||
| chr18:61817742
|
T | TA | 51 | a0001c0001t0038g0166a0001c0001t0038g0182a0001c0001t0043g0143others(48): Show | 51 | HG00423.hp1 HG00597.hp1 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.-135-1145dupT | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61817742 | ||||||
| chr18:61817742
|
T | TAAA | 64 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(61): Show | 64 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.-135-1147_-135-114 others(7): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61817742 | ||||||
| chr18:61817819
|
G | A | 1 | a0001c0008t0004g0063 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-135-1221C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61817819 | ||||||
| chr18:61817826
|
C | T | 2 | a0001c0001t0085g0140a0001c0001t0092g0141 | 2 | HG02572.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-135-1228G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61817826 | ||||||
| chr18:61817833
|
C | T | 1 | a0001c0001t0011g0135 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-135-1235G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61817833 | ||||||
| chr18:61817851
|
G | A | 123 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(120): Show | 123 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.-135-1253C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61817851 | ||||||
| chr18:61817874
|
C | A | 2 | a0001c0002t0062g0296a0001c0002t0063g0297 | 2 | HG01258.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.-135-1276G>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61817874 | ||||||
| chr18:61817925
|
T | C | 6 | a0001c0001t0078g0219a0001c0001t0079g0218a0001c0001t0097g0220others(3): Show | 6 | HG02145.hp2 HG02258.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.-135-1327A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61817925 | ||||||
| chr18:61817938
|
T | A | 12 | a0001c0002t0016g0171a0001c0002t0016g0174a0001c0002t0016g0175others(9): Show | 12 | HG00280.hp1 HG01255.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.-135-1340A>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61817938 | ||||||
| chr18:61818021
|
G | T | 124 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(121): Show | 124 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.-135-1423C>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61818021 | ||||||
| chr18:61818054
|
T | C | 8 | a0001c0002t0016g0171a0001c0002t0016g0174a0001c0002t0016g0175others(5): Show | 8 | HG01884.hp2 HG02280.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.-135-1456A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61818054 | ||||||
| chr18:61818109
|
A | C | 1 | a0001c0001t0080g0295 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-135-1511T>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61818109 | ||||||
| chr18:61818259
|
C | T | 3 | a0001c0002t0027g0134a0001c0002t0027g0179a0001c0002t0064g0178 | 3 | HG02257.hp1 HG02258.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-135-1661G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61818259 | ||||||
| chr18:61818308
|
G | A | 12 | a0001c0002t0016g0171a0001c0002t0016g0174a0001c0002t0016g0175others(9): Show | 12 | HG00280.hp1 HG01255.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.-135-1710C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61818308 | ||||||
| chr18:61818705
|
G | C | 12 | a0001c0002t0016g0171a0001c0002t0016g0174a0001c0002t0016g0175others(9): Show | 12 | HG00280.hp1 HG01255.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.-135-2107C>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61818705 | ||||||
| chr18:61818895
|
G | A | 6 | a0001c0001t0004g0150a0001c0001t0004g0204a0001c0001t0004g0242others(3): Show | 6 | HG00639.hp2 HG01106.hp2 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.-135-2297C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61818895 | ||||||
| chr18:61818949
|
C | T | 2 | a0001c0001t0001g0238a0001c0001t0033g0105 | 2 | NA18991.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.-135-2351G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61818949 | ||||||
| chr18:61818966
|
A | G | 12 | a0001c0002t0016g0171a0001c0002t0016g0174a0001c0002t0016g0175others(9): Show | 12 | HG00280.hp1 HG01255.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.-135-2368T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61818966 | ||||||
| chr18:61818989
|
C | G | 112 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(109): Show | 112 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.-135-2391G>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61818989 | ||||||
| chr18:61819032
|
A | T | 1 | a0001c0002t0015g0205 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-135-2434T>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61819032 | ||||||
| chr18:61819066
|
C | T | 1 | a0001c0001t0001g0092 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-135-2468G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61819066 | ||||||
| chr18:61819067
|
G | A | 1 | a0001c0002t0069g0083 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-135-2469C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61819067 | ||||||
| chr18:61819320
|
G | A | 4 | a0001c0001t0030g0207a0001c0001t0030g0209a0001c0001t0081g0244others(1): Show | 4 | HG00621.hp1 NA18949.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.-135-2722C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61819320 | ||||||
| chr18:61819331
|
C | T | 68 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(65): Show | 68 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.-135-2733G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61819331 | ||||||
| chr18:61819456
|
G | T | 1 | a0001c0001t0002g0050 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-135-2858C>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61819456 | ||||||
| chr18:61819499
|
G | A | 1 | a0001c0001t0099g0139 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-135-2901C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61819499 | ||||||
| chr18:61819554
|
G | A | 3 | a0001c0003t0017g0041a0001c0003t0017g0280a0001c0003t0017g0281 | 3 | HG00280.hp1 HG02886.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-135-2956C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61819554 | ||||||
| chr18:61819557
|
A | G | 1 | a0001c0001t0003g0230 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-135-2959T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61819557 | ||||||
| chr18:61819744
|
G | C | 4 | a0001c0001t0076g0300a0001c0002t0044g0097a0001c0002t0062g0296others(1): Show | 4 | HG01258.hp2 HG01934.hp1 NA18944.hp1 others(1): Show |
intron_variant | MODIFIER | c.-135-3146C>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61819744 | ||||||
| chr18:61819811
|
A | G | 1 | a0002c0005t0070g0192 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-135-3213T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61819811 | ||||||
| chr18:61819842
|
G | A | 68 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(65): Show | 68 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.-135-3244C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61819842 | ||||||
| chr18:61819854
|
C | G | 2 | a0001c0001t0001g0046a0001c0001t0004g0010 | 2 | HG02015.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.-135-3256G>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61819854 | ||||||
| chr18:61819857
|
C | A | 40 | a0001c0002t0005g0019a0001c0002t0005g0020a0001c0002t0005g0025others(37): Show | 40 | HG00423.hp1 HG00597.hp1 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.-135-3259G>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61819857 | ||||||
| chr18:61820020
|
C | CA | 9 | a0001c0001t0001g0121a0001c0001t0001g0243a0001c0001t0002g0007others(6): Show | 9 | HG01255.hp1 HG01981.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.-135-3423dupT | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61820020 | ||||||
| chr18:61820020
|
CA | C | 50 | a0001c0001t0001g0238a0001c0001t0013g0302a0001c0001t0013g0304others(47): Show | 50 | HG00280.hp1 HG00423.hp1 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.-135-3423delT | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61820020 | ||||||
| chr18:61820052
|
G | A | 40 | a0001c0002t0005g0019a0001c0002t0005g0020a0001c0002t0005g0025others(37): Show | 40 | HG00423.hp1 HG00597.hp1 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.-135-3454C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61820052 | ||||||
| chr18:61820142
|
A | C | 3 | a0001c0001t0002g0202a0001c0001t0007g0071a0001c0001t0041g0056 | 3 | HG03669.hp2 HG03834.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.-135-3544T>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61820142 | ||||||
| chr18:61820180
|
T | A | 1 | a0001c0001t0106g0082 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-135-3582A>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61820180 | ||||||
| chr18:61820236
|
G | A | 1 | a0001c0001t0021g0299 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-135-3638C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61820236 | ||||||
| chr18:61820283
|
C | G | 1 | a0002c0005t0070g0192 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-135-3685G>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61820283 | ||||||
| chr18:61820308
|
G | A | 5 | a0001c0001t0038g0166a0001c0001t0038g0182a0001c0001t0105g0183others(2): Show | 5 | HG02647.hp1 HG02922.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-135-3710C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61820308 | ||||||
| chr18:61820322
|
C | T | 1 | a0001c0001t0003g0153 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-135-3724G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61820322 | ||||||
| chr18:61820323
|
C | T | 27 | a0001c0002t0005g0019a0001c0002t0005g0020a0001c0002t0005g0025others(24): Show | 27 | HG00423.hp1 HG00597.hp1 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.-135-3725G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61820323 | ||||||
| chr18:61820328
|
C | CA | 113 | a0001c0001t0001g0060a0001c0001t0001g0092a0001c0001t0001g0106others(110): Show | 113 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(110): Show |
intron_variant | MODIFIER | c.-135-3731dupT | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61820328 | ||||||
| chr18:61820328
|
CACCAAAA others(3): Show |
C | 6 | a0001c0001t0006g0003a0001c0001t0043g0143a0001c0001t0043g0144others(3): Show | 6 | HG02451.hp1 HG02630.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.-135-3740_-135-373 others(14): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61820328 | ||||||
| chr18:61820328
|
CACCAAAA others(4): Show |
C | 4 | a0001c0001t0022g0260a0001c0001t0022g0277a0001c0001t0096g0024others(1): Show | 4 | HG02970.hp2 HG03098.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-135-3741_-135-373 others(15): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61820328 | ||||||
| chr18:61820328
|
CACCAAAA others(5): Show |
C | 1 | a0001c0001t0003g0235 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-135-3742_-135-373 others(16): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61820328 | ||||||
| chr18:61820328
|
CACCAAAA others(10): Show |
C | 1 | a0001c0001t0010g0065 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-135-3747_-135-373 others(21): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61820328 | ||||||
| chr18:61820330
|
C | A | 182 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0046others(179): Show | 183 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.-135-3732G>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61820330 | ||||||
| chr18:61820331
|
C | A | 113 | a0001c0001t0001g0060a0001c0001t0001g0092a0001c0001t0001g0106others(110): Show | 113 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(110): Show |
intron_variant | MODIFIER | c.-135-3733G>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61820331 | ||||||
| chr18:61820331
|
C | CAA | 22 | a0001c0001t0002g0029a0001c0001t0002g0272a0001c0001t0007g0111others(19): Show | 22 | HG01071.hp1 HG01175.hp2 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.-135-3735_-135-373 others(6): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61820331 | ||||||
| chr18:61820331
|
CA | C | 6 | a0001c0001t0003g0222a0001c0001t0003g0230a0001c0001t0003g0231others(3): Show | 6 | HG00639.hp1 HG01167.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.-135-3734delT | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61820331 | ||||||
| chr18:61820333
|
A | C | 1 | a0001c0001t0095g0236 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.-135-3735T>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61820333 | ||||||
| chr18:61820341
|
A | C | 6 | a0001c0001t0006g0003a0001c0001t0043g0143a0001c0001t0043g0144others(3): Show | 6 | HG02451.hp1 HG02630.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.-135-3743T>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61820341 | ||||||
| chr18:61820342
|
A | C | 4 | a0001c0001t0022g0260a0001c0001t0022g0277a0001c0001t0096g0024others(1): Show | 4 | HG02970.hp2 HG03098.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-135-3744T>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61820342 | ||||||
| chr18:61820343
|
A | C | 1 | a0001c0001t0003g0235 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-135-3745T>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61820343 | ||||||
| chr18:61820348
|
A | C | 1 | a0001c0001t0010g0065 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-135-3750T>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61820348 | ||||||
| chr18:61820502
|
C | T | 2 | a0001c0001t0123g0307a0001c0001t0125g0306 | 2 | HG02809.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-135-3904G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61820502 | ||||||
| chr18:61820515
|
T | C | 1 | a0002c0005t0070g0192 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-135-3917A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61820515 | ||||||
| chr18:61820554
|
C | T | 1 | a0001c0001t0113g0044 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-135-3956G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61820554 | ||||||
| chr18:61820666
|
A | G | 2 | a0001c0001t0102g0305a0001c0001t0104g0303 | 2 | HG02717.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-135-4068T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61820666 | ||||||
| chr18:61820674
|
T | G | 1 | a0001c0001t0001g0069 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-135-4076A>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61820674 | ||||||
| chr18:61820715
|
C | T | 1 | a0001c0001t0035g0027 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-135-4117G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61820715 | ||||||
| chr18:61820917
|
C | T | 40 | a0001c0002t0005g0019a0001c0002t0005g0020a0001c0002t0005g0025others(37): Show | 40 | HG00423.hp1 HG00597.hp1 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.-135-4319G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61820917 | ||||||
| chr18:61820963
|
G | A | 1 | a0002c0005t0070g0192 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-135-4365C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61820963 | ||||||
| chr18:61821172
|
C | T | 1 | a0001c0002t0066g0258 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-135-4574G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61821172 | ||||||
| chr18:61821212
|
G | C | 1 | a0002c0005t0070g0192 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-135-4614C>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61821212 | ||||||
| chr18:61821289
|
C | T | 3 | a0001c0003t0017g0041a0001c0003t0017g0280a0001c0003t0017g0281 | 3 | HG00280.hp1 HG02886.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-135-4691G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61821289 | ||||||
| chr18:61821325
|
T | C | 1 | a0001c0001t0006g0064 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-135-4727A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61821325 | ||||||
| chr18:61821348
|
T | C | 3 | a0001c0002t0044g0097a0001c0002t0062g0296a0001c0002t0063g0297 | 3 | HG01258.hp2 HG01934.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.-135-4750A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61821348 | ||||||
| chr18:61821397
|
T | C | 1 | a0001c0001t0039g0136 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-135-4799A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61821397 | ||||||
| chr18:61821430
|
C | T | 5 | a0001c0001t0010g0065a0001c0001t0010g0146a0001c0001t0010g0198others(2): Show | 5 | HG01243.hp2 HG03195.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.-135-4832G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61821430 | ||||||
| chr18:61821456
|
G | T | 1 | a0001c0001t0001g0103 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-135-4858C>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61821456 | ||||||
| chr18:61821471
|
A | G | 1 | a0001c0002t0044g0097 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-135-4873T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61821471 | ||||||
| chr18:61821648
|
C | T | 61 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(58): Show | 61 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.-135-5050G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61821648 | ||||||
| chr18:61821869
|
C | T | 1 | a0001c0001t0012g0164 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-135-5271G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61821869 | ||||||
| chr18:61821889
|
C | T | 2 | a0001c0001t0018g0249a0001c0001t0029g0257 | 2 | HG01255.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.-135-5291G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61821889 | ||||||
| chr18:61821898
|
A | T | 1 | a0002c0005t0070g0192 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-135-5300T>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61821898 | ||||||
| chr18:61821970
|
G | A | 1 | a0002c0005t0070g0192 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-135-5372C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61821970 | ||||||
| chr18:61822025
|
A | G | 4 | a0001c0001t0030g0207a0001c0001t0030g0209a0001c0001t0081g0244others(1): Show | 4 | HG00621.hp1 NA18949.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.-135-5427T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61822025 | ||||||
| chr18:61822120
|
C | T | 68 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(65): Show | 68 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.-135-5522G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61822120 | ||||||
| chr18:61822285
|
A | C | 1 | a0001c0001t0002g0163 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-135-5687T>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61822285 | ||||||
| chr18:61822394
|
A | G | 2 | a0001c0002t0005g0112a0001c0002t0005g0210 | 2 | HG00741.hp1 HG01167.hp1 |
intron_variant | MODIFIER | c.-135-5796T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61822394 | ||||||
| chr18:61822499
|
G | A | 2 | a0001c0001t0004g0085a0001c0001t0077g0045 | 2 | NA19065.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.-135-5901C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61822499 | ||||||
| chr18:61822501
|
A | T | 11 | a0001c0001t0038g0166a0001c0001t0038g0182a0001c0001t0078g0219others(8): Show | 11 | HG02145.hp2 HG02258.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.-135-5903T>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61822501 | ||||||
| chr18:61822512
|
A | T | 1 | a0001c0002t0005g0025 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-135-5914T>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61822512 | ||||||
| chr18:61822540
|
A | G | 1 | a0001c0001t0002g0039 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-135-5942T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61822540 | ||||||
| chr18:61822597
|
A | T | 1 | a0001c0001t0002g0012 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-135-5999T>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61822597 | ||||||
| chr18:61822805
|
A | G | 1 | a0001c0001t0107g0168 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-135-6207T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61822805 | ||||||
| chr18:61822900
|
C | A | 1 | a0001c0002t0066g0258 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-135-6302G>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61822900 | ||||||
| chr18:61822981
|
C | A | 1 | a0002c0005t0070g0192 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-135-6383G>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61822981 | ||||||
| chr18:61823071
|
G | C | 2 | a0001c0002t0045g0255a0001c0002t0067g0254 | 2 | HG02145.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-135-6473C>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61823071 | ||||||
| chr18:61823253
|
G | A | 1 | a0001c0002t0066g0258 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-135-6655C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61823253 | ||||||
| chr18:61823273
|
T | C | 43 | a0001c0002t0005g0019a0001c0002t0005g0020a0001c0002t0005g0025others(40): Show | 43 | HG00423.hp1 HG00597.hp1 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.-135-6675A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61823273 | ||||||
| chr18:61823371
|
C | G | 1 | a0001c0001t0095g0236 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.-135-6773G>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61823371 | ||||||
| chr18:61823462
|
AT | A | 68 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(65): Show | 68 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.-135-6865delA | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61823462 | ||||||
| chr18:61823488
|
A | G | 301 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0046others(298): Show | 302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.-135-6890T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61823488 | ||||||
| chr18:61823524
|
C | G | 1 | a0001c0002t0066g0258 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-135-6926G>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61823524 | ||||||
| chr18:61823535
|
C | G | 44 | a0001c0002t0005g0019a0001c0002t0005g0020a0001c0002t0005g0025others(41): Show | 44 | HG00423.hp1 HG00597.hp1 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.-135-6937G>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61823535 | ||||||
| chr18:61823841
|
G | A | 3 | a0001c0002t0027g0134a0001c0002t0027g0179a0001c0002t0064g0178 | 3 | HG02257.hp1 HG02258.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-135-7243C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61823841 | ||||||
| chr18:61823862
|
C | T | 1 | a0001c0001t0035g0027 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-135-7264G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61823862 | ||||||
| chr18:61823883
|
G | A | 1 | a0001c0001t0077g0045 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-135-7285C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61823883 | ||||||
| chr18:61823901
|
T | C | 8 | a0001c0002t0016g0171a0001c0002t0016g0174a0001c0002t0016g0175others(5): Show | 8 | HG01884.hp2 HG02280.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.-135-7303A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61823901 | ||||||
| chr18:61823923
|
G | A | 1 | a0002c0005t0070g0192 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-135-7325C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61823923 | ||||||
| chr18:61824139
|
G | C | 2 | a0001c0002t0045g0255a0001c0002t0067g0254 | 2 | HG02145.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-135-7541C>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61824139 | ||||||
| chr18:61824141
|
G | A | 2 | a0001c0002t0025g0172a0001c0002t0025g0173 | 2 | HG02280.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-135-7543C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61824141 | ||||||
| chr18:61824186
|
C | T | 12 | a0001c0002t0016g0171a0001c0002t0016g0174a0001c0002t0016g0175others(9): Show | 12 | HG00280.hp1 HG01255.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.-135-7588G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61824186 | ||||||
| chr18:61824343
|
T | C | 1 | a0002c0005t0070g0192 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-135-7745A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61824343 | ||||||
| chr18:61824364
|
G | T | 1 | a0001c0001t0001g0069 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-135-7766C>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61824364 | ||||||
| chr18:61824431
|
T | A | 17 | a0001c0001t0003g0147a0001c0001t0003g0149a0001c0001t0003g0153others(14): Show | 17 | HG00099.hp1 HG00423.hp2 HG00639.hp1 others(14): Show |
intron_variant | MODIFIER | c.-135-7833A>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61824431 | ||||||
| chr18:61824536
|
T | C | 40 | a0001c0002t0005g0019a0001c0002t0005g0020a0001c0002t0005g0025others(37): Show | 40 | HG00423.hp1 HG00597.hp1 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.-135-7938A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61824536 | ||||||
| chr18:61824538
|
G | T | 1 | a0001c0002t0047g0264 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-135-7940C>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61824538 | ||||||
| chr18:61824577
|
T | C | 1 | a0001c0003t0017g0041 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-135-7979A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61824577 | ||||||
| chr18:61824721
|
C | T | 3 | a0001c0002t0044g0097a0001c0002t0062g0296a0001c0002t0063g0297 | 3 | HG01258.hp2 HG01934.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.-135-8123G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61824721 | ||||||
| chr18:61824794
|
A | T | 1 | a0001c0001t0012g0156 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-135-8196T>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61824794 | ||||||
| chr18:61824944
|
T | C | 124 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(121): Show | 124 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.-135-8346A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61824944 | ||||||
| chr18:61825116
|
T | C | 2 | a0001c0001t0018g0249a0001c0001t0029g0257 | 2 | HG01255.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.-135-8518A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61825116 | ||||||
| chr18:61825381
|
G | A | 1 | a0001c0002t0050g0018 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.-135-8783C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61825381 | ||||||
| chr18:61825728
|
G | T | 1 | a0001c0001t0125g0306 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-135-9130C>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61825728 | ||||||
| chr18:61825740
|
C | T | 40 | a0001c0002t0005g0019a0001c0002t0005g0020a0001c0002t0005g0025others(37): Show | 40 | HG00423.hp1 HG00597.hp1 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.-135-9142G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61825740 | ||||||
| chr18:61825836
|
G | T | 40 | a0001c0002t0005g0019a0001c0002t0005g0020a0001c0002t0005g0025others(37): Show | 40 | HG00423.hp1 HG00597.hp1 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.-135-9238C>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61825836 | ||||||
| chr18:61826019
|
G | A | 1 | a0001c0001t0110g0181 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-135-9421C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61826019 | ||||||
| chr18:61826101
|
G | T | 69 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(66): Show | 69 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.-135-9503C>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61826101 | ||||||
| chr18:61826238
|
C | G | 87 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(84): Show | 87 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.-135-9640G>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61826238 | ||||||
| chr18:61826272
|
A | G | 87 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(84): Show | 87 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.-135-9674T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61826272 | ||||||
| chr18:61826307
|
C | T | 1 | a0001c0001t0020g0088 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-135-9709G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61826307 | ||||||
| chr18:61826511
|
T | G | 1 | a0001c0002t0068g0098 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-135-9913A>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61826511 | ||||||
| chr18:61826563
|
C | CT | 86 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(83): Show | 86 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.-135-9966dupA | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61826563 | ||||||
| chr18:61826579
|
C | T | 16 | a0001c0001t0043g0143a0001c0001t0043g0144a0001c0001t0122g0145others(13): Show | 16 | HG00280.hp1 HG01255.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.-135-9981G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61826579 | ||||||
| chr18:61826743
|
T | G | 1 | a0001c0001t0019g0286 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-135-10145A>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61826743 | ||||||
| chr18:61826804
|
C | T | 16 | a0001c0001t0043g0143a0001c0001t0043g0144a0001c0001t0122g0145others(13): Show | 16 | HG00280.hp1 HG01255.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.-135-10206G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61826804 | ||||||
| chr18:61826836
|
C | T | 95 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(92): Show | 95 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.-135-10238G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61826836 | ||||||
| chr18:61826857
|
G | A | 1 | a0001c0002t0053g0206 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-135-10259C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61826857 | ||||||
| chr18:61826973
|
A | T | 7 | a0001c0001t0010g0065a0001c0001t0010g0146a0001c0001t0010g0198others(4): Show | 7 | HG01243.hp2 HG02717.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.-135-10375T>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61826973 | ||||||
| chr18:61827022
|
A | G | 3 | a0001c0001t0001g0091a0001c0001t0008g0294a0001c0006t0001g0157 | 3 | HG00609.hp2 HG03831.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.-135-10424T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61827022 | ||||||
| chr18:61827032
|
A | G | 79 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(76): Show | 79 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.-135-10434T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61827032 | ||||||
| chr18:61827360
|
C | G | 1 | a0001c0002t0066g0258 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-135-10762G>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61827360 | ||||||
| chr18:61827536
|
G | A | 40 | a0001c0002t0005g0019a0001c0002t0005g0020a0001c0002t0005g0025others(37): Show | 40 | HG00423.hp1 HG00597.hp1 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.-135-10938C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61827536 | ||||||
| chr18:61827592
|
T | TTATA | 40 | a0001c0002t0005g0019a0001c0002t0005g0020a0001c0002t0005g0025others(37): Show | 40 | HG00423.hp1 HG00597.hp1 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.-135-10998_-135-10 others(10): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61827592 | ||||||
| chr18:61827597
|
G | T | 40 | a0001c0002t0005g0019a0001c0002t0005g0020a0001c0002t0005g0025others(37): Show | 40 | HG00423.hp1 HG00597.hp1 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.-135-10999C>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61827597 | ||||||
| chr18:61827693
|
A | G | 5 | a0001c0001t0038g0166a0001c0001t0038g0182a0001c0001t0105g0183others(2): Show | 5 | HG02647.hp1 HG02922.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-135-11095T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61827693 | ||||||
| chr18:61827893
|
C | T | 1 | a0001c0002t0056g0132 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-135-11295G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61827893 | ||||||
| chr18:61828138
|
C | T | 5 | a0001c0001t0043g0143a0001c0001t0043g0144a0001c0001t0122g0145others(2): Show | 5 | HG02451.hp1 HG02630.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.-135-11540G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61828138 | ||||||
| chr18:61828139
|
G | A | 1 | a0001c0001t0012g0156 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-135-11541C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61828139 | ||||||
| chr18:61828223
|
T | C | 1 | a0002c0005t0070g0192 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-135-11625A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61828223 | ||||||
| chr18:61828247
|
CCTTT | C | 69 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(66): Show | 69 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.-135-11653_-135-11 others(10): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61828247 | ||||||
| chr18:61828266
|
G | T | 1 | a0001c0001t0002g0225 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.-135-11668C>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61828266 | ||||||
| chr18:61828295
|
T | C | 143 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(140): Show | 143 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.-135-11697A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61828295 | ||||||
| chr18:61828343
|
C | T | 1 | a0001c0001t0001g0278 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-135-11745G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61828343 | ||||||
| chr18:61828373
|
C | G | 87 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(84): Show | 87 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.-135-11775G>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61828373 | ||||||
| chr18:61828447
|
C | T | 1 | a0001c0008t0004g0063 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-135-11849G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61828447 | ||||||
| chr18:61828448
|
G | A | 70 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(67): Show | 70 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.-135-11850C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61828448 | ||||||
| chr18:61828481
|
G | A | 52 | a0001c0001t0039g0136a0001c0001t0039g0138a0001c0001t0040g0184others(49): Show | 52 | HG00423.hp1 HG00597.hp1 HG00735.hp2 others(49): Show |
intron_variant | MODIFIER | c.-135-11883C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61828481 | ||||||
| chr18:61828629
|
G | GA | 85 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(82): Show | 85 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.-135-12032dupT | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61828629 | ||||||
| chr18:61828682
|
G | A | 1 | a0001c0001t0013g0084 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-135-12084C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61828682 | ||||||
| chr18:61828932
|
G | T | 69 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(66): Show | 69 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.-135-12334C>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61828932 | ||||||
| chr18:61829072
|
G | A | 1 | a0001c0001t0004g0053 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-135-12474C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61829072 | ||||||
| chr18:61829236
|
C | T | 1 | a0001c0002t0016g0175 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-135-12638G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61829236 | ||||||
| chr18:61829254
|
C | G | 4 | a0001c0001t0084g0195a0001c0002t0044g0097a0001c0002t0062g0296others(1): Show | 4 | HG01258.hp2 HG01934.hp1 HG01943.hp2 others(1): Show |
intron_variant | MODIFIER | c.-135-12656G>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61829254 | ||||||
| chr18:61829472
|
G | A | 1 | a0001c0001t0106g0082 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-135-12874C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61829472 | ||||||
| chr18:61829504
|
G | T | 44 | a0001c0001t0038g0166a0001c0001t0038g0182a0001c0001t0073g0110others(41): Show | 44 | HG00423.hp1 HG00597.hp1 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.-135-12906C>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61829504 | ||||||
| chr18:61829506
|
T | G | 85 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(82): Show | 85 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.-135-12908A>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61829506 | ||||||
| chr18:61829508
|
T | G | 85 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(82): Show | 85 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.-135-12910A>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61829508 | ||||||
| chr18:61829510
|
T | G | 85 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(82): Show | 85 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.-135-12912A>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61829510 | ||||||
| chr18:61829512
|
T | G | 85 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(82): Show | 85 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.-135-12914A>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61829512 | ||||||
| chr18:61829568
|
T | C | 1 | a0001c0001t0002g0012 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-135-12970A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61829568 | ||||||
| chr18:61829597
|
G | GGAGA | 75 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(72): Show | 75 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.-135-13003_-135-13 others(10): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61829597 | ||||||
| chr18:61829597
|
G | GGAGAGA | 36 | a0001c0001t0011g0066a0001c0001t0011g0135a0001c0002t0005g0019others(33): Show | 36 | HG00423.hp1 HG00597.hp1 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.-135-13005_-135-13 others(12): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61829597 | ||||||
| chr18:61829597
|
G | GGAGAGAG others(1): Show |
5 | a0001c0001t0084g0195a0001c0002t0044g0097a0001c0002t0048g0196others(2): Show | 5 | HG01258.hp2 HG01934.hp1 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.-135-13007_-135-13 others(14): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61829597 | ||||||
| chr18:61829597
|
GGAGA | G | 7 | a0001c0002t0016g0174a0001c0002t0016g0175a0001c0002t0025g0172others(4): Show | 7 | HG02280.hp1 HG02717.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.-135-13003_-135-13 others(10): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61829597 | ||||||
| chr18:61829629
|
T | A | 15 | a0001c0001t0011g0066a0001c0001t0011g0135a0001c0001t0043g0143others(12): Show | 15 | HG01255.hp1 HG02280.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.-135-13031A>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61829629 | ||||||
| chr18:61829637
|
G | A | 34 | a0001c0002t0005g0019a0001c0002t0005g0020a0001c0002t0005g0025others(31): Show | 34 | HG00423.hp1 HG00597.hp1 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.-135-13039C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61829637 | ||||||
| chr18:61829764
|
C | T | 34 | a0001c0002t0005g0019a0001c0002t0005g0020a0001c0002t0005g0025others(31): Show | 34 | HG00423.hp1 HG00597.hp1 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.-135-13166G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61829764 | ||||||
| chr18:61829820
|
C | T | 5 | a0001c0001t0118g0137a0001c0002t0028g0187a0001c0002t0028g0301others(2): Show | 5 | HG02622.hp1 HG02818.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.-135-13222G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61829820 | ||||||
| chr18:61829971
|
G | C | 1 | a0001c0001t0007g0081 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-135-13373C>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61829971 | ||||||
| chr18:61830025
|
C | CTT | 68 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(65): Show | 68 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.-135-13429_-135-13 others(8): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61830025 | ||||||
| chr18:61830114
|
C | T | 4 | a0001c0001t0084g0195a0001c0002t0044g0097a0001c0002t0062g0296others(1): Show | 4 | HG01258.hp2 HG01934.hp1 HG01943.hp2 others(1): Show |
intron_variant | MODIFIER | c.-135-13516G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61830114 | ||||||
| chr18:61830115
|
G | A | 1 | a0001c0002t0005g0211 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-135-13517C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61830115 | ||||||
| chr18:61830146
|
C | T | 1 | a0001c0001t0084g0195 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-135-13548G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61830146 | ||||||
| chr18:61830170
|
C | G | 70 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(67): Show | 70 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.-135-13572G>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61830170 | ||||||
| chr18:61830171
|
A | G | 119 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(116): Show | 119 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.-135-13573T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61830171 | ||||||
| chr18:61830278
|
G | A | 70 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(67): Show | 70 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.-135-13680C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61830278 | ||||||
| chr18:61830322
|
A | G | 117 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(114): Show | 117 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.-135-13724T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61830322 | ||||||
| chr18:61830530
|
G | A | 2 | a0001c0001t0011g0066a0001c0001t0011g0135 | 2 | HG03471.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-135-13932C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61830530 | ||||||
| chr18:61830562
|
C | T | 123 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(120): Show | 123 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.-135-13964G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61830562 | ||||||
| chr18:61830587
|
G | A | 70 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(67): Show | 70 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.-135-13989C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61830587 | ||||||
| chr18:61830607
|
T | A | 1 | a0001c0001t0001g0092 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-135-14009A>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61830607 | ||||||
| chr18:61830763
|
A | AAGG | 85 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(82): Show | 85 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.-135-14168_-135-14 others(9): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61830763 | ||||||
| chr18:61830771
|
T | C | 70 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(67): Show | 70 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.-135-14173A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61830771 | ||||||
| chr18:61830909
|
T | C | 40 | a0001c0001t0084g0195a0001c0002t0005g0019a0001c0002t0005g0020others(37): Show | 40 | HG00423.hp1 HG00597.hp1 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.-135-14311A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61830909 | ||||||
| chr18:61831123
|
C | A | 61 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(58): Show | 61 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.-135-14525G>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61831123 | ||||||
| chr18:61831182
|
G | A | 10 | a0001c0001t0011g0066a0001c0001t0011g0135a0001c0002t0016g0174others(7): Show | 10 | HG01255.hp1 HG02280.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.-135-14584C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61831182 | ||||||
| chr18:61831309
|
C | T | 1 | a0001c0001t0001g0108 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-135-14711G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61831309 | ||||||
| chr18:61831321
|
C | T | 1 | a0001c0001t0006g0271 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-135-14723G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61831321 | ||||||
| chr18:61831322
|
G | A | 61 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(58): Show | 61 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.-135-14724C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61831322 | ||||||
| chr18:61831554
|
G | A | 1 | a0001c0002t0063g0297 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-135-14956C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61831554 | ||||||
| chr18:61831680
|
GAACA | G | 76 | a0001c0001t0001g0028a0001c0001t0002g0005a0001c0001t0002g0006others(73): Show | 76 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.-135-15086_-135-15 others(10): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61831680 | ||||||
| chr18:61831780
|
TC | T | 76 | a0001c0001t0001g0028a0001c0001t0002g0005a0001c0001t0002g0006others(73): Show | 76 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.-135-15183delG | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61831780 | ||||||
| chr18:61831915
|
ATG | A | 31 | a0001c0002t0005g0019a0001c0002t0005g0020a0001c0002t0005g0025others(28): Show | 31 | HG00423.hp1 HG00597.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.-135-15319_-135-15 others(8): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61831915 | ||||||
| chr18:61831919
|
GT | G | 4 | a0001c0002t0015g0227a0001c0002t0026g0216a0001c0002t0026g0217others(1): Show | 4 | HG01261.hp1 HG02451.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-135-15322delA | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61831919 | ||||||
| chr18:61831921
|
GT | G | 69 | a0001c0001t0001g0028a0001c0001t0002g0005a0001c0001t0002g0006others(66): Show | 69 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.-135-15324delA | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61831921 | ||||||
| chr18:61831922
|
T | G | 35 | a0001c0002t0005g0019a0001c0002t0005g0020a0001c0002t0005g0025others(32): Show | 35 | HG00423.hp1 HG00597.hp1 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.-135-15324A>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61831922 | ||||||
| chr18:61831922
|
TG | T | 7 | a0001c0001t0010g0065a0001c0001t0010g0146a0001c0001t0010g0198others(4): Show | 7 | HG01243.hp2 HG02717.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.-135-15325delC | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61831922 | ||||||
| chr18:61831943
|
A | G | 1 | a0001c0002t0071g0190 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-135-15345T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61831943 | ||||||
| chr18:61832002
|
A | T | 10 | a0001c0001t0011g0066a0001c0001t0011g0135a0001c0002t0016g0174others(7): Show | 10 | HG01255.hp1 HG02280.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.-135-15404T>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61832002 | ||||||
| chr18:61832161
|
G | A | 1 | a0001c0001t0084g0195 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-135-15563C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61832161 | ||||||
| chr18:61832180
|
T | C | 1 | a0001c0001t0011g0267 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-135-15582A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61832180 | ||||||
| chr18:61832522
|
T | G | 7 | a0001c0001t0003g0222a0001c0001t0003g0232a0001c0001t0003g0235others(4): Show | 7 | HG02027.hp1 NA18943.hp1 NA18946.hp1 others(4): Show |
intron_variant | MODIFIER | c.-135-15924A>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61832522 | ||||||
| chr18:61832539
|
G | C | 3 | a0001c0001t0004g0057a0001c0001t0004g0058a0001c0001t0004g0133 | 3 | HG00280.hp2 HG01109.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.-135-15941C>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61832539 | ||||||
| chr18:61832588
|
T | C | 1 | a0001c0001t0041g0160 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-135-15990A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61832588 | ||||||
| chr18:61832660
|
T | A | 13 | a0001c0001t0039g0136a0001c0001t0039g0138a0001c0001t0040g0184others(10): Show | 13 | HG02055.hp1 HG02559.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-135-16062A>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61832660 | ||||||
| chr18:61832664
|
C | T | 116 | a0001c0001t0001g0028a0001c0001t0002g0005a0001c0001t0002g0006others(113): Show | 116 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.-135-16066G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61832664 | ||||||
| chr18:61832679
|
G | A | 67 | a0001c0001t0001g0028a0001c0001t0002g0005a0001c0001t0002g0006others(64): Show | 67 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.-135-16081C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61832679 | ||||||
| chr18:61832747
|
C | T | 116 | a0001c0001t0001g0028a0001c0001t0002g0005a0001c0001t0002g0006others(113): Show | 116 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.-135-16149G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61832747 | ||||||
| chr18:61832755
|
T | C | 1 | a0001c0001t0012g0156 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-135-16157A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61832755 | ||||||
| chr18:61832949
|
TAACATGG others(2): Show |
T | 5 | a0001c0001t0038g0166a0001c0001t0038g0182a0001c0001t0105g0183others(2): Show | 5 | HG02647.hp1 HG02922.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-135-16360_-135-16 others(15): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61832949 | ||||||
| chr18:61833028
|
C | G | 81 | a0001c0001t0001g0028a0001c0001t0002g0005a0001c0001t0002g0006others(78): Show | 81 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.-135-16430G>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61833028 | ||||||
| chr18:61833076
|
T | C | 116 | a0001c0001t0001g0028a0001c0001t0002g0005a0001c0001t0002g0006others(113): Show | 116 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.-135-16478A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61833076 | ||||||
| chr18:61833077
|
G | A | 67 | a0001c0001t0001g0028a0001c0001t0002g0005a0001c0001t0002g0006others(64): Show | 67 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.-135-16479C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61833077 | ||||||
| chr18:61833107
|
A | T | 55 | a0001c0001t0001g0028a0001c0001t0002g0005a0001c0001t0002g0006others(52): Show | 55 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(52): Show |
intron_variant | MODIFIER | c.-135-16509T>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61833107 | ||||||
| chr18:61833228
|
A | C | 10 | a0001c0001t0011g0066a0001c0001t0011g0135a0001c0002t0016g0174others(7): Show | 10 | HG01255.hp1 HG02280.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.-135-16630T>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61833228 | ||||||
| chr18:61833242
|
G | T | 1 | a0001c0001t0012g0239 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-135-16644C>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61833242 | ||||||
| chr18:61833389
|
C | A | 1 | a0001c0002t0005g0019 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.-135-16791G>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61833389 | ||||||
| chr18:61833408
|
C | A | 116 | a0001c0001t0001g0028a0001c0001t0002g0005a0001c0001t0002g0006others(113): Show | 116 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.-135-16810G>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61833408 | ||||||
| chr18:61833428
|
A | G | 1 | a0001c0001t0011g0135 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-135-16830T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61833428 | ||||||
| chr18:61833472
|
C | T | 1 | a0002c0005t0070g0192 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-135-16874G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61833472 | ||||||
| chr18:61833514
|
G | A | 116 | a0001c0001t0001g0028a0001c0001t0002g0005a0001c0001t0002g0006others(113): Show | 116 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.-135-16916C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61833514 | ||||||
| chr18:61833566
|
A | G | 4 | a0001c0001t0084g0195a0001c0002t0044g0097a0001c0002t0062g0296others(1): Show | 4 | HG01258.hp2 HG01934.hp1 HG01943.hp2 others(1): Show |
intron_variant | MODIFIER | c.-135-16968T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61833566 | ||||||
| chr18:61833569
|
T | C | 116 | a0001c0001t0001g0028a0001c0001t0002g0005a0001c0001t0002g0006others(113): Show | 116 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.-135-16971A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61833569 | ||||||
| chr18:61833612
|
C | T | 4 | a0001c0001t0084g0195a0001c0002t0044g0097a0001c0002t0062g0296others(1): Show | 4 | HG01258.hp2 HG01934.hp1 HG01943.hp2 others(1): Show |
intron_variant | MODIFIER | c.-135-17014G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61833612 | ||||||
| chr18:61833814
|
G | A | 5 | a0001c0001t0038g0166a0001c0001t0038g0182a0001c0001t0105g0183others(2): Show | 5 | HG02647.hp1 HG02922.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-135-17216C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61833814 | ||||||
| chr18:61833829
|
A | C | 116 | a0001c0001t0001g0028a0001c0001t0002g0005a0001c0001t0002g0006others(113): Show | 116 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.-135-17231T>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61833829 | ||||||
| chr18:61833884
|
TA | T | 116 | a0001c0001t0001g0028a0001c0001t0002g0005a0001c0001t0002g0006others(113): Show | 116 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.-135-17287delT | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61833884 | ||||||
| chr18:61833899
|
C | T | 306 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0046others(303): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.-135-17301G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61833899 | ||||||
| chr18:61833904
|
A | T | 68 | a0001c0001t0001g0028a0001c0001t0002g0005a0001c0001t0002g0006others(65): Show | 68 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.-135-17306T>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61833904 | ||||||
| chr18:61833917
|
T | A | 2 | a0001c0001t0123g0307a0001c0001t0125g0306 | 2 | HG02809.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-135-17319A>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61833917 | ||||||
| chr18:61833927
|
T | C | 1 | a0001c0001t0107g0168 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-135-17329A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61833927 | ||||||
| chr18:61833955
|
T | C | 116 | a0001c0001t0001g0028a0001c0001t0002g0005a0001c0001t0002g0006others(113): Show | 116 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.-135-17357A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61833955 | ||||||
| chr18:61834114
|
C | T | 116 | a0001c0001t0001g0028a0001c0001t0002g0005a0001c0001t0002g0006others(113): Show | 116 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.-135-17516G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61834114 | ||||||
| chr18:61834253
|
A | G | 3 | a0001c0002t0027g0134a0001c0002t0027g0179a0001c0002t0064g0178 | 3 | HG02257.hp1 HG02258.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-135-17655T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61834253 | ||||||
| chr18:61834266
|
C | T | 10 | a0001c0001t0011g0066a0001c0001t0011g0135a0001c0002t0016g0174others(7): Show | 10 | HG01255.hp1 HG02280.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.-135-17668G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61834266 | ||||||
| chr18:61834519
|
A | G | 68 | a0001c0001t0001g0028a0001c0001t0002g0005a0001c0001t0002g0006others(65): Show | 68 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.-135-17921T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61834519 | ||||||
| chr18:61834624
|
A | G | 2 | a0001c0001t0011g0066a0001c0001t0011g0135 | 2 | HG03471.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-135-18026T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61834624 | ||||||
| chr18:61834663
|
T | G | 5 | a0001c0001t0043g0143a0001c0001t0043g0144a0001c0001t0122g0145others(2): Show | 5 | HG02451.hp1 HG02630.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.-135-18065A>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61834663 | ||||||
| chr18:61834679
|
AT | A | 116 | a0001c0001t0001g0028a0001c0001t0002g0005a0001c0001t0002g0006others(113): Show | 116 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.-135-18082delA | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61834679 | ||||||
| chr18:61834718
|
T | C | 4 | a0001c0001t0084g0195a0001c0002t0044g0097a0001c0002t0062g0296others(1): Show | 4 | HG01258.hp2 HG01934.hp1 HG01943.hp2 others(1): Show |
intron_variant | MODIFIER | c.-135-18120A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61834718 | ||||||
| chr18:61834779
|
A | G | 14 | a0001c0001t0011g0066a0001c0001t0011g0135a0001c0001t0084g0195others(11): Show | 14 | HG01255.hp1 HG01258.hp2 HG01934.hp1 others(11): Show |
intron_variant | MODIFIER | c.-135-18181T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61834779 | ||||||
| chr18:61834791
|
A | T | 2 | a0001c0001t0085g0140a0001c0001t0092g0141 | 2 | HG02572.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-135-18193T>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61834791 | ||||||
| chr18:61834913
|
A | C | 5 | a0001c0001t0043g0143a0001c0001t0043g0144a0001c0001t0122g0145others(2): Show | 5 | HG02451.hp1 HG02630.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.-135-18315T>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61834913 | ||||||
| chr18:61834988
|
T | C | 68 | a0001c0001t0001g0028a0001c0001t0002g0005a0001c0001t0002g0006others(65): Show | 68 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.-135-18390A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61834988 | ||||||
| chr18:61835166
|
C | T | 116 | a0001c0001t0001g0028a0001c0001t0002g0005a0001c0001t0002g0006others(113): Show | 116 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.-135-18568G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61835166 | ||||||
| chr18:61835198
|
T | G | 55 | a0001c0001t0001g0028a0001c0001t0002g0005a0001c0001t0002g0006others(52): Show | 55 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(52): Show |
intron_variant | MODIFIER | c.-135-18600A>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61835198 | ||||||
| chr18:61835208
|
C | T | 8 | a0001c0002t0016g0174a0001c0002t0016g0175a0001c0002t0025g0172others(5): Show | 8 | HG01255.hp1 HG02280.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.-135-18610G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61835208 | ||||||
| chr18:61835273
|
T | C | 1 | a0001c0001t0003g0203 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-135-18675A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61835273 | ||||||
| chr18:61835292
|
C | T | 1 | a0001c0001t0002g0006 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-135-18694G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61835292 | ||||||
| chr18:61835388
|
C | T | 3 | a0001c0002t0005g0030a0001c0002t0005g0224a0001c0002t0051g0223 | 3 | NA18972.hp1 NA19009.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.-135-18790G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61835388 | ||||||
| chr18:61835489
|
G | A | 67 | a0001c0001t0001g0028a0001c0001t0002g0005a0001c0001t0002g0006others(64): Show | 67 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.-135-18891C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61835489 | ||||||
| chr18:61835612
|
T | G | 116 | a0001c0001t0001g0028a0001c0001t0002g0005a0001c0001t0002g0006others(113): Show | 116 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.-135-19014A>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61835612 | ||||||
| chr18:61835620
|
A | T | 5 | a0001c0001t0043g0143a0001c0001t0043g0144a0001c0001t0122g0145others(2): Show | 5 | HG02451.hp1 HG02630.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.-135-19022T>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61835620 | ||||||
| chr18:61835998
|
C | A | 4 | a0001c0001t0084g0195a0001c0002t0044g0097a0001c0002t0062g0296others(1): Show | 4 | HG01258.hp2 HG01934.hp1 HG01943.hp2 others(1): Show |
intron_variant | MODIFIER | c.-135-19400G>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61835998 | ||||||
| chr18:61836086
|
C | A | 1 | a0001c0001t0110g0181 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-135-19488G>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61836086 | ||||||
| chr18:61836123
|
G | T | 5 | a0001c0001t0043g0143a0001c0001t0043g0144a0001c0001t0122g0145others(2): Show | 5 | HG02451.hp1 HG02630.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.-135-19525C>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61836123 | ||||||
| chr18:61836428
|
T | C | 24 | a0001c0001t0011g0066a0001c0001t0011g0135a0001c0001t0039g0136others(21): Show | 24 | HG01255.hp1 HG02055.hp1 HG02280.hp1 others(21): Show |
intron_variant | MODIFIER | c.-135-19830A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61836428 | ||||||
| chr18:61836461
|
G | C | 1 | a0001c0001t0073g0110 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-135-19863C>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61836461 | ||||||
| chr18:61836677
|
C | A | 1 | a0001c0002t0053g0206 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-135-20079G>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61836677 | ||||||
| chr18:61836685
|
G | A | 1 | a0001c0002t0053g0206 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-135-20087C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61836685 | ||||||
| chr18:61836700
|
T | C | 1 | a0001c0001t0043g0144 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-135-20102A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61836700 | ||||||
| chr18:61836727
|
T | TA | 64 | a0001c0001t0001g0028a0001c0001t0002g0005a0001c0001t0002g0006others(61): Show | 64 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.-135-20130dupT | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61836727 | ||||||
| chr18:61836862
|
A | C | 3 | a0001c0002t0027g0134a0001c0002t0027g0179a0001c0002t0064g0178 | 3 | HG02257.hp1 HG02258.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-135-20264T>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61836862 | ||||||
| chr18:61836926
|
G | A | 2 | a0001c0001t0011g0066a0001c0001t0011g0135 | 2 | HG03471.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-135-20328C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61836926 | ||||||
| chr18:61836928
|
C | A | 117 | a0001c0001t0001g0028a0001c0001t0002g0005a0001c0001t0002g0006others(114): Show | 117 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.-135-20330G>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61836928 | ||||||
| chr18:61836969
|
T | C | 1 | a0001c0001t0104g0303 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-135-20371A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61836969 | ||||||
| chr18:61836997
|
C | A | 2 | a0001c0001t0111g0228a0001c0001t0115g0212 | 2 | NA19075.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.-135-20399G>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61836997 | ||||||
| chr18:61836997
|
C | T | 34 | a0001c0002t0005g0019a0001c0002t0005g0020a0001c0002t0005g0025others(31): Show | 34 | HG00423.hp1 HG00597.hp1 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.-135-20399G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61836997 | ||||||
| chr18:61837116
|
C | T | 35 | a0001c0001t0012g0164a0001c0002t0005g0019a0001c0002t0005g0020others(32): Show | 35 | HG00423.hp1 HG00597.hp1 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.-135-20518G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61837116 | ||||||
| chr18:61837117
|
G | A | 64 | a0001c0001t0001g0001a0001c0001t0001g0047a0001c0001t0001g0060others(61): Show | 65 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.-135-20519C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61837117 | ||||||
| chr18:61837308
|
T | C | 1 | a0001c0001t0004g0204 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-135-20710A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61837308 | ||||||
| chr18:61837327
|
A | C | 130 | a0001c0001t0001g0028a0001c0001t0002g0005a0001c0001t0002g0006others(127): Show | 130 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.-135-20729T>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61837327 | ||||||
| chr18:61837411
|
G | A | 1 | a0001c0002t0025g0173 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-135-20813C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61837411 | ||||||
| chr18:61837426
|
T | C | 4 | a0001c0001t0084g0195a0001c0002t0044g0097a0001c0002t0062g0296others(1): Show | 4 | HG01258.hp2 HG01934.hp1 HG01943.hp2 others(1): Show |
intron_variant | MODIFIER | c.-135-20828A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61837426 | ||||||
| chr18:61837426
|
T | G | 1 | a0001c0002t0053g0206 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-135-20828A>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61837426 | ||||||
| chr18:61837473
|
C | T | 3 | a0001c0001t0043g0143a0001c0001t0043g0144a0001c0001t0122g0145 | 3 | HG02451.hp1 HG02630.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-135-20875G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61837473 | ||||||
| chr18:61837881
|
G | A | 1 | a0001c0001t0001g0266 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-135-21283C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61837881 | ||||||
| chr18:61838017
|
AAC | A | 63 | a0001c0001t0001g0028a0001c0001t0002g0005a0001c0001t0002g0006others(60): Show | 63 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.-135-21421_-135-21 others(8): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61838017 | ||||||
| chr18:61838052
|
C | T | 1 | a0001c0002t0016g0171 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-135-21454G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61838052 | ||||||
| chr18:61838115
|
A | G | 130 | a0001c0001t0001g0028a0001c0001t0002g0005a0001c0001t0002g0006others(127): Show | 130 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.-135-21517T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61838115 | ||||||
| chr18:61838326
|
C | A | 4 | a0001c0001t0084g0195a0001c0002t0044g0097a0001c0002t0062g0296others(1): Show | 4 | HG01258.hp2 HG01934.hp1 HG01943.hp2 others(1): Show |
intron_variant | MODIFIER | c.-135-21728G>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61838326 | ||||||
| chr18:61838406
|
C | A | 1 | a0001c0001t0076g0300 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-135-21808G>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61838406 | ||||||
| chr18:61838407
|
G | A | 1 | a0001c0001t0014g0095 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-135-21809C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61838407 | ||||||
| chr18:61838529
|
G | A | 2 | a0001c0001t0011g0066a0001c0001t0011g0135 | 2 | HG03471.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-135-21931C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61838529 | ||||||
| chr18:61838564
|
T | A | 119 | a0001c0001t0001g0028a0001c0001t0002g0005a0001c0001t0002g0006others(116): Show | 119 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.-135-21966A>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61838564 | ||||||
| chr18:61838706
|
C | T | 1 | a0001c0008t0004g0063 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-135-22108G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61838706 | ||||||
| chr18:61838802
|
C | T | 2 | a0001c0001t0039g0136a0001c0001t0039g0138 | 2 | HG02055.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-135-22204G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61838802 | ||||||
| chr18:61839000
|
G | A | 2 | a0001c0001t0123g0307a0001c0001t0125g0306 | 2 | HG02809.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-135-22402C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61839000 | ||||||
| chr18:61839054
|
C | CA | 8 | a0001c0001t0001g0119a0001c0001t0001g0125a0001c0001t0001g0290others(5): Show | 8 | HG01433.hp2 HG01975.hp1 HG02027.hp1 others(5): Show |
intron_variant | MODIFIER | c.-135-22457dupT | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61839054 | ||||||
| chr18:61839054
|
CA | C | 56 | a0001c0001t0001g0028a0001c0001t0002g0005a0001c0001t0002g0006others(53): Show | 56 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.-135-22457delT | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61839054 | ||||||
| chr18:61839054
|
CAA | C | 33 | a0001c0001t0107g0168a0001c0002t0005g0019a0001c0002t0005g0020others(30): Show | 33 | HG00423.hp1 HG00597.hp1 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.-135-22458_-135-22 others(8): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61839054 | ||||||
| chr18:61839179
|
T | C | 13 | a0001c0001t0043g0143a0001c0001t0043g0144a0001c0001t0108g0180others(10): Show | 13 | HG02280.hp1 HG02451.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.-135-22581A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61839179 | ||||||
| chr18:61839301
|
C | G | 1 | a0001c0001t0033g0126 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-135-22703G>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61839301 | ||||||
| chr18:61839385
|
A | G | 22 | a0001c0001t0010g0065a0001c0001t0010g0146a0001c0001t0010g0198others(19): Show | 22 | HG01243.hp2 HG02280.hp1 HG02451.hp1 others(19): Show |
intron_variant | MODIFIER | c.-135-22787T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61839385 | ||||||
| chr18:61839415
|
G | C | 1 | a0001c0001t0114g0037 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-135-22817C>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61839415 | ||||||
| chr18:61839548
|
G | T | 1 | a0001c0001t0007g0071 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-135-22950C>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61839548 | ||||||
| chr18:61839671
|
G | A | 43 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(40): Show | 43 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(40): Show |
intron_variant | MODIFIER | c.-135-23073C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61839671 | ||||||
| chr18:61839684
|
G | A | 89 | a0001c0001t0001g0028a0001c0001t0002g0005a0001c0001t0002g0006others(86): Show | 89 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.-135-23086C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61839684 | ||||||
| chr18:61839714
|
C | T | 90 | a0001c0001t0001g0028a0001c0001t0002g0005a0001c0001t0002g0006others(87): Show | 90 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.-135-23116G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61839714 | ||||||
| chr18:61839756
|
G | A | 118 | a0001c0001t0001g0028a0001c0001t0002g0005a0001c0001t0002g0006others(115): Show | 118 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.-135-23158C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61839756 | ||||||
| chr18:61839757
|
T | C | 3 | a0001c0001t0011g0066a0001c0001t0011g0135a0002c0005t0070g0192 | 3 | HG03098.hp1 HG03471.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-135-23159A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61839757 | ||||||
| chr18:61840056
|
A | G | 5 | a0001c0001t0043g0143a0001c0001t0043g0144a0001c0001t0122g0145others(2): Show | 5 | HG02451.hp1 HG02630.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.-135-23458T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61840056 | ||||||
| chr18:61840094
|
A | G | 17 | a0001c0001t0039g0136a0001c0001t0039g0138a0001c0001t0040g0184others(14): Show | 17 | HG00735.hp2 HG01258.hp2 HG01934.hp1 others(14): Show |
intron_variant | MODIFIER | c.-135-23496T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61840094 | ||||||
| chr18:61840209
|
G | A | 1 | a0001c0002t0069g0083 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-135-23611C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61840209 | ||||||
| chr18:61840374
|
T | C | 1 | a0001c0001t0001g0090 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-135-23776A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61840374 | ||||||
| chr18:61840405
|
T | C | 91 | a0001c0001t0001g0028a0001c0001t0002g0005a0001c0001t0002g0006others(88): Show | 91 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.-135-23807A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61840405 | ||||||
| chr18:61840479
|
C | T | 5 | a0001c0001t0010g0065a0001c0001t0010g0146a0001c0001t0010g0198others(2): Show | 5 | HG01243.hp2 HG03195.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.-135-23881G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61840479 | ||||||
| chr18:61840503
|
T | A | 5 | a0001c0001t0043g0143a0001c0001t0043g0144a0001c0001t0122g0145others(2): Show | 5 | HG02451.hp1 HG02630.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.-135-23905A>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61840503 | ||||||
| chr18:61840611
|
G | A | 1 | a0001c0001t0106g0082 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-135-24013C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61840611 | ||||||
| chr18:61840813
|
C | G | 1 | a0001c0001t0099g0139 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-135-24215G>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61840813 | ||||||
| chr18:61840875
|
T | C | 1 | a0001c0001t0001g0240 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-135-24277A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61840875 | ||||||
| chr18:61840879
|
C | T | 21 | a0001c0001t0003g0194a0001c0001t0003g0201a0001c0001t0010g0065others(18): Show | 21 | HG01243.hp2 HG02280.hp1 HG02451.hp1 others(18): Show |
intron_variant | MODIFIER | c.-135-24281G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61840879 | ||||||
| chr18:61840978
|
A | C | 129 | a0001c0001t0001g0028a0001c0001t0002g0005a0001c0001t0002g0006others(126): Show | 129 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.-135-24380T>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61840978 | ||||||
| chr18:61841064
|
G | A | 5 | a0001c0001t0084g0195a0001c0002t0044g0097a0001c0002t0048g0196others(2): Show | 5 | HG01258.hp2 HG01934.hp1 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.-135-24466C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61841064 | ||||||
| chr18:61841104
|
C | T | 3 | a0001c0002t0026g0216a0001c0002t0026g0217a0001c0002t0061g0215 | 3 | HG02451.hp2 HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-135-24506G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61841104 | ||||||
| chr18:61841373
|
C | T | 2 | a0001c0001t0011g0268a0001c0001t0019g0285 | 2 | HG00140.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.-135-24775G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61841373 | ||||||
| chr18:61841471
|
G | A | 117 | a0001c0001t0001g0028a0001c0001t0002g0005a0001c0001t0002g0006others(114): Show | 117 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.-135-24873C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61841471 | ||||||
| chr18:61841516
|
A | C | 5 | a0001c0001t0084g0195a0001c0002t0044g0097a0001c0002t0048g0196others(2): Show | 5 | HG01258.hp2 HG01934.hp1 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.-135-24918T>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61841516 | ||||||
| chr18:61841575
|
T | A | 91 | a0001c0001t0001g0028a0001c0001t0002g0005a0001c0001t0002g0006others(88): Show | 91 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.-135-24977A>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61841575 | ||||||
| chr18:61841642
|
G | A | 117 | a0001c0001t0001g0028a0001c0001t0002g0005a0001c0001t0002g0006others(114): Show | 117 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.-135-25044C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61841642 | ||||||
| chr18:61841733
|
C | G | 5 | a0001c0001t0084g0195a0001c0002t0044g0097a0001c0002t0048g0196others(2): Show | 5 | HG01258.hp2 HG01934.hp1 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.-135-25135G>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61841733 | ||||||
| chr18:61841922
|
T | C | 91 | a0001c0001t0001g0028a0001c0001t0002g0005a0001c0001t0002g0006others(88): Show | 91 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.-135-25324A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61841922 | ||||||
| chr18:61841947
|
C | T | 117 | a0001c0001t0001g0028a0001c0001t0002g0005a0001c0001t0002g0006others(114): Show | 117 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.-135-25349G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61841947 | ||||||
| chr18:61842029
|
A | G | 12 | a0001c0001t0039g0136a0001c0001t0039g0138a0001c0001t0040g0184others(9): Show | 12 | HG00735.hp2 HG02055.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.-135-25431T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61842029 | ||||||
| chr18:61842053
|
A | T | 12 | a0001c0001t0039g0136a0001c0001t0039g0138a0001c0001t0040g0184others(9): Show | 12 | HG00735.hp2 HG02055.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.-135-25455T>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61842053 | ||||||
| chr18:61842126
|
T | C | 1 | a0001c0002t0015g0205 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-135-25528A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61842126 | ||||||
| chr18:61842271
|
T | C | 5 | a0001c0001t0084g0195a0001c0002t0044g0097a0001c0002t0048g0196others(2): Show | 5 | HG01258.hp2 HG01934.hp1 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.-135-25673A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61842271 | ||||||
| chr18:61842347
|
C | G | 1 | a0001c0002t0005g0211 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-135-25749G>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61842347 | ||||||
| chr18:61842474
|
G | A | 94 | a0001c0001t0001g0028a0001c0001t0002g0005a0001c0001t0002g0006others(91): Show | 94 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.-135-25876C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61842474 | ||||||
| chr18:61842631
|
G | A | 1 | a0001c0002t0068g0098 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-135-26033C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61842631 | ||||||
| chr18:61842633
|
G | A | 1 | a0001c0001t0080g0295 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-135-26035C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61842633 | ||||||
| chr18:61842732
|
T | C | 1 | a0001c0002t0027g0179 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-135-26134A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61842732 | ||||||
| chr18:61842749
|
C | A | 3 | a0001c0002t0044g0097a0001c0002t0062g0296a0001c0002t0063g0297 | 3 | HG01258.hp2 HG01934.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.-135-26151G>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61842749 | ||||||
| chr18:61842775
|
T | C | 2 | a0001c0001t0001g0001a0001c0001t0001g0100 | 3 | NA18944.hp2 NA19054.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.-135-26177A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61842775 | ||||||
| chr18:61842953
|
G | A | 1 | a0001c0001t0004g0177 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-135-26355C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61842953 | ||||||
| chr18:61843143
|
C | T | 5 | a0001c0001t0043g0143a0001c0001t0043g0144a0001c0001t0122g0145others(2): Show | 5 | HG02451.hp1 HG02630.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.-135-26545G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61843143 | ||||||
| chr18:61843147
|
T | TAAGTGCC others(35): Show |
2 | a0001c0001t0022g0282a0001c0001t0036g0283 | 2 | NA18960.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.-135-26591_-135-26 others(48): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61843147 | ||||||
| chr18:61843211
|
C | T | 2 | a0001c0001t0002g0039a0001c0001t0109g0072 | 2 | HG00735.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.-135-26613G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61843211 | ||||||
| chr18:61843327
|
C | T | 118 | a0001c0001t0001g0028a0001c0001t0002g0005a0001c0001t0002g0006others(115): Show | 118 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.-135-26729G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61843327 | ||||||
| chr18:61843434
|
G | A | 3 | a0001c0002t0026g0216a0001c0002t0026g0217a0001c0002t0061g0215 | 3 | HG02451.hp2 HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-135-26836C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61843434 | ||||||
| chr18:61843448
|
G | A | 1 | a0001c0001t0001g0290 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-135-26850C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61843448 | ||||||
| chr18:61843498
|
C | T | 7 | a0001c0002t0016g0174a0001c0002t0016g0175a0001c0002t0025g0172others(4): Show | 7 | HG02280.hp1 HG02717.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.-135-26900G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61843498 | ||||||
| chr18:61843510
|
T | C | 5 | a0001c0001t0043g0143a0001c0001t0043g0144a0001c0001t0122g0145others(2): Show | 5 | HG02451.hp1 HG02630.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.-135-26912A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61843510 | ||||||
| chr18:61843558
|
C | T | 1 | a0001c0001t0003g0231 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.-135-26960G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61843558 | ||||||
| chr18:61843651
|
G | A | 2 | a0001c0001t0022g0282a0001c0001t0036g0283 | 2 | NA18960.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.-135-27053C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61843651 | ||||||
| chr18:61843655
|
T | C | 1 | a0001c0001t0099g0139 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-135-27057A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61843655 | ||||||
| chr18:61843797
|
G | A | 1 | a0001c0001t0001g0266 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-135-27199C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61843797 | ||||||
| chr18:61843967
|
T | C | 96 | a0001c0001t0001g0028a0001c0001t0001g0238a0001c0001t0002g0005others(93): Show | 96 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.-135-27369A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61843967 | ||||||
| chr18:61843978
|
A | C | 7 | a0001c0001t0006g0017a0001c0001t0009g0023a0001c0001t0009g0031others(4): Show | 7 | NA18942.hp2 NA18949.hp1 NA19000.hp1 others(4): Show |
intron_variant | MODIFIER | c.-135-27380T>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61843978 | ||||||
| chr18:61844077
|
G | GGAAA | 48 | a0001c0001t0001g0060a0001c0001t0001g0067a0001c0001t0001g0086others(45): Show | 48 | HG00423.hp2 HG00438.hp1 HG00609.hp1 others(45): Show |
intron_variant | MODIFIER | c.-135-27483_-135-27 others(10): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844077 | ||||||
| chr18:61844077
|
G | GGAAAGAA others(1): Show |
24 | a0001c0001t0001g0092a0001c0001t0001g0186a0001c0001t0001g0291others(21): Show | 24 | HG00639.hp1 HG00738.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.-135-27487_-135-27 others(14): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844077 | ||||||
| chr18:61844077
|
G | GGAAAGAA others(5): Show |
6 | a0001c0001t0001g0248a0001c0001t0004g0150a0001c0001t0007g0114others(3): Show | 6 | HG00621.hp2 HG01106.hp1 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.-135-27491_-135-27 others(18): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844077 | ||||||
| chr18:61844077
|
G | GGAAAGAA others(9): Show |
3 | a0001c0001t0001g0116a0001c0001t0019g0289a0001c0001t0040g0184 | 3 | HG01192.hp1 HG02630.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.-135-27495_-135-27 others(22): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844077 | ||||||
| chr18:61844077
|
G | GGAAAGAA others(31): Show |
1 | a0001c0004t0101g0253 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-135-27480_-135-27 others(44): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844077 | ||||||
| chr18:61844077
|
G | GGAAAGAA others(35): Show |
3 | a0001c0002t0005g0221a0001c0002t0051g0223a0001c0002t0071g0190 | 3 | HG03710.hp1 NA18956.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.-135-27480_-135-27 others(48): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844077 | ||||||
| chr18:61844077
|
G | GGAAAGAA others(43): Show |
1 | a0001c0002t0005g0211 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-135-27480_-135-27 others(56): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844077 | ||||||
| chr18:61844077
|
G | GGAAAGAA others(43): Show |
1 | a0001c0002t0054g0214 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-135-27480_-135-27 others(56): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844077 | ||||||
| chr18:61844077
|
G | GGAAAGAA others(47): Show |
1 | a0001c0002t0026g0216 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-135-27480_-135-27 others(60): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844077 | ||||||
| chr18:61844077
|
G | GGAAAGAA others(44): Show |
1 | a0001c0002t0053g0206 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-135-27480_-135-27 others(57): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844077 | ||||||
| chr18:61844077
|
G | GGAAAGAA others(36): Show |
1 | a0001c0002t0023g0256 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-135-27480_-135-27 others(49): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844077 | ||||||
| chr18:61844077
|
G | GGAAAGAA others(31): Show |
1 | a0001c0002t0005g0030 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-135-27480_-135-27 others(44): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844077 | ||||||
| chr18:61844077
|
G | GGAAAGAA others(35): Show |
1 | a0001c0002t0005g0224 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.-135-27480_-135-27 others(48): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844077 | ||||||
| chr18:61844077
|
GGAAA | G | 39 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0068others(36): Show | 39 | HG00323.hp2 HG00408.hp2 HG01081.hp1 others(36): Show |
intron_variant | MODIFIER | c.-135-27483_-135-27 others(10): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844077 | ||||||
| chr18:61844077
|
GGAAAGAA others(1): Show |
G | 33 | a0001c0001t0001g0089a0001c0001t0001g0115a0001c0001t0001g0266others(30): Show | 33 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.-135-27487_-135-27 others(14): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844077 | ||||||
| chr18:61844077
|
GGAAAGAA others(5): Show |
G | 14 | a0001c0001t0001g0001a0001c0001t0001g0079a0001c0001t0001g0131others(11): Show | 15 | HG00280.hp1 HG01109.hp2 HG01123.hp1 others(12): Show |
intron_variant | MODIFIER | c.-135-27491_-135-27 others(18): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844077 | ||||||
| chr18:61844077
|
GGAAAGAA others(9): Show |
G | 6 | a0001c0001t0001g0100a0001c0001t0003g0194a0001c0001t0004g0177others(3): Show | 6 | HG00597.hp2 HG02602.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-135-27495_-135-27 others(22): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844077 | ||||||
| chr18:61844077
|
GGAAAGAA others(17): Show |
G | 2 | a0001c0001t0038g0182a0001c0002t0016g0171 | 2 | HG01884.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-135-27503_-135-27 others(30): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844077 | ||||||
| chr18:61844078
|
G | GAAAGAAA others(35): Show |
2 | a0001c0002t0005g0210a0001c0002t0026g0217 | 2 | HG01167.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.-135-27522_-135-27 others(48): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844078 | ||||||
| chr18:61844078
|
G | GAAAGAAA others(39): Show |
1 | a0001c0002t0005g0112 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-135-27526_-135-27 others(52): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844078 | ||||||
| chr18:61844082
|
G | GAAAGAAA others(31): Show |
1 | a0001c0002t0015g0226 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.-135-27522_-135-27 others(44): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844082 | ||||||
| chr18:61844082
|
G | GAAAGAAA others(35): Show |
1 | a0001c0002t0061g0215 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-135-27526_-135-27 others(48): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844082 | ||||||
| chr18:61844084
|
A | AGAAAGAA others(30): Show |
1 | a0001c0002t0055g0241 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-135-27487_-135-27 others(43): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844084 | ||||||
| chr18:61844086
|
G | A | 1 | a0001c0002t0055g0241 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-135-27488C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844086 | ||||||
| chr18:61844086
|
G | GAAAGAAA others(31): Show |
2 | a0001c0001t0002g0043a0001c0001t0002g0163 | 2 | HG00738.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.-135-27526_-135-27 others(44): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844086 | ||||||
| chr18:61844098
|
G | GAAAGAAA others(31): Show |
1 | a0001c0001t0009g0124 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.-135-27538_-135-27 others(44): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844098 | ||||||
| chr18:61844103
|
A | G | 1 | a0001c0001t0008g0073 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-135-27505T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844103 | ||||||
| chr18:61844110
|
G | GAA | 5 | a0001c0001t0006g0017a0001c0001t0111g0228a0001c0001t0115g0212others(2): Show | 5 | HG00423.hp1 HG02486.hp2 NA19067.hp1 others(2): Show |
intron_variant | MODIFIER | c.-135-27514_-135-27 others(8): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844110 | ||||||
| chr18:61844114
|
G | GAA | 7 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0015others(4): Show | 7 | HG00323.hp1 HG01167.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.-135-27518_-135-27 others(8): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844114 | ||||||
| chr18:61844118
|
G | GAA | 16 | a0001c0001t0002g0007a0001c0001t0002g0022a0001c0001t0002g0029others(13): Show | 16 | HG00099.hp2 HG00408.hp1 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.-135-27522_-135-27 others(8): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844118 | ||||||
| chr18:61844122
|
G | GAA | 19 | a0001c0001t0002g0012a0001c0001t0002g0039a0001c0001t0002g0051others(16): Show | 19 | HG00597.hp1 HG00735.hp1 HG01123.hp2 others(16): Show |
intron_variant | MODIFIER | c.-135-27526_-135-27 others(8): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844122 | ||||||
| chr18:61844126
|
G | GAA | 3 | a0001c0001t0001g0028a0001c0001t0007g0036a0001c0001t0041g0056 | 3 | HG00140.hp1 HG03834.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-135-27530_-135-27 others(8): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844126 | ||||||
| chr18:61844139
|
A | AAAGAAAG others(4): Show |
1 | a0001c0001t0004g0085 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-135-27542_-135-27 others(17): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844139 | ||||||
| chr18:61844139
|
A | AAAGAAAG others(8): Show |
1 | a0001c0001t0003g0153 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-135-27542_-135-27 others(21): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844139 | ||||||
| chr18:61844142
|
T | G | 60 | a0001c0001t0001g0028a0001c0001t0001g0238a0001c0001t0002g0005others(57): Show | 60 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.-135-27544A>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844142 | ||||||
| chr18:61844143
|
T | A | 60 | a0001c0001t0001g0028a0001c0001t0001g0238a0001c0001t0002g0005others(57): Show | 60 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.-135-27545A>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844143 | ||||||
| chr18:61844148
|
G | A | 60 | a0001c0001t0001g0028a0001c0001t0001g0238a0001c0001t0002g0005others(57): Show | 60 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.-135-27550C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844148 | ||||||
| chr18:61844149
|
A | AG | 3 | a0001c0001t0007g0071a0001c0001t0014g0095a0001c0002t0023g0021 | 3 | HG02080.hp1 HG02615.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.-135-27552_-135-27 others(7): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844149 | ||||||
| chr18:61844150
|
A | G | 57 | a0001c0001t0001g0028a0001c0001t0001g0238a0001c0001t0002g0005others(54): Show | 57 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.-135-27552T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844150 | ||||||
| chr18:61844153
|
G | A | 57 | a0001c0001t0001g0028a0001c0001t0001g0238a0001c0001t0002g0005others(54): Show | 57 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.-135-27555C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844153 | ||||||
| chr18:61844154
|
G | A | 3 | a0001c0001t0007g0071a0001c0001t0014g0095a0001c0002t0023g0021 | 3 | HG02080.hp1 HG02615.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.-135-27556C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844154 | ||||||
| chr18:61844157
|
G | A | 57 | a0001c0001t0001g0028a0001c0001t0001g0238a0001c0001t0002g0005others(54): Show | 57 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.-135-27559C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844157 | ||||||
| chr18:61844157
|
G | T | 3 | a0001c0001t0007g0071a0001c0001t0014g0095a0001c0002t0023g0021 | 3 | HG02080.hp1 HG02615.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.-135-27559C>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844157 | ||||||
| chr18:61844158
|
G | T | 3 | a0001c0001t0007g0071a0001c0001t0014g0095a0001c0002t0023g0021 | 3 | HG02080.hp1 HG02615.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.-135-27560C>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844158 | ||||||
| chr18:61844161
|
G | A | 57 | a0001c0001t0001g0028a0001c0001t0001g0238a0001c0001t0002g0005others(54): Show | 57 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.-135-27563C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844161 | ||||||
| chr18:61844162
|
G | A | 3 | a0001c0001t0007g0071a0001c0001t0014g0095a0001c0002t0023g0021 | 3 | HG02080.hp1 HG02615.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.-135-27564C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844162 | ||||||
| chr18:61844162
|
G | GAAATTAA | 18 | a0001c0001t0001g0028a0001c0001t0002g0007a0001c0001t0002g0029others(15): Show | 18 | HG00099.hp2 HG00597.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.-135-27565_-135-27 others(13): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844162 | ||||||
| chr18:61844162
|
G | T | 12 | a0001c0001t0002g0006a0001c0001t0002g0022a0001c0001t0002g0050others(9): Show | 12 | HG00408.hp1 HG00423.hp1 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.-135-27564C>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844162 | ||||||
| chr18:61844163
|
G | A | 27 | a0001c0001t0001g0238a0001c0001t0002g0005a0001c0001t0002g0009others(24): Show | 27 | HG00140.hp1 HG00323.hp1 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.-135-27565C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844163 | ||||||
| chr18:61844163
|
G | T | 12 | a0001c0001t0002g0006a0001c0001t0002g0022a0001c0001t0002g0050others(9): Show | 12 | HG00408.hp1 HG00423.hp1 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.-135-27565C>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844163 | ||||||
| chr18:61844164
|
AG | A | 3 | a0001c0001t0007g0071a0001c0001t0014g0095a0001c0002t0023g0021 | 3 | HG02080.hp1 HG02615.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.-135-27567delC | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844164 | ||||||
| chr18:61844165
|
G | A | 39 | a0001c0001t0001g0238a0001c0001t0002g0005a0001c0001t0002g0006others(36): Show | 39 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(36): Show |
intron_variant | MODIFIER | c.-135-27567C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844165 | ||||||
| chr18:61844165
|
G | GA | 18 | a0001c0001t0001g0028a0001c0001t0002g0007a0001c0001t0002g0029others(15): Show | 18 | HG00099.hp2 HG00597.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.-135-27568_-135-27 others(7): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844165 | ||||||
| chr18:61844166
|
G | A | 21 | a0001c0001t0001g0028a0001c0001t0002g0007a0001c0001t0002g0029others(18): Show | 21 | HG00099.hp2 HG00597.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.-135-27568C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844166 | ||||||
| chr18:61844166
|
G | GAAAGAAA others(13): Show |
1 | a0001c0001t0002g0009 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-135-27569_-135-27 others(26): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844166 | ||||||
| chr18:61844166
|
G | GAAATAAA others(9): Show |
1 | a0001c0001t0001g0238 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-135-27569_-135-27 others(22): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844166 | ||||||
| chr18:61844166
|
G | GAAATTAA others(5): Show |
25 | a0001c0001t0002g0005a0001c0001t0002g0012a0001c0001t0002g0015others(22): Show | 25 | HG00140.hp1 HG00323.hp1 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.-135-27569_-135-27 others(18): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844166 | ||||||
| chr18:61844166
|
G | GAGAA | 12 | a0001c0001t0002g0006a0001c0001t0002g0022a0001c0001t0002g0050others(9): Show | 12 | HG00408.hp1 HG00423.hp1 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.-135-27569_-135-27 others(10): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844166 | ||||||
| chr18:61844170
|
G | A | 25 | a0001c0001t0002g0043a0001c0001t0002g0163a0001c0001t0009g0124others(22): Show | 25 | HG00738.hp1 HG00741.hp1 HG01167.hp1 others(22): Show |
intron_variant | MODIFIER | c.-135-27572C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844170 | ||||||
| chr18:61844171
|
G | A | 60 | a0001c0001t0001g0028a0001c0001t0001g0238a0001c0001t0002g0005others(57): Show | 60 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.-135-27573C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844171 | ||||||
| chr18:61844176
|
AGAGAGGA others(10): Show |
A | 19 | a0001c0001t0002g0043a0001c0001t0002g0163a0001c0001t0009g0124others(16): Show | 19 | HG00738.hp1 HG00741.hp1 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.-135-27595_-135-27 others(23): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844176 | ||||||
| chr18:61844178
|
A | G | 61 | a0001c0001t0001g0028a0001c0001t0001g0238a0001c0001t0002g0005others(58): Show | 61 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.-135-27580T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844178 | ||||||
| chr18:61844186
|
G | A | 61 | a0001c0001t0001g0028a0001c0001t0001g0238a0001c0001t0002g0005others(58): Show | 61 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.-135-27588C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844186 | ||||||
| chr18:61844187
|
A | G | 61 | a0001c0001t0001g0028a0001c0001t0001g0238a0001c0001t0002g0005others(58): Show | 61 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.-135-27589T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844187 | ||||||
| chr18:61844187
|
AAGGAAGG others(5): Show |
A | 2 | a0001c0001t0001g0266a0001c0001t0001g0275 | 2 | HG01081.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.-135-27601_-135-27 others(18): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844187 | ||||||
| chr18:61844191
|
A | AAGGGAAG others(5): Show |
14 | a0001c0001t0010g0065a0001c0001t0010g0146a0001c0001t0010g0198others(11): Show | 14 | HG00735.hp2 HG01243.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.-135-27605_-135-27 others(18): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844191 | ||||||
| chr18:61844191
|
A | AAGGGAAG others(17): Show |
11 | a0001c0001t0003g0194a0001c0001t0003g0201a0001c0001t0011g0066others(8): Show | 11 | HG02280.hp1 HG02615.hp1 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.-135-27617_-135-27 others(30): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844191 | ||||||
| chr18:61844192
|
AG | A | 61 | a0001c0001t0001g0028a0001c0001t0001g0238a0001c0001t0002g0005others(58): Show | 61 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.-135-27595delC | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844192 | ||||||
| chr18:61844203
|
G | A | 1 | a0001c0001t0007g0081 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-135-27605C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844203 | ||||||
| chr18:61844212
|
A | AGGGAGGG others(12): Show |
1 | a0001c0001t0001g0189 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-135-27633_-135-27 others(25): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844212 | ||||||
| chr18:61844216
|
A | G | 1 | a0001c0001t0007g0081 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-135-27618T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844216 | ||||||
| chr18:61844221
|
A | G | 84 | a0001c0001t0001g0028a0001c0001t0001g0238a0001c0001t0002g0005others(81): Show | 84 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.-135-27623T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844221 | ||||||
| chr18:61844223
|
G | A | 84 | a0001c0001t0001g0028a0001c0001t0001g0238a0001c0001t0002g0005others(81): Show | 84 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.-135-27625C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844223 | ||||||
| chr18:61844231
|
C | T | 7 | a0001c0002t0016g0174a0001c0002t0016g0175a0001c0002t0025g0172others(4): Show | 7 | HG02280.hp1 HG02717.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.-135-27633G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844231 | ||||||
| chr18:61844255
|
CCATAGTA others(3): Show |
C | 1 | a0001c0001t0007g0081 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-135-27667_-135-27 others(16): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844255 | ||||||
| chr18:61844413
|
A | G | 1 | a0001c0001t0004g0154 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-135-27815T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844413 | ||||||
| chr18:61844426
|
A | G | 82 | a0001c0001t0001g0028a0001c0001t0001g0238a0001c0001t0002g0005others(79): Show | 82 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.-135-27828T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844426 | ||||||
| chr18:61844458
|
G | A | 1 | a0001c0002t0063g0297 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-135-27860C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844458 | ||||||
| chr18:61844798
|
G | A | 2 | a0001c0001t0022g0260a0001c0001t0022g0277 | 2 | HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-135-28200C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844798 | ||||||
| chr18:61844870
|
CA | C | 8 | a0001c0001t0001g0290a0001c0001t0030g0207a0001c0001t0030g0209others(5): Show | 8 | HG00621.hp1 HG01255.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.-135-28273delT | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844870 | ||||||
| chr18:61844874
|
A | C | 81 | a0001c0001t0001g0001a0001c0001t0001g0047a0001c0001t0001g0060others(78): Show | 82 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.-135-28276T>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844874 | ||||||
| chr18:61844903
|
C | T | 5 | a0001c0001t0043g0143a0001c0001t0043g0144a0001c0001t0122g0145others(2): Show | 5 | HG02451.hp1 HG02630.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.-135-28305G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844903 | ||||||
| chr18:61844916
|
G | A | 2 | a0001c0001t0002g0043a0001c0001t0114g0037 | 2 | HG00738.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.-135-28318C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844916 | ||||||
| chr18:61844968
|
C | T | 5 | a0001c0001t0084g0195a0001c0002t0044g0097a0001c0002t0048g0196others(2): Show | 5 | HG01258.hp2 HG01934.hp1 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.-135-28370G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844968 | ||||||
| chr18:61844969
|
A | G | 110 | a0001c0001t0001g0028a0001c0001t0001g0238a0001c0001t0002g0005others(107): Show | 110 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.-135-28371T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844969 | ||||||
| chr18:61844975
|
C | G | 1 | a0001c0008t0004g0063 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-135-28377G>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844975 | ||||||
| chr18:61844977
|
T | C | 1 | a0001c0001t0004g0058 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-135-28379A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844977 | ||||||
| chr18:61844994
|
C | T | 2 | a0001c0001t0117g0284a0001c0001t0119g0279 | 2 | HG02559.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.-135-28396G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844994 | ||||||
| chr18:61844996
|
C | T | 1 | a0001c0001t0008g0087 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-135-28398G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61844996 | ||||||
| chr18:61845083
|
T | C | 83 | a0001c0001t0001g0028a0001c0001t0001g0238a0001c0001t0002g0005others(80): Show | 83 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.-135-28485A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61845083 | ||||||
| chr18:61845437
|
G | A | 1 | a0001c0001t0002g0012 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-135-28839C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61845437 | ||||||
| chr18:61845451
|
C | T | 2 | a0001c0003t0017g0280a0001c0003t0017g0281 | 2 | HG00280.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-135-28853G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61845451 | ||||||
| chr18:61845796
|
C | G | 1 | a0001c0001t0110g0181 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-135-29198G>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61845796 | ||||||
| chr18:61845904
|
C | G | 15 | a0001c0001t0003g0194a0001c0001t0003g0201a0001c0001t0078g0219others(12): Show | 15 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.-135-29306G>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61845904 | ||||||
| chr18:61845920
|
T | TG | 13 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(10): Show | 13 | HG00099.hp2 HG01099.hp2 HG01123.hp2 others(10): Show |
intron_variant | MODIFIER | c.-135-29323dupC | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61845920 | ||||||
| chr18:61845922
|
G | T | 1 | a0001c0002t0071g0190 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-135-29324C>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61845922 | ||||||
| chr18:61845926
|
G | T | 1 | a0001c0001t0107g0168 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-135-29328C>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61845926 | ||||||
| chr18:61845927
|
GC | G | 5 | a0001c0001t0084g0195a0001c0002t0044g0097a0001c0002t0048g0196others(2): Show | 5 | HG01258.hp2 HG01934.hp1 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.-135-29330delG | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61845927 | ||||||
| chr18:61845928
|
C | G | 105 | a0001c0001t0001g0028a0001c0001t0001g0238a0001c0001t0002g0005others(102): Show | 105 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.-135-29330G>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61845928 | ||||||
| chr18:61845930
|
T | G | 51 | a0001c0001t0001g0046a0001c0001t0001g0240a0001c0001t0001g0243others(48): Show | 51 | HG00438.hp1 HG00621.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.-135-29332A>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61845930 | ||||||
| chr18:61845988
|
A | G | 1 | a0001c0001t0107g0168 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-135-29390T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61845988 | ||||||
| chr18:61846149
|
T | C | 1 | a0001c0001t0007g0111 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-135-29551A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61846149 | ||||||
| chr18:61846272
|
C | A | 14 | a0001c0001t0003g0194a0001c0001t0003g0201a0001c0001t0078g0219others(11): Show | 14 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.-135-29674G>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61846272 | ||||||
| chr18:61846683
|
G | C | 1 | a0001c0002t0053g0206 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-135-30085C>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61846683 | ||||||
| chr18:61846744
|
T | C | 5 | a0001c0001t0043g0143a0001c0001t0043g0144a0001c0001t0122g0145others(2): Show | 5 | HG02451.hp1 HG02630.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.-135-30146A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61846744 | ||||||
| chr18:61846761
|
C | T | 3 | a0001c0001t0037g0265a0001c0001t0037g0270a0003c0007t0103g0269 | 3 | HG01070.hp2 HG01243.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.-135-30163G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61846761 | ||||||
| chr18:61846794
|
A | T | 1 | a0001c0001t0004g0053 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-135-30196T>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61846794 | ||||||
| chr18:61846949
|
C | T | 7 | a0001c0002t0005g0112a0001c0002t0005g0210a0001c0002t0005g0211others(4): Show | 7 | HG00741.hp1 HG01167.hp1 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.-135-30351G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61846949 | ||||||
| chr18:61847032
|
T | C | 1 | a0001c0001t0003g0153 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-135-30434A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61847032 | ||||||
| chr18:61847083
|
G | A | 1 | a0001c0001t0107g0168 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-135-30485C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61847083 | ||||||
| chr18:61847090
|
C | T | 5 | a0001c0001t0084g0195a0001c0002t0044g0097a0001c0002t0048g0196others(2): Show | 5 | HG01258.hp2 HG01934.hp1 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.-135-30492G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61847090 | ||||||
| chr18:61847151
|
CAG | C | 5 | a0001c0001t0084g0195a0001c0002t0044g0097a0001c0002t0048g0196others(2): Show | 5 | HG01258.hp2 HG01934.hp1 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.-135-30555_-135-30 others(8): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61847151 | ||||||
| chr18:61847184
|
T | C | 1 | a0001c0001t0077g0045 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-135-30586A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61847184 | ||||||
| chr18:61847191
|
A | G | 1 | a0001c0001t0110g0181 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-135-30593T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61847191 | ||||||
| chr18:61847212
|
T | A | 1 | a0001c0001t0014g0262 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-135-30614A>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61847212 | ||||||
| chr18:61847383
|
G | C | 1 | a0001c0001t0019g0289 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-135-30785C>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61847383 | ||||||
| chr18:61847600
|
C | G | 1 | a0001c0001t0106g0082 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-135-31002G>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61847600 | ||||||
| chr18:61847613
|
A | C | 1 | a0001c0001t0106g0082 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-135-31015T>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61847613 | ||||||
| chr18:61847750
|
C | T | 110 | a0001c0001t0001g0028a0001c0001t0001g0238a0001c0001t0002g0005others(107): Show | 110 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.-135-31152G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61847750 | ||||||
| chr18:61848022
|
T | G | 1 | a0001c0001t0001g0060 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-135-31424A>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61848022 | ||||||
| chr18:61848105
|
C | T | 5 | a0001c0001t0043g0143a0001c0001t0043g0144a0001c0001t0122g0145others(2): Show | 5 | HG02451.hp1 HG02630.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.-135-31507G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61848105 | ||||||
| chr18:61848162
|
T | C | 7 | a0001c0001t0010g0065a0001c0001t0010g0146a0001c0001t0010g0198others(4): Show | 7 | HG01243.hp2 HG02622.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.-135-31564A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61848162 | ||||||
| chr18:61848195
|
A | G | 5 | a0001c0001t0043g0143a0001c0001t0043g0144a0001c0001t0122g0145others(2): Show | 5 | HG02451.hp1 HG02630.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.-135-31597T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61848195 | ||||||
| chr18:61848389
|
G | A | 1 | a0001c0001t0034g0059 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-135-31791C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61848389 | ||||||
| chr18:61848531
|
G | A | 132 | a0001c0001t0001g0028a0001c0001t0001g0238a0001c0001t0002g0005others(129): Show | 132 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.-135-31933C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61848531 | ||||||
| chr18:61848537
|
C | G | 1 | a0001c0001t0104g0303 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-135-31939G>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61848537 | ||||||
| chr18:61848558
|
T | A | 1 | a0001c0001t0012g0156 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-135-31960A>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61848558 | ||||||
| chr18:61848604
|
C | G | 22 | a0001c0001t0011g0066a0001c0001t0011g0135a0001c0001t0038g0166others(19): Show | 22 | HG00735.hp2 HG02055.hp1 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.-135-32006G>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61848604 | ||||||
| chr18:61848638
|
C | T | 5 | a0001c0001t0084g0195a0001c0002t0044g0097a0001c0002t0048g0196others(2): Show | 5 | HG01258.hp2 HG01934.hp1 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.-135-32040G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61848638 | ||||||
| chr18:61848962
|
C | T | 3 | a0001c0001t0004g0057a0001c0001t0004g0058a0001c0001t0004g0133 | 3 | HG00280.hp2 HG01109.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.-135-32364G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61848962 | ||||||
| chr18:61849087
|
G | T | 1 | a0001c0001t0104g0303 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-135-32489C>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61849087 | ||||||
| chr18:61849101
|
G | A | 11 | a0001c0001t0003g0194a0001c0001t0003g0201a0001c0001t0102g0305others(8): Show | 11 | HG02280.hp1 HG02615.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.-135-32503C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61849101 | ||||||
| chr18:61849328
|
A | C | 1 | a0001c0002t0066g0258 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-135-32730T>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61849328 | ||||||
| chr18:61849329
|
A | C | 1 | a0001c0001t0107g0168 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-135-32731T>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61849329 | ||||||
| chr18:61849392
|
A | G | 3 | a0001c0001t0001g0189a0001c0001t0074g0004a0001c0006t0001g0157 | 3 | HG00099.hp1 HG03704.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.-135-32794T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61849392 | ||||||
| chr18:61849517
|
C | A | 1 | a0001c0001t0001g0070 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-135-32919G>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61849517 | ||||||
| chr18:61849627
|
A | G | 2 | a0001c0001t0001g0116a0001c0001t0020g0118 | 2 | NA18969.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.-135-33029T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61849627 | ||||||
| chr18:61849634
|
A | G | 23 | a0001c0001t0001g0238a0001c0001t0111g0228a0001c0001t0115g0212others(20): Show | 23 | HG00423.hp1 HG00741.hp1 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.-135-33036T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61849634 | ||||||
| chr18:61849646
|
A | G | 1 | a0001c0002t0061g0215 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-135-33048T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61849646 | ||||||
| chr18:61849859
|
G | A | 2 | a0001c0001t0102g0305a0001c0001t0104g0303 | 2 | HG02717.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-135-33261C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61849859 | ||||||
| chr18:61849881
|
T | C | 1 | a0001c0001t0107g0168 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-135-33283A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61849881 | ||||||
| chr18:61849912
|
A | G | 1 | a0001c0001t0001g0186 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-135-33314T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61849912 | ||||||
| chr18:61849957
|
C | T | 1 | a0001c0001t0006g0271 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-135-33359G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61849957 | ||||||
| chr18:61850428
|
T | C | 3 | a0001c0001t0001g0189a0001c0001t0074g0004a0001c0006t0001g0157 | 3 | HG00099.hp1 HG03704.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.-135-33830A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61850428 | ||||||
| chr18:61850469
|
C | T | 1 | a0001c0002t0066g0258 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-135-33871G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61850469 | ||||||
| chr18:61850508
|
T | A | 1 | a0001c0002t0055g0241 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-135-33910A>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61850508 | ||||||
| chr18:61850563
|
G | A | 1 | a0001c0001t0122g0145 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-135-33965C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61850563 | ||||||
| chr18:61850571
|
G | C | 2 | a0001c0001t0011g0066a0001c0001t0011g0135 | 2 | HG03471.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-135-33973C>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61850571 | ||||||
| chr18:61850652
|
T | C | 132 | a0001c0001t0001g0028a0001c0001t0001g0238a0001c0001t0002g0005others(129): Show | 132 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.-135-34054A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61850652 | ||||||
| chr18:61850764
|
C | T | 8 | a0001c0001t0038g0166a0001c0001t0038g0182a0001c0001t0105g0183others(5): Show | 8 | HG02257.hp1 HG02258.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.-135-34166G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61850764 | ||||||
| chr18:61850928
|
G | A | 8 | a0001c0001t0010g0065a0001c0001t0010g0146a0001c0001t0010g0198others(5): Show | 8 | HG01243.hp2 HG02622.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.-135-34330C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61850928 | ||||||
| chr18:61850959
|
A | G | 1 | a0001c0001t0003g0194 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-135-34361T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61850959 | ||||||
| chr18:61851042
|
C | T | 1 | a0001c0001t0002g0026 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-135-34444G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61851042 | ||||||
| chr18:61851090
|
T | TA | 18 | a0001c0001t0001g0115a0001c0001t0006g0003a0001c0001t0007g0081others(15): Show | 18 | HG00735.hp2 HG01258.hp2 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.-135-34493dupT | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61851090 | ||||||
| chr18:61851090
|
T | TAA | 20 | a0001c0001t0003g0194a0001c0001t0003g0201a0001c0001t0038g0166others(17): Show | 20 | HG02055.hp1 HG02257.hp1 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.-135-34494_-135-34 others(8): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61851090 | ||||||
| chr18:61851165
|
C | A | 1 | a0001c0001t0088g0191 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-135-34567G>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61851165 | ||||||
| chr18:61851421
|
G | A | 24 | a0001c0001t0038g0166a0001c0001t0038g0182a0001c0001t0039g0136others(21): Show | 24 | HG01884.hp2 HG02055.hp1 HG02257.hp2 others(21): Show |
intron_variant | MODIFIER | c.-135-34823C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61851421 | ||||||
| chr18:61851425
|
G | T | 1 | a0001c0002t0068g0098 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-135-34827C>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61851425 | ||||||
| chr18:61851507
|
T | C | 1 | a0001c0001t0107g0168 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-135-34909A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61851507 | ||||||
| chr18:61851718
|
T | C | 79 | a0001c0001t0001g0028a0001c0001t0002g0005a0001c0001t0002g0006others(76): Show | 79 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.-135-35120A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61851718 | ||||||
| chr18:61851787
|
T | A | 1 | a0001c0001t0107g0168 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-135-35189A>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61851787 | ||||||
| chr18:61851787
|
T | C | 45 | a0001c0001t0003g0194a0001c0001t0003g0201a0001c0001t0010g0065others(42): Show | 45 | HG00735.hp2 HG01243.hp2 HG01258.hp2 others(42): Show |
intron_variant | MODIFIER | c.-135-35189A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61851787 | ||||||
| chr18:61852066
|
G | T | 9 | a0001c0001t0003g0194a0001c0001t0003g0201a0001c0001t0010g0198others(6): Show | 9 | HG02615.hp1 HG02717.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.-135-35468C>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61852066 | ||||||
| chr18:61852101
|
G | A | 34 | a0001c0001t0001g0238a0001c0001t0030g0207a0001c0001t0030g0209others(31): Show | 34 | HG00423.hp1 HG00621.hp1 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.-135-35503C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61852101 | ||||||
| chr18:61852256
|
T | G | 138 | a0001c0001t0001g0028a0001c0001t0001g0238a0001c0001t0002g0005others(135): Show | 138 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.-135-35658A>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61852256 | ||||||
| chr18:61852324
|
G | A | 6 | a0001c0001t0078g0219a0001c0001t0079g0218a0001c0001t0097g0220others(3): Show | 6 | HG02145.hp2 HG02258.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-135-35726C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61852324 | ||||||
| chr18:61852397
|
G | A | 3 | a0001c0001t0012g0164a0001c0001t0012g0165a0001c0002t0027g0134 | 3 | HG02257.hp1 HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.-135-35799C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61852397 | ||||||
| chr18:61852521
|
C | T | 2 | a0001c0001t0002g0099a0001c0001t0007g0080 | 2 | NA18945.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.-135-35923G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61852521 | ||||||
| chr18:61852553
|
T | C | 51 | a0001c0001t0001g0238a0001c0001t0003g0194a0001c0001t0003g0201others(48): Show | 51 | HG00423.hp1 HG00621.hp1 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.-135-35955A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61852553 | ||||||
| chr18:61852810
|
C | A | 1 | a0001c0001t0020g0118 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-135-36212G>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61852810 | ||||||
| chr18:61852932
|
A | G | 3 | a0001c0001t0040g0184a0001c0001t0040g0185a0001c0002t0060g0298 | 3 | HG02257.hp2 HG02559.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.-135-36334T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61852932 | ||||||
| chr18:61853127
|
C | T | 135 | a0001c0001t0001g0028a0001c0001t0001g0238a0001c0001t0002g0005others(132): Show | 135 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.-135-36529G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61853127 | ||||||
| chr18:61853296
|
C | CT | 32 | a0001c0001t0001g0067a0001c0001t0002g0009a0001c0001t0002g0038others(29): Show | 32 | HG00735.hp1 HG00735.hp2 HG01167.hp2 others(29): Show |
intron_variant | MODIFIER | c.-135-36699dupA | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61853296 | ||||||
| chr18:61853296
|
C | CTT | 56 | a0001c0001t0001g0028a0001c0001t0002g0005a0001c0001t0002g0006others(53): Show | 56 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(53): Show |
intron_variant | MODIFIER | c.-135-36700_-135-36 others(8): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61853296 | ||||||
| chr18:61853353
|
G | A | 3 | a0001c0002t0052g0293a0001c0002t0062g0296a0001c0002t0063g0297 | 3 | HG01258.hp2 HG01934.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.-135-36755C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61853353 | ||||||
| chr18:61853470
|
T | A | 1 | a0001c0001t0001g0186 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-135-36872A>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61853470 | ||||||
| chr18:61853541
|
C | T | 1 | a0001c0001t0003g0158 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-135-36943G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61853541 | ||||||
| chr18:61853559
|
C | T | 1 | a0002c0005t0070g0192 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-135-36961G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61853559 | ||||||
| chr18:61853814
|
T | C | 7 | a0001c0001t0080g0295a0001c0001t0084g0195a0001c0002t0044g0097others(4): Show | 7 | HG01258.hp2 HG01934.hp1 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.-135-37216A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61853814 | ||||||
| chr18:61853859
|
C | T | 1 | a0001c0001t0104g0303 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-135-37261G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61853859 | ||||||
| chr18:61853874
|
G | A | 17 | a0001c0001t0038g0182a0001c0001t0039g0136a0001c0001t0039g0138others(14): Show | 17 | HG02055.hp1 HG02257.hp2 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.-135-37276C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61853874 | ||||||
| chr18:61854102
|
C | T | 2 | a0001c0001t0106g0082a0001c0002t0069g0083 | 2 | HG00735.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-135-37504G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61854102 | ||||||
| chr18:61854116
|
G | C | 1 | a0001c0001t0009g0124 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.-135-37518C>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61854116 | ||||||
| chr18:61854178
|
C | A | 17 | a0001c0001t0038g0182a0001c0001t0039g0136a0001c0001t0039g0138others(14): Show | 17 | HG02055.hp1 HG02257.hp2 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.-135-37580G>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61854178 | ||||||
| chr18:61854211
|
T | C | 1 | a0001c0001t0034g0059 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-135-37613A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61854211 | ||||||
| chr18:61854339
|
G | GTTTTCCC others(2): Show |
3 | a0001c0001t0030g0207a0001c0001t0030g0209a0001c0001t0082g0208 | 3 | NA18949.hp2 NA18959.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.-135-37742_-135-37 others(15): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61854339 | ||||||
| chr18:61854410
|
A | G | 1 | a0001c0001t0003g0194 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-135-37812T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61854410 | ||||||
| chr18:61854433
|
G | A | 77 | a0001c0001t0001g0028a0001c0001t0001g0240a0001c0001t0002g0005others(74): Show | 77 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(74): Show |
intron_variant | MODIFIER | c.-135-37835C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61854433 | ||||||
| chr18:61854457
|
T | A | 11 | a0001c0001t0001g0238a0001c0001t0111g0228a0001c0001t0115g0212others(8): Show | 11 | HG00423.hp1 HG02155.hp1 HG02523.hp1 others(8): Show |
intron_variant | MODIFIER | c.-135-37859A>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61854457 | ||||||
| chr18:61854551
|
G | A | 1 | a0001c0002t0058g0169 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-135-37953C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61854551 | ||||||
| chr18:61854846
|
A | G | 1 | a0001c0002t0066g0258 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-136+37949T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61854846 | ||||||
| chr18:61854917
|
A | T | 34 | a0001c0001t0001g0238a0001c0001t0011g0066a0001c0001t0011g0135others(31): Show | 34 | HG00423.hp1 HG00621.hp1 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.-136+37878T>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61854917 | ||||||
| chr18:61855041
|
A | G | 77 | a0001c0001t0001g0001a0001c0001t0001g0047a0001c0001t0001g0060others(74): Show | 78 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.-136+37754T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61855041 | ||||||
| chr18:61855082
|
C | T | 1 | a0001c0001t0080g0295 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-136+37713G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61855082 | ||||||
| chr18:61855332
|
T | C | 75 | a0001c0001t0001g0001a0001c0001t0001g0047a0001c0001t0001g0060others(72): Show | 76 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.-136+37463A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61855332 | ||||||
| chr18:61855406
|
G | A | 32 | a0001c0001t0001g0238a0001c0001t0030g0207a0001c0001t0030g0209others(29): Show | 32 | HG00423.hp1 HG00621.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.-136+37389C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61855406 | ||||||
| chr18:61855422
|
G | A | 1 | a0001c0001t0088g0191 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-136+37373C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61855422 | ||||||
| chr18:61855676
|
CCCACACT others(6): Show |
C | 1 | a0001c0001t0032g0193 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-136+37106_-136+37 others(19): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61855676 | ||||||
| chr18:61855765
|
G | A | 1 | a0001c0001t0008g0075 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-136+37030C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61855765 | ||||||
| chr18:61855851
|
C | T | 1 | a0001c0002t0060g0298 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-136+36944G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61855851 | ||||||
| chr18:61855957
|
C | T | 1 | a0001c0002t0066g0258 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-136+36838G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61855957 | ||||||
| chr18:61855997
|
A | G | 1 | a0001c0002t0066g0258 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-136+36798T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61855997 | ||||||
| chr18:61856209
|
G | A | 76 | a0001c0001t0001g0001a0001c0001t0001g0047a0001c0001t0001g0060others(73): Show | 77 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.-136+36586C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61856209 | ||||||
| chr18:61856267
|
A | G | 2 | a0001c0003t0017g0280a0001c0003t0017g0281 | 2 | HG00280.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-136+36528T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61856267 | ||||||
| chr18:61856293
|
G | A | 2 | a0001c0001t0084g0195a0001c0002t0048g0196 | 2 | HG01943.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.-136+36502C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61856293 | ||||||
| chr18:61856392
|
C | T | 19 | a0001c0001t0001g0060a0001c0001t0001g0070a0001c0001t0001g0079others(16): Show | 19 | HG00609.hp2 HG00738.hp2 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.-136+36403G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61856392 | ||||||
| chr18:61856466
|
T | C | 5 | a0001c0001t0043g0143a0001c0001t0043g0144a0001c0001t0122g0145others(2): Show | 5 | HG02451.hp1 HG02630.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.-136+36329A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61856466 | ||||||
| chr18:61856517
|
C | G | 1 | a0001c0002t0047g0264 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-136+36278G>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61856517 | ||||||
| chr18:61856602
|
G | A | 2 | a0001c0001t0040g0184a0001c0001t0040g0185 | 2 | HG02559.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.-136+36193C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61856602 | ||||||
| chr18:61856995
|
C | T | 1 | a0001c0001t0077g0045 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-136+35800G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61856995 | ||||||
| chr18:61857028
|
G | A | 85 | a0001c0001t0001g0001a0001c0001t0001g0047a0001c0001t0001g0060others(82): Show | 86 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.-136+35767C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61857028 | ||||||
| chr18:61857079
|
C | T | 32 | a0001c0001t0001g0238a0001c0001t0030g0207a0001c0001t0030g0209others(29): Show | 32 | HG00423.hp1 HG00621.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.-136+35716G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61857079 | ||||||
| chr18:61857095
|
C | T | 4 | a0001c0001t0013g0084a0001c0001t0013g0094a0001c0001t0014g0095others(1): Show | 4 | HG02615.hp2 HG02647.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.-136+35700G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61857095 | ||||||
| chr18:61857160
|
C | T | 8 | a0001c0001t0008g0294a0001c0001t0080g0295a0001c0001t0084g0195others(5): Show | 8 | HG01258.hp2 HG01934.hp1 HG01943.hp2 others(5): Show |
intron_variant | MODIFIER | c.-136+35635G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61857160 | ||||||
| chr18:61857203
|
C | T | 1 | a0001c0002t0005g0211 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-136+35592G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61857203 | ||||||
| chr18:61857217
|
A | C | 17 | a0001c0001t0038g0182a0001c0001t0039g0136a0001c0001t0039g0138others(14): Show | 17 | HG02055.hp1 HG02257.hp2 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.-136+35578T>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61857217 | ||||||
| chr18:61857410
|
G | A | 85 | a0001c0001t0001g0001a0001c0001t0001g0047a0001c0001t0001g0060others(82): Show | 86 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.-136+35385C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61857410 | ||||||
| chr18:61857427
|
T | C | 1 | a0001c0001t0118g0137 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-136+35368A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61857427 | ||||||
| chr18:61857630
|
G | A | 1 | a0001c0001t0107g0168 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-136+35165C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61857630 | ||||||
| chr18:61857694
|
TAAAC | T | 38 | a0001c0001t0001g0238a0001c0001t0030g0207a0001c0001t0030g0209others(35): Show | 38 | HG00423.hp1 HG00621.hp1 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.-136+35097_-136+35 others(10): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61857694 | ||||||
| chr18:61857760
|
A | C | 1 | a0001c0004t0101g0253 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-136+35035T>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61857760 | ||||||
| chr18:61857981
|
C | T | 27 | a0001c0001t0038g0182a0001c0001t0039g0136a0001c0001t0039g0138others(24): Show | 27 | HG00735.hp2 HG01884.hp2 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.-136+34814G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61857981 | ||||||
| chr18:61858036
|
G | C | 1 | a0001c0001t0102g0305 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-136+34759C>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61858036 | ||||||
| chr18:61858077
|
C | T | 4 | a0001c0001t0001g0189a0001c0001t0012g0156a0001c0001t0074g0004others(1): Show | 4 | HG00099.hp1 HG02602.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.-136+34718G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61858077 | ||||||
| chr18:61858194
|
T | C | 1 | a0001c0001t0077g0045 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-136+34601A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61858194 | ||||||
| chr18:61858415
|
C | T | 1 | a0001c0002t0060g0298 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-136+34380G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61858415 | ||||||
| chr18:61858612
|
G | T | 7 | a0001c0001t0008g0294a0001c0001t0080g0295a0001c0001t0084g0195others(4): Show | 7 | HG01258.hp2 HG01934.hp1 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.-136+34183C>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61858612 | ||||||
| chr18:61858906
|
A | G | 2 | a0001c0001t0039g0136a0001c0001t0039g0138 | 2 | HG02055.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-136+33889T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61858906 | ||||||
| chr18:61858973
|
T | C | 1 | a0001c0002t0053g0206 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-136+33822A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61858973 | ||||||
| chr18:61858986
|
G | A | 1 | a0001c0002t0005g0211 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-136+33809C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61858986 | ||||||
| chr18:61859010
|
GA | G | 17 | a0001c0001t0038g0182a0001c0001t0039g0136a0001c0001t0039g0138others(14): Show | 17 | HG02055.hp1 HG02257.hp2 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.-136+33784delT | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61859010 | ||||||
| chr18:61859018
|
A | G | 4 | a0001c0001t0013g0302a0001c0001t0013g0304a0001c0001t0102g0305others(1): Show | 4 | HG02717.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-136+33777T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61859018 | ||||||
| chr18:61859126
|
C | T | 7 | a0001c0001t0008g0294a0001c0001t0080g0295a0001c0001t0084g0195others(4): Show | 7 | HG01258.hp2 HG01934.hp1 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.-136+33669G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61859126 | ||||||
| chr18:61859301
|
G | A | 1 | a0001c0001t0095g0236 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.-136+33494C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61859301 | ||||||
| chr18:61859364
|
G | A | 3 | a0001c0002t0016g0171a0001c0002t0025g0172a0001c0002t0025g0173 | 3 | HG01884.hp2 HG02280.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-136+33431C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61859364 | ||||||
| chr18:61859390
|
G | A | 44 | a0001c0001t0001g0238a0001c0001t0003g0194a0001c0001t0003g0201others(41): Show | 44 | HG00423.hp1 HG00621.hp1 HG00741.hp1 others(41): Show |
intron_variant | MODIFIER | c.-136+33405C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61859390 | ||||||
| chr18:61859391
|
G | T | 66 | a0001c0001t0001g0001a0001c0001t0001g0060a0001c0001t0001g0067others(63): Show | 67 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.-136+33404C>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61859391 | ||||||
| chr18:61859880
|
A | AAAAAG | 9 | a0001c0001t0039g0136a0001c0001t0039g0138a0001c0002t0016g0171others(6): Show | 9 | HG01884.hp2 HG02055.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.-136+32910_-136+32 others(11): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61859880 | ||||||
| chr18:61859880
|
A | AAAAAGAA others(3): Show |
8 | a0001c0001t0038g0182a0001c0001t0040g0185a0001c0001t0105g0183others(5): Show | 8 | HG02559.hp1 HG02647.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.-136+32905_-136+32 others(16): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61859880 | ||||||
| chr18:61859880
|
A | AAAAAGAA others(8): Show |
8 | a0001c0001t0040g0184a0001c0001t0099g0139a0001c0001t0107g0168others(5): Show | 8 | HG02257.hp2 HG02622.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.-136+32900_-136+32 others(21): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61859880 | ||||||
| chr18:61859880
|
A | AAAAAGAA others(13): Show |
2 | a0001c0002t0027g0179a0001c0002t0064g0178 | 2 | HG02258.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-136+32895_-136+32 others(26): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61859880 | ||||||
| chr18:61859980
|
T | C | 1 | a0001c0001t0001g0070 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-136+32815A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61859980 | ||||||
| chr18:61860030
|
C | T | 2 | a0001c0001t0039g0136a0001c0001t0039g0138 | 2 | HG02055.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-136+32765G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61860030 | ||||||
| chr18:61860034
|
A | C | 2 | a0001c0001t0037g0265a0001c0001t0037g0270 | 2 | HG01243.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.-136+32761T>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61860034 | ||||||
| chr18:61860037
|
ACAGAAAA others(4): Show |
A | 1 | a0001c0002t0005g0211 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-136+32747_-136+32 others(17): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61860037 | ||||||
| chr18:61860284
|
T | C | 2 | a0001c0001t0007g0113a0001c0001t0007g0114 | 2 | NA18946.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.-136+32511A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61860284 | ||||||
| chr18:61860382
|
G | A | 10 | a0001c0001t0107g0168a0001c0002t0016g0171a0001c0002t0016g0174others(7): Show | 10 | HG01884.hp2 HG02280.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.-136+32413C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61860382 | ||||||
| chr18:61860523
|
G | A | 29 | a0001c0001t0001g0238a0001c0001t0030g0207a0001c0001t0030g0209others(26): Show | 29 | HG00423.hp1 HG00621.hp1 HG01167.hp1 others(26): Show |
intron_variant | MODIFIER | c.-136+32272C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61860523 | ||||||
| chr18:61860558
|
A | G | 90 | a0001c0001t0001g0028a0001c0001t0001g0189a0001c0001t0001g0240others(87): Show | 90 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(87): Show |
intron_variant | MODIFIER | c.-136+32237T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61860558 | ||||||
| chr18:61860734
|
T | C | 1 | a0001c0001t0006g0061 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-136+32061A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61860734 | ||||||
| chr18:61860745
|
G | C | 30 | a0001c0001t0001g0238a0001c0001t0002g0043a0001c0001t0030g0207others(27): Show | 30 | HG00423.hp1 HG00621.hp1 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.-136+32050C>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61860745 | ||||||
| chr18:61860928
|
T | A | 1 | a0001c0001t0088g0191 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-136+31867A>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61860928 | ||||||
| chr18:61861189
|
T | C | 16 | a0001c0001t0038g0182a0001c0001t0039g0136a0001c0001t0039g0138others(13): Show | 16 | HG02055.hp1 HG02258.hp2 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.-136+31606A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61861189 | ||||||
| chr18:61861194
|
TCCACTCA | T | 10 | a0001c0001t0107g0168a0001c0002t0016g0171a0001c0002t0016g0174others(7): Show | 10 | HG01884.hp2 HG02280.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.-136+31594_-136+31 others(13): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61861194 | ||||||
| chr18:61861219
|
C | T | 3 | a0001c0002t0028g0187a0001c0002t0028g0301a0001c0002t0065g0188 | 3 | HG02622.hp1 HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-136+31576G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61861219 | ||||||
| chr18:61861350
|
T | A | 1 | a0001c0001t0001g0119 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-136+31445A>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61861350 | ||||||
| chr18:61861444
|
C | T | 44 | a0001c0001t0001g0238a0001c0001t0002g0202a0001c0001t0003g0194others(41): Show | 44 | HG00423.hp1 HG00621.hp1 HG01167.hp1 others(41): Show |
intron_variant | MODIFIER | c.-136+31351G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61861444 | ||||||
| chr18:61861481
|
C | A | 100 | a0001c0001t0001g0028a0001c0001t0001g0189a0001c0001t0001g0240others(97): Show | 100 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(97): Show |
intron_variant | MODIFIER | c.-136+31314G>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61861481 | ||||||
| chr18:61861541
|
C | G | 10 | a0001c0001t0002g0202a0001c0001t0003g0194a0001c0001t0003g0201others(7): Show | 10 | HG01346.hp1 HG02145.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.-136+31254G>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61861541 | ||||||
| chr18:61861752
|
C | G | 1 | a0001c0001t0118g0137 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-136+31043G>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61861752 | ||||||
| chr18:61861757
|
A | C | 1 | a0001c0002t0060g0298 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-136+31038T>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61861757 | ||||||
| chr18:61861759
|
C | G | 1 | a0001c0002t0060g0298 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-136+31036G>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61861759 | ||||||
| chr18:61861760
|
A | G | 1 | a0001c0002t0060g0298 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-136+31035T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61861760 | ||||||
| chr18:61861802
|
G | C | 1 | a0001c0002t0055g0241 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-136+30993C>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61861802 | ||||||
| chr18:61861940
|
A | C | 17 | a0001c0001t0038g0182a0001c0001t0039g0136a0001c0001t0039g0138others(14): Show | 17 | HG02055.hp1 HG02258.hp2 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.-136+30855T>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61861940 | ||||||
| chr18:61862195
|
C | T | 45 | a0001c0001t0001g0266a0001c0001t0001g0275a0001c0001t0001g0278others(42): Show | 45 | HG00140.hp2 HG00280.hp1 HG01070.hp2 others(42): Show |
intron_variant | MODIFIER | c.-136+30600G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61862195 | ||||||
| chr18:61862348
|
T | C | 5 | a0001c0001t0001g0060a0001c0001t0001g0070a0001c0001t0001g0115others(2): Show | 5 | NA18939.hp2 NA18948.hp1 NA18979.hp1 others(2): Show |
intron_variant | MODIFIER | c.-136+30447A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61862348 | ||||||
| chr18:61862534
|
A | C | 1 | a0001c0001t0086g0292 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-136+30261T>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61862534 | ||||||
| chr18:61862544
|
G | A | 3 | a0001c0001t0004g0053a0001c0001t0004g0057a0001c0001t0004g0058 | 3 | HG00280.hp2 HG01109.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.-136+30251C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61862544 | ||||||
| chr18:61862546
|
TA | T | 8 | a0001c0001t0010g0065a0001c0001t0010g0146a0001c0001t0012g0164others(5): Show | 8 | HG00735.hp2 HG01243.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.-136+30248delT | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61862546 | ||||||
| chr18:61862586
|
C | G | 1 | a0001c0001t0034g0059 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-136+30209G>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61862586 | ||||||
| chr18:61862633
|
T | C | 3 | a0001c0001t0012g0164a0001c0001t0012g0165a0001c0002t0027g0134 | 3 | HG02257.hp1 HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.-136+30162A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61862633 | ||||||
| chr18:61862681
|
A | C | 5 | a0001c0002t0016g0171a0001c0002t0016g0174a0001c0002t0016g0175others(2): Show | 5 | HG01884.hp2 HG02280.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.-136+30114T>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61862681 | ||||||
| chr18:61862695
|
C | T | 1 | a0001c0001t0088g0191 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-136+30100G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61862695 | ||||||
| chr18:61862755
|
G | T | 1 | a0002c0005t0070g0192 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-136+30040C>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61862755 | ||||||
| chr18:61862783
|
G | A | 7 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0119others(4): Show | 7 | HG01975.hp1 HG02523.hp2 NA18956.hp1 others(4): Show |
intron_variant | MODIFIER | c.-136+30012C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61862783 | ||||||
| chr18:61862828
|
C | T | 1 | a0001c0001t0086g0292 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-136+29967G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61862828 | ||||||
| chr18:61862849
|
T | C | 1 | a0001c0002t0060g0298 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-136+29946A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61862849 | ||||||
| chr18:61863254
|
G | A | 58 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0238others(55): Show | 58 | HG00423.hp1 HG00621.hp1 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.-136+29541C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61863254 | ||||||
| chr18:61863263
|
T | C | 1 | a0001c0001t0099g0139 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-136+29532A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61863263 | ||||||
| chr18:61863296
|
G | A | 1 | a0001c0001t0120g0155 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-136+29499C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61863296 | ||||||
| chr18:61863307
|
C | T | 1 | a0001c0001t0001g0122 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-136+29488G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61863307 | ||||||
| chr18:61863313
|
T | C | 2 | a0001c0001t0085g0140a0001c0001t0092g0141 | 2 | HG02572.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-136+29482A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61863313 | ||||||
| chr18:61863366
|
T | C | 14 | a0001c0001t0038g0182a0001c0001t0039g0136a0001c0001t0039g0138others(11): Show | 14 | HG02055.hp1 HG02257.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.-136+29429A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61863366 | ||||||
| chr18:61863429
|
G | A | 3 | a0001c0001t0040g0184a0001c0001t0040g0185a0001c0001t0109g0072 | 3 | HG02559.hp1 HG02630.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-136+29366C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61863429 | ||||||
| chr18:61863433
|
C | CA | 38 | a0001c0001t0001g0092a0001c0001t0001g0121a0001c0001t0002g0202others(35): Show | 38 | HG01255.hp1 HG01346.hp1 HG01884.hp2 others(35): Show |
intron_variant | MODIFIER | c.-136+29361dupT | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61863433 | ||||||
| chr18:61863433
|
CA | C | 89 | a0001c0001t0001g0028a0001c0001t0001g0069a0001c0001t0001g0096others(86): Show | 89 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(86): Show |
intron_variant | MODIFIER | c.-136+29361delT | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61863433 | ||||||
| chr18:61863433
|
CAAAAAAA others(3): Show |
C | 2 | a0001c0001t0001g0091a0001c0001t0100g0130 | 2 | HG00609.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.-136+29352_-136+29 others(16): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61863433 | ||||||
| chr18:61863482
|
C | T | 2 | a0001c0001t0014g0259a0001c0002t0066g0258 | 2 | HG01255.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-136+29313G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61863482 | ||||||
| chr18:61863834
|
C | T | 1 | a0001c0001t0120g0155 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-136+28961G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61863834 | ||||||
| chr18:61863930
|
C | T | 104 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0238others(101): Show | 104 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.-136+28865G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61863930 | ||||||
| chr18:61863974
|
C | T | 205 | a0001c0001t0001g0028a0001c0001t0001g0046a0001c0001t0001g0047others(202): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.-136+28821G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61863974 | ||||||
| chr18:61864017
|
T | C | 1 | a0001c0001t0088g0191 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-136+28778A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61864017 | ||||||
| chr18:61864123
|
C | T | 4 | a0001c0001t0006g0271a0001c0001t0037g0265a0001c0001t0037g0270others(1): Show | 4 | HG01070.hp2 HG01106.hp2 HG01243.hp1 others(1): Show |
intron_variant | MODIFIER | c.-136+28672G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61864123 | ||||||
| chr18:61864164
|
C | T | 2 | a0001c0001t0042g0048a0001c0001t0042g0049 | 2 | NA18965.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.-136+28631G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61864164 | ||||||
| chr18:61864269
|
A | G | 8 | a0001c0002t0016g0171a0001c0002t0016g0174a0001c0002t0016g0175others(5): Show | 8 | HG01884.hp2 HG02280.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.-136+28526T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61864269 | ||||||
| chr18:61864289
|
C | T | 7 | a0001c0001t0008g0294a0001c0001t0080g0295a0001c0001t0084g0195others(4): Show | 7 | HG01258.hp2 HG01934.hp1 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.-136+28506G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61864289 | ||||||
| chr18:61864298
|
C | T | 1 | a0001c0001t0004g0154 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-136+28497G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61864298 | ||||||
| chr18:61864574
|
T | C | 1 | a0001c0001t0001g0248 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-136+28221A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61864574 | ||||||
| chr18:61864680
|
G | A | 1 | a0001c0001t0002g0273 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-136+28115C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61864680 | ||||||
| chr18:61864700
|
C | T | 1 | a0002c0005t0070g0192 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-136+28095G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61864700 | ||||||
| chr18:61864739
|
G | T | 12 | a0001c0001t0107g0168a0001c0001t0123g0307a0001c0001t0125g0306others(9): Show | 12 | HG01884.hp2 HG02280.hp1 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.-136+28056C>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61864739 | ||||||
| chr18:61864770
|
G | A | 1 | a0001c0001t0088g0191 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-136+28025C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61864770 | ||||||
| chr18:61864780
|
C | T | 13 | a0001c0001t0038g0182a0001c0001t0039g0136a0001c0001t0039g0138others(10): Show | 13 | HG02055.hp1 HG02258.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-136+28015G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61864780 | ||||||
| chr18:61864784
|
C | T | 6 | a0001c0001t0014g0262a0001c0001t0014g0263a0001c0001t0022g0260others(3): Show | 6 | HG01109.hp1 HG02970.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.-136+28011G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61864784 | ||||||
| chr18:61864836
|
T | C | 13 | a0001c0001t0038g0182a0001c0001t0039g0136a0001c0001t0039g0138others(10): Show | 13 | HG02055.hp1 HG02258.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-136+27959A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61864836 | ||||||
| chr18:61864845
|
C | T | 3 | a0001c0001t0013g0084a0001c0001t0013g0094a0001c0001t0014g0095 | 3 | HG02615.hp2 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-136+27950G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61864845 | ||||||
| chr18:61864847
|
C | T | 1 | a0001c0001t0034g0059 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-136+27948G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61864847 | ||||||
| chr18:61864996
|
G | A | 13 | a0001c0001t0038g0182a0001c0001t0039g0136a0001c0001t0039g0138others(10): Show | 13 | HG02055.hp1 HG02258.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-136+27799C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61864996 | ||||||
| chr18:61865296
|
G | C | 3 | a0001c0001t0077g0045a0001c0001t0096g0024a0001c0001t0113g0044 | 3 | NA18951.hp2 NA18964.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.-136+27499C>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61865296 | ||||||
| chr18:61865417
|
G | A | 201 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0060others(198): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.-136+27378C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61865417 | ||||||
| chr18:61865440
|
A | G | 13 | a0001c0001t0038g0182a0001c0001t0039g0136a0001c0001t0039g0138others(10): Show | 13 | HG02055.hp1 HG02258.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-136+27355T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61865440 | ||||||
| chr18:61865494
|
T | C | 13 | a0001c0001t0038g0182a0001c0001t0039g0136a0001c0001t0039g0138others(10): Show | 13 | HG02055.hp1 HG02258.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-136+27301A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61865494 | ||||||
| chr18:61865525
|
G | A | 1 | a0001c0001t0107g0168 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-136+27270C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61865525 | ||||||
| chr18:61865525
|
G | C | 1 | a0001c0001t0110g0181 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-136+27270C>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61865525 | ||||||
| chr18:61865527
|
A | C | 1 | a0001c0002t0055g0241 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-136+27268T>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61865527 | ||||||
| chr18:61865628
|
C | T | 1 | a0001c0001t0003g0153 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-136+27167G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61865628 | ||||||
| chr18:61865643
|
G | C | 7 | a0001c0001t0078g0219a0001c0001t0079g0218a0001c0001t0097g0220others(4): Show | 7 | HG02145.hp2 HG02258.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.-136+27152C>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61865643 | ||||||
| chr18:61865720
|
T | C | 1 | a0001c0001t0001g0069 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-136+27075A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61865720 | ||||||
| chr18:61866323
|
C | T | 1 | a0001c0002t0016g0174 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-136+26472G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61866323 | ||||||
| chr18:61866422
|
A | C | 5 | a0001c0001t0002g0202a0001c0001t0003g0203a0001c0001t0004g0204others(2): Show | 5 | HG01346.hp1 HG02145.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.-136+26373T>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61866422 | ||||||
| chr18:61866455
|
C | CG | 306 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0046others(303): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.-136+26339dupC | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61866455 | ||||||
| chr18:61866459
|
C | T | 1 | a0001c0001t0091g0274 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-136+26336G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61866459 | ||||||
| chr18:61866460
|
G | A | 8 | a0001c0002t0016g0171a0001c0002t0016g0174a0001c0002t0016g0175others(5): Show | 8 | HG01884.hp2 HG02280.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.-136+26335C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61866460 | ||||||
| chr18:61866546
|
C | G | 2 | a0001c0001t0075g0276a0002c0005t0070g0192 | 2 | HG02897.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-136+26249G>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61866546 | ||||||
| chr18:61866548
|
C | T | 76 | a0001c0001t0001g0001a0001c0001t0001g0060a0001c0001t0001g0067others(73): Show | 77 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.-136+26247G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61866548 | ||||||
| chr18:61866554
|
T | C | 11 | a0001c0001t0075g0276a0001c0001t0107g0168a0001c0002t0016g0171others(8): Show | 11 | HG01884.hp2 HG02280.hp1 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.-136+26241A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61866554 | ||||||
| chr18:61866653
|
C | T | 4 | a0001c0001t0013g0302a0001c0001t0013g0304a0001c0001t0102g0305others(1): Show | 4 | HG02717.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-136+26142G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61866653 | ||||||
| chr18:61866687
|
A | G | 20 | a0001c0001t0008g0294a0001c0001t0038g0182a0001c0001t0039g0136others(17): Show | 20 | HG01258.hp2 HG01934.hp1 HG01943.hp2 others(17): Show |
intron_variant | MODIFIER | c.-136+26108T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61866687 | ||||||
| chr18:61866752
|
G | A | 1 | a0001c0001t0038g0182 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-136+26043C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61866752 | ||||||
| chr18:61866797
|
C | T | 1 | a0001c0001t0001g0067 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-136+25998G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61866797 | ||||||
| chr18:61866896
|
C | G | 12 | a0001c0001t0107g0168a0001c0001t0123g0307a0001c0001t0125g0306others(9): Show | 12 | HG01884.hp2 HG02280.hp1 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.-136+25899G>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61866896 | ||||||
| chr18:61866901
|
C | CA | 32 | a0001c0001t0001g0189a0001c0001t0001g0240a0001c0001t0002g0163others(29): Show | 32 | HG00423.hp2 HG00438.hp1 HG01943.hp1 others(29): Show |
intron_variant | MODIFIER | c.-136+25893dupT | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61866901 | ||||||
| chr18:61866961
|
G | A | 1 | a0001c0001t0001g0122 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-136+25834C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61866961 | ||||||
| chr18:61867143
|
T | C | 1 | a0001c0001t0001g0186 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-136+25652A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61867143 | ||||||
| chr18:61867335
|
T | C | 250 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0060others(247): Show | 251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.-136+25460A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61867335 | ||||||
| chr18:61867452
|
A | C | 1 | a0001c0002t0023g0256 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-136+25343T>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61867452 | ||||||
| chr18:61867537
|
A | G | 76 | a0001c0001t0001g0001a0001c0001t0001g0060a0001c0001t0001g0067others(73): Show | 77 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.-136+25258T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61867537 | ||||||
| chr18:61867566
|
T | C | 1 | a0001c0001t0002g0163 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-136+25229A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61867566 | ||||||
| chr18:61867596
|
G | A | 13 | a0001c0001t0038g0182a0001c0001t0039g0136a0001c0001t0039g0138others(10): Show | 13 | HG02055.hp1 HG02258.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-136+25199C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61867596 | ||||||
| chr18:61867651
|
G | A | 1 | a0001c0001t0001g0070 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-136+25144C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61867651 | ||||||
| chr18:61867657
|
A | C | 1 | a0001c0001t0032g0093 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-136+25138T>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61867657 | ||||||
| chr18:61867794
|
A | G | 15 | a0001c0001t0001g0079a0001c0001t0001g0086a0001c0001t0001g0091others(12): Show | 15 | HG00609.hp2 HG00738.hp2 HG01123.hp1 others(12): Show |
intron_variant | MODIFIER | c.-136+25001T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61867794 | ||||||
| chr18:61867903
|
C | T | 15 | a0001c0001t0011g0267a0001c0001t0011g0268a0001c0001t0019g0285others(12): Show | 15 | HG00140.hp2 HG01106.hp1 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.-136+24892G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61867903 | ||||||
| chr18:61867925
|
C | T | 91 | a0001c0001t0001g0028a0001c0001t0001g0189a0001c0001t0001g0240others(88): Show | 91 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(88): Show |
intron_variant | MODIFIER | c.-136+24870G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61867925 | ||||||
| chr18:61867950
|
A | G | 13 | a0001c0001t0038g0182a0001c0001t0039g0136a0001c0001t0039g0138others(10): Show | 13 | HG02055.hp1 HG02258.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-136+24845T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61867950 | ||||||
| chr18:61868079
|
G | T | 1 | a0001c0001t0088g0191 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-136+24716C>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61868079 | ||||||
| chr18:61868183
|
G | A | 13 | a0001c0001t0038g0182a0001c0001t0039g0136a0001c0001t0039g0138others(10): Show | 13 | HG02055.hp1 HG02258.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-136+24612C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61868183 | ||||||
| chr18:61868195
|
A | G | 97 | a0001c0001t0001g0028a0001c0001t0001g0046a0001c0001t0001g0047others(94): Show | 97 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(94): Show |
intron_variant | MODIFIER | c.-136+24600T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61868195 | ||||||
| chr18:61868213
|
T | C | 76 | a0001c0001t0001g0001a0001c0001t0001g0060a0001c0001t0001g0067others(73): Show | 77 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.-136+24582A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61868213 | ||||||
| chr18:61868340
|
C | G | 1 | a0002c0005t0070g0192 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-136+24455G>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61868340 | ||||||
| chr18:61868364
|
C | A | 1 | a0001c0001t0020g0088 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-136+24431G>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61868364 | ||||||
| chr18:61868445
|
G | A | 20 | a0001c0001t0008g0294a0001c0001t0038g0182a0001c0001t0039g0136others(17): Show | 20 | HG01258.hp2 HG01934.hp1 HG01943.hp2 others(17): Show |
intron_variant | MODIFIER | c.-136+24350C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61868445 | ||||||
| chr18:61868519
|
G | A | 13 | a0001c0001t0038g0182a0001c0001t0039g0136a0001c0001t0039g0138others(10): Show | 13 | HG02055.hp1 HG02258.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-136+24276C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61868519 | ||||||
| chr18:61868560
|
G | A | 1 | a0002c0005t0070g0192 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-136+24235C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61868560 | ||||||
| chr18:61868608
|
C | T | 2 | a0001c0002t0005g0224a0001c0002t0051g0223 | 2 | NA18972.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.-136+24187G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61868608 | ||||||
| chr18:61868658
|
A | G | 13 | a0001c0001t0038g0182a0001c0001t0039g0136a0001c0001t0039g0138others(10): Show | 13 | HG02055.hp1 HG02258.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-136+24137T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61868658 | ||||||
| chr18:61868715
|
T | TA | 69 | a0001c0001t0001g0001a0001c0001t0001g0060a0001c0001t0001g0067others(66): Show | 70 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.-136+24079dupT | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61868715 | ||||||
| chr18:61868985
|
G | C | 13 | a0001c0001t0038g0182a0001c0001t0039g0136a0001c0001t0039g0138others(10): Show | 13 | HG02055.hp1 HG02258.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-136+23810C>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61868985 | ||||||
| chr18:61869036
|
T | C | 13 | a0001c0001t0038g0182a0001c0001t0039g0136a0001c0001t0039g0138others(10): Show | 13 | HG02055.hp1 HG02258.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-136+23759A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61869036 | ||||||
| chr18:61869058
|
C | T | 5 | a0001c0001t0003g0194a0001c0001t0003g0201a0001c0001t0010g0198others(2): Show | 5 | HG02615.hp1 HG02723.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.-136+23737G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61869058 | ||||||
| chr18:61869120
|
C | T | 2 | a0001c0001t0011g0066a0001c0001t0011g0135 | 2 | HG03471.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-136+23675G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61869120 | ||||||
| chr18:61869284
|
T | C | 13 | a0001c0001t0038g0182a0001c0001t0039g0136a0001c0001t0039g0138others(10): Show | 13 | HG02055.hp1 HG02258.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-136+23511A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61869284 | ||||||
| chr18:61869472
|
T | C | 13 | a0001c0001t0038g0182a0001c0001t0039g0136a0001c0001t0039g0138others(10): Show | 13 | HG02055.hp1 HG02258.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-136+23323A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61869472 | ||||||
| chr18:61869778
|
C | T | 1 | a0001c0002t0060g0298 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-136+23017G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61869778 | ||||||
| chr18:61869897
|
C | A | 2 | a0001c0001t0018g0249a0001c0001t0029g0257 | 2 | HG01255.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.-136+22898G>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61869897 | ||||||
| chr18:61870091
|
G | A | 13 | a0001c0001t0038g0182a0001c0001t0039g0136a0001c0001t0039g0138others(10): Show | 13 | HG02055.hp1 HG02258.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-136+22704C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61870091 | ||||||
| chr18:61870308
|
G | T | 13 | a0001c0001t0038g0182a0001c0001t0039g0136a0001c0001t0039g0138others(10): Show | 13 | HG02055.hp1 HG02258.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-136+22487C>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61870308 | ||||||
| chr18:61870455
|
A | C | 31 | a0001c0001t0001g0266a0001c0001t0001g0275a0001c0001t0001g0278others(28): Show | 31 | HG00140.hp2 HG00280.hp1 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.-136+22340T>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61870455 | ||||||
| chr18:61870490
|
C | T | 3 | a0001c0001t0040g0184a0001c0001t0040g0185a0001c0001t0109g0072 | 3 | HG02559.hp1 HG02630.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-136+22305G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61870490 | ||||||
| chr18:61870742
|
T | A | 1 | a0001c0001t0007g0081 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-136+22053A>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61870742 | ||||||
| chr18:61870879
|
C | G | 216 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0046others(213): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.-136+21916G>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61870879 | ||||||
| chr18:61870880
|
C | A | 95 | a0001c0001t0001g0028a0001c0001t0001g0046a0001c0001t0001g0047others(92): Show | 95 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(92): Show |
intron_variant | MODIFIER | c.-136+21915G>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61870880 | ||||||
| chr18:61870914
|
C | T | 1 | a0001c0001t0006g0151 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-136+21881G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61870914 | ||||||
| chr18:61870973
|
C | T | 1 | a0001c0002t0060g0298 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-136+21822G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61870973 | ||||||
| chr18:61871078
|
T | G | 5 | a0001c0002t0016g0171a0001c0002t0016g0174a0001c0002t0016g0175others(2): Show | 5 | HG01884.hp2 HG02280.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.-136+21717A>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61871078 | ||||||
| chr18:61871092
|
C | A | 13 | a0001c0001t0038g0182a0001c0001t0039g0136a0001c0001t0039g0138others(10): Show | 13 | HG02055.hp1 HG02258.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-136+21703G>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61871092 | ||||||
| chr18:61871216
|
A | C | 1 | a0001c0001t0020g0088 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-136+21579T>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61871216 | ||||||
| chr18:61871221
|
A | T | 1 | a0001c0001t0008g0075 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-136+21574T>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61871221 | ||||||
| chr18:61871301
|
C | T | 4 | a0001c0001t0013g0302a0001c0001t0013g0304a0001c0001t0102g0305others(1): Show | 4 | HG02717.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-136+21494G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61871301 | ||||||
| chr18:61871416
|
T | C | 13 | a0001c0001t0038g0182a0001c0001t0039g0136a0001c0001t0039g0138others(10): Show | 13 | HG02055.hp1 HG02258.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-136+21379A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61871416 | ||||||
| chr18:61871551
|
C | T | 4 | a0001c0001t0001g0243a0001c0001t0004g0242a0001c0001t0006g0003others(1): Show | 4 | HG00639.hp2 HG01981.hp1 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.-136+21244G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61871551 | ||||||
| chr18:61871607
|
T | A | 1 | a0001c0001t0001g0240 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-136+21188A>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61871607 | ||||||
| chr18:61871707
|
C | G | 236 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0046others(233): Show | 237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.-136+21088G>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61871707 | ||||||
| chr18:61871776
|
C | A | 1 | a0001c0001t0001g0070 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-136+21019G>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61871776 | ||||||
| chr18:61871861
|
A | T | 13 | a0001c0001t0038g0182a0001c0001t0039g0136a0001c0001t0039g0138others(10): Show | 13 | HG02055.hp1 HG02258.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-136+20934T>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61871861 | ||||||
| chr18:61871892
|
T | C | 6 | a0001c0001t0011g0267a0001c0001t0011g0268a0001c0001t0019g0285others(3): Show | 6 | HG00140.hp2 HG01106.hp1 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.-136+20903A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61871892 | ||||||
| chr18:61871907
|
A | G | 13 | a0001c0001t0038g0182a0001c0001t0039g0136a0001c0001t0039g0138others(10): Show | 13 | HG02055.hp1 HG02258.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-136+20888T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61871907 | ||||||
| chr18:61871989
|
A | G | 20 | a0001c0001t0001g0266a0001c0001t0001g0275a0001c0001t0001g0278others(17): Show | 20 | HG00140.hp2 HG00280.hp1 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.-136+20806T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61871989 | ||||||
| chr18:61872057
|
C | T | 13 | a0001c0001t0038g0182a0001c0001t0039g0136a0001c0001t0039g0138others(10): Show | 13 | HG02055.hp1 HG02258.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-136+20738G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61872057 | ||||||
| chr18:61872061
|
T | C | 2 | a0001c0001t0123g0307a0001c0001t0125g0306 | 2 | HG02809.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-136+20734A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61872061 | ||||||
| chr18:61872118
|
T | A | 31 | a0001c0001t0001g0266a0001c0001t0001g0275a0001c0001t0001g0278others(28): Show | 31 | HG00140.hp2 HG00280.hp1 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.-136+20677A>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61872118 | ||||||
| chr18:61872193
|
A | G | 2 | a0001c0001t0001g0028a0001c0001t0035g0027 | 2 | HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-136+20602T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61872193 | ||||||
| chr18:61872410
|
A | G | 1 | a0001c0001t0008g0087 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-136+20385T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61872410 | ||||||
| chr18:61872425
|
G | A | 13 | a0001c0001t0038g0182a0001c0001t0039g0136a0001c0001t0039g0138others(10): Show | 13 | HG02055.hp1 HG02258.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-136+20370C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61872425 | ||||||
| chr18:61872541
|
A | G | 13 | a0001c0001t0038g0182a0001c0001t0039g0136a0001c0001t0039g0138others(10): Show | 13 | HG02055.hp1 HG02258.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-136+20254T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61872541 | ||||||
| chr18:61872542
|
T | C | 20 | a0001c0001t0008g0294a0001c0001t0038g0182a0001c0001t0039g0136others(17): Show | 20 | HG01258.hp2 HG01934.hp1 HG01943.hp2 others(17): Show |
intron_variant | MODIFIER | c.-136+20253A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61872542 | ||||||
| chr18:61872614
|
T | C | 251 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0046others(248): Show | 252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.-136+20181A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61872614 | ||||||
| chr18:61872689
|
T | C | 13 | a0001c0001t0038g0182a0001c0001t0039g0136a0001c0001t0039g0138others(10): Show | 13 | HG02055.hp1 HG02258.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-136+20106A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61872689 | ||||||
| chr18:61872779
|
G | C | 1 | a0001c0001t0003g0123 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.-136+20016C>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61872779 | ||||||
| chr18:61872931
|
T | G | 1 | a0001c0002t0060g0298 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-136+19864A>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61872931 | ||||||
| chr18:61872942
|
G | C | 1 | a0001c0001t0004g0053 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-136+19853C>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61872942 | ||||||
| chr18:61873043
|
T | C | 13 | a0001c0001t0038g0182a0001c0001t0039g0136a0001c0001t0039g0138others(10): Show | 13 | HG02055.hp1 HG02258.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-136+19752A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61873043 | ||||||
| chr18:61873046
|
G | T | 13 | a0001c0001t0038g0182a0001c0001t0039g0136a0001c0001t0039g0138others(10): Show | 13 | HG02055.hp1 HG02258.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-136+19749C>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61873046 | ||||||
| chr18:61873105
|
T | C | 13 | a0001c0001t0038g0182a0001c0001t0039g0136a0001c0001t0039g0138others(10): Show | 13 | HG02055.hp1 HG02258.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-136+19690A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61873105 | ||||||
| chr18:61873118
|
T | C | 1 | a0001c0001t0022g0277 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-136+19677A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61873118 | ||||||
| chr18:61873233
|
A | G | 1 | a0001c0001t0090g0074 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-136+19562T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61873233 | ||||||
| chr18:61873311
|
C | T | 1 | a0001c0002t0055g0241 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-136+19484G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61873311 | ||||||
| chr18:61873313
|
C | A | 86 | a0001c0001t0001g0028a0001c0001t0001g0046a0001c0001t0001g0047others(83): Show | 86 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(83): Show |
intron_variant | MODIFIER | c.-136+19482G>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61873313 | ||||||
| chr18:61873336
|
T | C | 1 | a0001c0001t0009g0124 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.-136+19459A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61873336 | ||||||
| chr18:61873441
|
G | A | 1 | a0001c0001t0001g0079 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-136+19354C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61873441 | ||||||
| chr18:61873614
|
A | G | 13 | a0001c0001t0038g0182a0001c0001t0039g0136a0001c0001t0039g0138others(10): Show | 13 | HG02055.hp1 HG02258.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-136+19181T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61873614 | ||||||
| chr18:61873620
|
C | T | 2 | a0001c0001t0001g0086a0001c0001t0004g0085 | 2 | NA19065.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.-136+19175G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61873620 | ||||||
| chr18:61873877
|
C | T | 7 | a0001c0001t0008g0294a0001c0001t0080g0295a0001c0001t0084g0195others(4): Show | 7 | HG01258.hp2 HG01934.hp1 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.-136+18918G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61873877 | ||||||
| chr18:61873962
|
C | T | 8 | a0001c0002t0016g0171a0001c0002t0016g0174a0001c0002t0016g0175others(5): Show | 8 | HG01884.hp2 HG02280.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.-136+18833G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61873962 | ||||||
| chr18:61874346
|
C | T | 1 | a0001c0001t0107g0168 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-136+18449G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61874346 | ||||||
| chr18:61874347
|
G | A | 6 | a0001c0001t0002g0050a0001c0001t0002g0051a0001c0001t0002g0054others(3): Show | 6 | HG00408.hp1 NA18943.hp2 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-136+18448C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61874347 | ||||||
| chr18:61874425
|
C | T | 13 | a0001c0001t0038g0182a0001c0001t0039g0136a0001c0001t0039g0138others(10): Show | 13 | HG02055.hp1 HG02258.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-136+18370G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61874425 | ||||||
| chr18:61874443
|
G | A | 7 | a0001c0001t0008g0294a0001c0001t0080g0295a0001c0001t0084g0195others(4): Show | 7 | HG01258.hp2 HG01934.hp1 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.-136+18352C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61874443 | ||||||
| chr18:61874476
|
C | G | 13 | a0001c0001t0038g0182a0001c0001t0039g0136a0001c0001t0039g0138others(10): Show | 13 | HG02055.hp1 HG02258.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-136+18319G>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61874476 | ||||||
| chr18:61874476
|
C | T | 2 | a0001c0001t0001g0131a0001c0001t0008g0073 | 2 | NA18965.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.-136+18319G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61874476 | ||||||
| chr18:61874477
|
A | G | 13 | a0001c0001t0038g0182a0001c0001t0039g0136a0001c0001t0039g0138others(10): Show | 13 | HG02055.hp1 HG02258.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-136+18318T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61874477 | ||||||
| chr18:61874523
|
A | T | 13 | a0001c0001t0038g0182a0001c0001t0039g0136a0001c0001t0039g0138others(10): Show | 13 | HG02055.hp1 HG02258.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-136+18272T>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61874523 | ||||||
| chr18:61874594
|
C | T | 13 | a0001c0001t0038g0182a0001c0001t0039g0136a0001c0001t0039g0138others(10): Show | 13 | HG02055.hp1 HG02258.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-136+18201G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61874594 | ||||||
| chr18:61874742
|
G | T | 1 | a0001c0001t0011g0267 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-136+18053C>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61874742 | ||||||
| chr18:61875022
|
T | C | 8 | a0001c0002t0016g0171a0001c0002t0016g0174a0001c0002t0016g0175others(5): Show | 8 | HG01884.hp2 HG02280.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.-136+17773A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61875022 | ||||||
| chr18:61875135
|
G | A | 7 | a0001c0001t0008g0294a0001c0001t0080g0295a0001c0001t0084g0195others(4): Show | 7 | HG01258.hp2 HG01934.hp1 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.-136+17660C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61875135 | ||||||
| chr18:61875264
|
G | T | 13 | a0001c0001t0038g0182a0001c0001t0039g0136a0001c0001t0039g0138others(10): Show | 13 | HG02055.hp1 HG02258.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-136+17531C>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61875264 | ||||||
| chr18:61875283
|
C | T | 13 | a0001c0001t0038g0182a0001c0001t0039g0136a0001c0001t0039g0138others(10): Show | 13 | HG02055.hp1 HG02258.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-136+17512G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61875283 | ||||||
| chr18:61875409
|
G | T | 13 | a0001c0001t0038g0182a0001c0001t0039g0136a0001c0001t0039g0138others(10): Show | 13 | HG02055.hp1 HG02258.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-136+17386C>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61875409 | ||||||
| chr18:61875454
|
T | C | 13 | a0001c0001t0038g0182a0001c0001t0039g0136a0001c0001t0039g0138others(10): Show | 13 | HG02055.hp1 HG02258.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-136+17341A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61875454 | ||||||
| chr18:61875495
|
C | A | 2 | a0001c0001t0106g0082a0001c0002t0069g0083 | 2 | HG00735.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-136+17300G>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61875495 | ||||||
| chr18:61875572
|
C | A | 3 | a0001c0001t0001g0060a0001c0001t0006g0061a0001c0001t0033g0126 | 3 | NA18948.hp1 NA18991.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.-136+17223G>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61875572 | ||||||
| chr18:61875581
|
T | TA | 13 | a0001c0001t0038g0182a0001c0001t0039g0136a0001c0001t0039g0138others(10): Show | 13 | HG02055.hp1 HG02258.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-136+17213_-136+17 others(7): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61875581 | ||||||
| chr18:61875635
|
C | T | 13 | a0001c0001t0038g0182a0001c0001t0039g0136a0001c0001t0039g0138others(10): Show | 13 | HG02055.hp1 HG02258.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-136+17160G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61875635 | ||||||
| chr18:61875776
|
G | A | 190 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0046others(187): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.-136+17019C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61875776 | ||||||
| chr18:61875787
|
C | T | 190 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0046others(187): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.-136+17008G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61875787 | ||||||
| chr18:61875944
|
C | A | 1 | a0001c0001t0107g0168 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-136+16851G>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61875944 | ||||||
| chr18:61876032
|
T | C | 2 | a0001c0001t0022g0282a0001c0001t0036g0283 | 2 | NA18960.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.-136+16763A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61876032 | ||||||
| chr18:61876152
|
A | G | 2 | a0001c0001t0084g0195a0001c0002t0048g0196 | 2 | HG01943.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.-136+16643T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61876152 | ||||||
| chr18:61876184
|
G | A | 1 | a0001c0001t0107g0168 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-136+16611C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61876184 | ||||||
| chr18:61876197
|
T | C | 78 | a0001c0001t0001g0001a0001c0001t0001g0060a0001c0001t0001g0067others(75): Show | 79 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.-136+16598A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61876197 | ||||||
| chr18:61876662
|
T | C | 1 | a0001c0001t0088g0191 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-136+16133A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61876662 | ||||||
| chr18:61876745
|
C | T | 114 | a0001c0001t0001g0028a0001c0001t0001g0046a0001c0001t0001g0047others(111): Show | 114 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(111): Show |
intron_variant | MODIFIER | c.-136+16050G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61876745 | ||||||
| chr18:61876779
|
C | T | 1 | a0001c0001t0099g0139 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-136+16016G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61876779 | ||||||
| chr18:61876801
|
G | A | 1 | a0001c0001t0007g0080 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.-136+15994C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61876801 | ||||||
| chr18:61876907
|
G | A | 1 | a0001c0001t0001g0125 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-136+15888C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61876907 | ||||||
| chr18:61877110
|
C | T | 1 | a0001c0001t0002g0026 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-136+15685G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61877110 | ||||||
| chr18:61877111
|
G | A | 3 | a0001c0001t0003g0147a0001c0001t0003g0149a0001c0001t0093g0148 | 3 | HG00423.hp2 HG02071.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.-136+15684C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61877111 | ||||||
| chr18:61877201
|
G | A | 1 | a0001c0001t0014g0263 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-136+15594C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61877201 | ||||||
| chr18:61877292
|
A | G | 2 | a0001c0002t0058g0169a0001c0002t0059g0170 | 2 | HG02717.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-136+15503T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61877292 | ||||||
| chr18:61877497
|
C | T | 7 | a0001c0001t0008g0294a0001c0001t0080g0295a0001c0001t0084g0195others(4): Show | 7 | HG01258.hp2 HG01934.hp1 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.-136+15298G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61877497 | ||||||
| chr18:61877602
|
T | C | 2 | a0001c0002t0016g0174a0001c0002t0016g0175 | 2 | HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-136+15193A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61877602 | ||||||
| chr18:61877646
|
G | T | 1 | a0001c0002t0047g0264 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-136+15149C>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61877646 | ||||||
| chr18:61877692
|
C | T | 205 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0046others(202): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.-136+15103G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61877692 | ||||||
| chr18:61877757
|
C | A | 1 | a0001c0001t0035g0197 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-136+15038G>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61877757 | ||||||
| chr18:61877767
|
T | G | 7 | a0001c0001t0008g0294a0001c0001t0080g0295a0001c0001t0084g0195others(4): Show | 7 | HG01258.hp2 HG01934.hp1 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.-136+15028A>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61877767 | ||||||
| chr18:61877968
|
C | A | 9 | a0001c0001t0002g0272a0001c0001t0002g0273a0001c0001t0006g0271others(6): Show | 9 | HG01070.hp2 HG01106.hp2 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.-136+14827G>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61877968 | ||||||
| chr18:61878068
|
C | A | 78 | a0001c0001t0001g0001a0001c0001t0001g0060a0001c0001t0001g0067others(75): Show | 79 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.-136+14727G>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61878068 | ||||||
| chr18:61878088
|
C | T | 1 | a0001c0002t0060g0298 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-136+14707G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61878088 | ||||||
| chr18:61878159
|
C | T | 1 | a0001c0002t0060g0298 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-136+14636G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61878159 | ||||||
| chr18:61878312
|
A | C | 5 | a0001c0001t0003g0194a0001c0001t0003g0201a0001c0001t0010g0198others(2): Show | 5 | HG02615.hp1 HG02723.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.-136+14483T>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61878312 | ||||||
| chr18:61878318
|
G | A | 1 | a0001c0001t0001g0238 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-136+14477C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61878318 | ||||||
| chr18:61878471
|
C | T | 2 | a0001c0001t0013g0084a0001c0001t0088g0191 | 2 | HG02723.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-136+14324G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61878471 | ||||||
| chr18:61878472
|
G | A | 7 | a0001c0001t0008g0294a0001c0001t0080g0295a0001c0001t0084g0195others(4): Show | 7 | HG01258.hp2 HG01934.hp1 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.-136+14323C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61878472 | ||||||
| chr18:61878656
|
C | T | 2 | a0001c0001t0013g0302a0001c0001t0013g0304 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-136+14139G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61878656 | ||||||
| chr18:61878749
|
C | T | 1 | a0001c0002t0058g0169 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-136+14046G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61878749 | ||||||
| chr18:61878818
|
C | G | 6 | a0001c0001t0011g0267a0001c0001t0011g0268a0001c0001t0019g0285others(3): Show | 6 | HG00140.hp2 HG01106.hp1 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.-136+13977G>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61878818 | ||||||
| chr18:61878942
|
G | A | 1 | a0001c0002t0023g0021 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-136+13853C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61878942 | ||||||
| chr18:61879020
|
T | G | 20 | a0001c0001t0001g0266a0001c0001t0001g0275a0001c0001t0001g0278others(17): Show | 20 | HG00140.hp2 HG00280.hp1 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.-136+13775A>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61879020 | ||||||
| chr18:61879191
|
G | A | 1 | a0001c0002t0005g0221 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-136+13604C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61879191 | ||||||
| chr18:61879274
|
T | G | 1 | a0001c0002t0060g0298 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-136+13521A>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61879274 | ||||||
| chr18:61879288
|
C | T | 1 | a0001c0002t0005g0025 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-136+13507G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61879288 | ||||||
| chr18:61879295
|
AT | A | 7 | a0001c0001t0008g0294a0001c0001t0080g0295a0001c0001t0084g0195others(4): Show | 7 | HG01258.hp2 HG01934.hp1 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.-136+13499delA | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61879295 | ||||||
| chr18:61879299
|
C | G | 2 | a0001c0001t0117g0284a0001c0001t0119g0279 | 2 | HG02559.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.-136+13496G>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61879299 | ||||||
| chr18:61879472
|
C | T | 1 | a0002c0005t0070g0192 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-136+13323G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61879472 | ||||||
| chr18:61879473
|
G | A | 1 | a0001c0001t0096g0024 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.-136+13322C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61879473 | ||||||
| chr18:61879521
|
C | T | 7 | a0001c0001t0008g0294a0001c0001t0080g0295a0001c0001t0084g0195others(4): Show | 7 | HG01258.hp2 HG01934.hp1 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.-136+13274G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61879521 | ||||||
| chr18:61879561
|
G | A | 7 | a0001c0001t0008g0294a0001c0001t0080g0295a0001c0001t0084g0195others(4): Show | 7 | HG01258.hp2 HG01934.hp1 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.-136+13234C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61879561 | ||||||
| chr18:61879793
|
A | G | 201 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0046others(198): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.-136+13002T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61879793 | ||||||
| chr18:61879833
|
C | T | 2 | a0001c0001t0106g0082a0001c0002t0069g0083 | 2 | HG00735.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-136+12962G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61879833 | ||||||
| chr18:61879837
|
C | T | 2 | a0001c0002t0045g0255a0001c0002t0067g0254 | 2 | HG02145.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-136+12958G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61879837 | ||||||
| chr18:61879842
|
G | A | 1 | a0001c0001t0012g0239 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-136+12953C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61879842 | ||||||
| chr18:61879920
|
C | G | 7 | a0001c0001t0008g0294a0001c0001t0080g0295a0001c0001t0084g0195others(4): Show | 7 | HG01258.hp2 HG01934.hp1 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.-136+12875G>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61879920 | ||||||
| chr18:61879953
|
G | A | 14 | a0001c0001t0002g0202a0001c0001t0003g0194a0001c0001t0003g0201others(11): Show | 14 | HG01346.hp1 HG02145.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.-136+12842C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61879953 | ||||||
| chr18:61879965
|
CA | C | 178 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0046others(175): Show | 179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.-136+12829delT | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61879965 | ||||||
| chr18:61879965
|
CAA | C | 11 | a0001c0001t0002g0022a0001c0001t0007g0081a0001c0001t0008g0294others(8): Show | 11 | HG01169.hp2 HG01258.hp2 HG01934.hp1 others(8): Show |
intron_variant | MODIFIER | c.-136+12828_-136+12 others(8): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61879965 | ||||||
| chr18:61879982
|
T | A | 6 | a0001c0001t0088g0191a0001c0001t0123g0307a0001c0001t0125g0306others(3): Show | 6 | HG02155.hp1 HG02735.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.-136+12813A>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61879982 | ||||||
| chr18:61879992
|
G | T | 206 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0046others(203): Show | 207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.-136+12803C>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61879992 | ||||||
| chr18:61880185
|
C | T | 7 | a0001c0001t0006g0017a0001c0002t0005g0019a0001c0002t0005g0020others(4): Show | 7 | HG00597.hp1 HG02080.hp1 HG03831.hp1 others(4): Show |
intron_variant | MODIFIER | c.-136+12610G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61880185 | ||||||
| chr18:61880279
|
T | A | 7 | a0001c0001t0078g0219a0001c0001t0079g0218a0001c0001t0097g0220others(4): Show | 7 | HG02145.hp2 HG02258.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.-136+12516A>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61880279 | ||||||
| chr18:61880545
|
T | G | 89 | a0001c0001t0001g0028a0001c0001t0001g0046a0001c0001t0001g0047others(86): Show | 89 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(86): Show |
intron_variant | MODIFIER | c.-136+12250A>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61880545 | ||||||
| chr18:61880638
|
T | A | 1 | a0002c0005t0070g0192 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-136+12157A>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61880638 | ||||||
| chr18:61880742
|
G | A | 1 | a0001c0001t0001g0278 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-136+12053C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61880742 | ||||||
| chr18:61880752
|
T | C | 3 | a0001c0001t0123g0307a0001c0001t0125g0306a0002c0005t0070g0192 | 3 | HG02809.hp1 HG03098.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-136+12043A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61880752 | ||||||
| chr18:61880913
|
C | CT | 12 | a0001c0001t0003g0142a0001c0001t0004g0150a0001c0001t0008g0294others(9): Show | 12 | HG01258.hp2 HG01934.hp1 HG01943.hp2 others(9): Show |
intron_variant | MODIFIER | c.-136+11881dupA | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61880913 | ||||||
| chr18:61880913
|
CT | C | 101 | a0001c0001t0001g0001a0001c0001t0001g0060a0001c0001t0001g0067others(98): Show | 102 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.-136+11881delA | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61880913 | ||||||
| chr18:61880913
|
CTT | C | 13 | a0001c0001t0038g0182a0001c0001t0039g0136a0001c0001t0039g0138others(10): Show | 13 | HG02055.hp1 HG02258.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-136+11880_-136+11 others(8): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61880913 | ||||||
| chr18:61880935
|
C | T | 199 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0046others(196): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.-136+11860G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61880935 | ||||||
| chr18:61881017
|
G | A | 3 | a0001c0001t0123g0307a0001c0001t0125g0306a0002c0005t0070g0192 | 3 | HG02809.hp1 HG03098.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-136+11778C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61881017 | ||||||
| chr18:61881020
|
TCTC | T | 7 | a0001c0001t0008g0294a0001c0001t0080g0295a0001c0001t0084g0195others(4): Show | 7 | HG01258.hp2 HG01934.hp1 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.-136+11772_-136+11 others(9): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61881020 | ||||||
| chr18:61881059
|
G | A | 1 | a0001c0001t0033g0126 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-136+11736C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61881059 | ||||||
| chr18:61881113
|
C | T | 3 | a0001c0001t0040g0184a0001c0001t0040g0185a0001c0001t0109g0072 | 3 | HG02559.hp1 HG02630.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-136+11682G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61881113 | ||||||
| chr18:61881222
|
C | T | 3 | a0001c0001t0010g0198a0001c0001t0010g0199a0001c0001t0010g0200 | 3 | HG03195.hp2 NA19030.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-136+11573G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61881222 | ||||||
| chr18:61881264
|
T | C | 1 | a0001c0001t0107g0168 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-136+11531A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61881264 | ||||||
| chr18:61881279
|
A | T | 9 | a0001c0001t0001g0079a0001c0001t0001g0131a0001c0001t0006g0077others(6): Show | 9 | HG00738.hp2 HG01123.hp1 HG01928.hp2 others(6): Show |
intron_variant | MODIFIER | c.-136+11516T>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61881279 | ||||||
| chr18:61881567
|
C | A | 198 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0046others(195): Show | 199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.-136+11228G>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61881567 | ||||||
| chr18:61881585
|
A | C | 87 | a0001c0001t0001g0028a0001c0001t0001g0046a0001c0001t0001g0047others(84): Show | 87 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(84): Show |
intron_variant | MODIFIER | c.-136+11210T>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61881585 | ||||||
| chr18:61881592
|
G | A | 193 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0046others(190): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.-136+11203C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61881592 | ||||||
| chr18:61881657
|
T | C | 3 | a0001c0001t0123g0307a0001c0001t0125g0306a0002c0005t0070g0192 | 3 | HG02809.hp1 HG03098.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-136+11138A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61881657 | ||||||
| chr18:61881742
|
G | T | 198 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0046others(195): Show | 199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.-136+11053C>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61881742 | ||||||
| chr18:61881752
|
G | A | 5 | a0001c0001t0088g0191a0001c0001t0123g0307a0001c0001t0125g0306others(2): Show | 5 | HG02257.hp2 HG02809.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.-136+11043C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61881752 | ||||||
| chr18:61881881
|
T | A | 2 | a0001c0001t0085g0140a0001c0001t0092g0141 | 2 | HG02572.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-136+10914A>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61881881 | ||||||
| chr18:61881916
|
C | A | 1 | a0001c0001t0121g0002 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-136+10879G>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61881916 | ||||||
| chr18:61882046
|
G | A | 2 | a0001c0003t0017g0280a0001c0003t0017g0281 | 2 | HG00280.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-136+10749C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61882046 | ||||||
| chr18:61882064
|
A | G | 6 | a0001c0001t0078g0219a0001c0001t0079g0218a0001c0001t0097g0220others(3): Show | 6 | HG02145.hp2 HG02258.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-136+10731T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61882064 | ||||||
| chr18:61882158
|
C | T | 4 | a0001c0001t0088g0191a0001c0001t0123g0307a0001c0001t0125g0306others(1): Show | 4 | HG02809.hp1 HG03098.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-136+10637G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61882158 | ||||||
| chr18:61882300
|
C | A | 1 | a0001c0002t0060g0298 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-136+10495G>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61882300 | ||||||
| chr18:61882371
|
G | A | 2 | a0001c0001t0001g0290a0001c0001t0001g0291 | 2 | HG02155.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.-136+10424C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61882371 | ||||||
| chr18:61882464
|
C | T | 1 | a0001c0002t0054g0214 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-136+10331G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61882464 | ||||||
| chr18:61882678
|
G | A | 1 | a0001c0002t0060g0298 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-136+10117C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61882678 | ||||||
| chr18:61882833
|
T | A | 250 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0046others(247): Show | 251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.-136+9962A>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61882833 | ||||||
| chr18:61883194
|
A | C | 3 | a0001c0001t0003g0147a0001c0001t0003g0149a0001c0001t0093g0148 | 3 | HG00423.hp2 HG02071.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.-136+9601T>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61883194 | ||||||
| chr18:61883209
|
A | G | 250 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0046others(247): Show | 251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.-136+9586T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61883209 | ||||||
| chr18:61883270
|
G | A | 1 | a0001c0002t0005g0213 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-136+9525C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61883270 | ||||||
| chr18:61883286
|
G | A | 7 | a0001c0001t0008g0294a0001c0001t0080g0295a0001c0001t0084g0195others(4): Show | 7 | HG01258.hp2 HG01934.hp1 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.-136+9509C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61883286 | ||||||
| chr18:61883384
|
T | C | 3 | a0001c0001t0001g0127a0001c0001t0004g0128a0001c0001t0083g0129 | 3 | NA18947.hp1 NA19060.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.-136+9411A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61883384 | ||||||
| chr18:61883758
|
C | T | 3 | a0001c0001t0040g0184a0001c0001t0040g0185a0001c0001t0109g0072 | 3 | HG02559.hp1 HG02630.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-136+9037G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61883758 | ||||||
| chr18:61883861
|
T | C | 1 | a0001c0001t0088g0191 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-136+8934A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61883861 | ||||||
| chr18:61883967
|
C | T | 198 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0046others(195): Show | 199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.-136+8828G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61883967 | ||||||
| chr18:61884053
|
A | G | 1 | a0001c0001t0007g0071 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-136+8742T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61884053 | ||||||
| chr18:61884078
|
T | C | 5 | a0001c0001t0002g0202a0001c0001t0003g0203a0001c0001t0004g0204others(2): Show | 5 | HG01346.hp1 HG02145.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.-136+8717A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61884078 | ||||||
| chr18:61884228
|
G | T | 6 | a0001c0001t0011g0267a0001c0001t0011g0268a0001c0001t0019g0285others(3): Show | 6 | HG00140.hp2 HG01106.hp1 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.-136+8567C>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61884228 | ||||||
| chr18:61884229
|
C | T | 6 | a0001c0001t0011g0267a0001c0001t0011g0268a0001c0001t0019g0285others(3): Show | 6 | HG00140.hp2 HG01106.hp1 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.-136+8566G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61884229 | ||||||
| chr18:61884243
|
A | AG | 198 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0046others(195): Show | 199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.-136+8551_-136+855 others(5): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61884243 | ||||||
| chr18:61884295
|
C | A | 1 | a0001c0002t0057g0176 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-136+8500G>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61884295 | ||||||
| chr18:61884390
|
G | A | 1 | a0001c0001t0004g0204 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-136+8405C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61884390 | ||||||
| chr18:61884399
|
T | C | 1 | a0001c0001t0029g0252 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-136+8396A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61884399 | ||||||
| chr18:61884444
|
CA | C | 9 | a0001c0001t0008g0294a0001c0001t0080g0295a0001c0001t0084g0195others(6): Show | 9 | HG01258.hp2 HG01934.hp1 HG01943.hp2 others(6): Show |
intron_variant | MODIFIER | c.-136+8350delT | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61884444 | ||||||
| chr18:61884444
|
CAA | C | 196 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0046others(193): Show | 197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.-136+8349_-136+835 others(6): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61884444 | ||||||
| chr18:61884453
|
A | T | 9 | a0001c0001t0107g0168a0001c0002t0016g0171a0001c0002t0016g0174others(6): Show | 9 | HG01884.hp2 HG02280.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.-136+8342T>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61884453 | ||||||
| chr18:61884637
|
C | T | 198 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0046others(195): Show | 199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.-136+8158G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61884637 | ||||||
| chr18:61884718
|
C | T | 1 | a0001c0001t0088g0191 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-136+8077G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61884718 | ||||||
| chr18:61884722
|
C | T | 1 | a0001c0001t0008g0294 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-136+8073G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61884722 | ||||||
| chr18:61884789
|
C | T | 4 | a0001c0001t0013g0302a0001c0001t0013g0304a0001c0001t0102g0305others(1): Show | 4 | HG02717.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-136+8006G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61884789 | ||||||
| chr18:61884814
|
C | T | 1 | a0001c0001t0021g0299 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-136+7981G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61884814 | ||||||
| chr18:61884906
|
T | C | 198 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0046others(195): Show | 199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.-136+7889A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61884906 | ||||||
| chr18:61885230
|
T | G | 1 | a0001c0008t0004g0063 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-136+7565A>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61885230 | ||||||
| chr18:61885310
|
T | TTTTGTTT others(1): Show |
198 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0046others(195): Show | 199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.-136+7477_-136+748 others(12): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61885310 | ||||||
| chr18:61885588
|
G | A | 1 | a0001c0002t0005g0055 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-136+7207C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61885588 | ||||||
| chr18:61885601
|
C | A | 2 | a0001c0001t0040g0184a0001c0001t0040g0185 | 2 | HG02559.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.-136+7194G>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61885601 | ||||||
| chr18:61885723
|
A | G | 1 | a0001c0001t0008g0167 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-136+7072T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61885723 | ||||||
| chr18:61885770
|
G | C | 1 | a0001c0001t0038g0182 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-136+7025C>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61885770 | ||||||
| chr18:61885818
|
G | A | 193 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0046others(190): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.-136+6977C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61885818 | ||||||
| chr18:61885856
|
C | T | 2 | a0001c0001t0001g0186a0001c0001t0032g0193 | 2 | HG00408.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.-136+6939G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61885856 | ||||||
| chr18:61885887
|
G | T | 198 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0046others(195): Show | 199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.-136+6908C>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61885887 | ||||||
| chr18:61885907
|
G | A | 193 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0046others(190): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.-136+6888C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61885907 | ||||||
| chr18:61885975
|
CTTTTGCT others(5): Show |
C | 7 | a0001c0001t0008g0294a0001c0001t0080g0295a0001c0001t0084g0195others(4): Show | 7 | HG01258.hp2 HG01934.hp1 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.-136+6808_-136+681 others(16): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61885975 | ||||||
| chr18:61885985
|
C | CT | 8 | a0001c0001t0030g0209a0001c0001t0082g0208a0001c0001t0115g0212others(5): Show | 8 | HG01167.hp1 HG01255.hp1 HG02735.hp2 others(5): Show |
intron_variant | MODIFIER | c.-136+6809dupA | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61885985 | ||||||
| chr18:61885985
|
CT | C | 21 | a0001c0001t0001g0240a0001c0001t0001g0243a0001c0001t0001g0248others(18): Show | 21 | HG00438.hp1 HG00621.hp1 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.-136+6809delA | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61885985 | ||||||
| chr18:61885985
|
CTT | C | 34 | a0001c0001t0001g0275a0001c0001t0001g0278a0001c0001t0002g0202others(31): Show | 34 | HG00140.hp2 HG00280.hp1 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.-136+6808_-136+680 others(6): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61885985 | ||||||
| chr18:61885985
|
CTTT | C | 8 | a0001c0001t0003g0201a0001c0001t0013g0302a0001c0001t0013g0304others(5): Show | 8 | HG01192.hp1 HG02559.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.-136+6807_-136+680 others(7): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61885985 | ||||||
| chr18:61885985
|
CTTTTTTT | C | 17 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0069others(14): Show | 17 | HG00323.hp1 HG00597.hp1 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.-136+6803_-136+680 others(11): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61885985 | ||||||
| chr18:61885985
|
CTTTTTTT others(1): Show |
C | 160 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0046others(157): Show | 161 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(158): Show |
intron_variant | MODIFIER | c.-136+6802_-136+680 others(12): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61885985 | ||||||
| chr18:61885985
|
CTTTTTTT others(2): Show |
C | 19 | a0001c0001t0002g0009a0001c0001t0002g0012a0001c0001t0004g0177others(16): Show | 19 | HG01192.hp2 HG02258.hp2 HG02602.hp1 others(16): Show |
intron_variant | MODIFIER | c.-136+6801_-136+680 others(13): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61885985 | ||||||
| chr18:61885985
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0105g0183 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-136+6800_-136+680 others(14): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61885985 | ||||||
| chr18:61885985
|
CTTTTTTT others(4): Show |
C | 1 | a0002c0005t0070g0192 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-136+6799_-136+680 others(15): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61885985 | ||||||
| chr18:61886127
|
T | C | 205 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0046others(202): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.-136+6668A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61886127 | ||||||
| chr18:61886201
|
T | G | 22 | a0001c0001t0038g0182a0001c0001t0039g0136a0001c0001t0039g0138others(19): Show | 22 | HG01884.hp2 HG02055.hp1 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.-136+6594A>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61886201 | ||||||
| chr18:61886296
|
T | C | 1 | a0001c0004t0101g0253 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-136+6499A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61886296 | ||||||
| chr18:61886561
|
T | C | 1 | a0001c0002t0065g0188 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-136+6234A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61886561 | ||||||
| chr18:61886641
|
A | G | 205 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0046others(202): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.-136+6154T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61886641 | ||||||
| chr18:61886688
|
C | G | 1 | a0001c0002t0052g0293 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-136+6107G>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61886688 | ||||||
| chr18:61886789
|
G | A | 78 | a0001c0001t0001g0001a0001c0001t0001g0060a0001c0001t0001g0067others(75): Show | 79 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.-136+6006C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61886789 | ||||||
| chr18:61886800
|
C | T | 2 | a0001c0001t0085g0140a0001c0001t0092g0141 | 2 | HG02572.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-136+5995G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61886800 | ||||||
| chr18:61886996
|
G | A | 1 | a0001c0001t0004g0177 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-136+5799C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61886996 | ||||||
| chr18:61887040
|
A | G | 5 | a0001c0001t0003g0194a0001c0001t0003g0201a0001c0001t0010g0198others(2): Show | 5 | HG02615.hp1 HG02723.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.-136+5755T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61887040 | ||||||
| chr18:61887131
|
G | A | 1 | a0002c0005t0070g0192 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-136+5664C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61887131 | ||||||
| chr18:61887408
|
GA | G | 197 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0046others(194): Show | 198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.-136+5386delT | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61887408 | ||||||
| chr18:61887414
|
G | A | 2 | a0001c0001t0004g0057a0001c0001t0004g0058 | 2 | HG00280.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.-136+5381C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61887414 | ||||||
| chr18:61887432
|
C | T | 1 | a0001c0001t0002g0012 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-136+5363G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61887432 | ||||||
| chr18:61887651
|
G | T | 13 | a0001c0001t0038g0182a0001c0001t0039g0136a0001c0001t0039g0138others(10): Show | 13 | HG02055.hp1 HG02258.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-136+5144C>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61887651 | ||||||
| chr18:61887688
|
T | C | 249 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0046others(246): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.-136+5107A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61887688 | ||||||
| chr18:61887701
|
C | CA | 14 | a0001c0001t0006g0287a0001c0001t0013g0304a0001c0001t0019g0285others(11): Show | 14 | HG01175.hp1 HG01433.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.-136+5093dupT | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61887701 | ||||||
| chr18:61887701
|
CA | C | 112 | a0001c0001t0001g0028a0001c0001t0001g0046a0001c0001t0001g0047others(109): Show | 112 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(109): Show |
intron_variant | MODIFIER | c.-136+5093delT | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61887701 | ||||||
| chr18:61887701
|
CAA | C | 79 | a0001c0001t0001g0001a0001c0001t0001g0060a0001c0001t0001g0067others(76): Show | 80 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.-136+5092_-136+509 others(6): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61887701 | ||||||
| chr18:61887832
|
C | A | 2 | a0001c0001t0014g0259a0001c0002t0066g0258 | 2 | HG01255.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-136+4963G>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61887832 | ||||||
| chr18:61887854
|
C | T | 1 | a0001c0001t0004g0010 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-136+4941G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61887854 | ||||||
| chr18:61888104
|
T | C | 197 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0046others(194): Show | 198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.-136+4691A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61888104 | ||||||
| chr18:61888172
|
G | A | 197 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0046others(194): Show | 198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.-136+4623C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61888172 | ||||||
| chr18:61888204
|
G | A | 2 | a0001c0001t0019g0289a0001c0001t0087g0288 | 2 | HG01106.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.-136+4591C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61888204 | ||||||
| chr18:61888239
|
C | G | 77 | a0001c0001t0001g0001a0001c0001t0001g0060a0001c0001t0001g0067others(74): Show | 78 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.-136+4556G>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61888239 | ||||||
| chr18:61888323
|
T | A | 200 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0046others(197): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.-136+4472A>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61888323 | ||||||
| chr18:61888423
|
T | C | 2 | a0001c0001t0040g0184a0001c0001t0040g0185 | 2 | HG02559.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.-136+4372A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61888423 | ||||||
| chr18:61888525
|
A | C | 3 | a0001c0001t0014g0262a0001c0001t0014g0263a0001c0001t0127g0261 | 3 | HG01109.hp1 HG03041.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-136+4270T>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61888525 | ||||||
| chr18:61888764
|
G | A | 2 | a0001c0001t0001g0186a0001c0001t0032g0193 | 2 | HG00408.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.-136+4031C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61888764 | ||||||
| chr18:61888831
|
C | T | 1 | a0001c0002t0015g0205 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-136+3964G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61888831 | ||||||
| chr18:61888840
|
T | C | 3 | a0001c0002t0028g0187a0001c0002t0028g0301a0001c0002t0065g0188 | 3 | HG02622.hp1 HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-136+3955A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61888840 | ||||||
| chr18:61889096
|
T | C | 1 | a0001c0001t0001g0189 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-136+3699A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61889096 | ||||||
| chr18:61889141
|
G | T | 1 | a0001c0002t0060g0298 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-136+3654C>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61889141 | ||||||
| chr18:61889188
|
A | G | 1 | a0001c0001t0010g0065 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-136+3607T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61889188 | ||||||
| chr18:61889464
|
C | T | 1 | a0001c0001t0006g0064 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-136+3331G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61889464 | ||||||
| chr18:61889484
|
G | C | 1 | a0001c0002t0071g0190 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-136+3311C>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61889484 | ||||||
| chr18:61889563
|
C | T | 2 | a0001c0001t0006g0062a0001c0008t0004g0063 | 2 | HG02071.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.-136+3232G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61889563 | ||||||
| chr18:61889718
|
C | T | 2 | a0001c0001t0001g0060a0001c0001t0006g0061 | 2 | NA18948.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.-136+3077G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61889718 | ||||||
| chr18:61889723
|
C | G | 1 | a0001c0001t0088g0191 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-136+3072G>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61889723 | ||||||
| chr18:61889879
|
T | A | 5 | a0001c0001t0088g0191a0001c0001t0123g0307a0001c0001t0125g0306others(2): Show | 5 | HG02257.hp2 HG02809.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.-136+2916A>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61889879 | ||||||
| chr18:61889958
|
C | T | 1 | a0001c0001t0022g0260 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-136+2837G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61889958 | ||||||
| chr18:61890048
|
C | A | 197 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0046others(194): Show | 198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.-136+2747G>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61890048 | ||||||
| chr18:61890218
|
C | G | 2 | a0001c0001t0123g0307a0001c0001t0125g0306 | 2 | HG02809.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-136+2577G>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61890218 | ||||||
| chr18:61890267
|
T | C | 1 | a0001c0001t0032g0193 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-136+2528A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61890267 | ||||||
| chr18:61890395
|
A | C | 56 | a0001c0001t0001g0028a0001c0001t0001g0046a0001c0001t0001g0047others(53): Show | 56 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(53): Show |
intron_variant | MODIFIER | c.-136+2400T>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61890395 | ||||||
| chr18:61890404
|
C | A | 2 | a0001c0001t0014g0259a0001c0002t0066g0258 | 2 | HG01255.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-136+2391G>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61890404 | ||||||
| chr18:61890537
|
A | G | 198 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0046others(195): Show | 199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.-136+2258T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61890537 | ||||||
| chr18:61890690
|
A | G | 198 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0046others(195): Show | 199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.-136+2105T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61890690 | ||||||
| chr18:61890764
|
T | A | 7 | a0001c0001t0008g0294a0001c0001t0080g0295a0001c0001t0084g0195others(4): Show | 7 | HG01258.hp2 HG01934.hp1 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.-136+2031A>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61890764 | ||||||
| chr18:61890819
|
T | C | 191 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0046others(188): Show | 192 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.-136+1976A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61890819 | ||||||
| chr18:61890827
|
C | T | 198 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0046others(195): Show | 199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.-136+1968G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61890827 | ||||||
| chr18:61890851
|
A | G | 7 | a0001c0001t0008g0294a0001c0001t0080g0295a0001c0001t0084g0195others(4): Show | 7 | HG01258.hp2 HG01934.hp1 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.-136+1944T>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61890851 | ||||||
| chr18:61891019
|
G | C | 7 | a0001c0001t0008g0294a0001c0001t0080g0295a0001c0001t0084g0195others(4): Show | 7 | HG01258.hp2 HG01934.hp1 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.-136+1776C>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61891019 | ||||||
| chr18:61891435
|
TA | T | 198 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0046others(195): Show | 199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.-136+1359delT | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61891435 | ||||||
| chr18:61891835
|
A | C | 42 | a0001c0001t0001g0266a0001c0001t0001g0275a0001c0001t0001g0278others(39): Show | 42 | HG00140.hp2 HG00280.hp1 HG01070.hp2 others(39): Show |
intron_variant | MODIFIER | c.-136+960T>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61891835 | ||||||
| chr18:61891863
|
G | C | 30 | a0001c0001t0001g0266a0001c0001t0001g0275a0001c0001t0001g0278others(27): Show | 30 | HG00140.hp2 HG00280.hp1 HG01070.hp2 others(27): Show |
intron_variant | MODIFIER | c.-136+932C>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61891863 | ||||||
| chr18:61891912
|
G | A | 7 | a0001c0001t0008g0294a0001c0001t0080g0295a0001c0001t0084g0195others(4): Show | 7 | HG01258.hp2 HG01934.hp1 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.-136+883C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61891912 | ||||||
| chr18:61891927
|
T | C | 3 | a0001c0001t0001g0290a0001c0001t0001g0291a0001c0001t0086g0292 | 3 | HG02129.hp2 HG02155.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.-136+868A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61891927 | ||||||
| chr18:61891982
|
C | G | 201 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0046others(198): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.-136+813G>C | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61891982 | ||||||
| chr18:61892014
|
G | A | 5 | a0001c0001t0008g0294a0001c0001t0080g0295a0001c0002t0052g0293others(2): Show | 5 | HG01258.hp2 HG01934.hp1 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.-136+781C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61892014 | ||||||
| chr18:61892071
|
G | A | 1 | a0001c0002t0060g0298 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-136+724C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61892071 | ||||||
| chr18:61892274
|
C | T | 1 | a0001c0001t0006g0003 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-136+521G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61892274 | ||||||
| chr18:61892383
|
G | A | 2 | a0001c0001t0021g0299a0001c0001t0076g0300 | 2 | NA18943.hp1 NA18944.hp1 |
intron_variant | MODIFIER | c.-136+412C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61892383 | ||||||
| chr18:61892457
|
T | C | 1 | a0001c0002t0028g0301 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-136+338A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61892457 | ||||||
| chr18:61892498
|
AAC | A | 4 | a0001c0001t0013g0302a0001c0001t0013g0304a0001c0001t0102g0305others(1): Show | 4 | HG02717.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-136+295_-136+296d others(4): Show |
RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61892498 | ||||||
| chr18:61892658
|
G | A | 2 | a0001c0001t0123g0307a0001c0001t0125g0306 | 2 | HG02809.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-136+137C>T | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61892658 | ||||||
| chr18:61892739
|
T | C | 2 | a0001c0002t0024g0308a0001c0002t0024g0309 | 2 | HG00423.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.-136+56A>G | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61892739 | ||||||
| chr18:61892794
|
C | T | 1 | a0001c0001t0121g0002 | 1 | HG01099.hp2 | splice_donor_variant&intron_variant | HIGH | c.-136+1G>A | RNF152 | ENSG00000176641.11 | transcript | ENST00000312828.4 | protein_coding | 1/1 | chr18 | 61892794 |